| geneid | 26018 |
|---|---|
| ensemblid | ENSG00000144749.14 |
| hgncid | 17360 |
| symbol | LRIG1 |
| name | leucine rich repeats and immunoglobulin like domains 1 |
| refseq_nuc | NM_015541.3 |
| refseq_prot | NP_056356.2 |
| ensembl_nuc | ENST00000273261.8 |
| ensembl_prot | ENSP00000273261.3 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 66378797 |
| end | 66501022 |
| strand | - |
| ver | v1.2 |
| region | chr3:66378797-66501022 |
| region5000 | chr3:66373797-66506022 |
| regionname0 | LRIG1_chr3_66378797_66501022 |
| regionname5000 | LRIG1_chr3_66373797_66506022 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 1093 | 60 | 6 | 25 | 16 | 4 | 8 | 12 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0002 | 0/0 | 1093 | 58 | 3 | 13 | 38 | 0 | 4 | 25 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0003 | 1/0 | 1093 | 29 | 16 | 1 | 11 | 0 | 0 | 9 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0004 | 0/0 | 1093 | 19 | 4 | 1 | 4 | 1 | 9 | 2 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0005 | 0/0 | 1093 | 15 | 9 | 4 | 2 | 0 | 0 | 2 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0006 | 0/0 | 1093 | 12 | 11 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0007 | 0/0 | 1093 | 12 | 5 | 0 | 5 | 0 | 2 | 4 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0008 | 0/0 | 1093 | 12 | 12 | 0 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0009 | 0/0 | 1093 | 9 | 3 | 1 | 4 | 0 | 1 | 3 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0010 | 0/0 | 1093 | 6 | 1 | 1 | 2 | 1 | 1 | 2 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0011 | 0/0 | 1093 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0012 | 0/0 | 1093 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0013 | 0/0 | 1093 | 2 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0014 | 0/0 | 1093 | 2 | 0 | 0 | 1 | 0 | 1 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0015 | 0/0 | 1093 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0016 | 0/0 | 1093 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0017 | 0/0 | 1093 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0018 | 0/0 | 1093 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0019 | 0/0 | 1093 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0020 | 0/0 | 1093 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0021 | 0/0 | 1093 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0022 | 0/0 | 1093 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0023 | 0/0 | 1093 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0024 | 0/0 | 1093 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0025 | 0/0 | 1093 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0026 | 0/0 | 1093 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0027 | 0/0 | 1093 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0028 | 0/0 | 1093 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0029 | 0/0 | 1093 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0030 | 0/0 | 1093 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0031 | 0/0 | 1093 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0032 | 0/0 | 1093 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0033 | 0/0 | 1093 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0034 | 0/0 | 1093 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0035 | 0/0 | 1093 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 3282 | 49 | 3 | 12 | 30 | 0 | 4 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| c0002 | 0/1 | 3282 | 40 | 4 | 14 | 12 | 3 | 6 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| c0003 | 0/0 | 3282 | 18 | 4 | 1 | 3 | 1 | 9 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| c0004 | 0/0 | 3282 | 15 | 9 | 4 | 2 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| c0005 | 1/0 | 3282 | 15 | 3 | 1 | 10 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| c0006 | 0/0 | 3282 | 12 | 12 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| c0007 | 0/0 | 3282 | 12 | 0 | 10 | 0 | 1 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| c0008 | 0/0 | 3282 | 11 | 4 | 0 | 5 | 0 | 2 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| c0009 | 0/0 | 3282 | 8 | 7 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| c0010 | 0/0 | 3282 | 7 | 7 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| c0011 | 0/0 | 3282 | 6 | 1 | 1 | 2 | 1 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| c0012 | 0/0 | 3282 | 5 | 4 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| c0013 | 0/0 | 3282 | 5 | 0 | 1 | 3 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| c0014 | 0/0 | 3282 | 5 | 0 | 1 | 3 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| c0015 | 0/0 | 3282 | 3 | 3 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| c0016 | 0/0 | 3282 | 3 | 3 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| c0017 | 0/0 | 3282 | 3 | 0 | 0 | 3 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| c0018 | 0/0 | 3282 | 3 | 0 | 0 | 3 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| c0019 | 0/0 | 3282 | 2 | 2 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| c0020 | 0/0 | 3282 | 2 | 1 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| c0021 | 0/0 | 3282 | 2 | 0 | 0 | 2 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| c0022 | 0/0 | 3282 | 2 | 0 | 1 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| c0023 | 0/0 | 3282 | 2 | 2 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| c0024 | 0/0 | 3282 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| c0025 | 0/0 | 3282 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| c0026 | 0/0 | 3282 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| c0027 | 0/0 | 3282 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| c0028 | 0/0 | 3282 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| c0029 | 0/0 | 3282 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| c0030 | 0/0 | 3282 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| c0031 | 0/0 | 3282 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| c0032 | 0/0 | 3282 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| c0033 | 0/0 | 3282 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| c0034 | 0/0 | 3282 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| c0035 | 0/0 | 3282 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| c0036 | 0/0 | 3282 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| c0037 | 0/0 | 3282 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| c0038 | 0/0 | 3282 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| c0039 | 0/0 | 3282 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| c0040 | 0/0 | 3282 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| c0041 | 0/0 | 3282 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| c0042 | 0/0 | 3282 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| c0043 | 0/0 | 3282 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| c0044 | 0/0 | 3282 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| c0045 | 0/0 | 3282 | 1 | 0 | 0 | 0 | 1 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| c0046 | 0/0 | 3282 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| c0047 | 0/0 | 3282 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| c0048 | 0/0 | 3282 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| c0049 | 0/0 | 3282 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| c0050 | 0/0 | 3282 | 1 | 0 | 0 | 0 | 1 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| c0051 | 0/0 | 3282 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| c0052 | 0/0 | 3282 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| c0053 | 0/0 | 3282 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| c0054 | 0/0 | 3282 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| c0055 | 0/0 | 3282 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| c0056 | 0/0 | 3282 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| c0057 | 0/0 | 3282 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 2082 | 120 | 14 | 26 | 62 | 5 | 12 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| t0002 | 0/0 | 2081 | 44 | 10 | 14 | 11 | 1 | 8 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| t0003 | 1/0 | 2082 | 17 | 5 | 1 | 9 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| t0004 | 0/0 | 2081 | 15 | 13 | 1 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| t0005 | 0/0 | 2081 | 7 | 7 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| t0006 | 0/0 | 2080 | 7 | 4 | 3 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| t0007 | 0/0 | 2080 | 5 | 1 | 1 | 1 | 1 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| t0008 | 0/0 | 2080 | 5 | 4 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| t0009 | 0/0 | 2081 | 4 | 4 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| t0010 | 0/0 | 2081 | 4 | 1 | 1 | 0 | 0 | 2 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| t0011 | 0/0 | 2081 | 3 | 0 | 0 | 3 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| t0012 | 0/0 | 2082 | 3 | 2 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| t0013 | 0/0 | 2086 | 3 | 3 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| t0014 | 0/0 | 2081 | 2 | 2 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| t0015 | 0/0 | 2082 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| t0016 | 0/0 | 2082 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| t0017 | 0/0 | 2084 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| t0018 | 0/0 | 2083 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| t0019 | 0/0 | 2083 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| t0020 | 0/0 | 2083 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| t0021 | 0/0 | 2082 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| t0022 | 0/0 | 2082 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| t0023 | 0/0 | 2081 | 1 | 0 | 0 | 0 | 1 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| t0024 | 0/0 | 2080 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| t0025 | 0/0 | 2082 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| t0026 | 0/0 | 2081 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| t0027 | 0/0 | 2086 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| t0028 | 0/0 | 2081 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| t0029 | 0/0 | 2080 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| t0030 | 0/0 | 2082 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| t0031 | 0/0 | 2082 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| t0032 | 0/0 | 2082 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| t0033 | 0/0 | 2082 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| t0034 | 0/0 | 2081 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| t0035 | 0/0 | 2082 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| t0036 | 0/0 | 2081 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| t0037 | 0/0 | 2082 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| t0038 | 0/0 | 2081 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| t0039 | 0/0 | 2082 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0111 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0249 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 0/1 | 3282 | 40 | 4 | 14 | 12 | 3 | 6 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0001c0007 | 0/0 | 3282 | 12 | 0 | 10 | 0 | 1 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0001c0014 | 0/0 | 3282 | 5 | 0 | 1 | 3 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0001c0023 | 0/0 | 3282 | 2 | 2 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0001c0040 | 0/0 | 3282 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0002c0001 | 0/0 | 3282 | 49 | 3 | 12 | 30 | 0 | 4 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0002c0018 | 0/0 | 3282 | 3 | 0 | 0 | 3 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0002c0021 | 0/0 | 3282 | 2 | 0 | 0 | 2 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0002c0022 | 0/0 | 3282 | 2 | 0 | 1 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0002c0041 | 0/0 | 3282 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0002c0048 | 0/0 | 3282 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0003c0005 | 1/0 | 3282 | 15 | 3 | 1 | 10 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0003c0010 | 0/0 | 3282 | 7 | 7 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0003c0012 | 0/0 | 3282 | 5 | 4 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0003c0031 | 0/0 | 3282 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0003c0036 | 0/0 | 3282 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0004c0003 | 0/0 | 3282 | 18 | 4 | 1 | 3 | 1 | 9 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0004c0053 | 0/0 | 3282 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0005c0004 | 0/0 | 3282 | 15 | 9 | 4 | 2 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0006c0009 | 0/0 | 3282 | 8 | 7 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0006c0019 | 0/0 | 3282 | 2 | 2 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0006c0026 | 0/0 | 3282 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0006c0035 | 0/0 | 3282 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0007c0008 | 0/0 | 3282 | 11 | 4 | 0 | 5 | 0 | 2 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0007c0033 | 0/0 | 3282 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0008c0006 | 0/0 | 3282 | 12 | 12 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0009c0013 | 0/0 | 3282 | 5 | 0 | 1 | 3 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0009c0015 | 0/0 | 3282 | 3 | 3 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0009c0037 | 0/0 | 3282 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0010c0011 | 0/0 | 3282 | 6 | 1 | 1 | 2 | 1 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0011c0016 | 0/0 | 3282 | 3 | 3 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0011c0030 | 0/0 | 3282 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0012c0017 | 0/0 | 3282 | 3 | 0 | 0 | 3 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0013c0020 | 0/0 | 3282 | 2 | 1 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0014c0042 | 0/0 | 3282 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0014c0043 | 0/0 | 3282 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0015c0024 | 0/0 | 3282 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0016c0038 | 0/0 | 3282 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0017c0025 | 0/0 | 3282 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0018c0028 | 0/0 | 3282 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0019c0029 | 0/0 | 3282 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0020c0027 | 0/0 | 3282 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0021c0034 | 0/0 | 3282 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0022c0032 | 0/0 | 3282 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0023c0051 | 0/0 | 3282 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0024c0055 | 0/0 | 3282 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0025c0054 | 0/0 | 3282 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0026c0039 | 0/0 | 3282 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0027c0050 | 0/0 | 3282 | 1 | 0 | 0 | 0 | 1 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0028c0049 | 0/0 | 3282 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0029c0052 | 0/0 | 3282 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0030c0046 | 0/0 | 3282 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0031c0047 | 0/0 | 3282 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0032c0045 | 0/0 | 3282 | 1 | 0 | 0 | 0 | 1 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0033c0044 | 0/0 | 3282 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0034c0056 | 0/0 | 3282 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0035c0057 | 0/0 | 3282 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001 | 0/1 | 5363 | 39 | 4 | 14 | 12 | 3 | 5 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0001c0002t0031 | 0/0 | 5363 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0001c0007t0001 | 0/0 | 5363 | 1 | 0 | 0 | 0 | 1 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0001c0007t0002 | 0/0 | 5362 | 11 | 0 | 10 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0001c0014t0010 | 0/0 | 5362 | 2 | 0 | 1 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0001c0014t0011 | 0/0 | 5362 | 2 | 0 | 0 | 2 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0001c0014t0028 | 0/0 | 5362 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0001c0023t0002 | 0/0 | 5362 | 2 | 2 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0001c0040t0001 | 0/0 | 5363 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0002c0001t0001 | 0/0 | 5363 | 46 | 3 | 11 | 28 | 0 | 4 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0002c0001t0015 | 0/0 | 5363 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0002c0001t0016 | 0/0 | 5363 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0002c0001t0032 | 0/0 | 5363 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0002c0018t0001 | 0/0 | 5363 | 3 | 0 | 0 | 3 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0002c0021t0001 | 0/0 | 5363 | 2 | 0 | 0 | 2 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0002c0022t0001 | 0/0 | 5363 | 2 | 0 | 1 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0002c0041t0001 | 0/0 | 5363 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0002c0048t0001 | 0/0 | 5363 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0003c0005t0001 | 0/0 | 5363 | 4 | 3 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0003c0005t0003 | 1/0 | 5363 | 11 | 0 | 1 | 9 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0003c0010t0002 | 0/0 | 5362 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0003c0010t0004 | 0/0 | 5362 | 6 | 6 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0003c0012t0001 | 0/0 | 5363 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0003c0012t0014 | 0/0 | 5362 | 2 | 2 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0003c0012t0017 | 0/0 | 5365 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0003c0012t0018 | 0/0 | 5364 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0003c0031t0001 | 0/0 | 5363 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0003c0036t0034 | 0/0 | 5362 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0004c0003t0001 | 0/0 | 5363 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0004c0003t0002 | 0/0 | 5362 | 15 | 3 | 1 | 3 | 1 | 7 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0004c0003t0026 | 0/0 | 5362 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0004c0003t0038 | 0/0 | 5362 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0004c0053t0002 | 0/0 | 5362 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0005c0004t0001 | 0/0 | 5363 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0005c0004t0006 | 0/0 | 5361 | 7 | 4 | 3 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0005c0004t0007 | 0/0 | 5361 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0005c0004t0008 | 0/0 | 5361 | 5 | 4 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0005c0004t0021 | 0/0 | 5363 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0006c0009t0002 | 0/0 | 5362 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0006c0009t0004 | 0/0 | 5362 | 7 | 6 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0006c0019t0012 | 0/0 | 5363 | 2 | 2 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0006c0026t0036 | 0/0 | 5362 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0006c0035t0033 | 0/0 | 5363 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0007c0008t0001 | 0/0 | 5363 | 5 | 1 | 0 | 4 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0007c0008t0003 | 0/0 | 5363 | 4 | 3 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0007c0008t0025 | 0/0 | 5363 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0007c0008t0037 | 0/0 | 5363 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0007c0033t0001 | 0/0 | 5363 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0008c0006t0005 | 0/0 | 5362 | 7 | 7 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0008c0006t0009 | 0/0 | 5362 | 4 | 4 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0008c0006t0020 | 0/0 | 5364 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0009c0013t0001 | 0/0 | 5363 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0009c0013t0002 | 0/0 | 5362 | 3 | 0 | 1 | 2 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0009c0013t0004 | 0/0 | 5362 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0009c0015t0002 | 0/0 | 5362 | 3 | 3 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0009c0037t0002 | 0/0 | 5362 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0010c0011t0001 | 0/0 | 5363 | 2 | 0 | 0 | 2 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0010c0011t0007 | 0/0 | 5361 | 3 | 0 | 1 | 0 | 1 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0010c0011t0024 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0011c0016t0013 | 0/0 | 5367 | 3 | 3 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0011c0030t0027 | 0/0 | 5367 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0012c0017t0002 | 0/0 | 5362 | 3 | 0 | 0 | 3 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0013c0020t0029 | 0/0 | 5361 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0013c0020t0035 | 0/0 | 5363 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0014c0042t0010 | 0/0 | 5362 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0014c0043t0022 | 0/0 | 5363 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0015c0024t0001 | 0/0 | 5363 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0016c0038t0003 | 0/0 | 5363 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0017c0025t0012 | 0/0 | 5363 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0018c0028t0003 | 0/0 | 5363 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0019c0029t0001 | 0/0 | 5363 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0020c0027t0004 | 0/0 | 5362 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0021c0034t0019 | 0/0 | 5364 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0022c0032t0007 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0023c0051t0002 | 0/0 | 5362 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0024c0055t0002 | 0/0 | 5362 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0025c0054t0002 | 0/0 | 5362 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0026c0039t0001 | 0/0 | 5363 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0027c0050t0023 | 0/0 | 5362 | 1 | 0 | 0 | 0 | 1 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0028c0049t0001 | 0/0 | 5363 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0029c0052t0039 | 0/0 | 5363 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0030c0046t0010 | 0/0 | 5362 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0031c0047t0030 | 0/0 | 5363 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0032c0045t0001 | 0/0 | 5363 | 1 | 0 | 0 | 0 | 1 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0033c0044t0001 | 0/0 | 5363 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0034c0056t0001 | 0/0 | 5363 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| a0035c0057t0011 | 0/0 | 5362 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | copy fasta | chr3 | 66373797 | 66506022 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0001c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0001c0002t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0001c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0001c0002t0001g0111 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0001c0002t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0001c0002t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0001c0002t0031g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0001c0007t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0001c0007t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0001c0007t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0001c0007t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0001c0007t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0001c0007t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0001c0007t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0001c0007t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0001c0007t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0001c0007t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0001c0007t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0001c0007t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0001c0014t0010g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0001c0014t0010g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0001c0014t0011g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0001c0014t0011g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0001c0014t0028g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0001c0023t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0001c0023t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0001c0040t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0002c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0002c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0002c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0002c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0002c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0002c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0002c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0002c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0002c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0002c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0002c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0002c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0002c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0002c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0002c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0002c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0002c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0002c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0002c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0002c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0002c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0002c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0002c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0002c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0002c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0002c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0002c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0002c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0002c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0002c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0002c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0002c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0002c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0002c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0002c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0002c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0002c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0002c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0002c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0002c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0002c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0002c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0002c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0002c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0002c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0002c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0002c0001t0015g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0002c0001t0016g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0002c0001t0032g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0002c0018t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0002c0018t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0002c0018t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0002c0021t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0002c0021t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0002c0022t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0002c0022t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0002c0041t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0002c0048t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0003c0005t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0003c0005t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0003c0005t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0003c0005t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0003c0005t0003g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0003c0005t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0003c0005t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0003c0005t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0003c0005t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0003c0005t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0003c0005t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0003c0005t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0003c0005t0003g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0003c0005t0003g0249 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0003c0010t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0003c0010t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0003c0010t0004g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0003c0010t0004g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0003c0010t0004g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0003c0010t0004g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0003c0010t0004g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0003c0012t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0003c0012t0014g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0003c0012t0014g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0003c0012t0017g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0003c0012t0018g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0003c0031t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0003c0036t0034g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0004c0003t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0004c0003t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0004c0003t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0004c0003t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0004c0003t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0004c0003t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0004c0003t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0004c0003t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0004c0003t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0004c0003t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0004c0003t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0004c0003t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0004c0003t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0004c0003t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0004c0003t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0004c0003t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0004c0003t0026g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0004c0003t0038g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0004c0053t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0005c0004t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0005c0004t0006g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0005c0004t0006g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0005c0004t0006g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0005c0004t0006g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0005c0004t0006g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0005c0004t0006g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0005c0004t0006g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0005c0004t0007g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0005c0004t0008g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0005c0004t0008g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0005c0004t0008g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0005c0004t0008g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0005c0004t0008g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0005c0004t0021g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0006c0009t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0006c0009t0004g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0006c0009t0004g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0006c0009t0004g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0006c0009t0004g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0006c0009t0004g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0006c0009t0004g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0006c0009t0004g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0006c0019t0012g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0006c0019t0012g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0006c0026t0036g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0006c0035t0033g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0007c0008t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0007c0008t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0007c0008t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0007c0008t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0007c0008t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0007c0008t0003g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0007c0008t0003g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0007c0008t0003g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0007c0008t0003g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0007c0008t0025g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0007c0008t0037g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0007c0033t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0008c0006t0005g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0008c0006t0005g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0008c0006t0005g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0008c0006t0005g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0008c0006t0005g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0008c0006t0005g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0008c0006t0005g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0008c0006t0009g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0008c0006t0009g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0008c0006t0009g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0008c0006t0009g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0008c0006t0020g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0009c0013t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0009c0013t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0009c0013t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0009c0013t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0009c0013t0004g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0009c0015t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0009c0015t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0009c0015t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0009c0037t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0010c0011t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0010c0011t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0010c0011t0007g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0010c0011t0007g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0010c0011t0007g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0010c0011t0024g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0011c0016t0013g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0011c0016t0013g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0011c0016t0013g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0011c0030t0027g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0012c0017t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0012c0017t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0012c0017t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0013c0020t0029g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0013c0020t0035g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0014c0042t0010g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0014c0043t0022g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0015c0024t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0016c0038t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0017c0025t0012g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0018c0028t0003g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0019c0029t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0020c0027t0004g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0021c0034t0019g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0022c0032t0007g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0023c0051t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0024c0055t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0025c0054t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0026c0039t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0027c0050t0023g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0028c0049t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0029c0052t0039g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0030c0046t0010g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0031c0047t0030g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0032c0045t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0033c0044t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0034c0056t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| a0035c0057t0011g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0004 | c0003 | t0002 | g0081 | EUR | GBR | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0079 | EUR | GBR | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG00280 | hp1 | a0010 | c0011 | t0007 | g0175 | EUR | FIN | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG00280 | hp2 | a0001 | c0007 | t0001 | g0116 | EUR | FIN | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG00544 | hp1 | a0012 | c0017 | t0002 | g0020 | EAS | CHS | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG00544 | hp2 | a0002 | c0001 | t0001 | g0047 | EAS | CHS | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG00558 | hp1 | a0002 | c0001 | t0001 | g0155 | EAS | CHS | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG00558 | hp2 | a0002 | c0021 | t0001 | g0113 | EAS | CHS | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG00609 | hp1 | a0014 | c0043 | t0022 | g0009 | EAS | CHS | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG00609 | hp2 | a0009 | c0037 | t0002 | g0018 | EAS | CHS | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG00621 | hp1 | a0002 | c0001 | t0032 | g0199 | EAS | CHS | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG00621 | hp2 | a0002 | c0001 | t0001 | g0156 | EAS | CHS | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0157 | EAS | CHS | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG00673 | hp2 | a0002 | c0018 | t0001 | g0050 | EAS | CHS | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG00735 | hp1 | a0006 | c0009 | t0004 | g0228 | AMR | PUR | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0061 | AMR | PUR | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG00738 | hp1 | a0002 | c0001 | t0001 | g0171 | AMR | PUR | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG00738 | hp2 | a0002 | c0001 | t0001 | g0160 | AMR | PUR | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG01069 | hp1 | a0002 | c0001 | t0001 | g0085 | AMR | PUR | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG01069 | hp2 | a0002 | c0001 | t0015 | g0002 | AMR | PUR | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0053 | AMR | PUR | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG01070 | hp2 | a0003 | c0005 | t0003 | g0241 | AMR | PUR | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0062 | AMR | PUR | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG01071 | hp2 | a0002 | c0001 | t0001 | g0087 | AMR | PUR | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG01074 | hp1 | a0002 | c0001 | t0001 | g0123 | AMR | PUR | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG01074 | hp2 | a0001 | c0007 | t0002 | g0128 | AMR | PUR | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG01099 | hp1 | a0005 | c0004 | t0006 | g0238 | AMR | PUR | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG01099 | hp2 | a0001 | c0007 | t0002 | g0163 | AMR | PUR | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG01167 | hp1 | a0002 | c0001 | t0001 | g0052 | AMR | PUR | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0070 | AMR | PUR | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0076 | AMR | PUR | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG01192 | hp2 | a0001 | c0007 | t0002 | g0131 | AMR | PUR | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG01243 | hp1 | a0002 | c0022 | t0001 | g0179 | AMR | PUR | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG01243 | hp2 | a0005 | c0004 | t0008 | g0254 | AMR | PUR | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG01255 | hp1 | a0001 | c0007 | t0002 | g0194 | AMR | CLM | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG01255 | hp2 | a0002 | c0001 | t0001 | g0121 | AMR | CLM | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG01256 | hp1 | a0004 | c0003 | t0002 | g0153 | AMR | CLM | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG01256 | hp2 | a0009 | c0013 | t0002 | g0024 | AMR | CLM | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG01261 | hp1 | a0001 | c0007 | t0002 | g0080 | AMR | CLM | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0084 | AMR | CLM | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0159 | AMR | CLM | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG01346 | hp2 | a0002 | c0001 | t0001 | g0166 | AMR | CLM | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG01358 | hp1 | a0005 | c0004 | t0006 | g0239 | AMR | CLM | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG01358 | hp2 | a0001 | c0007 | t0002 | g0132 | AMR | CLM | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG01433 | hp1 | a0001 | c0014 | t0010 | g0186 | AMR | CLM | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG01433 | hp2 | a0002 | c0001 | t0001 | g0164 | AMR | CLM | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG01496 | hp1 | a0023 | c0051 | t0002 | g0054 | AMR | CLM | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0066 | AMR | CLM | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG01515 | hp1 | a0027 | c0050 | t0023 | g0082 | EUR | IBS | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG01515 | hp2 | a0001 | c0002 | t0001 | g0063 | EUR | IBS | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG01884 | hp1 | a0003 | c0005 | t0001 | g0037 | AFR | ACB | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG01884 | hp2 | a0008 | c0006 | t0005 | g0242 | AFR | ACB | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0056 | AFR | ACB | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG01891 | hp2 | a0009 | c0015 | t0002 | g0034 | AFR | ACB | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0133 | AMR | PEL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG01928 | hp2 | a0001 | c0007 | t0002 | g0126 | AMR | PEL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG01934 | hp1 | a0001 | c0007 | t0002 | g0129 | AMR | PEL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0167 | AMR | PEL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG01952 | hp1 | a0017 | c0025 | t0012 | g0253 | AMR | PEL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0086 | AMR | PEL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG01981 | hp1 | a0002 | c0001 | t0001 | g0109 | AMR | PEL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG01981 | hp2 | a0005 | c0004 | t0006 | g0240 | AMR | PEL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0168 | AMR | PEL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG01993 | hp2 | a0001 | c0007 | t0002 | g0125 | AMR | PEL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0146 | EAS | KHV | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02027 | hp2 | a0013 | c0020 | t0029 | g0029 | EAS | KHV | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02040 | hp1 | a0002 | c0001 | t0001 | g0147 | EAS | KHV | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02040 | hp2 | a0003 | c0005 | t0003 | g0210 | EAS | KHV | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02055 | hp1 | a0003 | c0012 | t0014 | g0236 | AFR | ACB | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0178 | AFR | ACB | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02056 | hp1 | a0002 | c0018 | t0001 | g0192 | EAS | KHV | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02056 | hp2 | a0001 | c0002 | t0001 | g0189 | EAS | KHV | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02071 | hp1 | a0002 | c0001 | t0001 | g0180 | EAS | KHV | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02071 | hp2 | a0004 | c0003 | t0002 | g0103 | EAS | KHV | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02132 | hp1 | a0024 | c0055 | t0002 | g0139 | EAS | KHV | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02132 | hp2 | a0002 | c0001 | t0001 | g0195 | EAS | KHV | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02135 | hp1 | a0004 | c0003 | t0002 | g0181 | EAS | KHV | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0108 | EAS | KHV | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02145 | hp1 | a0016 | c0038 | t0003 | g0235 | AFR | ACB | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02145 | hp2 | a0030 | c0046 | t0010 | g0184 | AFR | ACB | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02148 | hp1 | a0001 | c0007 | t0002 | g0130 | AMR | PEL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0115 | AMR | PEL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02165 | hp1 | a0003 | c0012 | t0001 | g0040 | EAS | CDX | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02165 | hp2 | a0002 | c0001 | t0001 | g0170 | EAS | CDX | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02258 | hp1 | a0005 | c0004 | t0008 | g0248 | AFR | ACB | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02258 | hp2 | a0004 | c0003 | t0002 | g0161 | AFR | ACB | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02280 | hp1 | a0028 | c0049 | t0001 | g0067 | AFR | ACB | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02280 | hp2 | a0006 | c0019 | t0012 | g0244 | AFR | ACB | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0140 | AMR | PEL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02300 | hp2 | a0025 | c0054 | t0002 | g0196 | AMR | PEL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02451 | hp1 | a0007 | c0008 | t0001 | g0038 | AFR | ACB | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02451 | hp2 | a0005 | c0004 | t0008 | g0247 | AFR | ACB | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02523 | hp1 | a0007 | c0008 | t0025 | g0043 | EAS | KHV | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02523 | hp2 | a0034 | c0056 | t0001 | g0182 | EAS | KHV | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02572 | hp1 | a0003 | c0036 | t0034 | g0203 | AFR | GWD | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02572 | hp2 | a0005 | c0004 | t0008 | g0250 | AFR | GWD | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02622 | hp1 | a0008 | c0006 | t0009 | g0014 | AFR | GWD | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0065 | AFR | GWD | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02630 | hp1 | a0013 | c0020 | t0035 | g0208 | AFR | GWD | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02630 | hp2 | a0005 | c0004 | t0006 | g0222 | AFR | GWD | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02647 | hp1 | a0003 | c0010 | t0004 | g0231 | AFR | GWD | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02647 | hp2 | a0008 | c0006 | t0005 | g0219 | AFR | GWD | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02698 | hp1 | a0004 | c0003 | t0002 | g0057 | SAS | PJL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02698 | hp2 | a0010 | c0011 | t0007 | g0169 | SAS | PJL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02717 | hp1 | a0006 | c0035 | t0033 | g0207 | AFR | GWD | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02717 | hp2 | a0031 | c0047 | t0030 | g0162 | AFR | GWD | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02723 | hp1 | a0002 | c0001 | t0001 | g0174 | AFR | GWD | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02723 | hp2 | a0007 | c0008 | t0003 | g0256 | AFR | GWD | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02735 | hp1 | a0001 | c0002 | t0031 | g0069 | SAS | PJL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02735 | hp2 | a0004 | c0003 | t0002 | g0097 | SAS | PJL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0104 | SAS | PJL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02738 | hp2 | a0002 | c0001 | t0001 | g0187 | SAS | PJL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02809 | hp1 | a0003 | c0005 | t0001 | g0039 | AFR | GWD | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02809 | hp2 | a0006 | c0019 | t0012 | g0245 | AFR | GWD | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02818 | hp1 | a0003 | c0010 | t0004 | g0260 | AFR | GWD | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02818 | hp2 | a0005 | c0004 | t0006 | g0202 | AFR | GWD | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02886 | hp1 | a0008 | c0006 | t0005 | g0230 | AFR | GWD | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02886 | hp2 | a0005 | c0004 | t0021 | g0006 | AFR | GWD | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02896 | hp1 | a0001 | c0023 | t0002 | g0068 | AFR | GWD | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02896 | hp2 | a0022 | c0032 | t0007 | g0046 | AFR | GWD | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02897 | hp1 | a0003 | c0010 | t0004 | g0258 | AFR | GWD | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02897 | hp2 | a0001 | c0023 | t0002 | g0060 | AFR | GWD | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02922 | hp1 | a0009 | c0015 | t0002 | g0033 | AFR | ESN | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02922 | hp2 | a0003 | c0010 | t0004 | g0201 | AFR | ESN | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02965 | hp1 | a0008 | c0006 | t0005 | g0215 | AFR | ESN | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02965 | hp2 | a0011 | c0030 | t0027 | g0021 | AFR | ESN | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02970 | hp1 | a0006 | c0009 | t0004 | g0226 | AFR | ESN | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02970 | hp2 | a0006 | c0009 | t0004 | g0232 | AFR | ESN | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02976 | hp1 | a0003 | c0012 | t0017 | g0004 | AFR | ESN | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02976 | hp2 | a0003 | c0012 | t0018 | g0008 | AFR | ESN | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG03017 | hp1 | a0002 | c0001 | t0001 | g0059 | SAS | PJL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0078 | SAS | PJL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG03041 | hp1 | a0008 | c0006 | t0005 | g0200 | AFR | GWD | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG03041 | hp2 | a0006 | c0026 | t0036 | g0234 | AFR | GWD | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG03098 | hp1 | a0005 | c0004 | t0006 | g0220 | AFR | MSL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG03098 | hp2 | a0006 | c0009 | t0004 | g0251 | AFR | MSL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG03130 | hp1 | a0008 | c0006 | t0009 | g0035 | AFR | ESN | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG03130 | hp2 | a0003 | c0012 | t0014 | g0233 | AFR | ESN | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG03139 | hp1 | a0010 | c0011 | t0024 | g0064 | AFR | ESN | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG03139 | hp2 | a0002 | c0001 | t0001 | g0172 | AFR | ESN | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG03195 | hp1 | a0007 | c0033 | t0001 | g0027 | AFR | ESN | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG03195 | hp2 | a0003 | c0010 | t0004 | g0229 | AFR | ESN | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG03209 | hp1 | a0002 | c0001 | t0001 | g0173 | AFR | MSL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG03209 | hp2 | a0018 | c0028 | t0003 | g0259 | AFR | MSL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG03225 | hp1 | a0004 | c0003 | t0002 | g0088 | AFR | MSL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG03225 | hp2 | a0006 | c0009 | t0004 | g0224 | AFR | MSL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG03239 | hp1 | a0007 | c0008 | t0003 | g0213 | SAS | PJL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG03239 | hp2 | a0001 | c0007 | t0002 | g0100 | SAS | PJL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG03453 | hp1 | a0007 | c0008 | t0003 | g0252 | AFR | MSL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0074 | AFR | MSL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG03486 | hp1 | a0003 | c0031 | t0001 | g0036 | AFR | MSL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG03486 | hp2 | a0008 | c0006 | t0005 | g0223 | AFR | MSL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG03579 | hp1 | a0004 | c0003 | t0002 | g0089 | AFR | MSL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG03579 | hp2 | a0003 | c0005 | t0001 | g0028 | AFR | MSL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG03669 | hp1 | a0009 | c0013 | t0004 | g0214 | SAS | PJL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0122 | SAS | PJL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG03688 | hp1 | a0002 | c0001 | t0001 | g0124 | SAS | STU | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG03688 | hp2 | a0004 | c0003 | t0026 | g0190 | SAS | STU | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG03704 | hp1 | a0004 | c0003 | t0001 | g0151 | SAS | PJL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG03704 | hp2 | a0004 | c0003 | t0002 | g0105 | SAS | PJL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG03710 | hp1 | a0004 | c0003 | t0002 | g0141 | SAS | PJL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG03710 | hp2 | a0004 | c0003 | t0002 | g0193 | SAS | PJL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0075 | SAS | BEB | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG03834 | hp2 | a0014 | c0042 | t0010 | g0083 | SAS | BEB | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0106 | SAS | BEB | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG03927 | hp2 | a0033 | c0044 | t0001 | g0185 | SAS | BEB | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG03942 | hp1 | a0007 | c0008 | t0037 | g0261 | SAS | BEB | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG03942 | hp2 | a0004 | c0003 | t0002 | g0101 | SAS | BEB | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG04115 | hp1 | a0026 | c0039 | t0001 | g0073 | SAS | STU | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG04115 | hp2 | a0004 | c0003 | t0002 | g0107 | SAS | STU | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA18522 | hp1 | a0005 | c0004 | t0006 | g0221 | AFR | YRI | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA18522 | hp2 | a0008 | c0006 | t0009 | g0011 | AFR | YRI | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA18747 | hp1 | a0002 | c0001 | t0001 | g0110 | EAS | CHB | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA18747 | hp2 | a0002 | c0022 | t0001 | g0177 | EAS | CHB | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA18906 | hp1 | a0020 | c0027 | t0004 | g0227 | AFR | YRI | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA18906 | hp2 | a0004 | c0003 | t0038 | g0262 | AFR | YRI | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA18939 | hp1 | a0002 | c0001 | t0001 | g0090 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA18939 | hp2 | a0001 | c0014 | t0011 | g0058 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA18943 | hp2 | a0002 | c0001 | t0001 | g0048 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA18949 | hp1 | a0001 | c0014 | t0028 | g0118 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA18949 | hp2 | a0001 | c0002 | t0001 | g0136 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA18950 | hp1 | a0005 | c0004 | t0001 | g0019 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA18950 | hp2 | a0002 | c0001 | t0001 | g0183 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA18951 | hp1 | a0002 | c0001 | t0001 | g0145 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA18951 | hp2 | a0019 | c0029 | t0001 | g0022 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA18953 | hp1 | a0007 | c0008 | t0001 | g0030 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA18953 | hp2 | a0002 | c0001 | t0001 | g0119 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA18961 | hp1 | a0003 | c0005 | t0003 | g0217 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA18961 | hp2 | a0002 | c0001 | t0001 | g0191 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA18966 | hp1 | a0002 | c0001 | t0001 | g0137 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA18966 | hp2 | a0003 | c0005 | t0003 | g0001 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA18969 | hp1 | a0002 | c0041 | t0001 | g0114 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA18969 | hp2 | a0012 | c0017 | t0002 | g0023 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA18970 | hp1 | a0010 | c0011 | t0001 | g0091 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA18970 | hp2 | a0007 | c0008 | t0001 | g0031 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA18974 | hp1 | a0002 | c0001 | t0001 | g0143 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA18974 | hp2 | a0005 | c0004 | t0007 | g0017 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA18975 | hp1 | a0002 | c0001 | t0001 | g0158 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0198 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA18981 | hp1 | a0004 | c0053 | t0002 | g0197 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA18981 | hp2 | a0010 | c0011 | t0001 | g0095 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA18985 | hp1 | a0003 | c0005 | t0003 | g0218 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA18985 | hp2 | a0002 | c0001 | t0001 | g0165 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA18986 | hp1 | a0003 | c0005 | t0003 | g0001 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA18986 | hp2 | a0002 | c0021 | t0001 | g0112 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA18988 | hp1 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA18988 | hp2 | a0002 | c0001 | t0001 | g0102 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA18989 | hp1 | a0002 | c0001 | t0001 | g0188 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA18989 | hp2 | a0003 | c0005 | t0003 | g0216 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA18991 | hp1 | a0002 | c0001 | t0016 | g0003 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA18991 | hp2 | a0009 | c0013 | t0001 | g0041 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA18992 | hp1 | a0002 | c0001 | t0001 | g0148 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA18992 | hp2 | a0003 | c0005 | t0003 | g0209 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA18993 | hp1 | a0001 | c0040 | t0001 | g0096 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA18993 | hp2 | a0012 | c0017 | t0002 | g0015 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA18994 | hp1 | a0003 | c0005 | t0001 | g0026 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA18994 | hp2 | a0002 | c0001 | t0001 | g0149 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA19000 | hp1 | a0002 | c0018 | t0001 | g0176 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA19000 | hp2 | a0009 | c0013 | t0002 | g0044 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA19004 | hp1 | a0002 | c0001 | t0001 | g0154 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA19004 | hp2 | a0007 | c0008 | t0001 | g0016 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA19007 | hp1 | a0001 | c0014 | t0011 | g0117 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA19007 | hp2 | a0002 | c0001 | t0001 | g0152 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA19030 | hp1 | a0009 | c0015 | t0002 | g0032 | AFR | LWK | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA19030 | hp2 | a0003 | c0010 | t0004 | g0257 | AFR | LWK | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA19043 | hp1 | a0007 | c0008 | t0003 | g0237 | AFR | LWK | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA19043 | hp2 | a0011 | c0016 | t0013 | g0206 | AFR | LWK | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA19056 | hp1 | a0004 | c0003 | t0002 | g0098 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA19056 | hp2 | a0002 | c0001 | t0001 | g0135 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA19058 | hp1 | a0007 | c0008 | t0001 | g0013 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA19058 | hp2 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA19064 | hp1 | a0002 | c0001 | t0001 | g0142 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA19064 | hp2 | a0009 | c0013 | t0002 | g0042 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA19065 | hp1 | a0003 | c0005 | t0003 | g0211 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA19065 | hp2 | a0002 | c0048 | t0001 | g0099 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0051 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA19074 | hp2 | a0001 | c0002 | t0001 | g0077 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA19077 | hp1 | a0002 | c0001 | t0001 | g0144 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA19077 | hp2 | a0003 | c0005 | t0003 | g0212 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA19079 | hp1 | a0015 | c0024 | t0001 | g0025 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA19079 | hp2 | a0035 | c0057 | t0011 | g0138 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA19085 | hp1 | a0002 | c0001 | t0001 | g0072 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0049 | EAS | JPT | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA19240 | hp1 | a0005 | c0004 | t0008 | g0255 | AFR | YRI | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA19240 | hp2 | a0003 | c0010 | t0002 | g0010 | AFR | YRI | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0071 | EUR | TSI | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA20805 | hp2 | a0032 | c0045 | t0001 | g0120 | EUR | TSI | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA20905 | hp1 | a0001 | c0014 | t0010 | g0134 | SAS | GIH | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA20905 | hp2 | a0002 | c0001 | t0001 | g0150 | SAS | GIH | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG01123 | hp1 | a0010 | c0011 | t0007 | g0127 | AMR | CLM | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG01123 | hp2 | a0002 | c0001 | t0001 | g0055 | AMR | CLM | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02486 | hp1 | a0029 | c0052 | t0039 | g0263 | AFR | ACB | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02486 | hp2 | a0011 | c0016 | t0013 | g0204 | AFR | ACB | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02559 | hp1 | a0011 | c0016 | t0013 | g0205 | AFR | ACB | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG02559 | hp2 | a0008 | c0006 | t0009 | g0012 | AFR | ACB | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG03471 | hp1 | a0008 | c0006 | t0005 | g0243 | AFR | MSL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG03471 | hp2 | a0006 | c0009 | t0002 | g0045 | AFR | MSL | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG06807 | hp1 | a0006 | c0009 | t0004 | g0225 | AFR | USA | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| HG06807 | hp2 | a0008 | c0006 | t0020 | g0005 | AFR | USA | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA20300 | hp1 | a0006 | c0009 | t0004 | g0246 | AFR | USA | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| NA20300 | hp2 | a0021 | c0034 | t0019 | g0007 | AFR | USA | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0111 | REF | REF | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| homoSapiens_grch38 | hp1 | a0003 | c0005 | t0003 | g0249 | REF | REF | LRIG1_chr3_66373797_66506022 | LRIG1 | chr3 | 66373797 | 66506022 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:66380387
|
T | G | 8 | a0004a0009a0012others(5): Show | 36 | HG00099.hp1 HG00544.hp1 HG00609.hp2 others(33): Show |
missense_variant | MODERATE | c.3158A>C | p.Gln1053Pro | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 19/19 | 3773/5363 | 3158/3282 | 1053/1093 | chr3 | 66380387 | ||
| chr3:66380453
|
G | C | 7 | a0005a0010a0013others(4): Show | 27 | HG00280.hp1 HG01099.hp1 HG01123.hp1 others(24): Show |
missense_variant | MODERATE | c.3092C>G | p.Pro1031Arg | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 19/19 | 3707/5363 | 3092/3282 | 1031/1093 | chr3 | 66380453 | ||
| chr3:66380598
|
T | C | 1 | a0030 | 1 | HG02145.hp2 | missense_variant | MODERATE | c.3034A>G | p.Met1012Val | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 18/19 | 3649/5363 | 3034/3282 | 1012/1093 | chr3 | 66380598 | ||
| chr3:66380635
|
G | C | 1 | a0025 | 1 | HG02300.hp2 | missense_variant | MODERATE | c.2997C>G | p.Asn999Lys | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 18/19 | 3612/5363 | 2997/3282 | 999/1093 | chr3 | 66380635 | ||
| chr3:66380654
|
C | G | 2 | a0012a0024 | 4 | HG00544.hp1 HG02132.hp1 NA18969.hp2 others(1): Show |
missense_variant | MODERATE | c.2978G>C | p.Gly993Ala | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 18/19 | 3593/5363 | 2978/3282 | 993/1093 | chr3 | 66380654 | ||
| chr3:66380763
|
C | T | 5 | a0005a0010a0013others(2): Show | 25 | HG00280.hp1 HG01099.hp1 HG01123.hp1 others(22): Show |
missense_variant | MODERATE | c.2869G>A | p.Ala957Thr | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 18/19 | 3484/5363 | 2869/3282 | 957/1093 | chr3 | 66380763 | ||
| chr3:66380770
|
T | G | 1 | a0019 | 1 | NA18951.hp2 | missense_variant | MODERATE | c.2862A>C | p.Arg954Ser | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 18/19 | 3477/5363 | 2862/3282 | 954/1093 | chr3 | 66380770 | ||
| chr3:66380855
|
C | A | 1 | a0020 | 1 | NA18906.hp1 | missense_variant | MODERATE | c.2777G>T | p.Gly926Val | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 18/19 | 3392/5363 | 2777/3282 | 926/1093 | chr3 | 66380855 | ||
| chr3:66380856
|
C | T | 6 | a0006a0008a0017others(3): Show | 28 | HG00735.hp1 HG01515.hp1 HG01884.hp2 others(25): Show |
missense_variant | MODERATE | c.2776G>A | p.Gly926Ser | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 18/19 | 3391/5363 | 2776/3282 | 926/1093 | chr3 | 66380856 | ||
| chr3:66381622
|
G | A | 1 | a0023 | 1 | HG01496.hp1 | missense_variant | MODERATE | c.2627C>T | p.Pro876Leu | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 17/19 | 3242/5363 | 2627/3282 | 876/1093 | chr3 | 66381622 | ||
| chr3:66382293
|
T | C | 1 | a0029 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.2597A>G | p.Asn866Ser | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 16/19 | 3212/5363 | 2597/3282 | 866/1093 | chr3 | 66382293 | ||
| chr3:66382297
|
C | T | 1 | a0032 | 1 | NA20805.hp2 | missense_variant | MODERATE | c.2593G>A | p.Ala865Thr | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 16/19 | 3208/5363 | 2593/3282 | 865/1093 | chr3 | 66382297 | ||
| chr3:66382309
|
C | G | 1 | a0033 | 1 | HG03927.hp2 | missense_variant | MODERATE | c.2581G>C | p.Gly861Arg | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 16/19 | 3196/5363 | 2581/3282 | 861/1093 | chr3 | 66382309 | ||
| chr3:66383278
|
G | A | 1 | a0021 | 1 | NA20300.hp2 | missense_variant | MODERATE | c.2195C>T | p.Pro732Leu | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 15/19 | 2810/5363 | 2195/3282 | 732/1093 | chr3 | 66383278 | ||
| chr3:66383311
|
G | A | 2 | a0011a0014 | 6 | HG00609.hp1 HG02486.hp2 HG02559.hp1 others(3): Show |
missense_variant | MODERATE | c.2162C>T | p.Pro721Leu | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 15/19 | 2777/5363 | 2162/3282 | 721/1093 | chr3 | 66383311 | ||
| chr3:66383999
|
G | C | 1 | a0029 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.2063C>G | p.Thr688Ser | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 14/19 | 2678/5363 | 2063/3282 | 688/1093 | chr3 | 66383999 | ||
| chr3:66384219
|
T | C | 11 | a0002a0007a0013others(8): Show | 80 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(77): Show |
missense_variant | MODERATE | c.1843A>G | p.Met615Val | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 14/19 | 2458/5363 | 1843/3282 | 615/1093 | chr3 | 66384219 | ||
| chr3:66386113
|
C | T | 1 | a0021 | 1 | NA20300.hp2 | missense_variant | MODERATE | c.1657G>A | p.Gly553Arg | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 13/19 | 2272/5363 | 1657/3282 | 553/1093 | chr3 | 66386113 | ||
| chr3:66386121
|
G | A | 1 | a0022 | 1 | HG02896.hp2 | missense_variant | MODERATE | c.1649C>T | p.Ala550Val | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 13/19 | 2264/5363 | 1649/3282 | 550/1093 | chr3 | 66386121 | ||
| chr3:66386122
|
C | T | 1 | a0008 | 12 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(9): Show |
missense_variant | MODERATE | c.1648G>A | p.Ala550Thr | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 13/19 | 2263/5363 | 1648/3282 | 550/1093 | chr3 | 66386122 | ||
| chr3:66386255
|
C | T | 1 | a0017 | 1 | HG01952.hp1 | missense_variant | MODERATE | c.1515G>A | p.Met505Ile | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 13/19 | 2130/5363 | 1515/3282 | 505/1093 | chr3 | 66386255 | ||
| chr3:66410216
|
G | A | 1 | a0016 | 1 | HG02145.hp1 | missense_variant | MODERATE | c.848C>T | p.Thr283Met | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/19 | 1463/5363 | 848/3282 | 283/1093 | chr3 | 66410216 | ||
| chr3:66412879
|
C | T | 1 | a0015 | 1 | NA19079.hp1 | missense_variant | MODERATE | c.783G>A | p.Met261Ile | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/19 | 1398/5363 | 783/3282 | 261/1093 | chr3 | 66412879 | ||
| chr3:66412916
|
T | C | 1 | a0034 | 1 | HG02523.hp2 | missense_variant | MODERATE | c.746A>G | p.Lys249Arg | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/19 | 1361/5363 | 746/3282 | 249/1093 | chr3 | 66412916 | ||
| chr3:66451607
|
G | A | 1 | a0035 | 1 | NA19079.hp2 | missense_variant | MODERATE | c.317C>T | p.Ala106Val | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/19 | 932/5363 | 317/3282 | 106/1093 | chr3 | 66451607 | ||
| chr3:66500332
|
G | C | 18 | a0001a0002a0004others(15): Show | 158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
missense_variant | MODERATE | c.76C>G | p.Leu26Val | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/19 | 691/5363 | 76/3282 | 26/1093 | chr3 | 66500332 | ||
| chr3:66500338
|
G | C | 18 | a0001a0002a0004others(15): Show | 158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
missense_variant | MODERATE | c.70C>G | p.Leu24Val | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/19 | 685/5363 | 70/3282 | 24/1093 | chr3 | 66500338 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:66380395
|
C | T | 3 | a0009c0037a0012c0017a0024c0055 | 5 | HG00544.hp1 HG00609.hp2 HG02132.hp1 others(2): Show |
synonymous_variant | LOW | c.3150G>A | p.Ala1050Ala | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 19/19 | 3765/5363 | 3150/3282 | 1050/1093 | chr3 | 66380395 | ||
| chr3:66380446
|
G | A | 4 | a0001c0014a0014c0042a0030c0046others(1): Show | 8 | HG01433.hp1 HG02145.hp2 HG03834.hp2 others(5): Show |
synonymous_variant | LOW | c.3099C>T | p.Ser1033Ser | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 19/19 | 3714/5363 | 3099/3282 | 1033/1093 | chr3 | 66380446 | ||
| chr3:66380479
|
G | C | 1 | a0003c0036 | 1 | HG02572.hp1 | synonymous_variant | LOW | c.3066C>G | p.Ser1022Ser | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 19/19 | 3681/5363 | 3066/3282 | 1022/1093 | chr3 | 66380479 | ||
| chr3:66380680
|
G | A | 3 | a0006c0019a0011c0030a0017c0025 | 4 | HG01952.hp1 HG02280.hp2 HG02809.hp2 others(1): Show |
synonymous_variant | LOW | c.2952C>T | p.Ala984Ala | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 18/19 | 3567/5363 | 2952/3282 | 984/1093 | chr3 | 66380680 | ||
| chr3:66380737
|
C | T | 1 | a0002c0021 | 2 | HG00558.hp2 NA18986.hp2 |
synonymous_variant | LOW | c.2895G>A | p.Pro965Pro | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 18/19 | 3510/5363 | 2895/3282 | 965/1093 | chr3 | 66380737 | ||
| chr3:66380851
|
G | A | 2 | a0002c0018a0034c0056 | 4 | HG00673.hp2 HG02056.hp1 HG02523.hp2 others(1): Show |
synonymous_variant | LOW | c.2781C>T | p.Gly927Gly | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 18/19 | 3396/5363 | 2781/3282 | 927/1093 | chr3 | 66380851 | ||
| chr3:66381519
|
C | T | 1 | a0001c0007 | 12 | HG00280.hp2 HG01074.hp2 HG01099.hp2 others(9): Show |
synonymous_variant | LOW | c.2730G>A | p.Ala910Ala | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 17/19 | 3345/5363 | 2730/3282 | 910/1093 | chr3 | 66381519 | ||
| chr3:66383034
|
G | A | 3 | a0006c0009a0006c0026a0020c0027 | 10 | HG00735.hp1 HG02970.hp1 HG02970.hp2 others(7): Show |
synonymous_variant | LOW | c.2439C>T | p.Cys813Cys | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 15/19 | 3054/5363 | 2439/3282 | 813/1093 | chr3 | 66383034 | ||
| chr3:66383252
|
A | G | 42 | a0001c0007a0001c0014a0001c0023others(39): Show | 176 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(173): Show |
synonymous_variant | LOW | c.2221T>C | p.Leu741Leu | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 15/19 | 2836/5363 | 2221/3282 | 741/1093 | chr3 | 66383252 | ||
| chr3:66384097
|
G | A | 1 | a0003c0031 | 1 | HG03486.hp1 | synonymous_variant | LOW | c.1965C>T | p.Asp655Asp | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 14/19 | 2580/5363 | 1965/3282 | 655/1093 | chr3 | 66384097 | ||
| chr3:66384244
|
G | A | 1 | a0002c0022 | 2 | HG01243.hp1 NA18747.hp2 |
synonymous_variant | LOW | c.1818C>T | p.His606His | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 14/19 | 2433/5363 | 1818/3282 | 606/1093 | chr3 | 66384244 | ||
| chr3:66386114
|
G | A | 2 | a0004c0053a0025c0054 | 2 | HG02300.hp2 NA18981.hp1 |
synonymous_variant | LOW | c.1656C>T | p.Asp552Asp | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 13/19 | 2271/5363 | 1656/3282 | 552/1093 | chr3 | 66386114 | ||
| chr3:66386126
|
G | C | 3 | a0009c0037a0012c0017a0024c0055 | 5 | HG00544.hp1 HG00609.hp2 HG02132.hp1 others(2): Show |
synonymous_variant | LOW | c.1644C>G | p.Val548Val | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 13/19 | 2259/5363 | 1644/3282 | 548/1093 | chr3 | 66386126 | ||
| chr3:66386156
|
G | A | 1 | a0007c0033 | 1 | HG03195.hp1 | synonymous_variant | LOW | c.1614C>T | p.Thr538Thr | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 13/19 | 2229/5363 | 1614/3282 | 538/1093 | chr3 | 66386156 | ||
| chr3:66394191
|
G | A | 19 | a0001c0007a0001c0023a0003c0010others(16): Show | 78 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(75): Show |
synonymous_variant | LOW | c.1317C>T | p.Ser439Ser | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/19 | 1932/5363 | 1317/3282 | 439/1093 | chr3 | 66394191 | ||
| chr3:66417176
|
C | T | 2 | a0001c0040a0002c0041 | 2 | NA18969.hp1 NA18993.hp1 |
synonymous_variant | LOW | c.456G>A | p.Thr152Thr | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 4/19 | 1071/5363 | 456/3282 | 152/1093 | chr3 | 66417176 | ||
| chr3:66462470
|
A | G | 1 | a0026c0039 | 1 | HG04115.hp1 | synonymous_variant | LOW | c.258T>C | p.Ala86Ala | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/19 | 873/5363 | 258/3282 | 86/1093 | chr3 | 66462470 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:66378812
|
A | C | 1 | a0013c0020t0029 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1451T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 19/19 | 1451 | chr3 | 66378812 | |||||
| chr3:66379037
|
G | A | 2 | a0006c0019t0012a0017c0025t0012 | 3 | HG01952.hp1 HG02280.hp2 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1226C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 19/19 | 1226 | chr3 | 66379037 | |||||
| chr3:66379051
|
C | G | 7 | a0001c0014t0011a0001c0014t0028a0003c0012t0018others(4): Show | 17 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1212G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 19/19 | 1212 | chr3 | 66379051 | |||||
| chr3:66379132
|
T | TTTAAG | 2 | a0011c0016t0013a0011c0030t0027 | 4 | HG02486.hp2 HG02559.hp1 HG02965.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1126_*1130dupCTTA others(1): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 19/19 | 1130 | chr3 | 66379132 | |||||
| chr3:66379145
|
A | G | 1 | a0007c0008t0025 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1118T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 19/19 | 1118 | chr3 | 66379145 | |||||
| chr3:66379259
|
C | T | 2 | a0003c0012t0014a0004c0003t0026 | 3 | HG02055.hp1 HG03130.hp2 HG03688.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1004G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 19/19 | 1004 | chr3 | 66379259 | |||||
| chr3:66379331
|
C | T | 1 | a0006c0035t0033 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*932G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 19/19 | 932 | chr3 | 66379331 | |||||
| chr3:66379418
|
A | C | 1 | a0003c0036t0034 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*845T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 19/19 | 845 | chr3 | 66379418 | |||||
| chr3:66379586
|
G | A | 2 | a0003c0012t0014a0021c0034t0019 | 3 | HG02055.hp1 HG03130.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*677C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 19/19 | 677 | chr3 | 66379586 | |||||
| chr3:66379598
|
C | T | 1 | a0004c0003t0026 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*665G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 19/19 | 665 | chr3 | 66379598 | |||||
| chr3:66379705
|
G | C | 3 | a0008c0006t0005a0008c0006t0009a0008c0006t0020 | 12 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*558C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 19/19 | 558 | chr3 | 66379705 | |||||
| chr3:66379762
|
C | A | 1 | a0003c0012t0014 | 2 | HG02055.hp1 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*501G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 19/19 | 501 | chr3 | 66379762 | |||||
| chr3:66379791
|
G | A | 1 | a0003c0012t0014 | 2 | HG02055.hp1 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*472C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 19/19 | 472 | chr3 | 66379791 | |||||
| chr3:66379910
|
AC | A | 36 | a0001c0007t0002a0001c0014t0010a0001c0014t0011others(33): Show | 92 | HG00099.hp1 HG00544.hp1 HG00609.hp2 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*352delG | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 19/19 | 352 | chr3 | 66379910 | |||||
| chr3:66379924
|
T | A | 3 | a0001c0014t0010a0014c0042t0010a0030c0046t0010 | 4 | HG01433.hp1 HG02145.hp2 HG03834.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*339A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 19/19 | 339 | chr3 | 66379924 | |||||
| chr3:66379942
|
G | A | 1 | a0001c0014t0028 | 1 | NA18949.hp1 | 3_prime_UTR_variant | MODIFIER | c.*321C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 19/19 | 321 | chr3 | 66379942 | |||||
| chr3:66379952
|
ATT | A | 8 | a0005c0004t0006a0005c0004t0007a0005c0004t0008others(5): Show | 20 | HG00280.hp1 HG01099.hp1 HG01123.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*309_*310delAA | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 19/19 | 309 | chr3 | 66379952 | |||||
| chr3:66379953
|
T | C | 1 | a0029c0052t0039 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*310A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 19/19 | 310 | chr3 | 66379953 | |||||
| chr3:66379957
|
C | T | 2 | a0005c0004t0008a0010c0011t0024 | 6 | HG01243.hp2 HG02258.hp1 HG02451.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*306G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 19/19 | 306 | chr3 | 66379957 | |||||
| chr3:66379966
|
A | G | 1 | a0003c0012t0014 | 2 | HG02055.hp1 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*297T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 19/19 | 297 | chr3 | 66379966 | |||||
| chr3:66380043
|
C | G | 1 | a0027c0050t0023 | 1 | HG01515.hp1 | 3_prime_UTR_variant | MODIFIER | c.*220G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 19/19 | 220 | chr3 | 66380043 | |||||
| chr3:66380044
|
T | C | 2 | a0013c0020t0035a0031c0047t0030 | 2 | HG02630.hp1 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*219A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 19/19 | 219 | chr3 | 66380044 | |||||
| chr3:66380047
|
T | C | 1 | a0006c0026t0036 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*216A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 19/19 | 216 | chr3 | 66380047 | |||||
| chr3:66380151
|
G | A | 1 | a0001c0002t0031 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*112C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 19/19 | 112 | chr3 | 66380151 | |||||
| chr3:66500512
|
G | A | 1 | a0007c0008t0037 | 1 | HG03942.hp1 | 5_prime_UTR_variant | MODIFIER | c.-105C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/19 | 105 | chr3 | 66500512 | |||||
| chr3:66500574
|
C | A | 1 | a0002c0001t0032 | 1 | HG00621.hp1 | 5_prime_UTR_variant | MODIFIER | c.-167G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/19 | 167 | chr3 | 66500574 | |||||
| chr3:66500652
|
G | T | 67 | a0001c0002t0001a0001c0002t0031a0001c0007t0001others(64): Show | 200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
5_prime_UTR_variant | MODIFIER | c.-245C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/19 | 245 | chr3 | 66500652 | |||||
| chr3:66500920
|
G | T | 1 | a0014c0043t0022 | 1 | HG00609.hp1 | 5_prime_UTR_variant | MODIFIER | c.-513C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/19 | 513 | chr3 | 66500920 | |||||
| chr3:66500929
|
G | A | 2 | a0004c0003t0038a0029c0052t0039 | 2 | HG02486.hp1 NA18906.hp2 |
5_prime_UTR_variant | MODIFIER | c.-522C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/19 | 522 | chr3 | 66500929 | |||||
| chr3:66500930
|
A | AGC | 5 | a0003c0012t0017a0003c0012t0018a0005c0004t0021others(2): Show | 5 | HG02886.hp2 HG02976.hp1 HG02976.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-525_-524dupGC | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/19 | 524 | chr3 | 66500930 | |||||
| chr3:66500942
|
C | G | 1 | a0002c0001t0016 | 1 | NA18991.hp1 | 5_prime_UTR_variant | MODIFIER | c.-535G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/19 | 535 | chr3 | 66500942 | |||||
| chr3:66500955
|
G | T | 1 | a0002c0001t0015 | 1 | HG01069.hp2 | 5_prime_UTR_variant | MODIFIER | c.-548C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/19 | 548 | chr3 | 66500955 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:66380873
|
C | T | 1 | a0021c0034t0019g0007 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2771-12G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 17/18 | chr3 | 66380873 | ||||||
| chr3:66380971
|
A | C | 4 | a0001c0014t0011g0058a0001c0014t0011g0117a0001c0014t0028g0118others(1): Show | 4 | NA18939.hp2 NA18949.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.2771-110T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 17/18 | chr3 | 66380971 | ||||||
| chr3:66381030
|
A | C | 1 | a0003c0012t0018g0008 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2771-169T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 17/18 | chr3 | 66381030 | ||||||
| chr3:66381108
|
A | G | 204 | a0001c0007t0001g0116a0001c0007t0002g0080a0001c0007t0002g0100others(201): Show | 204 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.2771-247T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 17/18 | chr3 | 66381108 | ||||||
| chr3:66381111
|
G | A | 2 | a0007c0008t0001g0013a0007c0008t0001g0031 | 2 | NA18970.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.2771-250C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 17/18 | chr3 | 66381111 | ||||||
| chr3:66381178
|
A | G | 178 | a0001c0007t0001g0116a0001c0007t0002g0080a0001c0007t0002g0100others(175): Show | 178 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(175): Show |
intron_variant | MODIFIER | c.2770+301T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 17/18 | chr3 | 66381178 | ||||||
| chr3:66381180
|
A | AATAGCCC others(16): Show |
1 | a0003c0012t0018g0008 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2770+276_2770+298d others(25): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 17/18 | chr3 | 66381180 | ||||||
| chr3:66381186
|
C | T | 2 | a0003c0012t0014g0233a0003c0012t0014g0236 | 2 | HG02055.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2770+293G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 17/18 | chr3 | 66381186 | ||||||
| chr3:66381192
|
G | A | 12 | a0008c0006t0005g0200a0008c0006t0005g0215a0008c0006t0005g0219others(9): Show | 12 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.2770+287C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 17/18 | chr3 | 66381192 | ||||||
| chr3:66381222
|
G | A | 1 | a0022c0032t0007g0046 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2770+257C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 17/18 | chr3 | 66381222 | ||||||
| chr3:66381289
|
C | T | 35 | a0001c0014t0011g0058a0001c0014t0011g0117a0001c0014t0028g0118others(32): Show | 35 | HG00735.hp1 HG01884.hp2 HG01952.hp1 others(32): Show |
intron_variant | MODIFIER | c.2770+190G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 17/18 | chr3 | 66381289 | ||||||
| chr3:66381385
|
A | G | 1 | a0001c0014t0010g0186 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2770+94T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 17/18 | chr3 | 66381385 | ||||||
| chr3:66381394
|
G | C | 6 | a0006c0009t0004g0224a0006c0009t0004g0225a0006c0009t0004g0226others(3): Show | 6 | HG00735.hp1 HG02970.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.2770+85C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 17/18 | chr3 | 66381394 | ||||||
| chr3:66381663
|
C | G | 1 | a0003c0012t0018g0008 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2618-32G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 16/18 | chr3 | 66381663 | ||||||
| chr3:66381669
|
T | G | 1 | a0004c0003t0002g0181 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2618-38A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 16/18 | chr3 | 66381669 | ||||||
| chr3:66381732
|
T | A | 1 | a0028c0049t0001g0067 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2618-101A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 16/18 | chr3 | 66381732 | ||||||
| chr3:66381851
|
C | T | 1 | a0004c0003t0002g0101 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2618-220G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 16/18 | chr3 | 66381851 | ||||||
| chr3:66381852
|
A | G | 174 | a0001c0007t0001g0116a0001c0007t0002g0080a0001c0007t0002g0100others(171): Show | 174 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(171): Show |
intron_variant | MODIFIER | c.2618-221T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 16/18 | chr3 | 66381852 | ||||||
| chr3:66381883
|
G | A | 5 | a0001c0014t0010g0134a0001c0014t0010g0186a0003c0012t0018g0008others(2): Show | 5 | HG01433.hp1 HG02145.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2618-252C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 16/18 | chr3 | 66381883 | ||||||
| chr3:66381953
|
TC | T | 11 | a0003c0012t0018g0008a0006c0009t0002g0045a0006c0009t0004g0224others(8): Show | 11 | HG00735.hp1 HG02970.hp1 HG02970.hp2 others(8): Show |
intron_variant | MODIFIER | c.2617+319delG | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 16/18 | chr3 | 66381953 | ||||||
| chr3:66381991
|
G | A | 1 | a0002c0001t0001g0124 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2617+282C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 16/18 | chr3 | 66381991 | ||||||
| chr3:66381996
|
G | C | 3 | a0013c0020t0035g0208a0029c0052t0039g0263a0031c0047t0030g0162 | 3 | HG02486.hp1 HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.2617+277C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 16/18 | chr3 | 66381996 | ||||||
| chr3:66382022
|
A | G | 4 | a0001c0014t0011g0058a0001c0014t0011g0117a0001c0014t0028g0118others(1): Show | 4 | NA18939.hp2 NA18949.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.2617+251T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 16/18 | chr3 | 66382022 | ||||||
| chr3:66382077
|
G | A | 2 | a0001c0002t0001g0070a0001c0002t0001g0071 | 2 | HG01167.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.2617+196C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 16/18 | chr3 | 66382077 | ||||||
| chr3:66382114
|
T | C | 1 | a0018c0028t0003g0259 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2617+159A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 16/18 | chr3 | 66382114 | ||||||
| chr3:66382256
|
A | G | 204 | a0001c0007t0001g0116a0001c0007t0002g0080a0001c0007t0002g0100others(201): Show | 204 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.2617+17T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 16/18 | chr3 | 66382256 | ||||||
| chr3:66382421
|
G | A | 55 | a0001c0007t0001g0116a0001c0007t0002g0080a0001c0007t0002g0100others(52): Show | 55 | HG00280.hp2 HG00735.hp1 HG01074.hp2 others(52): Show |
intron_variant | MODIFIER | c.2492-23C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 15/18 | chr3 | 66382421 | ||||||
| chr3:66382423
|
A | C | 4 | a0011c0016t0013g0204a0011c0016t0013g0205a0011c0016t0013g0206others(1): Show | 4 | HG02486.hp2 HG02559.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2492-25T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 15/18 | chr3 | 66382423 | ||||||
| chr3:66382429
|
G | A | 5 | a0009c0037t0002g0018a0012c0017t0002g0015a0012c0017t0002g0020others(2): Show | 5 | HG00544.hp1 HG00609.hp2 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.2492-31C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 15/18 | chr3 | 66382429 | ||||||
| chr3:66382522
|
T | TG | 28 | a0001c0007t0001g0116a0001c0007t0002g0080a0001c0007t0002g0100others(25): Show | 28 | HG00280.hp2 HG00735.hp1 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.2492-125dupC | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 15/18 | chr3 | 66382522 | ||||||
| chr3:66382545
|
C | G | 4 | a0011c0016t0013g0204a0011c0016t0013g0205a0011c0016t0013g0206others(1): Show | 4 | HG02486.hp2 HG02559.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2492-147G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 15/18 | chr3 | 66382545 | ||||||
| chr3:66382563
|
G | A | 6 | a0006c0009t0004g0224a0006c0009t0004g0225a0006c0009t0004g0226others(3): Show | 6 | HG00735.hp1 HG02970.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.2492-165C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 15/18 | chr3 | 66382563 | ||||||
| chr3:66382578
|
A | ACACCCAG others(11): Show |
24 | a0005c0004t0001g0019a0005c0004t0006g0202a0005c0004t0006g0220others(21): Show | 24 | HG00280.hp1 HG01099.hp1 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.2492-198_2492-181d others(20): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 15/18 | chr3 | 66382578 | ||||||
| chr3:66382586
|
C | T | 100 | a0001c0007t0001g0116a0001c0007t0002g0080a0001c0007t0002g0100others(97): Show | 100 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.2492-188G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 15/18 | chr3 | 66382586 | ||||||
| chr3:66382649
|
G | A | 1 | a0001c0014t0010g0134 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2492-251C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 15/18 | chr3 | 66382649 | ||||||
| chr3:66382669
|
A | G | 204 | a0001c0007t0001g0116a0001c0007t0002g0080a0001c0007t0002g0100others(201): Show | 204 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.2492-271T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 15/18 | chr3 | 66382669 | ||||||
| chr3:66382717
|
C | T | 1 | a0004c0003t0002g0103 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2491+265G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 15/18 | chr3 | 66382717 | ||||||
| chr3:66382752
|
T | A | 177 | a0001c0007t0001g0116a0001c0007t0002g0080a0001c0007t0002g0100others(174): Show | 177 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(174): Show |
intron_variant | MODIFIER | c.2491+230A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 15/18 | chr3 | 66382752 | ||||||
| chr3:66382753
|
G | A | 4 | a0003c0005t0003g0001a0003c0005t0003g0209a0003c0005t0003g0211others(1): Show | 5 | NA18966.hp2 NA18986.hp1 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.2491+229C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 15/18 | chr3 | 66382753 | ||||||
| chr3:66382776
|
TGAGTATT others(21): Show |
T | 4 | a0002c0001t0001g0121a0003c0012t0014g0233a0003c0012t0014g0236others(1): Show | 4 | HG01255.hp2 HG02055.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2491+178_2491+205d others(30): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 15/18 | chr3 | 66382776 | ||||||
| chr3:66382887
|
C | T | 1 | a0004c0003t0002g0097 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2491+95G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 15/18 | chr3 | 66382887 | ||||||
| chr3:66382888
|
A | G | 177 | a0001c0007t0001g0116a0001c0007t0002g0080a0001c0007t0002g0100others(174): Show | 177 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(174): Show |
intron_variant | MODIFIER | c.2491+94T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 15/18 | chr3 | 66382888 | ||||||
| chr3:66383513
|
T | G | 89 | a0001c0007t0001g0116a0001c0007t0002g0080a0001c0007t0002g0100others(86): Show | 89 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.2072-112A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 14/18 | chr3 | 66383513 | ||||||
| chr3:66383611
|
G | A | 1 | a0004c0053t0002g0197 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2072-210C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 14/18 | chr3 | 66383611 | ||||||
| chr3:66383666
|
TTCTTGAC others(44): Show |
T | 23 | a0003c0012t0018g0008a0005c0004t0006g0202a0005c0004t0006g0220others(20): Show | 23 | HG00280.hp1 HG01099.hp1 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.2071+274_2072-266d others(53): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 14/18 | chr3 | 66383666 | ||||||
| chr3:66383732
|
A | G | 1 | a0021c0034t0019g0007 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2071+259T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 14/18 | chr3 | 66383732 | ||||||
| chr3:66383829
|
T | G | 1 | a0006c0019t0012g0245 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2071+162A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 14/18 | chr3 | 66383829 | ||||||
| chr3:66383941
|
C | G | 3 | a0002c0001t0001g0085a0002c0001t0001g0087a0002c0001t0001g0147 | 3 | HG01069.hp1 HG01071.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.2071+50G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 14/18 | chr3 | 66383941 | ||||||
| chr3:66383948
|
T | TCA | 24 | a0001c0002t0001g0066a0001c0002t0001g0071a0001c0002t0001g0084others(21): Show | 24 | HG00280.hp2 HG01074.hp2 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.2071+41_2071+42dup others(2): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 14/18 | chr3 | 66383948 | ||||||
| chr3:66383948
|
T | TCACA | 11 | a0005c0004t0006g0220a0005c0004t0006g0222a0005c0004t0008g0247others(8): Show | 11 | HG01243.hp2 HG02258.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.2071+39_2071+42dup others(4): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 14/18 | chr3 | 66383948 | ||||||
| chr3:66383948
|
T | TCACACA | 54 | a0002c0001t0001g0047a0002c0001t0001g0048a0002c0001t0001g0052others(51): Show | 54 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.2071+37_2071+42dup others(6): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 14/18 | chr3 | 66383948 | ||||||
| chr3:66383948
|
T | TCACACAC others(1): Show |
28 | a0002c0001t0001g0072a0002c0001t0001g0119a0002c0001t0001g0135others(25): Show | 28 | HG00621.hp1 HG00621.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.2071+35_2071+42dup others(8): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 14/18 | chr3 | 66383948 | ||||||
| chr3:66383948
|
T | TCACACAC others(3): Show |
15 | a0001c0023t0002g0060a0001c0023t0002g0068a0002c0001t0001g0149others(12): Show | 15 | HG00280.hp1 HG00735.hp1 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.2071+33_2071+42dup others(10): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 14/18 | chr3 | 66383948 | ||||||
| chr3:66383948
|
T | TCACACAC others(5): Show |
20 | a0005c0004t0006g0238a0005c0004t0007g0017a0006c0009t0004g0232others(17): Show | 20 | HG01099.hp1 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.2071+31_2071+42dup others(12): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 14/18 | chr3 | 66383948 | ||||||
| chr3:66383948
|
T | TCACACAC others(7): Show |
5 | a0001c0014t0010g0134a0001c0014t0010g0186a0008c0006t0005g0215others(2): Show | 5 | HG01433.hp1 HG02145.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2071+29_2071+42dup others(14): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 14/18 | chr3 | 66383948 | ||||||
| chr3:66383948
|
T | TCACACAC others(9): Show |
2 | a0006c0009t0002g0045a0030c0046t0010g0184 | 2 | HG02145.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2071+27_2071+42dup others(16): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 14/18 | chr3 | 66383948 | ||||||
| chr3:66383948
|
T | TCACACAC others(11): Show |
1 | a0026c0039t0001g0073 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2071+25_2071+42dup others(18): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 14/18 | chr3 | 66383948 | ||||||
| chr3:66383948
|
TCACACAC others(1): Show |
T | 3 | a0005c0004t0006g0202a0005c0004t0021g0006a0018c0028t0003g0259 | 3 | HG02818.hp2 HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2071+35_2071+42del others(8): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 14/18 | chr3 | 66383948 | ||||||
| chr3:66383948
|
TCACACAC others(5): Show |
T | 1 | a0005c0004t0006g0221 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2071+31_2071+42del others(12): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 14/18 | chr3 | 66383948 | ||||||
| chr3:66384307
|
G | A | 1 | a0003c0012t0017g0004 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1790-35C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 13/18 | chr3 | 66384307 | ||||||
| chr3:66384440
|
T | C | 1 | a0029c0052t0039g0263 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1790-168A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 13/18 | chr3 | 66384440 | ||||||
| chr3:66384454
|
T | C | 1 | a0018c0028t0003g0259 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1790-182A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 13/18 | chr3 | 66384454 | ||||||
| chr3:66384460
|
C | T | 1 | a0018c0028t0003g0259 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1790-188G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 13/18 | chr3 | 66384460 | ||||||
| chr3:66384581
|
TA | T | 4 | a0004c0003t0038g0262a0009c0015t0002g0032a0009c0015t0002g0033others(1): Show | 4 | HG01891.hp2 HG02922.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1790-310delT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 13/18 | chr3 | 66384581 | ||||||
| chr3:66384656
|
G | C | 1 | a0003c0012t0018g0008 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1790-384C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 13/18 | chr3 | 66384656 | ||||||
| chr3:66384671
|
G | C | 1 | a0002c0001t0001g0147 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1790-399C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 13/18 | chr3 | 66384671 | ||||||
| chr3:66384678
|
CAATGGGA others(34): Show |
C | 2 | a0001c0002t0001g0075a0010c0011t0007g0127 | 2 | HG01123.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1790-447_1790-407d others(43): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 13/18 | chr3 | 66384678 | ||||||
| chr3:66384693
|
T | A | 50 | a0002c0001t0001g0047a0002c0001t0001g0048a0002c0001t0001g0059others(47): Show | 50 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.1790-421A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 13/18 | chr3 | 66384693 | ||||||
| chr3:66384696
|
G | A | 1 | a0004c0003t0002g0193 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1790-424C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 13/18 | chr3 | 66384696 | ||||||
| chr3:66384703
|
T | C | 3 | a0001c0002t0001g0094a0003c0005t0001g0026a0019c0029t0001g0022 | 3 | NA18951.hp2 NA18994.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.1790-431A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 13/18 | chr3 | 66384703 | ||||||
| chr3:66384821
|
C | T | 1 | a0002c0001t0001g0152 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1790-549G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 13/18 | chr3 | 66384821 | ||||||
| chr3:66384905
|
G | A | 1 | a0034c0056t0001g0182 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1790-633C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 13/18 | chr3 | 66384905 | ||||||
| chr3:66385152
|
C | G | 1 | a0001c0002t0001g0063 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1789+829G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 13/18 | chr3 | 66385152 | ||||||
| chr3:66385457
|
T | TTTTTA | 4 | a0011c0016t0013g0204a0011c0016t0013g0205a0011c0016t0013g0206others(1): Show | 4 | HG02486.hp2 HG02559.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1789+523_1789+524i others(7): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 13/18 | chr3 | 66385457 | ||||||
| chr3:66385457
|
T | TTTTTG | 151 | a0001c0007t0001g0116a0001c0007t0002g0080a0001c0007t0002g0100others(148): Show | 151 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(148): Show |
intron_variant | MODIFIER | c.1789+519_1789+523d others(7): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 13/18 | chr3 | 66385457 | ||||||
| chr3:66385534
|
C | T | 26 | a0002c0001t0001g0171a0002c0001t0001g0172a0002c0001t0001g0173others(23): Show | 26 | HG00738.hp1 HG01099.hp1 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.1789+447G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 13/18 | chr3 | 66385534 | ||||||
| chr3:66385616
|
C | T | 15 | a0006c0035t0033g0207a0008c0006t0005g0200a0008c0006t0005g0215others(12): Show | 15 | HG01884.hp2 HG02280.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.1789+365G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 13/18 | chr3 | 66385616 | ||||||
| chr3:66385634
|
G | A | 3 | a0002c0001t0001g0055a0002c0001t0001g0160a0007c0008t0003g0213 | 3 | HG00738.hp2 HG01123.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1789+347C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 13/18 | chr3 | 66385634 | ||||||
| chr3:66385667
|
A | T | 1 | a0006c0009t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1789+314T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 13/18 | chr3 | 66385667 | ||||||
| chr3:66385672
|
C | T | 1 | a0001c0002t0001g0157 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1789+309G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 13/18 | chr3 | 66385672 | ||||||
| chr3:66385758
|
T | G | 97 | a0001c0014t0010g0134a0001c0014t0010g0186a0001c0014t0011g0058others(94): Show | 97 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.1789+223A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 13/18 | chr3 | 66385758 | ||||||
| chr3:66386330
|
G | A | 2 | a0004c0003t0002g0088a0004c0003t0002g0089 | 2 | HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1469-29C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66386330 | ||||||
| chr3:66386443
|
C | A | 1 | a0002c0001t0001g0137 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1469-142G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66386443 | ||||||
| chr3:66386452
|
G | T | 1 | a0002c0001t0001g0137 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1469-151C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66386452 | ||||||
| chr3:66386467
|
T | C | 57 | a0001c0007t0001g0116a0001c0007t0002g0080a0001c0007t0002g0100others(54): Show | 57 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.1469-166A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66386467 | ||||||
| chr3:66386603
|
C | G | 3 | a0006c0019t0012g0244a0006c0019t0012g0245a0017c0025t0012g0253 | 3 | HG01952.hp1 HG02280.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1469-302G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66386603 | ||||||
| chr3:66386652
|
G | A | 1 | a0030c0046t0010g0184 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1469-351C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66386652 | ||||||
| chr3:66386662
|
T | C | 93 | a0001c0014t0010g0134a0001c0014t0010g0186a0001c0014t0011g0058others(90): Show | 93 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.1469-361A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66386662 | ||||||
| chr3:66386692
|
G | C | 10 | a0008c0006t0005g0200a0008c0006t0005g0215a0008c0006t0005g0219others(7): Show | 10 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1469-391C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66386692 | ||||||
| chr3:66386760
|
A | AC | 13 | a0008c0006t0005g0200a0008c0006t0005g0215a0008c0006t0005g0219others(10): Show | 13 | HG01884.hp2 HG02145.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.1469-460_1469-459i others(3): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66386760 | ||||||
| chr3:66386835
|
G | A | 1 | a0001c0002t0001g0056 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1469-534C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66386835 | ||||||
| chr3:66387010
|
T | C | 1 | a0003c0012t0017g0004 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1469-709A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66387010 | ||||||
| chr3:66387032
|
C | G | 1 | a0019c0029t0001g0022 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1469-731G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66387032 | ||||||
| chr3:66387097
|
C | T | 22 | a0005c0004t0006g0202a0005c0004t0006g0220a0005c0004t0006g0221others(19): Show | 22 | HG00280.hp1 HG01099.hp1 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.1469-796G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66387097 | ||||||
| chr3:66387204
|
A | G | 1 | a0001c0007t0002g0194 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1469-903T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66387204 | ||||||
| chr3:66387246
|
G | C | 1 | a0001c0002t0031g0069 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1469-945C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66387246 | ||||||
| chr3:66387321
|
C | G | 1 | a0021c0034t0019g0007 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1469-1020G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66387321 | ||||||
| chr3:66387407
|
C | G | 1 | a0003c0012t0018g0008 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1469-1106G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66387407 | ||||||
| chr3:66387413
|
G | A | 1 | a0001c0002t0001g0189 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1469-1112C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66387413 | ||||||
| chr3:66387473
|
A | G | 13 | a0006c0035t0033g0207a0008c0006t0005g0200a0008c0006t0005g0215others(10): Show | 13 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.1469-1172T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66387473 | ||||||
| chr3:66387505
|
G | A | 5 | a0008c0006t0005g0219a0011c0016t0013g0204a0011c0016t0013g0205others(2): Show | 5 | HG02486.hp2 HG02559.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1469-1204C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66387505 | ||||||
| chr3:66387532
|
A | G | 23 | a0005c0004t0006g0202a0005c0004t0006g0220a0005c0004t0006g0221others(20): Show | 23 | HG00280.hp1 HG01099.hp1 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.1469-1231T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66387532 | ||||||
| chr3:66387566
|
C | T | 5 | a0004c0003t0002g0097a0004c0003t0002g0103a0004c0003t0002g0193others(2): Show | 5 | HG01256.hp2 HG02071.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.1469-1265G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66387566 | ||||||
| chr3:66387608
|
C | T | 2 | a0013c0020t0035g0208a0031c0047t0030g0162 | 2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1469-1307G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66387608 | ||||||
| chr3:66387738
|
A | G | 6 | a0001c0023t0002g0060a0001c0023t0002g0068a0003c0010t0004g0229others(3): Show | 6 | HG02055.hp1 HG02572.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1469-1437T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66387738 | ||||||
| chr3:66387785
|
C | G | 1 | a0029c0052t0039g0263 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1469-1484G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66387785 | ||||||
| chr3:66387836
|
G | A | 22 | a0002c0001t0001g0191a0005c0004t0006g0202a0005c0004t0006g0220others(19): Show | 22 | HG01099.hp1 HG01123.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.1469-1535C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66387836 | ||||||
| chr3:66387882
|
G | A | 23 | a0004c0003t0001g0151a0004c0003t0002g0057a0004c0003t0002g0081others(20): Show | 23 | HG00099.hp1 HG01256.hp1 HG01256.hp2 others(20): Show |
intron_variant | MODIFIER | c.1469-1581C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66387882 | ||||||
| chr3:66387883
|
G | C | 70 | a0002c0001t0001g0047a0002c0001t0001g0048a0002c0001t0001g0059others(67): Show | 70 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.1469-1582C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66387883 | ||||||
| chr3:66387916
|
G | T | 178 | a0001c0007t0001g0116a0001c0007t0002g0080a0001c0007t0002g0100others(175): Show | 178 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.1469-1615C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66387916 | ||||||
| chr3:66387941
|
C | CA | 104 | a0001c0002t0001g0061a0001c0007t0001g0116a0001c0007t0002g0080others(101): Show | 104 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.1469-1641dupT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66387941 | ||||||
| chr3:66387964
|
G | A | 73 | a0002c0001t0001g0047a0002c0001t0001g0048a0002c0001t0001g0052others(70): Show | 73 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.1469-1663C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66387964 | ||||||
| chr3:66388038
|
C | T | 1 | a0003c0005t0003g0241 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1469-1737G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66388038 | ||||||
| chr3:66388064
|
G | A | 1 | a0003c0005t0003g0211 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1469-1763C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66388064 | ||||||
| chr3:66388106
|
C | CA | 14 | a0001c0002t0001g0178a0001c0023t0002g0060a0001c0023t0002g0068others(11): Show | 14 | HG02055.hp1 HG02055.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1469-1806dupT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66388106 | ||||||
| chr3:66388106
|
C | CAA | 20 | a0001c0014t0010g0134a0001c0014t0010g0186a0003c0012t0014g0233others(17): Show | 20 | HG00280.hp1 HG01099.hp1 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.1469-1807_1469-180 others(6): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66388106 | ||||||
| chr3:66388106
|
C | CAAA | 9 | a0001c0014t0011g0058a0001c0014t0011g0117a0005c0004t0007g0017others(6): Show | 9 | HG01243.hp2 HG02572.hp2 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.1469-1808_1469-180 others(7): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66388106 | ||||||
| chr3:66388106
|
CA | C | 143 | a0001c0002t0001g0051a0001c0002t0001g0063a0001c0002t0001g0065others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.1469-1806delT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66388106 | ||||||
| chr3:66388106
|
CAA | C | 14 | a0001c0002t0001g0049a0001c0002t0001g0077a0001c0002t0001g0094others(11): Show | 14 | HG00735.hp1 HG02300.hp1 HG02897.hp1 others(11): Show |
intron_variant | MODIFIER | c.1469-1807_1469-180 others(6): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66388106 | ||||||
| chr3:66388272
|
A | C | 3 | a0004c0003t0002g0057a0004c0003t0002g0105a0004c0003t0002g0107 | 3 | HG02698.hp1 HG03704.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1469-1971T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66388272 | ||||||
| chr3:66388293
|
G | A | 1 | a0001c0002t0001g0092 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1469-1992C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66388293 | ||||||
| chr3:66388449
|
A | G | 6 | a0001c0023t0002g0060a0001c0023t0002g0068a0003c0010t0004g0229others(3): Show | 6 | HG02055.hp1 HG02572.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1469-2148T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66388449 | ||||||
| chr3:66388601
|
G | A | 4 | a0001c0014t0011g0058a0001c0014t0011g0117a0001c0014t0028g0118others(1): Show | 4 | NA18939.hp2 NA18949.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.1469-2300C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66388601 | ||||||
| chr3:66388649
|
A | T | 4 | a0001c0014t0011g0058a0001c0014t0011g0117a0001c0014t0028g0118others(1): Show | 4 | NA18939.hp2 NA18949.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.1469-2348T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66388649 | ||||||
| chr3:66388691
|
T | C | 12 | a0001c0007t0001g0116a0001c0007t0002g0080a0001c0007t0002g0100others(9): Show | 12 | HG00280.hp2 HG01074.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.1469-2390A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66388691 | ||||||
| chr3:66388708
|
T | G | 11 | a0001c0023t0002g0060a0001c0023t0002g0068a0003c0010t0004g0229others(8): Show | 11 | HG02055.hp1 HG02486.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1469-2407A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66388708 | ||||||
| chr3:66388777
|
A | G | 1 | a0003c0012t0018g0008 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1469-2476T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66388777 | ||||||
| chr3:66388816
|
G | A | 196 | a0001c0007t0001g0116a0001c0007t0002g0080a0001c0007t0002g0100others(193): Show | 196 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.1469-2515C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66388816 | ||||||
| chr3:66388900
|
C | T | 1 | a0006c0026t0036g0234 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1469-2599G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66388900 | ||||||
| chr3:66389031
|
T | C | 1 | a0013c0020t0035g0208 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1469-2730A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66389031 | ||||||
| chr3:66389049
|
G | A | 4 | a0001c0014t0011g0058a0001c0014t0011g0117a0001c0014t0028g0118others(1): Show | 4 | NA18939.hp2 NA18949.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.1469-2748C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66389049 | ||||||
| chr3:66389230
|
C | T | 1 | a0001c0002t0001g0061 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1469-2929G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66389230 | ||||||
| chr3:66389265
|
A | C | 14 | a0001c0014t0010g0134a0001c0014t0010g0186a0001c0014t0011g0058others(11): Show | 14 | HG01433.hp1 HG02145.hp2 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.1469-2964T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66389265 | ||||||
| chr3:66389315
|
G | GA | 4 | a0001c0014t0011g0058a0001c0014t0011g0117a0001c0014t0028g0118others(1): Show | 4 | NA18939.hp2 NA18949.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.1469-3015dupT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66389315 | ||||||
| chr3:66389366
|
T | A | 6 | a0001c0023t0002g0060a0001c0023t0002g0068a0003c0010t0004g0229others(3): Show | 6 | HG02055.hp1 HG02572.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1469-3065A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66389366 | ||||||
| chr3:66389367
|
T | A | 6 | a0001c0023t0002g0060a0001c0023t0002g0068a0003c0010t0004g0229others(3): Show | 6 | HG02055.hp1 HG02572.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1469-3066A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66389367 | ||||||
| chr3:66389426
|
T | C | 1 | a0015c0024t0001g0025 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1469-3125A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66389426 | ||||||
| chr3:66389471
|
A | G | 1 | a0001c0002t0001g0051 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1469-3170T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66389471 | ||||||
| chr3:66389596
|
A | G | 1 | a0003c0010t0004g0257 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1469-3295T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66389596 | ||||||
| chr3:66389662
|
C | G | 1 | a0004c0003t0002g0193 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1469-3361G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66389662 | ||||||
| chr3:66389751
|
T | C | 1 | a0006c0009t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1469-3450A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66389751 | ||||||
| chr3:66389831
|
A | C | 1 | a0004c0003t0002g0181 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1469-3530T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66389831 | ||||||
| chr3:66389998
|
T | C | 3 | a0004c0003t0002g0101a0004c0003t0002g0141a0004c0003t0026g0190 | 3 | HG03688.hp2 HG03710.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1469-3697A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66389998 | ||||||
| chr3:66390098
|
T | G | 4 | a0011c0016t0013g0204a0011c0016t0013g0205a0011c0016t0013g0206others(1): Show | 4 | HG02486.hp2 HG02559.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1469-3797A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66390098 | ||||||
| chr3:66390406
|
A | G | 24 | a0005c0004t0006g0202a0005c0004t0006g0220a0005c0004t0006g0221others(21): Show | 24 | HG00280.hp1 HG01099.hp1 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.1468+3634T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66390406 | ||||||
| chr3:66390545
|
A | C | 74 | a0002c0001t0001g0047a0002c0001t0001g0048a0002c0001t0001g0059others(71): Show | 74 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.1468+3495T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66390545 | ||||||
| chr3:66390558
|
T | G | 2 | a0004c0003t0002g0088a0004c0003t0002g0089 | 2 | HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1468+3482A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66390558 | ||||||
| chr3:66390619
|
T | C | 4 | a0001c0023t0002g0060a0001c0023t0002g0068a0003c0010t0004g0229others(1): Show | 4 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1468+3421A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66390619 | ||||||
| chr3:66390769
|
T | C | 4 | a0001c0014t0011g0058a0001c0014t0011g0117a0001c0014t0028g0118others(1): Show | 4 | NA18939.hp2 NA18949.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.1468+3271A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66390769 | ||||||
| chr3:66390774
|
T | C | 1 | a0006c0026t0036g0234 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1468+3266A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66390774 | ||||||
| chr3:66390825
|
C | T | 191 | a0001c0007t0001g0116a0001c0007t0002g0080a0001c0007t0002g0100others(188): Show | 191 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.1468+3215G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66390825 | ||||||
| chr3:66391020
|
GAT | G | 81 | a0001c0007t0001g0116a0001c0007t0002g0080a0001c0007t0002g0100others(78): Show | 81 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.1468+3018_1468+301 others(6): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66391020 | ||||||
| chr3:66391068
|
C | T | 21 | a0005c0004t0006g0202a0005c0004t0006g0220a0005c0004t0006g0221others(18): Show | 21 | HG01099.hp1 HG01123.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.1468+2972G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66391068 | ||||||
| chr3:66391122
|
C | T | 81 | a0001c0007t0001g0116a0001c0007t0002g0080a0001c0007t0002g0100others(78): Show | 81 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.1468+2918G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66391122 | ||||||
| chr3:66391166
|
T | C | 2 | a0006c0009t0004g0232a0006c0009t0004g0246 | 2 | HG02970.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1468+2874A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66391166 | ||||||
| chr3:66391237
|
C | T | 174 | a0001c0007t0001g0116a0001c0007t0002g0080a0001c0007t0002g0100others(171): Show | 174 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.1468+2803G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66391237 | ||||||
| chr3:66391454
|
T | C | 2 | a0013c0020t0035g0208a0031c0047t0030g0162 | 2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1468+2586A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66391454 | ||||||
| chr3:66391455
|
G | T | 87 | a0001c0007t0001g0116a0001c0007t0002g0080a0001c0007t0002g0100others(84): Show | 87 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.1468+2585C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66391455 | ||||||
| chr3:66391562
|
G | C | 1 | a0004c0003t0026g0190 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1468+2478C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66391562 | ||||||
| chr3:66391586
|
A | G | 5 | a0011c0016t0013g0204a0011c0016t0013g0205a0011c0016t0013g0206others(2): Show | 5 | HG02486.hp2 HG02559.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1468+2454T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66391586 | ||||||
| chr3:66391588
|
G | A | 2 | a0003c0012t0014g0233a0003c0012t0014g0236 | 2 | HG02055.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1468+2452C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66391588 | ||||||
| chr3:66391681
|
A | G | 1 | a0003c0010t0004g0257 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1468+2359T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66391681 | ||||||
| chr3:66391686
|
A | G | 1 | a0004c0003t0002g0193 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1468+2354T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66391686 | ||||||
| chr3:66391756
|
T | G | 71 | a0002c0001t0001g0047a0002c0001t0001g0048a0002c0001t0001g0059others(68): Show | 71 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.1468+2284A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66391756 | ||||||
| chr3:66391836
|
A | T | 4 | a0001c0014t0011g0058a0001c0014t0011g0117a0001c0014t0028g0118others(1): Show | 4 | NA18939.hp2 NA18949.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.1468+2204T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66391836 | ||||||
| chr3:66391942
|
T | C | 4 | a0001c0014t0011g0058a0001c0014t0011g0117a0001c0014t0028g0118others(1): Show | 4 | NA18939.hp2 NA18949.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.1468+2098A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66391942 | ||||||
| chr3:66392005
|
C | A | 1 | a0010c0011t0024g0064 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1468+2035G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66392005 | ||||||
| chr3:66392011
|
C | G | 195 | a0001c0007t0001g0116a0001c0007t0002g0080a0001c0007t0002g0100others(192): Show | 195 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.1468+2029G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66392011 | ||||||
| chr3:66392121
|
A | C | 74 | a0002c0001t0001g0047a0002c0001t0001g0048a0002c0001t0001g0059others(71): Show | 74 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.1468+1919T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66392121 | ||||||
| chr3:66392359
|
A | G | 4 | a0001c0014t0011g0058a0001c0014t0011g0117a0001c0014t0028g0118others(1): Show | 4 | NA18939.hp2 NA18949.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.1468+1681T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66392359 | ||||||
| chr3:66392454
|
T | C | 4 | a0001c0014t0011g0058a0001c0014t0011g0117a0001c0014t0028g0118others(1): Show | 4 | NA18939.hp2 NA18949.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.1468+1586A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66392454 | ||||||
| chr3:66392540
|
C | T | 1 | a0003c0010t0004g0229 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1468+1500G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66392540 | ||||||
| chr3:66392544
|
A | C | 21 | a0005c0004t0006g0202a0005c0004t0006g0220a0005c0004t0006g0221others(18): Show | 21 | HG00280.hp1 HG01099.hp1 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.1468+1496T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66392544 | ||||||
| chr3:66392577
|
T | A | 54 | a0001c0007t0001g0116a0001c0007t0002g0080a0001c0007t0002g0100others(51): Show | 54 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.1468+1463A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66392577 | ||||||
| chr3:66392596
|
T | C | 1 | a0018c0028t0003g0259 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1468+1444A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66392596 | ||||||
| chr3:66392603
|
G | C | 7 | a0003c0010t0002g0010a0003c0010t0004g0201a0003c0010t0004g0231others(4): Show | 7 | HG02258.hp2 HG02647.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1468+1437C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66392603 | ||||||
| chr3:66392757
|
G | A | 54 | a0001c0007t0001g0116a0001c0007t0002g0080a0001c0007t0002g0100others(51): Show | 54 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.1468+1283C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66392757 | ||||||
| chr3:66392813
|
T | C | 4 | a0001c0023t0002g0060a0001c0023t0002g0068a0003c0010t0004g0229others(1): Show | 4 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1468+1227A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66392813 | ||||||
| chr3:66392951
|
T | G | 4 | a0003c0005t0003g0001a0003c0005t0003g0209a0003c0005t0003g0211others(1): Show | 5 | NA18966.hp2 NA18986.hp1 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.1468+1089A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66392951 | ||||||
| chr3:66393138
|
A | G | 59 | a0001c0007t0001g0116a0001c0007t0002g0080a0001c0007t0002g0100others(56): Show | 59 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.1468+902T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66393138 | ||||||
| chr3:66393146
|
A | T | 4 | a0001c0023t0002g0060a0001c0023t0002g0068a0003c0010t0004g0229others(1): Show | 4 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1468+894T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66393146 | ||||||
| chr3:66393188
|
T | A | 1 | a0021c0034t0019g0007 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1468+852A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66393188 | ||||||
| chr3:66393430
|
T | C | 14 | a0006c0035t0033g0207a0008c0006t0005g0200a0008c0006t0005g0215others(11): Show | 14 | HG01884.hp2 HG02280.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1468+610A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66393430 | ||||||
| chr3:66393519
|
G | C | 4 | a0001c0014t0011g0058a0001c0014t0011g0117a0001c0014t0028g0118others(1): Show | 4 | NA18939.hp2 NA18949.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.1468+521C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66393519 | ||||||
| chr3:66393714
|
G | T | 84 | a0001c0007t0001g0116a0001c0007t0002g0080a0001c0007t0002g0100others(81): Show | 84 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.1468+326C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66393714 | ||||||
| chr3:66393906
|
T | C | 29 | a0004c0003t0001g0151a0004c0003t0002g0057a0004c0003t0002g0081others(26): Show | 29 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.1468+134A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66393906 | ||||||
| chr3:66393929
|
A | C | 1 | a0002c0001t0001g0144 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1468+111T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 12/18 | chr3 | 66393929 | ||||||
| chr3:66394273
|
A | C | 84 | a0001c0002t0001g0051a0001c0014t0011g0058a0001c0014t0011g0117others(81): Show | 84 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.1305-70T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66394273 | ||||||
| chr3:66394327
|
G | A | 1 | a0006c0035t0033g0207 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1305-124C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66394327 | ||||||
| chr3:66394459
|
A | G | 12 | a0006c0009t0002g0045a0006c0009t0004g0224a0006c0009t0004g0225others(9): Show | 12 | HG00735.hp1 HG01891.hp2 HG02922.hp1 others(9): Show |
intron_variant | MODIFIER | c.1305-256T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66394459 | ||||||
| chr3:66394552
|
C | T | 1 | a0008c0006t0020g0005 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1305-349G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66394552 | ||||||
| chr3:66394602
|
C | T | 1 | a0003c0012t0018g0008 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1305-399G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66394602 | ||||||
| chr3:66394710
|
A | G | 1 | a0003c0012t0018g0008 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1305-507T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66394710 | ||||||
| chr3:66394769
|
T | C | 1 | a0001c0002t0001g0065 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1305-566A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66394769 | ||||||
| chr3:66394840
|
C | A | 5 | a0006c0009t0004g0224a0006c0009t0004g0225a0006c0009t0004g0226others(2): Show | 5 | HG00735.hp1 HG02970.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1305-637G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66394840 | ||||||
| chr3:66394885
|
A | G | 1 | a0013c0020t0035g0208 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1305-682T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66394885 | ||||||
| chr3:66394896
|
T | C | 10 | a0001c0023t0002g0060a0001c0023t0002g0068a0003c0010t0004g0229others(7): Show | 10 | HG02055.hp1 HG02486.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1305-693A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66394896 | ||||||
| chr3:66395099
|
G | T | 1 | a0001c0002t0001g0140 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1305-896C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66395099 | ||||||
| chr3:66395144
|
C | T | 1 | a0002c0001t0001g0158 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1305-941G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66395144 | ||||||
| chr3:66395166
|
A | C | 4 | a0001c0023t0002g0060a0001c0023t0002g0068a0003c0010t0004g0229others(1): Show | 4 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1305-963T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66395166 | ||||||
| chr3:66395177
|
A | G | 12 | a0006c0009t0002g0045a0006c0009t0004g0224a0006c0009t0004g0225others(9): Show | 12 | HG00735.hp1 HG01891.hp2 HG02922.hp1 others(9): Show |
intron_variant | MODIFIER | c.1305-974T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66395177 | ||||||
| chr3:66395239
|
G | A | 13 | a0006c0035t0033g0207a0008c0006t0005g0200a0008c0006t0005g0215others(10): Show | 13 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.1305-1036C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66395239 | ||||||
| chr3:66395310
|
C | T | 1 | a0003c0005t0003g0218 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1305-1107G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66395310 | ||||||
| chr3:66395407
|
A | T | 1 | a0001c0007t0002g0126 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1305-1204T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66395407 | ||||||
| chr3:66395509
|
A | G | 2 | a0010c0011t0007g0169a0010c0011t0007g0175 | 2 | HG00280.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1305-1306T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66395509 | ||||||
| chr3:66395518
|
G | C | 57 | a0001c0007t0001g0116a0001c0007t0002g0080a0001c0007t0002g0100others(54): Show | 57 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.1305-1315C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66395518 | ||||||
| chr3:66395638
|
C | T | 3 | a0004c0003t0002g0161a0004c0003t0038g0262a0029c0052t0039g0263 | 3 | HG02258.hp2 HG02486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1305-1435G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66395638 | ||||||
| chr3:66395703
|
G | A | 1 | a0001c0002t0031g0069 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1305-1500C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66395703 | ||||||
| chr3:66395738
|
T | C | 13 | a0006c0009t0002g0045a0006c0009t0004g0224a0006c0009t0004g0225others(10): Show | 13 | HG00735.hp1 HG01891.hp2 HG02922.hp1 others(10): Show |
intron_variant | MODIFIER | c.1305-1535A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66395738 | ||||||
| chr3:66395850
|
A | C | 12 | a0008c0006t0005g0200a0008c0006t0005g0215a0008c0006t0005g0219others(9): Show | 12 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1305-1647T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66395850 | ||||||
| chr3:66395979
|
C | CA | 23 | a0005c0004t0006g0202a0005c0004t0006g0220a0005c0004t0006g0221others(20): Show | 23 | HG00280.hp1 HG01099.hp1 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.1305-1777dupT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66395979 | ||||||
| chr3:66396074
|
C | A | 2 | a0013c0020t0035g0208a0031c0047t0030g0162 | 2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1305-1871G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66396074 | ||||||
| chr3:66396082
|
C | T | 2 | a0001c0002t0001g0061a0003c0010t0004g0258 | 2 | HG00735.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1305-1879G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66396082 | ||||||
| chr3:66396092
|
G | A | 1 | a0005c0004t0001g0019 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1305-1889C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66396092 | ||||||
| chr3:66396182
|
A | T | 12 | a0008c0006t0005g0200a0008c0006t0005g0215a0008c0006t0005g0219others(9): Show | 12 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1304+1930T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66396182 | ||||||
| chr3:66396396
|
G | A | 20 | a0005c0004t0006g0202a0005c0004t0006g0220a0005c0004t0006g0221others(17): Show | 20 | HG00280.hp1 HG01099.hp1 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.1304+1716C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66396396 | ||||||
| chr3:66396809
|
T | G | 2 | a0006c0009t0004g0232a0006c0009t0004g0246 | 2 | HG02970.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1304+1303A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66396809 | ||||||
| chr3:66396875
|
A | T | 2 | a0001c0007t0002g0080a0001c0007t0002g0100 | 2 | HG01261.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1304+1237T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66396875 | ||||||
| chr3:66396880
|
A | G | 6 | a0003c0012t0014g0233a0003c0012t0014g0236a0011c0016t0013g0204others(3): Show | 6 | HG02055.hp1 HG02486.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1304+1232T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66396880 | ||||||
| chr3:66396929
|
C | T | 1 | a0006c0009t0004g0246 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1304+1183G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66396929 | ||||||
| chr3:66397070
|
C | T | 1 | a0009c0013t0002g0024 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1304+1042G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66397070 | ||||||
| chr3:66397110
|
C | T | 1 | a0011c0016t0013g0205 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1304+1002G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66397110 | ||||||
| chr3:66397237
|
G | A | 4 | a0001c0014t0010g0134a0001c0014t0010g0186a0014c0042t0010g0083others(1): Show | 4 | HG01433.hp1 HG02145.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.1304+875C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66397237 | ||||||
| chr3:66397440
|
T | C | 1 | a0018c0028t0003g0259 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1304+672A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66397440 | ||||||
| chr3:66397448
|
T | TA | 91 | a0001c0002t0001g0049a0001c0002t0001g0056a0001c0002t0001g0061others(88): Show | 92 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.1304+663dupT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66397448 | ||||||
| chr3:66397448
|
T | TAA | 69 | a0001c0002t0001g0053a0001c0002t0001g0136a0001c0002t0001g0178others(66): Show | 69 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.1304+662_1304+663d others(4): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66397448 | ||||||
| chr3:66397678
|
G | A | 4 | a0001c0023t0002g0060a0001c0023t0002g0068a0003c0010t0004g0229others(1): Show | 4 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1304+434C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66397678 | ||||||
| chr3:66397737
|
A | C | 4 | a0001c0023t0002g0060a0001c0023t0002g0068a0003c0010t0004g0229others(1): Show | 4 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1304+375T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66397737 | ||||||
| chr3:66397782
|
G | A | 235 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(232): Show | 236 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.1304+330C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66397782 | ||||||
| chr3:66397811
|
G | C | 1 | a0002c0001t0001g0144 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1304+301C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66397811 | ||||||
| chr3:66397842
|
T | G | 2 | a0006c0019t0012g0244a0006c0019t0012g0245 | 2 | HG02280.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1304+270A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66397842 | ||||||
| chr3:66397883
|
A | G | 94 | a0001c0002t0001g0051a0001c0014t0010g0134a0001c0014t0010g0186others(91): Show | 94 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.1304+229T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66397883 | ||||||
| chr3:66398007
|
G | A | 1 | a0030c0046t0010g0184 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1304+105C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66398007 | ||||||
| chr3:66398040
|
G | A | 2 | a0013c0020t0035g0208a0031c0047t0030g0162 | 2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1304+72C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 11/18 | chr3 | 66398040 | ||||||
| chr3:66398646
|
G | A | 5 | a0003c0012t0014g0233a0003c0012t0014g0236a0007c0008t0001g0038others(2): Show | 5 | HG02055.hp1 HG02451.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1232+324C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 10/18 | chr3 | 66398646 | ||||||
| chr3:66398652
|
G | A | 8 | a0005c0004t0006g0238a0005c0004t0006g0239a0005c0004t0006g0240others(5): Show | 8 | HG00280.hp1 HG01099.hp1 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.1232+318C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 10/18 | chr3 | 66398652 | ||||||
| chr3:66398718
|
G | A | 4 | a0001c0023t0002g0060a0001c0023t0002g0068a0003c0010t0004g0229others(1): Show | 4 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1232+252C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 10/18 | chr3 | 66398718 | ||||||
| chr3:66398718
|
G | C | 77 | a0001c0002t0001g0049a0001c0002t0001g0053a0001c0002t0001g0056others(74): Show | 78 | HG00099.hp2 HG00609.hp1 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.1232+252C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 10/18 | chr3 | 66398718 | ||||||
| chr3:66399203
|
C | T | 1 | a0002c0001t0001g0048 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1161-162G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66399203 | ||||||
| chr3:66399298
|
C | T | 2 | a0004c0003t0002g0081a0004c0003t0002g0153 | 2 | HG00099.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.1161-257G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66399298 | ||||||
| chr3:66399355
|
A | G | 12 | a0008c0006t0005g0200a0008c0006t0005g0215a0008c0006t0005g0219others(9): Show | 12 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1161-314T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66399355 | ||||||
| chr3:66399412
|
A | G | 3 | a0011c0016t0013g0204a0011c0016t0013g0205a0011c0016t0013g0206 | 3 | HG02486.hp2 HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1161-371T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66399412 | ||||||
| chr3:66399470
|
G | A | 2 | a0003c0012t0014g0233a0006c0009t0002g0045 | 2 | HG03130.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1161-429C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66399470 | ||||||
| chr3:66399559
|
G | A | 1 | a0002c0001t0001g0055 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1161-518C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66399559 | ||||||
| chr3:66399751
|
T | C | 5 | a0002c0001t0001g0052a0002c0001t0001g0055a0002c0001t0001g0160others(2): Show | 5 | HG00738.hp2 HG01123.hp2 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.1161-710A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66399751 | ||||||
| chr3:66399783
|
A | C | 1 | a0002c0001t0001g0174 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1161-742T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66399783 | ||||||
| chr3:66399835
|
C | T | 163 | a0001c0002t0001g0049a0001c0002t0001g0053a0001c0002t0001g0056others(160): Show | 164 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.1161-794G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66399835 | ||||||
| chr3:66399847
|
G | T | 3 | a0001c0014t0010g0134a0001c0014t0010g0186a0014c0042t0010g0083 | 3 | HG01433.hp1 HG03834.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1161-806C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66399847 | ||||||
| chr3:66400998
|
C | T | 1 | a0001c0002t0001g0108 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1161-1957G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66400998 | ||||||
| chr3:66401017
|
A | T | 241 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(238): Show | 242 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.1161-1976T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66401017 | ||||||
| chr3:66401059
|
C | T | 13 | a0006c0009t0002g0045a0006c0009t0004g0224a0006c0009t0004g0225others(10): Show | 13 | HG00735.hp1 HG01891.hp2 HG02922.hp1 others(10): Show |
intron_variant | MODIFIER | c.1161-2018G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66401059 | ||||||
| chr3:66401098
|
G | A | 33 | a0004c0003t0001g0151a0004c0003t0002g0057a0004c0003t0002g0081others(30): Show | 33 | HG00099.hp1 HG00544.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.1161-2057C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66401098 | ||||||
| chr3:66401172
|
G | A | 2 | a0004c0003t0038g0262a0029c0052t0039g0263 | 2 | HG02486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1161-2131C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66401172 | ||||||
| chr3:66401261
|
G | T | 239 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(236): Show | 240 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.1161-2220C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66401261 | ||||||
| chr3:66401279
|
G | A | 3 | a0011c0016t0013g0204a0011c0016t0013g0205a0011c0016t0013g0206 | 3 | HG02486.hp2 HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1161-2238C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66401279 | ||||||
| chr3:66401287
|
G | A | 2 | a0008c0006t0005g0242a0008c0006t0005g0243 | 2 | HG01884.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1161-2246C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66401287 | ||||||
| chr3:66401397
|
A | C | 56 | a0001c0007t0001g0116a0001c0007t0002g0080a0001c0007t0002g0100others(53): Show | 56 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.1161-2356T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66401397 | ||||||
| chr3:66401475
|
T | G | 10 | a0006c0009t0002g0045a0006c0009t0004g0224a0006c0009t0004g0225others(7): Show | 10 | HG00735.hp1 HG02970.hp1 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.1161-2434A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66401475 | ||||||
| chr3:66401483
|
T | C | 58 | a0001c0007t0001g0116a0001c0007t0002g0080a0001c0007t0002g0100others(55): Show | 58 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.1161-2442A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66401483 | ||||||
| chr3:66401529
|
A | G | 1 | a0020c0027t0004g0227 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1161-2488T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66401529 | ||||||
| chr3:66401613
|
C | T | 1 | a0003c0010t0004g0229 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1161-2572G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66401613 | ||||||
| chr3:66401628
|
G | A | 1 | a0023c0051t0002g0054 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1161-2587C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66401628 | ||||||
| chr3:66401696
|
A | G | 1 | a0016c0038t0003g0235 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1161-2655T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66401696 | ||||||
| chr3:66401844
|
C | T | 1 | a0004c0003t0026g0190 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1161-2803G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66401844 | ||||||
| chr3:66401886
|
G | A | 2 | a0013c0020t0035g0208a0031c0047t0030g0162 | 2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1161-2845C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66401886 | ||||||
| chr3:66402107
|
T | G | 62 | a0001c0007t0001g0116a0001c0007t0002g0125a0001c0007t0002g0126others(59): Show | 62 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.1161-3066A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66402107 | ||||||
| chr3:66402138
|
A | G | 71 | a0001c0002t0001g0049a0001c0002t0001g0053a0001c0002t0001g0056others(68): Show | 72 | HG00099.hp2 HG00609.hp1 HG00673.hp1 others(69): Show |
intron_variant | MODIFIER | c.1160+3060T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66402138 | ||||||
| chr3:66402167
|
A | G | 1 | a0002c0001t0001g0147 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1160+3031T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66402167 | ||||||
| chr3:66402301
|
C | T | 2 | a0003c0012t0014g0233a0003c0012t0014g0236 | 2 | HG02055.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1160+2897G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66402301 | ||||||
| chr3:66402408
|
A | ACTCT | 71 | a0001c0007t0001g0116a0001c0007t0002g0080a0001c0007t0002g0100others(68): Show | 71 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.1160+2786_1160+278 others(8): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66402408 | ||||||
| chr3:66402493
|
G | C | 1 | a0001c0002t0001g0104 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1160+2705C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66402493 | ||||||
| chr3:66402549
|
TTGCATGG others(16): Show |
T | 150 | a0001c0002t0001g0049a0001c0002t0001g0053a0001c0002t0001g0056others(147): Show | 151 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.1160+2626_1160+264 others(27): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66402549 | ||||||
| chr3:66402602
|
C | T | 13 | a0001c0007t0001g0116a0001c0007t0002g0080a0001c0007t0002g0100others(10): Show | 13 | HG00280.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.1160+2596G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66402602 | ||||||
| chr3:66403040
|
T | C | 9 | a0001c0023t0002g0060a0001c0023t0002g0068a0003c0010t0004g0229others(6): Show | 9 | HG02055.hp1 HG02572.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1160+2158A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66403040 | ||||||
| chr3:66403109
|
C | A | 10 | a0006c0009t0002g0045a0006c0009t0004g0224a0006c0009t0004g0225others(7): Show | 10 | HG00735.hp1 HG02970.hp1 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.1160+2089G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66403109 | ||||||
| chr3:66403126
|
A | G | 3 | a0002c0001t0001g0171a0002c0001t0001g0172a0002c0001t0001g0173 | 3 | HG00738.hp1 HG03139.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1160+2072T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66403126 | ||||||
| chr3:66403181
|
T | TC | 4 | a0001c0014t0011g0058a0001c0014t0011g0117a0001c0014t0028g0118others(1): Show | 4 | NA18939.hp2 NA18949.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.1160+2016dupG | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66403181 | ||||||
| chr3:66403217
|
T | C | 12 | a0008c0006t0005g0200a0008c0006t0005g0215a0008c0006t0005g0219others(9): Show | 12 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1160+1981A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66403217 | ||||||
| chr3:66403347
|
T | A | 56 | a0001c0007t0001g0116a0001c0007t0002g0080a0001c0007t0002g0100others(53): Show | 56 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.1160+1851A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66403347 | ||||||
| chr3:66403379
|
G | A | 12 | a0008c0006t0005g0200a0008c0006t0005g0215a0008c0006t0005g0219others(9): Show | 12 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1160+1819C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66403379 | ||||||
| chr3:66403411
|
CAG | C | 17 | a0001c0002t0001g0079a0005c0004t0006g0238a0005c0004t0006g0239others(14): Show | 17 | HG00099.hp2 HG01099.hp1 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.1160+1785_1160+178 others(6): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66403411 | ||||||
| chr3:66403513
|
A | T | 1 | a0002c0018t0001g0192 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1160+1685T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66403513 | ||||||
| chr3:66403584
|
C | A | 4 | a0011c0016t0013g0204a0011c0016t0013g0205a0011c0016t0013g0206others(1): Show | 4 | HG02486.hp2 HG02559.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1160+1614G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66403584 | ||||||
| chr3:66403699
|
G | A | 3 | a0009c0013t0001g0041a0009c0013t0002g0042a0009c0013t0002g0044 | 3 | NA18991.hp2 NA19000.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1160+1499C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66403699 | ||||||
| chr3:66403767
|
G | A | 68 | a0001c0002t0001g0049a0001c0002t0001g0053a0001c0002t0001g0056others(65): Show | 69 | HG00099.hp2 HG00609.hp1 HG00673.hp1 others(66): Show |
intron_variant | MODIFIER | c.1160+1431C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66403767 | ||||||
| chr3:66403872
|
C | T | 54 | a0001c0007t0001g0116a0001c0007t0002g0080a0001c0007t0002g0100others(51): Show | 54 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.1160+1326G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66403872 | ||||||
| chr3:66403920
|
C | T | 55 | a0001c0007t0001g0116a0001c0007t0002g0080a0001c0007t0002g0100others(52): Show | 55 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.1160+1278G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66403920 | ||||||
| chr3:66403982
|
G | A | 1 | a0007c0033t0001g0027 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1160+1216C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66403982 | ||||||
| chr3:66403997
|
G | C | 1 | a0002c0041t0001g0114 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1160+1201C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66403997 | ||||||
| chr3:66403998
|
G | A | 4 | a0005c0004t0006g0220a0005c0004t0006g0221a0005c0004t0006g0222others(1): Show | 4 | HG02630.hp2 HG02896.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1160+1200C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66403998 | ||||||
| chr3:66403998
|
G | C | 3 | a0003c0005t0001g0037a0003c0005t0001g0039a0003c0031t0001g0036 | 3 | HG01884.hp1 HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1160+1200C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66403998 | ||||||
| chr3:66404028
|
T | C | 1 | a0011c0030t0027g0021 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1160+1170A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66404028 | ||||||
| chr3:66404089
|
T | C | 12 | a0008c0006t0005g0200a0008c0006t0005g0215a0008c0006t0005g0219others(9): Show | 12 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1160+1109A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66404089 | ||||||
| chr3:66404106
|
A | C | 1 | a0021c0034t0019g0007 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1160+1092T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66404106 | ||||||
| chr3:66404183
|
C | T | 1 | a0002c0001t0001g0102 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1160+1015G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66404183 | ||||||
| chr3:66404555
|
C | T | 13 | a0006c0026t0036g0234a0008c0006t0005g0200a0008c0006t0005g0215others(10): Show | 13 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.1160+643G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66404555 | ||||||
| chr3:66404570
|
G | A | 233 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(230): Show | 234 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.1160+628C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66404570 | ||||||
| chr3:66404583
|
T | C | 1 | a0003c0010t0004g0257 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1160+615A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66404583 | ||||||
| chr3:66405039
|
C | G | 1 | a0001c0007t0002g0080 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1160+159G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66405039 | ||||||
| chr3:66405159
|
G | A | 1 | a0021c0034t0019g0007 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1160+39C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66405159 | ||||||
| chr3:66405170
|
G | A | 2 | a0005c0004t0007g0017a0026c0039t0001g0073 | 2 | HG04115.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.1160+28C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 9/18 | chr3 | 66405170 | ||||||
| chr3:66405306
|
C | T | 1 | a0002c0001t0032g0199 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1080-28G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 8/18 | chr3 | 66405306 | ||||||
| chr3:66405373
|
T | C | 68 | a0001c0007t0001g0116a0001c0007t0002g0080a0001c0007t0002g0100others(65): Show | 68 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.1080-95A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 8/18 | chr3 | 66405373 | ||||||
| chr3:66405463
|
C | T | 58 | a0001c0007t0001g0116a0001c0007t0002g0080a0001c0007t0002g0100others(55): Show | 58 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.1080-185G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 8/18 | chr3 | 66405463 | ||||||
| chr3:66405523
|
G | A | 1 | a0003c0012t0018g0008 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1080-245C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 8/18 | chr3 | 66405523 | ||||||
| chr3:66405618
|
C | T | 13 | a0001c0007t0001g0116a0001c0007t0002g0080a0001c0007t0002g0100others(10): Show | 13 | HG00280.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.1080-340G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 8/18 | chr3 | 66405618 | ||||||
| chr3:66405674
|
T | C | 13 | a0006c0026t0036g0234a0008c0006t0005g0200a0008c0006t0005g0215others(10): Show | 13 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.1080-396A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 8/18 | chr3 | 66405674 | ||||||
| chr3:66405689
|
A | T | 1 | a0005c0004t0006g0220 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1080-411T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 8/18 | chr3 | 66405689 | ||||||
| chr3:66405725
|
C | T | 1 | a0001c0002t0001g0079 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1080-447G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 8/18 | chr3 | 66405725 | ||||||
| chr3:66405749
|
G | A | 1 | a0013c0020t0035g0208 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1080-471C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 8/18 | chr3 | 66405749 | ||||||
| chr3:66406139
|
C | T | 1 | a0002c0001t0001g0048 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1080-861G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 8/18 | chr3 | 66406139 | ||||||
| chr3:66406297
|
A | T | 1 | a0002c0001t0001g0143 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1080-1019T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 8/18 | chr3 | 66406297 | ||||||
| chr3:66406407
|
G | A | 9 | a0001c0002t0001g0094a0001c0002t0001g0108a0001c0002t0001g0136others(6): Show | 9 | HG02056.hp2 HG02135.hp2 NA18949.hp2 others(6): Show |
intron_variant | MODIFIER | c.1079+941C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 8/18 | chr3 | 66406407 | ||||||
| chr3:66406484
|
T | C | 8 | a0001c0023t0002g0060a0001c0023t0002g0068a0003c0010t0004g0229others(5): Show | 8 | HG02055.hp1 HG02572.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1079+864A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 8/18 | chr3 | 66406484 | ||||||
| chr3:66406498
|
G | A | 4 | a0011c0016t0013g0204a0011c0016t0013g0205a0011c0016t0013g0206others(1): Show | 4 | HG02486.hp2 HG02559.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1079+850C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 8/18 | chr3 | 66406498 | ||||||
| chr3:66406532
|
C | T | 1 | a0006c0009t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1079+816G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 8/18 | chr3 | 66406532 | ||||||
| chr3:66406610
|
C | T | 1 | a0006c0009t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1079+738G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 8/18 | chr3 | 66406610 | ||||||
| chr3:66406638
|
G | T | 1 | a0003c0012t0017g0004 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1079+710C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 8/18 | chr3 | 66406638 | ||||||
| chr3:66406652
|
C | T | 59 | a0001c0007t0001g0116a0001c0007t0002g0080a0001c0007t0002g0100others(56): Show | 59 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.1079+696G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 8/18 | chr3 | 66406652 | ||||||
| chr3:66406671
|
T | C | 20 | a0001c0014t0010g0134a0001c0014t0010g0186a0006c0009t0004g0224others(17): Show | 20 | HG00735.hp1 HG01433.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.1079+677A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 8/18 | chr3 | 66406671 | ||||||
| chr3:66406769
|
A | G | 1 | a0002c0001t0001g0102 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1079+579T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 8/18 | chr3 | 66406769 | ||||||
| chr3:66406943
|
A | G | 3 | a0002c0001t0001g0135a0002c0001t0001g0149a0002c0001t0001g0154 | 3 | NA18994.hp2 NA19004.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.1079+405T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 8/18 | chr3 | 66406943 | ||||||
| chr3:66407020
|
C | T | 10 | a0006c0009t0004g0224a0006c0009t0004g0225a0006c0009t0004g0226others(7): Show | 10 | HG00735.hp1 HG02922.hp1 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.1079+328G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 8/18 | chr3 | 66407020 | ||||||
| chr3:66407159
|
T | G | 1 | a0001c0002t0001g0065 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1079+189A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 8/18 | chr3 | 66407159 | ||||||
| chr3:66407167
|
T | G | 1 | a0008c0006t0020g0005 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1079+181A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 8/18 | chr3 | 66407167 | ||||||
| chr3:66407303
|
T | G | 2 | a0004c0003t0038g0262a0029c0052t0039g0263 | 2 | HG02486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1079+45A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 8/18 | chr3 | 66407303 | ||||||
| chr3:66407584
|
A | G | 2 | a0001c0002t0001g0094a0003c0005t0001g0026 | 2 | NA18994.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.936-93T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66407584 | ||||||
| chr3:66407615
|
G | A | 1 | a0001c0002t0031g0069 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.936-124C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66407615 | ||||||
| chr3:66407622
|
T | C | 246 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(243): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.936-131A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66407622 | ||||||
| chr3:66407623
|
G | GCA | 86 | a0001c0002t0001g0049a0001c0002t0001g0053a0001c0002t0001g0056others(83): Show | 87 | HG00099.hp2 HG00609.hp1 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.936-134_936-133dup others(2): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66407623 | ||||||
| chr3:66407695
|
A | C | 1 | a0013c0020t0035g0208 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.936-204T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66407695 | ||||||
| chr3:66407714
|
T | C | 2 | a0006c0009t0002g0045a0018c0028t0003g0259 | 2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.936-223A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66407714 | ||||||
| chr3:66407804
|
C | T | 1 | a0001c0002t0001g0078 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.936-313G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66407804 | ||||||
| chr3:66407881
|
C | T | 4 | a0011c0016t0013g0204a0011c0016t0013g0205a0011c0016t0013g0206others(1): Show | 4 | HG02486.hp2 HG02559.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.936-390G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66407881 | ||||||
| chr3:66408042
|
C | G | 13 | a0006c0026t0036g0234a0008c0006t0005g0200a0008c0006t0005g0215others(10): Show | 13 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.936-551G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408042 | ||||||
| chr3:66408085
|
G | A | 5 | a0002c0001t0001g0052a0002c0001t0001g0055a0002c0001t0001g0160others(2): Show | 5 | HG00738.hp2 HG01123.hp2 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.936-594C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408085 | ||||||
| chr3:66408106
|
C | T | 10 | a0001c0007t0001g0116a0001c0007t0002g0125a0001c0007t0002g0126others(7): Show | 10 | HG00280.hp2 HG01074.hp2 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.936-615G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408106 | ||||||
| chr3:66408169
|
T | C | 2 | a0001c0002t0001g0056a0001c0002t0001g0074 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.936-678A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408169 | ||||||
| chr3:66408179
|
A | G | 7 | a0001c0023t0002g0060a0001c0023t0002g0068a0003c0010t0004g0229others(4): Show | 7 | HG02055.hp1 HG02572.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.936-688T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408179 | ||||||
| chr3:66408209
|
T | C | 59 | a0001c0007t0001g0116a0001c0007t0002g0080a0001c0007t0002g0100others(56): Show | 59 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.936-718A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408209 | ||||||
| chr3:66408219
|
G | A | 1 | a0007c0008t0001g0016 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.936-728C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408219 | ||||||
| chr3:66408277
|
T | C | 76 | a0001c0002t0001g0049a0001c0002t0001g0053a0001c0002t0001g0056others(73): Show | 77 | HG00099.hp2 HG00609.hp1 HG00673.hp1 others(74): Show |
intron_variant | MODIFIER | c.936-786A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408277 | ||||||
| chr3:66408521
|
C | T | 174 | a0001c0002t0001g0049a0001c0002t0001g0053a0001c0002t0001g0056others(171): Show | 175 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.936-1030G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408521 | ||||||
| chr3:66408683
|
G | A | 1 | a0011c0030t0027g0021 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.936-1192C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408683 | ||||||
| chr3:66408683
|
G | C | 5 | a0001c0014t0010g0134a0001c0014t0010g0186a0014c0042t0010g0083others(2): Show | 5 | HG01433.hp1 HG02145.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.936-1192C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408683 | ||||||
| chr3:66408808
|
C | T | 1 | a0002c0001t0001g0152 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.936-1317G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408808 | ||||||
| chr3:66408913
|
A | AGT | 23 | a0001c0002t0001g0074a0001c0002t0001g0075a0001c0002t0001g0076others(20): Show | 23 | HG00609.hp1 HG01192.hp1 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.935+1214_935+1215d others(4): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408913 | ||||||
| chr3:66408913
|
A | AGTGT | 28 | a0001c0002t0001g0063a0001c0002t0001g0070a0001c0002t0001g0078others(25): Show | 28 | HG01123.hp1 HG01123.hp2 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.935+1212_935+1215d others(6): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408913 | ||||||
| chr3:66408913
|
A | AGTGTGT | 17 | a0001c0002t0001g0049a0001c0002t0001g0053a0001c0002t0001g0062others(14): Show | 17 | HG00099.hp2 HG00738.hp2 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.935+1210_935+1215d others(8): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408913 | ||||||
| chr3:66408913
|
A | AGTGTGTG others(1): Show |
16 | a0001c0002t0001g0056a0001c0002t0001g0061a0001c0002t0001g0071others(13): Show | 16 | HG00735.hp2 HG01069.hp2 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.935+1208_935+1215d others(10): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408913 | ||||||
| chr3:66408913
|
A | AGTGTGTG others(3): Show |
14 | a0001c0002t0001g0146a0001c0002t0001g0198a0002c0001t0001g0137others(11): Show | 14 | HG00558.hp1 HG00558.hp2 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.935+1206_935+1215d others(12): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408913 | ||||||
| chr3:66408913
|
A | AGTGTGTG others(5): Show |
5 | a0002c0001t0001g0090a0002c0001t0001g0150a0002c0001t0001g0158others(2): Show | 5 | HG00673.hp2 HG02451.hp1 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.935+1204_935+1215d others(14): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408913 | ||||||
| chr3:66408913
|
A | AGTGTGTG others(7): Show |
12 | a0001c0002t0001g0051a0001c0002t0001g0136a0002c0001t0001g0110others(9): Show | 12 | HG02165.hp2 HG02723.hp2 HG03139.hp2 others(9): Show |
intron_variant | MODIFIER | c.935+1202_935+1215d others(16): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408913 | ||||||
| chr3:66408913
|
A | AGTGTGTG others(9): Show |
11 | a0001c0002t0001g0189a0002c0001t0001g0124a0002c0001t0001g0142others(8): Show | 11 | HG02040.hp1 HG02056.hp2 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.935+1200_935+1215d others(18): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408913 | ||||||
| chr3:66408913
|
A | AGTGTGTG others(11): Show |
3 | a0002c0001t0001g0145a0002c0001t0001g0156a0002c0001t0001g0171 | 3 | HG00621.hp2 HG00738.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.935+1198_935+1215d others(20): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408913 | ||||||
| chr3:66408913
|
A | AGTGTGTG others(13): Show |
4 | a0002c0001t0001g0135a0002c0001t0001g0149a0002c0001t0001g0180others(1): Show | 4 | HG02071.hp1 NA18950.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.935+1196_935+1215d others(22): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408913 | ||||||
| chr3:66408913
|
A | AGTGTGTG others(15): Show |
1 | a0002c0018t0001g0176 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.935+1194_935+1215d others(24): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408913 | ||||||
| chr3:66408913
|
A | AGTGTGTG others(17): Show |
5 | a0002c0001t0001g0047a0002c0001t0001g0059a0002c0001t0001g0102others(2): Show | 5 | HG00544.hp2 HG03017.hp1 NA18988.hp2 others(2): Show |
intron_variant | MODIFIER | c.935+1192_935+1215d others(26): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408913 | ||||||
| chr3:66408913
|
A | AGTGTGTG others(19): Show |
3 | a0002c0001t0001g0072a0002c0001t0001g0143a0002c0001t0001g0195 | 3 | HG02132.hp2 NA18974.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.935+1190_935+1215d others(28): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408913 | ||||||
| chr3:66408913
|
A | AGTGTGTG others(23): Show |
1 | a0002c0001t0001g0048 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.935+1186_935+1215d others(32): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408913 | ||||||
| chr3:66408913
|
AGT | A | 23 | a0002c0001t0001g0085a0002c0001t0001g0087a0002c0001t0001g0123others(20): Show | 23 | HG00544.hp1 HG00735.hp1 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.935+1214_935+1215d others(4): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408913 | ||||||
| chr3:66408913
|
AGTGT | A | 42 | a0001c0002t0001g0065a0001c0002t0001g0115a0001c0007t0002g0080others(39): Show | 42 | HG00099.hp1 HG00280.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.935+1212_935+1215d others(6): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408913 | ||||||
| chr3:66408913
|
AGTGTGT | A | 17 | a0001c0007t0001g0116a0001c0007t0002g0100a0001c0007t0002g0125others(14): Show | 17 | HG00280.hp2 HG01074.hp2 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.935+1210_935+1215d others(8): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408913 | ||||||
| chr3:66408913
|
AGTGTGTG others(1): Show |
A | 4 | a0004c0003t0001g0151a0004c0003t0002g0097a0004c0003t0002g0193others(1): Show | 4 | HG02735.hp2 HG03471.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.935+1208_935+1215d others(10): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408913 | ||||||
| chr3:66408913
|
AGTGTGTG others(3): Show |
A | 1 | a0004c0003t0002g0088 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.935+1206_935+1215d others(12): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408913 | ||||||
| chr3:66408913
|
AGTGTGTG others(5): Show |
A | 2 | a0003c0005t0003g0241a0009c0013t0004g0214 | 2 | HG01070.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.935+1204_935+1215d others(14): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408913 | ||||||
| chr3:66408943
|
T | TGTGTGC | 3 | a0001c0023t0002g0060a0001c0023t0002g0068a0003c0010t0004g0229 | 3 | HG02896.hp1 HG02897.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.935+1185_935+1186i others(8): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66408943 | ||||||
| chr3:66409135
|
C | T | 56 | a0001c0007t0001g0116a0001c0007t0002g0080a0001c0007t0002g0100others(53): Show | 56 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.935+994G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66409135 | ||||||
| chr3:66409188
|
A | G | 1 | a0018c0028t0003g0259 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.935+941T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66409188 | ||||||
| chr3:66409353
|
C | T | 3 | a0001c0040t0001g0096a0002c0041t0001g0114a0014c0043t0022g0009 | 3 | HG00609.hp1 NA18969.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.935+776G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66409353 | ||||||
| chr3:66409412
|
G | A | 1 | a0009c0037t0002g0018 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.935+717C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66409412 | ||||||
| chr3:66409535
|
C | G | 4 | a0001c0014t0011g0058a0001c0014t0011g0117a0001c0014t0028g0118others(1): Show | 4 | NA18939.hp2 NA18949.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.935+594G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66409535 | ||||||
| chr3:66409713
|
C | T | 4 | a0011c0016t0013g0204a0011c0016t0013g0205a0011c0016t0013g0206others(1): Show | 4 | HG02486.hp2 HG02559.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.935+416G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66409713 | ||||||
| chr3:66409835
|
G | C | 4 | a0011c0016t0013g0204a0011c0016t0013g0205a0011c0016t0013g0206others(1): Show | 4 | HG02486.hp2 HG02559.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.935+294C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66409835 | ||||||
| chr3:66409913
|
C | A | 56 | a0001c0007t0001g0116a0001c0007t0002g0080a0001c0007t0002g0100others(53): Show | 56 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.935+216G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 7/18 | chr3 | 66409913 | ||||||
| chr3:66410288
|
T | C | 4 | a0001c0014t0011g0058a0001c0014t0011g0117a0001c0014t0028g0118others(1): Show | 4 | NA18939.hp2 NA18949.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.792-16A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66410288 | ||||||
| chr3:66410395
|
C | A | 5 | a0001c0014t0010g0134a0001c0014t0010g0186a0014c0042t0010g0083others(2): Show | 5 | HG01433.hp1 HG02145.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.792-123G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66410395 | ||||||
| chr3:66410395
|
C | T | 1 | a0004c0003t0002g0153 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.792-123G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66410395 | ||||||
| chr3:66410434
|
T | C | 2 | a0002c0001t0001g0123a0002c0001t0001g0164 | 2 | HG01074.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.792-162A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66410434 | ||||||
| chr3:66410508
|
C | G | 85 | a0001c0002t0001g0051a0001c0002t0001g0146a0001c0014t0011g0058others(82): Show | 85 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.792-236G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66410508 | ||||||
| chr3:66410573
|
G | A | 1 | a0001c0002t0001g0056 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.792-301C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66410573 | ||||||
| chr3:66410618
|
G | A | 1 | a0011c0030t0027g0021 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.792-346C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66410618 | ||||||
| chr3:66410627
|
C | T | 3 | a0002c0001t0001g0170a0007c0008t0001g0013a0007c0008t0001g0031 | 3 | HG02165.hp2 NA18970.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.792-355G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66410627 | ||||||
| chr3:66410636
|
G | A | 1 | a0006c0009t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.792-364C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66410636 | ||||||
| chr3:66410809
|
G | T | 4 | a0011c0016t0013g0204a0011c0016t0013g0205a0011c0016t0013g0206others(1): Show | 4 | HG02486.hp2 HG02559.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.792-537C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66410809 | ||||||
| chr3:66410876
|
G | A | 1 | a0018c0028t0003g0259 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.792-604C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66410876 | ||||||
| chr3:66410944
|
C | A | 1 | a0002c0018t0001g0176 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.792-672G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66410944 | ||||||
| chr3:66410961
|
G | A | 1 | a0001c0002t0001g0076 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.792-689C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66410961 | ||||||
| chr3:66411051
|
G | A | 1 | a0004c0003t0001g0151 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.792-779C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66411051 | ||||||
| chr3:66411203
|
C | T | 12 | a0006c0026t0036g0234a0008c0006t0005g0200a0008c0006t0005g0215others(9): Show | 12 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.792-931G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66411203 | ||||||
| chr3:66411365
|
A | G | 1 | a0011c0030t0027g0021 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.792-1093T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66411365 | ||||||
| chr3:66411538
|
G | A | 1 | a0006c0009t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.792-1266C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66411538 | ||||||
| chr3:66411583
|
C | T | 12 | a0006c0026t0036g0234a0008c0006t0005g0200a0008c0006t0005g0215others(9): Show | 12 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.791+1288G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66411583 | ||||||
| chr3:66411623
|
C | T | 2 | a0003c0012t0014g0233a0003c0012t0014g0236 | 2 | HG02055.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.791+1248G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66411623 | ||||||
| chr3:66411771
|
T | C | 1 | a0002c0001t0032g0199 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.791+1100A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66411771 | ||||||
| chr3:66411812
|
A | G | 51 | a0001c0002t0001g0051a0002c0001t0001g0047a0002c0001t0001g0048others(48): Show | 51 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.791+1059T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66411812 | ||||||
| chr3:66411855
|
T | C | 1 | a0001c0002t0001g0140 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.791+1016A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66411855 | ||||||
| chr3:66411864
|
A | G | 1 | a0006c0009t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.791+1007T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66411864 | ||||||
| chr3:66412034
|
A | G | 1 | a0006c0009t0004g0224 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.791+837T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66412034 | ||||||
| chr3:66412083
|
G | A | 1 | a0001c0002t0001g0079 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.791+788C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66412083 | ||||||
| chr3:66412104
|
A | G | 79 | a0001c0002t0001g0049a0001c0002t0001g0053a0001c0002t0001g0056others(76): Show | 80 | HG00099.hp2 HG00609.hp1 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.791+767T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66412104 | ||||||
| chr3:66412170
|
C | G | 6 | a0003c0012t0018g0008a0006c0009t0002g0045a0011c0016t0013g0204others(3): Show | 6 | HG02486.hp2 HG02559.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.791+701G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66412170 | ||||||
| chr3:66412231
|
G | A | 4 | a0011c0016t0013g0204a0011c0016t0013g0205a0011c0016t0013g0206others(1): Show | 4 | HG02486.hp2 HG02559.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.791+640C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66412231 | ||||||
| chr3:66412259
|
C | A | 1 | a0006c0009t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.791+612G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66412259 | ||||||
| chr3:66412345
|
G | A | 1 | a0031c0047t0030g0162 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.791+526C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66412345 | ||||||
| chr3:66412362
|
G | A | 1 | a0006c0009t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.791+509C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66412362 | ||||||
| chr3:66412513
|
G | T | 1 | a0002c0001t0001g0174 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.791+358C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66412513 | ||||||
| chr3:66412549
|
A | G | 2 | a0002c0001t0001g0119a0007c0008t0001g0030 | 2 | NA18953.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.791+322T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66412549 | ||||||
| chr3:66412594
|
C | T | 1 | a0004c0003t0001g0151 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.791+277G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66412594 | ||||||
| chr3:66412723
|
C | T | 1 | a0016c0038t0003g0235 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.791+148G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66412723 | ||||||
| chr3:66412808
|
C | T | 8 | a0003c0012t0017g0004a0005c0004t0008g0247a0005c0004t0008g0248others(5): Show | 8 | HG01243.hp2 HG01952.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.791+63G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66412808 | ||||||
| chr3:66412827
|
G | A | 233 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(230): Show | 234 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.791+44C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66412827 | ||||||
| chr3:66412830
|
C | G | 58 | a0001c0007t0001g0116a0001c0007t0002g0080a0001c0007t0002g0100others(55): Show | 58 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.791+41G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66412830 | ||||||
| chr3:66412862
|
C | T | 11 | a0006c0026t0036g0234a0008c0006t0005g0200a0008c0006t0005g0215others(8): Show | 11 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.791+9G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 6/18 | chr3 | 66412862 | ||||||
| chr3:66413053
|
T | C | 1 | a0002c0001t0001g0191 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.648-39A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 5/18 | chr3 | 66413053 | ||||||
| chr3:66413212
|
C | G | 1 | a0008c0006t0009g0014 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.648-198G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 5/18 | chr3 | 66413212 | ||||||
| chr3:66413337
|
T | C | 1 | a0001c0002t0001g0189 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.648-323A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 5/18 | chr3 | 66413337 | ||||||
| chr3:66413487
|
C | A | 3 | a0001c0014t0011g0058a0001c0014t0011g0117a0001c0014t0028g0118 | 3 | NA18939.hp2 NA18949.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.648-473G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 5/18 | chr3 | 66413487 | ||||||
| chr3:66413628
|
T | C | 1 | a0005c0004t0007g0017 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.648-614A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 5/18 | chr3 | 66413628 | ||||||
| chr3:66413954
|
T | C | 1 | a0001c0007t0001g0116 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.648-940A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 5/18 | chr3 | 66413954 | ||||||
| chr3:66413970
|
GA | G | 11 | a0002c0001t0001g0110a0003c0010t0002g0010a0003c0010t0004g0201others(8): Show | 11 | HG02647.hp1 HG02818.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.647+949delT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 5/18 | chr3 | 66413970 | ||||||
| chr3:66414009
|
T | A | 86 | a0001c0002t0001g0051a0001c0002t0001g0146a0001c0014t0011g0058others(83): Show | 86 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.647+911A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 5/18 | chr3 | 66414009 | ||||||
| chr3:66414119
|
C | T | 3 | a0007c0008t0001g0038a0007c0008t0003g0252a0007c0008t0003g0256 | 3 | HG02451.hp1 HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.647+801G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 5/18 | chr3 | 66414119 | ||||||
| chr3:66414135
|
T | C | 73 | a0001c0002t0001g0051a0001c0002t0001g0146a0001c0014t0011g0058others(70): Show | 73 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.647+785A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 5/18 | chr3 | 66414135 | ||||||
| chr3:66414164
|
A | G | 1 | a0003c0012t0018g0008 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.647+756T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 5/18 | chr3 | 66414164 | ||||||
| chr3:66414207
|
G | C | 262 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(259): Show | 263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.647+713C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 5/18 | chr3 | 66414207 | ||||||
| chr3:66414313
|
T | C | 81 | a0001c0002t0001g0049a0001c0002t0001g0053a0001c0002t0001g0056others(78): Show | 82 | HG00099.hp2 HG00609.hp1 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.647+607A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 5/18 | chr3 | 66414313 | ||||||
| chr3:66414325
|
G | A | 5 | a0006c0009t0002g0045a0011c0016t0013g0204a0011c0016t0013g0205others(2): Show | 5 | HG02486.hp2 HG02559.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.647+595C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 5/18 | chr3 | 66414325 | ||||||
| chr3:66414345
|
T | C | 1 | a0001c0007t0001g0116 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.647+575A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 5/18 | chr3 | 66414345 | ||||||
| chr3:66414351
|
C | T | 1 | a0001c0007t0001g0116 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.647+569G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 5/18 | chr3 | 66414351 | ||||||
| chr3:66414352
|
A | C | 7 | a0001c0023t0002g0060a0001c0023t0002g0068a0003c0010t0004g0229others(4): Show | 7 | HG02055.hp1 HG02572.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.647+568T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 5/18 | chr3 | 66414352 | ||||||
| chr3:66414352
|
A | G | 1 | a0001c0007t0001g0116 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.647+568T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 5/18 | chr3 | 66414352 | ||||||
| chr3:66414354
|
A | G | 2 | a0001c0002t0001g0078a0001c0007t0001g0116 | 2 | HG00280.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.647+566T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 5/18 | chr3 | 66414354 | ||||||
| chr3:66414364
|
C | T | 2 | a0002c0022t0001g0177a0002c0022t0001g0179 | 2 | HG01243.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.647+556G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 5/18 | chr3 | 66414364 | ||||||
| chr3:66414391
|
C | G | 8 | a0003c0010t0002g0010a0003c0010t0004g0201a0003c0010t0004g0231others(5): Show | 8 | HG02647.hp1 HG02818.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.647+529G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 5/18 | chr3 | 66414391 | ||||||
| chr3:66414392
|
G | A | 1 | a0003c0012t0018g0008 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.647+528C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 5/18 | chr3 | 66414392 | ||||||
| chr3:66414403
|
T | A | 2 | a0013c0020t0035g0208a0021c0034t0019g0007 | 2 | HG02630.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.647+517A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 5/18 | chr3 | 66414403 | ||||||
| chr3:66414406
|
TAATA | T | 4 | a0005c0004t0007g0017a0011c0016t0013g0204a0011c0016t0013g0205others(1): Show | 4 | HG02486.hp2 HG02559.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.647+510_647+513del others(4): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 5/18 | chr3 | 66414406 | ||||||
| chr3:66414409
|
T | G | 1 | a0001c0002t0001g0108 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.647+511A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 5/18 | chr3 | 66414409 | ||||||
| chr3:66414418
|
AAAT | A | 4 | a0003c0012t0017g0004a0006c0019t0012g0244a0006c0019t0012g0245others(1): Show | 4 | HG01952.hp1 HG02280.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.647+499_647+501del others(3): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 5/18 | chr3 | 66414418 | ||||||
| chr3:66414560
|
A | T | 1 | a0002c0001t0016g0003 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.647+360T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 5/18 | chr3 | 66414560 | ||||||
| chr3:66414584
|
A | G | 1 | a0006c0009t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.647+336T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 5/18 | chr3 | 66414584 | ||||||
| chr3:66414755
|
C | G | 3 | a0009c0015t0002g0032a0009c0015t0002g0033a0009c0015t0002g0034 | 3 | HG01891.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.647+165G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 5/18 | chr3 | 66414755 | ||||||
| chr3:66414762
|
G | C | 4 | a0003c0012t0017g0004a0006c0019t0012g0244a0006c0019t0012g0245others(1): Show | 4 | HG01952.hp1 HG02280.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.647+158C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 5/18 | chr3 | 66414762 | ||||||
| chr3:66414835
|
T | C | 160 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(157): Show | 161 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(158): Show |
intron_variant | MODIFIER | c.647+85A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 5/18 | chr3 | 66414835 | ||||||
| chr3:66415278
|
C | T | 1 | a0006c0019t0012g0244 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.504-215G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 4/18 | chr3 | 66415278 | ||||||
| chr3:66415412
|
C | G | 1 | a0028c0049t0001g0067 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.504-349G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 4/18 | chr3 | 66415412 | ||||||
| chr3:66415456
|
T | C | 3 | a0001c0002t0001g0053a0001c0002t0001g0061a0001c0002t0001g0062 | 3 | HG00735.hp2 HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.504-393A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 4/18 | chr3 | 66415456 | ||||||
| chr3:66415503
|
G | C | 1 | a0013c0020t0035g0208 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.504-440C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 4/18 | chr3 | 66415503 | ||||||
| chr3:66415509
|
A | G | 1 | a0001c0002t0001g0074 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.504-446T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 4/18 | chr3 | 66415509 | ||||||
| chr3:66415611
|
G | C | 1 | a0002c0001t0001g0174 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.504-548C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 4/18 | chr3 | 66415611 | ||||||
| chr3:66415693
|
G | A | 1 | a0021c0034t0019g0007 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.504-630C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 4/18 | chr3 | 66415693 | ||||||
| chr3:66415717
|
C | T | 1 | a0013c0020t0035g0208 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.504-654G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 4/18 | chr3 | 66415717 | ||||||
| chr3:66415748
|
C | T | 1 | a0002c0001t0001g0090 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.504-685G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 4/18 | chr3 | 66415748 | ||||||
| chr3:66416015
|
A | C | 1 | a0003c0005t0001g0028 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.504-952T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 4/18 | chr3 | 66416015 | ||||||
| chr3:66416020
|
G | A | 60 | a0001c0002t0001g0049a0001c0002t0001g0077a0001c0002t0001g0140others(57): Show | 60 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.504-957C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 4/18 | chr3 | 66416020 | ||||||
| chr3:66416115
|
C | G | 60 | a0001c0002t0001g0049a0001c0002t0001g0077a0001c0002t0001g0140others(57): Show | 60 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.503+1014G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 4/18 | chr3 | 66416115 | ||||||
| chr3:66416174
|
C | T | 2 | a0003c0005t0003g0216a0003c0005t0003g0217 | 2 | NA18961.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.503+955G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 4/18 | chr3 | 66416174 | ||||||
| chr3:66416272
|
G | A | 1 | a0003c0012t0017g0004 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.503+857C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 4/18 | chr3 | 66416272 | ||||||
| chr3:66416383
|
G | A | 161 | a0001c0002t0001g0049a0001c0002t0001g0053a0001c0002t0001g0056others(158): Show | 162 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.503+746C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 4/18 | chr3 | 66416383 | ||||||
| chr3:66416685
|
A | G | 153 | a0001c0002t0001g0049a0001c0002t0001g0053a0001c0002t0001g0056others(150): Show | 154 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.503+444T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 4/18 | chr3 | 66416685 | ||||||
| chr3:66416739
|
A | G | 3 | a0002c0001t0001g0171a0002c0001t0001g0172a0002c0001t0001g0173 | 3 | HG00738.hp1 HG03139.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.503+390T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 4/18 | chr3 | 66416739 | ||||||
| chr3:66416797
|
C | T | 4 | a0011c0016t0013g0204a0011c0016t0013g0205a0011c0016t0013g0206others(1): Show | 4 | HG02486.hp2 HG02559.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.503+332G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 4/18 | chr3 | 66416797 | ||||||
| chr3:66416813
|
A | G | 182 | a0001c0002t0001g0049a0001c0002t0001g0053a0001c0002t0001g0056others(179): Show | 183 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.503+316T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 4/18 | chr3 | 66416813 | ||||||
| chr3:66416941
|
G | A | 68 | a0001c0002t0001g0049a0001c0002t0001g0077a0001c0002t0001g0140others(65): Show | 68 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.503+188C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 4/18 | chr3 | 66416941 | ||||||
| chr3:66416954
|
G | A | 3 | a0009c0015t0002g0032a0009c0015t0002g0033a0009c0015t0002g0034 | 3 | HG01891.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.503+175C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 4/18 | chr3 | 66416954 | ||||||
| chr3:66416977
|
G | C | 2 | a0006c0009t0002g0045a0018c0028t0003g0259 | 2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.503+152C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 4/18 | chr3 | 66416977 | ||||||
| chr3:66417312
|
G | A | 1 | a0005c0004t0007g0017 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.366-46C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66417312 | ||||||
| chr3:66417330
|
T | C | 2 | a0003c0005t0003g0210a0003c0005t0003g0218 | 2 | HG02040.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.366-64A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66417330 | ||||||
| chr3:66417539
|
T | C | 12 | a0006c0009t0004g0224a0006c0009t0004g0225a0006c0009t0004g0226others(9): Show | 12 | HG00735.hp1 HG01891.hp2 HG02922.hp1 others(9): Show |
intron_variant | MODIFIER | c.366-273A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66417539 | ||||||
| chr3:66417665
|
A | G | 65 | a0001c0002t0001g0051a0001c0002t0001g0146a0001c0014t0011g0058others(62): Show | 65 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.366-399T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66417665 | ||||||
| chr3:66417748
|
C | G | 3 | a0003c0005t0001g0037a0003c0005t0001g0039a0003c0031t0001g0036 | 3 | HG01884.hp1 HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.366-482G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66417748 | ||||||
| chr3:66417796
|
GA | G | 9 | a0001c0002t0001g0076a0001c0002t0001g0092a0006c0009t0002g0045others(6): Show | 9 | HG00280.hp1 HG01192.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.366-531delT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66417796 | ||||||
| chr3:66417796
|
GAA | G | 57 | a0001c0002t0001g0049a0001c0002t0001g0077a0001c0002t0001g0140others(54): Show | 57 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.366-532_366-531del others(2): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66417796 | ||||||
| chr3:66417816
|
G | A | 2 | a0007c0008t0003g0237a0016c0038t0003g0235 | 2 | HG02145.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.366-550C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66417816 | ||||||
| chr3:66417909
|
T | C | 1 | a0006c0009t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.366-643A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66417909 | ||||||
| chr3:66417979
|
C | T | 1 | a0002c0021t0001g0112 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.366-713G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66417979 | ||||||
| chr3:66417985
|
A | G | 61 | a0001c0002t0001g0049a0001c0002t0001g0077a0001c0002t0001g0140others(58): Show | 61 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.366-719T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66417985 | ||||||
| chr3:66418077
|
G | GT | 5 | a0001c0002t0001g0167a0006c0019t0012g0244a0006c0019t0012g0245others(2): Show | 5 | HG01934.hp2 HG01952.hp1 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.366-812dupA | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66418077 | ||||||
| chr3:66418083
|
T | G | 1 | a0005c0004t0006g0222 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.366-817A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66418083 | ||||||
| chr3:66418112
|
A | T | 2 | a0004c0003t0038g0262a0029c0052t0039g0263 | 2 | HG02486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.366-846T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66418112 | ||||||
| chr3:66418115
|
C | G | 2 | a0004c0003t0038g0262a0029c0052t0039g0263 | 2 | HG02486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.366-849G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66418115 | ||||||
| chr3:66418115
|
CAG | C | 44 | a0001c0002t0001g0049a0001c0002t0001g0077a0001c0002t0001g0140others(41): Show | 44 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.366-851_366-850del others(2): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66418115 | ||||||
| chr3:66418117
|
G | C | 2 | a0004c0003t0038g0262a0029c0052t0039g0263 | 2 | HG02486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.366-851C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66418117 | ||||||
| chr3:66418148
|
G | A | 1 | a0003c0012t0017g0004 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.366-882C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66418148 | ||||||
| chr3:66418172
|
A | G | 6 | a0003c0012t0017g0004a0006c0009t0002g0045a0006c0019t0012g0244others(3): Show | 6 | HG01952.hp1 HG02280.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.366-906T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66418172 | ||||||
| chr3:66418264
|
T | A | 4 | a0003c0010t0002g0010a0004c0003t0002g0105a0006c0009t0002g0045others(1): Show | 4 | HG02886.hp1 HG03471.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.366-998A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66418264 | ||||||
| chr3:66418340
|
G | A | 1 | a0030c0046t0010g0184 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.366-1074C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66418340 | ||||||
| chr3:66418398
|
G | A | 6 | a0001c0007t0002g0080a0001c0007t0002g0100a0001c0014t0010g0134others(3): Show | 6 | HG01261.hp1 HG01433.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.366-1132C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66418398 | ||||||
| chr3:66418698
|
C | T | 1 | a0002c0001t0001g0123 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.366-1432G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66418698 | ||||||
| chr3:66418699
|
G | A | 1 | a0023c0051t0002g0054 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.366-1433C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66418699 | ||||||
| chr3:66418844
|
G | C | 7 | a0001c0007t0002g0080a0001c0007t0002g0100a0001c0014t0010g0134others(4): Show | 7 | HG01261.hp1 HG01433.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.366-1578C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66418844 | ||||||
| chr3:66418859
|
A | G | 56 | a0001c0002t0001g0049a0001c0002t0001g0077a0001c0002t0001g0140others(53): Show | 56 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.366-1593T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66418859 | ||||||
| chr3:66418888
|
C | T | 59 | a0001c0002t0001g0049a0001c0002t0001g0077a0001c0002t0001g0140others(56): Show | 59 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.366-1622G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66418888 | ||||||
| chr3:66419038
|
T | C | 152 | a0001c0002t0001g0049a0001c0002t0001g0053a0001c0002t0001g0056others(149): Show | 153 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.366-1772A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66419038 | ||||||
| chr3:66419039
|
G | A | 1 | a0006c0009t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.366-1773C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66419039 | ||||||
| chr3:66419100
|
G | A | 140 | a0001c0002t0001g0049a0001c0002t0001g0053a0001c0002t0001g0056others(137): Show | 141 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.366-1834C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66419100 | ||||||
| chr3:66419113
|
G | A | 1 | a0001c0002t0001g0159 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.366-1847C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66419113 | ||||||
| chr3:66419151
|
G | A | 1 | a0002c0041t0001g0114 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.366-1885C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66419151 | ||||||
| chr3:66419157
|
G | A | 3 | a0006c0019t0012g0244a0006c0019t0012g0245a0017c0025t0012g0253 | 3 | HG01952.hp1 HG02280.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.366-1891C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66419157 | ||||||
| chr3:66419287
|
T | G | 1 | a0003c0005t0001g0028 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.366-2021A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66419287 | ||||||
| chr3:66419295
|
G | A | 1 | a0018c0028t0003g0259 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.366-2029C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66419295 | ||||||
| chr3:66419409
|
T | C | 16 | a0003c0005t0001g0028a0003c0010t0004g0257a0008c0006t0005g0200others(13): Show | 16 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.366-2143A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66419409 | ||||||
| chr3:66419411
|
C | T | 60 | a0001c0002t0001g0051a0001c0002t0001g0146a0002c0001t0001g0047others(57): Show | 60 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.366-2145G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66419411 | ||||||
| chr3:66419523
|
C | T | 1 | a0008c0006t0005g0223 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.366-2257G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66419523 | ||||||
| chr3:66419605
|
T | C | 1 | a0001c0002t0001g0078 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.366-2339A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66419605 | ||||||
| chr3:66419647
|
G | A | 31 | a0001c0002t0001g0049a0001c0002t0001g0077a0001c0002t0001g0140others(28): Show | 31 | HG00099.hp1 HG01256.hp1 HG01256.hp2 others(28): Show |
intron_variant | MODIFIER | c.366-2381C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66419647 | ||||||
| chr3:66419727
|
G | T | 11 | a0003c0010t0004g0257a0008c0006t0005g0200a0008c0006t0005g0215others(8): Show | 11 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.366-2461C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66419727 | ||||||
| chr3:66419788
|
C | G | 1 | a0008c0006t0020g0005 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.366-2522G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66419788 | ||||||
| chr3:66419891
|
T | C | 1 | a0002c0001t0001g0180 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.366-2625A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66419891 | ||||||
| chr3:66419994
|
C | T | 135 | a0001c0002t0001g0049a0001c0002t0001g0053a0001c0002t0001g0056others(132): Show | 136 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.366-2728G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66419994 | ||||||
| chr3:66420064
|
G | A | 1 | a0001c0002t0001g0159 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.366-2798C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66420064 | ||||||
| chr3:66420073
|
C | G | 79 | a0001c0002t0001g0053a0001c0002t0001g0056a0001c0002t0001g0061others(76): Show | 80 | HG00099.hp2 HG00609.hp1 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.366-2807G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66420073 | ||||||
| chr3:66420214
|
T | C | 10 | a0001c0007t0002g0080a0001c0007t0002g0100a0001c0014t0010g0134others(7): Show | 10 | HG01261.hp1 HG01433.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.366-2948A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66420214 | ||||||
| chr3:66420245
|
A | C | 1 | a0013c0020t0029g0029 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.366-2979T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66420245 | ||||||
| chr3:66420261
|
C | T | 1 | a0018c0028t0003g0259 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.366-2995G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66420261 | ||||||
| chr3:66420356
|
C | T | 1 | a0019c0029t0001g0022 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.366-3090G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66420356 | ||||||
| chr3:66420506
|
A | G | 82 | a0001c0002t0001g0051a0001c0002t0001g0053a0001c0002t0001g0056others(79): Show | 83 | HG00099.hp2 HG00544.hp2 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.366-3240T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66420506 | ||||||
| chr3:66420571
|
T | C | 1 | a0004c0003t0002g0089 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.366-3305A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66420571 | ||||||
| chr3:66420614
|
A | G | 1 | a0011c0030t0027g0021 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.366-3348T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66420614 | ||||||
| chr3:66420624
|
C | T | 5 | a0009c0037t0002g0018a0012c0017t0002g0015a0012c0017t0002g0020others(2): Show | 5 | HG00544.hp1 HG00609.hp2 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.366-3358G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66420624 | ||||||
| chr3:66420764
|
G | T | 1 | a0008c0006t0005g0215 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.366-3498C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66420764 | ||||||
| chr3:66420782
|
G | A | 1 | a0003c0005t0003g0241 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.366-3516C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66420782 | ||||||
| chr3:66420800
|
G | T | 14 | a0003c0005t0001g0028a0008c0006t0005g0200a0008c0006t0005g0215others(11): Show | 14 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.366-3534C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66420800 | ||||||
| chr3:66420814
|
C | T | 3 | a0004c0003t0002g0081a0004c0003t0002g0153a0027c0050t0023g0082 | 3 | HG00099.hp1 HG01256.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.366-3548G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66420814 | ||||||
| chr3:66420815
|
G | A | 41 | a0002c0001t0001g0048a0002c0001t0001g0059a0002c0001t0001g0085others(38): Show | 41 | HG00558.hp1 HG00621.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.366-3549C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66420815 | ||||||
| chr3:66420835
|
T | C | 77 | a0001c0002t0001g0051a0001c0002t0001g0053a0001c0002t0001g0056others(74): Show | 78 | HG00099.hp2 HG00544.hp2 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.366-3569A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66420835 | ||||||
| chr3:66420866
|
C | G | 1 | a0013c0020t0035g0208 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.366-3600G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66420866 | ||||||
| chr3:66420891
|
T | C | 1 | a0001c0007t0002g0132 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.366-3625A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66420891 | ||||||
| chr3:66420902
|
G | T | 3 | a0005c0004t0006g0220a0005c0004t0006g0221a0005c0004t0006g0222 | 3 | HG02630.hp2 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.366-3636C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66420902 | ||||||
| chr3:66420952
|
G | C | 4 | a0005c0004t0006g0238a0005c0004t0006g0239a0005c0004t0006g0240others(1): Show | 4 | HG01099.hp1 HG01123.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.366-3686C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66420952 | ||||||
| chr3:66421099
|
C | G | 75 | a0001c0002t0001g0053a0001c0002t0001g0056a0001c0002t0001g0061others(72): Show | 76 | HG00099.hp2 HG00609.hp1 HG00673.hp1 others(73): Show |
intron_variant | MODIFIER | c.366-3833G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66421099 | ||||||
| chr3:66421214
|
A | T | 10 | a0008c0006t0005g0200a0008c0006t0005g0215a0008c0006t0005g0219others(7): Show | 10 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.366-3948T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66421214 | ||||||
| chr3:66421235
|
T | C | 20 | a0001c0002t0001g0092a0001c0002t0001g0093a0005c0004t0001g0019others(17): Show | 20 | HG00544.hp1 HG00609.hp2 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.366-3969A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66421235 | ||||||
| chr3:66421248
|
A | G | 3 | a0011c0016t0013g0204a0011c0016t0013g0205a0011c0016t0013g0206 | 3 | HG02486.hp2 HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.366-3982T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66421248 | ||||||
| chr3:66421263
|
C | G | 131 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(128): Show | 132 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.366-3997G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66421263 | ||||||
| chr3:66421312
|
C | T | 3 | a0009c0015t0002g0032a0009c0015t0002g0033a0009c0015t0002g0034 | 3 | HG01891.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.366-4046G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66421312 | ||||||
| chr3:66421321
|
T | C | 241 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(238): Show | 242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.366-4055A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66421321 | ||||||
| chr3:66421322
|
G | T | 3 | a0009c0015t0002g0032a0009c0015t0002g0033a0009c0015t0002g0034 | 3 | HG01891.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.366-4056C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66421322 | ||||||
| chr3:66421375
|
T | C | 73 | a0001c0002t0001g0051a0001c0002t0001g0053a0001c0002t0001g0056others(70): Show | 74 | HG00099.hp2 HG00544.hp2 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.366-4109A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66421375 | ||||||
| chr3:66421462
|
G | C | 1 | a0013c0020t0035g0208 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.366-4196C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66421462 | ||||||
| chr3:66421470
|
A | G | 151 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(148): Show | 152 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.366-4204T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66421470 | ||||||
| chr3:66421555
|
C | G | 8 | a0003c0010t0002g0010a0003c0010t0004g0201a0003c0010t0004g0231others(5): Show | 8 | HG02647.hp1 HG02818.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.366-4289G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66421555 | ||||||
| chr3:66421588
|
C | T | 1 | a0013c0020t0035g0208 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.366-4322G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66421588 | ||||||
| chr3:66421618
|
C | T | 50 | a0001c0002t0001g0049a0001c0002t0001g0077a0001c0002t0001g0140others(47): Show | 50 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.366-4352G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66421618 | ||||||
| chr3:66421716
|
G | A | 4 | a0001c0023t0002g0060a0001c0023t0002g0068a0003c0010t0004g0229others(1): Show | 4 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.366-4450C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66421716 | ||||||
| chr3:66421811
|
G | C | 1 | a0006c0009t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.366-4545C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66421811 | ||||||
| chr3:66421866
|
T | C | 9 | a0001c0007t0002g0080a0001c0007t0002g0100a0001c0014t0010g0134others(6): Show | 9 | HG01261.hp1 HG01433.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.366-4600A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66421866 | ||||||
| chr3:66421981
|
T | C | 172 | a0001c0002t0001g0049a0001c0002t0001g0053a0001c0002t0001g0056others(169): Show | 173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.366-4715A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66421981 | ||||||
| chr3:66421996
|
G | A | 1 | a0001c0002t0001g0065 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.366-4730C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66421996 | ||||||
| chr3:66422015
|
T | A | 5 | a0003c0012t0017g0004a0006c0019t0012g0244a0006c0019t0012g0245others(2): Show | 5 | HG01952.hp1 HG02280.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.366-4749A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66422015 | ||||||
| chr3:66422052
|
T | G | 3 | a0011c0016t0013g0204a0011c0016t0013g0205a0011c0016t0013g0206 | 3 | HG02486.hp2 HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.366-4786A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66422052 | ||||||
| chr3:66422090
|
G | GC | 6 | a0006c0009t0004g0224a0006c0009t0004g0225a0006c0009t0004g0226others(3): Show | 6 | HG00735.hp1 HG02970.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.366-4825dupG | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66422090 | ||||||
| chr3:66422132
|
G | C | 2 | a0003c0012t0018g0008a0007c0008t0003g0237 | 2 | HG02976.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.366-4866C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66422132 | ||||||
| chr3:66422217
|
T | C | 1 | a0004c0053t0002g0197 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.366-4951A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66422217 | ||||||
| chr3:66422289
|
C | T | 1 | a0013c0020t0035g0208 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.366-5023G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66422289 | ||||||
| chr3:66422577
|
A | T | 3 | a0011c0016t0013g0204a0011c0016t0013g0205a0011c0016t0013g0206 | 3 | HG02486.hp2 HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.366-5311T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66422577 | ||||||
| chr3:66422660
|
A | T | 77 | a0001c0002t0001g0051a0001c0002t0001g0053a0001c0002t0001g0056others(74): Show | 78 | HG00099.hp2 HG00544.hp2 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.366-5394T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66422660 | ||||||
| chr3:66422718
|
T | G | 27 | a0001c0007t0002g0080a0001c0007t0002g0100a0001c0014t0010g0134others(24): Show | 27 | HG01261.hp1 HG01433.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.366-5452A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66422718 | ||||||
| chr3:66422748
|
C | G | 10 | a0001c0007t0002g0080a0001c0007t0002g0100a0001c0014t0010g0134others(7): Show | 10 | HG01261.hp1 HG01433.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.366-5482G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66422748 | ||||||
| chr3:66422828
|
T | C | 1 | a0001c0007t0002g0128 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.366-5562A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66422828 | ||||||
| chr3:66422873
|
C | T | 167 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(164): Show | 168 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.366-5607G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66422873 | ||||||
| chr3:66422885
|
A | G | 1 | a0004c0003t0002g0103 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.366-5619T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66422885 | ||||||
| chr3:66423062
|
G | A | 72 | a0001c0002t0001g0051a0001c0002t0001g0053a0001c0002t0001g0056others(69): Show | 73 | HG00099.hp2 HG00544.hp2 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.366-5796C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66423062 | ||||||
| chr3:66423088
|
A | G | 77 | a0001c0002t0001g0051a0001c0002t0001g0053a0001c0002t0001g0056others(74): Show | 78 | HG00099.hp2 HG00544.hp2 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.366-5822T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66423088 | ||||||
| chr3:66423238
|
A | G | 1 | a0006c0009t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.366-5972T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66423238 | ||||||
| chr3:66423240
|
G | A | 9 | a0001c0007t0002g0080a0001c0007t0002g0100a0001c0014t0010g0134others(6): Show | 9 | HG01261.hp1 HG01433.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.366-5974C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66423240 | ||||||
| chr3:66423249
|
T | C | 8 | a0003c0010t0002g0010a0003c0010t0004g0201a0003c0010t0004g0231others(5): Show | 8 | HG02647.hp1 HG02818.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.366-5983A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66423249 | ||||||
| chr3:66423308
|
C | T | 11 | a0008c0006t0005g0200a0008c0006t0005g0215a0008c0006t0005g0219others(8): Show | 11 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.366-6042G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66423308 | ||||||
| chr3:66423398
|
C | A | 1 | a0013c0020t0035g0208 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.366-6132G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66423398 | ||||||
| chr3:66423427
|
C | T | 2 | a0001c0002t0001g0178a0003c0005t0003g0241 | 2 | HG01070.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.366-6161G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66423427 | ||||||
| chr3:66423456
|
A | G | 1 | a0013c0020t0035g0208 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.366-6190T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66423456 | ||||||
| chr3:66423464
|
G | A | 1 | a0013c0020t0035g0208 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.366-6198C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66423464 | ||||||
| chr3:66423691
|
G | C | 1 | a0021c0034t0019g0007 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.366-6425C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66423691 | ||||||
| chr3:66423736
|
T | G | 54 | a0001c0002t0001g0049a0001c0002t0001g0077a0001c0002t0001g0140others(51): Show | 54 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.366-6470A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66423736 | ||||||
| chr3:66423749
|
T | C | 1 | a0008c0006t0005g0230 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.366-6483A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66423749 | ||||||
| chr3:66423750
|
T | C | 182 | a0001c0002t0001g0049a0001c0002t0001g0053a0001c0002t0001g0056others(179): Show | 183 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.366-6484A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66423750 | ||||||
| chr3:66423865
|
G | A | 71 | a0001c0002t0001g0053a0001c0002t0001g0056a0001c0002t0001g0061others(68): Show | 72 | HG00099.hp2 HG00609.hp1 HG00673.hp1 others(69): Show |
intron_variant | MODIFIER | c.366-6599C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66423865 | ||||||
| chr3:66424050
|
G | T | 2 | a0003c0012t0018g0008a0007c0008t0003g0237 | 2 | HG02976.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.366-6784C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66424050 | ||||||
| chr3:66424063
|
A | G | 53 | a0001c0002t0001g0049a0001c0002t0001g0077a0001c0002t0001g0140others(50): Show | 53 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(50): Show |
intron_variant | MODIFIER | c.366-6797T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66424063 | ||||||
| chr3:66424279
|
C | T | 1 | a0002c0001t0001g0059 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.366-7013G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66424279 | ||||||
| chr3:66424342
|
C | G | 7 | a0001c0007t0002g0080a0001c0007t0002g0100a0001c0014t0010g0134others(4): Show | 7 | HG01261.hp1 HG01433.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.366-7076G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66424342 | ||||||
| chr3:66424403
|
G | A | 10 | a0001c0007t0002g0080a0001c0007t0002g0100a0001c0014t0010g0134others(7): Show | 10 | HG01261.hp1 HG01433.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.366-7137C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66424403 | ||||||
| chr3:66424445
|
C | T | 13 | a0003c0005t0001g0028a0008c0006t0005g0200a0008c0006t0005g0215others(10): Show | 13 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.366-7179G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66424445 | ||||||
| chr3:66424530
|
A | G | 10 | a0001c0007t0002g0080a0001c0007t0002g0100a0001c0014t0010g0134others(7): Show | 10 | HG01261.hp1 HG01433.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.366-7264T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66424530 | ||||||
| chr3:66424533
|
A | G | 1 | a0002c0018t0001g0176 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.366-7267T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66424533 | ||||||
| chr3:66424745
|
T | C | 4 | a0001c0023t0002g0060a0001c0023t0002g0068a0003c0010t0004g0229others(1): Show | 4 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.366-7479A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66424745 | ||||||
| chr3:66425069
|
T | C | 1 | a0004c0003t0002g0161 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.366-7803A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66425069 | ||||||
| chr3:66425077
|
C | T | 9 | a0001c0007t0002g0080a0001c0007t0002g0100a0001c0014t0010g0134others(6): Show | 9 | HG01261.hp1 HG01433.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.366-7811G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66425077 | ||||||
| chr3:66425192
|
C | T | 1 | a0006c0009t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.366-7926G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66425192 | ||||||
| chr3:66425213
|
C | T | 50 | a0001c0002t0001g0049a0001c0002t0001g0077a0001c0002t0001g0140others(47): Show | 50 | HG00099.hp1 HG00280.hp2 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.366-7947G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66425213 | ||||||
| chr3:66425214
|
T | G | 1 | a0018c0028t0003g0259 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.366-7948A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66425214 | ||||||
| chr3:66425309
|
T | C | 1 | a0001c0014t0011g0058 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.366-8043A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66425309 | ||||||
| chr3:66425444
|
T | C | 67 | a0001c0002t0001g0053a0001c0002t0001g0056a0001c0002t0001g0061others(64): Show | 68 | HG00099.hp2 HG00609.hp1 HG00673.hp1 others(65): Show |
intron_variant | MODIFIER | c.366-8178A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66425444 | ||||||
| chr3:66425550
|
AG | A | 67 | a0001c0002t0001g0053a0001c0002t0001g0056a0001c0002t0001g0061others(64): Show | 68 | HG00099.hp2 HG00609.hp1 HG00673.hp1 others(65): Show |
intron_variant | MODIFIER | c.366-8285delC | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66425550 | ||||||
| chr3:66425611
|
T | C | 1 | a0021c0034t0019g0007 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.366-8345A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66425611 | ||||||
| chr3:66425677
|
A | G | 12 | a0008c0006t0005g0200a0008c0006t0005g0215a0008c0006t0005g0219others(9): Show | 12 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.366-8411T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66425677 | ||||||
| chr3:66425690
|
C | T | 1 | a0006c0009t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.366-8424G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66425690 | ||||||
| chr3:66425696
|
TG | T | 3 | a0007c0008t0001g0038a0007c0008t0003g0252a0007c0008t0003g0256 | 3 | HG02451.hp1 HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.366-8431delC | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66425696 | ||||||
| chr3:66425874
|
G | T | 1 | a0006c0009t0004g0246 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.366-8608C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66425874 | ||||||
| chr3:66425976
|
T | C | 1 | a0011c0030t0027g0021 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.366-8710A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66425976 | ||||||
| chr3:66426284
|
A | G | 9 | a0001c0007t0002g0080a0001c0007t0002g0100a0001c0014t0010g0134others(6): Show | 9 | HG01261.hp1 HG01433.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.366-9018T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66426284 | ||||||
| chr3:66426370
|
T | C | 4 | a0001c0023t0002g0060a0001c0023t0002g0068a0003c0010t0004g0229others(1): Show | 4 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.366-9104A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66426370 | ||||||
| chr3:66426707
|
G | T | 3 | a0009c0015t0002g0032a0009c0015t0002g0033a0009c0015t0002g0034 | 3 | HG01891.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.366-9441C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66426707 | ||||||
| chr3:66426763
|
T | C | 3 | a0001c0014t0011g0058a0001c0014t0011g0117a0001c0014t0028g0118 | 3 | NA18939.hp2 NA18949.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.366-9497A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66426763 | ||||||
| chr3:66426849
|
T | A | 3 | a0011c0016t0013g0204a0011c0016t0013g0205a0011c0016t0013g0206 | 3 | HG02486.hp2 HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.366-9583A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66426849 | ||||||
| chr3:66427094
|
C | T | 1 | a0010c0011t0007g0127 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.366-9828G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66427094 | ||||||
| chr3:66427219
|
C | G | 188 | a0001c0002t0001g0051a0001c0002t0001g0053a0001c0002t0001g0056others(185): Show | 189 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(186): Show |
intron_variant | MODIFIER | c.366-9953G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66427219 | ||||||
| chr3:66427378
|
G | A | 1 | a0013c0020t0035g0208 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.366-10112C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66427378 | ||||||
| chr3:66427404
|
A | G | 9 | a0001c0007t0002g0080a0001c0007t0002g0100a0001c0014t0010g0134others(6): Show | 9 | HG01261.hp1 HG01433.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.366-10138T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66427404 | ||||||
| chr3:66427514
|
C | T | 239 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(236): Show | 240 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.366-10248G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66427514 | ||||||
| chr3:66427563
|
C | A | 1 | a0006c0009t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.366-10297G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66427563 | ||||||
| chr3:66427894
|
C | A | 64 | a0001c0002t0001g0051a0001c0002t0001g0146a0001c0014t0011g0058others(61): Show | 64 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.366-10628G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66427894 | ||||||
| chr3:66427961
|
G | A | 4 | a0001c0002t0001g0051a0002c0001t0001g0047a0002c0001t0001g0195others(1): Show | 4 | HG00544.hp2 HG02132.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.366-10695C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66427961 | ||||||
| chr3:66427987
|
C | T | 1 | a0006c0009t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.366-10721G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66427987 | ||||||
| chr3:66427991
|
A | G | 5 | a0001c0023t0002g0060a0001c0023t0002g0068a0003c0010t0004g0229others(2): Show | 5 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.366-10725T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66427991 | ||||||
| chr3:66427994
|
T | C | 4 | a0003c0012t0017g0004a0006c0019t0012g0244a0006c0019t0012g0245others(1): Show | 4 | HG01952.hp1 HG02280.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.366-10728A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66427994 | ||||||
| chr3:66428047
|
T | C | 1 | a0007c0008t0025g0043 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.366-10781A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66428047 | ||||||
| chr3:66428071
|
T | C | 3 | a0011c0016t0013g0204a0011c0016t0013g0205a0011c0016t0013g0206 | 3 | HG02486.hp2 HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.366-10805A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66428071 | ||||||
| chr3:66428096
|
G | A | 1 | a0001c0002t0001g0070 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.366-10830C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66428096 | ||||||
| chr3:66428218
|
C | T | 1 | a0006c0009t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.366-10952G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66428218 | ||||||
| chr3:66428483
|
A | C | 70 | a0001c0002t0001g0053a0001c0002t0001g0056a0001c0002t0001g0061others(67): Show | 71 | HG00099.hp2 HG00609.hp1 HG00673.hp1 others(68): Show |
intron_variant | MODIFIER | c.366-11217T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66428483 | ||||||
| chr3:66428486
|
A | G | 70 | a0001c0002t0001g0053a0001c0002t0001g0056a0001c0002t0001g0061others(67): Show | 71 | HG00099.hp2 HG00609.hp1 HG00673.hp1 others(68): Show |
intron_variant | MODIFIER | c.366-11220T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66428486 | ||||||
| chr3:66428553
|
T | A | 65 | a0001c0002t0001g0051a0001c0002t0001g0146a0001c0014t0011g0058others(62): Show | 65 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.366-11287A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66428553 | ||||||
| chr3:66428581
|
C | T | 1 | a0006c0009t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.366-11315G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66428581 | ||||||
| chr3:66428607
|
T | G | 1 | a0018c0028t0003g0259 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.366-11341A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66428607 | ||||||
| chr3:66428904
|
C | T | 2 | a0002c0001t0001g0119a0007c0008t0001g0030 | 2 | NA18953.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.366-11638G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66428904 | ||||||
| chr3:66429010
|
C | T | 1 | a0004c0003t0002g0161 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.366-11744G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66429010 | ||||||
| chr3:66429037
|
G | C | 4 | a0005c0004t0006g0220a0005c0004t0006g0221a0005c0004t0006g0222others(1): Show | 4 | HG02630.hp2 HG02896.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.366-11771C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66429037 | ||||||
| chr3:66429063
|
G | A | 2 | a0004c0003t0002g0081a0004c0003t0002g0153 | 2 | HG00099.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.366-11797C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66429063 | ||||||
| chr3:66429222
|
T | C | 3 | a0001c0014t0011g0058a0001c0014t0011g0117a0001c0014t0028g0118 | 3 | NA18939.hp2 NA18949.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.366-11956A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66429222 | ||||||
| chr3:66429480
|
C | T | 4 | a0005c0004t0006g0220a0005c0004t0006g0221a0005c0004t0006g0222others(1): Show | 4 | HG02630.hp2 HG02896.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.366-12214G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66429480 | ||||||
| chr3:66429565
|
T | G | 28 | a0001c0007t0002g0080a0001c0007t0002g0100a0001c0014t0010g0134others(25): Show | 28 | HG00735.hp1 HG01261.hp1 HG01433.hp1 others(25): Show |
intron_variant | MODIFIER | c.366-12299A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66429565 | ||||||
| chr3:66429634
|
A | AT | 69 | a0001c0002t0001g0053a0001c0002t0001g0056a0001c0002t0001g0061others(66): Show | 70 | HG00099.hp2 HG00609.hp1 HG00673.hp1 others(67): Show |
intron_variant | MODIFIER | c.366-12369dupA | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66429634 | ||||||
| chr3:66429651
|
T | A | 2 | a0002c0001t0001g0124a0002c0001t0001g0150 | 2 | HG03688.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.366-12385A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66429651 | ||||||
| chr3:66429787
|
G | GGT | 22 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0014t0010g0134others(19): Show | 22 | HG00544.hp1 HG00609.hp2 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.366-12523_366-1252 others(6): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66429787 | ||||||
| chr3:66429787
|
G | T | 2 | a0001c0002t0001g0056a0001c0002t0001g0074 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.366-12521C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66429787 | ||||||
| chr3:66429787
|
GGT | G | 57 | a0001c0002t0001g0049a0001c0002t0001g0077a0001c0002t0001g0140others(54): Show | 57 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.366-12523_366-1252 others(6): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66429787 | ||||||
| chr3:66429787
|
GGTGT | G | 14 | a0001c0014t0011g0058a0001c0014t0011g0117a0001c0014t0028g0118others(11): Show | 14 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.366-12525_366-1252 others(8): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66429787 | ||||||
| chr3:66429789
|
T | G | 1 | a0015c0024t0001g0025 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.366-12523A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66429789 | ||||||
| chr3:66429833
|
G | A | 11 | a0008c0006t0005g0200a0008c0006t0005g0215a0008c0006t0005g0219others(8): Show | 11 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.366-12567C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66429833 | ||||||
| chr3:66429868
|
A | ATT | 243 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(240): Show | 244 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.366-12604_366-1260 others(6): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66429868 | ||||||
| chr3:66429878
|
A | G | 1 | a0004c0003t0026g0190 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.366-12612T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66429878 | ||||||
| chr3:66429908
|
A | AAAAAC | 18 | a0001c0014t0011g0058a0001c0014t0011g0117a0001c0014t0028g0118others(15): Show | 18 | HG01884.hp2 HG02486.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.366-12647_366-1264 others(9): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66429908 | ||||||
| chr3:66430078
|
T | C | 50 | a0001c0002t0001g0049a0001c0002t0001g0077a0001c0002t0001g0140others(47): Show | 50 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.366-12812A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66430078 | ||||||
| chr3:66430145
|
G | A | 1 | a0007c0008t0001g0038 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.366-12879C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66430145 | ||||||
| chr3:66430175
|
C | A | 55 | a0001c0002t0001g0049a0001c0002t0001g0077a0001c0002t0001g0140others(52): Show | 55 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(52): Show |
intron_variant | MODIFIER | c.366-12909G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66430175 | ||||||
| chr3:66430181
|
C | T | 3 | a0001c0014t0011g0058a0001c0014t0011g0117a0001c0014t0028g0118 | 3 | NA18939.hp2 NA18949.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.366-12915G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66430181 | ||||||
| chr3:66430182
|
A | G | 3 | a0001c0014t0011g0058a0001c0014t0011g0117a0001c0014t0028g0118 | 3 | NA18939.hp2 NA18949.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.366-12916T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66430182 | ||||||
| chr3:66430187
|
CAACAAA | C | 64 | a0001c0002t0001g0051a0001c0002t0001g0146a0002c0001t0001g0047others(61): Show | 64 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.366-12927_366-1292 others(10): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66430187 | ||||||
| chr3:66430190
|
CA | C | 56 | a0001c0002t0001g0049a0001c0002t0001g0077a0001c0002t0001g0140others(53): Show | 56 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.366-12925delT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66430190 | ||||||
| chr3:66430190
|
CAAA | C | 20 | a0001c0002t0001g0092a0001c0002t0001g0093a0005c0004t0001g0019others(17): Show | 20 | HG00544.hp1 HG00609.hp2 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.366-12927_366-1292 others(7): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66430190 | ||||||
| chr3:66430193
|
A | C | 81 | a0001c0002t0001g0053a0001c0002t0001g0056a0001c0002t0001g0061others(78): Show | 82 | HG00099.hp2 HG00609.hp1 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.366-12927T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66430193 | ||||||
| chr3:66430224
|
A | G | 3 | a0011c0016t0013g0204a0011c0016t0013g0205a0011c0016t0013g0206 | 3 | HG02486.hp2 HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.366-12958T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66430224 | ||||||
| chr3:66430376
|
G | A | 3 | a0011c0016t0013g0204a0011c0016t0013g0205a0011c0016t0013g0206 | 3 | HG02486.hp2 HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.366-13110C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66430376 | ||||||
| chr3:66430393
|
T | C | 20 | a0001c0002t0001g0092a0001c0002t0001g0093a0005c0004t0001g0019others(17): Show | 20 | HG00544.hp1 HG00609.hp2 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.366-13127A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66430393 | ||||||
| chr3:66430496
|
C | T | 1 | a0026c0039t0001g0073 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.366-13230G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66430496 | ||||||
| chr3:66430533
|
G | A | 1 | a0002c0001t0001g0048 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.366-13267C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66430533 | ||||||
| chr3:66430544
|
G | A | 10 | a0001c0002t0001g0092a0001c0002t0001g0093a0005c0004t0001g0019others(7): Show | 10 | HG00544.hp1 HG00609.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.366-13278C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66430544 | ||||||
| chr3:66430664
|
T | C | 10 | a0001c0002t0001g0111a0001c0007t0002g0080a0001c0007t0002g0100others(7): Show | 10 | HG01261.hp1 HG01433.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.366-13398A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66430664 | ||||||
| chr3:66430685
|
T | C | 4 | a0001c0023t0002g0060a0001c0023t0002g0068a0003c0010t0004g0229others(1): Show | 4 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.366-13419A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66430685 | ||||||
| chr3:66430790
|
C | T | 4 | a0005c0004t0006g0220a0005c0004t0006g0221a0005c0004t0006g0222others(1): Show | 4 | HG02630.hp2 HG02896.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.366-13524G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66430790 | ||||||
| chr3:66430840
|
G | A | 1 | a0001c0002t0001g0065 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.366-13574C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66430840 | ||||||
| chr3:66430870
|
C | A | 239 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(236): Show | 240 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.366-13604G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66430870 | ||||||
| chr3:66430967
|
C | T | 2 | a0004c0053t0002g0197a0025c0054t0002g0196 | 2 | HG02300.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.366-13701G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66430967 | ||||||
| chr3:66430981
|
T | C | 1 | a0006c0009t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.366-13715A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66430981 | ||||||
| chr3:66430990
|
C | T | 1 | a0004c0003t0002g0101 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.366-13724G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66430990 | ||||||
| chr3:66431001
|
C | T | 1 | a0002c0018t0001g0050 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.366-13735G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66431001 | ||||||
| chr3:66431029
|
C | T | 1 | a0008c0006t0005g0219 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.366-13763G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66431029 | ||||||
| chr3:66431173
|
G | A | 1 | a0006c0009t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.366-13907C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66431173 | ||||||
| chr3:66431250
|
T | G | 14 | a0003c0005t0001g0028a0008c0006t0005g0200a0008c0006t0005g0215others(11): Show | 14 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.366-13984A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66431250 | ||||||
| chr3:66431345
|
T | C | 3 | a0003c0012t0018g0008a0006c0009t0002g0045a0007c0008t0003g0237 | 3 | HG02976.hp2 HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.366-14079A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66431345 | ||||||
| chr3:66431572
|
T | C | 20 | a0001c0002t0001g0092a0001c0002t0001g0093a0005c0004t0001g0019others(17): Show | 20 | HG00544.hp1 HG00609.hp2 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.366-14306A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66431572 | ||||||
| chr3:66431574
|
T | C | 1 | a0021c0034t0019g0007 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.366-14308A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66431574 | ||||||
| chr3:66431620
|
C | T | 8 | a0003c0010t0002g0010a0003c0010t0004g0201a0003c0010t0004g0231others(5): Show | 8 | HG02647.hp1 HG02818.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.366-14354G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66431620 | ||||||
| chr3:66431638
|
A | G | 10 | a0001c0007t0001g0116a0001c0007t0002g0125a0001c0007t0002g0126others(7): Show | 10 | HG00280.hp2 HG01074.hp2 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.366-14372T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66431638 | ||||||
| chr3:66431646
|
T | C | 14 | a0003c0005t0001g0028a0008c0006t0005g0200a0008c0006t0005g0215others(11): Show | 14 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.366-14380A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66431646 | ||||||
| chr3:66431704
|
T | G | 4 | a0001c0023t0002g0060a0001c0023t0002g0068a0003c0010t0004g0229others(1): Show | 4 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.366-14438A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66431704 | ||||||
| chr3:66431890
|
A | G | 1 | a0027c0050t0023g0082 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.366-14624T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66431890 | ||||||
| chr3:66431916
|
C | T | 3 | a0001c0002t0001g0092a0001c0002t0001g0093a0010c0011t0001g0091 | 3 | NA18943.hp1 NA18970.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.366-14650G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66431916 | ||||||
| chr3:66431961
|
G | A | 1 | a0007c0033t0001g0027 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.366-14695C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66431961 | ||||||
| chr3:66431982
|
C | T | 10 | a0001c0007t0001g0116a0001c0007t0002g0125a0001c0007t0002g0126others(7): Show | 10 | HG00280.hp2 HG01074.hp2 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.366-14716G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66431982 | ||||||
| chr3:66432149
|
A | AG | 14 | a0003c0005t0001g0028a0008c0006t0005g0200a0008c0006t0005g0215others(11): Show | 14 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.366-14884_366-1488 others(5): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66432149 | ||||||
| chr3:66432181
|
G | C | 1 | a0001c0002t0001g0189 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.366-14915C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66432181 | ||||||
| chr3:66432186
|
T | C | 1 | a0021c0034t0019g0007 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.366-14920A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66432186 | ||||||
| chr3:66432286
|
G | A | 1 | a0022c0032t0007g0046 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.366-15020C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66432286 | ||||||
| chr3:66432489
|
C | G | 3 | a0001c0014t0011g0058a0001c0014t0011g0117a0001c0014t0028g0118 | 3 | NA18939.hp2 NA18949.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.366-15223G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66432489 | ||||||
| chr3:66432552
|
G | C | 6 | a0006c0009t0004g0224a0006c0009t0004g0225a0006c0009t0004g0226others(3): Show | 6 | HG00735.hp1 HG02970.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.366-15286C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66432552 | ||||||
| chr3:66432557
|
G | A | 1 | a0002c0001t0001g0121 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.366-15291C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66432557 | ||||||
| chr3:66432688
|
C | T | 1 | a0028c0049t0001g0067 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.366-15422G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66432688 | ||||||
| chr3:66432823
|
C | A | 1 | a0001c0002t0001g0178 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.366-15557G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66432823 | ||||||
| chr3:66433031
|
T | G | 1 | a0016c0038t0003g0235 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.366-15765A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66433031 | ||||||
| chr3:66433037
|
T | C | 10 | a0006c0009t0004g0224a0006c0009t0004g0225a0006c0009t0004g0226others(7): Show | 10 | HG00735.hp1 HG01891.hp2 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.366-15771A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66433037 | ||||||
| chr3:66433097
|
T | C | 32 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0002t0001g0111others(29): Show | 32 | HG00544.hp1 HG00609.hp2 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.366-15831A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66433097 | ||||||
| chr3:66433164
|
G | A | 11 | a0008c0006t0005g0200a0008c0006t0005g0215a0008c0006t0005g0219others(8): Show | 11 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.366-15898C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66433164 | ||||||
| chr3:66433277
|
G | T | 1 | a0021c0034t0019g0007 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.366-16011C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66433277 | ||||||
| chr3:66433476
|
G | A | 50 | a0001c0002t0001g0049a0001c0002t0001g0077a0001c0002t0001g0140others(47): Show | 50 | HG00099.hp1 HG00280.hp2 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.366-16210C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66433476 | ||||||
| chr3:66433543
|
T | A | 4 | a0005c0004t0006g0220a0005c0004t0006g0221a0005c0004t0006g0222others(1): Show | 4 | HG02630.hp2 HG02896.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.366-16277A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66433543 | ||||||
| chr3:66433629
|
A | G | 12 | a0008c0006t0005g0200a0008c0006t0005g0215a0008c0006t0005g0219others(9): Show | 12 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.366-16363T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66433629 | ||||||
| chr3:66433761
|
C | A | 3 | a0009c0015t0002g0032a0009c0015t0002g0033a0009c0015t0002g0034 | 3 | HG01891.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.366-16495G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66433761 | ||||||
| chr3:66433868
|
A | G | 1 | a0018c0028t0003g0259 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.366-16602T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66433868 | ||||||
| chr3:66434082
|
A | G | 1 | a0003c0005t0001g0028 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.366-16816T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66434082 | ||||||
| chr3:66434271
|
A | T | 1 | a0006c0009t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.366-17005T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66434271 | ||||||
| chr3:66434419
|
C | T | 4 | a0005c0004t0006g0220a0005c0004t0006g0221a0005c0004t0006g0222others(1): Show | 4 | HG02630.hp2 HG02896.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.365+17140G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66434419 | ||||||
| chr3:66434472
|
C | T | 11 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0002t0001g0140others(8): Show | 11 | HG00544.hp1 HG00609.hp2 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.365+17087G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66434472 | ||||||
| chr3:66434532
|
A | C | 79 | a0001c0002t0001g0053a0001c0002t0001g0056a0001c0002t0001g0061others(76): Show | 80 | HG00099.hp2 HG00609.hp1 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.365+17027T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66434532 | ||||||
| chr3:66434615
|
C | T | 1 | a0002c0022t0001g0177 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.365+16944G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66434615 | ||||||
| chr3:66434616
|
G | A | 10 | a0006c0009t0004g0224a0006c0009t0004g0225a0006c0009t0004g0226others(7): Show | 10 | HG00735.hp1 HG01891.hp2 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.365+16943C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66434616 | ||||||
| chr3:66434636
|
T | C | 1 | a0006c0009t0004g0246 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.365+16923A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66434636 | ||||||
| chr3:66434642
|
G | A | 22 | a0006c0009t0004g0224a0006c0009t0004g0225a0006c0009t0004g0226others(19): Show | 22 | HG00735.hp1 HG01884.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.365+16917C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66434642 | ||||||
| chr3:66434725
|
C | A | 10 | a0006c0009t0004g0224a0006c0009t0004g0225a0006c0009t0004g0226others(7): Show | 10 | HG00735.hp1 HG01891.hp2 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.365+16834G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66434725 | ||||||
| chr3:66434749
|
A | G | 3 | a0003c0005t0001g0037a0003c0005t0001g0039a0003c0031t0001g0036 | 3 | HG01884.hp1 HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.365+16810T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66434749 | ||||||
| chr3:66434755
|
T | TA | 44 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0002t0001g0136others(41): Show | 44 | HG00544.hp1 HG00609.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.365+16803dupT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66434755 | ||||||
| chr3:66434755
|
TA | T | 34 | a0001c0002t0001g0111a0001c0007t0001g0116a0001c0007t0002g0080others(31): Show | 34 | HG00280.hp2 HG01074.hp2 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.365+16803delT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66434755 | ||||||
| chr3:66434766
|
A | C | 1 | a0018c0028t0003g0259 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.365+16793T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66434766 | ||||||
| chr3:66434775
|
C | A | 87 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0002t0001g0140others(84): Show | 87 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.365+16784G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66434775 | ||||||
| chr3:66434797
|
A | C | 4 | a0001c0023t0002g0060a0001c0023t0002g0068a0003c0010t0004g0229others(1): Show | 4 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.365+16762T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66434797 | ||||||
| chr3:66434873
|
G | A | 11 | a0001c0007t0002g0194a0006c0009t0004g0224a0006c0009t0004g0225others(8): Show | 11 | HG00735.hp1 HG01255.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.365+16686C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66434873 | ||||||
| chr3:66434881
|
A | T | 2 | a0008c0006t0009g0011a0008c0006t0009g0012 | 2 | HG02559.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.365+16678T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66434881 | ||||||
| chr3:66435054
|
G | A | 50 | a0001c0002t0001g0049a0001c0002t0001g0077a0001c0007t0001g0116others(47): Show | 50 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.365+16505C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66435054 | ||||||
| chr3:66435071
|
A | ATGGC | 63 | a0001c0002t0001g0053a0001c0002t0001g0056a0001c0002t0001g0061others(60): Show | 64 | HG00099.hp2 HG00609.hp1 HG00673.hp1 others(61): Show |
intron_variant | MODIFIER | c.365+16487_365+1648 others(8): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66435071 | ||||||
| chr3:66435072
|
C | A | 63 | a0001c0002t0001g0053a0001c0002t0001g0056a0001c0002t0001g0061others(60): Show | 64 | HG00099.hp2 HG00609.hp1 HG00673.hp1 others(61): Show |
intron_variant | MODIFIER | c.365+16487G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66435072 | ||||||
| chr3:66435072
|
C | CGGCA | 16 | a0001c0002t0001g0111a0001c0007t0002g0080a0001c0007t0002g0100others(13): Show | 16 | HG01261.hp1 HG01433.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.365+16483_365+1648 others(8): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66435072 | ||||||
| chr3:66435082
|
A | G | 1 | a0007c0008t0003g0237 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.365+16477T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66435082 | ||||||
| chr3:66435116
|
A | G | 1 | a0001c0002t0001g0075 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.365+16443T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66435116 | ||||||
| chr3:66435161
|
C | T | 244 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(241): Show | 245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.365+16398G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66435161 | ||||||
| chr3:66435228
|
A | T | 12 | a0008c0006t0005g0200a0008c0006t0005g0215a0008c0006t0005g0219others(9): Show | 12 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.365+16331T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66435228 | ||||||
| chr3:66435274
|
G | C | 1 | a0004c0003t0002g0103 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.365+16285C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66435274 | ||||||
| chr3:66435285
|
A | G | 1 | a0002c0001t0001g0170 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.365+16274T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66435285 | ||||||
| chr3:66435316
|
T | C | 16 | a0001c0002t0001g0053a0001c0002t0001g0061a0001c0002t0001g0062others(13): Show | 17 | HG00673.hp1 HG00735.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.365+16243A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66435316 | ||||||
| chr3:66435396
|
TAAAAACA | T | 31 | a0001c0002t0001g0049a0001c0002t0001g0077a0002c0001t0032g0199others(28): Show | 31 | HG00099.hp1 HG00621.hp1 HG01256.hp1 others(28): Show |
intron_variant | MODIFIER | c.365+16156_365+1616 others(11): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66435396 | ||||||
| chr3:66435406
|
A | T | 21 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0002t0001g0140others(18): Show | 21 | HG00544.hp1 HG00609.hp2 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.365+16153T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66435406 | ||||||
| chr3:66435453
|
C | T | 1 | a0003c0005t0001g0028 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.365+16106G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66435453 | ||||||
| chr3:66435475
|
A | G | 1 | a0011c0030t0027g0021 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.365+16084T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66435475 | ||||||
| chr3:66435584
|
G | C | 4 | a0005c0004t0006g0220a0005c0004t0006g0221a0005c0004t0006g0222others(1): Show | 4 | HG02630.hp2 HG02896.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.365+15975C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66435584 | ||||||
| chr3:66435589
|
C | T | 10 | a0006c0009t0004g0224a0006c0009t0004g0225a0006c0009t0004g0226others(7): Show | 10 | HG00735.hp1 HG01891.hp2 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.365+15970G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66435589 | ||||||
| chr3:66435651
|
C | A | 47 | a0001c0002t0001g0051a0001c0002t0001g0146a0002c0001t0001g0047others(44): Show | 47 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.365+15908G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66435651 | ||||||
| chr3:66435670
|
T | C | 3 | a0001c0002t0001g0063a0001c0002t0001g0070a0001c0002t0001g0071 | 3 | HG01167.hp2 HG01515.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.365+15889A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66435670 | ||||||
| chr3:66435759
|
C | T | 1 | a0002c0001t0001g0143 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.365+15800G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66435759 | ||||||
| chr3:66435781
|
CT | C | 32 | a0001c0002t0001g0111a0001c0007t0002g0080a0001c0007t0002g0100others(29): Show | 32 | HG00738.hp1 HG01261.hp1 HG01433.hp1 others(29): Show |
intron_variant | MODIFIER | c.365+15777delA | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66435781 | ||||||
| chr3:66435781
|
CTT | C | 135 | a0001c0002t0001g0051a0001c0002t0001g0053a0001c0002t0001g0056others(132): Show | 136 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(133): Show |
intron_variant | MODIFIER | c.365+15776_365+1577 others(6): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66435781 | ||||||
| chr3:66435784
|
T | A | 2 | a0010c0011t0007g0169a0010c0011t0007g0175 | 2 | HG00280.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.365+15775A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66435784 | ||||||
| chr3:66435891
|
G | C | 21 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0002t0001g0140others(18): Show | 21 | HG00544.hp1 HG00609.hp2 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.365+15668C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66435891 | ||||||
| chr3:66435918
|
C | T | 1 | a0001c0002t0001g0198 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.365+15641G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66435918 | ||||||
| chr3:66435956
|
C | G | 10 | a0001c0002t0001g0111a0001c0007t0002g0080a0001c0007t0002g0100others(7): Show | 10 | HG01261.hp1 HG01433.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.365+15603G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66435956 | ||||||
| chr3:66436005
|
C | T | 63 | a0001c0002t0001g0051a0001c0002t0001g0146a0002c0001t0001g0047others(60): Show | 63 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.365+15554G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66436005 | ||||||
| chr3:66436025
|
C | T | 2 | a0003c0005t0001g0028a0011c0030t0027g0021 | 2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.365+15534G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66436025 | ||||||
| chr3:66436287
|
G | A | 4 | a0001c0002t0001g0051a0002c0001t0001g0047a0002c0001t0001g0195others(1): Show | 4 | HG00544.hp2 HG02132.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.365+15272C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66436287 | ||||||
| chr3:66436331
|
C | T | 1 | a0004c0003t0002g0161 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.365+15228G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66436331 | ||||||
| chr3:66436335
|
C | A | 48 | a0001c0002t0001g0049a0001c0002t0001g0077a0001c0007t0001g0116others(45): Show | 48 | HG00099.hp1 HG00280.hp2 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.365+15224G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66436335 | ||||||
| chr3:66436348
|
G | T | 3 | a0011c0016t0013g0204a0011c0016t0013g0205a0011c0016t0013g0206 | 3 | HG02486.hp2 HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.365+15211C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66436348 | ||||||
| chr3:66436363
|
C | T | 1 | a0011c0030t0027g0021 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.365+15196G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66436363 | ||||||
| chr3:66436437
|
C | T | 1 | a0011c0030t0027g0021 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.365+15122G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66436437 | ||||||
| chr3:66436454
|
T | C | 1 | a0003c0012t0018g0008 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.365+15105A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66436454 | ||||||
| chr3:66436466
|
A | G | 1 | a0003c0005t0001g0026 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.365+15093T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66436466 | ||||||
| chr3:66436493
|
G | A | 1 | a0011c0030t0027g0021 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.365+15066C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66436493 | ||||||
| chr3:66436505
|
C | T | 1 | a0002c0001t0001g0109 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.365+15054G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66436505 | ||||||
| chr3:66436528
|
G | A | 1 | a0001c0002t0001g0079 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.365+15031C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66436528 | ||||||
| chr3:66436607
|
G | A | 1 | a0021c0034t0019g0007 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.365+14952C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66436607 | ||||||
| chr3:66436665
|
AC | A | 10 | a0006c0009t0004g0224a0006c0009t0004g0225a0006c0009t0004g0226others(7): Show | 10 | HG00735.hp1 HG01891.hp2 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.365+14893delG | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66436665 | ||||||
| chr3:66436736
|
G | T | 1 | a0003c0005t0001g0028 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.365+14823C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66436736 | ||||||
| chr3:66436766
|
C | T | 1 | a0002c0001t0001g0166 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.365+14793G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66436766 | ||||||
| chr3:66436774
|
G | A | 1 | a0002c0001t0001g0109 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.365+14785C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66436774 | ||||||
| chr3:66436815
|
C | CA | 14 | a0003c0005t0001g0028a0008c0006t0005g0200a0008c0006t0005g0215others(11): Show | 14 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.365+14743dupT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66436815 | ||||||
| chr3:66437028
|
C | A | 1 | a0011c0030t0027g0021 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.365+14531G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66437028 | ||||||
| chr3:66437077
|
C | T | 1 | a0003c0010t0004g0257 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.365+14482G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66437077 | ||||||
| chr3:66437109
|
C | T | 14 | a0003c0005t0001g0028a0008c0006t0005g0200a0008c0006t0005g0215others(11): Show | 14 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.365+14450G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66437109 | ||||||
| chr3:66437118
|
A | G | 50 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0002t0001g0111others(47): Show | 50 | HG00544.hp1 HG00609.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.365+14441T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66437118 | ||||||
| chr3:66437189
|
G | A | 1 | a0004c0003t0002g0107 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.365+14370C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66437189 | ||||||
| chr3:66437228
|
T | G | 69 | a0001c0002t0001g0051a0001c0002t0001g0146a0001c0014t0011g0058others(66): Show | 69 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.365+14331A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66437228 | ||||||
| chr3:66437265
|
G | T | 1 | a0002c0001t0001g0059 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.365+14294C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66437265 | ||||||
| chr3:66437282
|
G | C | 3 | a0003c0005t0001g0037a0003c0005t0001g0039a0003c0031t0001g0036 | 3 | HG01884.hp1 HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.365+14277C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66437282 | ||||||
| chr3:66437306
|
A | C | 3 | a0009c0015t0002g0032a0009c0015t0002g0033a0009c0015t0002g0034 | 3 | HG01891.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.365+14253T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66437306 | ||||||
| chr3:66437314
|
G | C | 1 | a0018c0028t0003g0259 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.365+14245C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66437314 | ||||||
| chr3:66437337
|
A | G | 51 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0002t0001g0111others(48): Show | 51 | HG00544.hp1 HG00609.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.365+14222T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66437337 | ||||||
| chr3:66437346
|
C | G | 21 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0002t0001g0140others(18): Show | 21 | HG00544.hp1 HG00609.hp2 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.365+14213G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66437346 | ||||||
| chr3:66437406
|
C | A | 73 | a0001c0002t0001g0051a0001c0002t0001g0146a0001c0014t0011g0058others(70): Show | 73 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.365+14153G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66437406 | ||||||
| chr3:66437549
|
T | A | 1 | a0001c0014t0010g0134 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.365+14010A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66437549 | ||||||
| chr3:66437710
|
G | T | 50 | a0001c0002t0001g0049a0001c0002t0001g0077a0001c0007t0001g0116others(47): Show | 50 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.365+13849C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66437710 | ||||||
| chr3:66437722
|
G | A | 13 | a0003c0005t0001g0028a0008c0006t0005g0200a0008c0006t0005g0215others(10): Show | 13 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.365+13837C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66437722 | ||||||
| chr3:66437765
|
G | A | 13 | a0003c0005t0001g0028a0008c0006t0005g0200a0008c0006t0005g0215others(10): Show | 13 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.365+13794C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66437765 | ||||||
| chr3:66438026
|
T | C | 1 | a0002c0001t0032g0199 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.365+13533A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66438026 | ||||||
| chr3:66438030
|
T | C | 1 | a0021c0034t0019g0007 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.365+13529A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66438030 | ||||||
| chr3:66438103
|
G | A | 3 | a0003c0005t0001g0037a0003c0005t0001g0039a0003c0031t0001g0036 | 3 | HG01884.hp1 HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.365+13456C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66438103 | ||||||
| chr3:66438110
|
C | G | 1 | a0008c0006t0005g0223 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.365+13449G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66438110 | ||||||
| chr3:66438219
|
C | T | 4 | a0001c0023t0002g0060a0001c0023t0002g0068a0003c0010t0004g0229others(1): Show | 4 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.365+13340G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66438219 | ||||||
| chr3:66438232
|
C | T | 240 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(237): Show | 241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.365+13327G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66438232 | ||||||
| chr3:66438364
|
G | C | 11 | a0001c0002t0001g0111a0001c0007t0002g0080a0001c0007t0002g0100others(8): Show | 11 | HG01261.hp1 HG01433.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.365+13195C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66438364 | ||||||
| chr3:66438388
|
C | T | 1 | a0001c0007t0002g0129 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.365+13171G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66438388 | ||||||
| chr3:66438466
|
A | C | 4 | a0001c0023t0002g0060a0001c0023t0002g0068a0003c0010t0004g0229others(1): Show | 4 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.365+13093T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66438466 | ||||||
| chr3:66438611
|
T | C | 21 | a0001c0002t0001g0092a0001c0002t0001g0093a0005c0004t0001g0019others(18): Show | 21 | HG00544.hp1 HG00609.hp2 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.365+12948A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66438611 | ||||||
| chr3:66438714
|
G | A | 1 | a0013c0020t0035g0208 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.365+12845C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66438714 | ||||||
| chr3:66438948
|
C | A | 1 | a0003c0012t0018g0008 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.365+12611G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66438948 | ||||||
| chr3:66438990
|
G | T | 60 | a0001c0002t0001g0053a0001c0002t0001g0056a0001c0002t0001g0061others(57): Show | 61 | HG00099.hp2 HG00609.hp1 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.365+12569C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66438990 | ||||||
| chr3:66439011
|
A | C | 1 | a0023c0051t0002g0054 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.365+12548T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66439011 | ||||||
| chr3:66439070
|
A | G | 1 | a0003c0012t0014g0236 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.365+12489T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66439070 | ||||||
| chr3:66439187
|
G | A | 1 | a0005c0004t0006g0239 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.365+12372C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66439187 | ||||||
| chr3:66439200
|
C | T | 3 | a0009c0013t0001g0041a0009c0013t0002g0042a0009c0013t0002g0044 | 3 | NA18991.hp2 NA19000.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.365+12359G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66439200 | ||||||
| chr3:66439227
|
G | A | 2 | a0003c0005t0001g0028a0011c0030t0027g0021 | 2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.365+12332C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66439227 | ||||||
| chr3:66439369
|
A | G | 1 | a0008c0006t0005g0215 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.365+12190T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66439369 | ||||||
| chr3:66439419
|
A | G | 1 | a0006c0009t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.365+12140T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66439419 | ||||||
| chr3:66439561
|
CT | C | 6 | a0001c0002t0001g0071a0001c0002t0001g0079a0002c0001t0001g0121others(3): Show | 6 | HG00099.hp2 HG01255.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.365+11997delA | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66439561 | ||||||
| chr3:66439575
|
T | A | 184 | a0001c0002t0001g0051a0001c0002t0001g0053a0001c0002t0001g0056others(181): Show | 185 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(182): Show |
intron_variant | MODIFIER | c.365+11984A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66439575 | ||||||
| chr3:66439575
|
T | TA | 51 | a0001c0002t0001g0049a0001c0002t0001g0077a0001c0002t0001g0106others(48): Show | 51 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.365+11983dupT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66439575 | ||||||
| chr3:66439658
|
T | C | 14 | a0003c0005t0001g0028a0008c0006t0005g0200a0008c0006t0005g0215others(11): Show | 14 | HG01884.hp2 HG02559.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.365+11901A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66439658 | ||||||
| chr3:66439686
|
C | G | 1 | a0003c0010t0004g0201 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.365+11873G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66439686 | ||||||
| chr3:66439701
|
C | A | 132 | a0001c0002t0001g0051a0001c0002t0001g0053a0001c0002t0001g0056others(129): Show | 133 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(130): Show |
intron_variant | MODIFIER | c.365+11858G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66439701 | ||||||
| chr3:66439709
|
T | C | 20 | a0001c0002t0001g0092a0001c0002t0001g0093a0005c0004t0001g0019others(17): Show | 20 | HG00544.hp1 HG00609.hp2 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.365+11850A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66439709 | ||||||
| chr3:66439769
|
G | A | 1 | a0013c0020t0035g0208 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.365+11790C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66439769 | ||||||
| chr3:66439787
|
T | C | 3 | a0007c0008t0001g0038a0007c0008t0003g0252a0007c0008t0003g0256 | 3 | HG02451.hp1 HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.365+11772A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66439787 | ||||||
| chr3:66440019
|
A | AG | 39 | a0001c0002t0001g0092a0001c0002t0001g0093a0003c0005t0001g0028others(36): Show | 39 | HG00544.hp1 HG00609.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.365+11539dupC | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66440019 | ||||||
| chr3:66440019
|
A | G | 4 | a0001c0023t0002g0060a0001c0023t0002g0068a0003c0010t0004g0229others(1): Show | 4 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.365+11540T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66440019 | ||||||
| chr3:66440024
|
G | GA | 5 | a0001c0002t0001g0094a0001c0023t0002g0060a0001c0023t0002g0068others(2): Show | 5 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.365+11534dupT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66440024 | ||||||
| chr3:66440160
|
C | A | 1 | a0001c0002t0001g0051 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.365+11399G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66440160 | ||||||
| chr3:66440198
|
A | G | 1 | a0006c0009t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.365+11361T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66440198 | ||||||
| chr3:66440244
|
A | C | 3 | a0003c0005t0001g0037a0003c0005t0001g0039a0003c0031t0001g0036 | 3 | HG01884.hp1 HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.365+11315T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66440244 | ||||||
| chr3:66440246
|
CTCGAGGT others(4): Show |
C | 1 | a0001c0002t0001g0094 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.365+11302_365+1131 others(15): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66440246 | ||||||
| chr3:66440248
|
C | T | 1 | a0013c0020t0035g0208 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.365+11311G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66440248 | ||||||
| chr3:66440275
|
C | T | 1 | a0004c0003t0026g0190 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.365+11284G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66440275 | ||||||
| chr3:66440354
|
C | T | 1 | a0004c0003t0002g0141 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.365+11205G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66440354 | ||||||
| chr3:66440447
|
G | A | 238 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(235): Show | 239 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.365+11112C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66440447 | ||||||
| chr3:66440812
|
T | C | 1 | a0004c0003t0002g0181 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.365+10747A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66440812 | ||||||
| chr3:66440853
|
G | A | 1 | a0006c0009t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.365+10706C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66440853 | ||||||
| chr3:66441069
|
C | T | 4 | a0005c0004t0006g0220a0005c0004t0006g0221a0005c0004t0006g0222others(1): Show | 4 | HG02630.hp2 HG02896.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.365+10490G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66441069 | ||||||
| chr3:66441243
|
G | A | 48 | a0001c0002t0001g0049a0001c0002t0001g0077a0001c0007t0001g0116others(45): Show | 48 | HG00099.hp1 HG00280.hp2 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.365+10316C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66441243 | ||||||
| chr3:66441272
|
A | G | 3 | a0001c0014t0011g0058a0001c0014t0011g0117a0001c0014t0028g0118 | 3 | NA18939.hp2 NA18949.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.365+10287T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66441272 | ||||||
| chr3:66441398
|
C | G | 144 | a0001c0002t0001g0051a0001c0002t0001g0053a0001c0002t0001g0056others(141): Show | 145 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.365+10161G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66441398 | ||||||
| chr3:66441487
|
T | C | 3 | a0011c0016t0013g0204a0011c0016t0013g0205a0011c0016t0013g0206 | 3 | HG02486.hp2 HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.365+10072A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66441487 | ||||||
| chr3:66441957
|
G | A | 1 | a0001c0002t0001g0115 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.365+9602C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66441957 | ||||||
| chr3:66441976
|
C | T | 1 | a0002c0001t0001g0150 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.365+9583G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66441976 | ||||||
| chr3:66441998
|
C | T | 28 | a0001c0002t0001g0049a0001c0002t0001g0077a0004c0003t0001g0151others(25): Show | 28 | HG00099.hp1 HG01256.hp1 HG01256.hp2 others(25): Show |
intron_variant | MODIFIER | c.365+9561G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66441998 | ||||||
| chr3:66442028
|
C | T | 17 | a0001c0023t0002g0060a0001c0023t0002g0068a0003c0010t0004g0229others(14): Show | 17 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.365+9531G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66442028 | ||||||
| chr3:66442091
|
T | C | 1 | a0004c0003t0002g0101 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.365+9468A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66442091 | ||||||
| chr3:66442180
|
G | T | 61 | a0001c0002t0001g0053a0001c0002t0001g0056a0001c0002t0001g0061others(58): Show | 62 | HG00099.hp2 HG00609.hp1 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.365+9379C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66442180 | ||||||
| chr3:66442214
|
T | C | 4 | a0003c0005t0003g0001a0003c0005t0003g0209a0003c0005t0003g0211others(1): Show | 5 | NA18966.hp2 NA18986.hp1 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.365+9345A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66442214 | ||||||
| chr3:66442448
|
G | GGGA | 5 | a0001c0023t0002g0060a0001c0023t0002g0068a0003c0010t0004g0229others(2): Show | 5 | HG02572.hp1 HG02630.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.365+9108_365+9110d others(5): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66442448 | ||||||
| chr3:66442457
|
A | G | 8 | a0001c0002t0001g0066a0001c0002t0001g0084a0001c0002t0001g0086others(5): Show | 8 | HG01261.hp2 HG01433.hp2 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.365+9102T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66442457 | ||||||
| chr3:66442539
|
T | C | 1 | a0022c0032t0007g0046 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.365+9020A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66442539 | ||||||
| chr3:66442553
|
A | G | 1 | a0005c0004t0001g0019 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.365+9006T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66442553 | ||||||
| chr3:66442662
|
T | C | 1 | a0009c0037t0002g0018 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.365+8897A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66442662 | ||||||
| chr3:66442670
|
C | A | 3 | a0009c0015t0002g0032a0009c0015t0002g0033a0009c0015t0002g0034 | 3 | HG01891.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.365+8889G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66442670 | ||||||
| chr3:66442684
|
A | G | 2 | a0002c0001t0001g0188a0002c0041t0001g0114 | 2 | NA18969.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.365+8875T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66442684 | ||||||
| chr3:66442784
|
C | T | 1 | a0003c0005t0001g0037 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.365+8775G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66442784 | ||||||
| chr3:66442812
|
A | G | 1 | a0001c0002t0001g0066 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.365+8747T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66442812 | ||||||
| chr3:66442929
|
C | CCT | 5 | a0002c0001t0001g0188a0002c0021t0001g0112a0002c0021t0001g0113others(2): Show | 5 | HG00558.hp2 HG02027.hp2 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.365+8628_365+8629d others(4): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66442929 | ||||||
| chr3:66442957
|
A | C | 4 | a0001c0023t0002g0060a0001c0023t0002g0068a0003c0010t0004g0229others(1): Show | 4 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.365+8602T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66442957 | ||||||
| chr3:66442957
|
A | T | 42 | a0001c0002t0001g0056a0001c0002t0001g0063a0001c0002t0001g0065others(39): Show | 42 | HG00099.hp2 HG00609.hp1 HG01167.hp2 others(39): Show |
intron_variant | MODIFIER | c.365+8602T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66442957 | ||||||
| chr3:66442976
|
A | C | 1 | a0001c0002t0001g0079 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.365+8583T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66442976 | ||||||
| chr3:66443025
|
T | C | 1 | a0013c0020t0035g0208 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.365+8534A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66443025 | ||||||
| chr3:66443033
|
C | T | 1 | a0010c0011t0007g0127 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.365+8526G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66443033 | ||||||
| chr3:66443041
|
G | A | 73 | a0001c0002t0001g0051a0001c0002t0001g0146a0002c0001t0001g0047others(70): Show | 73 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.365+8518C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66443041 | ||||||
| chr3:66443162
|
G | A | 1 | a0003c0012t0017g0004 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.365+8397C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66443162 | ||||||
| chr3:66443316
|
A | AGGGGATG others(11): Show |
10 | a0006c0009t0004g0224a0006c0009t0004g0225a0006c0009t0004g0226others(7): Show | 10 | HG00735.hp1 HG01891.hp2 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.365+8225_365+8242d others(20): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66443316 | ||||||
| chr3:66443316
|
A | AGGGGATG others(30): Show |
9 | a0002c0001t0001g0119a0002c0001t0001g0135a0002c0001t0001g0143others(6): Show | 9 | HG00621.hp2 NA18951.hp1 NA18953.hp1 others(6): Show |
intron_variant | MODIFIER | c.365+8206_365+8242d others(39): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66443316 | ||||||
| chr3:66443316
|
AGGGGATG others(11): Show |
A | 49 | a0001c0002t0001g0049a0001c0002t0001g0077a0001c0007t0001g0116others(46): Show | 49 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.365+8225_365+8242d others(20): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66443316 | ||||||
| chr3:66443328
|
A | AGGGGCGG others(12): Show |
3 | a0006c0019t0012g0244a0006c0019t0012g0245a0017c0025t0012g0253 | 3 | HG01952.hp1 HG02280.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.365+8212_365+8230d others(21): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66443328 | ||||||
| chr3:66443328
|
AGGGGCGG others(12): Show |
A | 10 | a0001c0002t0001g0063a0001c0002t0001g0065a0001c0002t0001g0070others(7): Show | 10 | HG01167.hp2 HG01346.hp1 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.365+8212_365+8230d others(21): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66443328 | ||||||
| chr3:66443466
|
C | T | 4 | a0001c0023t0002g0060a0001c0023t0002g0068a0003c0010t0004g0229others(1): Show | 4 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.365+8093G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66443466 | ||||||
| chr3:66443670
|
T | C | 1 | a0008c0006t0005g0223 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.365+7889A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66443670 | ||||||
| chr3:66443779
|
A | G | 165 | a0001c0002t0001g0051a0001c0002t0001g0053a0001c0002t0001g0056others(162): Show | 166 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(163): Show |
intron_variant | MODIFIER | c.365+7780T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66443779 | ||||||
| chr3:66443995
|
G | A | 14 | a0001c0002t0001g0078a0001c0002t0001g0111a0001c0007t0002g0080others(11): Show | 14 | HG01261.hp1 HG01433.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.365+7564C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66443995 | ||||||
| chr3:66444065
|
C | T | 1 | a0003c0005t0001g0028 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.365+7494G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66444065 | ||||||
| chr3:66444300
|
G | T | 1 | a0001c0002t0031g0069 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.365+7259C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66444300 | ||||||
| chr3:66444326
|
A | T | 1 | a0003c0010t0002g0010 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.365+7233T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66444326 | ||||||
| chr3:66444368
|
T | TGC | 25 | a0001c0002t0001g0140a0005c0004t0001g0019a0006c0009t0004g0224others(22): Show | 25 | HG00544.hp1 HG00609.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.365+7189_365+7190d others(4): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66444368 | ||||||
| chr3:66444384
|
GC | G | 67 | a0001c0002t0001g0051a0001c0002t0001g0146a0002c0001t0001g0047others(64): Show | 67 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.365+7174delG | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66444384 | ||||||
| chr3:66444489
|
G | A | 1 | a0006c0009t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.365+7070C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66444489 | ||||||
| chr3:66444491
|
C | CT | 10 | a0001c0002t0001g0111a0001c0007t0002g0080a0001c0007t0002g0100others(7): Show | 10 | HG01261.hp1 HG01433.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.365+7067dupA | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66444491 | ||||||
| chr3:66444512
|
G | A | 1 | a0013c0020t0035g0208 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.365+7047C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66444512 | ||||||
| chr3:66444550
|
G | A | 1 | a0003c0012t0018g0008 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.365+7009C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66444550 | ||||||
| chr3:66444565
|
C | T | 3 | a0011c0016t0013g0204a0011c0016t0013g0205a0011c0016t0013g0206 | 3 | HG02486.hp2 HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.365+6994G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66444565 | ||||||
| chr3:66444869
|
TTA | T | 247 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(244): Show | 248 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.365+6688_365+6689d others(4): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66444869 | ||||||
| chr3:66444942
|
T | C | 67 | a0001c0002t0001g0053a0001c0002t0001g0056a0001c0002t0001g0061others(64): Show | 68 | HG00099.hp2 HG00609.hp1 HG00673.hp1 others(65): Show |
intron_variant | MODIFIER | c.365+6617A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66444942 | ||||||
| chr3:66444973
|
A | G | 10 | a0001c0002t0001g0111a0001c0007t0002g0080a0001c0007t0002g0100others(7): Show | 10 | HG01261.hp1 HG01433.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.365+6586T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66444973 | ||||||
| chr3:66445053
|
C | T | 48 | a0001c0002t0001g0049a0001c0002t0001g0077a0001c0007t0001g0116others(45): Show | 48 | HG00099.hp1 HG00280.hp2 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.365+6506G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66445053 | ||||||
| chr3:66445133
|
A | G | 5 | a0001c0023t0002g0060a0001c0023t0002g0068a0003c0010t0004g0229others(2): Show | 5 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.365+6426T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66445133 | ||||||
| chr3:66445171
|
T | A | 1 | a0004c0003t0002g0181 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.365+6388A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66445171 | ||||||
| chr3:66445274
|
G | GT | 12 | a0002c0001t0001g0158a0008c0006t0005g0200a0008c0006t0005g0215others(9): Show | 12 | HG01884.hp2 HG02622.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.365+6284dupA | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66445274 | ||||||
| chr3:66445331
|
T | C | 242 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(239): Show | 243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.365+6228A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66445331 | ||||||
| chr3:66445442
|
C | G | 1 | a0002c0001t0001g0142 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.365+6117G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66445442 | ||||||
| chr3:66445548
|
A | G | 3 | a0011c0016t0013g0204a0011c0016t0013g0205a0011c0016t0013g0206 | 3 | HG02486.hp2 HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.365+6011T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66445548 | ||||||
| chr3:66445774
|
G | A | 1 | a0003c0005t0003g0241 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.365+5785C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66445774 | ||||||
| chr3:66445803
|
A | G | 10 | a0001c0002t0001g0111a0001c0007t0002g0080a0001c0007t0002g0100others(7): Show | 10 | HG01261.hp1 HG01433.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.365+5756T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66445803 | ||||||
| chr3:66445961
|
A | G | 3 | a0011c0016t0013g0204a0011c0016t0013g0205a0011c0016t0013g0206 | 3 | HG02486.hp2 HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.365+5598T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66445961 | ||||||
| chr3:66445988
|
T | C | 11 | a0008c0006t0005g0200a0008c0006t0005g0215a0008c0006t0005g0219others(8): Show | 11 | HG01884.hp2 HG02622.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.365+5571A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66445988 | ||||||
| chr3:66446168
|
C | T | 95 | a0001c0002t0001g0049a0001c0002t0001g0077a0001c0002t0001g0111others(92): Show | 95 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.365+5391G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66446168 | ||||||
| chr3:66446187
|
C | A | 1 | a0001c0002t0001g0136 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.365+5372G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66446187 | ||||||
| chr3:66446262
|
C | T | 1 | a0004c0003t0002g0105 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.365+5297G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66446262 | ||||||
| chr3:66446299
|
G | A | 1 | a0013c0020t0035g0208 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.365+5260C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66446299 | ||||||
| chr3:66446403
|
C | CT | 11 | a0001c0002t0001g0133a0002c0001t0001g0156a0002c0001t0001g0180others(8): Show | 11 | HG00621.hp2 HG01928.hp1 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.365+5155dupA | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66446403 | ||||||
| chr3:66446403
|
CT | C | 15 | a0001c0002t0001g0111a0001c0007t0002g0080a0001c0007t0002g0100others(12): Show | 15 | HG01261.hp1 HG01433.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.365+5155delA | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66446403 | ||||||
| chr3:66446469
|
G | A | 3 | a0009c0013t0001g0041a0009c0013t0002g0042a0009c0013t0002g0044 | 3 | NA18991.hp2 NA19000.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.365+5090C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66446469 | ||||||
| chr3:66446537
|
C | T | 1 | a0003c0012t0018g0008 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.365+5022G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66446537 | ||||||
| chr3:66446751
|
C | T | 1 | a0001c0002t0001g0077 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.365+4808G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66446751 | ||||||
| chr3:66446851
|
CA | C | 67 | a0001c0002t0001g0051a0001c0002t0001g0146a0002c0001t0001g0047others(64): Show | 67 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.365+4707delT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66446851 | ||||||
| chr3:66446863
|
A | T | 1 | a0008c0006t0009g0014 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.365+4696T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66446863 | ||||||
| chr3:66446945
|
G | C | 2 | a0001c0002t0001g0070a0001c0002t0001g0071 | 2 | HG01167.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.365+4614C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66446945 | ||||||
| chr3:66447029
|
A | T | 1 | a0013c0020t0035g0208 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.365+4530T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66447029 | ||||||
| chr3:66447069
|
T | C | 10 | a0001c0002t0001g0111a0001c0007t0002g0080a0001c0007t0002g0100others(7): Show | 10 | HG01261.hp1 HG01433.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.365+4490A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66447069 | ||||||
| chr3:66447071
|
A | T | 1 | a0013c0020t0035g0208 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.365+4488T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66447071 | ||||||
| chr3:66447139
|
A | T | 238 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(235): Show | 239 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.365+4420T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66447139 | ||||||
| chr3:66447177
|
T | C | 3 | a0001c0014t0011g0058a0001c0014t0011g0117a0001c0014t0028g0118 | 3 | NA18939.hp2 NA18949.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.365+4382A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66447177 | ||||||
| chr3:66447273
|
C | G | 1 | a0008c0006t0009g0014 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.365+4286G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66447273 | ||||||
| chr3:66447290
|
T | C | 66 | a0001c0002t0001g0053a0001c0002t0001g0056a0001c0002t0001g0061others(63): Show | 67 | HG00099.hp2 HG00609.hp1 HG00673.hp1 others(64): Show |
intron_variant | MODIFIER | c.365+4269A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66447290 | ||||||
| chr3:66447353
|
C | T | 1 | a0003c0010t0004g0201 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.365+4206G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66447353 | ||||||
| chr3:66447718
|
C | T | 12 | a0006c0009t0004g0224a0006c0009t0004g0225a0006c0009t0004g0226others(9): Show | 12 | HG00735.hp1 HG01891.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.365+3841G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66447718 | ||||||
| chr3:66447741
|
G | A | 3 | a0011c0016t0013g0204a0011c0016t0013g0205a0011c0016t0013g0206 | 3 | HG02486.hp2 HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.365+3818C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66447741 | ||||||
| chr3:66447791
|
C | A | 226 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(223): Show | 227 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.365+3768G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66447791 | ||||||
| chr3:66447859
|
G | C | 2 | a0002c0001t0001g0158a0007c0008t0001g0016 | 2 | NA18975.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.365+3700C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66447859 | ||||||
| chr3:66448076
|
T | G | 9 | a0008c0006t0005g0200a0008c0006t0005g0215a0008c0006t0005g0219others(6): Show | 9 | HG01884.hp2 HG02647.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.365+3483A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66448076 | ||||||
| chr3:66448087
|
C | G | 8 | a0008c0006t0005g0200a0008c0006t0005g0215a0008c0006t0005g0219others(5): Show | 8 | HG01884.hp2 HG02647.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.365+3472G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66448087 | ||||||
| chr3:66448218
|
A | C | 254 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(251): Show | 255 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.365+3341T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66448218 | ||||||
| chr3:66448223
|
A | G | 1 | a0004c0003t0002g0161 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.365+3336T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66448223 | ||||||
| chr3:66448382
|
T | C | 4 | a0007c0008t0001g0038a0007c0008t0003g0252a0007c0008t0003g0256others(1): Show | 4 | HG02451.hp1 HG02723.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.365+3177A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66448382 | ||||||
| chr3:66448548
|
CT | C | 67 | a0001c0002t0001g0051a0001c0002t0001g0146a0002c0001t0001g0047others(64): Show | 67 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.365+3010delA | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66448548 | ||||||
| chr3:66448766
|
T | C | 3 | a0001c0014t0011g0058a0001c0014t0011g0117a0001c0014t0028g0118 | 3 | NA18939.hp2 NA18949.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.365+2793A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66448766 | ||||||
| chr3:66448794
|
C | T | 14 | a0001c0002t0001g0111a0001c0007t0002g0080a0001c0007t0002g0100others(11): Show | 14 | HG01261.hp1 HG01433.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.365+2765G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66448794 | ||||||
| chr3:66449044
|
G | A | 4 | a0007c0008t0001g0038a0007c0008t0003g0252a0007c0008t0003g0256others(1): Show | 4 | HG02451.hp1 HG02723.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.365+2515C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66449044 | ||||||
| chr3:66449315
|
C | T | 1 | a0013c0020t0035g0208 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.365+2244G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66449315 | ||||||
| chr3:66449396
|
A | G | 4 | a0007c0008t0001g0038a0007c0008t0003g0252a0007c0008t0003g0256others(1): Show | 4 | HG02451.hp1 HG02723.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.365+2163T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66449396 | ||||||
| chr3:66449435
|
C | A | 4 | a0007c0008t0001g0038a0007c0008t0003g0252a0007c0008t0003g0256others(1): Show | 4 | HG02451.hp1 HG02723.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.365+2124G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66449435 | ||||||
| chr3:66449467
|
A | G | 240 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(237): Show | 241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.365+2092T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66449467 | ||||||
| chr3:66449663
|
C | T | 9 | a0002c0001t0001g0171a0008c0006t0005g0200a0008c0006t0005g0215others(6): Show | 9 | HG00738.hp1 HG01884.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.365+1896G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66449663 | ||||||
| chr3:66449774
|
C | T | 240 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(237): Show | 241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.365+1785G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66449774 | ||||||
| chr3:66449784
|
A | G | 1 | a0021c0034t0019g0007 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.365+1775T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66449784 | ||||||
| chr3:66449821
|
A | G | 1 | a0006c0009t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.365+1738T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66449821 | ||||||
| chr3:66449959
|
C | T | 2 | a0001c0002t0001g0108a0002c0001t0001g0180 | 2 | HG02071.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.365+1600G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66449959 | ||||||
| chr3:66449977
|
T | C | 1 | a0013c0020t0035g0208 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.365+1582A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66449977 | ||||||
| chr3:66449996
|
C | A | 55 | a0001c0002t0001g0049a0001c0002t0001g0077a0001c0002t0001g0140others(52): Show | 55 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.365+1563G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66449996 | ||||||
| chr3:66450103
|
A | G | 1 | a0018c0028t0003g0259 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.365+1456T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66450103 | ||||||
| chr3:66450140
|
G | A | 10 | a0001c0002t0001g0111a0001c0007t0002g0080a0001c0007t0002g0100others(7): Show | 10 | HG01261.hp1 HG01433.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.365+1419C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66450140 | ||||||
| chr3:66450321
|
T | C | 10 | a0001c0002t0001g0111a0001c0007t0002g0080a0001c0007t0002g0100others(7): Show | 10 | HG01261.hp1 HG01433.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.365+1238A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66450321 | ||||||
| chr3:66450322
|
C | G | 1 | a0010c0011t0024g0064 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.365+1237G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66450322 | ||||||
| chr3:66450600
|
C | T | 2 | a0001c0002t0001g0071a0008c0006t0009g0014 | 2 | HG02622.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.365+959G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66450600 | ||||||
| chr3:66450671
|
G | C | 1 | a0013c0020t0029g0029 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.365+888C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66450671 | ||||||
| chr3:66450715
|
T | TTA | 2 | a0003c0012t0018g0008a0007c0008t0003g0237 | 2 | HG02976.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.365+842_365+843dup others(2): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66450715 | ||||||
| chr3:66450923
|
T | C | 12 | a0006c0009t0004g0224a0006c0009t0004g0225a0006c0009t0004g0226others(9): Show | 12 | HG00735.hp1 HG01891.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.365+636A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66450923 | ||||||
| chr3:66451178
|
C | T | 12 | a0006c0009t0004g0224a0006c0009t0004g0225a0006c0009t0004g0226others(9): Show | 12 | HG00735.hp1 HG01891.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.365+381G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66451178 | ||||||
| chr3:66451213
|
T | C | 1 | a0018c0028t0003g0259 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.365+346A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66451213 | ||||||
| chr3:66451298
|
C | T | 1 | a0004c0003t0002g0193 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.365+261G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66451298 | ||||||
| chr3:66451309
|
TA | T | 56 | a0001c0002t0001g0049a0001c0002t0001g0077a0001c0002t0001g0093others(53): Show | 56 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.365+249delT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66451309 | ||||||
| chr3:66451371
|
C | T | 1 | a0009c0013t0002g0024 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.365+188G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66451371 | ||||||
| chr3:66451487
|
C | A | 1 | a0013c0020t0035g0208 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.365+72G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66451487 | ||||||
| chr3:66451490
|
G | T | 1 | a0013c0020t0035g0208 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.365+69C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 3/18 | chr3 | 66451490 | ||||||
| chr3:66451670
|
T | C | 1 | a0006c0009t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.291-37A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66451670 | ||||||
| chr3:66451810
|
A | G | 185 | a0001c0002t0001g0051a0001c0002t0001g0053a0001c0002t0001g0056others(182): Show | 186 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(183): Show |
intron_variant | MODIFIER | c.291-177T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66451810 | ||||||
| chr3:66451827
|
C | G | 11 | a0001c0002t0001g0198a0003c0012t0014g0233a0003c0012t0014g0236others(8): Show | 11 | HG01099.hp1 HG01123.hp1 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.291-194G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66451827 | ||||||
| chr3:66451989
|
C | G | 1 | a0006c0009t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.291-356G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66451989 | ||||||
| chr3:66452166
|
T | TC | 10 | a0001c0002t0001g0111a0001c0007t0002g0080a0001c0007t0002g0100others(7): Show | 10 | HG01261.hp1 HG01433.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.291-534dupG | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66452166 | ||||||
| chr3:66452322
|
T | G | 3 | a0001c0014t0011g0058a0001c0014t0011g0117a0001c0014t0028g0118 | 3 | NA18939.hp2 NA18949.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.291-689A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66452322 | ||||||
| chr3:66452405
|
G | T | 4 | a0003c0005t0001g0028a0005c0004t0006g0220a0005c0004t0006g0221others(1): Show | 4 | HG02630.hp2 HG03098.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.291-772C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66452405 | ||||||
| chr3:66452507
|
C | G | 1 | a0014c0042t0010g0083 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.291-874G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66452507 | ||||||
| chr3:66452531
|
T | G | 12 | a0004c0003t0038g0262a0008c0006t0005g0200a0008c0006t0005g0215others(9): Show | 12 | HG01884.hp2 HG02486.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.291-898A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66452531 | ||||||
| chr3:66452551
|
G | A | 1 | a0005c0004t0001g0019 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.291-918C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66452551 | ||||||
| chr3:66452557
|
A | C | 69 | a0001c0002t0001g0053a0001c0002t0001g0056a0001c0002t0001g0061others(66): Show | 70 | HG00099.hp2 HG00609.hp1 HG00673.hp1 others(67): Show |
intron_variant | MODIFIER | c.291-924T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66452557 | ||||||
| chr3:66452783
|
T | C | 21 | a0005c0004t0001g0019a0006c0009t0004g0224a0006c0009t0004g0225others(18): Show | 21 | HG00544.hp1 HG00609.hp2 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.291-1150A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66452783 | ||||||
| chr3:66452872
|
T | G | 1 | a0018c0028t0003g0259 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.291-1239A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66452872 | ||||||
| chr3:66452942
|
C | T | 1 | a0001c0002t0001g0093 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.291-1309G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66452942 | ||||||
| chr3:66453198
|
G | A | 1 | a0021c0034t0019g0007 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.291-1565C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66453198 | ||||||
| chr3:66453234
|
T | C | 21 | a0005c0004t0001g0019a0006c0009t0004g0224a0006c0009t0004g0225others(18): Show | 21 | HG00544.hp1 HG00609.hp2 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.291-1601A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66453234 | ||||||
| chr3:66453510
|
C | G | 1 | a0001c0002t0001g0074 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.291-1877G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66453510 | ||||||
| chr3:66453584
|
A | G | 233 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(230): Show | 234 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.291-1951T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66453584 | ||||||
| chr3:66453625
|
G | C | 9 | a0001c0002t0001g0066a0001c0002t0001g0084a0001c0002t0001g0086others(6): Show | 9 | HG01261.hp2 HG01433.hp2 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.291-1992C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66453625 | ||||||
| chr3:66453638
|
G | A | 3 | a0011c0016t0013g0204a0011c0016t0013g0205a0011c0016t0013g0206 | 3 | HG02486.hp2 HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.291-2005C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66453638 | ||||||
| chr3:66453640
|
C | T | 68 | a0001c0002t0001g0051a0001c0002t0001g0146a0001c0014t0011g0058others(65): Show | 68 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.291-2007G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66453640 | ||||||
| chr3:66453692
|
C | G | 15 | a0001c0002t0001g0111a0001c0007t0002g0080a0001c0007t0002g0100others(12): Show | 15 | HG01261.hp1 HG01433.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.291-2059G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66453692 | ||||||
| chr3:66453695
|
G | T | 1 | a0021c0034t0019g0007 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.291-2062C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66453695 | ||||||
| chr3:66453749
|
A | G | 1 | a0021c0034t0019g0007 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.291-2116T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66453749 | ||||||
| chr3:66453800
|
G | C | 1 | a0018c0028t0003g0259 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.291-2167C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66453800 | ||||||
| chr3:66453955
|
T | C | 5 | a0001c0023t0002g0060a0001c0023t0002g0068a0003c0010t0004g0229others(2): Show | 5 | HG02572.hp1 HG02622.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.291-2322A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66453955 | ||||||
| chr3:66454068
|
C | T | 12 | a0006c0009t0004g0224a0006c0009t0004g0225a0006c0009t0004g0226others(9): Show | 12 | HG00735.hp1 HG01891.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.291-2435G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66454068 | ||||||
| chr3:66454134
|
C | T | 1 | a0002c0001t0001g0152 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.291-2501G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66454134 | ||||||
| chr3:66454458
|
T | A | 1 | a0003c0012t0017g0004 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.291-2825A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66454458 | ||||||
| chr3:66454514
|
C | T | 1 | a0001c0014t0010g0186 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.291-2881G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66454514 | ||||||
| chr3:66454632
|
T | C | 1 | a0005c0004t0007g0017 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.291-2999A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66454632 | ||||||
| chr3:66454740
|
C | T | 4 | a0007c0008t0001g0038a0007c0008t0003g0252a0007c0008t0003g0256others(1): Show | 4 | HG02451.hp1 HG02723.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.291-3107G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66454740 | ||||||
| chr3:66454745
|
C | T | 1 | a0002c0001t0001g0048 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.291-3112G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66454745 | ||||||
| chr3:66454765
|
A | G | 1 | a0005c0004t0021g0006 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.291-3132T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66454765 | ||||||
| chr3:66454799
|
A | G | 1 | a0007c0008t0003g0213 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.291-3166T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66454799 | ||||||
| chr3:66454965
|
G | A | 1 | a0028c0049t0001g0067 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.291-3332C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66454965 | ||||||
| chr3:66454972
|
C | T | 15 | a0006c0009t0004g0224a0006c0009t0004g0225a0006c0009t0004g0226others(12): Show | 15 | HG00735.hp1 HG01891.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.291-3339G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66454972 | ||||||
| chr3:66454980
|
G | A | 1 | a0008c0006t0005g0243 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.291-3347C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66454980 | ||||||
| chr3:66455026
|
C | T | 1 | a0005c0004t0006g0238 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.291-3393G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66455026 | ||||||
| chr3:66455276
|
T | C | 12 | a0006c0009t0004g0224a0006c0009t0004g0225a0006c0009t0004g0226others(9): Show | 12 | HG00735.hp1 HG01891.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.291-3643A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66455276 | ||||||
| chr3:66455717
|
G | C | 1 | a0002c0041t0001g0114 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.291-4084C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66455717 | ||||||
| chr3:66455779
|
T | C | 1 | a0005c0004t0001g0019 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.291-4146A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66455779 | ||||||
| chr3:66455820
|
C | T | 3 | a0011c0016t0013g0204a0011c0016t0013g0205a0011c0016t0013g0206 | 3 | HG02486.hp2 HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.291-4187G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66455820 | ||||||
| chr3:66455833
|
C | T | 2 | a0001c0002t0001g0198a0005c0004t0007g0017 | 2 | NA18974.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.291-4200G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66455833 | ||||||
| chr3:66455958
|
T | C | 134 | a0001c0002t0001g0049a0001c0002t0001g0053a0001c0002t0001g0056others(131): Show | 135 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.291-4325A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66455958 | ||||||
| chr3:66456111
|
T | C | 3 | a0006c0009t0004g0246a0008c0006t0009g0011a0008c0006t0009g0012 | 3 | HG02559.hp2 NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.291-4478A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66456111 | ||||||
| chr3:66456223
|
G | C | 1 | a0006c0009t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.291-4590C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66456223 | ||||||
| chr3:66456354
|
G | A | 1 | a0001c0007t0001g0116 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.291-4721C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66456354 | ||||||
| chr3:66456450
|
G | C | 68 | a0001c0002t0001g0051a0001c0002t0001g0146a0002c0001t0001g0047others(65): Show | 68 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.291-4817C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66456450 | ||||||
| chr3:66456537
|
C | T | 235 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(232): Show | 236 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.291-4904G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66456537 | ||||||
| chr3:66456572
|
T | TA | 58 | a0001c0002t0001g0049a0001c0002t0001g0077a0001c0002t0001g0094others(55): Show | 58 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.291-4940dupT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66456572 | ||||||
| chr3:66456572
|
TA | T | 69 | a0001c0002t0001g0051a0001c0002t0001g0053a0001c0002t0001g0071others(66): Show | 69 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.291-4940delT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66456572 | ||||||
| chr3:66456578
|
A | AG | 9 | a0001c0002t0001g0111a0001c0007t0002g0080a0001c0007t0002g0100others(6): Show | 9 | HG01261.hp1 HG01433.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.291-4946_291-4945i others(3): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66456578 | ||||||
| chr3:66456729
|
T | C | 2 | a0002c0001t0001g0085a0002c0001t0001g0087 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.291-5096A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66456729 | ||||||
| chr3:66456745
|
T | C | 3 | a0011c0016t0013g0204a0011c0016t0013g0205a0011c0016t0013g0206 | 3 | HG02486.hp2 HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.291-5112A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66456745 | ||||||
| chr3:66456859
|
T | G | 1 | a0014c0042t0010g0083 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.291-5226A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66456859 | ||||||
| chr3:66456998
|
G | A | 4 | a0003c0005t0001g0028a0005c0004t0006g0220a0005c0004t0006g0221others(1): Show | 4 | HG02630.hp2 HG03098.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.291-5365C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66456998 | ||||||
| chr3:66457018
|
A | G | 131 | a0001c0002t0001g0049a0001c0002t0001g0053a0001c0002t0001g0056others(128): Show | 132 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.291-5385T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66457018 | ||||||
| chr3:66457020
|
G | A | 63 | a0001c0002t0001g0053a0001c0002t0001g0056a0001c0002t0001g0061others(60): Show | 64 | HG00099.hp2 HG00609.hp1 HG00673.hp1 others(61): Show |
intron_variant | MODIFIER | c.291-5387C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66457020 | ||||||
| chr3:66457158
|
A | G | 3 | a0009c0015t0002g0032a0009c0015t0002g0033a0009c0015t0002g0034 | 3 | HG01891.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.290+5280T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66457158 | ||||||
| chr3:66457167
|
T | C | 9 | a0001c0002t0001g0111a0001c0007t0002g0080a0001c0007t0002g0100others(6): Show | 9 | HG01261.hp1 HG01433.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.290+5271A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66457167 | ||||||
| chr3:66457174
|
A | G | 262 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(259): Show | 263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.290+5264T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66457174 | ||||||
| chr3:66457340
|
T | C | 1 | a0002c0001t0001g0155 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.290+5098A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66457340 | ||||||
| chr3:66457525
|
C | A | 4 | a0007c0008t0001g0038a0007c0008t0003g0252a0007c0008t0003g0256others(1): Show | 4 | HG02451.hp1 HG02723.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.290+4913G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66457525 | ||||||
| chr3:66457566
|
T | C | 22 | a0001c0002t0001g0140a0005c0004t0001g0019a0006c0009t0004g0224others(19): Show | 22 | HG00544.hp1 HG00609.hp2 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.290+4872A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66457566 | ||||||
| chr3:66457580
|
G | A | 1 | a0007c0033t0001g0027 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.290+4858C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66457580 | ||||||
| chr3:66457635
|
G | T | 1 | a0013c0020t0035g0208 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.290+4803C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66457635 | ||||||
| chr3:66457658
|
A | C | 4 | a0001c0023t0002g0060a0001c0023t0002g0068a0003c0010t0004g0229others(1): Show | 4 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.290+4780T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66457658 | ||||||
| chr3:66457685
|
T | C | 4 | a0003c0005t0001g0028a0005c0004t0006g0220a0005c0004t0006g0221others(1): Show | 4 | HG02630.hp2 HG03098.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.290+4753A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66457685 | ||||||
| chr3:66457708
|
G | A | 62 | a0001c0002t0001g0053a0001c0002t0001g0056a0001c0002t0001g0061others(59): Show | 63 | HG00099.hp2 HG00609.hp1 HG00673.hp1 others(60): Show |
intron_variant | MODIFIER | c.290+4730C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66457708 | ||||||
| chr3:66458219
|
G | A | 1 | a0030c0046t0010g0184 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.290+4219C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66458219 | ||||||
| chr3:66458272
|
T | C | 1 | a0008c0006t0005g0230 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.290+4166A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66458272 | ||||||
| chr3:66458339
|
C | A | 1 | a0021c0034t0019g0007 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.290+4099G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66458339 | ||||||
| chr3:66458381
|
AGAAAATG others(17): Show |
A | 4 | a0007c0008t0001g0038a0007c0008t0003g0252a0007c0008t0003g0256others(1): Show | 4 | HG02451.hp1 HG02723.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.290+4033_290+4056d others(26): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66458381 | ||||||
| chr3:66458421
|
G | T | 1 | a0006c0009t0002g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.290+4017C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66458421 | ||||||
| chr3:66458520
|
G | A | 3 | a0001c0014t0011g0058a0001c0014t0011g0117a0001c0014t0028g0118 | 3 | NA18939.hp2 NA18949.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.290+3918C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66458520 | ||||||
| chr3:66458632
|
G | A | 4 | a0007c0008t0001g0038a0007c0008t0003g0252a0007c0008t0003g0256others(1): Show | 4 | HG02451.hp1 HG02723.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.290+3806C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66458632 | ||||||
| chr3:66458729
|
A | G | 3 | a0011c0016t0013g0204a0011c0016t0013g0205a0011c0016t0013g0206 | 3 | HG02486.hp2 HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.290+3709T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66458729 | ||||||
| chr3:66458833
|
A | G | 1 | a0013c0020t0035g0208 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.290+3605T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66458833 | ||||||
| chr3:66458909
|
T | C | 242 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(239): Show | 243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.290+3529A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66458909 | ||||||
| chr3:66458931
|
C | G | 68 | a0001c0002t0001g0051a0001c0002t0001g0146a0002c0001t0001g0047others(65): Show | 68 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.290+3507G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66458931 | ||||||
| chr3:66458987
|
C | A | 1 | a0004c0003t0002g0101 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.290+3451G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66458987 | ||||||
| chr3:66459014
|
C | CA | 151 | a0001c0002t0001g0051a0001c0002t0001g0053a0001c0002t0001g0056others(148): Show | 151 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(148): Show |
intron_variant | MODIFIER | c.290+3423dupT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66459014 | ||||||
| chr3:66459014
|
C | CAA | 4 | a0003c0005t0003g0001a0003c0005t0003g0209a0003c0005t0003g0211others(1): Show | 5 | NA18966.hp2 NA18986.hp1 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.290+3422_290+3423d others(4): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66459014 | ||||||
| chr3:66459160
|
C | A | 3 | a0009c0013t0001g0041a0009c0013t0002g0042a0009c0013t0002g0044 | 3 | NA18991.hp2 NA19000.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.290+3278G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66459160 | ||||||
| chr3:66459444
|
G | C | 172 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(169): Show | 173 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.290+2994C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66459444 | ||||||
| chr3:66459628
|
T | C | 4 | a0007c0008t0003g0252a0007c0008t0003g0256a0011c0030t0027g0021others(1): Show | 4 | HG02145.hp1 HG02723.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.290+2810A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66459628 | ||||||
| chr3:66459715
|
A | G | 6 | a0001c0007t0002g0194a0002c0001t0001g0059a0003c0012t0001g0040others(3): Show | 6 | HG01255.hp1 HG02165.hp1 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.290+2723T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66459715 | ||||||
| chr3:66459950
|
C | G | 2 | a0011c0030t0027g0021a0022c0032t0007g0046 | 2 | HG02896.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.290+2488G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66459950 | ||||||
| chr3:66460071
|
T | C | 6 | a0001c0007t0002g0194a0003c0012t0001g0040a0007c0008t0025g0043others(3): Show | 6 | HG01255.hp1 HG02165.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.290+2367A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66460071 | ||||||
| chr3:66460074
|
C | T | 1 | a0004c0003t0002g0101 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.290+2364G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66460074 | ||||||
| chr3:66460075
|
G | A | 6 | a0001c0007t0002g0194a0003c0012t0001g0040a0007c0008t0025g0043others(3): Show | 6 | HG01255.hp1 HG02165.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.290+2363C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66460075 | ||||||
| chr3:66460205
|
T | C | 36 | a0001c0002t0001g0133a0001c0007t0002g0125a0001c0007t0002g0126others(33): Show | 37 | HG01074.hp2 HG01099.hp1 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.290+2233A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66460205 | ||||||
| chr3:66460421
|
C | T | 231 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(228): Show | 232 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.290+2017G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66460421 | ||||||
| chr3:66460653
|
G | C | 6 | a0003c0010t0004g0201a0003c0010t0004g0257a0003c0010t0004g0258others(3): Show | 6 | HG02818.hp1 HG02818.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.290+1785C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66460653 | ||||||
| chr3:66460831
|
G | T | 3 | a0003c0012t0018g0008a0005c0004t0021g0006a0021c0034t0019g0007 | 3 | HG02886.hp2 HG02976.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.290+1607C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66460831 | ||||||
| chr3:66460868
|
G | A | 5 | a0003c0010t0004g0201a0003c0010t0004g0257a0003c0010t0004g0258others(2): Show | 5 | HG02818.hp1 HG02818.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.290+1570C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66460868 | ||||||
| chr3:66461261
|
C | T | 11 | a0003c0010t0004g0201a0003c0010t0004g0257a0003c0010t0004g0258others(8): Show | 11 | HG02630.hp2 HG02818.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.290+1177G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66461261 | ||||||
| chr3:66461356
|
C | T | 10 | a0001c0002t0001g0133a0001c0007t0002g0125a0001c0007t0002g0126others(7): Show | 10 | HG01074.hp2 HG01099.hp2 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.290+1082G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66461356 | ||||||
| chr3:66461666
|
T | G | 1 | a0003c0005t0001g0028 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.290+772A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66461666 | ||||||
| chr3:66461691
|
T | C | 3 | a0004c0003t0002g0081a0027c0050t0023g0082a0031c0047t0030g0162 | 3 | HG00099.hp1 HG01515.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.290+747A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66461691 | ||||||
| chr3:66461725
|
T | A | 1 | a0001c0002t0001g0104 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.290+713A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66461725 | ||||||
| chr3:66461822
|
T | A | 1 | a0001c0002t0001g0079 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.290+616A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66461822 | ||||||
| chr3:66461949
|
G | C | 255 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(252): Show | 256 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.290+489C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66461949 | ||||||
| chr3:66462001
|
T | C | 1 | a0005c0004t0008g0254 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.290+437A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66462001 | ||||||
| chr3:66462015
|
C | A | 5 | a0003c0012t0001g0040a0007c0008t0025g0043a0009c0013t0001g0041others(2): Show | 5 | HG02165.hp1 HG02523.hp1 NA18991.hp2 others(2): Show |
intron_variant | MODIFIER | c.290+423G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66462015 | ||||||
| chr3:66462020
|
A | C | 174 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(171): Show | 174 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.290+418T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66462020 | ||||||
| chr3:66462041
|
C | T | 5 | a0003c0012t0001g0040a0007c0008t0025g0043a0009c0013t0001g0041others(2): Show | 5 | HG02165.hp1 HG02523.hp1 NA18991.hp2 others(2): Show |
intron_variant | MODIFIER | c.290+397G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 2/18 | chr3 | 66462041 | ||||||
| chr3:66462810
|
G | GGTGTCCT others(19): Show |
1 | a0002c0048t0001g0099 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.219-302_219-301ins others(26): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66462810 | ||||||
| chr3:66462819
|
G | A | 7 | a0001c0023t0002g0060a0001c0023t0002g0068a0004c0003t0002g0088others(4): Show | 7 | HG02280.hp1 HG02486.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.219-310C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66462819 | ||||||
| chr3:66463012
|
T | C | 9 | a0001c0002t0001g0178a0001c0014t0010g0186a0002c0001t0001g0171others(6): Show | 9 | HG00738.hp1 HG01433.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.219-503A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66463012 | ||||||
| chr3:66463416
|
T | G | 4 | a0003c0012t0018g0008a0003c0036t0034g0203a0005c0004t0021g0006others(1): Show | 4 | HG02572.hp1 HG02886.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.219-907A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66463416 | ||||||
| chr3:66463523
|
G | T | 188 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(185): Show | 188 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.219-1014C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66463523 | ||||||
| chr3:66463650
|
C | T | 4 | a0003c0012t0014g0233a0003c0012t0014g0236a0006c0009t0004g0232others(1): Show | 4 | HG02055.hp1 HG02970.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.219-1141G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66463650 | ||||||
| chr3:66463770
|
T | C | 1 | a0002c0001t0001g0109 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.219-1261A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66463770 | ||||||
| chr3:66463876
|
A | T | 3 | a0005c0004t0006g0238a0005c0004t0006g0239a0005c0004t0006g0240 | 3 | HG01099.hp1 HG01358.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.219-1367T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66463876 | ||||||
| chr3:66463975
|
G | A | 1 | a0003c0005t0001g0039 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.219-1466C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66463975 | ||||||
| chr3:66464036
|
T | C | 2 | a0007c0033t0001g0027a0009c0013t0002g0024 | 2 | HG01256.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.219-1527A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66464036 | ||||||
| chr3:66464043
|
G | T | 45 | a0001c0002t0001g0133a0001c0007t0002g0125a0001c0007t0002g0126others(42): Show | 46 | HG01074.hp2 HG01099.hp1 HG01099.hp2 others(43): Show |
intron_variant | MODIFIER | c.219-1534C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66464043 | ||||||
| chr3:66464213
|
C | T | 170 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(167): Show | 170 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.219-1704G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66464213 | ||||||
| chr3:66464233
|
T | C | 2 | a0001c0002t0001g0122a0001c0007t0001g0116 | 2 | HG00280.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.219-1724A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66464233 | ||||||
| chr3:66464505
|
T | TA | 218 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(215): Show | 219 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.219-1997dupT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66464505 | ||||||
| chr3:66464505
|
T | TAA | 15 | a0001c0002t0001g0178a0001c0007t0002g0194a0002c0001t0001g0124others(12): Show | 15 | HG01255.hp1 HG01884.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.219-1998_219-1997d others(4): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66464505 | ||||||
| chr3:66464567
|
C | T | 7 | a0001c0023t0002g0060a0001c0023t0002g0068a0004c0003t0002g0088others(4): Show | 7 | HG02280.hp1 HG02486.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.219-2058G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66464567 | ||||||
| chr3:66464648
|
T | C | 6 | a0001c0007t0002g0194a0003c0012t0001g0040a0007c0008t0025g0043others(3): Show | 6 | HG01255.hp1 HG02165.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.219-2139A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66464648 | ||||||
| chr3:66464657
|
G | C | 2 | a0003c0005t0001g0039a0007c0008t0001g0038 | 2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.219-2148C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66464657 | ||||||
| chr3:66464845
|
T | C | 16 | a0003c0010t0004g0201a0003c0010t0004g0257a0003c0010t0004g0258others(13): Show | 16 | HG02572.hp1 HG02630.hp2 HG02818.hp1 others(13): Show |
intron_variant | MODIFIER | c.219-2336A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66464845 | ||||||
| chr3:66465251
|
A | G | 2 | a0004c0003t0001g0151a0004c0003t0002g0057 | 2 | HG02698.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.219-2742T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66465251 | ||||||
| chr3:66465357
|
A | AT | 44 | a0001c0002t0001g0133a0001c0007t0002g0125a0001c0007t0002g0126others(41): Show | 45 | HG01074.hp2 HG01099.hp1 HG01099.hp2 others(42): Show |
intron_variant | MODIFIER | c.219-2849dupA | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66465357 | ||||||
| chr3:66465357
|
A | ATT | 7 | a0001c0007t0002g0132a0003c0005t0001g0028a0003c0005t0001g0039others(4): Show | 7 | HG01358.hp2 HG02451.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.219-2850_219-2849d others(4): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66465357 | ||||||
| chr3:66465357
|
AT | A | 142 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(139): Show | 142 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(139): Show |
intron_variant | MODIFIER | c.219-2849delA | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66465357 | ||||||
| chr3:66465357
|
ATT | A | 11 | a0001c0002t0001g0079a0001c0002t0031g0069a0001c0007t0001g0116others(8): Show | 11 | HG00099.hp2 HG00280.hp2 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.219-2850_219-2849d others(4): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66465357 | ||||||
| chr3:66465392
|
C | T | 4 | a0003c0012t0014g0233a0003c0012t0014g0236a0006c0009t0004g0232others(1): Show | 4 | HG02055.hp1 HG02970.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.219-2883G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66465392 | ||||||
| chr3:66465457
|
G | A | 41 | a0001c0002t0001g0133a0001c0007t0002g0125a0001c0007t0002g0126others(38): Show | 42 | HG01074.hp2 HG01099.hp1 HG01099.hp2 others(39): Show |
intron_variant | MODIFIER | c.219-2948C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66465457 | ||||||
| chr3:66465605
|
A | T | 9 | a0001c0007t0002g0194a0003c0012t0001g0040a0007c0008t0025g0043others(6): Show | 9 | HG01255.hp1 HG02165.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.219-3096T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66465605 | ||||||
| chr3:66465683
|
A | C | 40 | a0001c0002t0001g0133a0001c0007t0002g0125a0001c0007t0002g0126others(37): Show | 41 | HG01074.hp2 HG01099.hp1 HG01099.hp2 others(38): Show |
intron_variant | MODIFIER | c.219-3174T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66465683 | ||||||
| chr3:66465790
|
C | T | 7 | a0002c0001t0001g0137a0002c0001t0001g0170a0002c0001t0015g0002others(4): Show | 7 | HG01069.hp2 HG02165.hp2 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.219-3281G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66465790 | ||||||
| chr3:66466021
|
T | C | 15 | a0003c0010t0004g0201a0003c0010t0004g0257a0003c0010t0004g0258others(12): Show | 15 | HG02572.hp1 HG02630.hp2 HG02818.hp1 others(12): Show |
intron_variant | MODIFIER | c.219-3512A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66466021 | ||||||
| chr3:66466212
|
T | C | 1 | a0004c0053t0002g0197 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.219-3703A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66466212 | ||||||
| chr3:66466214
|
A | G | 1 | a0004c0053t0002g0197 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.219-3705T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66466214 | ||||||
| chr3:66466215
|
G | A | 1 | a0007c0008t0003g0252 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.219-3706C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66466215 | ||||||
| chr3:66466310
|
T | C | 2 | a0003c0005t0001g0039a0007c0008t0001g0038 | 2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.219-3801A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66466310 | ||||||
| chr3:66466380
|
T | C | 1 | a0009c0013t0002g0024 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.219-3871A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66466380 | ||||||
| chr3:66466625
|
A | G | 1 | a0009c0013t0002g0024 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.219-4116T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66466625 | ||||||
| chr3:66466740
|
T | C | 3 | a0011c0016t0013g0204a0011c0016t0013g0205a0011c0016t0013g0206 | 3 | HG02486.hp2 HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.219-4231A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66466740 | ||||||
| chr3:66466934
|
T | C | 2 | a0004c0003t0001g0151a0004c0003t0002g0057 | 2 | HG02698.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.219-4425A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66466934 | ||||||
| chr3:66467058
|
C | G | 13 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0002t0001g0094others(10): Show | 13 | HG00544.hp1 HG00609.hp2 NA18943.hp1 others(10): Show |
intron_variant | MODIFIER | c.219-4549G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66467058 | ||||||
| chr3:66467206
|
G | A | 1 | a0005c0004t0007g0017 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.219-4697C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66467206 | ||||||
| chr3:66467246
|
C | T | 229 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(226): Show | 230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.219-4737G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66467246 | ||||||
| chr3:66467357
|
A | AT | 19 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0002t0001g0094others(16): Show | 19 | HG01099.hp1 HG01192.hp2 HG01358.hp1 others(16): Show |
intron_variant | MODIFIER | c.219-4849dupA | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66467357 | ||||||
| chr3:66467357
|
AT | A | 136 | a0001c0002t0001g0051a0001c0002t0001g0053a0001c0002t0001g0056others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.219-4849delA | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66467357 | ||||||
| chr3:66467357
|
ATT | A | 5 | a0004c0003t0038g0262a0007c0033t0001g0027a0008c0006t0009g0014others(2): Show | 5 | HG01256.hp2 HG02486.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.219-4850_219-4849d others(4): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66467357 | ||||||
| chr3:66467430
|
G | A | 8 | a0003c0005t0001g0028a0003c0012t0018g0008a0003c0036t0034g0203others(5): Show | 8 | HG01256.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.219-4921C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66467430 | ||||||
| chr3:66467446
|
G | A | 1 | a0003c0005t0001g0037 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.219-4937C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66467446 | ||||||
| chr3:66467563
|
G | A | 1 | a0001c0007t0002g0080 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.219-5054C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66467563 | ||||||
| chr3:66467572
|
A | G | 11 | a0003c0010t0004g0201a0003c0010t0004g0257a0003c0010t0004g0258others(8): Show | 11 | HG02630.hp2 HG02818.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.219-5063T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66467572 | ||||||
| chr3:66467582
|
T | C | 11 | a0003c0010t0004g0201a0003c0010t0004g0257a0003c0010t0004g0258others(8): Show | 11 | HG02630.hp2 HG02818.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.219-5073A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66467582 | ||||||
| chr3:66467597
|
G | A | 6 | a0001c0007t0002g0194a0003c0012t0001g0040a0007c0008t0025g0043others(3): Show | 6 | HG01255.hp1 HG02165.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.219-5088C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66467597 | ||||||
| chr3:66467611
|
T | G | 1 | a0004c0053t0002g0197 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.219-5102A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66467611 | ||||||
| chr3:66467615
|
C | A | 1 | a0004c0053t0002g0197 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.219-5106G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66467615 | ||||||
| chr3:66467643
|
G | A | 1 | a0001c0002t0001g0079 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.219-5134C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66467643 | ||||||
| chr3:66467652
|
C | T | 11 | a0003c0010t0004g0201a0003c0010t0004g0257a0003c0010t0004g0258others(8): Show | 11 | HG02630.hp2 HG02818.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.219-5143G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66467652 | ||||||
| chr3:66467719
|
T | C | 231 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(228): Show | 232 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.219-5210A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66467719 | ||||||
| chr3:66467744
|
A | G | 1 | a0018c0028t0003g0259 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.219-5235T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66467744 | ||||||
| chr3:66467896
|
A | G | 212 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(209): Show | 213 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.219-5387T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66467896 | ||||||
| chr3:66467959
|
T | C | 6 | a0001c0007t0002g0194a0003c0012t0001g0040a0007c0008t0025g0043others(3): Show | 6 | HG01255.hp1 HG02165.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.219-5450A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66467959 | ||||||
| chr3:66468014
|
T | G | 34 | a0001c0002t0001g0133a0001c0007t0002g0125a0001c0007t0002g0126others(31): Show | 35 | HG01074.hp2 HG01099.hp1 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.219-5505A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66468014 | ||||||
| chr3:66468114
|
T | C | 4 | a0003c0012t0018g0008a0003c0036t0034g0203a0005c0004t0021g0006others(1): Show | 4 | HG02572.hp1 HG02886.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.219-5605A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66468114 | ||||||
| chr3:66468129
|
A | G | 1 | a0001c0002t0001g0077 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.219-5620T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66468129 | ||||||
| chr3:66468137
|
A | T | 1 | a0018c0028t0003g0259 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.219-5628T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66468137 | ||||||
| chr3:66468193
|
T | C | 4 | a0006c0009t0004g0225a0006c0009t0004g0226a0008c0006t0005g0200others(1): Show | 4 | HG02970.hp1 HG03041.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.219-5684A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66468193 | ||||||
| chr3:66468253
|
G | A | 1 | a0008c0006t0009g0035 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.219-5744C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66468253 | ||||||
| chr3:66468256
|
A | G | 1 | a0003c0036t0034g0203 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.219-5747T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66468256 | ||||||
| chr3:66468294
|
T | C | 4 | a0003c0010t0004g0201a0003c0010t0004g0258a0003c0010t0004g0260others(1): Show | 4 | HG02818.hp1 HG02818.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.219-5785A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66468294 | ||||||
| chr3:66468348
|
G | A | 11 | a0003c0010t0004g0201a0003c0010t0004g0257a0003c0010t0004g0258others(8): Show | 11 | HG02630.hp2 HG02818.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.219-5839C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66468348 | ||||||
| chr3:66468402
|
T | C | 17 | a0003c0005t0001g0037a0003c0010t0002g0010a0003c0010t0004g0229others(14): Show | 17 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.219-5893A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66468402 | ||||||
| chr3:66468416
|
G | A | 2 | a0006c0009t0002g0045a0022c0032t0007g0046 | 2 | HG02896.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.219-5907C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66468416 | ||||||
| chr3:66468483
|
A | G | 3 | a0005c0004t0006g0220a0005c0004t0006g0221a0005c0004t0006g0222 | 3 | HG02630.hp2 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.219-5974T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66468483 | ||||||
| chr3:66468527
|
A | G | 4 | a0006c0009t0004g0225a0006c0009t0004g0226a0008c0006t0005g0200others(1): Show | 4 | HG02970.hp1 HG03041.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.219-6018T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66468527 | ||||||
| chr3:66468559
|
C | T | 2 | a0003c0005t0001g0039a0007c0008t0001g0038 | 2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.219-6050G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66468559 | ||||||
| chr3:66468993
|
G | C | 230 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(227): Show | 231 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.219-6484C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66468993 | ||||||
| chr3:66469385
|
G | A | 191 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(188): Show | 191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.219-6876C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66469385 | ||||||
| chr3:66469390
|
T | C | 15 | a0001c0002t0001g0053a0001c0002t0001g0056a0001c0002t0001g0061others(12): Show | 15 | HG00099.hp2 HG00609.hp1 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.219-6881A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66469390 | ||||||
| chr3:66469440
|
T | C | 2 | a0003c0005t0001g0039a0007c0008t0001g0038 | 2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.219-6931A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66469440 | ||||||
| chr3:66469600
|
C | A | 11 | a0003c0010t0004g0201a0003c0010t0004g0257a0003c0010t0004g0258others(8): Show | 11 | HG02630.hp2 HG02818.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.219-7091G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66469600 | ||||||
| chr3:66469702
|
C | G | 2 | a0003c0005t0001g0039a0007c0008t0001g0038 | 2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.219-7193G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66469702 | ||||||
| chr3:66469824
|
C | T | 4 | a0006c0009t0004g0246a0006c0019t0012g0244a0006c0019t0012g0245others(1): Show | 4 | HG01952.hp1 HG02280.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.219-7315G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66469824 | ||||||
| chr3:66469870
|
G | C | 6 | a0001c0007t0002g0194a0003c0012t0001g0040a0007c0008t0025g0043others(3): Show | 6 | HG01255.hp1 HG02165.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.219-7361C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66469870 | ||||||
| chr3:66469901
|
C | T | 6 | a0001c0007t0002g0194a0003c0012t0001g0040a0007c0008t0025g0043others(3): Show | 6 | HG01255.hp1 HG02165.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.219-7392G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66469901 | ||||||
| chr3:66469907
|
C | CA | 161 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(158): Show | 161 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.219-7399dupT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66469907 | ||||||
| chr3:66469907
|
C | CAA | 21 | a0001c0002t0001g0071a0001c0002t0001g0104a0001c0002t0001g0106others(18): Show | 21 | HG00735.hp1 HG01891.hp2 HG02559.hp2 others(18): Show |
intron_variant | MODIFIER | c.219-7400_219-7399d others(4): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66469907 | ||||||
| chr3:66469907
|
C | CAAA | 40 | a0001c0002t0001g0133a0001c0007t0002g0125a0001c0007t0002g0126others(37): Show | 41 | HG01074.hp2 HG01099.hp1 HG01099.hp2 others(38): Show |
intron_variant | MODIFIER | c.219-7401_219-7399d others(5): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66469907 | ||||||
| chr3:66470126
|
G | A | 3 | a0001c0002t0001g0070a0001c0002t0001g0071a0014c0042t0010g0083 | 3 | HG01167.hp2 HG03834.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.219-7617C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66470126 | ||||||
| chr3:66470382
|
A | C | 152 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(149): Show | 152 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.219-7873T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66470382 | ||||||
| chr3:66470582
|
G | T | 1 | a0005c0004t0001g0019 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.219-8073C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66470582 | ||||||
| chr3:66470662
|
A | G | 10 | a0001c0002t0001g0133a0001c0007t0002g0125a0001c0007t0002g0126others(7): Show | 10 | HG01074.hp2 HG01099.hp2 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.219-8153T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66470662 | ||||||
| chr3:66470675
|
A | C | 1 | a0002c0001t0001g0109 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.219-8166T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66470675 | ||||||
| chr3:66470823
|
T | C | 1 | a0002c0001t0032g0199 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.219-8314A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66470823 | ||||||
| chr3:66470946
|
C | A | 1 | a0009c0013t0002g0024 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.219-8437G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66470946 | ||||||
| chr3:66470978
|
C | A | 2 | a0003c0005t0001g0039a0007c0008t0001g0038 | 2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.219-8469G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66470978 | ||||||
| chr3:66471001
|
T | C | 1 | a0003c0005t0001g0026 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.219-8492A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66471001 | ||||||
| chr3:66471074
|
T | C | 2 | a0007c0033t0001g0027a0009c0013t0002g0024 | 2 | HG01256.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.219-8565A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66471074 | ||||||
| chr3:66471190
|
C | T | 67 | a0001c0002t0001g0063a0001c0002t0001g0108a0001c0002t0001g0111others(64): Show | 67 | HG00280.hp2 HG00558.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.219-8681G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66471190 | ||||||
| chr3:66471230
|
C | T | 15 | a0003c0010t0004g0201a0003c0010t0004g0257a0003c0010t0004g0258others(12): Show | 15 | HG02630.hp2 HG02818.hp1 HG02818.hp2 others(12): Show |
intron_variant | MODIFIER | c.219-8721G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66471230 | ||||||
| chr3:66471324
|
T | C | 17 | a0003c0005t0001g0037a0003c0010t0002g0010a0003c0010t0004g0229others(14): Show | 17 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.219-8815A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66471324 | ||||||
| chr3:66471378
|
CT | C | 153 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(150): Show | 153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.219-8870delA | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66471378 | ||||||
| chr3:66471387
|
C | T | 1 | a0004c0053t0002g0197 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.219-8878G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66471387 | ||||||
| chr3:66471447
|
G | C | 2 | a0006c0009t0002g0045a0022c0032t0007g0046 | 2 | HG02896.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.219-8938C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66471447 | ||||||
| chr3:66471995
|
G | A | 1 | a0008c0006t0009g0014 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.219-9486C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66471995 | ||||||
| chr3:66472103
|
G | A | 1 | a0002c0001t0001g0165 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.219-9594C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66472103 | ||||||
| chr3:66472171
|
G | C | 2 | a0005c0004t0021g0006a0021c0034t0019g0007 | 2 | HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.219-9662C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66472171 | ||||||
| chr3:66472209
|
C | T | 1 | a0018c0028t0003g0259 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.219-9700G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66472209 | ||||||
| chr3:66472235
|
C | T | 1 | a0002c0001t0001g0158 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.219-9726G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66472235 | ||||||
| chr3:66472303
|
C | CA | 13 | a0001c0007t0002g0125a0001c0007t0002g0128a0001c0007t0002g0129others(10): Show | 14 | HG01074.hp2 HG01123.hp1 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.219-9795dupT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66472303 | ||||||
| chr3:66472303
|
C | CAA | 8 | a0001c0002t0001g0133a0001c0007t0002g0126a0001c0007t0002g0130others(5): Show | 8 | HG01192.hp2 HG01358.hp2 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.219-9796_219-9795d others(4): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66472303 | ||||||
| chr3:66472303
|
C | CAAAA | 7 | a0006c0009t0004g0251a0007c0008t0003g0252a0007c0008t0003g0256others(4): Show | 7 | HG01884.hp2 HG02647.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.219-9798_219-9795d others(6): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66472303 | ||||||
| chr3:66472303
|
CAA | C | 7 | a0003c0005t0001g0028a0003c0012t0018g0008a0005c0004t0021g0006others(4): Show | 7 | HG02886.hp2 HG02970.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.219-9796_219-9795d others(4): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66472303 | ||||||
| chr3:66472303
|
CAAAA | C | 7 | a0001c0002t0001g0178a0002c0001t0001g0171a0002c0001t0001g0172others(4): Show | 7 | HG00738.hp1 HG02055.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.219-9798_219-9795d others(6): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66472303 | ||||||
| chr3:66472303
|
CAAAAA | C | 32 | a0001c0002t0001g0056a0001c0002t0001g0074a0001c0002t0001g0076others(29): Show | 32 | HG00558.hp1 HG00621.hp2 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.219-9799_219-9795d others(7): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66472303 | ||||||
| chr3:66472303
|
CAAAAAA | C | 148 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(145): Show | 148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.219-9800_219-9795d others(8): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66472303 | ||||||
| chr3:66472303
|
CAAAAAAA | C | 9 | a0001c0023t0002g0060a0002c0001t0001g0188a0005c0004t0001g0019others(6): Show | 9 | HG00544.hp1 HG02027.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.219-9801_219-9795d others(9): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66472303 | ||||||
| chr3:66472303
|
CAAAAAAA others(5): Show |
C | 3 | a0007c0033t0001g0027a0009c0013t0002g0024a0013c0020t0035g0208 | 3 | HG01256.hp2 HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.219-9806_219-9795d others(14): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66472303 | ||||||
| chr3:66472306
|
A | G | 1 | a0021c0034t0019g0007 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.219-9797T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66472306 | ||||||
| chr3:66472307
|
A | G | 1 | a0005c0004t0021g0006 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.219-9798T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66472307 | ||||||
| chr3:66472332
|
A | T | 25 | a0002c0001t0001g0188a0003c0005t0001g0026a0003c0005t0001g0039others(22): Show | 25 | HG00544.hp1 HG00609.hp2 HG02027.hp2 others(22): Show |
intron_variant | MODIFIER | c.219-9823T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66472332 | ||||||
| chr3:66472333
|
A | C | 1 | a0010c0011t0024g0064 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.219-9824T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66472333 | ||||||
| chr3:66472335
|
A | C | 1 | a0010c0011t0024g0064 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.219-9826T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66472335 | ||||||
| chr3:66472416
|
C | T | 3 | a0001c0002t0001g0104a0001c0007t0002g0100a0004c0003t0002g0097 | 3 | HG02735.hp2 HG02738.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.219-9907G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66472416 | ||||||
| chr3:66472439
|
C | T | 182 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.219-9930G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66472439 | ||||||
| chr3:66472676
|
C | T | 1 | a0003c0010t0004g0258 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.219-10167G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66472676 | ||||||
| chr3:66472747
|
T | C | 167 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(164): Show | 167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.219-10238A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66472747 | ||||||
| chr3:66472760
|
G | A | 1 | a0011c0030t0027g0021 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.219-10251C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66472760 | ||||||
| chr3:66472760
|
G | C | 1 | a0001c0002t0001g0178 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.219-10251C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66472760 | ||||||
| chr3:66472766
|
G | A | 196 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(193): Show | 196 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.219-10257C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66472766 | ||||||
| chr3:66472789
|
A | G | 4 | a0006c0009t0004g0246a0006c0019t0012g0244a0006c0019t0012g0245others(1): Show | 4 | HG01952.hp1 HG02280.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.219-10280T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66472789 | ||||||
| chr3:66472880
|
C | G | 2 | a0003c0005t0001g0039a0007c0008t0001g0038 | 2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.219-10371G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66472880 | ||||||
| chr3:66473022
|
C | T | 1 | a0004c0003t0002g0098 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.219-10513G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66473022 | ||||||
| chr3:66473039
|
T | C | 1 | a0003c0005t0001g0028 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.219-10530A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66473039 | ||||||
| chr3:66473269
|
A | C | 1 | a0009c0013t0002g0024 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.219-10760T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66473269 | ||||||
| chr3:66473509
|
T | C | 1 | a0003c0012t0001g0040 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.219-11000A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66473509 | ||||||
| chr3:66473538
|
C | T | 1 | a0004c0003t0002g0161 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.219-11029G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66473538 | ||||||
| chr3:66473657
|
T | C | 5 | a0003c0012t0001g0040a0007c0008t0025g0043a0009c0013t0001g0041others(2): Show | 5 | HG02165.hp1 HG02523.hp1 NA18991.hp2 others(2): Show |
intron_variant | MODIFIER | c.219-11148A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66473657 | ||||||
| chr3:66473681
|
G | A | 2 | a0003c0005t0001g0039a0007c0008t0001g0038 | 2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.219-11172C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66473681 | ||||||
| chr3:66473720
|
T | C | 1 | a0005c0004t0006g0202 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.219-11211A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66473720 | ||||||
| chr3:66473819
|
A | T | 225 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(222): Show | 226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.219-11310T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66473819 | ||||||
| chr3:66473846
|
G | C | 1 | a0004c0003t0002g0161 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.219-11337C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66473846 | ||||||
| chr3:66473989
|
A | G | 16 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0002t0001g0094others(13): Show | 16 | HG00544.hp1 HG00609.hp2 HG02965.hp2 others(13): Show |
intron_variant | MODIFIER | c.219-11480T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66473989 | ||||||
| chr3:66474181
|
T | C | 1 | a0004c0003t0026g0190 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.219-11672A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66474181 | ||||||
| chr3:66474293
|
C | T | 3 | a0011c0016t0013g0204a0011c0016t0013g0205a0011c0016t0013g0206 | 3 | HG02486.hp2 HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.219-11784G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66474293 | ||||||
| chr3:66474347
|
CT | C | 14 | a0001c0023t0002g0060a0003c0005t0001g0039a0003c0010t0004g0201others(11): Show | 14 | HG02451.hp1 HG02630.hp2 HG02809.hp1 others(11): Show |
intron_variant | MODIFIER | c.219-11839delA | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66474347 | ||||||
| chr3:66474347
|
CTT | C | 11 | a0002c0001t0001g0188a0003c0005t0001g0026a0005c0004t0001g0019others(8): Show | 11 | HG00544.hp1 HG00609.hp2 HG02965.hp2 others(8): Show |
intron_variant | MODIFIER | c.219-11840_219-1183 others(6): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66474347 | ||||||
| chr3:66474440
|
G | C | 2 | a0001c0002t0001g0075a0001c0002t0001g0076 | 2 | HG01192.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.219-11931C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66474440 | ||||||
| chr3:66474545
|
C | T | 1 | a0001c0007t0002g0100 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.219-12036G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66474545 | ||||||
| chr3:66474579
|
C | T | 5 | a0003c0012t0001g0040a0007c0008t0025g0043a0009c0013t0001g0041others(2): Show | 5 | HG02165.hp1 HG02523.hp1 NA18991.hp2 others(2): Show |
intron_variant | MODIFIER | c.219-12070G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66474579 | ||||||
| chr3:66474597
|
C | T | 3 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0002t0001g0094 | 3 | NA18943.hp1 NA18988.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.219-12088G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66474597 | ||||||
| chr3:66474598
|
G | A | 1 | a0008c0006t0005g0219 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.219-12089C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66474598 | ||||||
| chr3:66474760
|
C | T | 1 | a0003c0036t0034g0203 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.219-12251G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66474760 | ||||||
| chr3:66474816
|
G | C | 1 | a0003c0005t0003g0241 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.219-12307C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66474816 | ||||||
| chr3:66474874
|
T | C | 5 | a0003c0012t0001g0040a0007c0008t0025g0043a0009c0013t0001g0041others(2): Show | 5 | HG02165.hp1 HG02523.hp1 NA18991.hp2 others(2): Show |
intron_variant | MODIFIER | c.219-12365A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66474874 | ||||||
| chr3:66474878
|
T | C | 12 | a0001c0002t0001g0053a0001c0002t0001g0061a0001c0002t0001g0062others(9): Show | 12 | HG00099.hp2 HG00609.hp1 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.219-12369A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66474878 | ||||||
| chr3:66474969
|
G | A | 197 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(194): Show | 197 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.219-12460C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66474969 | ||||||
| chr3:66474999
|
G | A | 1 | a0003c0012t0018g0008 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.219-12490C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66474999 | ||||||
| chr3:66475001
|
G | A | 1 | a0003c0012t0018g0008 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.219-12492C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66475001 | ||||||
| chr3:66475055
|
C | T | 1 | a0001c0002t0001g0157 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.219-12546G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66475055 | ||||||
| chr3:66475099
|
T | C | 1 | a0018c0028t0003g0259 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.219-12590A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66475099 | ||||||
| chr3:66475274
|
T | A | 1 | a0003c0012t0018g0008 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.219-12765A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66475274 | ||||||
| chr3:66475389
|
A | C | 17 | a0001c0002t0001g0049a0001c0002t0001g0104a0001c0007t0002g0100others(14): Show | 17 | HG00544.hp2 HG02071.hp2 HG02300.hp2 others(14): Show |
intron_variant | MODIFIER | c.219-12880T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66475389 | ||||||
| chr3:66475476
|
A | T | 15 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0002t0001g0094others(12): Show | 15 | HG00544.hp1 HG00609.hp2 HG02965.hp2 others(12): Show |
intron_variant | MODIFIER | c.219-12967T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66475476 | ||||||
| chr3:66475539
|
T | C | 170 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(167): Show | 170 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.219-13030A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66475539 | ||||||
| chr3:66475587
|
G | A | 2 | a0003c0012t0018g0008a0008c0006t0005g0223 | 2 | HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.219-13078C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66475587 | ||||||
| chr3:66475595
|
G | A | 6 | a0001c0007t0002g0194a0003c0012t0001g0040a0007c0008t0025g0043others(3): Show | 6 | HG01255.hp1 HG02165.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.219-13086C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66475595 | ||||||
| chr3:66475697
|
G | A | 223 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(220): Show | 224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.219-13188C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66475697 | ||||||
| chr3:66475750
|
C | G | 2 | a0004c0003t0002g0088a0004c0003t0002g0089 | 2 | HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.219-13241G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66475750 | ||||||
| chr3:66475751
|
G | C | 1 | a0003c0012t0018g0008 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.219-13242C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66475751 | ||||||
| chr3:66475933
|
A | G | 6 | a0001c0007t0002g0194a0003c0012t0001g0040a0007c0008t0025g0043others(3): Show | 6 | HG01255.hp1 HG02165.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.219-13424T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66475933 | ||||||
| chr3:66475993
|
G | A | 1 | a0003c0005t0001g0028 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.219-13484C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66475993 | ||||||
| chr3:66476013
|
T | C | 2 | a0003c0005t0001g0039a0007c0008t0001g0038 | 2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.219-13504A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66476013 | ||||||
| chr3:66476155
|
T | C | 1 | a0001c0002t0001g0189 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.219-13646A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66476155 | ||||||
| chr3:66476178
|
G | A | 180 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(177): Show | 180 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.219-13669C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66476178 | ||||||
| chr3:66476981
|
G | C | 11 | a0003c0010t0004g0201a0003c0010t0004g0257a0003c0010t0004g0258others(8): Show | 11 | HG02630.hp2 HG02818.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.219-14472C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66476981 | ||||||
| chr3:66477234
|
GT | G | 210 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(207): Show | 210 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.219-14726delA | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66477234 | ||||||
| chr3:66477396
|
TG | T | 15 | a0003c0005t0003g0001a0003c0005t0003g0209a0003c0005t0003g0210others(12): Show | 16 | HG02040.hp2 HG02486.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.219-14888delC | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66477396 | ||||||
| chr3:66477856
|
A | T | 191 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(188): Show | 191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.219-15347T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66477856 | ||||||
| chr3:66477857
|
C | CA | 191 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(188): Show | 191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.219-15349_219-1534 others(5): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66477857 | ||||||
| chr3:66477858
|
T | A | 191 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(188): Show | 191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.219-15349A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66477858 | ||||||
| chr3:66477860
|
C | T | 191 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(188): Show | 191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.219-15351G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66477860 | ||||||
| chr3:66478032
|
G | A | 1 | a0008c0006t0009g0014 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.219-15523C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66478032 | ||||||
| chr3:66478159
|
C | T | 24 | a0003c0005t0001g0028a0003c0005t0001g0039a0003c0010t0004g0201others(21): Show | 24 | HG01256.hp2 HG02165.hp1 HG02451.hp1 others(21): Show |
intron_variant | MODIFIER | c.219-15650G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66478159 | ||||||
| chr3:66478160
|
G | A | 1 | a0001c0002t0001g0178 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.219-15651C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66478160 | ||||||
| chr3:66478279
|
A | G | 1 | a0003c0012t0018g0008 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.219-15770T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66478279 | ||||||
| chr3:66478320
|
T | C | 2 | a0007c0033t0001g0027a0009c0013t0002g0024 | 2 | HG01256.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.219-15811A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66478320 | ||||||
| chr3:66478350
|
G | A | 1 | a0004c0003t0002g0105 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.219-15841C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66478350 | ||||||
| chr3:66478378
|
G | A | 2 | a0003c0005t0001g0039a0007c0008t0001g0038 | 2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.219-15869C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66478378 | ||||||
| chr3:66478501
|
C | A | 1 | a0003c0005t0001g0028 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.219-15992G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66478501 | ||||||
| chr3:66478773
|
T | C | 3 | a0003c0012t0018g0008a0005c0004t0021g0006a0021c0034t0019g0007 | 3 | HG02886.hp2 HG02976.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.219-16264A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66478773 | ||||||
| chr3:66479101
|
C | T | 2 | a0007c0033t0001g0027a0009c0013t0002g0024 | 2 | HG01256.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.219-16592G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66479101 | ||||||
| chr3:66479207
|
C | T | 15 | a0003c0005t0003g0001a0003c0005t0003g0209a0003c0005t0003g0210others(12): Show | 16 | HG02040.hp2 HG02486.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.219-16698G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66479207 | ||||||
| chr3:66479263
|
A | G | 4 | a0003c0012t0014g0233a0003c0012t0014g0236a0006c0009t0004g0232others(1): Show | 4 | HG02055.hp1 HG02970.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.219-16754T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66479263 | ||||||
| chr3:66479308
|
T | C | 2 | a0003c0005t0001g0039a0007c0008t0001g0038 | 2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.219-16799A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66479308 | ||||||
| chr3:66479310
|
C | G | 5 | a0003c0010t0004g0201a0003c0010t0004g0257a0003c0010t0004g0258others(2): Show | 5 | HG02818.hp1 HG02818.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.219-16801G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66479310 | ||||||
| chr3:66479342
|
G | C | 1 | a0002c0001t0001g0156 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.219-16833C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66479342 | ||||||
| chr3:66479716
|
G | A | 13 | a0003c0005t0001g0039a0003c0010t0004g0201a0003c0010t0004g0257others(10): Show | 13 | HG02451.hp1 HG02630.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.219-17207C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66479716 | ||||||
| chr3:66479849
|
T | A | 193 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(190): Show | 193 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.219-17340A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66479849 | ||||||
| chr3:66479859
|
G | A | 11 | a0003c0010t0004g0201a0003c0010t0004g0257a0003c0010t0004g0258others(8): Show | 11 | HG02630.hp2 HG02818.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.219-17350C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66479859 | ||||||
| chr3:66479880
|
A | G | 154 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.219-17371T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66479880 | ||||||
| chr3:66480010
|
A | G | 20 | a0003c0005t0001g0037a0003c0010t0002g0010a0003c0010t0004g0229others(17): Show | 20 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.219-17501T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66480010 | ||||||
| chr3:66480040
|
C | T | 2 | a0003c0005t0001g0039a0007c0008t0001g0038 | 2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.219-17531G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66480040 | ||||||
| chr3:66480089
|
A | T | 167 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(164): Show | 167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.219-17580T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66480089 | ||||||
| chr3:66480447
|
T | C | 19 | a0003c0005t0001g0037a0003c0010t0002g0010a0003c0010t0004g0229others(16): Show | 19 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.219-17938A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66480447 | ||||||
| chr3:66480577
|
C | T | 13 | a0003c0005t0001g0039a0003c0010t0004g0201a0003c0010t0004g0257others(10): Show | 13 | HG02451.hp1 HG02630.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.219-18068G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66480577 | ||||||
| chr3:66480672
|
C | T | 45 | a0001c0002t0001g0063a0001c0002t0001g0108a0001c0002t0001g0140others(42): Show | 45 | HG00558.hp1 HG00621.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.219-18163G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66480672 | ||||||
| chr3:66480881
|
G | A | 2 | a0002c0018t0001g0176a0002c0022t0001g0177 | 2 | NA18747.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.219-18372C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66480881 | ||||||
| chr3:66481155
|
T | A | 1 | a0012c0017t0002g0015 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.219-18646A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66481155 | ||||||
| chr3:66481249
|
C | A | 1 | a0001c0007t0002g0080 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.219-18740G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66481249 | ||||||
| chr3:66481270
|
C | A | 1 | a0007c0008t0001g0016 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.219-18761G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66481270 | ||||||
| chr3:66481364
|
G | C | 3 | a0009c0015t0002g0032a0009c0015t0002g0033a0009c0015t0002g0034 | 3 | HG01891.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.218+18826C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66481364 | ||||||
| chr3:66481442
|
C | T | 159 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(156): Show | 159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.218+18748G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66481442 | ||||||
| chr3:66481460
|
G | C | 4 | a0002c0001t0001g0171a0002c0001t0001g0172a0002c0001t0001g0173others(1): Show | 4 | HG00738.hp1 HG02723.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+18730C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66481460 | ||||||
| chr3:66481520
|
T | TAC | 20 | a0003c0005t0001g0037a0003c0010t0002g0010a0003c0010t0004g0229others(17): Show | 20 | HG00735.hp1 HG01243.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.218+18668_218+1866 others(6): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66481520 | ||||||
| chr3:66481520
|
TAC | T | 5 | a0003c0005t0001g0028a0005c0004t0021g0006a0007c0033t0001g0027others(2): Show | 5 | HG01256.hp2 HG02886.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.218+18668_218+1866 others(6): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66481520 | ||||||
| chr3:66481520
|
TACAC | T | 11 | a0003c0010t0004g0201a0003c0010t0004g0257a0003c0010t0004g0258others(8): Show | 11 | HG02630.hp2 HG02818.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.218+18666_218+1866 others(8): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66481520 | ||||||
| chr3:66481691
|
C | T | 1 | a0003c0012t0018g0008 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.218+18499G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66481691 | ||||||
| chr3:66481835
|
C | T | 4 | a0005c0004t0021g0006a0007c0033t0001g0027a0009c0013t0002g0024others(1): Show | 4 | HG01256.hp2 HG02886.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.218+18355G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66481835 | ||||||
| chr3:66482245
|
T | C | 6 | a0003c0012t0017g0004a0005c0004t0021g0006a0007c0033t0001g0027others(3): Show | 6 | HG01256.hp2 HG02886.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.218+17945A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66482245 | ||||||
| chr3:66482342
|
A | G | 2 | a0002c0048t0001g0099a0004c0003t0002g0098 | 2 | NA19056.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.218+17848T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66482342 | ||||||
| chr3:66482387
|
G | A | 1 | a0003c0012t0018g0008 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.218+17803C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66482387 | ||||||
| chr3:66482720
|
T | C | 1 | a0002c0001t0001g0119 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.218+17470A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66482720 | ||||||
| chr3:66482754
|
T | C | 166 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(163): Show | 166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.218+17436A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66482754 | ||||||
| chr3:66482831
|
A | G | 4 | a0005c0004t0021g0006a0007c0033t0001g0027a0009c0013t0002g0024others(1): Show | 4 | HG01256.hp2 HG02886.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.218+17359T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66482831 | ||||||
| chr3:66482841
|
T | C | 2 | a0027c0050t0023g0082a0031c0047t0030g0162 | 2 | HG01515.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.218+17349A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66482841 | ||||||
| chr3:66483144
|
C | G | 17 | a0003c0005t0001g0039a0003c0010t0004g0201a0003c0010t0004g0257others(14): Show | 17 | HG02451.hp1 HG02630.hp1 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.218+17046G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66483144 | ||||||
| chr3:66483160
|
T | C | 17 | a0003c0005t0001g0039a0003c0010t0004g0201a0003c0010t0004g0257others(14): Show | 17 | HG02451.hp1 HG02630.hp1 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.218+17030A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66483160 | ||||||
| chr3:66483264
|
C | G | 16 | a0003c0005t0001g0039a0003c0010t0004g0201a0003c0010t0004g0257others(13): Show | 16 | HG02451.hp1 HG02630.hp2 HG02809.hp1 others(13): Show |
intron_variant | MODIFIER | c.218+16926G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66483264 | ||||||
| chr3:66483354
|
C | T | 23 | a0001c0007t0002g0194a0003c0005t0001g0039a0003c0010t0004g0201others(20): Show | 23 | HG01255.hp1 HG02165.hp1 HG02451.hp1 others(20): Show |
intron_variant | MODIFIER | c.218+16836G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66483354 | ||||||
| chr3:66483381
|
T | C | 6 | a0001c0007t0002g0194a0003c0012t0001g0040a0007c0008t0025g0043others(3): Show | 6 | HG01255.hp1 HG02165.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.218+16809A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66483381 | ||||||
| chr3:66483610
|
G | A | 1 | a0004c0053t0002g0197 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.218+16580C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66483610 | ||||||
| chr3:66483788
|
C | T | 1 | a0001c0002t0001g0136 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.218+16402G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66483788 | ||||||
| chr3:66483802
|
G | A | 1 | a0008c0006t0009g0014 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.218+16388C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66483802 | ||||||
| chr3:66483814
|
G | A | 1 | a0008c0006t0005g0223 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.218+16376C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66483814 | ||||||
| chr3:66483821
|
G | GC | 23 | a0001c0007t0002g0194a0003c0005t0001g0037a0003c0010t0002g0010others(20): Show | 23 | HG00735.hp1 HG01255.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.218+16368dupG | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66483821 | ||||||
| chr3:66483839
|
C | G | 25 | a0001c0007t0002g0194a0003c0005t0001g0039a0003c0010t0004g0201others(22): Show | 25 | HG01255.hp1 HG02165.hp1 HG02451.hp1 others(22): Show |
intron_variant | MODIFIER | c.218+16351G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66483839 | ||||||
| chr3:66483915
|
G | C | 1 | a0008c0006t0009g0035 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.218+16275C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66483915 | ||||||
| chr3:66483967
|
G | A | 2 | a0003c0005t0001g0039a0007c0008t0001g0038 | 2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.218+16223C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66483967 | ||||||
| chr3:66484024
|
G | C | 1 | a0019c0029t0001g0022 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.218+16166C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66484024 | ||||||
| chr3:66484120
|
T | C | 2 | a0003c0005t0001g0039a0007c0008t0001g0038 | 2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.218+16070A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66484120 | ||||||
| chr3:66484130
|
T | C | 19 | a0003c0005t0001g0037a0003c0010t0002g0010a0003c0010t0004g0229others(16): Show | 19 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.218+16060A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66484130 | ||||||
| chr3:66484212
|
T | C | 1 | a0003c0005t0001g0028 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.218+15978A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66484212 | ||||||
| chr3:66484229
|
C | T | 3 | a0011c0016t0013g0204a0011c0016t0013g0205a0011c0016t0013g0206 | 3 | HG02486.hp2 HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.218+15961G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66484229 | ||||||
| chr3:66484231
|
C | T | 20 | a0001c0007t0002g0194a0003c0005t0001g0039a0003c0010t0004g0201others(17): Show | 20 | HG01255.hp1 HG02165.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.218+15959G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66484231 | ||||||
| chr3:66484337
|
C | T | 6 | a0001c0007t0002g0194a0003c0012t0001g0040a0007c0008t0025g0043others(3): Show | 6 | HG01255.hp1 HG02165.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.218+15853G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66484337 | ||||||
| chr3:66484534
|
T | G | 6 | a0001c0007t0002g0194a0003c0012t0001g0040a0007c0008t0025g0043others(3): Show | 6 | HG01255.hp1 HG02165.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.218+15656A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66484534 | ||||||
| chr3:66484715
|
T | C | 12 | a0003c0010t0004g0201a0003c0010t0004g0257a0003c0010t0004g0258others(9): Show | 12 | HG02630.hp2 HG02818.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.218+15475A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66484715 | ||||||
| chr3:66484779
|
G | A | 4 | a0005c0004t0001g0019a0012c0017t0002g0015a0012c0017t0002g0020others(1): Show | 4 | HG00544.hp1 NA18950.hp1 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+15411C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66484779 | ||||||
| chr3:66484841
|
C | CA | 6 | a0005c0004t0006g0220a0005c0004t0006g0221a0005c0004t0006g0222others(3): Show | 6 | HG02630.hp2 HG02896.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.218+15348dupT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66484841 | ||||||
| chr3:66484936
|
T | C | 5 | a0003c0012t0001g0040a0007c0008t0025g0043a0009c0013t0001g0041others(2): Show | 5 | HG02165.hp1 HG02523.hp1 NA18991.hp2 others(2): Show |
intron_variant | MODIFIER | c.218+15254A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66484936 | ||||||
| chr3:66484974
|
T | C | 5 | a0003c0012t0001g0040a0007c0008t0025g0043a0009c0013t0001g0041others(2): Show | 5 | HG02165.hp1 HG02523.hp1 NA18991.hp2 others(2): Show |
intron_variant | MODIFIER | c.218+15216A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66484974 | ||||||
| chr3:66485155
|
CA | C | 170 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(167): Show | 170 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.218+15034delT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66485155 | ||||||
| chr3:66485155
|
CAA | C | 5 | a0002c0001t0001g0135a0004c0003t0002g0097a0004c0003t0002g0098others(2): Show | 5 | HG02735.hp2 HG02886.hp2 NA19056.hp1 others(2): Show |
intron_variant | MODIFIER | c.218+15033_218+1503 others(6): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66485155 | ||||||
| chr3:66485351
|
C | T | 5 | a0003c0012t0001g0040a0007c0008t0025g0043a0009c0013t0001g0041others(2): Show | 5 | HG02165.hp1 HG02523.hp1 NA18991.hp2 others(2): Show |
intron_variant | MODIFIER | c.218+14839G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66485351 | ||||||
| chr3:66485415
|
C | T | 2 | a0003c0005t0001g0039a0007c0008t0001g0038 | 2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.218+14775G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66485415 | ||||||
| chr3:66485456
|
T | C | 19 | a0003c0005t0001g0037a0003c0010t0002g0010a0003c0010t0004g0229others(16): Show | 19 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.218+14734A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66485456 | ||||||
| chr3:66485572
|
G | A | 3 | a0003c0012t0018g0008a0005c0004t0021g0006a0021c0034t0019g0007 | 3 | HG02886.hp2 HG02976.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.218+14618C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66485572 | ||||||
| chr3:66485649
|
A | G | 4 | a0003c0036t0034g0203a0006c0035t0033g0207a0007c0008t0003g0237others(1): Show | 4 | HG02572.hp1 HG02630.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.218+14541T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66485649 | ||||||
| chr3:66485692
|
C | G | 3 | a0001c0002t0001g0053a0001c0002t0001g0061a0001c0002t0001g0062 | 3 | HG00735.hp2 HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.218+14498G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66485692 | ||||||
| chr3:66485900
|
A | G | 20 | a0003c0005t0001g0037a0003c0010t0002g0010a0003c0010t0004g0229others(17): Show | 20 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.218+14290T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66485900 | ||||||
| chr3:66485974
|
T | C | 3 | a0005c0004t0006g0220a0005c0004t0006g0221a0005c0004t0006g0222 | 3 | HG02630.hp2 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.218+14216A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66485974 | ||||||
| chr3:66486002
|
C | T | 5 | a0003c0012t0001g0040a0007c0008t0025g0043a0009c0013t0001g0041others(2): Show | 5 | HG02165.hp1 HG02523.hp1 NA18991.hp2 others(2): Show |
intron_variant | MODIFIER | c.218+14188G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66486002 | ||||||
| chr3:66486042
|
C | T | 5 | a0003c0010t0004g0201a0003c0010t0004g0257a0003c0010t0004g0258others(2): Show | 5 | HG02818.hp1 HG02818.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.218+14148G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66486042 | ||||||
| chr3:66486071
|
T | G | 1 | a0001c0002t0001g0104 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.218+14119A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66486071 | ||||||
| chr3:66486153
|
A | G | 8 | a0005c0004t0008g0255a0007c0008t0003g0256a0007c0033t0001g0027others(5): Show | 8 | HG01256.hp2 HG01884.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.218+14037T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66486153 | ||||||
| chr3:66486292
|
T | C | 4 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0002t0001g0094others(1): Show | 4 | NA18943.hp1 NA18981.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.218+13898A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66486292 | ||||||
| chr3:66486355
|
G | A | 2 | a0004c0003t0002g0081a0027c0050t0023g0082 | 2 | HG00099.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.218+13835C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66486355 | ||||||
| chr3:66486358
|
C | G | 17 | a0003c0005t0003g0001a0003c0005t0003g0209a0003c0005t0003g0210others(14): Show | 18 | HG02040.hp2 HG02486.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.218+13832G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66486358 | ||||||
| chr3:66486359
|
T | G | 17 | a0003c0005t0003g0001a0003c0005t0003g0209a0003c0005t0003g0210others(14): Show | 18 | HG02040.hp2 HG02486.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.218+13831A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66486359 | ||||||
| chr3:66486388
|
G | A | 13 | a0002c0001t0001g0188a0003c0005t0001g0026a0004c0053t0002g0197others(10): Show | 13 | HG00544.hp1 HG00609.hp2 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.218+13802C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66486388 | ||||||
| chr3:66486441
|
T | G | 1 | a0004c0003t0002g0097 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.218+13749A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66486441 | ||||||
| chr3:66486466
|
A | C | 1 | a0003c0005t0001g0028 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.218+13724T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66486466 | ||||||
| chr3:66486736
|
C | T | 17 | a0003c0010t0004g0201a0003c0010t0004g0257a0003c0010t0004g0258others(14): Show | 17 | HG02630.hp2 HG02818.hp1 HG02818.hp2 others(14): Show |
intron_variant | MODIFIER | c.218+13454G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66486736 | ||||||
| chr3:66487003
|
A | G | 1 | a0008c0006t0005g0215 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.218+13187T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66487003 | ||||||
| chr3:66487020
|
A | G | 2 | a0005c0004t0008g0255a0007c0008t0003g0256 | 2 | HG02723.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.218+13170T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66487020 | ||||||
| chr3:66487118
|
A | C | 1 | a0003c0010t0004g0260 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.218+13072T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66487118 | ||||||
| chr3:66487187
|
A | T | 1 | a0001c0014t0010g0134 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.218+13003T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66487187 | ||||||
| chr3:66487353
|
TA | T | 22 | a0002c0001t0001g0188a0003c0005t0001g0026a0003c0005t0001g0028others(19): Show | 22 | HG00544.hp1 HG00609.hp2 HG01256.hp2 others(19): Show |
intron_variant | MODIFIER | c.218+12836delT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66487353 | ||||||
| chr3:66487474
|
T | C | 1 | a0001c0002t0001g0049 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.218+12716A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66487474 | ||||||
| chr3:66488030
|
A | G | 2 | a0003c0005t0001g0039a0007c0008t0001g0038 | 2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.218+12160T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66488030 | ||||||
| chr3:66488361
|
A | T | 1 | a0008c0006t0009g0014 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.218+11829T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66488361 | ||||||
| chr3:66488420
|
A | G | 1 | a0011c0030t0027g0021 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.218+11770T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66488420 | ||||||
| chr3:66488464
|
T | TA | 6 | a0002c0001t0001g0165a0003c0005t0001g0026a0007c0008t0001g0016others(3): Show | 6 | HG02145.hp2 HG03927.hp2 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.218+11725dupT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66488464 | ||||||
| chr3:66488472
|
A | AAAC | 14 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0002t0001g0094others(11): Show | 14 | HG00544.hp1 HG00609.hp2 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.218+11717_218+1171 others(7): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66488472 | ||||||
| chr3:66488473
|
AC | A | 21 | a0001c0002t0001g0053a0001c0002t0001g0084a0001c0002t0001g0111others(18): Show | 21 | HG00280.hp2 HG00558.hp2 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.218+11716delG | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66488473 | ||||||
| chr3:66488474
|
C | A | 158 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0056others(155): Show | 158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.218+11716G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66488474 | ||||||
| chr3:66488477
|
A | C | 4 | a0003c0005t0001g0039a0007c0008t0001g0038a0007c0033t0001g0027others(1): Show | 4 | HG01256.hp2 HG02451.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.218+11713T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66488477 | ||||||
| chr3:66488538
|
G | A | 1 | a0002c0001t0001g0123 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.218+11652C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66488538 | ||||||
| chr3:66488810
|
T | C | 1 | a0014c0042t0010g0083 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.218+11380A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66488810 | ||||||
| chr3:66488862
|
T | G | 3 | a0005c0004t0006g0238a0005c0004t0006g0239a0005c0004t0006g0240 | 3 | HG01099.hp1 HG01358.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.218+11328A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66488862 | ||||||
| chr3:66488867
|
C | G | 1 | a0002c0001t0001g0180 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.218+11323G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66488867 | ||||||
| chr3:66489026
|
C | T | 1 | a0001c0007t0002g0125 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.218+11164G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66489026 | ||||||
| chr3:66489105
|
G | A | 1 | a0003c0036t0034g0203 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.218+11085C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66489105 | ||||||
| chr3:66489204
|
T | C | 161 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(158): Show | 161 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.218+10986A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66489204 | ||||||
| chr3:66489278
|
C | A | 1 | a0008c0006t0009g0014 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.218+10912G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66489278 | ||||||
| chr3:66489358
|
C | T | 219 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(216): Show | 219 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.218+10832G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66489358 | ||||||
| chr3:66489382
|
T | C | 1 | a0001c0002t0001g0189 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.218+10808A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66489382 | ||||||
| chr3:66489422
|
T | G | 23 | a0001c0002t0001g0111a0001c0002t0001g0115a0001c0002t0001g0122others(20): Show | 23 | HG00280.hp2 HG00558.hp2 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.218+10768A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66489422 | ||||||
| chr3:66489432
|
G | A | 11 | a0003c0010t0004g0201a0003c0010t0004g0257a0003c0010t0004g0258others(8): Show | 11 | HG02630.hp2 HG02818.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.218+10758C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66489432 | ||||||
| chr3:66489465
|
T | C | 6 | a0001c0002t0001g0084a0001c0002t0001g0086a0001c0002t0001g0167others(3): Show | 6 | HG01069.hp1 HG01071.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.218+10725A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66489465 | ||||||
| chr3:66489525
|
A | ATG | 14 | a0003c0005t0003g0001a0003c0005t0003g0209a0003c0005t0003g0210others(11): Show | 15 | HG02040.hp2 HG02572.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.218+10663_218+1066 others(6): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66489525 | ||||||
| chr3:66489525
|
A | ATGTG | 4 | a0003c0005t0003g0241a0011c0016t0013g0204a0011c0016t0013g0205others(1): Show | 4 | HG01070.hp2 HG02486.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.218+10661_218+1066 others(8): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66489525 | ||||||
| chr3:66489525
|
ATG | A | 4 | a0003c0012t0001g0040a0009c0013t0001g0041a0009c0013t0002g0042others(1): Show | 4 | HG02165.hp1 NA18991.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+10663_218+1066 others(6): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66489525 | ||||||
| chr3:66489525
|
ATGTG | A | 3 | a0002c0001t0001g0124a0002c0001t0001g0191a0003c0005t0001g0028 | 3 | HG03579.hp2 HG03688.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.218+10661_218+1066 others(8): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66489525 | ||||||
| chr3:66489525
|
ATGTGTG | A | 197 | a0001c0002t0001g0051a0001c0002t0001g0053a0001c0002t0001g0056others(194): Show | 197 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.218+10659_218+1066 others(10): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66489525 | ||||||
| chr3:66489525
|
ATGTGTGT others(3): Show |
A | 1 | a0002c0001t0015g0002 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.218+10655_218+1066 others(14): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66489525 | ||||||
| chr3:66489525
|
ATGTGTGT others(5): Show |
A | 12 | a0003c0010t0004g0201a0003c0010t0004g0257a0003c0010t0004g0258others(9): Show | 12 | HG02630.hp2 HG02818.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.218+10653_218+1066 others(16): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66489525 | ||||||
| chr3:66489565
|
C | G | 2 | a0003c0010t0004g0231a0006c0009t0004g0224 | 2 | HG02647.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.218+10625G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66489565 | ||||||
| chr3:66489567
|
G | C | 2 | a0004c0003t0002g0088a0004c0003t0002g0089 | 2 | HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.218+10623C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66489567 | ||||||
| chr3:66489583
|
T | TTAAG | 12 | a0003c0010t0004g0201a0003c0010t0004g0257a0003c0010t0004g0258others(9): Show | 12 | HG02630.hp2 HG02818.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.218+10603_218+1060 others(8): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66489583 | ||||||
| chr3:66489679
|
A | G | 1 | a0002c0001t0001g0059 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.218+10511T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66489679 | ||||||
| chr3:66489684
|
T | G | 1 | a0008c0006t0009g0014 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.218+10506A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66489684 | ||||||
| chr3:66489965
|
GCAC | G | 5 | a0003c0012t0017g0004a0003c0012t0018g0008a0005c0004t0021g0006others(2): Show | 5 | HG02886.hp2 HG02976.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.218+10222_218+1022 others(7): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66489965 | ||||||
| chr3:66490121
|
T | C | 1 | a0008c0006t0005g0219 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.218+10069A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66490121 | ||||||
| chr3:66490132
|
T | C | 1 | a0022c0032t0007g0046 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.218+10058A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66490132 | ||||||
| chr3:66490192
|
C | CTCCAAA | 5 | a0003c0012t0017g0004a0003c0012t0018g0008a0005c0004t0021g0006others(2): Show | 5 | HG02886.hp2 HG02976.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.218+9992_218+9997d others(8): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66490192 | ||||||
| chr3:66490422
|
T | A | 1 | a0008c0006t0005g0223 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.218+9768A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66490422 | ||||||
| chr3:66490612
|
T | A | 8 | a0003c0010t0004g0201a0003c0010t0004g0257a0003c0010t0004g0258others(5): Show | 8 | HG02818.hp1 HG02818.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.218+9578A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66490612 | ||||||
| chr3:66490612
|
T | C | 159 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(156): Show | 159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.218+9578A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66490612 | ||||||
| chr3:66490645
|
TA | T | 36 | a0002c0001t0001g0110a0002c0022t0001g0179a0003c0005t0001g0028others(33): Show | 37 | HG00280.hp1 HG01099.hp1 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.218+9544delT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66490645 | ||||||
| chr3:66490645
|
TAA | T | 205 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(202): Show | 205 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.218+9543_218+9544d others(4): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66490645 | ||||||
| chr3:66490669
|
G | A | 1 | a0003c0005t0001g0028 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.218+9521C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66490669 | ||||||
| chr3:66490738
|
T | C | 33 | a0002c0001t0001g0188a0003c0005t0001g0026a0003c0005t0001g0037others(30): Show | 33 | HG00544.hp1 HG00609.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.218+9452A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66490738 | ||||||
| chr3:66490748
|
A | C | 5 | a0003c0012t0017g0004a0003c0012t0018g0008a0005c0004t0021g0006others(2): Show | 5 | HG02886.hp2 HG02976.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.218+9442T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66490748 | ||||||
| chr3:66490958
|
T | A | 1 | a0011c0030t0027g0021 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.218+9232A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66490958 | ||||||
| chr3:66491024
|
G | T | 219 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(216): Show | 219 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.218+9166C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66491024 | ||||||
| chr3:66491058
|
G | C | 11 | a0003c0010t0004g0201a0003c0010t0004g0257a0003c0010t0004g0258others(8): Show | 11 | HG02630.hp2 HG02818.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.218+9132C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66491058 | ||||||
| chr3:66491084
|
G | C | 2 | a0002c0001t0001g0090a0010c0011t0001g0091 | 2 | NA18939.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.218+9106C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66491084 | ||||||
| chr3:66491102
|
CT | C | 4 | a0003c0005t0001g0039a0007c0008t0001g0038a0007c0033t0001g0027others(1): Show | 4 | HG01256.hp2 HG02451.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.218+9087delA | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66491102 | ||||||
| chr3:66491242
|
C | T | 3 | a0002c0001t0001g0109a0002c0001t0001g0110a0002c0022t0001g0179 | 3 | HG01243.hp1 HG01981.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.218+8948G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66491242 | ||||||
| chr3:66491389
|
G | A | 11 | a0002c0001t0001g0188a0003c0005t0001g0026a0005c0004t0001g0019others(8): Show | 11 | HG00544.hp1 HG00609.hp2 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.218+8801C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66491389 | ||||||
| chr3:66491558
|
C | T | 8 | a0003c0010t0004g0201a0003c0010t0004g0257a0003c0010t0004g0258others(5): Show | 8 | HG02818.hp1 HG02818.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.218+8632G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66491558 | ||||||
| chr3:66491678
|
T | TA | 9 | a0001c0007t0002g0194a0003c0012t0001g0040a0007c0008t0001g0013others(6): Show | 9 | HG01255.hp1 HG02165.hp1 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.218+8511dupT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66491678 | ||||||
| chr3:66491836
|
C | T | 1 | a0001c0002t0001g0092 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.218+8354G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66491836 | ||||||
| chr3:66491838
|
T | C | 1 | a0011c0030t0027g0021 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.218+8352A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66491838 | ||||||
| chr3:66491951
|
A | G | 19 | a0003c0005t0001g0037a0003c0010t0002g0010a0003c0010t0004g0229others(16): Show | 19 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.218+8239T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66491951 | ||||||
| chr3:66491960
|
G | C | 1 | a0019c0029t0001g0022 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.218+8230C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66491960 | ||||||
| chr3:66491980
|
T | C | 2 | a0003c0005t0001g0039a0007c0008t0001g0038 | 2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.218+8210A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66491980 | ||||||
| chr3:66492008
|
C | G | 3 | a0005c0004t0006g0220a0005c0004t0006g0221a0005c0004t0006g0222 | 3 | HG02630.hp2 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.218+8182G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66492008 | ||||||
| chr3:66492250
|
G | C | 1 | a0008c0006t0020g0005 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.218+7940C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66492250 | ||||||
| chr3:66492336
|
T | C | 176 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(173): Show | 176 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.218+7854A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66492336 | ||||||
| chr3:66492339
|
G | T | 2 | a0001c0002t0001g0092a0001c0002t0001g0093 | 2 | NA18943.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.218+7851C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66492339 | ||||||
| chr3:66492387
|
G | A | 1 | a0002c0001t0001g0170 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.218+7803C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66492387 | ||||||
| chr3:66492439
|
A | G | 23 | a0001c0002t0001g0111a0001c0002t0001g0115a0001c0002t0001g0122others(20): Show | 23 | HG00280.hp2 HG00558.hp2 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.218+7751T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66492439 | ||||||
| chr3:66492456
|
C | T | 1 | a0003c0005t0001g0028 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.218+7734G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66492456 | ||||||
| chr3:66492468
|
C | T | 3 | a0005c0004t0006g0220a0005c0004t0006g0221a0005c0004t0006g0222 | 3 | HG02630.hp2 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.218+7722G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66492468 | ||||||
| chr3:66492711
|
T | C | 4 | a0002c0001t0001g0171a0002c0001t0001g0172a0002c0001t0001g0173others(1): Show | 4 | HG00738.hp1 HG02723.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+7479A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66492711 | ||||||
| chr3:66492715
|
T | TG | 23 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0002t0001g0094others(20): Show | 23 | HG00544.hp1 HG00609.hp2 HG01256.hp2 others(20): Show |
intron_variant | MODIFIER | c.218+7474_218+7475i others(3): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66492715 | ||||||
| chr3:66492739
|
T | G | 8 | a0003c0012t0001g0040a0007c0008t0001g0013a0007c0008t0001g0030others(5): Show | 8 | HG02165.hp1 HG02523.hp1 NA18953.hp1 others(5): Show |
intron_variant | MODIFIER | c.218+7451A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66492739 | ||||||
| chr3:66492744
|
T | C | 1 | a0016c0038t0003g0235 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.218+7446A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66492744 | ||||||
| chr3:66492777
|
G | A | 202 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.218+7413C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66492777 | ||||||
| chr3:66492866
|
T | C | 4 | a0007c0008t0025g0043a0009c0013t0001g0041a0009c0013t0002g0042others(1): Show | 4 | HG02523.hp1 NA18991.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+7324A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66492866 | ||||||
| chr3:66493047
|
G | A | 1 | a0010c0011t0007g0175 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.218+7143C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66493047 | ||||||
| chr3:66493072
|
GTCCTCCC | G | 12 | a0003c0010t0004g0201a0003c0010t0004g0257a0003c0010t0004g0258others(9): Show | 12 | HG02630.hp2 HG02818.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.218+7111_218+7117d others(9): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66493072 | ||||||
| chr3:66493114
|
G | T | 202 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.218+7076C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66493114 | ||||||
| chr3:66493116
|
G | A | 1 | a0001c0040t0001g0096 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.218+7074C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66493116 | ||||||
| chr3:66493160
|
C | T | 202 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.218+7030G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66493160 | ||||||
| chr3:66493180
|
T | C | 1 | a0012c0017t0002g0023 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.218+7010A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66493180 | ||||||
| chr3:66493212
|
T | A | 3 | a0003c0010t0002g0010a0008c0006t0009g0011a0008c0006t0009g0012 | 3 | HG02559.hp2 NA18522.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.218+6978A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66493212 | ||||||
| chr3:66493272
|
A | G | 202 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.218+6918T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66493272 | ||||||
| chr3:66493337
|
T | C | 2 | a0002c0018t0001g0176a0002c0022t0001g0177 | 2 | NA18747.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.218+6853A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66493337 | ||||||
| chr3:66493839
|
G | A | 217 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(214): Show | 217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.218+6351C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66493839 | ||||||
| chr3:66493843
|
G | A | 2 | a0005c0004t0021g0006a0021c0034t0019g0007 | 2 | HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.218+6347C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66493843 | ||||||
| chr3:66493912
|
A | G | 1 | a0018c0028t0003g0259 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.218+6278T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66493912 | ||||||
| chr3:66494008
|
G | A | 12 | a0003c0010t0004g0201a0003c0010t0004g0257a0003c0010t0004g0258others(9): Show | 12 | HG02630.hp2 HG02818.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.218+6182C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66494008 | ||||||
| chr3:66494108
|
A | G | 1 | a0007c0008t0037g0261 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.218+6082T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66494108 | ||||||
| chr3:66494325
|
C | T | 8 | a0003c0010t0004g0201a0003c0010t0004g0257a0003c0010t0004g0258others(5): Show | 8 | HG02818.hp1 HG02818.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.218+5865G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66494325 | ||||||
| chr3:66494655
|
C | T | 4 | a0003c0005t0001g0039a0007c0008t0001g0038a0007c0033t0001g0027others(1): Show | 4 | HG01256.hp2 HG02451.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.218+5535G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66494655 | ||||||
| chr3:66494975
|
T | C | 8 | a0003c0010t0004g0201a0003c0010t0004g0257a0003c0010t0004g0258others(5): Show | 8 | HG02818.hp1 HG02818.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.218+5215A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66494975 | ||||||
| chr3:66495066
|
A | G | 1 | a0003c0036t0034g0203 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.218+5124T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66495066 | ||||||
| chr3:66495284
|
C | T | 2 | a0006c0009t0002g0045a0022c0032t0007g0046 | 2 | HG02896.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.218+4906G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66495284 | ||||||
| chr3:66495426
|
G | A | 1 | a0001c0002t0001g0178 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.218+4764C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66495426 | ||||||
| chr3:66495664
|
C | G | 12 | a0003c0010t0004g0201a0003c0010t0004g0257a0003c0010t0004g0258others(9): Show | 12 | HG02630.hp2 HG02818.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.218+4526G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66495664 | ||||||
| chr3:66495764
|
T | G | 1 | a0008c0006t0005g0219 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.218+4426A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66495764 | ||||||
| chr3:66495787
|
C | A | 1 | a0007c0033t0001g0027 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.218+4403G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66495787 | ||||||
| chr3:66495946
|
G | C | 1 | a0004c0003t0002g0105 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.218+4244C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66495946 | ||||||
| chr3:66496121
|
T | C | 6 | a0003c0005t0001g0028a0003c0012t0017g0004a0003c0012t0018g0008others(3): Show | 6 | HG02886.hp2 HG02976.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.218+4069A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66496121 | ||||||
| chr3:66496222
|
G | A | 17 | a0001c0002t0001g0049a0001c0002t0001g0104a0001c0007t0002g0100others(14): Show | 17 | HG00544.hp2 HG02071.hp2 HG02300.hp2 others(14): Show |
intron_variant | MODIFIER | c.218+3968C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66496222 | ||||||
| chr3:66496276
|
T | C | 2 | a0003c0005t0001g0039a0007c0008t0001g0038 | 2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.218+3914A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66496276 | ||||||
| chr3:66496366
|
A | G | 1 | a0008c0006t0009g0014 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.218+3824T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66496366 | ||||||
| chr3:66496526
|
G | A | 1 | a0001c0002t0001g0106 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.218+3664C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66496526 | ||||||
| chr3:66496682
|
T | A | 2 | a0003c0005t0003g0216a0003c0005t0003g0217 | 2 | NA18961.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.218+3508A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66496682 | ||||||
| chr3:66496710
|
C | T | 1 | a0004c0003t0002g0057 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.218+3480G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66496710 | ||||||
| chr3:66496737
|
T | TA | 11 | a0003c0005t0001g0028a0003c0005t0001g0039a0003c0012t0017g0004others(8): Show | 11 | HG01256.hp2 HG02451.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.218+3452dupT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66496737 | ||||||
| chr3:66496786
|
C | G | 12 | a0003c0010t0004g0201a0003c0010t0004g0257a0003c0010t0004g0258others(9): Show | 12 | HG02630.hp2 HG02818.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.218+3404G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66496786 | ||||||
| chr3:66497004
|
A | C | 12 | a0003c0010t0004g0201a0003c0010t0004g0257a0003c0010t0004g0258others(9): Show | 12 | HG02630.hp2 HG02818.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.218+3186T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66497004 | ||||||
| chr3:66497011
|
C | T | 1 | a0001c0002t0001g0056 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.218+3179G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66497011 | ||||||
| chr3:66497104
|
T | C | 1 | a0003c0012t0014g0236 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.218+3086A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66497104 | ||||||
| chr3:66497211
|
T | A | 1 | a0003c0005t0001g0028 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.218+2979A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66497211 | ||||||
| chr3:66497372
|
A | T | 1 | a0001c0002t0001g0108 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.218+2818T>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66497372 | ||||||
| chr3:66497417
|
T | TG | 8 | a0003c0012t0001g0040a0007c0008t0001g0013a0007c0008t0001g0030others(5): Show | 8 | HG02165.hp1 HG02523.hp1 NA18953.hp1 others(5): Show |
intron_variant | MODIFIER | c.218+2772dupC | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66497417 | ||||||
| chr3:66497674
|
A | G | 1 | a0002c0001t0001g0055 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.218+2516T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66497674 | ||||||
| chr3:66497704
|
C | CA | 83 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.218+2485dupT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66497704 | ||||||
| chr3:66497704
|
C | CAA | 89 | a0001c0002t0001g0108a0001c0002t0001g0111a0001c0002t0001g0115others(86): Show | 89 | HG00280.hp1 HG00280.hp2 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.218+2484_218+2485d others(4): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66497704 | ||||||
| chr3:66497704
|
C | CAAA | 7 | a0001c0007t0002g0194a0002c0001t0001g0180a0002c0001t0001g0183others(4): Show | 7 | HG01243.hp1 HG01255.hp1 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.218+2483_218+2485d others(5): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66497704 | ||||||
| chr3:66497704
|
C | CAAAA | 6 | a0003c0010t0004g0201a0003c0010t0004g0260a0005c0004t0006g0202others(3): Show | 6 | HG02145.hp2 HG02818.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.218+2482_218+2485d others(6): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66497704 | ||||||
| chr3:66497704
|
C | CCAAA | 3 | a0005c0004t0006g0221a0005c0004t0006g0222a0008c0006t0005g0223 | 3 | HG02630.hp2 HG03486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.218+2485_218+2486i others(6): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66497704 | ||||||
| chr3:66497744
|
C | G | 2 | a0003c0005t0001g0039a0007c0008t0001g0038 | 2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.218+2446G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66497744 | ||||||
| chr3:66497847
|
C | A | 165 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.218+2343G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66497847 | ||||||
| chr3:66497921
|
C | G | 9 | a0003c0010t0004g0229a0003c0010t0004g0231a0006c0009t0004g0224others(6): Show | 9 | HG00735.hp1 HG02647.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.218+2269G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66497921 | ||||||
| chr3:66497970
|
T | C | 1 | a0001c0014t0010g0186 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.218+2220A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66497970 | ||||||
| chr3:66497996
|
C | T | 8 | a0003c0010t0004g0201a0003c0010t0004g0257a0003c0010t0004g0258others(5): Show | 8 | HG02818.hp1 HG02818.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.218+2194G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66497996 | ||||||
| chr3:66498061
|
G | T | 5 | a0003c0012t0014g0233a0003c0012t0014g0236a0006c0009t0004g0232others(2): Show | 5 | HG02055.hp1 HG02145.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.218+2129C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66498061 | ||||||
| chr3:66498232
|
A | C | 1 | a0009c0015t0002g0032 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.218+1958T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66498232 | ||||||
| chr3:66498377
|
C | A | 1 | a0002c0001t0001g0187 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.218+1813G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66498377 | ||||||
| chr3:66498405
|
G | C | 2 | a0006c0009t0002g0045a0022c0032t0007g0046 | 2 | HG02896.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.218+1785C>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66498405 | ||||||
| chr3:66498549
|
C | T | 5 | a0003c0012t0017g0004a0003c0012t0018g0008a0005c0004t0021g0006others(2): Show | 5 | HG02886.hp2 HG02976.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.218+1641G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66498549 | ||||||
| chr3:66498564
|
T | TA | 22 | a0001c0002t0001g0189a0002c0001t0001g0188a0002c0001t0001g0191others(19): Show | 22 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.218+1625dupT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66498564 | ||||||
| chr3:66498564
|
T | TAA | 7 | a0001c0007t0002g0194a0003c0010t0004g0231a0003c0012t0001g0040others(4): Show | 7 | HG01255.hp1 HG02165.hp1 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.218+1624_218+1625d others(4): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66498564 | ||||||
| chr3:66498564
|
TA | T | 8 | a0001c0002t0001g0053a0002c0001t0001g0052a0003c0012t0017g0004others(5): Show | 8 | HG01070.hp1 HG01167.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.218+1625delT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66498564 | ||||||
| chr3:66498564
|
TAA | T | 8 | a0003c0010t0004g0201a0003c0010t0004g0257a0003c0010t0004g0258others(5): Show | 8 | HG02818.hp1 HG02818.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.218+1624_218+1625d others(4): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66498564 | ||||||
| chr3:66498634
|
C | T | 8 | a0003c0010t0004g0201a0003c0010t0004g0257a0003c0010t0004g0258others(5): Show | 8 | HG02818.hp1 HG02818.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.218+1556G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66498634 | ||||||
| chr3:66498671
|
CA | C | 8 | a0003c0010t0004g0201a0003c0010t0004g0257a0003c0010t0004g0258others(5): Show | 8 | HG02818.hp1 HG02818.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.218+1518delT | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66498671 | ||||||
| chr3:66498680
|
T | C | 1 | a0004c0003t0002g0193 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.218+1510A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66498680 | ||||||
| chr3:66498788
|
T | A | 2 | a0003c0005t0001g0039a0007c0008t0001g0038 | 2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.218+1402A>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66498788 | ||||||
| chr3:66498818
|
C | G | 247 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(244): Show | 248 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.218+1372G>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66498818 | ||||||
| chr3:66498851
|
G | A | 2 | a0003c0005t0001g0039a0007c0008t0001g0038 | 2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.218+1339C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66498851 | ||||||
| chr3:66498909
|
G | T | 4 | a0001c0002t0001g0051a0002c0001t0001g0195a0002c0001t0032g0199others(1): Show | 4 | HG00621.hp1 HG00673.hp2 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+1281C>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66498909 | ||||||
| chr3:66498933
|
T | G | 2 | a0005c0004t0008g0255a0007c0008t0003g0256 | 2 | HG02723.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.218+1257A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66498933 | ||||||
| chr3:66498979
|
T | G | 4 | a0005c0004t0006g0220a0005c0004t0006g0221a0005c0004t0006g0222others(1): Show | 4 | HG02630.hp2 HG03098.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+1211A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66498979 | ||||||
| chr3:66499041
|
T | C | 2 | a0004c0003t0038g0262a0029c0052t0039g0263 | 2 | HG02486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.218+1149A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66499041 | ||||||
| chr3:66499096
|
G | A | 6 | a0001c0007t0002g0194a0003c0012t0001g0040a0007c0008t0025g0043others(3): Show | 6 | HG01255.hp1 HG02165.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.218+1094C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66499096 | ||||||
| chr3:66499152
|
T | G | 1 | a0002c0001t0001g0195 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.218+1038A>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66499152 | ||||||
| chr3:66499162
|
T | C | 9 | a0003c0010t0004g0229a0003c0010t0004g0231a0006c0009t0004g0224others(6): Show | 9 | HG00735.hp1 HG02647.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.218+1028A>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66499162 | ||||||
| chr3:66499179
|
A | C | 1 | a0001c0002t0001g0049 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.218+1011T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66499179 | ||||||
| chr3:66499202
|
TAC | T | 237 | a0001c0002t0001g0049a0001c0002t0001g0051a0001c0002t0001g0053others(234): Show | 238 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.218+986_218+987del others(2): Show |
LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66499202 | ||||||
| chr3:66499211
|
G | A | 1 | a0003c0012t0018g0008 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.218+979C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66499211 | ||||||
| chr3:66499236
|
A | G | 3 | a0003c0010t0002g0010a0008c0006t0009g0011a0008c0006t0009g0012 | 3 | HG02559.hp2 NA18522.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.218+954T>C | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66499236 | ||||||
| chr3:66499339
|
C | A | 2 | a0004c0053t0002g0197a0025c0054t0002g0196 | 2 | HG02300.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.218+851G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66499339 | ||||||
| chr3:66499372
|
C | T | 5 | a0003c0012t0017g0004a0003c0012t0018g0008a0005c0004t0021g0006others(2): Show | 5 | HG02886.hp2 HG02976.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.218+818G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66499372 | ||||||
| chr3:66499534
|
A | C | 8 | a0003c0010t0004g0201a0003c0010t0004g0257a0003c0010t0004g0258others(5): Show | 8 | HG02818.hp1 HG02818.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.218+656T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66499534 | ||||||
| chr3:66499749
|
C | T | 1 | a0008c0006t0005g0200 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.218+441G>A | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66499749 | ||||||
| chr3:66499800
|
A | C | 2 | a0002c0001t0001g0047a0002c0001t0001g0048 | 2 | HG00544.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.218+390T>G | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66499800 | ||||||
| chr3:66499893
|
C | A | 6 | a0003c0010t0004g0257a0003c0010t0004g0258a0003c0010t0004g0260others(3): Show | 6 | HG02818.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.218+297G>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66499893 | ||||||
| chr3:66500145
|
G | A | 1 | a0001c0002t0001g0198 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.218+45C>T | LRIG1 | ENSG00000144749.14 | transcript | ENST00000273261.8 | protein_coding | 1/18 | chr3 | 66500145 |