Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2814 | 236 | 84 | 45 | 66 | 11 | 29 | GRIN1_chr9_137134154_137173756 | GRIN1 | ATGAG others(2809): Show |
chr9 | 137134154 | 137173756 | ||
| a0001c0002 | 0/1 | 2814 | 32 | 1 | 16 | 0 | 5 | 9 | GRIN1_chr9_137134154_137173756 | GRIN1 | ATGAG others(2809): Show |
chr9 | 137134154 | 137173756 | ||
| a0001c0003 | 0/0 | 2814 | 15 | 2 | 0 | 10 | 0 | 3 | GRIN1_chr9_137134154_137173756 | GRIN1 | ATGAG others(2809): Show |
chr9 | 137134154 | 137173756 | ||
| a0001c0004 | 0/0 | 2814 | 5 | 0 | 0 | 5 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | ATGAG others(2809): Show |
chr9 | 137134154 | 137173756 | ||
| a0001c0005 | 0/0 | 2814 | 4 | 4 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | ATGAG others(2809): Show |
chr9 | 137134154 | 137173756 | ||
| a0001c0006 | 0/0 | 2814 | 2 | 2 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | ATGAG others(2809): Show |
chr9 | 137134154 | 137173756 | ||
| a0001c0007 | 0/0 | 2814 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | ATGAG others(2809): Show |
chr9 | 137134154 | 137173756 | ||
| a0001c0008 | 0/0 | 2814 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | ATGAG others(2809): Show |
chr9 | 137134154 | 137173756 | ||
| a0001c0009 | 0/0 | 2814 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | ATGAG others(2809): Show |
chr9 | 137134154 | 137173756 | ||
| a0001c0010 | 0/0 | 2814 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | ATGAG others(2809): Show |
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 | GCAGT others(4374): Show |
chr9 | 137134154 | 137173756 |
| a0001c0001t0003 | 0/0 | 4379 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | GCAGT others(4374): Show |
chr9 | 137134154 | 137173756 |
| a0001c0001t0004 | 0/0 | 4379 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | GCAGT others(4374): Show |
chr9 | 137134154 | 137173756 |
| a0001c0002t0001 | 0/1 | 4379 | 32 | 1 | 16 | 0 | 5 | 9 | GRIN1_chr9_137134154_137173756 | GRIN1 | GCAGT others(4374): Show |
chr9 | 137134154 | 137173756 |
| a0001c0003t0001 | 0/0 | 4379 | 15 | 2 | 0 | 10 | 0 | 3 | GRIN1_chr9_137134154_137173756 | GRIN1 | GCAGT others(4374): Show |
chr9 | 137134154 | 137173756 |
| a0001c0004t0001 | 0/0 | 4379 | 5 | 0 | 0 | 5 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | GCAGT others(4374): Show |
chr9 | 137134154 | 137173756 |
| a0001c0005t0001 | 0/0 | 4379 | 2 | 2 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | GCAGT others(4374): Show |
chr9 | 137134154 | 137173756 |
| a0001c0005t0002 | 0/0 | 4379 | 2 | 2 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | GCAGT others(4374): Show |
chr9 | 137134154 | 137173756 |
| a0001c0006t0001 | 0/0 | 4379 | 2 | 2 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | GCAGT others(4374): Show |
chr9 | 137134154 | 137173756 |
| a0001c0007t0001 | 0/0 | 4379 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | GCAGT others(4374): Show |
chr9 | 137134154 | 137173756 |
| a0001c0008t0001 | 0/0 | 4379 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | GCAGT others(4374): Show |
chr9 | 137134154 | 137173756 |
| a0001c0009t0001 | 0/0 | 4379 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | GCAGT others(4374): Show |
chr9 | 137134154 | 137173756 |
| a0001c0010t0001 | 0/0 | 4379 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | GCAGT others(4374): Show |
chr9 | 137134154 | 137173756 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | 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 |
| a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | 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 | 0 | 0 | 2 | 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 | 0 | 0 | 2 | 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 | 2 | 2 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 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 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0080 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 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 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0119 | 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 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 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 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0003g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0001t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0002t0001g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0002t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0002t0001g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0002t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0002t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0002t0001g0164 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0002t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0003t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0003t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0003t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0003t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0003t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0003t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0003t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0003t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0003t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0003t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0003t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0003t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0003t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0003t0001g0256 | 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 |
| a0001c0004t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0004t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0004t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0005t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0005t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0005t0002g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0006t0001g0111 | 0/0 | 1 | 1 | 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 |
| a0001c0007t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0008t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0009t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| a0001c0010t0001g0001 | 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 | g0201 | EUR | GBR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0017 | EUR | GBR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0195 | EUR | GBR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0240 | EUR | GBR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0022 | EUR | FIN | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0139 | EUR | FIN | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | CHS | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | CHS | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0042 | 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 | g0148 | EAS | CHS | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | CHS | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | CHS | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | CHS | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | CHS | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0023 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0020 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0173 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0175 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0172 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0183 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0145 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0023 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0024 | 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 | g0009 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0170 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0167 | 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 | g0020 | AMR | CLM | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | CLM | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0168 | AMR | CLM | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | CLM | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | CLM | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | CLM | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0141 | EUR | IBS | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0185 | EUR | IBS | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0076 | EUR | IBS | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0188 | EUR | IBS | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0184 | EUR | IBS | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0187 | EUR | IBS | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | ACB | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01928 | hp1 | a0001 | c0008 | t0001 | g0025 | AMR | PEL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0019 | AMR | PEL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PEL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02015 | hp1 | a0001 | c0003 | t0001 | g0236 | EAS | KHV | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02040 | hp1 | a0001 | c0003 | t0001 | g0075 | EAS | KHV | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02055 | hp1 | a0001 | c0006 | t0001 | g0111 | AFR | ACB | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02056 | hp1 | a0001 | c0010 | t0001 | g0001 | EAS | KHV | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02056 | hp2 | a0001 | c0003 | t0001 | g0224 | EAS | KHV | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0206 | 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 | g0235 | EAS | KHV | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0158 | 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 | g0140 | EAS | KHV | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | KHV | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CDX | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | CDX | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | ACB | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | ACB | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | PEL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | ACB | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PEL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0161 | AMR | PEL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PEL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0160 | 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 | g0149 | AFR | ACB | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02602 | hp2 | a0001 | c0003 | t0001 | g0135 | SAS | PJL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02717 | hp1 | a0001 | c0005 | t0002 | g0026 | AFR | GWD | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | GWD | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0022 | SAS | PJL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02809 | hp2 | a0001 | c0005 | t0001 | g0200 | AFR | GWD | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02818 | hp1 | a0001 | c0007 | t0001 | g0254 | AFR | GWD | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | GWD | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02896 | hp2 | a0001 | c0003 | t0001 | g0191 | AFR | GWD | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02897 | hp1 | a0001 | c0003 | t0001 | g0190 | AFR | GWD | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ESN | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02922 | hp2 | a0001 | c0006 | t0001 | g0127 | AFR | ESN | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ESN | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | ESN | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ESN | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ESN | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | ESN | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | ESN | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0147 | SAS | PJL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | ESN | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ESN | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ESN | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | ESN | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | ESN | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03209 | hp2 | a0001 | c0005 | t0001 | g0063 | 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 | g0268 | AFR | MSL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0196 | SAS | PJL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | MSL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | MSL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0021 | SAS | PJL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0171 | SAS | PJL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0021 | SAS | PJL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ESN | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | GWD | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | MSL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | MSL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0166 | SAS | PJL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | STU | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | STU | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0174 | SAS | PJL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0259 | SAS | BEB | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | BEB | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | BEB | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03834 | hp2 | a0001 | c0003 | t0001 | g0136 | SAS | BEB | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | BEB | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | BEB | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0243 | SAS | BEB | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03942 | hp2 | a0001 | c0003 | t0001 | g0134 | SAS | BEB | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0143 | SAS | STU | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0258 | SAS | STU | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | STU | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | STU | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | STU | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | STU | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | STU | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | STU | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | YRI | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | YRI | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | CHB | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | CHB | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | YRI | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | YRI | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA18942 | hp2 | a0001 | c0003 | t0001 | g0256 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA18952 | hp2 | a0001 | c0004 | t0001 | g0071 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA18960 | hp1 | a0001 | c0003 | t0001 | g0211 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA18980 | hp1 | a0001 | c0003 | t0001 | g0234 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA18985 | hp2 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0089 | 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 | g0096 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA19004 | hp1 | a0001 | c0004 | t0001 | g0070 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | LWK | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | LWK | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | LWK | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | LWK | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA19058 | hp2 | a0001 | c0003 | t0001 | g0046 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA19060 | hp1 | a0001 | c0001 | t0004 | g0118 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA19060 | hp2 | a0001 | c0004 | t0001 | g0069 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA19087 | hp1 | a0001 | c0003 | t0001 | g0004 | 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 | g0017 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA19091 | hp2 | a0001 | c0004 | t0001 | g0095 | EAS | JPT | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | YRI | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0194 | AFR | YRI | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | ASW | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ASW | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0179 | EUR | TSI | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0019 | EUR | TSI | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0226 | EUR | TSI | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0209 | EUR | TSI | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA20905 | hp1 | a0001 | c0009 | t0001 | g0180 | SAS | GIH | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | GIH | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0198 | AMR | CLM | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02559 | hp1 | a0001 | c0005 | t0002 | g0026 | AFR | ACB | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | MSL | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | USA | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | USA | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | USA | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | USA | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | LWK | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | LWK | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0164 | REF | REF | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0080 | REF | REF | GRIN1_chr9_137134154_137173756 | GRIN1 | chr9 | 137134154 | 137173756 |
| view | 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 |
|---|
| view | 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 | a0001c0002 a0001c0009 |
32 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(29): 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 | a0001c0002 a0001c0009 |
32 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(29): 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 |
| view | 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 |
| view | 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 | a0001c0001t0001g0269 | 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 | a0001c0001t0001g0267 a0001c0001t0001g0268 |
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 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0263 others(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 | 3 | a0001c0001t0001g0003 a0001c0001t0001g0027 a0001c0001t0001g0028 |
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 | 62 | a0001c0001t0001g0003 a0001c0001t0001g0025 a0001c0001t0001g0027 others(59): 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 | 62 | a0001c0001t0001g0003 a0001c0001t0001g0025 a0001c0001t0001g0027 others(59): 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 | a0001c0001t0001g0259 a0001c0001t0001g0260 |
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 | a0001c0001t0001g0029 a0001c0001t0001g0030 |
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 | a0001c0001t0001g0210 | 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 | a0001c0001t0001g0208 a0001c0001t0001g0209 |
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 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 others(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 | a0001c0001t0001g0203 | 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 | a0001c0001t0001g0202 | 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 | a0001c0001t0001g0024 a0001c0001t0001g0201 |
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 | 110 | a0001c0001t0001g0003 a0001c0001t0001g0025 a0001c0001t0001g0027 others(107): Show |
117 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(114): 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 | a0001c0001t0001g0258 | 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 | a0001c0001t0001g0031 | 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 | a0001c0005t0001g0200 | 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 | a0001c0001t0001g0025 a0001c0001t0001g0212 a0001c0001t0001g0213 others(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 | 5 | a0001c0001t0001g0162 a0001c0002t0001g0019 a0001c0002t0001g0020 others(2): 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 | a0001c0001t0001g0032 | 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 | a0001c0001t0001g0163 | 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 | a0001c0001t0001g0202 a0001c0001t0001g0267 a0001c0001t0001g0268 |
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 | a0001c0001t0001g0197 a0001c0001t0001g0199 a0001c0002t0001g0195 others(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 | a0001c0001t0001g0193 a0001c0002t0001g0194 |
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 | 41 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0165 others(38): Show |
46 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.393+430C>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137142577 | |||||||
| chr9:137142809 | C | G | 101 | a0001c0001t0001g0003 a0001c0001t0001g0025 a0001c0001t0001g0027 others(98): Show |
108 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(105): 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 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0202 a0001c0001t0001g0267 a0001c0001t0001g0268 |
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 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 |
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 | a0001c0001t0001g0202 a0001c0001t0001g0267 a0001c0001t0001g0268 |
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 | a0001c0001t0001g0255 a0001c0001t0001g0257 a0001c0003t0001g0256 others(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 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0032 others(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 | a0001c0001t0001g0138 | 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 | a0001c0001t0001g0025 a0001c0001t0001g0157 a0001c0001t0001g0158 others(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 | 46 | a0001c0001t0001g0137 a0001c0001t0001g0162 a0001c0001t0001g0163 others(43): Show |
51 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(48): 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 | a0001c0001t0001g0139 | 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 | 98 | a0001c0001t0001g0003 a0001c0001t0001g0025 a0001c0001t0001g0027 others(95): Show |
104 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(101): 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 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0032 others(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 | a0001c0001t0001g0229 a0001c0001t0001g0230 |
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 | a0001c0001t0001g0202 a0001c0001t0001g0267 a0001c0001t0001g0268 |
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 | a0001c0001t0001g0148 a0001c0001t0001g0261 a0001c0001t0001g0262 others(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 | 4 | a0001c0001t0001g0003 a0001c0001t0001g0027 a0001c0001t0001g0028 others(1): 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 | a0001c0001t0001g0025 a0001c0001t0001g0050 a0001c0001t0001g0137 others(57): Show |
65 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(62): 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 | a0001c0003t0001g0134 a0001c0003t0001g0135 |
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 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(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 | a0001c0001t0001g0227 | 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 | a0001c0001t0001g0203 | 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 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0005t0001g0200 |
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 | a0001c0001t0001g0130 a0001c0001t0001g0131 |
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 | a0001c0001t0001g0107 | 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 | a0001c0001t0001g0203 | 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 | a0001c0001t0001g0038 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0032 a0001c0001t0001g0038 a0001c0001t0001g0039 others(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 | a0001c0001t0001g0038 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0106 a0001c0001t0001g0202 a0001c0001t0001g0257 others(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 | a0001c0001t0001g0207 | 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 | a0001c0001t0001g0104 a0001c0001t0001g0105 |
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 | a0001c0001t0001g0138 a0001c0001t0001g0165 a0001c0001t0001g0267 others(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 | a0001c0002t0001g0166 | 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 | a0001c0001t0001g0016 a0001c0001t0001g0099 a0001c0001t0001g0100 others(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 | 11 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(8): 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 | 10 | a0001c0001t0001g0045 a0001c0001t0001g0128 a0001c0001t0001g0202 others(7): 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 | a0001c0001t0001g0243 | 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 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0001g0042 others(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 | a0001c0001t0001g0050 a0001c0001t0001g0202 a0001c0001t0001g0210 others(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 | a0001c0001t0001g0163 | 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 | a0001c0001t0001g0050 a0001c0001t0001g0132 a0001c0001t0001g0163 others(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 | a0001c0001t0001g0267 | 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 | a0001c0001t0001g0248 a0001c0001t0001g0267 a0001c0005t0001g0200 |
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 | a0001c0001t0001g0268 | 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 | a0001c0001t0001g0201 | 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 | a0001c0003t0001g0004 a0001c0003t0001g0046 a0001c0003t0001g0234 others(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 | a0001c0001t0001g0165 a0001c0001t0001g0207 a0001c0001t0001g0257 others(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 | a0001c0001t0001g0260 | 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 | a0001c0001t0001g0049 | 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 | a0001c0001t0001g0242 | 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 | a0001c0002t0001g0196 | 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 | a0001c0001t0001g0043 | 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 | a0001c0001t0001g0132 a0001c0001t0001g0232 a0001c0001t0001g0249 others(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 | a0001c0001t0001g0207 | 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 | a0001c0001t0001g0207 | 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 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0044 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0041 others(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 | a0001c0001t0001g0247 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0079 |
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 | a0001c0002t0001g0174 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0133 a0001c0001t0001g0153 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0041 others(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 | a0001c0003t0001g0004 a0001c0003t0001g0046 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0018 others(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 | a0001c0002t0001g0171 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0018 others(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 | a0001c0003t0001g0134 a0001c0003t0001g0135 |
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 | a0001c0001t0001g0003 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0031 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0031 others(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 | a0001c0001t0001g0201 a0001c0001t0001g0239 a0001c0001t0001g0265 |
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 | a0001c0001t0001g0176 | 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 | a0001c0002t0001g0171 | 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 | a0001c0002t0001g0171 | 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 | a0001c0001t0001g0106 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0018 others(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 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0197 others(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 | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(135): Show |
153 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(150): 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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0035 others(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 | a0001c0001t0001g0103 a0001c0001t0001g0192 a0001c0001t0001g0268 others(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 | a0001c0001t0001g0086 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0041 a0001c0001t0001g0132 others(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 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(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 | a0001c0006t0001g0127 | 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 | a0001c0001t0001g0225 | 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 | a0001c0001t0001g0097 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0041 a0001c0001t0001g0051 others(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 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0027 others(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 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0041 a0001c0001t0001g0137 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0041 a0001c0001t0001g0051 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0051 a0001c0001t0001g0052 others(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 | a0001c0001t0001g0041 a0001c0001t0001g0140 a0001c0001t0001g0165 others(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 | a0001c0001t0001g0132 a0001c0002t0001g0023 a0001c0002t0001g0147 others(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 | a0001c0001t0001g0132 a0001c0002t0001g0023 a0001c0002t0001g0147 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0027 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0051 a0001c0001t0001g0052 others(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 | a0001c0002t0001g0147 | 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 | a0001c0002t0001g0023 | 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 | a0001c0003t0001g0256 | 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 | a0001c0003t0001g0236 | 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 | a0001c0002t0001g0161 | 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 | a0001c0001t0001g0132 | 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 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0001t0001g0169 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0051 a0001c0001t0001g0052 others(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 | a0001c0001t0001g0247 | 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 | a0001c0001t0001g0152 | 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 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0001g0251 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0051 a0001c0001t0001g0052 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0125 |
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 | a0001c0001t0001g0005 a0001c0001t0001g0051 a0001c0001t0001g0052 others(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 | a0001c0001t0001g0108 a0001c0001t0001g0243 a0001c0001t0001g0245 others(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 | a0001c0003t0001g0136 | 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 | a0001c0003t0001g0136 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0051 a0001c0001t0001g0052 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0051 a0001c0001t0001g0052 others(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 | a0001c0003t0001g0136 | 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 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0001g0243 others(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 | a0001c0003t0001g0136 | 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 | a0001c0001t0001g0137 a0001c0001t0001g0247 |
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 | a0001c0001t0001g0005 a0001c0001t0001g0051 a0001c0001t0001g0052 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0051 a0001c0001t0001g0052 others(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 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0001g0243 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0051 a0001c0001t0001g0052 others(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 | a0001c0001t0001g0132 a0001c0001t0001g0243 a0001c0001t0001g0248 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0051 a0001c0001t0001g0052 others(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 | a0001c0001t0001g0132 a0001c0001t0001g0243 a0001c0001t0001g0248 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0051 a0001c0001t0001g0052 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0051 a0001c0001t0001g0052 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0041 a0001c0001t0001g0051 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0041 a0001c0001t0001g0051 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0041 a0001c0001t0001g0051 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0041 a0001c0001t0001g0042 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0041 a0001c0001t0001g0051 others(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 | a0001c0001t0001g0054 a0001c0001t0001g0192 a0001c0001t0001g0249 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0041 a0001c0001t0001g0051 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0032 a0001c0001t0001g0051 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0032 a0001c0001t0001g0051 others(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 | a0001c0001t0001g0032 a0001c0001t0001g0098 a0001c0001t0001g0163 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0018 others(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 | a0001c0001t0001g0097 | 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 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0031 others(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 | a0001c0001t0001g0097 | 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 | a0001c0001t0001g0097 | 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 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0031 others(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 | a0001c0001t0001g0237 a0001c0003t0001g0136 |
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 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0031 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0001t0001g0073 others(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 | a0001c0007t0001g0254 | 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 | a0001c0001t0001g0193 | 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 | a0001c0001t0001g0201 a0001c0001t0001g0212 a0001c0001t0001g0213 others(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 | a0001c0001t0001g0193 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0041 others(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 | a0001c0005t0001g0200 | 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 | a0001c0001t0001g0016 a0001c0001t0001g0041 a0001c0001t0001g0042 others(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 | a0001c0007t0001g0254 | 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 | a0001c0005t0001g0200 | 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 | a0001c0001t0001g0016 a0001c0001t0001g0041 a0001c0001t0001g0042 others(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 | a0001c0001t0001g0231 a0001c0001t0001g0232 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0041 a0001c0001t0001g0042 others(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 | 69 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(66): 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 | a0001c0001t0001g0049 | 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 | a0001c0001t0001g0193 a0001c0005t0001g0200 |
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 | a0001c0001t0001g0193 a0001c0005t0001g0200 |
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 | a0001c0001t0001g0193 a0001c0005t0001g0200 |
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 | a0001c0001t0001g0259 | 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 | a0001c0001t0001g0207 | 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 | a0001c0001t0001g0032 a0001c0001t0001g0133 a0001c0001t0001g0193 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0032 a0001c0001t0001g0051 others(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 | a0001c0006t0001g0111 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0028 others(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 | 56 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0013 others(53): 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 | 88 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0015 others(85): Show |
96 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.394-639C>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145087 | |||||||
| chr9:137145090 | G | A | 88 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0015 others(85): Show |
96 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(93): 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 | a0001c0001t0001g0208 | 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 | a0001c0001t0001g0255 | 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 | a0001c0001t0001g0192 a0001c0003t0001g0190 a0001c0003t0001g0191 |
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 | a0001c0001t0001g0091 a0001c0001t0001g0106 |
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 | 104 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(101): Show |
112 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(109): 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 | a0001c0001t0001g0016 a0001c0001t0001g0129 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0052 others(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 | a0001c0001t0001g0243 a0001c0001t0001g0245 a0001c0001t0001g0248 |
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 | a0001c0001t0001g0247 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0052 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0083 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0129 |
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 | a0001c0001t0001g0243 a0001c0001t0001g0248 |
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 | 80 | a0001c0001t0001g0005 a0001c0001t0001g0032 a0001c0001t0001g0041 others(77): Show |
85 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.394-582C>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145144 | |||||||
| chr9:137145147 | G | A | 76 | a0001c0001t0001g0005 a0001c0001t0001g0032 a0001c0001t0001g0041 others(73): Show |
81 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(78): 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 | a0001c0001t0001g0237 | 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 | a0001c0003t0001g0136 | 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 | a0001c0001t0001g0243 a0001c0001t0001g0245 a0001c0001t0001g0248 |
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 | a0001c0001t0001g0243 a0001c0001t0001g0245 a0001c0001t0001g0248 |
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 | a0001c0001t0001g0243 a0001c0001t0001g0248 |
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 | a0001c0001t0001g0243 a0001c0001t0001g0245 a0001c0001t0001g0248 |
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 | 89 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0028 others(86): Show |
96 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.394-553T>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | chr9 | 137145173 | |||||||
| chr9:137145189 | G | A | 83 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0028 others(80): Show |
90 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(87): 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 | a0001c0001t0001g0243 a0001c0001t0001g0246 a0001c0001t0001g0248 others(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 | 87 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0028 others(84): Show |
94 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(91): 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 | a0001c0003t0001g0236 | 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 | a0001c0002t0001g0170 | 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 | a0001c0001t0001g0243 a0001c0001t0001g0248 |
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 | a0001c0001t0001g0243 a0001c0001t0001g0246 a0001c0001t0001g0248 others(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 | 155 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(152): Show |
170 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(167): 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 | a0001c0001t0001g0243 a0001c0001t0001g0248 |
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 | 153 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(150): Show |
168 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(165): 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 | a0001c0001t0001g0243 a0001c0001t0001g0248 |
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 | a0001c0001t0001g0243 a0001c0001t0001g0246 a0001c0001t0001g0248 others(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 | a0001c0001t0001g0132 | 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 | a0001c0001t0001g0208 | 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 | a0001c0001t0001g0243 a0001c0001t0001g0246 a0001c0001t0001g0248 others(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 | a0001c0001t0001g0243 a0001c0001t0001g0246 a0001c0001t0001g0248 others(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 | a0001c0001t0001g0243 a0001c0001t0001g0246 a0001c0001t0001g0248 others(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 | a0001c0001t0001g0243 a0001c0001t0001g0248 |
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 | a0001c0001t0001g0245 a0001c0001t0001g0247 |
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 | a0001c0001t0001g0243 a0001c0001t0001g0246 a0001c0001t0001g0248 others(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 | a0001c0001t0001g0243 a0001c0001t0001g0248 |
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 | a0001c0001t0001g0246 a0001c0001t0001g0261 a0001c0005t0001g0200 |
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 | a0001c0001t0001g0246 a0001c0001t0001g0261 |
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 | a0001c0001t0001g0225 | 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 | a0001c0001t0001g0246 a0001c0001t0001g0261 |
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 | a0001c0001t0001g0246 a0001c0001t0001g0261 |
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 | a0001c0001t0001g0246 a0001c0001t0001g0261 |
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 | a0001c0001t0001g0039 a0001c0001t0001g0132 a0001c0001t0001g0225 |
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 | a0001c0001t0001g0246 a0001c0001t0001g0261 |
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 | a0001c0001t0001g0039 a0001c0001t0001g0132 a0001c0001t0001g0225 others(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 | a0001c0001t0001g0246 a0001c0001t0001g0261 |
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 | a0001c0001t0001g0246 a0001c0001t0001g0261 |
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 | a0001c0001t0001g0246 a0001c0001t0001g0261 |
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 | a0001c0001t0001g0246 a0001c0001t0001g0261 |
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 | a0001c0001t0001g0246 a0001c0001t0001g0248 a0001c0001t0001g0261 |
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 | a0001c0001t0001g0243 a0001c0001t0001g0246 a0001c0001t0001g0248 others(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 | a0001c0001t0001g0243 a0001c0001t0001g0246 a0001c0001t0001g0261 |
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 | a0001c0001t0001g0192 a0001c0003t0001g0190 a0001c0003t0001g0191 others(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 | a0001c0001t0001g0192 a0001c0003t0001g0190 a0001c0003t0001g0191 others(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 | a0001c0001t0001g0192 a0001c0003t0001g0190 a0001c0003t0001g0191 others(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 | a0001c0001t0001g0192 a0001c0001t0001g0243 a0001c0001t0001g0261 others(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 | a0001c0007t0001g0254 | 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 | a0001c0001t0001g0192 a0001c0001t0001g0243 a0001c0001t0001g0261 others(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 | a0001c0001t0001g0192 a0001c0001t0001g0243 a0001c0001t0001g0261 others(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 | a0001c0001t0001g0192 a0001c0001t0001g0243 a0001c0001t0001g0261 others(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 | a0001c0001t0001g0192 a0001c0001t0001g0243 a0001c0001t0001g0261 others(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 | a0001c0001t0001g0243 | 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 | a0001c0001t0001g0192 a0001c0001t0001g0239 a0001c0001t0001g0243 others(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 | a0001c0001t0001g0261 | 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 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(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 | a0001c0001t0001g0246 a0001c0001t0001g0248 |
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 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(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 | a0001c0001t0001g0192 a0001c0001t0001g0239 a0001c0001t0001g0253 others(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 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(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 | a0001c0001t0001g0192 a0001c0001t0001g0239 a0001c0001t0001g0253 others(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 | a0001c0001t0001g0192 a0001c0001t0001g0239 a0001c0001t0001g0253 others(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 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(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 | a0001c0001t0001g0132 a0001c0001t0001g0192 a0001c0001t0001g0239 others(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 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(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 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0193 others(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 | a0001c0001t0001g0051 a0001c0002t0001g0147 |
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 | a0001c0001t0001g0051 a0001c0002t0001g0147 |
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 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(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 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0193 others(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 | a0001c0001t0001g0051 | 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 | a0001c0002t0001g0147 | 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 | a0001c0001t0001g0192 a0001c0001t0001g0239 a0001c0001t0001g0253 others(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 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(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 | a0001c0002t0001g0175 a0001c0002t0001g0183 |
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 | a0001c0001t0001g0261 | 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 | a0001c0001t0001g0192 a0001c0003t0001g0190 a0001c0003t0001g0191 others(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 | a0001c0001t0001g0192 a0001c0001t0001g0261 a0001c0003t0001g0190 others(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 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(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 | a0001c0001t0001g0192 a0001c0001t0001g0261 a0001c0003t0001g0190 others(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 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(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 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(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 | a0001c0001t0001g0261 | 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 | a0001c0001t0001g0261 | 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 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(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 | a0001c0001t0001g0261 | 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 | a0001c0001t0001g0261 | 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 | a0001c0001t0001g0261 | 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 | a0001c0001t0001g0072 | 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 | a0001c0001t0001g0261 | 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 | a0001c0001t0001g0208 | 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 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(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 | a0001c0001t0001g0239 a0001c0001t0001g0246 a0001c0001t0001g0248 others(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 | a0001c0001t0001g0261 | 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 | a0001c0001t0001g0261 | 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 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(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 | a0001c0001t0001g0014 a0001c0001t0001g0068 a0001c0001t0001g0122 |
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 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(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 | a0001c0001t0001g0132 | 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 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(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 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(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 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(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 | a0001c0001t0001g0192 a0001c0003t0001g0190 a0001c0003t0001g0191 others(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 | a0001c0001t0001g0245 a0001c0001t0001g0247 |
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 | a0001c0001t0001g0132 | 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 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(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 | a0001c0001t0001g0162 a0001c0001t0001g0203 |
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 | a0001c0001t0001g0261 | 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 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(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 | a0001c0001t0001g0261 | 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 | a0001c0001t0001g0261 | 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 | a0001c0001t0001g0261 | 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 | a0001c0001t0001g0163 | 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 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(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 | a0001c0001t0001g0261 | 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 | 156 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(153): Show |
171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): 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 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(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 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(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 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(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 | 49 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(46): 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 | 49 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(46): 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 | a0001c0001t0001g0081 a0001c0001t0001g0082 |
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 | a0001c0001t0001g0244 | 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 | a0001c0001t0001g0244 | 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 | a0001c0001t0001g0239 a0001c0001t0001g0249 a0001c0001t0001g0250 others(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 | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(243): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): 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 | a0001c0004t0001g0040 a0001c0004t0001g0069 a0001c0004t0001g0070 others(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 | a0001c0001t0001g0058 | 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 | a0001c0001t0001g0227 | 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 | a0001c0001t0001g0148 | 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 | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(253): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): 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 | a0001c0002t0001g0167 a0001c0002t0001g0168 |
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 | a0001c0001t0001g0123 a0001c0001t0001g0125 |
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 | a0001c0001t0001g0050 | 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 | a0001c0001t0001g0163 a0001c0001t0001g0237 a0001c0001t0001g0255 others(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 | a0001c0001t0001g0239 a0001c0001t0001g0249 a0001c0001t0001g0250 others(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 | a0001c0001t0001g0225 | 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 | a0001c0001t0001g0132 | 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 | a0001c0001t0001g0094 | 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 | a0001c0001t0001g0067 | 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 | a0001c0006t0001g0111 | 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 | a0001c0001t0001g0030 a0001c0001t0001g0045 |
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 |
235 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(232): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): 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 | a0001c0001t0001g0144 | 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 | a0001c0001t0001g0243 a0001c0001t0001g0246 a0001c0001t0001g0248 |
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 | a0001c0001t0001g0009 a0001c0001t0001g0076 a0001c0001t0001g0077 others(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 | 242 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(239): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): 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 | a0001c0001t0001g0245 a0001c0001t0001g0247 |
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 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0001g0251 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0076 a0001c0001t0001g0077 others(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 | a0001c0007t0001g0254 | 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 | a0001c0001t0001g0028 | 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 | a0001c0001t0001g0152 | 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 | a0001c0001t0001g0152 | 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 | a0001c0001t0001g0240 | 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 | a0001c0007t0001g0254 | 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 | a0001c0002t0001g0141 | 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 | a0001c0001t0001g0204 a0001c0001t0001g0258 |
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 | a0001c0001t0001g0237 a0001c0001t0001g0255 a0001c0003t0001g0075 others(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 | a0001c0007t0001g0254 | 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 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0001g0251 others(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 | a0001c0001t0001g0203 | 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 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0097 others(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 | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(200): 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 | a0001c0002t0001g0167 a0001c0002t0001g0168 |
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 | a0001c0001t0001g0108 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0083 |
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 | a0001c0001t0001g0158 | 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 | a0001c0001t0001g0093 | 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 | a0001c0001t0001g0130 | 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 | a0001c0007t0001g0254 | 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 | a0001c0007t0001g0254 | 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 | a0001c0007t0001g0254 | 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 | a0001c0003t0001g0211 | 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 | a0001c0001t0001g0013 a0001c0001t0001g0054 a0001c0001t0001g0092 others(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 | a0001c0001t0001g0051 | 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 | a0001c0001t0001g0192 a0001c0003t0001g0190 a0001c0003t0001g0191 |
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 | a0001c0006t0001g0111 a0001c0006t0001g0127 |
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 | a0001c0005t0001g0200 a0001c0005t0002g0026 a0001c0007t0001g0254 |
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 | a0001c0003t0001g0211 | 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 | a0001c0001t0001g0215 | 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 | a0001c0003t0001g0235 | 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 | a0001c0003t0001g0004 a0001c0003t0001g0046 |
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 | 26 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0021 others(23): Show |
31 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(28): 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 | a0001c0001t0001g0091 | 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 | a0001c0001t0001g0091 | 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 | a0001c0005t0001g0200 a0001c0005t0002g0026 a0001c0007t0001g0254 |
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 | a0001c0001t0001g0084 | 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 | a0001c0001t0001g0048 | 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 | a0001c0001t0001g0243 a0001c0001t0001g0245 a0001c0001t0001g0246 others(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 | 26 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0021 others(23): Show |
31 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(28): 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 | a0001c0003t0001g0190 a0001c0003t0001g0191 |
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 | a0001c0001t0001g0212 | 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 | a0001c0001t0001g0205 | 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 | a0001c0001t0001g0115 | 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 | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(172): 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 | a0001c0001t0001g0029 a0001c0001t0001g0091 a0001c0001t0001g0097 others(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 | a0001c0001t0001g0132 a0001c0001t0001g0163 a0001c0001t0001g0202 others(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 | 41 | a0001c0001t0001g0237 a0001c0001t0001g0255 a0001c0002t0001g0019 others(38): Show |
48 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(45): 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 | a0001c0001t0001g0247 | 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 | a0001c0006t0001g0111 a0001c0006t0001g0127 |
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 | 238 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(235): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.671+3121C>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137152230 | |||||||
| chr9:137152639 | C | T | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(190): 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 | a0001c0001t0001g0248 | 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 | a0001c0001t0001g0158 | 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 | a0001c0004t0001g0069 | 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 | a0001c0001t0001g0076 a0001c0001t0001g0077 |
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 | a0001c0001t0001g0163 | 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 | a0001c0001t0001g0260 | 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 | a0001c0002t0001g0179 | 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 | a0001c0001t0001g0202 a0001c0001t0001g0257 a0001c0001t0001g0267 others(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 | a0001c0002t0001g0173 | 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 | 48 | a0001c0001t0001g0202 a0001c0001t0001g0237 a0001c0001t0001g0255 others(45): Show |
55 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(52): 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 | a0001c0001t0001g0132 | 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 | a0001c0001t0001g0142 | 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 | a0001c0001t0001g0216 a0001c0001t0001g0268 |
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 | a0001c0001t0001g0037 | 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 | a0001c0005t0001g0200 a0001c0005t0002g0026 |
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 | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(253): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): 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 | a0001c0001t0001g0267 | 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 | a0001c0001t0001g0260 | 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 | a0001c0001t0001g0153 | 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 | a0001c0001t0001g0243 a0001c0001t0001g0245 a0001c0001t0001g0246 others(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 | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(249): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): 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 | a0001c0001t0001g0072 a0001c0001t0001g0240 a0001c0001t0001g0241 others(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 | a0001c0002t0001g0021 | 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 | a0001c0001t0001g0042 a0001c0001t0001g0051 a0001c0001t0001g0068 others(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 | a0001c0001t0001g0013 a0001c0001t0001g0041 a0001c0001t0001g0043 others(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 | 69 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(66): 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 | 27 | a0001c0001t0001g0003 a0001c0001t0001g0027 a0001c0001t0001g0028 others(24): 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 | a0001c0001t0001g0012 a0001c0001t0001g0029 a0001c0001t0001g0047 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0025 others(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 | a0001c0001t0001g0073 a0001c0001t0001g0084 a0001c0001t0001g0086 others(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 | a0001c0001t0001g0267 | 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 | a0001c0001t0001g0085 a0001c0001t0001g0237 a0001c0001t0001g0255 others(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 | a0001c0001t0001g0257 a0001c0002t0001g0195 a0001c0003t0001g0046 others(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 | 21 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0021 others(18): Show |
26 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(23): 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 | a0001c0002t0001g0167 a0001c0002t0001g0172 a0001c0002t0001g0173 others(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 | a0001c0007t0001g0254 | 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 | a0001c0005t0001g0200 a0001c0005t0002g0026 |
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 | a0001c0007t0001g0254 | 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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0035 others(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 | a0001c0001t0001g0058 | 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 | a0001c0001t0001g0192 a0001c0001t0001g0210 |
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 | a0001c0005t0001g0200 a0001c0005t0002g0026 |
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 | a0001c0005t0001g0200 a0001c0005t0002g0026 |
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 | a0001c0001t0001g0031 a0001c0001t0001g0116 a0001c0001t0001g0239 others(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 | a0001c0001t0001g0129 | 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 | a0001c0007t0001g0254 | 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 | a0001c0001t0001g0039 a0001c0001t0001g0050 a0001c0001t0001g0192 others(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 | a0001c0001t0001g0241 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0038 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0007t0001g0254 | 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 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0242 |
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 | a0001c0005t0001g0200 a0001c0005t0002g0026 |
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 | a0001c0001t0001g0114 | 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 | a0001c0001t0001g0119 a0001c0001t0001g0120 |
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 | a0001c0006t0001g0111 a0001c0006t0001g0127 |
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 | 26 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0021 others(23): Show |
31 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(28): 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 | a0001c0001t0001g0132 a0001c0001t0001g0163 |
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 | 206 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(203): 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 | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(205): 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 | a0001c0001t0001g0132 | 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 | a0001c0001t0001g0202 a0001c0001t0001g0257 a0001c0001t0001g0267 others(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 | 26 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0021 others(23): Show |
31 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(28): 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 | a0001c0001t0001g0237 a0001c0001t0001g0255 a0001c0003t0001g0004 others(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 | a0001c0001t0001g0237 a0001c0001t0001g0255 a0001c0003t0001g0004 others(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 | 27 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0021 others(24): Show |
32 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.672-134A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137156535 | |||||||
| chr9:137156563 | A | C | 27 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0021 others(24): Show |
32 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.672-106A>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 4/19 | chr9 | 137156563 | |||||||
| chr9:137156589 | A | G | 27 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0021 others(24): Show |
32 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(29): 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 | a0001c0005t0001g0200 a0001c0005t0002g0026 |
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 | a0001c0001t0001g0239 | 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 | a0001c0001t0001g0132 | 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 | 30 | a0001c0001t0001g0109 a0001c0001t0001g0123 a0001c0002t0001g0019 others(27): Show |
35 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(32): 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 | a0001c0002t0001g0175 a0001c0002t0001g0183 a0001c0009t0001g0180 |
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 | a0001c0001t0001g0119 | 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 | a0001c0001t0001g0015 a0001c0001t0001g0112 a0001c0001t0001g0126 |
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 | a0001c0002t0001g0143 | 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 | a0001c0001t0001g0163 | 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 | a0001c0001t0001g0132 | 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 | a0001c0005t0001g0063 | 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 | a0001c0001t0001g0091 | 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 | a0001c0001t0001g0158 | 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 | a0001c0001t0001g0016 a0001c0001t0001g0129 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0139 | 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 | a0001c0001t0001g0176 | 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 | a0001c0003t0001g0004 a0001c0003t0001g0046 a0001c0003t0001g0075 others(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 | a0001c0007t0001g0254 | 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 | a0001c0003t0001g0190 a0001c0003t0001g0191 |
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 | a0001c0001t0001g0098 a0001c0001t0001g0243 a0001c0001t0001g0245 others(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 | 31 | a0001c0001t0001g0094 a0001c0001t0001g0132 a0001c0001t0001g0150 others(28): Show |
36 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(33): 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 | a0001c0001t0001g0090 | 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 | a0001c0001t0001g0233 | 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 | a0001c0001t0001g0158 | 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 | a0001c0007t0001g0254 | 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 | a0001c0001t0001g0012 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0269 | 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 | a0001c0001t0001g0259 | 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 | a0001c0001t0001g0202 a0001c0001t0001g0257 a0001c0001t0001g0267 others(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 | a0001c0001t0001g0117 | 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 | a0001c0003t0001g0224 | 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 | 28 | a0001c0001t0001g0094 a0001c0001t0001g0132 a0001c0002t0001g0019 others(25): Show |
33 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(30): 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 | a0001c0001t0001g0202 a0001c0001t0001g0257 a0001c0001t0001g0267 others(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 | a0001c0001t0001g0202 a0001c0001t0001g0257 a0001c0001t0001g0267 others(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 | 254 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(251): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): 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 | a0001c0001t0001g0043 | 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 | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(171): 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 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | 204 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(201): 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 | a0001c0001t0001g0217 | 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 | a0001c0001t0001g0094 a0001c0002t0001g0141 |
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 | 26 | a0001c0001t0001g0132 a0001c0002t0001g0019 a0001c0002t0001g0020 others(23): Show |
31 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.1468-253C>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 10/19 | chr9 | 137161671 | |||||||
| chr9:137161672 | A | G | 26 | a0001c0001t0001g0132 a0001c0002t0001g0019 a0001c0002t0001g0020 others(23): Show |
31 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.1468-252A>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 10/19 | chr9 | 137161672 | |||||||
| chr9:137161677 | C | A | 26 | a0001c0001t0001g0132 a0001c0002t0001g0019 a0001c0002t0001g0020 others(23): Show |
31 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.1468-247C>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 10/19 | chr9 | 137161677 | |||||||
| chr9:137161678 | T | C | 26 | a0001c0001t0001g0132 a0001c0002t0001g0019 a0001c0002t0001g0020 others(23): Show |
31 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.1468-246T>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 10/19 | chr9 | 137161678 | |||||||
| chr9:137161680 | C | G | 26 | a0001c0001t0001g0132 a0001c0002t0001g0019 a0001c0002t0001g0020 others(23): Show |
31 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.1468-244C>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 10/19 | chr9 | 137161680 | |||||||
| chr9:137161683 | G | T | 26 | a0001c0001t0001g0132 a0001c0002t0001g0019 a0001c0002t0001g0020 others(23): Show |
31 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.1468-241G>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 10/19 | chr9 | 137161683 | |||||||
| chr9:137161684 | C | G | 26 | a0001c0001t0001g0132 a0001c0002t0001g0019 a0001c0002t0001g0020 others(23): Show |
31 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.1468-240C>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 10/19 | chr9 | 137161684 | |||||||
| chr9:137161686 | G | GCA | 26 | a0001c0001t0001g0132 a0001c0002t0001g0019 a0001c0002t0001g0020 others(23): Show |
31 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(28): 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 | 26 | a0001c0001t0001g0132 a0001c0002t0001g0019 a0001c0002t0001g0020 others(23): Show |
31 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(28): 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 | 228 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(225): 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 | 26 | a0001c0001t0001g0132 a0001c0002t0001g0019 a0001c0002t0001g0020 others(23): Show |
31 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.1468-230G>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 10/19 | chr9 | 137161694 | |||||||
| chr9:137161696 | GT | G | 26 | a0001c0001t0001g0132 a0001c0002t0001g0019 a0001c0002t0001g0020 others(23): Show |
31 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.1468-227delT | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 10/19 | chr9 | 137161696 | |||||||
| chr9:137161699 | G | C | 26 | a0001c0001t0001g0132 a0001c0002t0001g0019 a0001c0002t0001g0020 others(23): Show |
31 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.1468-225G>C | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 10/19 | chr9 | 137161699 | |||||||
| chr9:137161701 | C | G | 26 | a0001c0001t0001g0132 a0001c0002t0001g0019 a0001c0002t0001g0020 others(23): Show |
31 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.1468-223C>G | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 10/19 | chr9 | 137161701 | |||||||
| chr9:137161705 | A | T | 26 | a0001c0001t0001g0132 a0001c0002t0001g0019 a0001c0002t0001g0020 others(23): Show |
31 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.1468-219A>T | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 10/19 | chr9 | 137161705 | |||||||
| chr9:137161706 | CG | C | 26 | a0001c0001t0001g0132 a0001c0002t0001g0019 a0001c0002t0001g0020 others(23): Show |
31 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.1468-217delG | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 10/19 | chr9 | 137161706 | |||||||
| chr9:137161715 | G | C | 1 | a0001c0001t0001g0108 | 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 | a0001c0001t0001g0089 | 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 | a0001c0001t0001g0048 a0001c0001t0001g0081 a0001c0001t0001g0133 others(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 | a0001c0003t0001g0190 a0001c0003t0001g0191 |
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 | a0001c0001t0001g0222 | 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 | a0001c0001t0001g0144 | 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 | a0001c0001t0001g0187 a0001c0001t0001g0188 |
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 | 5 | a0001c0001t0001g0003 a0001c0001t0001g0027 a0001c0001t0001g0028 others(2): 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 | a0001c0007t0001g0254 | 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 | a0001c0001t0001g0050 | 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 | a0001c0003t0001g0256 | 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 | a0001c0001t0001g0215 | 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 | a0001c0001t0001g0099 | 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 | a0001c0001t0001g0115 | 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 | a0001c0001t0001g0123 a0001c0001t0001g0125 |
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 | a0001c0001t0001g0018 | 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 | a0001c0001t0001g0098 a0001c0001t0001g0243 a0001c0001t0001g0245 others(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 | a0001c0001t0001g0062 | 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 | a0001c0001t0001g0163 | 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 | a0001c0007t0001g0254 | 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 | a0001c0003t0001g0190 a0001c0003t0001g0191 |
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 | a0001c0002t0001g0175 a0001c0002t0001g0183 |
2 | HG01074.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.2701-69G>A | GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 19/19 | chr9 | 137167342 |