Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 2891 |
|---|---|
| ensemblid | ENSG00000120251.22 |
| hgncid | 4572 |
| symbol | GRIA2 |
| name | glutamate ionotropic receptor AMPA type subunit 2 |
| refseq_nuc | NM_001083619.3 |
| refseq_prot | NP_001077088.2 |
| ensembl_nuc | ENST00000264426.14 |
| ensembl_prot | ENSP00000264426.9 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 157220728 |
| end | 157366075 |
| strand | + |
| ver | v1.2 |
| region | chr4:157220728-157366075 |
| region5000 | chr4:157215728-157371075 |
| regionname0 | GRIA2_chr4_157220728_157366075 |
| regionname5000 | GRIA2_chr4_157215728_157371075 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 883 | 216 | 68 | 36 | 82 | 10 | 20 | 66 | GRIA2_chr4_157215728_157371075 | GRIA2 | copy fasta | chr4 | 157215728 | 157371075 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 2652 | 112 | 36 | 19 | 40 | 8 | 9 | GRIA2_chr4_157215728_157371075 | GRIA2 | copy fasta | chr4 | 157215728 | 157371075 |
| c0002 | 0/0 | 2652 | 91 | 23 | 14 | 42 | 1 | 11 | GRIA2_chr4_157215728_157371075 | GRIA2 | copy fasta | chr4 | 157215728 | 157371075 |
| c0003 | 0/0 | 2652 | 10 | 9 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | copy fasta | chr4 | 157215728 | 157371075 |
| c0004 | 0/0 | 2652 | 2 | 0 | 2 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | copy fasta | chr4 | 157215728 | 157371075 |
| c0005 | 0/0 | 2652 | 1 | 0 | 0 | 0 | 1 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | copy fasta | chr4 | 157215728 | 157371075 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 2960 | 81 | 51 | 14 | 11 | 2 | 3 | GRIA2_chr4_157215728_157371075 | GRIA2 | copy fasta | chr4 | 157215728 | 157371075 |
| t0002 | 0/0 | 2960 | 64 | 3 | 14 | 33 | 2 | 12 | GRIA2_chr4_157215728_157371075 | GRIA2 | copy fasta | chr4 | 157215728 | 157371075 |
| t0003 | 0/0 | 2960 | 32 | 1 | 0 | 30 | 0 | 1 | GRIA2_chr4_157215728_157371075 | GRIA2 | copy fasta | chr4 | 157215728 | 157371075 |
| t0004 | 0/0 | 2960 | 24 | 6 | 7 | 4 | 6 | 1 | GRIA2_chr4_157215728_157371075 | GRIA2 | copy fasta | chr4 | 157215728 | 157371075 |
| t0005 | 0/0 | 2962 | 5 | 2 | 0 | 0 | 0 | 3 | GRIA2_chr4_157215728_157371075 | GRIA2 | copy fasta | chr4 | 157215728 | 157371075 |
| t0006 | 0/0 | 2960 | 2 | 0 | 0 | 2 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | copy fasta | chr4 | 157215728 | 157371075 |
| t0007 | 0/0 | 2960 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | copy fasta | chr4 | 157215728 | 157371075 |
| t0008 | 0/0 | 2960 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | copy fasta | chr4 | 157215728 | 157371075 |
| t0009 | 0/0 | 2962 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | copy fasta | chr4 | 157215728 | 157371075 |
| t0010 | 0/0 | 2960 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | copy fasta | chr4 | 157215728 | 157371075 |
| t0011 | 0/0 | 2960 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | copy fasta | chr4 | 157215728 | 157371075 |
| t0012 | 0/0 | 2960 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | copy fasta | chr4 | 157215728 | 157371075 |
| t0013 | 0/0 | 2960 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | copy fasta | chr4 | 157215728 | 157371075 |
| t0014 | 0/0 | 2960 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | copy fasta | chr4 | 157215728 | 157371075 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2652 | 112 | 36 | 19 | 40 | 8 | 9 | GRIA2_chr4_157215728_157371075 | GRIA2 | copy fasta | chr4 | 157215728 | 157371075 |
| a0001c0002 | 0/0 | 2652 | 91 | 23 | 14 | 42 | 1 | 11 | GRIA2_chr4_157215728_157371075 | GRIA2 | copy fasta | chr4 | 157215728 | 157371075 |
| a0001c0003 | 0/0 | 2652 | 10 | 9 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | copy fasta | chr4 | 157215728 | 157371075 |
| a0001c0004 | 0/0 | 2652 | 2 | 0 | 2 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | copy fasta | chr4 | 157215728 | 157371075 |
| a0001c0005 | 0/0 | 2652 | 1 | 0 | 0 | 0 | 1 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | copy fasta | chr4 | 157215728 | 157371075 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5611 | 41 | 25 | 10 | 2 | 2 | 2 | GRIA2_chr4_157215728_157371075 | GRIA2 | copy fasta | chr4 | 157215728 | 157371075 |
| a0001c0001t0002 | 0/0 | 5611 | 8 | 1 | 2 | 2 | 0 | 3 | GRIA2_chr4_157215728_157371075 | GRIA2 | copy fasta | chr4 | 157215728 | 157371075 |
| a0001c0001t0003 | 0/0 | 5611 | 31 | 1 | 0 | 29 | 0 | 1 | GRIA2_chr4_157215728_157371075 | GRIA2 | copy fasta | chr4 | 157215728 | 157371075 |
| a0001c0001t0004 | 0/0 | 5611 | 23 | 5 | 7 | 4 | 6 | 1 | GRIA2_chr4_157215728_157371075 | GRIA2 | copy fasta | chr4 | 157215728 | 157371075 |
| a0001c0001t0005 | 0/0 | 5613 | 3 | 1 | 0 | 0 | 0 | 2 | GRIA2_chr4_157215728_157371075 | GRIA2 | copy fasta | chr4 | 157215728 | 157371075 |
| a0001c0001t0006 | 0/0 | 5611 | 2 | 0 | 0 | 2 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | copy fasta | chr4 | 157215728 | 157371075 |
| a0001c0001t0008 | 0/0 | 5611 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | copy fasta | chr4 | 157215728 | 157371075 |
| a0001c0001t0010 | 0/0 | 5611 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | copy fasta | chr4 | 157215728 | 157371075 |
| a0001c0001t0011 | 0/0 | 5611 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | copy fasta | chr4 | 157215728 | 157371075 |
| a0001c0001t0014 | 0/0 | 5611 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | copy fasta | chr4 | 157215728 | 157371075 |
| a0001c0002t0001 | 0/0 | 5611 | 32 | 19 | 3 | 9 | 0 | 1 | GRIA2_chr4_157215728_157371075 | GRIA2 | copy fasta | chr4 | 157215728 | 157371075 |
| a0001c0002t0002 | 0/0 | 5611 | 53 | 2 | 10 | 31 | 1 | 9 | GRIA2_chr4_157215728_157371075 | GRIA2 | copy fasta | chr4 | 157215728 | 157371075 |
| a0001c0002t0003 | 0/0 | 5611 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | copy fasta | chr4 | 157215728 | 157371075 |
| a0001c0002t0004 | 0/0 | 5611 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | copy fasta | chr4 | 157215728 | 157371075 |
| a0001c0002t0005 | 0/0 | 5613 | 2 | 1 | 0 | 0 | 0 | 1 | GRIA2_chr4_157215728_157371075 | GRIA2 | copy fasta | chr4 | 157215728 | 157371075 |
| a0001c0002t0009 | 0/0 | 5613 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | copy fasta | chr4 | 157215728 | 157371075 |
| a0001c0002t0012 | 0/0 | 5611 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | copy fasta | chr4 | 157215728 | 157371075 |
| a0001c0003t0001 | 0/0 | 5611 | 8 | 7 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | copy fasta | chr4 | 157215728 | 157371075 |
| a0001c0003t0007 | 0/0 | 5611 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | copy fasta | chr4 | 157215728 | 157371075 |
| a0001c0003t0013 | 0/0 | 5611 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | copy fasta | chr4 | 157215728 | 157371075 |
| a0001c0004t0002 | 0/0 | 5611 | 2 | 0 | 2 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | copy fasta | chr4 | 157215728 | 157371075 |
| a0001c0005t0002 | 0/0 | 5611 | 1 | 0 | 0 | 0 | 1 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | copy fasta | chr4 | 157215728 | 157371075 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0003g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0003g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0004g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0004g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0004g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0004g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0004g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0004g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0004g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0004g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0004g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0004g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0004g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0004g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0004g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0004g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0004g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0004g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0004g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0004g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0004g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0004g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0004g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0005g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0005g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0006g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0006g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0008g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0010g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0011g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0014g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0005g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0005g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0009g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0012g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0003t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0003t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0003t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0003t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0003t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0003t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0003t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0003t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0003t0007g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0003t0013g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0004t0002g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0005t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0004 | g0071 | EUR | FIN | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG00280 | hp2 | a0001 | c0001 | t0004 | g0057 | EUR | FIN | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG00323 | hp1 | a0001 | c0001 | t0004 | g0067 | EUR | FIN | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG00323 | hp2 | a0001 | c0002 | t0002 | g0168 | EUR | FIN | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0174 | EAS | CHS | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG00423 | hp2 | a0001 | c0002 | t0002 | g0208 | EAS | CHS | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0103 | EAS | CHS | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG00438 | hp2 | a0001 | c0002 | t0002 | g0202 | EAS | CHS | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG00609 | hp1 | a0001 | c0002 | t0002 | g0114 | EAS | CHS | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0094 | EAS | CHS | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG00639 | hp2 | a0001 | c0001 | t0004 | g0064 | AMR | PUR | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG00642 | hp1 | a0001 | c0002 | t0002 | g0152 | AMR | PUR | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG00733 | hp1 | a0001 | c0002 | t0002 | g0193 | AMR | PUR | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG00738 | hp1 | a0001 | c0002 | t0002 | g0045 | AMR | PUR | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01070 | hp2 | a0001 | c0004 | t0002 | g0003 | AMR | PUR | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01071 | hp1 | a0001 | c0004 | t0002 | g0003 | AMR | PUR | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01071 | hp2 | a0001 | c0002 | t0002 | g0187 | AMR | PUR | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0129 | AMR | PUR | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01081 | hp1 | a0001 | c0002 | t0002 | g0125 | AMR | PUR | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0130 | AMR | PUR | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0068 | AMR | PUR | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0023 | AMR | PUR | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0127 | AMR | PUR | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01169 | hp2 | a0001 | c0002 | t0002 | g0190 | AMR | PUR | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01175 | hp2 | a0001 | c0001 | t0004 | g0047 | AMR | PUR | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01243 | hp2 | a0001 | c0002 | t0002 | g0044 | AMR | PUR | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0058 | AMR | CLM | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01261 | hp2 | a0001 | c0002 | t0002 | g0188 | AMR | CLM | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01433 | hp1 | a0001 | c0002 | t0002 | g0121 | AMR | CLM | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01433 | hp2 | a0001 | c0001 | t0004 | g0048 | AMR | CLM | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01496 | hp1 | a0001 | c0001 | t0004 | g0069 | AMR | CLM | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0197 | AMR | CLM | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01516 | hp1 | a0001 | c0001 | t0004 | g0027 | EUR | IBS | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01516 | hp2 | a0001 | c0005 | t0002 | g0161 | EUR | IBS | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01517 | hp1 | a0001 | c0001 | t0004 | g0070 | EUR | IBS | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01517 | hp2 | a0001 | c0001 | t0004 | g0028 | EUR | IBS | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01884 | hp2 | a0001 | c0003 | t0001 | g0032 | AFR | ACB | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0039 | AFR | ACB | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01952 | hp1 | a0001 | c0002 | t0002 | g0192 | AMR | PEL | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01952 | hp2 | a0001 | c0002 | t0012 | g0122 | AMR | PEL | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0143 | AFR | ACB | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0093 | AFR | ACB | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02071 | hp1 | a0001 | c0001 | t0014 | g0035 | EAS | KHV | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02071 | hp2 | a0001 | c0002 | t0002 | g0167 | EAS | KHV | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0095 | EAS | KHV | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02129 | hp2 | a0001 | c0002 | t0002 | g0163 | EAS | KHV | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0104 | EAS | KHV | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0172 | EAS | KHV | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0080 | EAS | KHV | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02135 | hp2 | a0001 | c0002 | t0002 | g0116 | EAS | KHV | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0102 | EAS | CDX | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0175 | EAS | CDX | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02258 | hp2 | a0001 | c0001 | t0005 | g0007 | AFR | ACB | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0180 | AFR | ACB | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02280 | hp2 | a0001 | c0003 | t0001 | g0031 | AFR | ACB | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0183 | AFR | ACB | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02622 | hp1 | a0001 | c0003 | t0001 | g0018 | AFR | GWD | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0041 | AFR | GWD | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02630 | hp2 | a0001 | c0003 | t0001 | g0030 | AFR | GWD | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02683 | hp1 | a0001 | c0002 | t0002 | g0126 | SAS | PJL | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02698 | hp1 | a0001 | c0002 | t0002 | g0153 | SAS | PJL | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02698 | hp2 | a0001 | c0002 | t0002 | g0123 | SAS | PJL | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02717 | hp1 | a0001 | c0003 | t0013 | g0016 | AFR | GWD | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0141 | AFR | GWD | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02735 | hp1 | a0001 | c0002 | t0005 | g0211 | SAS | PJL | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02735 | hp2 | a0001 | c0002 | t0002 | g0179 | SAS | PJL | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0209 | SAS | PJL | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02738 | hp2 | a0001 | c0002 | t0002 | g0198 | SAS | PJL | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0131 | AFR | GWD | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0134 | AFR | GWD | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0135 | AFR | GWD | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02895 | hp2 | a0001 | c0003 | t0007 | g0043 | AFR | GWD | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02922 | hp1 | a0001 | c0001 | t0008 | g0042 | AFR | ESN | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | ESN | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02976 | hp1 | a0001 | c0002 | t0004 | g0138 | AFR | ESN | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0181 | AFR | ESN | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0140 | AFR | GWD | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG03098 | hp1 | a0001 | c0002 | t0001 | g0137 | AFR | MSL | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | MSL | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0142 | AFR | ESN | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0040 | AFR | ESN | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0099 | AFR | ESN | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0194 | AFR | ESN | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG03209 | hp1 | a0001 | c0003 | t0001 | g0033 | AFR | MSL | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG03209 | hp2 | a0001 | c0002 | t0005 | g0205 | AFR | MSL | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0200 | AFR | MSL | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0101 | AFR | MSL | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | MSL | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | MSL | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0132 | AFR | MSL | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | MSL | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG03491 | hp1 | a0001 | c0001 | t0005 | g0004 | SAS | PJL | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG03491 | hp2 | a0001 | c0002 | t0002 | g0201 | SAS | PJL | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG03492 | hp1 | a0001 | c0001 | t0005 | g0004 | SAS | PJL | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG03492 | hp2 | a0001 | c0002 | t0002 | g0199 | SAS | PJL | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG03516 | hp1 | a0001 | c0003 | t0001 | g0017 | AFR | ESN | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG03516 | hp2 | a0001 | c0001 | t0010 | g0207 | AFR | ESN | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG03540 | hp2 | a0001 | c0002 | t0002 | g0155 | AFR | GWD | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0051 | AFR | MSL | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | MSL | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG03669 | hp1 | a0001 | c0001 | t0004 | g0108 | SAS | PJL | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG03669 | hp2 | a0001 | c0002 | t0002 | g0146 | SAS | PJL | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0149 | SAS | BEB | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0162 | SAS | BEB | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0105 | SAS | BEB | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0210 | SAS | BEB | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0177 | AFR | YRI | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | YRI | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18906 | hp1 | a0001 | c0003 | t0001 | g0021 | AFR | YRI | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | YRI | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18942 | hp1 | a0001 | c0002 | t0002 | g0160 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18943 | hp2 | a0001 | c0002 | t0009 | g0203 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18944 | hp2 | a0001 | c0002 | t0002 | g0117 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18950 | hp1 | a0001 | c0002 | t0002 | g0145 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18950 | hp2 | a0001 | c0001 | t0004 | g0072 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18951 | hp1 | a0001 | c0002 | t0002 | g0156 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18954 | hp2 | a0001 | c0002 | t0002 | g0176 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18956 | hp1 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18956 | hp2 | a0001 | c0002 | t0002 | g0118 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18964 | hp2 | a0001 | c0002 | t0002 | g0139 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18968 | hp2 | a0001 | c0002 | t0002 | g0169 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0166 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18975 | hp2 | a0001 | c0002 | t0003 | g0196 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18977 | hp1 | a0001 | c0001 | t0004 | g0086 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18977 | hp2 | a0001 | c0002 | t0002 | g0159 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18980 | hp1 | a0001 | c0001 | t0006 | g0100 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18980 | hp2 | a0001 | c0002 | t0002 | g0154 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18981 | hp2 | a0001 | c0002 | t0002 | g0120 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18984 | hp2 | a0001 | c0002 | t0002 | g0185 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18991 | hp1 | a0001 | c0002 | t0001 | g0173 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18991 | hp2 | a0001 | c0001 | t0004 | g0074 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0060 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18995 | hp2 | a0001 | c0002 | t0002 | g0148 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18999 | hp1 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0182 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0191 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA19001 | hp1 | a0001 | c0002 | t0002 | g0128 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA19001 | hp2 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA19003 | hp1 | a0001 | c0002 | t0002 | g0165 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA19003 | hp2 | a0001 | c0001 | t0004 | g0073 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA19006 | hp1 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA19006 | hp2 | a0001 | c0002 | t0002 | g0170 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA19010 | hp2 | a0001 | c0002 | t0002 | g0195 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | LWK | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | LWK | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA19057 | hp1 | a0001 | c0002 | t0002 | g0150 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0088 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA19063 | hp2 | a0001 | c0002 | t0002 | g0115 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA19064 | hp1 | a0001 | c0002 | t0001 | g0144 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA19065 | hp1 | a0001 | c0002 | t0002 | g0158 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0124 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA19077 | hp2 | a0001 | c0002 | t0002 | g0119 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA19078 | hp1 | a0001 | c0002 | t0002 | g0164 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA19078 | hp2 | a0001 | c0001 | t0003 | g0059 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA19085 | hp2 | a0001 | c0002 | t0002 | g0147 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA19087 | hp1 | a0001 | c0001 | t0006 | g0091 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA19087 | hp2 | a0001 | c0002 | t0002 | g0171 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA19089 | hp1 | a0001 | c0001 | t0003 | g0090 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA19089 | hp2 | a0001 | c0002 | t0002 | g0186 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | YRI | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | YRI | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0133 | AFR | ASW | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0178 | AFR | ASW | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0026 | EUR | TSI | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0065 | EUR | TSI | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA20905 | hp1 | a0001 | c0002 | t0002 | g0189 | SAS | GIH | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | GIH | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01123 | hp1 | a0001 | c0001 | t0004 | g0184 | AMR | CLM | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01123 | hp2 | a0001 | c0003 | t0001 | g0052 | AMR | CLM | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02109 | hp1 | a0001 | c0001 | t0011 | g0014 | AFR | ACB | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0157 | AFR | ACB | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0136 | AFR | ACB | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02559 | hp2 | a0001 | c0002 | t0002 | g0151 | AFR | ACB | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:157317678
|
T | C | 3 | a0001c0002a0001c0004a0001c0005 | 94 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(91): Show |
synonymous_variant | LOW | c.687T>C | p.His229His | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 5/16 | 1002/5611 | 687/2652 | 229/883 | chr4 | 157317678 | ||
| chr4:157332827
|
T | C | 1 | a0001c0003 | 10 | HG01123.hp2 HG01884.hp2 HG02280.hp2 others(7): Show |
synonymous_variant | LOW | c.891T>C | p.Ser297Ser | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 7/16 | 1206/5611 | 891/2652 | 297/883 | chr4 | 157332827 | ||
| chr4:157333320
|
C | T | 1 | a0001c0005 | 1 | HG01516.hp2 | synonymous_variant | LOW | c.1122C>T | p.Asn374Asn | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 8/16 | 1437/5611 | 1122/2652 | 374/883 | chr4 | 157333320 | ||
| chr4:157359946
|
G | A | 1 | a0001c0004 | 2 | HG01070.hp2 HG01071.hp1 |
synonymous_variant | LOW | c.2094G>A | p.Ala698Ala | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 13/16 | 2409/5611 | 2094/2652 | 698/883 | chr4 | 157359946 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:157220798
|
A | G | 1 | a0001c0001t0014 | 1 | HG02071.hp1 | 5_prime_UTR_variant | MODIFIER | c.-245A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 1/16 | 245 | chr4 | 157220798 | |||||
| chr4:157220851
|
G | A | 2 | a0001c0001t0008a0001c0003t0007 | 2 | HG02895.hp2 HG02922.hp1 |
5_prime_UTR_variant | MODIFIER | c.-192G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 1/16 | 192 | chr4 | 157220851 | |||||
| chr4:157221008
|
A | G | 1 | a0001c0003t0013 | 1 | HG02717.hp1 | 5_prime_UTR_variant | MODIFIER | c.-35A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 1/16 | 35 | chr4 | 157221008 | |||||
| chr4:157363513
|
A | T | 1 | a0001c0001t0006 | 2 | NA18980.hp1 NA19087.hp1 |
3_prime_UTR_variant | MODIFIER | c.*82A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 16/16 | 469 | chr4 | 157363513 | |||||
| chr4:157363913
|
A | T | 1 | a0001c0002t0012 | 1 | HG01952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*482A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 16/16 | 869 | chr4 | 157363913 | |||||
| chr4:157364445
|
T | C | 5 | a0001c0001t0002a0001c0002t0002a0001c0002t0009others(2): Show | 65 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*1014T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 16/16 | 1401 | chr4 | 157364445 | |||||
| chr4:157364468
|
A | AAT | 3 | a0001c0001t0005a0001c0002t0005a0001c0002t0009 | 6 | HG02258.hp2 HG02735.hp1 HG03209.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1051_*1052dupTA | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 16/16 | 1440 | INFO_REALIGN_3_PRIME | chr4 | 157364468 | ||||
| chr4:157364573
|
G | A | 2 | a0001c0001t0005a0001c0002t0005 | 5 | HG02258.hp2 HG02735.hp1 HG03209.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1142G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 16/16 | 1529 | chr4 | 157364573 | |||||
| chr4:157365250
|
C | T | 1 | a0001c0001t0011 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1819C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 16/16 | 2206 | chr4 | 157365250 | |||||
| chr4:157365312
|
G | A | 3 | a0001c0001t0003a0001c0001t0006a0001c0002t0003 | 34 | HG00438.hp1 HG00609.hp2 HG02055.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*1881G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 16/16 | 2268 | chr4 | 157365312 | |||||
| chr4:157365388
|
G | A | 1 | a0001c0001t0010 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1957G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 16/16 | 2344 | chr4 | 157365388 | |||||
| chr4:157365463
|
A | T | 6 | a0001c0001t0003a0001c0001t0004a0001c0001t0006others(3): Show | 59 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*2032A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 16/16 | 2419 | chr4 | 157365463 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:157221453
|
T | C | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00733.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.89-214T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 1/15 | chr4 | 157221453 | ||||||
| chr4:157221458
|
G | A | 207 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(204): Show | 210 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.89-209G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 1/15 | chr4 | 157221458 | ||||||
| chr4:157221588
|
T | G | 39 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(36): Show | 39 | HG00642.hp2 HG00733.hp2 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.89-79T>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 1/15 | chr4 | 157221588 | ||||||
| chr4:157221623
|
G | A | 2 | a0001c0002t0002g0044a0001c0002t0002g0045 | 2 | HG00738.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.89-44G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 1/15 | chr4 | 157221623 | ||||||
| chr4:157221940
|
A | G | 137 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(134): Show | 138 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.229+133A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157221940 | ||||||
| chr4:157222091
|
G | C | 1 | a0001c0001t0003g0046 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.229+284G>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157222091 | ||||||
| chr4:157222156
|
G | C | 1 | a0001c0001t0005g0007 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.229+349G>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157222156 | ||||||
| chr4:157222350
|
T | C | 202 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(199): Show | 205 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.229+543T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157222350 | ||||||
| chr4:157222538
|
C | G | 1 | a0001c0002t0002g0208 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.229+731C>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157222538 | ||||||
| chr4:157222734
|
A | G | 39 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(36): Show | 39 | HG00642.hp2 HG00733.hp2 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.229+927A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157222734 | ||||||
| chr4:157222796
|
A | C | 1 | a0001c0001t0004g0108 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.229+989A>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157222796 | ||||||
| chr4:157223058
|
G | A | 9 | a0001c0002t0002g0114a0001c0002t0002g0115a0001c0002t0002g0116others(6): Show | 9 | HG00609.hp1 HG01433.hp1 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.229+1251G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157223058 | ||||||
| chr4:157223074
|
A | C | 8 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(5): Show | 8 | HG01891.hp2 HG02622.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.229+1267A>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157223074 | ||||||
| chr4:157223214
|
C | G | 1 | a0001c0001t0014g0035 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.229+1407C>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157223214 | ||||||
| chr4:157223379
|
C | A | 1 | a0001c0002t0002g0123 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.229+1572C>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157223379 | ||||||
| chr4:157223524
|
A | G | 5 | a0001c0001t0004g0039a0001c0001t0008g0042a0001c0002t0001g0040others(2): Show | 5 | HG01891.hp2 HG02622.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.229+1717A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157223524 | ||||||
| chr4:157223656
|
A | G | 1 | a0001c0001t0014g0035 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.229+1849A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157223656 | ||||||
| chr4:157223770
|
T | C | 1 | a0001c0002t0001g0124 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.229+1963T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157223770 | ||||||
| chr4:157224128
|
A | G | 1 | a0001c0001t0003g0107 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.229+2321A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157224128 | ||||||
| chr4:157224661
|
G | T | 2 | a0001c0001t0001g0206a0001c0001t0010g0207 | 2 | HG00639.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.229+2854G>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157224661 | ||||||
| chr4:157224743
|
C | T | 5 | a0001c0001t0004g0039a0001c0001t0008g0042a0001c0002t0001g0040others(2): Show | 5 | HG01891.hp2 HG02622.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.229+2936C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157224743 | ||||||
| chr4:157225389
|
T | C | 1 | a0001c0001t0005g0007 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.229+3582T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157225389 | ||||||
| chr4:157225591
|
A | T | 2 | a0001c0002t0002g0121a0001c0002t0012g0122 | 2 | HG01433.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.229+3784A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157225591 | ||||||
| chr4:157225621
|
C | CT | 97 | a0001c0001t0001g0034a0001c0001t0001g0204a0001c0001t0001g0206others(94): Show | 98 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.229+3828dupT | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157225621 | |||||
| chr4:157225621
|
CT | C | 69 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0053others(66): Show | 71 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.229+3828delT | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157225621 | |||||
| chr4:157225797
|
TA | T | 4 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(1): Show | 4 | HG01884.hp2 HG02280.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.229+3997delA | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157225797 | |||||
| chr4:157225930
|
G | C | 1 | a0001c0001t0002g0127 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.229+4123G>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157225930 | ||||||
| chr4:157226044
|
T | A | 2 | a0001c0001t0004g0047a0001c0001t0004g0048 | 2 | HG01175.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.229+4237T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157226044 | ||||||
| chr4:157226134
|
A | T | 4 | a0001c0001t0003g0102a0001c0001t0003g0103a0001c0001t0003g0104others(1): Show | 4 | HG00438.hp1 HG02132.hp1 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.229+4327A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157226134 | ||||||
| chr4:157226288
|
C | T | 5 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111others(2): Show | 5 | HG02630.hp1 HG02886.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.229+4481C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157226288 | ||||||
| chr4:157226443
|
A | C | 2 | a0001c0001t0001g0204a0001c0002t0005g0205 | 2 | HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.229+4636A>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157226443 | ||||||
| chr4:157226483
|
G | T | 1 | a0001c0001t0004g0101 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.229+4676G>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157226483 | ||||||
| chr4:157226708
|
T | C | 5 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111others(2): Show | 5 | HG02630.hp1 HG02886.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.229+4901T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157226708 | ||||||
| chr4:157226882
|
T | G | 1 | a0001c0001t0001g0106 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.229+5075T>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157226882 | ||||||
| chr4:157227124
|
G | T | 10 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(7): Show | 10 | HG00733.hp2 HG00738.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.229+5317G>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157227124 | ||||||
| chr4:157227151
|
A | T | 11 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0005g0007others(8): Show | 11 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.229+5344A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157227151 | ||||||
| chr4:157227163
|
T | C | 1 | a0001c0002t0002g0128 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.229+5356T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157227163 | ||||||
| chr4:157227591
|
A | C | 98 | a0001c0001t0001g0204a0001c0001t0001g0206a0001c0001t0002g0127others(95): Show | 99 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.229+5784A>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157227591 | ||||||
| chr4:157227807
|
C | G | 5 | a0001c0001t0004g0039a0001c0001t0008g0042a0001c0002t0001g0040others(2): Show | 5 | HG01891.hp2 HG02622.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.229+6000C>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157227807 | ||||||
| chr4:157228169
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.229+6362C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157228169 | ||||||
| chr4:157228375
|
A | C | 1 | a0001c0002t0009g0203 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.229+6568A>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157228375 | ||||||
| chr4:157228558
|
C | T | 10 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(7): Show | 10 | HG00733.hp2 HG00738.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.229+6751C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157228558 | ||||||
| chr4:157228563
|
C | T | 1 | a0001c0001t0001g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.229+6756C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157228563 | ||||||
| chr4:157228564
|
G | A | 1 | a0001c0001t0004g0039 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.229+6757G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157228564 | ||||||
| chr4:157228576
|
T | C | 1 | a0001c0002t0001g0129 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.229+6769T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157228576 | ||||||
| chr4:157228707
|
C | A | 9 | a0001c0002t0001g0130a0001c0002t0001g0131a0001c0002t0001g0132others(6): Show | 9 | HG01081.hp2 HG02486.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.229+6900C>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157228707 | ||||||
| chr4:157228731
|
T | C | 1 | a0001c0001t0014g0035 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.229+6924T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157228731 | ||||||
| chr4:157228790
|
C | CA | 164 | a0001c0001t0001g0015a0001c0001t0001g0053a0001c0001t0001g0054others(161): Show | 168 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.229+7003dupA | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157228790 | |||||
| chr4:157228790
|
C | CAA | 30 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0019others(27): Show | 30 | HG00733.hp2 HG00738.hp2 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.229+7002_229+7003d others(4): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157228790 | |||||
| chr4:157228790
|
C | CAAA | 5 | a0001c0001t0004g0039a0001c0001t0008g0042a0001c0002t0001g0040others(2): Show | 5 | HG01891.hp2 HG02622.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.229+7001_229+7003d others(5): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157228790 | |||||
| chr4:157228790
|
C | CAAAA | 5 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(2): Show | 5 | HG00642.hp2 HG01168.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.229+7000_229+7003d others(6): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157228790 | |||||
| chr4:157228834
|
C | A | 4 | a0001c0001t0005g0007a0001c0003t0001g0017a0001c0003t0001g0018others(1): Show | 4 | HG02258.hp2 HG02622.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.229+7027C>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157228834 | ||||||
| chr4:157228856
|
A | C | 2 | a0001c0001t0001g0106a0001c0002t0002g0199 | 2 | HG03492.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.229+7049A>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157228856 | ||||||
| chr4:157229107
|
A | G | 207 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(204): Show | 210 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.229+7300A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157229107 | ||||||
| chr4:157229179
|
T | C | 1 | a0001c0002t0001g0140 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.229+7372T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157229179 | ||||||
| chr4:157229548
|
G | A | 29 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(26): Show | 29 | HG00642.hp2 HG01168.hp2 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.229+7741G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157229548 | ||||||
| chr4:157229987
|
T | A | 5 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111others(2): Show | 5 | HG02630.hp1 HG02886.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.229+8180T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157229987 | ||||||
| chr4:157230059
|
T | G | 8 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(5): Show | 8 | HG01891.hp2 HG02622.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.229+8252T>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157230059 | ||||||
| chr4:157230183
|
T | C | 1 | a0001c0001t0005g0007 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.229+8376T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157230183 | ||||||
| chr4:157230204
|
C | A | 1 | a0001c0001t0001g0204 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.229+8397C>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157230204 | ||||||
| chr4:157230256
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.229+8449T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157230256 | ||||||
| chr4:157230262
|
AT | A | 58 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0053others(55): Show | 60 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.229+8462delT | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157230262 | |||||
| chr4:157230262
|
ATT | A | 4 | a0001c0001t0003g0102a0001c0001t0003g0103a0001c0001t0003g0104others(1): Show | 4 | HG00438.hp1 HG02132.hp1 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.229+8461_229+8462d others(4): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157230262 | |||||
| chr4:157230370
|
G | C | 5 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111others(2): Show | 5 | HG02630.hp1 HG02886.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.229+8563G>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157230370 | ||||||
| chr4:157230495
|
A | C | 2 | a0001c0001t0001g0098a0001c0001t0014g0035 | 2 | HG02071.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.229+8688A>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157230495 | ||||||
| chr4:157230535
|
C | T | 64 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0053others(61): Show | 66 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.229+8728C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157230535 | ||||||
| chr4:157230539
|
T | C | 64 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0053others(61): Show | 66 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.229+8732T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157230539 | ||||||
| chr4:157230555
|
C | T | 64 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0053others(61): Show | 66 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.229+8748C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157230555 | ||||||
| chr4:157230559
|
T | C | 64 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0053others(61): Show | 66 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.229+8752T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157230559 | ||||||
| chr4:157230559
|
T | TTTCCTTC others(17): Show |
4 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(1): Show | 4 | HG01884.hp2 HG02280.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.229+8767_229+8768i others(26): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157230559 | |||||
| chr4:157230575
|
C | CTTCCTTC others(1): Show |
24 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(21): Show | 24 | HG00642.hp2 HG01168.hp2 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.229+8771_229+8772i others(10): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157230575 | |||||
| chr4:157230575
|
C | T | 70 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0053others(67): Show | 72 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.229+8768C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157230575 | ||||||
| chr4:157230579
|
T | C | 94 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(91): Show | 96 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.229+8772T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157230579 | ||||||
| chr4:157230579
|
T | TTTCC | 106 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(103): Show | 107 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.229+8788_229+8791d others(6): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157230579 | |||||
| chr4:157230638
|
C | CT | 8 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(5): Show | 8 | HG01891.hp2 HG02622.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.229+8839dupT | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157230638 | |||||
| chr4:157230652
|
A | G | 1 | a0001c0002t0003g0196 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.229+8845A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157230652 | ||||||
| chr4:157230681
|
T | C | 1 | a0001c0002t0001g0200 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.229+8874T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157230681 | ||||||
| chr4:157230858
|
T | C | 5 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(2): Show | 5 | HG01123.hp2 HG02559.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.229+9051T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157230858 | ||||||
| chr4:157230862
|
T | G | 1 | a0001c0002t0001g0131 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.229+9055T>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157230862 | ||||||
| chr4:157230870
|
T | A | 62 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0053others(59): Show | 64 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.229+9063T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157230870 | ||||||
| chr4:157230888
|
C | G | 1 | a0001c0002t0002g0195 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.229+9081C>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157230888 | ||||||
| chr4:157231046
|
T | G | 1 | a0001c0001t0003g0056 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.229+9239T>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157231046 | ||||||
| chr4:157231169
|
G | C | 1 | a0001c0001t0001g0206 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.229+9362G>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157231169 | ||||||
| chr4:157231239
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.229+9432G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157231239 | ||||||
| chr4:157231280
|
C | G | 1 | a0001c0001t0001g0106 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.229+9473C>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157231280 | ||||||
| chr4:157231554
|
T | G | 2 | a0001c0001t0004g0057a0001c0001t0004g0058 | 2 | HG00280.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.229+9747T>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157231554 | ||||||
| chr4:157231566
|
G | A | 1 | a0001c0002t0002g0114 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.229+9759G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157231566 | ||||||
| chr4:157231756
|
A | G | 115 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(112): Show | 118 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.229+9949A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157231756 | ||||||
| chr4:157231829
|
T | A | 1 | a0001c0002t0001g0040 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.229+10022T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157231829 | ||||||
| chr4:157231995
|
A | C | 1 | a0001c0002t0002g0193 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.229+10188A>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157231995 | ||||||
| chr4:157232051
|
A | G | 2 | a0001c0001t0001g0049a0001c0001t0001g0050 | 2 | HG01884.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.229+10244A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157232051 | ||||||
| chr4:157232212
|
G | A | 20 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(17): Show | 20 | HG00642.hp2 HG01168.hp2 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.229+10405G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157232212 | ||||||
| chr4:157232350
|
C | T | 1 | a0001c0002t0002g0192 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.229+10543C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157232350 | ||||||
| chr4:157232367
|
G | C | 75 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0053others(72): Show | 78 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.229+10560G>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157232367 | ||||||
| chr4:157232654
|
T | C | 2 | a0001c0002t0001g0132a0001c0002t0001g0133 | 2 | HG03486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.229+10847T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157232654 | ||||||
| chr4:157232752
|
T | C | 1 | a0001c0002t0002g0115 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.229+10945T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157232752 | ||||||
| chr4:157232795
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.229+10988G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157232795 | ||||||
| chr4:157232898
|
T | C | 10 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(7): Show | 10 | HG00733.hp2 HG00738.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.229+11091T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157232898 | ||||||
| chr4:157233273
|
G | A | 20 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(17): Show | 20 | HG00642.hp2 HG01168.hp2 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.229+11466G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157233273 | ||||||
| chr4:157233322
|
C | T | 114 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(111): Show | 117 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.229+11515C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157233322 | ||||||
| chr4:157233579
|
C | G | 1 | a0001c0002t0001g0191 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.229+11772C>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157233579 | ||||||
| chr4:157233680
|
C | T | 1 | a0001c0001t0001g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.229+11873C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157233680 | ||||||
| chr4:157233728
|
A | C | 1 | a0001c0001t0001g0106 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.229+11921A>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157233728 | ||||||
| chr4:157234082
|
T | C | 3 | a0001c0003t0001g0017a0001c0003t0001g0018a0001c0003t0013g0016 | 3 | HG02622.hp1 HG02717.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.229+12275T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157234082 | ||||||
| chr4:157234258
|
T | C | 3 | a0001c0003t0001g0017a0001c0003t0001g0018a0001c0003t0013g0016 | 3 | HG02622.hp1 HG02717.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.229+12451T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157234258 | ||||||
| chr4:157234325
|
T | C | 19 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(16): Show | 19 | HG00642.hp2 HG01168.hp2 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.229+12518T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157234325 | ||||||
| chr4:157234357
|
C | T | 1 | a0001c0001t0014g0035 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.229+12550C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157234357 | ||||||
| chr4:157234513
|
A | G | 1 | a0001c0002t0002g0202 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.229+12706A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157234513 | ||||||
| chr4:157234538
|
T | C | 66 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0049others(63): Show | 68 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.229+12731T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157234538 | ||||||
| chr4:157234601
|
C | T | 2 | a0001c0002t0001g0130a0001c0002t0004g0138 | 2 | HG01081.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.229+12794C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157234601 | ||||||
| chr4:157234778
|
G | T | 10 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(7): Show | 10 | HG00733.hp2 HG00738.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.229+12971G>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157234778 | ||||||
| chr4:157234891
|
G | T | 1 | a0001c0001t0001g0097 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.229+13084G>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157234891 | ||||||
| chr4:157234909
|
T | C | 1 | a0001c0003t0001g0021 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.229+13102T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157234909 | ||||||
| chr4:157235383
|
G | C | 8 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(5): Show | 8 | HG00642.hp2 HG01168.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.229+13576G>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157235383 | ||||||
| chr4:157235432
|
C | T | 1 | a0001c0001t0011g0014 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.229+13625C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157235432 | ||||||
| chr4:157235478
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.229+13671C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157235478 | ||||||
| chr4:157235604
|
A | T | 1 | a0001c0002t0002g0208 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.229+13797A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157235604 | ||||||
| chr4:157235618
|
G | T | 5 | a0001c0002t0002g0188a0001c0002t0002g0189a0001c0002t0002g0190others(2): Show | 5 | HG00733.hp1 HG01169.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.229+13811G>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157235618 | ||||||
| chr4:157235628
|
A | G | 5 | a0001c0001t0001g0212a0001c0001t0002g0209a0001c0001t0002g0210others(2): Show | 6 | HG02735.hp1 HG02738.hp1 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.229+13821A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157235628 | ||||||
| chr4:157235689
|
A | G | 1 | a0001c0001t0001g0096 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.229+13882A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157235689 | ||||||
| chr4:157235705
|
T | C | 1 | a0001c0001t0001g0019 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.229+13898T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157235705 | ||||||
| chr4:157236315
|
T | A | 127 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(124): Show | 130 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.229+14508T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157236315 | ||||||
| chr4:157236320
|
A | G | 5 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(2): Show | 5 | HG01123.hp2 HG02559.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.229+14513A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157236320 | ||||||
| chr4:157236456
|
T | C | 1 | a0001c0001t0014g0035 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.229+14649T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157236456 | ||||||
| chr4:157236550
|
T | A | 2 | a0001c0001t0004g0057a0001c0001t0004g0058 | 2 | HG00280.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.229+14743T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157236550 | ||||||
| chr4:157236696
|
G | A | 1 | a0001c0001t0004g0039 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.229+14889G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157236696 | ||||||
| chr4:157236697
|
G | A | 1 | a0001c0001t0004g0039 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.229+14890G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157236697 | ||||||
| chr4:157237077
|
T | C | 3 | a0001c0002t0001g0124a0001c0002t0001g0144a0001c0002t0001g0191 | 3 | NA19000.hp1 NA19064.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.229+15270T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157237077 | ||||||
| chr4:157237100
|
T | A | 75 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0053others(72): Show | 78 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.229+15293T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157237100 | ||||||
| chr4:157237244
|
C | T | 1 | a0001c0001t0010g0207 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.229+15437C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157237244 | ||||||
| chr4:157237289
|
GT | G | 96 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(93): Show | 98 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.229+15499delT | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157237289 | |||||
| chr4:157237488
|
C | T | 1 | a0001c0002t0002g0187 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.229+15681C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157237488 | ||||||
| chr4:157237628
|
A | G | 1 | a0001c0001t0001g0106 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.229+15821A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157237628 | ||||||
| chr4:157237686
|
A | T | 1 | a0001c0001t0001g0106 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.229+15879A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157237686 | ||||||
| chr4:157238022
|
G | A | 2 | a0001c0001t0002g0209a0001c0001t0002g0210 | 2 | HG02738.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.229+16215G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157238022 | ||||||
| chr4:157238286
|
G | T | 1 | a0001c0001t0014g0035 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.229+16479G>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157238286 | ||||||
| chr4:157238747
|
G | A | 3 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038 | 3 | HG03041.hp1 HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.229+16940G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157238747 | ||||||
| chr4:157239470
|
C | A | 1 | a0001c0001t0014g0035 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.229+17663C>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157239470 | ||||||
| chr4:157239541
|
A | C | 1 | a0001c0001t0003g0105 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.229+17734A>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157239541 | ||||||
| chr4:157239839
|
C | T | 1 | a0001c0001t0014g0035 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.229+18032C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157239839 | ||||||
| chr4:157239909
|
C | T | 10 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111others(7): Show | 11 | HG02630.hp1 HG02735.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.229+18102C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157239909 | ||||||
| chr4:157240034
|
G | T | 1 | a0001c0001t0001g0106 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.229+18227G>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157240034 | ||||||
| chr4:157240094
|
T | C | 4 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0002g0099others(1): Show | 4 | HG02486.hp1 HG02809.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.229+18287T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157240094 | ||||||
| chr4:157240111
|
T | C | 2 | a0001c0002t0002g0145a0001c0002t0003g0196 | 2 | NA18950.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.229+18304T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157240111 | ||||||
| chr4:157240151
|
A | G | 127 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(124): Show | 130 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.229+18344A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157240151 | ||||||
| chr4:157240454
|
C | T | 5 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111others(2): Show | 5 | HG02630.hp1 HG02886.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.229+18647C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157240454 | ||||||
| chr4:157240493
|
C | T | 4 | a0001c0001t0005g0007a0001c0003t0001g0017a0001c0003t0001g0018others(1): Show | 4 | HG02258.hp2 HG02622.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.229+18686C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157240493 | ||||||
| chr4:157240702
|
C | CT | 21 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(18): Show | 21 | HG00642.hp2 HG01168.hp2 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.229+18906dupT | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157240702 | |||||
| chr4:157240702
|
CT | C | 11 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(8): Show | 11 | HG00733.hp2 HG00738.hp2 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.229+18906delT | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157240702 | |||||
| chr4:157240770
|
A | G | 2 | a0001c0001t0001g0011a0001c0001t0001g0012 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.229+18963A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157240770 | ||||||
| chr4:157240799
|
G | A | 2 | a0001c0002t0002g0146a0001c0002t0002g0147 | 2 | HG03669.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.229+18992G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157240799 | ||||||
| chr4:157240858
|
T | C | 4 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0025others(1): Show | 4 | HG01070.hp1 HG01109.hp2 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.229+19051T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157240858 | ||||||
| chr4:157240942
|
G | C | 5 | a0001c0001t0003g0059a0001c0001t0003g0060a0001c0001t0003g0061others(2): Show | 5 | NA18951.hp2 NA18995.hp1 NA19057.hp2 others(2): Show |
intron_variant | MODIFIER | c.229+19135G>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157240942 | ||||||
| chr4:157240954
|
G | C | 1 | a0001c0002t0002g0148 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.229+19147G>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157240954 | ||||||
| chr4:157240998
|
T | TG | 62 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0053others(59): Show | 64 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.229+19192dupG | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157240998 | |||||
| chr4:157241007
|
A | G | 10 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111others(7): Show | 11 | HG02630.hp1 HG02735.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.229+19200A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157241007 | ||||||
| chr4:157241050
|
T | C | 1 | a0001c0001t0001g0034 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.229+19243T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157241050 | ||||||
| chr4:157241112
|
G | T | 1 | a0001c0001t0011g0014 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.229+19305G>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157241112 | ||||||
| chr4:157241155
|
A | G | 1 | a0001c0002t0002g0186 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.229+19348A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157241155 | ||||||
| chr4:157241157
|
G | A | 5 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111others(2): Show | 5 | HG02630.hp1 HG02886.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.229+19350G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157241157 | ||||||
| chr4:157241253
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.229+19446G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157241253 | ||||||
| chr4:157241274
|
T | G | 1 | a0001c0001t0004g0141 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.229+19467T>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157241274 | ||||||
| chr4:157241315
|
T | G | 1 | a0001c0001t0003g0063 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.229+19508T>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157241315 | ||||||
| chr4:157241360
|
T | C | 5 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111others(2): Show | 5 | HG02630.hp1 HG02886.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.229+19553T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157241360 | ||||||
| chr4:157241542
|
C | A | 6 | a0001c0001t0003g0002a0001c0001t0003g0056a0001c0001t0003g0089others(3): Show | 7 | NA18944.hp1 NA18980.hp1 NA19000.hp2 others(4): Show |
intron_variant | MODIFIER | c.229+19735C>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157241542 | ||||||
| chr4:157241582
|
C | A | 1 | a0001c0001t0003g0059 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.229+19775C>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157241582 | ||||||
| chr4:157241598
|
G | A | 1 | a0001c0001t0002g0149 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.229+19791G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157241598 | ||||||
| chr4:157241658
|
G | A | 1 | a0001c0001t0001g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.229+19851G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157241658 | ||||||
| chr4:157241837
|
T | A | 1 | a0001c0001t0001g0097 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.229+20030T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157241837 | ||||||
| chr4:157241868
|
C | T | 114 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(111): Show | 117 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.229+20061C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157241868 | ||||||
| chr4:157242303
|
T | C | 4 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(1): Show | 4 | HG00642.hp2 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.229+20496T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157242303 | ||||||
| chr4:157242390
|
A | G | 1 | a0001c0001t0001g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.229+20583A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157242390 | ||||||
| chr4:157242582
|
CT | C | 5 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0004g0057others(2): Show | 5 | HG00280.hp2 HG00639.hp2 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.229+20779delT | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157242582 | |||||
| chr4:157242649
|
C | T | 1 | a0001c0002t0002g0185 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.229+20842C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157242649 | ||||||
| chr4:157242817
|
A | T | 5 | a0001c0001t0001g0212a0001c0001t0002g0209a0001c0001t0002g0210others(2): Show | 6 | HG02735.hp1 HG02738.hp1 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.229+21010A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157242817 | ||||||
| chr4:157242891
|
T | C | 212 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(209): Show | 216 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.229+21084T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157242891 | ||||||
| chr4:157243328
|
A | G | 1 | a0001c0002t0002g0187 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.229+21521A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157243328 | ||||||
| chr4:157243347
|
A | G | 9 | a0001c0002t0001g0130a0001c0002t0001g0131a0001c0002t0001g0132others(6): Show | 9 | HG01081.hp2 HG02486.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.229+21540A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157243347 | ||||||
| chr4:157243477
|
A | G | 1 | a0001c0001t0001g0010 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.229+21670A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157243477 | ||||||
| chr4:157243488
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.229+21681T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157243488 | ||||||
| chr4:157243545
|
T | C | 17 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(14): Show | 17 | HG00642.hp2 HG01168.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.229+21738T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157243545 | ||||||
| chr4:157243805
|
T | A | 5 | a0001c0001t0001g0212a0001c0001t0002g0209a0001c0001t0002g0210others(2): Show | 6 | HG02735.hp1 HG02738.hp1 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.229+21998T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157243805 | ||||||
| chr4:157243882
|
C | T | 2 | a0001c0001t0003g0103a0001c0001t0003g0104 | 2 | HG00438.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.229+22075C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157243882 | ||||||
| chr4:157243935
|
A | G | 1 | a0001c0002t0002g0147 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.229+22128A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157243935 | ||||||
| chr4:157243969
|
G | A | 1 | a0001c0002t0002g0150 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.229+22162G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157243969 | ||||||
| chr4:157244115
|
G | T | 1 | a0001c0001t0014g0035 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.229+22308G>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157244115 | ||||||
| chr4:157244136
|
T | A | 6 | a0001c0001t0004g0067a0001c0001t0004g0068a0001c0001t0004g0069others(3): Show | 6 | HG00280.hp1 HG00323.hp1 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.229+22329T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157244136 | ||||||
| chr4:157244252
|
T | C | 1 | a0001c0001t0003g0105 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.229+22445T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157244252 | ||||||
| chr4:157244501
|
C | T | 3 | a0001c0001t0002g0149a0001c0001t0004g0183a0001c0001t0004g0184 | 3 | HG01123.hp1 HG02451.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.229+22694C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157244501 | ||||||
| chr4:157245027
|
T | C | 1 | a0001c0002t0002g0151 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.229+23220T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157245027 | ||||||
| chr4:157245046
|
A | G | 1 | a0001c0002t0001g0191 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.229+23239A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157245046 | ||||||
| chr4:157245260
|
A | T | 1 | a0001c0002t0001g0182 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.229+23453A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157245260 | ||||||
| chr4:157245366
|
A | T | 114 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(111): Show | 117 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.229+23559A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157245366 | ||||||
| chr4:157245537
|
A | G | 85 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0036others(82): Show | 88 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.229+23730A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157245537 | ||||||
| chr4:157245971
|
G | A | 1 | a0001c0001t0001g0005 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.229+24164G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157245971 | ||||||
| chr4:157246017
|
CTG | C | 2 | a0001c0001t0001g0019a0001c0001t0001g0020 | 2 | HG02486.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.229+24211_229+2421 others(6): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157246017 | ||||||
| chr4:157246068
|
G | T | 1 | a0001c0001t0014g0035 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.229+24261G>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157246068 | ||||||
| chr4:157246156
|
G | T | 212 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(209): Show | 216 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.229+24349G>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157246156 | ||||||
| chr4:157246192
|
T | A | 10 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(7): Show | 10 | HG00733.hp2 HG00738.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.229+24385T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157246192 | ||||||
| chr4:157246307
|
A | T | 1 | a0001c0001t0014g0035 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.229+24500A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157246307 | ||||||
| chr4:157246308
|
C | T | 1 | a0001c0001t0014g0035 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.229+24501C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157246308 | ||||||
| chr4:157246553
|
T | C | 1 | a0001c0001t0001g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.229+24746T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157246553 | ||||||
| chr4:157247057
|
A | G | 1 | a0001c0001t0002g0127 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.229+25250A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157247057 | ||||||
| chr4:157247160
|
T | C | 1 | a0001c0002t0002g0152 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.229+25353T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157247160 | ||||||
| chr4:157247194
|
C | G | 111 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(108): Show | 114 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.229+25387C>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157247194 | ||||||
| chr4:157247395
|
G | A | 29 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(26): Show | 29 | HG00642.hp2 HG00733.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.229+25588G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157247395 | ||||||
| chr4:157247482
|
T | C | 1 | a0001c0001t0004g0067 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.229+25675T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157247482 | ||||||
| chr4:157247564
|
TA | T | 66 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0049others(63): Show | 68 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.229+25758delA | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157247564 | ||||||
| chr4:157247613
|
C | T | 1 | a0001c0001t0014g0035 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.229+25806C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157247613 | ||||||
| chr4:157247701
|
G | T | 1 | a0001c0001t0003g0095 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.229+25894G>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157247701 | ||||||
| chr4:157247850
|
C | T | 1 | a0001c0003t0001g0021 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.229+26043C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157247850 | ||||||
| chr4:157247851
|
G | A | 1 | a0001c0002t0002g0152 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.229+26044G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157247851 | ||||||
| chr4:157247872
|
A | G | 2 | a0001c0002t0002g0119a0001c0002t0002g0120 | 2 | NA18981.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.229+26065A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157247872 | ||||||
| chr4:157247875
|
C | G | 1 | a0001c0001t0001g0049 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.229+26068C>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157247875 | ||||||
| chr4:157248027
|
C | T | 1 | a0001c0001t0001g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.229+26220C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157248027 | ||||||
| chr4:157248425
|
G | A | 4 | a0001c0001t0005g0007a0001c0003t0001g0017a0001c0003t0001g0018others(1): Show | 4 | HG02258.hp2 HG02622.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.229+26618G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157248425 | ||||||
| chr4:157248568
|
T | TGTATATA others(53): Show |
10 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(7): Show | 10 | HG00733.hp2 HG00738.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.229+26763_229+2676 others(64): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157248568 | |||||
| chr4:157248568
|
T | TGTGTATA others(73): Show |
1 | a0001c0001t0001g0204 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.229+26775_229+2677 others(84): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157248568 | |||||
| chr4:157248568
|
T | TGTGTATA others(89): Show |
1 | a0001c0002t0005g0211 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.229+26775_229+2677 others(100): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157248568 | |||||
| chr4:157248568
|
T | TGTGTATA others(41): Show |
3 | a0001c0001t0001g0206a0001c0002t0002g0123a0001c0002t0002g0153 | 3 | HG00639.hp1 HG02698.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.229+26774_229+2677 others(52): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157248568 | |||||
| chr4:157248568
|
T | TGTGTATA others(71): Show |
1 | a0001c0001t0003g0060 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.229+26774_229+2677 others(82): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157248568 | |||||
| chr4:157248568
|
T | TGTGTATA others(69): Show |
58 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0049others(55): Show | 60 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.229+26774_229+2677 others(80): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157248568 | |||||
| chr4:157248568
|
T | TGTGTATA others(85): Show |
1 | a0001c0001t0001g0096 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.229+26774_229+2677 others(96): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157248568 | |||||
| chr4:157248568
|
T | TGTGTATA others(113): Show |
5 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(2): Show | 5 | HG01123.hp2 HG02559.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.229+26774_229+2677 others(124): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157248568 | |||||
| chr4:157248568
|
T | TGTGTATA others(71): Show |
1 | a0001c0001t0001g0106 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.229+26774_229+2677 others(82): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157248568 | |||||
| chr4:157248568
|
T | TGTGTATA others(87): Show |
8 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(5): Show | 8 | HG02630.hp1 HG02886.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.229+26774_229+2677 others(98): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157248568 | |||||
| chr4:157248568
|
T | TGTGTATA others(73): Show |
1 | a0001c0001t0005g0007 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.229+26774_229+2677 others(84): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157248568 | |||||
| chr4:157248568
|
T | TGTGTATA others(73): Show |
7 | a0001c0003t0001g0017a0001c0003t0001g0018a0001c0003t0001g0021others(4): Show | 7 | HG01884.hp2 HG02280.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.229+26774_229+2677 others(84): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157248568 | |||||
| chr4:157248568
|
T | TGTGTATA others(89): Show |
5 | a0001c0001t0001g0212a0001c0001t0002g0127a0001c0001t0002g0209others(2): Show | 6 | HG01168.hp1 HG02738.hp1 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.229+26774_229+2677 others(100): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157248568 | |||||
| chr4:157248568
|
T | TGTGTATA others(105): Show |
1 | a0001c0003t0013g0016 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.229+26774_229+2677 others(116): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157248568 | |||||
| chr4:157248568
|
T | TGTGTATA others(87): Show |
2 | a0001c0002t0001g0040a0001c0002t0001g0041 | 2 | HG02622.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.229+26774_229+2677 others(98): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157248568 | |||||
| chr4:157248568
|
T | TGTGTATA others(103): Show |
1 | a0001c0003t0007g0043 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.229+26774_229+2677 others(114): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157248568 | |||||
| chr4:157248568
|
T | TGTGTATA others(59): Show |
1 | a0001c0001t0004g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.229+26774_229+2677 others(70): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157248568 | |||||
| chr4:157248568
|
T | TGTGTATA others(119): Show |
1 | a0001c0001t0008g0042 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.229+26774_229+2677 others(130): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157248568 | |||||
| chr4:157248568
|
T | TGTGTATA others(73): Show |
1 | a0001c0002t0001g0191 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.229+26774_229+2677 others(84): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157248568 | |||||
| chr4:157248568
|
T | TGTGTATA others(57): Show |
4 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0034others(1): Show | 4 | HG02109.hp1 HG02258.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.229+26774_229+2677 others(68): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157248568 | |||||
| chr4:157248568
|
T | TGTGTATA others(73): Show |
91 | a0001c0001t0002g0149a0001c0001t0004g0141a0001c0001t0004g0183others(88): Show | 92 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.229+26774_229+2677 others(84): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157248568 | |||||
| chr4:157248568
|
T | TGTGTATA others(87): Show |
4 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(1): Show | 4 | HG00642.hp2 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.229+26774_229+2677 others(98): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157248568 | |||||
| chr4:157248571
|
G | GTA | 4 | a0001c0001t0001g0015a0001c0001t0004g0039a0001c0001t0014g0035others(1): Show | 4 | HG01891.hp2 HG02071.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.229+26773_229+2677 others(6): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157248571 | |||||
| chr4:157248583
|
G | GTGTATAT others(129): Show |
1 | a0001c0001t0014g0035 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.229+26785_229+2678 others(140): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157248583 | |||||
| chr4:157248590
|
T | TATATACG others(105): Show |
1 | a0001c0001t0004g0039 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.229+26785_229+2678 others(116): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157248590 | |||||
| chr4:157248592
|
T | TATATACG others(67): Show |
1 | a0001c0001t0001g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.229+26785_229+2678 others(78): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157248592 | ||||||
| chr4:157248593
|
G | A | 2 | a0001c0001t0001g0019a0001c0001t0001g0020 | 2 | HG02486.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.229+26786G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157248593 | ||||||
| chr4:157248602
|
T | C | 12 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(9): Show | 12 | HG00642.hp2 HG01168.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.229+26795T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157248602 | ||||||
| chr4:157248603
|
G | A | 1 | a0001c0001t0001g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.229+26796G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157248603 | ||||||
| chr4:157248612
|
C | T | 1 | a0001c0001t0004g0039 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.229+26805C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157248612 | ||||||
| chr4:157248615
|
G | A | 1 | a0001c0001t0004g0039 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.229+26808G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157248615 | ||||||
| chr4:157248615
|
G | GTATATAT others(21): Show |
6 | a0001c0001t0001g0106a0001c0001t0008g0042a0001c0002t0001g0040others(3): Show | 6 | HG01074.hp2 HG02622.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.229+26818_229+2684 others(32): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157248615 | |||||
| chr4:157248625
|
G | C | 2 | a0001c0002t0002g0139a0001c0002t0002g0154 | 2 | NA18964.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.229+26818G>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157248625 | ||||||
| chr4:157248714
|
C | T | 8 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(5): Show | 8 | HG00642.hp2 HG01168.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.229+26907C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157248714 | ||||||
| chr4:157248732
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.229+26925C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157248732 | ||||||
| chr4:157248780
|
CTA | C | 3 | a0001c0002t0001g0131a0001c0002t0001g0137a0001c0002t0002g0198 | 3 | HG02738.hp2 HG02818.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.229+27006_229+2700 others(6): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157248780 | |||||
| chr4:157248780
|
CTATA | C | 4 | a0001c0001t0001g0212a0001c0001t0004g0141a0001c0002t0002g0114others(1): Show | 4 | HG00609.hp1 HG02683.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.229+27004_229+2700 others(8): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157248780 | |||||
| chr4:157248780
|
CTATATA | C | 18 | a0001c0001t0001g0204a0001c0001t0002g0149a0001c0001t0008g0042others(15): Show | 18 | HG02055.hp1 HG02280.hp1 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.229+27002_229+2700 others(10): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157248780 | |||||
| chr4:157248780
|
CTATATAT others(1): Show |
C | 76 | a0001c0001t0001g0106a0001c0001t0002g0127a0001c0001t0002g0209others(73): Show | 78 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.229+27000_229+2700 others(12): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157248780 | |||||
| chr4:157248780
|
CTATATAT others(3): Show |
C | 6 | a0001c0001t0001g0020a0001c0001t0004g0039a0001c0001t0004g0051others(3): Show | 6 | HG01891.hp2 HG02135.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.229+26998_229+2700 others(14): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157248780 | |||||
| chr4:157248780
|
CTATATAT others(5): Show |
C | 80 | a0001c0001t0001g0019a0001c0001t0001g0036a0001c0001t0001g0037others(77): Show | 82 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.229+26996_229+2700 others(16): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157248780 | |||||
| chr4:157248780
|
CTATATAT others(7): Show |
C | 5 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0004g0027others(2): Show | 5 | HG01243.hp1 HG01516.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.229+26994_229+2700 others(18): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157248780 | |||||
| chr4:157248780
|
CTATATAT others(9): Show |
C | 6 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(3): Show | 6 | HG00733.hp2 HG00738.hp2 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.229+26992_229+2700 others(20): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157248780 | |||||
| chr4:157248780
|
CTATATAT others(11): Show |
C | 9 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(6): Show | 9 | HG00642.hp2 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.229+26990_229+2700 others(22): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157248780 | |||||
| chr4:157248809
|
TATATAA | T | 3 | a0001c0002t0001g0130a0001c0002t0001g0181a0001c0002t0004g0138 | 3 | HG01081.hp2 HG02976.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.229+27006_229+2701 others(10): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157248809 | |||||
| chr4:157248813
|
T | A | 1 | a0001c0001t0004g0141 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.229+27006T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157248813 | ||||||
| chr4:157248867
|
ACT | A | 10 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(7): Show | 10 | HG00733.hp2 HG00738.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.229+27065_229+2706 others(6): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157248867 | |||||
| chr4:157248971
|
G | A | 1 | a0001c0002t0001g0134 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.229+27164G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157248971 | ||||||
| chr4:157249441
|
T | C | 8 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(5): Show | 8 | HG00642.hp2 HG01168.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.229+27634T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157249441 | ||||||
| chr4:157249566
|
A | G | 5 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111others(2): Show | 5 | HG02630.hp1 HG02886.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.229+27759A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157249566 | ||||||
| chr4:157249844
|
C | G | 1 | a0001c0001t0001g0034 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.229+28037C>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157249844 | ||||||
| chr4:157250600
|
T | C | 1 | a0001c0002t0002g0146 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.229+28793T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157250600 | ||||||
| chr4:157250644
|
T | C | 115 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(112): Show | 118 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.229+28837T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157250644 | ||||||
| chr4:157250656
|
A | G | 1 | a0001c0003t0001g0021 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.229+28849A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157250656 | ||||||
| chr4:157250912
|
C | T | 1 | a0001c0001t0001g0034 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.229+29105C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157250912 | ||||||
| chr4:157250984
|
T | C | 6 | a0001c0001t0004g0067a0001c0001t0004g0068a0001c0001t0004g0069others(3): Show | 6 | HG00280.hp1 HG00323.hp1 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.229+29177T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157250984 | ||||||
| chr4:157251183
|
C | A | 8 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(5): Show | 8 | HG00642.hp2 HG01168.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.229+29376C>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157251183 | ||||||
| chr4:157252117
|
T | C | 1 | a0001c0001t0011g0014 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.229+30310T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157252117 | ||||||
| chr4:157252445
|
T | C | 11 | a0001c0001t0005g0007a0001c0003t0001g0017a0001c0003t0001g0018others(8): Show | 11 | HG01123.hp2 HG01884.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.229+30638T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157252445 | ||||||
| chr4:157252578
|
T | C | 1 | a0001c0002t0002g0145 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.229+30771T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157252578 | ||||||
| chr4:157252758
|
T | C | 1 | a0001c0001t0003g0105 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.229+30951T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157252758 | ||||||
| chr4:157252779
|
T | C | 1 | a0001c0001t0001g0034 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.229+30972T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157252779 | ||||||
| chr4:157252812
|
A | T | 1 | a0001c0001t0001g0106 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.229+31005A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157252812 | ||||||
| chr4:157252886
|
A | C | 1 | a0001c0001t0014g0035 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.229+31079A>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157252886 | ||||||
| chr4:157253156
|
G | A | 1 | a0001c0002t0002g0155 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.229+31349G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157253156 | ||||||
| chr4:157253337
|
G | A | 67 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0049others(64): Show | 69 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.229+31530G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157253337 | ||||||
| chr4:157253399
|
G | T | 5 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111others(2): Show | 5 | HG02630.hp1 HG02886.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.229+31592G>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157253399 | ||||||
| chr4:157253432
|
G | T | 1 | a0001c0001t0001g0097 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.229+31625G>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157253432 | ||||||
| chr4:157253686
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.229+31879C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157253686 | ||||||
| chr4:157253731
|
C | G | 1 | a0001c0003t0007g0043 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.229+31924C>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157253731 | ||||||
| chr4:157253840
|
T | A | 1 | a0001c0001t0004g0101 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.229+32033T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157253840 | ||||||
| chr4:157253919
|
G | T | 6 | a0001c0001t0001g0212a0001c0001t0002g0127a0001c0001t0002g0209others(3): Show | 7 | HG01168.hp1 HG02735.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.229+32112G>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157253919 | ||||||
| chr4:157254005
|
C | T | 8 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(5): Show | 8 | HG00642.hp2 HG01168.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.229+32198C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157254005 | ||||||
| chr4:157254098
|
G | A | 1 | a0001c0001t0003g0060 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.229+32291G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157254098 | ||||||
| chr4:157254183
|
C | A | 8 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(5): Show | 8 | HG00642.hp2 HG01168.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.229+32376C>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157254183 | ||||||
| chr4:157254493
|
G | A | 1 | a0001c0001t0001g0010 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.229+32686G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157254493 | ||||||
| chr4:157254572
|
A | G | 1 | a0001c0002t0002g0151 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.229+32765A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157254572 | ||||||
| chr4:157254600
|
G | C | 1 | a0001c0001t0010g0207 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.229+32793G>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157254600 | ||||||
| chr4:157254686
|
C | T | 2 | a0001c0002t0001g0180a0001c0002t0005g0205 | 2 | HG02280.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.229+32879C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157254686 | ||||||
| chr4:157254809
|
T | C | 1 | a0001c0001t0014g0035 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.229+33002T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157254809 | ||||||
| chr4:157254962
|
G | A | 1 | a0001c0002t0002g0151 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.229+33155G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157254962 | ||||||
| chr4:157255241
|
A | T | 2 | a0001c0001t0001g0049a0001c0001t0001g0050 | 2 | HG01884.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.229+33434A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157255241 | ||||||
| chr4:157255264
|
T | TAC | 80 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0049others(77): Show | 82 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.229+33472_229+3347 others(6): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157255264 | |||||
| chr4:157255428
|
G | C | 118 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(115): Show | 121 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.229+33621G>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157255428 | ||||||
| chr4:157255482
|
A | G | 2 | a0001c0002t0002g0152a0001c0004t0002g0003 | 3 | HG00642.hp1 HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.229+33675A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157255482 | ||||||
| chr4:157255859
|
T | C | 5 | a0001c0001t0005g0007a0001c0003t0001g0017a0001c0003t0001g0018others(2): Show | 5 | HG02258.hp2 HG02622.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.229+34052T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157255859 | ||||||
| chr4:157255898
|
T | C | 4 | a0001c0001t0004g0039a0001c0001t0008g0042a0001c0002t0001g0040others(1): Show | 4 | HG01891.hp2 HG02622.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.229+34091T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157255898 | ||||||
| chr4:157255923
|
C | T | 3 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038 | 3 | HG03041.hp1 HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.229+34116C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157255923 | ||||||
| chr4:157255971
|
G | A | 3 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0002g0023 | 3 | HG01070.hp1 HG01109.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.229+34164G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157255971 | ||||||
| chr4:157256142
|
GTAATATT others(149): Show |
G | 3 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038 | 3 | HG03041.hp1 HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.229+34363_229+3451 others(4): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157256142 | |||||
| chr4:157256149
|
T | TATATATT others(27): Show |
1 | a0001c0002t0002g0176 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.229+34349_229+3438 others(38): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157256149 | |||||
| chr4:157256149
|
T | TATATATT others(36): Show |
15 | a0001c0001t0001g0055a0001c0001t0002g0078a0001c0001t0002g0084others(12): Show | 15 | HG00280.hp1 HG00438.hp1 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.229+34369_229+3441 others(47): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157256149 | |||||
| chr4:157256160
|
T | TATATATG others(34): Show |
2 | a0001c0001t0003g0093a0001c0001t0003g0094 | 2 | HG00609.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.229+34360_229+3440 others(45): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157256160 | |||||
| chr4:157256214
|
T | G | 1 | a0001c0002t0002g0126 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.229+34407T>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157256214 | ||||||
| chr4:157256219
|
A | T | 117 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(114): Show | 120 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.229+34412A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157256219 | ||||||
| chr4:157256233
|
AAT | A | 12 | a0001c0002t0001g0130a0001c0002t0001g0131a0001c0002t0001g0132others(9): Show | 13 | HG00438.hp2 HG01070.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.229+34438_229+3443 others(6): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157256233 | |||||
| chr4:157256235
|
T | C | 70 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(67): Show | 72 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.229+34428T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157256235 | ||||||
| chr4:157256235
|
TATATATA others(12): Show |
T | 8 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(5): Show | 8 | HG00642.hp2 HG01168.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.229+34431_229+3444 others(23): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157256235 | |||||
| chr4:157256237
|
T | TTATATAT others(11): Show |
1 | a0001c0001t0001g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.229+34430_229+3443 others(22): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157256237 | ||||||
| chr4:157256237
|
TA | T | 35 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0055others(32): Show | 36 | HG00280.hp1 HG00438.hp1 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.229+34431delA | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157256237 | ||||||
| chr4:157256238
|
A | ATATTACA others(121): Show |
10 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(7): Show | 10 | HG00733.hp2 HG00738.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.229+34434_229+3443 others(132): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157256238 | |||||
| chr4:157256238
|
A | ATATTACA others(78): Show |
2 | a0001c0001t0001g0097a0001c0001t0001g0204 | 2 | HG02818.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.229+34434_229+3443 others(89): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157256238 | |||||
| chr4:157256238
|
A | ATATTACA others(97): Show |
1 | a0001c0001t0001g0106 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.229+34434_229+3443 others(108): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157256238 | |||||
| chr4:157256238
|
A | ATATTACA others(35): Show |
57 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0053others(54): Show | 59 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.229+34434_229+3443 others(46): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157256238 | |||||
| chr4:157256238
|
A | T | 2 | a0001c0001t0001g0015a0001c0001t0001g0212 | 2 | HG02451.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.229+34431A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157256238 | ||||||
| chr4:157256244
|
A | G | 13 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(10): Show | 13 | HG00733.hp2 HG00738.hp2 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.229+34437A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157256244 | ||||||
| chr4:157256254
|
A | AT | 103 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0015others(100): Show | 106 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.229+34447_229+3444 others(5): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157256254 | ||||||
| chr4:157256254
|
A | ATATTATA others(61): Show |
1 | a0001c0001t0008g0042 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.229+34447_229+3444 others(72): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157256254 | ||||||
| chr4:157256254
|
A | ATATTATA others(42): Show |
3 | a0001c0001t0004g0039a0001c0002t0001g0040a0001c0002t0001g0041 | 3 | HG01891.hp2 HG02622.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.229+34447_229+3444 others(53): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157256254 | ||||||
| chr4:157256294
|
A | C | 1 | a0001c0002t0002g0179 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.229+34487A>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157256294 | ||||||
| chr4:157256413
|
T | C | 4 | a0001c0001t0004g0039a0001c0001t0008g0042a0001c0002t0001g0040others(1): Show | 4 | HG01891.hp2 HG02622.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.229+34606T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157256413 | ||||||
| chr4:157256742
|
T | G | 1 | a0001c0002t0002g0126 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.229+34935T>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157256742 | ||||||
| chr4:157256809
|
A | G | 1 | a0001c0001t0008g0042 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.229+35002A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157256809 | ||||||
| chr4:157256860
|
A | G | 11 | a0001c0001t0005g0007a0001c0003t0001g0017a0001c0003t0001g0018others(8): Show | 11 | HG01123.hp2 HG01884.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.229+35053A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157256860 | ||||||
| chr4:157256926
|
A | T | 1 | a0001c0001t0001g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.229+35119A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157256926 | ||||||
| chr4:157257100
|
C | G | 1 | a0001c0001t0002g0149 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.229+35293C>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157257100 | ||||||
| chr4:157257194
|
G | A | 5 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111others(2): Show | 5 | HG02630.hp1 HG02886.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.229+35387G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157257194 | ||||||
| chr4:157257409
|
C | T | 1 | a0001c0001t0003g0085 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.229+35602C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157257409 | ||||||
| chr4:157257411
|
T | G | 108 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0019others(105): Show | 111 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.229+35604T>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157257411 | ||||||
| chr4:157257726
|
T | C | 1 | a0001c0001t0001g0020 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.229+35919T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157257726 | ||||||
| chr4:157257893
|
A | T | 1 | a0001c0002t0002g0147 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.229+36086A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157257893 | ||||||
| chr4:157258281
|
T | A | 1 | a0001c0003t0001g0021 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.229+36474T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157258281 | ||||||
| chr4:157258350
|
C | T | 1 | a0001c0002t0005g0211 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.229+36543C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157258350 | ||||||
| chr4:157258422
|
G | A | 10 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(7): Show | 10 | HG00733.hp2 HG00738.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.229+36615G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157258422 | ||||||
| chr4:157258860
|
G | A | 1 | a0001c0001t0011g0014 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.229+37053G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157258860 | ||||||
| chr4:157259019
|
C | A | 1 | a0001c0003t0001g0052 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.229+37212C>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157259019 | ||||||
| chr4:157259152
|
C | A | 1 | a0001c0002t0002g0171 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.229+37345C>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157259152 | ||||||
| chr4:157259195
|
T | C | 1 | a0001c0002t0002g0156 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.229+37388T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157259195 | ||||||
| chr4:157259463
|
C | G | 1 | a0001c0001t0001g0113 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.229+37656C>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157259463 | ||||||
| chr4:157259584
|
A | T | 1 | a0001c0001t0001g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.229+37777A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157259584 | ||||||
| chr4:157259729
|
T | A | 118 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(115): Show | 121 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.229+37922T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157259729 | ||||||
| chr4:157259882
|
T | A | 10 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(7): Show | 10 | HG00733.hp2 HG00738.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.229+38075T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157259882 | ||||||
| chr4:157260149
|
T | C | 109 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(106): Show | 112 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.229+38342T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157260149 | ||||||
| chr4:157260169
|
T | A | 118 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(115): Show | 121 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.229+38362T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157260169 | ||||||
| chr4:157260363
|
C | A | 1 | a0001c0001t0004g0074 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.229+38556C>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157260363 | ||||||
| chr4:157260425
|
C | T | 2 | a0001c0002t0002g0170a0001c0002t0002g0185 | 2 | NA18984.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.229+38618C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157260425 | ||||||
| chr4:157260682
|
T | C | 10 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(7): Show | 10 | HG00733.hp2 HG00738.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.229+38875T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157260682 | ||||||
| chr4:157261008
|
C | A | 8 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(5): Show | 8 | HG00642.hp2 HG01168.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.229+39201C>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157261008 | ||||||
| chr4:157261187
|
C | T | 108 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0019others(105): Show | 111 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.229+39380C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157261187 | ||||||
| chr4:157261564
|
G | T | 5 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111others(2): Show | 5 | HG02630.hp1 HG02886.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.229+39757G>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157261564 | ||||||
| chr4:157261654
|
T | C | 6 | a0001c0001t0001g0212a0001c0001t0002g0127a0001c0001t0002g0209others(3): Show | 7 | HG01168.hp1 HG02735.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.229+39847T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157261654 | ||||||
| chr4:157261679
|
C | T | 18 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(15): Show | 19 | HG01168.hp1 HG01891.hp2 HG02622.hp2 others(16): Show |
intron_variant | MODIFIER | c.229+39872C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157261679 | ||||||
| chr4:157262093
|
A | T | 1 | a0001c0002t0001g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.229+40286A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157262093 | ||||||
| chr4:157262247
|
T | A | 3 | a0001c0002t0001g0124a0001c0002t0001g0144a0001c0002t0001g0191 | 3 | NA19000.hp1 NA19064.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.229+40440T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157262247 | ||||||
| chr4:157262944
|
G | A | 118 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(115): Show | 121 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.230-40608G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157262944 | ||||||
| chr4:157263127
|
C | A | 1 | a0001c0002t0002g0128 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.230-40425C>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157263127 | ||||||
| chr4:157263451
|
C | T | 1 | a0001c0001t0001g0204 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.230-40101C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157263451 | ||||||
| chr4:157263541
|
C | A | 1 | a0001c0002t0001g0140 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.230-40011C>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157263541 | ||||||
| chr4:157263555
|
C | G | 10 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(7): Show | 10 | HG00733.hp2 HG00738.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.230-39997C>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157263555 | ||||||
| chr4:157263893
|
A | G | 1 | a0001c0001t0001g0106 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.230-39659A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157263893 | ||||||
| chr4:157264260
|
C | T | 1 | a0001c0001t0011g0014 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.230-39292C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157264260 | ||||||
| chr4:157264330
|
T | C | 1 | a0001c0001t0005g0004 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.230-39222T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157264330 | ||||||
| chr4:157264363
|
C | T | 1 | a0001c0001t0002g0084 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.230-39189C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157264363 | ||||||
| chr4:157264631
|
G | T | 1 | a0001c0001t0003g0046 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.230-38921G>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157264631 | ||||||
| chr4:157264757
|
T | C | 10 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(7): Show | 10 | HG00733.hp2 HG00738.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.230-38795T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157264757 | ||||||
| chr4:157265101
|
T | C | 1 | a0001c0001t0004g0068 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.230-38451T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157265101 | ||||||
| chr4:157265190
|
G | A | 118 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(115): Show | 121 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.230-38362G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157265190 | ||||||
| chr4:157265372
|
G | C | 2 | a0001c0002t0001g0140a0001c0002t0001g0157 | 2 | HG02109.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.230-38180G>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157265372 | ||||||
| chr4:157266297
|
G | C | 1 | a0001c0001t0001g0026 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.230-37255G>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157266297 | ||||||
| chr4:157266450
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.230-37102G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157266450 | ||||||
| chr4:157266458
|
G | A | 2 | a0001c0002t0002g0171a0001c0003t0001g0021 | 2 | NA18906.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.230-37094G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157266458 | ||||||
| chr4:157266500
|
C | G | 8 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(5): Show | 8 | HG00642.hp2 HG01168.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.230-37052C>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157266500 | ||||||
| chr4:157266550
|
T | A | 1 | a0001c0001t0001g0204 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.230-37002T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157266550 | ||||||
| chr4:157266747
|
C | T | 3 | a0001c0002t0001g0132a0001c0002t0001g0134a0001c0002t0001g0178 | 3 | HG02886.hp1 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.230-36805C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157266747 | ||||||
| chr4:157267082
|
A | C | 1 | a0001c0002t0002g0198 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.230-36470A>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157267082 | ||||||
| chr4:157267171
|
A | G | 80 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0049others(77): Show | 82 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.230-36381A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157267171 | ||||||
| chr4:157267200
|
C | T | 1 | a0001c0002t0002g0139 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.230-36352C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157267200 | ||||||
| chr4:157267285
|
A | G | 212 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(209): Show | 216 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.230-36267A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157267285 | ||||||
| chr4:157267391
|
C | CA | 14 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(11): Show | 14 | HG00733.hp2 HG00738.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.230-36139dupA | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157267391 | |||||
| chr4:157267391
|
CA | C | 10 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(7): Show | 10 | HG01168.hp2 HG01169.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.230-36139delA | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157267391 | |||||
| chr4:157268047
|
A | G | 5 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111others(2): Show | 5 | HG02630.hp1 HG02886.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.230-35505A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157268047 | ||||||
| chr4:157268301
|
G | A | 13 | a0001c0001t0001g0106a0001c0001t0001g0204a0001c0001t0005g0007others(10): Show | 13 | HG01123.hp2 HG01884.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.230-35251G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157268301 | ||||||
| chr4:157268391
|
T | A | 1 | a0001c0002t0002g0208 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.230-35161T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157268391 | ||||||
| chr4:157268537
|
C | T | 8 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(5): Show | 8 | HG00642.hp2 HG01168.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.230-35015C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157268537 | ||||||
| chr4:157268607
|
C | T | 1 | a0001c0001t0005g0007 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.230-34945C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157268607 | ||||||
| chr4:157268776
|
G | A | 1 | a0001c0002t0002g0158 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.230-34776G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157268776 | ||||||
| chr4:157268998
|
A | G | 1 | a0001c0001t0003g0102 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.230-34554A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157268998 | ||||||
| chr4:157269469
|
G | A | 1 | a0001c0001t0004g0074 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.230-34083G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157269469 | ||||||
| chr4:157269624
|
A | C | 1 | a0001c0002t0002g0169 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.230-33928A>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157269624 | ||||||
| chr4:157269636
|
T | G | 108 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0019others(105): Show | 111 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.230-33916T>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157269636 | ||||||
| chr4:157269792
|
A | G | 4 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(1): Show | 4 | HG00642.hp2 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.230-33760A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157269792 | ||||||
| chr4:157270130
|
C | A | 2 | a0001c0001t0001g0049a0001c0001t0001g0050 | 2 | HG01884.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.230-33422C>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157270130 | ||||||
| chr4:157270256
|
G | A | 1 | a0001c0001t0001g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.230-33296G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157270256 | ||||||
| chr4:157270269
|
T | C | 1 | a0001c0001t0001g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.230-33283T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157270269 | ||||||
| chr4:157270444
|
G | A | 1 | a0001c0002t0002g0193 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.230-33108G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157270444 | ||||||
| chr4:157270493
|
C | T | 1 | a0001c0002t0002g0199 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.230-33059C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157270493 | ||||||
| chr4:157270612
|
T | C | 1 | a0001c0001t0001g0204 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.230-32940T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157270612 | ||||||
| chr4:157270661
|
G | A | 1 | a0001c0002t0002g0148 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.230-32891G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157270661 | ||||||
| chr4:157270747
|
G | A | 118 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(115): Show | 121 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.230-32805G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157270747 | ||||||
| chr4:157270925
|
G | GT | 57 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0019others(54): Show | 58 | HG00733.hp2 HG00738.hp2 HG01070.hp1 others(55): Show |
intron_variant | MODIFIER | c.230-32616dupT | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157270925 | |||||
| chr4:157270925
|
G | GTT | 55 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0065others(52): Show | 57 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.230-32617_230-3261 others(6): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157270925 | |||||
| chr4:157270936
|
T | G | 1 | a0001c0002t0002g0187 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.230-32616T>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157270936 | ||||||
| chr4:157271062
|
A | C | 1 | a0001c0001t0001g0097 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.230-32490A>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157271062 | ||||||
| chr4:157271274
|
C | T | 118 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(115): Show | 121 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.230-32278C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157271274 | ||||||
| chr4:157271286
|
C | T | 1 | a0001c0001t0011g0014 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.230-32266C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157271286 | ||||||
| chr4:157271624
|
G | A | 6 | a0001c0001t0004g0067a0001c0001t0004g0068a0001c0001t0004g0069others(3): Show | 6 | HG00280.hp1 HG00323.hp1 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.230-31928G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157271624 | ||||||
| chr4:157271756
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.230-31796T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157271756 | ||||||
| chr4:157271801
|
A | G | 10 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(7): Show | 10 | HG00733.hp2 HG00738.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.230-31751A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157271801 | ||||||
| chr4:157272013
|
C | T | 1 | a0001c0002t0002g0187 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.230-31539C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157272013 | ||||||
| chr4:157272143
|
C | G | 1 | a0001c0001t0001g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.230-31409C>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157272143 | ||||||
| chr4:157272283
|
T | C | 118 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(115): Show | 121 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.230-31269T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157272283 | ||||||
| chr4:157272630
|
G | C | 6 | a0001c0001t0002g0078a0001c0001t0003g0046a0001c0001t0003g0075others(3): Show | 6 | NA18943.hp1 NA18970.hp1 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.230-30922G>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157272630 | ||||||
| chr4:157272790
|
A | C | 8 | a0001c0002t0001g0130a0001c0002t0001g0131a0001c0002t0001g0132others(5): Show | 8 | HG01081.hp2 HG02818.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.230-30762A>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157272790 | ||||||
| chr4:157272910
|
G | T | 3 | a0001c0001t0002g0149a0001c0001t0004g0183a0001c0001t0004g0184 | 3 | HG01123.hp1 HG02451.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.230-30642G>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157272910 | ||||||
| chr4:157273386
|
G | A | 1 | a0001c0002t0001g0194 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.230-30166G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157273386 | ||||||
| chr4:157273388
|
A | G | 9 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(6): Show | 9 | HG00642.hp2 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.230-30164A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157273388 | ||||||
| chr4:157273450
|
CAA | C | 3 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038 | 3 | HG03041.hp1 HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.230-30101_230-3010 others(6): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157273450 | ||||||
| chr4:157273477
|
T | C | 1 | a0001c0002t0002g0114 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.230-30075T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157273477 | ||||||
| chr4:157273550
|
A | C | 1 | a0001c0001t0011g0014 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.230-30002A>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157273550 | ||||||
| chr4:157273577
|
T | C | 1 | a0001c0001t0003g0103 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.230-29975T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157273577 | ||||||
| chr4:157273983
|
T | TA | 2 | a0001c0001t0001g0011a0001c0001t0001g0012 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.230-29568dupA | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157273983 | |||||
| chr4:157274076
|
G | A | 1 | a0001c0002t0002g0128 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.230-29476G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157274076 | ||||||
| chr4:157274132
|
T | G | 1 | a0001c0001t0001g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.230-29420T>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157274132 | ||||||
| chr4:157274145
|
G | A | 118 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(115): Show | 121 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.230-29407G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157274145 | ||||||
| chr4:157274241
|
A | G | 118 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(115): Show | 121 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.230-29311A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157274241 | ||||||
| chr4:157274538
|
C | T | 3 | a0001c0001t0001g0212a0001c0001t0005g0004a0001c0002t0005g0211 | 4 | HG02735.hp1 HG03491.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.230-29014C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157274538 | ||||||
| chr4:157274636
|
C | T | 1 | a0001c0001t0001g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.230-28916C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157274636 | ||||||
| chr4:157274637
|
G | A | 1 | a0001c0001t0003g0085 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.230-28915G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157274637 | ||||||
| chr4:157274668
|
T | C | 118 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(115): Show | 121 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.230-28884T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157274668 | ||||||
| chr4:157274692
|
T | C | 1 | a0001c0001t0001g0009 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.230-28860T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157274692 | ||||||
| chr4:157274710
|
A | T | 118 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(115): Show | 121 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.230-28842A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157274710 | ||||||
| chr4:157274728
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.230-28824C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157274728 | ||||||
| chr4:157274732
|
T | G | 212 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(209): Show | 216 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.230-28820T>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157274732 | ||||||
| chr4:157274921
|
T | C | 118 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(115): Show | 121 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.230-28631T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157274921 | ||||||
| chr4:157274937
|
G | C | 108 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(105): Show | 111 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.230-28615G>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157274937 | ||||||
| chr4:157274937
|
G | T | 104 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(101): Show | 105 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.230-28615G>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157274937 | ||||||
| chr4:157274944
|
T | C | 10 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(7): Show | 10 | HG00733.hp2 HG00738.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.230-28608T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157274944 | ||||||
| chr4:157274945
|
C | T | 10 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(7): Show | 10 | HG00733.hp2 HG00738.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.230-28607C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157274945 | ||||||
| chr4:157274947
|
A | T | 10 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(7): Show | 10 | HG00733.hp2 HG00738.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.230-28605A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157274947 | ||||||
| chr4:157275025
|
G | A | 1 | a0001c0002t0002g0116 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.230-28527G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157275025 | ||||||
| chr4:157275150
|
C | G | 1 | a0001c0001t0002g0023 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.230-28402C>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157275150 | ||||||
| chr4:157275194
|
C | T | 9 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(6): Show | 9 | HG00642.hp2 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.230-28358C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157275194 | ||||||
| chr4:157275200
|
C | G | 1 | a0001c0002t0002g0168 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.230-28352C>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157275200 | ||||||
| chr4:157275243
|
A | C | 6 | a0001c0001t0001g0212a0001c0001t0002g0127a0001c0001t0002g0209others(3): Show | 7 | HG01168.hp1 HG02735.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.230-28309A>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157275243 | ||||||
| chr4:157275292
|
C | A | 1 | a0001c0002t0002g0117 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.230-28260C>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157275292 | ||||||
| chr4:157275407
|
C | A | 1 | a0001c0001t0001g0036 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.230-28145C>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157275407 | ||||||
| chr4:157275418
|
G | T | 1 | a0001c0001t0003g0092 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.230-28134G>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157275418 | ||||||
| chr4:157275428
|
C | T | 2 | a0001c0002t0002g0189a0001c0002t0002g0201 | 2 | HG03491.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.230-28124C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157275428 | ||||||
| chr4:157275447
|
C | T | 5 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111others(2): Show | 5 | HG02630.hp1 HG02886.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.230-28105C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157275447 | ||||||
| chr4:157275454
|
C | G | 80 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0049others(77): Show | 82 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.230-28098C>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157275454 | ||||||
| chr4:157275565
|
C | A | 118 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(115): Show | 121 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.230-27987C>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157275565 | ||||||
| chr4:157275630
|
G | C | 118 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(115): Show | 121 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.230-27922G>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157275630 | ||||||
| chr4:157275674
|
G | A | 20 | a0001c0001t0001g0081a0001c0001t0001g0096a0001c0001t0002g0078others(17): Show | 21 | HG02135.hp1 NA18943.hp1 NA18951.hp2 others(18): Show |
intron_variant | MODIFIER | c.230-27878G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157275674 | ||||||
| chr4:157275714
|
T | A | 118 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(115): Show | 121 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.230-27838T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157275714 | ||||||
| chr4:157275800
|
C | T | 1 | a0001c0001t0001g0204 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.230-27752C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157275800 | ||||||
| chr4:157276004
|
T | C | 1 | a0001c0001t0001g0109 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.230-27548T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157276004 | ||||||
| chr4:157276038
|
A | C | 3 | a0001c0002t0002g0148a0001c0002t0002g0169a0001c0002t0012g0122 | 3 | HG01952.hp2 NA18968.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.230-27514A>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157276038 | ||||||
| chr4:157276080
|
G | A | 67 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0049others(64): Show | 69 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.230-27472G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157276080 | ||||||
| chr4:157276084
|
C | G | 2 | a0001c0002t0002g0123a0001c0002t0002g0153 | 2 | HG02698.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.230-27468C>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157276084 | ||||||
| chr4:157276131
|
A | G | 1 | a0001c0003t0001g0021 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.230-27421A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157276131 | ||||||
| chr4:157276199
|
C | G | 1 | a0001c0002t0002g0116 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.230-27353C>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157276199 | ||||||
| chr4:157276231
|
G | T | 1 | a0001c0002t0001g0191 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.230-27321G>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157276231 | ||||||
| chr4:157276277
|
A | G | 1 | a0001c0001t0001g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.230-27275A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157276277 | ||||||
| chr4:157276459
|
C | G | 1 | a0001c0001t0014g0035 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.230-27093C>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157276459 | ||||||
| chr4:157276505
|
G | A | 1 | a0001c0002t0002g0116 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.230-27047G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157276505 | ||||||
| chr4:157276748
|
G | T | 1 | a0001c0002t0002g0167 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.230-26804G>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157276748 | ||||||
| chr4:157276792
|
A | G | 1 | a0001c0001t0004g0070 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.230-26760A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157276792 | ||||||
| chr4:157276854
|
C | G | 118 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(115): Show | 121 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.230-26698C>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157276854 | ||||||
| chr4:157277287
|
G | A | 1 | a0001c0001t0002g0084 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.230-26265G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157277287 | ||||||
| chr4:157277299
|
C | A | 1 | a0001c0002t0002g0168 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.230-26253C>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157277299 | ||||||
| chr4:157277441
|
A | G | 1 | a0001c0001t0002g0099 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.230-26111A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157277441 | ||||||
| chr4:157277627
|
G | C | 1 | a0001c0002t0001g0172 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.230-25925G>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157277627 | ||||||
| chr4:157277670
|
T | A | 1 | a0001c0001t0002g0149 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.230-25882T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157277670 | ||||||
| chr4:157277732
|
T | C | 1 | a0001c0001t0001g0204 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.230-25820T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157277732 | ||||||
| chr4:157277814
|
C | CTATATAT others(13): Show |
4 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(1): Show | 4 | HG02630.hp1 HG02886.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.230-25708_230-2568 others(24): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157277814 | |||||
| chr4:157277836
|
A | ATATATAT others(11): Show |
82 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0015others(79): Show | 85 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.230-25670_230-2565 others(22): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157277836 | |||||
| chr4:157277836
|
A | ATATATAT others(29): Show |
4 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0004g0027others(1): Show | 4 | HG01243.hp1 HG01516.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.230-25688_230-2565 others(40): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157277836 | |||||
| chr4:157277836
|
A | ATATATAT others(9): Show |
1 | a0001c0001t0008g0042 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.230-25709_230-2570 others(20): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157277836 | |||||
| chr4:157277838
|
A | ATATATAT others(9): Show |
5 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(2): Show | 5 | HG02559.hp1 HG03041.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.230-25706_230-2569 others(20): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157277838 | |||||
| chr4:157277838
|
A | ATATATAT others(37): Show |
3 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0034 | 3 | HG02258.hp1 HG02809.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.230-25698_230-2565 others(48): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157277838 | |||||
| chr4:157277838
|
A | ATATATAT others(63): Show |
4 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(1): Show | 4 | HG00642.hp2 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.230-25655_230-2565 others(74): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157277838 | |||||
| chr4:157277866
|
A | G | 1 | a0001c0001t0001g0112 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.230-25686A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157277866 | ||||||
| chr4:157277872
|
GTATATAT others(13): Show |
G | 1 | a0001c0002t0002g0168 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.230-25652_230-2563 others(24): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157277872 | |||||
| chr4:157277874
|
A | ATATATAT others(9): Show |
1 | a0001c0001t0014g0035 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.230-25670_230-2565 others(20): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157277874 | |||||
| chr4:157277881
|
T | TGTATATA others(31): Show |
1 | a0001c0001t0001g0204 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.230-25653_230-2565 others(42): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157277881 | |||||
| chr4:157277882
|
G | GTATATAT others(23): Show |
1 | a0001c0002t0002g0159 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.230-25648_230-2561 others(34): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157277882 | |||||
| chr4:157277882
|
G | GTATATAT others(41): Show |
1 | a0001c0001t0003g0063 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.230-25653_230-2565 others(52): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157277882 | |||||
| chr4:157277882
|
G | GTATATAT others(67): Show |
1 | a0001c0001t0011g0014 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.230-25655_230-2565 others(78): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157277882 | |||||
| chr4:157277890
|
G | GTATATAT others(13): Show |
2 | a0001c0001t0002g0084a0001c0001t0004g0086 | 2 | NA18942.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.230-25653_230-2565 others(24): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157277890 | |||||
| chr4:157277892
|
A | ATATATAT others(9): Show |
1 | a0001c0001t0001g0106 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.230-25653_230-2565 others(20): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157277892 | |||||
| chr4:157277892
|
A | ATATATAT others(11): Show |
1 | a0001c0002t0001g0040 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.230-25653_230-2565 others(22): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157277892 | |||||
| chr4:157277901
|
T | C | 1 | a0001c0001t0001g0204 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.230-25651T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157277901 | ||||||
| chr4:157277910
|
G | GTA | 3 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038 | 3 | HG03041.hp1 HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.230-25634_230-2563 others(6): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157277910 | |||||
| chr4:157277912
|
A | G | 1 | a0001c0001t0014g0035 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.230-25640A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157277912 | ||||||
| chr4:157278036
|
G | T | 1 | a0001c0001t0001g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.230-25516G>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157278036 | ||||||
| chr4:157278099
|
G | A | 4 | a0001c0001t0001g0015a0001c0001t0001g0036a0001c0001t0001g0037others(1): Show | 4 | HG02451.hp2 HG03041.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.230-25453G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157278099 | ||||||
| chr4:157278106
|
T | A | 2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | HG02809.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.230-25446T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157278106 | ||||||
| chr4:157278156
|
T | G | 3 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038 | 3 | HG03041.hp1 HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.230-25396T>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157278156 | ||||||
| chr4:157278316
|
C | T | 1 | a0001c0002t0002g0158 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.230-25236C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157278316 | ||||||
| chr4:157278380
|
T | C | 67 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0049others(64): Show | 69 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.230-25172T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157278380 | ||||||
| chr4:157278695
|
G | A | 1 | a0001c0001t0002g0209 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.230-24857G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157278695 | ||||||
| chr4:157278716
|
A | G | 1 | a0001c0003t0001g0021 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.230-24836A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157278716 | ||||||
| chr4:157278792
|
TA | T | 135 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(132): Show | 138 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.230-24751delA | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157278792 | |||||
| chr4:157278834
|
AGAAGATA others(4): Show |
A | 67 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0049others(64): Show | 69 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.230-24705_230-2469 others(15): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157278834 | |||||
| chr4:157278853
|
T | C | 1 | a0001c0001t0011g0014 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.230-24699T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157278853 | ||||||
| chr4:157279001
|
T | G | 1 | a0001c0001t0003g0090 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.230-24551T>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157279001 | ||||||
| chr4:157279078
|
C | A | 1 | a0001c0001t0005g0004 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.230-24474C>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157279078 | ||||||
| chr4:157279530
|
G | A | 1 | a0001c0002t0001g0140 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.230-24022G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157279530 | ||||||
| chr4:157279715
|
A | G | 1 | a0001c0001t0014g0035 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.230-23837A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157279715 | ||||||
| chr4:157279833
|
C | T | 1 | a0001c0001t0001g0034 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.230-23719C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157279833 | ||||||
| chr4:157279975
|
A | G | 1 | a0001c0001t0001g0034 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.230-23577A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157279975 | ||||||
| chr4:157280187
|
G | T | 5 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111others(2): Show | 5 | HG02630.hp1 HG02886.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.230-23365G>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157280187 | ||||||
| chr4:157280277
|
G | A | 1 | a0001c0002t0002g0208 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.230-23275G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157280277 | ||||||
| chr4:157280342
|
G | A | 118 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(115): Show | 121 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.230-23210G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157280342 | ||||||
| chr4:157280522
|
G | T | 1 | a0001c0002t0002g0168 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.230-23030G>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157280522 | ||||||
| chr4:157280720
|
A | C | 1 | a0001c0002t0001g0166 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.230-22832A>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157280720 | ||||||
| chr4:157281083
|
C | T | 4 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(1): Show | 4 | HG00642.hp2 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.230-22469C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157281083 | ||||||
| chr4:157281250
|
G | C | 80 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0049others(77): Show | 82 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.230-22302G>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157281250 | ||||||
| chr4:157281390
|
G | A | 17 | a0001c0001t0004g0141a0001c0002t0001g0130a0001c0002t0001g0131others(14): Show | 17 | HG01081.hp2 HG02055.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.230-22162G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157281390 | ||||||
| chr4:157281689
|
CA | C | 108 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0019others(105): Show | 111 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.230-21860delA | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157281689 | |||||
| chr4:157281840
|
T | G | 1 | a0001c0001t0001g0010 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.230-21712T>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157281840 | ||||||
| chr4:157282062
|
G | A | 1 | a0001c0002t0002g0199 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.230-21490G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157282062 | ||||||
| chr4:157282195
|
G | A | 1 | a0001c0002t0002g0155 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.230-21357G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157282195 | ||||||
| chr4:157282406
|
GGA | G | 18 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(15): Show | 19 | HG01168.hp1 HG01891.hp2 HG02622.hp2 others(16): Show |
intron_variant | MODIFIER | c.230-21142_230-2114 others(6): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157282406 | |||||
| chr4:157282432
|
T | C | 1 | a0001c0001t0014g0035 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.230-21120T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157282432 | ||||||
| chr4:157282574
|
C | T | 9 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(6): Show | 9 | HG00642.hp2 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.230-20978C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157282574 | ||||||
| chr4:157282657
|
G | A | 4 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(1): Show | 4 | HG00642.hp2 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.230-20895G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157282657 | ||||||
| chr4:157282802
|
G | A | 1 | a0001c0001t0004g0051 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.230-20750G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157282802 | ||||||
| chr4:157282862
|
G | C | 5 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111others(2): Show | 5 | HG02630.hp1 HG02886.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.230-20690G>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157282862 | ||||||
| chr4:157283081
|
A | C | 3 | a0001c0003t0001g0017a0001c0003t0001g0018a0001c0003t0013g0016 | 3 | HG02622.hp1 HG02717.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.230-20471A>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157283081 | ||||||
| chr4:157283140
|
A | G | 1 | a0001c0001t0001g0087 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.230-20412A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157283140 | ||||||
| chr4:157283231
|
A | T | 80 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0049others(77): Show | 82 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.230-20321A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157283231 | ||||||
| chr4:157283300
|
C | T | 9 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(6): Show | 9 | HG00642.hp2 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.230-20252C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157283300 | ||||||
| chr4:157283347
|
T | A | 1 | a0001c0001t0001g0050 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.230-20205T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157283347 | ||||||
| chr4:157283433
|
G | A | 1 | a0001c0003t0001g0017 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.230-20119G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157283433 | ||||||
| chr4:157283533
|
A | G | 1 | a0001c0001t0001g0204 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.230-20019A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157283533 | ||||||
| chr4:157283701
|
T | C | 1 | a0001c0001t0002g0209 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.230-19851T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157283701 | ||||||
| chr4:157283702
|
T | A | 1 | a0001c0001t0014g0035 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.230-19850T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157283702 | ||||||
| chr4:157284141
|
C | A | 1 | a0001c0001t0001g0204 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.230-19411C>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157284141 | ||||||
| chr4:157284359
|
C | T | 1 | a0001c0002t0005g0211 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.230-19193C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157284359 | ||||||
| chr4:157284386
|
T | C | 18 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(15): Show | 19 | HG01168.hp1 HG01891.hp2 HG02622.hp2 others(16): Show |
intron_variant | MODIFIER | c.230-19166T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157284386 | ||||||
| chr4:157284533
|
C | T | 1 | a0001c0002t0001g0200 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.230-19019C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157284533 | ||||||
| chr4:157285040
|
T | A | 18 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(15): Show | 19 | HG01168.hp1 HG01891.hp2 HG02622.hp2 others(16): Show |
intron_variant | MODIFIER | c.230-18512T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157285040 | ||||||
| chr4:157285557
|
T | TTG | 9 | a0001c0001t0001g0081a0001c0001t0001g0097a0001c0001t0003g0063others(6): Show | 9 | HG01081.hp1 HG02818.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.230-17969_230-1796 others(6): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157285557 | |||||
| chr4:157285557
|
TTG | T | 38 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(35): Show | 39 | HG00642.hp2 HG01123.hp2 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.230-17969_230-1796 others(6): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157285557 | |||||
| chr4:157285642
|
A | G | 2 | a0001c0001t0001g0011a0001c0001t0001g0012 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.230-17910A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157285642 | ||||||
| chr4:157285761
|
G | A | 2 | a0001c0002t0001g0040a0001c0002t0001g0041 | 2 | HG02622.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.230-17791G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157285761 | ||||||
| chr4:157286132
|
A | G | 1 | a0001c0002t0002g0128 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.230-17420A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157286132 | ||||||
| chr4:157286603
|
T | G | 2 | a0001c0002t0001g0172a0001c0002t0001g0173 | 2 | HG02132.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.230-16949T>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157286603 | ||||||
| chr4:157286652
|
AT | A | 118 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(115): Show | 121 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.230-16895delT | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157286652 | |||||
| chr4:157286833
|
G | T | 12 | a0001c0001t0001g0204a0001c0001t0005g0007a0001c0003t0001g0017others(9): Show | 12 | HG01123.hp2 HG01884.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.230-16719G>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157286833 | ||||||
| chr4:157287058
|
C | T | 108 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0019others(105): Show | 111 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.230-16494C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157287058 | ||||||
| chr4:157287375
|
C | A | 4 | a0001c0001t0004g0039a0001c0001t0008g0042a0001c0002t0001g0040others(1): Show | 4 | HG01891.hp2 HG02622.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.230-16177C>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157287375 | ||||||
| chr4:157287550
|
T | C | 1 | a0001c0001t0001g0212 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.230-16002T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157287550 | ||||||
| chr4:157287785
|
A | G | 1 | a0001c0001t0004g0108 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.230-15767A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157287785 | ||||||
| chr4:157287799
|
T | C | 4 | a0001c0001t0004g0039a0001c0001t0008g0042a0001c0002t0001g0040others(1): Show | 4 | HG01891.hp2 HG02622.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.230-15753T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157287799 | ||||||
| chr4:157287803
|
C | T | 3 | a0001c0001t0002g0127a0001c0001t0002g0209a0001c0001t0002g0210 | 3 | HG01168.hp1 HG02738.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.230-15749C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157287803 | ||||||
| chr4:157287804
|
G | A | 1 | a0001c0002t0002g0169 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.230-15748G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157287804 | ||||||
| chr4:157287865
|
C | T | 10 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(7): Show | 10 | HG00733.hp2 HG00738.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.230-15687C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157287865 | ||||||
| chr4:157287902
|
T | A | 108 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0019others(105): Show | 111 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.230-15650T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157287902 | ||||||
| chr4:157288056
|
T | G | 10 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(7): Show | 10 | HG00733.hp2 HG00738.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.230-15496T>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157288056 | ||||||
| chr4:157288096
|
C | T | 1 | a0001c0002t0002g0148 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.230-15456C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157288096 | ||||||
| chr4:157288188
|
T | C | 1 | a0001c0001t0001g0034 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.230-15364T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157288188 | ||||||
| chr4:157288443
|
G | A | 1 | a0001c0002t0002g0189 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.230-15109G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157288443 | ||||||
| chr4:157288579
|
A | G | 4 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(1): Show | 4 | HG00642.hp2 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.230-14973A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157288579 | ||||||
| chr4:157288684
|
C | A | 10 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(7): Show | 10 | HG00733.hp2 HG00738.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.230-14868C>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157288684 | ||||||
| chr4:157288884
|
G | A | 1 | a0001c0001t0001g0025 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.230-14668G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157288884 | ||||||
| chr4:157289213
|
A | G | 1 | a0001c0001t0001g0097 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.230-14339A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157289213 | ||||||
| chr4:157289603
|
C | T | 1 | a0001c0001t0014g0035 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.230-13949C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157289603 | ||||||
| chr4:157290046
|
G | A | 3 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038 | 3 | HG03041.hp1 HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.230-13506G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157290046 | ||||||
| chr4:157290115
|
G | T | 1 | a0001c0002t0002g0045 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.230-13437G>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157290115 | ||||||
| chr4:157290192
|
G | A | 1 | a0001c0001t0004g0101 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.230-13360G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157290192 | ||||||
| chr4:157290383
|
G | C | 1 | a0001c0001t0014g0035 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.230-13169G>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157290383 | ||||||
| chr4:157290501
|
CT | C | 84 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0036others(81): Show | 87 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.230-13036delT | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157290501 | |||||
| chr4:157290501
|
CTT | C | 14 | a0001c0001t0001g0204a0001c0001t0003g0095a0001c0001t0005g0007others(11): Show | 14 | HG01123.hp2 HG01884.hp2 HG02129.hp1 others(11): Show |
intron_variant | MODIFIER | c.230-13037_230-1303 others(6): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157290501 | |||||
| chr4:157290729
|
G | A | 2 | a0001c0002t0002g0121a0001c0002t0002g0192 | 2 | HG01433.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.230-12823G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157290729 | ||||||
| chr4:157290937
|
C | A | 5 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(2): Show | 5 | HG01123.hp2 HG01884.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.230-12615C>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157290937 | ||||||
| chr4:157291413
|
G | A | 1 | a0001c0001t0001g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.230-12139G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157291413 | ||||||
| chr4:157291668
|
T | C | 1 | a0001c0001t0002g0210 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.230-11884T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157291668 | ||||||
| chr4:157291700
|
C | A | 1 | a0001c0004t0002g0003 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.230-11852C>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157291700 | ||||||
| chr4:157291712
|
A | G | 1 | a0001c0002t0001g0181 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.230-11840A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157291712 | ||||||
| chr4:157291971
|
G | T | 1 | a0001c0001t0014g0035 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.230-11581G>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157291971 | ||||||
| chr4:157291979
|
C | G | 1 | a0001c0001t0001g0113 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.230-11573C>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157291979 | ||||||
| chr4:157292145
|
A | G | 2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | HG02809.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.230-11407A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157292145 | ||||||
| chr4:157292262
|
C | T | 1 | a0001c0002t0002g0167 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.230-11290C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157292262 | ||||||
| chr4:157292552
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.230-11000C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157292552 | ||||||
| chr4:157292723
|
T | G | 1 | a0001c0002t0001g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.230-10829T>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157292723 | ||||||
| chr4:157293078
|
A | G | 10 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(7): Show | 10 | HG00733.hp2 HG00738.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.230-10474A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157293078 | ||||||
| chr4:157293246
|
T | C | 4 | a0001c0001t0003g0102a0001c0001t0003g0103a0001c0001t0003g0104others(1): Show | 4 | HG00438.hp1 HG02132.hp1 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.230-10306T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157293246 | ||||||
| chr4:157293247
|
A | G | 1 | a0001c0001t0014g0035 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.230-10305A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157293247 | ||||||
| chr4:157293364
|
A | G | 11 | a0001c0001t0005g0007a0001c0003t0001g0017a0001c0003t0001g0018others(8): Show | 11 | HG01123.hp2 HG01884.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.230-10188A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157293364 | ||||||
| chr4:157293451
|
G | A | 1 | a0001c0002t0001g0166 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.230-10101G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157293451 | ||||||
| chr4:157294193
|
C | CT | 87 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0036others(84): Show | 90 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.230-9347dupT | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157294193 | |||||
| chr4:157294363
|
G | A | 6 | a0001c0001t0001g0212a0001c0001t0002g0127a0001c0001t0002g0209others(3): Show | 7 | HG01168.hp1 HG02735.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.230-9189G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157294363 | ||||||
| chr4:157294411
|
A | G | 1 | a0001c0002t0001g0129 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.230-9141A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157294411 | ||||||
| chr4:157294499
|
T | C | 3 | a0001c0002t0002g0150a0001c0002t0002g0170a0001c0002t0002g0185 | 3 | NA18984.hp2 NA19006.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.230-9053T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157294499 | ||||||
| chr4:157295148
|
A | G | 1 | a0001c0001t0014g0035 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.230-8404A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157295148 | ||||||
| chr4:157295177
|
C | T | 3 | a0001c0002t0001g0133a0001c0002t0001g0177a0001c0002t0001g0194 | 3 | HG03195.hp2 NA18522.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.230-8375C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157295177 | ||||||
| chr4:157295973
|
T | C | 1 | a0001c0002t0002g0187 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.230-7579T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157295973 | ||||||
| chr4:157296202
|
C | T | 1 | a0001c0001t0003g0090 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.230-7350C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157296202 | ||||||
| chr4:157296267
|
A | T | 212 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(209): Show | 216 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.230-7285A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157296267 | ||||||
| chr4:157296535
|
A | C | 1 | a0001c0001t0004g0184 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.230-7017A>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157296535 | ||||||
| chr4:157296772
|
C | T | 10 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(7): Show | 10 | HG00733.hp2 HG00738.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.230-6780C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157296772 | ||||||
| chr4:157296920
|
G | A | 4 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(1): Show | 4 | HG02559.hp1 HG02922.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.230-6632G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157296920 | ||||||
| chr4:157297011
|
G | A | 1 | a0001c0001t0002g0099 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.230-6541G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157297011 | ||||||
| chr4:157297375
|
G | A | 1 | a0001c0002t0002g0160 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.230-6177G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157297375 | ||||||
| chr4:157297399
|
A | G | 99 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0036others(96): Show | 102 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.230-6153A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157297399 | ||||||
| chr4:157297690
|
A | G | 1 | a0001c0001t0002g0099 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.230-5862A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157297690 | ||||||
| chr4:157297700
|
T | C | 1 | a0001c0001t0001g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.230-5852T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157297700 | ||||||
| chr4:157297720
|
G | A | 1 | a0001c0001t0001g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.230-5832G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157297720 | ||||||
| chr4:157297734
|
A | C | 1 | a0001c0001t0014g0035 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.230-5818A>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157297734 | ||||||
| chr4:157297785
|
CT | C | 81 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0049others(78): Show | 83 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.230-5760delT | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157297785 | |||||
| chr4:157297921
|
T | A | 34 | a0001c0001t0001g0081a0001c0001t0001g0096a0001c0001t0002g0078others(31): Show | 36 | HG00438.hp1 HG00609.hp2 HG02055.hp2 others(33): Show |
intron_variant | MODIFIER | c.230-5631T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157297921 | ||||||
| chr4:157298028
|
G | A | 1 | a0001c0001t0001g0212 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.230-5524G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157298028 | ||||||
| chr4:157298090
|
T | G | 8 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(5): Show | 8 | HG00642.hp2 HG01168.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.230-5462T>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157298090 | ||||||
| chr4:157298332
|
G | A | 99 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0036others(96): Show | 102 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.230-5220G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157298332 | ||||||
| chr4:157298450
|
T | C | 1 | a0001c0001t0004g0141 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.230-5102T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157298450 | ||||||
| chr4:157298611
|
C | CT | 20 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0019others(17): Show | 20 | HG00642.hp2 HG01123.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.230-4914dupT | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157298611 | |||||
| chr4:157298611
|
C | CTT | 8 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0113others(5): Show | 8 | HG01168.hp1 HG01516.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.230-4915_230-4914d others(4): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157298611 | |||||
| chr4:157298611
|
C | CTTT | 20 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(17): Show | 21 | HG00733.hp2 HG00738.hp2 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.230-4916_230-4914d others(5): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157298611 | |||||
| chr4:157298611
|
C | CTTTT | 5 | a0001c0001t0001g0026a0001c0001t0001g0038a0001c0001t0001g0204others(2): Show | 5 | HG01109.hp2 HG02738.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.230-4917_230-4914d others(6): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157298611 | |||||
| chr4:157298611
|
CT | C | 80 | a0001c0001t0001g0011a0001c0001t0001g0049a0001c0001t0002g0149others(77): Show | 81 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.230-4914delT | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157298611 | |||||
| chr4:157298611
|
CTT | C | 18 | a0001c0001t0001g0081a0001c0001t0001g0096a0001c0001t0002g0078others(15): Show | 19 | HG00438.hp2 HG02135.hp1 HG03041.hp2 others(16): Show |
intron_variant | MODIFIER | c.230-4915_230-4914d others(4): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157298611 | |||||
| chr4:157298716
|
A | T | 10 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(7): Show | 10 | HG00733.hp2 HG00738.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.230-4836A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157298716 | ||||||
| chr4:157299044
|
C | G | 212 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(209): Show | 216 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.230-4508C>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157299044 | ||||||
| chr4:157299193
|
C | T | 1 | a0001c0002t0005g0205 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.230-4359C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157299193 | ||||||
| chr4:157299298
|
A | G | 5 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0206others(2): Show | 5 | HG00280.hp2 HG00639.hp1 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.230-4254A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157299298 | ||||||
| chr4:157299601
|
CAGAGTGA others(6): Show |
C | 1 | a0001c0001t0011g0014 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.230-3947_230-3935d others(15): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157299601 | |||||
| chr4:157299884
|
A | G | 1 | a0001c0001t0001g0204 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.230-3668A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157299884 | ||||||
| chr4:157300082
|
C | T | 119 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(116): Show | 122 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.230-3470C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157300082 | ||||||
| chr4:157300143
|
G | T | 4 | a0001c0003t0001g0017a0001c0003t0001g0018a0001c0003t0007g0043others(1): Show | 4 | HG02622.hp1 HG02717.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.230-3409G>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157300143 | ||||||
| chr4:157300664
|
G | A | 5 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111others(2): Show | 5 | HG02630.hp1 HG02886.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.230-2888G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157300664 | ||||||
| chr4:157300851
|
A | G | 1 | a0001c0002t0002g0167 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.230-2701A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157300851 | ||||||
| chr4:157300898
|
C | T | 1 | a0001c0001t0014g0035 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.230-2654C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157300898 | ||||||
| chr4:157300998
|
C | T | 1 | a0001c0001t0005g0004 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.230-2554C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157300998 | ||||||
| chr4:157301543
|
C | G | 109 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0019others(106): Show | 112 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.230-2009C>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157301543 | ||||||
| chr4:157301627
|
A | G | 2 | a0001c0001t0001g0015a0001c0001t0014g0035 | 2 | HG02071.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.230-1925A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157301627 | ||||||
| chr4:157301753
|
G | T | 99 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0036others(96): Show | 102 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.230-1799G>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157301753 | ||||||
| chr4:157301818
|
G | A | 3 | a0001c0001t0002g0127a0001c0001t0002g0209a0001c0001t0002g0210 | 3 | HG01168.hp1 HG02738.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.230-1734G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157301818 | ||||||
| chr4:157302176
|
C | CA | 20 | a0001c0001t0001g0034a0001c0001t0001g0204a0001c0001t0003g0082others(17): Show | 20 | HG00438.hp1 HG01071.hp2 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.230-1357dupA | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr4 | 157302176 | |||||
| chr4:157302204
|
T | G | 119 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(116): Show | 122 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.230-1348T>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157302204 | ||||||
| chr4:157302356
|
A | T | 10 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(7): Show | 10 | HG00733.hp2 HG00738.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.230-1196A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157302356 | ||||||
| chr4:157302367
|
G | A | 8 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(5): Show | 8 | HG00642.hp2 HG01168.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.230-1185G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157302367 | ||||||
| chr4:157302623
|
G | A | 1 | a0001c0002t0002g0187 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.230-929G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157302623 | ||||||
| chr4:157302640
|
A | T | 1 | a0001c0001t0014g0035 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.230-912A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157302640 | ||||||
| chr4:157303019
|
G | A | 10 | a0001c0003t0001g0017a0001c0003t0001g0018a0001c0003t0001g0021others(7): Show | 10 | HG01123.hp2 HG01884.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.230-533G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157303019 | ||||||
| chr4:157303827
|
G | T | 1 | a0001c0002t0002g0168 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.469+36G>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157303827 | ||||||
| chr4:157304273
|
A | G | 1 | a0001c0001t0014g0035 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.469+482A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157304273 | ||||||
| chr4:157304365
|
A | T | 10 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(7): Show | 10 | HG00733.hp2 HG00738.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.469+574A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157304365 | ||||||
| chr4:157304509
|
T | C | 119 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(116): Show | 122 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.469+718T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157304509 | ||||||
| chr4:157304528
|
G | A | 119 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(116): Show | 122 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.469+737G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157304528 | ||||||
| chr4:157304750
|
G | T | 1 | a0001c0001t0004g0101 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.469+959G>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157304750 | ||||||
| chr4:157304789
|
A | T | 1 | a0001c0001t0001g0106 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.469+998A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157304789 | ||||||
| chr4:157304913
|
G | A | 1 | a0001c0002t0002g0151 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.469+1122G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157304913 | ||||||
| chr4:157305266
|
G | A | 1 | a0001c0002t0002g0164 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.469+1475G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157305266 | ||||||
| chr4:157305339
|
T | A | 1 | a0001c0002t0001g0166 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.469+1548T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157305339 | ||||||
| chr4:157305535
|
C | T | 1 | a0001c0001t0001g0009 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.469+1744C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157305535 | ||||||
| chr4:157305616
|
C | T | 1 | a0001c0001t0002g0084 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.469+1825C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157305616 | ||||||
| chr4:157305689
|
G | A | 1 | a0001c0001t0001g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.469+1898G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157305689 | ||||||
| chr4:157305833
|
T | C | 1 | a0001c0001t0001g0087 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.469+2042T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157305833 | ||||||
| chr4:157305998
|
G | A | 2 | a0001c0002t0001g0172a0001c0002t0001g0173 | 2 | HG02132.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.469+2207G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157305998 | ||||||
| chr4:157306109
|
A | G | 1 | a0001c0002t0001g0191 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.469+2318A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157306109 | ||||||
| chr4:157306291
|
A | G | 1 | a0001c0001t0004g0067 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.469+2500A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157306291 | ||||||
| chr4:157306707
|
G | T | 1 | a0001c0001t0005g0007 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.469+2916G>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157306707 | ||||||
| chr4:157306853
|
A | G | 1 | a0001c0002t0001g0191 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.469+3062A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157306853 | ||||||
| chr4:157307027
|
C | A | 2 | a0001c0002t0002g0119a0001c0002t0002g0120 | 2 | NA18981.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.469+3236C>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157307027 | ||||||
| chr4:157307088
|
T | C | 1 | a0001c0001t0004g0051 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.469+3297T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157307088 | ||||||
| chr4:157307104
|
G | T | 119 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(116): Show | 122 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.469+3313G>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157307104 | ||||||
| chr4:157307106
|
T | A | 119 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(116): Show | 122 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.469+3315T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157307106 | ||||||
| chr4:157307141
|
G | A | 8 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(5): Show | 8 | HG00642.hp2 HG01168.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.469+3350G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157307141 | ||||||
| chr4:157307180
|
G | T | 10 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(7): Show | 10 | HG00733.hp2 HG00738.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.469+3389G>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157307180 | ||||||
| chr4:157307197
|
G | C | 2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | HG02809.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.469+3406G>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157307197 | ||||||
| chr4:157307491
|
C | T | 2 | a0001c0002t0001g0130a0001c0002t0001g0181 | 2 | HG01081.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.469+3700C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157307491 | ||||||
| chr4:157307599
|
T | C | 10 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(7): Show | 10 | HG00733.hp2 HG00738.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.469+3808T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157307599 | ||||||
| chr4:157307682
|
G | T | 1 | a0001c0001t0001g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.469+3891G>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157307682 | ||||||
| chr4:157307916
|
G | C | 1 | a0001c0001t0001g0204 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.469+4125G>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157307916 | ||||||
| chr4:157307929
|
A | C | 1 | a0001c0002t0002g0208 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.469+4138A>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157307929 | ||||||
| chr4:157308019
|
T | C | 1 | a0001c0001t0001g0065 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.469+4228T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157308019 | ||||||
| chr4:157308039
|
T | C | 1 | a0001c0001t0014g0035 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.469+4248T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157308039 | ||||||
| chr4:157308395
|
G | T | 1 | a0001c0002t0001g0191 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.470-4284G>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157308395 | ||||||
| chr4:157308418
|
A | T | 1 | a0001c0002t0002g0126 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.470-4261A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157308418 | ||||||
| chr4:157308428
|
T | A | 8 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(5): Show | 8 | HG00642.hp2 HG01168.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.470-4251T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157308428 | ||||||
| chr4:157308479
|
T | G | 7 | a0001c0001t0001g0106a0001c0001t0001g0212a0001c0001t0002g0127others(4): Show | 8 | HG01168.hp1 HG02735.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.470-4200T>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157308479 | ||||||
| chr4:157308491
|
A | ATAGT | 119 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(116): Show | 122 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.470-4186_470-4185i others(6): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr4 | 157308491 | |||||
| chr4:157308601
|
T | A | 1 | a0001c0001t0001g0034 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.470-4078T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157308601 | ||||||
| chr4:157308746
|
T | G | 68 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0049others(65): Show | 70 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.470-3933T>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157308746 | ||||||
| chr4:157308747
|
G | C | 68 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0049others(65): Show | 70 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.470-3932G>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157308747 | ||||||
| chr4:157308821
|
G | C | 4 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0004g0027others(1): Show | 4 | HG01243.hp1 HG01516.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.470-3858G>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157308821 | ||||||
| chr4:157309025
|
G | C | 10 | a0001c0003t0001g0017a0001c0003t0001g0018a0001c0003t0001g0021others(7): Show | 10 | HG01123.hp2 HG01884.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.470-3654G>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157309025 | ||||||
| chr4:157309071
|
C | T | 1 | a0001c0001t0001g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.470-3608C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157309071 | ||||||
| chr4:157309311
|
G | A | 4 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(1): Show | 4 | HG00642.hp2 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.470-3368G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157309311 | ||||||
| chr4:157309349
|
G | GT | 11 | a0001c0001t0001g0013a0001c0001t0001g0053a0001c0001t0001g0054others(8): Show | 11 | HG01109.hp1 HG01175.hp1 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.470-3310dupT | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr4 | 157309349 | |||||
| chr4:157309400
|
G | T | 10 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(7): Show | 10 | HG00733.hp2 HG00738.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.470-3279G>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157309400 | ||||||
| chr4:157309421
|
G | A | 3 | a0001c0002t0002g0118a0001c0002t0002g0121a0001c0002t0002g0192 | 3 | HG01433.hp1 HG01952.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.470-3258G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157309421 | ||||||
| chr4:157309482
|
G | T | 1 | a0001c0002t0001g0142 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.470-3197G>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157309482 | ||||||
| chr4:157309548
|
C | T | 1 | a0001c0001t0014g0035 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.470-3131C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157309548 | ||||||
| chr4:157309571
|
T | C | 119 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(116): Show | 122 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.470-3108T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157309571 | ||||||
| chr4:157309754
|
C | G | 1 | a0001c0002t0002g0153 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.470-2925C>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157309754 | ||||||
| chr4:157310002
|
AAC | A | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | HG02922.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.470-2676_470-2675d others(4): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157310002 | ||||||
| chr4:157310209
|
T | C | 1 | a0001c0001t0003g0075 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.470-2470T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157310209 | ||||||
| chr4:157310360
|
T | C | 1 | a0001c0002t0002g0116 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.470-2319T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157310360 | ||||||
| chr4:157310382
|
C | T | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | HG02922.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.470-2297C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157310382 | ||||||
| chr4:157310520
|
C | T | 1 | a0001c0001t0004g0101 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.470-2159C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157310520 | ||||||
| chr4:157310609
|
A | G | 1 | a0001c0001t0001g0106 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.470-2070A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157310609 | ||||||
| chr4:157310628
|
T | G | 1 | a0001c0002t0002g0151 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.470-2051T>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157310628 | ||||||
| chr4:157310652
|
T | C | 2 | a0001c0001t0004g0057a0001c0001t0004g0058 | 2 | HG00280.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.470-2027T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157310652 | ||||||
| chr4:157310726
|
A | G | 119 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(116): Show | 122 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.470-1953A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157310726 | ||||||
| chr4:157311146
|
T | G | 1 | a0001c0001t0004g0028 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.470-1533T>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157311146 | ||||||
| chr4:157311198
|
A | T | 1 | a0001c0001t0014g0035 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.470-1481A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157311198 | ||||||
| chr4:157311533
|
C | A | 4 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(1): Show | 4 | HG02630.hp1 HG02886.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.470-1146C>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157311533 | ||||||
| chr4:157311630
|
T | A | 1 | a0001c0002t0001g0200 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.470-1049T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157311630 | ||||||
| chr4:157311714
|
T | A | 1 | a0001c0001t0004g0057 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.470-965T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157311714 | ||||||
| chr4:157311724
|
A | G | 1 | a0001c0003t0007g0043 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.470-955A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157311724 | ||||||
| chr4:157311736
|
C | T | 3 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038 | 3 | HG03041.hp1 HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.470-943C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157311736 | ||||||
| chr4:157311737
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.470-942G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157311737 | ||||||
| chr4:157311745
|
G | A | 1 | a0001c0002t0001g0191 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.470-934G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157311745 | ||||||
| chr4:157311833
|
T | A | 108 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0019others(105): Show | 111 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.470-846T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157311833 | ||||||
| chr4:157311833
|
T | G | 1 | a0001c0001t0001g0204 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.470-846T>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157311833 | ||||||
| chr4:157311959
|
A | G | 8 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(5): Show | 8 | HG00642.hp2 HG01168.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.470-720A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157311959 | ||||||
| chr4:157312094
|
C | CA | 4 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(1): Show | 4 | HG02559.hp1 HG02922.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.470-577dupA | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr4 | 157312094 | |||||
| chr4:157312293
|
T | A | 1 | a0001c0002t0002g0164 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.470-386T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157312293 | ||||||
| chr4:157312396
|
T | C | 2 | a0001c0002t0001g0174a0001c0002t0001g0175 | 2 | HG00423.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.470-283T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 3/15 | chr4 | 157312396 | ||||||
| chr4:157312997
|
A | G | 10 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(7): Show | 10 | HG00733.hp2 HG00738.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.666+122A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 4/15 | chr4 | 157312997 | ||||||
| chr4:157313220
|
A | G | 3 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038 | 3 | HG03041.hp1 HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.666+345A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 4/15 | chr4 | 157313220 | ||||||
| chr4:157313393
|
T | C | 5 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111others(2): Show | 5 | HG02630.hp1 HG02886.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.666+518T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 4/15 | chr4 | 157313393 | ||||||
| chr4:157313560
|
G | A | 1 | a0001c0002t0002g0192 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.666+685G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 4/15 | chr4 | 157313560 | ||||||
| chr4:157313711
|
A | ATG | 10 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(7): Show | 10 | HG00642.hp2 HG01168.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.666+855_666+856dup others(2): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr4 | 157313711 | |||||
| chr4:157313728
|
T | C | 1 | a0001c0001t0011g0014 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.666+853T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 4/15 | chr4 | 157313728 | ||||||
| chr4:157313883
|
T | A | 1 | a0001c0001t0008g0042 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.666+1008T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 4/15 | chr4 | 157313883 | ||||||
| chr4:157314180
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.666+1305C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 4/15 | chr4 | 157314180 | ||||||
| chr4:157314742
|
G | A | 1 | a0001c0001t0004g0064 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.666+1867G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 4/15 | chr4 | 157314742 | ||||||
| chr4:157315110
|
T | C | 1 | a0001c0001t0001g0053 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.666+2235T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 4/15 | chr4 | 157315110 | ||||||
| chr4:157315376
|
CCA | C | 61 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0053others(58): Show | 63 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.667-2281_667-2280d others(4): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 4/15 | chr4 | 157315376 | ||||||
| chr4:157315431
|
A | T | 4 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0025others(1): Show | 4 | HG01070.hp1 HG01109.hp2 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.667-2227A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 4/15 | chr4 | 157315431 | ||||||
| chr4:157315510
|
T | G | 1 | a0001c0001t0001g0087 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.667-2148T>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 4/15 | chr4 | 157315510 | ||||||
| chr4:157315527
|
GTTTGT | G | 109 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(106): Show | 112 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.667-2102_667-2098d others(7): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr4 | 157315527 | |||||
| chr4:157315531
|
GT | G | 6 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0004g0039others(3): Show | 6 | HG01891.hp2 HG02486.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.667-2123delT | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr4 | 157315531 | |||||
| chr4:157315532
|
T | G | 1 | a0001c0002t0002g0195 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.667-2126T>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 4/15 | chr4 | 157315532 | ||||||
| chr4:157315575
|
G | A | 1 | a0001c0001t0003g0061 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.667-2083G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 4/15 | chr4 | 157315575 | ||||||
| chr4:157315630
|
A | G | 1 | a0001c0001t0001g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.667-2028A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 4/15 | chr4 | 157315630 | ||||||
| chr4:157315634
|
C | T | 1 | a0001c0002t0001g0136 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.667-2024C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 4/15 | chr4 | 157315634 | ||||||
| chr4:157315662
|
C | T | 1 | a0001c0001t0014g0035 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.667-1996C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 4/15 | chr4 | 157315662 | ||||||
| chr4:157315690
|
A | C | 1 | a0001c0002t0002g0192 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.667-1968A>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 4/15 | chr4 | 157315690 | ||||||
| chr4:157315708
|
T | C | 1 | a0001c0002t0001g0180 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.667-1950T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 4/15 | chr4 | 157315708 | ||||||
| chr4:157315815
|
A | C | 1 | a0001c0002t0001g0041 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.667-1843A>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 4/15 | chr4 | 157315815 | ||||||
| chr4:157316065
|
A | G | 1 | a0001c0002t0001g0129 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.667-1593A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 4/15 | chr4 | 157316065 | ||||||
| chr4:157316253
|
C | A | 3 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0206 | 3 | HG00639.hp1 HG01074.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.667-1405C>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 4/15 | chr4 | 157316253 | ||||||
| chr4:157316280
|
C | T | 1 | a0001c0001t0003g0093 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.667-1378C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 4/15 | chr4 | 157316280 | ||||||
| chr4:157316953
|
C | T | 1 | a0001c0001t0001g0212 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.667-705C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 4/15 | chr4 | 157316953 | ||||||
| chr4:157316954
|
G | A | 1 | a0001c0001t0008g0042 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.667-704G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 4/15 | chr4 | 157316954 | ||||||
| chr4:157317348
|
T | C | 10 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(7): Show | 10 | HG00639.hp1 HG00642.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.667-310T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 4/15 | chr4 | 157317348 | ||||||
| chr4:157317455
|
C | T | 5 | a0001c0002t0002g0188a0001c0002t0002g0189a0001c0002t0002g0190others(2): Show | 5 | HG00733.hp1 HG01169.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.667-203C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 4/15 | chr4 | 157317455 | ||||||
| chr4:157317490
|
A | T | 2 | a0001c0002t0001g0140a0001c0002t0001g0157 | 2 | HG02109.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.667-168A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 4/15 | chr4 | 157317490 | ||||||
| chr4:157317546
|
C | A | 2 | a0001c0001t0001g0015a0001c0001t0014g0035 | 2 | HG02071.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.667-112C>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 4/15 | chr4 | 157317546 | ||||||
| chr4:157317831
|
C | G | 1 | a0001c0001t0011g0014 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.720+120C>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 5/15 | chr4 | 157317831 | ||||||
| chr4:157318005
|
T | C | 13 | a0001c0001t0001g0034a0001c0001t0001g0106a0001c0001t0001g0204others(10): Show | 13 | HG01123.hp2 HG01884.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.720+294T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 5/15 | chr4 | 157318005 | ||||||
| chr4:157319293
|
T | C | 2 | a0001c0002t0001g0130a0001c0002t0001g0181 | 2 | HG01081.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.720+1582T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 5/15 | chr4 | 157319293 | ||||||
| chr4:157319361
|
C | A | 5 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111others(2): Show | 5 | HG02630.hp1 HG02886.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.720+1650C>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 5/15 | chr4 | 157319361 | ||||||
| chr4:157319566
|
G | T | 1 | a0001c0001t0014g0035 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.720+1855G>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 5/15 | chr4 | 157319566 | ||||||
| chr4:157319567
|
C | T | 1 | a0001c0001t0014g0035 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.720+1856C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 5/15 | chr4 | 157319567 | ||||||
| chr4:157319638
|
T | C | 1 | a0001c0002t0002g0159 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.721-1800T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 5/15 | chr4 | 157319638 | ||||||
| chr4:157320107
|
C | T | 10 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(7): Show | 10 | HG00733.hp2 HG00738.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.721-1331C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 5/15 | chr4 | 157320107 | ||||||
| chr4:157320119
|
G | T | 1 | a0001c0001t0014g0035 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.721-1319G>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 5/15 | chr4 | 157320119 | ||||||
| chr4:157320131
|
T | C | 1 | a0001c0004t0002g0003 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.721-1307T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 5/15 | chr4 | 157320131 | ||||||
| chr4:157320797
|
G | A | 2 | a0001c0001t0004g0051a0001c0001t0004g0141 | 2 | HG02717.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.721-641G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 5/15 | chr4 | 157320797 | ||||||
| chr4:157320876
|
T | G | 212 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(209): Show | 216 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.721-562T>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 5/15 | chr4 | 157320876 | ||||||
| chr4:157320946
|
T | C | 1 | a0001c0001t0014g0035 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.721-492T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 5/15 | chr4 | 157320946 | ||||||
| chr4:157321342
|
A | G | 1 | a0001c0001t0002g0099 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.721-96A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 5/15 | chr4 | 157321342 | ||||||
| chr4:157321360
|
T | C | 13 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(10): Show | 13 | HG00639.hp1 HG00642.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.721-78T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 5/15 | chr4 | 157321360 | ||||||
| chr4:157321388
|
G | A | 92 | a0001c0002t0001g0040a0001c0002t0001g0041a0001c0002t0001g0124others(89): Show | 93 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.721-50G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 5/15 | chr4 | 157321388 | ||||||
| chr4:157321868
|
G | A | 1 | a0001c0002t0002g0169 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.882+269G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | chr4 | 157321868 | ||||||
| chr4:157322229
|
AAG | A | 6 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0029others(3): Show | 6 | HG01243.hp1 HG01516.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.882+643_882+644del others(2): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 157322229 | |||||
| chr4:157322242
|
A | AGT | 2 | a0001c0001t0008g0042a0001c0003t0001g0021 | 2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.882+682_882+683dup others(2): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 157322242 | |||||
| chr4:157322242
|
A | T | 1 | a0001c0001t0014g0035 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.882+643A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | chr4 | 157322242 | ||||||
| chr4:157322242
|
AGT | A | 80 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0020others(77): Show | 81 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.882+682_882+683del others(2): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 157322242 | |||||
| chr4:157322242
|
AGTGT | A | 65 | a0001c0001t0001g0006a0001c0001t0001g0049a0001c0001t0001g0050others(62): Show | 68 | HG00609.hp2 HG00639.hp2 HG00733.hp2 others(65): Show |
intron_variant | MODIFIER | c.882+680_882+683del others(4): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 157322242 | |||||
| chr4:157322242
|
AGTGTGT | A | 8 | a0001c0001t0002g0149a0001c0001t0003g0103a0001c0001t0004g0183others(5): Show | 8 | HG00438.hp1 HG01123.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.882+678_882+683del others(6): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 157322242 | |||||
| chr4:157322242
|
AGTGTGTG others(1): Show |
A | 11 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(8): Show | 11 | HG00639.hp1 HG00642.hp2 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.882+676_882+683del others(8): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 157322242 | |||||
| chr4:157322242
|
AGTGTGTG others(3): Show |
A | 6 | a0001c0001t0001g0034a0001c0001t0001g0109a0001c0001t0001g0110others(3): Show | 6 | HG02258.hp1 HG02630.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.882+674_882+683del others(10): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 157322242 | |||||
| chr4:157322246
|
T | A | 3 | a0001c0002t0001g0142a0001c0002t0002g0187a0001c0004t0002g0003 | 4 | HG01070.hp2 HG01071.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.882+647T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | chr4 | 157322246 | ||||||
| chr4:157322248
|
T | A | 1 | a0001c0001t0001g0204 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.882+649T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | chr4 | 157322248 | ||||||
| chr4:157322254
|
T | A | 4 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(1): Show | 4 | HG02630.hp1 HG02886.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.882+655T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | chr4 | 157322254 | ||||||
| chr4:157323089
|
A | C | 1 | a0001c0002t0002g0208 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.882+1490A>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | chr4 | 157323089 | ||||||
| chr4:157323168
|
T | G | 1 | a0001c0002t0009g0203 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.882+1569T>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | chr4 | 157323168 | ||||||
| chr4:157323292
|
G | A | 14 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(11): Show | 14 | HG00639.hp1 HG00642.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.882+1693G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | chr4 | 157323292 | ||||||
| chr4:157323313
|
G | A | 105 | a0001c0001t0001g0034a0001c0001t0001g0106a0001c0001t0001g0204others(102): Show | 106 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.882+1714G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | chr4 | 157323313 | ||||||
| chr4:157323336
|
C | CA | 5 | a0001c0001t0003g0056a0001c0001t0003g0080a0001c0001t0003g0092others(2): Show | 5 | HG02109.hp1 HG02132.hp1 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.882+1767dupA | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 157323336 | |||||
| chr4:157323336
|
C | CAAA | 7 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0036others(4): Show | 7 | HG00639.hp1 HG01074.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.882+1765_882+1767d others(5): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 157323336 | |||||
| chr4:157323336
|
C | CAAAA | 5 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(2): Show | 5 | HG00642.hp2 HG01168.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.882+1764_882+1767d others(6): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 157323336 | |||||
| chr4:157323336
|
CA | C | 69 | a0001c0001t0001g0049a0001c0001t0001g0055a0001c0001t0001g0096others(66): Show | 70 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.882+1767delA | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 157323336 | |||||
| chr4:157323336
|
CAA | C | 69 | a0001c0001t0001g0015a0001c0001t0001g0053a0001c0001t0001g0054others(66): Show | 71 | HG00323.hp2 HG00438.hp2 HG00733.hp1 others(68): Show |
intron_variant | MODIFIER | c.882+1766_882+1767d others(4): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 157323336 | |||||
| chr4:157323336
|
CAAA | C | 10 | a0001c0001t0001g0006a0001c0001t0001g0022a0001c0001t0001g0026others(7): Show | 10 | HG00733.hp2 HG01081.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.882+1765_882+1767d others(5): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 157323336 | |||||
| chr4:157323336
|
CAAAA | C | 6 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0025others(3): Show | 6 | HG00738.hp2 HG01070.hp1 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.882+1764_882+1767d others(6): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 157323336 | |||||
| chr4:157323336
|
CAAAAA | C | 9 | a0001c0001t0001g0034a0001c0003t0001g0017a0001c0003t0001g0018others(6): Show | 9 | HG01123.hp2 HG01884.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.882+1763_882+1767d others(7): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 157323336 | |||||
| chr4:157323383
|
C | A | 1 | a0001c0002t0001g0136 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.882+1784C>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | chr4 | 157323383 | ||||||
| chr4:157323580
|
T | A | 1 | a0001c0001t0003g0093 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.882+1981T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | chr4 | 157323580 | ||||||
| chr4:157323744
|
C | T | 1 | a0001c0003t0001g0021 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.882+2145C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | chr4 | 157323744 | ||||||
| chr4:157323746
|
G | A | 1 | a0001c0001t0014g0035 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.882+2147G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | chr4 | 157323746 | ||||||
| chr4:157323775
|
T | C | 2 | a0001c0002t0002g0189a0001c0002t0002g0201 | 2 | HG03491.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.882+2176T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | chr4 | 157323775 | ||||||
| chr4:157324052
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.882+2453T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | chr4 | 157324052 | ||||||
| chr4:157324292
|
G | A | 1 | a0001c0001t0004g0108 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.882+2693G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | chr4 | 157324292 | ||||||
| chr4:157324616
|
C | T | 1 | a0001c0001t0002g0149 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.882+3017C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | chr4 | 157324616 | ||||||
| chr4:157324666
|
A | G | 4 | a0001c0003t0001g0017a0001c0003t0001g0018a0001c0003t0007g0043others(1): Show | 4 | HG02622.hp1 HG02717.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.882+3067A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | chr4 | 157324666 | ||||||
| chr4:157324874
|
C | T | 2 | a0001c0001t0003g0093a0001c0001t0003g0094 | 2 | HG00609.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.882+3275C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | chr4 | 157324874 | ||||||
| chr4:157325195
|
A | C | 2 | a0001c0001t0001g0015a0001c0001t0014g0035 | 2 | HG02071.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.882+3596A>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | chr4 | 157325195 | ||||||
| chr4:157325274
|
A | AAT | 3 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038 | 3 | HG03041.hp1 HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.882+3679_882+3680d others(4): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 157325274 | |||||
| chr4:157325350
|
T | G | 1 | a0001c0002t0001g0181 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.882+3751T>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | chr4 | 157325350 | ||||||
| chr4:157325486
|
C | A | 4 | a0001c0002t0002g0044a0001c0002t0002g0045a0001c0002t0002g0125others(1): Show | 4 | HG00738.hp1 HG01081.hp1 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.882+3887C>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | chr4 | 157325486 | ||||||
| chr4:157325591
|
C | G | 1 | a0001c0001t0011g0014 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.882+3992C>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | chr4 | 157325591 | ||||||
| chr4:157325908
|
C | T | 2 | a0001c0001t0001g0015a0001c0001t0014g0035 | 2 | HG02071.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.882+4309C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | chr4 | 157325908 | ||||||
| chr4:157326164
|
GA | G | 2 | a0001c0002t0001g0130a0001c0002t0001g0181 | 2 | HG01081.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.882+4566delA | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | chr4 | 157326164 | ||||||
| chr4:157326795
|
C | T | 1 | a0001c0001t0001g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.882+5196C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | chr4 | 157326795 | ||||||
| chr4:157326805
|
A | C | 1 | a0001c0002t0001g0135 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.882+5206A>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | chr4 | 157326805 | ||||||
| chr4:157327165
|
G | T | 1 | a0001c0001t0014g0035 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.882+5566G>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | chr4 | 157327165 | ||||||
| chr4:157327363
|
A | G | 3 | a0001c0001t0001g0015a0001c0001t0001g0106a0001c0001t0014g0035 | 3 | HG02071.hp1 HG02451.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.883-5456A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | chr4 | 157327363 | ||||||
| chr4:157327512
|
G | A | 8 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(5): Show | 8 | HG00733.hp2 HG00738.hp2 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.883-5307G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | chr4 | 157327512 | ||||||
| chr4:157327769
|
A | G | 1 | a0001c0002t0002g0195 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.883-5050A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | chr4 | 157327769 | ||||||
| chr4:157327881
|
A | G | 177 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0015others(174): Show | 180 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.883-4938A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | chr4 | 157327881 | ||||||
| chr4:157327946
|
C | T | 2 | a0001c0002t0002g0190a0001c0002t0002g0193 | 2 | HG00733.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.883-4873C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | chr4 | 157327946 | ||||||
| chr4:157327991
|
G | A | 2 | a0001c0001t0003g0061a0001c0001t0003g0062 | 2 | NA18951.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.883-4828G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | chr4 | 157327991 | ||||||
| chr4:157328233
|
G | A | 1 | a0001c0002t0001g0157 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.883-4586G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | chr4 | 157328233 | ||||||
| chr4:157328604
|
C | G | 1 | a0001c0001t0001g0025 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.883-4215C>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | chr4 | 157328604 | ||||||
| chr4:157328805
|
T | C | 1 | a0001c0001t0001g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.883-4014T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | chr4 | 157328805 | ||||||
| chr4:157328999
|
G | A | 3 | a0001c0002t0001g0166a0001c0002t0001g0174a0001c0002t0001g0175 | 3 | HG00423.hp1 HG02165.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.883-3820G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | chr4 | 157328999 | ||||||
| chr4:157329464
|
G | A | 10 | a0001c0003t0001g0017a0001c0003t0001g0018a0001c0003t0001g0021others(7): Show | 10 | HG01123.hp2 HG01884.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.883-3355G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | chr4 | 157329464 | ||||||
| chr4:157329492
|
A | G | 190 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(187): Show | 193 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.883-3327A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | chr4 | 157329492 | ||||||
| chr4:157329494
|
T | C | 1 | a0001c0001t0008g0042 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.883-3325T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | chr4 | 157329494 | ||||||
| chr4:157329530
|
C | T | 13 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(10): Show | 13 | HG00639.hp1 HG00642.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.883-3289C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | chr4 | 157329530 | ||||||
| chr4:157329827
|
G | C | 1 | a0001c0001t0001g0019 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.883-2992G>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | chr4 | 157329827 | ||||||
| chr4:157330002
|
T | C | 10 | a0001c0003t0001g0017a0001c0003t0001g0018a0001c0003t0001g0021others(7): Show | 10 | HG01123.hp2 HG01884.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.883-2817T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | chr4 | 157330002 | ||||||
| chr4:157330144
|
A | T | 1 | a0001c0002t0002g0176 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.883-2675A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | chr4 | 157330144 | ||||||
| chr4:157330222
|
A | G | 1 | a0001c0002t0002g0199 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.883-2597A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | chr4 | 157330222 | ||||||
| chr4:157330350
|
G | A | 1 | a0001c0002t0002g0195 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.883-2469G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | chr4 | 157330350 | ||||||
| chr4:157330369
|
T | C | 8 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(5): Show | 8 | HG00733.hp2 HG00738.hp2 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.883-2450T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | chr4 | 157330369 | ||||||
| chr4:157330744
|
C | T | 1 | a0001c0001t0001g0065 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.883-2075C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | chr4 | 157330744 | ||||||
| chr4:157331091
|
C | T | 13 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(10): Show | 13 | HG00639.hp1 HG00642.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.883-1728C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | chr4 | 157331091 | ||||||
| chr4:157331147
|
G | A | 1 | a0001c0002t0002g0123 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.883-1672G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | chr4 | 157331147 | ||||||
| chr4:157331238
|
T | C | 6 | a0001c0001t0001g0212a0001c0001t0002g0127a0001c0001t0002g0209others(3): Show | 7 | HG01168.hp1 HG02735.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.883-1581T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | chr4 | 157331238 | ||||||
| chr4:157331243
|
C | T | 1 | a0001c0001t0011g0014 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.883-1576C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | chr4 | 157331243 | ||||||
| chr4:157331244
|
G | A | 4 | a0001c0003t0001g0017a0001c0003t0001g0018a0001c0003t0007g0043others(1): Show | 4 | HG02622.hp1 HG02717.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.883-1575G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | chr4 | 157331244 | ||||||
| chr4:157331782
|
A | G | 21 | a0001c0001t0001g0015a0001c0001t0001g0106a0001c0001t0001g0212others(18): Show | 22 | HG01123.hp2 HG01168.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.883-1037A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | chr4 | 157331782 | ||||||
| chr4:157331963
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.883-856G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | chr4 | 157331963 | ||||||
| chr4:157332020
|
A | G | 1 | a0001c0001t0003g0060 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.883-799A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | chr4 | 157332020 | ||||||
| chr4:157332034
|
A | G | 1 | a0001c0002t0001g0197 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.883-785A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | chr4 | 157332034 | ||||||
| chr4:157332527
|
G | GA | 104 | a0001c0001t0001g0034a0001c0001t0001g0081a0001c0001t0001g0106others(101): Show | 106 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.883-281dupA | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 157332527 | |||||
| chr4:157332545
|
T | G | 1 | a0001c0001t0014g0035 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.883-274T>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | chr4 | 157332545 | ||||||
| chr4:157332755
|
G | T | 1 | a0001c0001t0004g0101 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.883-64G>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 6/15 | chr4 | 157332755 | ||||||
| chr4:157333025
|
G | A | 1 | a0001c0002t0001g0180 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1050+39G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 7/15 | chr4 | 157333025 | ||||||
| chr4:157333657
|
A | T | 10 | a0001c0003t0001g0017a0001c0003t0001g0018a0001c0003t0001g0021others(7): Show | 10 | HG01123.hp2 HG01884.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1155+304A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 8/15 | chr4 | 157333657 | ||||||
| chr4:157333738
|
G | T | 3 | a0001c0002t0002g0148a0001c0002t0002g0169a0001c0002t0012g0122 | 3 | HG01952.hp2 NA18968.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.1156-272G>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 8/15 | chr4 | 157333738 | ||||||
| chr4:157334218
|
G | T | 1 | a0001c0002t0001g0200 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1266+98G>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 9/15 | chr4 | 157334218 | ||||||
| chr4:157334259
|
C | A | 1 | a0001c0001t0001g0109 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1266+139C>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 9/15 | chr4 | 157334259 | ||||||
| chr4:157334731
|
C | T | 1 | a0001c0002t0002g0125 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1266+611C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 9/15 | chr4 | 157334731 | ||||||
| chr4:157334902
|
A | G | 5 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111others(2): Show | 5 | HG02630.hp1 HG02886.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1267-769A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 9/15 | chr4 | 157334902 | ||||||
| chr4:157334935
|
A | T | 1 | a0001c0002t0002g0163 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1267-736A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 9/15 | chr4 | 157334935 | ||||||
| chr4:157334956
|
C | T | 1 | a0001c0001t0014g0035 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1267-715C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 9/15 | chr4 | 157334956 | ||||||
| chr4:157335011
|
A | G | 2 | a0001c0001t0001g0009a0001c0003t0007g0043 | 2 | HG02809.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1267-660A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 9/15 | chr4 | 157335011 | ||||||
| chr4:157335041
|
T | A | 1 | a0001c0002t0002g0123 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1267-630T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 9/15 | chr4 | 157335041 | ||||||
| chr4:157335298
|
C | T | 1 | a0001c0002t0002g0154 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1267-373C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 9/15 | chr4 | 157335298 | ||||||
| chr4:157335581
|
G | A | 1 | a0001c0001t0004g0068 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1267-90G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 9/15 | chr4 | 157335581 | ||||||
| chr4:157336156
|
T | A | 38 | a0001c0001t0001g0034a0001c0001t0001g0053a0001c0001t0001g0054others(35): Show | 38 | HG00423.hp1 HG01074.hp2 HG01952.hp2 others(35): Show |
intron_variant | MODIFIER | c.1474-221T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 10/15 | chr4 | 157336156 | ||||||
| chr4:157336166
|
C | G | 1 | a0001c0001t0001g0109 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1474-211C>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 10/15 | chr4 | 157336166 | ||||||
| chr4:157336203
|
G | A | 2 | a0001c0002t0002g0190a0001c0002t0002g0193 | 2 | HG00733.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1474-174G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 10/15 | chr4 | 157336203 | ||||||
| chr4:157336211
|
C | T | 1 | a0001c0001t0001g0204 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1474-166C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 10/15 | chr4 | 157336211 | ||||||
| chr4:157336760
|
C | A | 3 | a0001c0002t0001g0131a0001c0002t0001g0135a0001c0002t0001g0137 | 3 | HG02818.hp2 HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1844+13C>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 11/15 | chr4 | 157336760 | ||||||
| chr4:157337175
|
T | G | 1 | a0001c0001t0002g0084 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1844+428T>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 11/15 | chr4 | 157337175 | ||||||
| chr4:157337266
|
A | G | 3 | a0001c0002t0002g0171a0001c0002t0002g0186a0001c0002t0009g0203 | 3 | NA18943.hp2 NA19087.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.1844+519A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 11/15 | chr4 | 157337266 | ||||||
| chr4:157337267
|
G | A | 6 | a0001c0001t0001g0212a0001c0001t0005g0004a0001c0001t0005g0007others(3): Show | 7 | HG02071.hp1 HG02258.hp2 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.1844+520G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 11/15 | chr4 | 157337267 | ||||||
| chr4:157337284
|
C | A | 6 | a0001c0001t0001g0212a0001c0001t0005g0004a0001c0001t0005g0007others(3): Show | 7 | HG02071.hp1 HG02258.hp2 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.1844+537C>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 11/15 | chr4 | 157337284 | ||||||
| chr4:157337370
|
T | A | 1 | a0001c0002t0005g0211 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1844+623T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 11/15 | chr4 | 157337370 | ||||||
| chr4:157337429
|
A | G | 1 | a0001c0001t0001g0025 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1844+682A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 11/15 | chr4 | 157337429 | ||||||
| chr4:157337468
|
C | T | 2 | a0001c0002t0002g0170a0001c0002t0002g0185 | 2 | NA18984.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.1844+721C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 11/15 | chr4 | 157337468 | ||||||
| chr4:157337587
|
G | T | 1 | a0001c0002t0002g0195 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1844+840G>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 11/15 | chr4 | 157337587 | ||||||
| chr4:157337604
|
C | G | 1 | a0001c0002t0002g0187 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1844+857C>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 11/15 | chr4 | 157337604 | ||||||
| chr4:157337744
|
G | T | 5 | a0001c0003t0001g0017a0001c0003t0001g0018a0001c0003t0001g0021others(2): Show | 5 | HG02622.hp1 HG02717.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1844+997G>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 11/15 | chr4 | 157337744 | ||||||
| chr4:157337933
|
C | T | 3 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0206 | 3 | HG00639.hp1 HG01074.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1844+1186C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 11/15 | chr4 | 157337933 | ||||||
| chr4:157337996
|
G | A | 5 | a0001c0001t0001g0212a0001c0001t0005g0004a0001c0001t0005g0007others(2): Show | 6 | HG02258.hp2 HG02735.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.1844+1249G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 11/15 | chr4 | 157337996 | ||||||
| chr4:157338002
|
ATATGTG | A | 2 | a0001c0001t0004g0183a0001c0001t0004g0184 | 2 | HG01123.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1844+1259_1844+126 others(10): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr4 | 157338002 | |||||
| chr4:157338004
|
A | G | 1 | a0001c0002t0002g0123 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1844+1257A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 11/15 | chr4 | 157338004 | ||||||
| chr4:157338008
|
G | GTA | 9 | a0001c0001t0001g0054a0001c0001t0001g0212a0001c0002t0001g0178others(6): Show | 9 | HG01884.hp2 HG02280.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1844+1302_1844+130 others(6): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr4 | 157338008 | |||||
| chr4:157338008
|
G | GTATA | 3 | a0001c0002t0001g0136a0001c0002t0001g0142a0001c0002t0001g0162 | 3 | HG02486.hp2 HG03130.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1844+1300_1844+130 others(8): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr4 | 157338008 | |||||
| chr4:157338008
|
GTATA | G | 41 | a0001c0001t0001g0019a0001c0001t0001g0025a0001c0001t0001g0036others(38): Show | 41 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.1844+1300_1844+130 others(8): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr4 | 157338008 | |||||
| chr4:157338008
|
GTATATA | G | 39 | a0001c0001t0001g0022a0001c0001t0001g0034a0001c0001t0001g0050others(36): Show | 40 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(37): Show |
intron_variant | MODIFIER | c.1844+1298_1844+130 others(10): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr4 | 157338008 | |||||
| chr4:157338008
|
GTATATAT others(1): Show |
G | 33 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0026others(30): Show | 35 | HG00280.hp2 HG00438.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.1844+1296_1844+130 others(12): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr4 | 157338008 | |||||
| chr4:157338008
|
GTATATAT others(3): Show |
G | 8 | a0001c0001t0001g0106a0001c0001t0003g0089a0001c0001t0003g0094others(5): Show | 8 | HG00609.hp2 HG01081.hp2 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.1844+1294_1844+130 others(14): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr4 | 157338008 | |||||
| chr4:157338008
|
GTATATAT others(5): Show |
G | 1 | a0001c0002t0001g0200 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1844+1292_1844+130 others(16): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr4 | 157338008 | |||||
| chr4:157338008
|
GTATATAT others(7): Show |
G | 2 | a0001c0001t0001g0087a0001c0002t0001g0181 | 2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1844+1290_1844+130 others(18): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr4 | 157338008 | |||||
| chr4:157338008
|
GTATATAT others(9): Show |
G | 1 | a0001c0001t0003g0063 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1844+1288_1844+130 others(20): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr4 | 157338008 | |||||
| chr4:157338008
|
GTATATAT others(11): Show |
G | 2 | a0001c0001t0003g0082a0001c0001t0003g0083 | 2 | NA18956.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.1844+1286_1844+130 others(22): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr4 | 157338008 | |||||
| chr4:157338008
|
GTATATAT others(21): Show |
G | 1 | a0001c0001t0001g0111 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1844+1276_1844+130 others(32): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr4 | 157338008 | |||||
| chr4:157338010
|
A | G | 1 | a0001c0001t0001g0109 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1844+1263A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 11/15 | chr4 | 157338010 | ||||||
| chr4:157338014
|
A | G | 4 | a0001c0001t0004g0058a0001c0001t0004g0183a0001c0001t0004g0184others(1): Show | 4 | HG01123.hp1 HG01261.hp1 HG02071.hp2 others(1): Show |
intron_variant | MODIFIER | c.1844+1267A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 11/15 | chr4 | 157338014 | ||||||
| chr4:157338016
|
A | G | 3 | a0001c0001t0004g0183a0001c0001t0004g0184a0001c0005t0002g0161 | 3 | HG01123.hp1 HG01516.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1844+1269A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 11/15 | chr4 | 157338016 | ||||||
| chr4:157338018
|
A | G | 1 | a0001c0001t0004g0057 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1844+1271A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 11/15 | chr4 | 157338018 | ||||||
| chr4:157338021
|
TATATATA others(23): Show |
T | 9 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(6): Show | 9 | HG00639.hp1 HG00642.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.1844+1276_1844+130 others(34): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr4 | 157338021 | |||||
| chr4:157338023
|
TATATATA others(21): Show |
T | 1 | a0001c0003t0001g0021 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1844+1278_1844+130 others(32): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr4 | 157338023 | |||||
| chr4:157338049
|
T | C | 20 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0037others(17): Show | 21 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.1844+1302T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 11/15 | chr4 | 157338049 | ||||||
| chr4:157338049
|
T | TATATAC | 2 | a0001c0002t0001g0143a0001c0002t0001g0177 | 2 | HG02055.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1844+1303_1844+130 others(10): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr4 | 157338049 | |||||
| chr4:157338051
|
C | T | 22 | a0001c0001t0001g0009a0001c0002t0001g0162a0001c0002t0001g0182others(19): Show | 22 | HG01123.hp2 HG01433.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.1844+1304C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 11/15 | chr4 | 157338051 | ||||||
| chr4:157338055
|
C | T | 13 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0037others(10): Show | 14 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.1844+1308C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 11/15 | chr4 | 157338055 | ||||||
| chr4:157338056
|
ACAT | A | 13 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0037others(10): Show | 14 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.1844+1310_1844+131 others(7): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 11/15 | chr4 | 157338056 | ||||||
| chr4:157338057
|
C | T | 61 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0022others(58): Show | 61 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.1844+1310C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 11/15 | chr4 | 157338057 | ||||||
| chr4:157338058
|
AT | A | 62 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0022others(59): Show | 62 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.1844+1319delT | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr4 | 157338058 | |||||
| chr4:157338059
|
T | A | 1 | a0001c0002t0001g0194 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1844+1312T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 11/15 | chr4 | 157338059 | ||||||
| chr4:157338059
|
T | TA | 129 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0011others(126): Show | 132 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.1844+1312_1844+131 others(5): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 11/15 | chr4 | 157338059 | ||||||
| chr4:157338208
|
C | A | 2 | a0001c0001t0005g0007a0001c0002t0005g0205 | 2 | HG02258.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1844+1461C>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 11/15 | chr4 | 157338208 | ||||||
| chr4:157338268
|
C | T | 6 | a0001c0001t0001g0212a0001c0001t0005g0004a0001c0001t0005g0007others(3): Show | 7 | HG02071.hp1 HG02258.hp2 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.1844+1521C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 11/15 | chr4 | 157338268 | ||||||
| chr4:157338337
|
G | A | 2 | a0001c0001t0003g0093a0001c0001t0003g0094 | 2 | HG00609.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.1844+1590G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 11/15 | chr4 | 157338337 | ||||||
| chr4:157338355
|
G | A | 1 | a0001c0001t0001g0050 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1844+1608G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 11/15 | chr4 | 157338355 | ||||||
| chr4:157338452
|
G | C | 4 | a0001c0001t0003g0102a0001c0001t0003g0103a0001c0001t0003g0104others(1): Show | 4 | HG00438.hp1 HG02132.hp1 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.1844+1705G>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 11/15 | chr4 | 157338452 | ||||||
| chr4:157339131
|
T | C | 2 | a0001c0001t0001g0049a0001c0002t0001g0197 | 2 | HG01496.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1845-2133T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 11/15 | chr4 | 157339131 | ||||||
| chr4:157339573
|
T | A | 1 | a0001c0001t0005g0004 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1845-1691T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 11/15 | chr4 | 157339573 | ||||||
| chr4:157339891
|
T | C | 2 | a0001c0002t0001g0040a0001c0002t0001g0041 | 2 | HG02622.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1845-1373T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 11/15 | chr4 | 157339891 | ||||||
| chr4:157340057
|
C | A | 4 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(1): Show | 4 | HG02630.hp1 HG02886.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1845-1207C>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 11/15 | chr4 | 157340057 | ||||||
| chr4:157340169
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1845-1095C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 11/15 | chr4 | 157340169 | ||||||
| chr4:157340338
|
C | T | 1 | a0001c0003t0001g0032 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1845-926C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 11/15 | chr4 | 157340338 | ||||||
| chr4:157340673
|
G | A | 4 | a0001c0001t0001g0212a0001c0001t0005g0004a0001c0002t0002g0208others(1): Show | 5 | HG00423.hp2 HG02735.hp1 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.1845-591G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 11/15 | chr4 | 157340673 | ||||||
| chr4:157340985
|
T | A | 1 | a0001c0001t0001g0109 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1845-279T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 11/15 | chr4 | 157340985 | ||||||
| chr4:157341064
|
G | T | 5 | a0001c0001t0001g0212a0001c0001t0005g0004a0001c0001t0005g0007others(2): Show | 6 | HG02258.hp2 HG02735.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.1845-200G>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 11/15 | chr4 | 157341064 | ||||||
| chr4:157341142
|
T | C | 1 | a0001c0002t0001g0133 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1845-122T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 11/15 | chr4 | 157341142 | ||||||
| chr4:157341209
|
T | G | 1 | a0001c0001t0014g0035 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1845-55T>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 11/15 | chr4 | 157341209 | ||||||
| chr4:157341587
|
T | C | 9 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(6): Show | 9 | HG00733.hp2 HG00738.hp2 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.2043+125T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157341587 | ||||||
| chr4:157341650
|
A | C | 5 | a0001c0001t0001g0212a0001c0001t0005g0004a0001c0001t0005g0007others(2): Show | 6 | HG02258.hp2 HG02735.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.2043+188A>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157341650 | ||||||
| chr4:157341745
|
A | G | 2 | a0001c0001t0003g0093a0001c0001t0003g0094 | 2 | HG00609.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.2043+283A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157341745 | ||||||
| chr4:157342105
|
A | C | 1 | a0001c0002t0001g0181 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2043+643A>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157342105 | ||||||
| chr4:157342311
|
A | G | 2 | a0001c0001t0004g0057a0001c0001t0004g0058 | 2 | HG00280.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.2043+849A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157342311 | ||||||
| chr4:157342430
|
A | G | 34 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0046others(31): Show | 36 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.2043+968A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157342430 | ||||||
| chr4:157342624
|
G | A | 39 | a0001c0001t0001g0034a0001c0001t0001g0053a0001c0001t0001g0054others(36): Show | 39 | HG00423.hp1 HG01074.hp2 HG01952.hp2 others(36): Show |
intron_variant | MODIFIER | c.2043+1162G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157342624 | ||||||
| chr4:157342637
|
A | T | 8 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(5): Show | 8 | HG00733.hp2 HG00738.hp2 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.2043+1175A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157342637 | ||||||
| chr4:157343009
|
A | G | 206 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(203): Show | 210 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.2043+1547A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157343009 | ||||||
| chr4:157343044
|
G | C | 1 | a0001c0002t0002g0123 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2043+1582G>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157343044 | ||||||
| chr4:157343138
|
C | A | 1 | a0001c0002t0001g0174 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2043+1676C>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157343138 | ||||||
| chr4:157343281
|
C | T | 1 | a0001c0001t0014g0035 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2043+1819C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157343281 | ||||||
| chr4:157343297
|
TAGTC | T | 3 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0025 | 3 | HG01070.hp1 HG01891.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.2043+1838_2043+184 others(8): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | 157343297 | |||||
| chr4:157343470
|
C | T | 205 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(202): Show | 209 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.2043+2008C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157343470 | ||||||
| chr4:157343533
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2043+2071C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157343533 | ||||||
| chr4:157343632
|
T | C | 1 | a0001c0002t0012g0122 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2043+2170T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157343632 | ||||||
| chr4:157343817
|
T | C | 6 | a0001c0001t0004g0047a0001c0001t0004g0048a0001c0001t0004g0072others(3): Show | 6 | HG01175.hp2 HG01433.hp2 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.2043+2355T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157343817 | ||||||
| chr4:157343887
|
C | G | 1 | a0001c0002t0002g0169 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2043+2425C>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157343887 | ||||||
| chr4:157344095
|
A | G | 1 | a0001c0002t0002g0179 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2043+2633A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157344095 | ||||||
| chr4:157344385
|
A | G | 3 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0025 | 3 | HG01070.hp1 HG01891.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.2043+2923A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157344385 | ||||||
| chr4:157344543
|
T | C | 205 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(202): Show | 209 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.2043+3081T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157344543 | ||||||
| chr4:157344545
|
G | A | 2 | a0001c0002t0001g0040a0001c0002t0001g0041 | 2 | HG02622.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2043+3083G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157344545 | ||||||
| chr4:157344760
|
G | A | 3 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0025 | 3 | HG01070.hp1 HG01891.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.2043+3298G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157344760 | ||||||
| chr4:157345364
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2043+3902C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157345364 | ||||||
| chr4:157345728
|
C | T | 5 | a0001c0003t0001g0017a0001c0003t0001g0018a0001c0003t0001g0021others(2): Show | 5 | HG02622.hp1 HG02717.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.2043+4266C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157345728 | ||||||
| chr4:157345758
|
G | T | 1 | a0001c0002t0001g0166 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2043+4296G>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157345758 | ||||||
| chr4:157345886
|
T | C | 1 | a0001c0002t0002g0150 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2043+4424T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157345886 | ||||||
| chr4:157346158
|
C | T | 2 | a0001c0001t0001g0109a0001c0001t0011g0014 | 2 | HG02109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2043+4696C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157346158 | ||||||
| chr4:157346325
|
A | G | 1 | a0001c0001t0003g0076 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.2043+4863A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157346325 | ||||||
| chr4:157346351
|
T | C | 6 | a0001c0001t0004g0047a0001c0001t0004g0048a0001c0001t0004g0072others(3): Show | 6 | HG01175.hp2 HG01433.hp2 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.2043+4889T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157346351 | ||||||
| chr4:157346383
|
C | T | 55 | a0001c0001t0001g0050a0001c0001t0001g0097a0001c0001t0002g0149others(52): Show | 57 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.2043+4921C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157346383 | ||||||
| chr4:157346384
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2043+4922G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157346384 | ||||||
| chr4:157346469
|
G | A | 1 | a0001c0001t0004g0101 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2043+5007G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157346469 | ||||||
| chr4:157346590
|
G | A | 1 | a0001c0002t0001g0144 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.2043+5128G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157346590 | ||||||
| chr4:157346945
|
T | C | 1 | a0001c0001t0001g0212 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2043+5483T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157346945 | ||||||
| chr4:157347356
|
A | G | 2 | a0001c0001t0001g0026a0001c0001t0001g0029 | 2 | HG01243.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.2043+5894A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157347356 | ||||||
| chr4:157347472
|
GATTAATC others(4): Show |
G | 1 | a0001c0001t0001g0204 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2043+6012_2043+602 others(15): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | 157347472 | |||||
| chr4:157347801
|
G | A | 1 | a0001c0001t0004g0070 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.2043+6339G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157347801 | ||||||
| chr4:157347908
|
G | A | 1 | a0001c0001t0014g0035 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2043+6446G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157347908 | ||||||
| chr4:157347922
|
G | A | 1 | a0001c0002t0002g0195 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2043+6460G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157347922 | ||||||
| chr4:157347923
|
A | G | 1 | a0001c0002t0002g0195 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2043+6461A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157347923 | ||||||
| chr4:157348072
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2043+6610C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157348072 | ||||||
| chr4:157348090
|
G | A | 116 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0015others(113): Show | 117 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.2043+6628G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157348090 | ||||||
| chr4:157348344
|
T | A | 1 | a0001c0002t0002g0139 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2043+6882T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157348344 | ||||||
| chr4:157348527
|
C | T | 1 | a0001c0002t0002g0156 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.2043+7065C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157348527 | ||||||
| chr4:157348599
|
T | C | 4 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(1): Show | 4 | HG00642.hp2 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.2043+7137T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157348599 | ||||||
| chr4:157348680
|
T | A | 1 | a0001c0001t0003g0059 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.2043+7218T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157348680 | ||||||
| chr4:157348808
|
G | T | 1 | a0001c0002t0002g0146 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2043+7346G>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157348808 | ||||||
| chr4:157348993
|
T | A | 1 | a0001c0001t0011g0014 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2043+7531T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157348993 | ||||||
| chr4:157349042
|
T | A | 2 | a0001c0001t0006g0091a0001c0001t0006g0100 | 2 | NA18980.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.2043+7580T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157349042 | ||||||
| chr4:157349238
|
A | T | 2 | a0001c0001t0004g0047a0001c0001t0004g0048 | 2 | HG01175.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.2043+7776A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157349238 | ||||||
| chr4:157349252
|
C | T | 18 | a0001c0001t0001g0034a0001c0001t0001g0081a0001c0001t0001g0096others(15): Show | 18 | HG00423.hp1 HG01074.hp2 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.2043+7790C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157349252 | ||||||
| chr4:157349254
|
G | A | 115 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0015others(112): Show | 116 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.2043+7792G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157349254 | ||||||
| chr4:157349315
|
T | C | 5 | a0001c0001t0003g0095a0001c0001t0003g0102a0001c0001t0003g0103others(2): Show | 5 | HG00438.hp1 HG02129.hp1 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.2043+7853T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157349315 | ||||||
| chr4:157349339
|
G | T | 1 | a0001c0001t0014g0035 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2043+7877G>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157349339 | ||||||
| chr4:157349450
|
T | C | 1 | a0001c0001t0003g0059 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.2043+7988T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157349450 | ||||||
| chr4:157349576
|
A | G | 42 | a0001c0001t0001g0034a0001c0001t0001g0053a0001c0001t0001g0054others(39): Show | 42 | HG00423.hp1 HG01074.hp2 HG01952.hp2 others(39): Show |
intron_variant | MODIFIER | c.2043+8114A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157349576 | ||||||
| chr4:157349871
|
C | T | 2 | a0001c0001t0001g0087a0001c0001t0001g0106 | 2 | HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2043+8409C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157349871 | ||||||
| chr4:157350098
|
T | C | 4 | a0001c0001t0005g0004a0001c0001t0005g0007a0001c0002t0005g0205others(1): Show | 5 | HG02258.hp2 HG02735.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.2043+8636T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157350098 | ||||||
| chr4:157350310
|
G | A | 1 | a0001c0002t0001g0130 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2043+8848G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157350310 | ||||||
| chr4:157350931
|
C | CT | 11 | a0001c0001t0001g0009a0001c0001t0004g0047a0001c0001t0004g0057others(8): Show | 12 | HG00280.hp2 HG01081.hp2 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.2044-8948dupT | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | 157350931 | |||||
| chr4:157350941
|
T | TA | 2 | a0001c0001t0001g0109a0001c0001t0011g0014 | 2 | HG02109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2044-8955_2044-895 others(5): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157350941 | ||||||
| chr4:157351055
|
G | A | 1 | a0001c0002t0002g0169 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2044-8841G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157351055 | ||||||
| chr4:157351225
|
A | G | 206 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(203): Show | 210 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.2044-8671A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157351225 | ||||||
| chr4:157351280
|
G | A | 4 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(1): Show | 4 | HG02630.hp1 HG02886.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2044-8616G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157351280 | ||||||
| chr4:157351413
|
G | A | 1 | a0001c0002t0012g0122 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2044-8483G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157351413 | ||||||
| chr4:157351426
|
A | G | 1 | a0001c0002t0001g0129 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2044-8470A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157351426 | ||||||
| chr4:157351525
|
T | A | 3 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0206 | 3 | HG00639.hp1 HG01074.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.2044-8371T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157351525 | ||||||
| chr4:157351600
|
G | T | 1 | a0001c0001t0001g0038 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2044-8296G>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157351600 | ||||||
| chr4:157351628
|
C | T | 8 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(5): Show | 8 | HG00733.hp2 HG00738.hp2 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.2044-8268C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157351628 | ||||||
| chr4:157351665
|
C | T | 1 | a0001c0001t0011g0014 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2044-8231C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157351665 | ||||||
| chr4:157351673
|
A | G | 1 | a0001c0001t0001g0109 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2044-8223A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157351673 | ||||||
| chr4:157351929
|
C | G | 1 | a0001c0001t0001g0087 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2044-7967C>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157351929 | ||||||
| chr4:157351973
|
T | C | 2 | a0001c0001t0001g0109a0001c0001t0011g0014 | 2 | HG02109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2044-7923T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157351973 | ||||||
| chr4:157351979
|
A | T | 2 | a0001c0001t0005g0004a0001c0002t0005g0211 | 3 | HG02735.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2044-7917A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157351979 | ||||||
| chr4:157352061
|
A | C | 8 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(5): Show | 8 | HG00733.hp2 HG00738.hp2 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.2044-7835A>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157352061 | ||||||
| chr4:157352070
|
C | T | 1 | a0001c0001t0004g0067 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2044-7826C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157352070 | ||||||
| chr4:157352087
|
C | G | 1 | a0001c0002t0001g0180 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2044-7809C>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157352087 | ||||||
| chr4:157352242
|
A | G | 1 | a0001c0001t0004g0067 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2044-7654A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157352242 | ||||||
| chr4:157352518
|
G | A | 1 | a0001c0002t0002g0168 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2044-7378G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157352518 | ||||||
| chr4:157352592
|
C | T | 4 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(1): Show | 4 | HG02630.hp1 HG02886.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2044-7304C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157352592 | ||||||
| chr4:157352651
|
T | C | 2 | a0001c0001t0005g0007a0001c0002t0005g0205 | 2 | HG02258.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2044-7245T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157352651 | ||||||
| chr4:157352718
|
T | TA | 68 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(65): Show | 71 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.2044-7158dupA | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | 157352718 | |||||
| chr4:157352718
|
T | TAA | 24 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(21): Show | 24 | HG00639.hp1 HG00642.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.2044-7159_2044-715 others(6): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | 157352718 | |||||
| chr4:157352718
|
T | TAAA | 39 | a0001c0001t0001g0034a0001c0001t0001g0053a0001c0001t0001g0054others(36): Show | 39 | HG00423.hp1 HG01074.hp2 HG01123.hp2 others(36): Show |
intron_variant | MODIFIER | c.2044-7160_2044-715 others(7): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | 157352718 | |||||
| chr4:157352718
|
T | TAAAA | 8 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(5): Show | 8 | HG02280.hp1 HG02630.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.2044-7161_2044-715 others(8): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | 157352718 | |||||
| chr4:157352748
|
C | T | 5 | a0001c0001t0004g0039a0001c0001t0004g0051a0001c0001t0004g0141others(2): Show | 5 | HG01891.hp2 HG02717.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2044-7148C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157352748 | ||||||
| chr4:157353126
|
G | T | 57 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0046others(54): Show | 59 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.2044-6770G>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157353126 | ||||||
| chr4:157353347
|
T | C | 204 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(201): Show | 208 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.2044-6549T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157353347 | ||||||
| chr4:157353396
|
C | T | 1 | a0001c0002t0001g0180 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2044-6500C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157353396 | ||||||
| chr4:157353397
|
G | A | 1 | a0001c0001t0014g0035 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2044-6499G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157353397 | ||||||
| chr4:157353408
|
C | T | 1 | a0001c0001t0014g0035 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2044-6488C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157353408 | ||||||
| chr4:157353445
|
C | T | 1 | a0001c0002t0002g0160 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.2044-6451C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157353445 | ||||||
| chr4:157353486
|
C | T | 1 | a0001c0001t0001g0204 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2044-6410C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157353486 | ||||||
| chr4:157353512
|
T | A | 1 | a0001c0001t0001g0204 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2044-6384T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157353512 | ||||||
| chr4:157353512
|
T | TA | 3 | a0001c0001t0001g0106a0001c0001t0003g0092a0001c0001t0006g0091 | 3 | HG03540.hp1 NA19001.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.2044-6382dupA | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | 157353512 | |||||
| chr4:157353514
|
AT | A | 17 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(14): Show | 17 | HG00639.hp1 HG00642.hp2 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.2044-6381delT | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157353514 | ||||||
| chr4:157353515
|
T | A | 186 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(183): Show | 190 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.2044-6381T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157353515 | ||||||
| chr4:157353518
|
A | T | 2 | a0001c0001t0004g0183a0001c0001t0004g0184 | 2 | HG01123.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.2044-6378A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157353518 | ||||||
| chr4:157353520
|
A | T | 1 | a0001c0002t0002g0195 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2044-6376A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157353520 | ||||||
| chr4:157353555
|
A | C | 1 | a0001c0001t0001g0015 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2044-6341A>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157353555 | ||||||
| chr4:157353601
|
G | A | 33 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0046others(30): Show | 35 | HG00438.hp1 HG00609.hp2 HG02055.hp2 others(32): Show |
intron_variant | MODIFIER | c.2044-6295G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157353601 | ||||||
| chr4:157353643
|
A | G | 5 | a0001c0001t0001g0109a0001c0001t0005g0004a0001c0001t0005g0007others(2): Show | 6 | HG02258.hp2 HG02735.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.2044-6253A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157353643 | ||||||
| chr4:157353924
|
C | A | 1 | a0001c0001t0004g0039 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2044-5972C>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157353924 | ||||||
| chr4:157354077
|
T | C | 8 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(5): Show | 8 | HG00733.hp2 HG00738.hp2 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.2044-5819T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157354077 | ||||||
| chr4:157354130
|
C | T | 2 | a0001c0001t0001g0049a0001c0002t0001g0197 | 2 | HG01496.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2044-5766C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157354130 | ||||||
| chr4:157354143
|
GGAATGTC others(4): Show |
G | 1 | a0001c0002t0002g0123 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2044-5749_2044-573 others(15): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | 157354143 | |||||
| chr4:157354374
|
A | G | 1 | a0001c0001t0001g0087 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2044-5522A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157354374 | ||||||
| chr4:157354405
|
C | T | 42 | a0001c0001t0001g0034a0001c0001t0001g0053a0001c0001t0001g0054others(39): Show | 42 | HG00423.hp1 HG01074.hp2 HG01952.hp2 others(39): Show |
intron_variant | MODIFIER | c.2044-5491C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157354405 | ||||||
| chr4:157354666
|
A | G | 1 | a0001c0001t0004g0074 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2044-5230A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157354666 | ||||||
| chr4:157354692
|
G | A | 8 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(5): Show | 8 | HG00733.hp2 HG00738.hp2 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.2044-5204G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157354692 | ||||||
| chr4:157354862
|
A | C | 123 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(120): Show | 125 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.2044-5034A>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157354862 | ||||||
| chr4:157354977
|
G | C | 4 | a0001c0001t0005g0004a0001c0001t0005g0007a0001c0002t0005g0205others(1): Show | 5 | HG02258.hp2 HG02735.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.2044-4919G>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157354977 | ||||||
| chr4:157355144
|
T | C | 1 | a0001c0001t0001g0087 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2044-4752T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355144 | ||||||
| chr4:157355277
|
C | T | 2 | a0001c0002t0001g0040a0001c0002t0001g0041 | 2 | HG02622.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2044-4619C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355277 | ||||||
| chr4:157355303
|
G | A | 1 | a0001c0001t0001g0050 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2044-4593G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355303 | ||||||
| chr4:157355528
|
C | CA | 64 | a0001c0001t0002g0023a0001c0001t0002g0078a0001c0001t0002g0084others(61): Show | 65 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.2044-4356dupA | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | 157355528 | |||||
| chr4:157355600
|
A | ATATTTAT others(12): Show |
1 | a0001c0003t0001g0021 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2044-4283_2044-428 others(23): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | 157355600 | |||||
| chr4:157355600
|
A | ATATTTAT others(7): Show |
124 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(121): Show | 126 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.2044-4256_2044-424 others(18): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | 157355600 | |||||
| chr4:157355600
|
A | ATATTTAT others(33): Show |
1 | a0001c0002t0001g0175 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2044-4269_2044-426 others(44): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | 157355600 | |||||
| chr4:157355600
|
A | ATTTATAT others(5): Show |
14 | a0001c0001t0003g0002a0001c0001t0003g0056a0001c0001t0003g0089others(11): Show | 15 | HG00438.hp1 HG00609.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.2044-4295_2044-429 others(16): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | 157355600 | |||||
| chr4:157355622
|
A | ATATATTT others(7): Show |
1 | a0001c0001t0014g0035 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2044-4261_2044-426 others(18): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | 157355622 | |||||
| chr4:157355670
|
T | A | 2 | a0001c0002t0002g0154a0001c0002t0002g0158 | 2 | NA18980.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.2044-4226T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355670 | ||||||
| chr4:157355686
|
ATATT | A | 2 | a0001c0002t0001g0172a0001c0002t0001g0173 | 2 | HG02132.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.2044-4202_2044-419 others(8): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | 157355686 | |||||
| chr4:157355694
|
TTA | T | 61 | a0001c0001t0002g0023a0001c0001t0002g0078a0001c0001t0002g0084others(58): Show | 62 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.2044-4194_2044-419 others(6): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | 157355694 | |||||
| chr4:157355700
|
A | T | 1 | a0001c0002t0002g0158 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2044-4196A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355700 | ||||||
| chr4:157355706
|
G | T | 2 | a0001c0002t0002g0154a0001c0002t0002g0158 | 2 | NA18980.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.2044-4190G>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355706 | ||||||
| chr4:157355706
|
GTATATAT others(5): Show |
G | 4 | a0001c0001t0004g0072a0001c0001t0004g0073a0001c0002t0001g0130others(1): Show | 4 | HG01081.hp2 HG02976.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.2044-4155_2044-414 others(16): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | 157355706 | |||||
| chr4:157355716
|
A | ATTTATAT others(5): Show |
1 | a0001c0002t0002g0154 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2044-4173_2044-417 others(16): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | 157355716 | |||||
| chr4:157355726
|
TTATTTAT others(36): Show |
T | 1 | a0001c0001t0002g0099 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2044-4154_2044-411 others(47): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | 157355726 | |||||
| chr4:157355738
|
TTATTTAT others(24): Show |
T | 54 | a0001c0001t0002g0023a0001c0001t0002g0078a0001c0001t0002g0127others(51): Show | 55 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.2044-4143_2044-411 others(35): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | 157355738 | |||||
| chr4:157355741
|
TTTATATA others(5): Show |
T | 19 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(16): Show | 19 | HG02055.hp1 HG02109.hp2 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.2044-4154_2044-414 others(16): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355741 | ||||||
| chr4:157355742
|
T | A | 1 | a0001c0002t0002g0158 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2044-4154T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355742 | ||||||
| chr4:157355746
|
A | T | 1 | a0001c0002t0002g0158 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2044-4150A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355746 | ||||||
| chr4:157355752
|
A | G | 1 | a0001c0002t0002g0154 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2044-4144A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355752 | ||||||
| chr4:157355753
|
C | T | 41 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0015others(38): Show | 41 | HG00423.hp1 HG00733.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.2044-4143C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355753 | ||||||
| chr4:157355758
|
A | ATTTATTT others(6): Show |
1 | a0001c0002t0002g0154 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2044-4136_2044-413 others(17): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | 157355758 | |||||
| chr4:157355762
|
G | T | 2 | a0001c0002t0002g0154a0001c0002t0002g0158 | 2 | NA18980.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.2044-4134G>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355762 | ||||||
| chr4:157355773
|
TTATATAT others(3): Show |
T | 8 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0002g0149others(5): Show | 8 | HG00738.hp1 HG01071.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.2044-4114_2044-410 others(14): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | 157355773 | |||||
| chr4:157355780
|
T | TTAG | 7 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(4): Show | 7 | HG00733.hp2 HG00738.hp2 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.2044-4115_2044-411 others(7): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | 157355780 | |||||
| chr4:157355783
|
A | T | 1 | a0001c0001t0002g0084 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2044-4113A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355783 | ||||||
| chr4:157355791
|
TA | T | 7 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(4): Show | 7 | HG00733.hp2 HG00738.hp2 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.2044-4104delA | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355791 | ||||||
| chr4:157355792
|
A | T | 1 | a0001c0001t0002g0084 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2044-4104A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355792 | ||||||
| chr4:157355793
|
G | A | 1 | a0001c0001t0002g0084 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2044-4103G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355793 | ||||||
| chr4:157355793
|
G | T | 7 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(4): Show | 7 | HG00733.hp2 HG00738.hp2 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.2044-4103G>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355793 | ||||||
| chr4:157355794
|
T | A | 7 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(4): Show | 7 | HG00733.hp2 HG00738.hp2 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.2044-4102T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355794 | ||||||
| chr4:157355802
|
A | T | 7 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(4): Show | 7 | HG00733.hp2 HG00738.hp2 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.2044-4094A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355802 | ||||||
| chr4:157355804
|
T | G | 1 | a0001c0001t0002g0084 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2044-4092T>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355804 | ||||||
| chr4:157355810
|
A | AT | 7 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(4): Show | 7 | HG00733.hp2 HG00738.hp2 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.2044-4084dupT | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | 157355810 | |||||
| chr4:157355810
|
AT | A | 8 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0002g0149others(5): Show | 8 | HG00738.hp1 HG01071.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.2044-4084delT | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | 157355810 | |||||
| chr4:157355814
|
G | T | 15 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0015others(12): Show | 15 | HG00733.hp2 HG00738.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.2044-4082G>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355814 | ||||||
| chr4:157355817
|
A | T | 8 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0002g0149others(5): Show | 8 | HG00738.hp1 HG01071.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.2044-4079A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355817 | ||||||
| chr4:157355820
|
T | C | 1 | a0001c0001t0002g0084 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2044-4076T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355820 | ||||||
| chr4:157355823
|
A | G | 7 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(4): Show | 7 | HG00733.hp2 HG00738.hp2 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.2044-4073A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355823 | ||||||
| chr4:157355825
|
T | A | 7 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(4): Show | 7 | HG00733.hp2 HG00738.hp2 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.2044-4071T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355825 | ||||||
| chr4:157355829
|
A | T | 8 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0002g0149others(5): Show | 8 | HG00738.hp1 HG01071.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.2044-4067A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355829 | ||||||
| chr4:157355830
|
T | TTAAC | 7 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(4): Show | 7 | HG00733.hp2 HG00738.hp2 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.2044-4066_2044-406 others(8): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355830 | ||||||
| chr4:157355833
|
A | T | 1 | a0001c0001t0001g0034 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2044-4063A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355833 | ||||||
| chr4:157355835
|
T | A | 8 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0002g0149others(5): Show | 8 | HG00738.hp1 HG01071.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.2044-4061T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355835 | ||||||
| chr4:157355837
|
T | A | 7 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(4): Show | 7 | HG00733.hp2 HG00738.hp2 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.2044-4059T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355837 | ||||||
| chr4:157355837
|
T | G | 8 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0002g0149others(5): Show | 8 | HG00738.hp1 HG01071.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.2044-4059T>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355837 | ||||||
| chr4:157355838
|
T | A | 1 | a0001c0001t0002g0084 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2044-4058T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355838 | ||||||
| chr4:157355845
|
T | TAACA | 8 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0002g0149others(5): Show | 8 | HG00738.hp1 HG01071.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.2044-4051_2044-405 others(8): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355845 | ||||||
| chr4:157355845
|
T | TAATA | 7 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(4): Show | 7 | HG00733.hp2 HG00738.hp2 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.2044-4051_2044-405 others(8): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355845 | ||||||
| chr4:157355849
|
TTA | T | 62 | a0001c0001t0002g0023a0001c0001t0002g0078a0001c0001t0002g0099others(59): Show | 63 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.2044-4039_2044-403 others(6): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | 157355849 | |||||
| chr4:157355851
|
A | T | 1 | a0001c0001t0014g0035 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2044-4045A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355851 | ||||||
| chr4:157355856
|
T | A | 1 | a0001c0001t0002g0084 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2044-4040T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355856 | ||||||
| chr4:157355856
|
T | TAA | 7 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(4): Show | 7 | HG00733.hp2 HG00738.hp2 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.2044-4039_2044-403 others(6): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | 157355856 | |||||
| chr4:157355859
|
G | A | 8 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(5): Show | 8 | HG00733.hp2 HG00738.hp2 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.2044-4037G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355859 | ||||||
| chr4:157355859
|
G | T | 8 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0002g0149others(5): Show | 8 | HG00738.hp1 HG01071.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.2044-4037G>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355859 | ||||||
| chr4:157355860
|
T | A | 8 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0002g0149others(5): Show | 8 | HG00738.hp1 HG01071.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.2044-4036T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355860 | ||||||
| chr4:157355868
|
A | T | 8 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0002g0149others(5): Show | 8 | HG00738.hp1 HG01071.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.2044-4028A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355868 | ||||||
| chr4:157355870
|
C | T | 16 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0015others(13): Show | 16 | HG00733.hp2 HG00738.hp1 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.2044-4026C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355870 | ||||||
| chr4:157355874
|
T | TAA | 8 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0002g0149others(5): Show | 8 | HG00738.hp1 HG01071.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.2044-4022_2044-402 others(6): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355874 | ||||||
| chr4:157355875
|
T | A | 8 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0002g0149others(5): Show | 8 | HG00738.hp1 HG01071.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.2044-4021T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355875 | ||||||
| chr4:157355875
|
T | TTATATAT others(29): Show |
1 | a0001c0001t0001g0024 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2044-4013_2044-401 others(40): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | 157355875 | |||||
| chr4:157355875
|
T | TTATATAT others(31): Show |
4 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0025others(1): Show | 4 | HG00733.hp2 HG00738.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.2044-4013_2044-401 others(42): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | 157355875 | |||||
| chr4:157355875
|
T | TTATATAT others(59): Show |
1 | a0001c0001t0001g0212 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2044-4013_2044-401 others(70): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | 157355875 | |||||
| chr4:157355875
|
T | TTATATAT others(31): Show |
1 | a0001c0001t0001g0022 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2044-4013_2044-401 others(42): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | 157355875 | |||||
| chr4:157355893
|
T | A | 1 | a0001c0001t0002g0084 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2044-4003T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355893 | ||||||
| chr4:157355897
|
A | T | 1 | a0001c0001t0002g0084 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2044-3999A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355897 | ||||||
| chr4:157355902
|
A | T | 1 | a0001c0001t0002g0084 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2044-3994A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355902 | ||||||
| chr4:157355902
|
AAT | A | 123 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(120): Show | 124 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.2044-3983_2044-398 others(6): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | 157355902 | |||||
| chr4:157355904
|
T | TATATATA others(19): Show |
3 | a0001c0001t0003g0002a0001c0001t0003g0090a0001c0001t0008g0042 | 4 | HG02922.hp1 NA18944.hp1 NA19085.hp1 others(1): Show |
intron_variant | MODIFIER | c.2044-3984_2044-398 others(30): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | 157355904 | |||||
| chr4:157355904
|
T | TATATATA others(47): Show |
2 | a0001c0001t0005g0007a0001c0002t0005g0205 | 2 | HG02258.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2044-3984_2044-398 others(58): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | 157355904 | |||||
| chr4:157355904
|
T | TATATATA others(75): Show |
2 | a0001c0001t0005g0004a0001c0002t0005g0211 | 3 | HG02735.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2044-3984_2044-398 others(86): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | 157355904 | |||||
| chr4:157355904
|
T | TATATATA others(29): Show |
12 | a0001c0001t0001g0097a0001c0001t0010g0207a0001c0003t0001g0017others(9): Show | 12 | HG01123.hp2 HG01884.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.2044-3984_2044-398 others(40): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | 157355904 | |||||
| chr4:157355905
|
A | T | 1 | a0001c0001t0002g0084 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2044-3991A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355905 | ||||||
| chr4:157355906
|
T | A | 1 | a0001c0001t0002g0084 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2044-3990T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355906 | ||||||
| chr4:157355908
|
T | TATATTA | 63 | a0001c0001t0002g0023a0001c0001t0002g0078a0001c0001t0002g0099others(60): Show | 64 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.2044-3984_2044-398 others(10): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | 157355908 | |||||
| chr4:157355916
|
A | T | 64 | a0001c0001t0002g0023a0001c0001t0002g0078a0001c0001t0002g0084others(61): Show | 65 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.2044-3980A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355916 | ||||||
| chr4:157355918
|
T | C | 2 | a0001c0001t0001g0109a0001c0001t0011g0014 | 2 | HG02109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2044-3978T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355918 | ||||||
| chr4:157355922
|
T | TAA | 62 | a0001c0001t0002g0023a0001c0001t0002g0078a0001c0001t0002g0099others(59): Show | 63 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.2044-3974_2044-397 others(6): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355922 | ||||||
| chr4:157355923
|
T | A | 63 | a0001c0001t0002g0023a0001c0001t0002g0078a0001c0001t0002g0099others(60): Show | 64 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.2044-3973T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355923 | ||||||
| chr4:157355924
|
T | A | 1 | a0001c0002t0002g0171 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2044-3972T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355924 | ||||||
| chr4:157355925
|
A | T | 1 | a0001c0001t0014g0035 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2044-3971A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355925 | ||||||
| chr4:157355926
|
T | TATATAA | 5 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0049others(2): Show | 5 | HG01496.hp2 HG01884.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.2044-3965_2044-396 others(10): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | 157355926 | |||||
| chr4:157355931
|
ATT | A | 7 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(4): Show | 7 | HG00639.hp1 HG00642.hp2 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.2044-3963_2044-396 others(6): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | 157355931 | |||||
| chr4:157355932
|
T | TATATTA | 7 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(4): Show | 7 | HG00733.hp2 HG00738.hp2 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.2044-3964_2044-396 others(10): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355932 | ||||||
| chr4:157355933
|
T | A | 8 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(5): Show | 8 | HG00733.hp2 HG00738.hp2 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.2044-3963T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355933 | ||||||
| chr4:157355933
|
T | TAA | 5 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0049others(2): Show | 5 | HG01496.hp2 HG01884.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.2044-3963_2044-396 others(6): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355933 | ||||||
| chr4:157355934
|
T | A | 7 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(4): Show | 7 | HG00639.hp1 HG00642.hp2 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.2044-3962T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355934 | ||||||
| chr4:157355942
|
A | T | 13 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(10): Show | 13 | HG00733.hp2 HG00738.hp2 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.2044-3954A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355942 | ||||||
| chr4:157355943
|
A | ATATATTT others(51): Show |
1 | a0001c0001t0001g0026 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2044-3948_2044-394 others(62): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | 157355943 | |||||
| chr4:157355943
|
ATATATAT others(1): Show |
A | 4 | a0001c0001t0001g0109a0001c0001t0011g0014a0001c0002t0001g0130others(1): Show | 4 | HG01081.hp2 HG02109.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.2044-3941_2044-393 others(12): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | 157355943 | |||||
| chr4:157355949
|
A | G | 41 | a0001c0001t0001g0034a0001c0001t0001g0053a0001c0001t0001g0054others(38): Show | 41 | HG00423.hp1 HG01074.hp2 HG01952.hp2 others(38): Show |
intron_variant | MODIFIER | c.2044-3947A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355949 | ||||||
| chr4:157355949
|
A | T | 12 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(9): Show | 12 | HG00733.hp2 HG00738.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.2044-3947A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355949 | ||||||
| chr4:157355951
|
T | A | 12 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(9): Show | 12 | HG00733.hp2 HG00738.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.2044-3945T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355951 | ||||||
| chr4:157355951
|
T | TTATATAT others(3): Show |
93 | a0001c0001t0001g0015a0001c0001t0001g0053a0001c0001t0001g0054others(90): Show | 95 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.2044-3943_2044-393 others(14): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | 157355951 | |||||
| chr4:157355963
|
G | A | 96 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(93): Show | 98 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.2044-3933G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355963 | ||||||
| chr4:157355970
|
A | T | 96 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(93): Show | 98 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.2044-3926A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355970 | ||||||
| chr4:157355971
|
A | ATATATAT others(1): Show |
2 | a0001c0002t0002g0154a0001c0002t0002g0160 | 2 | NA18942.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.2044-3918_2044-391 others(12): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | 157355971 | |||||
| chr4:157355971
|
A | ATATATGT others(3): Show |
1 | a0001c0001t0002g0084 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2044-3920_2044-391 others(14): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | 157355971 | |||||
| chr4:157355971
|
A | ATGTATAT others(1): Show |
61 | a0001c0001t0002g0023a0001c0001t0002g0078a0001c0001t0002g0099others(58): Show | 62 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.2044-3924_2044-392 others(12): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | 157355971 | |||||
| chr4:157355972
|
T | TATATTA | 4 | a0001c0001t0005g0004a0001c0001t0005g0007a0001c0002t0005g0205others(1): Show | 5 | HG02258.hp2 HG02735.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.2044-3920_2044-391 others(10): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | 157355972 | |||||
| chr4:157355973
|
A | G | 28 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(25): Show | 28 | HG00423.hp1 HG00639.hp1 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.2044-3923A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355973 | ||||||
| chr4:157355973
|
ATATATAT others(1): Show |
A | 21 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(18): Show | 21 | HG02055.hp1 HG02071.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.2044-3907_2044-390 others(12): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | 157355973 | |||||
| chr4:157355978
|
T | TTA | 21 | a0001c0001t0001g0034a0001c0001t0001g0081a0001c0001t0001g0096others(18): Show | 21 | HG00423.hp1 HG01074.hp2 HG01952.hp2 others(18): Show |
intron_variant | MODIFIER | c.2044-3918_2044-391 others(6): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355978 | ||||||
| chr4:157355979
|
A | T | 7 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(4): Show | 7 | HG00639.hp1 HG00642.hp2 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.2044-3917A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355979 | ||||||
| chr4:157355980
|
T | A | 7 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(4): Show | 7 | HG00639.hp1 HG00642.hp2 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.2044-3916T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355980 | ||||||
| chr4:157355981
|
T | A | 28 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(25): Show | 28 | HG00423.hp1 HG00639.hp1 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.2044-3915T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355981 | ||||||
| chr4:157355989
|
T | A | 7 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(4): Show | 7 | HG00639.hp1 HG00642.hp2 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.2044-3907T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355989 | ||||||
| chr4:157355991
|
A | T | 7 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(4): Show | 7 | HG00639.hp1 HG00642.hp2 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.2044-3905A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355991 | ||||||
| chr4:157355995
|
A | T | 1 | a0001c0001t0002g0084 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2044-3901A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157355995 | ||||||
| chr4:157356003
|
A | G | 4 | a0001c0001t0005g0004a0001c0001t0005g0007a0001c0002t0005g0205others(1): Show | 5 | HG02258.hp2 HG02735.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.2044-3893A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157356003 | ||||||
| chr4:157356007
|
G | A | 4 | a0001c0001t0005g0004a0001c0001t0005g0007a0001c0002t0005g0205others(1): Show | 5 | HG02258.hp2 HG02735.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.2044-3889G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157356007 | ||||||
| chr4:157356009
|
A | T | 4 | a0001c0001t0005g0004a0001c0001t0005g0007a0001c0002t0005g0205others(1): Show | 5 | HG02258.hp2 HG02735.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.2044-3887A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157356009 | ||||||
| chr4:157356010
|
T | A | 4 | a0001c0001t0005g0004a0001c0001t0005g0007a0001c0002t0005g0205others(1): Show | 5 | HG02258.hp2 HG02735.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.2044-3886T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157356010 | ||||||
| chr4:157356011
|
T | A | 4 | a0001c0001t0005g0004a0001c0001t0005g0007a0001c0002t0005g0205others(1): Show | 5 | HG02258.hp2 HG02735.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.2044-3885T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157356011 | ||||||
| chr4:157356035
|
T | A | 4 | a0001c0001t0005g0004a0001c0001t0005g0007a0001c0002t0005g0205others(1): Show | 5 | HG02258.hp2 HG02735.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.2044-3861T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157356035 | ||||||
| chr4:157356047
|
G | A | 1 | a0001c0001t0002g0084 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2044-3849G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157356047 | ||||||
| chr4:157356047
|
G | GTATTTAT others(67): Show |
12 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(9): Show | 12 | HG00639.hp1 HG00642.hp2 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.2044-3795_2044-372 others(78): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | 157356047 | |||||
| chr4:157356059
|
A | T | 1 | a0001c0001t0002g0084 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2044-3837A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157356059 | ||||||
| chr4:157356061
|
T | A | 1 | a0001c0001t0002g0084 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2044-3835T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157356061 | ||||||
| chr4:157356062
|
T | A | 57 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0046others(54): Show | 59 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.2044-3834T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157356062 | ||||||
| chr4:157356065
|
A | T | 1 | a0001c0001t0002g0084 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2044-3831A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157356065 | ||||||
| chr4:157356073
|
A | T | 1 | a0001c0001t0002g0084 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2044-3823A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157356073 | ||||||
| chr4:157356075
|
T | A | 1 | a0001c0001t0002g0084 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2044-3821T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157356075 | ||||||
| chr4:157356079
|
T | A | 1 | a0001c0001t0002g0084 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2044-3817T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157356079 | ||||||
| chr4:157356079
|
T | TTATATAT others(1): Show |
4 | a0001c0001t0005g0004a0001c0001t0005g0007a0001c0002t0005g0205others(1): Show | 5 | HG02258.hp2 HG02735.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.2044-3814_2044-381 others(12): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | 157356079 | |||||
| chr4:157356079
|
T | TTATTTAT others(35): Show |
68 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0015others(65): Show | 69 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.2044-3749_2044-370 others(46): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | 157356079 | |||||
| chr4:157356079
|
T | TTATTTAT others(77): Show |
1 | a0001c0002t0002g0153 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2044-3791_2044-370 others(88): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | 157356079 | |||||
| chr4:157356079
|
T | TTATTTAT others(151): Show |
1 | a0001c0002t0002g0139 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2044-3708_2044-370 others(162): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | 157356079 | |||||
| chr4:157356079
|
T | TTATTTAT others(67): Show |
1 | a0001c0002t0002g0195 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2044-3764_2044-376 others(78): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | 157356079 | |||||
| chr4:157356111
|
TTATTTAT others(3): Show |
T | 3 | a0001c0001t0004g0057a0001c0001t0004g0058a0001c0001t0014g0035 | 3 | HG00280.hp2 HG01261.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.2044-3763_2044-375 others(14): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | 157356111 | |||||
| chr4:157356121
|
A | ATATTTAT others(25): Show |
1 | a0001c0001t0002g0127 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2044-3753_2044-372 others(36): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | 157356121 | |||||
| chr4:157356129
|
A | ATATT | 4 | a0001c0001t0005g0004a0001c0001t0005g0007a0001c0002t0005g0205others(1): Show | 5 | HG02258.hp2 HG02735.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.2044-3764_2044-376 others(8): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | 157356129 | |||||
| chr4:157356149
|
T | TTATTTAT others(25): Show |
2 | a0001c0001t0011g0014a0001c0001t0014g0035 | 2 | HG02071.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.2044-3719_2044-368 others(36): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | 157356149 | |||||
| chr4:157356163
|
A | ATATTTAT others(25): Show |
1 | a0001c0002t0002g0165 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2044-3708_2044-370 others(36): Show |
GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | 157356163 | |||||
| chr4:157356185
|
T | A | 2 | a0001c0001t0004g0072a0001c0001t0004g0073 | 2 | NA18950.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.2044-3711T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157356185 | ||||||
| chr4:157356190
|
T | C | 1 | a0001c0001t0001g0034 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2044-3706T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157356190 | ||||||
| chr4:157356203
|
A | G | 1 | a0001c0002t0002g0202 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2044-3693A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157356203 | ||||||
| chr4:157356216
|
T | G | 200 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(197): Show | 204 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.2044-3680T>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157356216 | ||||||
| chr4:157356281
|
A | T | 1 | a0001c0001t0001g0087 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2044-3615A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157356281 | ||||||
| chr4:157356418
|
T | C | 42 | a0001c0001t0001g0034a0001c0001t0001g0053a0001c0001t0001g0054others(39): Show | 42 | HG00423.hp1 HG01074.hp2 HG01952.hp2 others(39): Show |
intron_variant | MODIFIER | c.2044-3478T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157356418 | ||||||
| chr4:157356530
|
A | C | 12 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(9): Show | 12 | HG00639.hp1 HG00642.hp2 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.2044-3366A>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157356530 | ||||||
| chr4:157356661
|
T | A | 12 | a0001c0001t0001g0097a0001c0001t0010g0207a0001c0003t0001g0017others(9): Show | 12 | HG01123.hp2 HG01884.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.2044-3235T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157356661 | ||||||
| chr4:157356684
|
C | T | 52 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0046others(49): Show | 54 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.2044-3212C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157356684 | ||||||
| chr4:157356706
|
A | C | 34 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0046others(31): Show | 36 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.2044-3190A>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157356706 | ||||||
| chr4:157356746
|
AT | A | 5 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(2): Show | 5 | HG01123.hp2 HG01884.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2044-3144delT | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | 157356746 | |||||
| chr4:157357006
|
T | A | 1 | a0001c0002t0002g0125 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2044-2890T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157357006 | ||||||
| chr4:157357180
|
T | A | 1 | a0001c0001t0001g0009 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2044-2716T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157357180 | ||||||
| chr4:157357210
|
C | T | 8 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(5): Show | 8 | HG00733.hp2 HG00738.hp2 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.2044-2686C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157357210 | ||||||
| chr4:157357395
|
T | A | 1 | a0001c0001t0001g0024 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2044-2501T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157357395 | ||||||
| chr4:157357408
|
G | T | 1 | a0001c0001t0014g0035 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2044-2488G>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157357408 | ||||||
| chr4:157357695
|
T | C | 4 | a0001c0001t0005g0004a0001c0001t0005g0007a0001c0002t0005g0205others(1): Show | 5 | HG02258.hp2 HG02735.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.2044-2201T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157357695 | ||||||
| chr4:157357842
|
C | G | 1 | a0001c0002t0002g0158 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2044-2054C>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157357842 | ||||||
| chr4:157357965
|
A | C | 12 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(9): Show | 12 | HG00639.hp1 HG00642.hp2 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.2044-1931A>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157357965 | ||||||
| chr4:157358189
|
G | A | 2 | a0001c0002t0001g0040a0001c0002t0001g0041 | 2 | HG02622.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2044-1707G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157358189 | ||||||
| chr4:157358367
|
G | A | 1 | a0001c0002t0001g0142 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2044-1529G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157358367 | ||||||
| chr4:157358474
|
G | A | 4 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(1): Show | 4 | HG00642.hp2 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.2044-1422G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157358474 | ||||||
| chr4:157358787
|
A | G | 1 | a0001c0002t0004g0138 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2044-1109A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157358787 | ||||||
| chr4:157358802
|
A | G | 42 | a0001c0001t0001g0034a0001c0001t0001g0053a0001c0001t0001g0054others(39): Show | 42 | HG00423.hp1 HG01074.hp2 HG01952.hp2 others(39): Show |
intron_variant | MODIFIER | c.2044-1094A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157358802 | ||||||
| chr4:157358915
|
C | T | 18 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(15): Show | 18 | HG02055.hp1 HG02109.hp2 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.2044-981C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157358915 | ||||||
| chr4:157358941
|
T | A | 1 | a0001c0002t0002g0199 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.2044-955T>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157358941 | ||||||
| chr4:157358952
|
A | T | 1 | a0001c0002t0002g0114 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2044-944A>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157358952 | ||||||
| chr4:157359092
|
T | C | 1 | a0001c0001t0011g0014 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2044-804T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157359092 | ||||||
| chr4:157359127
|
C | A | 203 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(200): Show | 207 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.2044-769C>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157359127 | ||||||
| chr4:157359267
|
T | C | 1 | a0001c0001t0011g0014 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2044-629T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157359267 | ||||||
| chr4:157359407
|
A | G | 11 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(8): Show | 11 | HG02486.hp2 HG02559.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.2044-489A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157359407 | ||||||
| chr4:157359441
|
G | A | 1 | a0001c0001t0001g0087 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2044-455G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157359441 | ||||||
| chr4:157359527
|
G | C | 1 | a0001c0001t0001g0204 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2044-369G>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157359527 | ||||||
| chr4:157359877
|
C | T | 12 | a0001c0001t0001g0097a0001c0001t0010g0207a0001c0003t0001g0017others(9): Show | 12 | HG01123.hp2 HG01884.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.2044-19C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 12/15 | chr4 | 157359877 | ||||||
| chr4:157360219
|
C | G | 12 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(9): Show | 12 | HG00639.hp1 HG00642.hp2 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.2291+76C>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 13/15 | chr4 | 157360219 | ||||||
| chr4:157360371
|
T | G | 123 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(120): Show | 125 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.2291+228T>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 13/15 | chr4 | 157360371 | ||||||
| chr4:157361270
|
T | C | 2 | a0001c0001t0001g0109a0001c0001t0011g0014 | 2 | HG02109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2406+146T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 14/15 | chr4 | 157361270 | ||||||
| chr4:157361864
|
T | C | 1 | a0001c0002t0009g0203 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.2406+740T>C | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 14/15 | chr4 | 157361864 | ||||||
| chr4:157362066
|
G | A | 1 | a0001c0001t0002g0209 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2407-733G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 14/15 | chr4 | 157362066 | ||||||
| chr4:157362149
|
G | A | 5 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032others(2): Show | 5 | HG01123.hp2 HG01884.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2407-650G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 14/15 | chr4 | 157362149 | ||||||
| chr4:157362190
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2407-609C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 14/15 | chr4 | 157362190 | ||||||
| chr4:157362353
|
A | G | 1 | a0001c0002t0001g0143 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2407-446A>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 14/15 | chr4 | 157362353 | ||||||
| chr4:157362395
|
G | A | 1 | a0001c0002t0002g0148 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2407-404G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 14/15 | chr4 | 157362395 | ||||||
| chr4:157362419
|
G | A | 2 | a0001c0001t0003g0002a0001c0001t0003g0090 | 3 | NA18944.hp1 NA19085.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.2407-380G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 14/15 | chr4 | 157362419 | ||||||
| chr4:157362483
|
C | T | 1 | a0001c0003t0001g0021 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2407-316C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 14/15 | chr4 | 157362483 | ||||||
| chr4:157363418
|
C | G | 4 | a0001c0001t0005g0004a0001c0001t0005g0007a0001c0002t0005g0205others(1): Show | 5 | HG02258.hp2 HG02735.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.*4-17C>G | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 15/15 | chr4 | 157363418 |