Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2649 | 112 | 36 | 19 | 40 | 8 | 9 | GRIA2_chr4_157215728_157371075 | GRIA2 | ATGCA others(2644): Show |
chr4 | 157215728 | 157371075 | ||
| a0001c0002 | 0/0 | 2649 | 91 | 23 | 14 | 42 | 1 | 11 | GRIA2_chr4_157215728_157371075 | GRIA2 | ATGCA others(2644): Show |
chr4 | 157215728 | 157371075 | ||
| a0001c0003 | 0/0 | 2649 | 10 | 9 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | ATGCA others(2644): Show |
chr4 | 157215728 | 157371075 | ||
| a0001c0004 | 0/0 | 2649 | 2 | 0 | 2 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | ATGCA others(2644): Show |
chr4 | 157215728 | 157371075 | ||
| a0001c0005 | 0/0 | 2649 | 1 | 0 | 0 | 0 | 1 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | ATGCA others(2644): Show |
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 | GAGTG others(5606): Show |
chr4 | 157215728 | 157371075 |
| a0001c0001t0002 | 0/0 | 5611 | 8 | 1 | 2 | 2 | 0 | 3 | GRIA2_chr4_157215728_157371075 | GRIA2 | GAGTG others(5606): Show |
chr4 | 157215728 | 157371075 |
| a0001c0001t0003 | 0/0 | 5611 | 31 | 1 | 0 | 29 | 0 | 1 | GRIA2_chr4_157215728_157371075 | GRIA2 | GAGTG others(5606): Show |
chr4 | 157215728 | 157371075 |
| a0001c0001t0004 | 0/0 | 5611 | 23 | 5 | 7 | 4 | 6 | 1 | GRIA2_chr4_157215728_157371075 | GRIA2 | GAGTG others(5606): Show |
chr4 | 157215728 | 157371075 |
| a0001c0001t0005 | 0/0 | 5613 | 3 | 1 | 0 | 0 | 0 | 2 | GRIA2_chr4_157215728_157371075 | GRIA2 | GAGTG others(5608): Show |
chr4 | 157215728 | 157371075 |
| a0001c0001t0006 | 0/0 | 5611 | 2 | 0 | 0 | 2 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | GAGTG others(5606): Show |
chr4 | 157215728 | 157371075 |
| a0001c0001t0008 | 0/0 | 5611 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | GAGTG others(5606): Show |
chr4 | 157215728 | 157371075 |
| a0001c0001t0010 | 0/0 | 5611 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | GAGTG others(5606): Show |
chr4 | 157215728 | 157371075 |
| a0001c0001t0011 | 0/0 | 5611 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | GAGTG others(5606): Show |
chr4 | 157215728 | 157371075 |
| a0001c0001t0014 | 0/0 | 5611 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | GAGTG others(5606): Show |
chr4 | 157215728 | 157371075 |
| a0001c0002t0001 | 0/0 | 5611 | 32 | 19 | 3 | 9 | 0 | 1 | GRIA2_chr4_157215728_157371075 | GRIA2 | GAGTG others(5606): Show |
chr4 | 157215728 | 157371075 |
| a0001c0002t0002 | 0/0 | 5611 | 53 | 2 | 10 | 31 | 1 | 9 | GRIA2_chr4_157215728_157371075 | GRIA2 | GAGTG others(5606): Show |
chr4 | 157215728 | 157371075 |
| a0001c0002t0003 | 0/0 | 5611 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | GAGTG others(5606): Show |
chr4 | 157215728 | 157371075 |
| a0001c0002t0004 | 0/0 | 5611 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | GAGTG others(5606): Show |
chr4 | 157215728 | 157371075 |
| a0001c0002t0005 | 0/0 | 5613 | 2 | 1 | 0 | 0 | 0 | 1 | GRIA2_chr4_157215728_157371075 | GRIA2 | GAGTG others(5608): Show |
chr4 | 157215728 | 157371075 |
| a0001c0002t0009 | 0/0 | 5613 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | GAGTG others(5608): Show |
chr4 | 157215728 | 157371075 |
| a0001c0002t0012 | 0/0 | 5611 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | GAGTG others(5606): Show |
chr4 | 157215728 | 157371075 |
| a0001c0003t0001 | 0/0 | 5611 | 8 | 7 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | GAGTG others(5606): Show |
chr4 | 157215728 | 157371075 |
| a0001c0003t0007 | 0/0 | 5611 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | GAGTG others(5606): Show |
chr4 | 157215728 | 157371075 |
| a0001c0003t0013 | 0/0 | 5611 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | GAGTG others(5606): Show |
chr4 | 157215728 | 157371075 |
| a0001c0004t0002 | 0/0 | 5611 | 2 | 0 | 2 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | GAGTG others(5606): Show |
chr4 | 157215728 | 157371075 |
| a0001c0005t0002 | 0/0 | 5611 | 1 | 0 | 0 | 0 | 1 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | GAGTG others(5606): Show |
chr4 | 157215728 | 157371075 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 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 | 1 | 0 | 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 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0001g0016 | 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 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0001g0035 | 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 |
| a0001c0001t0001g0039 | 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 |
| a0001c0001t0001g0051 | 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 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0001g0108 | 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 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0002g0208 | 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 |
| a0001c0001t0003g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0003g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0003g0057 | 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 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0003g0074 | 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 |
| 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 |
| a0001c0001t0003g0081 | 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 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0003g0087 | 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 |
| a0001c0001t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | 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 |
| a0001c0001t0003g0101 | 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 | 0 | 0 | 1 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0004g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 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 |
| a0001c0001t0004g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0004g0040 | 0/0 | 1 | 1 | 0 | 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 |
| a0001c0001t0004g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0004g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0004g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0004g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0004g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0004g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 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 | 0 | 1 | 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 |
| a0001c0001t0004g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0004g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0004g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0004g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0004g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0004g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0005g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0005g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0006g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0006g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0008g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0010g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0011g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0001t0014g0036 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0002t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 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 |
| a0001c0002t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0001g0141 | 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 | 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 |
| a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0001g0171 | 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 |
| a0001c0002t0001g0179 | 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 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0001g0199 | 0/0 | 1 | 1 | 0 | 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 |
| a0001c0002t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0002t0002g0161 | 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 |
| a0001c0002t0002g0166 | 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 |
| 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 |
| a0001c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 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 | 0 | 0 | 0 | 1 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0191 | 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 |
| a0001c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0004g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0005g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0005g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0009g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0002t0012g0121 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0003t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0003t0001g0022 | 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 |
| a0001c0003t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0003t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0003t0007g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0003t0013g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0004t0002g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| a0001c0005t0002g0164 | 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 | g0072 | EUR | FIN | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG00280 | hp2 | a0001 | c0001 | t0004 | g0058 | EUR | FIN | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG00323 | hp1 | a0001 | c0001 | t0004 | g0068 | EUR | FIN | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG00323 | hp2 | a0001 | c0002 | t0002 | g0173 | EUR | FIN | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0162 | EAS | CHS | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG00423 | hp2 | a0001 | c0002 | t0002 | g0207 | EAS | CHS | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0102 | EAS | CHS | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG00438 | hp2 | a0001 | c0002 | t0002 | g0201 | EAS | CHS | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG00609 | hp1 | a0001 | c0002 | t0002 | g0113 | EAS | CHS | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0092 | EAS | CHS | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG00639 | hp2 | a0001 | c0001 | t0004 | g0065 | AMR | PUR | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG00642 | hp1 | a0001 | c0002 | t0002 | g0151 | AMR | PUR | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG00733 | hp1 | a0001 | c0002 | t0002 | g0192 | AMR | PUR | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG00738 | hp1 | a0001 | c0002 | t0002 | g0046 | AMR | PUR | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01070 | hp2 | a0001 | c0004 | t0002 | g0004 | AMR | PUR | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01071 | hp1 | a0001 | c0004 | t0002 | g0004 | AMR | PUR | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01071 | hp2 | a0001 | c0002 | t0002 | g0186 | AMR | PUR | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0128 | AMR | PUR | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01081 | hp1 | a0001 | c0002 | t0002 | g0124 | AMR | PUR | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0129 | AMR | PUR | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0069 | AMR | PUR | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0024 | AMR | PUR | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0126 | AMR | PUR | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01169 | hp2 | a0001 | c0002 | t0002 | g0189 | AMR | PUR | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01175 | hp2 | a0001 | c0001 | t0004 | g0048 | AMR | PUR | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01243 | hp2 | a0001 | c0002 | t0002 | g0045 | AMR | PUR | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0059 | AMR | CLM | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01261 | hp2 | a0001 | c0002 | t0002 | g0187 | AMR | CLM | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01433 | hp1 | a0001 | c0002 | t0002 | g0120 | AMR | CLM | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01433 | hp2 | a0001 | c0001 | t0004 | g0049 | AMR | CLM | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01496 | hp1 | a0001 | c0001 | t0004 | g0070 | AMR | CLM | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0196 | AMR | CLM | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01516 | hp1 | a0001 | c0001 | t0004 | g0028 | EUR | IBS | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01516 | hp2 | a0001 | c0005 | t0002 | g0164 | EUR | IBS | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01517 | hp1 | a0001 | c0001 | t0004 | g0071 | EUR | IBS | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01517 | hp2 | a0001 | c0001 | t0004 | g0029 | EUR | IBS | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01884 | hp2 | a0001 | c0003 | t0001 | g0033 | AFR | ACB | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0040 | AFR | ACB | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01952 | hp1 | a0001 | c0002 | t0002 | g0191 | AMR | PEL | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01952 | hp2 | a0001 | c0002 | t0012 | g0121 | AMR | PEL | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0142 | AFR | ACB | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0091 | AFR | ACB | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02071 | hp1 | a0001 | c0001 | t0014 | g0036 | EAS | KHV | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02071 | hp2 | a0001 | c0002 | t0002 | g0172 | EAS | KHV | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0094 | EAS | KHV | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02129 | hp2 | a0001 | c0002 | t0002 | g0169 | EAS | KHV | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0103 | EAS | KHV | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0159 | 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 | g0115 | EAS | KHV | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0101 | EAS | CDX | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0168 | EAS | CDX | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02258 | hp2 | a0001 | c0001 | t0005 | g0008 | AFR | ACB | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0179 | AFR | ACB | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02280 | hp2 | a0001 | c0003 | t0001 | g0032 | AFR | ACB | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0182 | AFR | ACB | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02622 | hp1 | a0001 | c0003 | t0001 | g0019 | AFR | GWD | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0042 | AFR | GWD | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02630 | hp2 | a0001 | c0003 | t0001 | g0031 | AFR | GWD | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02683 | hp1 | a0001 | c0002 | t0002 | g0125 | SAS | PJL | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02698 | hp1 | a0001 | c0002 | t0002 | g0152 | SAS | PJL | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02698 | hp2 | a0001 | c0002 | t0002 | g0122 | SAS | PJL | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02717 | hp1 | a0001 | c0003 | t0013 | g0017 | AFR | GWD | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0140 | AFR | GWD | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02735 | hp1 | a0001 | c0002 | t0005 | g0210 | SAS | PJL | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02735 | hp2 | a0001 | c0002 | t0002 | g0176 | SAS | PJL | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0208 | SAS | PJL | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02738 | hp2 | a0001 | c0002 | t0002 | g0197 | SAS | PJL | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0130 | AFR | GWD | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0133 | AFR | GWD | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0110 | 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 | g0044 | AFR | GWD | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02922 | hp1 | a0001 | c0001 | t0008 | g0043 | AFR | ESN | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ESN | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02976 | hp1 | a0001 | c0002 | t0004 | g0137 | AFR | ESN | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0180 | AFR | ESN | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0139 | AFR | GWD | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG03098 | hp1 | a0001 | c0002 | t0001 | g0136 | AFR | MSL | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | MSL | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0141 | AFR | ESN | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0041 | AFR | ESN | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0098 | AFR | ESN | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0193 | AFR | ESN | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG03209 | hp1 | a0001 | c0003 | t0001 | g0034 | AFR | MSL | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG03209 | hp2 | a0001 | c0002 | t0005 | g0204 | AFR | MSL | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0199 | AFR | MSL | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0100 | AFR | MSL | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | MSL | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0097 | 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 | g0108 | AFR | MSL | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG03491 | hp1 | a0001 | c0001 | t0005 | g0005 | SAS | PJL | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG03491 | hp2 | a0001 | c0002 | t0002 | g0200 | SAS | PJL | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG03492 | hp1 | a0001 | c0001 | t0005 | g0005 | SAS | PJL | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG03492 | hp2 | a0001 | c0002 | t0002 | g0198 | SAS | PJL | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG03516 | hp1 | a0001 | c0003 | t0001 | g0018 | AFR | ESN | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG03516 | hp2 | a0001 | c0001 | t0010 | g0206 | AFR | ESN | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG03540 | hp2 | a0001 | c0002 | t0002 | g0154 | AFR | GWD | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0052 | AFR | MSL | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | MSL | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG03669 | hp1 | a0001 | c0001 | t0004 | g0107 | SAS | PJL | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG03669 | hp2 | a0001 | c0002 | t0002 | g0145 | SAS | PJL | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0148 | SAS | BEB | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0165 | SAS | BEB | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0104 | SAS | BEB | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0209 | 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 | g0050 | AFR | YRI | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18906 | hp1 | a0001 | c0003 | t0001 | g0022 | AFR | YRI | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | YRI | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18942 | hp1 | a0001 | c0002 | t0002 | g0161 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18943 | hp2 | a0001 | c0002 | t0009 | g0202 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18944 | hp2 | a0001 | c0002 | t0002 | g0116 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18950 | hp1 | a0001 | c0002 | t0002 | g0144 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18950 | hp2 | a0001 | c0001 | t0004 | g0001 | 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 | g0062 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18954 | hp2 | a0001 | c0002 | t0002 | g0167 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18956 | hp1 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18956 | hp2 | a0001 | c0002 | t0002 | g0117 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0081 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18964 | hp2 | a0001 | c0002 | t0002 | g0138 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18968 | hp2 | a0001 | c0002 | t0002 | g0174 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0171 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18975 | hp2 | a0001 | c0002 | t0003 | g0195 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18977 | hp1 | a0001 | c0001 | t0004 | g0085 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18977 | hp2 | a0001 | c0002 | t0002 | g0163 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18980 | hp1 | a0001 | c0001 | t0006 | g0099 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18980 | hp2 | a0001 | c0002 | t0002 | g0153 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18981 | hp2 | a0001 | c0002 | t0002 | g0119 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18984 | hp2 | a0001 | c0002 | t0002 | g0184 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18991 | hp1 | a0001 | c0002 | t0001 | g0160 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18991 | hp2 | a0001 | c0001 | t0004 | g0073 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18995 | hp2 | a0001 | c0002 | t0002 | g0147 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18999 | hp1 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0181 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0190 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0088 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA19001 | hp1 | a0001 | c0002 | t0002 | g0127 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA19001 | hp2 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA19003 | hp1 | a0001 | c0002 | t0002 | g0166 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA19003 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA19006 | hp1 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA19006 | hp2 | a0001 | c0002 | t0002 | g0175 | 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 | g0194 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | LWK | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | LWK | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA19057 | hp1 | a0001 | c0002 | t0002 | g0149 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA19063 | hp2 | a0001 | c0002 | t0002 | g0114 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA19064 | hp1 | a0001 | c0002 | t0001 | g0143 | 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 | g0095 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0123 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA19077 | hp2 | a0001 | c0002 | t0002 | g0118 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA19078 | hp1 | a0001 | c0002 | t0002 | g0170 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA19078 | hp2 | a0001 | c0001 | t0003 | g0060 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA19085 | hp2 | a0001 | c0002 | t0002 | g0146 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA19087 | hp1 | a0001 | c0001 | t0006 | g0090 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA19087 | hp2 | a0001 | c0002 | t0002 | g0155 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA19089 | hp1 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA19089 | hp2 | a0001 | c0002 | t0002 | g0185 | EAS | JPT | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | YRI | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | YRI | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0131 | 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 | g0027 | EUR | TSI | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0066 | EUR | TSI | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA20905 | hp1 | a0001 | c0002 | t0002 | g0188 | SAS | GIH | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | GIH | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01123 | hp1 | a0001 | c0001 | t0004 | g0183 | AMR | CLM | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG01123 | hp2 | a0001 | c0003 | t0001 | g0053 | AMR | CLM | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02109 | hp1 | a0001 | c0001 | t0011 | g0015 | 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 | g0021 | AFR | ACB | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0134 | AFR | ACB | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | ACB | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| HG02559 | hp2 | a0001 | c0002 | t0002 | g0150 | AFR | ACB | GRIA2_chr4_157215728_157371075 | GRIA2 | chr4 | 157215728 | 157371075 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:157317678 | T | C | 3 | a0001c0002 a0001c0004 a0001c0005 |
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 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | a0001c0001t0008 a0001c0003t0007 |
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 | a0001c0001t0002 a0001c0002t0002 a0001c0002t0009 others(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 | a0001c0001t0005 a0001c0002t0005 a0001c0002t0009 |
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 | a0001c0001t0005 a0001c0002t0005 |
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 | a0001c0001t0003 a0001c0001t0006 a0001c0002t0003 |
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 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(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 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:157221453 | T | C | 2 | a0001c0001t0001g0006 a0001c0001t0001g0007 |
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 | 206 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(203): 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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(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 | a0001c0002t0002g0045 a0001c0002t0002g0046 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(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 | a0001c0001t0003g0047 | 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 | a0001c0001t0005g0008 | 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 | 201 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(198): 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 | a0001c0002t0002g0207 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(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 | a0001c0001t0004g0107 | 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 | a0001c0002t0002g0113 a0001c0002t0002g0114 a0001c0002t0002g0115 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(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 | a0001c0001t0014g0036 | 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 | a0001c0002t0002g0122 | 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 | a0001c0001t0004g0040 a0001c0001t0008g0043 a0001c0002t0001g0041 others(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 | a0001c0001t0014g0036 | 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 | a0001c0002t0001g0123 | 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 | a0001c0001t0003g0106 | 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 | a0001c0001t0001g0205 a0001c0001t0010g0206 |
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 | a0001c0001t0004g0040 a0001c0001t0008g0043 a0001c0002t0001g0041 others(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 | a0001c0001t0005g0008 | 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 | a0001c0002t0002g0120 a0001c0002t0012g0121 |
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 | a0001c0001t0001g0035 a0001c0001t0001g0203 a0001c0001t0001g0205 others(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 | 68 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0054 others(65): 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 | a0001c0003t0001g0031 a0001c0003t0001g0032 a0001c0003t0001g0033 others(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 | a0001c0001t0002g0126 | 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 | a0001c0001t0004g0048 a0001c0001t0004g0049 |
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 | a0001c0001t0003g0101 a0001c0001t0003g0102 a0001c0001t0003g0103 others(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 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(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 | a0001c0001t0001g0203 a0001c0002t0005g0204 |
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 | a0001c0001t0004g0100 | 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 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0005g0008 others(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 | a0001c0002t0002g0127 | 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 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0002g0126 others(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 | a0001c0001t0004g0040 a0001c0001t0008g0043 a0001c0002t0001g0041 others(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 | a0001c0001t0001g0105 | 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 | a0001c0002t0009g0202 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(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 | a0001c0001t0001g0016 | 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 | a0001c0001t0004g0040 | 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 | a0001c0002t0001g0128 | 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 | a0001c0002t0001g0129 a0001c0002t0001g0130 a0001c0002t0001g0131 others(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 | a0001c0001t0014g0036 | 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 | 163 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0055 others(160): 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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0020 others(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 | a0001c0001t0004g0040 a0001c0001t0008g0043 a0001c0002t0001g0041 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0005g0008 a0001c0003t0001g0018 a0001c0003t0001g0019 others(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 | a0001c0001t0001g0105 a0001c0002t0002g0198 |
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 | 206 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(203): 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 | a0001c0002t0001g0139 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(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 | a0001c0001t0005g0008 | 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 | a0001c0001t0001g0203 | 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 | a0001c0001t0001g0105 | 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 | 57 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0054 others(54): 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 | a0001c0001t0003g0101 a0001c0001t0003g0102 a0001c0001t0003g0103 others(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 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(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 | a0001c0001t0001g0097 a0001c0001t0014g0036 |
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 | 63 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0054 others(60): 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 | 63 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0054 others(60): 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 | 63 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0054 others(60): 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 | 63 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0054 others(60): 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 | a0001c0003t0001g0031 a0001c0003t0001g0032 a0001c0003t0001g0033 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | 69 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0054 others(66): 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 | 93 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(90): 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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(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 | a0001c0002t0003g0195 | 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 | a0001c0002t0001g0199 | 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 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(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 | a0001c0002t0001g0130 | 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 | 61 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0054 others(58): 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 | a0001c0002t0002g0194 | 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 | a0001c0001t0003g0057 | 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 | a0001c0001t0001g0205 | 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 | a0001c0001t0001g0035 | 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 | a0001c0001t0001g0105 | 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 | a0001c0001t0004g0058 a0001c0001t0004g0059 |
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 | a0001c0002t0002g0113 | 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 | 114 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(111): 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 | a0001c0002t0001g0041 | 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 | a0001c0002t0002g0192 | 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 | a0001c0001t0001g0050 a0001c0001t0001g0051 |
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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0002t0002g0191 | 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 | 74 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0054 others(71): 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 | a0001c0002t0001g0131 a0001c0002t0001g0132 |
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 | a0001c0002t0002g0114 | 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 | a0001c0001t0001g0035 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | 113 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(110): 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 | a0001c0002t0001g0190 | 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 | a0001c0001t0001g0016 | 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 | a0001c0001t0001g0105 | 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 | a0001c0003t0001g0018 a0001c0003t0001g0019 a0001c0003t0013g0017 |
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 | a0001c0003t0001g0018 a0001c0003t0001g0019 a0001c0003t0013g0017 |
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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0014g0036 | 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 | a0001c0002t0002g0201 | 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 | 65 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0050 others(62): 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 | a0001c0002t0001g0129 a0001c0002t0004g0137 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(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 | a0001c0001t0001g0096 | 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 | a0001c0003t0001g0022 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0011g0015 | 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 | a0001c0001t0001g0105 | 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 | a0001c0002t0002g0207 | 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 | a0001c0002t0002g0187 a0001c0002t0002g0188 a0001c0002t0002g0189 others(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 | a0001c0001t0001g0211 a0001c0001t0002g0208 a0001c0001t0002g0209 others(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 | a0001c0001t0001g0095 | 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 | a0001c0001t0001g0020 | 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 | 126 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(123): 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 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(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 | a0001c0001t0014g0036 | 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 | a0001c0001t0004g0058 a0001c0001t0004g0059 |
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 | a0001c0001t0004g0040 | 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 | a0001c0001t0004g0040 | 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 | a0001c0002t0001g0123 a0001c0002t0001g0143 a0001c0002t0001g0190 |
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 | 74 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0054 others(71): 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 | a0001c0001t0010g0206 | 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 | 95 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(92): 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 | a0001c0002t0002g0186 | 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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0105 | 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 | a0001c0001t0002g0208 a0001c0001t0002g0209 |
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 | a0001c0001t0014g0036 | 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 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 |
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 | a0001c0001t0014g0036 | 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 | a0001c0001t0003g0104 | 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 | a0001c0001t0014g0036 | 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 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0002g0098 others(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 | a0001c0002t0002g0144 a0001c0002t0003g0195 |
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 | 126 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(123): 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 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(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 | a0001c0001t0005g0008 a0001c0003t0001g0018 a0001c0003t0001g0019 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
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 | a0001c0002t0002g0145 a0001c0002t0002g0146 |
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 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0026 others(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 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0003g0062 others(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 | a0001c0002t0002g0147 | 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 | 61 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0054 others(58): 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 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(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 | a0001c0001t0001g0035 | 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 | a0001c0001t0011g0015 | 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 | a0001c0002t0002g0185 | 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 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(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 | a0001c0001t0001g0105 | 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 | a0001c0001t0004g0140 | 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 | a0001c0001t0003g0064 | 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 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(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 | a0001c0001t0003g0003 a0001c0001t0003g0057 a0001c0001t0003g0088 others(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 | a0001c0001t0003g0060 | 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 | a0001c0001t0002g0148 | 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 | a0001c0001t0001g0016 | 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 | a0001c0001t0001g0096 | 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 | 113 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(110): 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 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0016 | 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 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0004g0058 others(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 | a0001c0002t0002g0184 | 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 | a0001c0001t0001g0211 a0001c0001t0002g0208 a0001c0001t0002g0209 others(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 | |||||||
| chr4:157243328 | A | G | 1 | a0001c0002t0002g0186 | 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 | a0001c0002t0001g0129 a0001c0002t0001g0130 a0001c0002t0001g0131 others(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 | a0001c0001t0001g0011 | 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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0211 a0001c0001t0002g0208 a0001c0001t0002g0209 others(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 | a0001c0001t0003g0102 a0001c0001t0003g0103 |
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 | a0001c0002t0002g0146 | 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 | a0001c0002t0002g0149 | 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 | a0001c0001t0014g0036 | 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 | a0001c0001t0004g0068 a0001c0001t0004g0069 a0001c0001t0004g0070 others(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 | a0001c0001t0003g0104 | 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 | a0001c0001t0002g0148 a0001c0001t0004g0182 a0001c0001t0004g0183 |
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 | a0001c0002t0002g0150 | 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 | a0001c0002t0001g0190 | 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 | a0001c0002t0001g0181 | 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 | 113 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(110): 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 | 84 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0037 others(81): 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 | a0001c0001t0001g0006 | 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 | a0001c0001t0001g0020 a0001c0001t0001g0021 |
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 | a0001c0001t0014g0036 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.229+24261G>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157246068 | |||||||
| chr4:157246192 | T | A | 10 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(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 | a0001c0001t0014g0036 | 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 | a0001c0001t0014g0036 | 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 | a0001c0001t0001g0016 | 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 | a0001c0001t0002g0126 | 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 | a0001c0002t0002g0151 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(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 | a0001c0001t0004g0068 | 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 | 65 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0050 others(62): 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 | a0001c0001t0014g0036 | 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 | a0001c0001t0003g0094 | 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 | a0001c0003t0001g0022 | 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 | a0001c0002t0002g0151 | 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 | a0001c0002t0002g0118 a0001c0002t0002g0119 |
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 | a0001c0001t0001g0050 | 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 | a0001c0001t0001g0016 | 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 | a0001c0001t0005g0008 a0001c0003t0001g0018 a0001c0003t0001g0019 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(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 | a0001c0001t0001g0203 | 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 | a0001c0002t0005g0210 | 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 | a0001c0001t0001g0205 a0001c0002t0002g0122 a0001c0002t0002g0152 |
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 | a0001c0001t0003g0061 | 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 |
57 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0050 others(54): 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 | a0001c0001t0001g0095 | 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 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(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 | a0001c0001t0005g0008 | 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 | a0001c0003t0001g0018 a0001c0003t0001g0019 a0001c0003t0001g0022 others(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 | a0001c0001t0001g0211 a0001c0001t0002g0126 a0001c0001t0002g0208 others(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 | a0001c0003t0013g0017 | 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 | a0001c0002t0001g0041 a0001c0002t0001g0042 |
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 | a0001c0003t0007g0044 | 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 | a0001c0001t0004g0072 | 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 | a0001c0001t0008g0043 | 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 | a0001c0002t0001g0190 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0035 others(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 | a0001c0001t0002g0148 a0001c0001t0004g0140 a0001c0001t0004g0182 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0016 a0001c0001t0004g0040 a0001c0001t0014g0036 others(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 | a0001c0001t0014g0036 | 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 | a0001c0001t0004g0040 | 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 | a0001c0001t0001g0016 | 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 | a0001c0001t0001g0020 a0001c0001t0001g0021 |
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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0016 | 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 | a0001c0001t0004g0040 | 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 | a0001c0001t0004g0040 | 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 | a0001c0001t0001g0105 a0001c0001t0008g0043 a0001c0002t0001g0041 others(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 | a0001c0002t0002g0138 a0001c0002t0002g0153 |
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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0105 | 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 | a0001c0002t0001g0130 a0001c0002t0001g0136 a0001c0002t0002g0197 |
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 | a0001c0001t0001g0211 a0001c0001t0004g0140 a0001c0002t0002g0113 others(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 | a0001c0001t0001g0203 a0001c0001t0002g0148 a0001c0001t0008g0043 others(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 | a0001c0001t0001g0105 a0001c0001t0002g0126 a0001c0001t0002g0208 others(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 | a0001c0001t0001g0021 a0001c0001t0004g0040 a0001c0001t0004g0052 others(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 | 79 | a0001c0001t0001g0020 a0001c0001t0001g0037 a0001c0001t0001g0038 others(76): 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 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0004g0028 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0002t0001g0129 a0001c0002t0001g0180 a0001c0002t0004g0137 |
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 | a0001c0001t0004g0140 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(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 | a0001c0002t0001g0133 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(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 | a0001c0001t0001g0035 | 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 | a0001c0002t0002g0145 | 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 | 114 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(111): 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 | a0001c0003t0001g0022 | 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 | a0001c0001t0001g0035 | 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 | a0001c0001t0004g0068 a0001c0001t0004g0069 a0001c0001t0004g0070 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0011g0015 | 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 | a0001c0001t0005g0008 a0001c0003t0001g0018 a0001c0003t0001g0019 others(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 | a0001c0002t0002g0144 | 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 | a0001c0001t0003g0104 | 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 | a0001c0001t0001g0035 | 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 | a0001c0001t0001g0105 | 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 | a0001c0001t0014g0036 | 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 | a0001c0002t0002g0154 | 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 | 66 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0050 others(63): 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 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(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 | a0001c0001t0001g0096 | 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 | a0001c0001t0001g0105 | 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 | a0001c0003t0007g0044 | 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 | a0001c0001t0004g0100 | 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 | a0001c0001t0001g0211 a0001c0001t0002g0126 a0001c0001t0002g0208 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0003g0061 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0011 | 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 | a0001c0002t0002g0150 | 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 | a0001c0001t0010g0206 | 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 | a0001c0002t0001g0179 a0001c0002t0005g0204 |
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 | a0001c0001t0014g0036 | 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 | a0001c0002t0002g0150 | 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 | a0001c0001t0001g0050 a0001c0001t0001g0051 |
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 | 79 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0050 others(76): 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 | 117 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(114): 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 | a0001c0002t0002g0151 a0001c0004t0002g0004 |
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 | a0001c0001t0005g0008 a0001c0003t0001g0018 a0001c0003t0001g0019 others(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 | a0001c0001t0004g0040 a0001c0001t0008g0043 a0001c0002t0001g0041 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 |
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 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0002g0024 |
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 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 |
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 | a0001c0002t0002g0167 | 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 | a0001c0001t0001g0056 a0001c0001t0002g0077 a0001c0001t0002g0083 others(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 | a0001c0001t0003g0091 a0001c0001t0003g0092 |
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 | a0001c0002t0002g0125 | 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 | 116 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(113): 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 | a0001c0002t0001g0129 a0001c0002t0001g0130 a0001c0002t0001g0132 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0016 | 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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0056 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(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 | a0001c0001t0001g0096 a0001c0001t0001g0203 |
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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0054 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0211 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(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 | 102 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0016 others(99): 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 | a0001c0001t0008g0043 | 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 | a0001c0001t0004g0040 a0001c0002t0001g0041 a0001c0002t0001g0042 |
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 | a0001c0002t0002g0176 | 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 | a0001c0001t0004g0040 a0001c0001t0008g0043 a0001c0002t0001g0041 others(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 | a0001c0002t0002g0125 | 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 | a0001c0001t0008g0043 | 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 | a0001c0001t0005g0008 a0001c0003t0001g0018 a0001c0003t0001g0019 others(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 | a0001c0001t0001g0016 | 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 | a0001c0001t0002g0148 | 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 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(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 | a0001c0001t0003g0084 | 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 | 107 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0020 others(104): 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 | a0001c0001t0001g0021 | 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 | a0001c0002t0002g0146 | 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 | a0001c0003t0001g0022 | 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 | a0001c0002t0005g0210 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(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 | a0001c0001t0011g0015 | 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 | a0001c0003t0001g0053 | 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 | a0001c0002t0002g0155 | 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 | a0001c0001t0001g0112 | 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 | a0001c0001t0001g0016 | 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 | 117 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(114): 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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(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 | 108 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0010 others(105): 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 | 117 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(114): 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 | a0001c0001t0004g0073 | 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 | a0001c0002t0002g0175 a0001c0002t0002g0184 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | 107 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0020 others(104): 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 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(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 | a0001c0001t0001g0211 a0001c0001t0002g0126 a0001c0001t0002g0208 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(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 | a0001c0002t0001g0123 a0001c0002t0001g0143 a0001c0002t0001g0190 |
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 | 117 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(114): 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 | a0001c0002t0002g0127 | 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 | a0001c0001t0001g0203 | 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 | a0001c0002t0001g0139 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(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 | a0001c0001t0001g0105 | 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 | a0001c0001t0011g0015 | 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 | a0001c0001t0005g0005 | 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 | a0001c0001t0002g0083 | 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 | a0001c0001t0003g0047 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(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 | a0001c0001t0004g0069 | 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 | 117 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(114): 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 | a0001c0002t0001g0139 a0001c0002t0001g0157 |
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 | a0001c0001t0001g0027 | 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 | a0001c0001t0001g0105 | 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 | a0001c0002t0002g0155 a0001c0003t0001g0022 |
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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0203 | 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 | a0001c0002t0001g0132 a0001c0002t0001g0133 a0001c0002t0001g0178 |
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 | a0001c0002t0002g0197 | 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 | 79 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0050 others(76): 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 | a0001c0002t0002g0138 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.230-36352C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157267200 | |||||||
| chr4:157267391 | C | CA | 14 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(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 | a0001c0001t0001g0105 a0001c0001t0001g0203 a0001c0001t0005g0008 others(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 | a0001c0002t0002g0207 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0005g0008 | 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 | a0001c0001t0003g0101 | 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 | a0001c0001t0004g0073 | 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 | a0001c0002t0002g0174 | 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 | 107 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0020 others(104): 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 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0050 a0001c0001t0001g0051 |
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 | a0001c0001t0001g0016 | 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 | a0001c0001t0001g0016 | 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 | a0001c0002t0002g0192 | 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 | a0001c0002t0002g0198 | 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 | a0001c0001t0001g0203 | 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 | a0001c0002t0002g0147 | 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 | 117 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(114): 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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0020 others(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 | 54 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0066 others(51): 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 | a0001c0002t0002g0186 | 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 | a0001c0001t0001g0096 | 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 | 117 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(114): 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 | a0001c0001t0011g0015 | 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 | a0001c0001t0004g0068 a0001c0001t0004g0069 a0001c0001t0004g0070 others(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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(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 | a0001c0002t0002g0186 | 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 | a0001c0001t0001g0016 | 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 | 117 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(114): 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 | a0001c0001t0002g0077 a0001c0001t0003g0047 a0001c0001t0003g0074 others(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 | a0001c0002t0001g0129 a0001c0002t0001g0130 a0001c0002t0001g0132 others(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 | a0001c0001t0002g0148 a0001c0001t0004g0182 a0001c0001t0004g0183 |
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 | a0001c0002t0001g0193 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 |
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 | a0001c0002t0002g0113 | 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 | a0001c0001t0011g0015 | 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 | a0001c0001t0003g0102 | 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 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
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 | a0001c0002t0002g0127 | 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 | a0001c0001t0001g0016 | 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 | 117 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(114): 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 | 117 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(114): 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 | a0001c0001t0001g0211 a0001c0001t0005g0005 a0001c0002t0005g0210 |
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 | a0001c0001t0001g0016 | 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 | a0001c0001t0003g0084 | 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 | 117 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(114): 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 | a0001c0001t0001g0010 | 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 | 117 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(114): 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 | a0001c0001t0001g0105 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.230-28824C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157274728 | |||||||
| chr4:157274921 | T | C | 117 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(114): 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 | T | 104 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(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 | a0001c0002t0002g0115 | 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 | a0001c0001t0002g0024 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0002t0002g0173 | 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 | a0001c0001t0001g0211 a0001c0001t0002g0126 a0001c0001t0002g0208 others(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 | a0001c0002t0002g0116 | 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 | a0001c0001t0001g0037 | 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 | a0001c0001t0003g0093 | 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 | a0001c0002t0002g0188 a0001c0002t0002g0200 |
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 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(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 | 79 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0050 others(76): 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 | 117 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(114): 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 | 117 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(114): 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 | a0001c0001t0001g0078 a0001c0001t0001g0095 a0001c0001t0002g0077 others(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 | 117 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(114): 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 | a0001c0001t0001g0203 | 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 | a0001c0001t0001g0108 | 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 | a0001c0002t0002g0147 a0001c0002t0002g0174 a0001c0002t0012g0121 |
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 | 66 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0050 others(63): 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 | a0001c0002t0002g0122 a0001c0002t0002g0152 |
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 | a0001c0003t0001g0022 | 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 | a0001c0002t0002g0115 | 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 | a0001c0002t0001g0190 | 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 | a0001c0001t0001g0016 | 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 | a0001c0001t0014g0036 | 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 | a0001c0002t0002g0115 | 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 | a0001c0002t0002g0172 | 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 | a0001c0001t0004g0071 | 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 | 117 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(114): 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 | a0001c0001t0002g0083 | 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 | a0001c0002t0002g0173 | 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 | a0001c0001t0002g0098 | 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 | a0001c0002t0001g0159 | 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 | a0001c0001t0002g0148 | 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 | a0001c0001t0001g0203 | 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 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(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 |
81 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0016 others(78): 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 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0004g0028 others(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 | a0001c0001t0008g0043 | 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 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0035 |
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 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0111 | 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 | a0001c0002t0002g0173 | 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 | a0001c0001t0014g0036 | 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 | a0001c0001t0001g0203 | 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 | a0001c0002t0002g0163 | 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 | a0001c0001t0003g0064 | 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 | a0001c0001t0011g0015 | 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 | a0001c0001t0002g0083 a0001c0001t0004g0085 |
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 | a0001c0001t0001g0105 | 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 | a0001c0002t0001g0041 | 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 | a0001c0001t0001g0203 | 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 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 |
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 | a0001c0001t0014g0036 | 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 | a0001c0001t0001g0016 | 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 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0038 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0011 |
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 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 |
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 | 66 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0050 others(63): 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 | a0001c0001t0002g0208 | 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 | a0001c0003t0001g0022 | 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 | 134 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(131): 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 | 66 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0050 others(63): 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 | a0001c0001t0011g0015 | 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 | a0001c0001t0003g0089 | 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 | a0001c0001t0005g0005 | 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 | a0001c0002t0001g0139 | 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 | a0001c0001t0014g0036 | 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 | a0001c0001t0001g0035 | 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 | a0001c0001t0001g0035 | 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 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(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 | a0001c0002t0002g0207 | 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 | 117 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(114): 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 | a0001c0002t0002g0173 | 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 | a0001c0002t0001g0171 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | 79 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0050 others(76): 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 | a0001c0001t0004g0140 a0001c0002t0001g0129 a0001c0002t0001g0130 others(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 | 107 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0020 others(104): 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 | a0001c0001t0001g0011 | 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 | a0001c0002t0002g0198 | 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 | a0001c0002t0002g0154 | 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 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(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 | a0001c0001t0014g0036 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0004g0052 | 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 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(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 | a0001c0003t0001g0018 a0001c0003t0001g0019 a0001c0003t0013g0017 |
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 | a0001c0001t0001g0086 | 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 | 79 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0050 others(76): 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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0051 | 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 | a0001c0003t0001g0018 | 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 | a0001c0001t0001g0203 | 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 | a0001c0001t0002g0208 | 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 | a0001c0001t0014g0036 | 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 | a0001c0001t0001g0203 | 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 | a0001c0002t0005g0210 | 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 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(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 | a0001c0002t0001g0199 | 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 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(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 | a0001c0001t0001g0078 a0001c0001t0001g0096 a0001c0001t0003g0064 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
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 | a0001c0002t0001g0041 a0001c0002t0001g0042 |
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 | a0001c0002t0002g0127 | 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 | a0001c0002t0001g0159 a0001c0002t0001g0160 |
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 | 117 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(114): 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 | a0001c0001t0001g0203 a0001c0001t0005g0008 a0001c0003t0001g0018 others(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 | 107 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0020 others(104): 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 | a0001c0001t0004g0040 a0001c0001t0008g0043 a0001c0002t0001g0041 others(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 | a0001c0001t0001g0211 | 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 | a0001c0001t0004g0107 | 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 | a0001c0001t0004g0040 a0001c0001t0008g0043 a0001c0002t0001g0041 others(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 | a0001c0001t0002g0126 a0001c0001t0002g0208 a0001c0001t0002g0209 |
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 | a0001c0002t0002g0174 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(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 | 107 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0020 others(104): 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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(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 | a0001c0002t0002g0147 | 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 | a0001c0001t0001g0035 | 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 | a0001c0002t0002g0188 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(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 | a0001c0001t0001g0026 | 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 | a0001c0001t0001g0096 | 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 | a0001c0001t0014g0036 | 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 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 |
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 | a0001c0002t0002g0046 | 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 | a0001c0001t0004g0100 | 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 | a0001c0001t0014g0036 | 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 | 83 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0037 others(80): 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 | a0001c0001t0001g0203 a0001c0001t0003g0094 a0001c0001t0005g0008 others(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 | a0001c0002t0002g0120 a0001c0002t0002g0191 |
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 | a0001c0003t0001g0031 a0001c0003t0001g0032 a0001c0003t0001g0033 others(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 | a0001c0001t0001g0016 | 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 | a0001c0001t0002g0209 | 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 | a0001c0004t0002g0004 | 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 | a0001c0002t0001g0180 | 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 | a0001c0001t0014g0036 | 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 | a0001c0001t0001g0112 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0011 |
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 | a0001c0002t0002g0172 | 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 | a0001c0001t0001g0096 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(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 | a0001c0001t0003g0101 a0001c0001t0003g0102 a0001c0001t0003g0103 others(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 | a0001c0001t0014g0036 | 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 | a0001c0001t0005g0008 a0001c0003t0001g0018 a0001c0003t0001g0019 others(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 | a0001c0002t0001g0171 | 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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0037 others(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 | a0001c0001t0001g0211 a0001c0001t0002g0126 a0001c0001t0002g0208 others(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 | a0001c0002t0001g0128 | 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 | a0001c0002t0002g0149 a0001c0002t0002g0175 a0001c0002t0002g0184 |
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 | a0001c0001t0014g0036 | 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 | a0001c0002t0001g0131 a0001c0002t0001g0177 a0001c0002t0001g0193 |
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 | a0001c0002t0002g0186 | 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 | a0001c0001t0003g0089 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.230-7350C>T | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 2/15 | chr4 | 157296202 | |||||||
| chr4:157296535 | A | C | 1 | a0001c0001t0004g0183 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(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 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(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 | a0001c0001t0002g0098 | 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 | a0001c0002t0002g0161 | 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 | 98 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0037 others(95): 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 | a0001c0001t0002g0098 | 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 | a0001c0001t0001g0016 | 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 | a0001c0001t0001g0016 | 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 | a0001c0001t0014g0036 | 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 | 80 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0050 others(77): 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 | a0001c0001t0001g0078 a0001c0001t0001g0095 a0001c0001t0002g0077 others(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 | a0001c0001t0001g0211 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | 98 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0037 others(95): 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 | a0001c0001t0004g0140 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0020 others(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 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0112 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0039 a0001c0001t0001g0203 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0050 a0001c0001t0002g0148 others(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 | a0001c0001t0001g0078 a0001c0001t0001g0095 a0001c0001t0002g0077 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(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 | |||||||
| chr4:157299193 | C | T | 1 | a0001c0002t0005g0204 | 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 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0205 others(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 | a0001c0001t0011g0015 | 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 | a0001c0001t0001g0203 | 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 | 118 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(115): 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 | a0001c0003t0001g0018 a0001c0003t0001g0019 a0001c0003t0007g0044 others(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 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(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 | a0001c0002t0002g0172 | 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 | a0001c0001t0014g0036 | 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 | a0001c0001t0005g0005 | 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 | 108 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0020 others(105): 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 | a0001c0001t0001g0016 a0001c0001t0014g0036 |
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 | 98 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0037 others(95): 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 | a0001c0001t0002g0126 a0001c0001t0002g0208 a0001c0001t0002g0209 |
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 | a0001c0001t0001g0035 a0001c0001t0001g0203 a0001c0001t0003g0081 others(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 | 118 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(115): 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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0002t0002g0186 | 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 | a0001c0001t0014g0036 | 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 | a0001c0003t0001g0018 a0001c0003t0001g0019 a0001c0003t0001g0022 others(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 | a0001c0002t0002g0173 | 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 | a0001c0001t0014g0036 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(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 | 118 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(115): 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 | 118 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(115): 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 | a0001c0001t0004g0100 | 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 | a0001c0001t0001g0105 | 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 | a0001c0002t0002g0150 | 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 | a0001c0002t0002g0170 | 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 | a0001c0002t0001g0171 | 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 | a0001c0001t0001g0010 | 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 | a0001c0001t0002g0083 | 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 | a0001c0001t0001g0016 | 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 | a0001c0001t0001g0086 | 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 | a0001c0002t0001g0159 a0001c0002t0001g0160 |
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 | a0001c0002t0001g0190 | 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 | a0001c0001t0004g0068 | 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 | a0001c0001t0005g0008 | 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 | a0001c0002t0001g0190 | 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 | a0001c0002t0002g0118 a0001c0002t0002g0119 |
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 | a0001c0001t0004g0052 | 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 | 118 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(115): 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 | 118 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(115): 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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0011 |
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 | a0001c0002t0001g0129 a0001c0002t0001g0180 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(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 | a0001c0001t0001g0016 | 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 | a0001c0001t0001g0203 | 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 | a0001c0002t0002g0207 | 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 | a0001c0001t0001g0066 | 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 | a0001c0001t0014g0036 | 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 | a0001c0002t0001g0190 | 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 | a0001c0002t0002g0125 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0105 a0001c0001t0001g0211 a0001c0001t0002g0126 others(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 | 118 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(115): 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 | a0001c0001t0001g0035 | 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 | 67 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0050 others(64): 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 | 67 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0050 others(64): 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 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0004g0028 others(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 | a0001c0003t0001g0018 a0001c0003t0001g0019 a0001c0003t0001g0022 others(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 | a0001c0001t0001g0016 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0014 a0001c0001t0001g0054 a0001c0001t0001g0055 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(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 | a0001c0002t0002g0117 a0001c0002t0002g0120 a0001c0002t0002g0191 |
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 | a0001c0002t0001g0141 | 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 | a0001c0001t0014g0036 | 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 | 118 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(115): 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 | a0001c0002t0002g0152 | 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 | a0001c0001t0001g0054 a0001c0001t0001g0055 |
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 | a0001c0001t0003g0074 | 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 | a0001c0002t0002g0115 | 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 | a0001c0001t0001g0054 a0001c0001t0001g0055 |
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 | a0001c0001t0004g0100 | 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 | a0001c0001t0001g0105 | 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 | a0001c0002t0002g0150 | 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 | a0001c0001t0004g0058 a0001c0001t0004g0059 |
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 | 118 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(115): 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 | a0001c0001t0004g0029 | 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 | a0001c0001t0014g0036 | 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 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(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 | a0001c0002t0001g0199 | 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 | a0001c0001t0004g0058 | 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 | a0001c0003t0007g0044 | 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 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 |
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 | a0001c0001t0001g0109 | 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 | a0001c0002t0001g0190 | 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 | 107 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0020 others(104): 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 | a0001c0001t0001g0203 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(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 | a0001c0002t0002g0170 | 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 | a0001c0002t0001g0162 a0001c0002t0001g0168 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 |
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 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(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 | a0001c0002t0002g0191 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0011g0015 | 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 | a0001c0001t0008g0043 | 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 | a0001c0001t0001g0108 | 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 | a0001c0001t0004g0065 | 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 | a0001c0001t0001g0054 | 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 | 60 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0054 others(57): 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 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0026 others(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 | a0001c0001t0001g0086 | 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 | 108 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(105): 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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0004g0040 others(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 | a0001c0002t0002g0194 | 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 | a0001c0001t0003g0062 | 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 | a0001c0001t0001g0016 | 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 | a0001c0002t0001g0134 | 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 | a0001c0001t0014g0036 | 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 | a0001c0002t0002g0191 | 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 | a0001c0002t0001g0179 | 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 | a0001c0002t0001g0042 | 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 | a0001c0002t0001g0128 | 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 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0205 |
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 | a0001c0001t0003g0091 | 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 | a0001c0001t0001g0211 | 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 | a0001c0001t0008g0043 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0002t0002g0187 a0001c0002t0002g0188 a0001c0002t0002g0189 others(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 | a0001c0002t0001g0139 a0001c0002t0001g0157 |
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 | a0001c0001t0001g0016 a0001c0001t0014g0036 |
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 | a0001c0001t0011g0015 | 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 | a0001c0001t0001g0035 a0001c0001t0001g0105 a0001c0001t0001g0203 others(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 | a0001c0002t0001g0129 a0001c0002t0001g0180 |
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 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(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 | a0001c0001t0014g0036 | 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 | a0001c0001t0014g0036 | 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 | a0001c0002t0002g0163 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(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 | a0001c0001t0014g0036 | 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 | a0001c0004t0002g0004 | 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 | a0001c0001t0004g0052 a0001c0001t0004g0140 |
2 | HG02717.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.721-641G>A | GRIA2 | ENSG00000120251.22 | transcript | ENST00000264426.14 | protein_coding | 5/15 | chr4 | 157320797 | |||||||
| chr4:157320946 | T | C | 1 | a0001c0001t0014g0036 | 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 | a0001c0001t0002g0098 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0002t0001g0041 a0001c0002t0001g0042 a0001c0002t0001g0123 others(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 | a0001c0002t0002g0174 | 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 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0030 others(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 | a0001c0001t0008g0043 a0001c0003t0001g0022 |
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 | a0001c0001t0014g0036 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0021 others(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 | 64 | a0001c0001t0001g0007 a0001c0001t0001g0050 a0001c0001t0001g0051 others(61): 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 | a0001c0001t0002g0148 a0001c0001t0003g0102 a0001c0001t0004g0182 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0035 a0001c0001t0001g0108 a0001c0001t0001g0109 others(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 | a0001c0002t0001g0141 a0001c0002t0002g0186 a0001c0004t0002g0004 |
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 | a0001c0001t0001g0203 | 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 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(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 | a0001c0002t0002g0207 | 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 | a0001c0002t0009g0202 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0035 a0001c0001t0001g0105 a0001c0001t0001g0203 others(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 | a0001c0001t0003g0057 a0001c0001t0003g0080 a0001c0001t0003g0093 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0037 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0014 others(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 | 68 | a0001c0001t0001g0050 a0001c0001t0001g0056 a0001c0001t0001g0095 others(65): 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 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0055 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0027 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0025 a0001c0001t0001g0026 others(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 | a0001c0001t0001g0035 a0001c0003t0001g0018 a0001c0003t0001g0019 others(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 | a0001c0002t0001g0134 | 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 | a0001c0001t0003g0091 | 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 | a0001c0003t0001g0022 | 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 | a0001c0001t0014g0036 | 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 | a0001c0002t0002g0188 a0001c0002t0002g0200 |
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 | a0001c0001t0001g0105 | 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 | a0001c0001t0004g0107 | 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 | a0001c0001t0002g0148 | 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 | a0001c0003t0001g0018 a0001c0003t0001g0019 a0001c0003t0007g0044 others(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 | a0001c0001t0003g0091 a0001c0001t0003g0092 |
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 | a0001c0001t0001g0016 a0001c0001t0014g0036 |
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 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 |
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 | a0001c0002t0001g0180 | 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 | a0001c0002t0002g0045 a0001c0002t0002g0046 a0001c0002t0002g0124 others(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 | a0001c0001t0011g0015 | 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 | a0001c0001t0001g0016 a0001c0001t0014g0036 |
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 | a0001c0002t0001g0129 a0001c0002t0001g0180 |
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 | a0001c0001t0001g0016 | 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 | a0001c0001t0014g0036 | 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 | a0001c0001t0001g0016 a0001c0001t0001g0105 a0001c0001t0014g0036 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(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 | a0001c0002t0002g0194 | 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 | 176 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0016 others(173): 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 | a0001c0002t0002g0189 a0001c0002t0002g0192 |
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 | a0001c0001t0003g0062 a0001c0001t0003g0063 |
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 | a0001c0001t0001g0026 | 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 | a0001c0001t0001g0016 | 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 | a0001c0002t0001g0162 a0001c0002t0001g0168 a0001c0002t0001g0171 |
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 | a0001c0003t0001g0018 a0001c0003t0001g0019 a0001c0003t0001g0022 others(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 | 189 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(186): 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 | a0001c0001t0008g0043 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0020 | 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 | a0001c0003t0001g0018 a0001c0003t0001g0019 a0001c0003t0001g0022 others(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 | a0001c0002t0002g0167 | 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 | a0001c0002t0002g0198 | 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 | a0001c0002t0002g0194 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(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 | a0001c0001t0001g0066 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0002t0002g0122 | 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 | a0001c0001t0001g0211 a0001c0001t0002g0126 a0001c0001t0002g0208 others(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 | a0001c0001t0011g0015 | 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 | a0001c0003t0001g0018 a0001c0003t0001g0019 a0001c0003t0007g0044 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0105 a0001c0001t0001g0211 others(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 | a0001c0001t0001g0105 | 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 | a0001c0001t0003g0061 | 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 | a0001c0002t0001g0196 | 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 | a0001c0001t0001g0035 a0001c0001t0001g0078 a0001c0001t0001g0105 others(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 | a0001c0001t0014g0036 | 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 | a0001c0001t0004g0100 | 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 | a0001c0002t0001g0179 | 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 | a0001c0003t0001g0018 a0001c0003t0001g0019 a0001c0003t0001g0022 others(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 | a0001c0002t0002g0147 a0001c0002t0002g0174 a0001c0002t0012g0121 |
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 | a0001c0002t0001g0199 | 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 | a0001c0001t0001g0108 | 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 | a0001c0002t0002g0124 | 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 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(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 | a0001c0002t0002g0169 | 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 | a0001c0001t0014g0036 | 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 | a0001c0001t0001g0010 a0001c0003t0007g0044 |
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 | a0001c0002t0002g0122 | 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 | a0001c0002t0002g0153 | 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 | a0001c0001t0004g0069 | 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 | a0001c0001t0001g0035 a0001c0001t0001g0054 a0001c0001t0001g0055 others(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 | a0001c0001t0001g0108 | 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 | a0001c0002t0002g0189 a0001c0002t0002g0192 |
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 | a0001c0001t0001g0203 | 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 | a0001c0002t0001g0130 a0001c0002t0001g0135 a0001c0002t0001g0136 |
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 | a0001c0001t0002g0083 | 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 | a0001c0002t0002g0155 a0001c0002t0002g0185 a0001c0002t0009g0202 |
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 | a0001c0001t0001g0211 a0001c0001t0005g0005 a0001c0001t0005g0008 others(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 | a0001c0001t0001g0211 a0001c0001t0005g0005 a0001c0001t0005g0008 others(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 | a0001c0002t0005g0210 | 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 | a0001c0001t0001g0026 | 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 | a0001c0002t0002g0175 a0001c0002t0002g0184 |
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 | a0001c0002t0002g0194 | 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 | a0001c0002t0002g0186 | 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 | a0001c0003t0001g0018 a0001c0003t0001g0019 a0001c0003t0001g0022 others(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 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0205 |
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 | a0001c0001t0001g0211 a0001c0001t0005g0005 a0001c0001t0005g0008 others(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 | a0001c0001t0004g0182 a0001c0001t0004g0183 |
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 | a0001c0002t0002g0122 | 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 | a0001c0001t0001g0055 a0001c0001t0001g0211 a0001c0002t0001g0178 others(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 | a0001c0002t0001g0134 a0001c0002t0001g0141 a0001c0002t0001g0165 |
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 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0037 others(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 | a0001c0001t0001g0023 a0001c0001t0001g0035 a0001c0001t0001g0051 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0025 a0001c0001t0001g0027 others(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 | a0001c0001t0001g0105 a0001c0001t0003g0088 a0001c0001t0003g0092 others(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 | a0001c0002t0001g0199 | 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 | a0001c0001t0001g0086 a0001c0002t0001g0180 |
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 | a0001c0001t0003g0064 | 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 | a0001c0001t0003g0081 a0001c0001t0003g0082 |
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 | a0001c0001t0001g0110 | 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 | a0001c0001t0001g0108 | 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 | a0001c0001t0004g0059 a0001c0001t0004g0182 a0001c0001t0004g0183 others(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 | a0001c0001t0004g0182 a0001c0001t0004g0183 a0001c0005t0002g0164 |
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 | a0001c0001t0004g0058 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0003t0001g0022 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0038 others(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 | a0001c0002t0001g0142 a0001c0002t0001g0177 |
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 | a0001c0001t0001g0010 a0001c0002t0001g0165 a0001c0002t0001g0181 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0038 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0038 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0023 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0023 others(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 | a0001c0002t0001g0193 | 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 | 128 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(125): 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 | a0001c0001t0005g0008 a0001c0002t0005g0204 |
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 | a0001c0001t0001g0211 a0001c0001t0005g0005 a0001c0001t0005g0008 others(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 | a0001c0001t0003g0091 a0001c0001t0003g0092 |
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 | a0001c0001t0001g0051 | 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 | a0001c0001t0003g0101 a0001c0001t0003g0102 a0001c0001t0003g0103 others(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 | a0001c0001t0001g0050 a0001c0002t0001g0196 |
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 | a0001c0001t0005g0005 | 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 | a0001c0002t0001g0041 a0001c0002t0001g0042 |
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 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(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 | a0001c0001t0001g0108 | 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 | a0001c0003t0001g0033 | 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 | a0001c0001t0001g0211 a0001c0001t0005g0005 a0001c0002t0002g0207 others(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 | a0001c0001t0001g0108 | 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 | a0001c0001t0001g0211 a0001c0001t0005g0005 a0001c0001t0005g0008 others(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 | a0001c0002t0001g0131 | 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 | a0001c0001t0014g0036 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(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 | a0001c0001t0001g0211 a0001c0001t0005g0005 a0001c0001t0005g0008 others(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 | a0001c0001t0003g0091 a0001c0001t0003g0092 |
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 | a0001c0002t0001g0180 | 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 | a0001c0001t0004g0058 a0001c0001t0004g0059 |
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 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0047 others(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 | a0001c0001t0001g0035 a0001c0001t0001g0054 a0001c0001t0001g0055 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(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 | 205 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(202): 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 | a0001c0002t0002g0122 | 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 | a0001c0002t0001g0162 | 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 | a0001c0001t0014g0036 | 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 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0026 |
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 | 204 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(201): 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 | a0001c0001t0001g0096 | 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 | a0001c0002t0012g0121 | 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 | 5 | a0001c0001t0004g0001 a0001c0001t0004g0048 a0001c0001t0004g0049 others(2): 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 | a0001c0002t0002g0174 | 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 | a0001c0002t0002g0176 | 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 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0026 |
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 | 204 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(201): 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 | a0001c0002t0001g0041 a0001c0002t0001g0042 |
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 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0026 |
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 | a0001c0001t0001g0105 | 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 | a0001c0003t0001g0018 a0001c0003t0001g0019 a0001c0003t0001g0022 others(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 | a0001c0002t0001g0171 | 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 | a0001c0002t0002g0149 | 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 | a0001c0001t0001g0108 a0001c0001t0011g0015 |
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 | 5 | a0001c0001t0004g0001 a0001c0001t0004g0048 a0001c0001t0004g0049 others(2): 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 | 54 | a0001c0001t0001g0051 a0001c0001t0001g0096 a0001c0001t0002g0148 others(51): 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 | a0001c0001t0001g0105 | 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 | a0001c0001t0004g0100 | 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 | a0001c0002t0001g0143 | 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 | a0001c0001t0001g0211 | 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 | a0001c0001t0001g0027 a0001c0001t0001g0030 |
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 | a0001c0001t0001g0203 | 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 | a0001c0001t0004g0071 | 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 | a0001c0001t0014g0036 | 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 | a0001c0002t0002g0194 | 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 | a0001c0002t0002g0194 | 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 | a0001c0001t0001g0108 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0016 others(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 | a0001c0002t0002g0138 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0003g0060 | 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 | a0001c0002t0002g0145 | 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 | a0001c0001t0011g0015 | 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 | a0001c0001t0006g0090 a0001c0001t0006g0099 |
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 | a0001c0001t0004g0048 a0001c0001t0004g0049 |
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 | a0001c0001t0001g0035 a0001c0001t0001g0078 a0001c0001t0001g0095 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0016 others(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 | a0001c0001t0003g0094 a0001c0001t0003g0101 a0001c0001t0003g0102 others(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 | a0001c0001t0014g0036 | 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 | a0001c0001t0003g0060 | 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 | a0001c0001t0001g0035 a0001c0001t0001g0054 a0001c0001t0001g0055 others(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 | a0001c0001t0001g0086 a0001c0001t0001g0105 |
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 | a0001c0001t0005g0005 a0001c0001t0005g0008 a0001c0002t0005g0204 others(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 | a0001c0002t0001g0129 | 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 | a0001c0001t0001g0010 a0001c0001t0004g0048 a0001c0001t0004g0058 others(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 | a0001c0001t0001g0108 a0001c0001t0011g0015 |
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 | a0001c0002t0002g0174 | 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 | 205 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(202): 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 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(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 | a0001c0002t0012g0121 | 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 | a0001c0002t0001g0128 | 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 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0205 |
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 | a0001c0001t0001g0039 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(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 | a0001c0001t0011g0015 | 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 | a0001c0001t0001g0108 | 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 | a0001c0001t0001g0086 | 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 | a0001c0001t0001g0108 a0001c0001t0011g0015 |
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 | a0001c0001t0005g0005 a0001c0002t0005g0210 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(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 | a0001c0001t0004g0068 | 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 | a0001c0002t0001g0179 | 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 | a0001c0001t0004g0068 | 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 | a0001c0002t0002g0173 | 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 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(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 | a0001c0001t0005g0008 a0001c0002t0005g0204 |
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 | 67 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(64): 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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0035 a0001c0001t0001g0054 a0001c0001t0001g0055 others(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 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(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 | a0001c0001t0004g0040 a0001c0001t0004g0052 a0001c0001t0004g0140 others(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 | 56 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0047 others(53): 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 | 203 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(200): 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 | a0001c0002t0001g0179 | 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 | a0001c0001t0014g0036 | 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 | a0001c0001t0014g0036 | 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 | a0001c0002t0002g0161 | 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 | a0001c0001t0001g0203 | 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 | a0001c0001t0001g0203 | 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 | a0001c0001t0001g0105 a0001c0001t0003g0093 a0001c0001t0006g0090 |
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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | 185 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(182): 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 | a0001c0001t0004g0182 a0001c0001t0004g0183 |
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 | a0001c0002t0002g0194 | 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 | a0001c0001t0001g0016 | 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 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0047 others(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 | a0001c0001t0001g0108 a0001c0001t0005g0005 a0001c0001t0005g0008 others(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 | a0001c0001t0004g0040 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(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 | a0001c0001t0001g0050 a0001c0002t0001g0196 |
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 | a0001c0002t0002g0122 | 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 | a0001c0001t0001g0086 | 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 | a0001c0001t0001g0035 a0001c0001t0001g0054 a0001c0001t0001g0055 others(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 | a0001c0001t0004g0073 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(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 | 122 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(119): 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 | a0001c0001t0005g0005 a0001c0001t0005g0008 a0001c0002t0005g0204 others(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 | a0001c0001t0001g0086 | 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 | a0001c0002t0001g0041 a0001c0002t0001g0042 |
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 | a0001c0001t0001g0051 | 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 | a0001c0001t0002g0024 a0001c0001t0002g0077 a0001c0001t0002g0083 others(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 | a0001c0003t0001g0022 | 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 |
123 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(120): 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 | a0001c0002t0001g0168 | 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 | a0001c0001t0003g0003 a0001c0001t0003g0057 a0001c0001t0003g0088 others(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 | a0001c0001t0014g0036 | 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 | a0001c0002t0002g0153 a0001c0002t0002g0158 |
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 | a0001c0002t0001g0159 a0001c0002t0001g0160 |
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 | a0001c0001t0002g0024 a0001c0001t0002g0077 a0001c0001t0002g0083 others(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 | a0001c0002t0002g0153 a0001c0002t0002g0158 |
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 | 3 | a0001c0001t0004g0001 a0001c0002t0001g0129 a0001c0002t0001g0180 |
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 | a0001c0002t0002g0153 | 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 | a0001c0001t0002g0098 | 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 | a0001c0001t0002g0024 a0001c0001t0002g0077 a0001c0001t0002g0126 others(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 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(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 | a0001c0002t0002g0153 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0016 others(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 | a0001c0002t0002g0153 | 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 | a0001c0002t0002g0153 a0001c0002t0002g0158 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0002g0148 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(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 | a0001c0001t0002g0083 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(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 | a0001c0001t0002g0083 | 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 | a0001c0001t0002g0083 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(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 | a0001c0001t0002g0083 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0002g0148 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0016 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0002g0148 others(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 | a0001c0001t0002g0083 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0002g0148 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(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 | a0001c0001t0001g0035 | 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 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0002g0148 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0002g0148 others(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 | a0001c0001t0002g0083 | 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 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0002g0148 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(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 | a0001c0001t0002g0024 a0001c0001t0002g0077 a0001c0001t0002g0098 others(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 | a0001c0001t0014g0036 | 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 | a0001c0001t0002g0083 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0002g0148 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0002g0148 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0002g0148 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0016 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0002g0148 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0002g0148 others(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 | a0001c0001t0001g0025 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0026 others(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 | a0001c0001t0001g0211 | 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 | a0001c0001t0001g0023 | 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 | a0001c0001t0002g0083 | 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 | a0001c0001t0002g0083 | 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 | a0001c0001t0002g0083 | 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 | 122 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(119): 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 | a0001c0001t0003g0003 a0001c0001t0003g0089 a0001c0001t0008g0043 |
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 | a0001c0001t0005g0008 a0001c0002t0005g0204 |
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 | a0001c0001t0005g0005 a0001c0002t0005g0210 |
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 | a0001c0001t0001g0096 a0001c0001t0010g0206 a0001c0003t0001g0018 others(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 | a0001c0001t0002g0083 | 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 | a0001c0001t0002g0083 | 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 | a0001c0001t0002g0024 a0001c0001t0002g0077 a0001c0001t0002g0098 others(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 | a0001c0001t0002g0024 a0001c0001t0002g0077 a0001c0001t0002g0083 others(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 | a0001c0001t0001g0108 a0001c0001t0011g0015 |
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 | a0001c0001t0002g0024 a0001c0001t0002g0077 a0001c0001t0002g0098 others(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 | a0001c0001t0002g0024 a0001c0001t0002g0077 a0001c0001t0002g0098 others(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 | a0001c0002t0002g0155 | 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 | a0001c0001t0014g0036 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0050 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0050 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0027 | 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 | a0001c0001t0001g0108 a0001c0001t0011g0015 a0001c0002t0001g0129 others(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 | a0001c0001t0001g0035 a0001c0001t0001g0054 a0001c0001t0001g0055 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0010 others(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 |
92 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0055 others(89): 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 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0002t0002g0153 a0001c0002t0002g0161 |
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 | a0001c0001t0002g0083 | 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 | a0001c0001t0002g0024 a0001c0001t0002g0077 a0001c0001t0002g0098 others(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 | a0001c0001t0005g0005 a0001c0001t0005g0008 a0001c0002t0005g0204 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(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 | a0001c0001t0001g0035 a0001c0001t0001g0078 a0001c0001t0001g0095 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0002g0083 | 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 | a0001c0001t0005g0005 a0001c0001t0005g0008 a0001c0002t0005g0204 others(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 | a0001c0001t0005g0005 a0001c0001t0005g0008 a0001c0002t0005g0204 others(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 | a0001c0001t0005g0005 a0001c0001t0005g0008 a0001c0002t0005g0204 others(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 | a0001c0001t0005g0005 a0001c0001t0005g0008 a0001c0002t0005g0204 others(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 | a0001c0001t0005g0005 a0001c0001t0005g0008 a0001c0002t0005g0204 others(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 | a0001c0001t0005g0005 a0001c0001t0005g0008 a0001c0002t0005g0204 others(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 | a0001c0001t0002g0083 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0002g0083 | 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 | a0001c0001t0002g0083 | 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 | 56 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0047 others(53): 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 | a0001c0001t0002g0083 | 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 | a0001c0001t0002g0083 | 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 | a0001c0001t0002g0083 | 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 | a0001c0001t0002g0083 | 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 | a0001c0001t0005g0005 a0001c0001t0005g0008 a0001c0002t0005g0204 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0016 others(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 | a0001c0002t0002g0152 | 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 | a0001c0002t0002g0138 | 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 | a0001c0002t0002g0194 | 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 | a0001c0001t0004g0058 a0001c0001t0004g0059 a0001c0001t0014g0036 |
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 | a0001c0001t0002g0126 | 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 | a0001c0001t0005g0005 a0001c0001t0005g0008 a0001c0002t0005g0204 others(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 | a0001c0001t0011g0015 a0001c0001t0014g0036 |
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 | a0001c0002t0002g0166 | 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 | 1 | a0001c0001t0004g0001 | 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 | a0001c0001t0001g0035 | 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 | a0001c0002t0002g0201 | 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 | 199 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(196): 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 | a0001c0001t0001g0086 | 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 | a0001c0001t0001g0035 a0001c0001t0001g0054 a0001c0001t0001g0055 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0096 a0001c0001t0010g0206 a0001c0003t0001g0018 others(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 | 51 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0047 others(48): 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 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0047 others(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 | a0001c0003t0001g0031 a0001c0003t0001g0032 a0001c0003t0001g0033 others(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 | a0001c0002t0002g0124 | 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 | a0001c0001t0001g0010 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(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 | a0001c0001t0001g0025 | 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 | a0001c0001t0014g0036 | 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 | a0001c0001t0005g0005 a0001c0001t0005g0008 a0001c0002t0005g0204 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0002t0001g0041 a0001c0002t0001g0042 |
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 | a0001c0002t0001g0141 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0002t0004g0137 | 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 | a0001c0001t0001g0035 a0001c0001t0001g0054 a0001c0001t0001g0055 others(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 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(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 | a0001c0002t0002g0198 | 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 | a0001c0002t0002g0113 | 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 | a0001c0001t0011g0015 | 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 | 202 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(199): 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 | a0001c0001t0011g0015 | 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 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(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 | a0001c0001t0001g0086 | 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 | a0001c0001t0001g0203 | 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 | a0001c0001t0001g0096 a0001c0001t0010g0206 a0001c0003t0001g0018 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | 122 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(119): 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 | a0001c0001t0001g0108 a0001c0001t0011g0015 |
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 | a0001c0002t0009g0202 | 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 | a0001c0001t0002g0208 | 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 | a0001c0003t0001g0031 a0001c0003t0001g0032 a0001c0003t0001g0033 others(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 | a0001c0001t0001g0108 | 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 | a0001c0002t0001g0142 | 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 | a0001c0002t0002g0147 | 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 | a0001c0001t0003g0003 a0001c0001t0003g0089 |
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 | a0001c0003t0001g0022 | 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 | a0001c0001t0005g0005 a0001c0001t0005g0008 a0001c0002t0005g0204 others(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 |