Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 100130742 |
|---|---|
| ensemblid | ENSG00000214954.9 |
| hgncid | 34303 |
| symbol | LRRC69 |
| name | leucine rich repeat containing 69 |
| refseq_nuc | NM_001129890.2 |
| refseq_prot | NP_001123362.1 |
| ensembl_nuc | ENST00000448384.3 |
| ensembl_prot | ENSP00000400803.2 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 91102619 |
| end | 91219257 |
| strand | + |
| ver | v1.2 |
| region | chr8:91102619-91219257 |
| region5000 | chr8:91097619-91224257 |
| regionname0 | LRRC69_chr8_91102619_91219257 |
| regionname5000 | LRRC69_chr8_91097619_91224257 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 347 | 184 | 71 | 28 | 67 | 6 | 10 | 56 | LRRC69_chr8_91097619_91224257 | LRRC69 | copy fasta | chr8 | 91097619 | 91224257 |
| a0002 | 0/0 | 347 | 133 | 17 | 22 | 74 | 6 | 14 | 56 | LRRC69_chr8_91097619_91224257 | LRRC69 | copy fasta | chr8 | 91097619 | 91224257 |
| a0003 | 0/0 | 347 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | copy fasta | chr8 | 91097619 | 91224257 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1044 | 176 | 65 | 27 | 66 | 6 | 10 | LRRC69_chr8_91097619_91224257 | LRRC69 | copy fasta | chr8 | 91097619 | 91224257 |
| c0002 | 0/0 | 1044 | 131 | 16 | 21 | 74 | 6 | 14 | LRRC69_chr8_91097619_91224257 | LRRC69 | copy fasta | chr8 | 91097619 | 91224257 |
| c0003 | 0/0 | 1044 | 7 | 6 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | copy fasta | chr8 | 91097619 | 91224257 |
| c0004 | 0/0 | 1044 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | copy fasta | chr8 | 91097619 | 91224257 |
| c0005 | 0/0 | 1044 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | copy fasta | chr8 | 91097619 | 91224257 |
| c0006 | 0/0 | 1044 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | copy fasta | chr8 | 91097619 | 91224257 |
| c0007 | 0/0 | 1044 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | copy fasta | chr8 | 91097619 | 91224257 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 301 | 302 | 72 | 50 | 142 | 12 | 24 | LRRC69_chr8_91097619_91224257 | LRRC69 | copy fasta | chr8 | 91097619 | 91224257 |
| t0002 | 0/0 | 301 | 13 | 13 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | copy fasta | chr8 | 91097619 | 91224257 |
| t0003 | 0/0 | 301 | 3 | 3 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | copy fasta | chr8 | 91097619 | 91224257 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0011 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0240 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1044 | 176 | 65 | 27 | 66 | 6 | 10 | LRRC69_chr8_91097619_91224257 | LRRC69 | copy fasta | chr8 | 91097619 | 91224257 |
| a0001c0003 | 0/0 | 1044 | 7 | 6 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | copy fasta | chr8 | 91097619 | 91224257 |
| a0001c0004 | 0/0 | 1044 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | copy fasta | chr8 | 91097619 | 91224257 |
| a0002c0002 | 0/0 | 1044 | 131 | 16 | 21 | 74 | 6 | 14 | LRRC69_chr8_91097619_91224257 | LRRC69 | copy fasta | chr8 | 91097619 | 91224257 |
| a0002c0006 | 0/0 | 1044 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | copy fasta | chr8 | 91097619 | 91224257 |
| a0002c0007 | 0/0 | 1044 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | copy fasta | chr8 | 91097619 | 91224257 |
| a0003c0005 | 0/0 | 1044 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | copy fasta | chr8 | 91097619 | 91224257 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1344 | 162 | 51 | 27 | 66 | 6 | 10 | LRRC69_chr8_91097619_91224257 | LRRC69 | copy fasta | chr8 | 91097619 | 91224257 |
| a0001c0001t0002 | 0/0 | 1344 | 11 | 11 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | copy fasta | chr8 | 91097619 | 91224257 |
| a0001c0001t0003 | 0/0 | 1344 | 3 | 3 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | copy fasta | chr8 | 91097619 | 91224257 |
| a0001c0003t0001 | 0/0 | 1344 | 7 | 6 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | copy fasta | chr8 | 91097619 | 91224257 |
| a0001c0004t0001 | 0/0 | 1344 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | copy fasta | chr8 | 91097619 | 91224257 |
| a0002c0002t0001 | 0/0 | 1344 | 130 | 15 | 21 | 74 | 6 | 14 | LRRC69_chr8_91097619_91224257 | LRRC69 | copy fasta | chr8 | 91097619 | 91224257 |
| a0002c0002t0002 | 0/0 | 1344 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | copy fasta | chr8 | 91097619 | 91224257 |
| a0002c0006t0002 | 0/0 | 1344 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | copy fasta | chr8 | 91097619 | 91224257 |
| a0002c0007t0001 | 0/0 | 1344 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | copy fasta | chr8 | 91097619 | 91224257 |
| a0003c0005t0001 | 0/0 | 1344 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | copy fasta | chr8 | 91097619 | 91224257 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0011 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0240 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0003g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0001t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0003t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0003t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0003t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0003t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0003t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0003t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0003t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0001c0004t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0002t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0006t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0002c0007t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| a0003c0005t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0111 | EUR | GBR | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0252 | EUR | GBR | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG00140 | hp1 | a0002 | c0002 | t0001 | g0104 | EUR | GBR | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0020 | EUR | GBR | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG00408 | hp1 | a0002 | c0002 | t0001 | g0105 | EAS | CHS | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG00408 | hp2 | a0003 | c0005 | t0001 | g0245 | EAS | CHS | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | CHS | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | CHS | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0033 | EAS | CHS | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | CHS | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG00544 | hp1 | a0002 | c0002 | t0001 | g0137 | EAS | CHS | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | CHS | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0130 | EAS | CHS | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | CHS | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0069 | EAS | CHS | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0136 | EAS | CHS | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG00639 | hp1 | a0002 | c0007 | t0001 | g0061 | AMR | PUR | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | CHS | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG00673 | hp2 | a0002 | c0002 | t0001 | g0093 | EAS | CHS | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG00733 | hp2 | a0002 | c0002 | t0001 | g0092 | AMR | PUR | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0077 | AMR | PUR | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0096 | AMR | PUR | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0308 | AMR | PUR | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG01070 | hp2 | a0002 | c0002 | t0001 | g0043 | AMR | PUR | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG01081 | hp1 | a0001 | c0003 | t0001 | g0287 | AMR | PUR | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0135 | AMR | PUR | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0063 | AMR | PUR | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0072 | AMR | PUR | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0078 | AMR | PUR | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0039 | AMR | PUR | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG01109 | hp2 | a0002 | c0002 | t0001 | g0086 | AMR | PUR | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0113 | AMR | PUR | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0084 | AMR | PUR | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0307 | AMR | CLM | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG01256 | hp2 | a0002 | c0002 | t0001 | g0119 | AMR | CLM | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | CLM | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0134 | AMR | CLM | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0062 | AMR | CLM | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0304 | AMR | CLM | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | CLM | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0067 | AMR | CLM | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | CLM | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0189 | EUR | IBS | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0123 | EUR | IBS | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0200 | EUR | IBS | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG01516 | hp2 | a0002 | c0002 | t0001 | g0125 | EUR | IBS | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0201 | EUR | IBS | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG01517 | hp2 | a0002 | c0002 | t0001 | g0122 | EUR | IBS | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0019 | AFR | ACB | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG01891 | hp1 | a0001 | c0003 | t0001 | g0285 | AFR | ACB | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | ACB | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG01934 | hp1 | a0002 | c0002 | t0001 | g0012 | AMR | PEL | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG01943 | hp1 | a0002 | c0002 | t0001 | g0049 | AMR | PEL | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | PEL | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0027 | AMR | PEL | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PEL | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0101 | AMR | PEL | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02015 | hp2 | a0002 | c0002 | t0001 | g0053 | EAS | KHV | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0126 | EAS | KHV | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | KHV | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | KHV | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02055 | hp1 | a0002 | c0002 | t0001 | g0066 | AFR | ACB | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02056 | hp1 | a0002 | c0002 | t0001 | g0083 | EAS | KHV | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0050 | EAS | KHV | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0139 | EAS | KHV | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02074 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | KHV | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0048 | EAS | KHV | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02129 | hp1 | a0002 | c0002 | t0001 | g0131 | EAS | KHV | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02129 | hp2 | a0002 | c0002 | t0001 | g0030 | EAS | KHV | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PEL | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02148 | hp2 | a0002 | c0002 | t0001 | g0042 | AMR | PEL | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0305 | AFR | ACB | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0277 | AFR | ACB | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0303 | AFR | ACB | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02280 | hp2 | a0002 | c0002 | t0001 | g0060 | AFR | ACB | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02572 | hp2 | a0001 | c0003 | t0001 | g0284 | AFR | GWD | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0085 | SAS | PJL | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0120 | SAS | PJL | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02622 | hp1 | a0002 | c0002 | t0001 | g0065 | AFR | GWD | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0306 | SAS | PJL | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02698 | hp2 | a0002 | c0002 | t0001 | g0138 | SAS | PJL | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02717 | hp2 | a0002 | c0002 | t0001 | g0070 | AFR | GWD | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02723 | hp2 | a0002 | c0002 | t0001 | g0005 | AFR | GWD | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02738 | hp2 | a0002 | c0002 | t0001 | g0081 | SAS | PJL | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0281 | AFR | GWD | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0178 | AFR | GWD | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02818 | hp2 | a0001 | c0003 | t0001 | g0283 | AFR | GWD | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02895 | hp2 | a0002 | c0002 | t0001 | g0129 | AFR | GWD | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | GWD | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0187 | AFR | GWD | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02897 | hp2 | a0002 | c0002 | t0001 | g0005 | AFR | GWD | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | ESN | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | ESN | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ESN | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | ESN | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ESN | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ESN | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0181 | AFR | GWD | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG03098 | hp1 | a0001 | c0003 | t0001 | g0282 | AFR | MSL | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG03098 | hp2 | a0002 | c0006 | t0002 | g0154 | AFR | MSL | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ESN | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG03139 | hp1 | a0002 | c0002 | t0001 | g0038 | AFR | ESN | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | ESN | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ESN | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG03195 | hp2 | a0002 | c0002 | t0001 | g0075 | AFR | ESN | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0160 | AFR | MSL | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | MSL | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0159 | AFR | MSL | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | MSL | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG03239 | hp2 | a0002 | c0002 | t0001 | g0112 | SAS | PJL | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG03486 | hp1 | a0001 | c0003 | t0001 | g0302 | AFR | MSL | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0158 | AFR | MSL | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG03490 | hp1 | a0002 | c0002 | t0001 | g0035 | SAS | PJL | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0180 | AFR | GWD | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | GWD | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG03579 | hp1 | a0002 | c0002 | t0001 | g0055 | AFR | MSL | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | MSL | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0114 | SAS | PJL | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0132 | SAS | PJL | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0091 | SAS | BEB | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0089 | SAS | BEB | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0082 | SAS | BEB | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0259 | SAS | BEB | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0102 | SAS | BEB | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0309 | SAS | BEB | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0088 | SAS | BEB | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | BEB | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0097 | SAS | STU | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | STU | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | YRI | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0156 | AFR | YRI | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18747 | hp1 | a0002 | c0002 | t0001 | g0054 | EAS | CHB | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | CHB | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | YRI | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | YRI | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18939 | hp1 | a0002 | c0002 | t0001 | g0064 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18939 | hp2 | a0002 | c0002 | t0001 | g0040 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18944 | hp1 | a0002 | c0002 | t0001 | g0031 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18945 | hp1 | a0001 | c0004 | t0001 | g0270 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18945 | hp2 | a0002 | c0002 | t0001 | g0090 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18947 | hp1 | a0002 | c0002 | t0001 | g0071 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18949 | hp1 | a0002 | c0002 | t0001 | g0056 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0128 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18952 | hp1 | a0002 | c0002 | t0001 | g0037 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18952 | hp2 | a0002 | c0002 | t0001 | g0108 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18953 | hp1 | a0002 | c0002 | t0001 | g0103 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18954 | hp1 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18957 | hp1 | a0002 | c0002 | t0001 | g0106 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18959 | hp1 | a0002 | c0002 | t0001 | g0275 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18961 | hp1 | a0002 | c0002 | t0001 | g0099 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18962 | hp1 | a0002 | c0002 | t0001 | g0032 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18964 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18967 | hp2 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18969 | hp2 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18970 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18973 | hp2 | a0002 | c0002 | t0001 | g0079 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18977 | hp2 | a0002 | c0002 | t0001 | g0127 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0073 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18980 | hp2 | a0002 | c0002 | t0001 | g0107 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18981 | hp2 | a0002 | c0002 | t0001 | g0208 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18984 | hp1 | a0002 | c0002 | t0001 | g0274 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18989 | hp1 | a0002 | c0002 | t0001 | g0141 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18990 | hp1 | a0002 | c0002 | t0001 | g0034 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18992 | hp1 | a0002 | c0002 | t0001 | g0140 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18993 | hp1 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18993 | hp2 | a0002 | c0002 | t0001 | g0095 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18998 | hp2 | a0002 | c0002 | t0001 | g0044 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18999 | hp1 | a0002 | c0002 | t0001 | g0036 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18999 | hp2 | a0002 | c0002 | t0001 | g0310 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA19000 | hp2 | a0002 | c0002 | t0001 | g0273 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA19001 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA19001 | hp2 | a0002 | c0002 | t0001 | g0207 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA19002 | hp1 | a0002 | c0002 | t0001 | g0100 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA19006 | hp1 | a0002 | c0002 | t0001 | g0109 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA19010 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0110 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | LWK | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA19030 | hp2 | a0002 | c0002 | t0002 | g0041 | AFR | LWK | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA19043 | hp1 | a0002 | c0002 | t0001 | g0074 | AFR | LWK | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | LWK | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA19054 | hp2 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA19057 | hp1 | a0002 | c0002 | t0001 | g0076 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA19058 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA19060 | hp2 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0098 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA19068 | hp2 | a0002 | c0002 | t0001 | g0094 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA19072 | hp2 | a0002 | c0002 | t0001 | g0142 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA19074 | hp2 | a0002 | c0002 | t0001 | g0029 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA19082 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA19083 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA19084 | hp1 | a0002 | c0002 | t0001 | g0311 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | YRI | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | YRI | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | ASW | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA20129 | hp2 | a0002 | c0002 | t0001 | g0068 | AFR | ASW | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0250 | EUR | TSI | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0118 | EUR | TSI | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0300 | AMR | CLM | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | CLM | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0157 | AFR | ACB | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | ACB | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02486 | hp1 | a0001 | c0003 | t0001 | g0286 | AFR | ACB | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02486 | hp2 | a0002 | c0002 | t0001 | g0051 | AFR | ACB | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0161 | AFR | ACB | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | MSL | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | MSL | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | USA | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | USA | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18955 | hp1 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA18955 | hp2 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0087 | AFR | USA | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | USA | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0155 | AFR | LWK | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0179 | AFR | LWK | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0011 | REF | REF | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0240 | REF | REF | LRRC69_chr8_91097619_91224257 | LRRC69 | chr8 | 91097619 | 91224257 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:91124500
|
C | T | 1 | a0002 | 133 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(130): Show |
missense_variant | MODERATE | c.191C>T | p.Thr64Ile | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 2/8 | 234/1344 | 191/1044 | 64/347 | chr8 | 91124500 | ||
| chr8:91218920
|
G | A | 1 | a0003 | 1 | HG00408.hp2 | missense_variant | MODERATE | c.964G>A | p.Val322Met | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 8/8 | 1007/1344 | 964/1044 | 322/347 | chr8 | 91218920 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:91124537
|
G | A | 1 | a0002c0006 | 1 | HG03098.hp2 | synonymous_variant | LOW | c.228G>A | p.Pro76Pro | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 2/8 | 271/1344 | 228/1044 | 76/347 | chr8 | 91124537 | ||
| chr8:91133143
|
T | C | 1 | a0001c0003 | 7 | HG01081.hp1 HG01891.hp1 HG02486.hp1 others(4): Show |
synonymous_variant | LOW | c.417T>C | p.Tyr139Tyr | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 4/8 | 460/1344 | 417/1044 | 139/347 | chr8 | 91133143 | ||
| chr8:91133302
|
G | A | 1 | a0001c0004 | 1 | NA18945.hp1 | synonymous_variant | LOW | c.576G>A | p.Pro192Pro | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 4/8 | 619/1344 | 576/1044 | 192/347 | chr8 | 91133302 | ||
| chr8:91218922
|
G | A | 1 | a0002c0007 | 1 | HG00639.hp1 | synonymous_variant | LOW | c.966G>A | p.Val322Val | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 8/8 | 1009/1344 | 966/1044 | 322/347 | chr8 | 91218922 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:91219087
|
C | T | 3 | a0001c0001t0002a0002c0002t0002a0002c0006t0002 | 13 | HG02109.hp1 HG02257.hp2 HG02559.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*87C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 8/8 | 87 | chr8 | 91219087 | |||||
| chr8:91219107
|
A | G | 1 | a0001c0001t0003 | 3 | HG02818.hp1 HG03540.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*107A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 8/8 | 107 | chr8 | 91219107 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:91103182
|
G | T | 1 | a0001c0001t0001g0312 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.183+338G>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91103182 | ||||||
| chr8:91103312
|
C | T | 2 | a0002c0002t0001g0310a0002c0002t0001g0311 | 2 | NA18999.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.183+468C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91103312 | ||||||
| chr8:91103926
|
C | A | 5 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG00735.hp2 HG02615.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.183+1082C>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91103926 | ||||||
| chr8:91103976
|
A | G | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG01069.hp1 HG01256.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.183+1132A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91103976 | ||||||
| chr8:91104015
|
C | G | 2 | a0001c0001t0001g0304a0001c0001t0001g0305 | 2 | HG01261.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.183+1171C>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91104015 | ||||||
| chr8:91104123
|
A | G | 29 | a0001c0001t0001g0001a0001c0001t0001g0276a0001c0001t0001g0278others(26): Show | 31 | HG00423.hp2 HG00558.hp2 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.183+1279A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91104123 | ||||||
| chr8:91104513
|
T | C | 6 | a0001c0001t0001g0276a0001c0001t0001g0278a0001c0001t0001g0279others(3): Show | 6 | HG02257.hp2 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.183+1669T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91104513 | ||||||
| chr8:91105010
|
G | A | 1 | a0001c0001t0001g0011 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.183+2166G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91105010 | ||||||
| chr8:91105261
|
A | C | 3 | a0002c0002t0001g0273a0002c0002t0001g0274a0002c0002t0001g0275 | 3 | NA18959.hp1 NA18984.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.183+2417A>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91105261 | ||||||
| chr8:91105363
|
C | G | 1 | a0001c0001t0001g0272 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.183+2519C>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91105363 | ||||||
| chr8:91105464
|
G | T | 5 | a0001c0001t0001g0267a0001c0001t0001g0268a0001c0001t0001g0269others(2): Show | 5 | NA18945.hp1 NA18954.hp2 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.183+2620G>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91105464 | ||||||
| chr8:91105500
|
A | T | 1 | a0001c0001t0001g0266 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.183+2656A>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91105500 | ||||||
| chr8:91105586
|
G | A | 145 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(142): Show | 149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.183+2742G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91105586 | ||||||
| chr8:91105659
|
C | CA | 211 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(208): Show | 217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.183+2833dupA | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 91105659 | |||||
| chr8:91105708
|
G | C | 158 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(155): Show | 162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.183+2864G>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91105708 | ||||||
| chr8:91105713
|
C | CTTAGAGA others(1): Show |
29 | a0001c0001t0001g0001a0001c0001t0001g0276a0001c0001t0001g0278others(26): Show | 31 | HG00423.hp2 HG00558.hp2 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.183+2872_183+2879d others(10): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 91105713 | |||||
| chr8:91105866
|
T | C | 161 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(158): Show | 165 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.183+3022T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91105866 | ||||||
| chr8:91105997
|
T | A | 3 | a0002c0002t0001g0012a0002c0002t0001g0310a0002c0002t0001g0311 | 3 | HG01934.hp1 NA18999.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.183+3153T>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91105997 | ||||||
| chr8:91106313
|
A | G | 1 | a0001c0001t0002g0181 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.183+3469A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91106313 | ||||||
| chr8:91106549
|
A | C | 1 | a0001c0001t0002g0281 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.183+3705A>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91106549 | ||||||
| chr8:91106616
|
A | T | 1 | a0002c0002t0001g0138 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.183+3772A>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91106616 | ||||||
| chr8:91106650
|
G | A | 1 | a0001c0001t0001g0183 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.183+3806G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91106650 | ||||||
| chr8:91106821
|
C | T | 3 | a0001c0001t0003g0178a0001c0001t0003g0179a0001c0001t0003g0180 | 3 | HG02818.hp1 HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.183+3977C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91106821 | ||||||
| chr8:91106968
|
AT | A | 30 | a0001c0001t0001g0001a0001c0001t0001g0188a0001c0001t0001g0276others(27): Show | 32 | HG00423.hp2 HG00558.hp2 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.183+4136delT | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 91106968 | |||||
| chr8:91106969
|
T | A | 176 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(173): Show | 180 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.183+4125T>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91106969 | ||||||
| chr8:91106970
|
T | A | 190 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(187): Show | 196 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.183+4126T>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91106970 | ||||||
| chr8:91107260
|
G | A | 161 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(158): Show | 165 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.183+4416G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91107260 | ||||||
| chr8:91107464
|
C | T | 1 | a0001c0001t0001g0265 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.183+4620C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91107464 | ||||||
| chr8:91107674
|
T | C | 3 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0191 | 3 | HG01099.hp1 HG01515.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.183+4830T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91107674 | ||||||
| chr8:91107987
|
G | C | 6 | a0002c0002t0001g0013a0002c0002t0001g0014a0002c0002t0001g0015others(3): Show | 6 | NA18954.hp1 NA18964.hp2 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.183+5143G>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91107987 | ||||||
| chr8:91108106
|
C | T | 1 | a0002c0002t0001g0142 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.183+5262C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91108106 | ||||||
| chr8:91108727
|
GTTAT | G | 3 | a0001c0001t0003g0178a0001c0001t0003g0179a0001c0001t0003g0180 | 3 | HG02818.hp1 HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.183+5898_183+5901d others(6): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 91108727 | |||||
| chr8:91108807
|
T | A | 1 | a0002c0002t0001g0019 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.183+5963T>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91108807 | ||||||
| chr8:91108987
|
T | C | 3 | a0001c0001t0001g0304a0001c0001t0001g0305a0002c0006t0002g0154 | 3 | HG01261.hp2 HG02257.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.183+6143T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91108987 | ||||||
| chr8:91109161
|
AC | A | 160 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(157): Show | 164 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.183+6319delC | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 91109161 | |||||
| chr8:91109242
|
C | T | 3 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0191 | 3 | HG01099.hp1 HG01515.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.183+6398C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91109242 | ||||||
| chr8:91109302
|
G | T | 23 | a0001c0001t0001g0001a0001c0001t0001g0288a0001c0001t0001g0289others(20): Show | 25 | HG00423.hp2 HG00558.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.183+6458G>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91109302 | ||||||
| chr8:91109336
|
C | T | 1 | a0001c0001t0002g0161 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.183+6492C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91109336 | ||||||
| chr8:91109477
|
G | A | 160 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(157): Show | 164 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.183+6633G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91109477 | ||||||
| chr8:91109642
|
C | A | 29 | a0001c0001t0001g0001a0001c0001t0001g0276a0001c0001t0001g0278others(26): Show | 31 | HG00423.hp2 HG00558.hp2 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.183+6798C>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91109642 | ||||||
| chr8:91109691
|
A | T | 2 | a0002c0002t0001g0136a0002c0002t0001g0137 | 2 | HG00544.hp1 HG00609.hp2 |
intron_variant | MODIFIER | c.183+6847A>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91109691 | ||||||
| chr8:91109698
|
G | T | 1 | a0002c0002t0001g0135 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.183+6854G>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91109698 | ||||||
| chr8:91109760
|
C | T | 1 | a0002c0002t0001g0134 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.183+6916C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91109760 | ||||||
| chr8:91110141
|
A | G | 160 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(157): Show | 164 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.183+7297A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91110141 | ||||||
| chr8:91110223
|
T | C | 3 | a0001c0001t0001g0304a0001c0001t0001g0305a0002c0006t0002g0154 | 3 | HG01261.hp2 HG02257.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.183+7379T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91110223 | ||||||
| chr8:91110298
|
G | A | 4 | a0002c0002t0001g0002a0002c0002t0001g0021a0002c0002t0001g0022others(1): Show | 5 | NA18960.hp1 NA18969.hp2 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.183+7454G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91110298 | ||||||
| chr8:91110363
|
G | A | 1 | a0001c0001t0001g0192 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.183+7519G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91110363 | ||||||
| chr8:91110455
|
C | T | 3 | a0001c0001t0003g0178a0001c0001t0003g0179a0001c0001t0003g0180 | 3 | HG02818.hp1 HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.183+7611C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91110455 | ||||||
| chr8:91110459
|
G | A | 3 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0191 | 3 | HG01099.hp1 HG01515.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.183+7615G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91110459 | ||||||
| chr8:91110512
|
A | G | 204 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(201): Show | 210 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.183+7668A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91110512 | ||||||
| chr8:91110513
|
A | C | 204 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(201): Show | 210 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.183+7669A>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91110513 | ||||||
| chr8:91110603
|
CA | C | 157 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(154): Show | 161 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.183+7760delA | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91110603 | ||||||
| chr8:91110780
|
C | T | 9 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(6): Show | 9 | HG02109.hp1 HG02559.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.183+7936C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91110780 | ||||||
| chr8:91110802
|
A | G | 108 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(105): Show | 111 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.183+7958A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91110802 | ||||||
| chr8:91110908
|
A | G | 1 | a0001c0001t0002g0160 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.183+8064A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91110908 | ||||||
| chr8:91110980
|
T | C | 11 | a0001c0001t0001g0020a0001c0001t0001g0193a0001c0001t0001g0194others(8): Show | 11 | HG00140.hp2 HG00733.hp1 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.183+8136T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91110980 | ||||||
| chr8:91111112
|
G | A | 204 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(201): Show | 210 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.183+8268G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91111112 | ||||||
| chr8:91111407
|
G | A | 3 | a0001c0001t0003g0178a0001c0001t0003g0179a0001c0001t0003g0180 | 3 | HG02818.hp1 HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.183+8563G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91111407 | ||||||
| chr8:91111409
|
A | G | 2 | a0001c0001t0001g0304a0001c0001t0001g0305 | 2 | HG01261.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.183+8565A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91111409 | ||||||
| chr8:91111958
|
A | C | 1 | a0001c0001t0001g0303 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.183+9114A>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91111958 | ||||||
| chr8:91111966
|
A | G | 1 | a0001c0003t0001g0302 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.183+9122A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91111966 | ||||||
| chr8:91112165
|
A | G | 3 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186 | 3 | HG02886.hp1 HG02965.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.183+9321A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91112165 | ||||||
| chr8:91112278
|
A | T | 3 | a0001c0001t0003g0178a0001c0001t0003g0179a0001c0001t0003g0180 | 3 | HG02818.hp1 HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.183+9434A>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91112278 | ||||||
| chr8:91112535
|
A | G | 29 | a0001c0001t0001g0001a0001c0001t0001g0276a0001c0001t0001g0278others(26): Show | 31 | HG00423.hp2 HG00558.hp2 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.183+9691A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91112535 | ||||||
| chr8:91112654
|
G | A | 3 | a0001c0001t0003g0178a0001c0001t0003g0179a0001c0001t0003g0180 | 3 | HG02818.hp1 HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.183+9810G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91112654 | ||||||
| chr8:91112729
|
G | A | 1 | a0001c0001t0001g0303 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.183+9885G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91112729 | ||||||
| chr8:91113161
|
A | G | 29 | a0001c0001t0001g0001a0001c0001t0001g0276a0001c0001t0001g0278others(26): Show | 31 | HG00423.hp2 HG00558.hp2 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.183+10317A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91113161 | ||||||
| chr8:91113292
|
A | G | 6 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(3): Show | 6 | HG02818.hp1 HG02886.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.183+10448A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91113292 | ||||||
| chr8:91113721
|
A | G | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(1): Show | 4 | HG00735.hp2 HG02922.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.184-10772A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91113721 | ||||||
| chr8:91113786
|
G | T | 1 | a0001c0001t0001g0309 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.184-10707G>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91113786 | ||||||
| chr8:91113861
|
A | G | 2 | a0002c0002t0001g0053a0002c0002t0001g0054 | 2 | HG02015.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.184-10632A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91113861 | ||||||
| chr8:91113961
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.184-10532G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91113961 | ||||||
| chr8:91113972
|
C | CA | 7 | a0001c0001t0001g0162a0001c0001t0001g0188a0001c0001t0001g0193others(4): Show | 7 | HG01433.hp1 HG02027.hp2 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.184-10499dupA | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 91113972 | |||||
| chr8:91113972
|
C | CAAAA | 22 | a0001c0001t0001g0001a0001c0001t0001g0288a0001c0001t0001g0289others(19): Show | 24 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.184-10502_184-1049 others(8): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 91113972 | |||||
| chr8:91113972
|
C | CAAAAA | 131 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(128): Show | 134 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.184-10503_184-1049 others(9): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 91113972 | |||||
| chr8:91113972
|
C | CAAAAAA | 46 | a0001c0001t0001g0007a0001c0001t0001g0045a0001c0001t0001g0046others(43): Show | 47 | HG00438.hp1 HG00438.hp2 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.184-10504_184-1049 others(10): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 91113972 | |||||
| chr8:91113972
|
CA | C | 9 | a0001c0001t0001g0177a0001c0001t0001g0189a0001c0001t0001g0190others(6): Show | 9 | HG01069.hp1 HG01099.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.184-10499delA | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 91113972 | |||||
| chr8:91114125
|
C | T | 2 | a0001c0001t0001g0308a0001c0001t0001g0309 | 2 | HG01069.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.184-10368C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91114125 | ||||||
| chr8:91114229
|
G | A | 160 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(157): Show | 164 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.184-10264G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91114229 | ||||||
| chr8:91114232
|
A | G | 36 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047others(33): Show | 37 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(34): Show |
intron_variant | MODIFIER | c.184-10261A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91114232 | ||||||
| chr8:91114443
|
A | ATGTGTGT others(3): Show |
3 | a0002c0002t0001g0012a0002c0002t0001g0310a0002c0002t0001g0311 | 3 | HG01934.hp1 NA18999.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.184-10046_184-1003 others(14): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 91114443 | |||||
| chr8:91114455
|
G | GTA | 45 | a0001c0001t0001g0001a0001c0001t0001g0163a0001c0001t0001g0184others(42): Show | 47 | HG00423.hp2 HG00558.hp2 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.184-10028_184-1002 others(6): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 91114455 | |||||
| chr8:91114455
|
G | GTGTGTGT others(3): Show |
82 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(79): Show | 85 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.184-10037_184-1003 others(14): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 91114455 | |||||
| chr8:91114455
|
G | GTGTGTGT others(5): Show |
75 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(72): Show | 76 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.184-10037_184-1003 others(16): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 91114455 | |||||
| chr8:91114649
|
A | G | 1 | a0001c0001t0001g0182 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.184-9844A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91114649 | ||||||
| chr8:91114706
|
A | G | 1 | a0001c0001t0001g0301 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.184-9787A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91114706 | ||||||
| chr8:91114864
|
A | G | 2 | a0001c0001t0001g0262a0001c0001t0001g0263 | 2 | HG00673.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.184-9629A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91114864 | ||||||
| chr8:91114988
|
TA | T | 3 | a0002c0002t0001g0126a0002c0002t0001g0127a0002c0002t0001g0128 | 3 | HG02027.hp1 NA18951.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.184-9500delA | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 91114988 | |||||
| chr8:91115174
|
A | G | 1 | a0002c0002t0001g0125 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.184-9319A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91115174 | ||||||
| chr8:91115209
|
G | A | 148 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(145): Show | 152 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.184-9284G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91115209 | ||||||
| chr8:91115235
|
C | T | 141 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(138): Show | 145 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.184-9258C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91115235 | ||||||
| chr8:91115384
|
T | C | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG01069.hp1 HG01256.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.184-9109T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91115384 | ||||||
| chr8:91115385
|
G | T | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG01069.hp1 HG01256.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.184-9108G>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91115385 | ||||||
| chr8:91115403
|
A | G | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG01069.hp1 HG01256.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.184-9090A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91115403 | ||||||
| chr8:91115686
|
A | G | 2 | a0002c0002t0001g0122a0002c0002t0001g0123 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.184-8807A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91115686 | ||||||
| chr8:91116129
|
A | G | 1 | a0002c0002t0001g0044 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.184-8364A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91116129 | ||||||
| chr8:91116273
|
C | T | 1 | a0001c0001t0001g0202 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.184-8220C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91116273 | ||||||
| chr8:91116539
|
C | CAT | 129 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(126): Show | 133 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.184-7941_184-7940d others(4): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 91116539 | |||||
| chr8:91116539
|
C | CATAT | 3 | a0002c0002t0001g0019a0002c0002t0001g0021a0002c0002t0001g0064 | 3 | HG01884.hp2 NA18939.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.184-7943_184-7940d others(6): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 91116539 | |||||
| chr8:91116539
|
CATATAT | C | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG01069.hp1 HG01256.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.184-7945_184-7940d others(8): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 91116539 | |||||
| chr8:91116612
|
C | T | 131 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(128): Show | 135 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.184-7881C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91116612 | ||||||
| chr8:91116646
|
G | A | 1 | a0001c0001t0001g0209 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.184-7847G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91116646 | ||||||
| chr8:91116751
|
T | G | 1 | a0001c0001t0001g0312 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.184-7742T>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91116751 | ||||||
| chr8:91116815
|
G | A | 230 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(227): Show | 236 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(233): Show |
intron_variant | MODIFIER | c.184-7678G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91116815 | ||||||
| chr8:91116903
|
A | G | 1 | a0002c0002t0001g0120 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.184-7590A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91116903 | ||||||
| chr8:91116924
|
C | T | 6 | a0001c0001t0001g0276a0001c0001t0001g0278a0001c0001t0001g0279others(3): Show | 6 | HG02257.hp2 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.184-7569C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91116924 | ||||||
| chr8:91116994
|
T | C | 3 | a0002c0002t0001g0077a0002c0002t0001g0078a0002c0002t0001g0120 | 3 | HG00735.hp1 HG01106.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.184-7499T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91116994 | ||||||
| chr8:91117166
|
T | C | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG01069.hp1 HG01256.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.184-7327T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91117166 | ||||||
| chr8:91117208
|
C | T | 228 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(225): Show | 234 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.184-7285C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91117208 | ||||||
| chr8:91117225
|
A | G | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG01069.hp1 HG01256.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.184-7268A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91117225 | ||||||
| chr8:91117246
|
A | G | 131 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(128): Show | 135 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.184-7247A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91117246 | ||||||
| chr8:91117308
|
G | C | 1 | a0002c0002t0001g0022 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.184-7185G>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91117308 | ||||||
| chr8:91117412
|
T | C | 1 | a0002c0002t0001g0142 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.184-7081T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91117412 | ||||||
| chr8:91117482
|
G | A | 9 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(6): Show | 9 | HG00735.hp2 HG02145.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.184-7011G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91117482 | ||||||
| chr8:91117531
|
T | C | 2 | a0001c0001t0001g0262a0001c0001t0001g0263 | 2 | HG00673.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.184-6962T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91117531 | ||||||
| chr8:91117559
|
C | CT | 15 | a0001c0001t0001g0047a0001c0001t0001g0059a0001c0001t0001g0163others(12): Show | 15 | HG00438.hp2 HG01256.hp1 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.184-6910dupT | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 91117559 | |||||
| chr8:91117559
|
C | CTT | 6 | a0001c0001t0001g0276a0001c0001t0001g0278a0001c0001t0001g0279others(3): Show | 6 | HG02257.hp2 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.184-6911_184-6910d others(4): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 91117559 | |||||
| chr8:91117559
|
CT | C | 28 | a0001c0001t0001g0001a0001c0001t0001g0057a0001c0001t0001g0164others(25): Show | 30 | HG00423.hp2 HG00558.hp2 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.184-6910delT | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 91117559 | |||||
| chr8:91117559
|
CTT | C | 128 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(125): Show | 132 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.184-6911_184-6910d others(4): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 91117559 | |||||
| chr8:91117594
|
CTG | C | 98 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(95): Show | 101 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.184-6897_184-6896d others(4): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 91117594 | |||||
| chr8:91117797
|
C | T | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG01069.hp1 HG01256.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.184-6696C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91117797 | ||||||
| chr8:91118073
|
C | T | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG01069.hp1 HG01256.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.184-6420C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91118073 | ||||||
| chr8:91118088
|
A | G | 132 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(129): Show | 136 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.184-6405A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91118088 | ||||||
| chr8:91118188
|
A | G | 1 | a0001c0001t0001g0303 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.184-6305A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91118188 | ||||||
| chr8:91118243
|
G | A | 2 | a0002c0002t0001g0079a0002c0002t0001g0080 | 2 | NA18955.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.184-6250G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91118243 | ||||||
| chr8:91118308
|
C | T | 1 | a0002c0002t0002g0041 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.184-6185C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91118308 | ||||||
| chr8:91118351
|
C | A | 1 | a0001c0001t0001g0203 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.184-6142C>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91118351 | ||||||
| chr8:91118351
|
C | CA | 26 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0052others(23): Show | 26 | HG00423.hp1 HG00438.hp2 HG01361.hp1 others(23): Show |
intron_variant | MODIFIER | c.184-6099dupA | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 91118351 | |||||
| chr8:91118351
|
C | CAA | 10 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0217others(7): Show | 10 | HG01243.hp1 HG01433.hp2 HG04184.hp2 others(7): Show |
intron_variant | MODIFIER | c.184-6100_184-6099d others(4): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 91118351 | |||||
| chr8:91118351
|
C | CAAAA | 9 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(6): Show | 9 | HG01069.hp2 HG01168.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.184-6102_184-6099d others(6): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 91118351 | |||||
| chr8:91118351
|
C | CAAAAA | 6 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0194others(3): Show | 6 | HG00733.hp1 HG00741.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.184-6103_184-6099d others(7): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 91118351 | |||||
| chr8:91118351
|
C | CAAAAAAA others(7): Show |
1 | a0001c0001t0001g0011 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.184-6112_184-6099d others(16): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 91118351 | |||||
| chr8:91118351
|
CA | C | 9 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0001g0189others(6): Show | 9 | HG00673.hp1 HG01099.hp1 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.184-6099delA | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 91118351 | |||||
| chr8:91118351
|
CAAAAAAA others(2): Show |
C | 6 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(3): Show | 6 | HG00735.hp2 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.184-6107_184-6099d others(11): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 91118351 | |||||
| chr8:91118351
|
CAAAAAAA others(3): Show |
C | 4 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0133others(1): Show | 4 | HG02922.hp1 HG03209.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.184-6108_184-6099d others(12): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 91118351 | |||||
| chr8:91118351
|
CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0001g0174 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.184-6112_184-6099d others(16): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 91118351 | |||||
| chr8:91118351
|
CAAAAAAA others(8): Show |
C | 2 | a0001c0001t0002g0157a0001c0001t0002g0161 | 2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.184-6113_184-6099d others(17): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 91118351 | |||||
| chr8:91118351
|
CAAAAAAA others(9): Show |
C | 6 | a0001c0001t0001g0183a0001c0001t0002g0158a0001c0001t0002g0159others(3): Show | 6 | HG02896.hp2 HG03041.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.184-6114_184-6099d others(18): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 91118351 | |||||
| chr8:91118351
|
CAAAAAAA others(10): Show |
C | 3 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257 | 3 | HG02004.hp1 NA18944.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.184-6115_184-6099d others(19): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 91118351 | |||||
| chr8:91118351
|
CAAAAAAA others(11): Show |
C | 2 | a0001c0001t0001g0202a0001c0001t0001g0258 | 2 | HG01074.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.184-6116_184-6099d others(20): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 91118351 | |||||
| chr8:91118351
|
CAAAAAAA others(12): Show |
C | 3 | a0001c0001t0001g0124a0001c0001t0001g0308a0001c0001t0001g0309 | 3 | HG01069.hp1 HG03942.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.184-6117_184-6099d others(21): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 91118351 | |||||
| chr8:91118351
|
CAAAAAAA others(13): Show |
C | 10 | a0001c0001t0001g0259a0001c0001t0001g0289a0001c0001t0001g0290others(7): Show | 10 | HG00423.hp2 HG01256.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.184-6118_184-6099d others(22): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 91118351 | |||||
| chr8:91118351
|
CAAAAAAA others(14): Show |
C | 18 | a0001c0001t0001g0001a0001c0001t0001g0162a0001c0001t0001g0177others(15): Show | 20 | HG00558.hp2 HG01081.hp1 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.184-6119_184-6099d others(23): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 91118351 | |||||
| chr8:91118351
|
CAAAAAAA others(15): Show |
C | 17 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(14): Show | 17 | HG01884.hp1 HG01891.hp2 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.184-6120_184-6099d others(24): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 91118351 | |||||
| chr8:91118351
|
CAAAAAAA others(16): Show |
C | 13 | a0002c0002t0001g0081a0002c0002t0001g0082a0002c0002t0001g0083others(10): Show | 13 | HG01243.hp2 HG02056.hp1 HG02071.hp1 others(10): Show |
intron_variant | MODIFIER | c.184-6121_184-6099d others(25): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 91118351 | |||||
| chr8:91118351
|
CAAAAAAA others(17): Show |
C | 117 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(114): Show | 121 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.184-6122_184-6099d others(26): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 91118351 | |||||
| chr8:91118351
|
CAAAAAAA others(18): Show |
C | 1 | a0002c0002t0001g0119 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.184-6123_184-6099d others(27): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 91118351 | |||||
| chr8:91118396
|
C | G | 1 | a0001c0001t0001g0197 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.184-6097C>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91118396 | ||||||
| chr8:91118531
|
G | A | 132 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(129): Show | 136 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.184-5962G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91118531 | ||||||
| chr8:91118571
|
G | C | 202 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(199): Show | 208 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.184-5922G>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91118571 | ||||||
| chr8:91118582
|
G | A | 1 | a0002c0002t0001g0065 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.184-5911G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91118582 | ||||||
| chr8:91118611
|
C | T | 132 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(129): Show | 136 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.184-5882C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91118611 | ||||||
| chr8:91118730
|
G | T | 1 | a0001c0001t0001g0148 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.184-5763G>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91118730 | ||||||
| chr8:91118781
|
C | T | 1 | a0002c0002t0001g0135 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.184-5712C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91118781 | ||||||
| chr8:91118861
|
A | G | 132 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(129): Show | 136 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.184-5632A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91118861 | ||||||
| chr8:91119099
|
G | A | 6 | a0001c0001t0001g0276a0001c0001t0001g0278a0001c0001t0001g0279others(3): Show | 6 | HG02257.hp2 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.184-5394G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91119099 | ||||||
| chr8:91119490
|
A | G | 132 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(129): Show | 136 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.184-5003A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91119490 | ||||||
| chr8:91119780
|
C | G | 131 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(128): Show | 135 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.184-4713C>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91119780 | ||||||
| chr8:91119901
|
A | G | 132 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(129): Show | 136 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.184-4592A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91119901 | ||||||
| chr8:91119944
|
G | C | 2 | a0001c0001t0001g0217a0001c0001t0001g0222 | 2 | HG01433.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.184-4549G>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91119944 | ||||||
| chr8:91119958
|
A | G | 1 | a0001c0001t0001g0234 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.184-4535A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91119958 | ||||||
| chr8:91120044
|
A | T | 1 | a0002c0002t0001g0040 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.184-4449A>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91120044 | ||||||
| chr8:91120087
|
A | T | 10 | a0001c0001t0001g0020a0001c0001t0001g0205a0001c0001t0001g0217others(7): Show | 10 | HG00099.hp2 HG00140.hp2 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.184-4406A>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91120087 | ||||||
| chr8:91120098
|
G | T | 9 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(6): Show | 9 | HG02109.hp1 HG02559.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.184-4395G>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91120098 | ||||||
| chr8:91120114
|
G | A | 132 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(129): Show | 136 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.184-4379G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91120114 | ||||||
| chr8:91120186
|
A | G | 1 | a0002c0002t0001g0064 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.184-4307A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91120186 | ||||||
| chr8:91120368
|
T | G | 6 | a0001c0001t0001g0276a0001c0001t0001g0278a0001c0001t0001g0279others(3): Show | 6 | HG02257.hp2 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.184-4125T>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91120368 | ||||||
| chr8:91120578
|
T | C | 37 | a0001c0001t0001g0001a0001c0001t0001g0143a0001c0001t0001g0144others(34): Show | 39 | HG00423.hp2 HG00558.hp2 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.184-3915T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91120578 | ||||||
| chr8:91120619
|
C | T | 1 | a0002c0002t0001g0131 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.184-3874C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91120619 | ||||||
| chr8:91120858
|
A | G | 1 | a0001c0001t0001g0204 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.184-3635A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91120858 | ||||||
| chr8:91121221
|
T | C | 1 | a0001c0001t0001g0305 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.184-3272T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91121221 | ||||||
| chr8:91121419
|
T | A | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG01069.hp1 HG01256.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.184-3074T>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91121419 | ||||||
| chr8:91121451
|
G | C | 1 | a0001c0001t0001g0235 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.184-3042G>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91121451 | ||||||
| chr8:91121730
|
G | A | 46 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(43): Show | 48 | HG00423.hp2 HG00558.hp2 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.184-2763G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91121730 | ||||||
| chr8:91121813
|
A | T | 1 | a0002c0002t0001g0051 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.184-2680A>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91121813 | ||||||
| chr8:91121962
|
A | G | 15 | a0001c0001t0001g0001a0001c0001t0001g0288a0001c0001t0001g0289others(12): Show | 17 | HG00423.hp2 HG00558.hp2 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.184-2531A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91121962 | ||||||
| chr8:91122036
|
T | C | 9 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(6): Show | 9 | HG02109.hp1 HG02559.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.184-2457T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91122036 | ||||||
| chr8:91122169
|
C | A | 3 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202 | 3 | HG01074.hp2 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.184-2324C>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91122169 | ||||||
| chr8:91122202
|
T | C | 68 | a0002c0002t0001g0002a0002c0002t0001g0013a0002c0002t0001g0014others(65): Show | 69 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(66): Show |
intron_variant | MODIFIER | c.184-2291T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91122202 | ||||||
| chr8:91122360
|
C | T | 16 | a0001c0001t0001g0001a0001c0001t0001g0288a0001c0001t0001g0289others(13): Show | 18 | HG00423.hp2 HG00558.hp2 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.184-2133C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91122360 | ||||||
| chr8:91122509
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.184-1984G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91122509 | ||||||
| chr8:91122551
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.184-1942C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91122551 | ||||||
| chr8:91122587
|
C | T | 129 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0004others(126): Show | 133 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.184-1906C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91122587 | ||||||
| chr8:91122663
|
G | A | 3 | a0002c0002t0001g0081a0002c0002t0001g0082a0002c0002t0001g0132 | 3 | HG02738.hp2 HG03704.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.184-1830G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91122663 | ||||||
| chr8:91122760
|
G | A | 4 | a0001c0001t0001g0205a0001c0001t0001g0251a0001c0001t0001g0252others(1): Show | 4 | HG00099.hp2 HG01257.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.184-1733G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91122760 | ||||||
| chr8:91122824
|
C | T | 3 | a0002c0002t0001g0038a0002c0002t0001g0039a0002c0002t0001g0043 | 3 | HG01070.hp2 HG01109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.184-1669C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91122824 | ||||||
| chr8:91123520
|
C | T | 1 | a0002c0002t0001g0037 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.184-973C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91123520 | ||||||
| chr8:91123679
|
G | A | 9 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(6): Show | 9 | HG00735.hp2 HG02145.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.184-814G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91123679 | ||||||
| chr8:91123864
|
C | T | 3 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0196 | 3 | HG00733.hp1 HG01433.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.184-629C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91123864 | ||||||
| chr8:91124008
|
G | C | 3 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186 | 3 | HG02886.hp1 HG02965.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.184-485G>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91124008 | ||||||
| chr8:91124062
|
G | A | 1 | a0002c0002t0001g0085 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.184-431G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91124062 | ||||||
| chr8:91124078
|
A | T | 129 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0004others(126): Show | 133 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.184-415A>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91124078 | ||||||
| chr8:91124217
|
T | A | 1 | a0002c0002t0001g0066 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.184-276T>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91124217 | ||||||
| chr8:91124329
|
CTTTG | C | 36 | a0001c0001t0001g0001a0001c0001t0001g0143a0001c0001t0001g0144others(33): Show | 38 | HG00423.hp2 HG00558.hp2 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.184-158_184-155del others(4): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 91124329 | |||||
| chr8:91124337
|
G | A | 129 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0004others(126): Show | 133 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.184-156G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 1/7 | chr8 | 91124337 | ||||||
| chr8:91124791
|
A | G | 129 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0004others(126): Show | 133 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.310+172A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 2/7 | chr8 | 91124791 | ||||||
| chr8:91125218
|
G | A | 129 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0004others(126): Show | 133 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.310+599G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 2/7 | chr8 | 91125218 | ||||||
| chr8:91125313
|
G | T | 1 | a0001c0001t0001g0304 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.310+694G>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 2/7 | chr8 | 91125313 | ||||||
| chr8:91125373
|
G | A | 2 | a0001c0001t0001g0223a0001c0001t0001g0254 | 2 | HG02040.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.310+754G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 2/7 | chr8 | 91125373 | ||||||
| chr8:91125497
|
T | G | 10 | a0002c0002t0001g0002a0002c0002t0001g0013a0002c0002t0001g0014others(7): Show | 11 | NA18954.hp1 NA18960.hp1 NA18964.hp2 others(8): Show |
intron_variant | MODIFIER | c.310+878T>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 2/7 | chr8 | 91125497 | ||||||
| chr8:91125543
|
A | T | 4 | a0001c0001t0001g0163a0001c0001t0003g0178a0001c0001t0003g0179others(1): Show | 4 | HG02818.hp1 HG03130.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.310+924A>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 2/7 | chr8 | 91125543 | ||||||
| chr8:91126036
|
G | T | 1 | a0001c0001t0001g0304 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.311-1052G>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 2/7 | chr8 | 91126036 | ||||||
| chr8:91126040
|
T | C | 1 | a0001c0001t0001g0306 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.311-1048T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 2/7 | chr8 | 91126040 | ||||||
| chr8:91126225
|
C | T | 1 | a0002c0002t0001g0036 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.311-863C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 2/7 | chr8 | 91126225 | ||||||
| chr8:91126423
|
A | G | 1 | a0001c0001t0001g0300 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.311-665A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 2/7 | chr8 | 91126423 | ||||||
| chr8:91126460
|
T | C | 1 | a0001c0001t0001g0164 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.311-628T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 2/7 | chr8 | 91126460 | ||||||
| chr8:91126702
|
G | C | 1 | a0002c0002t0002g0041 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.311-386G>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 2/7 | chr8 | 91126702 | ||||||
| chr8:91126749
|
C | A | 9 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(6): Show | 9 | HG02109.hp1 HG02559.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.311-339C>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 2/7 | chr8 | 91126749 | ||||||
| chr8:91127026
|
T | C | 95 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(92): Show | 98 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.311-62T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 2/7 | chr8 | 91127026 | ||||||
| chr8:91127182
|
C | T | 1 | a0001c0001t0001g0213 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.383+22C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 3/7 | chr8 | 91127182 | ||||||
| chr8:91127301
|
G | A | 1 | a0002c0002t0001g0077 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.383+141G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 3/7 | chr8 | 91127301 | ||||||
| chr8:91127467
|
G | A | 4 | a0001c0001t0001g0163a0001c0001t0003g0178a0001c0001t0003g0179others(1): Show | 4 | HG02818.hp1 HG03130.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.383+307G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 3/7 | chr8 | 91127467 | ||||||
| chr8:91127560
|
CAT | C | 4 | a0001c0001t0001g0163a0001c0001t0003g0178a0001c0001t0003g0179others(1): Show | 4 | HG02818.hp1 HG03130.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.383+401_383+402del others(2): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 3/7 | chr8 | 91127560 | ||||||
| chr8:91127601
|
C | CA | 29 | a0001c0001t0001g0047a0001c0001t0001g0163a0001c0001t0001g0188others(26): Show | 29 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.383+470dupA | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 91127601 | |||||
| chr8:91127601
|
CA | C | 28 | a0001c0001t0001g0164a0001c0001t0001g0168a0001c0001t0001g0169others(25): Show | 28 | HG01099.hp1 HG01515.hp1 HG01978.hp2 others(25): Show |
intron_variant | MODIFIER | c.383+470delA | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 91127601 | |||||
| chr8:91127601
|
CAA | C | 55 | a0001c0001t0001g0115a0001c0001t0001g0289a0001c0001t0001g0290others(52): Show | 56 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.383+469_383+470del others(2): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 91127601 | |||||
| chr8:91127601
|
CAAA | C | 96 | a0001c0001t0001g0001a0001c0001t0001g0059a0001c0001t0001g0116others(93): Show | 101 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.383+468_383+470del others(3): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 91127601 | |||||
| chr8:91127601
|
CAAAA | C | 24 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(21): Show | 24 | HG00735.hp2 HG01515.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.383+467_383+470del others(4): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 91127601 | |||||
| chr8:91127601
|
CAAAAAAA others(5): Show |
C | 3 | a0001c0001t0002g0157a0001c0001t0002g0159a0001c0001t0002g0161 | 3 | HG02109.hp1 HG02559.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.383+459_383+470del others(12): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 91127601 | |||||
| chr8:91127603
|
A | T | 5 | a0001c0001t0001g0278a0001c0001t0001g0279a0001c0001t0001g0280others(2): Show | 5 | HG02257.hp2 HG02809.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.383+443A>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 3/7 | chr8 | 91127603 | ||||||
| chr8:91127631
|
G | T | 1 | a0002c0002t0001g0054 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.383+471G>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 3/7 | chr8 | 91127631 | ||||||
| chr8:91127632
|
G | T | 1 | a0002c0002t0001g0054 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.383+472G>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 3/7 | chr8 | 91127632 | ||||||
| chr8:91128111
|
G | GTA | 6 | a0001c0001t0001g0276a0001c0001t0001g0278a0001c0001t0001g0279others(3): Show | 6 | HG02257.hp2 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.383+957_383+958dup others(2): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 91128111 | |||||
| chr8:91128174
|
G | T | 1 | a0002c0002t0001g0035 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.383+1014G>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 3/7 | chr8 | 91128174 | ||||||
| chr8:91128181
|
T | C | 9 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(6): Show | 9 | HG02109.hp1 HG02559.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.383+1021T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 3/7 | chr8 | 91128181 | ||||||
| chr8:91128200
|
G | A | 129 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0004others(126): Show | 133 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.383+1040G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 3/7 | chr8 | 91128200 | ||||||
| chr8:91128223
|
A | G | 2 | a0002c0002t0001g0028a0002c0002t0001g0034 | 2 | NA18955.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.383+1063A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 3/7 | chr8 | 91128223 | ||||||
| chr8:91128361
|
G | A | 95 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0005others(92): Show | 98 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.383+1201G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 3/7 | chr8 | 91128361 | ||||||
| chr8:91128399
|
A | T | 6 | a0001c0001t0001g0276a0001c0001t0001g0278a0001c0001t0001g0279others(3): Show | 6 | HG02257.hp2 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.383+1239A>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 3/7 | chr8 | 91128399 | ||||||
| chr8:91128578
|
A | G | 1 | a0001c0001t0001g0209 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.383+1418A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 3/7 | chr8 | 91128578 | ||||||
| chr8:91128701
|
G | C | 3 | a0002c0002t0001g0126a0002c0002t0001g0127a0002c0002t0001g0128 | 3 | HG02027.hp1 NA18951.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.383+1541G>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 3/7 | chr8 | 91128701 | ||||||
| chr8:91129009
|
A | C | 1 | a0001c0001t0001g0304 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.383+1849A>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 3/7 | chr8 | 91129009 | ||||||
| chr8:91129117
|
G | A | 4 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0191others(1): Show | 4 | HG01099.hp1 HG01515.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.383+1957G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 3/7 | chr8 | 91129117 | ||||||
| chr8:91129275
|
G | A | 6 | a0002c0002t0001g0013a0002c0002t0001g0014a0002c0002t0001g0015others(3): Show | 6 | NA18954.hp1 NA18964.hp2 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.383+2115G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 3/7 | chr8 | 91129275 | ||||||
| chr8:91129299
|
A | G | 1 | a0001c0001t0001g0304 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.383+2139A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 3/7 | chr8 | 91129299 | ||||||
| chr8:91129300
|
T | C | 129 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0004others(126): Show | 133 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.383+2140T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 3/7 | chr8 | 91129300 | ||||||
| chr8:91129458
|
AATGAACA others(5): Show |
A | 1 | a0002c0006t0002g0154 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.383+2301_383+2312d others(14): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 91129458 | |||||
| chr8:91130017
|
C | T | 2 | a0002c0002t0001g0081a0002c0002t0001g0132 | 2 | HG02738.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.383+2857C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 3/7 | chr8 | 91130017 | ||||||
| chr8:91130303
|
T | C | 2 | a0001c0001t0001g0200a0001c0001t0001g0201 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.384-2807T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 3/7 | chr8 | 91130303 | ||||||
| chr8:91130469
|
T | C | 1 | a0001c0001t0001g0304 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.384-2641T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 3/7 | chr8 | 91130469 | ||||||
| chr8:91130472
|
G | A | 128 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0004others(125): Show | 132 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.384-2638G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 3/7 | chr8 | 91130472 | ||||||
| chr8:91130477
|
G | A | 202 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(199): Show | 208 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.384-2633G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 3/7 | chr8 | 91130477 | ||||||
| chr8:91130545
|
G | A | 1 | a0002c0002t0001g0142 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.384-2565G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 3/7 | chr8 | 91130545 | ||||||
| chr8:91130555
|
G | A | 15 | a0001c0001t0001g0276a0001c0001t0001g0278a0001c0001t0001g0279others(12): Show | 15 | HG02109.hp1 HG02257.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.384-2555G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 3/7 | chr8 | 91130555 | ||||||
| chr8:91130707
|
G | T | 1 | a0001c0001t0001g0210 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.384-2403G>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 3/7 | chr8 | 91130707 | ||||||
| chr8:91130789
|
C | T | 6 | a0001c0001t0001g0276a0001c0001t0001g0278a0001c0001t0001g0279others(3): Show | 6 | HG02257.hp2 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.384-2321C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 3/7 | chr8 | 91130789 | ||||||
| chr8:91130799
|
G | A | 1 | a0001c0001t0001g0304 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.384-2311G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 3/7 | chr8 | 91130799 | ||||||
| chr8:91131055
|
A | G | 1 | a0001c0001t0001g0209 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.384-2055A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 3/7 | chr8 | 91131055 | ||||||
| chr8:91131098
|
T | C | 4 | a0001c0001t0001g0163a0001c0001t0003g0178a0001c0001t0003g0179others(1): Show | 4 | HG02818.hp1 HG03130.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.384-2012T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 3/7 | chr8 | 91131098 | ||||||
| chr8:91131211
|
A | G | 9 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(6): Show | 9 | HG00735.hp2 HG02145.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.384-1899A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 3/7 | chr8 | 91131211 | ||||||
| chr8:91131235
|
C | CT | 143 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(140): Show | 147 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.384-1862dupT | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 91131235 | |||||
| chr8:91131244
|
T | G | 1 | a0001c0001t0001g0059 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.384-1866T>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 3/7 | chr8 | 91131244 | ||||||
| chr8:91131244
|
T | TG | 5 | a0002c0002t0001g0084a0002c0002t0001g0093a0002c0002t0001g0136others(2): Show | 5 | HG00544.hp1 HG00609.hp2 HG00673.hp2 others(2): Show |
intron_variant | MODIFIER | c.384-1866_384-1865i others(3): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 3/7 | chr8 | 91131244 | ||||||
| chr8:91131245
|
T | TG | 5 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(2): Show | 5 | HG00609.hp1 HG01884.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.384-1865_384-1864i others(3): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 3/7 | chr8 | 91131245 | ||||||
| chr8:91131249
|
G | T | 6 | a0002c0002t0001g0013a0002c0002t0001g0014a0002c0002t0001g0015others(3): Show | 6 | NA18954.hp1 NA18964.hp2 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.384-1861G>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 3/7 | chr8 | 91131249 | ||||||
| chr8:91131271
|
A | C | 1 | a0002c0002t0001g0051 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.384-1839A>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 3/7 | chr8 | 91131271 | ||||||
| chr8:91131280
|
T | C | 202 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(199): Show | 208 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.384-1830T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 3/7 | chr8 | 91131280 | ||||||
| chr8:91131281
|
C | T | 1 | a0002c0007t0001g0061 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.384-1829C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 3/7 | chr8 | 91131281 | ||||||
| chr8:91131387
|
A | G | 1 | a0001c0001t0001g0308 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.384-1723A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 3/7 | chr8 | 91131387 | ||||||
| chr8:91131435
|
A | G | 9 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(6): Show | 9 | HG00735.hp2 HG02145.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.384-1675A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 3/7 | chr8 | 91131435 | ||||||
| chr8:91131701
|
T | A | 23 | a0001c0001t0001g0001a0001c0001t0001g0288a0001c0001t0001g0289others(20): Show | 25 | HG00423.hp2 HG00558.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.384-1409T>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 3/7 | chr8 | 91131701 | ||||||
| chr8:91132093
|
C | T | 38 | a0001c0001t0001g0001a0001c0001t0001g0143a0001c0001t0001g0144others(35): Show | 40 | HG00423.hp2 HG00558.hp2 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.384-1017C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 3/7 | chr8 | 91132093 | ||||||
| chr8:91132107
|
C | T | 129 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0004others(126): Show | 133 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.384-1003C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 3/7 | chr8 | 91132107 | ||||||
| chr8:91132139
|
CTT | C | 5 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG00735.hp2 HG02615.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.384-970_384-969del others(2): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 3/7 | chr8 | 91132139 | ||||||
| chr8:91132243
|
A | G | 1 | a0001c0001t0001g0306 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.384-867A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 3/7 | chr8 | 91132243 | ||||||
| chr8:91132524
|
A | G | 1 | a0001c0001t0001g0304 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.384-586A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 3/7 | chr8 | 91132524 | ||||||
| chr8:91132693
|
C | G | 1 | a0002c0006t0002g0154 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.384-417C>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 3/7 | chr8 | 91132693 | ||||||
| chr8:91132778
|
G | A | 2 | a0001c0001t0001g0223a0001c0001t0001g0254 | 2 | HG02040.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.384-332G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 3/7 | chr8 | 91132778 | ||||||
| chr8:91132944
|
A | C | 51 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(48): Show | 53 | HG00423.hp2 HG00558.hp2 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.384-166A>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 3/7 | chr8 | 91132944 | ||||||
| chr8:91132972
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.384-138G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 3/7 | chr8 | 91132972 | ||||||
| chr8:91133094
|
G | GT | 11 | a0001c0001t0001g0312a0002c0002t0001g0060a0002c0002t0001g0062others(8): Show | 11 | HG00099.hp1 HG00639.hp1 HG00733.hp2 others(8): Show |
splice_acceptor_variant&intron_variant | HIGH | c.384-3dupT | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 91133094 | |||||
| chr8:91133575
|
A | G | 7 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(4): Show | 7 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.579+270A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 4/7 | chr8 | 91133575 | ||||||
| chr8:91133631
|
T | C | 1 | a0002c0002t0001g0081 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.579+326T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 4/7 | chr8 | 91133631 | ||||||
| chr8:91133823
|
G | A | 136 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(133): Show | 140 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.579+518G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 4/7 | chr8 | 91133823 | ||||||
| chr8:91134499
|
T | TC | 202 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(199): Show | 208 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.580-1168dupC | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 91134499 | |||||
| chr8:91134558
|
C | T | 1 | a0001c0001t0001g0121 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.580-1110C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 4/7 | chr8 | 91134558 | ||||||
| chr8:91134570
|
C | T | 1 | a0002c0002t0001g0083 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.580-1098C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 4/7 | chr8 | 91134570 | ||||||
| chr8:91135301
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.580-367C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 4/7 | chr8 | 91135301 | ||||||
| chr8:91135481
|
A | T | 15 | a0001c0001t0001g0276a0001c0001t0001g0278a0001c0001t0001g0279others(12): Show | 15 | HG02109.hp1 HG02257.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.580-187A>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 4/7 | chr8 | 91135481 | ||||||
| chr8:91135510
|
G | C | 1 | a0001c0001t0002g0156 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.580-158G>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 4/7 | chr8 | 91135510 | ||||||
| chr8:91135575
|
T | A | 1 | a0001c0001t0001g0210 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.580-93T>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 4/7 | chr8 | 91135575 | ||||||
| chr8:91135967
|
C | T | 202 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(199): Show | 208 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.651+228C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91135967 | ||||||
| chr8:91136005
|
G | C | 8 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(5): Show | 8 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.651+266G>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91136005 | ||||||
| chr8:91136251
|
A | G | 1 | a0001c0001t0001g0312 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.651+512A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91136251 | ||||||
| chr8:91136330
|
A | G | 2 | a0002c0002t0001g0085a0002c0002t0001g0091 | 2 | HG02602.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.651+591A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91136330 | ||||||
| chr8:91136452
|
G | T | 5 | a0002c0002t0001g0003a0002c0002t0001g0028a0002c0002t0001g0034others(2): Show | 6 | HG02071.hp1 NA18939.hp2 NA18955.hp2 others(3): Show |
intron_variant | MODIFIER | c.651+713G>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91136452 | ||||||
| chr8:91136604
|
C | T | 1 | a0001c0001t0001g0248 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.651+865C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91136604 | ||||||
| chr8:91136742
|
T | C | 1 | a0001c0001t0002g0181 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.651+1003T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91136742 | ||||||
| chr8:91136905
|
C | G | 3 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186 | 3 | HG02886.hp1 HG02965.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.651+1166C>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91136905 | ||||||
| chr8:91137068
|
C | T | 1 | a0001c0001t0002g0161 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.651+1329C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91137068 | ||||||
| chr8:91137201
|
T | C | 225 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(222): Show | 231 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.651+1462T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91137201 | ||||||
| chr8:91137327
|
G | T | 202 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(199): Show | 208 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.651+1588G>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91137327 | ||||||
| chr8:91137520
|
T | G | 39 | a0001c0001t0001g0001a0001c0001t0001g0143a0001c0001t0001g0144others(36): Show | 41 | HG00423.hp2 HG00558.hp2 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.651+1781T>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91137520 | ||||||
| chr8:91137541
|
C | G | 1 | a0001c0001t0001g0216 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.651+1802C>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91137541 | ||||||
| chr8:91137675
|
T | C | 1 | a0001c0001t0001g0305 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.651+1936T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91137675 | ||||||
| chr8:91138117
|
A | T | 1 | a0002c0002t0001g0083 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.651+2378A>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91138117 | ||||||
| chr8:91138225
|
G | A | 1 | a0001c0001t0001g0153 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.651+2486G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91138225 | ||||||
| chr8:91138542
|
C | A | 5 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(2): Show | 5 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.651+2803C>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91138542 | ||||||
| chr8:91138551
|
A | AT | 9 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(6): Show | 9 | HG01884.hp1 HG02055.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.651+2825dupT | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91138551 | |||||
| chr8:91138551
|
A | ATT | 36 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(33): Show | 36 | HG00735.hp2 HG01081.hp1 HG02109.hp1 others(33): Show |
intron_variant | MODIFIER | c.651+2824_651+2825d others(4): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91138551 | |||||
| chr8:91138551
|
A | ATTT | 26 | a0001c0001t0001g0001a0001c0001t0001g0288a0001c0001t0001g0289others(23): Show | 28 | HG00423.hp2 HG00558.hp2 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.651+2823_651+2825d others(5): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91138551 | |||||
| chr8:91138551
|
AT | A | 18 | a0001c0001t0001g0183a0001c0001t0001g0204a0001c0001t0001g0216others(15): Show | 18 | HG01070.hp2 HG01109.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.651+2825delT | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91138551 | |||||
| chr8:91138738
|
A | G | 14 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(11): Show | 14 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.651+2999A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91138738 | ||||||
| chr8:91138992
|
G | A | 1 | a0001c0001t0001g0153 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.651+3253G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91138992 | ||||||
| chr8:91139049
|
GA | G | 14 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(11): Show | 14 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.651+3323delA | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91139049 | |||||
| chr8:91139230
|
A | C | 1 | a0001c0001t0001g0146 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.651+3491A>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91139230 | ||||||
| chr8:91139292
|
A | C | 1 | a0002c0002t0001g0051 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.651+3553A>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91139292 | ||||||
| chr8:91139323
|
C | T | 1 | a0001c0001t0001g0213 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.651+3584C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91139323 | ||||||
| chr8:91139528
|
GC | G | 311 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(308): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.651+3792delC | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91139528 | |||||
| chr8:91139537
|
A | G | 3 | a0002c0002t0001g0090a0002c0002t0001g0108a0002c0002t0001g0142 | 3 | NA18945.hp2 NA18952.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.651+3798A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91139537 | ||||||
| chr8:91139636
|
C | T | 1 | a0002c0002t0001g0107 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.651+3897C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91139636 | ||||||
| chr8:91139713
|
G | A | 14 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(11): Show | 14 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.651+3974G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91139713 | ||||||
| chr8:91140022
|
A | G | 9 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(6): Show | 9 | HG00735.hp2 HG01261.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.651+4283A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91140022 | ||||||
| chr8:91140087
|
G | A | 132 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(129): Show | 136 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.651+4348G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91140087 | ||||||
| chr8:91140091
|
C | CA | 10 | a0001c0001t0001g0162a0001c0001t0001g0165a0001c0001t0001g0166others(7): Show | 10 | HG02145.hp1 HG02572.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.651+4373dupA | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91140091 | |||||
| chr8:91140091
|
CA | C | 30 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0268others(27): Show | 30 | HG01943.hp1 HG01978.hp2 HG02015.hp2 others(27): Show |
intron_variant | MODIFIER | c.651+4373delA | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91140091 | |||||
| chr8:91140091
|
CAA | C | 170 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(167): Show | 176 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.651+4372_651+4373d others(4): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91140091 | |||||
| chr8:91140107
|
A | T | 1 | a0001c0001t0001g0256 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.651+4368A>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91140107 | ||||||
| chr8:91140592
|
CATT | C | 9 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(6): Show | 9 | HG02109.hp1 HG02559.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.651+4856_651+4858d others(5): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91140592 | |||||
| chr8:91140628
|
TTCAATAT others(317): Show |
T | 202 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(199): Show | 208 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.651+4906_651+5229d others(2): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91140628 | |||||
| chr8:91140639
|
A | AT | 20 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0052others(17): Show | 20 | HG00423.hp1 HG00438.hp2 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.651+4932dupT | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91140639 | |||||
| chr8:91140639
|
A | ATT | 17 | a0001c0001t0001g0020a0001c0001t0001g0059a0001c0001t0001g0162others(14): Show | 17 | HG00140.hp2 HG02027.hp2 HG02071.hp2 others(14): Show |
intron_variant | MODIFIER | c.651+4931_651+4932d others(4): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91140639 | |||||
| chr8:91140639
|
AT | A | 21 | a0001c0001t0001g0011a0001c0001t0001g0121a0001c0001t0001g0183others(18): Show | 21 | HG00099.hp2 HG00733.hp1 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.651+4932delT | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91140639 | |||||
| chr8:91140641
|
T | C | 1 | a0001c0004t0001g0270 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.651+4902T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91140641 | ||||||
| chr8:91140671
|
T | C | 1 | a0001c0001t0001g0195 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.651+4932T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91140671 | ||||||
| chr8:91141001
|
C | T | 15 | a0001c0001t0001g0276a0001c0001t0001g0278a0001c0001t0001g0279others(12): Show | 15 | HG02109.hp1 HG02257.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.651+5262C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91141001 | ||||||
| chr8:91141132
|
A | G | 4 | a0001c0001t0001g0168a0001c0001t0001g0212a0001c0001t0001g0214others(1): Show | 4 | HG02896.hp1 HG02897.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.651+5393A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91141132 | ||||||
| chr8:91141150
|
C | T | 9 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(6): Show | 9 | HG02109.hp1 HG02559.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.651+5411C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91141150 | ||||||
| chr8:91141163
|
T | C | 25 | a0002c0002t0001g0004a0002c0002t0001g0012a0002c0002t0001g0055others(22): Show | 26 | HG00558.hp1 HG00609.hp1 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.651+5424T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91141163 | ||||||
| chr8:91141415
|
T | A | 14 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(11): Show | 14 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.651+5676T>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91141415 | ||||||
| chr8:91141982
|
CTCAGTCT others(16): Show |
C | 3 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186 | 3 | HG02886.hp1 HG02965.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.651+6251_651+6273d others(25): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91141982 | |||||
| chr8:91142094
|
C | G | 1 | a0001c0001t0001g0216 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.651+6355C>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91142094 | ||||||
| chr8:91142117
|
C | T | 1 | a0001c0001t0001g0211 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.651+6378C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91142117 | ||||||
| chr8:91142320
|
G | A | 8 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(5): Show | 8 | HG00735.hp2 HG02559.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.651+6581G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91142320 | ||||||
| chr8:91142327
|
A | G | 1 | a0001c0001t0001g0163 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.651+6588A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91142327 | ||||||
| chr8:91142630
|
C | T | 1 | a0001c0001t0001g0303 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.651+6891C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91142630 | ||||||
| chr8:91142661
|
T | C | 1 | a0002c0002t0001g0054 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.651+6922T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91142661 | ||||||
| chr8:91142886
|
C | A | 138 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(135): Show | 142 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.651+7147C>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91142886 | ||||||
| chr8:91143143
|
G | A | 5 | a0001c0001t0001g0267a0001c0001t0001g0268a0001c0001t0001g0269others(2): Show | 5 | NA18945.hp1 NA18954.hp2 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.651+7404G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91143143 | ||||||
| chr8:91143144
|
C | A | 5 | a0001c0001t0001g0267a0001c0001t0001g0268a0001c0001t0001g0269others(2): Show | 5 | NA18945.hp1 NA18954.hp2 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.651+7405C>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91143144 | ||||||
| chr8:91143173
|
A | G | 1 | a0001c0001t0001g0257 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.651+7434A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91143173 | ||||||
| chr8:91143242
|
C | T | 1 | a0001c0001t0001g0266 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.651+7503C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91143242 | ||||||
| chr8:91143422
|
C | G | 9 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(6): Show | 9 | HG00735.hp2 HG01261.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.651+7683C>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91143422 | ||||||
| chr8:91143681
|
C | T | 3 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186 | 3 | HG02886.hp1 HG02965.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.651+7942C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91143681 | ||||||
| chr8:91144313
|
T | C | 137 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(134): Show | 141 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.651+8574T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91144313 | ||||||
| chr8:91144494
|
C | A | 1 | a0001c0001t0001g0183 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.651+8755C>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91144494 | ||||||
| chr8:91144512
|
A | T | 5 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(2): Show | 5 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.651+8773A>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91144512 | ||||||
| chr8:91144598
|
C | T | 1 | a0001c0001t0001g0198 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.651+8859C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91144598 | ||||||
| chr8:91144620
|
C | T | 203 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(200): Show | 209 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.651+8881C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91144620 | ||||||
| chr8:91144675
|
A | G | 1 | a0002c0002t0001g0037 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.651+8936A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91144675 | ||||||
| chr8:91144707
|
AGCATATC | A | 35 | a0001c0001t0001g0249a0002c0002t0001g0003a0002c0002t0001g0024others(32): Show | 36 | HG00438.hp1 HG00544.hp1 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.651+8969_651+8975d others(9): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91144707 | ||||||
| chr8:91144861
|
A | G | 9 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(6): Show | 9 | HG00735.hp2 HG02559.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.651+9122A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91144861 | ||||||
| chr8:91144933
|
T | C | 55 | a0001c0001t0001g0001a0001c0001t0001g0143a0001c0001t0001g0144others(52): Show | 57 | HG00423.hp2 HG00558.hp2 HG01081.hp1 others(54): Show |
intron_variant | MODIFIER | c.651+9194T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91144933 | ||||||
| chr8:91145111
|
C | T | 203 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(200): Show | 209 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.651+9372C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91145111 | ||||||
| chr8:91145248
|
A | G | 1 | a0003c0005t0001g0245 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.651+9509A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91145248 | ||||||
| chr8:91145512
|
C | G | 1 | a0001c0001t0001g0312 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.651+9773C>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91145512 | ||||||
| chr8:91145576
|
G | A | 1 | a0002c0002t0001g0070 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.651+9837G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91145576 | ||||||
| chr8:91145637
|
A | C | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+9898A>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91145637 | ||||||
| chr8:91145826
|
G | A | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+10087G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91145826 | ||||||
| chr8:91145918
|
T | C | 1 | a0001c0001t0001g0059 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.651+10179T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91145918 | ||||||
| chr8:91146145
|
A | G | 1 | a0001c0001t0001g0299 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.651+10406A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91146145 | ||||||
| chr8:91146153
|
G | C | 1 | a0001c0001t0003g0179 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.651+10414G>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91146153 | ||||||
| chr8:91146203
|
T | G | 1 | a0001c0001t0001g0175 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.651+10464T>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91146203 | ||||||
| chr8:91146211
|
A | G | 202 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(199): Show | 208 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.651+10472A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91146211 | ||||||
| chr8:91146301
|
C | A | 3 | a0001c0001t0003g0178a0001c0001t0003g0179a0001c0001t0003g0180 | 3 | HG02818.hp1 HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.651+10562C>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91146301 | ||||||
| chr8:91146416
|
G | T | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+10677G>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91146416 | ||||||
| chr8:91146469
|
G | A | 1 | a0002c0002t0001g0048 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.651+10730G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91146469 | ||||||
| chr8:91146534
|
T | TTCTC | 203 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(200): Show | 209 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.651+10800_651+1080 others(8): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91146534 | |||||
| chr8:91146671
|
T | C | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+10932T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91146671 | ||||||
| chr8:91146692
|
A | G | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+10953A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91146692 | ||||||
| chr8:91146795
|
A | G | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+11056A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91146795 | ||||||
| chr8:91146870
|
A | C | 132 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(129): Show | 136 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.651+11131A>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91146870 | ||||||
| chr8:91147051
|
G | A | 202 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(199): Show | 208 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.651+11312G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91147051 | ||||||
| chr8:91147217
|
A | G | 18 | a0002c0002t0001g0024a0002c0002t0001g0025a0002c0002t0001g0026others(15): Show | 18 | HG01943.hp1 HG01978.hp2 HG02015.hp2 others(15): Show |
intron_variant | MODIFIER | c.651+11478A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91147217 | ||||||
| chr8:91147229
|
CTATATTA others(34): Show |
C | 2 | a0002c0002t0001g0005a0002c0002t0001g0129 | 3 | HG02723.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.651+11511_651+1155 others(45): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91147229 | |||||
| chr8:91147251
|
A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0059 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.651+11520_651+1154 others(28): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91147251 | |||||
| chr8:91147269
|
C | CAT | 200 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(197): Show | 205 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.651+11535_651+1153 others(6): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91147269 | |||||
| chr8:91147281
|
A | G | 9 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(6): Show | 9 | HG00735.hp2 HG01261.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.651+11542A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91147281 | ||||||
| chr8:91147286
|
CAT | C | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+11550_651+1155 others(6): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91147286 | |||||
| chr8:91147341
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.651+11602C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91147341 | ||||||
| chr8:91147565
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.651+11826C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91147565 | ||||||
| chr8:91147603
|
G | C | 15 | a0001c0001t0001g0276a0001c0001t0001g0278a0001c0001t0001g0279others(12): Show | 15 | HG02109.hp1 HG02257.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.651+11864G>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91147603 | ||||||
| chr8:91147636
|
T | G | 1 | a0001c0001t0001g0059 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.651+11897T>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91147636 | ||||||
| chr8:91147645
|
C | T | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+11906C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91147645 | ||||||
| chr8:91147673
|
G | A | 5 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(2): Show | 5 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.651+11934G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91147673 | ||||||
| chr8:91147859
|
C | G | 1 | a0002c0002t0001g0082 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.651+12120C>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91147859 | ||||||
| chr8:91147862
|
C | T | 1 | a0002c0002t0001g0091 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.651+12123C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91147862 | ||||||
| chr8:91147865
|
G | T | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+12126G>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91147865 | ||||||
| chr8:91147872
|
C | G | 1 | a0001c0001t0001g0059 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.651+12133C>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91147872 | ||||||
| chr8:91147946
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.651+12207G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91147946 | ||||||
| chr8:91147974
|
C | A | 15 | a0001c0001t0001g0276a0001c0001t0001g0278a0001c0001t0001g0279others(12): Show | 15 | HG02109.hp1 HG02257.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.651+12235C>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91147974 | ||||||
| chr8:91147975
|
C | G | 15 | a0001c0001t0001g0276a0001c0001t0001g0278a0001c0001t0001g0279others(12): Show | 15 | HG02109.hp1 HG02257.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.651+12236C>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91147975 | ||||||
| chr8:91148058
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.651+12319C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91148058 | ||||||
| chr8:91148081
|
T | G | 1 | a0001c0001t0001g0167 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.651+12342T>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91148081 | ||||||
| chr8:91148231
|
G | C | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+12492G>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91148231 | ||||||
| chr8:91148397
|
A | G | 1 | a0001c0001t0001g0260 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.651+12658A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91148397 | ||||||
| chr8:91148457
|
C | T | 1 | a0002c0002t0001g0114 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.651+12718C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91148457 | ||||||
| chr8:91148490
|
C | T | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+12751C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91148490 | ||||||
| chr8:91148497
|
C | G | 1 | a0002c0002t0001g0141 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.651+12758C>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91148497 | ||||||
| chr8:91148519
|
C | T | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+12780C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91148519 | ||||||
| chr8:91148613
|
G | A | 13 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(10): Show | 13 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.651+12874G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91148613 | ||||||
| chr8:91148711
|
C | T | 22 | a0001c0001t0001g0001a0001c0001t0001g0288a0001c0001t0001g0289others(19): Show | 24 | HG00423.hp2 HG00558.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.651+12972C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91148711 | ||||||
| chr8:91148792
|
T | G | 6 | a0002c0002t0001g0013a0002c0002t0001g0014a0002c0002t0001g0015others(3): Show | 6 | NA18954.hp1 NA18964.hp2 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.651+13053T>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91148792 | ||||||
| chr8:91148841
|
G | T | 131 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(128): Show | 135 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.651+13102G>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91148841 | ||||||
| chr8:91148977
|
A | T | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+13238A>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91148977 | ||||||
| chr8:91148994
|
A | G | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+13255A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91148994 | ||||||
| chr8:91149025
|
T | C | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+13286T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91149025 | ||||||
| chr8:91149027
|
G | A | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+13288G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91149027 | ||||||
| chr8:91149035
|
C | T | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+13296C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91149035 | ||||||
| chr8:91149037
|
T | A | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+13298T>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91149037 | ||||||
| chr8:91149052
|
T | C | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+13313T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91149052 | ||||||
| chr8:91149054
|
C | G | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+13315C>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91149054 | ||||||
| chr8:91149058
|
G | C | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+13319G>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91149058 | ||||||
| chr8:91149122
|
C | T | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+13383C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91149122 | ||||||
| chr8:91149123
|
A | G | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+13384A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91149123 | ||||||
| chr8:91149179
|
A | G | 2 | a0002c0002t0001g0005a0002c0002t0001g0129 | 3 | HG02723.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.651+13440A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91149179 | ||||||
| chr8:91149193
|
C | G | 1 | a0001c0001t0001g0248 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.651+13454C>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91149193 | ||||||
| chr8:91149350
|
T | C | 1 | a0001c0001t0001g0213 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.651+13611T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91149350 | ||||||
| chr8:91149356
|
T | G | 1 | a0001c0001t0001g0213 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.651+13617T>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91149356 | ||||||
| chr8:91149440
|
C | T | 1 | a0002c0002t0001g0106 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.651+13701C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91149440 | ||||||
| chr8:91149547
|
T | C | 34 | a0001c0001t0001g0249a0002c0002t0001g0003a0002c0002t0001g0024others(31): Show | 35 | HG00438.hp1 HG00544.hp1 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.651+13808T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91149547 | ||||||
| chr8:91149658
|
C | G | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+13919C>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91149658 | ||||||
| chr8:91149681
|
G | A | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+13942G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91149681 | ||||||
| chr8:91149801
|
G | A | 2 | a0001c0001t0002g0158a0001c0001t0002g0181 | 2 | HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.651+14062G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91149801 | ||||||
| chr8:91149808
|
G | T | 2 | a0002c0002t0001g0105a0002c0002t0001g0106 | 2 | HG00408.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.651+14069G>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91149808 | ||||||
| chr8:91149891
|
A | G | 1 | a0001c0001t0001g0193 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.651+14152A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91149891 | ||||||
| chr8:91149912
|
T | C | 1 | a0001c0001t0001g0261 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.651+14173T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91149912 | ||||||
| chr8:91150069
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.651+14330C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91150069 | ||||||
| chr8:91150097
|
C | T | 15 | a0001c0001t0001g0276a0001c0001t0001g0278a0001c0001t0001g0279others(12): Show | 15 | HG02109.hp1 HG02257.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.651+14358C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91150097 | ||||||
| chr8:91150296
|
C | G | 1 | a0002c0002t0001g0070 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.651+14557C>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91150296 | ||||||
| chr8:91150426
|
A | G | 201 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(198): Show | 207 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.651+14687A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91150426 | ||||||
| chr8:91150497
|
T | C | 25 | a0001c0001t0001g0001a0001c0001t0001g0288a0001c0001t0001g0289others(22): Show | 27 | HG00423.hp2 HG00558.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.651+14758T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91150497 | ||||||
| chr8:91150511
|
G | A | 18 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(15): Show | 18 | HG00408.hp2 HG01884.hp1 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.651+14772G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91150511 | ||||||
| chr8:91150569
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.651+14830G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91150569 | ||||||
| chr8:91150624
|
C | A | 5 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(2): Show | 5 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.651+14885C>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91150624 | ||||||
| chr8:91150627
|
T | G | 5 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(2): Show | 5 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.651+14888T>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91150627 | ||||||
| chr8:91150630
|
C | T | 5 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(2): Show | 5 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.651+14891C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91150630 | ||||||
| chr8:91150633
|
C | T | 5 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(2): Show | 5 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.651+14894C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91150633 | ||||||
| chr8:91150636
|
A | C | 1 | a0002c0002t0001g0055 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.651+14897A>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91150636 | ||||||
| chr8:91150865
|
G | A | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+15126G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91150865 | ||||||
| chr8:91150871
|
A | C | 1 | a0001c0001t0001g0246 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.651+15132A>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91150871 | ||||||
| chr8:91150893
|
C | G | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+15154C>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91150893 | ||||||
| chr8:91151177
|
G | T | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+15438G>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91151177 | ||||||
| chr8:91151297
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.651+15558G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91151297 | ||||||
| chr8:91151307
|
A | G | 3 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186 | 3 | HG02886.hp1 HG02965.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.651+15568A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91151307 | ||||||
| chr8:91151310
|
A | G | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+15571A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91151310 | ||||||
| chr8:91151373
|
C | T | 2 | a0001c0001t0001g0163a0002c0006t0002g0154 | 2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.651+15634C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91151373 | ||||||
| chr8:91151491
|
G | A | 34 | a0001c0001t0001g0249a0002c0002t0001g0003a0002c0002t0001g0024others(31): Show | 35 | HG00438.hp1 HG00544.hp1 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.651+15752G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91151491 | ||||||
| chr8:91151505
|
A | C | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+15766A>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91151505 | ||||||
| chr8:91151539
|
G | A | 202 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(199): Show | 208 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.651+15800G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91151539 | ||||||
| chr8:91151685
|
G | C | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+15946G>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91151685 | ||||||
| chr8:91151718
|
A | G | 1 | a0002c0002t0001g0136 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.651+15979A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91151718 | ||||||
| chr8:91151829
|
T | C | 1 | a0001c0001t0001g0206 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.651+16090T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91151829 | ||||||
| chr8:91151963
|
G | A | 25 | a0001c0001t0001g0001a0001c0001t0001g0288a0001c0001t0001g0289others(22): Show | 27 | HG00423.hp2 HG00558.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.651+16224G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91151963 | ||||||
| chr8:91152119
|
T | C | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+16380T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91152119 | ||||||
| chr8:91152206
|
G | C | 201 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(198): Show | 207 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.651+16467G>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91152206 | ||||||
| chr8:91152231
|
G | A | 25 | a0001c0001t0001g0001a0001c0001t0001g0288a0001c0001t0001g0289others(22): Show | 27 | HG00423.hp2 HG00558.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.651+16492G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91152231 | ||||||
| chr8:91152400
|
G | T | 9 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(6): Show | 9 | HG00735.hp2 HG01261.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.651+16661G>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91152400 | ||||||
| chr8:91152649
|
C | T | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+16910C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91152649 | ||||||
| chr8:91152817
|
G | A | 5 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(2): Show | 5 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.651+17078G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91152817 | ||||||
| chr8:91152830
|
A | G | 3 | a0002c0002t0001g0026a0002c0002t0001g0031a0002c0002t0001g0140 | 3 | NA18944.hp1 NA18992.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.651+17091A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91152830 | ||||||
| chr8:91152843
|
A | G | 5 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(2): Show | 5 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.651+17104A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91152843 | ||||||
| chr8:91153062
|
G | A | 14 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(11): Show | 14 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.651+17323G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91153062 | ||||||
| chr8:91153121
|
G | A | 14 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(11): Show | 14 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.651+17382G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91153121 | ||||||
| chr8:91153210
|
T | G | 1 | a0001c0001t0001g0169 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.651+17471T>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91153210 | ||||||
| chr8:91153283
|
C | T | 1 | a0002c0006t0002g0154 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.651+17544C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91153283 | ||||||
| chr8:91153425
|
A | G | 14 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(11): Show | 14 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.651+17686A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91153425 | ||||||
| chr8:91153503
|
TAACA | T | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+17769_651+1777 others(8): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91153503 | |||||
| chr8:91153524
|
G | C | 202 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(199): Show | 208 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.651+17785G>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91153524 | ||||||
| chr8:91153778
|
A | G | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+18039A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91153778 | ||||||
| chr8:91153863
|
C | T | 1 | a0001c0001t0001g0238 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.651+18124C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91153863 | ||||||
| chr8:91154004
|
A | C | 1 | a0001c0001t0001g0221 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.651+18265A>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91154004 | ||||||
| chr8:91154007
|
G | C | 3 | a0001c0003t0001g0282a0001c0003t0001g0283a0001c0003t0001g0285 | 3 | HG01891.hp1 HG02818.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.651+18268G>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91154007 | ||||||
| chr8:91154055
|
T | C | 131 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(128): Show | 135 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.651+18316T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91154055 | ||||||
| chr8:91154147
|
C | A | 131 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(128): Show | 135 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.651+18408C>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91154147 | ||||||
| chr8:91154201
|
T | C | 1 | a0002c0002t0001g0067 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.651+18462T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91154201 | ||||||
| chr8:91154281
|
G | T | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+18542G>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91154281 | ||||||
| chr8:91154359
|
C | T | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+18620C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91154359 | ||||||
| chr8:91154513
|
A | T | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+18774A>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91154513 | ||||||
| chr8:91154548
|
A | C | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+18809A>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91154548 | ||||||
| chr8:91154595
|
C | A | 97 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(94): Show | 100 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.651+18856C>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91154595 | ||||||
| chr8:91154658
|
C | T | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+18919C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91154658 | ||||||
| chr8:91154696
|
A | G | 14 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(11): Show | 14 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.651+18957A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91154696 | ||||||
| chr8:91154718
|
A | C | 1 | a0002c0006t0002g0154 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.651+18979A>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91154718 | ||||||
| chr8:91154855
|
T | C | 1 | a0002c0002t0001g0083 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.651+19116T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91154855 | ||||||
| chr8:91154922
|
G | A | 1 | a0002c0002t0001g0125 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.651+19183G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91154922 | ||||||
| chr8:91154976
|
G | A | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+19237G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91154976 | ||||||
| chr8:91155085
|
C | A | 1 | a0002c0002t0001g0056 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.651+19346C>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91155085 | ||||||
| chr8:91155116
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.651+19377C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91155116 | ||||||
| chr8:91155202
|
T | C | 64 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(61): Show | 66 | HG00423.hp2 HG00558.hp2 HG00735.hp2 others(63): Show |
intron_variant | MODIFIER | c.651+19463T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91155202 | ||||||
| chr8:91155232
|
T | TA | 39 | a0001c0001t0001g0001a0001c0001t0001g0143a0001c0001t0001g0144others(36): Show | 41 | HG00423.hp2 HG00558.hp2 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.651+19501dupA | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91155232 | |||||
| chr8:91155372
|
TG | T | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+19638delG | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91155372 | |||||
| chr8:91155390
|
T | C | 1 | a0002c0002t0001g0096 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.651+19651T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91155390 | ||||||
| chr8:91155432
|
A | G | 6 | a0001c0001t0001g0276a0001c0001t0001g0278a0001c0001t0001g0279others(3): Show | 6 | HG02257.hp2 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.651+19693A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91155432 | ||||||
| chr8:91155448
|
C | T | 1 | a0002c0002t0001g0034 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.651+19709C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91155448 | ||||||
| chr8:91155498
|
A | G | 1 | a0002c0002t0001g0078 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.651+19759A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91155498 | ||||||
| chr8:91155802
|
C | T | 1 | a0002c0002t0001g0032 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.651+20063C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91155802 | ||||||
| chr8:91155807
|
G | A | 201 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(198): Show | 207 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.651+20068G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91155807 | ||||||
| chr8:91155837
|
A | G | 39 | a0001c0001t0001g0001a0001c0001t0001g0143a0001c0001t0001g0144others(36): Show | 41 | HG00423.hp2 HG00558.hp2 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.651+20098A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91155837 | ||||||
| chr8:91155867
|
G | GTA | 68 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(65): Show | 70 | HG00423.hp2 HG00558.hp2 HG00735.hp2 others(67): Show |
intron_variant | MODIFIER | c.651+20141_651+2014 others(6): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91155867 | |||||
| chr8:91155880
|
T | C | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+20141T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91155880 | ||||||
| chr8:91155882
|
C | CACAACAT others(23): Show |
1 | a0002c0002t0001g0311 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.651+20162_651+2019 others(34): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91155882 | |||||
| chr8:91155882
|
CACAACAT others(8): Show |
C | 2 | a0001c0001t0001g0175a0002c0002t0001g0073 | 2 | NA18979.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.651+20177_651+2019 others(19): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91155882 | |||||
| chr8:91155884
|
C | A | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+20145C>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91155884 | ||||||
| chr8:91155885
|
A | C | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+20146A>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91155885 | ||||||
| chr8:91155887
|
C | T | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+20148C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91155887 | ||||||
| chr8:91156010
|
A | G | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+20271A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91156010 | ||||||
| chr8:91156050
|
A | ATTTCT | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+20315_651+2031 others(9): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91156050 | |||||
| chr8:91156090
|
G | T | 3 | a0001c0001t0003g0178a0001c0001t0003g0179a0001c0001t0003g0180 | 3 | HG02818.hp1 HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.651+20351G>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91156090 | ||||||
| chr8:91156167
|
C | T | 2 | a0002c0002t0001g0122a0002c0002t0001g0123 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.651+20428C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91156167 | ||||||
| chr8:91156316
|
T | C | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+20577T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91156316 | ||||||
| chr8:91156362
|
G | T | 9 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(6): Show | 9 | HG00735.hp2 HG01261.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.651+20623G>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91156362 | ||||||
| chr8:91156481
|
T | C | 64 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(61): Show | 66 | HG00423.hp2 HG00558.hp2 HG00735.hp2 others(63): Show |
intron_variant | MODIFIER | c.651+20742T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91156481 | ||||||
| chr8:91156499
|
A | G | 15 | a0001c0001t0001g0276a0001c0001t0001g0278a0001c0001t0001g0279others(12): Show | 15 | HG02109.hp1 HG02257.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.651+20760A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91156499 | ||||||
| chr8:91156617
|
G | T | 201 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(198): Show | 207 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.651+20878G>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91156617 | ||||||
| chr8:91156640
|
T | A | 3 | a0002c0002t0001g0026a0002c0002t0001g0031a0002c0002t0001g0140 | 3 | NA18944.hp1 NA18992.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.651+20901T>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91156640 | ||||||
| chr8:91156641
|
A | T | 2 | a0002c0002t0001g0054a0002c0002t0001g0134 | 2 | HG01257.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.651+20902A>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91156641 | ||||||
| chr8:91156645
|
A | C | 2 | a0002c0002t0001g0085a0002c0002t0001g0091 | 2 | HG02602.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.651+20906A>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91156645 | ||||||
| chr8:91156997
|
T | C | 1 | a0002c0002t0001g0094 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.651+21258T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91156997 | ||||||
| chr8:91157185
|
G | A | 3 | a0001c0003t0001g0286a0001c0003t0001g0287a0001c0003t0001g0302 | 3 | HG01081.hp1 HG02486.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.651+21446G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91157185 | ||||||
| chr8:91157550
|
G | T | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+21811G>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91157550 | ||||||
| chr8:91157776
|
A | C | 1 | a0002c0002t0001g0094 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.651+22037A>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91157776 | ||||||
| chr8:91157877
|
G | A | 1 | a0001c0001t0001g0172 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.651+22138G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91157877 | ||||||
| chr8:91157925
|
C | T | 8 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(5): Show | 8 | HG00735.hp2 HG02559.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.651+22186C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91157925 | ||||||
| chr8:91157941
|
G | C | 1 | a0001c0001t0001g0151 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.651+22202G>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91157941 | ||||||
| chr8:91157976
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.651+22237G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91157976 | ||||||
| chr8:91158124
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.651+22385C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91158124 | ||||||
| chr8:91158132
|
A | T | 1 | a0001c0001t0001g0304 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.651+22393A>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91158132 | ||||||
| chr8:91158160
|
A | G | 9 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(6): Show | 9 | HG00735.hp2 HG01261.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.651+22421A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91158160 | ||||||
| chr8:91158362
|
T | C | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+22623T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91158362 | ||||||
| chr8:91158421
|
A | G | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+22682A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91158421 | ||||||
| chr8:91158429
|
A | G | 5 | a0001c0001t0001g0216a0001c0001t0001g0241a0001c0001t0001g0244others(2): Show | 5 | HG00673.hp1 NA18747.hp2 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.651+22690A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91158429 | ||||||
| chr8:91158607
|
A | G | 1 | a0001c0001t0001g0248 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.651+22868A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91158607 | ||||||
| chr8:91158720
|
T | C | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+22981T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91158720 | ||||||
| chr8:91158955
|
T | C | 7 | a0001c0001t0001g0163a0001c0001t0001g0306a0001c0001t0001g0307others(4): Show | 7 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.651+23216T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91158955 | ||||||
| chr8:91158992
|
C | A | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+23253C>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91158992 | ||||||
| chr8:91159157
|
CATCACAC others(3): Show |
C | 34 | a0001c0001t0001g0249a0002c0002t0001g0003a0002c0002t0001g0024others(31): Show | 35 | HG00438.hp1 HG00544.hp1 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.651+23421_651+2343 others(14): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91159157 | |||||
| chr8:91159314
|
T | G | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+23575T>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91159314 | ||||||
| chr8:91159436
|
G | A | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+23697G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91159436 | ||||||
| chr8:91159439
|
T | A | 1 | a0001c0001t0001g0312 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.651+23700T>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91159439 | ||||||
| chr8:91159469
|
A | T | 6 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(3): Show | 6 | HG02622.hp2 HG03130.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+23730A>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91159469 | ||||||
| chr8:91159671
|
T | C | 1 | a0001c0001t0001g0163 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.651+23932T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91159671 | ||||||
| chr8:91159673
|
C | T | 5 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(2): Show | 5 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.651+23934C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91159673 | ||||||
| chr8:91159690
|
T | C | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+23951T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91159690 | ||||||
| chr8:91159766
|
T | C | 202 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(199): Show | 208 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.651+24027T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91159766 | ||||||
| chr8:91159875
|
A | AAAC | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+24136_651+2413 others(7): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91159875 | ||||||
| chr8:91159876
|
G | A | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+24137G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91159876 | ||||||
| chr8:91159878
|
G | T | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+24139G>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91159878 | ||||||
| chr8:91159971
|
AAAC | A | 7 | a0001c0003t0001g0282a0001c0003t0001g0283a0001c0003t0001g0284others(4): Show | 7 | HG01081.hp1 HG01891.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.651+24250_651+2425 others(7): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91159971 | |||||
| chr8:91160021
|
G | A | 1 | a0002c0002t0001g0083 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.651+24282G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91160021 | ||||||
| chr8:91160044
|
T | G | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+24305T>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91160044 | ||||||
| chr8:91160049
|
C | G | 9 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(6): Show | 9 | HG00735.hp2 HG01261.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.651+24310C>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91160049 | ||||||
| chr8:91160116
|
T | A | 9 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(6): Show | 9 | HG00735.hp2 HG01261.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.651+24377T>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91160116 | ||||||
| chr8:91160151
|
G | C | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+24412G>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91160151 | ||||||
| chr8:91160163
|
A | ATTTTTTC others(7): Show |
6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+24433_651+2443 others(18): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91160163 | |||||
| chr8:91160203
|
C | T | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+24464C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91160203 | ||||||
| chr8:91160273
|
G | C | 131 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(128): Show | 135 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.651+24534G>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91160273 | ||||||
| chr8:91160311
|
T | A | 6 | a0001c0001t0001g0267a0001c0001t0001g0268a0001c0001t0001g0269others(3): Show | 6 | HG02280.hp1 NA18945.hp1 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.651+24572T>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91160311 | ||||||
| chr8:91160316
|
A | G | 1 | a0001c0001t0001g0163 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.651+24577A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91160316 | ||||||
| chr8:91160325
|
A | C | 202 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(199): Show | 208 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.651+24586A>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91160325 | ||||||
| chr8:91160686
|
C | G | 131 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(128): Show | 135 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.651+24947C>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91160686 | ||||||
| chr8:91160708
|
C | T | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+24969C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91160708 | ||||||
| chr8:91161041
|
A | G | 1 | a0001c0001t0001g0304 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.651+25302A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91161041 | ||||||
| chr8:91161190
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.651+25451C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91161190 | ||||||
| chr8:91161209
|
A | G | 15 | a0001c0001t0001g0001a0001c0001t0001g0288a0001c0001t0001g0289others(12): Show | 17 | HG00423.hp2 HG00558.hp2 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.651+25470A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91161209 | ||||||
| chr8:91161285
|
T | C | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+25546T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91161285 | ||||||
| chr8:91161328
|
A | G | 1 | a0001c0001t0001g0150 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.651+25589A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91161328 | ||||||
| chr8:91161365
|
G | A | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+25626G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91161365 | ||||||
| chr8:91161586
|
T | C | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+25847T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91161586 | ||||||
| chr8:91161760
|
T | C | 1 | a0001c0001t0001g0163 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.651+26021T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91161760 | ||||||
| chr8:91161887
|
G | A | 70 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(67): Show | 72 | HG00423.hp2 HG00558.hp2 HG00735.hp2 others(69): Show |
intron_variant | MODIFIER | c.651+26148G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91161887 | ||||||
| chr8:91162026
|
G | C | 15 | a0001c0001t0001g0276a0001c0001t0001g0278a0001c0001t0001g0279others(12): Show | 15 | HG02109.hp1 HG02257.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.651+26287G>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91162026 | ||||||
| chr8:91162027
|
G | C | 14 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(11): Show | 14 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.651+26288G>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91162027 | ||||||
| chr8:91162116
|
G | C | 14 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(11): Show | 14 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.651+26377G>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91162116 | ||||||
| chr8:91162277
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.651+26538G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91162277 | ||||||
| chr8:91162402
|
A | G | 1 | a0002c0002t0001g0068 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.651+26663A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91162402 | ||||||
| chr8:91162460
|
A | G | 1 | a0001c0001t0001g0163 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.651+26721A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91162460 | ||||||
| chr8:91162808
|
C | T | 202 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(199): Show | 208 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.652-26714C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91162808 | ||||||
| chr8:91163073
|
C | T | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.652-26449C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91163073 | ||||||
| chr8:91163108
|
A | T | 3 | a0001c0001t0001g0212a0001c0001t0001g0214a0001c0001t0001g0215 | 3 | HG02896.hp1 HG02897.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.652-26414A>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91163108 | ||||||
| chr8:91163165
|
G | A | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.652-26357G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91163165 | ||||||
| chr8:91163248
|
A | G | 7 | a0001c0001t0002g0157a0001c0001t0002g0158a0001c0001t0002g0159others(4): Show | 7 | HG02109.hp1 HG02559.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.652-26274A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91163248 | ||||||
| chr8:91163325
|
C | A | 1 | a0001c0001t0001g0163 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.652-26197C>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91163325 | ||||||
| chr8:91163345
|
C | T | 3 | a0001c0001t0003g0178a0001c0001t0003g0179a0001c0001t0003g0180 | 3 | HG02818.hp1 HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.652-26177C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91163345 | ||||||
| chr8:91163446
|
T | C | 2 | a0001c0001t0001g0212a0001c0001t0001g0214 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.652-26076T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91163446 | ||||||
| chr8:91163451
|
T | A | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.652-26071T>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91163451 | ||||||
| chr8:91163718
|
A | G | 3 | a0001c0001t0001g0249a0002c0002t0001g0033a0002c0002t0001g0035 | 3 | HG00438.hp1 HG03490.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.652-25804A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91163718 | ||||||
| chr8:91163734
|
A | G | 1 | a0002c0006t0002g0154 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.652-25788A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91163734 | ||||||
| chr8:91163793
|
TAAAA | T | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.652-25728_652-2572 others(8): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91163793 | ||||||
| chr8:91163818
|
TA | T | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.652-25703delA | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91163818 | ||||||
| chr8:91164121
|
G | C | 201 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(198): Show | 207 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.652-25401G>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91164121 | ||||||
| chr8:91164121
|
G | T | 2 | a0001c0001t0001g0124a0001c0001t0001g0259 | 2 | HG03834.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.652-25401G>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91164121 | ||||||
| chr8:91164162
|
C | A | 1 | a0001c0001t0001g0006 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.652-25360C>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91164162 | ||||||
| chr8:91164171
|
C | G | 1 | a0002c0002t0001g0104 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.652-25351C>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91164171 | ||||||
| chr8:91164279
|
GT | G | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.652-25241delT | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91164279 | |||||
| chr8:91164400
|
G | A | 1 | a0001c0001t0001g0312 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.652-25122G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91164400 | ||||||
| chr8:91164456
|
A | G | 1 | a0001c0001t0001g0202 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.652-25066A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91164456 | ||||||
| chr8:91164707
|
C | A | 1 | a0001c0001t0001g0182 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.652-24815C>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91164707 | ||||||
| chr8:91164833
|
T | C | 3 | a0002c0002t0001g0012a0002c0002t0001g0310a0002c0002t0001g0311 | 3 | HG01934.hp1 NA18999.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.652-24689T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91164833 | ||||||
| chr8:91164926
|
A | G | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.652-24596A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91164926 | ||||||
| chr8:91164958
|
C | T | 5 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(2): Show | 5 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.652-24564C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91164958 | ||||||
| chr8:91164991
|
C | T | 14 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(11): Show | 14 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.652-24531C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91164991 | ||||||
| chr8:91165019
|
T | C | 2 | a0002c0002t0001g0079a0002c0002t0001g0080 | 2 | NA18955.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.652-24503T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91165019 | ||||||
| chr8:91165123
|
C | T | 3 | a0001c0001t0001g0212a0001c0001t0001g0214a0001c0001t0001g0215 | 3 | HG02896.hp1 HG02897.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.652-24399C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91165123 | ||||||
| chr8:91165128
|
C | T | 1 | a0001c0001t0001g0153 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.652-24394C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91165128 | ||||||
| chr8:91165579
|
G | A | 1 | a0002c0002t0001g0109 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.652-23943G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91165579 | ||||||
| chr8:91165709
|
A | G | 57 | a0001c0001t0001g0001a0001c0001t0001g0143a0001c0001t0001g0144others(54): Show | 59 | HG00423.hp2 HG00558.hp2 HG01081.hp1 others(56): Show |
intron_variant | MODIFIER | c.652-23813A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91165709 | ||||||
| chr8:91165807
|
T | A | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.652-23715T>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91165807 | ||||||
| chr8:91165872
|
A | G | 1 | a0001c0001t0001g0133 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.652-23650A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91165872 | ||||||
| chr8:91166381
|
T | C | 1 | a0002c0002t0001g0096 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.652-23141T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91166381 | ||||||
| chr8:91166492
|
G | GA | 15 | a0001c0001t0001g0052a0001c0001t0001g0124a0001c0001t0001g0143others(12): Show | 15 | HG00423.hp1 HG01081.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.652-23006dupA | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91166492 | |||||
| chr8:91166492
|
G | GAA | 38 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0059others(35): Show | 40 | HG00423.hp2 HG00558.hp2 HG02055.hp2 others(37): Show |
intron_variant | MODIFIER | c.652-23007_652-2300 others(6): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91166492 | |||||
| chr8:91166492
|
G | GAAA | 15 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0133others(12): Show | 15 | HG01123.hp1 HG01884.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.652-23008_652-2300 others(7): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91166492 | |||||
| chr8:91166492
|
GA | G | 14 | a0001c0001t0001g0145a0001c0001t0001g0167a0001c0001t0001g0171others(11): Show | 14 | HG00408.hp2 HG01891.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.652-23006delA | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91166492 | |||||
| chr8:91166492
|
GAAAA | G | 40 | a0001c0001t0001g0256a0001c0001t0001g0306a0001c0001t0001g0307others(37): Show | 41 | HG00438.hp1 HG01069.hp1 HG01070.hp2 others(38): Show |
intron_variant | MODIFIER | c.652-23009_652-2300 others(8): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91166492 | |||||
| chr8:91166492
|
GAAAAA | G | 6 | a0001c0001t0001g0249a0001c0001t0001g0257a0002c0002t0001g0095others(3): Show | 6 | HG00544.hp1 HG00609.hp2 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.652-23010_652-2300 others(9): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91166492 | |||||
| chr8:91166492
|
GAAAAAAA | G | 83 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(80): Show | 84 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.652-23012_652-2300 others(11): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91166492 | |||||
| chr8:91166492
|
GAAAAAAA others(1): Show |
G | 5 | a0002c0002t0001g0004a0002c0002t0001g0005a0002c0002t0001g0129others(2): Show | 7 | HG02040.hp2 HG02074.hp1 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.652-23013_652-2300 others(12): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91166492 | |||||
| chr8:91166513
|
A | C | 1 | a0001c0001t0001g0045 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.652-23009A>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91166513 | ||||||
| chr8:91166623
|
A | G | 1 | a0001c0001t0001g0175 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.652-22899A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91166623 | ||||||
| chr8:91166982
|
TCA | T | 42 | a0001c0001t0001g0001a0001c0001t0001g0143a0001c0001t0001g0144others(39): Show | 44 | HG00423.hp2 HG00558.hp2 HG01081.hp1 others(41): Show |
intron_variant | MODIFIER | c.652-22537_652-2253 others(6): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91166982 | |||||
| chr8:91166999
|
A | T | 14 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(11): Show | 14 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.652-22523A>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91166999 | ||||||
| chr8:91167263
|
C | T | 1 | a0001c0003t0001g0284 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.652-22259C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91167263 | ||||||
| chr8:91167264
|
G | A | 1 | a0002c0002t0001g0019 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.652-22258G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91167264 | ||||||
| chr8:91167457
|
G | A | 1 | a0001c0001t0001g0234 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.652-22065G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91167457 | ||||||
| chr8:91167595
|
T | G | 1 | a0001c0001t0001g0304 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.652-21927T>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91167595 | ||||||
| chr8:91167619
|
C | T | 1 | a0001c0001t0001g0303 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.652-21903C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91167619 | ||||||
| chr8:91167737
|
T | C | 143 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(140): Show | 147 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.652-21785T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91167737 | ||||||
| chr8:91167850
|
T | C | 10 | a0001c0001t0001g0162a0001c0001t0001g0165a0001c0001t0001g0166others(7): Show | 10 | HG02145.hp1 HG02572.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.652-21672T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91167850 | ||||||
| chr8:91168148
|
A | C | 5 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(2): Show | 5 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.652-21374A>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91168148 | ||||||
| chr8:91168190
|
G | T | 1 | a0001c0001t0001g0288 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.652-21332G>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91168190 | ||||||
| chr8:91168191
|
C | T | 1 | a0001c0001t0001g0288 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.652-21331C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91168191 | ||||||
| chr8:91168264
|
G | A | 1 | a0001c0001t0001g0020 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.652-21258G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91168264 | ||||||
| chr8:91168317
|
T | C | 1 | a0002c0002t0001g0063 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.652-21205T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91168317 | ||||||
| chr8:91168359
|
ACCCCCAT | A | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.652-21161_652-2115 others(11): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91168359 | |||||
| chr8:91168368
|
T | G | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.652-21154T>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91168368 | ||||||
| chr8:91168391
|
C | A | 5 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(2): Show | 5 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.652-21131C>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91168391 | ||||||
| chr8:91168551
|
T | C | 1 | a0002c0002t0001g0125 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.652-20971T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91168551 | ||||||
| chr8:91168683
|
T | C | 1 | a0002c0006t0002g0154 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.652-20839T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91168683 | ||||||
| chr8:91168736
|
GT | G | 203 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(200): Show | 209 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.652-20777delT | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91168736 | |||||
| chr8:91168925
|
T | C | 129 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(126): Show | 133 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.652-20597T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91168925 | ||||||
| chr8:91168986
|
A | C | 204 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(201): Show | 210 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.652-20536A>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91168986 | ||||||
| chr8:91169242
|
C | G | 204 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(201): Show | 210 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.652-20280C>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91169242 | ||||||
| chr8:91169300
|
G | A | 33 | a0001c0001t0001g0249a0002c0002t0001g0003a0002c0002t0001g0024others(30): Show | 34 | HG00438.hp1 HG00544.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.652-20222G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91169300 | ||||||
| chr8:91169328
|
A | G | 75 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(72): Show | 77 | HG00423.hp2 HG00558.hp2 HG00735.hp2 others(74): Show |
intron_variant | MODIFIER | c.652-20194A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91169328 | ||||||
| chr8:91169413
|
A | G | 1 | a0001c0001t0001g0243 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.652-20109A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91169413 | ||||||
| chr8:91169523
|
A | AT | 17 | a0001c0001t0001g0059a0001c0001t0001g0276a0001c0001t0001g0278others(14): Show | 17 | HG02109.hp1 HG02145.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.652-19989dupT | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91169523 | |||||
| chr8:91169523
|
AT | A | 130 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(127): Show | 134 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.652-19989delT | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91169523 | |||||
| chr8:91169661
|
TC | T | 244 | a0001c0001t0001g0011a0001c0001t0001g0020a0001c0001t0001g0045others(241): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.652-19857delC | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91169661 | |||||
| chr8:91169664
|
CCT | C | 55 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(52): Show | 57 | HG00423.hp2 HG00558.hp2 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.652-19856_652-1985 others(6): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91169664 | |||||
| chr8:91169665
|
C | T | 12 | a0001c0001t0001g0174a0001c0001t0001g0176a0001c0001t0001g0194others(9): Show | 12 | HG00140.hp1 HG00735.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.652-19857C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91169665 | ||||||
| chr8:91169666
|
T | C | 12 | a0001c0001t0001g0174a0001c0001t0001g0176a0001c0001t0001g0194others(9): Show | 12 | HG00140.hp1 HG00735.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.652-19856T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91169666 | ||||||
| chr8:91169667
|
C | T | 55 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(52): Show | 57 | HG00423.hp2 HG00558.hp2 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.652-19855C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91169667 | ||||||
| chr8:91169671
|
C | A | 1 | a0001c0001t0001g0167 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.652-19851C>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91169671 | ||||||
| chr8:91169672
|
C | G | 28 | a0001c0001t0001g0001a0001c0001t0001g0164a0001c0001t0001g0170others(25): Show | 30 | HG00423.hp2 HG00558.hp2 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.652-19850C>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91169672 | ||||||
| chr8:91169672
|
C | T | 3 | a0001c0001t0001g0308a0001c0001t0001g0309a0002c0002t0001g0135 | 3 | HG01069.hp1 HG01081.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.652-19850C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91169672 | ||||||
| chr8:91169673
|
C | G | 8 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(5): Show | 8 | HG00735.hp2 HG02559.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.652-19849C>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91169673 | ||||||
| chr8:91169675
|
A | C | 311 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(308): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.652-19847A>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91169675 | ||||||
| chr8:91169677
|
C | A | 1 | a0001c0001t0001g0264 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.652-19845C>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91169677 | ||||||
| chr8:91169701
|
G | A | 6 | a0001c0001t0001g0164a0001c0001t0001g0170a0001c0001t0001g0173others(3): Show | 6 | HG02818.hp1 HG02976.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.652-19821G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91169701 | ||||||
| chr8:91169769
|
C | T | 22 | a0001c0001t0001g0001a0001c0001t0001g0288a0001c0001t0001g0289others(19): Show | 24 | HG00423.hp2 HG00558.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.652-19753C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91169769 | ||||||
| chr8:91169770
|
A | G | 204 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(201): Show | 210 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.652-19752A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91169770 | ||||||
| chr8:91169919
|
A | G | 1 | a0002c0002t0001g0106 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.652-19603A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91169919 | ||||||
| chr8:91170003
|
C | T | 204 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(201): Show | 210 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.652-19519C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91170003 | ||||||
| chr8:91170209
|
C | T | 202 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(199): Show | 208 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.652-19313C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91170209 | ||||||
| chr8:91170304
|
T | TG | 204 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(201): Show | 210 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.652-19217dupG | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91170304 | |||||
| chr8:91170348
|
A | G | 3 | a0002c0002t0001g0136a0002c0002t0001g0137a0002c0002t0001g0208 | 3 | HG00544.hp1 HG00609.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.652-19174A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91170348 | ||||||
| chr8:91170523
|
C | CA | 204 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(201): Show | 210 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.652-18996dupA | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91170523 | |||||
| chr8:91170559
|
G | GA | 204 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(201): Show | 210 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.652-18963_652-1896 others(5): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91170559 | ||||||
| chr8:91170596
|
G | A | 204 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(201): Show | 210 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.652-18926G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91170596 | ||||||
| chr8:91170598
|
G | A | 204 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(201): Show | 210 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.652-18924G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91170598 | ||||||
| chr8:91170714
|
C | G | 175 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(172): Show | 179 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.652-18808C>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91170714 | ||||||
| chr8:91170732
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.652-18790C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91170732 | ||||||
| chr8:91170773
|
C | T | 204 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(201): Show | 210 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.652-18749C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91170773 | ||||||
| chr8:91170902
|
G | A | 14 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(11): Show | 14 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.652-18620G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91170902 | ||||||
| chr8:91171073
|
C | T | 6 | a0001c0001t0001g0164a0001c0001t0001g0170a0001c0001t0001g0173others(3): Show | 6 | HG02818.hp1 HG02976.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.652-18449C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91171073 | ||||||
| chr8:91171106
|
A | G | 29 | a0001c0001t0001g0249a0002c0002t0001g0003a0002c0002t0001g0024others(26): Show | 30 | HG00438.hp1 HG00544.hp1 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.652-18416A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91171106 | ||||||
| chr8:91171158
|
A | C | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | HG01884.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.652-18364A>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91171158 | ||||||
| chr8:91171297
|
T | TAG | 204 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(201): Show | 210 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.652-18224_652-1822 others(6): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91171297 | |||||
| chr8:91171307
|
A | G | 204 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(201): Show | 210 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.652-18215A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91171307 | ||||||
| chr8:91171309
|
G | A | 204 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(201): Show | 210 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.652-18213G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91171309 | ||||||
| chr8:91171339
|
C | T | 204 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(201): Show | 210 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.652-18183C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91171339 | ||||||
| chr8:91171402
|
C | T | 1 | a0001c0001t0001g0308 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.652-18120C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91171402 | ||||||
| chr8:91171430
|
T | C | 204 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(201): Show | 210 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.652-18092T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91171430 | ||||||
| chr8:91171439
|
A | T | 5 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(2): Show | 5 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.652-18083A>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91171439 | ||||||
| chr8:91171468
|
A | C | 1 | a0001c0001t0001g0163 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.652-18054A>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91171468 | ||||||
| chr8:91171529
|
A | G | 204 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(201): Show | 210 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.652-17993A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91171529 | ||||||
| chr8:91171610
|
G | A | 204 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(201): Show | 210 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.652-17912G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91171610 | ||||||
| chr8:91171627
|
G | A | 1 | a0002c0006t0002g0154 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.652-17895G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91171627 | ||||||
| chr8:91171887
|
T | G | 16 | a0001c0001t0001g0276a0001c0001t0001g0278a0001c0001t0001g0279others(13): Show | 16 | HG02109.hp1 HG02257.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.652-17635T>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91171887 | ||||||
| chr8:91171958
|
T | A | 1 | a0002c0002t0001g0123 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.652-17564T>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91171958 | ||||||
| chr8:91171958
|
T | TA | 202 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(199): Show | 208 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.652-17564_652-1756 others(5): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91171958 | ||||||
| chr8:91171959
|
T | A | 203 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(200): Show | 209 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.652-17563T>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91171959 | ||||||
| chr8:91172046
|
A | G | 1 | a0001c0001t0001g0163 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.652-17476A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91172046 | ||||||
| chr8:91172279
|
A | G | 1 | a0001c0001t0001g0217 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.652-17243A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91172279 | ||||||
| chr8:91172509
|
A | T | 14 | a0002c0002t0001g0004a0002c0002t0001g0012a0002c0002t0001g0056others(11): Show | 15 | HG00558.hp1 HG01106.hp1 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.652-17013A>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91172509 | ||||||
| chr8:91172586
|
G | A | 22 | a0001c0001t0001g0001a0001c0001t0001g0288a0001c0001t0001g0289others(19): Show | 24 | HG00423.hp2 HG00558.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.652-16936G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91172586 | ||||||
| chr8:91172640
|
C | T | 1 | a0001c0001t0001g0229 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.652-16882C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91172640 | ||||||
| chr8:91172745
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.652-16777C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91172745 | ||||||
| chr8:91172897
|
T | G | 1 | a0001c0001t0001g0150 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.652-16625T>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91172897 | ||||||
| chr8:91172940
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.652-16582C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91172940 | ||||||
| chr8:91173118
|
G | T | 204 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(201): Show | 210 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.652-16404G>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91173118 | ||||||
| chr8:91173170
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.652-16352G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91173170 | ||||||
| chr8:91173358
|
T | C | 1 | a0001c0001t0001g0262 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.652-16164T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91173358 | ||||||
| chr8:91173507
|
T | G | 204 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(201): Show | 210 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.652-16015T>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91173507 | ||||||
| chr8:91173515
|
G | T | 204 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(201): Show | 210 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.652-16007G>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91173515 | ||||||
| chr8:91173532
|
A | G | 204 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(201): Show | 210 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.652-15990A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91173532 | ||||||
| chr8:91173537
|
T | C | 204 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(201): Show | 210 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.652-15985T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91173537 | ||||||
| chr8:91173542
|
A | T | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.652-15980A>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91173542 | ||||||
| chr8:91173597
|
A | G | 1 | a0002c0002t0001g0141 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.652-15925A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91173597 | ||||||
| chr8:91173870
|
C | T | 205 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(202): Show | 211 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.652-15652C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91173870 | ||||||
| chr8:91173942
|
A | AC | 14 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(11): Show | 14 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.652-15580_652-1557 others(5): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91173942 | ||||||
| chr8:91174036
|
A | AGTGTAGT others(62): Show |
5 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(2): Show | 5 | HG01070.hp1 HG01071.hp2 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.652-15466_652-1546 others(73): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91174036 | |||||
| chr8:91174036
|
A | AGTGTAGT others(61): Show |
1 | a0001c0001t0001g0304 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.652-15466_652-1546 others(72): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91174036 | |||||
| chr8:91174036
|
A | AGTGTAGT others(61): Show |
17 | a0001c0001t0001g0303a0002c0002t0001g0019a0002c0002t0001g0029others(14): Show | 17 | HG00408.hp1 HG00673.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.652-15466_652-1546 others(72): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91174036 | |||||
| chr8:91174036
|
A | AGTGTAGT others(62): Show |
1 | a0001c0001t0001g0163 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.652-15466_652-1546 others(73): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91174036 | |||||
| chr8:91174036
|
A | AGTGTAGT others(61): Show |
10 | a0002c0002t0001g0060a0002c0002t0001g0062a0002c0002t0001g0084others(7): Show | 10 | HG00099.hp1 HG00639.hp1 HG00733.hp2 others(7): Show |
intron_variant | MODIFIER | c.652-15466_652-1546 others(72): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91174036 | |||||
| chr8:91174036
|
A | AGTGTAGT others(62): Show |
30 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0164others(27): Show | 32 | HG00423.hp2 HG00558.hp2 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.652-15466_652-1546 others(73): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91174036 | |||||
| chr8:91174036
|
A | AGTGTAGT others(62): Show |
95 | a0001c0001t0001g0249a0002c0002t0001g0002a0002c0002t0001g0003others(92): Show | 99 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.652-15466_652-1546 others(73): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91174036 | |||||
| chr8:91174036
|
A | AGTGTAGT others(63): Show |
1 | a0001c0001t0001g0307 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.652-15466_652-1546 others(74): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91174036 | |||||
| chr8:91174036
|
A | AGTGTAGT others(61): Show |
3 | a0001c0001t0001g0145a0001c0001t0001g0148a0002c0002t0001g0037 | 3 | HG03225.hp2 NA18952.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.652-15466_652-1546 others(72): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91174036 | |||||
| chr8:91174036
|
A | AGTGTAGT others(62): Show |
1 | a0002c0002t0001g0038 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.652-15466_652-1546 others(73): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91174036 | |||||
| chr8:91174036
|
A | AGTGTAGT others(63): Show |
22 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(19): Show | 22 | HG00735.hp2 HG02109.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.652-15466_652-1546 others(74): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91174036 | |||||
| chr8:91174036
|
A | AGTGTAGT others(64): Show |
5 | a0001c0001t0001g0306a0001c0001t0001g0308a0001c0001t0001g0309others(2): Show | 5 | HG01069.hp1 HG01081.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.652-15466_652-1546 others(75): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91174036 | |||||
| chr8:91174036
|
A | AGTGTAGT others(62): Show |
4 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0147others(1): Show | 4 | HG00741.hp1 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.652-15466_652-1546 others(73): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91174036 | |||||
| chr8:91174036
|
A | AGTGTAGT others(63): Show |
9 | a0001c0001t0001g0143a0001c0001t0001g0149a0001c0001t0001g0150others(6): Show | 9 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.652-15466_652-1546 others(74): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91174036 | |||||
| chr8:91174036
|
A | AGTGTAGT others(62): Show |
1 | a0001c0001t0001g0059 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.652-15466_652-1546 others(73): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91174036 | |||||
| chr8:91174206
|
TC | T | 3 | a0002c0002t0001g0002a0002c0002t0001g0022a0002c0002t0001g0023 | 4 | NA18960.hp1 NA19010.hp2 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.652-15314delC | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91174206 | |||||
| chr8:91174279
|
T | A | 5 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(2): Show | 5 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.652-15243T>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91174279 | ||||||
| chr8:91174354
|
C | T | 4 | a0001c0001t0001g0276a0001c0001t0001g0278a0001c0001t0001g0279others(1): Show | 4 | HG02970.hp2 HG03471.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.652-15168C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91174354 | ||||||
| chr8:91174404
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.652-15118G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91174404 | ||||||
| chr8:91174494
|
T | C | 205 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(202): Show | 211 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.652-15028T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91174494 | ||||||
| chr8:91174610
|
A | C | 205 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(202): Show | 211 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.652-14912A>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91174610 | ||||||
| chr8:91174705
|
A | G | 205 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(202): Show | 211 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.652-14817A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91174705 | ||||||
| chr8:91174721
|
A | G | 205 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(202): Show | 211 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.652-14801A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91174721 | ||||||
| chr8:91174785
|
C | T | 96 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(93): Show | 99 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.652-14737C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91174785 | ||||||
| chr8:91174841
|
T | A | 1 | a0001c0001t0001g0209 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.652-14681T>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91174841 | ||||||
| chr8:91174844
|
G | A | 28 | a0001c0001t0001g0001a0001c0001t0001g0164a0001c0001t0001g0170others(25): Show | 30 | HG00423.hp2 HG00558.hp2 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.652-14678G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91174844 | ||||||
| chr8:91174860
|
GGAGAGGT others(3637): Show |
G | 1 | a0001c0001t0001g0213 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.652-14658_652-1101 others(4): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91174860 | |||||
| chr8:91174889
|
TA | T | 205 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(202): Show | 211 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.652-14629delA | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91174889 | |||||
| chr8:91174979
|
G | A | 205 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(202): Show | 211 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.652-14543G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91174979 | ||||||
| chr8:91175074
|
G | T | 1 | a0001c0001t0001g0257 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.652-14448G>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91175074 | ||||||
| chr8:91175276
|
C | T | 14 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(11): Show | 14 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.652-14246C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91175276 | ||||||
| chr8:91175278
|
CA | C | 16 | a0001c0001t0001g0276a0001c0001t0001g0278a0001c0001t0001g0279others(13): Show | 16 | HG02109.hp1 HG02257.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.652-14243delA | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91175278 | ||||||
| chr8:91175297
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.652-14225G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91175297 | ||||||
| chr8:91175364
|
A | G | 1 | a0001c0001t0001g0192 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.652-14158A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91175364 | ||||||
| chr8:91175510
|
G | A | 205 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(202): Show | 211 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.652-14012G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91175510 | ||||||
| chr8:91175815
|
GT | G | 205 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(202): Show | 211 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.652-13695delT | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91175815 | |||||
| chr8:91175834
|
G | A | 205 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(202): Show | 211 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.652-13688G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91175834 | ||||||
| chr8:91175958
|
T | C | 205 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(202): Show | 211 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.652-13564T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91175958 | ||||||
| chr8:91175973
|
T | G | 1 | a0001c0001t0001g0011 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.652-13549T>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91175973 | ||||||
| chr8:91176050
|
T | A | 1 | a0002c0002t0001g0093 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.652-13472T>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91176050 | ||||||
| chr8:91176115
|
CAT | C | 17 | a0001c0001t0001g0162a0001c0001t0001g0165a0001c0001t0001g0166others(14): Show | 17 | HG00544.hp2 HG01891.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.652-13388_652-1338 others(6): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91176115 | |||||
| chr8:91176131
|
TA | T | 75 | a0001c0001t0001g0011a0001c0001t0001g0020a0001c0001t0001g0045others(72): Show | 75 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.652-13390delA | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91176131 | ||||||
| chr8:91176132
|
A | ATTTT | 6 | a0001c0001t0001g0145a0001c0001t0001g0149a0001c0001t0001g0150others(3): Show | 6 | HG01884.hp1 HG02055.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.652-13389_652-1338 others(8): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91176132 | |||||
| chr8:91176132
|
A | T | 6 | a0001c0001t0001g0176a0001c0001t0001g0184a0001c0001t0001g0223others(3): Show | 6 | HG00423.hp1 HG02040.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.652-13390A>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91176132 | ||||||
| chr8:91176133
|
TA | T | 5 | a0001c0001t0001g0195a0001c0001t0001g0197a0001c0001t0001g0198others(2): Show | 5 | HG00741.hp2 HG01069.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.652-13388delA | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91176133 | ||||||
| chr8:91176134
|
A | ATATATAT others(20): Show |
1 | a0001c0001t0001g0304 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.652-13387_652-1338 others(31): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91176134 | |||||
| chr8:91176134
|
A | ATATATAT others(13): Show |
1 | a0001c0001t0001g0296 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.652-13387_652-1338 others(24): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91176134 | |||||
| chr8:91176134
|
A | ATATATAT others(7): Show |
1 | a0002c0002t0002g0041 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.652-13387_652-1338 others(18): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91176134 | |||||
| chr8:91176134
|
A | ATATATAT others(8): Show |
1 | a0002c0002t0001g0088 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.652-13387_652-1338 others(19): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91176134 | |||||
| chr8:91176134
|
A | ATATATAT others(10): Show |
1 | a0001c0001t0001g0303 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.652-13387_652-1338 others(21): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91176134 | |||||
| chr8:91176134
|
A | ATATATAT others(11): Show |
1 | a0002c0002t0001g0127 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.652-13387_652-1338 others(22): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91176134 | |||||
| chr8:91176134
|
A | ATATATAT others(13): Show |
1 | a0001c0001t0001g0297 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.652-13387_652-1338 others(24): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91176134 | |||||
| chr8:91176134
|
A | ATATATAT others(14): Show |
6 | a0001c0001t0001g0001a0001c0001t0001g0289a0001c0001t0001g0291others(3): Show | 8 | HG00423.hp2 NA18942.hp2 NA18984.hp2 others(5): Show |
intron_variant | MODIFIER | c.652-13387_652-1338 others(25): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91176134 | |||||
| chr8:91176134
|
A | ATATATAT others(15): Show |
2 | a0001c0001t0001g0006a0001c0001t0001g0290 | 2 | HG02615.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.652-13387_652-1338 others(26): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91176134 | |||||
| chr8:91176134
|
A | ATATATAT others(16): Show |
1 | a0001c0001t0001g0299 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.652-13387_652-1338 others(27): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91176134 | |||||
| chr8:91176134
|
A | ATATATAT others(5): Show |
1 | a0002c0002t0001g0039 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.652-13387_652-1338 others(16): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91176134 | |||||
| chr8:91176134
|
A | ATATATAT others(6): Show |
1 | a0002c0002t0001g0091 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.652-13387_652-1338 others(17): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91176134 | |||||
| chr8:91176134
|
A | ATATATAT others(7): Show |
5 | a0001c0001t0001g0276a0001c0001t0001g0278a0001c0001t0001g0279others(2): Show | 5 | HG02257.hp2 HG02970.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.652-13387_652-1338 others(18): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91176134 | |||||
| chr8:91176134
|
A | ATATATAT others(9): Show |
1 | a0002c0002t0001g0126 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.652-13387_652-1338 others(20): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91176134 | |||||
| chr8:91176134
|
A | ATATATAT others(11): Show |
3 | a0001c0001t0001g0293a0001c0001t0001g0300a0001c0001t0001g0301 | 3 | HG01123.hp1 NA18966.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.652-13387_652-1338 others(22): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91176134 | |||||
| chr8:91176134
|
A | ATATATAT others(12): Show |
2 | a0001c0001t0001g0288a0001c0001t0001g0294 | 2 | NA18972.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.652-13387_652-1338 others(23): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91176134 | |||||
| chr8:91176134
|
A | ATATATAT others(3): Show |
1 | a0001c0001t0001g0249 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.652-13387_652-1338 others(14): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91176134 | |||||
| chr8:91176134
|
A | ATATATAT others(4): Show |
5 | a0002c0002t0001g0026a0002c0002t0001g0044a0002c0002t0001g0051others(2): Show | 5 | HG02015.hp2 HG02486.hp2 NA18992.hp1 others(2): Show |
intron_variant | MODIFIER | c.652-13387_652-1338 others(15): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91176134 | |||||
| chr8:91176134
|
A | ATATATAT others(5): Show |
10 | a0002c0002t0001g0027a0002c0002t0001g0032a0002c0002t0001g0036others(7): Show | 10 | HG01256.hp2 HG01943.hp1 HG01978.hp2 others(7): Show |
intron_variant | MODIFIER | c.652-13387_652-1338 others(16): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91176134 | |||||
| chr8:91176134
|
A | ATATATAT others(6): Show |
10 | a0002c0002t0001g0077a0002c0002t0001g0078a0002c0002t0001g0081others(7): Show | 10 | HG00408.hp1 HG00735.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.652-13387_652-1338 others(17): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91176134 | |||||
| chr8:91176134
|
A | ATATATAT others(7): Show |
6 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0281others(3): Show | 6 | HG02809.hp1 HG04199.hp1 NA18522.hp2 others(3): Show |
intron_variant | MODIFIER | c.652-13387_652-1338 others(18): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91176134 | |||||
| chr8:91176134
|
A | ATATATAT others(8): Show |
8 | a0001c0001t0002g0157a0001c0001t0002g0158a0001c0001t0002g0159others(5): Show | 8 | HG02109.hp1 HG02559.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.652-13387_652-1338 others(19): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91176134 | |||||
| chr8:91176134
|
A | ATATATAT others(9): Show |
5 | a0001c0003t0001g0287a0001c0003t0001g0302a0002c0002t0001g0004others(2): Show | 6 | HG01081.hp1 HG02040.hp2 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.652-13387_652-1338 others(20): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91176134 | |||||
| chr8:91176134
|
A | ATATATAT others(10): Show |
2 | a0001c0003t0001g0284a0001c0003t0001g0286 | 2 | HG02486.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.652-13387_652-1338 others(21): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91176134 | |||||
| chr8:91176134
|
A | ATATATAT others(11): Show |
2 | a0001c0001t0001g0007a0001c0001t0001g0009 | 2 | HG00735.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.652-13387_652-1338 others(22): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91176134 | |||||
| chr8:91176134
|
A | ATATATAT others(12): Show |
3 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0133 | 3 | HG02970.hp1 HG03209.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.652-13387_652-1338 others(23): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91176134 | |||||
| chr8:91176134
|
A | ATATATAT others(3): Show |
2 | a0002c0002t0001g0033a0002c0002t0001g0139 | 2 | HG00438.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.652-13387_652-1338 others(14): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91176134 | |||||
| chr8:91176134
|
A | ATATATAT others(4): Show |
15 | a0002c0002t0001g0003a0002c0002t0001g0024a0002c0002t0001g0025others(12): Show | 16 | HG00544.hp1 HG00609.hp2 HG00673.hp2 others(13): Show |
intron_variant | MODIFIER | c.652-13387_652-1338 others(15): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91176134 | |||||
| chr8:91176134
|
A | ATATATAT others(5): Show |
6 | a0001c0001t0001g0116a0002c0002t0001g0042a0002c0002t0001g0054others(3): Show | 6 | HG01070.hp1 HG02148.hp2 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.652-13387_652-1338 others(16): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91176134 | |||||
| chr8:91176134
|
A | ATATATAT others(6): Show |
32 | a0001c0001t0001g0115a0001c0001t0001g0117a0002c0002t0001g0002others(29): Show | 33 | HG00140.hp1 HG00741.hp1 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.652-13387_652-1338 others(17): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91176134 | |||||
| chr8:91176134
|
A | ATATATAT others(7): Show |
1 | a0002c0002t0001g0066 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.652-13387_652-1338 others(18): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91176134 | |||||
| chr8:91176134
|
A | ATATATAT others(8): Show |
5 | a0001c0001t0001g0059a0002c0002t0001g0071a0002c0002t0001g0073others(2): Show | 5 | HG00558.hp1 HG02145.hp2 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.652-13387_652-1338 others(19): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91176134 | |||||
| chr8:91176134
|
A | ATATATAT others(10): Show |
3 | a0001c0003t0001g0282a0001c0003t0001g0283a0001c0003t0001g0285 | 3 | HG01891.hp1 HG02818.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.652-13387_652-1338 others(21): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91176134 | |||||
| chr8:91176134
|
A | ATATATAT others(12): Show |
1 | a0001c0001t0001g0057 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.652-13387_652-1338 others(23): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91176134 | |||||
| chr8:91176134
|
A | ATATATAT others(13): Show |
1 | a0001c0001t0001g0058 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.652-13387_652-1338 others(24): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91176134 | |||||
| chr8:91176134
|
A | ATATATTT others(3): Show |
1 | a0002c0002t0001g0092 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.652-13387_652-1338 others(14): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91176134 | |||||
| chr8:91176134
|
A | ATATATTT others(4): Show |
1 | a0002c0002t0001g0035 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.652-13387_652-1338 others(15): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91176134 | |||||
| chr8:91176134
|
A | ATATATTT others(5): Show |
11 | a0002c0002t0001g0055a0002c0002t0001g0060a0002c0002t0001g0062others(8): Show | 11 | HG00099.hp1 HG00639.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.652-13387_652-1338 others(16): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91176134 | |||||
| chr8:91176134
|
A | ATATATTT others(6): Show |
14 | a0002c0002t0001g0005a0002c0002t0001g0012a0002c0002t0001g0021others(11): Show | 15 | HG01934.hp1 HG02717.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.652-13387_652-1338 others(17): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91176134 | |||||
| chr8:91176134
|
A | ATATATTT others(7): Show |
1 | a0001c0001t0003g0178 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.652-13387_652-1338 others(18): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91176134 | |||||
| chr8:91176134
|
A | ATATATTT others(8): Show |
7 | a0001c0001t0001g0164a0001c0001t0001g0170a0001c0001t0001g0173others(4): Show | 7 | HG01106.hp1 HG01361.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.652-13387_652-1338 others(19): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91176134 | |||||
| chr8:91176134
|
A | ATATTTTT others(4): Show |
1 | a0002c0002t0001g0113 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.652-13387_652-1338 others(15): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91176134 | |||||
| chr8:91176134
|
A | ATATTTTT others(6): Show |
2 | a0002c0002t0001g0056a0002c0002t0001g0063 | 2 | HG01099.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.652-13387_652-1338 others(17): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91176134 | |||||
| chr8:91176134
|
A | ATATTTTT others(7): Show |
1 | a0001c0001t0001g0163 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.652-13387_652-1338 others(18): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91176134 | |||||
| chr8:91176134
|
A | T | 104 | a0001c0001t0001g0011a0001c0001t0001g0020a0001c0001t0001g0045others(101): Show | 104 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.652-13388A>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91176134 | ||||||
| chr8:91176212
|
A | G | 205 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(202): Show | 211 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.652-13310A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91176212 | ||||||
| chr8:91176226
|
C | G | 205 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(202): Show | 211 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.652-13296C>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91176226 | ||||||
| chr8:91176607
|
C | T | 28 | a0001c0001t0001g0001a0001c0001t0001g0164a0001c0001t0001g0170others(25): Show | 30 | HG00423.hp2 HG00558.hp2 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.652-12915C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91176607 | ||||||
| chr8:91176687
|
C | T | 205 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(202): Show | 211 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.652-12835C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91176687 | ||||||
| chr8:91176712
|
A | C | 205 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(202): Show | 211 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.652-12810A>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91176712 | ||||||
| chr8:91176713
|
G | C | 22 | a0001c0001t0001g0001a0001c0001t0001g0288a0001c0001t0001g0289others(19): Show | 24 | HG00423.hp2 HG00558.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.652-12809G>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91176713 | ||||||
| chr8:91176745
|
C | T | 1 | a0002c0006t0002g0154 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.652-12777C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91176745 | ||||||
| chr8:91176798
|
A | G | 1 | a0001c0001t0001g0059 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.652-12724A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91176798 | ||||||
| chr8:91176808
|
C | T | 9 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(6): Show | 9 | HG00735.hp2 HG01261.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.652-12714C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91176808 | ||||||
| chr8:91176877
|
TAATGTTA others(32): Show |
T | 9 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(6): Show | 9 | HG00735.hp2 HG01261.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.652-12642_652-1260 others(43): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91176877 | |||||
| chr8:91177163
|
A | G | 1 | a0002c0006t0002g0154 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.652-12359A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91177163 | ||||||
| chr8:91177279
|
T | G | 1 | a0002c0002t0001g0065 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.652-12243T>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91177279 | ||||||
| chr8:91177364
|
C | A | 17 | a0001c0001t0001g0059a0001c0001t0001g0276a0001c0001t0001g0278others(14): Show | 17 | HG02109.hp1 HG02145.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.652-12158C>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91177364 | ||||||
| chr8:91177408
|
CTATT | C | 18 | a0001c0001t0001g0276a0001c0001t0001g0278a0001c0001t0001g0279others(15): Show | 18 | HG00558.hp1 HG02109.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.652-12113_652-1211 others(8): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91177408 | ||||||
| chr8:91177673
|
A | G | 10 | a0001c0001t0001g0216a0001c0001t0001g0224a0001c0001t0001g0226others(7): Show | 10 | HG00423.hp1 HG00673.hp1 HG02148.hp1 others(7): Show |
intron_variant | MODIFIER | c.652-11849A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91177673 | ||||||
| chr8:91177677
|
T | C | 205 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(202): Show | 211 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.652-11845T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91177677 | ||||||
| chr8:91177772
|
A | T | 5 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(2): Show | 5 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.652-11750A>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91177772 | ||||||
| chr8:91177850
|
C | CT | 130 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(127): Show | 134 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.652-11656dupT | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91177850 | |||||
| chr8:91177850
|
C | CTT | 32 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(29): Show | 32 | HG00735.hp2 HG01069.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.652-11657_652-1165 others(6): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91177850 | |||||
| chr8:91177850
|
C | CTTT | 40 | a0001c0001t0001g0001a0001c0001t0001g0164a0001c0001t0001g0170others(37): Show | 42 | HG00423.hp2 HG00558.hp2 HG01081.hp1 others(39): Show |
intron_variant | MODIFIER | c.652-11658_652-1165 others(7): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91177850 | |||||
| chr8:91177883
|
G | C | 205 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(202): Show | 211 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.652-11639G>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91177883 | ||||||
| chr8:91177942
|
G | A | 205 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(202): Show | 211 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.652-11580G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91177942 | ||||||
| chr8:91178006
|
A | G | 205 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(202): Show | 211 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.652-11516A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91178006 | ||||||
| chr8:91178049
|
C | T | 205 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(202): Show | 211 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.652-11473C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91178049 | ||||||
| chr8:91178050
|
G | C | 3 | a0001c0001t0003g0178a0001c0001t0003g0179a0001c0001t0003g0180 | 3 | HG02818.hp1 HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.652-11472G>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91178050 | ||||||
| chr8:91178144
|
G | A | 205 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(202): Show | 211 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.652-11378G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91178144 | ||||||
| chr8:91178381
|
C | T | 205 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(202): Show | 211 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.652-11141C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91178381 | ||||||
| chr8:91178392
|
A | G | 2 | a0001c0001t0001g0223a0001c0001t0001g0254 | 2 | HG02040.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.652-11130A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91178392 | ||||||
| chr8:91178418
|
C | G | 1 | a0002c0002t0001g0134 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.652-11104C>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91178418 | ||||||
| chr8:91178604
|
G | C | 1 | a0001c0001t0001g0176 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.652-10918G>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91178604 | ||||||
| chr8:91178699
|
T | C | 1 | a0001c0001t0001g0163 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.652-10823T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91178699 | ||||||
| chr8:91178783
|
A | G | 205 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(202): Show | 211 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.652-10739A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91178783 | ||||||
| chr8:91178799
|
G | T | 28 | a0001c0001t0001g0001a0001c0001t0001g0164a0001c0001t0001g0170others(25): Show | 30 | HG00423.hp2 HG00558.hp2 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.652-10723G>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91178799 | ||||||
| chr8:91178809
|
G | T | 144 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(141): Show | 148 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.652-10713G>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91178809 | ||||||
| chr8:91178912
|
TGCTTTTT others(18): Show |
T | 1 | a0001c0001t0001g0213 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.652-10607_652-1058 others(29): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91178912 | |||||
| chr8:91179136
|
C | T | 1 | a0002c0002t0001g0108 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.652-10386C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91179136 | ||||||
| chr8:91179192
|
G | C | 1 | a0001c0001t0001g0306 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.652-10330G>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91179192 | ||||||
| chr8:91179279
|
G | T | 16 | a0001c0001t0001g0276a0001c0001t0001g0278a0001c0001t0001g0279others(13): Show | 16 | HG02109.hp1 HG02257.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.652-10243G>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91179279 | ||||||
| chr8:91179488
|
T | C | 1 | a0001c0001t0001g0006 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.652-10034T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91179488 | ||||||
| chr8:91179506
|
C | T | 205 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(202): Show | 211 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.652-10016C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91179506 | ||||||
| chr8:91179571
|
A | T | 205 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(202): Show | 211 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.652-9951A>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91179571 | ||||||
| chr8:91179573
|
C | T | 2 | a0001c0001t0001g0150a0002c0002t0001g0078 | 2 | HG01106.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.652-9949C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91179573 | ||||||
| chr8:91179574
|
T | G | 205 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(202): Show | 211 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.652-9948T>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91179574 | ||||||
| chr8:91179595
|
G | T | 205 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(202): Show | 211 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.652-9927G>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91179595 | ||||||
| chr8:91179663
|
T | A | 1 | a0001c0001t0001g0210 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.652-9859T>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91179663 | ||||||
| chr8:91179666
|
G | A | 2 | a0002c0002t0001g0085a0002c0002t0001g0091 | 2 | HG02602.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.652-9856G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91179666 | ||||||
| chr8:91179676
|
C | T | 130 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(127): Show | 134 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.652-9846C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91179676 | ||||||
| chr8:91179706
|
T | C | 1 | a0001c0001t0001g0008 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.652-9816T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91179706 | ||||||
| chr8:91179762
|
G | A | 205 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(202): Show | 211 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.652-9760G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91179762 | ||||||
| chr8:91179798
|
G | A | 1 | a0001c0001t0001g0304 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.652-9724G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91179798 | ||||||
| chr8:91179847
|
T | A | 205 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(202): Show | 211 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.652-9675T>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91179847 | ||||||
| chr8:91179868
|
A | T | 16 | a0001c0001t0001g0276a0001c0001t0001g0278a0001c0001t0001g0279others(13): Show | 16 | HG02109.hp1 HG02257.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.652-9654A>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91179868 | ||||||
| chr8:91179886
|
G | A | 6 | a0001c0001t0001g0164a0001c0001t0001g0170a0001c0001t0001g0173others(3): Show | 6 | HG02818.hp1 HG02976.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.652-9636G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91179886 | ||||||
| chr8:91179979
|
A | G | 8 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(5): Show | 8 | HG00735.hp2 HG02559.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.652-9543A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91179979 | ||||||
| chr8:91180271
|
A | G | 205 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(202): Show | 211 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.652-9251A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91180271 | ||||||
| chr8:91180299
|
T | C | 14 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(11): Show | 14 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.652-9223T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91180299 | ||||||
| chr8:91180396
|
C | A | 10 | a0001c0001t0001g0162a0001c0001t0001g0165a0001c0001t0001g0166others(7): Show | 10 | HG02145.hp1 HG02572.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.652-9126C>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91180396 | ||||||
| chr8:91180442
|
A | G | 9 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(6): Show | 9 | HG00735.hp2 HG01261.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.652-9080A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91180442 | ||||||
| chr8:91180477
|
GT | G | 205 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(202): Show | 211 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.652-9044delT | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91180477 | ||||||
| chr8:91180499
|
T | G | 1 | a0002c0002t0001g0027 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.652-9023T>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91180499 | ||||||
| chr8:91180638
|
T | C | 1 | a0002c0002t0001g0083 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.652-8884T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91180638 | ||||||
| chr8:91180642
|
C | CT | 14 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(11): Show | 14 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.652-8879dupT | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91180642 | |||||
| chr8:91180862
|
G | C | 16 | a0001c0001t0001g0276a0001c0001t0001g0278a0001c0001t0001g0279others(13): Show | 16 | HG02109.hp1 HG02257.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.652-8660G>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91180862 | ||||||
| chr8:91180875
|
A | G | 1 | a0002c0002t0001g0084 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.652-8647A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91180875 | ||||||
| chr8:91180955
|
A | G | 205 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(202): Show | 211 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.652-8567A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91180955 | ||||||
| chr8:91180984
|
GA | G | 16 | a0001c0001t0001g0162a0001c0001t0001g0165a0001c0001t0001g0166others(13): Show | 16 | HG01891.hp2 HG02145.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.652-8536delA | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91180984 | |||||
| chr8:91181071
|
A | G | 1 | a0002c0002t0001g0085 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.652-8451A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91181071 | ||||||
| chr8:91181105
|
A | T | 1 | a0002c0002t0001g0141 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.652-8417A>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91181105 | ||||||
| chr8:91181125
|
G | A | 205 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(202): Show | 211 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.652-8397G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91181125 | ||||||
| chr8:91181133
|
G | T | 205 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(202): Show | 211 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.652-8389G>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91181133 | ||||||
| chr8:91181482
|
C | T | 205 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(202): Show | 211 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.652-8040C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91181482 | ||||||
| chr8:91181523
|
A | G | 2 | a0002c0002t0001g0088a0002c0002t0001g0089 | 2 | HG03831.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.652-7999A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91181523 | ||||||
| chr8:91181590
|
C | T | 1 | a0001c0001t0001g0235 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.652-7932C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91181590 | ||||||
| chr8:91181626
|
G | C | 1 | a0001c0001t0001g0045 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.652-7896G>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91181626 | ||||||
| chr8:91182281
|
C | T | 4 | a0001c0001t0001g0168a0001c0001t0001g0212a0001c0001t0001g0214others(1): Show | 4 | HG02896.hp1 HG02897.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.652-7241C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91182281 | ||||||
| chr8:91183184
|
G | A | 1 | a0001c0001t0001g0304 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.652-6338G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91183184 | ||||||
| chr8:91183197
|
T | C | 1 | a0001c0001t0001g0168 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.652-6325T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91183197 | ||||||
| chr8:91183422
|
G | T | 1 | a0002c0002t0001g0065 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.652-6100G>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91183422 | ||||||
| chr8:91183554
|
G | C | 205 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(202): Show | 211 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.652-5968G>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91183554 | ||||||
| chr8:91183614
|
T | TA | 20 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(17): Show | 20 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(17): Show |
intron_variant | MODIFIER | c.652-5897dupA | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91183614 | |||||
| chr8:91183651
|
G | A | 4 | a0001c0001t0001g0203a0002c0002t0001g0002a0002c0002t0001g0022others(1): Show | 5 | HG02071.hp2 NA18960.hp1 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.652-5871G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91183651 | ||||||
| chr8:91183682
|
C | T | 2 | a0002c0002t0001g0122a0002c0002t0001g0123 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.652-5840C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91183682 | ||||||
| chr8:91183707
|
A | G | 1 | a0002c0002t0001g0035 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.652-5815A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91183707 | ||||||
| chr8:91183881
|
G | A | 1 | a0002c0002t0001g0136 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.652-5641G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91183881 | ||||||
| chr8:91183974
|
A | G | 1 | a0002c0002t0001g0064 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.652-5548A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91183974 | ||||||
| chr8:91184187
|
G | A | 5 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG00735.hp2 HG02615.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.652-5335G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91184187 | ||||||
| chr8:91184234
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.652-5288G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91184234 | ||||||
| chr8:91185125
|
A | G | 1 | a0001c0001t0001g0188 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.652-4397A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91185125 | ||||||
| chr8:91185150
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.652-4372C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91185150 | ||||||
| chr8:91185167
|
C | T | 1 | a0001c0001t0001g0235 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.652-4355C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91185167 | ||||||
| chr8:91185287
|
A | G | 1 | a0001c0001t0001g0221 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.652-4235A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91185287 | ||||||
| chr8:91185363
|
C | CTG | 157 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(154): Show | 161 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.652-4141_652-4140d others(4): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91185363 | |||||
| chr8:91185582
|
T | TG | 206 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(203): Show | 212 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.652-3940_652-3939i others(3): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91185582 | ||||||
| chr8:91185583
|
T | G | 206 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(203): Show | 212 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.652-3939T>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91185583 | ||||||
| chr8:91185763
|
C | G | 3 | a0002c0002t0001g0077a0002c0002t0001g0078a0002c0002t0001g0120 | 3 | HG00735.hp1 HG01106.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.652-3759C>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91185763 | ||||||
| chr8:91185786
|
C | G | 2 | a0002c0002t0001g0067a0002c0002t0001g0072 | 2 | HG01106.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.652-3736C>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91185786 | ||||||
| chr8:91185983
|
G | A | 205 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(202): Show | 211 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.652-3539G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91185983 | ||||||
| chr8:91186005
|
C | T | 1 | a0002c0002t0001g0077 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.652-3517C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91186005 | ||||||
| chr8:91186044
|
T | C | 8 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(5): Show | 8 | HG00735.hp2 HG02559.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.652-3478T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91186044 | ||||||
| chr8:91186341
|
A | T | 3 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0196 | 3 | HG00733.hp1 HG01433.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.652-3181A>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91186341 | ||||||
| chr8:91186458
|
C | A | 1 | a0002c0002t0001g0125 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.652-3064C>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91186458 | ||||||
| chr8:91186460
|
G | A | 1 | a0002c0002t0001g0125 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.652-3062G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91186460 | ||||||
| chr8:91186461
|
T | A | 1 | a0002c0002t0001g0125 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.652-3061T>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91186461 | ||||||
| chr8:91186525
|
T | G | 2 | a0002c0002t0001g0068a0002c0002t0001g0075 | 2 | HG03195.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.652-2997T>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91186525 | ||||||
| chr8:91186546
|
G | T | 2 | a0002c0002t0001g0053a0002c0002t0001g0054 | 2 | HG02015.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.652-2976G>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91186546 | ||||||
| chr8:91186720
|
G | T | 3 | a0001c0003t0001g0282a0001c0003t0001g0283a0001c0003t0001g0285 | 3 | HG01891.hp1 HG02818.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.652-2802G>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91186720 | ||||||
| chr8:91186778
|
C | T | 1 | a0001c0001t0001g0257 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.652-2744C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91186778 | ||||||
| chr8:91186882
|
T | C | 2 | a0002c0002t0001g0005a0002c0002t0001g0129 | 3 | HG02723.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.652-2640T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91186882 | ||||||
| chr8:91187006
|
G | A | 2 | a0002c0002t0001g0005a0002c0002t0001g0129 | 3 | HG02723.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.652-2516G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91187006 | ||||||
| chr8:91187104
|
G | A | 1 | a0001c0003t0001g0287 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.652-2418G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91187104 | ||||||
| chr8:91187548
|
C | T | 3 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0133 | 3 | HG02559.hp2 HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.652-1974C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91187548 | ||||||
| chr8:91187664
|
T | C | 198 | a0001c0001t0001g0001a0001c0001t0001g0115a0001c0001t0001g0116others(195): Show | 204 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.652-1858T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91187664 | ||||||
| chr8:91187671
|
T | C | 198 | a0001c0001t0001g0001a0001c0001t0001g0115a0001c0001t0001g0116others(195): Show | 204 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.652-1851T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91187671 | ||||||
| chr8:91187706
|
G | A | 1 | a0001c0001t0001g0248 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.652-1816G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91187706 | ||||||
| chr8:91187774
|
G | A | 210 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(207): Show | 216 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.652-1748G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91187774 | ||||||
| chr8:91187782
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.652-1740C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91187782 | ||||||
| chr8:91188007
|
TG | T | 13 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(10): Show | 13 | HG02109.hp1 HG02257.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.652-1513delG | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91188007 | |||||
| chr8:91188398
|
C | T | 10 | a0001c0001t0001g0162a0001c0001t0001g0166a0001c0001t0001g0167others(7): Show | 10 | HG02145.hp1 HG02572.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.652-1124C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91188398 | ||||||
| chr8:91188835
|
G | GT | 43 | a0001c0001t0001g0124a0001c0001t0001g0149a0001c0001t0001g0163others(40): Show | 43 | HG01261.hp2 HG01891.hp2 HG01934.hp2 others(40): Show |
intron_variant | MODIFIER | c.652-672dupT | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91188835 | |||||
| chr8:91188850
|
T | C | 13 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(10): Show | 13 | HG00735.hp2 HG01069.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.652-672T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91188850 | ||||||
| chr8:91188935
|
T | C | 198 | a0001c0001t0001g0001a0001c0001t0001g0115a0001c0001t0001g0116others(195): Show | 204 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.652-587T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91188935 | ||||||
| chr8:91188967
|
G | A | 13 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(10): Show | 13 | HG02109.hp1 HG02257.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.652-555G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91188967 | ||||||
| chr8:91189122
|
G | T | 1 | a0001c0001t0001g0147 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.652-400G>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | chr8 | 91189122 | ||||||
| chr8:91189369
|
ATTACT | A | 8 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(5): Show | 8 | HG00735.hp2 HG02559.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.652-149_652-145del others(5): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 91189369 | |||||
| chr8:91189680
|
A | G | 13 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(10): Show | 13 | HG02109.hp1 HG02257.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.753+57A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91189680 | ||||||
| chr8:91190062
|
A | G | 2 | a0001c0001t0001g0209a0001c0001t0001g0304 | 2 | HG01261.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.753+439A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91190062 | ||||||
| chr8:91190195
|
G | A | 1 | a0002c0002t0001g0083 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.753+572G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91190195 | ||||||
| chr8:91190268
|
GT | G | 7 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(4): Show | 7 | HG00735.hp2 HG01123.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.753+658delT | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr8 | 91190268 | |||||
| chr8:91190317
|
C | T | 6 | a0002c0002t0001g0086a0002c0002t0001g0087a0002c0002t0001g0095others(3): Show | 6 | HG01109.hp2 NA18961.hp1 NA18993.hp2 others(3): Show |
intron_variant | MODIFIER | c.753+694C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91190317 | ||||||
| chr8:91190383
|
G | A | 4 | a0001c0003t0001g0282a0001c0003t0001g0283a0001c0003t0001g0285others(1): Show | 4 | HG01891.hp1 HG02015.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.753+760G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91190383 | ||||||
| chr8:91190413
|
C | T | 138 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(135): Show | 142 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.753+790C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91190413 | ||||||
| chr8:91190464
|
A | G | 1 | a0001c0001t0001g0230 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.753+841A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91190464 | ||||||
| chr8:91190465
|
G | A | 1 | a0001c0001t0001g0230 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.753+842G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91190465 | ||||||
| chr8:91190899
|
T | C | 3 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257 | 3 | HG02004.hp1 NA18944.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.753+1276T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91190899 | ||||||
| chr8:91190931
|
C | T | 3 | a0001c0003t0001g0282a0001c0003t0001g0283a0001c0003t0001g0285 | 3 | HG01891.hp1 HG02818.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.753+1308C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91190931 | ||||||
| chr8:91191028
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.753+1405G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91191028 | ||||||
| chr8:91191041
|
A | AC | 33 | a0001c0001t0001g0121a0001c0001t0001g0162a0001c0001t0001g0166others(30): Show | 33 | HG00544.hp2 HG00609.hp1 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.753+1431dupC | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr8 | 91191041 | |||||
| chr8:91191041
|
AC | A | 142 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(139): Show | 146 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.753+1431delC | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr8 | 91191041 | |||||
| chr8:91191041
|
ACC | A | 16 | a0001c0001t0001g0059a0001c0001t0001g0143a0001c0001t0001g0144others(13): Show | 16 | HG00099.hp1 HG01884.hp1 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.753+1430_753+1431d others(4): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr8 | 91191041 | |||||
| chr8:91191044
|
C | G | 5 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0277others(2): Show | 5 | HG02257.hp2 HG02809.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.753+1421C>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91191044 | ||||||
| chr8:91191045
|
C | CA | 10 | a0001c0001t0001g0001a0001c0001t0001g0289a0001c0001t0001g0290others(7): Show | 12 | HG00423.hp2 HG00558.hp2 NA18942.hp2 others(9): Show |
intron_variant | MODIFIER | c.753+1422_753+1423i others(3): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91191045 | ||||||
| chr8:91191045
|
C | G | 10 | a0001c0001t0002g0157a0001c0001t0002g0158a0001c0001t0002g0159others(7): Show | 10 | HG02109.hp1 HG02559.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.753+1422C>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91191045 | ||||||
| chr8:91191045
|
C | T | 5 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(2): Show | 5 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.753+1422C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91191045 | ||||||
| chr8:91191046
|
C | A | 13 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(10): Show | 13 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.753+1423C>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91191046 | ||||||
| chr8:91191048
|
C | G | 1 | a0002c0002t0001g0104 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.753+1425C>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91191048 | ||||||
| chr8:91191049
|
C | T | 1 | a0001c0001t0001g0312 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.753+1426C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91191049 | ||||||
| chr8:91191051
|
C | A | 8 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(5): Show | 8 | HG00735.hp2 HG02559.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.753+1428C>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91191051 | ||||||
| chr8:91191051
|
C | G | 1 | a0001c0001t0001g0217 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.753+1428C>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91191051 | ||||||
| chr8:91191051
|
C | T | 5 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(2): Show | 5 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.753+1428C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91191051 | ||||||
| chr8:91191052
|
C | G | 36 | a0001c0001t0001g0249a0001c0001t0001g0260a0001c0001t0001g0266others(33): Show | 37 | HG00438.hp1 HG00544.hp1 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.753+1429C>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91191052 | ||||||
| chr8:91191286
|
A | G | 3 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186 | 3 | HG02886.hp1 HG02965.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.753+1663A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91191286 | ||||||
| chr8:91191292
|
T | C | 9 | a0001c0001t0001g0251a0002c0002t0001g0094a0002c0002t0001g0096others(6): Show | 9 | HG00741.hp1 HG01257.hp1 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.753+1669T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91191292 | ||||||
| chr8:91191410
|
T | G | 1 | a0002c0002t0001g0013 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.753+1787T>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91191410 | ||||||
| chr8:91191534
|
T | C | 138 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(135): Show | 142 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.753+1911T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91191534 | ||||||
| chr8:91191651
|
T | A | 1 | a0001c0001t0001g0279 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.753+2028T>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91191651 | ||||||
| chr8:91191842
|
T | A | 5 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(2): Show | 5 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.753+2219T>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91191842 | ||||||
| chr8:91191899
|
G | C | 16 | a0001c0001t0001g0001a0001c0001t0001g0182a0001c0001t0001g0288others(13): Show | 18 | HG00423.hp2 HG00558.hp2 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.753+2276G>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91191899 | ||||||
| chr8:91191921
|
T | G | 2 | a0002c0002t0001g0088a0002c0002t0001g0089 | 2 | HG03831.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.753+2298T>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91191921 | ||||||
| chr8:91191979
|
A | G | 13 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(10): Show | 13 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.753+2356A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91191979 | ||||||
| chr8:91191994
|
C | G | 13 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(10): Show | 13 | HG02109.hp1 HG02257.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.753+2371C>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91191994 | ||||||
| chr8:91191996
|
T | C | 1 | a0002c0002t0001g0207 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.753+2373T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91191996 | ||||||
| chr8:91192092
|
G | A | 1 | a0002c0002t0001g0094 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.753+2469G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91192092 | ||||||
| chr8:91192325
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.753+2702C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91192325 | ||||||
| chr8:91192393
|
T | C | 2 | a0001c0001t0001g0059a0002c0002t0001g0092 | 2 | HG00733.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.753+2770T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91192393 | ||||||
| chr8:91192488
|
C | T | 8 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(5): Show | 8 | HG00735.hp2 HG02559.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.753+2865C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91192488 | ||||||
| chr8:91192630
|
T | G | 3 | a0001c0003t0001g0282a0001c0003t0001g0283a0001c0003t0001g0285 | 3 | HG01891.hp1 HG02818.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.753+3007T>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91192630 | ||||||
| chr8:91192682
|
T | C | 1 | a0001c0001t0001g0163 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.753+3059T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91192682 | ||||||
| chr8:91192696
|
T | C | 2 | a0002c0002t0001g0111a0002c0002t0001g0112 | 2 | HG00099.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.753+3073T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91192696 | ||||||
| chr8:91192738
|
G | A | 8 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(5): Show | 8 | HG00735.hp2 HG02559.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.753+3115G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91192738 | ||||||
| chr8:91192755
|
T | C | 210 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(207): Show | 216 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.753+3132T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91192755 | ||||||
| chr8:91192813
|
A | G | 104 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(101): Show | 107 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.753+3190A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91192813 | ||||||
| chr8:91193047
|
G | C | 13 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(10): Show | 13 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.753+3424G>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91193047 | ||||||
| chr8:91193054
|
C | T | 3 | a0001c0003t0001g0282a0001c0003t0001g0283a0001c0003t0001g0285 | 3 | HG01891.hp1 HG02818.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.753+3431C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91193054 | ||||||
| chr8:91193169
|
G | A | 21 | a0001c0001t0001g0001a0001c0001t0001g0163a0001c0001t0001g0182others(18): Show | 23 | HG00423.hp2 HG00558.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.753+3546G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91193169 | ||||||
| chr8:91193230
|
A | G | 6 | a0001c0001t0001g0164a0001c0001t0001g0170a0001c0001t0001g0173others(3): Show | 6 | HG02818.hp1 HG02976.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.753+3607A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91193230 | ||||||
| chr8:91193261
|
T | C | 13 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(10): Show | 13 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.753+3638T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91193261 | ||||||
| chr8:91193297
|
G | T | 1 | a0002c0002t0001g0082 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.753+3674G>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91193297 | ||||||
| chr8:91193446
|
C | A | 5 | a0001c0001t0001g0267a0001c0001t0001g0268a0001c0001t0001g0269others(2): Show | 5 | NA18945.hp1 NA18954.hp2 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.753+3823C>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91193446 | ||||||
| chr8:91193463
|
A | C | 34 | a0001c0001t0001g0249a0001c0001t0001g0260a0002c0002t0001g0003others(31): Show | 35 | HG00438.hp1 HG00544.hp1 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.753+3840A>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91193463 | ||||||
| chr8:91193476
|
A | G | 1 | a0001c0001t0001g0307 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.753+3853A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91193476 | ||||||
| chr8:91193558
|
C | T | 99 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(96): Show | 102 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.753+3935C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91193558 | ||||||
| chr8:91193562
|
A | C | 1 | a0001c0001t0001g0253 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.753+3939A>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91193562 | ||||||
| chr8:91193564
|
A | G | 13 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(10): Show | 13 | HG02109.hp1 HG02257.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.753+3941A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91193564 | ||||||
| chr8:91193564
|
A | T | 4 | a0001c0001t0001g0011a0001c0001t0001g0237a0001c0001t0001g0243others(1): Show | 4 | HG00639.hp2 HG01123.hp2 NA20805.hp1 others(1): Show |
intron_variant | MODIFIER | c.753+3941A>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91193564 | ||||||
| chr8:91193572
|
T | A | 1 | a0001c0001t0001g0230 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.753+3949T>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91193572 | ||||||
| chr8:91193575
|
G | T | 1 | a0001c0001t0001g0230 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.753+3952G>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91193575 | ||||||
| chr8:91193651
|
T | A | 1 | a0001c0001t0001g0230 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.753+4028T>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91193651 | ||||||
| chr8:91193652
|
C | G | 5 | a0001c0001t0001g0267a0001c0001t0001g0268a0001c0001t0001g0269others(2): Show | 5 | NA18945.hp1 NA18954.hp2 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.753+4029C>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91193652 | ||||||
| chr8:91193869
|
G | C | 2 | a0001c0001t0001g0209a0001c0001t0001g0304 | 2 | HG01261.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.753+4246G>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91193869 | ||||||
| chr8:91193946
|
T | C | 13 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(10): Show | 13 | HG02109.hp1 HG02257.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.753+4323T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91193946 | ||||||
| chr8:91194013
|
A | G | 3 | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0001t0001g0152 | 3 | HG01884.hp1 HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.753+4390A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91194013 | ||||||
| chr8:91194107
|
C | CAT | 311 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(308): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.753+4484_753+4485i others(4): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91194107 | ||||||
| chr8:91194146
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.753+4523C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91194146 | ||||||
| chr8:91194160
|
C | T | 1 | a0001c0001t0001g0191 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.753+4537C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91194160 | ||||||
| chr8:91194204
|
A | T | 6 | a0001c0001t0001g0164a0001c0001t0001g0170a0001c0001t0001g0173others(3): Show | 6 | HG02818.hp1 HG02976.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.753+4581A>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91194204 | ||||||
| chr8:91194213
|
G | A | 6 | a0001c0001t0001g0164a0001c0001t0001g0170a0001c0001t0001g0173others(3): Show | 6 | HG02818.hp1 HG02976.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.753+4590G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91194213 | ||||||
| chr8:91194241
|
C | T | 2 | a0001c0001t0001g0045a0001c0001t0001g0047 | 2 | HG00438.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.753+4618C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91194241 | ||||||
| chr8:91194259
|
T | C | 3 | a0001c0003t0001g0282a0001c0003t0001g0283a0001c0003t0001g0285 | 3 | HG01891.hp1 HG02818.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.753+4636T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91194259 | ||||||
| chr8:91194330
|
A | C | 3 | a0001c0003t0001g0282a0001c0003t0001g0283a0001c0003t0001g0285 | 3 | HG01891.hp1 HG02818.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.753+4707A>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91194330 | ||||||
| chr8:91194375
|
G | T | 8 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(5): Show | 8 | HG00735.hp2 HG02559.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.753+4752G>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91194375 | ||||||
| chr8:91194383
|
T | C | 3 | a0001c0003t0001g0282a0001c0003t0001g0283a0001c0003t0001g0285 | 3 | HG01891.hp1 HG02818.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.753+4760T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91194383 | ||||||
| chr8:91194386
|
A | C | 3 | a0001c0003t0001g0282a0001c0003t0001g0283a0001c0003t0001g0285 | 3 | HG01891.hp1 HG02818.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.753+4763A>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91194386 | ||||||
| chr8:91194389
|
G | T | 3 | a0001c0003t0001g0282a0001c0003t0001g0283a0001c0003t0001g0285 | 3 | HG01891.hp1 HG02818.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.753+4766G>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91194389 | ||||||
| chr8:91194392
|
T | C | 3 | a0001c0003t0001g0282a0001c0003t0001g0283a0001c0003t0001g0285 | 3 | HG01891.hp1 HG02818.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.753+4769T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91194392 | ||||||
| chr8:91194590
|
C | T | 13 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(10): Show | 13 | HG02109.hp1 HG02257.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.753+4967C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91194590 | ||||||
| chr8:91194626
|
T | A | 1 | a0001c0001t0001g0163 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.753+5003T>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91194626 | ||||||
| chr8:91194701
|
T | A | 1 | a0001c0001t0001g0059 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.753+5078T>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91194701 | ||||||
| chr8:91194701
|
T | C | 13 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(10): Show | 13 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.753+5078T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91194701 | ||||||
| chr8:91194716
|
C | T | 1 | a0001c0003t0001g0285 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.753+5093C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91194716 | ||||||
| chr8:91194767
|
T | A | 2 | a0001c0001t0001g0166a0001c0001t0001g0194 | 2 | HG01934.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.753+5144T>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91194767 | ||||||
| chr8:91194831
|
G | C | 1 | a0001c0001t0001g0303 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.753+5208G>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91194831 | ||||||
| chr8:91194838
|
T | A | 1 | a0001c0001t0001g0306 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.753+5215T>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91194838 | ||||||
| chr8:91194926
|
T | C | 13 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(10): Show | 13 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.753+5303T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91194926 | ||||||
| chr8:91194935
|
T | G | 2 | a0001c0001t0001g0221a0002c0002t0001g0032 | 2 | NA18962.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.753+5312T>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91194935 | ||||||
| chr8:91194966
|
G | C | 13 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(10): Show | 13 | HG02109.hp1 HG02257.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.753+5343G>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91194966 | ||||||
| chr8:91195206
|
A | G | 8 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(5): Show | 8 | HG00735.hp2 HG02559.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.754-5407A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91195206 | ||||||
| chr8:91195209
|
T | C | 8 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(5): Show | 8 | HG00735.hp2 HG02559.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.754-5404T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91195209 | ||||||
| chr8:91195227
|
G | T | 1 | a0002c0002t0001g0028 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.754-5386G>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91195227 | ||||||
| chr8:91195285
|
AGGTGT | A | 3 | a0001c0003t0001g0282a0001c0003t0001g0283a0001c0003t0001g0285 | 3 | HG01891.hp1 HG02818.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.754-5318_754-5314d others(7): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr8 | 91195285 | |||||
| chr8:91195338
|
G | A | 30 | a0001c0001t0001g0249a0001c0001t0001g0260a0002c0002t0001g0003others(27): Show | 31 | HG00438.hp1 HG00544.hp1 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.754-5275G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91195338 | ||||||
| chr8:91195361
|
C | T | 8 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(5): Show | 8 | HG00735.hp2 HG02559.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.754-5252C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91195361 | ||||||
| chr8:91195372
|
G | C | 1 | a0001c0001t0001g0262 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.754-5241G>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91195372 | ||||||
| chr8:91195429
|
A | G | 1 | a0001c0001t0001g0059 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.754-5184A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91195429 | ||||||
| chr8:91195502
|
G | C | 1 | a0002c0002t0001g0037 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.754-5111G>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91195502 | ||||||
| chr8:91195502
|
G | T | 16 | a0001c0001t0001g0001a0001c0001t0001g0182a0001c0001t0001g0288others(13): Show | 18 | HG00423.hp2 HG00558.hp2 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.754-5111G>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91195502 | ||||||
| chr8:91195634
|
A | C | 1 | a0001c0001t0001g0215 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.754-4979A>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91195634 | ||||||
| chr8:91195664
|
A | C | 1 | a0001c0001t0001g0303 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.754-4949A>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91195664 | ||||||
| chr8:91195775
|
T | A | 151 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(148): Show | 155 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.754-4838T>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91195775 | ||||||
| chr8:91195828
|
C | G | 34 | a0001c0001t0001g0249a0001c0001t0001g0260a0002c0002t0001g0003others(31): Show | 35 | HG00438.hp1 HG00544.hp1 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.754-4785C>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91195828 | ||||||
| chr8:91195953
|
A | G | 1 | a0001c0001t0002g0160 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.754-4660A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91195953 | ||||||
| chr8:91195974
|
G | A | 3 | a0001c0001t0001g0224a0001c0001t0001g0242a0001c0001t0001g0258 | 3 | HG00423.hp1 NA18942.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.754-4639G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91195974 | ||||||
| chr8:91196105
|
G | A | 151 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(148): Show | 155 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.754-4508G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91196105 | ||||||
| chr8:91196202
|
C | G | 2 | a0001c0001t0001g0059a0002c0002t0001g0127 | 2 | HG02145.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.754-4411C>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91196202 | ||||||
| chr8:91196204
|
C | T | 9 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(6): Show | 9 | HG01099.hp2 HG02622.hp2 HG03130.hp1 others(6): Show |
intron_variant | MODIFIER | c.754-4409C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91196204 | ||||||
| chr8:91196213
|
T | C | 1 | a0001c0001t0001g0059 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.754-4400T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91196213 | ||||||
| chr8:91196234
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.754-4379C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91196234 | ||||||
| chr8:91196296
|
G | C | 20 | a0001c0001t0001g0059a0001c0001t0001g0143a0001c0001t0001g0144others(17): Show | 20 | HG00438.hp1 HG01069.hp1 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.754-4317G>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91196296 | ||||||
| chr8:91196355
|
T | G | 27 | a0001c0001t0001g0001a0001c0001t0001g0059a0001c0001t0001g0164others(24): Show | 29 | HG00423.hp2 HG00558.hp2 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.754-4258T>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91196355 | ||||||
| chr8:91196357
|
T | C | 1 | a0001c0001t0001g0059 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.754-4256T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91196357 | ||||||
| chr8:91196485
|
G | T | 2 | a0001c0001t0001g0224a0001c0001t0001g0242 | 2 | HG00423.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.754-4128G>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91196485 | ||||||
| chr8:91196490
|
C | T | 1 | a0002c0002t0001g0118 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.754-4123C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91196490 | ||||||
| chr8:91196606
|
C | T | 3 | a0002c0002t0001g0038a0002c0002t0001g0039a0002c0002t0001g0043 | 3 | HG01070.hp2 HG01109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.754-4007C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91196606 | ||||||
| chr8:91196607
|
G | A | 1 | a0002c0002t0001g0102 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.754-4006G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91196607 | ||||||
| chr8:91196631
|
T | C | 1 | a0001c0001t0001g0059 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.754-3982T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91196631 | ||||||
| chr8:91196821
|
G | A | 13 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(10): Show | 13 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.754-3792G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91196821 | ||||||
| chr8:91197063
|
C | G | 2 | a0002c0002t0001g0017a0002c0002t0001g0018 | 2 | NA18970.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.754-3550C>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91197063 | ||||||
| chr8:91197100
|
G | C | 99 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(96): Show | 102 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.754-3513G>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91197100 | ||||||
| chr8:91197192
|
C | T | 1 | a0001c0001t0001g0306 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.754-3421C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91197192 | ||||||
| chr8:91197214
|
C | T | 1 | a0001c0001t0001g0306 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.754-3399C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91197214 | ||||||
| chr8:91197225
|
A | G | 1 | a0001c0001t0001g0306 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.754-3388A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91197225 | ||||||
| chr8:91197227
|
A | T | 1 | a0001c0001t0001g0306 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.754-3386A>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91197227 | ||||||
| chr8:91197368
|
A | G | 1 | a0002c0002t0001g0094 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.754-3245A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91197368 | ||||||
| chr8:91197386
|
C | T | 1 | a0001c0001t0001g0249 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.754-3227C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91197386 | ||||||
| chr8:91197406
|
T | G | 1 | a0002c0002t0001g0108 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.754-3207T>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91197406 | ||||||
| chr8:91197416
|
C | G | 211 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(208): Show | 217 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.754-3197C>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91197416 | ||||||
| chr8:91197446
|
C | T | 208 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(205): Show | 214 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(211): Show |
intron_variant | MODIFIER | c.754-3167C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91197446 | ||||||
| chr8:91197450
|
C | T | 208 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(205): Show | 214 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(211): Show |
intron_variant | MODIFIER | c.754-3163C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91197450 | ||||||
| chr8:91197451
|
G | A | 1 | a0001c0001t0001g0162 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.754-3162G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91197451 | ||||||
| chr8:91197452
|
C | T | 7 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(4): Show | 7 | HG02622.hp2 HG03130.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.754-3161C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91197452 | ||||||
| chr8:91197455
|
C | T | 5 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(2): Show | 5 | HG01070.hp1 HG01071.hp2 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.754-3158C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91197455 | ||||||
| chr8:91197491
|
C | T | 8 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(5): Show | 8 | HG00735.hp2 HG02559.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.754-3122C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91197491 | ||||||
| chr8:91197597
|
C | G | 2 | a0001c0001t0001g0217a0001c0001t0001g0222 | 2 | HG01433.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.754-3016C>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91197597 | ||||||
| chr8:91197611
|
T | C | 5 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(2): Show | 5 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.754-3002T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91197611 | ||||||
| chr8:91197689
|
A | G | 5 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(2): Show | 5 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.754-2924A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91197689 | ||||||
| chr8:91197798
|
C | T | 1 | a0002c0002t0001g0125 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.754-2815C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91197798 | ||||||
| chr8:91197799
|
G | A | 5 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(2): Show | 5 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.754-2814G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91197799 | ||||||
| chr8:91197811
|
G | A | 5 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(2): Show | 5 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.754-2802G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91197811 | ||||||
| chr8:91197854
|
A | G | 1 | a0001c0001t0001g0189 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.754-2759A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91197854 | ||||||
| chr8:91198018
|
T | A | 101 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(98): Show | 104 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.754-2595T>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91198018 | ||||||
| chr8:91198194
|
A | G | 1 | a0001c0001t0001g0300 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.754-2419A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91198194 | ||||||
| chr8:91198294
|
T | G | 101 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(98): Show | 104 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.754-2319T>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91198294 | ||||||
| chr8:91198536
|
T | C | 2 | a0001c0001t0001g0209a0001c0001t0001g0304 | 2 | HG01261.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.754-2077T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91198536 | ||||||
| chr8:91198555
|
ATAATT | A | 4 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(1): Show | 4 | HG01074.hp2 HG01516.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.754-2053_754-2049d others(7): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr8 | 91198555 | |||||
| chr8:91198577
|
A | ATAAG | 210 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(207): Show | 216 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.754-2035_754-2032d others(6): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr8 | 91198577 | |||||
| chr8:91198577
|
A | G | 1 | a0002c0002t0001g0026 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.754-2036A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91198577 | ||||||
| chr8:91198660
|
A | G | 19 | a0001c0001t0001g0001a0001c0001t0001g0288a0001c0001t0001g0289others(16): Show | 21 | HG00423.hp2 HG00558.hp2 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.754-1953A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91198660 | ||||||
| chr8:91198865
|
A | G | 1 | a0001c0001t0001g0164 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.754-1748A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91198865 | ||||||
| chr8:91199086
|
G | A | 208 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(205): Show | 214 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(211): Show |
intron_variant | MODIFIER | c.754-1527G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91199086 | ||||||
| chr8:91199123
|
A | C | 2 | a0001c0001t0002g0277a0001c0001t0002g0281 | 2 | HG02257.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.754-1490A>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91199123 | ||||||
| chr8:91199142
|
A | G | 13 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(10): Show | 13 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.754-1471A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91199142 | ||||||
| chr8:91199327
|
G | A | 4 | a0001c0001t0001g0276a0001c0001t0001g0278a0001c0001t0001g0279others(1): Show | 4 | HG02970.hp2 HG03471.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.754-1286G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91199327 | ||||||
| chr8:91199469
|
A | G | 13 | a0002c0002t0001g0004a0002c0002t0001g0056a0002c0002t0001g0064others(10): Show | 14 | HG00408.hp2 HG00558.hp1 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.754-1144A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91199469 | ||||||
| chr8:91199522
|
AAAATT | A | 15 | a0001c0001t0001g0001a0001c0001t0001g0288a0001c0001t0001g0289others(12): Show | 17 | HG00423.hp2 HG00558.hp2 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.754-1083_754-1079d others(7): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr8 | 91199522 | |||||
| chr8:91199882
|
C | G | 6 | a0001c0001t0001g0164a0001c0001t0001g0170a0001c0001t0001g0173others(3): Show | 6 | HG02818.hp1 HG02976.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.754-731C>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91199882 | ||||||
| chr8:91199898
|
C | G | 34 | a0001c0001t0001g0249a0001c0001t0001g0260a0002c0002t0001g0003others(31): Show | 35 | HG00438.hp1 HG00544.hp1 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.754-715C>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91199898 | ||||||
| chr8:91200153
|
A | G | 3 | a0001c0003t0001g0282a0001c0003t0001g0283a0001c0003t0001g0285 | 3 | HG01891.hp1 HG02818.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.754-460A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91200153 | ||||||
| chr8:91200437
|
A | G | 13 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(10): Show | 13 | HG02109.hp1 HG02257.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.754-176A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 6/7 | chr8 | 91200437 | ||||||
| chr8:91200794
|
T | A | 2 | a0001c0001t0001g0194a0001c0001t0001g0196 | 2 | HG00733.hp1 HG01934.hp2 |
splice_donor_variant&intron_variant | HIGH | c.933+2T>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91200794 | ||||||
| chr8:91200799
|
G | T | 1 | a0001c0001t0001g0143 | 1 | HG03195.hp1 | splice_region_variant&intron_variant | LOW | c.933+7G>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91200799 | ||||||
| chr8:91201094
|
T | G | 3 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202 | 3 | HG01074.hp2 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.933+302T>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91201094 | ||||||
| chr8:91201208
|
G | A | 35 | a0001c0001t0001g0249a0001c0001t0001g0260a0002c0002t0001g0003others(32): Show | 36 | HG00438.hp1 HG00544.hp1 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.933+416G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91201208 | ||||||
| chr8:91201393
|
T | C | 8 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(5): Show | 8 | HG00735.hp2 HG02559.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.933+601T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91201393 | ||||||
| chr8:91201514
|
A | AT | 169 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(166): Show | 173 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.933+731dupT | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 91201514 | |||||
| chr8:91201514
|
A | ATT | 38 | a0001c0001t0001g0001a0001c0001t0001g0164a0001c0001t0001g0170others(35): Show | 40 | HG00423.hp2 HG00558.hp2 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.933+730_933+731dup others(2): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 91201514 | |||||
| chr8:91201599
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.933+807G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91201599 | ||||||
| chr8:91201759
|
C | G | 5 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(2): Show | 5 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.933+967C>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91201759 | ||||||
| chr8:91202193
|
G | A | 1 | a0001c0001t0001g0238 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.933+1401G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91202193 | ||||||
| chr8:91202204
|
TAAAACA | T | 8 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(5): Show | 8 | HG00735.hp2 HG02559.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.933+1437_933+1442d others(8): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 91202204 | |||||
| chr8:91202233
|
CACA | C | 13 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(10): Show | 13 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.933+1446_933+1448d others(5): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 91202233 | |||||
| chr8:91202235
|
CAACA | C | 4 | a0001c0001t0001g0304a0002c0002t0001g0032a0002c0002t0001g0036others(1): Show | 4 | HG01261.hp2 NA18962.hp1 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.933+1458_933+1461d others(6): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 91202235 | |||||
| chr8:91202302
|
T | G | 3 | a0001c0003t0001g0282a0001c0003t0001g0283a0001c0003t0001g0285 | 3 | HG01891.hp1 HG02818.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.933+1510T>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91202302 | ||||||
| chr8:91202311
|
G | A | 1 | a0001c0001t0001g0307 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.933+1519G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91202311 | ||||||
| chr8:91202392
|
A | G | 1 | a0001c0001t0001g0266 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.933+1600A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91202392 | ||||||
| chr8:91202660
|
G | A | 2 | a0002c0002t0001g0122a0002c0002t0001g0123 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.933+1868G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91202660 | ||||||
| chr8:91202661
|
T | C | 1 | a0001c0001t0001g0007 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.933+1869T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91202661 | ||||||
| chr8:91202700
|
A | T | 9 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047others(6): Show | 9 | HG00438.hp2 HG00544.hp2 NA18961.hp2 others(6): Show |
intron_variant | MODIFIER | c.933+1908A>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91202700 | ||||||
| chr8:91202843
|
G | A | 3 | a0001c0003t0001g0282a0001c0003t0001g0283a0001c0003t0001g0285 | 3 | HG01891.hp1 HG02818.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.933+2051G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91202843 | ||||||
| chr8:91203359
|
G | A | 3 | a0001c0003t0001g0282a0001c0003t0001g0283a0001c0003t0001g0285 | 3 | HG01891.hp1 HG02818.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.933+2567G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91203359 | ||||||
| chr8:91203390
|
C | CT | 13 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(10): Show | 13 | HG02109.hp1 HG02257.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.933+2611dupT | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 91203390 | |||||
| chr8:91203678
|
C | T | 1 | a0001c0001t0001g0246 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.933+2886C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91203678 | ||||||
| chr8:91203695
|
A | G | 212 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(209): Show | 218 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.933+2903A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91203695 | ||||||
| chr8:91203706
|
A | G | 35 | a0001c0001t0001g0249a0001c0001t0001g0260a0001c0001t0001g0266others(32): Show | 36 | HG00438.hp1 HG00544.hp1 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.933+2914A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91203706 | ||||||
| chr8:91203821
|
T | C | 3 | a0001c0003t0001g0282a0001c0003t0001g0283a0001c0003t0001g0285 | 3 | HG01891.hp1 HG02818.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.933+3029T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91203821 | ||||||
| chr8:91203847
|
C | T | 1 | a0001c0001t0001g0006 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.933+3055C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91203847 | ||||||
| chr8:91203857
|
C | T | 1 | a0002c0002t0001g0100 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.933+3065C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91203857 | ||||||
| chr8:91203894
|
C | T | 5 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(2): Show | 5 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.933+3102C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91203894 | ||||||
| chr8:91203901
|
CGAGGTCA others(9): Show |
C | 3 | a0002c0002t0001g0055a0002c0002t0001g0065a0002c0002t0001g0074 | 3 | HG02622.hp1 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.933+3112_933+3127d others(18): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 91203901 | |||||
| chr8:91203947
|
G | A | 5 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(2): Show | 5 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.933+3155G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91203947 | ||||||
| chr8:91204036
|
G | T | 1 | a0001c0001t0001g0224 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.933+3244G>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91204036 | ||||||
| chr8:91204121
|
C | CA | 8 | a0001c0001t0001g0162a0001c0001t0001g0166a0001c0001t0001g0231others(5): Show | 8 | HG00639.hp2 HG00735.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.933+3349dupA | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 91204121 | |||||
| chr8:91204121
|
CA | C | 15 | a0001c0001t0001g0165a0001c0001t0001g0176a0001c0001t0001g0210others(12): Show | 15 | HG01069.hp1 HG01070.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.933+3349delA | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 91204121 | |||||
| chr8:91204588
|
C | A | 1 | a0001c0001t0001g0304 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.933+3796C>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91204588 | ||||||
| chr8:91204837
|
C | A | 2 | a0001c0001t0001g0195a0001c0001t0001g0199 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.933+4045C>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91204837 | ||||||
| chr8:91204976
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.933+4184G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91204976 | ||||||
| chr8:91205137
|
C | T | 1 | a0001c0003t0001g0283 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.933+4345C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91205137 | ||||||
| chr8:91205340
|
C | T | 10 | a0001c0001t0001g0162a0001c0001t0001g0166a0001c0001t0001g0167others(7): Show | 10 | HG02145.hp1 HG02572.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.933+4548C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91205340 | ||||||
| chr8:91205525
|
G | A | 2 | a0001c0001t0001g0209a0001c0001t0001g0304 | 2 | HG01261.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.933+4733G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91205525 | ||||||
| chr8:91205534
|
G | T | 13 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(10): Show | 13 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.933+4742G>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91205534 | ||||||
| chr8:91205901
|
T | G | 10 | a0002c0002t0001g0060a0002c0002t0001g0062a0002c0002t0001g0084others(7): Show | 10 | HG00099.hp1 HG00639.hp1 HG00733.hp2 others(7): Show |
intron_variant | MODIFIER | c.933+5109T>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91205901 | ||||||
| chr8:91206388
|
G | A | 5 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(2): Show | 5 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.933+5596G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91206388 | ||||||
| chr8:91206404
|
T | C | 1 | a0001c0001t0001g0052 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.933+5612T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91206404 | ||||||
| chr8:91206455
|
C | T | 13 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(10): Show | 13 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.933+5663C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91206455 | ||||||
| chr8:91206456
|
A | G | 13 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(10): Show | 13 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.933+5664A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91206456 | ||||||
| chr8:91206486
|
A | G | 13 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(10): Show | 13 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.933+5694A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91206486 | ||||||
| chr8:91206548
|
C | T | 209 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(206): Show | 215 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.933+5756C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91206548 | ||||||
| chr8:91206617
|
T | A | 1 | a0001c0001t0001g0163 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.933+5825T>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91206617 | ||||||
| chr8:91206893
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.933+6101G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91206893 | ||||||
| chr8:91207035
|
T | C | 4 | a0001c0001t0001g0276a0001c0001t0001g0278a0001c0001t0001g0279others(1): Show | 4 | HG02970.hp2 HG03471.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.933+6243T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91207035 | ||||||
| chr8:91207336
|
T | A | 3 | a0002c0002t0001g0077a0002c0002t0001g0078a0002c0002t0001g0120 | 3 | HG00735.hp1 HG01106.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.933+6544T>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91207336 | ||||||
| chr8:91207514
|
T | A | 1 | a0001c0001t0001g0153 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.933+6722T>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91207514 | ||||||
| chr8:91207769
|
A | G | 1 | a0001c0001t0001g0163 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.933+6977A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91207769 | ||||||
| chr8:91208897
|
G | A | 3 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186 | 3 | HG02886.hp1 HG02965.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.933+8105G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91208897 | ||||||
| chr8:91209192
|
C | T | 1 | a0002c0002t0001g0311 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.933+8400C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91209192 | ||||||
| chr8:91209268
|
AAC | A | 35 | a0001c0001t0001g0249a0001c0001t0001g0260a0001c0001t0001g0266others(32): Show | 36 | HG00438.hp1 HG00544.hp1 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.933+8480_933+8481d others(4): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 91209268 | |||||
| chr8:91209381
|
G | A | 13 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(10): Show | 13 | HG02109.hp1 HG02257.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.933+8589G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91209381 | ||||||
| chr8:91209423
|
G | A | 5 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(2): Show | 5 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.933+8631G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91209423 | ||||||
| chr8:91209437
|
CAATA | C | 206 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(203): Show | 212 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.933+8676_933+8679d others(6): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 91209437 | |||||
| chr8:91209605
|
G | A | 1 | a0002c0002t0001g0082 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.933+8813G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91209605 | ||||||
| chr8:91209756
|
T | A | 1 | a0002c0002t0001g0089 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.933+8964T>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91209756 | ||||||
| chr8:91209912
|
T | C | 1 | a0002c0002t0001g0017 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.934-8978T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91209912 | ||||||
| chr8:91210034
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.934-8856C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91210034 | ||||||
| chr8:91210055
|
A | G | 233 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(230): Show | 239 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.934-8835A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91210055 | ||||||
| chr8:91210221
|
T | C | 6 | a0001c0001t0001g0164a0001c0001t0001g0170a0001c0001t0001g0173others(3): Show | 6 | HG02818.hp1 HG02976.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.934-8669T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91210221 | ||||||
| chr8:91210536
|
T | G | 2 | a0001c0001t0001g0231a0001c0001t0001g0236 | 2 | NA18949.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.934-8354T>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91210536 | ||||||
| chr8:91210562
|
G | GAC | 15 | a0001c0001t0001g0057a0001c0001t0001g0184a0001c0001t0001g0185others(12): Show | 16 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(13): Show |
intron_variant | MODIFIER | c.934-8296_934-8295d others(4): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 91210562 | |||||
| chr8:91210562
|
G | GACAC | 20 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(17): Show | 20 | HG00735.hp2 HG01884.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.934-8298_934-8295d others(6): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 91210562 | |||||
| chr8:91210562
|
G | GACACAC | 6 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0276others(3): Show | 6 | HG02922.hp1 HG02970.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.934-8300_934-8295d others(8): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 91210562 | |||||
| chr8:91210562
|
G | GACACACA others(3): Show |
17 | a0001c0001t0001g0001a0001c0001t0001g0164a0001c0001t0001g0170others(14): Show | 19 | HG00423.hp2 HG00558.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.934-8304_934-8295d others(12): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 91210562 | |||||
| chr8:91210562
|
G | GACACACA others(5): Show |
5 | a0001c0001t0001g0182a0001c0001t0001g0288a0001c0001t0001g0293others(2): Show | 5 | HG02895.hp1 NA18966.hp2 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.934-8306_934-8295d others(14): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 91210562 | |||||
| chr8:91210562
|
G | GACACACA others(7): Show |
3 | a0001c0003t0001g0286a0001c0003t0001g0287a0001c0003t0001g0302 | 3 | HG01081.hp1 HG02486.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.934-8308_934-8295d others(16): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 91210562 | |||||
| chr8:91210562
|
G | GACACACA others(9): Show |
1 | a0001c0003t0001g0284 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.934-8310_934-8295d others(18): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 91210562 | |||||
| chr8:91210562
|
GAC | G | 3 | a0001c0001t0001g0168a0001c0001t0001g0172a0001c0001t0001g0228 | 3 | HG02723.hp1 HG03490.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.934-8296_934-8295d others(4): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 91210562 | |||||
| chr8:91210562
|
GACAC | G | 4 | a0001c0001t0001g0174a0002c0002t0001g0136a0002c0002t0001g0137others(1): Show | 4 | HG00544.hp1 HG00609.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.934-8298_934-8295d others(6): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 91210562 | |||||
| chr8:91210562
|
GACACAC | G | 10 | a0001c0001t0001g0162a0001c0001t0001g0166a0001c0001t0001g0167others(7): Show | 10 | HG01261.hp2 HG01891.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.934-8300_934-8295d others(8): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 91210562 | |||||
| chr8:91210562
|
GACACACA others(1): Show |
G | 99 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(96): Show | 102 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.934-8302_934-8295d others(10): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 91210562 | |||||
| chr8:91210562
|
GACACACA others(3): Show |
G | 1 | a0002c0002t0001g0071 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.934-8304_934-8295d others(12): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 91210562 | |||||
| chr8:91210562
|
GACACACA others(13): Show |
G | 12 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(9): Show | 12 | HG02109.hp1 HG02257.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.934-8314_934-8295d others(22): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 91210562 | |||||
| chr8:91210655
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.934-8235G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91210655 | ||||||
| chr8:91211188
|
G | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(206): Show | 215 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.934-7702G>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91211188 | ||||||
| chr8:91211262
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.934-7628G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91211262 | ||||||
| chr8:91211265
|
A | G | 1 | a0001c0001t0001g0182 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.934-7625A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91211265 | ||||||
| chr8:91211277
|
T | G | 35 | a0001c0001t0001g0249a0001c0001t0001g0260a0001c0001t0001g0266others(32): Show | 36 | HG00438.hp1 HG00544.hp1 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.934-7613T>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91211277 | ||||||
| chr8:91211440
|
T | A | 4 | a0001c0001t0001g0011a0001c0001t0001g0237a0001c0001t0001g0243others(1): Show | 4 | HG00639.hp2 HG01123.hp2 NA20805.hp1 others(1): Show |
intron_variant | MODIFIER | c.934-7450T>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91211440 | ||||||
| chr8:91211509
|
G | A | 2 | a0002c0002t0001g0053a0002c0002t0001g0054 | 2 | HG02015.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.934-7381G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91211509 | ||||||
| chr8:91211552
|
A | G | 1 | a0001c0001t0001g0265 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.934-7338A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91211552 | ||||||
| chr8:91211595
|
A | AAT | 58 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(55): Show | 59 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.934-7274_934-7273d others(4): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 91211595 | |||||
| chr8:91211595
|
A | AATAT | 4 | a0001c0001t0001g0163a0001c0001t0001g0174a0001c0001t0002g0155others(1): Show | 4 | HG02280.hp2 HG02572.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.934-7276_934-7273d others(6): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 91211595 | |||||
| chr8:91211595
|
AAT | A | 8 | a0002c0002t0001g0033a0002c0002t0001g0055a0002c0002t0001g0065others(5): Show | 8 | HG00438.hp1 HG02622.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.934-7274_934-7273d others(4): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 91211595 | |||||
| chr8:91211612
|
A | T | 2 | a0001c0001t0001g0209a0001c0001t0001g0304 | 2 | HG01261.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.934-7278A>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91211612 | ||||||
| chr8:91211614
|
A | AT | 4 | a0001c0001t0001g0306a0001c0001t0001g0308a0001c0001t0001g0309others(1): Show | 4 | HG01069.hp1 HG01081.hp2 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.934-7275dupT | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 91211614 | |||||
| chr8:91211614
|
A | T | 9 | a0001c0001t0001g0059a0001c0001t0001g0209a0001c0001t0001g0300others(6): Show | 9 | HG01081.hp1 HG01123.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.934-7276A>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91211614 | ||||||
| chr8:91211615
|
TA | T | 14 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(11): Show | 14 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.934-7274delA | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91211615 | ||||||
| chr8:91211616
|
A | ATT | 8 | a0002c0002t0001g0081a0002c0002t0001g0090a0002c0002t0001g0096others(5): Show | 8 | HG00741.hp1 HG02602.hp2 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.934-7265_934-7264d others(4): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 91211616 | |||||
| chr8:91211616
|
A | T | 32 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(29): Show | 32 | HG00558.hp1 HG00735.hp2 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.934-7274A>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91211616 | ||||||
| chr8:91211616
|
AT | A | 6 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0133others(3): Show | 6 | HG01361.hp2 HG02486.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.934-7264delT | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 91211616 | |||||
| chr8:91211617
|
T | TA | 3 | a0001c0001t0001g0307a0002c0002t0001g0018a0002c0002t0001g0207 | 3 | HG01256.hp1 NA19001.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.934-7273_934-7272i others(3): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91211617 | ||||||
| chr8:91211618
|
T | A | 47 | a0001c0001t0001g0046a0001c0001t0001g0162a0001c0001t0001g0167others(44): Show | 47 | HG00639.hp1 HG00673.hp2 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.934-7272T>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91211618 | ||||||
| chr8:91211619
|
T | A | 1 | a0002c0002t0001g0051 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.934-7271T>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91211619 | ||||||
| chr8:91211619
|
T | TTTTA | 10 | a0001c0001t0001g0164a0001c0001t0001g0170a0001c0001t0001g0173others(7): Show | 10 | HG01081.hp1 HG02486.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.934-7268_934-7267i others(6): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 91211619 | |||||
| chr8:91211619
|
T | TTTTTA | 10 | a0001c0001t0001g0001a0001c0001t0001g0289a0001c0001t0001g0290others(7): Show | 12 | HG00423.hp2 HG00558.hp2 NA18942.hp2 others(9): Show |
intron_variant | MODIFIER | c.934-7267_934-7266i others(7): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 91211619 | |||||
| chr8:91211620
|
T | A | 16 | a0001c0001t0001g0167a0001c0001t0001g0251a0001c0001t0002g0155others(13): Show | 16 | HG01257.hp1 HG02109.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.934-7270T>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91211620 | ||||||
| chr8:91211622
|
T | A | 12 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(9): Show | 12 | HG02109.hp1 HG02257.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.934-7268T>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91211622 | ||||||
| chr8:91211626
|
T | A | 1 | a0001c0001t0001g0166 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.934-7264T>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91211626 | ||||||
| chr8:91211647
|
T | G | 9 | a0001c0001t0001g0162a0001c0001t0001g0166a0001c0001t0001g0167others(6): Show | 9 | HG02145.hp1 HG02572.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.934-7243T>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91211647 | ||||||
| chr8:91211852
|
T | C | 2 | a0001c0001t0001g0209a0001c0001t0001g0304 | 2 | HG01261.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.934-7038T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91211852 | ||||||
| chr8:91211870
|
A | T | 1 | a0002c0002t0001g0113 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.934-7020A>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91211870 | ||||||
| chr8:91212040
|
T | C | 1 | a0001c0001t0001g0059 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.934-6850T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91212040 | ||||||
| chr8:91212070
|
T | A | 2 | a0002c0002t0001g0081a0002c0002t0001g0132 | 2 | HG02738.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.934-6820T>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91212070 | ||||||
| chr8:91212134
|
A | G | 1 | a0001c0001t0001g0059 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.934-6756A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91212134 | ||||||
| chr8:91212316
|
T | G | 1 | a0001c0001t0001g0256 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.934-6574T>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91212316 | ||||||
| chr8:91212320
|
GT | G | 7 | a0001c0001t0001g0192a0001c0001t0001g0206a0001c0001t0001g0218others(4): Show | 7 | HG01943.hp2 HG02027.hp2 NA18973.hp1 others(4): Show |
intron_variant | MODIFIER | c.934-6567delT | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 91212320 | |||||
| chr8:91212536
|
C | A | 1 | a0001c0001t0001g0167 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.934-6354C>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91212536 | ||||||
| chr8:91212774
|
A | G | 1 | a0001c0001t0001g0163 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.934-6116A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91212774 | ||||||
| chr8:91212948
|
G | A | 2 | a0001c0001t0001g0209a0001c0001t0001g0304 | 2 | HG01261.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.934-5942G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91212948 | ||||||
| chr8:91212965
|
C | T | 1 | a0002c0002t0001g0077 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.934-5925C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91212965 | ||||||
| chr8:91213004
|
G | A | 140 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(137): Show | 144 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.934-5886G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91213004 | ||||||
| chr8:91213015
|
A | G | 1 | a0001c0001t0001g0215 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.934-5875A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91213015 | ||||||
| chr8:91213238
|
G | A | 2 | a0001c0001t0001g0209a0001c0001t0001g0304 | 2 | HG01261.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.934-5652G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91213238 | ||||||
| chr8:91213295
|
T | A | 5 | a0001c0001t0001g0276a0001c0001t0001g0278a0001c0001t0001g0279others(2): Show | 5 | HG02280.hp1 HG02970.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.934-5595T>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91213295 | ||||||
| chr8:91213452
|
T | G | 5 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(2): Show | 5 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.934-5438T>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91213452 | ||||||
| chr8:91213541
|
C | T | 1 | a0001c0003t0001g0284 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.934-5349C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91213541 | ||||||
| chr8:91213572
|
T | A | 3 | a0002c0002t0001g0055a0002c0002t0001g0065a0002c0002t0001g0074 | 3 | HG02622.hp1 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.934-5318T>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91213572 | ||||||
| chr8:91214014
|
A | G | 1 | a0002c0002t0001g0142 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.934-4876A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91214014 | ||||||
| chr8:91214098
|
T | C | 2 | a0002c0002t0001g0310a0002c0002t0001g0311 | 2 | NA18999.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.934-4792T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91214098 | ||||||
| chr8:91214126
|
T | G | 226 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(223): Show | 232 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.934-4764T>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91214126 | ||||||
| chr8:91214314
|
G | A | 2 | a0001c0001t0001g0209a0001c0001t0001g0304 | 2 | HG01261.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.934-4576G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91214314 | ||||||
| chr8:91214375
|
A | T | 1 | a0001c0001t0001g0309 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.934-4515A>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91214375 | ||||||
| chr8:91214627
|
A | C | 1 | a0001c0001t0001g0192 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.934-4263A>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91214627 | ||||||
| chr8:91214750
|
T | C | 8 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(5): Show | 8 | HG00735.hp2 HG02559.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.934-4140T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91214750 | ||||||
| chr8:91214806
|
A | T | 1 | a0001c0001t0002g0281 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.934-4084A>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91214806 | ||||||
| chr8:91214847
|
A | C | 72 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(69): Show | 73 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.934-4043A>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91214847 | ||||||
| chr8:91214969
|
T | C | 2 | a0001c0001t0001g0209a0001c0001t0001g0304 | 2 | HG01261.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.934-3921T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91214969 | ||||||
| chr8:91215090
|
G | A | 8 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047others(5): Show | 8 | HG00438.hp2 NA18961.hp2 NA18964.hp1 others(5): Show |
intron_variant | MODIFIER | c.934-3800G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91215090 | ||||||
| chr8:91215121
|
A | C | 3 | a0002c0002t0001g0126a0002c0002t0001g0127a0002c0002t0001g0128 | 3 | HG02027.hp1 NA18951.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.934-3769A>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91215121 | ||||||
| chr8:91215347
|
A | G | 1 | a0001c0001t0001g0059 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.934-3543A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91215347 | ||||||
| chr8:91215475
|
A | G | 1 | a0002c0002t0001g0028 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.934-3415A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91215475 | ||||||
| chr8:91215480
|
G | A | 5 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(2): Show | 5 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.934-3410G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91215480 | ||||||
| chr8:91215546
|
T | C | 1 | a0001c0001t0001g0007 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.934-3344T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91215546 | ||||||
| chr8:91215690
|
A | G | 13 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(10): Show | 13 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.934-3200A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91215690 | ||||||
| chr8:91215729
|
C | T | 208 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(205): Show | 214 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(211): Show |
intron_variant | MODIFIER | c.934-3161C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91215729 | ||||||
| chr8:91215855
|
A | G | 2 | a0001c0001t0001g0059a0001c0001t0001g0170 | 2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.934-3035A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91215855 | ||||||
| chr8:91216143
|
G | A | 30 | a0001c0001t0001g0249a0001c0001t0001g0260a0002c0002t0001g0003others(27): Show | 31 | HG00438.hp1 HG00544.hp1 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.934-2747G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91216143 | ||||||
| chr8:91216164
|
G | A | 5 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(2): Show | 5 | HG01069.hp1 HG01081.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.934-2726G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91216164 | ||||||
| chr8:91216289
|
G | A | 140 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(137): Show | 144 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.934-2601G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91216289 | ||||||
| chr8:91216346
|
C | T | 1 | a0002c0002t0001g0125 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.934-2544C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91216346 | ||||||
| chr8:91216503
|
G | C | 1 | a0001c0001t0001g0218 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.934-2387G>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91216503 | ||||||
| chr8:91216704
|
T | G | 1 | a0002c0002t0001g0034 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.934-2186T>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91216704 | ||||||
| chr8:91216820
|
G | A | 26 | a0001c0001t0001g0001a0001c0001t0001g0164a0001c0001t0001g0170others(23): Show | 28 | HG00423.hp2 HG00558.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.934-2070G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91216820 | ||||||
| chr8:91216883
|
C | T | 10 | a0001c0001t0001g0162a0001c0001t0001g0166a0001c0001t0001g0167others(7): Show | 10 | HG02145.hp1 HG02572.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.934-2007C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91216883 | ||||||
| chr8:91217024
|
T | A | 1 | a0002c0002t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.934-1866T>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217024 | ||||||
| chr8:91217026
|
C | G | 1 | a0002c0002t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.934-1864C>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217026 | ||||||
| chr8:91217028
|
T | G | 1 | a0002c0002t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.934-1862T>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217028 | ||||||
| chr8:91217034
|
G | T | 1 | a0002c0002t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.934-1856G>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217034 | ||||||
| chr8:91217035
|
C | A | 1 | a0002c0002t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.934-1855C>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217035 | ||||||
| chr8:91217037
|
G | A | 1 | a0002c0002t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.934-1853G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217037 | ||||||
| chr8:91217039
|
C | A | 1 | a0002c0002t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.934-1851C>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217039 | ||||||
| chr8:91217047
|
T | C | 1 | a0002c0002t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.934-1843T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217047 | ||||||
| chr8:91217048
|
C | A | 1 | a0002c0002t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.934-1842C>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217048 | ||||||
| chr8:91217048
|
C | T | 13 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(10): Show | 13 | HG02109.hp1 HG02257.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.934-1842C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217048 | ||||||
| chr8:91217053
|
G | T | 208 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(205): Show | 214 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(211): Show |
intron_variant | MODIFIER | c.934-1837G>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217053 | ||||||
| chr8:91217054
|
T | A | 1 | a0002c0002t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.934-1836T>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217054 | ||||||
| chr8:91217062
|
C | A | 1 | a0002c0002t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.934-1828C>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217062 | ||||||
| chr8:91217064
|
C | G | 1 | a0002c0002t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.934-1826C>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217064 | ||||||
| chr8:91217066
|
T | A | 1 | a0002c0002t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.934-1824T>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217066 | ||||||
| chr8:91217068
|
T | G | 1 | a0002c0002t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.934-1822T>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217068 | ||||||
| chr8:91217071
|
A | G | 1 | a0002c0002t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.934-1819A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217071 | ||||||
| chr8:91217073
|
C | A | 1 | a0002c0002t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.934-1817C>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217073 | ||||||
| chr8:91217091
|
C | T | 1 | a0002c0002t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.934-1799C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217091 | ||||||
| chr8:91217093
|
T | G | 1 | a0002c0002t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.934-1797T>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217093 | ||||||
| chr8:91217097
|
T | C | 1 | a0002c0002t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.934-1793T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217097 | ||||||
| chr8:91217098
|
T | A | 1 | a0002c0002t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.934-1792T>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217098 | ||||||
| chr8:91217099
|
T | A | 1 | a0002c0002t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.934-1791T>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217099 | ||||||
| chr8:91217100
|
C | T | 1 | a0002c0002t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.934-1790C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217100 | ||||||
| chr8:91217101
|
T | G | 1 | a0002c0002t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.934-1789T>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217101 | ||||||
| chr8:91217104
|
T | C | 1 | a0002c0002t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.934-1786T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217104 | ||||||
| chr8:91217107
|
T | G | 1 | a0002c0002t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.934-1783T>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217107 | ||||||
| chr8:91217108
|
G | A | 1 | a0002c0002t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.934-1782G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217108 | ||||||
| chr8:91217111
|
T | A | 1 | a0002c0002t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.934-1779T>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217111 | ||||||
| chr8:91217112
|
G | A | 1 | a0002c0002t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.934-1778G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217112 | ||||||
| chr8:91217114
|
G | C | 1 | a0002c0002t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.934-1776G>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217114 | ||||||
| chr8:91217116
|
G | C | 1 | a0002c0002t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.934-1774G>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217116 | ||||||
| chr8:91217117
|
T | C | 1 | a0002c0002t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.934-1773T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217117 | ||||||
| chr8:91217122
|
T | G | 1 | a0002c0002t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.934-1768T>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217122 | ||||||
| chr8:91217123
|
T | A | 1 | a0002c0002t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.934-1767T>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217123 | ||||||
| chr8:91217127
|
G | A | 1 | a0002c0002t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.934-1763G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217127 | ||||||
| chr8:91217130
|
T | G | 1 | a0002c0002t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.934-1760T>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217130 | ||||||
| chr8:91217133
|
C | A | 1 | a0002c0002t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.934-1757C>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217133 | ||||||
| chr8:91217136
|
A | T | 1 | a0002c0002t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.934-1754A>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217136 | ||||||
| chr8:91217137
|
C | G | 1 | a0002c0002t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.934-1753C>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217137 | ||||||
| chr8:91217138
|
T | A | 1 | a0002c0002t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.934-1752T>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217138 | ||||||
| chr8:91217140
|
G | A | 1 | a0002c0002t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.934-1750G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217140 | ||||||
| chr8:91217142
|
T | A | 1 | a0002c0002t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.934-1748T>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217142 | ||||||
| chr8:91217145
|
T | C | 1 | a0002c0002t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.934-1745T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217145 | ||||||
| chr8:91217156
|
G | C | 1 | a0002c0002t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.934-1734G>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217156 | ||||||
| chr8:91217158
|
G | A | 1 | a0002c0002t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.934-1732G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217158 | ||||||
| chr8:91217159
|
G | A | 1 | a0002c0002t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.934-1731G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217159 | ||||||
| chr8:91217165
|
A | T | 1 | a0002c0002t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.934-1725A>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217165 | ||||||
| chr8:91217168
|
G | A | 1 | a0002c0002t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.934-1722G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217168 | ||||||
| chr8:91217169
|
T | C | 1 | a0002c0002t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.934-1721T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217169 | ||||||
| chr8:91217170
|
T | C | 1 | a0002c0002t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.934-1720T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217170 | ||||||
| chr8:91217172
|
G | A | 1 | a0002c0002t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.934-1718G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217172 | ||||||
| chr8:91217175
|
G | A | 1 | a0002c0002t0001g0108 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.934-1715G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217175 | ||||||
| chr8:91217179
|
A | G | 1 | a0002c0002t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.934-1711A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217179 | ||||||
| chr8:91217180
|
T | A | 1 | a0002c0002t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.934-1710T>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217180 | ||||||
| chr8:91217181
|
C | T | 1 | a0002c0002t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.934-1709C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217181 | ||||||
| chr8:91217183
|
T | C | 1 | a0002c0002t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.934-1707T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217183 | ||||||
| chr8:91217185
|
G | A | 1 | a0002c0002t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.934-1705G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217185 | ||||||
| chr8:91217186
|
T | C | 1 | a0002c0002t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.934-1704T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217186 | ||||||
| chr8:91217194
|
C | T | 1 | a0002c0002t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.934-1696C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217194 | ||||||
| chr8:91217196
|
C | A | 1 | a0002c0002t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.934-1694C>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217196 | ||||||
| chr8:91217198
|
T | G | 1 | a0002c0002t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.934-1692T>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217198 | ||||||
| chr8:91217199
|
T | G | 1 | a0002c0002t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.934-1691T>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217199 | ||||||
| chr8:91217200
|
G | A | 1 | a0002c0002t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.934-1690G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217200 | ||||||
| chr8:91217343
|
G | A | 1 | a0001c0001t0001g0220 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.934-1547G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217343 | ||||||
| chr8:91217449
|
G | A | 39 | a0001c0001t0001g0001a0001c0001t0001g0164a0001c0001t0001g0170others(36): Show | 41 | HG00423.hp2 HG00558.hp2 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.934-1441G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217449 | ||||||
| chr8:91217526
|
C | G | 1 | a0002c0002t0001g0021 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.934-1364C>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217526 | ||||||
| chr8:91217629
|
G | A | 4 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(1): Show | 4 | HG01884.hp1 HG02055.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.934-1261G>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217629 | ||||||
| chr8:91217672
|
T | C | 8 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(5): Show | 8 | HG00735.hp2 HG02559.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.934-1218T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217672 | ||||||
| chr8:91217779
|
C | A | 1 | a0002c0002t0001g0012 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.934-1111C>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217779 | ||||||
| chr8:91217925
|
G | T | 1 | a0002c0002t0001g0207 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.934-965G>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91217925 | ||||||
| chr8:91218278
|
A | T | 1 | a0001c0001t0001g0163 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.934-612A>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91218278 | ||||||
| chr8:91218353
|
C | CACTAAGA others(4): Show |
234 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(231): Show | 240 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.934-536_934-535ins others(11): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr8 | 91218353 | |||||
| chr8:91218355
|
A | G | 234 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(231): Show | 240 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.934-535A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91218355 | ||||||
| chr8:91218359
|
A | AGAAAT | 234 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(231): Show | 240 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.934-531_934-530ins others(5): Show |
LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91218359 | ||||||
| chr8:91218360
|
T | A | 234 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(231): Show | 240 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.934-530T>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91218360 | ||||||
| chr8:91218441
|
A | G | 1 | a0001c0001t0001g0059 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.934-449A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91218441 | ||||||
| chr8:91218496
|
A | G | 1 | a0001c0001t0001g0163 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.934-394A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91218496 | ||||||
| chr8:91218531
|
C | T | 8 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(5): Show | 8 | HG00735.hp2 HG02559.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.934-359C>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91218531 | ||||||
| chr8:91218558
|
C | A | 1 | a0002c0002t0001g0099 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.934-332C>A | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91218558 | ||||||
| chr8:91218630
|
G | T | 5 | a0001c0001t0001g0276a0001c0001t0001g0278a0001c0001t0001g0279others(2): Show | 5 | HG02280.hp1 HG02970.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.934-260G>T | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91218630 | ||||||
| chr8:91218642
|
A | G | 13 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0157others(10): Show | 13 | HG02109.hp1 HG02257.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.934-248A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91218642 | ||||||
| chr8:91218646
|
A | G | 4 | a0001c0001t0001g0276a0001c0001t0001g0278a0001c0001t0001g0279others(1): Show | 4 | HG02970.hp2 HG03471.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.934-244A>G | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91218646 | ||||||
| chr8:91218848
|
T | C | 1 | a0002c0002t0001g0037 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.934-42T>C | LRRC69 | ENSG00000214954.9 | transcript | ENST00000448384.3 | protein_coding | 7/7 | chr8 | 91218848 |