Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 2902 |
|---|---|
| ensemblid | ENSG00000176884.17 |
| hgncid | 4584 |
| symbol | GRIN1 |
| name | glutamate ionotropic receptor NMDA type subunit 1 |
| refseq_nuc | NM_007327.4 |
| refseq_prot | NP_015566.1 |
| ensembl_nuc | ENST00000371561.8 |
| ensembl_prot | ENSP00000360616.3 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 137139154 |
| end | 137168756 |
| strand | + |
| ver | v1.2 |
| region | chr9:137139154-137168756 |
| region5000 | chr9:137134154-137173756 |
| regionname0 | GRIN1_chr9_137139154_137168756 |
| regionname5000 | GRIN1_chr9_137134154_137173756 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 938 | 298 | 94 | 62 | 82 | 16 | 42 | 46 | GRIN1_chr9_137134154_137173756 | GRIN1 | copy fasta | chr9 | 137134154 | 137173756 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 2817 | 236 | 84 | 45 | 66 | 11 | 29 | GRIN1_chr9_137134154_137173756 | GRIN1 | copy fasta | chr9 | 137134154 | 137173756 |
| c0002 | 0/1 | 2817 | 32 | 1 | 16 | 0 | 5 | 9 | GRIN1_chr9_137134154_137173756 | GRIN1 | copy fasta | chr9 | 137134154 | 137173756 |
| c0003 | 0/0 | 2817 | 15 | 2 | 0 | 10 | 0 | 3 | GRIN1_chr9_137134154_137173756 | GRIN1 | copy fasta | chr9 | 137134154 | 137173756 |
| c0004 | 0/0 | 2817 | 5 | 0 | 0 | 5 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | copy fasta | chr9 | 137134154 | 137173756 |
| c0005 | 0/0 | 2817 | 4 | 4 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | copy fasta | chr9 | 137134154 | 137173756 |
| c0006 | 0/0 | 2817 | 2 | 2 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | copy fasta | chr9 | 137134154 | 137173756 |
| c0007 | 0/0 | 2817 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | copy fasta | chr9 | 137134154 | 137173756 |
| c0008 | 0/0 | 2817 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | copy fasta | chr9 | 137134154 | 137173756 |
| c0009 | 0/0 | 2817 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | copy fasta | chr9 | 137134154 | 137173756 |
| c0010 | 0/0 | 2817 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | copy fasta | chr9 | 137134154 | 137173756 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 1563 | 294 | 92 | 62 | 81 | 15 | 42 | GRIN1_chr9_137134154_137173756 | GRIN1 | copy fasta | chr9 | 137134154 | 137173756 |
| t0002 | 0/0 | 1563 | 2 | 2 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | copy fasta | chr9 | 137134154 | 137173756 |
| t0003 | 0/0 | 1563 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | copy fasta | chr9 | 137134154 | 137173756 |
| t0004 | 0/0 | 1563 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | copy fasta | chr9 | 137134154 | 137173756 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0007 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0015 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0020 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0021 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0098 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2817 | 236 | 84 | 45 | 66 | 11 | 29 | GRIN1_chr9_137134154_137173756 | GRIN1 | copy fasta | chr9 | 137134154 | 137173756 |
| a0001c0002 | 0/1 | 2817 | 32 | 1 | 16 | 0 | 5 | 9 | GRIN1_chr9_137134154_137173756 | GRIN1 | copy fasta | chr9 | 137134154 | 137173756 |
| a0001c0003 | 0/0 | 2817 | 15 | 2 | 0 | 10 | 0 | 3 | GRIN1_chr9_137134154_137173756 | GRIN1 | copy fasta | chr9 | 137134154 | 137173756 |
| a0001c0004 | 0/0 | 2817 | 5 | 0 | 0 | 5 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | copy fasta | chr9 | 137134154 | 137173756 |
| a0001c0005 | 0/0 | 2817 | 4 | 4 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | copy fasta | chr9 | 137134154 | 137173756 |
| a0001c0006 | 0/0 | 2817 | 2 | 2 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | copy fasta | chr9 | 137134154 | 137173756 |
| a0001c0007 | 0/0 | 2817 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | copy fasta | chr9 | 137134154 | 137173756 |
| a0001c0008 | 0/0 | 2817 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | copy fasta | chr9 | 137134154 | 137173756 |
| a0001c0009 | 0/0 | 2817 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | copy fasta | chr9 | 137134154 | 137173756 |
| a0001c0010 | 0/0 | 2817 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | copy fasta | chr9 | 137134154 | 137173756 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 4379 | 234 | 84 | 45 | 65 | 10 | 29 | GRIN1_chr9_137134154_137173756 | GRIN1 | copy fasta | chr9 | 137134154 | 137173756 |
| a0001c0001t0003 | 0/0 | 4379 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | copy fasta | chr9 | 137134154 | 137173756 |
| a0001c0001t0004 | 0/0 | 4379 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | copy fasta | chr9 | 137134154 | 137173756 |
| a0001c0002t0001 | 0/1 | 4379 | 32 | 1 | 16 | 0 | 5 | 9 | GRIN1_chr9_137134154_137173756 | GRIN1 | copy fasta | chr9 | 137134154 | 137173756 |
| a0001c0003t0001 | 0/0 | 4379 | 15 | 2 | 0 | 10 | 0 | 3 | GRIN1_chr9_137134154_137173756 | GRIN1 | copy fasta | chr9 | 137134154 | 137173756 |
| a0001c0004t0001 | 0/0 | 4379 | 5 | 0 | 0 | 5 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | copy fasta | chr9 | 137134154 | 137173756 |
| a0001c0005t0001 | 0/0 | 4379 | 2 | 2 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | copy fasta | chr9 | 137134154 | 137173756 |
| a0001c0005t0002 | 0/0 | 4379 | 2 | 2 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | copy fasta | chr9 | 137134154 | 137173756 |
| a0001c0006t0001 | 0/0 | 4379 | 2 | 2 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | copy fasta | chr9 | 137134154 | 137173756 |
| a0001c0007t0001 | 0/0 | 4379 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | copy fasta | chr9 | 137134154 | 137173756 |
| a0001c0008t0001 | 0/0 | 4379 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | copy fasta | chr9 | 137134154 | 137173756 |
| a0001c0009t0001 | 0/0 | 4379 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | copy fasta | chr9 | 137134154 | 137173756 |
| a0001c0010t0001 | 0/0 | 4379 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | copy fasta | chr9 | 137134154 | 137173756 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0098 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0003g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0004g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0002t0001g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0002t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0002t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0002t0001g0020 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0003t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0003t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0003t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0003t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0003t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0003t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0003t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0003t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0003t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0003t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0003t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0003t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0004t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0004t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0004t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0004t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0004t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0005t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0005t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0005t0002g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0006t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0006t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0007t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0008t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0009t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0010t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0206 | EUR | GBR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0015 | EUR | GBR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0200 | EUR | GBR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0247 | EUR | GBR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0020 | EUR | FIN | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0142 | EUR | FIN | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | CHS | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | CHS | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | CHS | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | CHS | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | CHS | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | CHS | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | CHS | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | CHS | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0018 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | CHS | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | CHS | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0166 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0179 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0171 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0189 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0182 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0148 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0018 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0176 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0185 | AMR | CLM | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0164 | AMR | CLM | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | CLM | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0186 | AMR | CLM | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | CLM | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | CLM | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0144 | EUR | IBS | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0194 | EUR | IBS | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0095 | EUR | IBS | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0191 | EUR | IBS | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0193 | EUR | IBS | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0190 | EUR | IBS | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | ACB | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | ACB | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01928 | hp1 | a0001 | c0008 | t0001 | g0225 | AMR | PEL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PEL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PEL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0017 | AMR | PEL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PEL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02015 | hp1 | a0001 | c0003 | t0001 | g0240 | EAS | KHV | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02040 | hp1 | a0001 | c0003 | t0001 | g0050 | EAS | KHV | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02055 | hp1 | a0001 | c0006 | t0001 | g0127 | AFR | ACB | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02056 | hp1 | a0001 | c0010 | t0001 | g0049 | EAS | KHV | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02056 | hp2 | a0001 | c0003 | t0001 | g0218 | EAS | KHV | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02080 | hp2 | a0001 | c0004 | t0001 | g0040 | EAS | KHV | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02083 | hp1 | a0001 | c0003 | t0001 | g0244 | EAS | KHV | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | KHV | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | KHV | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | ACB | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CDX | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | CDX | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | ACB | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | ACB | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | ACB | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | PEL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | ACB | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PEL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0163 | AMR | PEL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0165 | AMR | PEL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02602 | hp2 | a0001 | c0003 | t0001 | g0138 | SAS | PJL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02717 | hp1 | a0001 | c0005 | t0002 | g0022 | AFR | GWD | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | GWD | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0252 | SAS | PJL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0188 | SAS | PJL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02809 | hp2 | a0001 | c0005 | t0001 | g0205 | AFR | GWD | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02818 | hp1 | a0001 | c0007 | t0001 | g0261 | AFR | GWD | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | GWD | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | GWD | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02896 | hp2 | a0001 | c0003 | t0001 | g0196 | AFR | GWD | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02897 | hp1 | a0001 | c0003 | t0001 | g0195 | AFR | GWD | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ESN | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02922 | hp2 | a0001 | c0006 | t0001 | g0130 | AFR | ESN | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ESN | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ESN | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ESN | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ESN | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | ESN | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ESN | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0150 | SAS | PJL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | GWD | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ESN | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ESN | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ESN | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ESN | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ESN | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03209 | hp2 | a0001 | c0005 | t0001 | g0078 | AFR | MSL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | MSL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | MSL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0201 | SAS | PJL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | MSL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | MSL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0019 | SAS | PJL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0181 | SAS | PJL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0254 | SAS | PJL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0019 | SAS | PJL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ESN | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | GWD | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | MSL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0255 | SAS | PJL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0169 | SAS | PJL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | STU | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | STU | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0180 | SAS | PJL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0266 | SAS | BEB | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | BEB | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | BEB | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03834 | hp2 | a0001 | c0003 | t0001 | g0139 | SAS | BEB | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | BEB | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | BEB | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | BEB | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03942 | hp2 | a0001 | c0003 | t0001 | g0137 | SAS | BEB | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0145 | SAS | STU | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | STU | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | STU | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | STU | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | STU | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | STU | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | STU | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | STU | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | YRI | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | YRI | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | CHB | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | CHB | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | YRI | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | YRI | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA18942 | hp2 | a0001 | c0003 | t0001 | g0262 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA18952 | hp2 | a0001 | c0004 | t0001 | g0087 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA18960 | hp1 | a0001 | c0003 | t0001 | g0217 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA18980 | hp1 | a0001 | c0003 | t0001 | g0239 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA18985 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA19004 | hp1 | a0001 | c0004 | t0001 | g0086 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | LWK | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | LWK | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | LWK | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | LWK | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA19058 | hp2 | a0001 | c0003 | t0001 | g0032 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA19060 | hp1 | a0001 | c0001 | t0004 | g0119 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA19060 | hp2 | a0001 | c0004 | t0001 | g0085 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA19087 | hp1 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA19091 | hp2 | a0001 | c0004 | t0001 | g0069 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | YRI | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0198 | AFR | YRI | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | ASW | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ASW | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0173 | EUR | TSI | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0017 | EUR | TSI | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0232 | EUR | TSI | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0214 | EUR | TSI | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA20905 | hp1 | a0001 | c0009 | t0001 | g0174 | SAS | GIH | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | GIH | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0203 | AMR | CLM | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02559 | hp1 | a0001 | c0005 | t0002 | g0022 | AFR | ACB | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | MSL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | USA | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | USA | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | USA | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | USA | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | LWK | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | LWK | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0020 | REF | REF | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0098 | REF | REF | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:137139732
|
C | T | 1 | a0001c0010 | 1 | HG02056.hp1 | synonymous_variant | LOW | c.246C>T | p.Leu82Leu | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 1/20 | 579/4379 | 246/2817 | 82/938 | chr9 | 137139732 | ||
| chr9:137145857
|
G | A | 1 | a0001c0007 | 1 | HG02818.hp1 | synonymous_variant | LOW | c.525G>A | p.Ala175Ala | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 3/20 | 858/4379 | 525/2817 | 175/938 | chr9 | 137145857 | ||
| chr9:137156690
|
A | C | 1 | a0001c0009 | 1 | NA20905.hp1 | synonymous_variant | LOW | c.693A>C | p.Val231Val | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 5/20 | 1026/4379 | 693/2817 | 231/938 | chr9 | 137156690 | ||
| chr9:137156765
|
G | C | 1 | a0001c0004 | 5 | HG02080.hp2 NA18952.hp2 NA19004.hp1 others(2): Show |
synonymous_variant | LOW | c.768G>C | p.Gly256Gly | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 5/20 | 1101/4379 | 768/2817 | 256/938 | chr9 | 137156765 | ||
| chr9:137156786
|
A | G | 2 | a0001c0002a0001c0009 | 33 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(30): Show |
synonymous_variant | LOW | c.789A>G | p.Pro263Pro | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 5/20 | 1122/4379 | 789/2817 | 263/938 | chr9 | 137156786 | ||
| chr9:137156924
|
G | A | 2 | a0001c0002a0001c0009 | 33 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(30): Show |
synonymous_variant | LOW | c.855G>A | p.Val285Val | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 6/20 | 1188/4379 | 855/2817 | 285/938 | chr9 | 137156924 | ||
| chr9:137162004
|
G | A | 1 | a0001c0003 | 15 | HG02015.hp1 HG02040.hp1 HG02056.hp2 others(12): Show |
synonymous_variant | LOW | c.1548G>A | p.Pro516Pro | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 11/20 | 1881/4379 | 1548/2817 | 516/938 | chr9 | 137162004 | ||
| chr9:137162040
|
G | A | 1 | a0001c0006 | 2 | HG02055.hp1 HG02922.hp2 |
synonymous_variant | LOW | c.1584G>A | p.Glu528Glu | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 11/20 | 1917/4379 | 1584/2817 | 528/938 | chr9 | 137162040 | ||
| chr9:137162461
|
G | C | 1 | a0001c0007 | 1 | HG02818.hp1 | synonymous_variant | LOW | c.1809G>C | p.Leu603Leu | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 13/20 | 2142/4379 | 1809/2817 | 603/938 | chr9 | 137162461 | ||
| chr9:137162464
|
C | T | 1 | a0001c0008 | 1 | HG01928.hp1 | synonymous_variant | LOW | c.1812C>T | p.Ser604Ser | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 13/20 | 2145/4379 | 1812/2817 | 604/938 | chr9 | 137162464 | ||
| chr9:137163238
|
G | C | 1 | a0001c0005 | 4 | HG02559.hp1 HG02717.hp1 HG02809.hp2 others(1): Show |
synonymous_variant | LOW | c.2241G>C | p.Val747Val | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 16/20 | 2574/4379 | 2241/2817 | 747/938 | chr9 | 137163238 | ||
| chr9:137163241
|
G | C | 1 | a0001c0005 | 4 | HG02559.hp1 HG02717.hp1 HG02809.hp2 others(1): Show |
synonymous_variant | LOW | c.2244G>C | p.Thr748Thr | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 16/20 | 2577/4379 | 2244/2817 | 748/938 | chr9 | 137163241 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:137167535
|
C | T | 1 | a0001c0001t0004 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 20/20 | 8 | chr9 | 137167535 | |||||
| chr9:137168440
|
T | G | 1 | a0001c0005t0002 | 2 | HG02559.hp1 HG02717.hp1 |
3_prime_UTR_variant | MODIFIER | c.*913T>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 20/20 | 913 | chr9 | 137168440 | |||||
| chr9:137168624
|
C | G | 1 | a0001c0001t0003 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1097C>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 20/20 | 1097 | chr9 | 137168624 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:137139799
|
A | G | 1 | a0001c0001t0001g0276 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.258+55A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 1/19 | chr9 | 137139799 | ||||||
| chr9:137139832
|
C | T | 2 | a0001c0001t0001g0274a0001c0001t0001g0275 | 2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.258+88C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 1/19 | chr9 | 137139832 | ||||||
| chr9:137139844
|
G | GT | 6 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(3): Show | 6 | HG00423.hp1 HG02273.hp2 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.258+101dupT | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr9 | 137139844 | |||||
| chr9:137139948
|
T | A | 4 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(1): Show | 4 | HG01891.hp2 HG02280.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.258+204T>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 1/19 | chr9 | 137139948 | ||||||
| chr9:137139979
|
C | T | 63 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(60): Show | 64 | HG00140.hp2 HG00423.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.258+235C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 1/19 | chr9 | 137139979 | ||||||
| chr9:137140083
|
T | C | 63 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(60): Show | 64 | HG00140.hp2 HG00423.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.258+339T>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 1/19 | chr9 | 137140083 | ||||||
| chr9:137140176
|
C | T | 2 | a0001c0001t0001g0266a0001c0001t0001g0267 | 2 | HG00609.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.258+432C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 1/19 | chr9 | 137140176 | ||||||
| chr9:137140385
|
G | A | 2 | a0001c0001t0001g0027a0001c0001t0001g0028 | 2 | NA18980.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.258+641G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 1/19 | chr9 | 137140385 | ||||||
| chr9:137140399
|
G | T | 1 | a0001c0001t0001g0215 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.258+655G>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 1/19 | chr9 | 137140399 | ||||||
| chr9:137140551
|
C | G | 2 | a0001c0001t0001g0213a0001c0001t0001g0214 | 2 | HG03834.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.258+807C>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 1/19 | chr9 | 137140551 | ||||||
| chr9:137140559
|
A | G | 4 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0211others(1): Show | 4 | HG00597.hp1 HG02080.hp1 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.258+815A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 1/19 | chr9 | 137140559 | ||||||
| chr9:137140627
|
A | G | 1 | a0001c0001t0001g0208 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.258+883A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 1/19 | chr9 | 137140627 | ||||||
| chr9:137140812
|
C | T | 1 | a0001c0001t0001g0207 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.258+1068C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 1/19 | chr9 | 137140812 | ||||||
| chr9:137140816
|
A | G | 2 | a0001c0001t0001g0021a0001c0001t0001g0206 | 3 | HG00099.hp1 HG01175.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.258+1072A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 1/19 | chr9 | 137140816 | ||||||
| chr9:137141280
|
A | C | 113 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(110): Show | 118 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.259-733A>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 1/19 | chr9 | 137141280 | ||||||
| chr9:137141327
|
C | T | 1 | a0001c0001t0001g0265 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.259-686C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 1/19 | chr9 | 137141327 | ||||||
| chr9:137141449
|
C | A | 1 | a0001c0001t0001g0029 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.259-564C>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 1/19 | chr9 | 137141449 | ||||||
| chr9:137141591
|
G | T | 1 | a0001c0005t0001g0205 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.259-422G>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 1/19 | chr9 | 137141591 | ||||||
| chr9:137141643
|
G | A | 31 | a0001c0001t0001g0216a0001c0001t0001g0219a0001c0001t0001g0220others(28): Show | 31 | HG00423.hp1 HG00609.hp1 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.259-370G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 1/19 | chr9 | 137141643 | ||||||
| chr9:137141810
|
G | A | 6 | a0001c0001t0001g0167a0001c0002t0001g0017a0001c0002t0001g0163others(3): Show | 7 | HG00733.hp2 HG01346.hp1 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.259-203G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 1/19 | chr9 | 137141810 | ||||||
| chr9:137141872
|
G | C | 1 | a0001c0001t0001g0030 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.259-141G>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 1/19 | chr9 | 137141872 | ||||||
| chr9:137142231
|
C | A | 1 | a0001c0001t0001g0168 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.393+84C>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137142231 | ||||||
| chr9:137142303
|
G | A | 3 | a0001c0001t0001g0207a0001c0001t0001g0274a0001c0001t0001g0275 | 3 | HG02258.hp1 HG03225.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.393+156G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137142303 | ||||||
| chr9:137142459
|
TCACACAT others(4): Show |
T | 5 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0002t0001g0200others(2): Show | 5 | HG00140.hp1 HG01123.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.393+327_393+337del others(11): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 137142459 | |||||
| chr9:137142488
|
C | T | 2 | a0001c0001t0001g0199a0001c0002t0001g0198 | 2 | HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.393+341C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137142488 | ||||||
| chr9:137142577
|
C | A | 43 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0170others(40): Show | 47 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.393+430C>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137142577 | ||||||
| chr9:137142809
|
C | G | 104 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(101): Show | 109 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.393+662C>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137142809 | ||||||
| chr9:137142893
|
C | T | 5 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(2): Show | 5 | HG02647.hp1 HG02723.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.393+746C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137142893 | ||||||
| chr9:137142902
|
G | A | 3 | a0001c0001t0001g0207a0001c0001t0001g0274a0001c0001t0001g0275 | 3 | HG02258.hp1 HG03225.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.393+755G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137142902 | ||||||
| chr9:137143060
|
C | G | 3 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154 | 3 | HG01884.hp1 HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.393+913C>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137143060 | ||||||
| chr9:137143265
|
C | G | 3 | a0001c0001t0001g0207a0001c0001t0001g0274a0001c0001t0001g0275 | 3 | HG02258.hp1 HG03225.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.393+1118C>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137143265 | ||||||
| chr9:137143353
|
C | T | 4 | a0001c0001t0001g0263a0001c0001t0001g0264a0001c0003t0001g0262others(1): Show | 4 | HG02818.hp1 HG02976.hp1 NA18939.hp1 others(1): Show |
intron_variant | MODIFIER | c.393+1206C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137143353 | ||||||
| chr9:137143494
|
C | T | 15 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0030others(12): Show | 16 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(13): Show |
intron_variant | MODIFIER | c.393+1347C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137143494 | ||||||
| chr9:137143529
|
G | T | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.393+1382G>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137143529 | ||||||
| chr9:137143531
|
G | A | 38 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0215others(35): Show | 38 | HG00423.hp1 HG00609.hp1 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.393+1384G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137143531 | ||||||
| chr9:137143649
|
C | T | 48 | a0001c0001t0001g0140a0001c0001t0001g0167a0001c0001t0001g0168others(45): Show | 52 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.393+1502C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137143649 | ||||||
| chr9:137143865
|
G | C | 1 | a0001c0001t0001g0142 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.393+1718G>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137143865 | ||||||
| chr9:137143947
|
A | G | 101 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(98): Show | 105 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.394-1779A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137143947 | ||||||
| chr9:137143989
|
G | T | 15 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0030others(12): Show | 16 | HG00099.hp2 HG00558.hp2 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.394-1737G>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137143989 | ||||||
| chr9:137144095
|
C | T | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | HG01496.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.394-1631C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144095 | ||||||
| chr9:137144175
|
G | A | 3 | a0001c0001t0001g0207a0001c0001t0001g0274a0001c0001t0001g0275 | 3 | HG02258.hp1 HG03225.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.394-1551G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144175 | ||||||
| chr9:137144259
|
A | G | 7 | a0001c0001t0001g0151a0001c0001t0001g0268a0001c0001t0001g0269others(4): Show | 7 | HG00423.hp1 HG00558.hp2 HG02273.hp2 others(4): Show |
intron_variant | MODIFIER | c.394-1467A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144259 | ||||||
| chr9:137144312
|
ATGGTGGG others(52): Show |
A | 5 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG01891.hp2 HG02280.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.394-1410_394-1352d others(61): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 137144312 | |||||
| chr9:137144350
|
T | G | 60 | a0001c0001t0001g0033a0001c0001t0001g0140a0001c0001t0001g0168others(57): Show | 66 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.394-1376T>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144350 | ||||||
| chr9:137144377
|
G | A | 2 | a0001c0003t0001g0137a0001c0003t0001g0138 | 2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.394-1349G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144377 | ||||||
| chr9:137144382
|
C | T | 42 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(39): Show | 45 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.394-1344C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144382 | ||||||
| chr9:137144383
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.394-1343G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144383 | ||||||
| chr9:137144392
|
C | T | 1 | a0001c0001t0001g0234 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.394-1334C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144392 | ||||||
| chr9:137144420
|
C | A | 1 | a0001c0001t0001g0035 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.394-1306C>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144420 | ||||||
| chr9:137144425
|
C | T | 1 | a0001c0001t0001g0208 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.394-1301C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144425 | ||||||
| chr9:137144426
|
G | A | 3 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0005t0001g0205 | 3 | HG02572.hp2 HG02809.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.394-1300G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144426 | ||||||
| chr9:137144429
|
C | T | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | HG00673.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.394-1297C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144429 | ||||||
| chr9:137144436
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.394-1290C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144436 | ||||||
| chr9:137144457
|
A | C | 1 | a0001c0001t0001g0208 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.394-1269A>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144457 | ||||||
| chr9:137144465
|
T | C | 11 | a0001c0001t0001g0038a0001c0001t0001g0111a0001c0001t0001g0112others(8): Show | 11 | HG00140.hp1 HG00738.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.394-1261T>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144465 | ||||||
| chr9:137144468
|
T | C | 21 | a0001c0001t0001g0030a0001c0001t0001g0038a0001c0001t0001g0039others(18): Show | 22 | HG00140.hp1 HG00738.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.394-1258T>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144468 | ||||||
| chr9:137144470
|
C | T | 11 | a0001c0001t0001g0038a0001c0001t0001g0111a0001c0001t0001g0112others(8): Show | 11 | HG00140.hp1 HG00738.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.394-1256C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144470 | ||||||
| chr9:137144482
|
A | G | 5 | a0001c0001t0001g0109a0001c0001t0001g0207a0001c0001t0001g0264others(2): Show | 5 | HG02258.hp1 HG02976.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.394-1244A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144482 | ||||||
| chr9:137144501
|
A | T | 1 | a0001c0001t0001g0212 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.394-1225A>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144501 | ||||||
| chr9:137144511
|
C | T | 2 | a0001c0001t0001g0107a0001c0001t0001g0108 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.394-1215C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144511 | ||||||
| chr9:137144516
|
G | A | 4 | a0001c0001t0001g0141a0001c0001t0001g0184a0001c0001t0001g0274others(1): Show | 4 | HG01168.hp2 HG02258.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.394-1210G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144516 | ||||||
| chr9:137144518
|
G | A | 1 | a0001c0002t0001g0169 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.394-1208G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144518 | ||||||
| chr9:137144523
|
C | T | 8 | a0001c0001t0001g0014a0001c0001t0001g0102a0001c0001t0001g0103others(5): Show | 9 | HG01934.hp1 HG02965.hp1 HG03579.hp2 others(6): Show |
intron_variant | MODIFIER | c.394-1203C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144523 | ||||||
| chr9:137144524
|
G | A | 12 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(9): Show | 13 | HG00438.hp1 HG00544.hp1 HG00544.hp2 others(10): Show |
intron_variant | MODIFIER | c.394-1202G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144524 | ||||||
| chr9:137144527
|
C | T | 11 | a0001c0001t0001g0045a0001c0001t0001g0131a0001c0001t0001g0207others(8): Show | 12 | HG00733.hp2 HG01261.hp1 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.394-1199C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144527 | ||||||
| chr9:137144528
|
G | A | 1 | a0001c0001t0001g0250 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.394-1198G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144528 | ||||||
| chr9:137144538
|
T | C | 27 | a0001c0001t0001g0039a0001c0001t0001g0041a0001c0001t0001g0042others(24): Show | 28 | HG00438.hp1 HG00544.hp1 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.394-1188T>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144538 | ||||||
| chr9:137144547
|
T | C | 9 | a0001c0001t0001g0033a0001c0001t0001g0207a0001c0001t0001g0215others(6): Show | 9 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.394-1179T>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144547 | ||||||
| chr9:137144571
|
T | C | 1 | a0001c0001t0001g0168 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.394-1155T>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144571 | ||||||
| chr9:137144572
|
G | A | 21 | a0001c0001t0001g0033a0001c0001t0001g0135a0001c0001t0001g0168others(18): Show | 22 | HG01109.hp1 HG01884.hp2 HG02015.hp1 others(19): Show |
intron_variant | MODIFIER | c.394-1154G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144572 | ||||||
| chr9:137144587
|
G | A | 1 | a0001c0001t0001g0274 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.394-1139G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144587 | ||||||
| chr9:137144592
|
C | T | 3 | a0001c0001t0001g0255a0001c0001t0001g0274a0001c0005t0001g0205 | 3 | HG02258.hp1 HG02809.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.394-1134C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144592 | ||||||
| chr9:137144603
|
C | T | 1 | a0001c0001t0001g0275 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.394-1123C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144603 | ||||||
| chr9:137144606
|
G | A | 1 | a0001c0001t0001g0206 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.394-1120G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144606 | ||||||
| chr9:137144608
|
T | TTGCGCCA others(1): Show |
6 | a0001c0003t0001g0001a0001c0003t0001g0032a0001c0003t0001g0239others(3): Show | 7 | HG02015.hp1 HG02083.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.394-1115_394-1114i others(10): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 137144608 | |||||
| chr9:137144643
|
TA | T | 6 | a0001c0001t0001g0184a0001c0001t0001g0212a0001c0001t0001g0264others(3): Show | 6 | HG00597.hp1 HG01167.hp2 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.394-1069delA | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 137144643 | |||||
| chr9:137144680
|
A | C | 1 | a0001c0001t0001g0267 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.394-1046A>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144680 | ||||||
| chr9:137144694
|
GGAGGGGG others(110): Show |
G | 1 | a0001c0001t0001g0048 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.394-996_394-880del | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 137144694 | |||||
| chr9:137144694
|
GGAGGGGG others(685): Show |
G | 1 | a0001c0001t0001g0249 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.394-996_394-305del | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 137144694 | |||||
| chr9:137144695
|
G | GAGGGGGT others(50): Show |
1 | a0001c0002t0001g0201 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.394-999_394-998ins others(57): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 137144695 | |||||
| chr9:137144695
|
GAGGGGGT others(226): Show |
G | 1 | a0001c0001t0001g0041 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.394-1014_394-782de others(1): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 137144695 | |||||
| chr9:137144696
|
AG | A | 7 | a0001c0001t0001g0135a0001c0001t0001g0243a0001c0001t0001g0256others(4): Show | 7 | HG02258.hp2 HG02717.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.394-1025delG | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 137144696 | |||||
| chr9:137144705
|
C | A | 1 | a0001c0001t0001g0212 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.394-1021C>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144705 | ||||||
| chr9:137144706
|
A | G | 1 | a0001c0001t0001g0212 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.394-1020A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144706 | ||||||
| chr9:137144708
|
GGTCTAGA others(169): Show |
G | 14 | a0001c0001t0001g0014a0001c0001t0001g0043a0001c0001t0001g0044others(11): Show | 15 | HG00544.hp1 HG00544.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.394-986_394-811del | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 137144708 | |||||
| chr9:137144712
|
T | C | 7 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0042others(4): Show | 9 | HG02056.hp1 HG02165.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.394-1014T>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144712 | ||||||
| chr9:137144712
|
T | TAGAAAGT others(335): Show |
1 | a0001c0001t0001g0252 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.394-940_394-939ins others(342): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 137144712 | |||||
| chr9:137144712
|
T | TAGAAAGT others(223): Show |
2 | a0001c0001t0001g0011a0001c0001t0001g0101 | 3 | HG00642.hp2 HG01192.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.394-997_394-996ins others(230): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 137144712 | |||||
| chr9:137144712
|
TAGAAAGT others(50): Show |
T | 1 | a0001c0002t0001g0180 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.394-996_394-940del others(57): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 137144712 | |||||
| chr9:137144712
|
TAGAAAGT others(226): Show |
T | 6 | a0001c0001t0001g0003a0001c0001t0001g0136a0001c0001t0001g0155others(3): Show | 7 | HG02572.hp1 HG02723.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.394-998_394-766del | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 137144712 | |||||
| chr9:137144725
|
C | CAG | 6 | a0001c0001t0001g0036a0001c0001t0001g0042a0001c0001t0001g0055others(3): Show | 6 | HG02083.hp1 HG02165.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.394-1000_394-999du others(3): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 137144725 | |||||
| chr9:137144727
|
GGGGTGTG others(167): Show |
G | 1 | a0001c0001t0001g0054 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.394-998_394-825del | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144727 | ||||||
| chr9:137144727
|
GGGGTGTG others(281): Show |
G | 2 | a0001c0003t0001g0001a0001c0003t0001g0032 | 3 | NA18985.hp2 NA19058.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.394-998_394-711del | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144727 | ||||||
| chr9:137144728
|
G | A | 25 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0051others(22): Show | 26 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.394-998G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144728 | ||||||
| chr9:137144730
|
G | T | 1 | a0001c0002t0001g0181 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.394-996G>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144730 | ||||||
| chr9:137144731
|
T | G | 28 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0051others(25): Show | 29 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(26): Show |
intron_variant | MODIFIER | c.394-995T>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144731 | ||||||
| chr9:137144731
|
T | TGTGGGGA others(166): Show |
2 | a0001c0003t0001g0137a0001c0003t0001g0138 | 2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.394-958_394-957ins others(173): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 137144731 | |||||
| chr9:137144731
|
TGTGGGGA others(397): Show |
T | 1 | a0001c0001t0001g0026 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.394-986_394-583del | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 137144731 | |||||
| chr9:137144731
|
TGTGGGGA others(511): Show |
T | 1 | a0001c0001t0001g0039 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.394-941_394-424del | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 137144731 | |||||
| chr9:137144740
|
A | C | 26 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0029others(23): Show | 28 | HG01109.hp1 HG01192.hp1 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.394-986A>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144740 | ||||||
| chr9:137144743
|
A | G | 27 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0029others(24): Show | 29 | HG01109.hp1 HG01192.hp1 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.394-983A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144743 | ||||||
| chr9:137144743
|
AGTGAGAG others(169): Show |
A | 3 | a0001c0001t0001g0206a0001c0001t0001g0245a0001c0001t0001g0268 | 3 | HG00099.hp1 HG02280.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.394-941_394-766del | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 137144743 | |||||
| chr9:137144743
|
AGTGAGAG others(454): Show |
A | 1 | a0001c0001t0001g0170 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.394-941_394-481del | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 137144743 | |||||
| chr9:137144747
|
A | G | 1 | a0001c0002t0001g0181 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.394-979A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144747 | ||||||
| chr9:137144752
|
A | G | 1 | a0001c0002t0001g0181 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.394-974A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144752 | ||||||
| chr9:137144754
|
GGGGGTCC others(111): Show |
G | 1 | a0001c0001t0001g0109 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.394-967_394-850del | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 137144754 | |||||
| chr9:137144765
|
GGTCCAGA others(112): Show |
G | 9 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0053others(6): Show | 10 | HG00099.hp2 HG00558.hp2 HG00673.hp1 others(7): Show |
intron_variant | MODIFIER | c.394-957_394-839del | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 137144765 | |||||
| chr9:137144769
|
C | T | 8 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0202others(5): Show | 8 | HG00140.hp1 HG01123.hp2 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.394-957C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144769 | ||||||
| chr9:137144769
|
CAGAAAGT others(112): Show |
C | 142 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(139): Show | 154 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.394-939_394-821del | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 137144769 | |||||
| chr9:137144769
|
CAGAAAGT others(397): Show |
C | 8 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0033others(5): Show | 10 | HG01243.hp2 HG01261.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.394-939_394-536del | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 137144769 | |||||
| chr9:137144784
|
GGGTGGTA others(110): Show |
G | 5 | a0001c0001t0001g0102a0001c0001t0001g0197a0001c0001t0001g0275others(2): Show | 5 | HG01109.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.394-941_394-825del | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144784 | ||||||
| chr9:137144784
|
GGGTGGTA others(395): Show |
G | 1 | a0001c0001t0001g0057 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.394-941_394-540del | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144784 | ||||||
| chr9:137144785
|
G | A | 25 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0135others(22): Show | 26 | HG02015.hp1 HG02083.hp1 HG02135.hp2 others(23): Show |
intron_variant | MODIFIER | c.394-941G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144785 | ||||||
| chr9:137144785
|
GGTGGTAG others(169): Show |
G | 5 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(2): Show | 5 | HG01516.hp2 HG01517.hp2 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.394-939_394-764del | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 137144785 | |||||
| chr9:137144785
|
GGTGGTAG others(283): Show |
G | 1 | a0001c0006t0001g0130 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.394-939_394-650del | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 137144785 | |||||
| chr9:137144785
|
GGTGGTAG others(454): Show |
G | 1 | a0001c0001t0001g0233 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.394-939_394-479del | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 137144785 | |||||
| chr9:137144786
|
GTGGTAGG others(168): Show |
G | 1 | a0001c0001t0001g0094 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.394-939_394-765del | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144786 | ||||||
| chr9:137144787
|
T | G | 51 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0070others(48): Show | 53 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.394-939T>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144787 | ||||||
| chr9:137144788
|
G | T | 26 | a0001c0001t0001g0070a0001c0001t0001g0089a0001c0001t0001g0090others(23): Show | 27 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.394-938G>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144788 | ||||||
| chr9:137144791
|
A | G | 62 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0024others(59): Show | 64 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.394-935A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144791 | ||||||
| chr9:137144797
|
A | C | 31 | a0001c0001t0001g0070a0001c0001t0001g0089a0001c0001t0001g0090others(28): Show | 32 | HG00642.hp1 HG00735.hp1 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.394-929A>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144797 | ||||||
| chr9:137144800
|
G | A | 20 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0140others(17): Show | 21 | HG00140.hp1 HG01123.hp2 HG02015.hp1 others(18): Show |
intron_variant | MODIFIER | c.394-926G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144800 | ||||||
| chr9:137144804
|
G | A | 51 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0070others(48): Show | 53 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.394-922G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144804 | ||||||
| chr9:137144807
|
GACA | G | 37 | a0001c0001t0001g0002a0001c0001t0001g0070a0001c0001t0001g0089others(34): Show | 38 | HG00140.hp1 HG01069.hp1 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.394-918_394-916del others(3): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144807 | ||||||
| chr9:137144807
|
GACACGAG others(55): Show |
G | 8 | a0001c0001t0001g0042a0001c0001t0001g0143a0001c0001t0001g0183others(5): Show | 8 | HG00735.hp1 HG01123.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.394-918_394-857del others(62): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144807 | ||||||
| chr9:137144808
|
A | G | 6 | a0001c0001t0001g0135a0001c0002t0001g0018a0001c0002t0001g0150others(3): Show | 7 | HG00642.hp1 HG01175.hp1 HG02015.hp1 others(4): Show |
intron_variant | MODIFIER | c.394-918A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144808 | ||||||
| chr9:137144809
|
C | A | 6 | a0001c0001t0001g0135a0001c0002t0001g0018a0001c0002t0001g0150others(3): Show | 7 | HG00642.hp1 HG01175.hp1 HG02015.hp1 others(4): Show |
intron_variant | MODIFIER | c.394-917C>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144809 | ||||||
| chr9:137144811
|
C | G | 54 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0024others(51): Show | 56 | HG00140.hp1 HG00642.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.394-915C>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144811 | ||||||
| chr9:137144812
|
G | A | 37 | a0001c0001t0001g0002a0001c0001t0001g0070a0001c0001t0001g0089others(34): Show | 38 | HG00140.hp1 HG01069.hp1 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.394-914G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144812 | ||||||
| chr9:137144812
|
G | GGGGTCCC others(47): Show |
1 | a0001c0002t0001g0150 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.394-914_394-913ins others(54): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144812 | ||||||
| chr9:137144812
|
G | GGGGTCCC others(104): Show |
1 | a0001c0002t0001g0018 | 2 | HG00642.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.394-914_394-913ins others(111): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144812 | ||||||
| chr9:137144812
|
G | GGGGTCCC others(47): Show |
1 | a0001c0003t0001g0262 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.394-914_394-913ins others(54): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144812 | ||||||
| chr9:137144812
|
G | GGGGTCCC others(104): Show |
1 | a0001c0003t0001g0240 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.394-914_394-913ins others(111): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144812 | ||||||
| chr9:137144812
|
G | GGGGTCCC others(104): Show |
1 | a0001c0002t0001g0163 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.394-914_394-913ins others(111): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144812 | ||||||
| chr9:137144812
|
G | GGGGTCCC others(218): Show |
1 | a0001c0001t0001g0135 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.394-914_394-913ins others(225): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144812 | ||||||
| chr9:137144825
|
GGTCTAGA others(52): Show |
G | 4 | a0001c0001t0001g0025a0001c0001t0001g0031a0001c0001t0001g0187others(1): Show | 4 | HG02630.hp2 HG03017.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.394-879_394-821del others(59): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 137144825 | |||||
| chr9:137144829
|
T | C | 34 | a0001c0001t0001g0002a0001c0001t0001g0070a0001c0001t0001g0089others(31): Show | 36 | HG00140.hp1 HG00642.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.394-897T>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144829 | ||||||
| chr9:137144829
|
T | TAGAAAGT others(50): Show |
1 | a0001c0001t0001g0252 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.394-880_394-879ins others(57): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 137144829 | |||||
| chr9:137144829
|
TAGAAAGT others(109): Show |
T | 1 | a0001c0001t0001g0159 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.394-881_394-766del | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 137144829 | |||||
| chr9:137144844
|
GGGTGGCA others(50): Show |
G | 5 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(2): Show | 5 | HG02258.hp2 HG02717.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.394-881_394-825del others(57): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144844 | ||||||
| chr9:137144845
|
G | A | 32 | a0001c0001t0001g0002a0001c0001t0001g0070a0001c0001t0001g0089others(29): Show | 34 | HG00642.hp1 HG01069.hp1 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.394-881G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144845 | ||||||
| chr9:137144845
|
GGTGGCAG others(223): Show |
G | 3 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0126 | 3 | HG01891.hp2 HG02280.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.394-879_394-650del | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 137144845 | |||||
| chr9:137144847
|
T | G | 38 | a0001c0001t0001g0002a0001c0001t0001g0070a0001c0001t0001g0089others(35): Show | 40 | HG00140.hp1 HG00642.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.394-879T>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144847 | ||||||
| chr9:137144848
|
G | T | 6 | a0001c0001t0001g0112a0001c0001t0001g0250a0001c0001t0001g0254others(3): Show | 6 | HG00140.hp1 HG03491.hp2 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.394-878G>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144848 | ||||||
| chr9:137144849
|
G | T | 1 | a0001c0003t0001g0139 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.394-877G>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144849 | ||||||
| chr9:137144850
|
C | G | 1 | a0001c0003t0001g0139 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.394-876C>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144850 | ||||||
| chr9:137144850
|
C | T | 40 | a0001c0001t0001g0002a0001c0001t0001g0070a0001c0001t0001g0089others(37): Show | 42 | HG00140.hp1 HG00642.hp1 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.394-876C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144850 | ||||||
| chr9:137144851
|
A | G | 40 | a0001c0001t0001g0002a0001c0001t0001g0070a0001c0001t0001g0089others(37): Show | 42 | HG00140.hp1 HG00642.hp1 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.394-875A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144851 | ||||||
| chr9:137144854
|
G | A | 1 | a0001c0003t0001g0139 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.394-872G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144854 | ||||||
| chr9:137144855
|
A | AC | 8 | a0001c0001t0001g0135a0001c0001t0001g0140a0001c0001t0001g0250others(5): Show | 8 | HG02015.hp1 HG02083.hp1 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.394-871_394-870ins others(1): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144855 | ||||||
| chr9:137144855
|
A | C | 1 | a0001c0003t0001g0139 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.394-871A>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144855 | ||||||
| chr9:137144856
|
T | A | 2 | a0001c0001t0001g0140a0001c0001t0001g0252 | 2 | HG02735.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.394-870T>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144856 | ||||||
| chr9:137144856
|
T | C | 39 | a0001c0001t0001g0002a0001c0001t0001g0070a0001c0001t0001g0089others(36): Show | 41 | HG00140.hp1 HG00642.hp1 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.394-870T>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144856 | ||||||
| chr9:137144857
|
G | A | 32 | a0001c0001t0001g0002a0001c0001t0001g0070a0001c0001t0001g0089others(29): Show | 34 | HG00140.hp1 HG00642.hp1 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.394-869G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144857 | ||||||
| chr9:137144860
|
A | G | 9 | a0001c0001t0001g0135a0001c0001t0001g0140a0001c0001t0001g0250others(6): Show | 9 | HG02015.hp1 HG02083.hp1 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.394-866A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144860 | ||||||
| chr9:137144860
|
AT | A | 32 | a0001c0001t0001g0002a0001c0001t0001g0070a0001c0001t0001g0089others(29): Show | 34 | HG00140.hp1 HG00642.hp1 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.394-865delT | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144860 | ||||||
| chr9:137144863
|
G | A | 7 | a0001c0001t0001g0135a0001c0001t0001g0250a0001c0001t0001g0255others(4): Show | 7 | HG02015.hp1 HG02083.hp1 HG03654.hp1 others(4): Show |
intron_variant | MODIFIER | c.394-863G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144863 | ||||||
| chr9:137144863
|
G | T | 32 | a0001c0001t0001g0002a0001c0001t0001g0070a0001c0001t0001g0089others(29): Show | 34 | HG00140.hp1 HG00642.hp1 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.394-863G>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144863 | ||||||
| chr9:137144866
|
GACA | G | 7 | a0001c0001t0001g0135a0001c0001t0001g0250a0001c0001t0001g0255others(4): Show | 7 | HG02015.hp1 HG02083.hp1 HG03654.hp1 others(4): Show |
intron_variant | MODIFIER | c.394-859_394-857del others(3): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144866 | ||||||
| chr9:137144867
|
AC | A | 32 | a0001c0001t0001g0002a0001c0001t0001g0070a0001c0001t0001g0089others(29): Show | 34 | HG00140.hp1 HG00642.hp1 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.394-858delC | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144867 | ||||||
| chr9:137144869
|
A | G | 32 | a0001c0001t0001g0002a0001c0001t0001g0070a0001c0001t0001g0089others(29): Show | 34 | HG00140.hp1 HG00642.hp1 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.394-857A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144869 | ||||||
| chr9:137144870
|
C | G | 48 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0070others(45): Show | 50 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.394-856C>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144870 | ||||||
| chr9:137144871
|
G | A | 47 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0070others(44): Show | 49 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.394-855G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144871 | ||||||
| chr9:137144884
|
A | G | 50 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0070others(47): Show | 52 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.394-842A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144884 | ||||||
| chr9:137144888
|
T | C | 45 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0043others(42): Show | 47 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.394-838T>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144888 | ||||||
| chr9:137144904
|
G | A | 34 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0070others(31): Show | 36 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.394-822G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144904 | ||||||
| chr9:137144905
|
GGT | G | 10 | a0001c0001t0001g0054a0001c0001t0001g0197a0001c0001t0001g0256others(7): Show | 10 | HG01109.hp1 HG02132.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.394-817_394-816del others(2): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 137144905 | |||||
| chr9:137144907
|
T | G | 35 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0070others(32): Show | 37 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.394-819T>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144907 | ||||||
| chr9:137144916
|
C | A | 34 | a0001c0001t0001g0002a0001c0001t0001g0030a0001c0001t0001g0070others(31): Show | 36 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.394-810C>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144916 | ||||||
| chr9:137144919
|
G | A | 34 | a0001c0001t0001g0002a0001c0001t0001g0030a0001c0001t0001g0070others(31): Show | 36 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.394-807G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144919 | ||||||
| chr9:137144945
|
C | T | 4 | a0001c0001t0001g0030a0001c0001t0001g0100a0001c0001t0001g0168others(1): Show | 4 | HG01070.hp1 HG01515.hp1 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.394-781C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144945 | ||||||
| chr9:137144961
|
A | G | 22 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0016others(19): Show | 25 | HG01069.hp1 HG01070.hp1 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.394-765A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144961 | ||||||
| chr9:137144963
|
G | T | 1 | a0001c0001t0001g0094 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.394-763G>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144963 | ||||||
| chr9:137144964
|
G | T | 23 | a0001c0001t0001g0012a0001c0001t0001g0016a0001c0001t0001g0029others(20): Show | 25 | HG01069.hp1 HG01070.hp1 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.394-762G>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144964 | ||||||
| chr9:137144965
|
G | T | 1 | a0001c0001t0001g0094 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.394-761G>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144965 | ||||||
| chr9:137144966
|
T | G | 1 | a0001c0001t0001g0094 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.394-760T>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144966 | ||||||
| chr9:137144973
|
A | C | 28 | a0001c0001t0001g0012a0001c0001t0001g0016a0001c0001t0001g0029others(25): Show | 30 | HG00621.hp1 HG01069.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.394-753A>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144973 | ||||||
| chr9:137144976
|
A | AGTGAGAG others(50): Show |
2 | a0001c0001t0001g0241a0001c0003t0001g0139 | 2 | HG02135.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.394-697_394-696ins others(57): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 137144976 | |||||
| chr9:137144976
|
A | G | 28 | a0001c0001t0001g0012a0001c0001t0001g0016a0001c0001t0001g0029others(25): Show | 30 | HG00621.hp1 HG01069.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.394-750A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144976 | ||||||
| chr9:137144976
|
AGTGAGAG others(221): Show |
A | 8 | a0001c0001t0001g0025a0001c0001t0001g0031a0001c0001t0001g0091others(5): Show | 8 | HG01168.hp1 HG02630.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.394-639_394-412del | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 137144976 | |||||
| chr9:137144981
|
G | A | 1 | a0001c0007t0001g0261 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.394-745G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137144981 | ||||||
| chr9:137145002
|
C | CAGAAAGT others(112): Show |
1 | a0001c0001t0001g0199 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.394-709_394-708ins others(119): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 137145002 | |||||
| chr9:137145002
|
C | T | 5 | a0001c0001t0001g0206a0001c0001t0001g0229a0001c0001t0001g0230others(2): Show | 5 | HG00099.hp1 HG01934.hp2 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.394-724C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145002 | ||||||
| chr9:137145018
|
A | C | 1 | a0001c0001t0001g0199 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.394-708A>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145018 | ||||||
| chr9:137145018
|
A | G | 29 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0042others(26): Show | 32 | HG00099.hp1 HG00544.hp1 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.394-708A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145018 | ||||||
| chr9:137145020
|
G | T | 1 | a0001c0005t0001g0205 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.394-706G>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145020 | ||||||
| chr9:137145021
|
G | T | 27 | a0001c0001t0001g0014a0001c0001t0001g0042a0001c0001t0001g0043others(24): Show | 29 | HG00099.hp1 HG00544.hp1 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.394-705G>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145021 | ||||||
| chr9:137145021
|
GGTGGGGA others(164): Show |
G | 1 | a0001c0007t0001g0261 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.394-696_394-526del | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 137145021 | |||||
| chr9:137145024
|
G | A | 1 | a0001c0005t0001g0205 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.394-702G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145024 | ||||||
| chr9:137145030
|
A | C | 25 | a0001c0001t0001g0014a0001c0001t0001g0042a0001c0001t0001g0043others(22): Show | 26 | HG00544.hp1 HG01496.hp1 HG01516.hp2 others(23): Show |
intron_variant | MODIFIER | c.394-696A>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145030 | ||||||
| chr9:137145031
|
G | A | 2 | a0001c0001t0001g0242a0001c0001t0001g0243 | 2 | HG02886.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.394-695G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145031 | ||||||
| chr9:137145033
|
A | G | 27 | a0001c0001t0001g0014a0001c0001t0001g0042a0001c0001t0001g0043others(24): Show | 28 | HG00544.hp1 HG01496.hp1 HG01516.hp2 others(25): Show |
intron_variant | MODIFIER | c.394-693A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145033 | ||||||
| chr9:137145033
|
AGTGAGAG others(164): Show |
A | 71 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0013others(68): Show | 76 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.394-639_394-469del | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 137145033 | |||||
| chr9:137145036
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.394-690G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145036 | ||||||
| chr9:137145037
|
A | G | 2 | a0001c0001t0001g0199a0001c0005t0001g0205 | 2 | HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.394-689A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145037 | ||||||
| chr9:137145041
|
G | C | 2 | a0001c0001t0001g0199a0001c0005t0001g0205 | 2 | HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.394-685G>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145041 | ||||||
| chr9:137145042
|
A | G | 2 | a0001c0001t0001g0199a0001c0005t0001g0205 | 2 | HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.394-684A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145042 | ||||||
| chr9:137145044
|
GGGGGTCC others(163): Show |
G | 1 | a0001c0001t0001g0266 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.394-677_394-508del | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 137145044 | |||||
| chr9:137145054
|
GGGTCCAG others(163): Show |
G | 1 | a0001c0001t0001g0212 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.394-669_394-500del | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 137145054 | |||||
| chr9:137145059
|
C | T | 5 | a0001c0001t0001g0030a0001c0001t0001g0136a0001c0001t0001g0199others(2): Show | 5 | HG01070.hp1 HG01515.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.394-667C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145059 | ||||||
| chr9:137145075
|
A | G | 17 | a0001c0001t0001g0002a0001c0001t0001g0030a0001c0001t0001g0070others(14): Show | 18 | HG00099.hp1 HG00621.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.394-651A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145075 | ||||||
| chr9:137145076
|
GGGGTGGG others(163): Show |
G | 1 | a0001c0006t0001g0127 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.394-646_394-477del | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 137145076 | |||||
| chr9:137145078
|
G | T | 19 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0024others(16): Show | 20 | HG00099.hp1 HG00621.hp1 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.394-648G>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145078 | ||||||
| chr9:137145078
|
GGTGGGGA others(107): Show |
G | 57 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(54): Show | 61 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.394-610_394-497del | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 137145078 | |||||
| chr9:137145087
|
C | A | 89 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0014others(86): Show | 97 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.394-639C>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145087 | ||||||
| chr9:137145090
|
G | A | 89 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0014others(86): Show | 97 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.394-636G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145090 | ||||||
| chr9:137145090
|
G | GGTGAGAG others(50): Show |
1 | a0001c0001t0001g0213 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.394-611_394-610ins others(57): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 137145090 | |||||
| chr9:137145090
|
G | GGTGAGAG others(107): Show |
1 | a0001c0001t0001g0263 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.394-611_394-610ins others(114): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 137145090 | |||||
| chr9:137145092
|
TGAGAGGA others(109): Show |
T | 3 | a0001c0001t0001g0197a0001c0003t0001g0195a0001c0003t0001g0196 | 3 | HG01109.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.394-630_394-515del | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 137145092 | |||||
| chr9:137145101
|
GGGGGTCC others(106): Show |
G | 2 | a0001c0001t0001g0058a0001c0001t0001g0109 | 2 | HG00741.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.394-620_394-508del | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 137145101 | |||||
| chr9:137145116
|
T | C | 105 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0012others(102): Show | 113 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.394-610T>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145116 | ||||||
| chr9:137145130
|
AGAG | A | 2 | a0001c0001t0001g0014a0001c0001t0001g0132 | 3 | HG02965.hp1 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.394-594_394-592del others(3): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 137145130 | |||||
| chr9:137145132
|
A | G | 10 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0089others(7): Show | 10 | HG01891.hp2 HG02257.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.394-594A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145132 | ||||||
| chr9:137145134
|
G | T | 3 | a0001c0001t0001g0250a0001c0001t0001g0254a0001c0001t0001g0255 | 3 | HG03491.hp2 HG03654.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.394-592G>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145134 | ||||||
| chr9:137145135
|
G | GGTGGGGA others(167): Show |
1 | a0001c0001t0001g0252 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.394-583_394-582ins others(174): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 137145135 | |||||
| chr9:137145135
|
G | T | 7 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0089others(4): Show | 7 | HG01891.hp2 HG02257.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.394-591G>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145135 | ||||||
| chr9:137145135
|
GGTGGGGA others(50): Show |
G | 12 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0059others(9): Show | 14 | HG00280.hp2 HG01934.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.394-553_394-497del others(57): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 137145135 | |||||
| chr9:137145137
|
TGGGGACC others(104): Show |
T | 2 | a0001c0001t0001g0014a0001c0001t0001g0132 | 3 | HG02965.hp1 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.394-586_394-476del | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 137145137 | |||||
| chr9:137145138
|
G | A | 2 | a0001c0001t0001g0250a0001c0001t0001g0255 | 2 | HG03654.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.394-588G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145138 | ||||||
| chr9:137145144
|
C | A | 81 | a0001c0001t0001g0002a0001c0001t0001g0030a0001c0001t0001g0042others(78): Show | 86 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.394-582C>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145144 | ||||||
| chr9:137145147
|
G | A | 77 | a0001c0001t0001g0002a0001c0001t0001g0030a0001c0001t0001g0042others(74): Show | 82 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.394-579G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145147 | ||||||
| chr9:137145147
|
G | GGTGAGAG others(50): Show |
1 | a0001c0001t0001g0241 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.394-554_394-553ins others(57): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 137145147 | |||||
| chr9:137145147
|
G | GGTGAGAG others(164): Show |
1 | a0001c0003t0001g0139 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.394-554_394-553ins others(171): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 137145147 | |||||
| chr9:137145151
|
A | G | 3 | a0001c0001t0001g0250a0001c0001t0001g0254a0001c0001t0001g0255 | 3 | HG03491.hp2 HG03654.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.394-575A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145151 | ||||||
| chr9:137145154
|
G | GACA | 3 | a0001c0001t0001g0250a0001c0001t0001g0254a0001c0001t0001g0255 | 3 | HG03491.hp2 HG03654.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.394-572_394-571ins others(3): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145154 | ||||||
| chr9:137145155
|
G | C | 2 | a0001c0001t0001g0250a0001c0001t0001g0255 | 2 | HG03654.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.394-571G>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145155 | ||||||
| chr9:137145156
|
A | G | 3 | a0001c0001t0001g0250a0001c0001t0001g0254a0001c0001t0001g0255 | 3 | HG03491.hp2 HG03654.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.394-570A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145156 | ||||||
| chr9:137145173
|
T | C | 91 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0024others(88): Show | 97 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.394-553T>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145173 | ||||||
| chr9:137145189
|
G | A | 85 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0024others(82): Show | 91 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.394-537G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145189 | ||||||
| chr9:137145191
|
G | T | 4 | a0001c0001t0001g0250a0001c0001t0001g0253a0001c0001t0001g0255others(1): Show | 4 | HG03017.hp1 HG03654.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.394-535G>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145191 | ||||||
| chr9:137145192
|
T | G | 89 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0024others(86): Show | 95 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.394-534T>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145192 | ||||||
| chr9:137145192
|
T | TGGGGACA others(732): Show |
1 | a0001c0003t0001g0240 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.394-533_394-532ins others(739): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 137145192 | |||||
| chr9:137145192
|
T | TGTGGGGA others(278): Show |
1 | a0001c0002t0001g0176 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.394-526_394-525ins others(285): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 137145192 | |||||
| chr9:137145194
|
T | C | 2 | a0001c0001t0001g0250a0001c0001t0001g0255 | 2 | HG03654.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.394-532T>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145194 | ||||||
| chr9:137145195
|
G | A | 4 | a0001c0001t0001g0250a0001c0001t0001g0253a0001c0001t0001g0255others(1): Show | 4 | HG03017.hp1 HG03654.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.394-531G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145195 | ||||||
| chr9:137145201
|
C | A | 159 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(156): Show | 171 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.394-525C>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145201 | ||||||
| chr9:137145201
|
C | T | 2 | a0001c0001t0001g0250a0001c0001t0001g0255 | 2 | HG03654.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.394-525C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145201 | ||||||
| chr9:137145204
|
G | A | 157 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(154): Show | 169 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.394-522G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145204 | ||||||
| chr9:137145205
|
G | A | 2 | a0001c0001t0001g0250a0001c0001t0001g0255 | 2 | HG03654.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.394-521G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145205 | ||||||
| chr9:137145208
|
A | G | 4 | a0001c0001t0001g0250a0001c0001t0001g0253a0001c0001t0001g0255others(1): Show | 4 | HG03017.hp1 HG03654.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.394-518A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145208 | ||||||
| chr9:137145209
|
G | A | 1 | a0001c0001t0001g0135 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.394-517G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145209 | ||||||
| chr9:137145210
|
A | GGGAAGGG others(50): Show |
1 | a0001c0001t0001g0213 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.394-517_394-516ins others(57): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145210 | ||||||
| chr9:137145211
|
G | GACA | 4 | a0001c0001t0001g0250a0001c0001t0001g0253a0001c0001t0001g0255others(1): Show | 4 | HG03017.hp1 HG03654.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.394-515_394-514ins others(3): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145211 | ||||||
| chr9:137145212
|
G | C | 4 | a0001c0001t0001g0250a0001c0001t0001g0253a0001c0001t0001g0255others(1): Show | 4 | HG03017.hp1 HG03654.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.394-514G>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145212 | ||||||
| chr9:137145213
|
A | G | 4 | a0001c0001t0001g0250a0001c0001t0001g0253a0001c0001t0001g0255others(1): Show | 4 | HG03017.hp1 HG03654.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.394-513A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145213 | ||||||
| chr9:137145226
|
G | A | 2 | a0001c0001t0001g0250a0001c0001t0001g0255 | 2 | HG03654.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.394-500G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145226 | ||||||
| chr9:137145230
|
C | CAGAAAGT others(53): Show |
2 | a0001c0001t0001g0252a0001c0001t0001g0254 | 2 | HG02735.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.394-481_394-480ins others(60): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 137145230 | |||||
| chr9:137145230
|
C | T | 4 | a0001c0001t0001g0250a0001c0001t0001g0253a0001c0001t0001g0255others(1): Show | 4 | HG03017.hp1 HG03654.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.394-496C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145230 | ||||||
| chr9:137145246
|
A | C | 2 | a0001c0001t0001g0250a0001c0001t0001g0255 | 2 | HG03654.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.394-480A>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145246 | ||||||
| chr9:137145246
|
A | G | 3 | a0001c0001t0001g0253a0001c0001t0001g0270a0001c0005t0001g0205 | 3 | HG02809.hp2 HG03017.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.394-480A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145246 | ||||||
| chr9:137145248
|
G | T | 2 | a0001c0001t0001g0253a0001c0001t0001g0270 | 2 | HG03017.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.394-478G>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145248 | ||||||
| chr9:137145249
|
G | T | 1 | a0001c0001t0001g0233 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.394-477G>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145249 | ||||||
| chr9:137145251
|
T | C | 2 | a0001c0001t0001g0253a0001c0001t0001g0270 | 2 | HG03017.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.394-475T>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145251 | ||||||
| chr9:137145252
|
G | A | 2 | a0001c0001t0001g0253a0001c0001t0001g0270 | 2 | HG03017.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.394-474G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145252 | ||||||
| chr9:137145257
|
C | T | 2 | a0001c0001t0001g0253a0001c0001t0001g0270 | 2 | HG03017.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.394-469C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145257 | ||||||
| chr9:137145258
|
A | C | 3 | a0001c0001t0001g0039a0001c0001t0001g0135a0001c0001t0001g0233 | 3 | HG00738.hp2 HG02451.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.394-468A>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145258 | ||||||
| chr9:137145258
|
A | G | 2 | a0001c0001t0001g0253a0001c0001t0001g0270 | 2 | HG03017.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.394-468A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145258 | ||||||
| chr9:137145261
|
A | G | 4 | a0001c0001t0001g0039a0001c0001t0001g0135a0001c0001t0001g0233others(1): Show | 4 | HG00738.hp2 HG02451.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.394-465A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145261 | ||||||
| chr9:137145263
|
T | G | 2 | a0001c0001t0001g0253a0001c0001t0001g0270 | 2 | HG03017.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.394-463T>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145263 | ||||||
| chr9:137145268
|
G | A | 2 | a0001c0001t0001g0253a0001c0001t0001g0270 | 2 | HG03017.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.394-458G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145268 | ||||||
| chr9:137145269
|
G | C | 2 | a0001c0001t0001g0253a0001c0001t0001g0270 | 2 | HG03017.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.394-457G>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145269 | ||||||
| chr9:137145270
|
A | G | 2 | a0001c0001t0001g0253a0001c0001t0001g0270 | 2 | HG03017.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.394-456A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145270 | ||||||
| chr9:137145283
|
G | A | 3 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0270 | 3 | HG03017.hp1 HG03654.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.394-443G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145283 | ||||||
| chr9:137145287
|
C | T | 4 | a0001c0001t0001g0250a0001c0001t0001g0253a0001c0001t0001g0255others(1): Show | 4 | HG03017.hp1 HG03654.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.394-439C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145287 | ||||||
| chr9:137145303
|
A | C | 3 | a0001c0001t0001g0250a0001c0001t0001g0253a0001c0001t0001g0270 | 3 | HG03017.hp1 HG03942.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.394-423A>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145303 | ||||||
| chr9:137145303
|
A | G | 5 | a0001c0001t0001g0197a0001c0003t0001g0195a0001c0003t0001g0196others(2): Show | 5 | HG01109.hp1 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.394-423A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145303 | ||||||
| chr9:137145305
|
G | T | 5 | a0001c0001t0001g0197a0001c0003t0001g0195a0001c0003t0001g0196others(2): Show | 5 | HG01109.hp1 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.394-421G>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145305 | ||||||
| chr9:137145309
|
G | A | 5 | a0001c0001t0001g0197a0001c0003t0001g0195a0001c0003t0001g0196others(2): Show | 5 | HG01109.hp1 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.394-417G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145309 | ||||||
| chr9:137145318
|
A | G | 7 | a0001c0001t0001g0197a0001c0001t0001g0250a0001c0001t0001g0270others(4): Show | 7 | HG01109.hp1 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.394-408A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145318 | ||||||
| chr9:137145319
|
G | A | 1 | a0001c0007t0001g0261 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.394-407G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145319 | ||||||
| chr9:137145322
|
A | G | 7 | a0001c0001t0001g0197a0001c0001t0001g0250a0001c0001t0001g0270others(4): Show | 7 | HG01109.hp1 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.394-404A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145322 | ||||||
| chr9:137145325
|
G | GACA | 7 | a0001c0001t0001g0197a0001c0001t0001g0250a0001c0001t0001g0270others(4): Show | 7 | HG01109.hp1 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.394-401_394-400ins others(3): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145325 | ||||||
| chr9:137145326
|
G | C | 7 | a0001c0001t0001g0197a0001c0001t0001g0250a0001c0001t0001g0270others(4): Show | 7 | HG01109.hp1 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.394-400G>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145326 | ||||||
| chr9:137145327
|
A | G | 7 | a0001c0001t0001g0197a0001c0001t0001g0250a0001c0001t0001g0270others(4): Show | 7 | HG01109.hp1 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.394-399A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145327 | ||||||
| chr9:137145340
|
G | A | 1 | a0001c0001t0001g0250 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.394-386G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145340 | ||||||
| chr9:137145344
|
C | T | 10 | a0001c0001t0001g0197a0001c0001t0001g0245a0001c0001t0001g0250others(7): Show | 10 | HG01109.hp1 HG02280.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.394-382C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145344 | ||||||
| chr9:137145359
|
G | T | 1 | a0001c0001t0001g0270 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.394-367G>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145359 | ||||||
| chr9:137145360
|
G | A | 24 | a0001c0001t0001g0070a0001c0001t0001g0089a0001c0001t0001g0090others(21): Show | 25 | HG00642.hp1 HG01069.hp1 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.394-366G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145360 | ||||||
| chr9:137145360
|
G | C | 2 | a0001c0001t0001g0253a0001c0001t0001g0255 | 2 | HG03017.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.394-366G>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145360 | ||||||
| chr9:137145362
|
T | G | 27 | a0001c0001t0001g0070a0001c0001t0001g0089a0001c0001t0001g0090others(24): Show | 28 | HG00642.hp1 HG01069.hp1 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.394-364T>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145362 | ||||||
| chr9:137145365
|
T | C | 6 | a0001c0001t0001g0197a0001c0001t0001g0245a0001c0001t0001g0260others(3): Show | 6 | HG01109.hp1 HG02280.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.394-361T>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145365 | ||||||
| chr9:137145366
|
A | G | 27 | a0001c0001t0001g0070a0001c0001t0001g0089a0001c0001t0001g0090others(24): Show | 28 | HG00642.hp1 HG01069.hp1 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.394-360A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145366 | ||||||
| chr9:137145370
|
AC | A | 6 | a0001c0001t0001g0197a0001c0001t0001g0245a0001c0001t0001g0260others(3): Show | 6 | HG01109.hp1 HG02280.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.394-355delC | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145370 | ||||||
| chr9:137145372
|
A | T | 6 | a0001c0001t0001g0197a0001c0001t0001g0245a0001c0001t0001g0260others(3): Show | 6 | HG01109.hp1 HG02280.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.394-354A>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145372 | ||||||
| chr9:137145375
|
G | A | 23 | a0001c0001t0001g0070a0001c0001t0001g0089a0001c0001t0001g0090others(20): Show | 24 | HG00642.hp1 HG01069.hp1 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.394-351G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145375 | ||||||
| chr9:137145376
|
G | A | 7 | a0001c0001t0001g0135a0001c0001t0001g0197a0001c0001t0001g0245others(4): Show | 7 | HG01109.hp1 HG02280.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.394-350G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145376 | ||||||
| chr9:137145379
|
G | A | 24 | a0001c0001t0001g0070a0001c0001t0001g0089a0001c0001t0001g0090others(21): Show | 25 | HG00642.hp1 HG01069.hp1 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.394-347G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145379 | ||||||
| chr9:137145382
|
GACA | G | 23 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0199others(20): Show | 24 | HG00642.hp1 HG01069.hp1 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.394-343_394-341del others(3): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145382 | ||||||
| chr9:137145383
|
A | G | 2 | a0001c0001t0001g0070a0001c0002t0001g0150 | 2 | HG03017.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.394-343A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145383 | ||||||
| chr9:137145384
|
C | A | 2 | a0001c0001t0001g0070a0001c0002t0001g0150 | 2 | HG03017.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.394-342C>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145384 | ||||||
| chr9:137145386
|
C | G | 25 | a0001c0001t0001g0070a0001c0001t0001g0089a0001c0001t0001g0090others(22): Show | 26 | HG00642.hp1 HG01069.hp1 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.394-340C>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145386 | ||||||
| chr9:137145387
|
G | A | 23 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0199others(20): Show | 24 | HG00642.hp1 HG01069.hp1 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.394-339G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145387 | ||||||
| chr9:137145387
|
G | GGGGTCCC others(47): Show |
1 | a0001c0001t0001g0070 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.394-339_394-338ins others(54): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145387 | ||||||
| chr9:137145387
|
G | GGGGTCCC others(218): Show |
1 | a0001c0002t0001g0150 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.394-339_394-338ins others(225): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145387 | ||||||
| chr9:137145400
|
G | A | 6 | a0001c0001t0001g0197a0001c0001t0001g0245a0001c0001t0001g0260others(3): Show | 6 | HG01109.hp1 HG02280.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.394-326G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145400 | ||||||
| chr9:137145404
|
T | C | 20 | a0001c0001t0001g0070a0001c0001t0001g0089a0001c0001t0001g0090others(17): Show | 21 | HG00642.hp1 HG01069.hp1 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.394-322T>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145404 | ||||||
| chr9:137145419
|
G | A | 2 | a0001c0002t0001g0171a0001c0002t0001g0182 | 2 | HG01074.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.394-307G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145419 | ||||||
| chr9:137145420
|
G | A | 1 | a0001c0001t0001g0270 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.394-306G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145420 | ||||||
| chr9:137145420
|
G | C | 4 | a0001c0001t0001g0197a0001c0003t0001g0195a0001c0003t0001g0196others(1): Show | 4 | HG01109.hp1 HG02818.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.394-306G>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145420 | ||||||
| chr9:137145422
|
T | G | 5 | a0001c0001t0001g0197a0001c0001t0001g0270a0001c0003t0001g0195others(2): Show | 5 | HG01109.hp1 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.394-304T>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145422 | ||||||
| chr9:137145425
|
C | T | 26 | a0001c0001t0001g0070a0001c0001t0001g0089a0001c0001t0001g0090others(23): Show | 27 | HG00642.hp1 HG01069.hp1 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.394-301C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145425 | ||||||
| chr9:137145426
|
A | G | 5 | a0001c0001t0001g0197a0001c0001t0001g0270a0001c0003t0001g0195others(2): Show | 5 | HG01109.hp1 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.394-300A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145426 | ||||||
| chr9:137145430
|
A | AC | 23 | a0001c0001t0001g0070a0001c0001t0001g0089a0001c0001t0001g0090others(20): Show | 24 | HG00642.hp1 HG01069.hp1 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.394-296_394-295ins others(1): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145430 | ||||||
| chr9:137145431
|
T | A | 23 | a0001c0001t0001g0070a0001c0001t0001g0089a0001c0001t0001g0090others(20): Show | 24 | HG00642.hp1 HG01069.hp1 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.394-295T>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145431 | ||||||
| chr9:137145431
|
T | C | 1 | a0001c0001t0001g0270 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.394-295T>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145431 | ||||||
| chr9:137145432
|
G | A | 1 | a0001c0001t0001g0270 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.394-294G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145432 | ||||||
| chr9:137145435
|
A | G | 23 | a0001c0001t0001g0070a0001c0001t0001g0089a0001c0001t0001g0090others(20): Show | 24 | HG00642.hp1 HG01069.hp1 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.394-291A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145435 | ||||||
| chr9:137145438
|
G | T | 1 | a0001c0001t0001g0270 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.394-288G>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145438 | ||||||
| chr9:137145444
|
A | G | 1 | a0001c0001t0001g0270 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.394-282A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145444 | ||||||
| chr9:137145445
|
C | G | 1 | a0001c0001t0001g0270 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.394-281C>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145445 | ||||||
| chr9:137145445
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.394-281C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145445 | ||||||
| chr9:137145446
|
G | A | 1 | a0001c0001t0001g0270 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.394-280G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145446 | ||||||
| chr9:137145459
|
A | AGTCTAGA others(53): Show |
1 | a0001c0001t0001g0213 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.394-247_394-188dup others(60): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 137145459 | |||||
| chr9:137145459
|
A | G | 25 | a0001c0001t0001g0033a0001c0001t0001g0070a0001c0001t0001g0089others(22): Show | 26 | HG00642.hp1 HG01069.hp1 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.394-267A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145459 | ||||||
| chr9:137145459
|
AGTCTAGA others(53): Show |
A | 9 | a0001c0001t0001g0245a0001c0001t0001g0253a0001c0001t0001g0255others(6): Show | 9 | HG02080.hp2 HG02280.hp2 HG03017.hp1 others(6): Show |
intron_variant | MODIFIER | c.394-247_394-188del others(60): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 137145459 | |||||
| chr9:137145463
|
T | C | 1 | a0001c0001t0001g0270 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.394-263T>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145463 | ||||||
| chr9:137145479
|
C | A | 1 | a0001c0001t0001g0270 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.394-247C>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145479 | ||||||
| chr9:137145479
|
C | G | 28 | a0001c0001t0001g0070a0001c0001t0001g0089a0001c0001t0001g0090others(25): Show | 29 | HG00642.hp1 HG01069.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.394-247C>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145479 | ||||||
| chr9:137145479
|
CGGGGTGG others(112): Show |
C | 3 | a0001c0001t0001g0013a0001c0001t0001g0084a0001c0001t0001g0123 | 4 | HG02145.hp2 NA18522.hp1 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.394-224_394-106del | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 137145479 | |||||
| chr9:137145481
|
G | T | 28 | a0001c0001t0001g0070a0001c0001t0001g0089a0001c0001t0001g0090others(25): Show | 29 | HG00642.hp1 HG01069.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.394-245G>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145481 | ||||||
| chr9:137145483
|
G | A | 1 | a0001c0001t0001g0135 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.394-243G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145483 | ||||||
| chr9:137145484
|
T | C | 23 | a0001c0001t0001g0070a0001c0001t0001g0089a0001c0001t0001g0090others(20): Show | 24 | HG00642.hp1 HG01069.hp1 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.394-242T>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145484 | ||||||
| chr9:137145485
|
G | A | 28 | a0001c0001t0001g0070a0001c0001t0001g0089a0001c0001t0001g0090others(25): Show | 29 | HG00642.hp1 HG01069.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.394-241G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145485 | ||||||
| chr9:137145489
|
AC | A | 24 | a0001c0001t0001g0070a0001c0001t0001g0089a0001c0001t0001g0090others(21): Show | 25 | HG00642.hp1 HG01069.hp1 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.394-236delC | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145489 | ||||||
| chr9:137145490
|
CA | C | 4 | a0001c0001t0001g0197a0001c0003t0001g0195a0001c0003t0001g0196others(1): Show | 4 | HG01109.hp1 HG02818.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.394-235delA | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145490 | ||||||
| chr9:137145491
|
A | AGGAGTGA others(109): Show |
2 | a0001c0001t0001g0252a0001c0001t0001g0254 | 2 | HG02735.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.394-233_394-232ins others(116): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 137145491 | |||||
| chr9:137145491
|
A | AGGGGTGG others(52): Show |
1 | a0001c0001t0001g0135 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.394-198_394-140dup others(59): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 137145491 | |||||
| chr9:137145491
|
A | T | 24 | a0001c0001t0001g0070a0001c0001t0001g0089a0001c0001t0001g0090others(21): Show | 25 | HG00642.hp1 HG01069.hp1 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.394-235A>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145491 | ||||||
| chr9:137145491
|
AGGGGTGG others(52): Show |
A | 2 | a0001c0001t0001g0167a0001c0001t0001g0208 | 2 | HG01993.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.394-198_394-140del others(59): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 137145491 | |||||
| chr9:137145494
|
G | A | 1 | a0001c0001t0001g0270 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.394-232G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145494 | ||||||
| chr9:137145495
|
G | A | 26 | a0001c0001t0001g0070a0001c0001t0001g0089a0001c0001t0001g0090others(23): Show | 27 | HG00642.hp1 HG01069.hp1 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.394-231G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145495 | ||||||
| chr9:137145498
|
G | A | 1 | a0001c0001t0001g0270 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.394-228G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145498 | ||||||
| chr9:137145505
|
C | G | 1 | a0001c0001t0001g0270 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.394-221C>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145505 | ||||||
| chr9:137145506
|
G | A | 1 | a0001c0001t0001g0270 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.394-220G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145506 | ||||||
| chr9:137145511
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.394-215G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145511 | ||||||
| chr9:137145519
|
G | A | 26 | a0001c0001t0001g0070a0001c0001t0001g0089a0001c0001t0001g0090others(23): Show | 27 | HG00642.hp1 HG01069.hp1 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.394-207G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145519 | ||||||
| chr9:137145523
|
T | C | 1 | a0001c0001t0001g0270 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.394-203T>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145523 | ||||||
| chr9:137145528
|
AGTGTCCC others(52): Show |
A | 160 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(157): Show | 172 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.394-188_394-130del others(59): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 137145528 | |||||
| chr9:137145539
|
G | C | 18 | a0001c0001t0001g0070a0001c0001t0001g0089a0001c0001t0001g0090others(15): Show | 19 | HG00642.hp1 HG01069.hp1 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.394-187G>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145539 | ||||||
| chr9:137145541
|
T | G | 18 | a0001c0001t0001g0070a0001c0001t0001g0089a0001c0001t0001g0090others(15): Show | 19 | HG00642.hp1 HG01069.hp1 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.394-185T>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145541 | ||||||
| chr9:137145545
|
A | G | 18 | a0001c0001t0001g0070a0001c0001t0001g0089a0001c0001t0001g0090others(15): Show | 19 | HG00642.hp1 HG01069.hp1 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.394-181A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145545 | ||||||
| chr9:137145550
|
C | CA | 50 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0021others(47): Show | 55 | HG00099.hp1 HG00597.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.394-176_394-175ins others(1): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145550 | ||||||
| chr9:137145587
|
C | A | 50 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0021others(47): Show | 55 | HG00099.hp1 HG00597.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.394-139C>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145587 | ||||||
| chr9:137145621
|
G | A | 2 | a0001c0001t0001g0051a0001c0001t0001g0052 | 2 | HG02071.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.394-105G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145621 | ||||||
| chr9:137145627
|
G | C | 1 | a0001c0001t0001g0251 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.394-99G>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145627 | ||||||
| chr9:137145688
|
G | A | 1 | a0001c0001t0001g0251 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.394-38G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145688 | ||||||
| chr9:137145694
|
A | G | 6 | a0001c0001t0001g0245a0001c0001t0001g0256a0001c0001t0001g0257others(3): Show | 6 | HG02258.hp2 HG02280.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.394-32A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145694 | ||||||
| chr9:137145704
|
G | A | 252 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(249): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.394-22G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145704 | ||||||
| chr9:137145715
|
G | A | 5 | a0001c0004t0001g0040a0001c0004t0001g0069a0001c0004t0001g0085others(2): Show | 5 | HG02080.hp2 NA18952.hp2 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.394-11G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145715 | ||||||
| chr9:137146003
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.570+101G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 3/19 | chr9 | 137146003 | ||||||
| chr9:137146031
|
G | A | 1 | a0001c0001t0001g0234 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.570+129G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 3/19 | chr9 | 137146031 | ||||||
| chr9:137146038
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.570+136C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 3/19 | chr9 | 137146038 | ||||||
| chr9:137146165
|
G | C | 262 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(259): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.570+263G>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 3/19 | chr9 | 137146165 | ||||||
| chr9:137146169
|
G | A | 2 | a0001c0002t0001g0185a0001c0002t0001g0186 | 2 | HG01261.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.570+267G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 3/19 | chr9 | 137146169 | ||||||
| chr9:137146222
|
G | A | 2 | a0001c0001t0001g0124a0001c0001t0001g0126 | 2 | HG02602.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.570+320G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 3/19 | chr9 | 137146222 | ||||||
| chr9:137146304
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.570+402G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 3/19 | chr9 | 137146304 | ||||||
| chr9:137146368
|
C | T | 14 | a0001c0001t0001g0168a0001c0001t0001g0241a0001c0001t0001g0263others(11): Show | 15 | HG01884.hp2 HG02015.hp1 HG02040.hp1 others(12): Show |
intron_variant | MODIFIER | c.570+466C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 3/19 | chr9 | 137146368 | ||||||
| chr9:137146452
|
T | C | 7 | a0001c0001t0001g0245a0001c0001t0001g0256a0001c0001t0001g0257others(4): Show | 7 | HG02258.hp2 HG02280.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.570+550T>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 3/19 | chr9 | 137146452 | ||||||
| chr9:137146638
|
C | T | 1 | a0001c0001t0001g0233 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.570+736C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 3/19 | chr9 | 137146638 | ||||||
| chr9:137146641
|
C | G | 1 | a0001c0001t0001g0135 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.570+739C>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 3/19 | chr9 | 137146641 | ||||||
| chr9:137146947
|
G | T | 1 | a0001c0001t0001g0068 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.570+1045G>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 3/19 | chr9 | 137146947 | ||||||
| chr9:137146973
|
C | T | 1 | a0001c0001t0001g0083 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.570+1071C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 3/19 | chr9 | 137146973 | ||||||
| chr9:137147003
|
G | GCCCGACA others(18): Show |
1 | a0001c0006t0001g0127 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.570+1121_570+1122i others(27): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr9 | 137147003 | |||||
| chr9:137147016
|
C | CTCCCCCC others(18): Show |
2 | a0001c0001t0001g0028a0001c0001t0001g0045 | 2 | NA18980.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.570+1124_570+1125i others(27): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr9 | 137147016 | |||||
| chr9:137147017
|
T | TCCCCCCA others(18): Show |
241 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(238): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.570+1124_570+1125i others(27): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr9 | 137147017 | |||||
| chr9:137147017
|
T | TCCCCCCA others(19): Show |
1 | a0001c0001t0001g0146 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.570+1124_570+1125i others(28): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr9 | 137147017 | |||||
| chr9:137147022
|
C | CCAGCACC others(18): Show |
3 | a0001c0001t0001g0250a0001c0001t0001g0253a0001c0001t0001g0255 | 3 | HG03017.hp1 HG03654.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.570+1124_570+1125i others(27): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr9 | 137147022 | |||||
| chr9:137147027
|
G | A | 28 | a0001c0001t0001g0011a0001c0001t0001g0095a0001c0001t0001g0096others(25): Show | 30 | HG00609.hp1 HG00642.hp2 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.570+1125G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 3/19 | chr9 | 137147027 | ||||||
| chr9:137147041
|
TC | T | 248 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(245): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.570+1146delC | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr9 | 137147041 | |||||
| chr9:137147042
|
C | CCCCCACA others(17): Show |
2 | a0001c0001t0001g0252a0001c0001t0001g0254 | 2 | HG02735.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.570+1144_570+1145i others(26): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr9 | 137147042 | |||||
| chr9:137147042
|
C | CCCCCCCA others(17): Show |
5 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(2): Show | 5 | HG02258.hp2 HG02717.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.570+1142_570+1165d others(26): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr9 | 137147042 | |||||
| chr9:137147042
|
C | CCCCCCCA others(17): Show |
21 | a0001c0001t0001g0011a0001c0001t0001g0095a0001c0001t0001g0096others(18): Show | 23 | HG00609.hp1 HG00642.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.570+1149_570+1150i others(26): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr9 | 137147042 | |||||
| chr9:137147056
|
G | A | 1 | a0001c0007t0001g0261 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.570+1154G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 3/19 | chr9 | 137147056 | ||||||
| chr9:137147077
|
C | T | 1 | a0001c0001t0001g0024 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.570+1175C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 3/19 | chr9 | 137147077 | ||||||
| chr9:137147080
|
G | C | 1 | a0001c0001t0001g0159 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.570+1178G>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 3/19 | chr9 | 137147080 | ||||||
| chr9:137147082
|
C | A | 1 | a0001c0001t0001g0159 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.570+1180C>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 3/19 | chr9 | 137147082 | ||||||
| chr9:137147114
|
G | A | 1 | a0001c0001t0001g0247 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.570+1212G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 3/19 | chr9 | 137147114 | ||||||
| chr9:137147138
|
C | T | 1 | a0001c0007t0001g0261 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.570+1236C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 3/19 | chr9 | 137147138 | ||||||
| chr9:137147146
|
C | T | 1 | a0001c0002t0001g0144 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.570+1244C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 3/19 | chr9 | 137147146 | ||||||
| chr9:137147268
|
C | T | 2 | a0001c0001t0001g0209a0001c0001t0001g0265 | 2 | HG04115.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.570+1366C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 3/19 | chr9 | 137147268 | ||||||
| chr9:137147279
|
G | A | 7 | a0001c0001t0001g0241a0001c0001t0001g0263a0001c0003t0001g0050others(4): Show | 7 | HG02040.hp1 HG02135.hp2 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.570+1377G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 3/19 | chr9 | 137147279 | ||||||
| chr9:137147383
|
C | T | 1 | a0001c0007t0001g0261 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.570+1481C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 3/19 | chr9 | 137147383 | ||||||
| chr9:137147623
|
TA | T | 6 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(3): Show | 6 | HG02258.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.571-1384delA | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr9 | 137147623 | |||||
| chr9:137147660
|
G | A | 1 | a0001c0001t0001g0208 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.571-1349G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 3/19 | chr9 | 137147660 | ||||||
| chr9:137147849
|
G | A | 4 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0094others(1): Show | 4 | HG00621.hp1 HG03831.hp1 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.571-1160G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 3/19 | chr9 | 137147849 | ||||||
| chr9:137147868
|
G | A | 207 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(204): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.571-1141G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 3/19 | chr9 | 137147868 | ||||||
| chr9:137147880
|
C | T | 2 | a0001c0002t0001g0185a0001c0002t0001g0186 | 2 | HG01261.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.571-1129C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 3/19 | chr9 | 137147880 | ||||||
| chr9:137147973
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.571-1036C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 3/19 | chr9 | 137147973 | ||||||
| chr9:137148007
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0059 | 3 | HG02015.hp2 NA18990.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.571-1002G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 3/19 | chr9 | 137148007 | ||||||
| chr9:137148439
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.571-570C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 3/19 | chr9 | 137148439 | ||||||
| chr9:137148544
|
C | G | 1 | a0001c0001t0001g0060 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.571-465C>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 3/19 | chr9 | 137148544 | ||||||
| chr9:137148960
|
C | A | 1 | a0001c0001t0001g0133 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.571-49C>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 3/19 | chr9 | 137148960 | ||||||
| chr9:137149315
|
T | C | 1 | a0001c0007t0001g0261 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.671+206T>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137149315 | ||||||
| chr9:137149394
|
C | G | 1 | a0001c0001t0001g0039 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.671+285C>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137149394 | ||||||
| chr9:137149413
|
G | A | 1 | a0001c0007t0001g0261 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.671+304G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137149413 | ||||||
| chr9:137149888
|
T | G | 1 | a0001c0007t0001g0261 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.671+779T>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137149888 | ||||||
| chr9:137150058
|
T | G | 1 | a0001c0003t0001g0217 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.671+949T>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137150058 | ||||||
| chr9:137150201
|
C | G | 6 | a0001c0001t0001g0006a0001c0001t0001g0054a0001c0001t0001g0067others(3): Show | 7 | HG00621.hp2 HG02132.hp2 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.671+1092C>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137150201 | ||||||
| chr9:137150309
|
C | G | 1 | a0001c0001t0001g0070 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.671+1200C>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137150309 | ||||||
| chr9:137150428
|
G | C | 3 | a0001c0001t0001g0197a0001c0003t0001g0195a0001c0003t0001g0196 | 3 | HG01109.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.671+1319G>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137150428 | ||||||
| chr9:137150603
|
C | CCCCTTCC others(63): Show |
2 | a0001c0006t0001g0127a0001c0006t0001g0130 | 2 | HG02055.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.671+1495_671+1496i others(72): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 137150603 | |||||
| chr9:137150646
|
A | C | 3 | a0001c0005t0001g0205a0001c0005t0002g0022a0001c0007t0001g0261 | 4 | HG02559.hp1 HG02717.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.671+1537A>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137150646 | ||||||
| chr9:137150682
|
G | A | 1 | a0001c0003t0001g0217 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.671+1573G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137150682 | ||||||
| chr9:137150780
|
TGCCCAGA others(25): Show |
T | 1 | a0001c0001t0001g0228 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.671+1682_671+1713d others(34): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 137150780 | |||||
| chr9:137150873
|
C | A | 1 | a0001c0003t0001g0244 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.671+1764C>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137150873 | ||||||
| chr9:137150949
|
AAAAAGAC others(26): Show |
A | 2 | a0001c0003t0001g0001a0001c0003t0001g0032 | 3 | NA18985.hp2 NA19058.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.671+1861_671+1893d others(35): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 137150949 | |||||
| chr9:137151057
|
G | T | 28 | a0001c0002t0001g0017a0001c0002t0001g0018a0001c0002t0001g0019others(25): Show | 32 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.671+1948G>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137151057 | ||||||
| chr9:137151105
|
C | G | 1 | a0001c0001t0001g0058 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.671+1996C>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137151105 | ||||||
| chr9:137151106
|
G | C | 1 | a0001c0001t0001g0058 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.671+1997G>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137151106 | ||||||
| chr9:137151126
|
C | T | 3 | a0001c0005t0001g0205a0001c0005t0002g0022a0001c0007t0001g0261 | 4 | HG02559.hp1 HG02717.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.671+2017C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137151126 | ||||||
| chr9:137151139
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.671+2030G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137151139 | ||||||
| chr9:137151183
|
ACCCGCCC others(10): Show |
A | 1 | a0001c0001t0001g0046 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.671+2093_671+2109d others(19): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 137151183 | |||||
| chr9:137151249
|
G | A | 5 | a0001c0001t0001g0250a0001c0001t0001g0252a0001c0001t0001g0253others(2): Show | 5 | HG02735.hp1 HG03017.hp1 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.671+2140G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137151249 | ||||||
| chr9:137151407
|
C | T | 28 | a0001c0002t0001g0017a0001c0002t0001g0018a0001c0002t0001g0019others(25): Show | 32 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.671+2298C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137151407 | ||||||
| chr9:137151650
|
A | T | 2 | a0001c0003t0001g0195a0001c0003t0001g0196 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.671+2541A>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137151650 | ||||||
| chr9:137151655
|
C | A | 1 | a0001c0001t0001g0229 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.671+2546C>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137151655 | ||||||
| chr9:137151858
|
G | A | 1 | a0001c0001t0001g0210 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.671+2749G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137151858 | ||||||
| chr9:137151872
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.671+2763G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137151872 | ||||||
| chr9:137151899
|
C | CT | 179 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(176): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.671+2811dupT | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 137151899 | |||||
| chr9:137151899
|
C | CTT | 7 | a0001c0001t0001g0027a0001c0001t0001g0058a0001c0001t0001g0094others(4): Show | 7 | HG00621.hp1 HG00741.hp1 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.671+2810_671+2811d others(4): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 137151899 | |||||
| chr9:137151899
|
CT | C | 7 | a0001c0001t0001g0135a0001c0001t0001g0168a0001c0001t0001g0207others(4): Show | 7 | HG01884.hp2 HG02258.hp1 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.671+2811delT | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 137151899 | |||||
| chr9:137151899
|
CTT | C | 43 | a0001c0001t0001g0241a0001c0001t0001g0263a0001c0002t0001g0017others(40): Show | 49 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.671+2810_671+2811d others(4): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 137151899 | |||||
| chr9:137152142
|
A | G | 1 | a0001c0001t0001g0252 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.671+3033A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137152142 | ||||||
| chr9:137152216
|
T | C | 2 | a0001c0006t0001g0127a0001c0006t0001g0130 | 2 | HG02055.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.671+3107T>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137152216 | ||||||
| chr9:137152230
|
C | A | 244 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(241): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.671+3121C>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137152230 | ||||||
| chr9:137152639
|
C | T | 197 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(194): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.671+3530C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137152639 | ||||||
| chr9:137152642
|
C | T | 1 | a0001c0001t0001g0255 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.671+3533C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137152642 | ||||||
| chr9:137152659
|
G | A | 1 | a0001c0001t0001g0161 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.671+3550G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137152659 | ||||||
| chr9:137152726
|
GGCACACA others(43): Show |
G | 1 | a0001c0004t0001g0085 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.671+3618_671+3667d others(52): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137152726 | ||||||
| chr9:137152859
|
T | C | 2 | a0001c0001t0001g0095a0001c0001t0001g0096 | 2 | HG01106.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.671+3750T>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137152859 | ||||||
| chr9:137152906
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.672-3763G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137152906 | ||||||
| chr9:137152948
|
T | TACACCAT others(4): Show |
1 | a0001c0001t0001g0267 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.672-3717_672-3707d others(13): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 137152948 | |||||
| chr9:137152964
|
G | A | 1 | a0001c0002t0001g0173 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.672-3705G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137152964 | ||||||
| chr9:137153249
|
A | G | 4 | a0001c0001t0001g0207a0001c0001t0001g0264a0001c0001t0001g0274others(1): Show | 4 | HG02258.hp1 HG02976.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.672-3420A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137153249 | ||||||
| chr9:137153369
|
C | T | 1 | a0001c0001t0001g0045 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.672-3300C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137153369 | ||||||
| chr9:137153453
|
A | G | 1 | a0001c0002t0001g0179 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.672-3216A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137153453 | ||||||
| chr9:137153549
|
A | G | 50 | a0001c0001t0001g0207a0001c0001t0001g0241a0001c0001t0001g0263others(47): Show | 56 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.672-3120A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137153549 | ||||||
| chr9:137153643
|
C | T | 1 | a0001c0001t0001g0135 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.672-3026C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137153643 | ||||||
| chr9:137153674
|
C | A | 1 | a0001c0001t0001g0147 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.672-2995C>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137153674 | ||||||
| chr9:137153701
|
G | A | 2 | a0001c0001t0001g0223a0001c0001t0001g0275 | 2 | HG01346.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.672-2968G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137153701 | ||||||
| chr9:137153722
|
C | T | 1 | a0001c0001t0001g0036 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.672-2947C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137153722 | ||||||
| chr9:137153745
|
C | T | 2 | a0001c0005t0001g0205a0001c0005t0002g0022 | 3 | HG02559.hp1 HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.672-2924C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137153745 | ||||||
| chr9:137153746
|
A | G | 262 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(259): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.672-2923A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137153746 | ||||||
| chr9:137153915
|
G | A | 1 | a0001c0001t0001g0274 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.672-2754G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137153915 | ||||||
| chr9:137154020
|
C | T | 1 | a0001c0001t0001g0267 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.672-2649C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137154020 | ||||||
| chr9:137154047
|
G | A | 1 | a0001c0001t0001g0155 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.672-2622G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137154047 | ||||||
| chr9:137154131
|
T | G | 5 | a0001c0001t0001g0250a0001c0001t0001g0252a0001c0001t0001g0253others(2): Show | 5 | HG02735.hp1 HG03017.hp1 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.672-2538T>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137154131 | ||||||
| chr9:137154133
|
G | T | 257 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(254): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.672-2536G>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137154133 | ||||||
| chr9:137154135
|
G | T | 4 | a0001c0001t0001g0088a0001c0001t0001g0247a0001c0001t0001g0248others(1): Show | 4 | HG00140.hp2 HG01358.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.672-2534G>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137154135 | ||||||
| chr9:137154238
|
C | A | 1 | a0001c0002t0001g0019 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.672-2431C>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137154238 | ||||||
| chr9:137154432
|
C | CT | 12 | a0001c0001t0001g0043a0001c0001t0001g0067a0001c0001t0001g0070others(9): Show | 12 | HG00544.hp1 HG00621.hp2 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.672-2198dupT | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 137154432 | |||||
| chr9:137154432
|
C | CTT | 17 | a0001c0001t0001g0006a0001c0001t0001g0041a0001c0001t0001g0042others(14): Show | 18 | HG00280.hp2 HG00438.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.672-2199_672-2198d others(4): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 137154432 | |||||
| chr9:137154432
|
CT | C | 71 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(68): Show | 78 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.672-2198delT | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 137154432 | |||||
| chr9:137154432
|
CTT | C | 28 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(25): Show | 28 | HG01168.hp2 HG01515.hp1 HG01517.hp1 others(25): Show |
intron_variant | MODIFIER | c.672-2199_672-2198d others(4): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 137154432 | |||||
| chr9:137154432
|
CTTTTTTT | C | 12 | a0001c0001t0001g0010a0001c0001t0001g0027a0001c0001t0001g0047others(9): Show | 13 | HG00609.hp1 HG00738.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.672-2204_672-2198d others(9): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 137154432 | |||||
| chr9:137154432
|
CTTTTTTT others(1): Show |
C | 33 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0035others(30): Show | 35 | HG00140.hp2 HG00609.hp2 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.672-2205_672-2198d others(10): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 137154432 | |||||
| chr9:137154432
|
CTTTTTTT others(2): Show |
C | 7 | a0001c0001t0001g0057a0001c0001t0001g0091a0001c0001t0001g0093others(4): Show | 7 | HG01167.hp1 HG02895.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.672-2206_672-2198d others(11): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 137154432 | |||||
| chr9:137154432
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0274 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.672-2207_672-2198d others(12): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 137154432 | |||||
| chr9:137154432
|
CTTTTTTT others(4): Show |
C | 12 | a0001c0001t0001g0062a0001c0001t0001g0241a0001c0001t0001g0263others(9): Show | 13 | HG01106.hp1 HG02040.hp1 HG02083.hp1 others(10): Show |
intron_variant | MODIFIER | c.672-2208_672-2198d others(13): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 137154432 | |||||
| chr9:137154432
|
CTTTTTTT others(5): Show |
C | 6 | a0001c0001t0001g0264a0001c0002t0001g0200a0001c0003t0001g0032others(3): Show | 6 | HG00140.hp1 HG02015.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.672-2209_672-2198d others(14): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 137154432 | |||||
| chr9:137154432
|
CTTTTTTT others(6): Show |
C | 23 | a0001c0002t0001g0017a0001c0002t0001g0018a0001c0002t0001g0019others(20): Show | 27 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.672-2210_672-2198d others(15): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 137154432 | |||||
| chr9:137154432
|
CTTTTTTT others(7): Show |
C | 4 | a0001c0002t0001g0179a0001c0002t0001g0180a0001c0002t0001g0185others(1): Show | 4 | HG01069.hp1 HG01099.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.672-2211_672-2198d others(16): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 137154432 | |||||
| chr9:137154432
|
CTTTTTTT others(8): Show |
C | 1 | a0001c0007t0001g0261 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.672-2212_672-2198d others(17): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 137154432 | |||||
| chr9:137154432
|
CTTTTTTT others(13): Show |
C | 2 | a0001c0005t0001g0205a0001c0005t0002g0022 | 3 | HG02559.hp1 HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.672-2217_672-2198d others(22): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 137154432 | |||||
| chr9:137154448
|
T | A | 1 | a0001c0007t0001g0261 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.672-2221T>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137154448 | ||||||
| chr9:137154514
|
C | T | 9 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0035others(6): Show | 11 | HG01243.hp2 HG01261.hp2 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.672-2155C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137154514 | ||||||
| chr9:137154553
|
A | G | 1 | a0001c0001t0001g0073 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.672-2116A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137154553 | ||||||
| chr9:137154571
|
G | A | 2 | a0001c0001t0001g0197a0001c0001t0001g0215 | 2 | HG01109.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.672-2098G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137154571 | ||||||
| chr9:137154614
|
G | A | 2 | a0001c0005t0001g0205a0001c0005t0002g0022 | 3 | HG02559.hp1 HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.672-2055G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137154614 | ||||||
| chr9:137154639
|
A | G | 2 | a0001c0005t0001g0205a0001c0005t0002g0022 | 3 | HG02559.hp1 HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.672-2030A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137154639 | ||||||
| chr9:137154642
|
G | A | 8 | a0001c0001t0001g0029a0001c0001t0001g0129a0001c0001t0001g0245others(5): Show | 8 | HG02258.hp2 HG02280.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.672-2027G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137154642 | ||||||
| chr9:137154744
|
G | T | 1 | a0001c0001t0001g0132 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.672-1925G>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137154744 | ||||||
| chr9:137154773
|
G | T | 1 | a0001c0007t0001g0261 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.672-1896G>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137154773 | ||||||
| chr9:137154788
|
G | A | 4 | a0001c0001t0001g0033a0001c0001t0001g0039a0001c0001t0001g0197others(1): Show | 4 | HG01109.hp1 HG02451.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.672-1881G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137154788 | ||||||
| chr9:137154895
|
A | G | 1 | a0001c0001t0001g0054 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.672-1774A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137154895 | ||||||
| chr9:137154970
|
C | G | 1 | a0001c0001t0001g0248 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.672-1699C>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137154970 | ||||||
| chr9:137155044
|
A | G | 16 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(13): Show | 19 | HG01243.hp2 HG01261.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.672-1625A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137155044 | ||||||
| chr9:137155084
|
G | A | 11 | a0001c0001t0001g0038a0001c0001t0001g0111a0001c0001t0001g0112others(8): Show | 11 | HG00738.hp1 HG01099.hp1 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.672-1585G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137155084 | ||||||
| chr9:137155203
|
T | C | 1 | a0001c0007t0001g0261 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.672-1466T>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137155203 | ||||||
| chr9:137155204
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.672-1465G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137155204 | ||||||
| chr9:137155324
|
T | G | 3 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0001g0249 | 3 | HG00140.hp2 HG01358.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.672-1345T>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137155324 | ||||||
| chr9:137155423
|
G | A | 2 | a0001c0005t0001g0205a0001c0005t0002g0022 | 3 | HG02559.hp1 HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.672-1246G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137155423 | ||||||
| chr9:137155432
|
A | C | 1 | a0001c0001t0001g0117 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.672-1237A>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137155432 | ||||||
| chr9:137155473
|
C | A | 2 | a0001c0001t0001g0120a0001c0001t0001g0121 | 2 | HG00423.hp2 HG00438.hp2 |
intron_variant | MODIFIER | c.672-1196C>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137155473 | ||||||
| chr9:137155495
|
C | T | 2 | a0001c0006t0001g0127a0001c0006t0001g0130 | 2 | HG02055.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.672-1174C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137155495 | ||||||
| chr9:137155598
|
CAA | C | 28 | a0001c0002t0001g0017a0001c0002t0001g0018a0001c0002t0001g0019others(25): Show | 32 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.672-1069_672-1068d others(4): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 137155598 | |||||
| chr9:137155902
|
C | T | 2 | a0001c0001t0001g0135a0001c0001t0001g0168 | 2 | HG01884.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.672-767C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137155902 | ||||||
| chr9:137156092
|
A | G | 210 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(207): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.672-577A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137156092 | ||||||
| chr9:137156100
|
G | C | 212 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(209): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.672-569G>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137156100 | ||||||
| chr9:137156127
|
G | C | 1 | a0001c0001t0001g0039 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.672-542G>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137156127 | ||||||
| chr9:137156176
|
C | G | 1 | a0001c0001t0001g0135 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.672-493C>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137156176 | ||||||
| chr9:137156268
|
A | G | 1 | a0001c0004t0001g0040 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.672-401A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137156268 | ||||||
| chr9:137156339
|
A | G | 6 | a0001c0001t0001g0207a0001c0001t0001g0264a0001c0001t0001g0274others(3): Show | 7 | HG02258.hp1 HG02559.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.672-330A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137156339 | ||||||
| chr9:137156379
|
CCCCTGCT others(32): Show |
C | 28 | a0001c0002t0001g0017a0001c0002t0001g0018a0001c0002t0001g0019others(25): Show | 32 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.672-267_672-229del others(39): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 137156379 | |||||
| chr9:137156521
|
G | A | 15 | a0001c0001t0001g0241a0001c0001t0001g0263a0001c0003t0001g0001others(12): Show | 16 | HG02015.hp1 HG02040.hp1 HG02083.hp1 others(13): Show |
intron_variant | MODIFIER | c.672-148G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137156521 | ||||||
| chr9:137156522
|
C | T | 15 | a0001c0001t0001g0241a0001c0001t0001g0263a0001c0003t0001g0001others(12): Show | 16 | HG02015.hp1 HG02040.hp1 HG02083.hp1 others(13): Show |
intron_variant | MODIFIER | c.672-147C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137156522 | ||||||
| chr9:137156535
|
A | G | 29 | a0001c0002t0001g0017a0001c0002t0001g0018a0001c0002t0001g0019others(26): Show | 33 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.672-134A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137156535 | ||||||
| chr9:137156563
|
A | C | 29 | a0001c0002t0001g0017a0001c0002t0001g0018a0001c0002t0001g0019others(26): Show | 33 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.672-106A>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137156563 | ||||||
| chr9:137156589
|
A | G | 29 | a0001c0002t0001g0017a0001c0002t0001g0018a0001c0002t0001g0019others(26): Show | 33 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.672-80A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137156589 | ||||||
| chr9:137157188
|
C | T | 2 | a0001c0005t0001g0205a0001c0005t0002g0022 | 3 | HG02559.hp1 HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.968+151C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 6/19 | chr9 | 137157188 | ||||||
| chr9:137157206
|
C | A | 1 | a0001c0001t0001g0245 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.968+169C>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 6/19 | chr9 | 137157206 | ||||||
| chr9:137157255
|
G | A | 1 | a0001c0001t0001g0135 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.968+218G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 6/19 | chr9 | 137157255 | ||||||
| chr9:137157311
|
A | G | 32 | a0001c0001t0001g0111a0001c0001t0001g0124a0001c0002t0001g0017others(29): Show | 36 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.968+274A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 6/19 | chr9 | 137157311 | ||||||
| chr9:137157457
|
G | A | 3 | a0001c0002t0001g0171a0001c0002t0001g0182a0001c0009t0001g0174 | 3 | HG01074.hp2 HG01167.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.968+420G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 6/19 | chr9 | 137157457 | ||||||
| chr9:137157575
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.968+538G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 6/19 | chr9 | 137157575 | ||||||
| chr9:137157745
|
T | C | 3 | a0001c0001t0001g0012a0001c0001t0001g0114a0001c0001t0001g0115 | 4 | HG02630.hp1 HG02976.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.969-634T>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 6/19 | chr9 | 137157745 | ||||||
| chr9:137157748
|
A | G | 1 | a0001c0002t0001g0145 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.969-631A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 6/19 | chr9 | 137157748 | ||||||
| chr9:137157848
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.969-531G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 6/19 | chr9 | 137157848 | ||||||
| chr9:137158026
|
G | C | 1 | a0001c0001t0001g0135 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.969-353G>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 6/19 | chr9 | 137158026 | ||||||
| chr9:137158032
|
G | A | 1 | a0001c0005t0001g0078 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.969-347G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 6/19 | chr9 | 137158032 | ||||||
| chr9:137158067
|
G | C | 1 | a0001c0001t0001g0058 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.969-312G>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 6/19 | chr9 | 137158067 | ||||||
| chr9:137158067
|
G | T | 1 | a0001c0001t0001g0161 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.969-312G>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 6/19 | chr9 | 137158067 | ||||||
| chr9:137158144
|
A | G | 2 | a0001c0001t0001g0014a0001c0001t0001g0132 | 3 | HG02965.hp1 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.969-235A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 6/19 | chr9 | 137158144 | ||||||
| chr9:137158202
|
G | A | 15 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(12): Show | 18 | HG01243.hp2 HG01261.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.969-177G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 6/19 | chr9 | 137158202 | ||||||
| chr9:137158572
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1113+49G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 7/19 | chr9 | 137158572 | ||||||
| chr9:137158731
|
T | G | 1 | a0001c0001t0001g0170 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1197+27T>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 8/19 | chr9 | 137158731 | ||||||
| chr9:137158898
|
G | A | 12 | a0001c0003t0001g0001a0001c0003t0001g0032a0001c0003t0001g0050others(9): Show | 13 | HG02015.hp1 HG02040.hp1 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.1197+194G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 8/19 | chr9 | 137158898 | ||||||
| chr9:137159287
|
A | T | 1 | a0001c0007t0001g0261 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1197+583A>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 8/19 | chr9 | 137159287 | ||||||
| chr9:137159605
|
G | A | 2 | a0001c0003t0001g0195a0001c0003t0001g0196 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1197+901G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 8/19 | chr9 | 137159605 | ||||||
| chr9:137159627
|
C | T | 6 | a0001c0001t0001g0100a0001c0001t0001g0250a0001c0001t0001g0252others(3): Show | 6 | HG02735.hp1 HG03017.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.1197+923C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 8/19 | chr9 | 137159627 | ||||||
| chr9:137159684
|
T | C | 33 | a0001c0001t0001g0068a0001c0001t0001g0135a0001c0001t0001g0153others(30): Show | 37 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1197+980T>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 8/19 | chr9 | 137159684 | ||||||
| chr9:137159753
|
A | G | 1 | a0001c0001t0001g0066 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1197+1049A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 8/19 | chr9 | 137159753 | ||||||
| chr9:137159768
|
C | T | 1 | a0001c0001t0001g0238 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1197+1064C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 8/19 | chr9 | 137159768 | ||||||
| chr9:137160024
|
T | C | 1 | a0001c0001t0001g0161 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1198-1032T>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 8/19 | chr9 | 137160024 | ||||||
| chr9:137160436
|
C | CTTTTTTT others(4): Show |
1 | a0001c0007t0001g0261 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1198-619_1198-609d others(13): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 137160436 | |||||
| chr9:137160537
|
C | T | 1 | a0001c0001t0001g0010 | 2 | HG03453.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1198-519C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 8/19 | chr9 | 137160537 | ||||||
| chr9:137160539
|
C | T | 15 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(12): Show | 18 | HG01243.hp2 HG01261.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.1198-517C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 8/19 | chr9 | 137160539 | ||||||
| chr9:137160547
|
A | G | 1 | a0001c0001t0001g0276 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1198-509A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 8/19 | chr9 | 137160547 | ||||||
| chr9:137160806
|
C | T | 1 | a0001c0001t0001g0266 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1198-250C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 8/19 | chr9 | 137160806 | ||||||
| chr9:137160825
|
C | G | 4 | a0001c0001t0001g0207a0001c0001t0001g0264a0001c0001t0001g0274others(1): Show | 4 | HG02258.hp1 HG02976.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1198-231C>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 8/19 | chr9 | 137160825 | ||||||
| chr9:137160978
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1198-78G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 8/19 | chr9 | 137160978 | ||||||
| chr9:137161238
|
C | T | 1 | a0001c0003t0001g0218 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1339+41C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 9/19 | chr9 | 137161238 | ||||||
| chr9:137161251
|
G | A | 30 | a0001c0001t0001g0068a0001c0001t0001g0135a0001c0002t0001g0017others(27): Show | 34 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.1340-38G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 9/19 | chr9 | 137161251 | ||||||
| chr9:137161271
|
C | CGTA | 4 | a0001c0001t0001g0207a0001c0001t0001g0264a0001c0001t0001g0274others(1): Show | 4 | HG02258.hp1 HG02976.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1340-18_1340-17ins others(3): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 9/19 | chr9 | 137161271 | ||||||
| chr9:137161272
|
C | A | 4 | a0001c0001t0001g0207a0001c0001t0001g0264a0001c0001t0001g0274others(1): Show | 4 | HG02258.hp1 HG02976.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1340-17C>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 9/19 | chr9 | 137161272 | ||||||
| chr9:137161424
|
G | A | 260 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(257): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
splice_region_variant&intron_variant | LOW | c.1467+8G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 10/19 | chr9 | 137161424 | ||||||
| chr9:137161567
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1467+151C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 10/19 | chr9 | 137161567 | ||||||
| chr9:137161576
|
G | A | 178 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(175): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.1467+160G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 10/19 | chr9 | 137161576 | ||||||
| chr9:137161598
|
C | T | 14 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(11): Show | 17 | HG01243.hp2 HG01261.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1467+182C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 10/19 | chr9 | 137161598 | ||||||
| chr9:137161618
|
T | C | 208 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(205): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.1467+202T>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 10/19 | chr9 | 137161618 | ||||||
| chr9:137161641
|
G | A | 1 | a0001c0001t0001g0224 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1467+225G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 10/19 | chr9 | 137161641 | ||||||
| chr9:137161645
|
T | TCGGAGTG others(9): Show |
2 | a0001c0001t0001g0068a0001c0002t0001g0144 | 2 | HG01515.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.1467+239_1467+254d others(18): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr9 | 137161645 | |||||
| chr9:137161671
|
C | T | 28 | a0001c0001t0001g0135a0001c0002t0001g0017a0001c0002t0001g0018others(25): Show | 32 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.1468-253C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 10/19 | chr9 | 137161671 | ||||||
| chr9:137161672
|
A | G | 28 | a0001c0001t0001g0135a0001c0002t0001g0017a0001c0002t0001g0018others(25): Show | 32 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.1468-252A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 10/19 | chr9 | 137161672 | ||||||
| chr9:137161677
|
C | A | 28 | a0001c0001t0001g0135a0001c0002t0001g0017a0001c0002t0001g0018others(25): Show | 32 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.1468-247C>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 10/19 | chr9 | 137161677 | ||||||
| chr9:137161678
|
T | C | 28 | a0001c0001t0001g0135a0001c0002t0001g0017a0001c0002t0001g0018others(25): Show | 32 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.1468-246T>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 10/19 | chr9 | 137161678 | ||||||
| chr9:137161680
|
C | G | 28 | a0001c0001t0001g0135a0001c0002t0001g0017a0001c0002t0001g0018others(25): Show | 32 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.1468-244C>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 10/19 | chr9 | 137161680 | ||||||
| chr9:137161683
|
G | T | 28 | a0001c0001t0001g0135a0001c0002t0001g0017a0001c0002t0001g0018others(25): Show | 32 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.1468-241G>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 10/19 | chr9 | 137161683 | ||||||
| chr9:137161684
|
C | G | 28 | a0001c0001t0001g0135a0001c0002t0001g0017a0001c0002t0001g0018others(25): Show | 32 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.1468-240C>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 10/19 | chr9 | 137161684 | ||||||
| chr9:137161686
|
G | GCA | 28 | a0001c0001t0001g0135a0001c0002t0001g0017a0001c0002t0001g0018others(25): Show | 32 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.1468-238_1468-237i others(4): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 10/19 | chr9 | 137161686 | ||||||
| chr9:137161690
|
T | C | 28 | a0001c0001t0001g0135a0001c0002t0001g0017a0001c0002t0001g0018others(25): Show | 32 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.1468-234T>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 10/19 | chr9 | 137161690 | ||||||
| chr9:137161691
|
CTGGAGTG others(9): Show |
C | 232 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(229): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.1468-219_1468-204d others(18): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr9 | 137161691 | |||||
| chr9:137161694
|
G | C | 28 | a0001c0001t0001g0135a0001c0002t0001g0017a0001c0002t0001g0018others(25): Show | 32 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.1468-230G>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 10/19 | chr9 | 137161694 | ||||||
| chr9:137161696
|
GT | G | 28 | a0001c0001t0001g0135a0001c0002t0001g0017a0001c0002t0001g0018others(25): Show | 32 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.1468-227delT | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 10/19 | chr9 | 137161696 | ||||||
| chr9:137161699
|
G | C | 28 | a0001c0001t0001g0135a0001c0002t0001g0017a0001c0002t0001g0018others(25): Show | 32 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.1468-225G>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 10/19 | chr9 | 137161699 | ||||||
| chr9:137161701
|
C | G | 28 | a0001c0001t0001g0135a0001c0002t0001g0017a0001c0002t0001g0018others(25): Show | 32 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.1468-223C>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 10/19 | chr9 | 137161701 | ||||||
| chr9:137161705
|
A | T | 28 | a0001c0001t0001g0135a0001c0002t0001g0017a0001c0002t0001g0018others(25): Show | 32 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.1468-219A>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 10/19 | chr9 | 137161705 | ||||||
| chr9:137161706
|
CG | C | 28 | a0001c0001t0001g0135a0001c0002t0001g0017a0001c0002t0001g0018others(25): Show | 32 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.1468-217delG | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 10/19 | chr9 | 137161706 | ||||||
| chr9:137161715
|
G | C | 1 | a0001c0001t0001g0112 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1468-209G>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 10/19 | chr9 | 137161715 | ||||||
| chr9:137161750
|
C | T | 1 | a0001c0001t0001g0065 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1468-174C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 10/19 | chr9 | 137161750 | ||||||
| chr9:137162108
|
C | CG | 6 | a0001c0001t0001g0046a0001c0001t0001g0051a0001c0001t0001g0136others(3): Show | 6 | HG01123.hp1 HG01928.hp2 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.1632+24dupG | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr9 | 137162108 | |||||
| chr9:137162773
|
A | G | 2 | a0001c0003t0001g0195a0001c0003t0001g0196 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2013+34A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 14/19 | chr9 | 137162773 | ||||||
| chr9:137163043
|
G | C | 1 | a0001c0001t0001g0221 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2171+40G>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 15/19 | chr9 | 137163043 | ||||||
| chr9:137163466
|
T | A | 1 | a0001c0001t0001g0146 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2334-93T>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 16/19 | chr9 | 137163466 | ||||||
| chr9:137163745
|
G | A | 2 | a0001c0001t0001g0190a0001c0001t0001g0191 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.2444-14G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 17/19 | chr9 | 137163745 | ||||||
| chr9:137163749
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2444-10C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 17/19 | chr9 | 137163749 | ||||||
| chr9:137164337
|
G | A | 6 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(3): Show | 6 | HG01891.hp2 HG02280.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2589+433G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 18/19 | chr9 | 137164337 | ||||||
| chr9:137164349
|
C | T | 1 | a0001c0007t0001g0261 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2589+445C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 18/19 | chr9 | 137164349 | ||||||
| chr9:137164825
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2590-361G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 18/19 | chr9 | 137164825 | ||||||
| chr9:137165558
|
C | T | 1 | a0001c0003t0001g0262 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2700+262C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 19/19 | chr9 | 137165558 | ||||||
| chr9:137165816
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2700+520C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 19/19 | chr9 | 137165816 | ||||||
| chr9:137165970
|
A | T | 1 | a0001c0001t0001g0105 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2700+674A>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 19/19 | chr9 | 137165970 | ||||||
| chr9:137166012
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2700+716C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 19/19 | chr9 | 137166012 | ||||||
| chr9:137166481
|
G | A | 2 | a0001c0001t0001g0124a0001c0001t0001g0126 | 2 | HG02602.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2701-930G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 19/19 | chr9 | 137166481 | ||||||
| chr9:137166489
|
G | C | 1 | a0001c0001t0001g0016 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2701-922G>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 19/19 | chr9 | 137166489 | ||||||
| chr9:137166534
|
CG | C | 6 | a0001c0001t0001g0100a0001c0001t0001g0250a0001c0001t0001g0253others(3): Show | 6 | HG02040.hp1 HG03017.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.2701-873delG | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr9 | 137166534 | |||||
| chr9:137166914
|
C | T | 1 | a0001c0001t0001g0077 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2701-497C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 19/19 | chr9 | 137166914 | ||||||
| chr9:137166994
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2701-417G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 19/19 | chr9 | 137166994 | ||||||
| chr9:137167087
|
C | T | 1 | a0001c0007t0001g0261 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2701-324C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 19/19 | chr9 | 137167087 | ||||||
| chr9:137167246
|
G | A | 2 | a0001c0003t0001g0195a0001c0003t0001g0196 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2701-165G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 19/19 | chr9 | 137167246 | ||||||
| chr9:137167342
|
G | A | 2 | a0001c0002t0001g0171a0001c0002t0001g0182 | 2 | HG01074.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.2701-69G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 19/19 | chr9 | 137167342 |