Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 6653 |
|---|---|
| ensemblid | ENSG00000137642.13 |
| hgncid | 11185 |
| symbol | SORL1 |
| name | sortilin related receptor 1 |
| refseq_nuc | NM_003105.6 |
| refseq_prot | NP_003096.2 |
| ensembl_nuc | ENST00000260197.12 |
| ensembl_prot | ENSP00000260197.6 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 121452314 |
| end | 121633763 |
| strand | + |
| ver | v1.2 |
| region | chr11:121452314-121633763 |
| region5000 | chr11:121447314-121638763 |
| regionname0 | SORL1_chr11_121452314_121633763 |
| regionname5000 | SORL1_chr11_121447314_121638763 |
| 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 | 0/1 | 2214 | 215 | 52 | 40 | 92 | 7 | 23 | 71 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0002 | 0/0 | 2214 | 31 | 8 | 9 | 12 | 0 | 2 | 11 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0003 | 0/0 | 2214 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0004 | 0/0 | 2214 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0005 | 0/0 | 2214 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0006 | 0/0 | 2214 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0007 | 1/0 | 2214 | 2 | 1 | 0 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0008 | 0/0 | 2214 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0009 | 0/0 | 2214 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0010 | 0/0 | 2214 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0011 | 0/0 | 2214 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0012 | 0/0 | 2214 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0013 | 0/0 | 2214 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0014 | 0/0 | 2214 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0015 | 0/0 | 2214 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0016 | 0/0 | 2214 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| 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 | 0/0 | 6645 | 46 | 1 | 5 | 33 | 1 | 6 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0002 | 0/0 | 6645 | 38 | 2 | 2 | 32 | 0 | 2 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0003 | 0/1 | 6645 | 33 | 9 | 12 | 4 | 0 | 7 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0004 | 0/0 | 6645 | 15 | 2 | 5 | 3 | 3 | 2 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0005 | 0/0 | 6645 | 14 | 1 | 6 | 5 | 0 | 2 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0006 | 0/0 | 6645 | 6 | 0 | 4 | 0 | 0 | 2 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0007 | 0/0 | 6645 | 6 | 0 | 0 | 6 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0008 | 0/0 | 6645 | 6 | 1 | 1 | 2 | 0 | 2 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0009 | 0/0 | 6645 | 5 | 5 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0010 | 0/0 | 6645 | 5 | 5 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0011 | 0/0 | 6645 | 5 | 0 | 3 | 0 | 2 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0012 | 0/0 | 6645 | 5 | 5 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0013 | 0/0 | 6645 | 5 | 0 | 0 | 5 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0014 | 0/0 | 6645 | 4 | 3 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0015 | 0/0 | 6645 | 4 | 0 | 1 | 3 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0016 | 0/0 | 6645 | 4 | 0 | 3 | 0 | 1 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0017 | 0/0 | 6645 | 3 | 0 | 3 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0018 | 0/0 | 6645 | 3 | 0 | 0 | 3 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0019 | 0/0 | 6645 | 3 | 0 | 0 | 3 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0020 | 0/0 | 6645 | 3 | 2 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0021 | 0/0 | 6645 | 2 | 2 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0022 | 0/0 | 6645 | 2 | 2 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0023 | 0/0 | 6645 | 2 | 1 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0024 | 0/0 | 6645 | 2 | 0 | 0 | 0 | 0 | 2 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0025 | 0/0 | 6645 | 2 | 2 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0026 | 0/0 | 6645 | 2 | 1 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0027 | 0/0 | 6645 | 2 | 2 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0028 | 0/0 | 6645 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0029 | 0/0 | 6645 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0030 | 0/0 | 6645 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0031 | 0/0 | 6645 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0032 | 0/0 | 6645 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0033 | 0/0 | 6645 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0034 | 0/0 | 6645 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0035 | 0/0 | 6645 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0036 | 0/0 | 6645 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0037 | 0/0 | 6645 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0038 | 0/0 | 6645 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0039 | 0/0 | 6645 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0040 | 0/0 | 6645 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0041 | 0/0 | 6645 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0042 | 0/0 | 6645 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0043 | 0/0 | 6645 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0044 | 0/0 | 6645 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0045 | 0/0 | 6645 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0046 | 0/0 | 6645 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0047 | 0/0 | 6645 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0048 | 0/0 | 6645 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0049 | 0/0 | 6645 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0050 | 0/0 | 6645 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0051 | 1/0 | 6645 | 1 | 0 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0052 | 0/0 | 6645 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0053 | 0/0 | 6645 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0054 | 0/0 | 6645 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0055 | 0/0 | 6645 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0056 | 0/0 | 6645 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0057 | 0/0 | 6645 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0058 | 0/0 | 6645 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0059 | 0/0 | 6645 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0060 | 0/0 | 6645 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0061 | 0/0 | 6645 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0062 | 0/0 | 6645 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0063 | 0/0 | 6645 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0064 | 0/0 | 6645 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0065 | 0/0 | 6645 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0066 | 0/0 | 6645 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0067 | 0/0 | 6645 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0068 | 0/0 | 6645 | 1 | 0 | 0 | 0 | 1 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0069 | 0/0 | 6645 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0070 | 0/0 | 6645 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0071 | 0/0 | 6645 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| c0072 | 0/0 | 6645 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 4224 | 88 | 1 | 19 | 51 | 4 | 13 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| t0002 | 1/1 | 4219 | 66 | 15 | 16 | 22 | 0 | 11 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| t0003 | 0/0 | 4219 | 24 | 23 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| t0004 | 0/0 | 4219 | 22 | 0 | 3 | 19 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| t0005 | 0/0 | 4219 | 12 | 10 | 2 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| t0006 | 0/0 | 4219 | 7 | 0 | 0 | 6 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| t0007 | 0/0 | 4219 | 7 | 7 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| t0008 | 0/0 | 4219 | 5 | 4 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| t0009 | 0/0 | 4219 | 4 | 0 | 4 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| t0010 | 0/0 | 4219 | 3 | 3 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| t0011 | 0/0 | 4219 | 3 | 3 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| t0012 | 0/0 | 4219 | 3 | 0 | 1 | 0 | 2 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| t0013 | 0/0 | 4219 | 3 | 3 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| t0014 | 0/0 | 4219 | 3 | 3 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| t0015 | 0/0 | 4219 | 2 | 0 | 0 | 2 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| t0016 | 0/0 | 4219 | 2 | 1 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| t0017 | 0/0 | 4219 | 2 | 0 | 0 | 2 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| t0018 | 0/0 | 4219 | 2 | 0 | 1 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| t0019 | 0/0 | 4224 | 2 | 0 | 1 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| t0020 | 0/0 | 4219 | 2 | 0 | 1 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| t0021 | 0/0 | 4219 | 1 | 0 | 0 | 0 | 1 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| t0022 | 0/0 | 4224 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| t0023 | 0/0 | 4224 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| t0024 | 0/0 | 4224 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| t0025 | 0/0 | 4224 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| t0026 | 0/0 | 4224 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| t0027 | 0/0 | 4219 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| t0028 | 0/0 | 4219 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| t0029 | 0/0 | 4224 | 1 | 0 | 0 | 0 | 1 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| t0030 | 0/0 | 4219 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| 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 | 2 | 0 | 0 | 2 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0095 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0253 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| 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 | 0/0 | 6645 | 46 | 1 | 5 | 33 | 1 | 6 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0002 | 0/0 | 6645 | 38 | 2 | 2 | 32 | 0 | 2 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0003 | 0/1 | 6645 | 33 | 9 | 12 | 4 | 0 | 7 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0004 | 0/0 | 6645 | 15 | 2 | 5 | 3 | 3 | 2 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0006 | 0/0 | 6645 | 6 | 0 | 4 | 0 | 0 | 2 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0008 | 0/0 | 6645 | 6 | 1 | 1 | 2 | 0 | 2 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0009 | 0/0 | 6645 | 5 | 5 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0010 | 0/0 | 6645 | 5 | 5 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0011 | 0/0 | 6645 | 5 | 0 | 3 | 0 | 2 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0012 | 0/0 | 6645 | 5 | 5 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0013 | 0/0 | 6645 | 5 | 0 | 0 | 5 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0015 | 0/0 | 6645 | 4 | 0 | 1 | 3 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0016 | 0/0 | 6645 | 4 | 0 | 3 | 0 | 1 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0018 | 0/0 | 6645 | 3 | 0 | 0 | 3 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0019 | 0/0 | 6645 | 3 | 0 | 0 | 3 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0020 | 0/0 | 6645 | 3 | 2 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0021 | 0/0 | 6645 | 2 | 2 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0022 | 0/0 | 6645 | 2 | 2 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0023 | 0/0 | 6645 | 2 | 1 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0028 | 0/0 | 6645 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0031 | 0/0 | 6645 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0032 | 0/0 | 6645 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0033 | 0/0 | 6645 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0035 | 0/0 | 6645 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0036 | 0/0 | 6645 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0038 | 0/0 | 6645 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0039 | 0/0 | 6645 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0040 | 0/0 | 6645 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0042 | 0/0 | 6645 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0045 | 0/0 | 6645 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0046 | 0/0 | 6645 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0052 | 0/0 | 6645 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0053 | 0/0 | 6645 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0057 | 0/0 | 6645 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0058 | 0/0 | 6645 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0060 | 0/0 | 6645 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0061 | 0/0 | 6645 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0062 | 0/0 | 6645 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0063 | 0/0 | 6645 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0065 | 0/0 | 6645 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0066 | 0/0 | 6645 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0067 | 0/0 | 6645 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0002c0005 | 0/0 | 6645 | 14 | 1 | 6 | 5 | 0 | 2 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0002c0007 | 0/0 | 6645 | 6 | 0 | 0 | 6 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0002c0014 | 0/0 | 6645 | 4 | 3 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0002c0025 | 0/0 | 6645 | 2 | 2 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0002c0026 | 0/0 | 6645 | 2 | 1 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0002c0030 | 0/0 | 6645 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0002c0048 | 0/0 | 6645 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0002c0049 | 0/0 | 6645 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0003c0027 | 0/0 | 6645 | 2 | 2 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0003c0034 | 0/0 | 6645 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0003c0069 | 0/0 | 6645 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0003c0070 | 0/0 | 6645 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0003c0071 | 0/0 | 6645 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0004c0041 | 0/0 | 6645 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0004c0056 | 0/0 | 6645 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0004c0059 | 0/0 | 6645 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0005c0017 | 0/0 | 6645 | 3 | 0 | 3 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0006c0043 | 0/0 | 6645 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0006c0055 | 0/0 | 6645 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0007c0051 | 1/0 | 6645 | 1 | 0 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0007c0072 | 0/0 | 6645 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0008c0024 | 0/0 | 6645 | 2 | 0 | 0 | 0 | 0 | 2 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0009c0054 | 0/0 | 6645 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0010c0037 | 0/0 | 6645 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0011c0044 | 0/0 | 6645 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0012c0064 | 0/0 | 6645 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0013c0047 | 0/0 | 6645 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0014c0068 | 0/0 | 6645 | 1 | 0 | 0 | 0 | 1 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0015c0050 | 0/0 | 6645 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0016c0029 | 0/0 | 6645 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 10868 | 35 | 0 | 5 | 24 | 1 | 5 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0001t0002 | 0/0 | 10863 | 9 | 1 | 0 | 7 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0001t0004 | 0/0 | 10863 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0001t0025 | 0/0 | 10868 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0002t0001 | 0/0 | 10868 | 12 | 0 | 2 | 9 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0002t0002 | 0/0 | 10863 | 2 | 0 | 0 | 2 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0002t0003 | 0/0 | 10863 | 2 | 2 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0002t0004 | 0/0 | 10863 | 14 | 0 | 0 | 14 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0002t0006 | 0/0 | 10863 | 7 | 0 | 0 | 6 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0002t0015 | 0/0 | 10863 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0003t0001 | 0/0 | 10868 | 2 | 0 | 0 | 0 | 0 | 2 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0003t0002 | 0/1 | 10863 | 18 | 1 | 7 | 4 | 0 | 5 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0003t0003 | 0/0 | 10863 | 2 | 2 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0003t0005 | 0/0 | 10863 | 2 | 2 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0003t0007 | 0/0 | 10863 | 3 | 3 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0003t0008 | 0/0 | 10863 | 2 | 1 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0003t0012 | 0/0 | 10863 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0003t0018 | 0/0 | 10863 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0003t0019 | 0/0 | 10868 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0003t0023 | 0/0 | 10868 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0004t0001 | 0/0 | 10868 | 7 | 1 | 1 | 2 | 2 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0004t0002 | 0/0 | 10863 | 2 | 0 | 1 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0004t0003 | 0/0 | 10863 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0004t0004 | 0/0 | 10863 | 2 | 0 | 2 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0004t0009 | 0/0 | 10863 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0004t0022 | 0/0 | 10868 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0004t0029 | 0/0 | 10868 | 1 | 0 | 0 | 0 | 1 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0006t0001 | 0/0 | 10868 | 4 | 0 | 3 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0006t0009 | 0/0 | 10863 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0006t0028 | 0/0 | 10863 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0008t0001 | 0/0 | 10868 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0008t0002 | 0/0 | 10863 | 3 | 1 | 0 | 1 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0008t0004 | 0/0 | 10863 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0008t0018 | 0/0 | 10863 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0009t0003 | 0/0 | 10863 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0009t0008 | 0/0 | 10863 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0009t0010 | 0/0 | 10863 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0009t0011 | 0/0 | 10863 | 2 | 2 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0010t0002 | 0/0 | 10863 | 2 | 2 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0010t0003 | 0/0 | 10863 | 2 | 2 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0010t0005 | 0/0 | 10863 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0011t0001 | 0/0 | 10868 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0011t0002 | 0/0 | 10863 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0011t0012 | 0/0 | 10863 | 1 | 0 | 0 | 0 | 1 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0011t0020 | 0/0 | 10863 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0011t0021 | 0/0 | 10863 | 1 | 0 | 0 | 0 | 1 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0012t0002 | 0/0 | 10863 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0012t0005 | 0/0 | 10863 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0012t0007 | 0/0 | 10863 | 3 | 3 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0013t0002 | 0/0 | 10863 | 4 | 0 | 0 | 4 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0013t0027 | 0/0 | 10863 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0015t0001 | 0/0 | 10868 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0015t0004 | 0/0 | 10863 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0015t0005 | 0/0 | 10863 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0015t0015 | 0/0 | 10863 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0016t0001 | 0/0 | 10868 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0016t0002 | 0/0 | 10863 | 2 | 0 | 2 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0016t0012 | 0/0 | 10863 | 1 | 0 | 0 | 0 | 1 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0018t0002 | 0/0 | 10863 | 3 | 0 | 0 | 3 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0019t0001 | 0/0 | 10868 | 3 | 0 | 0 | 3 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0020t0003 | 0/0 | 10863 | 3 | 2 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0021t0003 | 0/0 | 10863 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0021t0016 | 0/0 | 10863 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0022t0003 | 0/0 | 10863 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0022t0008 | 0/0 | 10863 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0023t0002 | 0/0 | 10863 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0023t0003 | 0/0 | 10863 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0028t0001 | 0/0 | 10868 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0031t0010 | 0/0 | 10863 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0032t0003 | 0/0 | 10863 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0033t0003 | 0/0 | 10863 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0035t0001 | 0/0 | 10868 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0036t0003 | 0/0 | 10863 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0038t0002 | 0/0 | 10863 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0039t0002 | 0/0 | 10863 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0040t0001 | 0/0 | 10868 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0042t0002 | 0/0 | 10863 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0045t0020 | 0/0 | 10863 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0046t0002 | 0/0 | 10863 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0052t0001 | 0/0 | 10868 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0053t0001 | 0/0 | 10868 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0057t0002 | 0/0 | 10863 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0058t0011 | 0/0 | 10863 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0060t0003 | 0/0 | 10863 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0061t0030 | 0/0 | 10863 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0062t0003 | 0/0 | 10863 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0063t0010 | 0/0 | 10863 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0065t0003 | 0/0 | 10863 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0066t0016 | 0/0 | 10863 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0001c0067t0013 | 0/0 | 10863 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0002c0005t0001 | 0/0 | 10868 | 9 | 0 | 3 | 4 | 0 | 2 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0002c0005t0003 | 0/0 | 10863 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0002c0005t0004 | 0/0 | 10863 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0002c0005t0009 | 0/0 | 10863 | 2 | 0 | 2 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0002c0005t0019 | 0/0 | 10868 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0002c0007t0001 | 0/0 | 10868 | 4 | 0 | 0 | 4 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0002c0007t0017 | 0/0 | 10863 | 2 | 0 | 0 | 2 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0002c0014t0002 | 0/0 | 10863 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0002c0014t0004 | 0/0 | 10863 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0002c0014t0014 | 0/0 | 10863 | 2 | 2 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0002c0025t0003 | 0/0 | 10863 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0002c0025t0005 | 0/0 | 10863 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0002c0026t0005 | 0/0 | 10863 | 2 | 1 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0002c0030t0002 | 0/0 | 10863 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0002c0048t0002 | 0/0 | 10863 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0002c0049t0003 | 0/0 | 10863 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0003c0027t0005 | 0/0 | 10863 | 2 | 2 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0003c0034t0003 | 0/0 | 10863 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0003c0069t0008 | 0/0 | 10863 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0003c0070t0005 | 0/0 | 10863 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0003c0071t0014 | 0/0 | 10863 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0004c0041t0013 | 0/0 | 10863 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0004c0056t0013 | 0/0 | 10863 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0004c0059t0002 | 0/0 | 10863 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0005c0017t0001 | 0/0 | 10868 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0005c0017t0002 | 0/0 | 10863 | 2 | 0 | 2 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0006c0043t0026 | 0/0 | 10868 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0006c0055t0002 | 0/0 | 10863 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0007c0051t0002 | 1/0 | 10863 | 1 | 0 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0007c0072t0002 | 0/0 | 10863 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0008c0024t0002 | 0/0 | 10863 | 2 | 0 | 0 | 0 | 0 | 2 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0009c0054t0004 | 0/0 | 10863 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0010c0037t0005 | 0/0 | 10863 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0011c0044t0002 | 0/0 | 10863 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0012c0064t0024 | 0/0 | 10868 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0013c0047t0007 | 0/0 | 10863 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0014c0068t0001 | 0/0 | 10868 | 1 | 0 | 0 | 0 | 1 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0015c0050t0002 | 0/0 | 10863 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| a0016c0029t0001 | 0/0 | 10868 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | copy fasta | chr11 | 121447314 | 121638763 |
| 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 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0001t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0001t0004g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0001t0025g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0002t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0002t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0002t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0002t0004g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0002t0004g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0002t0004g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0002t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0002t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0002t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0002t0004g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0002t0004g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0002t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0002t0004g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0002t0004g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0002t0004g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0002t0004g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0002t0004g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0002t0006g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0002t0006g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0002t0006g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0002t0006g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0002t0006g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0002t0006g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0002t0015g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0003t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0003t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0003t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0003t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0003t0002g0095 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0003t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0003t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0003t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0003t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0003t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0003t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0003t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0003t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0003t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0003t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0003t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0003t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0003t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0003t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0003t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0003t0003g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0003t0003g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0003t0005g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0003t0005g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0003t0007g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0003t0007g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0003t0007g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0003t0008g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0003t0008g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0003t0012g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0003t0018g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0003t0019g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0003t0023g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0004t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0004t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0004t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0004t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0004t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0004t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0004t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0004t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0004t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0004t0003g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0004t0004g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0004t0004g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0004t0009g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0004t0022g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0004t0029g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0006t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0006t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0006t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0006t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0006t0009g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0006t0028g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0008t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0008t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0008t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0008t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0008t0004g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0008t0018g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0009t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0009t0008g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0009t0010g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0009t0011g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0009t0011g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0010t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0010t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0010t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0010t0003g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0010t0005g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0011t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0011t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0011t0012g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0011t0020g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0011t0021g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0012t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0012t0005g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0012t0007g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0012t0007g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0012t0007g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0013t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0013t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0013t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0013t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0013t0027g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0015t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0015t0004g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0015t0005g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0015t0015g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0016t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0016t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0016t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0016t0012g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0018t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0018t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0018t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0019t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0019t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0019t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0020t0003g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0020t0003g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0020t0003g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0021t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0021t0016g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0022t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0022t0008g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0023t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0023t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0028t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0031t0010g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0032t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0033t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0035t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0036t0003g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0038t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0039t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0040t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0042t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0045t0020g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0046t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0052t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0053t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0057t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0058t0011g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0060t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0061t0030g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0062t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0063t0010g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0065t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0066t0016g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0001c0067t0013g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0002c0005t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0002c0005t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0002c0005t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0002c0005t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0002c0005t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0002c0005t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0002c0005t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0002c0005t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0002c0005t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0002c0005t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0002c0005t0004g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0002c0005t0009g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0002c0005t0009g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0002c0005t0019g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0002c0007t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0002c0007t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0002c0007t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0002c0007t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0002c0007t0017g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0002c0007t0017g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0002c0014t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0002c0014t0004g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0002c0014t0014g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0002c0014t0014g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0002c0025t0003g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0002c0025t0005g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0002c0026t0005g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0002c0026t0005g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0002c0030t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0002c0048t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0002c0049t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0003c0027t0005g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0003c0027t0005g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0003c0034t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0003c0069t0008g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0003c0070t0005g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0003c0071t0014g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0004c0041t0013g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0004c0056t0013g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0004c0059t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0005c0017t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0005c0017t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0005c0017t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0006c0043t0026g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0006c0055t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0007c0051t0002g0253 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0007c0072t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0008c0024t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0008c0024t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0009c0054t0004g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0010c0037t0005g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0011c0044t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0012c0064t0024g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0013c0047t0007g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0014c0068t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0015c0050t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| a0016c0029t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0014 | c0068 | t0001 | g0195 | EUR | GBR | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG00099 | hp2 | a0001 | c0004 | t0029 | g0187 | EUR | GBR | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG00280 | hp1 | a0001 | c0004 | t0001 | g0238 | EUR | FIN | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG00280 | hp2 | a0001 | c0011 | t0021 | g0243 | EUR | FIN | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG00323 | hp1 | a0001 | c0016 | t0012 | g0210 | EUR | FIN | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG00323 | hp2 | a0001 | c0004 | t0001 | g0236 | EUR | FIN | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG00438 | hp1 | a0001 | c0001 | t0025 | g0119 | EAS | CHS | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0116 | EAS | CHS | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG00544 | hp1 | a0002 | c0005 | t0019 | g0062 | EAS | CHS | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | CHS | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG00639 | hp1 | a0001 | c0003 | t0002 | g0225 | AMR | PUR | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG00642 | hp1 | a0005 | c0017 | t0002 | g0237 | AMR | PUR | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG00642 | hp2 | a0002 | c0026 | t0005 | g0245 | AMR | PUR | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG00735 | hp1 | a0002 | c0030 | t0002 | g0212 | AMR | PUR | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG00738 | hp1 | a0001 | c0008 | t0001 | g0136 | AMR | PUR | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG00738 | hp2 | a0002 | c0005 | t0004 | g0043 | AMR | PUR | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG00741 | hp1 | a0001 | c0003 | t0002 | g0133 | AMR | PUR | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG00741 | hp2 | a0001 | c0003 | t0002 | g0229 | AMR | PUR | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG01071 | hp1 | a0005 | c0017 | t0001 | g0240 | AMR | PUR | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG01071 | hp2 | a0001 | c0004 | t0002 | g0134 | AMR | PUR | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG01074 | hp1 | a0001 | c0003 | t0002 | g0096 | AMR | PUR | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG01074 | hp2 | a0001 | c0011 | t0002 | g0271 | AMR | PUR | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG01081 | hp2 | a0002 | c0048 | t0002 | g0201 | AMR | PUR | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG01099 | hp1 | a0001 | c0015 | t0005 | g0270 | AMR | PUR | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG01099 | hp2 | a0001 | c0003 | t0018 | g0191 | AMR | PUR | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG01109 | hp1 | a0001 | c0003 | t0002 | g0098 | AMR | PUR | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG01109 | hp2 | a0001 | c0020 | t0003 | g0248 | AMR | PUR | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG01167 | hp1 | a0001 | c0004 | t0009 | g0015 | AMR | PUR | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG01167 | hp2 | a0001 | c0003 | t0023 | g0183 | AMR | PUR | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG01169 | hp1 | a0001 | c0003 | t0012 | g0184 | AMR | PUR | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG01169 | hp2 | a0001 | c0016 | t0001 | g0196 | AMR | PUR | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG01175 | hp1 | a0005 | c0017 | t0002 | g0241 | AMR | PUR | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG01192 | hp1 | a0001 | c0016 | t0002 | g0044 | AMR | PUR | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG01192 | hp2 | a0001 | c0011 | t0020 | g0106 | AMR | PUR | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG01243 | hp1 | a0001 | c0066 | t0016 | g0194 | AMR | PUR | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG01243 | hp2 | a0001 | c0006 | t0001 | g0068 | AMR | PUR | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG01256 | hp1 | a0001 | c0016 | t0002 | g0121 | AMR | CLM | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG01256 | hp2 | a0001 | c0004 | t0004 | g0012 | AMR | CLM | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG01258 | hp1 | a0001 | c0004 | t0004 | g0011 | AMR | CLM | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG01258 | hp2 | a0001 | c0003 | t0002 | g0097 | AMR | CLM | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG01361 | hp1 | a0001 | c0003 | t0019 | g0209 | AMR | CLM | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG01361 | hp2 | a0001 | c0006 | t0001 | g0072 | AMR | CLM | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG01433 | hp1 | a0002 | c0005 | t0001 | g0205 | AMR | CLM | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG01433 | hp2 | a0001 | c0011 | t0001 | g0107 | AMR | CLM | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG01496 | hp1 | a0001 | c0003 | t0008 | g0208 | AMR | CLM | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG01496 | hp2 | a0001 | c0006 | t0009 | g0200 | AMR | CLM | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG01884 | hp1 | a0001 | c0004 | t0001 | g0110 | AFR | ACB | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG01884 | hp2 | a0001 | c0012 | t0007 | g0175 | AFR | ACB | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG01891 | hp1 | a0001 | c0010 | t0005 | g0239 | AFR | ACB | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG01891 | hp2 | a0002 | c0049 | t0003 | g0162 | AFR | ACB | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG01934 | hp1 | a0001 | c0040 | t0001 | g0137 | AMR | PEL | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG01934 | hp2 | a0002 | c0005 | t0009 | g0041 | AMR | PEL | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG01952 | hp1 | a0002 | c0005 | t0001 | g0008 | AMR | PEL | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG01952 | hp2 | a0001 | c0003 | t0002 | g0094 | AMR | PEL | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG01993 | hp1 | a0001 | c0023 | t0002 | g0070 | AMR | PEL | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG01993 | hp2 | a0001 | c0004 | t0001 | g0082 | AMR | PEL | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG02027 | hp1 | a0001 | c0002 | t0006 | g0020 | EAS | KHV | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG02040 | hp1 | a0001 | c0002 | t0004 | g0003 | EAS | KHV | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG02080 | hp2 | a0001 | c0002 | t0006 | g0014 | EAS | KHV | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG02148 | hp1 | a0001 | c0002 | t0001 | g0130 | AMR | PEL | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG02148 | hp2 | a0001 | c0006 | t0001 | g0118 | AMR | PEL | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | CDX | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG02155 | hp2 | a0001 | c0002 | t0006 | g0218 | EAS | CDX | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG02165 | hp1 | a0001 | c0002 | t0004 | g0007 | EAS | CDX | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CDX | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG02257 | hp1 | a0001 | c0003 | t0005 | g0228 | AFR | ACB | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0185 | AFR | ACB | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG02258 | hp1 | a0003 | c0069 | t0008 | g0164 | AFR | ACB | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG02258 | hp2 | a0001 | c0010 | t0002 | g0234 | AFR | ACB | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0129 | AMR | PEL | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG02273 | hp2 | a0002 | c0005 | t0001 | g0042 | AMR | PEL | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PEL | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG02300 | hp2 | a0002 | c0005 | t0009 | g0120 | AMR | PEL | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG02451 | hp1 | a0001 | c0003 | t0005 | g0226 | AFR | ACB | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG02451 | hp2 | a0001 | c0003 | t0007 | g0261 | AFR | ACB | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | KHV | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0188 | EAS | KHV | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG02622 | hp1 | a0001 | c0002 | t0003 | g0151 | AFR | GWD | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG02622 | hp2 | a0001 | c0008 | t0002 | g0177 | AFR | GWD | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG02630 | hp1 | a0001 | c0009 | t0003 | g0147 | AFR | GWD | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG02630 | hp2 | a0004 | c0056 | t0013 | g0148 | AFR | GWD | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG02647 | hp1 | a0002 | c0025 | t0003 | g0260 | AFR | GWD | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG02647 | hp2 | a0006 | c0055 | t0002 | g0246 | AFR | GWD | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG02683 | hp2 | a0001 | c0003 | t0002 | g0115 | SAS | PJL | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG02723 | hp1 | a0001 | c0022 | t0003 | g0213 | AFR | GWD | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG02723 | hp2 | a0001 | c0032 | t0003 | g0149 | AFR | GWD | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG02735 | hp1 | a0001 | c0003 | t0002 | g0135 | SAS | PJL | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG02735 | hp2 | a0001 | c0006 | t0028 | g0031 | SAS | PJL | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0139 | SAS | PJL | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG02738 | hp2 | a0011 | c0044 | t0002 | g0069 | SAS | PJL | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG02809 | hp1 | a0001 | c0031 | t0010 | g0214 | AFR | GWD | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG02809 | hp2 | a0001 | c0010 | t0003 | g0257 | AFR | GWD | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG02818 | hp1 | a0001 | c0063 | t0010 | g0251 | AFR | GWD | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG02818 | hp2 | a0012 | c0064 | t0024 | g0168 | AFR | GWD | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG02886 | hp1 | a0002 | c0014 | t0002 | g0172 | AFR | GWD | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG02886 | hp2 | a0001 | c0023 | t0003 | g0193 | AFR | GWD | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG02896 | hp1 | a0002 | c0026 | t0005 | g0161 | AFR | GWD | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG02896 | hp2 | a0001 | c0021 | t0016 | g0206 | AFR | GWD | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG02922 | hp1 | a0001 | c0010 | t0002 | g0190 | AFR | ESN | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG02922 | hp2 | a0006 | c0043 | t0026 | g0215 | AFR | ESN | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG02965 | hp1 | a0002 | c0025 | t0005 | g0179 | AFR | ESN | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG02965 | hp2 | a0001 | c0003 | t0007 | g0265 | AFR | ESN | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG02970 | hp1 | a0001 | c0003 | t0007 | g0264 | AFR | ESN | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG02970 | hp2 | a0001 | c0065 | t0003 | g0152 | AFR | ESN | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG02976 | hp1 | a0001 | c0057 | t0002 | g0160 | AFR | ESN | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG02976 | hp2 | a0004 | c0041 | t0013 | g0189 | AFR | ESN | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG03017 | hp1 | a0001 | c0006 | t0001 | g0157 | SAS | PJL | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG03098 | hp1 | a0001 | c0012 | t0002 | g0178 | AFR | MSL | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG03098 | hp2 | a0003 | c0027 | t0005 | g0173 | AFR | MSL | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG03130 | hp1 | a0002 | c0014 | t0014 | g0252 | AFR | ESN | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG03130 | hp2 | a0003 | c0070 | t0005 | g0145 | AFR | ESN | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG03139 | hp1 | a0001 | c0003 | t0008 | g0263 | AFR | ESN | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG03139 | hp2 | a0001 | c0009 | t0011 | g0255 | AFR | ESN | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG03195 | hp1 | a0001 | c0038 | t0002 | g0186 | AFR | ESN | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG03195 | hp2 | a0001 | c0022 | t0008 | g0211 | AFR | ESN | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG03209 | hp1 | a0003 | c0027 | t0005 | g0181 | AFR | MSL | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG03209 | hp2 | a0004 | c0059 | t0002 | g0171 | AFR | MSL | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG03225 | hp1 | a0001 | c0039 | t0002 | g0267 | AFR | MSL | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG03225 | hp2 | a0001 | c0021 | t0003 | g0216 | AFR | MSL | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG03453 | hp1 | a0002 | c0014 | t0014 | g0217 | AFR | MSL | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG03453 | hp2 | a0003 | c0034 | t0003 | g0227 | AFR | MSL | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG03486 | hp1 | a0001 | c0009 | t0010 | g0165 | AFR | MSL | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG03486 | hp2 | a0001 | c0061 | t0030 | g0249 | AFR | MSL | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG03490 | hp1 | a0008 | c0024 | t0002 | g0033 | SAS | PJL | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG03490 | hp2 | a0001 | c0008 | t0018 | g0192 | SAS | PJL | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG03492 | hp1 | a0008 | c0024 | t0002 | g0034 | SAS | PJL | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG03492 | hp2 | a0001 | c0003 | t0001 | g0019 | SAS | PJL | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG03516 | hp1 | a0003 | c0071 | t0014 | g0146 | AFR | ESN | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG03516 | hp2 | a0001 | c0067 | t0013 | g0204 | AFR | ESN | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG03540 | hp1 | a0001 | c0003 | t0002 | g0230 | AFR | GWD | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG03540 | hp2 | a0001 | c0046 | t0002 | g0174 | AFR | GWD | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG03688 | hp1 | a0001 | c0045 | t0020 | g0102 | SAS | STU | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG03688 | hp2 | a0002 | c0005 | t0001 | g0223 | SAS | STU | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0167 | SAS | PJL | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG03710 | hp2 | a0001 | c0003 | t0001 | g0113 | SAS | PJL | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG03831 | hp1 | a0001 | c0003 | t0002 | g0117 | SAS | BEB | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG03831 | hp2 | a0002 | c0005 | t0001 | g0032 | SAS | BEB | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG03834 | hp1 | a0001 | c0008 | t0002 | g0131 | SAS | BEB | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | BEB | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | STU | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG04115 | hp2 | a0001 | c0003 | t0002 | g0101 | SAS | STU | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG04184 | hp1 | a0001 | c0004 | t0002 | g0132 | SAS | BEB | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG04184 | hp2 | a0001 | c0002 | t0006 | g0114 | SAS | BEB | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG04199 | hp1 | a0001 | c0004 | t0001 | g0100 | SAS | STU | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG04199 | hp2 | a0001 | c0035 | t0001 | g0071 | SAS | STU | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0112 | EAS | CHB | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0083 | EAS | CHB | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA18747 | hp1 | a0001 | c0052 | t0001 | g0219 | EAS | CHB | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0092 | EAS | CHB | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA18906 | hp1 | a0001 | c0020 | t0003 | g0269 | AFR | YRI | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA18906 | hp2 | a0001 | c0009 | t0008 | g0207 | AFR | YRI | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA18939 | hp1 | a0001 | c0003 | t0002 | g0128 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA18941 | hp1 | a0001 | c0001 | t0004 | g0099 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA18941 | hp2 | a0001 | c0002 | t0001 | g0103 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA18942 | hp2 | a0002 | c0007 | t0017 | g0123 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA18951 | hp1 | a0002 | c0007 | t0001 | g0124 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA18951 | hp2 | a0001 | c0002 | t0004 | g0090 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA18952 | hp1 | a0001 | c0003 | t0002 | g0080 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA18957 | hp1 | a0001 | c0018 | t0002 | g0156 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA18959 | hp2 | a0001 | c0008 | t0004 | g0005 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA18961 | hp1 | a0001 | c0042 | t0002 | g0002 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA18961 | hp2 | a0001 | c0015 | t0015 | g0067 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA18965 | hp1 | a0001 | c0002 | t0004 | g0079 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA18966 | hp1 | a0001 | c0002 | t0004 | g0084 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA18966 | hp2 | a0001 | c0008 | t0002 | g0222 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA18969 | hp2 | a0002 | c0007 | t0001 | g0221 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA18972 | hp1 | a0001 | c0018 | t0002 | g0081 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA18972 | hp2 | a0001 | c0053 | t0001 | g0065 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA18974 | hp1 | a0001 | c0003 | t0002 | g0231 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA18974 | hp2 | a0002 | c0005 | t0001 | g0074 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA18983 | hp1 | a0001 | c0002 | t0002 | g0109 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA18983 | hp2 | a0001 | c0002 | t0006 | g0001 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA18984 | hp1 | a0001 | c0019 | t0001 | g0028 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA18984 | hp2 | a0001 | c0013 | t0002 | g0016 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA18985 | hp1 | a0001 | c0013 | t0002 | g0035 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA18985 | hp2 | a0001 | c0002 | t0004 | g0078 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA18989 | hp2 | a0001 | c0013 | t0002 | g0054 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA18990 | hp1 | a0002 | c0014 | t0004 | g0076 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA18991 | hp1 | a0002 | c0005 | t0001 | g0203 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA18991 | hp2 | a0001 | c0002 | t0004 | g0143 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA18995 | hp2 | a0001 | c0002 | t0004 | g0077 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA18999 | hp1 | a0001 | c0004 | t0001 | g0088 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA18999 | hp2 | a0001 | c0002 | t0006 | g0104 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA19000 | hp2 | a0001 | c0002 | t0015 | g0017 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA19001 | hp1 | a0001 | c0013 | t0002 | g0018 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA19001 | hp2 | a0001 | c0002 | t0001 | g0158 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA19002 | hp1 | a0001 | c0002 | t0004 | g0085 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA19005 | hp2 | a0001 | c0015 | t0001 | g0022 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA19007 | hp1 | a0001 | c0002 | t0002 | g0091 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA19009 | hp1 | a0002 | c0005 | t0001 | g0127 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0235 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA19012 | hp1 | a0002 | c0007 | t0017 | g0122 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA19012 | hp2 | a0001 | c0003 | t0002 | g0232 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA19043 | hp1 | a0001 | c0036 | t0003 | g0266 | AFR | LWK | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA19043 | hp2 | a0001 | c0058 | t0011 | g0166 | AFR | LWK | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA19056 | hp1 | a0016 | c0029 | t0001 | g0064 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA19056 | hp2 | a0001 | c0004 | t0022 | g0086 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA19063 | hp2 | a0001 | c0018 | t0002 | g0013 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA19066 | hp2 | a0002 | c0005 | t0001 | g0202 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA19068 | hp1 | a0001 | c0002 | t0004 | g0233 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA19074 | hp1 | a0001 | c0002 | t0004 | g0087 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA19074 | hp2 | a0001 | c0028 | t0001 | g0046 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA19077 | hp1 | a0002 | c0007 | t0001 | g0060 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA19081 | hp1 | a0001 | c0002 | t0004 | g0093 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA19083 | hp1 | a0001 | c0019 | t0001 | g0030 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA19083 | hp2 | a0001 | c0002 | t0004 | g0126 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA19085 | hp1 | a0001 | c0019 | t0001 | g0029 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA19085 | hp2 | a0002 | c0007 | t0001 | g0073 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA19086 | hp1 | a0001 | c0002 | t0004 | g0108 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA19086 | hp2 | a0001 | c0013 | t0027 | g0140 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA19090 | hp1 | a0001 | c0004 | t0001 | g0144 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA19090 | hp2 | a0001 | c0015 | t0004 | g0056 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA19091 | hp2 | a0001 | c0002 | t0006 | g0001 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA19240 | hp1 | a0001 | c0012 | t0007 | g0176 | AFR | YRI | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA19240 | hp2 | a0001 | c0003 | t0003 | g0254 | AFR | YRI | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA20129 | hp1 | a0007 | c0072 | t0002 | g0256 | AFR | ASW | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA20129 | hp2 | a0001 | c0003 | t0003 | g0262 | AFR | ASW | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0057 | EUR | TSI | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA20805 | hp2 | a0001 | c0011 | t0012 | g0242 | EUR | TSI | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA20905 | hp1 | a0001 | c0003 | t0002 | g0105 | SAS | GIH | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | GIH | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG02109 | hp1 | a0001 | c0010 | t0003 | g0258 | AFR | ACB | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG02109 | hp2 | a0001 | c0002 | t0003 | g0150 | AFR | ACB | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG02486 | hp1 | a0001 | c0020 | t0003 | g0268 | AFR | ACB | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG02486 | hp2 | a0001 | c0009 | t0011 | g0170 | AFR | ACB | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG02559 | hp1 | a0001 | c0062 | t0003 | g0250 | AFR | ACB | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG02559 | hp2 | a0001 | c0060 | t0003 | g0163 | AFR | ACB | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG03471 | hp1 | a0001 | c0012 | t0007 | g0244 | AFR | MSL | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG03471 | hp2 | a0015 | c0050 | t0002 | g0180 | AFR | MSL | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG06807 | hp1 | a0002 | c0005 | t0003 | g0159 | AFR | USA | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| HG06807 | hp2 | a0001 | c0012 | t0005 | g0247 | AFR | USA | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA18955 | hp2 | a0009 | c0054 | t0004 | g0021 | EAS | JPT | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA20300 | hp1 | a0001 | c0033 | t0003 | g0169 | AFR | USA | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA20300 | hp2 | a0010 | c0037 | t0005 | g0259 | AFR | USA | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA21309 | hp1 | a0001 | c0004 | t0003 | g0224 | AFR | LWK | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| NA21309 | hp2 | a0013 | c0047 | t0007 | g0182 | AFR | LWK | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0003 | t0002 | g0095 | REF | REF | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| homoSapiens_grch38 | hp1 | a0007 | c0051 | t0002 | g0253 | REF | REF | SORL1_chr11_121447314_121638763 | SORL1 | chr11 | 121447314 | 121638763 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:121452532
|
G | C | 1 | a0016 | 1 | NA19056.hp1 | missense_variant | MODERATE | c.201G>C | p.Arg67Ser | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/48 | 219/10863 | 201/6645 | 67/2214 | chr11 | 121452532 | ||
| chr11:121496918
|
G | A | 1 | a0005 | 3 | HG00642.hp1 HG01071.hp1 HG01175.hp1 |
missense_variant | MODERATE | c.808G>A | p.Glu270Lys | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/48 | 826/10863 | 808/6645 | 270/2214 | chr11 | 121496918 | ||
| chr11:121522975
|
G | A | 3 | a0002a0008a0015 | 34 | HG00544.hp1 HG00642.hp2 HG00735.hp1 others(31): Show |
missense_variant | MODERATE | c.1582G>A | p.Ala528Thr | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/48 | 1600/10863 | 1582/6645 | 528/2214 | chr11 | 121522975 | ||
| chr11:121532543
|
A | G | 1 | a0014 | 1 | HG00099.hp1 | missense_variant | MODERATE | c.1676A>G | p.Asn559Ser | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/48 | 1694/10863 | 1676/6645 | 559/2214 | chr11 | 121532543 | ||
| chr11:121545293
|
C | T | 1 | a0013 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.1915C>T | p.Arg639Trp | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/48 | 1933/10863 | 1915/6645 | 639/2214 | chr11 | 121545293 | ||
| chr11:121567110
|
C | G | 13 | a0001a0002a0004others(10): Show | 263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
missense_variant | MODERATE | c.3220C>G | p.Gln1074Glu | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 22/48 | 3238/10863 | 3220/6645 | 1074/2214 | chr11 | 121567110 | ||
| chr11:121574249
|
A | G | 1 | a0011 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.3346A>G | p.Ile1116Val | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 24/48 | 3364/10863 | 3346/6645 | 1116/2214 | chr11 | 121574249 | ||
| chr11:121589294
|
T | G | 1 | a0008 | 2 | HG03490.hp1 HG03492.hp1 |
missense_variant | MODERATE | c.3982T>G | p.Phe1328Val | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 29/48 | 4000/10863 | 3982/6645 | 1328/2214 | chr11 | 121589294 | ||
| chr11:121591081
|
G | A | 1 | a0009 | 1 | NA18955.hp2 | missense_variant | MODERATE | c.4294G>A | p.Val1432Met | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 31/48 | 4312/10863 | 4294/6645 | 1432/2214 | chr11 | 121591081 | ||
| chr11:121615048
|
G | A | 1 | a0010 | 1 | NA20300.hp2 | missense_variant | MODERATE | c.5597G>A | p.Arg1866Gln | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 41/48 | 5615/10863 | 5597/6645 | 1866/2214 | chr11 | 121615048 | ||
| chr11:121621073
|
G | A | 13 | a0001a0002a0003others(10): Show | 266 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(263): Show |
missense_variant | MODERATE | c.5899G>A | p.Val1967Ile | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 44/48 | 5917/10863 | 5899/6645 | 1967/2214 | chr11 | 121621073 | ||
| chr11:121625161
|
A | G | 2 | a0006a0012 | 3 | HG02647.hp2 HG02818.hp2 HG02922.hp2 |
missense_variant | MODERATE | c.6248A>G | p.Lys2083Arg | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 46/48 | 6266/10863 | 6248/6645 | 2083/2214 | chr11 | 121625161 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:121452511
|
G | A | 1 | a0001c0028 | 1 | NA19074.hp2 | synonymous_variant | LOW | c.180G>A | p.Leu60Leu | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/48 | 198/10863 | 180/6645 | 60/2214 | chr11 | 121452511 | ||
| chr11:121452568
|
G | A | 4 | a0001c0021a0001c0022a0001c0031others(1): Show | 6 | HG00735.hp1 HG02723.hp1 HG02809.hp1 others(3): Show |
synonymous_variant | LOW | c.237G>A | p.Arg79Arg | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/48 | 255/10863 | 237/6645 | 79/2214 | chr11 | 121452568 | ||
| chr11:121478231
|
G | A | 1 | a0001c0032 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.516G>A | p.Ala172Ala | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/48 | 534/10863 | 516/6645 | 172/2214 | chr11 | 121478231 | ||
| chr11:121496917
|
T | C | 28 | a0001c0002a0001c0003a0001c0004others(25): Show | 135 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(132): Show |
synonymous_variant | LOW | c.807T>C | p.His269His | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/48 | 825/10863 | 807/6645 | 269/2214 | chr11 | 121496917 | ||
| chr11:121522675
|
G | A | 1 | a0001c0033 | 1 | NA20300.hp1 | synonymous_variant | LOW | c.1494G>A | p.Glu498Glu | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 10/48 | 1512/10863 | 1494/6645 | 498/2214 | chr11 | 121522675 | ||
| chr11:121532520
|
C | T | 5 | a0003c0027a0003c0069a0003c0070others(2): Show | 6 | HG02258.hp1 HG03098.hp2 HG03130.hp2 others(3): Show |
synonymous_variant | LOW | c.1653C>T | p.Ala551Ala | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/48 | 1671/10863 | 1653/6645 | 551/2214 | chr11 | 121532520 | ||
| chr11:121543611
|
G | A | 1 | a0002c0048 | 1 | HG01081.hp2 | synonymous_variant | LOW | c.1749G>A | p.Val583Val | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 13/48 | 1767/10863 | 1749/6645 | 583/2214 | chr11 | 121543611 | ||
| chr11:121545355
|
A | G | 1 | a0001c0067 | 1 | HG03516.hp2 | synonymous_variant | LOW | c.1977A>G | p.Thr659Thr | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/48 | 1995/10863 | 1977/6645 | 659/2214 | chr11 | 121545355 | ||
| chr11:121545397
|
C | T | 2 | a0001c0033a0001c0046 | 2 | HG03540.hp2 NA20300.hp1 |
synonymous_variant | LOW | c.2019C>T | p.Ser673Ser | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/48 | 2037/10863 | 2019/6645 | 673/2214 | chr11 | 121545397 | ||
| chr11:121550041
|
C | T | 4 | a0001c0065a0001c0066a0001c0067others(1): Show | 4 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(1): Show |
synonymous_variant | LOW | c.2133C>T | p.Ser711Ser | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 15/48 | 2151/10863 | 2133/6645 | 711/2214 | chr11 | 121550041 | ||
| chr11:121555246
|
A | T | 4 | a0001c0011a0001c0016a0001c0045others(1): Show | 11 | HG00280.hp2 HG00323.hp1 HG01074.hp2 others(8): Show |
synonymous_variant | LOW | c.2499A>T | p.Thr833Thr | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 18/48 | 2517/10863 | 2499/6645 | 833/2214 | chr11 | 121555246 | ||
| chr11:121570194
|
C | T | 4 | a0003c0027a0003c0034a0003c0071others(1): Show | 5 | HG03098.hp2 HG03209.hp1 HG03453.hp2 others(2): Show |
synonymous_variant | LOW | c.3261C>T | p.Asn1087Asn | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 23/48 | 3279/10863 | 3261/6645 | 1087/2214 | chr11 | 121570194 | ||
| chr11:121577381
|
T | G | 12 | a0001c0001a0001c0004a0001c0028others(9): Show | 85 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(82): Show |
synonymous_variant | LOW | c.3561T>G | p.Ser1187Ser | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 25/48 | 3579/10863 | 3561/6645 | 1187/2214 | chr11 | 121577381 | ||
| chr11:121583543
|
G | A | 1 | a0001c0065 | 1 | HG02970.hp2 | synonymous_variant | LOW | c.3666G>A | p.Thr1222Thr | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 26/48 | 3684/10863 | 3666/6645 | 1222/2214 | chr11 | 121583543 | ||
| chr11:121586253
|
C | T | 26 | a0001c0003a0001c0008a0001c0010others(23): Show | 92 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(89): Show |
synonymous_variant | LOW | c.3738C>T | p.Asn1246Asn | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 27/48 | 3756/10863 | 3738/6645 | 1246/2214 | chr11 | 121586253 | ||
| chr11:121586313
|
C | T | 4 | a0001c0033a0001c0060a0001c0063others(1): Show | 4 | HG02559.hp2 HG02818.hp1 HG02922.hp2 others(1): Show |
synonymous_variant | LOW | c.3798C>T | p.Ser1266Ser | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 27/48 | 3816/10863 | 3798/6645 | 1266/2214 | chr11 | 121586313 | ||
| chr11:121589386
|
C | T | 1 | a0001c0052 | 1 | NA18747.hp1 | synonymous_variant | LOW | c.4074C>T | p.Asn1358Asn | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 29/48 | 4092/10863 | 4074/6645 | 1358/2214 | chr11 | 121589386 | ||
| chr11:121590137
|
C | T | 15 | a0001c0009a0001c0013a0001c0018others(12): Show | 32 | HG01891.hp2 HG02486.hp2 HG02630.hp1 others(29): Show |
synonymous_variant | LOW | c.4176C>T | p.Asn1392Asn | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 30/48 | 4194/10863 | 4176/6645 | 1392/2214 | chr11 | 121590137 | ||
| chr11:121595696
|
G | A | 2 | a0001c0036a0001c0038 | 2 | HG03195.hp1 NA19043.hp1 |
synonymous_variant | LOW | c.4443G>A | p.Pro1481Pro | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 32/48 | 4461/10863 | 4443/6645 | 1481/2214 | chr11 | 121595696 | ||
| chr11:121605213
|
T | A | 19 | a0001c0001a0001c0004a0001c0006others(16): Show | 99 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(96): Show |
synonymous_variant | LOW | c.4752T>A | p.Ala1584Ala | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 34/48 | 4770/10863 | 4752/6645 | 1584/2214 | chr11 | 121605213 | ||
| chr11:121614899
|
T | C | 1 | a0001c0040 | 1 | HG01934.hp1 | synonymous_variant | LOW | c.5448T>C | p.Tyr1816Tyr | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 41/48 | 5466/10863 | 5448/6645 | 1816/2214 | chr11 | 121614899 | ||
| chr11:121618854
|
G | A | 15 | a0001c0010a0001c0012a0001c0020others(12): Show | 27 | HG00642.hp2 HG01109.hp2 HG01884.hp2 others(24): Show |
synonymous_variant | LOW | c.5685G>A | p.Lys1895Lys | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 42/48 | 5703/10863 | 5685/6645 | 1895/2214 | chr11 | 121618854 | ||
| chr11:121619860
|
C | T | 1 | a0001c0045 | 1 | HG03688.hp1 | synonymous_variant | LOW | c.5832C>T | p.Gly1944Gly | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 43/48 | 5850/10863 | 5832/6645 | 1944/2214 | chr11 | 121619860 | ||
| chr11:121625195
|
G | A | 1 | a0003c0070 | 1 | HG03130.hp2 | synonymous_variant | LOW | c.6282G>A | p.Thr2094Thr | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 46/48 | 6300/10863 | 6282/6645 | 2094/2214 | chr11 | 121625195 | ||
| chr11:121627706
|
C | T | 1 | a0004c0056 | 1 | HG02630.hp2 | synonymous_variant | LOW | c.6516C>T | p.Phe2172Phe | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 47/48 | 6534/10863 | 6516/6645 | 2172/2214 | chr11 | 121627706 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:121629830
|
T | C | 2 | a0001c0002t0015a0001c0015t0015 | 2 | NA18961.hp2 NA19000.hp2 |
3_prime_UTR_variant | MODIFIER | c.*267T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 48/48 | 267 | chr11 | 121629830 | |||||
| chr11:121629870
|
G | A | 2 | a0001c0021t0016a0001c0066t0016 | 2 | HG01243.hp1 HG02896.hp2 |
3_prime_UTR_variant | MODIFIER | c.*307G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 48/48 | 307 | chr11 | 121629870 | |||||
| chr11:121629912
|
A | T | 3 | a0001c0061t0030a0002c0014t0014a0003c0071t0014 | 4 | HG03130.hp1 HG03453.hp1 HG03486.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*349A>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 48/48 | 349 | chr11 | 121629912 | |||||
| chr11:121629978
|
G | C | 3 | a0001c0009t0010a0001c0031t0010a0001c0063t0010 | 3 | HG02809.hp1 HG02818.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*415G>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 48/48 | 415 | chr11 | 121629978 | |||||
| chr11:121630122
|
T | C | 1 | a0002c0007t0017 | 2 | NA18942.hp2 NA19012.hp1 |
3_prime_UTR_variant | MODIFIER | c.*559T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 48/48 | 559 | chr11 | 121630122 | |||||
| chr11:121630164
|
C | T | 2 | a0001c0021t0016a0001c0066t0016 | 2 | HG01243.hp1 HG02896.hp2 |
3_prime_UTR_variant | MODIFIER | c.*601C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 48/48 | 601 | chr11 | 121630164 | |||||
| chr11:121630211
|
G | A | 6 | a0001c0003t0008a0001c0009t0008a0001c0009t0011others(3): Show | 8 | HG01496.hp1 HG02258.hp1 HG02486.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*648G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 48/48 | 648 | chr11 | 121630211 | |||||
| chr11:121630321
|
T | G | 1 | a0001c0011t0021 | 1 | HG00280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*758T>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 48/48 | 758 | chr11 | 121630321 | |||||
| chr11:121630352
|
A | G | 3 | a0001c0003t0007a0001c0012t0007a0013c0047t0007 | 7 | HG01884.hp2 HG02451.hp2 HG02965.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*789A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 48/48 | 789 | chr11 | 121630352 | |||||
| chr11:121630529
|
G | A | 24 | a0001c0001t0001a0001c0001t0025a0001c0002t0001others(21): Show | 92 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*966G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 48/48 | 966 | chr11 | 121630529 | |||||
| chr11:121630571
|
C | T | 3 | a0001c0067t0013a0004c0041t0013a0004c0056t0013 | 3 | HG02630.hp2 HG02976.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1008C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 48/48 | 1008 | chr11 | 121630571 | |||||
| chr11:121630583
|
A | G | 1 | a0001c0002t0006 | 7 | HG02027.hp1 HG02080.hp2 HG02155.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1020A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 48/48 | 1020 | chr11 | 121630583 | |||||
| chr11:121630697
|
T | C | 29 | a0001c0001t0001a0001c0001t0025a0001c0002t0001others(26): Show | 97 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*1134T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 48/48 | 1134 | chr11 | 121630697 | |||||
| chr11:121631046
|
G | A | 84 | a0001c0001t0001a0001c0001t0004a0001c0001t0025others(81): Show | 182 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(179): Show |
3_prime_UTR_variant | MODIFIER | c.*1483G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 48/48 | 1483 | chr11 | 121631046 | |||||
| chr11:121631083
|
G | A | 1 | a0001c0004t0022 | 1 | NA19056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1520G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 48/48 | 1520 | chr11 | 121631083 | |||||
| chr11:121631337
|
T | A | 3 | a0001c0003t0012a0001c0011t0012a0001c0016t0012 | 3 | HG00323.hp1 HG01169.hp1 NA20805.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1774T>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 48/48 | 1774 | chr11 | 121631337 | |||||
| chr11:121631364
|
C | CTTTTT | 28 | a0001c0001t0001a0001c0001t0025a0001c0002t0001others(25): Show | 96 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*1802_*1803insTTTT others(1): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 48/48 | 1803 | INFO_REALIGN_3_PRIME | chr11 | 121631364 | ||||
| chr11:121632036
|
C | G | 28 | a0001c0001t0001a0001c0001t0025a0001c0002t0001others(25): Show | 96 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*2473C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 48/48 | 2473 | chr11 | 121632036 | |||||
| chr11:121632059
|
A | G | 28 | a0001c0001t0001a0001c0001t0025a0001c0002t0001others(25): Show | 96 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*2496A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 48/48 | 2496 | chr11 | 121632059 | |||||
| chr11:121632185
|
T | C | 28 | a0001c0001t0001a0001c0001t0025a0001c0002t0001others(25): Show | 96 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*2622T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 48/48 | 2622 | chr11 | 121632185 | |||||
| chr11:121632353
|
G | A | 14 | a0001c0003t0005a0001c0009t0010a0001c0009t0011others(11): Show | 18 | HG00642.hp2 HG01099.hp1 HG01891.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2790G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 48/48 | 2790 | chr11 | 121632353 | |||||
| chr11:121632419
|
T | C | 3 | a0001c0004t0009a0001c0006t0009a0002c0005t0009 | 4 | HG01167.hp1 HG01496.hp2 HG01934.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2856T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 48/48 | 2856 | chr11 | 121632419 | |||||
| chr11:121632663
|
A | T | 1 | a0001c0006t0028 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3100A>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 48/48 | 3100 | chr11 | 121632663 | |||||
| chr11:121632779
|
C | G | 1 | a0001c0001t0025 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3216C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 48/48 | 3216 | chr11 | 121632779 | |||||
| chr11:121632941
|
A | C | 1 | a0001c0013t0027 | 1 | NA19086.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3378A>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 48/48 | 3378 | chr11 | 121632941 | |||||
| chr11:121633166
|
A | G | 1 | a0012c0064t0024 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3603A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 48/48 | 3603 | chr11 | 121633166 | |||||
| chr11:121633223
|
G | A | 1 | a0001c0061t0030 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3660G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 48/48 | 3660 | chr11 | 121633223 | |||||
| chr11:121633472
|
A | C | 11 | a0001c0001t0004a0001c0002t0004a0001c0002t0015others(8): Show | 26 | HG00738.hp2 HG01256.hp2 HG01258.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*3909A>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 48/48 | 3909 | chr11 | 121633472 | |||||
| chr11:121633551
|
C | G | 1 | a0001c0003t0023 | 1 | HG01167.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3988C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 48/48 | 3988 | chr11 | 121633551 | |||||
| chr11:121633693
|
C | T | 2 | a0001c0011t0020a0001c0045t0020 | 2 | HG01192.hp2 HG03688.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4130C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 48/48 | 4130 | chr11 | 121633693 | |||||
| chr11:121633732
|
A | G | 3 | a0001c0067t0013a0004c0041t0013a0004c0056t0013 | 3 | HG02630.hp2 HG02976.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4169A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 48/48 | 4169 | chr11 | 121633732 | |||||
| chr11:121633754
|
C | G | 3 | a0001c0061t0030a0002c0014t0014a0003c0071t0014 | 4 | HG03130.hp1 HG03453.hp1 HG03486.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4191C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 48/48 | 4191 | chr11 | 121633754 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:121452768
|
G | C | 144 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(141): Show | 145 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.285+152G>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121452768 | ||||||
| chr11:121452773
|
C | CA | 5 | a0001c0009t0003g0147a0001c0032t0003g0149a0003c0070t0005g0145others(2): Show | 5 | HG02630.hp1 HG02630.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.285+158dupA | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr11 | 121452773 | |||||
| chr11:121453498
|
T | C | 17 | a0001c0001t0001g0153a0001c0001t0001g0155a0001c0001t0002g0154others(14): Show | 17 | HG01891.hp2 HG02080.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.285+882T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121453498 | ||||||
| chr11:121453901
|
T | A | 1 | a0001c0042t0002g0002 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.285+1285T>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121453901 | ||||||
| chr11:121453921
|
T | A | 1 | a0001c0001t0002g0167 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.285+1305T>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121453921 | ||||||
| chr11:121454254
|
T | C | 3 | a0001c0002t0003g0150a0001c0002t0003g0151a0001c0065t0003g0152 | 3 | HG02109.hp2 HG02622.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.285+1638T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121454254 | ||||||
| chr11:121454353
|
T | C | 71 | a0001c0001t0001g0153a0001c0001t0001g0155a0001c0001t0001g0197others(68): Show | 71 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.285+1737T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121454353 | ||||||
| chr11:121454475
|
A | C | 1 | a0001c0011t0002g0271 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.285+1859A>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121454475 | ||||||
| chr11:121454646
|
C | G | 3 | a0001c0015t0005g0270a0001c0020t0003g0268a0001c0020t0003g0269 | 3 | HG01099.hp1 HG02486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.285+2030C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121454646 | ||||||
| chr11:121454725
|
G | C | 5 | a0001c0001t0001g0006a0001c0001t0002g0004a0001c0002t0004g0003others(2): Show | 6 | HG00558.hp1 HG02040.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.285+2109G>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121454725 | ||||||
| chr11:121454791
|
G | A | 1 | a0012c0064t0024g0168 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.285+2175G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121454791 | ||||||
| chr11:121454827
|
T | C | 1 | a0001c0002t0004g0007 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.285+2211T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121454827 | ||||||
| chr11:121454906
|
T | C | 9 | a0001c0001t0001g0009a0001c0002t0001g0010a0001c0002t0006g0014others(6): Show | 9 | HG01167.hp1 HG01256.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.285+2290T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121454906 | ||||||
| chr11:121455008
|
T | G | 1 | a0001c0033t0003g0169 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.285+2392T>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121455008 | ||||||
| chr11:121455055
|
G | A | 1 | a0001c0009t0011g0170 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.285+2439G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121455055 | ||||||
| chr11:121455094
|
T | C | 1 | a0002c0014t0014g0217 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.285+2478T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121455094 | ||||||
| chr11:121455201
|
A | G | 5 | a0001c0001t0002g0141a0001c0001t0002g0142a0001c0002t0004g0143others(2): Show | 5 | NA18977.hp2 NA18991.hp2 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.285+2585A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121455201 | ||||||
| chr11:121455283
|
G | A | 12 | a0001c0008t0002g0177a0001c0012t0002g0178a0001c0012t0007g0175others(9): Show | 12 | HG01884.hp2 HG02622.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.285+2667G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121455283 | ||||||
| chr11:121455324
|
T | C | 2 | a0001c0003t0012g0184a0001c0003t0023g0183 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.285+2708T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121455324 | ||||||
| chr11:121455445
|
C | G | 69 | a0001c0001t0001g0153a0001c0001t0001g0155a0001c0001t0001g0197others(66): Show | 69 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.285+2829C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121455445 | ||||||
| chr11:121455502
|
G | A | 12 | a0001c0001t0001g0153a0001c0001t0001g0155a0001c0001t0002g0154others(9): Show | 12 | HG01891.hp2 HG02080.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.285+2886G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121455502 | ||||||
| chr11:121455540
|
C | G | 3 | a0001c0002t0003g0150a0001c0002t0003g0151a0001c0065t0003g0152 | 3 | HG02109.hp2 HG02622.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.285+2924C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121455540 | ||||||
| chr11:121455566
|
G | C | 1 | a0001c0001t0002g0185 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.285+2950G>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121455566 | ||||||
| chr11:121455915
|
C | T | 1 | a0001c0001t0002g0185 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.285+3299C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121455915 | ||||||
| chr11:121455941
|
C | T | 1 | a0001c0002t0001g0139 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.285+3325C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121455941 | ||||||
| chr11:121455942
|
G | A | 1 | a0001c0002t0015g0017 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.285+3326G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121455942 | ||||||
| chr11:121455984
|
C | T | 48 | a0001c0001t0001g0153a0001c0001t0001g0155a0001c0001t0001g0197others(45): Show | 48 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.285+3368C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121455984 | ||||||
| chr11:121455991
|
T | TA | 20 | a0001c0001t0001g0220a0001c0002t0001g0188a0001c0002t0003g0150others(17): Show | 20 | HG00099.hp2 HG01099.hp2 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.285+3393dupA | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr11 | 121455991 | |||||
| chr11:121456154
|
A | T | 1 | a0013c0047t0007g0182 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.285+3538A>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121456154 | ||||||
| chr11:121456841
|
C | A | 1 | a0001c0003t0001g0019 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.285+4225C>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121456841 | ||||||
| chr11:121456877
|
C | T | 1 | a0001c0001t0001g0138 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.285+4261C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121456877 | ||||||
| chr11:121457069
|
A | G | 31 | a0001c0003t0003g0262a0001c0003t0007g0261a0001c0003t0007g0264others(28): Show | 31 | HG00738.hp1 HG01099.hp2 HG01167.hp2 others(28): Show |
intron_variant | MODIFIER | c.285+4453A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121457069 | ||||||
| chr11:121457150
|
G | A | 203 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(200): Show | 204 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.285+4534G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121457150 | ||||||
| chr11:121457160
|
C | A | 1 | a0001c0002t0006g0020 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.285+4544C>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121457160 | ||||||
| chr11:121457184
|
G | C | 6 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(3): Show | 6 | NA18955.hp2 NA18969.hp1 NA18989.hp1 others(3): Show |
intron_variant | MODIFIER | c.285+4568G>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121457184 | ||||||
| chr11:121457204
|
G | A | 1 | a0001c0001t0001g0027 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.285+4588G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121457204 | ||||||
| chr11:121457208
|
G | A | 1 | a0001c0008t0001g0136 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.285+4592G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121457208 | ||||||
| chr11:121457328
|
C | A | 164 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0024others(161): Show | 164 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.285+4712C>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121457328 | ||||||
| chr11:121457435
|
A | G | 3 | a0001c0032t0003g0149a0001c0060t0003g0163a0002c0049t0003g0162 | 3 | HG01891.hp2 HG02559.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.285+4819A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121457435 | ||||||
| chr11:121457640
|
G | A | 5 | a0001c0002t0003g0150a0001c0002t0003g0151a0001c0009t0003g0147others(2): Show | 5 | HG02109.hp2 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.285+5024G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121457640 | ||||||
| chr11:121457706
|
G | A | 1 | a0001c0001t0002g0167 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.285+5090G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121457706 | ||||||
| chr11:121457793
|
A | G | 50 | a0001c0001t0001g0027a0001c0001t0001g0111a0001c0001t0002g0167others(47): Show | 51 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.285+5177A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121457793 | ||||||
| chr11:121458073
|
T | A | 1 | a0001c0003t0002g0230 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.285+5457T>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121458073 | ||||||
| chr11:121458245
|
T | C | 111 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(108): Show | 111 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.285+5629T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121458245 | ||||||
| chr11:121458332
|
T | C | 43 | a0001c0001t0001g0111a0001c0002t0001g0112a0001c0002t0001g0116others(40): Show | 44 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.285+5716T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121458332 | ||||||
| chr11:121458559
|
T | C | 28 | a0001c0002t0001g0139a0001c0002t0003g0150a0001c0002t0003g0151others(25): Show | 28 | HG00099.hp2 HG00735.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.285+5943T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121458559 | ||||||
| chr11:121458671
|
C | T | 2 | a0001c0003t0002g0117a0001c0006t0001g0118 | 2 | HG02148.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.285+6055C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121458671 | ||||||
| chr11:121458687
|
C | T | 268 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(265): Show | 269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.285+6071C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121458687 | ||||||
| chr11:121458739
|
A | G | 268 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(265): Show | 269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.285+6123A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121458739 | ||||||
| chr11:121458802
|
C | T | 1 | a0004c0056t0013g0148 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.285+6186C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121458802 | ||||||
| chr11:121458869
|
G | A | 1 | a0001c0040t0001g0137 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.285+6253G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121458869 | ||||||
| chr11:121459088
|
G | T | 8 | a0002c0014t0002g0172a0002c0025t0005g0179a0002c0026t0005g0161others(5): Show | 8 | HG02258.hp1 HG02886.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.285+6472G>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121459088 | ||||||
| chr11:121459217
|
C | T | 1 | a0001c0009t0010g0165 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.285+6601C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121459217 | ||||||
| chr11:121459378
|
A | G | 98 | a0001c0001t0001g0089a0001c0001t0001g0111a0001c0002t0001g0010others(95): Show | 99 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.285+6762A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121459378 | ||||||
| chr11:121459436
|
A | C | 4 | a0001c0009t0011g0170a0001c0009t0011g0255a0004c0056t0013g0148others(1): Show | 4 | HG02486.hp2 HG02630.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.285+6820A>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121459436 | ||||||
| chr11:121459476
|
A | G | 96 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0024others(93): Show | 96 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.285+6860A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121459476 | ||||||
| chr11:121459666
|
T | C | 269 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(266): Show | 270 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.285+7050T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121459666 | ||||||
| chr11:121459746
|
C | T | 1 | a0001c0008t0002g0222 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.285+7130C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121459746 | ||||||
| chr11:121459793
|
T | C | 7 | a0001c0003t0002g0229a0001c0004t0002g0132a0001c0011t0001g0107others(4): Show | 7 | HG00741.hp2 HG01074.hp2 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.285+7177T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121459793 | ||||||
| chr11:121459898
|
G | A | 1 | a0001c0021t0003g0216 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.285+7282G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121459898 | ||||||
| chr11:121460283
|
G | A | 1 | a0002c0026t0005g0245 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.285+7667G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121460283 | ||||||
| chr11:121460394
|
A | AT | 201 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(198): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.285+7798dupT | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr11 | 121460394 | |||||
| chr11:121460394
|
A | ATT | 54 | a0001c0001t0001g0027a0001c0001t0001g0089a0001c0002t0001g0010others(51): Show | 54 | HG00280.hp2 HG00642.hp2 HG01109.hp1 others(51): Show |
intron_variant | MODIFIER | c.285+7797_285+7798d others(4): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr11 | 121460394 | |||||
| chr11:121460871
|
G | A | 1 | a0001c0020t0003g0268 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.285+8255G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121460871 | ||||||
| chr11:121461146
|
C | T | 1 | a0001c0001t0002g0125 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.285+8530C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121461146 | ||||||
| chr11:121461180
|
T | TA | 127 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(124): Show | 127 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.285+8578dupA | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr11 | 121461180 | |||||
| chr11:121461307
|
C | T | 1 | a0001c0009t0010g0165 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.285+8691C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121461307 | ||||||
| chr11:121461662
|
G | C | 1 | a0001c0003t0002g0117 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.286-8345G>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121461662 | ||||||
| chr11:121461698
|
C | T | 1 | a0001c0063t0010g0251 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.286-8309C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121461698 | ||||||
| chr11:121461728
|
G | A | 1 | a0001c0038t0002g0186 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.286-8279G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121461728 | ||||||
| chr11:121461774
|
G | A | 4 | a0001c0009t0011g0170a0001c0009t0011g0255a0004c0056t0013g0148others(1): Show | 4 | HG02486.hp2 HG02630.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.286-8233G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121461774 | ||||||
| chr11:121461818
|
G | A | 1 | a0001c0023t0002g0070 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.286-8189G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121461818 | ||||||
| chr11:121461835
|
A | G | 1 | a0001c0009t0010g0165 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.286-8172A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121461835 | ||||||
| chr11:121461912
|
C | T | 1 | a0001c0032t0003g0149 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.286-8095C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121461912 | ||||||
| chr11:121461963
|
C | T | 1 | a0001c0038t0002g0186 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.286-8044C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121461963 | ||||||
| chr11:121462206
|
T | C | 2 | a0001c0008t0002g0177a0001c0012t0002g0178 | 2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.286-7801T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121462206 | ||||||
| chr11:121462574
|
G | A | 2 | a0001c0003t0002g0080a0001c0003t0002g0128 | 2 | NA18939.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.286-7433G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121462574 | ||||||
| chr11:121462663
|
C | T | 1 | a0001c0032t0003g0149 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.286-7344C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121462663 | ||||||
| chr11:121462702
|
A | G | 1 | a0001c0046t0002g0174 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.286-7305A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121462702 | ||||||
| chr11:121462882
|
C | T | 4 | a0003c0027t0005g0173a0003c0027t0005g0181a0003c0069t0008g0164others(1): Show | 4 | HG02258.hp1 HG03098.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.286-7125C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121462882 | ||||||
| chr11:121462889
|
C | T | 1 | a0001c0022t0008g0211 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.286-7118C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121462889 | ||||||
| chr11:121463031
|
T | A | 2 | a0003c0027t0005g0173a0003c0027t0005g0181 | 2 | HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.286-6976T>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121463031 | ||||||
| chr11:121463048
|
C | T | 1 | a0001c0021t0003g0216 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.286-6959C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121463048 | ||||||
| chr11:121463104
|
A | G | 3 | a0001c0003t0002g0095a0001c0003t0002g0096a0001c0003t0002g0097 | 3 | HG01074.hp1 HG01258.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.286-6903A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121463104 | ||||||
| chr11:121463132
|
G | A | 4 | a0001c0009t0010g0165a0001c0065t0003g0152a0001c0066t0016g0194others(1): Show | 4 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.286-6875G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121463132 | ||||||
| chr11:121463178
|
C | T | 1 | a0001c0022t0008g0211 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.286-6829C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121463178 | ||||||
| chr11:121463232
|
G | A | 1 | a0010c0037t0005g0259 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.286-6775G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121463232 | ||||||
| chr11:121463260
|
A | AT | 134 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.286-6737dupT | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr11 | 121463260 | |||||
| chr11:121463337
|
A | C | 1 | a0001c0003t0003g0254 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.286-6670A>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121463337 | ||||||
| chr11:121463546
|
G | A | 1 | a0001c0002t0001g0129 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.286-6461G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121463546 | ||||||
| chr11:121463608
|
T | TCACTACT others(12): Show |
2 | a0001c0004t0003g0224a0001c0060t0003g0163 | 2 | HG02559.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.286-6398_286-6397i others(21): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr11 | 121463608 | |||||
| chr11:121463747
|
T | C | 1 | a0001c0004t0001g0110 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.286-6260T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121463747 | ||||||
| chr11:121463844
|
G | A | 38 | a0001c0001t0001g0023a0001c0002t0004g0007a0001c0008t0018g0192others(35): Show | 38 | HG00642.hp2 HG01081.hp2 HG01433.hp1 others(35): Show |
intron_variant | MODIFIER | c.286-6163G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121463844 | ||||||
| chr11:121463901
|
A | G | 269 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(266): Show | 270 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.286-6106A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121463901 | ||||||
| chr11:121464243
|
A | G | 4 | a0001c0009t0010g0165a0001c0065t0003g0152a0001c0066t0016g0194others(1): Show | 4 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.286-5764A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121464243 | ||||||
| chr11:121464424
|
G | A | 2 | a0001c0008t0002g0177a0001c0012t0002g0178 | 2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.286-5583G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121464424 | ||||||
| chr11:121464454
|
T | C | 39 | a0001c0001t0001g0023a0001c0001t0002g0125a0001c0002t0004g0007others(36): Show | 39 | HG00558.hp2 HG00642.hp2 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.286-5553T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121464454 | ||||||
| chr11:121464523
|
A | AT | 4 | a0001c0009t0011g0170a0001c0009t0011g0255a0004c0056t0013g0148others(1): Show | 4 | HG02486.hp2 HG02630.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.286-5483dupT | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr11 | 121464523 | |||||
| chr11:121464773
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.286-5234G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121464773 | ||||||
| chr11:121464875
|
C | T | 1 | a0015c0050t0002g0180 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.286-5132C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121464875 | ||||||
| chr11:121464889
|
A | C | 1 | a0005c0017t0001g0240 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.286-5118A>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121464889 | ||||||
| chr11:121464889
|
A | G | 2 | a0001c0008t0002g0177a0001c0012t0002g0178 | 2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.286-5118A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121464889 | ||||||
| chr11:121464984
|
TTCTCTGC others(64): Show |
T | 1 | a0001c0018t0002g0081 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.286-5022_286-4952d others(73): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121464984 | ||||||
| chr11:121465019
|
A | G | 133 | a0001c0001t0001g0023a0001c0001t0001g0089a0001c0001t0001g0111others(130): Show | 134 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.286-4988A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121465019 | ||||||
| chr11:121465206
|
T | G | 128 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0024others(125): Show | 128 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.286-4801T>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121465206 | ||||||
| chr11:121465348
|
A | C | 1 | a0001c0018t0002g0156 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.286-4659A>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121465348 | ||||||
| chr11:121465467
|
A | G | 2 | a0001c0008t0002g0177a0001c0012t0002g0178 | 2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.286-4540A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121465467 | ||||||
| chr11:121465484
|
T | C | 40 | a0001c0001t0001g0089a0001c0002t0001g0010a0001c0002t0001g0083others(37): Show | 40 | HG00280.hp2 HG01167.hp1 HG01256.hp2 others(37): Show |
intron_variant | MODIFIER | c.286-4523T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121465484 | ||||||
| chr11:121465566
|
C | T | 2 | a0001c0008t0002g0177a0001c0012t0002g0178 | 2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.286-4441C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121465566 | ||||||
| chr11:121465635
|
C | A | 1 | a0001c0009t0010g0165 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.286-4372C>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121465635 | ||||||
| chr11:121465762
|
C | T | 135 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0024others(132): Show | 135 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.286-4245C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121465762 | ||||||
| chr11:121466155
|
A | C | 3 | a0001c0001t0002g0185a0001c0057t0002g0160a0002c0005t0003g0159 | 3 | HG02257.hp2 HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.286-3852A>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121466155 | ||||||
| chr11:121466183
|
A | G | 4 | a0001c0009t0010g0165a0001c0065t0003g0152a0001c0066t0016g0194others(1): Show | 4 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.286-3824A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121466183 | ||||||
| chr11:121466196
|
G | A | 2 | a0001c0008t0002g0177a0001c0012t0002g0178 | 2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.286-3811G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121466196 | ||||||
| chr11:121466208
|
A | G | 4 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0002g0026others(1): Show | 4 | NA18961.hp2 NA18969.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.286-3799A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121466208 | ||||||
| chr11:121466410
|
G | A | 1 | a0001c0013t0002g0035 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.286-3597G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121466410 | ||||||
| chr11:121466468
|
G | A | 1 | a0001c0002t0004g0108 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.286-3539G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121466468 | ||||||
| chr11:121466474
|
C | T | 2 | a0001c0008t0002g0177a0001c0012t0002g0178 | 2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.286-3533C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121466474 | ||||||
| chr11:121466516
|
G | C | 1 | a0001c0003t0019g0209 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.286-3491G>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121466516 | ||||||
| chr11:121466668
|
T | C | 1 | a0001c0003t0002g0229 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.286-3339T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121466668 | ||||||
| chr11:121466676
|
G | A | 2 | a0001c0008t0002g0177a0001c0012t0002g0178 | 2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.286-3331G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121466676 | ||||||
| chr11:121466677
|
C | T | 39 | a0001c0001t0001g0089a0001c0002t0001g0010a0001c0002t0001g0083others(36): Show | 39 | HG00280.hp2 HG01167.hp1 HG01256.hp2 others(36): Show |
intron_variant | MODIFIER | c.286-3330C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121466677 | ||||||
| chr11:121466800
|
G | A | 1 | a0001c0035t0001g0071 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.286-3207G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121466800 | ||||||
| chr11:121467030
|
C | CT | 131 | a0001c0001t0001g0089a0001c0001t0001g0138a0001c0001t0002g0185others(128): Show | 132 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.286-2960dupT | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr11 | 121467030 | |||||
| chr11:121467030
|
C | CTT | 40 | a0001c0001t0002g0125a0001c0002t0001g0116a0001c0002t0004g0007others(37): Show | 40 | HG00438.hp2 HG00558.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.286-2961_286-2960d others(4): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr11 | 121467030 | |||||
| chr11:121467072
|
C | T | 6 | a0001c0004t0002g0132a0001c0011t0001g0107a0001c0011t0002g0271others(3): Show | 6 | HG01074.hp2 HG01192.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.286-2935C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121467072 | ||||||
| chr11:121467115
|
C | T | 1 | a0001c0009t0010g0165 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.286-2892C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121467115 | ||||||
| chr11:121467122
|
C | T | 262 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(259): Show | 263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.286-2885C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121467122 | ||||||
| chr11:121467191
|
G | A | 1 | a0001c0039t0002g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.286-2816G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121467191 | ||||||
| chr11:121467284
|
G | A | 94 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(91): Show | 94 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.286-2723G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121467284 | ||||||
| chr11:121467539
|
A | AT | 5 | a0001c0003t0003g0254a0001c0003t0005g0228a0001c0018t0002g0081others(2): Show | 5 | HG02257.hp1 HG03195.hp1 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.286-2458dupT | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr11 | 121467539 | |||||
| chr11:121467539
|
AT | A | 37 | a0001c0001t0002g0125a0001c0002t0004g0007a0001c0008t0018g0192others(34): Show | 37 | HG00558.hp2 HG00642.hp2 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.286-2458delT | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr11 | 121467539 | |||||
| chr11:121467610
|
C | T | 2 | a0003c0069t0008g0164a0003c0071t0014g0146 | 2 | HG02258.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.286-2397C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121467610 | ||||||
| chr11:121467745
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.286-2262C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121467745 | ||||||
| chr11:121468176
|
A | T | 1 | a0002c0005t0001g0074 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.286-1831A>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121468176 | ||||||
| chr11:121468369
|
G | A | 8 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(5): Show | 8 | HG00544.hp2 HG02040.hp2 NA18747.hp1 others(5): Show |
intron_variant | MODIFIER | c.286-1638G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121468369 | ||||||
| chr11:121468393
|
T | C | 1 | a0001c0046t0002g0174 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.286-1614T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121468393 | ||||||
| chr11:121469283
|
G | A | 1 | a0003c0027t0005g0181 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.286-724G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121469283 | ||||||
| chr11:121469480
|
A | G | 1 | a0001c0006t0009g0200 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.286-527A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121469480 | ||||||
| chr11:121469498
|
T | C | 1 | a0001c0011t0020g0106 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.286-509T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121469498 | ||||||
| chr11:121469518
|
A | G | 1 | a0001c0011t0020g0106 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.286-489A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121469518 | ||||||
| chr11:121469524
|
C | T | 223 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(220): Show | 224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.286-483C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121469524 | ||||||
| chr11:121469684
|
A | G | 1 | a0001c0018t0002g0081 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.286-323A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 1/47 | chr11 | 121469684 | ||||||
| chr11:121470161
|
A | G | 5 | a0001c0003t0002g0229a0001c0004t0002g0132a0001c0011t0001g0107others(2): Show | 5 | HG00741.hp2 HG01074.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.402+38A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 2/47 | chr11 | 121470161 | ||||||
| chr11:121470219
|
T | A | 1 | a0006c0043t0026g0215 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.402+96T>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 2/47 | chr11 | 121470219 | ||||||
| chr11:121470441
|
C | T | 23 | a0001c0002t0001g0139a0001c0002t0003g0150a0001c0003t0002g0105others(20): Show | 23 | HG00099.hp2 HG00735.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.402+318C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 2/47 | chr11 | 121470441 | ||||||
| chr11:121470553
|
G | A | 42 | a0001c0002t0004g0007a0001c0008t0002g0177a0001c0008t0018g0192others(39): Show | 42 | HG00642.hp2 HG01081.hp2 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.402+430G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 2/47 | chr11 | 121470553 | ||||||
| chr11:121470599
|
G | T | 38 | a0001c0002t0004g0007a0001c0008t0002g0177a0001c0008t0018g0192others(35): Show | 38 | HG00642.hp2 HG01081.hp2 HG01433.hp1 others(35): Show |
intron_variant | MODIFIER | c.402+476G>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 2/47 | chr11 | 121470599 | ||||||
| chr11:121470760
|
C | T | 1 | a0001c0053t0001g0065 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.402+637C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 2/47 | chr11 | 121470760 | ||||||
| chr11:121470858
|
A | G | 6 | a0001c0002t0001g0092a0001c0002t0002g0091a0001c0002t0002g0109others(3): Show | 6 | NA18747.hp2 NA18951.hp2 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.402+735A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 2/47 | chr11 | 121470858 | ||||||
| chr11:121470864
|
T | A | 1 | a0001c0004t0003g0224 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.402+741T>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 2/47 | chr11 | 121470864 | ||||||
| chr11:121470891
|
G | A | 6 | a0001c0004t0002g0132a0001c0011t0001g0107a0001c0011t0002g0271others(3): Show | 6 | HG01074.hp2 HG01192.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.402+768G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 2/47 | chr11 | 121470891 | ||||||
| chr11:121470911
|
A | T | 1 | a0016c0029t0001g0064 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.402+788A>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 2/47 | chr11 | 121470911 | ||||||
| chr11:121471041
|
A | G | 1 | a0001c0021t0003g0216 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.402+918A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 2/47 | chr11 | 121471041 | ||||||
| chr11:121471166
|
C | T | 37 | a0001c0001t0001g0089a0001c0002t0001g0010a0001c0002t0001g0083others(34): Show | 37 | HG01167.hp1 HG01256.hp2 HG01258.hp1 others(34): Show |
intron_variant | MODIFIER | c.402+1043C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 2/47 | chr11 | 121471166 | ||||||
| chr11:121471249
|
C | T | 1 | a0001c0031t0010g0214 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.402+1126C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 2/47 | chr11 | 121471249 | ||||||
| chr11:121471378
|
G | A | 49 | a0001c0001t0001g0111a0001c0002t0001g0112a0001c0002t0001g0116others(46): Show | 50 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.402+1255G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 2/47 | chr11 | 121471378 | ||||||
| chr11:121471399
|
T | C | 1 | a0001c0039t0002g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.402+1276T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 2/47 | chr11 | 121471399 | ||||||
| chr11:121471531
|
C | T | 1 | a0001c0038t0002g0186 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.402+1408C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 2/47 | chr11 | 121471531 | ||||||
| chr11:121471566
|
A | G | 7 | a0001c0003t0002g0229a0001c0004t0002g0132a0001c0011t0001g0107others(4): Show | 7 | HG00741.hp2 HG01074.hp2 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.402+1443A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 2/47 | chr11 | 121471566 | ||||||
| chr11:121471774
|
G | A | 1 | a0001c0002t0003g0150 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.402+1651G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 2/47 | chr11 | 121471774 | ||||||
| chr11:121471920
|
G | A | 1 | a0001c0032t0003g0149 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.402+1797G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 2/47 | chr11 | 121471920 | ||||||
| chr11:121472254
|
A | T | 4 | a0001c0009t0010g0165a0001c0065t0003g0152a0001c0066t0016g0194others(1): Show | 4 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.402+2131A>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 2/47 | chr11 | 121472254 | ||||||
| chr11:121472337
|
T | A | 39 | a0001c0001t0001g0089a0001c0002t0001g0010a0001c0002t0001g0083others(36): Show | 39 | HG00280.hp2 HG01167.hp1 HG01256.hp2 others(36): Show |
intron_variant | MODIFIER | c.402+2214T>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 2/47 | chr11 | 121472337 | ||||||
| chr11:121472405
|
G | T | 2 | a0001c0008t0002g0177a0001c0012t0002g0178 | 2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.402+2282G>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 2/47 | chr11 | 121472405 | ||||||
| chr11:121472634
|
G | A | 12 | a0001c0003t0003g0262a0001c0003t0005g0226a0001c0003t0005g0228others(9): Show | 12 | HG01496.hp1 HG02257.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.402+2511G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 2/47 | chr11 | 121472634 | ||||||
| chr11:121472726
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.402+2603C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 2/47 | chr11 | 121472726 | ||||||
| chr11:121472852
|
C | T | 85 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0024others(82): Show | 85 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.402+2729C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 2/47 | chr11 | 121472852 | ||||||
| chr11:121472853
|
G | A | 4 | a0001c0009t0010g0165a0001c0065t0003g0152a0001c0066t0016g0194others(1): Show | 4 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.402+2730G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 2/47 | chr11 | 121472853 | ||||||
| chr11:121472885
|
G | T | 167 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0024others(164): Show | 168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.402+2762G>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 2/47 | chr11 | 121472885 | ||||||
| chr11:121472968
|
G | GA | 264 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(261): Show | 265 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.402+2856dupA | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr11 | 121472968 | |||||
| chr11:121473172
|
C | A | 1 | a0001c0022t0008g0211 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.402+3049C>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 2/47 | chr11 | 121473172 | ||||||
| chr11:121473574
|
AG | A | 61 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0024others(58): Show | 61 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.402+3455delG | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr11 | 121473574 | |||||
| chr11:121473826
|
C | T | 1 | a0003c0071t0014g0146 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.402+3703C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 2/47 | chr11 | 121473826 | ||||||
| chr11:121473847
|
A | T | 1 | a0003c0027t0005g0173 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.402+3724A>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 2/47 | chr11 | 121473847 | ||||||
| chr11:121473947
|
A | G | 6 | a0001c0003t0003g0262a0001c0003t0005g0226a0001c0003t0005g0228others(3): Show | 6 | HG02257.hp1 HG02451.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.402+3824A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 2/47 | chr11 | 121473947 | ||||||
| chr11:121473958
|
T | A | 1 | a0001c0031t0010g0214 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.402+3835T>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 2/47 | chr11 | 121473958 | ||||||
| chr11:121473983
|
C | T | 1 | a0001c0022t0008g0211 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.402+3860C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 2/47 | chr11 | 121473983 | ||||||
| chr11:121474096
|
A | G | 1 | a0001c0011t0020g0106 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.402+3973A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 2/47 | chr11 | 121474096 | ||||||
| chr11:121474134
|
C | A | 1 | a0001c0003t0002g0133 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.403-3984C>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 2/47 | chr11 | 121474134 | ||||||
| chr11:121474144
|
T | C | 1 | a0001c0001t0025g0119 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.403-3974T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 2/47 | chr11 | 121474144 | ||||||
| chr11:121474216
|
C | G | 4 | a0001c0009t0010g0165a0001c0065t0003g0152a0001c0066t0016g0194others(1): Show | 4 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.403-3902C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 2/47 | chr11 | 121474216 | ||||||
| chr11:121474278
|
G | A | 1 | a0002c0005t0001g0032 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.403-3840G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 2/47 | chr11 | 121474278 | ||||||
| chr11:121474811
|
C | T | 4 | a0001c0009t0010g0165a0001c0065t0003g0152a0001c0066t0016g0194others(1): Show | 4 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.403-3307C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 2/47 | chr11 | 121474811 | ||||||
| chr11:121475308
|
TA | T | 218 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0024others(215): Show | 219 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.403-2805delA | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr11 | 121475308 | |||||
| chr11:121475858
|
T | C | 7 | a0001c0001t0001g0039a0001c0001t0001g0040a0002c0005t0001g0008others(4): Show | 7 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.403-2260T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 2/47 | chr11 | 121475858 | ||||||
| chr11:121475892
|
T | C | 269 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(266): Show | 270 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.403-2226T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 2/47 | chr11 | 121475892 | ||||||
| chr11:121476196
|
G | A | 2 | a0001c0003t0003g0254a0001c0038t0002g0186 | 2 | HG03195.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.403-1922G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 2/47 | chr11 | 121476196 | ||||||
| chr11:121476323
|
C | T | 1 | a0001c0038t0002g0186 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.403-1795C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 2/47 | chr11 | 121476323 | ||||||
| chr11:121476388
|
T | C | 269 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(266): Show | 270 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.403-1730T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 2/47 | chr11 | 121476388 | ||||||
| chr11:121476692
|
TTCCC | T | 2 | a0001c0008t0002g0177a0001c0012t0002g0178 | 2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.403-1416_403-1413d others(6): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr11 | 121476692 | |||||
| chr11:121476698
|
C | T | 37 | a0001c0001t0002g0125a0001c0002t0004g0007a0001c0008t0018g0192others(34): Show | 37 | HG00558.hp2 HG00642.hp2 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.403-1420C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 2/47 | chr11 | 121476698 | ||||||
| chr11:121476804
|
C | T | 4 | a0001c0009t0011g0170a0001c0009t0011g0255a0004c0056t0013g0148others(1): Show | 4 | HG02486.hp2 HG02630.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.403-1314C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 2/47 | chr11 | 121476804 | ||||||
| chr11:121476806
|
C | T | 1 | a0001c0001t0001g0199 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.403-1312C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 2/47 | chr11 | 121476806 | ||||||
| chr11:121476875
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.403-1243G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 2/47 | chr11 | 121476875 | ||||||
| chr11:121476956
|
T | C | 3 | a0001c0065t0003g0152a0001c0066t0016g0194a0012c0064t0024g0168 | 3 | HG01243.hp1 HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.403-1162T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 2/47 | chr11 | 121476956 | ||||||
| chr11:121477110
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.403-1008C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 2/47 | chr11 | 121477110 | ||||||
| chr11:121477204
|
T | A | 1 | a0001c0001t0001g0027 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.403-914T>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 2/47 | chr11 | 121477204 | ||||||
| chr11:121477251
|
C | T | 1 | a0002c0005t0019g0062 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.403-867C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 2/47 | chr11 | 121477251 | ||||||
| chr11:121477263
|
A | C | 269 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(266): Show | 270 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.403-855A>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 2/47 | chr11 | 121477263 | ||||||
| chr11:121477311
|
T | C | 1 | a0002c0005t0001g0223 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.403-807T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 2/47 | chr11 | 121477311 | ||||||
| chr11:121477324
|
A | G | 1 | a0002c0005t0019g0062 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.403-794A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 2/47 | chr11 | 121477324 | ||||||
| chr11:121477638
|
G | C | 7 | a0001c0004t0002g0132a0001c0004t0003g0224a0001c0011t0001g0107others(4): Show | 7 | HG01074.hp2 HG01192.hp2 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.403-480G>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 2/47 | chr11 | 121477638 | ||||||
| chr11:121477893
|
G | A | 1 | a0001c0006t0001g0157 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.403-225G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 2/47 | chr11 | 121477893 | ||||||
| chr11:121478032
|
CA | C | 172 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0024others(169): Show | 172 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.403-66delA | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr11 | 121478032 | |||||
| chr11:121478032
|
CAAAAA | C | 46 | a0001c0001t0001g0111a0001c0002t0001g0112a0001c0002t0001g0116others(43): Show | 47 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.403-70_403-66delAA others(3): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr11 | 121478032 | |||||
| chr11:121478049
|
A | G | 1 | a0001c0001t0001g0061 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.403-69A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 2/47 | chr11 | 121478049 | ||||||
| chr11:121478402
|
A | G | 47 | a0001c0001t0001g0111a0001c0002t0001g0112a0001c0002t0001g0116others(44): Show | 48 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.528+159A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121478402 | ||||||
| chr11:121478663
|
C | G | 38 | a0001c0001t0001g0089a0001c0002t0001g0010a0001c0002t0001g0083others(35): Show | 38 | HG00280.hp2 HG01167.hp1 HG01256.hp2 others(35): Show |
intron_variant | MODIFIER | c.528+420C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121478663 | ||||||
| chr11:121478671
|
C | T | 1 | a0002c0007t0001g0060 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.528+428C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121478671 | ||||||
| chr11:121478752
|
G | A | 2 | a0001c0008t0002g0177a0001c0012t0002g0178 | 2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.528+509G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121478752 | ||||||
| chr11:121478764
|
G | C | 2 | a0003c0027t0005g0173a0003c0027t0005g0181 | 2 | HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.528+521G>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121478764 | ||||||
| chr11:121478795
|
T | C | 1 | a0001c0058t0011g0166 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.528+552T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121478795 | ||||||
| chr11:121478820
|
G | T | 1 | a0001c0011t0001g0107 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.528+577G>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121478820 | ||||||
| chr11:121478838
|
G | A | 1 | a0001c0009t0008g0207 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.528+595G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121478838 | ||||||
| chr11:121478843
|
G | A | 1 | a0001c0004t0001g0082 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.528+600G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121478843 | ||||||
| chr11:121478870
|
A | G | 269 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(266): Show | 270 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.528+627A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121478870 | ||||||
| chr11:121478953
|
T | C | 4 | a0001c0009t0010g0165a0001c0065t0003g0152a0001c0066t0016g0194others(1): Show | 4 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.528+710T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121478953 | ||||||
| chr11:121479354
|
C | T | 1 | a0001c0004t0002g0132 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.528+1111C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121479354 | ||||||
| chr11:121479441
|
C | G | 1 | a0001c0003t0019g0209 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.528+1198C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121479441 | ||||||
| chr11:121479538
|
G | A | 4 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0002g0026others(1): Show | 4 | NA18961.hp2 NA18969.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.528+1295G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121479538 | ||||||
| chr11:121479772
|
T | C | 1 | a0001c0060t0003g0163 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.528+1529T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121479772 | ||||||
| chr11:121480126
|
C | G | 1 | a0001c0009t0003g0147 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.528+1883C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121480126 | ||||||
| chr11:121480287
|
A | G | 6 | a0001c0001t0004g0099a0002c0005t0001g0074a0002c0005t0001g0205others(3): Show | 6 | HG01433.hp1 HG03490.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.528+2044A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121480287 | ||||||
| chr11:121480607
|
CAGCTCCT others(1337): Show |
C | 1 | a0001c0022t0008g0211 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.528+2403_528+3746d others(2): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | INFO_REALIGN_3_PRIME | chr11 | 121480607 | |||||
| chr11:121480646
|
T | C | 1 | a0001c0016t0002g0044 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.528+2403T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121480646 | ||||||
| chr11:121480669
|
C | CCCCTAGT others(152): Show |
1 | a0001c0018t0002g0081 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.528+2449_528+2450i others(161): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | INFO_REALIGN_3_PRIME | chr11 | 121480669 | |||||
| chr11:121480691
|
A | AGGCAGGC others(155): Show |
8 | a0001c0003t0002g0229a0001c0004t0002g0132a0001c0004t0003g0224others(5): Show | 8 | HG00741.hp2 HG01074.hp2 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.528+2494_528+2495i others(164): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | INFO_REALIGN_3_PRIME | chr11 | 121480691 | |||||
| chr11:121480691
|
A | AGGCAGGC others(101): Show |
2 | a0001c0008t0002g0177a0001c0012t0002g0178 | 2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.528+2498_528+2499i others(110): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | INFO_REALIGN_3_PRIME | chr11 | 121480691 | |||||
| chr11:121480691
|
A | AGGCAGGC others(209): Show |
1 | a0001c0003t0002g0133 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.528+2506_528+2507i others(218): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | INFO_REALIGN_3_PRIME | chr11 | 121480691 | |||||
| chr11:121480734
|
C | T | 25 | a0001c0002t0001g0139a0001c0002t0003g0150a0001c0003t0002g0105others(22): Show | 25 | HG00099.hp2 HG00735.hp1 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.528+2491C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121480734 | ||||||
| chr11:121480750
|
A | AGCTCCAT others(155): Show |
3 | a0001c0065t0003g0152a0001c0066t0016g0194a0012c0064t0024g0168 | 3 | HG01243.hp1 HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.528+2552_528+2553i others(164): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | INFO_REALIGN_3_PRIME | chr11 | 121480750 | |||||
| chr11:121480750
|
A | AGCTCCAT others(155): Show |
36 | a0001c0001t0001g0089a0001c0002t0001g0010a0001c0002t0001g0083others(33): Show | 36 | HG01167.hp1 HG01256.hp2 HG01258.hp1 others(33): Show |
intron_variant | MODIFIER | c.528+2552_528+2553i others(164): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | INFO_REALIGN_3_PRIME | chr11 | 121480750 | |||||
| chr11:121480750
|
A | AGCTCCAT others(101): Show |
1 | a0001c0001t0001g0059 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.528+2552_528+2553i others(110): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | INFO_REALIGN_3_PRIME | chr11 | 121480750 | |||||
| chr11:121480750
|
A | AGCTCCAT others(155): Show |
146 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(143): Show | 147 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.528+2552_528+2553i others(164): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | INFO_REALIGN_3_PRIME | chr11 | 121480750 | |||||
| chr11:121480750
|
A | AGCTCCAT others(155): Show |
2 | a0001c0009t0008g0207a0001c0033t0003g0169 | 2 | NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.528+2552_528+2553i others(164): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | INFO_REALIGN_3_PRIME | chr11 | 121480750 | |||||
| chr11:121480750
|
A | AGCTCCAT others(155): Show |
39 | a0001c0002t0004g0007a0001c0008t0018g0192a0001c0009t0011g0170others(36): Show | 39 | HG00642.hp2 HG01081.hp2 HG01433.hp1 others(36): Show |
intron_variant | MODIFIER | c.528+2552_528+2553i others(164): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | INFO_REALIGN_3_PRIME | chr11 | 121480750 | |||||
| chr11:121480750
|
A | G | 13 | a0001c0003t0002g0133a0001c0003t0002g0229a0001c0003t0003g0254others(10): Show | 13 | HG00741.hp1 HG00741.hp2 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.528+2507A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121480750 | ||||||
| chr11:121480796
|
T | A | 29 | a0001c0001t0001g0039a0001c0002t0001g0139a0001c0002t0003g0150others(26): Show | 29 | HG00099.hp2 HG00735.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.528+2553T>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121480796 | ||||||
| chr11:121480800
|
G | A | 29 | a0001c0001t0001g0039a0001c0002t0001g0139a0001c0002t0003g0150others(26): Show | 29 | HG00099.hp2 HG00735.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.528+2557G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121480800 | ||||||
| chr11:121480804
|
A | G | 1 | a0001c0001t0001g0059 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.528+2561A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121480804 | ||||||
| chr11:121480853
|
A | C | 29 | a0001c0001t0001g0039a0001c0002t0001g0139a0001c0002t0003g0150others(26): Show | 29 | HG00099.hp2 HG00735.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.528+2610A>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121480853 | ||||||
| chr11:121480858
|
GGCTCCAT others(101): Show |
G | 26 | a0001c0002t0001g0139a0001c0002t0003g0150a0001c0003t0002g0105others(23): Show | 26 | HG00099.hp2 HG00735.hp1 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.528+2626_528+2733d others(2): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | INFO_REALIGN_3_PRIME | chr11 | 121480858 | |||||
| chr11:121480869
|
T | C | 7 | a0001c0001t0001g0039a0001c0003t0002g0101a0001c0004t0001g0100others(4): Show | 7 | HG00735.hp2 HG01243.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.528+2626T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121480869 | ||||||
| chr11:121480872
|
T | C | 3 | a0001c0001t0001g0039a0001c0003t0002g0101a0001c0004t0001g0100 | 3 | HG00735.hp2 HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.528+2629T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121480872 | ||||||
| chr11:121480882
|
T | C | 3 | a0001c0001t0001g0039a0001c0003t0002g0101a0001c0004t0001g0100 | 3 | HG00735.hp2 HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.528+2639T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121480882 | ||||||
| chr11:121480885
|
T | C | 3 | a0001c0001t0001g0039a0001c0003t0002g0101a0001c0004t0001g0100 | 3 | HG00735.hp2 HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.528+2642T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121480885 | ||||||
| chr11:121480888
|
G | C | 3 | a0001c0001t0001g0039a0001c0003t0002g0101a0001c0004t0001g0100 | 3 | HG00735.hp2 HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.528+2645G>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121480888 | ||||||
| chr11:121480916
|
T | C | 3 | a0001c0001t0001g0039a0001c0003t0002g0101a0001c0004t0001g0100 | 3 | HG00735.hp2 HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.528+2673T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121480916 | ||||||
| chr11:121481001
|
A | G | 29 | a0001c0001t0001g0039a0001c0002t0001g0139a0001c0002t0003g0150others(26): Show | 29 | HG00099.hp2 HG00735.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.528+2758A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121481001 | ||||||
| chr11:121481024
|
T | C | 29 | a0001c0001t0001g0039a0001c0002t0001g0139a0001c0002t0003g0150others(26): Show | 29 | HG00099.hp2 HG00735.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.528+2781T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121481024 | ||||||
| chr11:121481031
|
C | T | 3 | a0001c0001t0001g0039a0001c0003t0002g0101a0001c0004t0001g0100 | 3 | HG00735.hp2 HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.528+2788C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121481031 | ||||||
| chr11:121481034
|
C | T | 3 | a0001c0001t0001g0039a0001c0003t0002g0101a0001c0004t0001g0100 | 3 | HG00735.hp2 HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.528+2791C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121481034 | ||||||
| chr11:121481044
|
C | T | 3 | a0001c0001t0001g0039a0001c0003t0002g0101a0001c0004t0001g0100 | 3 | HG00735.hp2 HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.528+2801C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121481044 | ||||||
| chr11:121481047
|
C | T | 3 | a0001c0001t0001g0039a0001c0003t0002g0101a0001c0004t0001g0100 | 3 | HG00735.hp2 HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.528+2804C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121481047 | ||||||
| chr11:121481050
|
C | G | 3 | a0001c0001t0001g0039a0001c0003t0002g0101a0001c0004t0001g0100 | 3 | HG00735.hp2 HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.528+2807C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121481050 | ||||||
| chr11:121481063
|
A | G | 1 | a0001c0003t0002g0229 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.528+2820A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121481063 | ||||||
| chr11:121481064
|
C | T | 1 | a0001c0003t0002g0229 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.528+2821C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121481064 | ||||||
| chr11:121481074
|
G | A | 26 | a0001c0002t0001g0139a0001c0002t0003g0150a0001c0003t0002g0105others(23): Show | 26 | HG00099.hp2 HG00735.hp1 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.528+2831G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121481074 | ||||||
| chr11:121481078
|
T | C | 28 | a0001c0002t0001g0139a0001c0002t0003g0150a0001c0003t0002g0105others(25): Show | 28 | HG00099.hp2 HG00735.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.528+2835T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121481078 | ||||||
| chr11:121481097
|
T | G | 1 | a0001c0038t0002g0186 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.528+2854T>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121481097 | ||||||
| chr11:121481109
|
A | G | 29 | a0001c0002t0001g0139a0001c0002t0003g0150a0001c0003t0002g0101others(26): Show | 29 | HG00099.hp2 HG00735.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.528+2866A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121481109 | ||||||
| chr11:121481121
|
G | A | 29 | a0001c0002t0001g0139a0001c0002t0003g0150a0001c0003t0002g0101others(26): Show | 29 | HG00099.hp2 HG00735.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.528+2878G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121481121 | ||||||
| chr11:121481128
|
G | A | 2 | a0001c0003t0002g0101a0001c0004t0001g0100 | 2 | HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.528+2885G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121481128 | ||||||
| chr11:121481129
|
A | G | 29 | a0001c0002t0001g0139a0001c0002t0003g0150a0001c0003t0002g0101others(26): Show | 29 | HG00099.hp2 HG00735.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.528+2886A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121481129 | ||||||
| chr11:121481132
|
C | T | 1 | a0001c0003t0002g0229 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.528+2889C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121481132 | ||||||
| chr11:121481138
|
C | G | 4 | a0001c0009t0010g0165a0001c0065t0003g0152a0001c0066t0016g0194others(1): Show | 4 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.528+2895C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121481138 | ||||||
| chr11:121481139
|
T | C | 4 | a0001c0003t0002g0101a0001c0003t0002g0229a0001c0003t0007g0261others(1): Show | 4 | HG00741.hp2 HG02451.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.528+2896T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121481139 | ||||||
| chr11:121481142
|
T | C | 3 | a0001c0003t0002g0101a0001c0003t0002g0229a0001c0004t0001g0100 | 3 | HG00741.hp2 HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.528+2899T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121481142 | ||||||
| chr11:121481152
|
T | C | 3 | a0001c0003t0002g0101a0001c0003t0002g0229a0001c0004t0001g0100 | 3 | HG00741.hp2 HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.528+2909T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121481152 | ||||||
| chr11:121481155
|
T | C | 3 | a0001c0003t0002g0101a0001c0003t0002g0229a0001c0004t0001g0100 | 3 | HG00741.hp2 HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.528+2912T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121481155 | ||||||
| chr11:121481158
|
G | C | 3 | a0001c0003t0002g0101a0001c0003t0002g0229a0001c0004t0001g0100 | 3 | HG00741.hp2 HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.528+2915G>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121481158 | ||||||
| chr11:121481163
|
G | A | 3 | a0001c0003t0002g0101a0001c0003t0002g0229a0001c0004t0001g0100 | 3 | HG00741.hp2 HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.528+2920G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121481163 | ||||||
| chr11:121481186
|
C | T | 29 | a0001c0002t0001g0139a0001c0002t0003g0150a0001c0003t0002g0101others(26): Show | 29 | HG00099.hp2 HG00735.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.528+2943C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121481186 | ||||||
| chr11:121481210
|
T | C | 170 | a0001c0001t0001g0089a0001c0001t0001g0111a0001c0001t0002g0125others(167): Show | 171 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.528+2967T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121481210 | ||||||
| chr11:121481236
|
A | AGCTCCAT others(905): Show |
1 | a0002c0005t0001g0074 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.528+3042_528+3043i others(914): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | INFO_REALIGN_3_PRIME | chr11 | 121481236 | |||||
| chr11:121481236
|
A | G | 3 | a0001c0003t0002g0101a0001c0003t0002g0229a0001c0004t0001g0100 | 3 | HG00741.hp2 HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.528+2993A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121481236 | ||||||
| chr11:121481238
|
CTCCATCT others(419): Show |
C | 26 | a0001c0002t0001g0139a0001c0002t0003g0150a0001c0003t0002g0105others(23): Show | 26 | HG00099.hp2 HG00735.hp1 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.528+3051_528+3476d others(2): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | INFO_REALIGN_3_PRIME | chr11 | 121481238 | |||||
| chr11:121481240
|
C | T | 3 | a0001c0003t0002g0101a0001c0003t0002g0229a0001c0004t0001g0100 | 3 | HG00741.hp2 HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.528+2997C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121481240 | ||||||
| chr11:121481255
|
C | G | 1 | a0001c0003t0002g0229 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.528+3012C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121481255 | ||||||
| chr11:121481263
|
C | T | 2 | a0001c0008t0002g0177a0001c0012t0002g0178 | 2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.528+3020C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121481263 | ||||||
| chr11:121481271
|
G | A | 2 | a0001c0003t0002g0101a0001c0004t0001g0100 | 2 | HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.528+3028G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121481271 | ||||||
| chr11:121481283
|
A | G | 2 | a0001c0003t0002g0101a0001c0004t0001g0100 | 2 | HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.528+3040A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121481283 | ||||||
| chr11:121481291
|
G | A | 2 | a0001c0003t0002g0101a0001c0004t0001g0100 | 2 | HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.528+3048G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121481291 | ||||||
| chr11:121481301
|
C | T | 3 | a0001c0003t0002g0101a0001c0003t0002g0229a0001c0004t0001g0100 | 3 | HG00741.hp2 HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.528+3058C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121481301 | ||||||
| chr11:121481304
|
C | T | 3 | a0001c0003t0002g0101a0001c0003t0002g0229a0001c0004t0001g0100 | 3 | HG00741.hp2 HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.528+3061C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121481304 | ||||||
| chr11:121481314
|
C | T | 2 | a0001c0003t0002g0101a0001c0004t0001g0100 | 2 | HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.528+3071C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121481314 | ||||||
| chr11:121481317
|
C | T | 2 | a0001c0003t0002g0101a0001c0004t0001g0100 | 2 | HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.528+3074C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121481317 | ||||||
| chr11:121481320
|
C | G | 2 | a0001c0003t0002g0101a0001c0004t0001g0100 | 2 | HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.528+3077C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121481320 | ||||||
| chr11:121481340
|
A | G | 3 | a0001c0003t0002g0101a0001c0004t0001g0100a0001c0008t0002g0131 | 3 | HG03834.hp1 HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.528+3097A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121481340 | ||||||
| chr11:121481344
|
A | G | 2 | a0001c0003t0002g0101a0001c0004t0001g0100 | 2 | HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.528+3101A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121481344 | ||||||
| chr11:121481368
|
T | C | 2 | a0001c0003t0002g0101a0001c0004t0001g0100 | 2 | HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.528+3125T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121481368 | ||||||
| chr11:121481371
|
T | C | 2 | a0001c0003t0002g0101a0001c0004t0001g0100 | 2 | HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.528+3128T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121481371 | ||||||
| chr11:121481374
|
A | C | 2 | a0001c0003t0002g0101a0001c0004t0001g0100 | 2 | HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.528+3131A>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121481374 | ||||||
| chr11:121481398
|
G | A | 2 | a0001c0003t0002g0101a0001c0004t0001g0100 | 2 | HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.528+3155G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121481398 | ||||||
| chr11:121481426
|
T | C | 2 | a0001c0003t0002g0101a0001c0004t0001g0100 | 2 | HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.528+3183T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121481426 | ||||||
| chr11:121481426
|
TCCTAGTG others(47): Show |
T | 1 | a0002c0025t0003g0260 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.528+3236_528+3289d others(56): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | INFO_REALIGN_3_PRIME | chr11 | 121481426 | |||||
| chr11:121481462
|
C | T | 2 | a0001c0009t0008g0207a0001c0033t0003g0169 | 2 | NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.528+3219C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121481462 | ||||||
| chr11:121481538
|
A | G | 2 | a0001c0009t0008g0207a0001c0033t0003g0169 | 2 | NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.528+3295A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121481538 | ||||||
| chr11:121481656
|
T | C | 2 | a0001c0003t0002g0117a0001c0006t0001g0118 | 2 | HG02148.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.528+3413T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121481656 | ||||||
| chr11:121481697
|
G | A | 26 | a0001c0002t0001g0139a0001c0002t0003g0150a0001c0003t0002g0105others(23): Show | 26 | HG00099.hp2 HG00735.hp1 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.528+3454G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121481697 | ||||||
| chr11:121481771
|
G | C | 1 | a0001c0001t0001g0027 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.528+3528G>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121481771 | ||||||
| chr11:121481774
|
C | CCATCTCC others(47): Show |
1 | a0002c0005t0001g0032 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.528+3562_528+3615d others(56): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | INFO_REALIGN_3_PRIME | chr11 | 121481774 | |||||
| chr11:121481774
|
C | CCATCTCC others(101): Show |
1 | a0001c0021t0003g0216 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.528+3600_528+3707d others(110): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | INFO_REALIGN_3_PRIME | chr11 | 121481774 | |||||
| chr11:121481805
|
GCACAGAT others(47): Show |
G | 41 | a0001c0001t0001g0089a0001c0002t0001g0010a0001c0002t0001g0083others(38): Show | 41 | HG01167.hp1 HG01256.hp2 HG01258.hp1 others(38): Show |
intron_variant | MODIFIER | c.528+3616_528+3669d others(56): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | INFO_REALIGN_3_PRIME | chr11 | 121481805 | |||||
| chr11:121481859
|
ACACAGAT others(47): Show |
A | 1 | a0001c0002t0001g0158 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.528+3654_528+3707d others(56): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | INFO_REALIGN_3_PRIME | chr11 | 121481859 | |||||
| chr11:121481882
|
T | C | 1 | a0001c0001t0002g0167 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.528+3639T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121481882 | ||||||
| chr11:121482226
|
G | A | 1 | a0001c0006t0028g0031 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.528+3983G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121482226 | ||||||
| chr11:121482305
|
T | C | 1 | a0001c0003t0003g0254 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.528+4062T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121482305 | ||||||
| chr11:121482307
|
T | C | 5 | a0001c0003t0002g0229a0001c0004t0002g0132a0001c0011t0001g0107others(2): Show | 5 | HG00741.hp2 HG01074.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.528+4064T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121482307 | ||||||
| chr11:121482368
|
T | G | 14 | a0001c0002t0004g0003a0001c0002t0004g0007a0002c0005t0001g0074others(11): Show | 14 | HG01081.hp2 HG01433.hp1 HG02040.hp1 others(11): Show |
intron_variant | MODIFIER | c.528+4125T>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121482368 | ||||||
| chr11:121482696
|
C | T | 1 | a0002c0025t0003g0260 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.528+4453C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121482696 | ||||||
| chr11:121483084
|
T | A | 1 | a0004c0059t0002g0171 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.528+4841T>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121483084 | ||||||
| chr11:121483138
|
A | G | 1 | a0001c0022t0008g0211 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.529-4894A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121483138 | ||||||
| chr11:121483417
|
C | T | 1 | a0001c0003t0002g0229 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.529-4615C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121483417 | ||||||
| chr11:121483473
|
T | C | 4 | a0001c0009t0010g0165a0001c0065t0003g0152a0001c0066t0016g0194others(1): Show | 4 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.529-4559T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121483473 | ||||||
| chr11:121483690
|
C | G | 4 | a0001c0009t0010g0165a0001c0065t0003g0152a0001c0066t0016g0194others(1): Show | 4 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.529-4342C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121483690 | ||||||
| chr11:121484020
|
G | A | 5 | a0001c0002t0004g0233a0001c0003t0002g0094a0001c0003t0002g0098others(2): Show | 5 | HG01109.hp1 HG01952.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.529-4012G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121484020 | ||||||
| chr11:121484550
|
G | A | 5 | a0001c0002t0004g0233a0001c0003t0002g0094a0001c0003t0002g0098others(2): Show | 5 | HG01109.hp1 HG01952.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.529-3482G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121484550 | ||||||
| chr11:121484588
|
C | T | 4 | a0002c0014t0002g0172a0002c0025t0005g0179a0002c0026t0005g0161others(1): Show | 4 | HG02886.hp1 HG02896.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.529-3444C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121484588 | ||||||
| chr11:121484811
|
T | A | 1 | a0001c0006t0001g0072 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.529-3221T>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121484811 | ||||||
| chr11:121484836
|
C | T | 4 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0002g0026others(1): Show | 4 | NA18961.hp2 NA18969.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.529-3196C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121484836 | ||||||
| chr11:121484866
|
A | G | 1 | a0001c0032t0003g0149 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.529-3166A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121484866 | ||||||
| chr11:121485465
|
C | T | 1 | a0001c0001t0002g0026 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.529-2567C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121485465 | ||||||
| chr11:121485470
|
A | G | 41 | a0001c0001t0001g0023a0001c0002t0004g0003a0001c0002t0004g0007others(38): Show | 41 | HG00642.hp2 HG01081.hp2 HG01433.hp1 others(38): Show |
intron_variant | MODIFIER | c.529-2562A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121485470 | ||||||
| chr11:121485840
|
A | C | 1 | a0001c0004t0001g0088 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.529-2192A>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121485840 | ||||||
| chr11:121486176
|
C | T | 44 | a0001c0001t0001g0111a0001c0002t0001g0112a0001c0002t0001g0116others(41): Show | 45 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.529-1856C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121486176 | ||||||
| chr11:121486188
|
C | G | 1 | a0001c0046t0002g0174 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.529-1844C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121486188 | ||||||
| chr11:121486223
|
C | G | 1 | a0001c0001t0001g0058 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.529-1809C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121486223 | ||||||
| chr11:121486259
|
C | T | 25 | a0001c0002t0001g0139a0001c0002t0003g0150a0001c0003t0002g0105others(22): Show | 25 | HG00099.hp2 HG00735.hp1 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.529-1773C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121486259 | ||||||
| chr11:121486484
|
T | C | 3 | a0001c0001t0001g0045a0001c0001t0004g0099a0001c0008t0002g0222 | 3 | NA18941.hp1 NA18942.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.529-1548T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121486484 | ||||||
| chr11:121486511
|
A | G | 1 | a0001c0022t0008g0211 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.529-1521A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121486511 | ||||||
| chr11:121486541
|
A | G | 5 | a0001c0003t0002g0229a0001c0004t0002g0132a0001c0011t0001g0107others(2): Show | 5 | HG00741.hp2 HG01074.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.529-1491A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121486541 | ||||||
| chr11:121486543
|
G | A | 18 | a0001c0002t0004g0003a0001c0002t0004g0007a0001c0012t0005g0247others(15): Show | 18 | HG01081.hp2 HG01109.hp2 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.529-1489G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121486543 | ||||||
| chr11:121486652
|
C | T | 3 | a0001c0065t0003g0152a0001c0066t0016g0194a0012c0064t0024g0168 | 3 | HG01243.hp1 HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.529-1380C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121486652 | ||||||
| chr11:121486655
|
A | G | 26 | a0001c0002t0001g0139a0001c0002t0003g0150a0001c0003t0002g0105others(23): Show | 26 | HG00099.hp2 HG00735.hp1 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.529-1377A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121486655 | ||||||
| chr11:121486669
|
T | C | 3 | a0001c0065t0003g0152a0001c0066t0016g0194a0012c0064t0024g0168 | 3 | HG01243.hp1 HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.529-1363T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121486669 | ||||||
| chr11:121486673
|
T | G | 3 | a0001c0065t0003g0152a0001c0066t0016g0194a0012c0064t0024g0168 | 3 | HG01243.hp1 HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.529-1359T>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121486673 | ||||||
| chr11:121486681
|
C | G | 3 | a0001c0065t0003g0152a0001c0066t0016g0194a0012c0064t0024g0168 | 3 | HG01243.hp1 HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.529-1351C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121486681 | ||||||
| chr11:121486714
|
C | T | 1 | a0001c0038t0002g0186 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.529-1318C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121486714 | ||||||
| chr11:121486726
|
G | A | 40 | a0001c0002t0004g0003a0001c0002t0004g0007a0001c0003t0002g0230others(37): Show | 40 | HG00642.hp2 HG01081.hp2 HG01167.hp2 others(37): Show |
intron_variant | MODIFIER | c.529-1306G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121486726 | ||||||
| chr11:121486886
|
G | A | 1 | a0001c0003t0018g0191 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.529-1146G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121486886 | ||||||
| chr11:121486911
|
A | G | 6 | a0001c0009t0003g0147a0001c0009t0010g0165a0001c0046t0002g0174others(3): Show | 6 | HG01243.hp1 HG02630.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.529-1121A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121486911 | ||||||
| chr11:121486948
|
C | T | 2 | a0001c0008t0002g0177a0001c0012t0002g0178 | 2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.529-1084C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121486948 | ||||||
| chr11:121487037
|
C | T | 1 | a0001c0002t0001g0158 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.529-995C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121487037 | ||||||
| chr11:121487043
|
A | G | 1 | a0001c0038t0002g0186 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.529-989A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121487043 | ||||||
| chr11:121487057
|
T | C | 269 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(266): Show | 270 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.529-975T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121487057 | ||||||
| chr11:121487085
|
A | G | 5 | a0001c0002t0004g0003a0001c0002t0004g0007a0002c0005t0001g0202others(2): Show | 5 | HG02040.hp1 HG02165.hp1 NA18990.hp1 others(2): Show |
intron_variant | MODIFIER | c.529-947A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121487085 | ||||||
| chr11:121487442
|
G | A | 84 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0024others(81): Show | 84 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.529-590G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121487442 | ||||||
| chr11:121487472
|
A | G | 1 | a0001c0003t0003g0254 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.529-560A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121487472 | ||||||
| chr11:121487519
|
C | A | 261 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(258): Show | 262 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.529-513C>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121487519 | ||||||
| chr11:121487553
|
T | C | 38 | a0001c0001t0002g0125a0001c0008t0018g0192a0001c0065t0003g0152others(35): Show | 38 | HG00544.hp1 HG00558.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.529-479T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121487553 | ||||||
| chr11:121487652
|
G | A | 125 | a0001c0002t0001g0010a0001c0002t0001g0083a0001c0002t0001g0092others(122): Show | 126 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.529-380G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121487652 | ||||||
| chr11:121487721
|
C | T | 90 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(87): Show | 90 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.529-311C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121487721 | ||||||
| chr11:121487868
|
A | T | 1 | a0001c0003t0018g0191 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.529-164A>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 3/47 | chr11 | 121487868 | ||||||
| chr11:121488411
|
A | T | 2 | a0001c0008t0002g0177a0001c0012t0002g0178 | 2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.690+218A>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 4/47 | chr11 | 121488411 | ||||||
| chr11:121488528
|
A | G | 3 | a0001c0065t0003g0152a0001c0066t0016g0194a0012c0064t0024g0168 | 3 | HG01243.hp1 HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.690+335A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 4/47 | chr11 | 121488528 | ||||||
| chr11:121488556
|
T | C | 92 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(89): Show | 92 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.690+363T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 4/47 | chr11 | 121488556 | ||||||
| chr11:121488744
|
G | A | 3 | a0001c0009t0008g0207a0001c0009t0011g0170a0001c0009t0011g0255 | 3 | HG02486.hp2 HG03139.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.690+551G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 4/47 | chr11 | 121488744 | ||||||
| chr11:121488976
|
G | A | 1 | a0001c0002t0001g0139 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.690+783G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 4/47 | chr11 | 121488976 | ||||||
| chr11:121489276
|
G | A | 1 | a0001c0046t0002g0174 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.691-767G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 4/47 | chr11 | 121489276 | ||||||
| chr11:121489363
|
C | T | 1 | a0001c0033t0003g0169 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.691-680C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 4/47 | chr11 | 121489363 | ||||||
| chr11:121489417
|
C | G | 4 | a0001c0003t0002g0080a0001c0003t0002g0128a0001c0018t0002g0081others(1): Show | 4 | NA18939.hp1 NA18952.hp1 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.691-626C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 4/47 | chr11 | 121489417 | ||||||
| chr11:121489460
|
A | G | 92 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(89): Show | 92 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.691-583A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 4/47 | chr11 | 121489460 | ||||||
| chr11:121489794
|
C | G | 2 | a0001c0001t0001g0155a0001c0008t0004g0005 | 2 | NA18959.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.691-249C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 4/47 | chr11 | 121489794 | ||||||
| chr11:121489832
|
G | T | 1 | a0002c0030t0002g0212 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.691-211G>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 4/47 | chr11 | 121489832 | ||||||
| chr11:121489970
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.691-73C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 4/47 | chr11 | 121489970 | ||||||
| chr11:121490000
|
G | A | 1 | a0001c0015t0015g0067 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.691-43G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 4/47 | chr11 | 121490000 | ||||||
| chr11:121490009
|
A | G | 1 | a0001c0001t0025g0119 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.691-34A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 4/47 | chr11 | 121490009 | ||||||
| chr11:121490175
|
T | A | 92 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(89): Show | 92 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.758+65T>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | chr11 | 121490175 | ||||||
| chr11:121490306
|
G | A | 35 | a0001c0008t0018g0192a0002c0005t0001g0008a0002c0005t0001g0032others(32): Show | 35 | HG00544.hp1 HG00642.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.758+196G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | chr11 | 121490306 | ||||||
| chr11:121490429
|
G | GT | 270 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(267): Show | 271 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.758+324dupT | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | INFO_REALIGN_3_PRIME | chr11 | 121490429 | |||||
| chr11:121490472
|
G | A | 39 | a0001c0002t0001g0010a0001c0002t0001g0083a0001c0002t0001g0092others(36): Show | 39 | HG01167.hp1 HG01256.hp2 HG01258.hp1 others(36): Show |
intron_variant | MODIFIER | c.758+362G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | chr11 | 121490472 | ||||||
| chr11:121490541
|
A | G | 1 | a0001c0002t0004g0087 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.758+431A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | chr11 | 121490541 | ||||||
| chr11:121490689
|
C | T | 8 | a0001c0003t0002g0229a0001c0004t0003g0224a0001c0011t0001g0107others(5): Show | 8 | HG00741.hp2 HG01074.hp2 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.758+579C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | chr11 | 121490689 | ||||||
| chr11:121490695
|
C | T | 7 | a0001c0003t0003g0262a0001c0003t0005g0226a0001c0003t0005g0228others(4): Show | 7 | HG01993.hp1 HG02257.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.758+585C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | chr11 | 121490695 | ||||||
| chr11:121490740
|
C | CA | 209 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(206): Show | 210 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.758+650dupA | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | INFO_REALIGN_3_PRIME | chr11 | 121490740 | |||||
| chr11:121490740
|
C | CAA | 16 | a0001c0001t0001g0027a0001c0001t0001g0066a0001c0001t0001g0138others(13): Show | 16 | HG02027.hp2 HG02080.hp2 HG02148.hp1 others(13): Show |
intron_variant | MODIFIER | c.758+649_758+650dup others(2): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | INFO_REALIGN_3_PRIME | chr11 | 121490740 | |||||
| chr11:121490830
|
A | C | 2 | a0001c0009t0011g0170a0001c0009t0011g0255 | 2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.758+720A>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | chr11 | 121490830 | ||||||
| chr11:121490968
|
C | T | 1 | a0001c0033t0003g0169 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.758+858C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | chr11 | 121490968 | ||||||
| chr11:121490983
|
T | C | 3 | a0001c0065t0003g0152a0001c0066t0016g0194a0012c0064t0024g0168 | 3 | HG01243.hp1 HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.758+873T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | chr11 | 121490983 | ||||||
| chr11:121491082
|
G | A | 2 | a0001c0003t0008g0208a0001c0003t0008g0263 | 2 | HG01496.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.758+972G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | chr11 | 121491082 | ||||||
| chr11:121491115
|
G | A | 85 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0024others(82): Show | 85 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.758+1005G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | chr11 | 121491115 | ||||||
| chr11:121491550
|
A | G | 1 | a0001c0003t0007g0261 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.758+1440A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | chr11 | 121491550 | ||||||
| chr11:121491607
|
G | A | 38 | a0001c0002t0001g0010a0001c0002t0001g0083a0001c0002t0001g0092others(35): Show | 38 | HG01167.hp1 HG01256.hp2 HG01258.hp1 others(35): Show |
intron_variant | MODIFIER | c.758+1497G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | chr11 | 121491607 | ||||||
| chr11:121492145
|
G | A | 1 | a0013c0047t0007g0182 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.758+2035G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | chr11 | 121492145 | ||||||
| chr11:121492194
|
C | T | 1 | a0007c0072t0002g0256 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.758+2084C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | chr11 | 121492194 | ||||||
| chr11:121492253
|
C | T | 1 | a0001c0001t0002g0125 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.758+2143C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | chr11 | 121492253 | ||||||
| chr11:121492300
|
G | C | 1 | a0001c0046t0002g0174 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.758+2190G>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | chr11 | 121492300 | ||||||
| chr11:121492337
|
T | C | 269 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(266): Show | 270 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.758+2227T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | chr11 | 121492337 | ||||||
| chr11:121492362
|
A | T | 3 | a0001c0065t0003g0152a0001c0066t0016g0194a0012c0064t0024g0168 | 3 | HG01243.hp1 HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.758+2252A>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | chr11 | 121492362 | ||||||
| chr11:121492549
|
A | G | 1 | a0002c0005t0003g0159 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.758+2439A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | chr11 | 121492549 | ||||||
| chr11:121492664
|
T | C | 3 | a0001c0060t0003g0163a0001c0067t0013g0204a0004c0059t0002g0171 | 3 | HG02559.hp2 HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.758+2554T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | chr11 | 121492664 | ||||||
| chr11:121492703
|
C | T | 1 | a0001c0046t0002g0174 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.758+2593C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | chr11 | 121492703 | ||||||
| chr11:121492737
|
T | G | 3 | a0001c0065t0003g0152a0001c0066t0016g0194a0012c0064t0024g0168 | 3 | HG01243.hp1 HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.758+2627T>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | chr11 | 121492737 | ||||||
| chr11:121492806
|
A | AT | 207 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(204): Show | 208 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.758+2711dupT | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | INFO_REALIGN_3_PRIME | chr11 | 121492806 | |||||
| chr11:121492806
|
A | ATT | 50 | a0001c0002t0001g0010a0001c0002t0001g0083a0001c0002t0001g0092others(47): Show | 50 | HG00280.hp2 HG01167.hp1 HG01256.hp2 others(47): Show |
intron_variant | MODIFIER | c.758+2710_758+2711d others(4): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | INFO_REALIGN_3_PRIME | chr11 | 121492806 | |||||
| chr11:121493046
|
A | G | 1 | a0001c0006t0001g0157 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.758+2936A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | chr11 | 121493046 | ||||||
| chr11:121493049
|
G | A | 4 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(1): Show | 4 | HG00544.hp2 HG02040.hp2 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.758+2939G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | chr11 | 121493049 | ||||||
| chr11:121493067
|
C | T | 1 | a0007c0072t0002g0256 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.758+2957C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | chr11 | 121493067 | ||||||
| chr11:121493119
|
C | T | 28 | a0001c0002t0001g0139a0001c0002t0003g0150a0001c0002t0003g0151others(25): Show | 28 | HG00099.hp2 HG01167.hp2 HG01169.hp1 others(25): Show |
intron_variant | MODIFIER | c.758+3009C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | chr11 | 121493119 | ||||||
| chr11:121493136
|
C | G | 263 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(260): Show | 264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.758+3026C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | chr11 | 121493136 | ||||||
| chr11:121493145
|
A | T | 1 | a0006c0043t0026g0215 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.758+3035A>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | chr11 | 121493145 | ||||||
| chr11:121493294
|
A | G | 92 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(89): Show | 92 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.758+3184A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | chr11 | 121493294 | ||||||
| chr11:121493318
|
G | A | 9 | a0001c0003t0002g0229a0001c0004t0003g0224a0001c0011t0001g0107others(6): Show | 9 | HG00741.hp2 HG01074.hp2 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.758+3208G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | chr11 | 121493318 | ||||||
| chr11:121493404
|
C | T | 1 | a0001c0003t0003g0254 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.758+3294C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | chr11 | 121493404 | ||||||
| chr11:121493431
|
A | G | 47 | a0001c0002t0001g0112a0001c0002t0001g0116a0001c0002t0001g0158others(44): Show | 48 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.758+3321A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | chr11 | 121493431 | ||||||
| chr11:121493476
|
T | C | 137 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(134): Show | 138 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.758+3366T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | chr11 | 121493476 | ||||||
| chr11:121493477
|
G | A | 4 | a0001c0003t0002g0133a0001c0010t0003g0257a0001c0010t0003g0258others(1): Show | 4 | HG00741.hp1 HG02109.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.758+3367G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | chr11 | 121493477 | ||||||
| chr11:121493707
|
T | C | 4 | a0001c0002t0003g0150a0001c0002t0003g0151a0001c0009t0003g0147others(1): Show | 4 | HG02109.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.759-3162T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | chr11 | 121493707 | ||||||
| chr11:121493761
|
T | A | 8 | a0001c0003t0002g0229a0001c0004t0003g0224a0001c0011t0001g0107others(5): Show | 8 | HG00741.hp2 HG01074.hp2 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.759-3108T>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | chr11 | 121493761 | ||||||
| chr11:121493762
|
A | G | 1 | a0001c0067t0013g0204 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.759-3107A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | chr11 | 121493762 | ||||||
| chr11:121493802
|
A | G | 3 | a0001c0065t0003g0152a0001c0066t0016g0194a0012c0064t0024g0168 | 3 | HG01243.hp1 HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.759-3067A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | chr11 | 121493802 | ||||||
| chr11:121494031
|
C | G | 1 | a0002c0025t0003g0260 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.759-2838C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | chr11 | 121494031 | ||||||
| chr11:121494031
|
C | T | 1 | a0001c0033t0003g0169 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.759-2838C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | chr11 | 121494031 | ||||||
| chr11:121494106
|
A | C | 133 | a0001c0002t0001g0010a0001c0002t0001g0083a0001c0002t0001g0092others(130): Show | 134 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.759-2763A>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | chr11 | 121494106 | ||||||
| chr11:121494254
|
A | G | 87 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0024others(84): Show | 87 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.759-2615A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | chr11 | 121494254 | ||||||
| chr11:121494297
|
C | T | 1 | a0001c0032t0003g0149 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.759-2572C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | chr11 | 121494297 | ||||||
| chr11:121494376
|
C | T | 1 | a0001c0046t0002g0174 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.759-2493C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | chr11 | 121494376 | ||||||
| chr11:121494626
|
A | C | 1 | a0001c0008t0018g0192 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.759-2243A>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | chr11 | 121494626 | ||||||
| chr11:121494815
|
G | T | 5 | a0001c0003t0002g0229a0001c0011t0001g0107a0001c0011t0002g0271others(2): Show | 5 | HG00741.hp2 HG01074.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.759-2054G>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | chr11 | 121494815 | ||||||
| chr11:121494967
|
A | G | 1 | a0001c0001t0001g0066 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.759-1902A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | chr11 | 121494967 | ||||||
| chr11:121494981
|
T | C | 16 | a0001c0001t0002g0125a0002c0005t0001g0074a0002c0005t0001g0202others(13): Show | 16 | HG00558.hp2 HG00735.hp1 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.759-1888T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | chr11 | 121494981 | ||||||
| chr11:121495011
|
G | T | 10 | a0001c0002t0001g0139a0001c0003t0002g0105a0001c0003t0012g0184others(7): Show | 10 | HG00099.hp2 HG01167.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.759-1858G>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | chr11 | 121495011 | ||||||
| chr11:121495151
|
A | G | 93 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(90): Show | 93 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.759-1718A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | chr11 | 121495151 | ||||||
| chr11:121495165
|
C | T | 1 | a0002c0005t0019g0062 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.759-1704C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | chr11 | 121495165 | ||||||
| chr11:121495216
|
G | A | 3 | a0001c0065t0003g0152a0001c0066t0016g0194a0012c0064t0024g0168 | 3 | HG01243.hp1 HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.759-1653G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | chr11 | 121495216 | ||||||
| chr11:121495463
|
C | T | 1 | a0001c0032t0003g0149 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.759-1406C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | chr11 | 121495463 | ||||||
| chr11:121495789
|
T | A | 2 | a0001c0001t0001g0111a0001c0016t0002g0121 | 2 | HG01256.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.759-1080T>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | chr11 | 121495789 | ||||||
| chr11:121496125
|
T | C | 1 | a0001c0009t0011g0170 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.759-744T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | chr11 | 121496125 | ||||||
| chr11:121496327
|
C | G | 1 | a0002c0005t0003g0159 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.759-542C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | chr11 | 121496327 | ||||||
| chr11:121496338
|
C | T | 1 | a0001c0038t0002g0186 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.759-531C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | chr11 | 121496338 | ||||||
| chr11:121496531
|
G | A | 5 | a0001c0002t0004g0233a0001c0003t0002g0094a0001c0003t0002g0098others(2): Show | 5 | HG01109.hp1 HG01952.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.759-338G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | chr11 | 121496531 | ||||||
| chr11:121496644
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.759-225C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | chr11 | 121496644 | ||||||
| chr11:121496701
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.759-168C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | chr11 | 121496701 | ||||||
| chr11:121496740
|
C | T | 1 | a0002c0005t0003g0159 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.759-129C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | chr11 | 121496740 | ||||||
| chr11:121496848
|
CT | C | 75 | a0001c0001t0002g0125a0001c0002t0001g0010a0001c0002t0001g0083others(72): Show | 75 | HG00544.hp1 HG00558.hp2 HG00642.hp2 others(72): Show |
splice_region_variant&intron_variant | LOW | c.759-8delT | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 5/47 | INFO_REALIGN_3_PRIME | chr11 | 121496848 | |||||
| chr11:121497212
|
C | T | 91 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(88): Show | 91 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.939+163C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121497212 | ||||||
| chr11:121497454
|
A | G | 169 | a0001c0001t0002g0125a0001c0002t0001g0010a0001c0002t0001g0083others(166): Show | 170 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.939+405A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121497454 | ||||||
| chr11:121497768
|
G | C | 1 | a0001c0001t0004g0099 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.939+719G>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121497768 | ||||||
| chr11:121497855
|
C | G | 1 | a0001c0012t0007g0244 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.939+806C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121497855 | ||||||
| chr11:121497919
|
A | G | 1 | a0001c0015t0004g0056 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.939+870A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121497919 | ||||||
| chr11:121497919
|
A | T | 8 | a0001c0003t0002g0229a0001c0004t0003g0224a0001c0011t0001g0107others(5): Show | 8 | HG00741.hp2 HG01074.hp2 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.939+870A>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121497919 | ||||||
| chr11:121498005
|
C | G | 1 | a0001c0002t0003g0151 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.939+956C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121498005 | ||||||
| chr11:121498022
|
A | G | 1 | a0001c0002t0004g0077 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.939+973A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121498022 | ||||||
| chr11:121498255
|
G | A | 5 | a0001c0012t0005g0247a0001c0020t0003g0248a0001c0061t0030g0249others(2): Show | 5 | HG01109.hp2 HG02559.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.939+1206G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121498255 | ||||||
| chr11:121498380
|
A | G | 1 | a0001c0009t0010g0165 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.939+1331A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121498380 | ||||||
| chr11:121498541
|
A | G | 38 | a0001c0002t0001g0010a0001c0002t0001g0083a0001c0002t0001g0092others(35): Show | 38 | HG01167.hp1 HG01256.hp2 HG01258.hp1 others(35): Show |
intron_variant | MODIFIER | c.939+1492A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121498541 | ||||||
| chr11:121498657
|
C | G | 1 | a0001c0001t0001g0045 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.939+1608C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121498657 | ||||||
| chr11:121498679
|
G | A | 81 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0024others(78): Show | 81 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.939+1630G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121498679 | ||||||
| chr11:121498836
|
A | G | 79 | a0001c0002t0001g0112a0001c0002t0001g0116a0001c0002t0001g0139others(76): Show | 80 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.939+1787A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121498836 | ||||||
| chr11:121498875
|
C | CA | 146 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(143): Show | 147 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.939+1840dupA | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr11 | 121498875 | |||||
| chr11:121499069
|
T | C | 1 | a0001c0001t0001g0006 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.939+2020T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121499069 | ||||||
| chr11:121499092
|
G | T | 88 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0024others(85): Show | 88 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.939+2043G>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121499092 | ||||||
| chr11:121499314
|
A | G | 93 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(90): Show | 93 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.939+2265A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121499314 | ||||||
| chr11:121499445
|
T | G | 3 | a0001c0060t0003g0163a0001c0067t0013g0204a0004c0059t0002g0171 | 3 | HG02559.hp2 HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.939+2396T>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121499445 | ||||||
| chr11:121499645
|
A | G | 40 | a0001c0001t0001g0023a0001c0015t0001g0022a0001c0019t0001g0028others(37): Show | 40 | HG00544.hp1 HG00642.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.939+2596A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121499645 | ||||||
| chr11:121499719
|
T | C | 1 | a0001c0060t0003g0163 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.939+2670T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121499719 | ||||||
| chr11:121499795
|
G | A | 3 | a0001c0065t0003g0152a0001c0066t0016g0194a0012c0064t0024g0168 | 3 | HG01243.hp1 HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.939+2746G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121499795 | ||||||
| chr11:121500007
|
C | T | 36 | a0001c0002t0001g0139a0001c0002t0003g0150a0001c0002t0003g0151others(33): Show | 36 | HG00099.hp2 HG00741.hp2 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.939+2958C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121500007 | ||||||
| chr11:121500249
|
A | G | 1 | a0001c0008t0002g0131 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.939+3200A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121500249 | ||||||
| chr11:121500275
|
A | G | 2 | a0001c0011t0012g0242a0001c0011t0021g0243 | 2 | HG00280.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.939+3226A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121500275 | ||||||
| chr11:121500406
|
C | T | 2 | a0001c0001t0001g0055a0001c0013t0002g0054 | 2 | NA18939.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.939+3357C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121500406 | ||||||
| chr11:121500411
|
G | A | 87 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0024others(84): Show | 87 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.939+3362G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121500411 | ||||||
| chr11:121500590
|
C | T | 6 | a0001c0002t0003g0150a0001c0002t0003g0151a0001c0009t0003g0147others(3): Show | 6 | HG02109.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.939+3541C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121500590 | ||||||
| chr11:121500789
|
A | G | 2 | a0001c0008t0002g0177a0001c0012t0002g0178 | 2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.939+3740A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121500789 | ||||||
| chr11:121500945
|
C | T | 1 | a0001c0018t0002g0013 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.939+3896C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121500945 | ||||||
| chr11:121501058
|
G | A | 1 | a0001c0032t0003g0149 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.939+4009G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121501058 | ||||||
| chr11:121501138
|
G | A | 1 | a0001c0018t0002g0156 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.939+4089G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121501138 | ||||||
| chr11:121501280
|
T | A | 1 | a0012c0064t0024g0168 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.939+4231T>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121501280 | ||||||
| chr11:121501291
|
A | G | 1 | a0002c0014t0004g0076 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.939+4242A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121501291 | ||||||
| chr11:121501373
|
C | T | 32 | a0002c0005t0001g0008a0002c0005t0001g0032a0002c0005t0001g0042others(29): Show | 32 | HG00544.hp1 HG00642.hp2 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.939+4324C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121501373 | ||||||
| chr11:121501397
|
T | C | 3 | a0001c0065t0003g0152a0001c0066t0016g0194a0012c0064t0024g0168 | 3 | HG01243.hp1 HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.939+4348T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121501397 | ||||||
| chr11:121501434
|
T | C | 1 | a0001c0046t0002g0174 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.939+4385T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121501434 | ||||||
| chr11:121501498
|
A | G | 1 | a0001c0009t0010g0165 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.939+4449A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121501498 | ||||||
| chr11:121501592
|
G | A | 1 | a0006c0043t0026g0215 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.939+4543G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121501592 | ||||||
| chr11:121501623
|
A | T | 1 | a0001c0016t0002g0044 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.939+4574A>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121501623 | ||||||
| chr11:121501697
|
C | T | 48 | a0001c0002t0001g0112a0001c0002t0001g0116a0001c0002t0001g0158others(45): Show | 49 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.939+4648C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121501697 | ||||||
| chr11:121501727
|
G | A | 45 | a0001c0002t0001g0112a0001c0002t0001g0116a0001c0002t0001g0158others(42): Show | 46 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.939+4678G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121501727 | ||||||
| chr11:121501867
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.939+4818A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121501867 | ||||||
| chr11:121502098
|
T | C | 177 | a0001c0001t0001g0023a0001c0001t0002g0125a0001c0002t0001g0010others(174): Show | 178 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.939+5049T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121502098 | ||||||
| chr11:121502124
|
C | CT | 44 | a0001c0001t0001g0025a0001c0001t0001g0063a0001c0001t0001g0138others(41): Show | 45 | HG00438.hp1 HG00438.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.939+5104dupT | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr11 | 121502124 | |||||
| chr11:121502124
|
C | CTT | 15 | a0001c0001t0001g0027a0001c0002t0006g0114a0001c0002t0006g0218others(12): Show | 15 | HG00280.hp1 HG00323.hp2 HG00642.hp1 others(12): Show |
intron_variant | MODIFIER | c.939+5103_939+5104d others(4): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr11 | 121502124 | |||||
| chr11:121502124
|
C | CTTTTTT | 5 | a0002c0005t0001g0074a0002c0005t0001g0205a0002c0026t0005g0161others(2): Show | 5 | HG01433.hp1 HG02896.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.939+5099_939+5104d others(8): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr11 | 121502124 | |||||
| chr11:121502124
|
C | CTTTTTTT | 14 | a0001c0009t0008g0207a0002c0005t0001g0042a0002c0005t0001g0202others(11): Show | 14 | HG00544.hp1 HG00738.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.939+5098_939+5104d others(9): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr11 | 121502124 | |||||
| chr11:121502124
|
C | CTTTTTTT others(1): Show |
18 | a0001c0001t0001g0023a0001c0001t0002g0125a0001c0015t0001g0022others(15): Show | 18 | HG00558.hp2 HG00642.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.939+5097_939+5104d others(10): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr11 | 121502124 | |||||
| chr11:121502124
|
C | CTTTTTTT others(3): Show |
1 | a0002c0048t0002g0201 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.939+5095_939+5104d others(12): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr11 | 121502124 | |||||
| chr11:121502124
|
CT | C | 5 | a0001c0001t0001g0220a0001c0012t0007g0244a0001c0060t0003g0163others(2): Show | 5 | HG02523.hp1 HG02559.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.939+5104delT | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr11 | 121502124 | |||||
| chr11:121502124
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0002t0001g0139 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.939+5094_939+5104d others(13): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr11 | 121502124 | |||||
| chr11:121502124
|
CTTTTTTT others(5): Show |
C | 80 | a0001c0002t0001g0010a0001c0002t0001g0092a0001c0002t0001g0103others(77): Show | 80 | HG00099.hp2 HG00280.hp2 HG00741.hp2 others(77): Show |
intron_variant | MODIFIER | c.939+5093_939+5104d others(14): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr11 | 121502124 | |||||
| chr11:121502124
|
CTTTTTTT others(6): Show |
C | 4 | a0001c0002t0001g0083a0001c0002t0004g0090a0001c0032t0003g0149others(1): Show | 4 | HG02723.hp2 HG03195.hp1 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.939+5092_939+5104d others(15): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr11 | 121502124 | |||||
| chr11:121502155
|
A | T | 2 | a0001c0009t0011g0170a0001c0009t0011g0255 | 2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.939+5106A>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121502155 | ||||||
| chr11:121502221
|
C | T | 3 | a0001c0065t0003g0152a0001c0066t0016g0194a0012c0064t0024g0168 | 3 | HG01243.hp1 HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.939+5172C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121502221 | ||||||
| chr11:121502223
|
C | T | 1 | a0001c0033t0003g0169 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.939+5174C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121502223 | ||||||
| chr11:121502239
|
CATTCTCC others(7334): Show |
C | 1 | a0001c0001t0001g0024 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.939+5224_940-3390d others(2): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr11 | 121502239 | |||||
| chr11:121502261
|
G | A | 3 | a0001c0001t0001g0153a0001c0001t0002g0053a0001c0001t0002g0154 | 3 | HG02080.hp1 NA19002.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.939+5212G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121502261 | ||||||
| chr11:121502390
|
A | G | 2 | a0001c0009t0011g0170a0001c0009t0011g0255 | 2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.939+5341A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121502390 | ||||||
| chr11:121502435
|
C | T | 1 | a0001c0001t0001g0198 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.939+5386C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121502435 | ||||||
| chr11:121502458
|
C | T | 1 | a0001c0052t0001g0219 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.939+5409C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121502458 | ||||||
| chr11:121502466
|
G | A | 2 | a0001c0031t0010g0214a0002c0025t0003g0260 | 2 | HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.939+5417G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121502466 | ||||||
| chr11:121502520
|
A | G | 1 | a0001c0003t0008g0208 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.939+5471A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121502520 | ||||||
| chr11:121502541
|
A | G | 3 | a0001c0002t0003g0150a0001c0002t0003g0151a0001c0022t0003g0213 | 3 | HG02109.hp2 HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.939+5492A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121502541 | ||||||
| chr11:121502544
|
C | T | 1 | a0003c0070t0005g0145 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.939+5495C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121502544 | ||||||
| chr11:121502657
|
C | T | 3 | a0001c0065t0003g0152a0001c0066t0016g0194a0012c0064t0024g0168 | 3 | HG01243.hp1 HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.939+5608C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121502657 | ||||||
| chr11:121502692
|
A | G | 12 | a0001c0003t0003g0262a0001c0003t0005g0226a0001c0003t0005g0228others(9): Show | 12 | HG01496.hp1 HG02257.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.939+5643A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121502692 | ||||||
| chr11:121502718
|
C | T | 2 | a0001c0001t0002g0026a0001c0053t0001g0065 | 2 | NA18969.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.939+5669C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121502718 | ||||||
| chr11:121502719
|
G | T | 1 | a0007c0072t0002g0256 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.939+5670G>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121502719 | ||||||
| chr11:121503018
|
G | A | 1 | a0001c0021t0003g0216 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.939+5969G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121503018 | ||||||
| chr11:121503058
|
C | T | 48 | a0001c0002t0001g0112a0001c0002t0001g0116a0001c0002t0001g0158others(45): Show | 49 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.939+6009C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121503058 | ||||||
| chr11:121503151
|
C | G | 1 | a0001c0022t0008g0211 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.939+6102C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121503151 | ||||||
| chr11:121503265
|
G | T | 1 | a0001c0009t0008g0207 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.939+6216G>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121503265 | ||||||
| chr11:121503616
|
T | G | 3 | a0001c0065t0003g0152a0001c0066t0016g0194a0012c0064t0024g0168 | 3 | HG01243.hp1 HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.939+6567T>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121503616 | ||||||
| chr11:121504103
|
C | T | 33 | a0001c0001t0002g0125a0002c0005t0001g0008a0002c0005t0001g0032others(30): Show | 33 | HG00544.hp1 HG00558.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.939+7054C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121504103 | ||||||
| chr11:121504182
|
G | A | 2 | a0001c0065t0003g0152a0001c0066t0016g0194 | 2 | HG01243.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.939+7133G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121504182 | ||||||
| chr11:121504390
|
C | T | 3 | a0001c0006t0028g0031a0001c0008t0002g0177a0001c0012t0002g0178 | 3 | HG02622.hp2 HG02735.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.939+7341C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121504390 | ||||||
| chr11:121504423
|
T | A | 1 | a0001c0003t0003g0254 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.939+7374T>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121504423 | ||||||
| chr11:121504458
|
G | T | 1 | a0001c0001t0001g0009 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.939+7409G>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121504458 | ||||||
| chr11:121504469
|
A | G | 3 | a0001c0010t0003g0257a0001c0010t0003g0258a0001c0039t0002g0267 | 3 | HG02109.hp1 HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.939+7420A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121504469 | ||||||
| chr11:121504498
|
T | C | 1 | a0001c0003t0002g0095 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.939+7449T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121504498 | ||||||
| chr11:121504732
|
T | C | 3 | a0001c0065t0003g0152a0001c0066t0016g0194a0012c0064t0024g0168 | 3 | HG01243.hp1 HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.939+7683T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121504732 | ||||||
| chr11:121504810
|
A | G | 1 | a0001c0003t0003g0254 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.939+7761A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121504810 | ||||||
| chr11:121504882
|
T | G | 41 | a0001c0001t0001g0023a0001c0001t0002g0125a0001c0009t0010g0165others(38): Show | 41 | HG00544.hp1 HG00558.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.939+7833T>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121504882 | ||||||
| chr11:121504940
|
G | A | 1 | a0001c0003t0003g0254 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.939+7891G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121504940 | ||||||
| chr11:121505053
|
A | T | 3 | a0001c0065t0003g0152a0001c0066t0016g0194a0012c0064t0024g0168 | 3 | HG01243.hp1 HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.940-7950A>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121505053 | ||||||
| chr11:121505242
|
A | G | 42 | a0001c0002t0001g0010a0001c0002t0001g0083a0001c0002t0001g0092others(39): Show | 42 | HG00280.hp2 HG01167.hp1 HG01256.hp2 others(39): Show |
intron_variant | MODIFIER | c.940-7761A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121505242 | ||||||
| chr11:121505254
|
C | T | 45 | a0001c0002t0001g0112a0001c0002t0001g0116a0001c0002t0001g0158others(42): Show | 46 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.940-7749C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121505254 | ||||||
| chr11:121505274
|
G | C | 3 | a0001c0065t0003g0152a0001c0066t0016g0194a0012c0064t0024g0168 | 3 | HG01243.hp1 HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.940-7729G>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121505274 | ||||||
| chr11:121505391
|
A | C | 1 | a0001c0021t0016g0206 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.940-7612A>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121505391 | ||||||
| chr11:121505425
|
A | T | 1 | a0001c0058t0011g0166 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.940-7578A>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121505425 | ||||||
| chr11:121505610
|
A | G | 1 | a0001c0001t0001g0057 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.940-7393A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121505610 | ||||||
| chr11:121506086
|
C | T | 45 | a0001c0002t0001g0112a0001c0002t0001g0116a0001c0002t0001g0158others(42): Show | 46 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.940-6917C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121506086 | ||||||
| chr11:121506112
|
T | C | 3 | a0001c0065t0003g0152a0001c0066t0016g0194a0012c0064t0024g0168 | 3 | HG01243.hp1 HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.940-6891T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121506112 | ||||||
| chr11:121506412
|
A | C | 2 | a0001c0008t0002g0177a0001c0012t0002g0178 | 2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.940-6591A>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121506412 | ||||||
| chr11:121506438
|
G | C | 3 | a0001c0008t0002g0177a0001c0009t0010g0165a0001c0012t0002g0178 | 3 | HG02622.hp2 HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.940-6565G>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121506438 | ||||||
| chr11:121506632
|
C | T | 1 | a0001c0058t0011g0166 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.940-6371C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121506632 | ||||||
| chr11:121506644
|
A | G | 50 | a0001c0002t0001g0112a0001c0002t0001g0116a0001c0002t0001g0158others(47): Show | 51 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.940-6359A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121506644 | ||||||
| chr11:121506938
|
T | C | 2 | a0001c0011t0020g0106a0001c0045t0020g0102 | 2 | HG01192.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.940-6065T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121506938 | ||||||
| chr11:121506957
|
C | G | 2 | a0001c0011t0020g0106a0001c0045t0020g0102 | 2 | HG01192.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.940-6046C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121506957 | ||||||
| chr11:121507046
|
A | G | 1 | a0001c0046t0002g0174 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.940-5957A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121507046 | ||||||
| chr11:121507061
|
T | C | 1 | a0001c0008t0001g0136 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.940-5942T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121507061 | ||||||
| chr11:121507070
|
T | A | 1 | a0001c0002t0006g0020 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.940-5933T>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121507070 | ||||||
| chr11:121507087
|
C | A | 48 | a0001c0002t0001g0112a0001c0002t0001g0116a0001c0002t0001g0158others(45): Show | 49 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.940-5916C>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121507087 | ||||||
| chr11:121507113
|
A | C | 1 | a0001c0031t0010g0214 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.940-5890A>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121507113 | ||||||
| chr11:121507311
|
T | G | 1 | a0001c0058t0011g0166 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.940-5692T>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121507311 | ||||||
| chr11:121507507
|
A | G | 1 | a0007c0072t0002g0256 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.940-5496A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121507507 | ||||||
| chr11:121507645
|
T | A | 45 | a0001c0002t0001g0112a0001c0002t0001g0116a0001c0002t0001g0158others(42): Show | 46 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.940-5358T>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121507645 | ||||||
| chr11:121507722
|
T | A | 3 | a0001c0060t0003g0163a0001c0067t0013g0204a0004c0059t0002g0171 | 3 | HG02559.hp2 HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.940-5281T>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121507722 | ||||||
| chr11:121507933
|
T | C | 2 | a0001c0032t0003g0149a0006c0043t0026g0215 | 2 | HG02723.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.940-5070T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121507933 | ||||||
| chr11:121508103
|
T | C | 1 | a0001c0033t0003g0169 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.940-4900T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121508103 | ||||||
| chr11:121508130
|
T | C | 1 | a0001c0016t0002g0121 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.940-4873T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121508130 | ||||||
| chr11:121508414
|
T | C | 2 | a0002c0007t0017g0122a0002c0007t0017g0123 | 2 | NA18942.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.940-4589T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121508414 | ||||||
| chr11:121508442
|
C | G | 1 | a0001c0002t0001g0158 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.940-4561C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121508442 | ||||||
| chr11:121508519
|
A | G | 1 | a0001c0004t0022g0086 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.940-4484A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121508519 | ||||||
| chr11:121508956
|
G | A | 4 | a0001c0002t0004g0077a0001c0002t0004g0078a0001c0002t0004g0084others(1): Show | 4 | NA18966.hp1 NA18985.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.940-4047G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121508956 | ||||||
| chr11:121509065
|
T | C | 1 | a0001c0001t0002g0167 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.940-3938T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121509065 | ||||||
| chr11:121509089
|
A | G | 264 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(261): Show | 265 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.940-3914A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121509089 | ||||||
| chr11:121509101
|
T | C | 1 | a0007c0072t0002g0256 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.940-3902T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121509101 | ||||||
| chr11:121509165
|
T | C | 1 | a0001c0033t0003g0169 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.940-3838T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121509165 | ||||||
| chr11:121509665
|
C | T | 6 | a0001c0003t0007g0261a0001c0003t0007g0264a0001c0003t0007g0265others(3): Show | 6 | HG01496.hp1 HG02451.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.940-3338C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121509665 | ||||||
| chr11:121509724
|
C | G | 1 | a0001c0003t0002g0229 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.940-3279C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121509724 | ||||||
| chr11:121509989
|
T | A | 1 | a0001c0004t0001g0082 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.940-3014T>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121509989 | ||||||
| chr11:121510198
|
GTTAAGTA others(12): Show |
G | 1 | a0001c0046t0002g0174 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.940-2801_940-2783d others(21): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr11 | 121510198 | |||||
| chr11:121510256
|
G | A | 82 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0024others(79): Show | 82 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.940-2747G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121510256 | ||||||
| chr11:121510388
|
G | A | 1 | a0001c0003t0002g0135 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.940-2615G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121510388 | ||||||
| chr11:121510780
|
A | G | 50 | a0001c0002t0001g0112a0001c0002t0001g0116a0001c0002t0001g0158others(47): Show | 51 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.940-2223A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121510780 | ||||||
| chr11:121510844
|
G | C | 1 | a0002c0007t0001g0060 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.940-2159G>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121510844 | ||||||
| chr11:121511354
|
G | A | 4 | a0001c0003t0003g0262a0001c0003t0005g0226a0001c0003t0005g0228others(1): Show | 4 | HG02257.hp1 HG02451.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.940-1649G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121511354 | ||||||
| chr11:121511407
|
C | G | 1 | a0006c0043t0026g0215 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.940-1596C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121511407 | ||||||
| chr11:121511463
|
A | T | 85 | a0001c0002t0001g0010a0001c0002t0001g0083a0001c0002t0001g0092others(82): Show | 85 | HG00099.hp2 HG00280.hp2 HG00741.hp2 others(82): Show |
intron_variant | MODIFIER | c.940-1540A>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121511463 | ||||||
| chr11:121511551
|
A | G | 1 | a0002c0005t0003g0159 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.940-1452A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121511551 | ||||||
| chr11:121511978
|
C | T | 8 | a0001c0012t0005g0247a0001c0012t0007g0175a0001c0012t0007g0176others(5): Show | 8 | HG01109.hp2 HG01884.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.940-1025C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121511978 | ||||||
| chr11:121512162
|
A | G | 30 | a0001c0002t0001g0139a0001c0002t0003g0150a0001c0002t0003g0151others(27): Show | 30 | HG00099.hp2 HG01167.hp2 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.940-841A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121512162 | ||||||
| chr11:121512201
|
G | A | 1 | a0001c0022t0008g0211 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.940-802G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121512201 | ||||||
| chr11:121512363
|
T | C | 1 | a0001c0001t0001g0009 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.940-640T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121512363 | ||||||
| chr11:121512439
|
C | T | 3 | a0001c0001t0001g0089a0001c0001t0001g0197a0001c0001t0001g0199 | 3 | HG01175.hp2 HG02300.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.940-564C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121512439 | ||||||
| chr11:121512519
|
A | C | 3 | a0001c0065t0003g0152a0001c0066t0016g0194a0012c0064t0024g0168 | 3 | HG01243.hp1 HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.940-484A>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121512519 | ||||||
| chr11:121512653
|
C | T | 1 | a0001c0046t0002g0174 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.940-350C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121512653 | ||||||
| chr11:121512674
|
C | T | 1 | a0001c0038t0002g0186 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.940-329C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121512674 | ||||||
| chr11:121512722
|
A | T | 3 | a0001c0015t0005g0270a0001c0020t0003g0268a0001c0020t0003g0269 | 3 | HG01099.hp1 HG02486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.940-281A>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121512722 | ||||||
| chr11:121512804
|
C | T | 1 | a0001c0046t0002g0174 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.940-199C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 6/47 | chr11 | 121512804 | ||||||
| chr11:121513156
|
A | C | 1 | a0007c0072t0002g0256 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1041+52A>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 7/47 | chr11 | 121513156 | ||||||
| chr11:121513215
|
C | G | 2 | a0001c0067t0013g0204a0004c0059t0002g0171 | 2 | HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1041+111C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 7/47 | chr11 | 121513215 | ||||||
| chr11:121513637
|
C | T | 1 | a0001c0016t0001g0196 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1042-515C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 7/47 | chr11 | 121513637 | ||||||
| chr11:121513729
|
C | T | 2 | a0001c0003t0007g0264a0001c0003t0007g0265 | 2 | HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1042-423C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 7/47 | chr11 | 121513729 | ||||||
| chr11:121513811
|
G | A | 2 | a0001c0032t0003g0149a0006c0043t0026g0215 | 2 | HG02723.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1042-341G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 7/47 | chr11 | 121513811 | ||||||
| chr11:121513940
|
C | A | 1 | a0001c0003t0002g0115 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1042-212C>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 7/47 | chr11 | 121513940 | ||||||
| chr11:121514000
|
A | C | 1 | a0001c0002t0004g0093 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1042-152A>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 7/47 | chr11 | 121514000 | ||||||
| chr11:121514404
|
T | G | 1 | a0001c0010t0005g0239 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1211+83T>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 8/47 | chr11 | 121514404 | ||||||
| chr11:121514552
|
TCTGAGA | T | 39 | a0001c0002t0001g0010a0001c0002t0001g0083a0001c0002t0001g0092others(36): Show | 39 | HG01167.hp1 HG01256.hp2 HG01258.hp1 others(36): Show |
intron_variant | MODIFIER | c.1211+232_1211+237d others(8): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 8/47 | chr11 | 121514552 | ||||||
| chr11:121514624
|
G | C | 1 | a0001c0033t0003g0169 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1211+303G>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 8/47 | chr11 | 121514624 | ||||||
| chr11:121514834
|
C | A | 1 | a0001c0038t0002g0186 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1211+513C>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 8/47 | chr11 | 121514834 | ||||||
| chr11:121514852
|
G | A | 1 | a0001c0002t0004g0093 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1211+531G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 8/47 | chr11 | 121514852 | ||||||
| chr11:121514924
|
G | A | 1 | a0001c0060t0003g0163 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1211+603G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 8/47 | chr11 | 121514924 | ||||||
| chr11:121515090
|
C | T | 39 | a0001c0002t0001g0010a0001c0002t0001g0083a0001c0002t0001g0092others(36): Show | 39 | HG01167.hp1 HG01256.hp2 HG01258.hp1 others(36): Show |
intron_variant | MODIFIER | c.1211+769C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 8/47 | chr11 | 121515090 | ||||||
| chr11:121515290
|
T | A | 1 | a0001c0033t0003g0169 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1211+969T>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 8/47 | chr11 | 121515290 | ||||||
| chr11:121515324
|
CA | C | 82 | a0001c0002t0001g0010a0001c0002t0001g0083a0001c0002t0001g0092others(79): Show | 82 | HG00099.hp2 HG00741.hp2 HG01074.hp2 others(79): Show |
intron_variant | MODIFIER | c.1211+1004delA | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 8/47 | chr11 | 121515324 | ||||||
| chr11:121515375
|
G | A | 1 | a0001c0021t0003g0216 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1211+1054G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 8/47 | chr11 | 121515375 | ||||||
| chr11:121515444
|
C | T | 1 | a0001c0001t0001g0055 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1211+1123C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 8/47 | chr11 | 121515444 | ||||||
| chr11:121515523
|
A | G | 1 | a0001c0008t0004g0005 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1211+1202A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 8/47 | chr11 | 121515523 | ||||||
| chr11:121515814
|
G | A | 1 | a0001c0022t0008g0211 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1211+1493G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 8/47 | chr11 | 121515814 | ||||||
| chr11:121515944
|
A | G | 1 | a0001c0001t0001g0039 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1211+1623A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 8/47 | chr11 | 121515944 | ||||||
| chr11:121516027
|
G | A | 40 | a0001c0008t0002g0177a0001c0009t0010g0165a0001c0012t0002g0178others(37): Show | 40 | HG00544.hp1 HG00642.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.1211+1706G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 8/47 | chr11 | 121516027 | ||||||
| chr11:121516046
|
A | G | 1 | a0001c0033t0003g0169 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1211+1725A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 8/47 | chr11 | 121516046 | ||||||
| chr11:121516695
|
G | T | 3 | a0001c0001t0001g0089a0001c0001t0001g0197a0001c0001t0001g0199 | 3 | HG01175.hp2 HG02300.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.1211+2374G>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 8/47 | chr11 | 121516695 | ||||||
| chr11:121516919
|
G | A | 1 | a0007c0072t0002g0256 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1211+2598G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 8/47 | chr11 | 121516919 | ||||||
| chr11:121516989
|
A | G | 1 | a0001c0008t0002g0222 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1211+2668A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 8/47 | chr11 | 121516989 | ||||||
| chr11:121517030
|
C | T | 1 | a0001c0013t0002g0035 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1211+2709C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 8/47 | chr11 | 121517030 | ||||||
| chr11:121517031
|
G | A | 1 | a0013c0047t0007g0182 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1211+2710G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 8/47 | chr11 | 121517031 | ||||||
| chr11:121517228
|
T | C | 3 | a0001c0065t0003g0152a0001c0066t0016g0194a0012c0064t0024g0168 | 3 | HG01243.hp1 HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1211+2907T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 8/47 | chr11 | 121517228 | ||||||
| chr11:121517272
|
A | T | 89 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(86): Show | 89 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.1211+2951A>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 8/47 | chr11 | 121517272 | ||||||
| chr11:121517396
|
G | A | 1 | a0001c0028t0001g0046 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1211+3075G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 8/47 | chr11 | 121517396 | ||||||
| chr11:121517551
|
A | G | 1 | a0001c0033t0003g0169 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1212-3106A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 8/47 | chr11 | 121517551 | ||||||
| chr11:121517677
|
G | T | 2 | a0001c0008t0002g0177a0001c0012t0002g0178 | 2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1212-2980G>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 8/47 | chr11 | 121517677 | ||||||
| chr11:121517998
|
T | C | 1 | a0001c0002t0006g0014 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1212-2659T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 8/47 | chr11 | 121517998 | ||||||
| chr11:121518262
|
G | T | 1 | a0001c0003t0003g0254 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1212-2395G>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 8/47 | chr11 | 121518262 | ||||||
| chr11:121518527
|
A | T | 1 | a0001c0058t0011g0166 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1212-2130A>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 8/47 | chr11 | 121518527 | ||||||
| chr11:121518793
|
T | G | 45 | a0001c0001t0001g0057a0001c0002t0001g0112a0001c0002t0001g0116others(42): Show | 46 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.1212-1864T>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 8/47 | chr11 | 121518793 | ||||||
| chr11:121518831
|
T | C | 1 | a0001c0001t0001g0006 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1212-1826T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 8/47 | chr11 | 121518831 | ||||||
| chr11:121518833
|
C | CA | 4 | a0001c0009t0010g0165a0001c0065t0003g0152a0001c0066t0016g0194others(1): Show | 4 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1212-1823dupA | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 8/47 | INFO_REALIGN_3_PRIME | chr11 | 121518833 | |||||
| chr11:121518951
|
CT | C | 46 | a0001c0002t0003g0150a0001c0003t0002g0229a0001c0004t0003g0224others(43): Show | 46 | HG00544.hp1 HG00642.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.1212-1691delT | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 8/47 | INFO_REALIGN_3_PRIME | chr11 | 121518951 | |||||
| chr11:121519051
|
G | A | 1 | a0001c0032t0003g0149 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1212-1606G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 8/47 | chr11 | 121519051 | ||||||
| chr11:121519301
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1212-1356C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 8/47 | chr11 | 121519301 | ||||||
| chr11:121519305
|
C | G | 1 | a0001c0009t0008g0207 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1212-1352C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 8/47 | chr11 | 121519305 | ||||||
| chr11:121519371
|
C | T | 1 | a0001c0002t0006g0114 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1212-1286C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 8/47 | chr11 | 121519371 | ||||||
| chr11:121519374
|
A | G | 1 | a0001c0009t0008g0207 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1212-1283A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 8/47 | chr11 | 121519374 | ||||||
| chr11:121519393
|
A | G | 1 | a0001c0009t0010g0165 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1212-1264A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 8/47 | chr11 | 121519393 | ||||||
| chr11:121519438
|
C | T | 1 | a0001c0021t0003g0216 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1212-1219C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 8/47 | chr11 | 121519438 | ||||||
| chr11:121519474
|
C | T | 38 | a0001c0001t0001g0059a0001c0002t0001g0010a0001c0002t0001g0083others(35): Show | 38 | HG01167.hp1 HG01256.hp2 HG01258.hp1 others(35): Show |
intron_variant | MODIFIER | c.1212-1183C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 8/47 | chr11 | 121519474 | ||||||
| chr11:121519634
|
G | A | 6 | a0001c0003t0003g0262a0001c0003t0005g0226a0001c0003t0005g0228others(3): Show | 6 | HG02257.hp1 HG02451.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1212-1023G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 8/47 | chr11 | 121519634 | ||||||
| chr11:121519970
|
G | C | 1 | a0001c0012t0007g0244 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1212-687G>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 8/47 | chr11 | 121519970 | ||||||
| chr11:121520095
|
T | TA | 5 | a0001c0003t0002g0229a0001c0011t0001g0107a0001c0011t0002g0271others(2): Show | 5 | HG00741.hp2 HG01074.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.1212-554dupA | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 8/47 | INFO_REALIGN_3_PRIME | chr11 | 121520095 | |||||
| chr11:121520192
|
G | T | 1 | a0001c0009t0008g0207 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1212-465G>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 8/47 | chr11 | 121520192 | ||||||
| chr11:121520369
|
A | G | 35 | a0001c0002t0003g0150a0002c0005t0001g0008a0002c0005t0001g0032others(32): Show | 35 | HG00544.hp1 HG00642.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.1212-288A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 8/47 | chr11 | 121520369 | ||||||
| chr11:121520460
|
G | A | 1 | a0001c0009t0010g0165 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1212-197G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 8/47 | chr11 | 121520460 | ||||||
| chr11:121520956
|
G | A | 1 | a0010c0037t0005g0259 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1404+107G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 9/47 | chr11 | 121520956 | ||||||
| chr11:121521025
|
T | C | 3 | a0001c0060t0003g0163a0001c0067t0013g0204a0004c0059t0002g0171 | 3 | HG02559.hp2 HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1404+176T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 9/47 | chr11 | 121521025 | ||||||
| chr11:121521064
|
GA | G | 126 | a0001c0001t0001g0059a0001c0002t0001g0010a0001c0002t0001g0083others(123): Show | 126 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.1404+231delA | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 9/47 | INFO_REALIGN_3_PRIME | chr11 | 121521064 | |||||
| chr11:121521064
|
GAA | G | 47 | a0001c0001t0001g0057a0001c0002t0001g0112a0001c0002t0001g0116others(44): Show | 48 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.1404+230_1404+231d others(4): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 9/47 | INFO_REALIGN_3_PRIME | chr11 | 121521064 | |||||
| chr11:121521218
|
T | G | 3 | a0001c0008t0002g0177a0001c0012t0002g0178a0007c0072t0002g0256 | 3 | HG02622.hp2 HG03098.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1404+369T>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 9/47 | chr11 | 121521218 | ||||||
| chr11:121521600
|
A | G | 1 | a0001c0035t0001g0071 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1404+751A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 9/47 | chr11 | 121521600 | ||||||
| chr11:121522095
|
A | T | 1 | a0002c0007t0001g0124 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1405-491A>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 9/47 | chr11 | 121522095 | ||||||
| chr11:121522193
|
A | G | 1 | a0001c0032t0003g0149 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1405-393A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 9/47 | chr11 | 121522193 | ||||||
| chr11:121522444
|
C | T | 1 | a0001c0046t0002g0174 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1405-142C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 9/47 | chr11 | 121522444 | ||||||
| chr11:121522466
|
C | A | 5 | a0001c0012t0005g0247a0001c0020t0003g0248a0001c0061t0030g0249others(2): Show | 5 | HG01109.hp2 HG02559.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1405-120C>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 9/47 | chr11 | 121522466 | ||||||
| chr11:121522489
|
G | A | 3 | a0001c0065t0003g0152a0001c0066t0016g0194a0012c0064t0024g0168 | 3 | HG01243.hp1 HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1405-97G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 9/47 | chr11 | 121522489 | ||||||
| chr11:121522503
|
C | G | 262 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(259): Show | 263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.1405-83C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 9/47 | chr11 | 121522503 | ||||||
| chr11:121522517
|
C | T | 35 | a0001c0009t0010g0165a0002c0005t0001g0008a0002c0005t0001g0032others(32): Show | 35 | HG00544.hp1 HG00642.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.1405-69C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 9/47 | chr11 | 121522517 | ||||||
| chr11:121522741
|
G | A | 35 | a0001c0009t0010g0165a0002c0005t0001g0008a0002c0005t0001g0032others(32): Show | 35 | HG00544.hp1 HG00642.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.1522+38G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 10/47 | chr11 | 121522741 | ||||||
| chr11:121522798
|
C | T | 3 | a0001c0060t0003g0163a0001c0067t0013g0204a0004c0059t0002g0171 | 3 | HG02559.hp2 HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1522+95C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 10/47 | chr11 | 121522798 | ||||||
| chr11:121523093
|
A | G | 1 | a0010c0037t0005g0259 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1596+104A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121523093 | ||||||
| chr11:121523190
|
A | G | 1 | a0001c0003t0002g0117 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1596+201A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121523190 | ||||||
| chr11:121523370
|
GGCT | G | 3 | a0001c0009t0008g0207a0001c0009t0011g0170a0001c0009t0011g0255 | 3 | HG02486.hp2 HG03139.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1596+385_1596+387d others(5): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | INFO_REALIGN_3_PRIME | chr11 | 121523370 | |||||
| chr11:121523482
|
T | G | 1 | a0001c0032t0003g0149 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1596+493T>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121523482 | ||||||
| chr11:121523578
|
C | T | 48 | a0001c0001t0001g0057a0001c0002t0001g0112a0001c0002t0001g0116others(45): Show | 49 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.1596+589C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121523578 | ||||||
| chr11:121523802
|
C | T | 86 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(83): Show | 86 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.1596+813C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121523802 | ||||||
| chr11:121523928
|
C | G | 1 | a0001c0018t0002g0081 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1596+939C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121523928 | ||||||
| chr11:121524031
|
G | C | 37 | a0001c0002t0001g0010a0001c0002t0001g0083a0001c0002t0001g0092others(34): Show | 37 | HG01167.hp1 HG01256.hp2 HG01258.hp1 others(34): Show |
intron_variant | MODIFIER | c.1596+1042G>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121524031 | ||||||
| chr11:121524065
|
T | C | 262 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(259): Show | 263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.1596+1076T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121524065 | ||||||
| chr11:121524069
|
C | T | 2 | a0002c0025t0003g0260a0002c0049t0003g0162 | 2 | HG01891.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1596+1080C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121524069 | ||||||
| chr11:121524139
|
A | G | 1 | a0007c0072t0002g0256 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1596+1150A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121524139 | ||||||
| chr11:121524193
|
C | A | 2 | a0001c0003t0002g0101a0001c0004t0001g0100 | 2 | HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1596+1204C>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121524193 | ||||||
| chr11:121524215
|
C | T | 1 | a0001c0001t0004g0099 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1596+1226C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121524215 | ||||||
| chr11:121524269
|
C | T | 2 | a0001c0003t0003g0254a0006c0043t0026g0215 | 2 | HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1596+1280C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121524269 | ||||||
| chr11:121524325
|
G | A | 1 | a0001c0001t0001g0057 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1596+1336G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121524325 | ||||||
| chr11:121524398
|
C | T | 1 | a0001c0003t0018g0191 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1596+1409C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121524398 | ||||||
| chr11:121524410
|
G | A | 1 | a0006c0055t0002g0246 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1596+1421G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121524410 | ||||||
| chr11:121524509
|
G | A | 1 | a0002c0005t0009g0041 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1596+1520G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121524509 | ||||||
| chr11:121524719
|
C | T | 265 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(262): Show | 266 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.1596+1730C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121524719 | ||||||
| chr11:121524904
|
G | A | 69 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(66): Show | 69 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.1596+1915G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121524904 | ||||||
| chr11:121525047
|
C | T | 3 | a0001c0065t0003g0152a0001c0066t0016g0194a0012c0064t0024g0168 | 3 | HG01243.hp1 HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1596+2058C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121525047 | ||||||
| chr11:121525081
|
C | T | 92 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(89): Show | 92 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.1596+2092C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121525081 | ||||||
| chr11:121525127
|
A | G | 1 | a0002c0026t0005g0161 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1596+2138A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121525127 | ||||||
| chr11:121525420
|
T | C | 1 | a0001c0046t0002g0174 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1596+2431T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121525420 | ||||||
| chr11:121525699
|
A | G | 1 | a0001c0016t0001g0196 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1596+2710A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121525699 | ||||||
| chr11:121525902
|
C | T | 34 | a0002c0005t0001g0008a0002c0005t0001g0032a0002c0005t0001g0042others(31): Show | 34 | HG00544.hp1 HG00642.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.1596+2913C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121525902 | ||||||
| chr11:121525903
|
C | A | 34 | a0002c0005t0001g0008a0002c0005t0001g0032a0002c0005t0001g0042others(31): Show | 34 | HG00544.hp1 HG00642.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.1596+2914C>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121525903 | ||||||
| chr11:121526011
|
G | A | 8 | a0001c0003t0002g0229a0001c0004t0003g0224a0001c0011t0001g0107others(5): Show | 8 | HG00741.hp2 HG01074.hp2 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.1596+3022G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121526011 | ||||||
| chr11:121526500
|
G | C | 2 | a0008c0024t0002g0033a0008c0024t0002g0034 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1596+3511G>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121526500 | ||||||
| chr11:121526570
|
A | G | 3 | a0001c0065t0003g0152a0001c0066t0016g0194a0012c0064t0024g0168 | 3 | HG01243.hp1 HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1596+3581A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121526570 | ||||||
| chr11:121526605
|
T | C | 1 | a0001c0004t0003g0224 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1596+3616T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121526605 | ||||||
| chr11:121526628
|
C | T | 3 | a0001c0009t0008g0207a0001c0009t0011g0170a0001c0009t0011g0255 | 3 | HG02486.hp2 HG03139.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1596+3639C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121526628 | ||||||
| chr11:121526660
|
G | A | 3 | a0001c0008t0002g0177a0001c0058t0011g0166a0007c0072t0002g0256 | 3 | HG02622.hp2 NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1596+3671G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121526660 | ||||||
| chr11:121526756
|
A | G | 265 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(262): Show | 266 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.1596+3767A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121526756 | ||||||
| chr11:121526929
|
CTCT | C | 4 | a0001c0022t0008g0211a0001c0060t0003g0163a0001c0067t0013g0204others(1): Show | 4 | HG02559.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1596+3946_1596+394 others(7): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | INFO_REALIGN_3_PRIME | chr11 | 121526929 | |||||
| chr11:121527004
|
A | G | 1 | a0001c0058t0011g0166 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1596+4015A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121527004 | ||||||
| chr11:121527124
|
A | G | 42 | a0001c0001t0001g0059a0001c0002t0001g0010a0001c0002t0001g0083others(39): Show | 42 | HG01167.hp1 HG01243.hp1 HG01256.hp2 others(39): Show |
intron_variant | MODIFIER | c.1596+4135A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121527124 | ||||||
| chr11:121527197
|
A | AT | 216 | a0001c0001t0001g0006a0001c0001t0001g0023a0001c0001t0001g0024others(213): Show | 217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.1596+4219dupT | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | INFO_REALIGN_3_PRIME | chr11 | 121527197 | |||||
| chr11:121527724
|
T | C | 1 | a0001c0019t0001g0028 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1596+4735T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121527724 | ||||||
| chr11:121527729
|
C | T | 26 | a0001c0001t0001g0057a0001c0002t0003g0151a0001c0003t0002g0105others(23): Show | 26 | HG00099.hp2 HG01167.hp2 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.1597-4735C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121527729 | ||||||
| chr11:121527801
|
T | G | 35 | a0001c0001t0002g0004a0001c0001t0002g0125a0001c0002t0001g0139others(32): Show | 35 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.1597-4663T>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121527801 | ||||||
| chr11:121527869
|
G | A | 149 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(146): Show | 149 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.1597-4595G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121527869 | ||||||
| chr11:121528039
|
A | T | 1 | a0001c0003t0018g0191 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1597-4425A>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121528039 | ||||||
| chr11:121528116
|
A | G | 1 | a0001c0003t0007g0261 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1597-4348A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121528116 | ||||||
| chr11:121528194
|
C | T | 1 | a0005c0017t0001g0240 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1597-4270C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121528194 | ||||||
| chr11:121528200
|
G | A | 1 | a0001c0004t0002g0134 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1597-4264G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121528200 | ||||||
| chr11:121528256
|
A | G | 265 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(262): Show | 266 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.1597-4208A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121528256 | ||||||
| chr11:121528350
|
T | C | 6 | a0001c0013t0002g0054a0001c0015t0001g0022a0001c0019t0001g0028others(3): Show | 6 | NA18955.hp2 NA18984.hp1 NA18989.hp2 others(3): Show |
intron_variant | MODIFIER | c.1597-4114T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121528350 | ||||||
| chr11:121528358
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1597-4106C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121528358 | ||||||
| chr11:121528445
|
C | T | 3 | a0001c0022t0008g0211a0001c0060t0003g0163a0004c0059t0002g0171 | 3 | HG02559.hp2 HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1597-4019C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121528445 | ||||||
| chr11:121528451
|
C | T | 1 | a0004c0056t0013g0148 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1597-4013C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121528451 | ||||||
| chr11:121528452
|
G | A | 1 | a0001c0002t0001g0010 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1597-4012G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121528452 | ||||||
| chr11:121528568
|
A | T | 45 | a0001c0002t0001g0112a0001c0002t0001g0116a0001c0002t0001g0158others(42): Show | 46 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.1597-3896A>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121528568 | ||||||
| chr11:121528715
|
A | G | 4 | a0001c0065t0003g0152a0001c0066t0016g0194a0001c0067t0013g0204others(1): Show | 4 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1597-3749A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121528715 | ||||||
| chr11:121528892
|
A | G | 2 | a0001c0008t0002g0177a0007c0072t0002g0256 | 2 | HG02622.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1597-3572A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121528892 | ||||||
| chr11:121529162
|
T | A | 3 | a0001c0022t0008g0211a0001c0060t0003g0163a0004c0059t0002g0171 | 3 | HG02559.hp2 HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1597-3302T>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121529162 | ||||||
| chr11:121529257
|
C | T | 2 | a0001c0002t0004g0143a0001c0004t0001g0144 | 2 | NA18991.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.1597-3207C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121529257 | ||||||
| chr11:121529448
|
C | A | 1 | a0001c0039t0002g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1597-3016C>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121529448 | ||||||
| chr11:121529753
|
C | T | 3 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0008t0002g0131 | 3 | HG00735.hp2 HG01081.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1597-2711C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121529753 | ||||||
| chr11:121529913
|
A | C | 2 | a0001c0003t0003g0254a0006c0043t0026g0215 | 2 | HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1597-2551A>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121529913 | ||||||
| chr11:121529936
|
C | T | 2 | a0001c0002t0003g0150a0001c0032t0003g0149 | 2 | HG02109.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1597-2528C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121529936 | ||||||
| chr11:121529967
|
A | G | 1 | a0001c0018t0002g0156 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1597-2497A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121529967 | ||||||
| chr11:121530003
|
A | T | 2 | a0001c0003t0003g0254a0006c0043t0026g0215 | 2 | HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1597-2461A>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121530003 | ||||||
| chr11:121530053
|
C | T | 34 | a0001c0001t0002g0004a0001c0001t0002g0125a0001c0002t0001g0139others(31): Show | 34 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.1597-2411C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121530053 | ||||||
| chr11:121530148
|
A | C | 32 | a0001c0001t0001g0057a0001c0002t0003g0151a0001c0003t0002g0105others(29): Show | 32 | HG00099.hp2 HG01167.hp2 HG01169.hp1 others(29): Show |
intron_variant | MODIFIER | c.1597-2316A>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121530148 | ||||||
| chr11:121530348
|
CTT | C | 26 | a0001c0001t0001g0057a0001c0002t0003g0151a0001c0003t0002g0105others(23): Show | 26 | HG00099.hp2 HG01167.hp2 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.1597-2115_1597-211 others(6): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121530348 | ||||||
| chr11:121530839
|
G | A | 4 | a0001c0065t0003g0152a0001c0066t0016g0194a0001c0067t0013g0204others(1): Show | 4 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1597-1625G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121530839 | ||||||
| chr11:121530961
|
C | T | 1 | a0001c0001t0004g0099 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1597-1503C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121530961 | ||||||
| chr11:121530973
|
T | G | 6 | a0002c0014t0002g0172a0002c0025t0003g0260a0002c0025t0005g0179others(3): Show | 6 | HG01891.hp2 HG02647.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1597-1491T>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121530973 | ||||||
| chr11:121531162
|
G | A | 1 | a0001c0057t0002g0160 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1597-1302G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121531162 | ||||||
| chr11:121531293
|
T | C | 11 | a0001c0003t0003g0262a0001c0003t0005g0226a0001c0003t0005g0228others(8): Show | 11 | HG01496.hp1 HG02257.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1597-1171T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121531293 | ||||||
| chr11:121531318
|
C | T | 1 | a0001c0008t0002g0177 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1597-1146C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121531318 | ||||||
| chr11:121531376
|
A | C | 39 | a0001c0001t0001g0057a0001c0002t0003g0151a0001c0003t0002g0105others(36): Show | 39 | HG00099.hp2 HG00741.hp2 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.1597-1088A>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121531376 | ||||||
| chr11:121531377
|
G | C | 1 | a0004c0059t0002g0171 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1597-1087G>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121531377 | ||||||
| chr11:121531401
|
A | G | 35 | a0001c0001t0002g0004a0001c0002t0001g0139a0001c0002t0003g0150others(32): Show | 35 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.1597-1063A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121531401 | ||||||
| chr11:121531430
|
G | T | 1 | a0002c0005t0019g0062 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1597-1034G>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121531430 | ||||||
| chr11:121531500
|
G | A | 34 | a0001c0001t0001g0059a0001c0002t0001g0010a0001c0002t0001g0083others(31): Show | 34 | HG01496.hp2 HG02027.hp1 HG02040.hp1 others(31): Show |
intron_variant | MODIFIER | c.1597-964G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121531500 | ||||||
| chr11:121531676
|
T | C | 27 | a0001c0001t0001g0057a0001c0002t0003g0151a0001c0003t0002g0105others(24): Show | 27 | HG00099.hp2 HG01167.hp2 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.1597-788T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121531676 | ||||||
| chr11:121531682
|
A | C | 1 | a0001c0038t0002g0186 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1597-782A>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121531682 | ||||||
| chr11:121531931
|
C | T | 2 | a0001c0003t0003g0254a0006c0043t0026g0215 | 2 | HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1597-533C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121531931 | ||||||
| chr11:121531932
|
G | A | 13 | a0001c0003t0002g0229a0001c0003t0007g0261a0001c0010t0003g0257others(10): Show | 13 | HG00741.hp2 HG01074.hp2 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.1597-532G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121531932 | ||||||
| chr11:121531934
|
G | A | 94 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(91): Show | 94 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.1597-530G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 11/47 | chr11 | 121531934 | ||||||
| chr11:121532636
|
T | C | 264 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(261): Show | 265 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.1685+84T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121532636 | ||||||
| chr11:121532687
|
CT | C | 6 | a0001c0002t0004g0090a0001c0016t0012g0210a0001c0022t0008g0211others(3): Show | 6 | HG00323.hp1 HG02559.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.1685+151delT | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | INFO_REALIGN_3_PRIME | chr11 | 121532687 | |||||
| chr11:121532784
|
G | A | 1 | a0001c0038t0002g0186 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1685+232G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121532784 | ||||||
| chr11:121533110
|
G | T | 1 | a0001c0003t0019g0209 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1685+558G>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121533110 | ||||||
| chr11:121533138
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1685+586A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121533138 | ||||||
| chr11:121533161
|
CAAT | C | 13 | a0001c0003t0002g0229a0001c0003t0007g0261a0001c0010t0003g0257others(10): Show | 13 | HG00741.hp2 HG01074.hp2 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.1685+626_1685+628d others(5): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | INFO_REALIGN_3_PRIME | chr11 | 121533161 | |||||
| chr11:121533175
|
A | T | 1 | a0001c0004t0001g0144 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1685+623A>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121533175 | ||||||
| chr11:121533717
|
G | T | 1 | a0001c0020t0003g0269 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1685+1165G>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121533717 | ||||||
| chr11:121533842
|
T | C | 4 | a0001c0022t0008g0211a0001c0060t0003g0163a0004c0059t0002g0171others(1): Show | 4 | HG02559.hp2 HG02922.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1685+1290T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121533842 | ||||||
| chr11:121533941
|
G | T | 1 | a0001c0016t0002g0044 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1685+1389G>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121533941 | ||||||
| chr11:121534105
|
G | A | 1 | a0001c0038t0002g0186 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1685+1553G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121534105 | ||||||
| chr11:121534354
|
G | A | 2 | a0001c0009t0011g0170a0001c0009t0011g0255 | 2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1685+1802G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121534354 | ||||||
| chr11:121534556
|
C | T | 2 | a0001c0001t0002g0185a0001c0057t0002g0160 | 2 | HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1685+2004C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121534556 | ||||||
| chr11:121534906
|
A | G | 2 | a0001c0033t0003g0169a0001c0046t0002g0174 | 2 | HG03540.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1685+2354A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121534906 | ||||||
| chr11:121535019
|
G | A | 1 | a0001c0016t0002g0121 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1685+2467G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121535019 | ||||||
| chr11:121535089
|
GT | G | 140 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.1685+2550delT | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | INFO_REALIGN_3_PRIME | chr11 | 121535089 | |||||
| chr11:121535130
|
G | T | 264 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(261): Show | 265 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.1685+2578G>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121535130 | ||||||
| chr11:121535195
|
C | G | 4 | a0001c0065t0003g0152a0001c0066t0016g0194a0001c0067t0013g0204others(1): Show | 4 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1685+2643C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121535195 | ||||||
| chr11:121535326
|
A | C | 2 | a0001c0061t0030g0249a0001c0062t0003g0250 | 2 | HG02559.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1685+2774A>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121535326 | ||||||
| chr11:121535395
|
C | T | 1 | a0001c0009t0010g0165 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1685+2843C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121535395 | ||||||
| chr11:121535440
|
C | G | 5 | a0001c0008t0002g0177a0001c0009t0008g0207a0001c0009t0011g0170others(2): Show | 5 | HG02486.hp2 HG02622.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1685+2888C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121535440 | ||||||
| chr11:121535486
|
G | T | 1 | a0001c0001t0001g0052 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1685+2934G>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121535486 | ||||||
| chr11:121535670
|
G | GT | 48 | a0001c0002t0001g0112a0001c0002t0001g0116a0001c0002t0001g0158others(45): Show | 49 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.1685+3132dupT | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | INFO_REALIGN_3_PRIME | chr11 | 121535670 | |||||
| chr11:121535999
|
T | C | 14 | a0001c0001t0001g0057a0001c0002t0003g0151a0001c0003t0002g0105others(11): Show | 14 | HG00099.hp2 HG01167.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.1685+3447T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121535999 | ||||||
| chr11:121536047
|
G | A | 1 | a0001c0008t0002g0131 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1685+3495G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121536047 | ||||||
| chr11:121536075
|
G | C | 1 | a0001c0003t0002g0115 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1685+3523G>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121536075 | ||||||
| chr11:121536286
|
G | A | 1 | a0001c0006t0001g0068 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1685+3734G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121536286 | ||||||
| chr11:121536427
|
G | GT | 13 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0051others(10): Show | 13 | HG01099.hp2 HG03516.hp1 HG03516.hp2 others(10): Show |
intron_variant | MODIFIER | c.1685+3894dupT | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | INFO_REALIGN_3_PRIME | chr11 | 121536427 | |||||
| chr11:121536427
|
G | T | 38 | a0001c0001t0001g0059a0001c0002t0001g0010a0001c0002t0001g0083others(35): Show | 38 | HG00280.hp2 HG01496.hp2 HG02027.hp1 others(35): Show |
intron_variant | MODIFIER | c.1685+3875G>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121536427 | ||||||
| chr11:121536427
|
GT | G | 14 | a0001c0003t0002g0229a0001c0003t0007g0261a0001c0004t0001g0236others(11): Show | 14 | HG00323.hp2 HG00741.hp2 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.1685+3894delT | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | INFO_REALIGN_3_PRIME | chr11 | 121536427 | |||||
| chr11:121536576
|
C | CT | 82 | a0001c0001t0001g0059a0001c0001t0001g0075a0001c0002t0001g0010others(79): Show | 83 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.1685+4037dupT | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | INFO_REALIGN_3_PRIME | chr11 | 121536576 | |||||
| chr11:121536823
|
A | C | 6 | a0001c0002t0004g0077a0001c0002t0004g0078a0001c0002t0004g0079others(3): Show | 6 | NA18965.hp1 NA18966.hp1 NA18985.hp2 others(3): Show |
intron_variant | MODIFIER | c.1685+4271A>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121536823 | ||||||
| chr11:121537049
|
G | A | 1 | a0001c0016t0001g0196 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1685+4497G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121537049 | ||||||
| chr11:121537169
|
C | T | 1 | a0001c0003t0003g0254 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1685+4617C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121537169 | ||||||
| chr11:121537246
|
T | C | 13 | a0001c0003t0002g0229a0001c0003t0007g0261a0001c0010t0003g0257others(10): Show | 13 | HG00741.hp2 HG01074.hp2 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.1685+4694T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121537246 | ||||||
| chr11:121537504
|
A | G | 1 | a0001c0001t0001g0038 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1685+4952A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121537504 | ||||||
| chr11:121537587
|
T | C | 2 | a0001c0009t0011g0170a0001c0009t0011g0255 | 2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1685+5035T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121537587 | ||||||
| chr11:121537662
|
G | C | 1 | a0002c0026t0005g0161 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1685+5110G>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121537662 | ||||||
| chr11:121537896
|
A | G | 1 | a0001c0038t0002g0186 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1685+5344A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121537896 | ||||||
| chr11:121537985
|
T | C | 264 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(261): Show | 265 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.1685+5433T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121537985 | ||||||
| chr11:121538056
|
C | T | 1 | a0001c0002t0006g0104 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1686-5492C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121538056 | ||||||
| chr11:121538176
|
G | A | 2 | a0001c0033t0003g0169a0001c0046t0002g0174 | 2 | HG03540.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1686-5372G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121538176 | ||||||
| chr11:121538183
|
A | AT | 248 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(245): Show | 249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.1686-5352dupT | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | INFO_REALIGN_3_PRIME | chr11 | 121538183 | |||||
| chr11:121538183
|
A | ATT | 12 | a0001c0065t0003g0152a0001c0066t0016g0194a0001c0067t0013g0204others(9): Show | 12 | HG00544.hp1 HG00738.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.1686-5353_1686-535 others(6): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | INFO_REALIGN_3_PRIME | chr11 | 121538183 | |||||
| chr11:121538247
|
C | G | 129 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(126): Show | 129 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.1686-5301C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121538247 | ||||||
| chr11:121538314
|
C | T | 1 | a0001c0001t0001g0197 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1686-5234C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121538314 | ||||||
| chr11:121538345
|
C | G | 4 | a0001c0003t0001g0019a0001c0004t0001g0110a0001c0004t0001g0236others(1): Show | 4 | HG00280.hp1 HG00323.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.1686-5203C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121538345 | ||||||
| chr11:121538357
|
C | T | 1 | a0001c0022t0003g0213 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1686-5191C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121538357 | ||||||
| chr11:121538510
|
T | C | 2 | a0001c0001t0001g0057a0001c0006t0028g0031 | 2 | HG02735.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1686-5038T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121538510 | ||||||
| chr11:121538549
|
A | T | 2 | a0001c0001t0001g0023a0001c0001t0001g0055 | 2 | NA18939.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.1686-4999A>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121538549 | ||||||
| chr11:121538699
|
G | A | 1 | a0001c0002t0001g0112 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1686-4849G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121538699 | ||||||
| chr11:121538778
|
A | G | 4 | a0001c0001t0001g0059a0001c0004t0002g0132a0001c0011t0012g0242others(1): Show | 4 | HG00280.hp2 HG04115.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.1686-4770A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121538778 | ||||||
| chr11:121538782
|
G | A | 2 | a0001c0001t0001g0059a0001c0004t0002g0132 | 2 | HG04115.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1686-4766G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121538782 | ||||||
| chr11:121538871
|
G | A | 1 | a0001c0002t0001g0188 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1686-4677G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121538871 | ||||||
| chr11:121538919
|
C | T | 2 | a0001c0009t0011g0170a0001c0009t0011g0255 | 2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1686-4629C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121538919 | ||||||
| chr11:121539205
|
A | G | 130 | a0001c0001t0001g0059a0001c0001t0002g0004a0001c0001t0002g0125others(127): Show | 131 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.1686-4343A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121539205 | ||||||
| chr11:121539270
|
G | T | 38 | a0001c0002t0001g0112a0001c0002t0001g0116a0001c0002t0001g0158others(35): Show | 39 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.1686-4278G>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121539270 | ||||||
| chr11:121539302
|
A | G | 1 | a0001c0046t0002g0174 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1686-4246A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121539302 | ||||||
| chr11:121539452
|
C | T | 264 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(261): Show | 265 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.1686-4096C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121539452 | ||||||
| chr11:121539591
|
T | C | 1 | a0001c0060t0003g0163 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1686-3957T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121539591 | ||||||
| chr11:121539617
|
AT | A | 15 | a0001c0003t0002g0229a0001c0003t0007g0261a0001c0009t0011g0170others(12): Show | 15 | HG00741.hp2 HG01074.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.1686-3923delT | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | INFO_REALIGN_3_PRIME | chr11 | 121539617 | |||||
| chr11:121539629
|
C | G | 38 | a0001c0001t0001g0059a0001c0002t0001g0010a0001c0002t0001g0083others(35): Show | 38 | HG00280.hp2 HG01496.hp2 HG02027.hp1 others(35): Show |
intron_variant | MODIFIER | c.1686-3919C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121539629 | ||||||
| chr11:121539659
|
G | A | 1 | a0001c0001t0001g0040 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1686-3889G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121539659 | ||||||
| chr11:121539668
|
CT | C | 4 | a0001c0065t0003g0152a0001c0066t0016g0194a0001c0067t0013g0204others(1): Show | 4 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1686-3871delT | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | INFO_REALIGN_3_PRIME | chr11 | 121539668 | |||||
| chr11:121539988
|
T | C | 1 | a0001c0008t0002g0177 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1686-3560T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121539988 | ||||||
| chr11:121540103
|
T | C | 1 | a0002c0005t0001g0127 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1686-3445T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121540103 | ||||||
| chr11:121540332
|
A | G | 136 | a0001c0001t0001g0059a0001c0001t0002g0004a0001c0001t0002g0125others(133): Show | 137 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.1686-3216A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121540332 | ||||||
| chr11:121540403
|
G | A | 106 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(103): Show | 106 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.1686-3145G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121540403 | ||||||
| chr11:121540419
|
G | A | 1 | a0002c0030t0002g0212 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1686-3129G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121540419 | ||||||
| chr11:121540522
|
C | CA | 108 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(105): Show | 108 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.1686-3012dupA | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | INFO_REALIGN_3_PRIME | chr11 | 121540522 | |||||
| chr11:121540522
|
C | CAAAAAAA others(4): Show |
1 | a0001c0016t0002g0044 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1686-3022_1686-301 others(15): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | INFO_REALIGN_3_PRIME | chr11 | 121540522 | |||||
| chr11:121540522
|
C | CAAAAAAA others(8): Show |
1 | a0001c0002t0004g0007 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1686-3012_1686-301 others(19): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | INFO_REALIGN_3_PRIME | chr11 | 121540522 | |||||
| chr11:121540522
|
C | CAAAAAAA others(9): Show |
25 | a0001c0001t0001g0059a0001c0002t0001g0010a0001c0002t0001g0083others(22): Show | 25 | HG01496.hp2 HG02148.hp1 HG02273.hp1 others(22): Show |
intron_variant | MODIFIER | c.1686-3012_1686-301 others(20): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | INFO_REALIGN_3_PRIME | chr11 | 121540522 | |||||
| chr11:121540522
|
C | CAAAAAAA others(10): Show |
11 | a0001c0002t0001g0103a0001c0002t0004g0003a0001c0002t0004g0078others(8): Show | 11 | HG02027.hp1 HG02040.hp1 HG03540.hp2 others(8): Show |
intron_variant | MODIFIER | c.1686-3012_1686-301 others(21): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | INFO_REALIGN_3_PRIME | chr11 | 121540522 | |||||
| chr11:121540522
|
C | CAAAAAAA others(11): Show |
10 | a0001c0031t0010g0214a0001c0033t0003g0169a0001c0058t0011g0166others(7): Show | 10 | HG00738.hp2 HG01952.hp1 HG02273.hp2 others(7): Show |
intron_variant | MODIFIER | c.1686-3012_1686-301 others(22): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | INFO_REALIGN_3_PRIME | chr11 | 121540522 | |||||
| chr11:121540522
|
C | CAAAAAAA others(12): Show |
45 | a0001c0002t0001g0112a0001c0002t0001g0235a0001c0002t0003g0150others(42): Show | 46 | HG00280.hp2 HG00544.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.1686-3012_1686-301 others(23): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | INFO_REALIGN_3_PRIME | chr11 | 121540522 | |||||
| chr11:121540522
|
C | CAAAAAAA others(13): Show |
20 | a0001c0001t0002g0004a0001c0002t0001g0116a0001c0002t0001g0158others(17): Show | 20 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(17): Show |
intron_variant | MODIFIER | c.1686-3012_1686-301 others(24): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | INFO_REALIGN_3_PRIME | chr11 | 121540522 | |||||
| chr11:121540522
|
C | CAAAAAAA others(14): Show |
4 | a0001c0002t0001g0139a0001c0003t0018g0191a0001c0065t0003g0152others(1): Show | 4 | HG01099.hp2 HG02647.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.1686-3012_1686-301 others(25): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | INFO_REALIGN_3_PRIME | chr11 | 121540522 | |||||
| chr11:121540522
|
C | CAAAAAAA others(15): Show |
7 | a0001c0010t0003g0257a0001c0010t0003g0258a0001c0036t0003g0266others(4): Show | 7 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1686-3012_1686-301 others(26): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | INFO_REALIGN_3_PRIME | chr11 | 121540522 | |||||
| chr11:121540522
|
C | CAAAAAAA others(16): Show |
5 | a0001c0011t0002g0271a0001c0012t0002g0178a0001c0039t0002g0267others(2): Show | 5 | HG01074.hp2 HG02818.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1686-3012_1686-301 others(27): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | INFO_REALIGN_3_PRIME | chr11 | 121540522 | |||||
| chr11:121540522
|
C | CAAAAAAA others(17): Show |
3 | a0001c0003t0002g0229a0001c0011t0020g0106a0001c0045t0020g0102 | 3 | HG00741.hp2 HG01192.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1686-3012_1686-301 others(28): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | INFO_REALIGN_3_PRIME | chr11 | 121540522 | |||||
| chr11:121540522
|
C | CAAAAAAA others(20): Show |
1 | a0001c0011t0001g0107 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1686-3012_1686-301 others(31): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | INFO_REALIGN_3_PRIME | chr11 | 121540522 | |||||
| chr11:121541203
|
C | CT | 93 | a0001c0001t0001g0059a0001c0001t0002g0004a0001c0001t0002g0125others(90): Show | 93 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.1686-2329dupT | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | INFO_REALIGN_3_PRIME | chr11 | 121541203 | |||||
| chr11:121541210
|
T | TTG | 40 | a0001c0002t0001g0112a0001c0002t0001g0116a0001c0002t0001g0158others(37): Show | 41 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.1686-2337_1686-233 others(6): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | INFO_REALIGN_3_PRIME | chr11 | 121541210 | |||||
| chr11:121541556
|
A | G | 137 | a0001c0001t0001g0059a0001c0001t0002g0004a0001c0001t0002g0125others(134): Show | 138 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.1686-1992A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121541556 | ||||||
| chr11:121541617
|
C | T | 1 | a0001c0021t0003g0216 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1686-1931C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121541617 | ||||||
| chr11:121541840
|
G | A | 1 | a0001c0031t0010g0214 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1686-1708G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121541840 | ||||||
| chr11:121541870
|
C | T | 2 | a0001c0033t0003g0169a0001c0046t0002g0174 | 2 | HG03540.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1686-1678C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121541870 | ||||||
| chr11:121542128
|
C | A | 15 | a0001c0001t0001g0057a0001c0002t0003g0151a0001c0003t0002g0105others(12): Show | 15 | HG00099.hp2 HG01167.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1686-1420C>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121542128 | ||||||
| chr11:121542182
|
C | T | 1 | a0001c0010t0003g0258 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1686-1366C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121542182 | ||||||
| chr11:121542238
|
C | T | 1 | a0001c0006t0001g0118 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1686-1310C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121542238 | ||||||
| chr11:121542382
|
C | CT | 3 | a0001c0002t0015g0017a0001c0015t0015g0067a0001c0042t0002g0002 | 3 | NA18961.hp1 NA18961.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.1686-1162dupT | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | INFO_REALIGN_3_PRIME | chr11 | 121542382 | |||||
| chr11:121542448
|
G | T | 38 | a0001c0001t0001g0059a0001c0002t0001g0010a0001c0002t0001g0083others(35): Show | 38 | HG00280.hp2 HG01496.hp2 HG02027.hp1 others(35): Show |
intron_variant | MODIFIER | c.1686-1100G>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121542448 | ||||||
| chr11:121542463
|
A | AT | 37 | a0001c0001t0002g0004a0001c0001t0002g0125a0001c0002t0001g0139others(34): Show | 37 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.1686-1076dupT | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | INFO_REALIGN_3_PRIME | chr11 | 121542463 | |||||
| chr11:121542508
|
A | G | 4 | a0001c0065t0003g0152a0001c0066t0016g0194a0001c0067t0013g0204others(1): Show | 4 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1686-1040A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121542508 | ||||||
| chr11:121542634
|
C | T | 3 | a0001c0060t0003g0163a0004c0059t0002g0171a0006c0043t0026g0215 | 3 | HG02559.hp2 HG02922.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1686-914C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121542634 | ||||||
| chr11:121542744
|
G | A | 37 | a0001c0001t0002g0004a0001c0001t0002g0125a0001c0002t0001g0139others(34): Show | 37 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.1686-804G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121542744 | ||||||
| chr11:121542812
|
A | AATTAT | 37 | a0001c0001t0002g0004a0001c0001t0002g0125a0001c0002t0001g0139others(34): Show | 37 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.1686-719_1686-715d others(7): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | INFO_REALIGN_3_PRIME | chr11 | 121542812 | |||||
| chr11:121542831
|
A | C | 1 | a0001c0038t0002g0186 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1686-717A>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121542831 | ||||||
| chr11:121542912
|
T | C | 1 | a0001c0038t0002g0186 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1686-636T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121542912 | ||||||
| chr11:121543071
|
G | C | 4 | a0001c0065t0003g0152a0001c0066t0016g0194a0001c0067t0013g0204others(1): Show | 4 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1686-477G>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121543071 | ||||||
| chr11:121543190
|
CAAAAAAA others(5): Show |
C | 4 | a0001c0065t0003g0152a0001c0066t0016g0194a0001c0067t0013g0204others(1): Show | 4 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1686-340_1686-329d others(14): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | INFO_REALIGN_3_PRIME | chr11 | 121543190 | |||||
| chr11:121543200
|
GA | G | 38 | a0001c0001t0001g0059a0001c0002t0001g0010a0001c0002t0001g0083others(35): Show | 38 | HG00280.hp2 HG01496.hp2 HG02027.hp1 others(35): Show |
intron_variant | MODIFIER | c.1686-337delA | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | INFO_REALIGN_3_PRIME | chr11 | 121543200 | |||||
| chr11:121543326
|
C | T | 16 | a0001c0001t0002g0004a0001c0001t0002g0125a0001c0002t0001g0139others(13): Show | 16 | HG00558.hp1 HG00558.hp2 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.1686-222C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 12/47 | chr11 | 121543326 | ||||||
| chr11:121543747
|
A | C | 38 | a0001c0001t0001g0059a0001c0002t0001g0010a0001c0002t0001g0083others(35): Show | 38 | HG00280.hp2 HG01496.hp2 HG02027.hp1 others(35): Show |
intron_variant | MODIFIER | c.1864+21A>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 13/47 | chr11 | 121543747 | ||||||
| chr11:121543767
|
G | T | 38 | a0001c0002t0001g0112a0001c0002t0001g0116a0001c0002t0001g0158others(35): Show | 39 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.1864+41G>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 13/47 | chr11 | 121543767 | ||||||
| chr11:121543791
|
C | T | 2 | a0001c0033t0003g0169a0001c0046t0002g0174 | 2 | HG03540.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1864+65C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 13/47 | chr11 | 121543791 | ||||||
| chr11:121543841
|
G | A | 106 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(103): Show | 106 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.1864+115G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 13/47 | chr11 | 121543841 | ||||||
| chr11:121543849
|
C | T | 1 | a0006c0055t0002g0246 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1864+123C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 13/47 | chr11 | 121543849 | ||||||
| chr11:121543866
|
A | T | 6 | a0001c0001t0001g0006a0001c0001t0001g0045a0001c0001t0002g0026others(3): Show | 6 | HG02165.hp2 NA18941.hp1 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.1864+140A>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 13/47 | chr11 | 121543866 | ||||||
| chr11:121543919
|
C | T | 264 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(261): Show | 265 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.1864+193C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 13/47 | chr11 | 121543919 | ||||||
| chr11:121544070
|
G | C | 37 | a0001c0001t0002g0004a0001c0001t0002g0125a0001c0002t0001g0139others(34): Show | 37 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.1864+344G>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 13/47 | chr11 | 121544070 | ||||||
| chr11:121544188
|
A | G | 13 | a0001c0003t0002g0229a0001c0003t0007g0261a0001c0010t0003g0257others(10): Show | 13 | HG00741.hp2 HG01074.hp2 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.1864+462A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 13/47 | chr11 | 121544188 | ||||||
| chr11:121544414
|
T | C | 1 | a0001c0008t0018g0192 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1864+688T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 13/47 | chr11 | 121544414 | ||||||
| chr11:121544468
|
G | A | 4 | a0001c0009t0008g0207a0001c0009t0011g0170a0001c0009t0011g0255others(1): Show | 4 | HG02486.hp2 HG03139.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1864+742G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 13/47 | chr11 | 121544468 | ||||||
| chr11:121544493
|
G | T | 1 | a0002c0030t0002g0212 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1865-750G>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 13/47 | chr11 | 121544493 | ||||||
| chr11:121544603
|
C | T | 19 | a0001c0003t0001g0019a0001c0003t0001g0113a0001c0003t0002g0115others(16): Show | 19 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.1865-640C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 13/47 | chr11 | 121544603 | ||||||
| chr11:121544712
|
C | T | 1 | a0002c0005t0009g0041 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1865-531C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 13/47 | chr11 | 121544712 | ||||||
| chr11:121544902
|
G | C | 1 | a0001c0009t0008g0207 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1865-341G>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 13/47 | chr11 | 121544902 | ||||||
| chr11:121545013
|
G | C | 1 | a0001c0032t0003g0149 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1865-230G>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 13/47 | chr11 | 121545013 | ||||||
| chr11:121545098
|
A | G | 264 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(261): Show | 265 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.1865-145A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 13/47 | chr11 | 121545098 | ||||||
| chr11:121545478
|
A | C | 97 | a0001c0001t0001g0059a0001c0002t0001g0010a0001c0002t0001g0083others(94): Show | 98 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.2051+49A>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/47 | chr11 | 121545478 | ||||||
| chr11:121545682
|
A | G | 37 | a0001c0001t0002g0004a0001c0001t0002g0125a0001c0002t0001g0139others(34): Show | 37 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.2051+253A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/47 | chr11 | 121545682 | ||||||
| chr11:121546067
|
G | A | 5 | a0001c0001t0001g0052a0001c0001t0001g0058a0001c0003t0002g0080others(2): Show | 5 | HG02155.hp1 NA18939.hp1 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.2051+638G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/47 | chr11 | 121546067 | ||||||
| chr11:121546118
|
G | T | 1 | a0001c0036t0003g0266 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2051+689G>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/47 | chr11 | 121546118 | ||||||
| chr11:121546119
|
T | G | 136 | a0001c0001t0001g0059a0001c0001t0002g0004a0001c0001t0002g0125others(133): Show | 137 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.2051+690T>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/47 | chr11 | 121546119 | ||||||
| chr11:121546261
|
T | C | 1 | a0004c0059t0002g0171 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2051+832T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/47 | chr11 | 121546261 | ||||||
| chr11:121546298
|
G | A | 1 | a0001c0016t0012g0210 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2051+869G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/47 | chr11 | 121546298 | ||||||
| chr11:121546415
|
G | A | 38 | a0001c0002t0001g0112a0001c0002t0001g0116a0001c0002t0001g0158others(35): Show | 39 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.2051+986G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/47 | chr11 | 121546415 | ||||||
| chr11:121546466
|
T | C | 1 | a0001c0023t0003g0193 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2051+1037T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/47 | chr11 | 121546466 | ||||||
| chr11:121546689
|
A | C | 4 | a0001c0022t0008g0211a0001c0060t0003g0163a0004c0059t0002g0171others(1): Show | 4 | HG02559.hp2 HG02922.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2051+1260A>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/47 | chr11 | 121546689 | ||||||
| chr11:121546708
|
G | A | 1 | a0001c0016t0002g0121 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2051+1279G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/47 | chr11 | 121546708 | ||||||
| chr11:121546930
|
C | G | 2 | a0001c0009t0011g0170a0001c0009t0011g0255 | 2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2051+1501C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/47 | chr11 | 121546930 | ||||||
| chr11:121547332
|
G | GT | 103 | a0001c0001t0001g0059a0001c0001t0001g0138a0001c0001t0002g0142others(100): Show | 104 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.2051+1916dupT | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/47 | INFO_REALIGN_3_PRIME | chr11 | 121547332 | |||||
| chr11:121547332
|
G | GTT | 37 | a0001c0001t0002g0004a0001c0001t0002g0125a0001c0002t0001g0139others(34): Show | 37 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.2051+1915_2051+191 others(6): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/47 | INFO_REALIGN_3_PRIME | chr11 | 121547332 | |||||
| chr11:121547345
|
T | C | 1 | a0001c0009t0008g0207 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2051+1916T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/47 | chr11 | 121547345 | ||||||
| chr11:121547361
|
T | A | 1 | a0013c0047t0007g0182 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2051+1932T>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/47 | chr11 | 121547361 | ||||||
| chr11:121547417
|
C | CAAAA | 54 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(51): Show | 54 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.2051+2013_2051+201 others(8): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/47 | INFO_REALIGN_3_PRIME | chr11 | 121547417 | |||||
| chr11:121547417
|
C | CAAAAA | 42 | a0001c0001t0001g0006a0001c0001t0001g0023a0001c0001t0001g0027others(39): Show | 42 | HG00323.hp1 HG00735.hp2 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.2051+2012_2051+201 others(9): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/47 | INFO_REALIGN_3_PRIME | chr11 | 121547417 | |||||
| chr11:121547417
|
C | CAAAAAA | 17 | a0001c0001t0002g0125a0001c0001t0002g0142a0001c0001t0025g0119others(14): Show | 17 | HG00438.hp1 HG00558.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.2051+2011_2051+201 others(10): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/47 | INFO_REALIGN_3_PRIME | chr11 | 121547417 | |||||
| chr11:121547417
|
C | CAAAAAAA others(3): Show |
7 | a0001c0001t0002g0004a0001c0003t0003g0254a0001c0003t0007g0261others(4): Show | 7 | HG00558.hp1 HG02109.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.2051+2007_2051+201 others(14): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/47 | INFO_REALIGN_3_PRIME | chr11 | 121547417 | |||||
| chr11:121547417
|
C | CAAAAAAA others(4): Show |
5 | a0001c0009t0011g0255a0001c0010t0003g0257a0001c0036t0003g0266others(2): Show | 5 | HG02809.hp2 HG03139.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.2051+2006_2051+201 others(15): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/47 | INFO_REALIGN_3_PRIME | chr11 | 121547417 | |||||
| chr11:121547417
|
C | CAAAAAAA others(5): Show |
5 | a0001c0003t0002g0229a0001c0009t0011g0170a0001c0011t0002g0271others(2): Show | 5 | HG00741.hp2 HG01074.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2051+2005_2051+201 others(16): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/47 | INFO_REALIGN_3_PRIME | chr11 | 121547417 | |||||
| chr11:121547417
|
C | CAAAAAAA others(6): Show |
4 | a0001c0009t0008g0207a0001c0011t0001g0107a0001c0011t0020g0106others(1): Show | 4 | HG01192.hp1 HG01192.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.2051+2004_2051+201 others(17): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/47 | INFO_REALIGN_3_PRIME | chr11 | 121547417 | |||||
| chr11:121547417
|
C | CAAAAAAA others(7): Show |
2 | a0001c0002t0003g0150a0002c0007t0001g0073 | 2 | HG02109.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.2051+2003_2051+201 others(18): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/47 | INFO_REALIGN_3_PRIME | chr11 | 121547417 | |||||
| chr11:121547417
|
C | CAAAAAAA others(8): Show |
1 | a0001c0012t0002g0178 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2051+2002_2051+201 others(19): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/47 | INFO_REALIGN_3_PRIME | chr11 | 121547417 | |||||
| chr11:121547417
|
C | CAAAAAAA others(11): Show |
1 | a0001c0031t0010g0214 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2051+1999_2051+201 others(22): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/47 | INFO_REALIGN_3_PRIME | chr11 | 121547417 | |||||
| chr11:121547417
|
C | CAAAAAAA others(13): Show |
1 | a0002c0049t0003g0162 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2051+1997_2051+201 others(24): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/47 | INFO_REALIGN_3_PRIME | chr11 | 121547417 | |||||
| chr11:121547417
|
C | CAAAAAAA others(14): Show |
1 | a0002c0005t0003g0159 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2051+1996_2051+201 others(25): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/47 | INFO_REALIGN_3_PRIME | chr11 | 121547417 | |||||
| chr11:121547417
|
C | CAAAAAAA others(17): Show |
1 | a0002c0025t0003g0260 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2051+1993_2051+201 others(28): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/47 | INFO_REALIGN_3_PRIME | chr11 | 121547417 | |||||
| chr11:121547417
|
C | CAAAAAAA others(18): Show |
1 | a0002c0007t0001g0221 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2051+1992_2051+201 others(29): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/47 | INFO_REALIGN_3_PRIME | chr11 | 121547417 | |||||
| chr11:121547417
|
C | CAAAAAAA others(19): Show |
3 | a0002c0005t0001g0202a0002c0005t0001g0205a0002c0014t0014g0217 | 3 | HG01433.hp1 HG03453.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.2051+1991_2051+201 others(30): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/47 | INFO_REALIGN_3_PRIME | chr11 | 121547417 | |||||
| chr11:121547417
|
C | CAAAAAAA others(20): Show |
3 | a0002c0026t0005g0245a0008c0024t0002g0033a0008c0024t0002g0034 | 3 | HG00642.hp2 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2051+1990_2051+201 others(31): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/47 | INFO_REALIGN_3_PRIME | chr11 | 121547417 | |||||
| chr11:121547417
|
C | CAAAAAAA others(21): Show |
1 | a0002c0048t0002g0201 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2051+1989_2051+201 others(32): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/47 | INFO_REALIGN_3_PRIME | chr11 | 121547417 | |||||
| chr11:121547417
|
C | CAAAAAAA others(22): Show |
1 | a0001c0058t0011g0166 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2051+2016_2051+201 others(33): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/47 | INFO_REALIGN_3_PRIME | chr11 | 121547417 | |||||
| chr11:121547417
|
C | CAAAAAAA others(23): Show |
2 | a0002c0007t0001g0124a0002c0007t0017g0123 | 2 | NA18942.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.2051+2016_2051+201 others(34): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/47 | INFO_REALIGN_3_PRIME | chr11 | 121547417 | |||||
| chr11:121547417
|
C | CAAAAAAA others(24): Show |
3 | a0003c0027t0005g0181a0003c0069t0008g0164a0007c0072t0002g0256 | 3 | HG02258.hp1 HG03209.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2051+2016_2051+201 others(35): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/47 | INFO_REALIGN_3_PRIME | chr11 | 121547417 | |||||
| chr11:121547417
|
C | CAAAAAAA others(25): Show |
4 | a0001c0002t0001g0139a0002c0007t0017g0122a0003c0027t0005g0173others(1): Show | 4 | HG02738.hp1 HG03098.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2051+2016_2051+201 others(36): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/47 | INFO_REALIGN_3_PRIME | chr11 | 121547417 | |||||
| chr11:121547417
|
C | CAAAAAAA others(26): Show |
2 | a0002c0005t0001g0074a0002c0007t0001g0060 | 2 | NA18974.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.2051+2016_2051+201 others(37): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/47 | INFO_REALIGN_3_PRIME | chr11 | 121547417 | |||||
| chr11:121547417
|
CA | C | 39 | a0001c0001t0001g0059a0001c0002t0001g0010a0001c0002t0001g0112others(36): Show | 40 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.2051+2016delA | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/47 | INFO_REALIGN_3_PRIME | chr11 | 121547417 | |||||
| chr11:121547417
|
CAA | C | 31 | a0001c0002t0001g0083a0001c0002t0001g0092a0001c0002t0001g0103others(28): Show | 31 | HG00280.hp2 HG01496.hp2 HG02027.hp1 others(28): Show |
intron_variant | MODIFIER | c.2051+2015_2051+201 others(6): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/47 | INFO_REALIGN_3_PRIME | chr11 | 121547417 | |||||
| chr11:121547417
|
CAAAA | C | 9 | a0001c0022t0008g0211a0002c0005t0001g0008a0002c0005t0001g0042others(6): Show | 9 | HG00544.hp1 HG00738.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.2051+2013_2051+201 others(8): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/47 | INFO_REALIGN_3_PRIME | chr11 | 121547417 | |||||
| chr11:121547706
|
C | T | 37 | a0001c0001t0002g0004a0001c0001t0002g0125a0001c0002t0001g0139others(34): Show | 37 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.2052-2254C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/47 | chr11 | 121547706 | ||||||
| chr11:121547807
|
G | A | 1 | a0002c0005t0001g0127 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2052-2153G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/47 | chr11 | 121547807 | ||||||
| chr11:121547838
|
C | T | 1 | a0001c0032t0003g0149 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2052-2122C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/47 | chr11 | 121547838 | ||||||
| chr11:121547895
|
A | G | 3 | a0001c0012t0005g0247a0001c0020t0003g0248a0006c0055t0002g0246 | 3 | HG01109.hp2 HG02647.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2052-2065A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/47 | chr11 | 121547895 | ||||||
| chr11:121548097
|
C | T | 92 | a0001c0001t0001g0059a0001c0002t0001g0010a0001c0002t0001g0083others(89): Show | 93 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.2052-1863C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/47 | chr11 | 121548097 | ||||||
| chr11:121548125
|
C | A | 1 | a0001c0052t0001g0219 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2052-1835C>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/47 | chr11 | 121548125 | ||||||
| chr11:121548127
|
T | A | 1 | a0001c0052t0001g0219 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2052-1833T>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/47 | chr11 | 121548127 | ||||||
| chr11:121548145
|
A | G | 1 | a0001c0002t0004g0126 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.2052-1815A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/47 | chr11 | 121548145 | ||||||
| chr11:121548531
|
G | A | 1 | a0001c0038t0002g0186 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2052-1429G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/47 | chr11 | 121548531 | ||||||
| chr11:121548923
|
C | T | 2 | a0001c0061t0030g0249a0001c0062t0003g0250 | 2 | HG02559.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2052-1037C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/47 | chr11 | 121548923 | ||||||
| chr11:121548957
|
A | C | 2 | a0001c0002t0003g0150a0001c0032t0003g0149 | 2 | HG02109.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.2052-1003A>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/47 | chr11 | 121548957 | ||||||
| chr11:121548991
|
C | G | 4 | a0001c0065t0003g0152a0001c0066t0016g0194a0001c0067t0013g0204others(1): Show | 4 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.2052-969C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/47 | chr11 | 121548991 | ||||||
| chr11:121549044
|
C | T | 1 | a0001c0038t0002g0186 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2052-916C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/47 | chr11 | 121549044 | ||||||
| chr11:121549292
|
G | A | 1 | a0001c0003t0003g0254 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2052-668G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/47 | chr11 | 121549292 | ||||||
| chr11:121549349
|
A | G | 38 | a0001c0001t0001g0059a0001c0002t0001g0010a0001c0002t0001g0083others(35): Show | 38 | HG00280.hp2 HG01496.hp2 HG02027.hp1 others(35): Show |
intron_variant | MODIFIER | c.2052-611A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/47 | chr11 | 121549349 | ||||||
| chr11:121549388
|
A | AT | 38 | a0001c0001t0001g0059a0001c0002t0001g0010a0001c0002t0001g0083others(35): Show | 38 | HG00280.hp2 HG01496.hp2 HG02027.hp1 others(35): Show |
intron_variant | MODIFIER | c.2052-563dupT | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/47 | INFO_REALIGN_3_PRIME | chr11 | 121549388 | |||||
| chr11:121549446
|
G | T | 134 | a0001c0001t0001g0059a0001c0001t0002g0004a0001c0002t0001g0010others(131): Show | 135 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.2052-514G>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/47 | chr11 | 121549446 | ||||||
| chr11:121549475
|
C | T | 38 | a0001c0002t0001g0112a0001c0002t0001g0116a0001c0002t0001g0158others(35): Show | 39 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.2052-485C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/47 | chr11 | 121549475 | ||||||
| chr11:121549532
|
T | A | 1 | a0001c0003t0001g0019 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.2052-428T>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/47 | chr11 | 121549532 | ||||||
| chr11:121549670
|
A | AG | 136 | a0001c0001t0001g0059a0001c0001t0002g0004a0001c0001t0002g0125others(133): Show | 137 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.2052-290_2052-289i others(3): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/47 | chr11 | 121549670 | ||||||
| chr11:121549672
|
A | G | 136 | a0001c0001t0001g0059a0001c0001t0002g0004a0001c0001t0002g0125others(133): Show | 137 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.2052-288A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/47 | chr11 | 121549672 | ||||||
| chr11:121549674
|
T | A | 136 | a0001c0001t0001g0059a0001c0001t0002g0004a0001c0001t0002g0125others(133): Show | 137 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.2052-286T>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/47 | chr11 | 121549674 | ||||||
| chr11:121549724
|
A | AT | 45 | a0001c0001t0001g0009a0001c0001t0001g0047a0001c0001t0001g0048others(42): Show | 45 | HG00741.hp2 HG01071.hp2 HG01074.hp1 others(42): Show |
intron_variant | MODIFIER | c.2052-222dupT | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/47 | INFO_REALIGN_3_PRIME | chr11 | 121549724 | |||||
| chr11:121549724
|
AT | A | 40 | a0001c0001t0002g0004a0001c0001t0002g0125a0001c0002t0001g0139others(37): Show | 40 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.2052-222delT | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 14/47 | INFO_REALIGN_3_PRIME | chr11 | 121549724 | |||||
| chr11:121550240
|
G | A | 2 | a0001c0033t0003g0169a0001c0046t0002g0174 | 2 | HG03540.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2180+152G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 15/47 | chr11 | 121550240 | ||||||
| chr11:121550321
|
C | G | 1 | a0002c0025t0003g0260 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2180+233C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 15/47 | chr11 | 121550321 | ||||||
| chr11:121550425
|
G | C | 264 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(261): Show | 265 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.2181-160G>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 15/47 | chr11 | 121550425 | ||||||
| chr11:121550445
|
G | C | 1 | a0001c0003t0018g0191 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2181-140G>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 15/47 | chr11 | 121550445 | ||||||
| chr11:121550465
|
T | C | 4 | a0001c0022t0008g0211a0001c0060t0003g0163a0004c0059t0002g0171others(1): Show | 4 | HG02559.hp2 HG02922.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2181-120T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 15/47 | chr11 | 121550465 | ||||||
| chr11:121550474
|
A | G | 4 | a0001c0065t0003g0152a0001c0066t0016g0194a0001c0067t0013g0204others(1): Show | 4 | HG01243.hp1 HG02818.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.2181-111A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 15/47 | chr11 | 121550474 | ||||||
| chr11:121550723
|
A | G | 1 | a0001c0003t0003g0254 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2266+53A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 16/47 | chr11 | 121550723 | ||||||
| chr11:121550735
|
C | T | 11 | a0001c0003t0002g0229a0001c0010t0003g0257a0001c0010t0003g0258others(8): Show | 11 | HG00741.hp2 HG01074.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.2266+65C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 16/47 | chr11 | 121550735 | ||||||
| chr11:121550744
|
G | A | 1 | a0001c0036t0003g0266 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2266+74G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 16/47 | chr11 | 121550744 | ||||||
| chr11:121550790
|
C | G | 1 | a0002c0048t0002g0201 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2266+120C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 16/47 | chr11 | 121550790 | ||||||
| chr11:121551007
|
G | T | 3 | a0001c0009t0008g0207a0001c0009t0011g0170a0001c0009t0011g0255 | 3 | HG02486.hp2 HG03139.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2266+337G>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 16/47 | chr11 | 121551007 | ||||||
| chr11:121551141
|
C | G | 1 | a0001c0058t0011g0166 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2266+471C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 16/47 | chr11 | 121551141 | ||||||
| chr11:121551195
|
C | T | 3 | a0003c0027t0005g0173a0003c0027t0005g0181a0007c0072t0002g0256 | 3 | HG03098.hp2 HG03209.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2266+525C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 16/47 | chr11 | 121551195 | ||||||
| chr11:121551260
|
A | C | 14 | a0001c0001t0001g0057a0001c0002t0001g0139a0001c0002t0003g0151others(11): Show | 14 | HG00642.hp1 HG01081.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.2266+590A>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 16/47 | chr11 | 121551260 | ||||||
| chr11:121551410
|
T | C | 3 | a0001c0001t0001g0089a0001c0001t0001g0197a0001c0002t0004g0007 | 3 | HG02165.hp1 HG02300.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.2266+740T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 16/47 | chr11 | 121551410 | ||||||
| chr11:121551527
|
A | G | 6 | a0001c0022t0008g0211a0002c0049t0003g0162a0003c0027t0005g0173others(3): Show | 6 | HG01891.hp2 HG02630.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.2266+857A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 16/47 | chr11 | 121551527 | ||||||
| chr11:121551548
|
T | C | 2 | a0001c0001t0002g0185a0001c0057t0002g0160 | 2 | HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2266+878T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 16/47 | chr11 | 121551548 | ||||||
| chr11:121551868
|
T | G | 3 | a0003c0027t0005g0173a0003c0027t0005g0181a0007c0072t0002g0256 | 3 | HG03098.hp2 HG03209.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2266+1198T>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 16/47 | chr11 | 121551868 | ||||||
| chr11:121551893
|
C | T | 1 | a0001c0015t0005g0270 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2266+1223C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 16/47 | chr11 | 121551893 | ||||||
| chr11:121551933
|
G | T | 1 | a0001c0009t0010g0165 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2266+1263G>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 16/47 | chr11 | 121551933 | ||||||
| chr11:121552124
|
A | G | 1 | a0001c0065t0003g0152 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2266+1454A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 16/47 | chr11 | 121552124 | ||||||
| chr11:121552538
|
C | G | 1 | a0002c0030t0002g0212 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2267-1399C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 16/47 | chr11 | 121552538 | ||||||
| chr11:121552585
|
C | T | 1 | a0001c0003t0002g0097 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.2267-1352C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 16/47 | chr11 | 121552585 | ||||||
| chr11:121552843
|
C | T | 42 | a0001c0001t0001g0059a0001c0002t0001g0010a0001c0002t0001g0083others(39): Show | 42 | HG00735.hp1 HG01081.hp2 HG01243.hp2 others(39): Show |
intron_variant | MODIFIER | c.2267-1094C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 16/47 | chr11 | 121552843 | ||||||
| chr11:121552931
|
G | A | 20 | a0001c0013t0002g0016a0001c0013t0002g0018a0001c0013t0002g0054others(17): Show | 20 | HG00544.hp1 HG01891.hp2 HG02647.hp1 others(17): Show |
intron_variant | MODIFIER | c.2267-1006G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 16/47 | chr11 | 121552931 | ||||||
| chr11:121553589
|
G | A | 1 | a0001c0004t0003g0224 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2267-348G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 16/47 | chr11 | 121553589 | ||||||
| chr11:121554173
|
G | A | 18 | a0001c0013t0002g0016a0001c0013t0002g0018a0001c0013t0002g0054others(15): Show | 18 | HG01891.hp2 HG02647.hp1 HG02809.hp1 others(15): Show |
intron_variant | MODIFIER | c.2439+64G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 17/47 | chr11 | 121554173 | ||||||
| chr11:121554461
|
G | A | 1 | a0001c0002t0002g0109 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2439+352G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 17/47 | chr11 | 121554461 | ||||||
| chr11:121554578
|
G | A | 3 | a0001c0066t0016g0194a0002c0014t0014g0217a0002c0014t0014g0252 | 3 | HG01243.hp1 HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2439+469G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 17/47 | chr11 | 121554578 | ||||||
| chr11:121554937
|
A | G | 1 | a0001c0002t0001g0188 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2440-250A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 17/47 | chr11 | 121554937 | ||||||
| chr11:121554952
|
A | G | 4 | a0001c0009t0011g0170a0001c0009t0011g0255a0001c0057t0002g0160others(1): Show | 4 | HG02486.hp2 HG02976.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2440-235A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 17/47 | chr11 | 121554952 | ||||||
| chr11:121555118
|
C | A | 1 | a0001c0001t0001g0063 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2440-69C>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 17/47 | chr11 | 121555118 | ||||||
| chr11:121555142
|
C | T | 11 | a0001c0002t0001g0139a0001c0002t0003g0151a0001c0006t0001g0068others(8): Show | 11 | HG00735.hp1 HG01081.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.2440-45C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 17/47 | chr11 | 121555142 | ||||||
| chr11:121555333
|
G | A | 19 | a0001c0013t0002g0016a0001c0013t0002g0018a0001c0013t0002g0054others(16): Show | 19 | HG00544.hp1 HG01891.hp2 HG02647.hp1 others(16): Show |
intron_variant | MODIFIER | c.2571+15G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 18/47 | chr11 | 121555333 | ||||||
| chr11:121555498
|
T | G | 95 | a0001c0002t0001g0103a0001c0002t0001g0112a0001c0002t0001g0116others(92): Show | 96 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.2571+180T>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 18/47 | chr11 | 121555498 | ||||||
| chr11:121555682
|
TATA | T | 24 | a0001c0002t0001g0103a0001c0002t0001g0112a0001c0002t0001g0116others(21): Show | 25 | HG00438.hp2 HG01109.hp1 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.2571+367_2571+369d others(5): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 18/47 | INFO_REALIGN_3_PRIME | chr11 | 121555682 | |||||
| chr11:121555742
|
T | TATC | 4 | a0001c0009t0011g0170a0001c0009t0011g0255a0001c0057t0002g0160others(1): Show | 4 | HG02486.hp2 HG02976.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2571+442_2571+444d others(5): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 18/47 | INFO_REALIGN_3_PRIME | chr11 | 121555742 | |||||
| chr11:121555767
|
A | G | 1 | a0001c0002t0003g0150 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2571+449A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 18/47 | chr11 | 121555767 | ||||||
| chr11:121555788
|
T | C | 1 | a0001c0002t0004g0003 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2571+470T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 18/47 | chr11 | 121555788 | ||||||
| chr11:121555821
|
C | G | 1 | a0001c0038t0002g0186 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2571+503C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 18/47 | chr11 | 121555821 | ||||||
| chr11:121555864
|
C | G | 3 | a0001c0002t0003g0151a0001c0009t0003g0147a0001c0022t0003g0213 | 3 | HG02622.hp1 HG02630.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.2571+546C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 18/47 | chr11 | 121555864 | ||||||
| chr11:121555871
|
T | G | 1 | a0001c0001t0001g0199 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2571+553T>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 18/47 | chr11 | 121555871 | ||||||
| chr11:121555871
|
TTGTC | T | 18 | a0001c0013t0002g0016a0001c0013t0002g0018a0001c0013t0002g0054others(15): Show | 18 | HG01891.hp2 HG02647.hp1 HG02809.hp1 others(15): Show |
intron_variant | MODIFIER | c.2571+556_2571+559d others(6): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 18/47 | INFO_REALIGN_3_PRIME | chr11 | 121555871 | |||||
| chr11:121556055
|
T | G | 5 | a0001c0010t0002g0190a0001c0010t0002g0234a0001c0010t0003g0257others(2): Show | 5 | HG02109.hp1 HG02258.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.2571+737T>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 18/47 | chr11 | 121556055 | ||||||
| chr11:121556068
|
C | T | 1 | a0001c0003t0002g0230 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2571+750C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 18/47 | chr11 | 121556068 | ||||||
| chr11:121556161
|
T | A | 18 | a0001c0013t0002g0016a0001c0013t0002g0018a0001c0013t0002g0054others(15): Show | 18 | HG01891.hp2 HG02647.hp1 HG02809.hp1 others(15): Show |
intron_variant | MODIFIER | c.2571+843T>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 18/47 | chr11 | 121556161 | ||||||
| chr11:121556313
|
T | A | 4 | a0001c0009t0011g0170a0001c0009t0011g0255a0001c0057t0002g0160others(1): Show | 4 | HG02486.hp2 HG02976.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2571+995T>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 18/47 | chr11 | 121556313 | ||||||
| chr11:121556550
|
A | G | 262 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(259): Show | 263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.2572-764A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 18/47 | chr11 | 121556550 | ||||||
| chr11:121556643
|
G | C | 10 | a0001c0002t0003g0150a0001c0003t0007g0261a0001c0009t0011g0170others(7): Show | 10 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.2572-671G>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 18/47 | chr11 | 121556643 | ||||||
| chr11:121556859
|
G | A | 23 | a0001c0002t0001g0139a0001c0002t0003g0151a0001c0006t0001g0068others(20): Show | 23 | HG00735.hp1 HG01081.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.2572-455G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 18/47 | chr11 | 121556859 | ||||||
| chr11:121556975
|
C | T | 1 | a0001c0015t0005g0270 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2572-339C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 18/47 | chr11 | 121556975 | ||||||
| chr11:121557276
|
C | T | 9 | a0001c0009t0008g0207a0001c0021t0016g0206a0001c0066t0016g0194others(6): Show | 9 | HG01243.hp1 HG02886.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.2572-38C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 18/47 | chr11 | 121557276 | ||||||
| chr11:121557548
|
C | T | 1 | a0001c0032t0003g0149 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2663+143C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 19/47 | chr11 | 121557548 | ||||||
| chr11:121557731
|
A | G | 11 | a0001c0011t0001g0107a0001c0011t0002g0271a0001c0011t0012g0242others(8): Show | 11 | HG00280.hp2 HG00323.hp1 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.2663+326A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 19/47 | chr11 | 121557731 | ||||||
| chr11:121558070
|
A | G | 9 | a0001c0001t0001g0025a0001c0001t0001g0038a0001c0001t0001g0040others(6): Show | 9 | HG01081.hp1 HG01175.hp2 HG02300.hp1 others(6): Show |
intron_variant | MODIFIER | c.2664-521A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 19/47 | chr11 | 121558070 | ||||||
| chr11:121558255
|
T | G | 1 | a0001c0067t0013g0204 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2664-336T>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 19/47 | chr11 | 121558255 | ||||||
| chr11:121558256
|
A | G | 10 | a0001c0011t0001g0107a0001c0011t0002g0271a0001c0011t0012g0242others(7): Show | 10 | HG00280.hp2 HG00323.hp1 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.2664-335A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 19/47 | chr11 | 121558256 | ||||||
| chr11:121558278
|
G | A | 2 | a0001c0010t0005g0239a0002c0026t0005g0161 | 2 | HG01891.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.2664-313G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 19/47 | chr11 | 121558278 | ||||||
| chr11:121558853
|
G | A | 1 | a0001c0015t0005g0270 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2910+16G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 20/47 | chr11 | 121558853 | ||||||
| chr11:121559188
|
A | G | 1 | a0001c0038t0002g0186 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2911-331A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 20/47 | chr11 | 121559188 | ||||||
| chr11:121559394
|
T | C | 4 | a0001c0002t0003g0151a0001c0009t0003g0147a0001c0021t0003g0216others(1): Show | 4 | HG02622.hp1 HG02630.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2911-125T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 20/47 | chr11 | 121559394 | ||||||
| chr11:121559471
|
A | G | 3 | a0001c0009t0011g0170a0001c0009t0011g0255a0001c0058t0011g0166 | 3 | HG02486.hp2 HG03139.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2911-48A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 20/47 | chr11 | 121559471 | ||||||
| chr11:121559480
|
C | T | 2 | a0002c0048t0002g0201a0004c0056t0013g0148 | 2 | HG01081.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2911-39C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 20/47 | chr11 | 121559480 | ||||||
| chr11:121559972
|
A | C | 1 | a0001c0031t0010g0214 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3049+315A>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121559972 | ||||||
| chr11:121560093
|
G | A | 3 | a0001c0004t0004g0011a0001c0004t0004g0012a0002c0005t0001g0127 | 3 | HG01256.hp2 HG01258.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.3049+436G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121560093 | ||||||
| chr11:121560163
|
C | T | 31 | a0001c0002t0001g0139a0001c0002t0003g0151a0001c0006t0001g0068others(28): Show | 31 | HG00280.hp2 HG00323.hp1 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.3049+506C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121560163 | ||||||
| chr11:121560456
|
A | G | 3 | a0001c0032t0003g0149a0001c0046t0002g0174a0002c0005t0003g0159 | 3 | HG02723.hp2 HG03540.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.3049+799A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121560456 | ||||||
| chr11:121560517
|
T | C | 2 | a0001c0003t0002g0117a0001c0003t0019g0209 | 2 | HG01361.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.3049+860T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121560517 | ||||||
| chr11:121560541
|
A | G | 1 | a0001c0023t0003g0193 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3049+884A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121560541 | ||||||
| chr11:121560618
|
A | G | 5 | a0001c0003t0007g0261a0001c0033t0003g0169a0001c0060t0003g0163others(2): Show | 5 | HG02451.hp2 HG02559.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.3049+961A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121560618 | ||||||
| chr11:121560645
|
A | T | 11 | a0001c0002t0001g0139a0001c0002t0003g0151a0001c0006t0001g0068others(8): Show | 11 | HG00735.hp1 HG01081.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.3049+988A>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121560645 | ||||||
| chr11:121560757
|
A | T | 1 | a0001c0008t0002g0131 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.3049+1100A>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121560757 | ||||||
| chr11:121561168
|
G | A | 4 | a0001c0009t0011g0170a0001c0009t0011g0255a0001c0057t0002g0160others(1): Show | 4 | HG02486.hp2 HG02976.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.3049+1511G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121561168 | ||||||
| chr11:121561183
|
C | G | 19 | a0001c0013t0002g0016a0001c0013t0002g0018a0001c0013t0002g0035others(16): Show | 19 | HG01891.hp2 HG02647.hp1 HG02809.hp1 others(16): Show |
intron_variant | MODIFIER | c.3049+1526C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121561183 | ||||||
| chr11:121561377
|
G | A | 1 | a0001c0038t0002g0186 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3049+1720G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121561377 | ||||||
| chr11:121561408
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.3049+1751C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121561408 | ||||||
| chr11:121561426
|
T | C | 1 | a0001c0057t0002g0160 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3049+1769T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121561426 | ||||||
| chr11:121561543
|
G | A | 1 | a0001c0002t0006g0104 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.3049+1886G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121561543 | ||||||
| chr11:121561578
|
C | A | 151 | a0001c0002t0001g0010a0001c0002t0001g0083a0001c0002t0001g0092others(148): Show | 152 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.3049+1921C>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121561578 | ||||||
| chr11:121561589
|
G | A | 1 | a0001c0002t0001g0112 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3049+1932G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121561589 | ||||||
| chr11:121561633
|
TA | T | 15 | a0001c0013t0002g0016a0001c0013t0002g0018a0001c0013t0002g0035others(12): Show | 15 | NA18942.hp2 NA18951.hp1 NA18957.hp1 others(12): Show |
intron_variant | MODIFIER | c.3049+1977delA | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121561633 | ||||||
| chr11:121561690
|
G | GA | 212 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(209): Show | 213 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.3049+2050dupA | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | INFO_REALIGN_3_PRIME | chr11 | 121561690 | |||||
| chr11:121561690
|
G | GAA | 22 | a0001c0001t0001g0025a0001c0001t0001g0038a0001c0001t0001g0061others(19): Show | 22 | HG00642.hp1 HG01099.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.3049+2049_3049+205 others(6): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | INFO_REALIGN_3_PRIME | chr11 | 121561690 | |||||
| chr11:121561758
|
A | G | 9 | a0001c0009t0008g0207a0001c0021t0016g0206a0001c0066t0016g0194others(6): Show | 9 | HG01243.hp1 HG02886.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.3049+2101A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121561758 | ||||||
| chr11:121561774
|
G | C | 57 | a0001c0002t0001g0103a0001c0002t0001g0112a0001c0002t0001g0116others(54): Show | 58 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.3049+2117G>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121561774 | ||||||
| chr11:121561938
|
T | G | 54 | a0001c0002t0001g0103a0001c0002t0001g0112a0001c0002t0001g0116others(51): Show | 55 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(52): Show |
intron_variant | MODIFIER | c.3049+2281T>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121561938 | ||||||
| chr11:121561997
|
C | T | 13 | a0001c0002t0001g0139a0001c0002t0003g0150a0001c0002t0003g0151others(10): Show | 13 | HG00735.hp1 HG01081.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.3049+2340C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121561997 | ||||||
| chr11:121562079
|
T | C | 10 | a0001c0011t0001g0107a0001c0011t0002g0271a0001c0011t0012g0242others(7): Show | 10 | HG00280.hp2 HG00323.hp1 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.3049+2422T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121562079 | ||||||
| chr11:121562158
|
G | C | 1 | a0001c0001t0001g0036 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.3049+2501G>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121562158 | ||||||
| chr11:121562211
|
C | T | 29 | a0001c0002t0001g0010a0001c0002t0001g0083a0001c0002t0001g0092others(26): Show | 29 | HG01496.hp2 HG02040.hp1 HG02148.hp1 others(26): Show |
intron_variant | MODIFIER | c.3049+2554C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121562211 | ||||||
| chr11:121562218
|
T | C | 1 | a0001c0002t0003g0150 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3049+2561T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121562218 | ||||||
| chr11:121562241
|
C | G | 3 | a0001c0003t0007g0261a0001c0060t0003g0163a0006c0043t0026g0215 | 3 | HG02451.hp2 HG02559.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.3049+2584C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121562241 | ||||||
| chr11:121562280
|
G | T | 1 | a0001c0002t0006g0104 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.3049+2623G>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121562280 | ||||||
| chr11:121562298
|
T | C | 2 | a0001c0020t0003g0248a0006c0055t0002g0246 | 2 | HG01109.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.3049+2641T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121562298 | ||||||
| chr11:121562540
|
C | T | 1 | a0001c0001t0001g0057 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3049+2883C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121562540 | ||||||
| chr11:121562565
|
C | T | 5 | a0001c0002t0001g0083a0001c0002t0001g0092a0001c0002t0004g0003others(2): Show | 5 | HG02040.hp1 HG02165.hp1 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.3049+2908C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121562565 | ||||||
| chr11:121562630
|
C | T | 3 | a0001c0011t0001g0107a0001c0011t0002g0271a0001c0016t0002g0121 | 3 | HG01074.hp2 HG01256.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.3049+2973C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121562630 | ||||||
| chr11:121562648
|
T | C | 6 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0036others(3): Show | 6 | HG00544.hp2 HG02040.hp2 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.3049+2991T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121562648 | ||||||
| chr11:121562967
|
A | G | 3 | a0001c0003t0002g0080a0001c0003t0002g0128a0001c0008t0002g0222 | 3 | NA18939.hp1 NA18952.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.3049+3310A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121562967 | ||||||
| chr11:121563084
|
T | C | 21 | a0001c0013t0002g0016a0001c0013t0002g0018a0001c0013t0002g0035others(18): Show | 21 | HG01891.hp2 HG02647.hp1 HG02723.hp2 others(18): Show |
intron_variant | MODIFIER | c.3049+3427T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121563084 | ||||||
| chr11:121563174
|
T | G | 1 | a0001c0003t0002g0094 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.3049+3517T>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121563174 | ||||||
| chr11:121563217
|
C | A | 30 | a0001c0002t0001g0010a0001c0002t0001g0083a0001c0002t0001g0092others(27): Show | 30 | HG01496.hp2 HG01993.hp1 HG02040.hp1 others(27): Show |
intron_variant | MODIFIER | c.3049+3560C>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121563217 | ||||||
| chr11:121563456
|
T | C | 145 | a0001c0002t0001g0010a0001c0002t0001g0083a0001c0002t0001g0092others(142): Show | 146 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.3050-3484T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121563456 | ||||||
| chr11:121563526
|
G | T | 3 | a0001c0011t0020g0106a0001c0016t0002g0044a0001c0045t0020g0102 | 3 | HG01192.hp1 HG01192.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.3050-3414G>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121563526 | ||||||
| chr11:121563642
|
C | T | 4 | a0001c0009t0011g0170a0001c0009t0011g0255a0001c0057t0002g0160others(1): Show | 4 | HG02486.hp2 HG02976.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.3050-3298C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121563642 | ||||||
| chr11:121563719
|
T | C | 20 | a0001c0013t0002g0016a0001c0013t0002g0018a0001c0013t0002g0035others(17): Show | 20 | HG01891.hp2 HG02647.hp1 HG02809.hp1 others(17): Show |
intron_variant | MODIFIER | c.3050-3221T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121563719 | ||||||
| chr11:121563847
|
C | T | 29 | a0001c0002t0001g0139a0001c0002t0003g0150a0001c0002t0003g0151others(26): Show | 29 | HG00735.hp1 HG01081.hp2 HG01099.hp1 others(26): Show |
intron_variant | MODIFIER | c.3050-3093C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121563847 | ||||||
| chr11:121563987
|
T | C | 15 | a0001c0009t0008g0207a0001c0009t0010g0165a0001c0009t0011g0170others(12): Show | 15 | HG01243.hp1 HG02486.hp2 HG02886.hp1 others(12): Show |
intron_variant | MODIFIER | c.3050-2953T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121563987 | ||||||
| chr11:121564041
|
T | G | 12 | a0001c0002t0001g0139a0001c0002t0003g0151a0001c0006t0001g0068others(9): Show | 12 | HG00735.hp1 HG01081.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.3050-2899T>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121564041 | ||||||
| chr11:121564108
|
T | A | 1 | a0001c0038t0002g0186 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3050-2832T>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121564108 | ||||||
| chr11:121564467
|
T | A | 2 | a0001c0009t0010g0165a0001c0065t0003g0152 | 2 | HG02970.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.3050-2473T>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121564467 | ||||||
| chr11:121564483
|
G | A | 4 | a0001c0009t0011g0170a0001c0009t0011g0255a0001c0057t0002g0160others(1): Show | 4 | HG02486.hp2 HG02976.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.3050-2457G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121564483 | ||||||
| chr11:121564681
|
A | G | 19 | a0001c0002t0002g0091a0001c0002t0002g0109a0001c0002t0004g0077others(16): Show | 19 | NA18951.hp2 NA18955.hp2 NA18961.hp2 others(16): Show |
intron_variant | MODIFIER | c.3050-2259A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121564681 | ||||||
| chr11:121564701
|
G | C | 4 | a0001c0009t0011g0170a0001c0009t0011g0255a0001c0057t0002g0160others(1): Show | 4 | HG02486.hp2 HG02976.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.3050-2239G>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121564701 | ||||||
| chr11:121564744
|
A | AT | 52 | a0001c0002t0001g0010a0001c0002t0001g0083a0001c0002t0001g0092others(49): Show | 52 | HG00544.hp1 HG01496.hp2 HG01891.hp2 others(49): Show |
intron_variant | MODIFIER | c.3050-2186dupT | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | INFO_REALIGN_3_PRIME | chr11 | 121564744 | |||||
| chr11:121564761
|
G | A | 86 | a0001c0002t0001g0010a0001c0002t0001g0083a0001c0002t0001g0092others(83): Show | 86 | HG00544.hp1 HG00735.hp1 HG01081.hp2 others(83): Show |
intron_variant | MODIFIER | c.3050-2179G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121564761 | ||||||
| chr11:121564878
|
T | C | 52 | a0001c0002t0001g0010a0001c0002t0001g0083a0001c0002t0001g0092others(49): Show | 52 | HG00544.hp1 HG01496.hp2 HG01891.hp2 others(49): Show |
intron_variant | MODIFIER | c.3050-2062T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121564878 | ||||||
| chr11:121565257
|
G | T | 36 | a0001c0003t0003g0254a0001c0003t0003g0262a0001c0003t0007g0264others(33): Show | 36 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.3050-1683G>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121565257 | ||||||
| chr11:121565295
|
G | A | 30 | a0001c0002t0001g0010a0001c0002t0001g0083a0001c0002t0001g0092others(27): Show | 30 | HG01496.hp2 HG01993.hp1 HG02040.hp1 others(27): Show |
intron_variant | MODIFIER | c.3050-1645G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121565295 | ||||||
| chr11:121565453
|
T | C | 1 | a0001c0066t0016g0194 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3050-1487T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121565453 | ||||||
| chr11:121565474
|
G | A | 1 | a0001c0062t0003g0250 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3050-1466G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121565474 | ||||||
| chr11:121565561
|
G | T | 71 | a0001c0002t0001g0010a0001c0002t0001g0083a0001c0002t0001g0092others(68): Show | 71 | HG00735.hp1 HG01081.hp2 HG01099.hp1 others(68): Show |
intron_variant | MODIFIER | c.3050-1379G>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121565561 | ||||||
| chr11:121565649
|
A | G | 1 | a0001c0008t0004g0005 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.3050-1291A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121565649 | ||||||
| chr11:121565802
|
A | G | 1 | a0001c0004t0029g0187 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.3050-1138A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121565802 | ||||||
| chr11:121565822
|
G | T | 1 | a0001c0002t0001g0116 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3050-1118G>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121565822 | ||||||
| chr11:121565860
|
C | G | 1 | a0001c0003t0007g0261 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3050-1080C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121565860 | ||||||
| chr11:121565930
|
C | A | 2 | a0001c0002t0003g0151a0001c0022t0003g0213 | 2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.3050-1010C>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121565930 | ||||||
| chr11:121566195
|
T | C | 1 | a0001c0001t0001g0059 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3050-745T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121566195 | ||||||
| chr11:121566199
|
G | C | 1 | a0004c0056t0013g0148 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3050-741G>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121566199 | ||||||
| chr11:121566220
|
T | C | 1 | a0004c0056t0013g0148 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3050-720T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121566220 | ||||||
| chr11:121566229
|
A | G | 1 | a0001c0001t0004g0099 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.3050-711A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121566229 | ||||||
| chr11:121566246
|
T | C | 145 | a0001c0002t0001g0010a0001c0002t0001g0083a0001c0002t0001g0092others(142): Show | 146 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.3050-694T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121566246 | ||||||
| chr11:121566275
|
T | G | 1 | a0001c0015t0005g0270 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.3050-665T>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121566275 | ||||||
| chr11:121566331
|
T | C | 1 | a0001c0003t0002g0225 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3050-609T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121566331 | ||||||
| chr11:121566353
|
G | A | 262 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(259): Show | 263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.3050-587G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121566353 | ||||||
| chr11:121566367
|
T | TA | 51 | a0001c0002t0001g0010a0001c0002t0001g0083a0001c0002t0001g0092others(48): Show | 51 | HG01496.hp2 HG01891.hp2 HG01993.hp1 others(48): Show |
intron_variant | MODIFIER | c.3050-562dupA | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | INFO_REALIGN_3_PRIME | chr11 | 121566367 | |||||
| chr11:121566379
|
T | A | 2 | a0001c0004t0001g0144a0002c0005t0001g0203 | 2 | NA18991.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.3050-561T>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121566379 | ||||||
| chr11:121566389
|
G | A | 1 | a0001c0065t0003g0152 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.3050-551G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121566389 | ||||||
| chr11:121566558
|
A | T | 60 | a0001c0002t0001g0103a0001c0002t0001g0112a0001c0002t0001g0116others(57): Show | 61 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.3050-382A>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121566558 | ||||||
| chr11:121566702
|
G | A | 11 | a0001c0002t0001g0139a0001c0002t0003g0151a0001c0006t0001g0068others(8): Show | 11 | HG00735.hp1 HG01081.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.3050-238G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121566702 | ||||||
| chr11:121566725
|
A | C | 1 | a0001c0001t0002g0141 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.3050-215A>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121566725 | ||||||
| chr11:121566862
|
A | G | 185 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(182): Show | 186 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.3050-78A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 21/47 | chr11 | 121566862 | ||||||
| chr11:121567211
|
C | T | 1 | a0001c0008t0002g0131 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.3223+98C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 22/47 | chr11 | 121567211 | ||||||
| chr11:121567317
|
C | T | 1 | a0011c0044t0002g0069 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3223+204C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 22/47 | chr11 | 121567317 | ||||||
| chr11:121567371
|
G | A | 3 | a0001c0001t0001g0025a0001c0001t0002g0141a0001c0001t0002g0142 | 3 | NA18977.hp2 NA19007.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.3223+258G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 22/47 | chr11 | 121567371 | ||||||
| chr11:121567494
|
C | G | 1 | a0002c0005t0003g0159 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3223+381C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 22/47 | chr11 | 121567494 | ||||||
| chr11:121567898
|
T | A | 12 | a0001c0002t0001g0139a0001c0002t0003g0151a0001c0006t0001g0068others(9): Show | 12 | HG00735.hp1 HG01081.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.3223+785T>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 22/47 | chr11 | 121567898 | ||||||
| chr11:121567909
|
TAAAGAGA others(4): Show |
T | 2 | a0001c0003t0003g0254a0001c0003t0003g0262 | 2 | NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.3223+806_3223+816d others(13): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 22/47 | INFO_REALIGN_3_PRIME | chr11 | 121567909 | |||||
| chr11:121567932
|
G | A | 1 | a0001c0038t0002g0186 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3223+819G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 22/47 | chr11 | 121567932 | ||||||
| chr11:121568222
|
C | T | 6 | a0001c0009t0010g0165a0001c0009t0011g0170a0001c0009t0011g0255others(3): Show | 6 | HG02486.hp2 HG02970.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.3223+1109C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 22/47 | chr11 | 121568222 | ||||||
| chr11:121568250
|
C | A | 2 | a0001c0061t0030g0249a0001c0062t0003g0250 | 2 | HG02559.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.3223+1137C>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 22/47 | chr11 | 121568250 | ||||||
| chr11:121568472
|
G | A | 12 | a0001c0002t0001g0139a0001c0002t0003g0151a0001c0006t0001g0068others(9): Show | 12 | HG00735.hp1 HG01081.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.3223+1359G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 22/47 | chr11 | 121568472 | ||||||
| chr11:121568910
|
T | C | 1 | a0001c0038t0002g0186 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3224-1247T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 22/47 | chr11 | 121568910 | ||||||
| chr11:121568956
|
T | C | 242 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(239): Show | 243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.3224-1201T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 22/47 | chr11 | 121568956 | ||||||
| chr11:121569009
|
C | T | 60 | a0001c0002t0001g0103a0001c0002t0001g0112a0001c0002t0001g0116others(57): Show | 61 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.3224-1148C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 22/47 | chr11 | 121569009 | ||||||
| chr11:121569010
|
G | A | 1 | a0015c0050t0002g0180 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3224-1147G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 22/47 | chr11 | 121569010 | ||||||
| chr11:121569163
|
ATGCCTG | A | 4 | a0001c0033t0003g0169a0001c0060t0003g0163a0001c0063t0010g0251others(1): Show | 4 | HG02559.hp2 HG02818.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.3224-992_3224-987d others(8): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 22/47 | INFO_REALIGN_3_PRIME | chr11 | 121569163 | |||||
| chr11:121569169
|
G | A | 131 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(128): Show | 131 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.3224-988G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 22/47 | chr11 | 121569169 | ||||||
| chr11:121569207
|
G | A | 1 | a0001c0038t0002g0186 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3224-950G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 22/47 | chr11 | 121569207 | ||||||
| chr11:121569269
|
G | C | 2 | a0001c0003t0003g0254a0001c0003t0003g0262 | 2 | NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.3224-888G>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 22/47 | chr11 | 121569269 | ||||||
| chr11:121569521
|
C | T | 12 | a0001c0002t0001g0139a0001c0002t0003g0151a0001c0006t0001g0068others(9): Show | 12 | HG00735.hp1 HG01081.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.3224-636C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 22/47 | chr11 | 121569521 | ||||||
| chr11:121569522
|
G | A | 135 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(132): Show | 135 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.3224-635G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 22/47 | chr11 | 121569522 | ||||||
| chr11:121569523
|
G | C | 1 | a0001c0004t0001g0110 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3224-634G>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 22/47 | chr11 | 121569523 | ||||||
| chr11:121569712
|
A | G | 6 | a0001c0009t0008g0207a0001c0021t0016g0206a0002c0014t0002g0172others(3): Show | 6 | HG02886.hp1 HG02896.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.3224-445A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 22/47 | chr11 | 121569712 | ||||||
| chr11:121569790
|
C | T | 1 | a0001c0021t0003g0216 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3224-367C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 22/47 | chr11 | 121569790 | ||||||
| chr11:121569791
|
A | G | 262 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(259): Show | 263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.3224-366A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 22/47 | chr11 | 121569791 | ||||||
| chr11:121569899
|
T | G | 2 | a0001c0001t0001g0052a0001c0028t0001g0046 | 2 | NA19068.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.3224-258T>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 22/47 | chr11 | 121569899 | ||||||
| chr11:121570296
|
G | A | 1 | a0001c0015t0005g0270 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.3337+26G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 23/47 | chr11 | 121570296 | ||||||
| chr11:121570306
|
T | A | 1 | a0001c0001t0001g0066 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.3337+36T>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 23/47 | chr11 | 121570306 | ||||||
| chr11:121570560
|
C | A | 1 | a0001c0008t0001g0136 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.3337+290C>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 23/47 | chr11 | 121570560 | ||||||
| chr11:121570635
|
T | G | 2 | a0001c0003t0005g0226a0001c0003t0005g0228 | 2 | HG02257.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.3337+365T>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 23/47 | chr11 | 121570635 | ||||||
| chr11:121570677
|
A | G | 3 | a0001c0001t0001g0052a0001c0001t0001g0058a0001c0028t0001g0046 | 3 | HG02155.hp1 NA19068.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.3337+407A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 23/47 | chr11 | 121570677 | ||||||
| chr11:121570679
|
G | T | 11 | a0001c0002t0001g0139a0001c0002t0003g0151a0001c0006t0001g0068others(8): Show | 11 | HG00735.hp1 HG01081.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.3337+409G>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 23/47 | chr11 | 121570679 | ||||||
| chr11:121570744
|
TTAGTAAT others(3): Show |
T | 1 | a0011c0044t0002g0069 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3337+478_3337+487d others(12): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 23/47 | INFO_REALIGN_3_PRIME | chr11 | 121570744 | |||||
| chr11:121570800
|
G | A | 2 | a0001c0002t0003g0150a0001c0038t0002g0186 | 2 | HG02109.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.3337+530G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 23/47 | chr11 | 121570800 | ||||||
| chr11:121570811
|
A | G | 243 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(240): Show | 244 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.3337+541A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 23/47 | chr11 | 121570811 | ||||||
| chr11:121571087
|
T | C | 1 | a0001c0019t0001g0029 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.3337+817T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 23/47 | chr11 | 121571087 | ||||||
| chr11:121571480
|
A | G | 90 | a0001c0002t0001g0010a0001c0002t0001g0083a0001c0002t0001g0092others(87): Show | 91 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.3337+1210A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 23/47 | chr11 | 121571480 | ||||||
| chr11:121571516
|
A | G | 1 | a0001c0038t0002g0186 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3337+1246A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 23/47 | chr11 | 121571516 | ||||||
| chr11:121571674
|
G | A | 1 | a0002c0048t0002g0201 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.3337+1404G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 23/47 | chr11 | 121571674 | ||||||
| chr11:121571731
|
T | C | 1 | a0001c0002t0001g0103 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.3337+1461T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 23/47 | chr11 | 121571731 | ||||||
| chr11:121571910
|
A | G | 17 | a0001c0003t0002g0105a0001c0003t0002g0115a0001c0003t0002g0117others(14): Show | 17 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(14): Show |
intron_variant | MODIFIER | c.3337+1640A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 23/47 | chr11 | 121571910 | ||||||
| chr11:121572205
|
C | G | 2 | a0001c0004t0001g0100a0001c0035t0001g0071 | 2 | HG04199.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.3337+1935C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 23/47 | chr11 | 121572205 | ||||||
| chr11:121572223
|
C | T | 1 | a0001c0038t0002g0186 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3337+1953C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 23/47 | chr11 | 121572223 | ||||||
| chr11:121572251
|
A | G | 1 | a0001c0004t0003g0224 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3337+1981A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 23/47 | chr11 | 121572251 | ||||||
| chr11:121572328
|
G | A | 80 | a0001c0002t0001g0103a0001c0002t0001g0112a0001c0002t0001g0116others(77): Show | 81 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.3338-1913G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 23/47 | chr11 | 121572328 | ||||||
| chr11:121572351
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.3338-1890C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 23/47 | chr11 | 121572351 | ||||||
| chr11:121572420
|
C | T | 6 | a0001c0009t0010g0165a0001c0009t0011g0170a0001c0009t0011g0255others(3): Show | 6 | HG02486.hp2 HG02970.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.3338-1821C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 23/47 | chr11 | 121572420 | ||||||
| chr11:121572481
|
C | T | 1 | a0001c0011t0002g0271 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.3338-1760C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 23/47 | chr11 | 121572481 | ||||||
| chr11:121572675
|
G | A | 4 | a0001c0033t0003g0169a0001c0060t0003g0163a0001c0063t0010g0251others(1): Show | 4 | HG02559.hp2 HG02818.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.3338-1566G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 23/47 | chr11 | 121572675 | ||||||
| chr11:121572954
|
C | T | 60 | a0001c0002t0001g0103a0001c0002t0001g0112a0001c0002t0001g0116others(57): Show | 61 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.3338-1287C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 23/47 | chr11 | 121572954 | ||||||
| chr11:121573085
|
G | A | 146 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(143): Show | 146 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.3338-1156G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 23/47 | chr11 | 121573085 | ||||||
| chr11:121573683
|
T | A | 1 | a0001c0001t0001g0047 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.3338-558T>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 23/47 | chr11 | 121573683 | ||||||
| chr11:121574048
|
G | T | 2 | a0001c0009t0008g0207a0004c0059t0002g0171 | 2 | HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3338-193G>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 23/47 | chr11 | 121574048 | ||||||
| chr11:121574084
|
A | G | 3 | a0001c0066t0016g0194a0002c0014t0014g0217a0002c0014t0014g0252 | 3 | HG01243.hp1 HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.3338-157A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 23/47 | chr11 | 121574084 | ||||||
| chr11:121574102
|
G | C | 30 | a0001c0002t0001g0010a0001c0002t0001g0083a0001c0002t0001g0092others(27): Show | 30 | HG01496.hp2 HG01993.hp1 HG02040.hp1 others(27): Show |
intron_variant | MODIFIER | c.3338-139G>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 23/47 | chr11 | 121574102 | ||||||
| chr11:121574201
|
T | C | 1 | a0001c0046t0002g0174 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3338-40T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 23/47 | chr11 | 121574201 | ||||||
| chr11:121574375
|
T | C | 262 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(259): Show | 263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.3460+12T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 24/47 | chr11 | 121574375 | ||||||
| chr11:121574565
|
C | T | 80 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(77): Show | 80 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.3460+202C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 24/47 | chr11 | 121574565 | ||||||
| chr11:121574593
|
C | T | 1 | a0001c0058t0011g0166 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3460+230C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 24/47 | chr11 | 121574593 | ||||||
| chr11:121574604
|
C | T | 1 | a0004c0056t0013g0148 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3460+241C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 24/47 | chr11 | 121574604 | ||||||
| chr11:121574874
|
A | G | 1 | a0001c0003t0002g0101 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3460+511A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 24/47 | chr11 | 121574874 | ||||||
| chr11:121575137
|
T | A | 2 | a0002c0025t0003g0260a0002c0049t0003g0162 | 2 | HG01891.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.3460+774T>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 24/47 | chr11 | 121575137 | ||||||
| chr11:121575146
|
T | C | 15 | a0001c0009t0008g0207a0001c0009t0010g0165a0001c0009t0011g0170others(12): Show | 15 | HG01243.hp1 HG02486.hp2 HG02886.hp1 others(12): Show |
intron_variant | MODIFIER | c.3460+783T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 24/47 | chr11 | 121575146 | ||||||
| chr11:121575231
|
A | G | 30 | a0001c0002t0001g0010a0001c0002t0001g0083a0001c0002t0001g0092others(27): Show | 30 | HG01496.hp2 HG01993.hp1 HG02040.hp1 others(27): Show |
intron_variant | MODIFIER | c.3460+868A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 24/47 | chr11 | 121575231 | ||||||
| chr11:121575350
|
C | A | 155 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(152): Show | 155 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.3460+987C>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 24/47 | chr11 | 121575350 | ||||||
| chr11:121575375
|
T | G | 1 | a0001c0003t0002g0101 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3460+1012T>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 24/47 | chr11 | 121575375 | ||||||
| chr11:121575466
|
G | A | 2 | a0001c0001t0001g0048a0001c0001t0001g0075 | 2 | HG03017.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.3460+1103G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 24/47 | chr11 | 121575466 | ||||||
| chr11:121575509
|
C | G | 30 | a0001c0002t0001g0010a0001c0002t0001g0083a0001c0002t0001g0092others(27): Show | 30 | HG01496.hp2 HG01993.hp1 HG02040.hp1 others(27): Show |
intron_variant | MODIFIER | c.3460+1146C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 24/47 | chr11 | 121575509 | ||||||
| chr11:121575780
|
G | A | 2 | a0001c0060t0003g0163a0006c0043t0026g0215 | 2 | HG02559.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.3460+1417G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 24/47 | chr11 | 121575780 | ||||||
| chr11:121575839
|
T | C | 13 | a0001c0002t0001g0139a0001c0002t0003g0151a0001c0006t0001g0068others(10): Show | 13 | HG00735.hp1 HG01081.hp2 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.3461-1442T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 24/47 | chr11 | 121575839 | ||||||
| chr11:121575890
|
T | C | 232 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(229): Show | 233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.3461-1391T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 24/47 | chr11 | 121575890 | ||||||
| chr11:121576104
|
C | G | 159 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(156): Show | 159 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.3461-1177C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 24/47 | chr11 | 121576104 | ||||||
| chr11:121576302
|
C | T | 85 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(82): Show | 85 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.3461-979C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 24/47 | chr11 | 121576302 | ||||||
| chr11:121576364
|
G | A | 7 | a0001c0003t0003g0254a0001c0003t0003g0262a0001c0008t0002g0177others(4): Show | 7 | HG01884.hp2 HG02622.hp2 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.3461-917G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 24/47 | chr11 | 121576364 | ||||||
| chr11:121576384
|
C | T | 6 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0036others(3): Show | 6 | HG00544.hp2 HG02040.hp2 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.3461-897C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 24/47 | chr11 | 121576384 | ||||||
| chr11:121576479
|
T | C | 85 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(82): Show | 85 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.3461-802T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 24/47 | chr11 | 121576479 | ||||||
| chr11:121576774
|
G | C | 1 | a0001c0060t0003g0163 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3461-507G>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 24/47 | chr11 | 121576774 | ||||||
| chr11:121576884
|
A | C | 15 | a0001c0009t0008g0207a0001c0009t0010g0165a0001c0009t0011g0170others(12): Show | 15 | HG01243.hp1 HG02486.hp2 HG02886.hp1 others(12): Show |
intron_variant | MODIFIER | c.3461-397A>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 24/47 | chr11 | 121576884 | ||||||
| chr11:121577098
|
A | G | 262 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(259): Show | 263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.3461-183A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 24/47 | chr11 | 121577098 | ||||||
| chr11:121577444
|
G | C | 2 | a0001c0001t0001g0048a0001c0001t0001g0075 | 2 | HG03017.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.3580+44G>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 25/47 | chr11 | 121577444 | ||||||
| chr11:121577474
|
C | G | 85 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(82): Show | 85 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.3580+74C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 25/47 | chr11 | 121577474 | ||||||
| chr11:121577545
|
G | A | 19 | a0001c0013t0002g0016a0001c0013t0002g0018a0001c0013t0002g0035others(16): Show | 19 | HG01891.hp2 HG02647.hp1 HG02809.hp1 others(16): Show |
intron_variant | MODIFIER | c.3580+145G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 25/47 | chr11 | 121577545 | ||||||
| chr11:121577629
|
G | A | 69 | a0001c0001t0001g0063a0001c0002t0001g0010a0001c0002t0001g0083others(66): Show | 69 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.3580+229G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 25/47 | chr11 | 121577629 | ||||||
| chr11:121577850
|
G | A | 13 | a0001c0009t0008g0207a0001c0009t0011g0170a0001c0009t0011g0255others(10): Show | 13 | HG01243.hp1 HG02486.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.3580+450G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 25/47 | chr11 | 121577850 | ||||||
| chr11:121577875
|
G | A | 1 | a0005c0017t0001g0240 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.3580+475G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 25/47 | chr11 | 121577875 | ||||||
| chr11:121578243
|
A | G | 3 | a0001c0001t0001g0061a0001c0004t0009g0015a0002c0005t0004g0043 | 3 | HG00738.hp2 HG01167.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.3580+843A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 25/47 | chr11 | 121578243 | ||||||
| chr11:121578263
|
T | C | 30 | a0001c0002t0001g0010a0001c0002t0001g0083a0001c0002t0001g0092others(27): Show | 30 | HG01496.hp2 HG01993.hp1 HG02040.hp1 others(27): Show |
intron_variant | MODIFIER | c.3580+863T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 25/47 | chr11 | 121578263 | ||||||
| chr11:121578324
|
T | A | 1 | a0001c0038t0002g0186 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3580+924T>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 25/47 | chr11 | 121578324 | ||||||
| chr11:121578325
|
C | A | 1 | a0001c0038t0002g0186 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3580+925C>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 25/47 | chr11 | 121578325 | ||||||
| chr11:121578397
|
G | T | 2 | a0001c0004t0001g0144a0002c0005t0001g0203 | 2 | NA18991.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.3580+997G>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 25/47 | chr11 | 121578397 | ||||||
| chr11:121578491
|
A | G | 1 | a0001c0036t0003g0266 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3580+1091A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 25/47 | chr11 | 121578491 | ||||||
| chr11:121579097
|
G | A | 3 | a0001c0011t0001g0107a0001c0011t0002g0271a0001c0016t0002g0121 | 3 | HG01074.hp2 HG01256.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.3580+1697G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 25/47 | chr11 | 121579097 | ||||||
| chr11:121579139
|
CT | C | 84 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(81): Show | 84 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.3580+1741delT | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 25/47 | INFO_REALIGN_3_PRIME | chr11 | 121579139 | |||||
| chr11:121579241
|
T | C | 1 | a0001c0001t0001g0047 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.3580+1841T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 25/47 | chr11 | 121579241 | ||||||
| chr11:121579271
|
C | T | 1 | a0001c0002t0002g0109 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.3580+1871C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 25/47 | chr11 | 121579271 | ||||||
| chr11:121579355
|
A | G | 1 | a0001c0006t0001g0157 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3580+1955A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 25/47 | chr11 | 121579355 | ||||||
| chr11:121579512
|
G | A | 12 | a0001c0002t0001g0139a0001c0002t0003g0151a0001c0006t0001g0068others(9): Show | 12 | HG00735.hp1 HG01081.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.3580+2112G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 25/47 | chr11 | 121579512 | ||||||
| chr11:121579566
|
A | G | 4 | a0001c0033t0003g0169a0001c0060t0003g0163a0001c0063t0010g0251others(1): Show | 4 | HG02559.hp2 HG02818.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.3580+2166A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 25/47 | chr11 | 121579566 | ||||||
| chr11:121579623
|
G | A | 30 | a0001c0002t0001g0010a0001c0002t0001g0083a0001c0002t0001g0092others(27): Show | 30 | HG01496.hp2 HG01993.hp1 HG02040.hp1 others(27): Show |
intron_variant | MODIFIER | c.3580+2223G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 25/47 | chr11 | 121579623 | ||||||
| chr11:121579660
|
C | T | 1 | a0001c0022t0008g0211 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3580+2260C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 25/47 | chr11 | 121579660 | ||||||
| chr11:121579985
|
T | C | 1 | a0001c0038t0002g0186 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3580+2585T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 25/47 | chr11 | 121579985 | ||||||
| chr11:121580270
|
G | A | 1 | a0001c0002t0001g0139 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3580+2870G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 25/47 | chr11 | 121580270 | ||||||
| chr11:121580335
|
CTG | C | 5 | a0001c0002t0001g0116a0001c0002t0006g0001a0001c0002t0006g0014others(2): Show | 6 | HG00438.hp2 HG02080.hp2 HG02155.hp2 others(3): Show |
intron_variant | MODIFIER | c.3580+2938_3580+293 others(6): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 25/47 | INFO_REALIGN_3_PRIME | chr11 | 121580335 | |||||
| chr11:121580500
|
G | A | 50 | a0001c0002t0001g0103a0001c0002t0001g0112a0001c0002t0001g0116others(47): Show | 51 | HG00099.hp1 HG00438.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.3581-2958G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 25/47 | chr11 | 121580500 | ||||||
| chr11:121580595
|
A | G | 15 | a0001c0009t0008g0207a0001c0009t0010g0165a0001c0009t0011g0170others(12): Show | 15 | HG01243.hp1 HG02486.hp2 HG02886.hp1 others(12): Show |
intron_variant | MODIFIER | c.3581-2863A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 25/47 | chr11 | 121580595 | ||||||
| chr11:121580604
|
C | CT | 164 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0024others(161): Show | 164 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.3581-2836dupT | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 25/47 | INFO_REALIGN_3_PRIME | chr11 | 121580604 | |||||
| chr11:121580604
|
C | CTT | 5 | a0001c0001t0001g0023a0001c0001t0001g0038a0001c0001t0001g0220others(2): Show | 5 | HG02523.hp1 HG02818.hp1 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.3581-2837_3581-283 others(6): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 25/47 | INFO_REALIGN_3_PRIME | chr11 | 121580604 | |||||
| chr11:121580668
|
G | A | 2 | a0001c0003t0012g0184a0001c0003t0023g0183 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.3581-2790G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 25/47 | chr11 | 121580668 | ||||||
| chr11:121580708
|
C | T | 3 | a0001c0004t0004g0011a0001c0004t0004g0012a0002c0005t0001g0127 | 3 | HG01256.hp2 HG01258.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.3581-2750C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 25/47 | chr11 | 121580708 | ||||||
| chr11:121580716
|
C | G | 4 | a0001c0009t0011g0170a0001c0009t0011g0255a0001c0057t0002g0160others(1): Show | 4 | HG02486.hp2 HG02976.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.3581-2742C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 25/47 | chr11 | 121580716 | ||||||
| chr11:121580843
|
G | A | 84 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(81): Show | 84 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.3581-2615G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 25/47 | chr11 | 121580843 | ||||||
| chr11:121580918
|
C | CT | 33 | a0001c0002t0001g0010a0001c0002t0001g0083a0001c0002t0001g0092others(30): Show | 33 | HG00642.hp1 HG01175.hp1 HG01496.hp2 others(30): Show |
intron_variant | MODIFIER | c.3581-2524dupT | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 25/47 | INFO_REALIGN_3_PRIME | chr11 | 121580918 | |||||
| chr11:121580918
|
CT | C | 14 | a0001c0001t0001g0024a0001c0002t0001g0139a0001c0002t0003g0151others(11): Show | 14 | HG00735.hp1 HG01081.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.3581-2524delT | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 25/47 | INFO_REALIGN_3_PRIME | chr11 | 121580918 | |||||
| chr11:121580929
|
T | C | 3 | a0001c0066t0016g0194a0002c0014t0014g0217a0002c0014t0014g0252 | 3 | HG01243.hp1 HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.3581-2529T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 25/47 | chr11 | 121580929 | ||||||
| chr11:121580952
|
G | A | 4 | a0001c0009t0011g0170a0001c0009t0011g0255a0001c0057t0002g0160others(1): Show | 4 | HG02486.hp2 HG02976.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.3581-2506G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 25/47 | chr11 | 121580952 | ||||||
| chr11:121580992
|
A | G | 29 | a0001c0002t0001g0010a0001c0002t0001g0083a0001c0002t0001g0092others(26): Show | 29 | HG01496.hp2 HG02040.hp1 HG02148.hp1 others(26): Show |
intron_variant | MODIFIER | c.3581-2466A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 25/47 | chr11 | 121580992 | ||||||
| chr11:121581104
|
T | G | 241 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(238): Show | 242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.3581-2354T>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 25/47 | chr11 | 121581104 | ||||||
| chr11:121581164
|
C | T | 3 | a0001c0066t0016g0194a0002c0014t0014g0217a0002c0014t0014g0252 | 3 | HG01243.hp1 HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.3581-2294C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 25/47 | chr11 | 121581164 | ||||||
| chr11:121581217
|
T | C | 56 | a0001c0002t0001g0103a0001c0002t0001g0112a0001c0002t0001g0116others(53): Show | 57 | HG00099.hp1 HG00438.hp2 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.3581-2241T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 25/47 | chr11 | 121581217 | ||||||
| chr11:121581231
|
C | T | 185 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(182): Show | 185 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.3581-2227C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 25/47 | chr11 | 121581231 | ||||||
| chr11:121581269
|
C | G | 185 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(182): Show | 185 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.3581-2189C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 25/47 | chr11 | 121581269 | ||||||
| chr11:121581324
|
C | T | 1 | a0001c0018t0002g0013 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.3581-2134C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 25/47 | chr11 | 121581324 | ||||||
| chr11:121581325
|
A | G | 262 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(259): Show | 263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.3581-2133A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 25/47 | chr11 | 121581325 | ||||||
| chr11:121581427
|
G | T | 1 | a0001c0011t0012g0242 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.3581-2031G>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 25/47 | chr11 | 121581427 | ||||||
| chr11:121581546
|
TA | T | 11 | a0001c0002t0001g0139a0001c0002t0003g0151a0001c0006t0001g0068others(8): Show | 11 | HG00735.hp1 HG01081.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.3581-1902delA | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 25/47 | INFO_REALIGN_3_PRIME | chr11 | 121581546 | |||||
| chr11:121581645
|
G | A | 74 | a0001c0002t0001g0010a0001c0002t0001g0083a0001c0002t0001g0092others(71): Show | 74 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.3581-1813G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 25/47 | chr11 | 121581645 | ||||||
| chr11:121581942
|
T | A | 85 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(82): Show | 85 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.3581-1516T>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 25/47 | chr11 | 121581942 | ||||||
| chr11:121582313
|
T | C | 4 | a0001c0033t0003g0169a0001c0060t0003g0163a0001c0063t0010g0251others(1): Show | 4 | HG02559.hp2 HG02818.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.3581-1145T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 25/47 | chr11 | 121582313 | ||||||
| chr11:121582517
|
G | A | 1 | a0001c0031t0010g0214 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3581-941G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 25/47 | chr11 | 121582517 | ||||||
| chr11:121582651
|
G | A | 1 | a0001c0003t0002g0135 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.3581-807G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 25/47 | chr11 | 121582651 | ||||||
| chr11:121582783
|
T | G | 15 | a0001c0009t0008g0207a0001c0009t0010g0165a0001c0009t0011g0170others(12): Show | 15 | HG01243.hp1 HG02486.hp2 HG02886.hp1 others(12): Show |
intron_variant | MODIFIER | c.3581-675T>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 25/47 | chr11 | 121582783 | ||||||
| chr11:121582808
|
T | G | 21 | a0001c0013t0002g0016a0001c0013t0002g0018a0001c0013t0002g0035others(18): Show | 21 | HG00544.hp1 HG01891.hp2 HG02647.hp1 others(18): Show |
intron_variant | MODIFIER | c.3581-650T>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 25/47 | chr11 | 121582808 | ||||||
| chr11:121582810
|
T | G | 11 | a0001c0002t0001g0139a0001c0002t0003g0151a0001c0006t0001g0068others(8): Show | 11 | HG00735.hp1 HG01081.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.3581-648T>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 25/47 | chr11 | 121582810 | ||||||
| chr11:121582954
|
T | C | 1 | a0015c0050t0002g0180 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3581-504T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 25/47 | chr11 | 121582954 | ||||||
| chr11:121582998
|
C | T | 12 | a0001c0002t0001g0139a0001c0002t0003g0151a0001c0006t0001g0068others(9): Show | 12 | HG00735.hp1 HG01081.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.3581-460C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 25/47 | chr11 | 121582998 | ||||||
| chr11:121583070
|
A | T | 68 | a0001c0002t0001g0010a0001c0002t0001g0083a0001c0002t0001g0092others(65): Show | 68 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.3581-388A>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 25/47 | chr11 | 121583070 | ||||||
| chr11:121583074
|
C | T | 30 | a0001c0002t0001g0010a0001c0002t0001g0083a0001c0002t0001g0092others(27): Show | 30 | HG01496.hp2 HG01993.hp1 HG02040.hp1 others(27): Show |
intron_variant | MODIFIER | c.3581-384C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 25/47 | chr11 | 121583074 | ||||||
| chr11:121583137
|
C | T | 1 | a0001c0001t0001g0038 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.3581-321C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 25/47 | chr11 | 121583137 | ||||||
| chr11:121583164
|
G | T | 1 | a0001c0060t0003g0163 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3581-294G>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 25/47 | chr11 | 121583164 | ||||||
| chr11:121583189
|
C | G | 12 | a0001c0002t0001g0139a0001c0002t0003g0151a0001c0006t0001g0068others(9): Show | 12 | HG00735.hp1 HG01081.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.3581-269C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 25/47 | chr11 | 121583189 | ||||||
| chr11:121583435
|
T | C | 1 | a0001c0002t0004g0093 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.3581-23T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 25/47 | chr11 | 121583435 | ||||||
| chr11:121583440
|
C | G | 37 | a0001c0003t0003g0254a0001c0003t0003g0262a0001c0003t0007g0261others(34): Show | 37 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.3581-18C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 25/47 | chr11 | 121583440 | ||||||
| chr11:121583680
|
C | T | 1 | a0001c0002t0003g0150 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3706+97C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 26/47 | chr11 | 121583680 | ||||||
| chr11:121584273
|
T | C | 1 | a0001c0001t0002g0185 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3706+690T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 26/47 | chr11 | 121584273 | ||||||
| chr11:121584515
|
T | TA | 82 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(79): Show | 82 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.3706+933dupA | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr11 | 121584515 | |||||
| chr11:121584528
|
C | T | 1 | a0001c0002t0003g0150 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3706+945C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 26/47 | chr11 | 121584528 | ||||||
| chr11:121584597
|
C | CT | 11 | a0001c0011t0020g0106a0001c0013t0002g0018a0001c0013t0002g0054others(8): Show | 11 | HG01192.hp1 HG01192.hp2 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.3706+1026dupT | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr11 | 121584597 | |||||
| chr11:121584613
|
A | G | 1 | a0001c0038t0002g0186 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3706+1030A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 26/47 | chr11 | 121584613 | ||||||
| chr11:121584636
|
G | A | 5 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0061others(2): Show | 5 | HG00738.hp2 HG01167.hp1 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.3706+1053G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 26/47 | chr11 | 121584636 | ||||||
| chr11:121584682
|
C | T | 37 | a0001c0003t0003g0254a0001c0003t0003g0262a0001c0003t0007g0261others(34): Show | 37 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.3706+1099C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 26/47 | chr11 | 121584682 | ||||||
| chr11:121584689
|
G | T | 2 | a0001c0009t0008g0207a0004c0059t0002g0171 | 2 | HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3706+1106G>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 26/47 | chr11 | 121584689 | ||||||
| chr11:121584841
|
A | G | 1 | a0001c0004t0003g0224 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3706+1258A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 26/47 | chr11 | 121584841 | ||||||
| chr11:121584886
|
G | A | 2 | a0001c0004t0004g0011a0001c0004t0004g0012 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.3706+1303G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 26/47 | chr11 | 121584886 | ||||||
| chr11:121584943
|
A | G | 13 | a0001c0002t0001g0139a0001c0002t0003g0151a0001c0006t0001g0068others(10): Show | 13 | HG00735.hp1 HG01081.hp2 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.3707-1279A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 26/47 | chr11 | 121584943 | ||||||
| chr11:121585036
|
T | C | 2 | a0002c0025t0003g0260a0002c0049t0003g0162 | 2 | HG01891.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.3707-1186T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 26/47 | chr11 | 121585036 | ||||||
| chr11:121585221
|
C | T | 50 | a0001c0002t0001g0103a0001c0002t0001g0112a0001c0002t0001g0116others(47): Show | 51 | HG00099.hp1 HG00438.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.3707-1001C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 26/47 | chr11 | 121585221 | ||||||
| chr11:121585352
|
G | A | 30 | a0001c0002t0001g0010a0001c0002t0001g0083a0001c0002t0001g0092others(27): Show | 30 | HG01496.hp2 HG01993.hp1 HG02040.hp1 others(27): Show |
intron_variant | MODIFIER | c.3707-870G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 26/47 | chr11 | 121585352 | ||||||
| chr11:121585380
|
G | A | 1 | a0010c0037t0005g0259 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3707-842G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 26/47 | chr11 | 121585380 | ||||||
| chr11:121585495
|
GTA | G | 8 | a0001c0009t0011g0170a0001c0009t0011g0255a0001c0021t0016g0206others(5): Show | 8 | HG02486.hp2 HG02886.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.3707-722_3707-721d others(4): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr11 | 121585495 | |||||
| chr11:121585498
|
T | TACAC | 10 | a0001c0002t0004g0077a0001c0002t0004g0079a0001c0002t0004g0084others(7): Show | 10 | HG01243.hp1 HG01993.hp1 HG03130.hp1 others(7): Show |
intron_variant | MODIFIER | c.3707-723_3707-722i others(6): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr11 | 121585498 | |||||
| chr11:121585498
|
T | TACACAC | 5 | a0001c0002t0001g0083a0001c0002t0003g0150a0001c0002t0004g0078others(2): Show | 5 | HG02109.hp2 NA18612.hp2 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.3707-723_3707-722i others(8): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr11 | 121585498 | |||||
| chr11:121585498
|
T | TACACACA others(1): Show |
15 | a0001c0002t0001g0010a0001c0002t0001g0092a0001c0002t0001g0129others(12): Show | 15 | HG02165.hp1 HG02273.hp1 NA18747.hp2 others(12): Show |
intron_variant | MODIFIER | c.3707-723_3707-722i others(10): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr11 | 121585498 | |||||
| chr11:121585498
|
T | TACACACA others(3): Show |
3 | a0001c0002t0001g0130a0001c0002t0004g0003a0001c0002t0004g0090 | 3 | HG02040.hp1 HG02148.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.3707-723_3707-722i others(12): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr11 | 121585498 | |||||
| chr11:121585498
|
T | TACACACA others(5): Show |
1 | a0001c0006t0009g0200 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3707-723_3707-722i others(14): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr11 | 121585498 | |||||
| chr11:121585500
|
T | C | 34 | a0001c0002t0001g0010a0001c0002t0001g0083a0001c0002t0001g0092others(31): Show | 34 | HG01243.hp1 HG01496.hp2 HG01993.hp1 others(31): Show |
intron_variant | MODIFIER | c.3707-722T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 26/47 | chr11 | 121585500 | ||||||
| chr11:121585500
|
T | TAC | 22 | a0001c0001t0001g0038a0001c0001t0001g0048a0001c0001t0001g0153others(19): Show | 22 | HG00099.hp2 HG00438.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.3707-685_3707-684d others(4): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr11 | 121585500 | |||||
| chr11:121585500
|
T | TACAC | 58 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(55): Show | 58 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.3707-687_3707-684d others(6): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr11 | 121585500 | |||||
| chr11:121585500
|
T | TACACAC | 7 | a0001c0001t0001g0023a0001c0001t0001g0049a0001c0001t0001g0051others(4): Show | 7 | HG02027.hp2 HG02738.hp1 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.3707-689_3707-684d others(8): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr11 | 121585500 | |||||
| chr11:121585500
|
T | TACACACA others(1): Show |
4 | a0001c0001t0001g0006a0001c0001t0004g0099a0001c0004t0001g0110others(1): Show | 4 | HG01099.hp1 HG01884.hp1 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.3707-691_3707-684d others(10): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr11 | 121585500 | |||||
| chr11:121585500
|
T | TACACACA others(3): Show |
6 | a0001c0001t0001g0009a0001c0001t0002g0167a0001c0002t0003g0151others(3): Show | 6 | HG00280.hp1 HG00323.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.3707-693_3707-684d others(12): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr11 | 121585500 | |||||
| chr11:121585500
|
T | TACACACA others(7): Show |
1 | a0001c0009t0003g0147 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3707-697_3707-684d others(16): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr11 | 121585500 | |||||
| chr11:121585500
|
TAC | T | 3 | a0001c0003t0002g0133a0001c0008t0002g0177a0001c0012t0007g0175 | 3 | HG00741.hp1 HG01884.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.3707-685_3707-684d others(4): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr11 | 121585500 | |||||
| chr11:121585500
|
TACAC | T | 6 | a0001c0003t0002g0230a0001c0009t0010g0165a0002c0005t0019g0062others(3): Show | 6 | HG00544.hp1 HG02258.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.3707-687_3707-684d others(6): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr11 | 121585500 | |||||
| chr11:121585500
|
TACACAC | T | 21 | a0001c0013t0002g0016a0001c0013t0002g0018a0001c0013t0002g0035others(18): Show | 21 | HG01891.hp2 HG02647.hp1 HG02809.hp1 others(18): Show |
intron_variant | MODIFIER | c.3707-689_3707-684d others(8): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr11 | 121585500 | |||||
| chr11:121585500
|
TACACACA others(3): Show |
T | 2 | a0001c0046t0002g0174a0002c0005t0003g0159 | 2 | HG03540.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.3707-693_3707-684d others(12): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr11 | 121585500 | |||||
| chr11:121585502
|
C | T | 1 | a0001c0065t0003g0152 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.3707-720C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 26/47 | chr11 | 121585502 | ||||||
| chr11:121585506
|
C | T | 1 | a0001c0009t0010g0165 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3707-716C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 26/47 | chr11 | 121585506 | ||||||
| chr11:121585841
|
G | C | 1 | a0001c0052t0001g0219 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.3707-381G>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 26/47 | chr11 | 121585841 | ||||||
| chr11:121585947
|
C | G | 71 | a0001c0002t0001g0010a0001c0002t0001g0083a0001c0002t0001g0092others(68): Show | 71 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.3707-275C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 26/47 | chr11 | 121585947 | ||||||
| chr11:121586339
|
T | G | 1 | a0001c0023t0002g0070 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.3814+10T>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 27/47 | chr11 | 121586339 | ||||||
| chr11:121586468
|
C | T | 3 | a0001c0003t0005g0226a0001c0003t0005g0228a0004c0041t0013g0189 | 3 | HG02257.hp1 HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.3814+139C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 27/47 | chr11 | 121586468 | ||||||
| chr11:121586693
|
TGGGGGGG | T | 18 | a0001c0002t0001g0112a0001c0002t0001g0130a0001c0002t0001g0158others(15): Show | 18 | HG00642.hp1 HG00741.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.3814+369_3814+375d others(9): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 27/47 | INFO_REALIGN_3_PRIME | chr11 | 121586693 | |||||
| chr11:121586695
|
G | A | 3 | a0001c0009t0011g0170a0001c0009t0011g0255a0001c0058t0011g0166 | 3 | HG02486.hp2 HG03139.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3814+366G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 27/47 | chr11 | 121586695 | ||||||
| chr11:121586697
|
G | T | 1 | a0002c0025t0005g0179 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3814+368G>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 27/47 | chr11 | 121586697 | ||||||
| chr11:121586697
|
GGGGGGGG others(1): Show |
G | 139 | a0001c0001t0001g0048a0001c0001t0001g0050a0001c0001t0001g0052others(136): Show | 140 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.3814+376_3814+383d others(10): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 27/47 | INFO_REALIGN_3_PRIME | chr11 | 121586697 | |||||
| chr11:121586698
|
G | C | 2 | a0001c0002t0004g0079a0001c0065t0003g0152 | 2 | HG02970.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.3814+369G>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 27/47 | chr11 | 121586698 | ||||||
| chr11:121586705
|
C | G | 57 | a0001c0001t0001g0006a0001c0001t0001g0025a0001c0001t0001g0036others(54): Show | 57 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.3814+376C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 27/47 | chr11 | 121586705 | ||||||
| chr11:121586705
|
CG | C | 16 | a0001c0002t0003g0151a0001c0009t0003g0147a0001c0013t0002g0016others(13): Show | 16 | HG01891.hp2 HG02622.hp1 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.3814+386delG | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 27/47 | INFO_REALIGN_3_PRIME | chr11 | 121586705 | |||||
| chr11:121586706
|
G | C | 152 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0050others(149): Show | 153 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.3814+377G>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 27/47 | chr11 | 121586706 | ||||||
| chr11:121586706
|
G | GC | 21 | a0001c0001t0001g0006a0001c0001t0001g0025a0001c0001t0001g0045others(18): Show | 21 | HG00280.hp1 HG00639.hp2 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.3814+377_3814+378i others(3): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 27/47 | chr11 | 121586706 | ||||||
| chr11:121586706
|
G | GGC | 18 | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0040others(15): Show | 18 | HG00323.hp2 HG00544.hp2 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.3814+378_3814+379i others(4): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 27/47 | INFO_REALIGN_3_PRIME | chr11 | 121586706 | |||||
| chr11:121586709
|
G | T | 7 | a0001c0020t0003g0248a0001c0020t0003g0268a0001c0020t0003g0269others(4): Show | 7 | HG01109.hp2 HG02486.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.3814+380G>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 27/47 | chr11 | 121586709 | ||||||
| chr11:121586868
|
TGATTTAA others(14): Show |
T | 1 | a0001c0002t0001g0103 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.3814+541_3814+561d others(23): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 27/47 | INFO_REALIGN_3_PRIME | chr11 | 121586868 | |||||
| chr11:121586875
|
A | G | 1 | a0001c0003t0002g0101 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3814+546A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 27/47 | chr11 | 121586875 | ||||||
| chr11:121587053
|
T | G | 7 | a0001c0002t0001g0139a0001c0006t0001g0068a0001c0006t0001g0072others(4): Show | 7 | HG00735.hp1 HG01243.hp2 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.3814+724T>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 27/47 | chr11 | 121587053 | ||||||
| chr11:121587395
|
G | A | 1 | a0002c0005t0019g0062 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.3815-625G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 27/47 | chr11 | 121587395 | ||||||
| chr11:121587471
|
G | A | 2 | a0002c0007t0017g0122a0002c0007t0017g0123 | 2 | NA18942.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.3815-549G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 27/47 | chr11 | 121587471 | ||||||
| chr11:121587770
|
A | G | 2 | a0001c0061t0030g0249a0001c0062t0003g0250 | 2 | HG02559.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.3815-250A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 27/47 | chr11 | 121587770 | ||||||
| chr11:121587787
|
A | G | 1 | a0015c0050t0002g0180 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3815-233A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 27/47 | chr11 | 121587787 | ||||||
| chr11:121587936
|
G | A | 29 | a0001c0002t0001g0010a0001c0002t0001g0083a0001c0002t0001g0092others(26): Show | 29 | HG02040.hp1 HG02148.hp1 HG02165.hp1 others(26): Show |
intron_variant | MODIFIER | c.3815-84G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 27/47 | chr11 | 121587936 | ||||||
| chr11:121588235
|
A | G | 1 | a0004c0056t0013g0148 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3946+84A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 28/47 | chr11 | 121588235 | ||||||
| chr11:121588279
|
A | C | 1 | a0001c0033t0003g0169 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3946+128A>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 28/47 | chr11 | 121588279 | ||||||
| chr11:121588355
|
C | T | 1 | a0004c0056t0013g0148 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3946+204C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 28/47 | chr11 | 121588355 | ||||||
| chr11:121588416
|
C | T | 4 | a0001c0009t0008g0207a0002c0025t0005g0179a0004c0059t0002g0171others(1): Show | 4 | HG02965.hp1 HG03209.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.3946+265C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 28/47 | chr11 | 121588416 | ||||||
| chr11:121588456
|
G | T | 1 | a0001c0002t0003g0150 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3946+305G>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 28/47 | chr11 | 121588456 | ||||||
| chr11:121588575
|
C | T | 3 | a0001c0033t0003g0169a0001c0060t0003g0163a0006c0043t0026g0215 | 3 | HG02559.hp2 HG02922.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.3946+424C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 28/47 | chr11 | 121588575 | ||||||
| chr11:121588794
|
C | G | 1 | a0001c0015t0005g0270 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.3947-465C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 28/47 | chr11 | 121588794 | ||||||
| chr11:121588798
|
C | G | 1 | a0007c0072t0002g0256 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3947-461C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 28/47 | chr11 | 121588798 | ||||||
| chr11:121588813
|
C | T | 57 | a0001c0002t0001g0103a0001c0002t0001g0112a0001c0002t0001g0116others(54): Show | 58 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.3947-446C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 28/47 | chr11 | 121588813 | ||||||
| chr11:121588943
|
C | T | 1 | a0001c0032t0003g0149 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3947-316C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 28/47 | chr11 | 121588943 | ||||||
| chr11:121589055
|
C | T | 7 | a0001c0008t0018g0192a0001c0011t0001g0107a0001c0011t0002g0271others(4): Show | 7 | HG01074.hp2 HG01192.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.3947-204C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 28/47 | chr11 | 121589055 | ||||||
| chr11:121589056
|
G | A | 1 | a0001c0002t0003g0150 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3947-203G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 28/47 | chr11 | 121589056 | ||||||
| chr11:121589192
|
AC | A | 4 | a0002c0005t0001g0074a0002c0005t0001g0205a0008c0024t0002g0033others(1): Show | 4 | HG01433.hp1 HG03490.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.3947-65delC | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 28/47 | INFO_REALIGN_3_PRIME | chr11 | 121589192 | |||||
| chr11:121589538
|
C | T | 2 | a0001c0001t0001g0153a0001c0001t0002g0154 | 2 | HG02080.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.4078+148C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 29/47 | chr11 | 121589538 | ||||||
| chr11:121589615
|
T | C | 36 | a0001c0009t0003g0147a0001c0009t0008g0207a0001c0009t0010g0165others(33): Show | 36 | HG00544.hp1 HG01891.hp2 HG02486.hp2 others(33): Show |
intron_variant | MODIFIER | c.4078+225T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 29/47 | chr11 | 121589615 | ||||||
| chr11:121589820
|
A | G | 1 | a0001c0004t0029g0187 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.4079-220A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 29/47 | chr11 | 121589820 | ||||||
| chr11:121589911
|
C | T | 1 | a0001c0003t0001g0019 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.4079-129C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 29/47 | chr11 | 121589911 | ||||||
| chr11:121589955
|
G | A | 97 | a0001c0002t0001g0010a0001c0002t0001g0083a0001c0002t0001g0092others(94): Show | 98 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.4079-85G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 29/47 | chr11 | 121589955 | ||||||
| chr11:121590179
|
G | C | 1 | a0001c0002t0003g0150 | 1 | HG02109.hp2 | splice_region_variant&intron_variant | LOW | c.4213+5G>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 30/47 | chr11 | 121590179 | ||||||
| chr11:121590523
|
A | G | 1 | a0001c0008t0002g0177 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.4213+349A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 30/47 | chr11 | 121590523 | ||||||
| chr11:121590673
|
T | C | 3 | a0001c0033t0003g0169a0001c0060t0003g0163a0006c0043t0026g0215 | 3 | HG02559.hp2 HG02922.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.4214-328T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 30/47 | chr11 | 121590673 | ||||||
| chr11:121590831
|
C | T | 1 | a0001c0002t0001g0158 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.4214-170C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 30/47 | chr11 | 121590831 | ||||||
| chr11:121590884
|
G | C | 32 | a0001c0002t0001g0010a0001c0002t0001g0083a0001c0002t0001g0092others(29): Show | 32 | HG01993.hp1 HG02040.hp1 HG02148.hp1 others(29): Show |
intron_variant | MODIFIER | c.4214-117G>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 30/47 | chr11 | 121590884 | ||||||
| chr11:121591289
|
C | G | 1 | a0004c0056t0013g0148 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4369+133C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 31/47 | chr11 | 121591289 | ||||||
| chr11:121591705
|
G | T | 1 | a0001c0032t0003g0149 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.4369+549G>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 31/47 | chr11 | 121591705 | ||||||
| chr11:121591939
|
A | G | 3 | a0001c0003t0005g0226a0001c0003t0005g0228a0004c0041t0013g0189 | 3 | HG02257.hp1 HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.4369+783A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 31/47 | chr11 | 121591939 | ||||||
| chr11:121592017
|
A | G | 3 | a0001c0001t0001g0153a0001c0001t0002g0053a0001c0001t0002g0154 | 3 | HG02080.hp1 NA19002.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.4369+861A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 31/47 | chr11 | 121592017 | ||||||
| chr11:121592215
|
C | T | 4 | a0001c0003t0002g0095a0001c0003t0002g0096a0001c0003t0002g0097others(1): Show | 4 | HG01074.hp1 HG01099.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.4369+1059C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 31/47 | chr11 | 121592215 | ||||||
| chr11:121592484
|
C | T | 2 | a0001c0003t0002g0115a0001c0003t0002g0230 | 2 | HG02683.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.4369+1328C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 31/47 | chr11 | 121592484 | ||||||
| chr11:121592721
|
A | G | 125 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(122): Show | 125 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.4369+1565A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 31/47 | chr11 | 121592721 | ||||||
| chr11:121592908
|
T | G | 260 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(257): Show | 261 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.4369+1752T>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 31/47 | chr11 | 121592908 | ||||||
| chr11:121593154
|
A | G | 3 | a0001c0001t0001g0023a0001c0001t0001g0051a0001c0001t0001g0055 | 3 | NA18939.hp2 NA18989.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.4369+1998A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 31/47 | chr11 | 121593154 | ||||||
| chr11:121593186
|
C | G | 59 | a0001c0002t0001g0103a0001c0002t0001g0112a0001c0002t0001g0116others(56): Show | 60 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.4369+2030C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 31/47 | chr11 | 121593186 | ||||||
| chr11:121593225
|
G | A | 1 | a0001c0015t0005g0270 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.4369+2069G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 31/47 | chr11 | 121593225 | ||||||
| chr11:121593253
|
G | A | 1 | a0013c0047t0007g0182 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4369+2097G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 31/47 | chr11 | 121593253 | ||||||
| chr11:121593275
|
A | G | 98 | a0001c0002t0001g0010a0001c0002t0001g0083a0001c0002t0001g0092others(95): Show | 99 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.4369+2119A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 31/47 | chr11 | 121593275 | ||||||
| chr11:121593351
|
A | G | 1 | a0001c0001t0001g0051 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.4369+2195A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 31/47 | chr11 | 121593351 | ||||||
| chr11:121593379
|
G | A | 161 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(158): Show | 161 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.4369+2223G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 31/47 | chr11 | 121593379 | ||||||
| chr11:121593547
|
A | T | 1 | a0001c0067t0013g0204 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.4370-2076A>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 31/47 | chr11 | 121593547 | ||||||
| chr11:121593621
|
CCCTTGTT others(24): Show |
C | 1 | a0001c0067t0013g0204 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.4370-1995_4370-196 others(35): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 31/47 | INFO_REALIGN_3_PRIME | chr11 | 121593621 | |||||
| chr11:121593721
|
C | T | 1 | a0001c0002t0003g0150 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4370-1902C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 31/47 | chr11 | 121593721 | ||||||
| chr11:121593867
|
C | T | 5 | a0001c0006t0001g0068a0001c0006t0001g0072a0001c0006t0001g0118others(2): Show | 5 | HG00735.hp1 HG01243.hp2 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.4370-1756C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 31/47 | chr11 | 121593867 | ||||||
| chr11:121593991
|
T | A | 4 | a0001c0009t0011g0170a0001c0009t0011g0255a0001c0057t0002g0160others(1): Show | 4 | HG02486.hp2 HG02976.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.4370-1632T>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 31/47 | chr11 | 121593991 | ||||||
| chr11:121594115
|
AT | A | 222 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(219): Show | 223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.4370-1495delT | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 31/47 | INFO_REALIGN_3_PRIME | chr11 | 121594115 | |||||
| chr11:121594237
|
A | G | 94 | a0001c0002t0001g0010a0001c0002t0001g0083a0001c0002t0001g0092others(91): Show | 95 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.4370-1386A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 31/47 | chr11 | 121594237 | ||||||
| chr11:121594401
|
T | G | 2 | a0001c0036t0003g0266a0001c0038t0002g0186 | 2 | HG03195.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.4370-1222T>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 31/47 | chr11 | 121594401 | ||||||
| chr11:121594568
|
G | A | 1 | a0001c0015t0004g0056 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.4370-1055G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 31/47 | chr11 | 121594568 | ||||||
| chr11:121595110
|
G | A | 1 | a0001c0001t0001g0155 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.4370-513G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 31/47 | chr11 | 121595110 | ||||||
| chr11:121595301
|
T | G | 2 | a0001c0020t0003g0268a0001c0020t0003g0269 | 2 | HG02486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.4370-322T>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 31/47 | chr11 | 121595301 | ||||||
| chr11:121595311
|
C | T | 5 | a0001c0006t0001g0068a0001c0006t0001g0072a0001c0006t0001g0118others(2): Show | 5 | HG00735.hp1 HG01243.hp2 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.4370-312C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 31/47 | chr11 | 121595311 | ||||||
| chr11:121595349
|
C | G | 1 | a0001c0015t0005g0270 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.4370-274C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 31/47 | chr11 | 121595349 | ||||||
| chr11:121595889
|
G | A | 2 | a0001c0001t0001g0198a0001c0004t0002g0134 | 2 | HG01071.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.4519+117G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 32/47 | chr11 | 121595889 | ||||||
| chr11:121595930
|
C | T | 1 | a0001c0002t0006g0114 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.4519+158C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 32/47 | chr11 | 121595930 | ||||||
| chr11:121596021
|
G | T | 1 | a0001c0003t0019g0209 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.4519+249G>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 32/47 | chr11 | 121596021 | ||||||
| chr11:121596048
|
G | T | 2 | a0001c0010t0005g0239a0002c0026t0005g0161 | 2 | HG01891.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.4519+276G>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 32/47 | chr11 | 121596048 | ||||||
| chr11:121596115
|
A | G | 2 | a0002c0007t0001g0060a0002c0007t0001g0073 | 2 | NA19077.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.4519+343A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 32/47 | chr11 | 121596115 | ||||||
| chr11:121596246
|
T | C | 2 | a0001c0036t0003g0266a0001c0038t0002g0186 | 2 | HG03195.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.4519+474T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 32/47 | chr11 | 121596246 | ||||||
| chr11:121596499
|
A | G | 3 | a0001c0003t0005g0226a0001c0003t0005g0228a0004c0041t0013g0189 | 3 | HG02257.hp1 HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.4519+727A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 32/47 | chr11 | 121596499 | ||||||
| chr11:121596510
|
G | A | 1 | a0001c0013t0002g0016 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.4519+738G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 32/47 | chr11 | 121596510 | ||||||
| chr11:121596560
|
C | T | 1 | a0004c0056t0013g0148 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4519+788C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 32/47 | chr11 | 121596560 | ||||||
| chr11:121596805
|
A | G | 1 | a0001c0002t0002g0091 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.4519+1033A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 32/47 | chr11 | 121596805 | ||||||
| chr11:121596833
|
T | G | 1 | a0006c0055t0002g0246 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4519+1061T>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 32/47 | chr11 | 121596833 | ||||||
| chr11:121597211
|
G | A | 40 | a0001c0003t0001g0019a0001c0003t0002g0080a0001c0003t0002g0094others(37): Show | 40 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(37): Show |
intron_variant | MODIFIER | c.4519+1439G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 32/47 | chr11 | 121597211 | ||||||
| chr11:121597456
|
G | T | 3 | a0001c0013t0002g0018a0001c0013t0027g0140a0001c0018t0002g0013 | 3 | NA19001.hp1 NA19063.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.4519+1684G>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 32/47 | chr11 | 121597456 | ||||||
| chr11:121597547
|
C | T | 19 | a0001c0009t0003g0147a0001c0009t0010g0165a0001c0013t0002g0016others(16): Show | 19 | HG02630.hp1 HG02647.hp1 HG02723.hp1 others(16): Show |
intron_variant | MODIFIER | c.4519+1775C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 32/47 | chr11 | 121597547 | ||||||
| chr11:121597554
|
C | T | 1 | a0001c0002t0003g0150 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4519+1782C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 32/47 | chr11 | 121597554 | ||||||
| chr11:121597752
|
G | A | 1 | a0001c0004t0002g0132 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.4519+1980G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 32/47 | chr11 | 121597752 | ||||||
| chr11:121597885
|
G | A | 1 | a0004c0059t0002g0171 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4519+2113G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 32/47 | chr11 | 121597885 | ||||||
| chr11:121597909
|
G | A | 1 | a0003c0071t0014g0146 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4519+2137G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 32/47 | chr11 | 121597909 | ||||||
| chr11:121597914
|
A | G | 3 | a0001c0001t0001g0024a0001c0001t0001g0047a0001c0042t0002g0002 | 3 | NA18961.hp1 NA18990.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.4519+2142A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 32/47 | chr11 | 121597914 | ||||||
| chr11:121598155
|
A | G | 3 | a0001c0033t0003g0169a0001c0060t0003g0163a0006c0043t0026g0215 | 3 | HG02559.hp2 HG02922.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.4519+2383A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 32/47 | chr11 | 121598155 | ||||||
| chr11:121598583
|
G | A | 33 | a0001c0002t0001g0010a0001c0002t0001g0083a0001c0002t0001g0092others(30): Show | 33 | HG01993.hp1 HG02040.hp1 HG02148.hp1 others(30): Show |
intron_variant | MODIFIER | c.4519+2811G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 32/47 | chr11 | 121598583 | ||||||
| chr11:121599272
|
C | T | 21 | a0001c0002t0003g0151a0001c0009t0003g0147a0001c0009t0010g0165others(18): Show | 21 | HG01099.hp1 HG02622.hp1 HG02630.hp1 others(18): Show |
intron_variant | MODIFIER | c.4519+3500C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 32/47 | chr11 | 121599272 | ||||||
| chr11:121599395
|
T | A | 1 | a0001c0003t0002g0231 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.4519+3623T>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 32/47 | chr11 | 121599395 | ||||||
| chr11:121599561
|
C | A | 54 | a0001c0002t0001g0103a0001c0002t0001g0112a0001c0002t0001g0116others(51): Show | 55 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.4519+3789C>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 32/47 | chr11 | 121599561 | ||||||
| chr11:121599564
|
A | G | 1 | a0001c0039t0002g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4519+3792A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 32/47 | chr11 | 121599564 | ||||||
| chr11:121599647
|
T | A | 1 | a0001c0001t0001g0059 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.4519+3875T>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 32/47 | chr11 | 121599647 | ||||||
| chr11:121599726
|
A | G | 32 | a0001c0002t0001g0010a0001c0002t0001g0083a0001c0002t0001g0092others(29): Show | 32 | HG01993.hp1 HG02040.hp1 HG02148.hp1 others(29): Show |
intron_variant | MODIFIER | c.4519+3954A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 32/47 | chr11 | 121599726 | ||||||
| chr11:121599767
|
C | CT | 34 | a0001c0003t0002g0135a0001c0003t0007g0261a0001c0003t0007g0264others(31): Show | 34 | HG00642.hp2 HG01074.hp2 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.4519+4007dupT | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 32/47 | INFO_REALIGN_3_PRIME | chr11 | 121599767 | |||||
| chr11:121599911
|
C | G | 38 | a0001c0002t0001g0010a0001c0002t0001g0083a0001c0002t0001g0092others(35): Show | 38 | HG01993.hp1 HG02040.hp1 HG02148.hp1 others(35): Show |
intron_variant | MODIFIER | c.4519+4139C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 32/47 | chr11 | 121599911 | ||||||
| chr11:121599937
|
C | T | 41 | a0001c0002t0001g0010a0001c0002t0001g0083a0001c0002t0001g0092others(38): Show | 41 | HG01993.hp1 HG02040.hp1 HG02148.hp1 others(38): Show |
intron_variant | MODIFIER | c.4519+4165C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 32/47 | chr11 | 121599937 | ||||||
| chr11:121600132
|
T | C | 1 | a0001c0002t0004g0085 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.4520-4061T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 32/47 | chr11 | 121600132 | ||||||
| chr11:121600178
|
G | A | 3 | a0001c0009t0011g0170a0001c0009t0011g0255a0001c0058t0011g0166 | 3 | HG02486.hp2 HG03139.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.4520-4015G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 32/47 | chr11 | 121600178 | ||||||
| chr11:121600218
|
G | A | 2 | a0001c0003t0002g0117a0001c0003t0019g0209 | 2 | HG01361.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.4520-3975G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 32/47 | chr11 | 121600218 | ||||||
| chr11:121600490
|
C | T | 1 | a0002c0049t0003g0162 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.4520-3703C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 32/47 | chr11 | 121600490 | ||||||
| chr11:121600543
|
A | G | 1 | a0001c0002t0001g0188 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.4520-3650A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 32/47 | chr11 | 121600543 | ||||||
| chr11:121600686
|
C | T | 2 | a0001c0001t0001g0006a0001c0001t0001g0009 | 2 | HG02165.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.4520-3507C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 32/47 | chr11 | 121600686 | ||||||
| chr11:121600748
|
C | G | 1 | a0001c0004t0003g0224 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.4520-3445C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 32/47 | chr11 | 121600748 | ||||||
| chr11:121600781
|
G | A | 1 | a0001c0002t0003g0150 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4520-3412G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 32/47 | chr11 | 121600781 | ||||||
| chr11:121600899
|
C | CT | 35 | a0001c0003t0002g0135a0001c0003t0007g0261a0001c0003t0007g0264others(32): Show | 35 | HG00642.hp2 HG01074.hp2 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.4520-3285dupT | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 32/47 | INFO_REALIGN_3_PRIME | chr11 | 121600899 | |||||
| chr11:121600899
|
CT | C | 25 | a0001c0001t0001g0036a0001c0002t0003g0150a0001c0002t0003g0151others(22): Show | 25 | HG00544.hp1 HG00544.hp2 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.4520-3285delT | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 32/47 | INFO_REALIGN_3_PRIME | chr11 | 121600899 | |||||
| chr11:121600908
|
T | A | 1 | a0001c0015t0005g0270 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.4520-3285T>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 32/47 | chr11 | 121600908 | ||||||
| chr11:121601224
|
A | T | 1 | a0001c0002t0001g0112 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.4520-2969A>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 32/47 | chr11 | 121601224 | ||||||
| chr11:121601517
|
T | A | 7 | a0001c0021t0016g0206a0001c0033t0003g0169a0001c0060t0003g0163others(4): Show | 7 | HG01243.hp1 HG02559.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.4520-2676T>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 32/47 | chr11 | 121601517 | ||||||
| chr11:121601583
|
G | GT | 70 | a0001c0001t0001g0024a0001c0001t0001g0036a0001c0001t0001g0057others(67): Show | 71 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.4520-2593dupT | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 32/47 | INFO_REALIGN_3_PRIME | chr11 | 121601583 | |||||
| chr11:121601583
|
G | GTT | 93 | a0001c0002t0001g0010a0001c0002t0001g0083a0001c0002t0001g0092others(90): Show | 93 | HG00642.hp2 HG01074.hp2 HG01109.hp2 others(90): Show |
intron_variant | MODIFIER | c.4520-2594_4520-259 others(6): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 32/47 | INFO_REALIGN_3_PRIME | chr11 | 121601583 | |||||
| chr11:121601583
|
G | T | 2 | a0001c0002t0003g0151a0001c0015t0005g0270 | 2 | HG01099.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.4520-2610G>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 32/47 | chr11 | 121601583 | ||||||
| chr11:121601782
|
C | T | 3 | a0001c0003t0003g0254a0001c0003t0003g0262a0001c0067t0013g0204 | 3 | HG03516.hp2 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.4520-2411C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 32/47 | chr11 | 121601782 | ||||||
| chr11:121601869
|
G | A | 35 | a0001c0003t0002g0135a0001c0003t0007g0261a0001c0003t0007g0264others(32): Show | 35 | HG00642.hp2 HG01074.hp2 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.4520-2324G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 32/47 | chr11 | 121601869 | ||||||
| chr11:121602284
|
G | A | 53 | a0001c0002t0001g0103a0001c0002t0001g0112a0001c0002t0001g0116others(50): Show | 54 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.4520-1909G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 32/47 | chr11 | 121602284 | ||||||
| chr11:121602625
|
G | A | 1 | a0001c0057t0002g0160 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4520-1568G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 32/47 | chr11 | 121602625 | ||||||
| chr11:121602672
|
G | T | 1 | a0001c0006t0001g0157 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.4520-1521G>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 32/47 | chr11 | 121602672 | ||||||
| chr11:121602682
|
T | C | 43 | a0001c0002t0001g0010a0001c0002t0001g0083a0001c0002t0001g0092others(40): Show | 43 | HG01993.hp1 HG02040.hp1 HG02109.hp2 others(40): Show |
intron_variant | MODIFIER | c.4520-1511T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 32/47 | chr11 | 121602682 | ||||||
| chr11:121602778
|
C | T | 1 | a0005c0017t0001g0240 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.4520-1415C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 32/47 | chr11 | 121602778 | ||||||
| chr11:121602889
|
T | C | 34 | a0001c0003t0007g0261a0001c0003t0007g0264a0001c0003t0007g0265others(31): Show | 34 | HG00642.hp2 HG01074.hp2 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.4520-1304T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 32/47 | chr11 | 121602889 | ||||||
| chr11:121603053
|
C | T | 1 | a0002c0026t0005g0245 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.4520-1140C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 32/47 | chr11 | 121603053 | ||||||
| chr11:121603316
|
T | C | 42 | a0001c0002t0001g0010a0001c0002t0001g0083a0001c0002t0001g0092others(39): Show | 42 | HG01993.hp1 HG02040.hp1 HG02109.hp2 others(39): Show |
intron_variant | MODIFIER | c.4520-877T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 32/47 | chr11 | 121603316 | ||||||
| chr11:121603480
|
G | A | 3 | a0001c0011t0001g0107a0001c0011t0002g0271a0001c0016t0002g0121 | 3 | HG01074.hp2 HG01256.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.4520-713G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 32/47 | chr11 | 121603480 | ||||||
| chr11:121603530
|
A | G | 38 | a0001c0002t0001g0010a0001c0002t0001g0083a0001c0002t0001g0092others(35): Show | 38 | HG01993.hp1 HG02040.hp1 HG02148.hp1 others(35): Show |
intron_variant | MODIFIER | c.4520-663A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 32/47 | chr11 | 121603530 | ||||||
| chr11:121603894
|
T | C | 4 | a0001c0021t0016g0206a0001c0066t0016g0194a0002c0014t0014g0217others(1): Show | 4 | HG01243.hp1 HG02896.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.4520-299T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 32/47 | chr11 | 121603894 | ||||||
| chr11:121604334
|
G | A | 3 | a0001c0003t0003g0254a0001c0003t0003g0262a0001c0067t0013g0204 | 3 | HG03516.hp2 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.4651+10G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 33/47 | chr11 | 121604334 | ||||||
| chr11:121604496
|
C | T | 1 | a0001c0010t0003g0257 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4651+172C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 33/47 | chr11 | 121604496 | ||||||
| chr11:121604515
|
C | T | 1 | a0001c0001t0002g0004 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.4651+191C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 33/47 | chr11 | 121604515 | ||||||
| chr11:121604553
|
A | AT | 7 | a0001c0021t0016g0206a0001c0033t0003g0169a0001c0060t0003g0163others(4): Show | 7 | HG01243.hp1 HG02559.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.4651+242dupT | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 33/47 | INFO_REALIGN_3_PRIME | chr11 | 121604553 | |||||
| chr11:121604553
|
AT | A | 75 | a0001c0002t0001g0103a0001c0002t0001g0112a0001c0002t0001g0116others(72): Show | 76 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.4651+242delT | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 33/47 | INFO_REALIGN_3_PRIME | chr11 | 121604553 | |||||
| chr11:121604849
|
A | G | 1 | a0001c0013t0027g0140 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.4652-264A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 33/47 | chr11 | 121604849 | ||||||
| chr11:121604958
|
A | G | 1 | a0001c0004t0029g0187 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.4652-155A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 33/47 | chr11 | 121604958 | ||||||
| chr11:121605089
|
T | A | 270 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(267): Show | 271 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.4652-24T>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 33/47 | chr11 | 121605089 | ||||||
| chr11:121605282
|
A | G | 1 | a0004c0056t0013g0148 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4778+43A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 34/47 | chr11 | 121605282 | ||||||
| chr11:121605335
|
G | A | 1 | a0001c0004t0003g0224 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.4779-67G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 34/47 | chr11 | 121605335 | ||||||
| chr11:121605631
|
G | T | 1 | a0001c0001t0001g0050 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.4948+60G>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 35/47 | chr11 | 121605631 | ||||||
| chr11:121605793
|
A | G | 7 | a0001c0021t0016g0206a0001c0033t0003g0169a0001c0060t0003g0163others(4): Show | 7 | HG01243.hp1 HG02559.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.4948+222A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 35/47 | chr11 | 121605793 | ||||||
| chr11:121606047
|
C | T | 1 | a0001c0033t0003g0169 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.4948+476C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 35/47 | chr11 | 121606047 | ||||||
| chr11:121606387
|
G | A | 77 | a0001c0002t0001g0103a0001c0002t0001g0112a0001c0002t0001g0116others(74): Show | 78 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.4949-458G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 35/47 | chr11 | 121606387 | ||||||
| chr11:121606514
|
G | A | 3 | a0001c0009t0011g0170a0001c0009t0011g0255a0001c0058t0011g0166 | 3 | HG02486.hp2 HG03139.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.4949-331G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 35/47 | chr11 | 121606514 | ||||||
| chr11:121606622
|
A | G | 1 | a0001c0016t0002g0044 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.4949-223A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 35/47 | chr11 | 121606622 | ||||||
| chr11:121606685
|
A | G | 1 | a0001c0002t0003g0150 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4949-160A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 35/47 | chr11 | 121606685 | ||||||
| chr11:121607107
|
C | T | 32 | a0001c0002t0001g0010a0001c0002t0001g0083a0001c0002t0001g0092others(29): Show | 32 | HG01993.hp1 HG02040.hp1 HG02148.hp1 others(29): Show |
intron_variant | MODIFIER | c.5062-79C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 36/47 | chr11 | 121607107 | ||||||
| chr11:121607527
|
G | A | 3 | a0001c0033t0003g0169a0001c0060t0003g0163a0006c0043t0026g0215 | 3 | HG02559.hp2 HG02922.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.5166+237G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 37/47 | chr11 | 121607527 | ||||||
| chr11:121607748
|
G | A | 269 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(266): Show | 270 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.5167-356G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 37/47 | chr11 | 121607748 | ||||||
| chr11:121607786
|
C | T | 98 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(95): Show | 98 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.5167-318C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 37/47 | chr11 | 121607786 | ||||||
| chr11:121607959
|
C | G | 1 | a0001c0001t0001g0039 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.5167-145C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 37/47 | chr11 | 121607959 | ||||||
| chr11:121608053
|
G | A | 3 | a0001c0003t0003g0254a0001c0003t0003g0262a0001c0067t0013g0204 | 3 | HG03516.hp2 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.5167-51G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 37/47 | chr11 | 121608053 | ||||||
| chr11:121608249
|
C | T | 89 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(86): Show | 89 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.5239+73C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 38/47 | chr11 | 121608249 | ||||||
| chr11:121608420
|
T | C | 1 | a0001c0004t0001g0088 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.5239+244T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 38/47 | chr11 | 121608420 | ||||||
| chr11:121608438
|
C | T | 1 | a0001c0036t0003g0266 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.5239+262C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 38/47 | chr11 | 121608438 | ||||||
| chr11:121608641
|
A | G | 1 | a0001c0015t0001g0022 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.5239+465A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 38/47 | chr11 | 121608641 | ||||||
| chr11:121608742
|
T | C | 2 | a0008c0024t0002g0033a0008c0024t0002g0034 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.5239+566T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 38/47 | chr11 | 121608742 | ||||||
| chr11:121608778
|
A | G | 3 | a0001c0033t0003g0169a0001c0060t0003g0163a0006c0043t0026g0215 | 3 | HG02559.hp2 HG02922.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.5239+602A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 38/47 | chr11 | 121608778 | ||||||
| chr11:121608794
|
G | A | 3 | a0001c0033t0003g0169a0001c0060t0003g0163a0006c0043t0026g0215 | 3 | HG02559.hp2 HG02922.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.5239+618G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 38/47 | chr11 | 121608794 | ||||||
| chr11:121608976
|
T | G | 36 | a0001c0002t0003g0150a0001c0003t0002g0135a0001c0003t0007g0261others(33): Show | 36 | HG00642.hp2 HG01074.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.5239+800T>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 38/47 | chr11 | 121608976 | ||||||
| chr11:121608983
|
C | T | 1 | a0001c0065t0003g0152 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.5239+807C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 38/47 | chr11 | 121608983 | ||||||
| chr11:121609805
|
G | A | 2 | a0002c0005t0001g0202a0016c0029t0001g0064 | 2 | NA19056.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.5240-1271G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 38/47 | chr11 | 121609805 | ||||||
| chr11:121609861
|
G | C | 3 | a0001c0004t0004g0011a0001c0004t0004g0012a0002c0005t0001g0127 | 3 | HG01256.hp2 HG01258.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.5240-1215G>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 38/47 | chr11 | 121609861 | ||||||
| chr11:121609870
|
A | G | 2 | a0001c0001t0001g0027a0001c0001t0001g0049 | 2 | NA18965.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.5240-1206A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 38/47 | chr11 | 121609870 | ||||||
| chr11:121609900
|
T | C | 158 | a0001c0002t0001g0010a0001c0002t0001g0083a0001c0002t0001g0092others(155): Show | 159 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.5240-1176T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 38/47 | chr11 | 121609900 | ||||||
| chr11:121609969
|
C | T | 1 | a0003c0069t0008g0164 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.5240-1107C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 38/47 | chr11 | 121609969 | ||||||
| chr11:121609982
|
G | A | 1 | a0001c0038t0002g0186 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.5240-1094G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 38/47 | chr11 | 121609982 | ||||||
| chr11:121610000
|
C | T | 3 | a0001c0009t0011g0170a0001c0009t0011g0255a0001c0058t0011g0166 | 3 | HG02486.hp2 HG03139.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.5240-1076C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 38/47 | chr11 | 121610000 | ||||||
| chr11:121610089
|
C | G | 1 | a0001c0003t0002g0101 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.5240-987C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 38/47 | chr11 | 121610089 | ||||||
| chr11:121610134
|
C | T | 1 | a0001c0004t0001g0144 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.5240-942C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 38/47 | chr11 | 121610134 | ||||||
| chr11:121610172
|
A | G | 1 | a0001c0003t0002g0133 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.5240-904A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 38/47 | chr11 | 121610172 | ||||||
| chr11:121610330
|
G | C | 1 | a0003c0034t0003g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5240-746G>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 38/47 | chr11 | 121610330 | ||||||
| chr11:121610487
|
G | A | 3 | a0001c0003t0001g0019a0001c0008t0001g0136a0014c0068t0001g0195 | 3 | HG00099.hp1 HG00738.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.5240-589G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 38/47 | chr11 | 121610487 | ||||||
| chr11:121610532
|
A | G | 1 | a0001c0004t0022g0086 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.5240-544A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 38/47 | chr11 | 121610532 | ||||||
| chr11:121610698
|
C | T | 99 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(96): Show | 99 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.5240-378C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 38/47 | chr11 | 121610698 | ||||||
| chr11:121611512
|
C | T | 1 | a0001c0001t0002g0185 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.5322+354C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 39/47 | chr11 | 121611512 | ||||||
| chr11:121611543
|
G | A | 1 | a0003c0071t0014g0146 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.5322+385G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 39/47 | chr11 | 121611543 | ||||||
| chr11:121611549
|
T | G | 1 | a0001c0032t0003g0149 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.5322+391T>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 39/47 | chr11 | 121611549 | ||||||
| chr11:121611607
|
C | T | 1 | a0001c0003t0002g0105 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.5322+449C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 39/47 | chr11 | 121611607 | ||||||
| chr11:121611687
|
C | T | 1 | a0001c0001t0001g0023 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.5322+529C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 39/47 | chr11 | 121611687 | ||||||
| chr11:121611823
|
T | G | 1 | a0001c0001t0001g0111 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.5322+665T>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 39/47 | chr11 | 121611823 | ||||||
| chr11:121611867
|
A | T | 1 | a0001c0020t0003g0268 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.5322+709A>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 39/47 | chr11 | 121611867 | ||||||
| chr11:121611888
|
C | A | 1 | a0001c0001t0001g0050 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.5322+730C>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 39/47 | chr11 | 121611888 | ||||||
| chr11:121612023
|
C | T | 1 | a0001c0001t0001g0057 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.5323-713C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 39/47 | chr11 | 121612023 | ||||||
| chr11:121612121
|
C | G | 1 | a0001c0003t0002g0098 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.5323-615C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 39/47 | chr11 | 121612121 | ||||||
| chr11:121612215
|
A | C | 3 | a0001c0003t0003g0254a0001c0003t0003g0262a0001c0067t0013g0204 | 3 | HG03516.hp2 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.5323-521A>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 39/47 | chr11 | 121612215 | ||||||
| chr11:121612229
|
C | A | 50 | a0001c0002t0001g0103a0001c0002t0001g0112a0001c0002t0001g0116others(47): Show | 51 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.5323-507C>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 39/47 | chr11 | 121612229 | ||||||
| chr11:121612230
|
G | A | 1 | a0001c0001t0002g0053 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.5323-506G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 39/47 | chr11 | 121612230 | ||||||
| chr11:121612519
|
C | G | 1 | a0001c0013t0002g0016 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.5323-217C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 39/47 | chr11 | 121612519 | ||||||
| chr11:121612522
|
G | A | 1 | a0001c0002t0003g0150 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.5323-214G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 39/47 | chr11 | 121612522 | ||||||
| chr11:121612608
|
C | A | 34 | a0001c0003t0007g0261a0001c0003t0007g0264a0001c0003t0007g0265others(31): Show | 34 | HG00642.hp2 HG01074.hp2 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.5323-128C>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 39/47 | chr11 | 121612608 | ||||||
| chr11:121612692
|
C | T | 118 | a0001c0002t0001g0010a0001c0002t0001g0083a0001c0002t0001g0092others(115): Show | 119 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.5323-44C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 39/47 | chr11 | 121612692 | ||||||
| chr11:121612896
|
G | A | 1 | a0002c0007t0001g0124 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.5419+64G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 40/47 | chr11 | 121612896 | ||||||
| chr11:121612942
|
G | A | 152 | a0001c0002t0001g0010a0001c0002t0001g0083a0001c0002t0001g0092others(149): Show | 153 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.5419+110G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 40/47 | chr11 | 121612942 | ||||||
| chr11:121612986
|
A | G | 1 | a0001c0057t0002g0160 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.5419+154A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 40/47 | chr11 | 121612986 | ||||||
| chr11:121613070
|
T | C | 1 | a0001c0004t0001g0110 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.5419+238T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 40/47 | chr11 | 121613070 | ||||||
| chr11:121613157
|
T | A | 2 | a0001c0060t0003g0163a0006c0043t0026g0215 | 2 | HG02559.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.5419+325T>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 40/47 | chr11 | 121613157 | ||||||
| chr11:121613203
|
G | A | 72 | a0001c0002t0001g0103a0001c0002t0001g0112a0001c0002t0001g0116others(69): Show | 73 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.5419+371G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 40/47 | chr11 | 121613203 | ||||||
| chr11:121613467
|
G | A | 4 | a0001c0021t0016g0206a0001c0066t0016g0194a0002c0014t0014g0217others(1): Show | 4 | HG01243.hp1 HG02896.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.5419+635G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 40/47 | chr11 | 121613467 | ||||||
| chr11:121613810
|
G | A | 1 | a0001c0046t0002g0174 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.5419+978G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 40/47 | chr11 | 121613810 | ||||||
| chr11:121613847
|
G | A | 1 | a0001c0004t0002g0132 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.5419+1015G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 40/47 | chr11 | 121613847 | ||||||
| chr11:121614168
|
A | G | 1 | a0001c0003t0007g0265 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.5420-703A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 40/47 | chr11 | 121614168 | ||||||
| chr11:121614616
|
A | C | 3 | a0001c0003t0003g0254a0001c0003t0003g0262a0001c0067t0013g0204 | 3 | HG03516.hp2 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.5420-255A>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 40/47 | chr11 | 121614616 | ||||||
| chr11:121614640
|
G | A | 1 | a0002c0005t0001g0127 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.5420-231G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 40/47 | chr11 | 121614640 | ||||||
| chr11:121614774
|
G | C | 1 | a0001c0001t0002g0125 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.5420-97G>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 40/47 | chr11 | 121614774 | ||||||
| chr11:121614781
|
A | G | 1 | a0001c0002t0006g0104 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.5420-90A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 40/47 | chr11 | 121614781 | ||||||
| chr11:121614790
|
T | A | 12 | a0001c0003t0003g0254a0001c0003t0003g0262a0001c0009t0008g0207others(9): Show | 12 | HG01243.hp1 HG02896.hp2 HG02965.hp1 others(9): Show |
intron_variant | MODIFIER | c.5420-81T>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 40/47 | chr11 | 121614790 | ||||||
| chr11:121614804
|
T | G | 3 | a0001c0003t0003g0254a0001c0003t0003g0262a0001c0067t0013g0204 | 3 | HG03516.hp2 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.5420-67T>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 40/47 | chr11 | 121614804 | ||||||
| chr11:121615265
|
A | G | 1 | a0001c0036t0003g0266 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.5604+210A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 41/47 | chr11 | 121615265 | ||||||
| chr11:121615313
|
C | A | 3 | a0001c0032t0003g0149a0001c0046t0002g0174a0002c0005t0003g0159 | 3 | HG02723.hp2 HG03540.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.5604+258C>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 41/47 | chr11 | 121615313 | ||||||
| chr11:121615333
|
C | T | 12 | a0001c0003t0003g0254a0001c0003t0003g0262a0001c0009t0008g0207others(9): Show | 12 | HG01243.hp1 HG02896.hp2 HG02965.hp1 others(9): Show |
intron_variant | MODIFIER | c.5604+278C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 41/47 | chr11 | 121615333 | ||||||
| chr11:121615595
|
C | T | 6 | a0001c0012t0005g0247a0001c0012t0007g0175a0001c0012t0007g0176others(3): Show | 6 | HG01884.hp2 HG01891.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.5604+540C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 41/47 | chr11 | 121615595 | ||||||
| chr11:121615649
|
T | C | 1 | a0001c0001t0001g0198 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.5604+594T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 41/47 | chr11 | 121615649 | ||||||
| chr11:121615843
|
C | A | 158 | a0001c0001t0002g0141a0001c0002t0001g0010a0001c0002t0001g0083others(155): Show | 159 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.5604+788C>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 41/47 | chr11 | 121615843 | ||||||
| chr11:121615851
|
C | T | 1 | a0001c0036t0003g0266 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.5604+796C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 41/47 | chr11 | 121615851 | ||||||
| chr11:121615924
|
G | A | 5 | a0001c0009t0003g0147a0001c0022t0003g0213a0001c0022t0008g0211others(2): Show | 5 | HG02630.hp1 HG02723.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.5604+869G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 41/47 | chr11 | 121615924 | ||||||
| chr11:121616038
|
A | G | 2 | a0001c0004t0001g0236a0001c0004t0001g0238 | 2 | HG00280.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.5604+983A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 41/47 | chr11 | 121616038 | ||||||
| chr11:121616068
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.5604+1013C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 41/47 | chr11 | 121616068 | ||||||
| chr11:121616073
|
A | G | 5 | a0001c0009t0008g0207a0002c0025t0005g0179a0004c0059t0002g0171others(2): Show | 5 | HG02965.hp1 HG03209.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.5604+1018A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 41/47 | chr11 | 121616073 | ||||||
| chr11:121616105
|
A | G | 263 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(260): Show | 264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.5604+1050A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 41/47 | chr11 | 121616105 | ||||||
| chr11:121616239
|
G | A | 1 | a0001c0023t0002g0070 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.5604+1184G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 41/47 | chr11 | 121616239 | ||||||
| chr11:121616541
|
C | T | 6 | a0001c0003t0003g0254a0001c0003t0003g0262a0001c0021t0016g0206others(3): Show | 6 | HG01243.hp1 HG02818.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.5604+1486C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 41/47 | chr11 | 121616541 | ||||||
| chr11:121616637
|
G | A | 4 | a0001c0002t0001g0092a0001c0002t0004g0003a0001c0002t0004g0007others(1): Show | 4 | HG02040.hp1 HG02165.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.5604+1582G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 41/47 | chr11 | 121616637 | ||||||
| chr11:121616663
|
C | T | 96 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(93): Show | 96 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.5604+1608C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 41/47 | chr11 | 121616663 | ||||||
| chr11:121616768
|
A | G | 1 | a0001c0058t0011g0166 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.5604+1713A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 41/47 | chr11 | 121616768 | ||||||
| chr11:121616781
|
T | C | 1 | a0001c0001t0001g0027 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.5604+1726T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 41/47 | chr11 | 121616781 | ||||||
| chr11:121616898
|
A | G | 27 | a0001c0003t0002g0135a0001c0010t0002g0190a0001c0010t0002g0234others(24): Show | 27 | HG00642.hp2 HG01109.hp2 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.5604+1843A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 41/47 | chr11 | 121616898 | ||||||
| chr11:121617077
|
A | G | 1 | a0001c0015t0001g0022 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.5605-1697A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 41/47 | chr11 | 121617077 | ||||||
| chr11:121617324
|
G | A | 4 | a0003c0027t0005g0173a0003c0027t0005g0181a0003c0070t0005g0145others(1): Show | 4 | HG03098.hp2 HG03130.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.5605-1450G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 41/47 | chr11 | 121617324 | ||||||
| chr11:121617329
|
A | G | 265 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(262): Show | 266 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.5605-1445A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 41/47 | chr11 | 121617329 | ||||||
| chr11:121617535
|
T | G | 1 | a0001c0002t0001g0112 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.5605-1239T>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 41/47 | chr11 | 121617535 | ||||||
| chr11:121617539
|
G | GT | 43 | a0001c0001t0002g0141a0001c0001t0002g0185a0001c0002t0001g0103others(40): Show | 43 | HG00544.hp1 HG00735.hp1 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.5605-1235_5605-123 others(5): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 41/47 | chr11 | 121617539 | ||||||
| chr11:121617613
|
C | A | 1 | a0001c0004t0001g0100 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.5605-1161C>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 41/47 | chr11 | 121617613 | ||||||
| chr11:121617889
|
C | T | 2 | a0001c0021t0016g0206a0001c0066t0016g0194 | 2 | HG01243.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.5605-885C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 41/47 | chr11 | 121617889 | ||||||
| chr11:121617930
|
G | C | 4 | a0003c0027t0005g0173a0003c0027t0005g0181a0003c0070t0005g0145others(1): Show | 4 | HG03098.hp2 HG03130.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.5605-844G>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 41/47 | chr11 | 121617930 | ||||||
| chr11:121618237
|
T | A | 1 | a0013c0047t0007g0182 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.5605-537T>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 41/47 | chr11 | 121618237 | ||||||
| chr11:121618253
|
A | G | 4 | a0001c0009t0008g0207a0001c0022t0008g0211a0002c0014t0014g0217others(1): Show | 4 | HG03130.hp1 HG03195.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.5605-521A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 41/47 | chr11 | 121618253 | ||||||
| chr11:121618707
|
G | A | 176 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(173): Show | 177 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.5605-67G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 41/47 | chr11 | 121618707 | ||||||
| chr11:121619063
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.5724+170G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 42/47 | chr11 | 121619063 | ||||||
| chr11:121619096
|
G | A | 29 | a0001c0001t0002g0141a0001c0001t0002g0185a0001c0002t0001g0103others(26): Show | 29 | HG00544.hp1 HG01496.hp1 HG02257.hp2 others(26): Show |
intron_variant | MODIFIER | c.5724+203G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 42/47 | chr11 | 121619096 | ||||||
| chr11:121619208
|
A | G | 1 | a0001c0001t0001g0061 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.5724+315A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 42/47 | chr11 | 121619208 | ||||||
| chr11:121619265
|
G | A | 2 | a0001c0033t0003g0169a0001c0065t0003g0152 | 2 | HG02970.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.5724+372G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 42/47 | chr11 | 121619265 | ||||||
| chr11:121619488
|
C | T | 1 | a0001c0001t0001g0198 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.5725-265C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 42/47 | chr11 | 121619488 | ||||||
| chr11:121619583
|
G | T | 1 | a0001c0040t0001g0137 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.5725-170G>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 42/47 | chr11 | 121619583 | ||||||
| chr11:121619585
|
A | G | 5 | a0001c0015t0005g0270a0001c0021t0003g0216a0001c0021t0016g0206others(2): Show | 5 | HG01099.hp1 HG01243.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.5725-168A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 42/47 | chr11 | 121619585 | ||||||
| chr11:121619714
|
T | C | 4 | a0001c0002t0003g0150a0001c0003t0003g0254a0001c0003t0003g0262others(1): Show | 4 | HG02109.hp2 HG02965.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.5725-39T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 42/47 | chr11 | 121619714 | ||||||
| chr11:121620072
|
G | T | 1 | a0001c0002t0004g0007 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.5889+155G>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 43/47 | chr11 | 121620072 | ||||||
| chr11:121620549
|
C | T | 27 | a0001c0010t0002g0190a0001c0010t0002g0234a0001c0010t0003g0257others(24): Show | 27 | HG00642.hp2 HG01109.hp2 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.5890-515C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 43/47 | chr11 | 121620549 | ||||||
| chr11:121620598
|
C | A | 92 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(89): Show | 92 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.5890-466C>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 43/47 | chr11 | 121620598 | ||||||
| chr11:121620616
|
G | C | 169 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(166): Show | 169 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.5890-448G>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 43/47 | chr11 | 121620616 | ||||||
| chr11:121620696
|
A | G | 4 | a0001c0009t0003g0147a0001c0036t0003g0266a0001c0062t0003g0250others(1): Show | 4 | HG02559.hp1 HG02630.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.5890-368A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 43/47 | chr11 | 121620696 | ||||||
| chr11:121620833
|
A | G | 51 | a0001c0001t0002g0125a0001c0002t0001g0112a0001c0002t0001g0116others(48): Show | 52 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.5890-231A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 43/47 | chr11 | 121620833 | ||||||
| chr11:121620938
|
C | T | 6 | a0003c0027t0005g0173a0003c0027t0005g0181a0003c0070t0005g0145others(3): Show | 6 | HG02818.hp2 HG02922.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.5890-126C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 43/47 | chr11 | 121620938 | ||||||
| chr11:121620971
|
C | T | 1 | a0001c0003t0002g0096 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.5890-93C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 43/47 | chr11 | 121620971 | ||||||
| chr11:121621712
|
G | A | 1 | a0001c0016t0012g0210 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.6065-450G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 44/47 | chr11 | 121621712 | ||||||
| chr11:121621790
|
G | A | 35 | a0001c0001t0001g0038a0001c0001t0001g0040a0001c0001t0001g0089others(32): Show | 35 | HG01081.hp1 HG01175.hp2 HG02040.hp1 others(32): Show |
intron_variant | MODIFIER | c.6065-372G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 44/47 | chr11 | 121621790 | ||||||
| chr11:121621890
|
A | G | 1 | a0001c0001t0001g0045 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.6065-272A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 44/47 | chr11 | 121621890 | ||||||
| chr11:121622292
|
T | G | 53 | a0001c0001t0002g0125a0001c0002t0001g0112a0001c0002t0001g0116others(50): Show | 54 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.6171+24T>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 45/47 | chr11 | 121622292 | ||||||
| chr11:121622362
|
G | T | 1 | a0001c0002t0004g0233 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.6171+94G>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 45/47 | chr11 | 121622362 | ||||||
| chr11:121622363
|
T | TA | 264 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(261): Show | 265 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.6171+104dupA | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 45/47 | INFO_REALIGN_3_PRIME | chr11 | 121622363 | |||||
| chr11:121622445
|
C | T | 1 | a0001c0019t0001g0028 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.6171+177C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 45/47 | chr11 | 121622445 | ||||||
| chr11:121622559
|
C | T | 11 | a0001c0002t0003g0150a0001c0003t0003g0254a0001c0003t0003g0262others(8): Show | 11 | HG01099.hp1 HG01243.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.6171+291C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 45/47 | chr11 | 121622559 | ||||||
| chr11:121622646
|
C | T | 1 | a0001c0004t0022g0086 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.6171+378C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 45/47 | chr11 | 121622646 | ||||||
| chr11:121622811
|
A | G | 1 | a0001c0063t0010g0251 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.6171+543A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 45/47 | chr11 | 121622811 | ||||||
| chr11:121622815
|
G | A | 4 | a0001c0009t0011g0170a0001c0009t0011g0255a0001c0058t0011g0166others(1): Show | 4 | HG02486.hp2 HG02647.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.6171+547G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 45/47 | chr11 | 121622815 | ||||||
| chr11:121622997
|
A | G | 4 | a0003c0027t0005g0173a0003c0027t0005g0181a0003c0070t0005g0145others(1): Show | 4 | HG03098.hp2 HG03130.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.6171+729A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 45/47 | chr11 | 121622997 | ||||||
| chr11:121623015
|
T | C | 4 | a0001c0004t0004g0011a0001c0004t0004g0012a0001c0004t0009g0015others(1): Show | 4 | HG00738.hp2 HG01167.hp1 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.6171+747T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 45/47 | chr11 | 121623015 | ||||||
| chr11:121623218
|
C | T | 1 | a0001c0003t0002g0230 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.6171+950C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 45/47 | chr11 | 121623218 | ||||||
| chr11:121623303
|
A | G | 1 | a0001c0003t0002g0133 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.6171+1035A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 45/47 | chr11 | 121623303 | ||||||
| chr11:121623318
|
C | T | 10 | a0001c0006t0001g0068a0001c0006t0001g0072a0001c0006t0001g0118others(7): Show | 10 | HG00735.hp1 HG01243.hp2 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.6171+1050C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 45/47 | chr11 | 121623318 | ||||||
| chr11:121623380
|
C | T | 5 | a0003c0027t0005g0173a0003c0027t0005g0181a0003c0070t0005g0145others(2): Show | 5 | HG02922.hp2 HG03098.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.6171+1112C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 45/47 | chr11 | 121623380 | ||||||
| chr11:121623460
|
G | T | 1 | a0001c0012t0005g0247 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.6171+1192G>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 45/47 | chr11 | 121623460 | ||||||
| chr11:121623569
|
T | C | 27 | a0001c0002t0002g0091a0001c0002t0004g0077a0001c0002t0004g0078others(24): Show | 27 | HG02922.hp2 HG03098.hp2 HG03130.hp2 others(24): Show |
intron_variant | MODIFIER | c.6171+1301T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 45/47 | chr11 | 121623569 | ||||||
| chr11:121623595
|
A | G | 1 | a0003c0027t0005g0173 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.6171+1327A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 45/47 | chr11 | 121623595 | ||||||
| chr11:121623606
|
A | G | 5 | a0001c0012t0007g0175a0001c0012t0007g0176a0001c0012t0007g0244others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.6171+1338A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 45/47 | chr11 | 121623606 | ||||||
| chr11:121623654
|
C | T | 2 | a0001c0013t0002g0018a0001c0018t0002g0013 | 2 | NA19001.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.6171+1386C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 45/47 | chr11 | 121623654 | ||||||
| chr11:121623655
|
G | A | 8 | a0001c0004t0003g0224a0001c0006t0028g0031a0001c0011t0001g0107others(5): Show | 8 | HG01074.hp2 HG01192.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.6171+1387G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 45/47 | chr11 | 121623655 | ||||||
| chr11:121623658
|
G | A | 4 | a0001c0009t0003g0147a0001c0036t0003g0266a0001c0062t0003g0250others(1): Show | 4 | HG02559.hp1 HG02630.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.6171+1390G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 45/47 | chr11 | 121623658 | ||||||
| chr11:121623678
|
T | A | 1 | a0001c0001t0001g0155 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.6172-1407T>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 45/47 | chr11 | 121623678 | ||||||
| chr11:121623690
|
G | T | 5 | a0003c0027t0005g0173a0003c0027t0005g0181a0003c0070t0005g0145others(2): Show | 5 | HG02922.hp2 HG03098.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.6172-1395G>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 45/47 | chr11 | 121623690 | ||||||
| chr11:121624289
|
A | G | 1 | a0002c0005t0001g0074 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.6172-796A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 45/47 | chr11 | 121624289 | ||||||
| chr11:121624432
|
T | C | 192 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(189): Show | 192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.6172-653T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 45/47 | chr11 | 121624432 | ||||||
| chr11:121624541
|
G | A | 9 | a0001c0003t0007g0261a0001c0003t0008g0208a0001c0003t0008g0263others(6): Show | 9 | HG01496.hp1 HG02258.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.6172-544G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 45/47 | chr11 | 121624541 | ||||||
| chr11:121624655
|
G | A | 2 | a0001c0013t0002g0018a0001c0018t0002g0013 | 2 | NA19001.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.6172-430G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 45/47 | chr11 | 121624655 | ||||||
| chr11:121624690
|
C | T | 2 | a0001c0033t0003g0169a0001c0065t0003g0152 | 2 | HG02970.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.6172-395C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 45/47 | chr11 | 121624690 | ||||||
| chr11:121624846
|
G | A | 184 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(181): Show | 184 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.6172-239G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 45/47 | chr11 | 121624846 | ||||||
| chr11:121624968
|
G | A | 2 | a0001c0033t0003g0169a0001c0065t0003g0152 | 2 | HG02970.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.6172-117G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 45/47 | chr11 | 121624968 | ||||||
| chr11:121625287
|
G | A | 1 | a0001c0011t0012g0242 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.6364+10G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 46/47 | chr11 | 121625287 | ||||||
| chr11:121625476
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.6364+199G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 46/47 | chr11 | 121625476 | ||||||
| chr11:121625541
|
G | A | 7 | a0001c0003t0005g0226a0001c0003t0005g0228a0001c0010t0005g0239others(4): Show | 7 | HG00642.hp2 HG01099.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.6364+264G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 46/47 | chr11 | 121625541 | ||||||
| chr11:121625949
|
A | C | 2 | a0001c0001t0001g0050a0001c0001t0001g0052 | 2 | NA18957.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.6364+672A>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 46/47 | chr11 | 121625949 | ||||||
| chr11:121626175
|
C | A | 1 | a0002c0005t0001g0202 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.6364+898C>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 46/47 | chr11 | 121626175 | ||||||
| chr11:121626224
|
C | T | 93 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(90): Show | 93 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.6364+947C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 46/47 | chr11 | 121626224 | ||||||
| chr11:121626453
|
GT | G | 175 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(172): Show | 175 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.6365-1089delT | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 46/47 | INFO_REALIGN_3_PRIME | chr11 | 121626453 | |||||
| chr11:121626781
|
C | A | 12 | a0001c0003t0005g0226a0001c0003t0005g0228a0001c0010t0005g0239others(9): Show | 12 | HG00642.hp2 HG01099.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.6365-774C>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 46/47 | chr11 | 121626781 | ||||||
| chr11:121626956
|
G | A | 1 | a0012c0064t0024g0168 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.6365-599G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 46/47 | chr11 | 121626956 | ||||||
| chr11:121627175
|
T | C | 91 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(88): Show | 91 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.6365-380T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 46/47 | chr11 | 121627175 | ||||||
| chr11:121627420
|
G | A | 1 | a0004c0056t0013g0148 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.6365-135G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 46/47 | chr11 | 121627420 | ||||||
| chr11:121627803
|
G | A | 1 | a0012c0064t0024g0168 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.6577+36G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 47/47 | chr11 | 121627803 | ||||||
| chr11:121628268
|
A | T | 11 | a0001c0002t0003g0151a0001c0004t0003g0224a0001c0010t0003g0257others(8): Show | 11 | HG01109.hp2 HG02486.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.6577+501A>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 47/47 | chr11 | 121628268 | ||||||
| chr11:121628354
|
C | G | 1 | a0001c0003t0001g0113 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.6577+587C>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 47/47 | chr11 | 121628354 | ||||||
| chr11:121628494
|
A | G | 1 | a0001c0020t0003g0248 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.6577+727A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 47/47 | chr11 | 121628494 | ||||||
| chr11:121628627
|
G | A | 179 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0023others(176): Show | 179 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.6577+860G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 47/47 | chr11 | 121628627 | ||||||
| chr11:121628770
|
G | A | 26 | a0001c0001t0004g0099a0001c0002t0004g0003a0001c0002t0004g0007others(23): Show | 26 | HG00738.hp2 HG01256.hp2 HG01258.hp1 others(23): Show |
intron_variant | MODIFIER | c.6578-726G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 47/47 | chr11 | 121628770 | ||||||
| chr11:121628800
|
T | C | 2 | a0005c0017t0002g0237a0005c0017t0002g0241 | 2 | HG00642.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.6578-696T>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 47/47 | chr11 | 121628800 | ||||||
| chr11:121628908
|
G | A | 1 | a0001c0002t0001g0083 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.6578-588G>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 47/47 | chr11 | 121628908 | ||||||
| chr11:121628915
|
T | A | 1 | a0004c0059t0002g0171 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.6578-581T>A | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 47/47 | chr11 | 121628915 | ||||||
| chr11:121629027
|
G | C | 1 | a0001c0001t0002g0004 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.6578-469G>C | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 47/47 | chr11 | 121629027 | ||||||
| chr11:121629150
|
C | CTAG | 4 | a0001c0061t0030g0249a0002c0014t0014g0217a0002c0014t0014g0252others(1): Show | 4 | HG03130.hp1 HG03453.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.6578-344_6578-342d others(5): Show |
SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 47/47 | INFO_REALIGN_3_PRIME | chr11 | 121629150 | |||||
| chr11:121629193
|
C | T | 1 | a0005c0017t0001g0240 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.6578-303C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 47/47 | chr11 | 121629193 | ||||||
| chr11:121629268
|
C | T | 6 | a0001c0009t0010g0165a0001c0021t0016g0206a0001c0031t0010g0214others(3): Show | 6 | HG01243.hp1 HG01891.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.6578-228C>T | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 47/47 | chr11 | 121629268 | ||||||
| chr11:121629276
|
A | G | 1 | a0001c0006t0001g0157 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.6578-220A>G | SORL1 | ENSG00000137642.13 | transcript | ENST00000260197.12 | protein_coding | 47/47 | chr11 | 121629276 |