Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2906 |
| ensemblid | ENSG00000105464.4 |
| hgncid | 4588 |
| symbol | GRIN2D |
| name | glutamate ionotropic receptor NMDA type subunit 2D |
| refseq_nuc | NM_000836.4 |
| refseq_prot | NP_000827.2 |
| ensembl_nuc | ENST00000263269.4 |
| ensembl_prot | ENSP00000263269.2 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 48393668 |
| end | 48444931 |
| strand | + |
| ver | v1.2 |
| region | chr19:48393668-48444931 |
| region5000 | chr19:48388668-48449931 |
| regionname0 | GRIN2D_chr19_48393668_48444931 |
| regionname5000 | GRIN2D_chr19_48388668_48449931 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1336 | 362 | 91 | 74 | 146 | 10 | 39 | 109 | GRIN2D_chr19_48388668_48449931 | GRIN2D | MRGAG others(1331): Show |
chr19 | 48388668 | 48449931 |
| a0002 | 0/0 | 1336 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | MRGAG others(1331): Show |
chr19 | 48388668 | 48449931 |
| a0003 | 0/0 | 1336 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | MRGAG others(1331): Show |
chr19 | 48388668 | 48449931 |
| a0004 | 0/0 | 1336 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | MRGAG others(1331): Show |
chr19 | 48388668 | 48449931 |
| a0005 | 0/0 | 1330 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | MRGAG others(1325): Show |
chr19 | 48388668 | 48449931 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 4008 | 227 | 51 | 50 | 89 | 7 | 29 | GRIN2D_chr19_48388668_48449931 | GRIN2D | ATGCG others(4003): Show |
chr19 | 48388668 | 48449931 | ||
| a0001c0002 | 1/0 | 4008 | 61 | 30 | 4 | 17 | 1 | 8 | GRIN2D_chr19_48388668_48449931 | GRIN2D | ATGCG others(4003): Show |
chr19 | 48388668 | 48449931 | ||
| a0001c0003 | 0/0 | 4008 | 36 | 0 | 3 | 31 | 1 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | ATGCG others(4003): Show |
chr19 | 48388668 | 48449931 | ||
| a0001c0004 | 0/0 | 4008 | 12 | 4 | 4 | 4 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | ATGCG others(4003): Show |
chr19 | 48388668 | 48449931 | ||
| a0001c0005 | 0/0 | 4008 | 5 | 0 | 4 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | ATGCG others(4003): Show |
chr19 | 48388668 | 48449931 | ||
| a0001c0006 | 0/0 | 4008 | 3 | 1 | 2 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | ATGCG others(4003): Show |
chr19 | 48388668 | 48449931 | ||
| a0001c0007 | 0/0 | 4008 | 2 | 1 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | ATGCG others(4003): Show |
chr19 | 48388668 | 48449931 | ||
| a0001c0008 | 0/0 | 4008 | 2 | 0 | 2 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | ATGCG others(4003): Show |
chr19 | 48388668 | 48449931 | ||
| a0001c0009 | 0/0 | 4008 | 2 | 2 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | ATGCG others(4003): Show |
chr19 | 48388668 | 48449931 | ||
| a0001c0010 | 0/0 | 4008 | 2 | 2 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | ATGCG others(4003): Show |
chr19 | 48388668 | 48449931 | ||
| a0001c0011 | 0/0 | 4008 | 2 | 0 | 2 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | ATGCG others(4003): Show |
chr19 | 48388668 | 48449931 | ||
| a0001c0012 | 0/0 | 4008 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | ATGCG others(4003): Show |
chr19 | 48388668 | 48449931 | ||
| a0001c0013 | 0/0 | 4008 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | ATGCG others(4003): Show |
chr19 | 48388668 | 48449931 | ||
| a0001c0015 | 0/0 | 4008 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | ATGCG others(4003): Show |
chr19 | 48388668 | 48449931 | ||
| a0001c0018 | 0/0 | 4008 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | ATGCG others(4003): Show |
chr19 | 48388668 | 48449931 | ||
| a0001c0020 | 0/0 | 4008 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | ATGCG others(4003): Show |
chr19 | 48388668 | 48449931 | ||
| a0001c0021 | 0/0 | 4008 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | ATGCG others(4003): Show |
chr19 | 48388668 | 48449931 | ||
| a0001c0022 | 0/0 | 4008 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | ATGCG others(4003): Show |
chr19 | 48388668 | 48449931 | ||
| a0001c0023 | 0/0 | 4008 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | ATGCG others(4003): Show |
chr19 | 48388668 | 48449931 | ||
| a0002c0014 | 0/0 | 4008 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | ATGCG others(4003): Show |
chr19 | 48388668 | 48449931 | ||
| a0003c0019 | 0/0 | 4008 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | ATGCG others(4003): Show |
chr19 | 48388668 | 48449931 | ||
| a0004c0017 | 0/0 | 4008 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | ATGCG others(4003): Show |
chr19 | 48388668 | 48449931 | ||
| a0005c0016 | 0/0 | 3990 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | ATGCG others(3985): Show |
chr19 | 48388668 | 48449931 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 5511 | 159 | 33 | 42 | 62 | 4 | 17 | GRIN2D_chr19_48388668_48449931 | GRIN2D | ATCCC others(5506): Show |
chr19 | 48388668 | 48449931 |
| a0001c0001t0002 | 0/0 | 5511 | 60 | 14 | 7 | 24 | 3 | 12 | GRIN2D_chr19_48388668_48449931 | GRIN2D | ATCCC others(5506): Show |
chr19 | 48388668 | 48449931 |
| a0001c0001t0004 | 0/0 | 5511 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | ATCCC others(5506): Show |
chr19 | 48388668 | 48449931 |
| a0001c0001t0005 | 0/0 | 5511 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | ATCCC others(5506): Show |
chr19 | 48388668 | 48449931 |
| a0001c0001t0006 | 0/0 | 5511 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | ATCCC others(5506): Show |
chr19 | 48388668 | 48449931 |
| a0001c0001t0008 | 0/0 | 5511 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | ATCCC others(5506): Show |
chr19 | 48388668 | 48449931 |
| a0001c0001t0009 | 0/0 | 5511 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | ATCCC others(5506): Show |
chr19 | 48388668 | 48449931 |
| a0001c0001t0010 | 0/0 | 5511 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | ATCCC others(5506): Show |
chr19 | 48388668 | 48449931 |
| a0001c0001t0011 | 0/0 | 5511 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | ATCCC others(5506): Show |
chr19 | 48388668 | 48449931 |
| a0001c0001t0013 | 0/0 | 5511 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | ATCCC others(5506): Show |
chr19 | 48388668 | 48449931 |
| a0001c0002t0002 | 1/0 | 5511 | 58 | 29 | 3 | 16 | 1 | 8 | GRIN2D_chr19_48388668_48449931 | GRIN2D | ATCCC others(5506): Show |
chr19 | 48388668 | 48449931 |
| a0001c0002t0003 | 0/0 | 5511 | 2 | 1 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | ATCCC others(5506): Show |
chr19 | 48388668 | 48449931 |
| a0001c0002t0012 | 0/0 | 5511 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | ATCCC others(5506): Show |
chr19 | 48388668 | 48449931 |
| a0001c0003t0002 | 0/0 | 5511 | 35 | 0 | 3 | 30 | 1 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | ATCCC others(5506): Show |
chr19 | 48388668 | 48449931 |
| a0001c0003t0015 | 0/0 | 5557 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | ATCCC others(5552): Show |
chr19 | 48388668 | 48449931 |
| a0001c0004t0002 | 0/0 | 5511 | 12 | 4 | 4 | 4 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | ATCCC others(5506): Show |
chr19 | 48388668 | 48449931 |
| a0001c0005t0001 | 0/0 | 5511 | 5 | 0 | 4 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | ATCCC others(5506): Show |
chr19 | 48388668 | 48449931 |
| a0001c0006t0001 | 0/0 | 5511 | 2 | 1 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | ATCCC others(5506): Show |
chr19 | 48388668 | 48449931 |
| a0001c0006t0002 | 0/0 | 5511 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | ATCCC others(5506): Show |
chr19 | 48388668 | 48449931 |
| a0001c0007t0004 | 0/0 | 5511 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | ATCCC others(5506): Show |
chr19 | 48388668 | 48449931 |
| a0001c0007t0007 | 0/0 | 5511 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | ATCCC others(5506): Show |
chr19 | 48388668 | 48449931 |
| a0001c0008t0001 | 0/0 | 5511 | 2 | 0 | 2 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | ATCCC others(5506): Show |
chr19 | 48388668 | 48449931 |
| a0001c0009t0001 | 0/0 | 5511 | 2 | 2 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | ATCCC others(5506): Show |
chr19 | 48388668 | 48449931 |
| a0001c0010t0002 | 0/0 | 5511 | 2 | 2 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | ATCCC others(5506): Show |
chr19 | 48388668 | 48449931 |
| a0001c0011t0002 | 0/0 | 5511 | 2 | 0 | 2 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | ATCCC others(5506): Show |
chr19 | 48388668 | 48449931 |
| a0001c0012t0014 | 0/0 | 5511 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | ATCCC others(5506): Show |
chr19 | 48388668 | 48449931 |
| a0001c0013t0001 | 0/0 | 5511 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | ATCCC others(5506): Show |
chr19 | 48388668 | 48449931 |
| a0001c0015t0002 | 0/0 | 5511 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | ATCCC others(5506): Show |
chr19 | 48388668 | 48449931 |
| a0001c0018t0002 | 0/0 | 5511 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | ATCCC others(5506): Show |
chr19 | 48388668 | 48449931 |
| a0001c0020t0002 | 0/0 | 5511 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | ATCCC others(5506): Show |
chr19 | 48388668 | 48449931 |
| a0001c0021t0001 | 0/0 | 5511 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | ATCCC others(5506): Show |
chr19 | 48388668 | 48449931 |
| a0001c0022t0002 | 0/0 | 5511 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | ATCCC others(5506): Show |
chr19 | 48388668 | 48449931 |
| a0001c0023t0002 | 0/0 | 5511 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | ATCCC others(5506): Show |
chr19 | 48388668 | 48449931 |
| a0002c0014t0001 | 0/0 | 5511 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | ATCCC others(5506): Show |
chr19 | 48388668 | 48449931 |
| a0003c0019t0001 | 0/0 | 5511 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | ATCCC others(5506): Show |
chr19 | 48388668 | 48449931 |
| a0004c0017t0001 | 0/0 | 5511 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | ATCCC others(5506): Show |
chr19 | 48388668 | 48449931 |
| a0005c0016t0001 | 0/0 | 5493 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | ATCCC others(5488): Show |
chr19 | 48388668 | 48449931 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0262 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0002g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0002g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0004g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0005g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0006g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0008g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0009g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0010g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0011g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0001t0013g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0002t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0002t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0002t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0002t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0002t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0002t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0002t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0002t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0002t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0002t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0002t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0002t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0002t0002g0148 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0002t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0002t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0002t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0002t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0002t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0002t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0002t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0002t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0002t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0002t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0002t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0002t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0002t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0002t0002g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0002t0002g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0002t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0002t0002g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0002t0002g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0002t0002g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0002t0002g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0002t0002g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0002t0002g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0002t0002g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0002t0002g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0002t0002g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0002t0002g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0002t0003g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0002t0003g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0002t0012g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0003t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0003t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0003t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0003t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0003t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0003t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0003t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0003t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0003t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0003t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0003t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0003t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0003t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0003t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0003t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0003t0002g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0003t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0003t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0003t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0003t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0003t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0003t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0003t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0003t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0003t0002g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0003t0002g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0003t0002g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0003t0002g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0003t0002g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0003t0002g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0003t0002g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0003t0002g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0003t0002g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0003t0002g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0003t0015g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0004t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0004t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0004t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0004t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0004t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0004t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0004t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0004t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0004t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0004t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0004t0002g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0004t0002g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0005t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0005t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0005t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0005t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0005t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0006t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0006t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0006t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0007t0004g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0007t0007g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0008t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0008t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0009t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0009t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0010t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0010t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0011t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0011t0002g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0012t0014g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0013t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0015t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0018t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0020t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0021t0001g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0022t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0001c0023t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0002c0014t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0003c0019t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0004c0017t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| a0005c0016t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0156 | EUR | GBR | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG00099 | hp2 | a0001 | c0003 | t0002 | g0073 | EUR | GBR | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG00140 | hp1 | a0001 | c0002 | t0002 | g0204 | EUR | GBR | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG00140 | hp2 | a0001 | c0023 | t0002 | g0270 | EUR | GBR | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0134 | EUR | FIN | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0061 | EUR | FIN | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG00408 | hp1 | a0002 | c0014 | t0001 | g0139 | EAS | CHS | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0313 | EAS | CHS | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0344 | EAS | CHS | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | CHS | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | CHS | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | CHS | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG00558 | hp1 | a0001 | c0015 | t0002 | g0318 | EAS | CHS | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG00597 | hp1 | a0001 | c0003 | t0002 | g0363 | EAS | CHS | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | CHS | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | CHS | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG00609 | hp2 | a0001 | c0003 | t0002 | g0329 | EAS | CHS | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG00639 | hp2 | a0001 | c0008 | t0001 | g0143 | AMR | PUR | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG00642 | hp2 | a0001 | c0006 | t0001 | g0025 | AMR | PUR | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG00673 | hp1 | a0001 | c0003 | t0002 | g0331 | EAS | CHS | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG00673 | hp2 | a0001 | c0003 | t0002 | g0260 | EAS | CHS | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG00733 | hp1 | a0001 | c0007 | t0004 | g0309 | AMR | PUR | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0146 | AMR | PUR | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0056 | AMR | PUR | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0055 | AMR | PUR | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG00741 | hp1 | a0001 | c0021 | t0001 | g0355 | AMR | PUR | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG01069 | hp2 | a0001 | c0003 | t0002 | g0361 | AMR | PUR | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG01070 | hp2 | a0001 | c0004 | t0002 | g0214 | AMR | PUR | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG01071 | hp2 | a0001 | c0004 | t0002 | g0213 | AMR | PUR | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0162 | AMR | PUR | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG01099 | hp2 | a0001 | c0005 | t0001 | g0022 | AMR | PUR | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG01106 | hp2 | a0001 | c0003 | t0002 | g0057 | AMR | PUR | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG01109 | hp1 | a0001 | c0002 | t0002 | g0341 | AMR | PUR | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG01167 | hp2 | a0001 | c0011 | t0002 | g0300 | AMR | PUR | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG01169 | hp1 | a0001 | c0011 | t0002 | g0299 | AMR | PUR | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG01169 | hp2 | a0001 | c0002 | t0002 | g0231 | AMR | PUR | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG01243 | hp1 | a0001 | c0002 | t0003 | g0007 | AMR | PUR | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0250 | AMR | CLM | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | CLM | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0251 | AMR | CLM | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG01261 | hp1 | a0001 | c0002 | t0002 | g0102 | AMR | CLM | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG01358 | hp2 | a0001 | c0008 | t0001 | g0043 | AMR | CLM | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | CLM | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG01433 | hp2 | a0001 | c0012 | t0014 | g0302 | AMR | CLM | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG01496 | hp1 | a0001 | c0006 | t0002 | g0027 | AMR | CLM | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG01496 | hp2 | a0001 | c0005 | t0001 | g0072 | AMR | CLM | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG01884 | hp1 | a0001 | c0002 | t0002 | g0304 | AFR | ACB | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0224 | AFR | ACB | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | ACB | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG01891 | hp2 | a0001 | c0002 | t0002 | g0135 | AFR | ACB | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG01928 | hp2 | a0001 | c0005 | t0001 | g0346 | AMR | PEL | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0159 | AMR | PEL | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG01952 | hp1 | a0001 | c0005 | t0001 | g0290 | AMR | PEL | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PEL | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG01975 | hp2 | a0001 | c0004 | t0002 | g0353 | AMR | PEL | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | PEL | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02015 | hp2 | a0001 | c0022 | t0002 | g0334 | EAS | KHV | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02040 | hp1 | a0001 | c0002 | t0002 | g0293 | EAS | KHV | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | ACB | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02056 | hp1 | a0001 | c0002 | t0012 | g0092 | EAS | KHV | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | KHV | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02074 | hp2 | a0001 | c0003 | t0002 | g0327 | EAS | KHV | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02083 | hp1 | a0001 | c0003 | t0002 | g0002 | EAS | KHV | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02083 | hp2 | a0001 | c0003 | t0002 | g0343 | EAS | KHV | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | KHV | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02135 | hp1 | a0001 | c0003 | t0002 | g0330 | EAS | KHV | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02135 | hp2 | a0001 | c0002 | t0002 | g0121 | EAS | KHV | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02145 | hp2 | a0001 | c0004 | t0002 | g0280 | AFR | ACB | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PEL | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | CDX | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | CDX | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02257 | hp1 | a0001 | c0001 | t0010 | g0322 | AFR | ACB | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0029 | AFR | ACB | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0352 | AMR | PEL | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02280 | hp2 | a0001 | c0002 | t0002 | g0091 | AFR | ACB | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02293 | hp1 | a0001 | c0001 | t0008 | g0220 | AMR | PEL | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02293 | hp2 | a0001 | c0004 | t0002 | g0351 | AMR | PEL | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02300 | hp1 | a0001 | c0003 | t0002 | g0356 | AMR | PEL | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0264 | AFR | ACB | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02523 | hp1 | a0001 | c0001 | t0005 | g0059 | EAS | KHV | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02523 | hp2 | a0001 | c0004 | t0002 | g0188 | EAS | KHV | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02572 | hp1 | a0001 | c0002 | t0002 | g0142 | AFR | GWD | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | GWD | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02615 | hp1 | a0001 | c0002 | t0002 | g0287 | AFR | GWD | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02622 | hp1 | a0001 | c0009 | t0001 | g0223 | AFR | GWD | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02630 | hp1 | a0001 | c0002 | t0002 | g0316 | AFR | GWD | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | GWD | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0137 | SAS | PJL | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02683 | hp2 | a0001 | c0002 | t0002 | g0298 | SAS | PJL | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02723 | hp1 | a0001 | c0002 | t0002 | g0039 | AFR | GWD | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02723 | hp2 | a0001 | c0002 | t0002 | g0283 | AFR | GWD | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02738 | hp1 | a0001 | c0002 | t0002 | g0339 | SAS | PJL | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02738 | hp2 | a0001 | c0002 | t0002 | g0229 | SAS | PJL | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02809 | hp1 | a0001 | c0004 | t0002 | g0274 | AFR | GWD | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0167 | AFR | GWD | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02818 | hp1 | a0001 | c0002 | t0002 | g0319 | AFR | GWD | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0180 | AFR | GWD | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02886 | hp1 | a0001 | c0004 | t0002 | g0099 | AFR | GWD | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02886 | hp2 | a0001 | c0002 | t0002 | g0077 | AFR | GWD | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02895 | hp1 | a0001 | c0010 | t0002 | g0210 | AFR | GWD | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02897 | hp1 | a0001 | c0010 | t0002 | g0209 | AFR | GWD | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0227 | AFR | GWD | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02922 | hp2 | a0001 | c0002 | t0002 | g0178 | AFR | ESN | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02965 | hp1 | a0001 | c0002 | t0002 | g0028 | AFR | ESN | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | ESN | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0265 | AFR | ESN | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | ESN | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02976 | hp2 | a0001 | c0002 | t0002 | g0282 | AFR | ESN | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0235 | SAS | PJL | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG03017 | hp2 | a0001 | c0002 | t0002 | g0205 | SAS | PJL | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG03041 | hp1 | a0001 | c0002 | t0002 | g0305 | AFR | GWD | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG03041 | hp2 | a0001 | c0002 | t0002 | g0165 | AFR | GWD | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | MSL | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG03098 | hp2 | a0001 | c0002 | t0002 | g0208 | AFR | MSL | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG03130 | hp2 | a0001 | c0004 | t0002 | g0281 | AFR | ESN | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0303 | AFR | ESN | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG03139 | hp2 | a0001 | c0002 | t0002 | g0109 | AFR | ESN | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG03209 | hp1 | a0001 | c0001 | t0006 | g0006 | AFR | MSL | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG03209 | hp2 | a0001 | c0002 | t0002 | g0306 | AFR | MSL | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG03225 | hp1 | a0001 | c0002 | t0003 | g0008 | AFR | MSL | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG03225 | hp2 | a0001 | c0002 | t0002 | g0093 | AFR | MSL | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0285 | SAS | PJL | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0295 | SAS | PJL | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG03453 | hp2 | a0001 | c0002 | t0002 | g0038 | AFR | MSL | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG03486 | hp1 | a0001 | c0009 | t0001 | g0116 | AFR | MSL | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0226 | AFR | MSL | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0263 | AFR | ESN | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG03516 | hp2 | a0001 | c0002 | t0002 | g0307 | AFR | ESN | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0222 | AFR | GWD | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0308 | AFR | GWD | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0179 | AFR | MSL | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG03579 | hp2 | a0001 | c0007 | t0007 | g0310 | AFR | MSL | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0271 | SAS | PJL | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0342 | SAS | PJL | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG03688 | hp1 | a0001 | c0002 | t0002 | g0297 | SAS | STU | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0258 | SAS | STU | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG03704 | hp1 | a0001 | c0020 | t0002 | g0206 | SAS | PJL | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG03710 | hp1 | a0004 | c0017 | t0001 | g0115 | SAS | PJL | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0233 | SAS | PJL | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | BEB | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | BEB | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0120 | SAS | BEB | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0080 | SAS | BEB | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG03927 | hp1 | a0001 | c0002 | t0002 | g0237 | SAS | BEB | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | BEB | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | BEB | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0321 | SAS | BEB | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG04115 | hp1 | a0001 | c0002 | t0002 | g0314 | SAS | STU | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | STU | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG04184 | hp1 | a0001 | c0003 | t0002 | g0326 | SAS | BEB | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | BEB | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | STU | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0052 | SAS | STU | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0340 | SAS | STU | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG04204 | hp2 | a0001 | c0002 | t0002 | g0053 | SAS | STU | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | YRI | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA18612 | hp1 | a0001 | c0002 | t0002 | g0193 | EAS | CHB | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA18612 | hp2 | a0001 | c0003 | t0002 | g0078 | EAS | CHB | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | CHB | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA18747 | hp2 | a0001 | c0003 | t0002 | g0324 | EAS | CHB | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA18906 | hp1 | a0001 | c0001 | t0011 | g0323 | AFR | YRI | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | YRI | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA18941 | hp1 | a0001 | c0003 | t0002 | g0104 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0336 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA18942 | hp2 | a0001 | c0002 | t0002 | g0041 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0359 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA18945 | hp1 | a0001 | c0018 | t0002 | g0049 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA18945 | hp2 | a0001 | c0003 | t0002 | g0333 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA18951 | hp2 | a0001 | c0003 | t0002 | g0347 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA18952 | hp2 | a0001 | c0003 | t0002 | g0019 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA18954 | hp2 | a0001 | c0005 | t0001 | g0184 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA18956 | hp2 | a0001 | c0013 | t0001 | g0246 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA18959 | hp1 | a0001 | c0002 | t0002 | g0194 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA18959 | hp2 | a0001 | c0003 | t0002 | g0085 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA18962 | hp1 | a0001 | c0002 | t0002 | g0292 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0337 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA18963 | hp1 | a0001 | c0003 | t0002 | g0332 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA18964 | hp1 | a0001 | c0002 | t0002 | g0273 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA18965 | hp2 | a0001 | c0003 | t0015 | g0362 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA18966 | hp1 | a0001 | c0002 | t0002 | g0247 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA18966 | hp2 | a0001 | c0002 | t0002 | g0046 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA18967 | hp1 | a0001 | c0003 | t0002 | g0261 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0335 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA18971 | hp1 | a0001 | c0003 | t0002 | g0345 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0358 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA18977 | hp1 | a0001 | c0004 | t0002 | g0107 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA18979 | hp2 | a0001 | c0002 | t0002 | g0094 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA18982 | hp2 | a0001 | c0003 | t0002 | g0357 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0320 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA18990 | hp2 | a0001 | c0003 | t0002 | g0338 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA19000 | hp2 | a0001 | c0002 | t0002 | g0186 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA19002 | hp1 | a0001 | c0004 | t0002 | g0106 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0350 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA19005 | hp1 | a0001 | c0003 | t0002 | g0312 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA19009 | hp1 | a0001 | c0004 | t0002 | g0083 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA19009 | hp2 | a0001 | c0002 | t0002 | g0067 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0364 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | LWK | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0228 | AFR | LWK | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA19054 | hp1 | a0001 | c0003 | t0002 | g0002 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA19056 | hp1 | a0001 | c0002 | t0002 | g0074 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA19059 | hp1 | a0001 | c0003 | t0002 | g0086 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA19060 | hp2 | a0001 | c0002 | t0002 | g0192 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA19064 | hp2 | a0001 | c0002 | t0002 | g0242 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA19065 | hp2 | a0005 | c0016 | t0001 | g0016 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA19066 | hp2 | a0001 | c0003 | t0002 | g0253 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA19068 | hp2 | a0001 | c0001 | t0013 | g0017 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA19074 | hp2 | a0001 | c0003 | t0002 | g0360 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA19080 | hp1 | a0001 | c0003 | t0002 | g0084 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA19082 | hp2 | a0001 | c0002 | t0002 | g0266 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA19084 | hp2 | a0001 | c0003 | t0002 | g0348 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA19085 | hp1 | a0001 | c0003 | t0002 | g0328 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA19087 | hp2 | a0001 | c0003 | t0002 | g0325 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA19089 | hp2 | a0001 | c0003 | t0002 | g0349 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA19240 | hp1 | a0001 | c0002 | t0002 | g0141 | AFR | YRI | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | YRI | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA20129 | hp1 | a0001 | c0002 | t0002 | g0207 | AFR | ASW | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ASW | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0294 | EUR | TSI | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0147 | EUR | TSI | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0354 | EUR | TSI | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0256 | EUR | TSI | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0047 | SAS | GIH | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0296 | SAS | GIH | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02109 | hp2 | a0001 | c0002 | t0002 | g0301 | AFR | ACB | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02486 | hp1 | a0001 | c0002 | t0002 | g0288 | AFR | ACB | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02486 | hp2 | a0001 | c0002 | t0002 | g0211 | AFR | ACB | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02559 | hp1 | a0003 | c0019 | t0001 | g0118 | AFR | ACB | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | ACB | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | MSL | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG03471 | hp2 | a0001 | c0002 | t0002 | g0311 | AFR | MSL | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | USA | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| HG06807 | hp2 | a0001 | c0002 | t0002 | g0013 | AFR | USA | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA18955 | hp1 | a0001 | c0001 | t0009 | g0070 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | USA | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA20300 | hp2 | a0001 | c0002 | t0002 | g0284 | AFR | USA | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| NA21309 | hp2 | a0001 | c0006 | t0001 | g0026 | AFR | LWK | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0262 | REF | REF | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0002 | g0148 | REF | REF | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:48405155 | G | A | 1 | a0002 | 1 | HG00408.hp1 | missense_variant | MODERATE | c.887G>A | p.Gly296Glu | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/14 | 1393/5511 | 887/4011 | 296/1336 | chr19 | 48405155 | |||
| chr19:48442871 | C | T | 1 | a0003 | 1 | HG02559.hp1 | missense_variant | MODERATE | c.2945C>T | p.Ala982Val | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 14/14 | 3451/5511 | 2945/4011 | 982/1336 | chr19 | 48442871 | |||
| chr19:48443623 | CCGCACCG others(11): Show |
C | 1 | a0005 | 1 | NA19065.hp2 | conservative_inframe_deletion | MODERATE | c.3706_3723delCCGCGG others(12): Show |
p.Pro1236_Arg1241del | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 14/14 | 4212/5511 | 3706/4011 | 1236/1336 | INFO_REALIGN_3_PRIME | chr19 | 48443623 | ||
| chr19:48443875 | G | A | 1 | a0004 | 1 | HG03710.hp1 | missense_variant | MODERATE | c.3949G>A | p.Gly1317Ser | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 14/14 | 4455/5511 | 3949/4011 | 1317/1336 | chr19 | 48443875 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:48398806 | G | A | 2 | a0001c0007 a0001c0012 |
3 | HG00733.hp1 HG01433.hp2 HG03579.hp2 |
synonymous_variant | LOW | c.414G>A | p.Ser138Ser | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/14 | 920/5511 | 414/4011 | 138/1336 | chr19 | 48398806 | |||
| chr19:48404823 | G | A | 1 | a0001c0013 | 1 | NA18956.hp2 | synonymous_variant | LOW | c.555G>A | p.Thr185Thr | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/14 | 1061/5511 | 555/4011 | 185/1336 | chr19 | 48404823 | |||
| chr19:48404887 | C | T | 1 | a0001c0011 | 2 | HG01167.hp2 HG01169.hp1 |
synonymous_variant | LOW | c.619C>T | p.Leu207Leu | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/14 | 1125/5511 | 619/4011 | 207/1336 | chr19 | 48404887 | |||
| chr19:48404991 | G | T | 1 | a0001c0023 | 1 | HG00140.hp2 | synonymous_variant | LOW | c.723G>T | p.Ala241Ala | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/14 | 1229/5511 | 723/4011 | 241/1336 | chr19 | 48404991 | |||
| chr19:48414561 | G | A | 1 | a0001c0015 | 1 | HG00558.hp1 | synonymous_variant | LOW | c.1389G>A | p.Arg463Arg | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 6/14 | 1895/5511 | 1389/4011 | 463/1336 | chr19 | 48414561 | |||
| chr19:48414900 | C | T | 3 | a0001c0003 a0001c0005 a0001c0022 |
42 | HG00099.hp2 HG00597.hp1 HG00609.hp2 others(39): Show |
synonymous_variant | LOW | c.1449C>T | p.Cys483Cys | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 7/14 | 1955/5511 | 1449/4011 | 483/1336 | chr19 | 48414900 | |||
| chr19:48415002 | C | T | 1 | a0001c0006 | 3 | HG00642.hp2 HG01496.hp1 NA21309.hp2 |
synonymous_variant | LOW | c.1551C>T | p.Ile517Ile | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 7/14 | 2057/5511 | 1551/4011 | 517/1336 | chr19 | 48415002 | |||
| chr19:48441787 | C | T | 1 | a0001c0021 | 1 | HG00741.hp1 | synonymous_variant | LOW | c.2271C>T | p.Ile757Ile | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 12/14 | 2777/5511 | 2271/4011 | 757/1336 | chr19 | 48441787 | |||
| chr19:48442623 | T | C | 16 | a0001c0001 a0001c0004 a0001c0005 others(13): Show |
261 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(258): Show |
synonymous_variant | LOW | c.2697T>C | p.Ala899Ala | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 14/14 | 3203/5511 | 2697/4011 | 899/1336 | chr19 | 48442623 | |||
| chr19:48442836 | G | A | 1 | a0001c0008 | 2 | HG00639.hp2 HG01358.hp2 |
synonymous_variant | LOW | c.2910G>A | p.Pro970Pro | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 14/14 | 3416/5511 | 2910/4011 | 970/1336 | chr19 | 48442836 | |||
| chr19:48443068 | T | C | 14 | a0001c0001 a0001c0005 a0001c0006 others(11): Show |
248 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(245): Show |
synonymous_variant | LOW | c.3142T>C | p.Leu1048Leu | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 14/14 | 3648/5511 | 3142/4011 | 1048/1336 | chr19 | 48443068 | |||
| chr19:48443148 | A | G | 14 | a0001c0001 a0001c0005 a0001c0006 others(11): Show |
248 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(245): Show |
synonymous_variant | LOW | c.3222A>G | p.Pro1074Pro | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 14/14 | 3728/5511 | 3222/4011 | 1074/1336 | chr19 | 48443148 | |||
| chr19:48443172 | G | C | 1 | a0001c0009 | 2 | HG02622.hp1 HG03486.hp1 |
synonymous_variant | LOW | c.3246G>C | p.Thr1082Thr | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 14/14 | 3752/5511 | 3246/4011 | 1082/1336 | chr19 | 48443172 | |||
| chr19:48443373 | C | T | 1 | a0001c0018 | 1 | NA18945.hp1 | synonymous_variant | LOW | c.3447C>T | p.Pro1149Pro | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 14/14 | 3953/5511 | 3447/4011 | 1149/1336 | chr19 | 48443373 | |||
| chr19:48443778 | G | C | 1 | a0001c0020 | 1 | HG03704.hp1 | synonymous_variant | LOW | c.3852G>C | p.Ala1284Ala | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 14/14 | 4358/5511 | 3852/4011 | 1284/1336 | chr19 | 48443778 | |||
| chr19:48443805 | C | T | 1 | a0001c0010 | 2 | HG02895.hp1 HG02897.hp1 |
synonymous_variant | LOW | c.3879C>T | p.His1293His | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 14/14 | 4385/5511 | 3879/4011 | 1293/1336 | chr19 | 48443805 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:48393745 | C | CGCCGCCG others(39): Show |
1 | a0001c0003t0015 | 1 | NA18965.hp2 | 5_prime_UTR_variant | MODIFIER | c.-428_-383dupGCCGCC others(40): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 1/14 | 4601 | INFO_REALIGN_3_PRIME | chr19 | 48393745 | |||||
| chr19:48393806 | G | T | 3 | a0001c0001t0004 a0001c0007t0004 a0001c0012t0014 |
3 | HG00733.hp1 HG01433.hp2 HG03540.hp2 |
5_prime_UTR_variant | MODIFIER | c.-368G>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 1/14 | 4587 | chr19 | 48393806 | ||||||
| chr19:48393833 | C | T | 1 | a0001c0001t0013 | 1 | NA19068.hp2 | 5_prime_UTR_variant | MODIFIER | c.-341C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 1/14 | 4560 | chr19 | 48393833 | ||||||
| chr19:48393835 | C | T | 1 | a0001c0002t0012 | 1 | HG02056.hp1 | 5_prime_UTR_variant | MODIFIER | c.-339C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 1/14 | 4558 | chr19 | 48393835 | ||||||
| chr19:48394682 | G | A | 1 | a0001c0001t0005 | 1 | HG02523.hp1 | 5_prime_UTR_variant | MODIFIER | c.-281G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 2/14 | 3711 | chr19 | 48394682 | ||||||
| chr19:48394826 | G | A | 2 | a0001c0001t0006 a0001c0002t0003 |
3 | HG01243.hp1 HG03209.hp1 HG03225.hp1 |
5_prime_UTR_variant | MODIFIER | c.-137G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 2/14 | 3567 | chr19 | 48394826 | ||||||
| chr19:48394838 | C | T | 2 | a0001c0001t0010 a0001c0001t0011 |
2 | HG02257.hp1 NA18906.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-125C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 2/14 | chr19 | 48394838 | |||||||
| chr19:48394853 | T | C | 4 | a0001c0001t0004 a0001c0007t0004 a0001c0007t0007 others(1): Show |
4 | HG00733.hp1 HG01433.hp2 HG03540.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-110T>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 2/14 | 3540 | chr19 | 48394853 | ||||||
| chr19:48444069 | G | T | 19 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(16): Show |
183 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*132G>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 14/14 | 132 | chr19 | 48444069 | ||||||
| chr19:48444108 | G | C | 1 | a0001c0001t0008 | 1 | HG02293.hp1 | 3_prime_UTR_variant | MODIFIER | c.*171G>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 14/14 | 171 | chr19 | 48444108 | ||||||
| chr19:48444249 | C | T | 1 | a0001c0001t0009 | 1 | NA18955.hp1 | 3_prime_UTR_variant | MODIFIER | c.*312C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 14/14 | 312 | chr19 | 48444249 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:48393986 | C | A | 106 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(103): Show |
106 | HG00099.hp2 HG00280.hp2 HG00621.hp2 others(103): Show |
intron_variant | MODIFIER | c.-306+118C>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 1/13 | chr19 | 48393986 | |||||||
| chr19:48394009 | C | T | 6 | a0001c0001t0002g0103 a0001c0001t0002g0105 a0001c0001t0002g0108 others(3): Show |
6 | NA18941.hp1 NA18977.hp1 NA19002.hp1 others(3): Show |
intron_variant | MODIFIER | c.-306+141C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 1/13 | chr19 | 48394009 | |||||||
| chr19:48394022 | C | G | 7 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 others(4): Show |
7 | HG01261.hp1 HG02109.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.-306+154C>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 1/13 | chr19 | 48394022 | |||||||
| chr19:48394255 | A | G | 293 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(290): Show |
294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.-306+387A>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 1/13 | chr19 | 48394255 | |||||||
| chr19:48394317 | G | A | 1 | a0001c0001t0001g0177 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-305-341G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 1/13 | chr19 | 48394317 | |||||||
| chr19:48394322 | G | T | 10 | a0001c0001t0001g0175 a0001c0001t0001g0364 a0001c0001t0002g0358 others(7): Show |
10 | HG00597.hp1 HG01069.hp2 HG02300.hp1 others(7): Show |
intron_variant | MODIFIER | c.-305-336G>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 1/13 | chr19 | 48394322 | |||||||
| chr19:48394366 | G | A | 1 | a0001c0001t0001g0176 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-305-292G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 1/13 | chr19 | 48394366 | |||||||
| chr19:48394460 | T | G | 1 | a0001c0001t0001g0177 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-305-198T>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 1/13 | chr19 | 48394460 | |||||||
| chr19:48394529 | G | C | 2 | a0001c0003t0002g0356 a0001c0003t0002g0357 |
2 | HG02300.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.-305-129G>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 1/13 | chr19 | 48394529 | |||||||
| chr19:48394603 | G | A | 7 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(4): Show |
7 | HG01243.hp1 HG02055.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.-305-55G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 1/13 | chr19 | 48394603 | |||||||
| chr19:48394959 | A | G | 1 | a0001c0001t0001g0174 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-27+23A>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 2/13 | chr19 | 48394959 | |||||||
| chr19:48394990 | T | A | 1 | a0001c0002t0002g0178 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-27+54T>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 2/13 | chr19 | 48394990 | |||||||
| chr19:48395017 | C | A | 123 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0175 others(120): Show |
123 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.-27+81C>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 2/13 | chr19 | 48395017 | |||||||
| chr19:48395101 | CCT | C | 5 | a0001c0001t0001g0294 a0001c0001t0002g0295 a0001c0001t0002g0296 others(2): Show |
5 | HG02683.hp2 HG03239.hp2 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.-27+175_-27+176del others(2): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 48395101 | ||||||
| chr19:48395291 | G | C | 14 | a0001c0001t0001g0177 a0001c0001t0001g0303 a0001c0001t0002g0179 others(11): Show |
14 | HG00733.hp1 HG01167.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.-27+355G>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 2/13 | chr19 | 48395291 | |||||||
| chr19:48395295 | C | A | 1 | a0001c0002t0002g0311 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-27+359C>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 2/13 | chr19 | 48395295 | |||||||
| chr19:48395295 | C | T | 138 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(135): Show |
139 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.-27+359C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 2/13 | chr19 | 48395295 | |||||||
| chr19:48395518 | G | T | 1 | a0001c0001t0001g0095 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-27+582G>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 2/13 | chr19 | 48395518 | |||||||
| chr19:48395529 | C | T | 11 | a0001c0001t0001g0173 a0001c0001t0001g0285 a0001c0001t0001g0286 others(8): Show |
11 | HG02055.hp1 HG02258.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-27+593C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 2/13 | chr19 | 48395529 | |||||||
| chr19:48395548 | C | T | 1 | a0001c0001t0001g0172 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-27+612C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 2/13 | chr19 | 48395548 | |||||||
| chr19:48395562 | G | C | 1 | a0001c0001t0002g0180 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-27+626G>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 2/13 | chr19 | 48395562 | |||||||
| chr19:48395768 | G | C | 183 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(180): Show |
185 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(182): Show |
intron_variant | MODIFIER | c.-27+832G>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 2/13 | chr19 | 48395768 | |||||||
| chr19:48395854 | G | A | 1 | a0001c0001t0002g0320 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-27+918G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 2/13 | chr19 | 48395854 | |||||||
| chr19:48395960 | G | A | 1 | a0001c0003t0002g0361 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-27+1024G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 2/13 | chr19 | 48395960 | |||||||
| chr19:48396040 | T | C | 16 | a0001c0001t0001g0294 a0001c0001t0002g0029 a0001c0001t0002g0295 others(13): Show |
16 | HG00140.hp1 HG02258.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.-27+1104T>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 2/13 | chr19 | 48396040 | |||||||
| chr19:48396062 | C | T | 1 | a0001c0001t0001g0203 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-27+1126C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 2/13 | chr19 | 48396062 | |||||||
| chr19:48396067 | T | A | 1 | a0001c0001t0002g0030 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-27+1131T>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 2/13 | chr19 | 48396067 | |||||||
| chr19:48396104 | G | A | 1 | a0001c0003t0015g0362 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-27+1168G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 2/13 | chr19 | 48396104 | |||||||
| chr19:48396112 | T | C | 1 | a0001c0001t0001g0175 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-27+1176T>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 2/13 | chr19 | 48396112 | |||||||
| chr19:48396113 | T | C | 3 | a0001c0002t0002g0301 a0001c0011t0002g0299 a0001c0011t0002g0300 |
3 | HG01167.hp2 HG01169.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.-27+1177T>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 2/13 | chr19 | 48396113 | |||||||
| chr19:48396177 | G | A | 9 | a0001c0001t0001g0294 a0001c0001t0002g0295 a0001c0001t0002g0296 others(6): Show |
9 | HG00140.hp1 HG02683.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.-27+1241G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 2/13 | chr19 | 48396177 | |||||||
| chr19:48396191 | G | A | 120 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(117): Show |
120 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(117): Show |
intron_variant | MODIFIER | c.-27+1255G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 2/13 | chr19 | 48396191 | |||||||
| chr19:48396297 | G | C | 124 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(121): Show |
124 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(121): Show |
intron_variant | MODIFIER | c.-27+1361G>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 2/13 | chr19 | 48396297 | |||||||
| chr19:48396368 | G | A | 1 | a0001c0002t0002g0288 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-27+1432G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 2/13 | chr19 | 48396368 | |||||||
| chr19:48396423 | G | C | 3 | a0001c0002t0002g0301 a0001c0011t0002g0299 a0001c0011t0002g0300 |
3 | HG01167.hp2 HG01169.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.-27+1487G>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 2/13 | chr19 | 48396423 | |||||||
| chr19:48396462 | G | A | 1 | a0001c0012t0014g0302 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-27+1526G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 2/13 | chr19 | 48396462 | |||||||
| chr19:48396784 | G | C | 2 | a0001c0002t0002g0282 a0001c0002t0002g0283 |
2 | HG02723.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-26-1583G>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 2/13 | chr19 | 48396784 | |||||||
| chr19:48396797 | T | A | 1 | a0001c0001t0002g0030 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-26-1570T>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 2/13 | chr19 | 48396797 | |||||||
| chr19:48396801 | C | G | 4 | a0001c0001t0001g0350 a0001c0001t0001g0352 a0001c0004t0002g0351 others(1): Show |
4 | HG01975.hp2 HG02273.hp2 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.-26-1566C>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 2/13 | chr19 | 48396801 | |||||||
| chr19:48397011 | G | A | 11 | a0001c0001t0001g0294 a0001c0001t0002g0029 a0001c0001t0002g0295 others(8): Show |
11 | HG00140.hp1 HG02258.hp2 HG02683.hp2 others(8): Show |
intron_variant | MODIFIER | c.-26-1356G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 2/13 | chr19 | 48397011 | |||||||
| chr19:48397049 | C | T | 2 | a0001c0001t0002g0029 a0001c0002t0002g0028 |
2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-26-1318C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 2/13 | chr19 | 48397049 | |||||||
| chr19:48397237 | G | A | 36 | a0001c0001t0001g0340 a0001c0001t0001g0342 a0001c0001t0001g0344 others(33): Show |
37 | HG00423.hp1 HG00597.hp1 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.-26-1130G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 2/13 | chr19 | 48397237 | |||||||
| chr19:48397378 | C | T | 6 | a0001c0001t0002g0103 a0001c0001t0002g0105 a0001c0001t0002g0108 others(3): Show |
6 | NA18941.hp1 NA18977.hp1 NA19002.hp1 others(3): Show |
intron_variant | MODIFIER | c.-26-989C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 2/13 | chr19 | 48397378 | |||||||
| chr19:48397384 | C | T | 1 | a0001c0002t0012g0092 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-26-983C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 2/13 | chr19 | 48397384 | |||||||
| chr19:48397394 | T | C | 1 | a0001c0001t0001g0294 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-26-973T>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 2/13 | chr19 | 48397394 | |||||||
| chr19:48397575 | T | C | 1 | a0003c0019t0001g0118 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-26-792T>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 2/13 | chr19 | 48397575 | |||||||
| chr19:48397704 | C | T | 8 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0087 others(5): Show |
8 | HG00639.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.-26-663C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 2/13 | chr19 | 48397704 | |||||||
| chr19:48398869 | C | A | 1 | a0001c0001t0001g0212 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.465+12C>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48398869 | |||||||
| chr19:48398879 | C | T | 1 | a0001c0001t0001g0202 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.465+22C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48398879 | |||||||
| chr19:48398930 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0002g0024 |
2 | HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.465+73C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48398930 | |||||||
| chr19:48399003 | G | A | 1 | a0001c0001t0001g0005 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.465+146G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48399003 | |||||||
| chr19:48399081 | G | A | 2 | a0001c0004t0002g0213 a0001c0004t0002g0214 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.465+224G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48399081 | |||||||
| chr19:48399128 | T | C | 1 | a0001c0001t0001g0215 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.465+271T>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48399128 | |||||||
| chr19:48399257 | A | C | 3 | a0001c0001t0001g0279 a0001c0004t0002g0280 a0001c0004t0002g0281 |
3 | HG01891.hp1 HG02145.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.465+400A>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48399257 | |||||||
| chr19:48399373 | G | A | 11 | a0001c0001t0001g0294 a0001c0001t0002g0029 a0001c0001t0002g0295 others(8): Show |
11 | HG00140.hp1 HG02258.hp2 HG02683.hp2 others(8): Show |
intron_variant | MODIFIER | c.465+516G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48399373 | |||||||
| chr19:48399400 | T | C | 2 | a0001c0001t0002g0179 a0001c0002t0002g0284 |
2 | HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.465+543T>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48399400 | |||||||
| chr19:48399678 | G | A | 2 | a0001c0004t0002g0213 a0001c0004t0002g0214 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.465+821G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48399678 | |||||||
| chr19:48399744 | A | AAG | 279 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(276): Show |
280 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.465+888_465+889dup others(2): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 48399744 | ||||||
| chr19:48399747 | T | C | 1 | a0001c0002t0002g0013 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.465+890T>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48399747 | |||||||
| chr19:48399888 | G | C | 1 | a0001c0004t0002g0274 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.465+1031G>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48399888 | |||||||
| chr19:48399889 | C | T | 3 | a0001c0002t0002g0301 a0001c0011t0002g0299 a0001c0011t0002g0300 |
3 | HG01167.hp2 HG01169.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.465+1032C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48399889 | |||||||
| chr19:48400028 | G | C | 1 | a0001c0001t0002g0119 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.465+1171G>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48400028 | |||||||
| chr19:48400130 | G | A | 3 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0315 |
3 | NA18948.hp1 NA18983.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.465+1273G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48400130 | |||||||
| chr19:48400298 | A | G | 1 | a0001c0015t0002g0318 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.465+1441A>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48400298 | |||||||
| chr19:48400480 | G | A | 1 | a0001c0002t0002g0194 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.465+1623G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48400480 | |||||||
| chr19:48400577 | C | G | 1 | a0001c0002t0002g0284 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.465+1720C>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48400577 | |||||||
| chr19:48400602 | G | T | 5 | a0001c0003t0002g0084 a0001c0003t0002g0085 a0001c0003t0002g0086 others(2): Show |
5 | NA18747.hp2 NA18959.hp2 NA19009.hp1 others(2): Show |
intron_variant | MODIFIER | c.465+1745G>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48400602 | |||||||
| chr19:48400756 | C | A | 1 | a0001c0001t0001g0279 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.465+1899C>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48400756 | |||||||
| chr19:48400982 | G | A | 5 | a0001c0001t0001g0195 a0001c0001t0001g0218 a0001c0001t0001g0219 others(2): Show |
5 | HG00642.hp1 HG01109.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+2125G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48400982 | |||||||
| chr19:48401081 | C | CA | 14 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0225 others(11): Show |
14 | HG00621.hp1 HG01884.hp2 HG02135.hp2 others(11): Show |
intron_variant | MODIFIER | c.465+2240dupA | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 48401081 | ||||||
| chr19:48401081 | CA | C | 229 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(226): Show |
230 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.465+2240delA | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 48401081 | ||||||
| chr19:48401150 | G | A | 7 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(4): Show |
7 | HG01243.hp1 HG02055.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.465+2293G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48401150 | |||||||
| chr19:48401264 | G | A | 274 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(271): Show |
275 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.465+2407G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48401264 | |||||||
| chr19:48401265 | G | A | 276 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(273): Show |
277 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.465+2408G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48401265 | |||||||
| chr19:48401265 | GA | G | 6 | a0001c0001t0001g0164 a0001c0001t0001g0166 a0001c0001t0002g0167 others(3): Show |
6 | HG01346.hp1 HG02809.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.465+2415delA | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 48401265 | ||||||
| chr19:48401266 | A | G | 8 | a0001c0001t0001g0117 a0001c0001t0001g0168 a0001c0001t0001g0169 others(5): Show |
8 | HG01975.hp1 HG01978.hp1 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.465+2409A>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48401266 | |||||||
| chr19:48401267 | A | G | 6 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(3): Show |
6 | HG01975.hp1 HG01978.hp1 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.465+2410A>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48401267 | |||||||
| chr19:48401284 | A | C | 1 | a0001c0004t0002g0274 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.465+2427A>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48401284 | |||||||
| chr19:48401368 | T | A | 1 | a0001c0002t0002g0231 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.465+2511T>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48401368 | |||||||
| chr19:48401432 | C | G | 76 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(73): Show |
76 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.465+2575C>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48401432 | |||||||
| chr19:48401439 | C | T | 3 | a0001c0002t0002g0301 a0001c0011t0002g0299 a0001c0011t0002g0300 |
3 | HG01167.hp2 HG01169.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.465+2582C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48401439 | |||||||
| chr19:48401643 | G | A | 14 | a0001c0001t0001g0294 a0001c0001t0002g0029 a0001c0001t0002g0295 others(11): Show |
14 | HG00140.hp1 HG01167.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.465+2786G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48401643 | |||||||
| chr19:48401888 | G | A | 36 | a0001c0001t0001g0232 a0001c0001t0001g0303 a0001c0001t0001g0340 others(33): Show |
37 | HG00423.hp1 HG00597.hp1 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.466-2846G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48401888 | |||||||
| chr19:48402035 | G | A | 5 | a0001c0001t0001g0303 a0001c0002t0002g0304 a0001c0002t0002g0305 others(2): Show |
5 | HG01884.hp1 HG03041.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.466-2699G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48402035 | |||||||
| chr19:48402049 | G | A | 12 | a0001c0001t0001g0294 a0001c0001t0002g0295 a0001c0001t0002g0296 others(9): Show |
12 | HG00140.hp1 HG01167.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.466-2685G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48402049 | |||||||
| chr19:48402093 | TGAAA | T | 6 | a0001c0001t0001g0164 a0001c0001t0001g0166 a0001c0001t0002g0167 others(3): Show |
6 | HG01346.hp1 HG02809.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.466-2634_466-2631d others(6): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 48402093 | ||||||
| chr19:48402115 | G | GGAAA | 19 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0112 others(16): Show |
20 | HG00408.hp1 HG00558.hp2 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.466-2568_466-2565d others(6): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 48402115 | ||||||
| chr19:48402115 | G | GGAAAGAA others(1): Show |
16 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(13): Show |
16 | HG00280.hp1 HG00738.hp1 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.466-2572_466-2565d others(10): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 48402115 | ||||||
| chr19:48402115 | G | GGAAAGAA others(5): Show |
9 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0125 others(6): Show |
9 | HG00408.hp2 HG00741.hp2 HG03492.hp2 others(6): Show |
intron_variant | MODIFIER | c.466-2576_466-2565d others(14): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 48402115 | ||||||
| chr19:48402115 | G | GGAAAGAA others(9): Show |
1 | a0001c0002t0002g0283 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.466-2580_466-2565d others(18): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 48402115 | ||||||
| chr19:48402115 | G | GGAAAGAA others(13): Show |
3 | a0001c0001t0001g0166 a0001c0001t0002g0167 a0001c0002t0002g0109 |
3 | HG01346.hp1 HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.466-2584_466-2565d others(22): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 48402115 | ||||||
| chr19:48402115 | G | GGAAAGAA others(17): Show |
1 | a0001c0002t0002g0165 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.466-2588_466-2565d others(26): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 48402115 | ||||||
| chr19:48402115 | G | GGAAAGAA others(21): Show |
1 | a0001c0002t0002g0282 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.466-2592_466-2565d others(30): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 48402115 | ||||||
| chr19:48402115 | G | GGAAAGAA others(29): Show |
1 | a0001c0001t0001g0164 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.466-2600_466-2565d others(38): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 48402115 | ||||||
| chr19:48402115 | G | GGAAGAAA others(8): Show |
1 | a0001c0002t0002g0091 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.466-2616_466-2615i others(17): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 48402115 | ||||||
| chr19:48402115 | GGAAA | G | 32 | a0001c0001t0001g0014 a0001c0001t0001g0040 a0001c0001t0001g0075 others(29): Show |
32 | HG00099.hp1 HG00733.hp1 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.466-2568_466-2565d others(6): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 48402115 | ||||||
| chr19:48402115 | GGAAAGAA others(1): Show |
G | 141 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(138): Show |
142 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.466-2572_466-2565d others(10): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 48402115 | ||||||
| chr19:48402115 | GGAAAGAA others(5): Show |
G | 3 | a0001c0001t0011g0323 a0001c0002t0002g0316 a0001c0002t0002g0319 |
3 | HG02630.hp1 HG02818.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.466-2576_466-2565d others(14): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 48402115 | ||||||
| chr19:48402115 | GGAAAGAA others(9): Show |
G | 1 | a0001c0001t0001g0364 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.466-2580_466-2565d others(18): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 48402115 | ||||||
| chr19:48402115 | GGAAAGAA others(13): Show |
G | 3 | a0001c0001t0001g0123 a0001c0001t0001g0163 a0001c0001t0001g0236 |
3 | NA18956.hp1 NA18970.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.466-2584_466-2565d others(22): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 48402115 | ||||||
| chr19:48402115 | GGAAAGAA others(17): Show |
G | 8 | a0001c0001t0001g0294 a0001c0001t0002g0295 a0001c0001t0002g0296 others(5): Show |
8 | HG00140.hp1 HG02683.hp2 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.466-2588_466-2565d others(26): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 48402115 | ||||||
| chr19:48402115 | GGAAAGAA others(25): Show |
G | 1 | a0001c0002t0002g0314 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.466-2596_466-2565d others(34): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 48402115 | ||||||
| chr19:48402136 | G | T | 6 | a0001c0001t0001g0350 a0001c0002t0002g0229 a0001c0002t0002g0237 others(3): Show |
6 | HG00733.hp1 HG01433.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.466-2598G>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48402136 | |||||||
| chr19:48402140 | G | T | 129 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(126): Show |
130 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.466-2594G>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48402140 | |||||||
| chr19:48402144 | G | T | 3 | a0001c0001t0011g0323 a0001c0002t0002g0316 a0001c0002t0002g0319 |
3 | HG02630.hp1 HG02818.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.466-2590G>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48402144 | |||||||
| chr19:48402148 | G | T | 1 | a0001c0001t0001g0364 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.466-2586G>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48402148 | |||||||
| chr19:48402165 | A | AAAGAAAG others(8): Show |
1 | a0001c0001t0001g0124 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.466-2565_466-2564i others(17): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 48402165 | ||||||
| chr19:48402166 | A | AAGAAAGA others(3): Show |
1 | a0001c0001t0001g0097 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.466-2565_466-2564i others(12): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 48402166 | ||||||
| chr19:48402166 | A | AAGAAAGA others(29): Show |
2 | a0001c0002t0002g0284 a0001c0011t0002g0299 |
2 | HG01169.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.466-2565_466-2564i others(38): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 48402166 | ||||||
| chr19:48402166 | A | AAGAAAGA others(23): Show |
1 | a0001c0001t0002g0179 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.466-2565_466-2564i others(32): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 48402166 | ||||||
| chr19:48402166 | A | AAGAAAGA others(25): Show |
1 | a0001c0011t0002g0300 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.466-2565_466-2564i others(34): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 48402166 | ||||||
| chr19:48402166 | A | AAGAAAGA others(13): Show |
6 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0018 others(3): Show |
6 | HG00639.hp1 HG01358.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.466-2565_466-2564i others(22): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 48402166 | ||||||
| chr19:48402166 | A | AAGAAAGA others(9): Show |
3 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0096 |
3 | HG03098.hp1 NA18995.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.466-2565_466-2564i others(18): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 48402166 | ||||||
| chr19:48402166 | A | AAGAAAGA others(5): Show |
13 | a0001c0001t0001g0004 a0001c0001t0001g0048 a0001c0001t0001g0050 others(10): Show |
13 | HG01257.hp2 HG02015.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.466-2565_466-2564i others(14): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 48402166 | ||||||
| chr19:48402166 | A | AAGAAAGA others(1): Show |
22 | a0001c0001t0001g0011 a0001c0001t0001g0023 a0001c0001t0001g0031 others(19): Show |
22 | HG00609.hp1 HG00735.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.466-2565_466-2564i others(10): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 48402166 | ||||||
| chr19:48402166 | A | AAGAG | 32 | a0001c0001t0001g0021 a0001c0001t0001g0033 a0001c0001t0001g0034 others(29): Show |
32 | HG00280.hp2 HG00621.hp2 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.466-2564_466-2561d others(6): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 48402166 | ||||||
| chr19:48402166 | A | G | 190 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(187): Show |
191 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.466-2568A>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48402166 | |||||||
| chr19:48402545 | G | A | 1 | a0001c0002t0012g0092 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.466-2189G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48402545 | |||||||
| chr19:48402580 | A | G | 15 | a0001c0001t0001g0051 a0001c0001t0001g0294 a0001c0001t0002g0029 others(12): Show |
15 | HG00140.hp1 HG01167.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.466-2154A>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48402580 | |||||||
| chr19:48402675 | C | T | 4 | a0001c0001t0001g0134 a0001c0002t0002g0135 a0001c0002t0002g0141 others(1): Show |
4 | HG00280.hp1 HG01891.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.466-2059C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48402675 | |||||||
| chr19:48402723 | C | CA | 70 | a0001c0001t0001g0112 a0001c0001t0001g0117 a0001c0001t0001g0124 others(67): Show |
70 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.466-1987dupA | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 48402723 | ||||||
| chr19:48402723 | C | CAA | 10 | a0001c0001t0001g0081 a0001c0001t0001g0136 a0001c0001t0001g0168 others(7): Show |
10 | HG00423.hp2 HG01099.hp1 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.466-1988_466-1987d others(4): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 48402723 | ||||||
| chr19:48402723 | C | CAAA | 10 | a0001c0001t0001g0294 a0001c0001t0002g0029 a0001c0001t0002g0295 others(7): Show |
10 | HG00140.hp1 HG02258.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.466-1989_466-1987d others(5): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 48402723 | ||||||
| chr19:48402723 | CA | C | 129 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(126): Show |
129 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(126): Show |
intron_variant | MODIFIER | c.466-1987delA | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 48402723 | ||||||
| chr19:48402723 | CAA | C | 44 | a0001c0001t0001g0289 a0001c0001t0001g0340 a0001c0001t0001g0342 others(41): Show |
45 | HG00099.hp2 HG00423.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.466-1988_466-1987d others(4): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 48402723 | ||||||
| chr19:48402765 | C | CGA | 24 | a0001c0001t0001g0015 a0001c0001t0001g0058 a0001c0001t0001g0075 others(21): Show |
24 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.466-1930_466-1929d others(4): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 48402765 | ||||||
| chr19:48402765 | C | CGAGA | 16 | a0001c0001t0001g0018 a0001c0001t0001g0044 a0001c0001t0001g0098 others(13): Show |
16 | HG00408.hp1 HG01099.hp2 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.466-1932_466-1929d others(6): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 48402765 | ||||||
| chr19:48402765 | C | CGAGAGA | 27 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(24): Show |
27 | HG01243.hp2 HG01261.hp1 HG02040.hp2 others(24): Show |
intron_variant | MODIFIER | c.466-1934_466-1929d others(8): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 48402765 | ||||||
| chr19:48402765 | C | CGAGAGAG others(1): Show |
29 | a0001c0001t0001g0012 a0001c0001t0001g0023 a0001c0001t0001g0031 others(26): Show |
29 | HG00099.hp2 HG00609.hp1 HG01257.hp2 others(26): Show |
intron_variant | MODIFIER | c.466-1936_466-1929d others(10): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 48402765 | ||||||
| chr19:48402765 | C | CGAGAGAG others(3): Show |
22 | a0001c0001t0001g0034 a0001c0001t0001g0050 a0001c0001t0001g0054 others(19): Show |
22 | HG00280.hp2 HG00621.hp2 HG01258.hp1 others(19): Show |
intron_variant | MODIFIER | c.466-1938_466-1929d others(12): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 48402765 | ||||||
| chr19:48402765 | C | CGAGAGAG others(5): Show |
11 | a0001c0001t0001g0032 a0001c0001t0001g0064 a0001c0001t0001g0065 others(8): Show |
11 | HG00738.hp2 HG01256.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.466-1940_466-1929d others(14): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 48402765 | ||||||
| chr19:48402765 | C | CGAGAGAG others(7): Show |
4 | a0001c0001t0001g0071 a0001c0001t0001g0087 a0001c0001t0002g0056 others(1): Show |
4 | HG00639.hp1 HG00735.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.466-1942_466-1929d others(16): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 48402765 | ||||||
| chr19:48402765 | C | CGAGAGAG others(9): Show |
3 | a0001c0001t0001g0175 a0001c0001t0002g0035 a0001c0004t0002g0281 |
3 | HG02976.hp1 HG03130.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.466-1944_466-1929d others(18): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 48402765 | ||||||
| chr19:48402765 | CGA | C | 10 | a0001c0001t0001g0134 a0001c0001t0001g0164 a0001c0001t0001g0166 others(7): Show |
10 | HG00280.hp1 HG00558.hp1 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.466-1930_466-1929d others(4): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 48402765 | ||||||
| chr19:48402765 | CGAGA | C | 18 | a0001c0001t0001g0129 a0001c0001t0001g0144 a0001c0001t0001g0200 others(15): Show |
19 | HG00140.hp2 HG00423.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.466-1932_466-1929d others(6): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 48402765 | ||||||
| chr19:48402765 | CGAGAGA | C | 51 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0081 others(48): Show |
51 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.466-1934_466-1929d others(8): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 48402765 | ||||||
| chr19:48402765 | CGAGAGAG others(1): Show |
C | 72 | a0001c0001t0001g0010 a0001c0001t0001g0177 a0001c0001t0001g0195 others(69): Show |
72 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.466-1936_466-1929d others(10): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 48402765 | ||||||
| chr19:48402765 | CGAGAGAG others(3): Show |
C | 6 | a0001c0001t0001g0101 a0001c0001t0001g0275 a0001c0001t0001g0278 others(3): Show |
6 | HG00408.hp2 HG02109.hp1 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.466-1938_466-1929d others(12): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 48402765 | ||||||
| chr19:48402765 | CGAGAGAG others(5): Show |
C | 11 | a0001c0001t0001g0294 a0001c0001t0002g0029 a0001c0001t0002g0295 others(8): Show |
11 | HG00140.hp1 HG02258.hp2 HG02683.hp2 others(8): Show |
intron_variant | MODIFIER | c.466-1940_466-1929d others(14): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 48402765 | ||||||
| chr19:48402765 | CGAGAGAG others(7): Show |
C | 1 | a0001c0002t0002g0041 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.466-1942_466-1929d others(16): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 48402765 | ||||||
| chr19:48402765 | CGAGAGAG others(13): Show |
C | 1 | a0001c0001t0002g0321 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.466-1948_466-1929d others(22): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 48402765 | ||||||
| chr19:48402802 | G | A | 5 | a0001c0001t0001g0272 a0001c0001t0001g0286 a0001c0001t0010g0322 others(2): Show |
5 | HG02055.hp1 HG02257.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-1932G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48402802 | |||||||
| chr19:48403060 | G | A | 5 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0243 others(2): Show |
5 | NA18975.hp1 NA18982.hp1 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.466-1674G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48403060 | |||||||
| chr19:48403125 | G | A | 1 | a0001c0001t0001g0245 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.466-1609G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48403125 | |||||||
| chr19:48403198 | C | CA | 11 | a0001c0001t0001g0112 a0001c0001t0001g0128 a0001c0001t0001g0130 others(8): Show |
11 | HG01361.hp2 HG02451.hp1 HG03471.hp2 others(8): Show |
intron_variant | MODIFIER | c.466-1511dupA | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 48403198 | ||||||
| chr19:48403198 | CA | C | 28 | a0001c0001t0001g0081 a0001c0001t0001g0166 a0001c0001t0001g0196 others(25): Show |
28 | HG00609.hp2 HG01070.hp2 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.466-1511delA | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 48403198 | ||||||
| chr19:48403198 | CAA | C | 117 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(114): Show |
118 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.466-1512_466-1511d others(4): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 48403198 | ||||||
| chr19:48403198 | CAAA | C | 10 | a0001c0001t0001g0245 a0001c0001t0001g0269 a0001c0001t0001g0279 others(7): Show |
10 | HG00733.hp1 HG01167.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.466-1513_466-1511d others(5): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 48403198 | ||||||
| chr19:48403198 | CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0001g0187 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.466-1524_466-1511d others(16): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 48403198 | ||||||
| chr19:48403198 | CAAAAAAA others(8): Show |
C | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(100): Show |
103 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.466-1525_466-1511d others(17): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 48403198 | ||||||
| chr19:48403230 | A | G | 270 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(267): Show |
271 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.466-1504A>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48403230 | |||||||
| chr19:48403262 | T | C | 9 | a0001c0001t0001g0294 a0001c0001t0002g0295 a0001c0001t0002g0296 others(6): Show |
9 | HG00140.hp1 HG02683.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.466-1472T>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48403262 | |||||||
| chr19:48403336 | T | C | 3 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0289 |
3 | NA19003.hp1 NA19059.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.466-1398T>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48403336 | |||||||
| chr19:48403374 | T | G | 1 | a0001c0003t0002g0357 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.466-1360T>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48403374 | |||||||
| chr19:48403436 | T | G | 78 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(75): Show |
78 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.466-1298T>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48403436 | |||||||
| chr19:48403454 | G | A | 8 | a0001c0001t0001g0145 a0001c0001t0001g0153 a0001c0001t0001g0154 others(5): Show |
8 | HG00639.hp2 HG00642.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.466-1280G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48403454 | |||||||
| chr19:48403503 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.466-1231G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48403503 | |||||||
| chr19:48403555 | A | T | 1 | a0001c0003t0002g0078 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.466-1179A>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48403555 | |||||||
| chr19:48403618 | T | G | 1 | a0001c0001t0001g0101 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.466-1116T>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48403618 | |||||||
| chr19:48404000 | G | A | 2 | a0001c0001t0002g0295 a0001c0001t0002g0296 |
2 | HG03239.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.466-734G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48404000 | |||||||
| chr19:48404026 | G | T | 129 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(126): Show |
130 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.466-708G>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48404026 | |||||||
| chr19:48404132 | C | T | 2 | a0001c0002t0002g0316 a0001c0002t0002g0319 |
2 | HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.466-602C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48404132 | |||||||
| chr19:48404172 | G | A | 8 | a0001c0001t0001g0225 a0001c0001t0002g0180 a0001c0001t0002g0222 others(5): Show |
8 | HG01884.hp2 HG02622.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.466-562G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48404172 | |||||||
| chr19:48404186 | G | A | 4 | a0001c0001t0001g0340 a0001c0001t0001g0342 a0001c0002t0002g0339 others(1): Show |
4 | HG01109.hp1 HG02738.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.466-548G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48404186 | |||||||
| chr19:48404212 | T | C | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(104): Show |
107 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(104): Show |
intron_variant | MODIFIER | c.466-522T>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48404212 | |||||||
| chr19:48404240 | C | CA | 38 | a0001c0001t0001g0164 a0001c0001t0001g0166 a0001c0001t0001g0217 others(35): Show |
38 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(35): Show |
intron_variant | MODIFIER | c.466-476dupA | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 48404240 | ||||||
| chr19:48404240 | CA | C | 119 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(116): Show |
120 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.466-476delA | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 48404240 | ||||||
| chr19:48404241 | A | C | 2 | a0001c0002t0002g0229 a0001c0002t0002g0237 |
2 | HG02738.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.466-493A>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48404241 | |||||||
| chr19:48404399 | A | G | 1 | a0004c0017t0001g0115 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.466-335A>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48404399 | |||||||
| chr19:48404507 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.466-227C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48404507 | |||||||
| chr19:48404564 | G | C | 79 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(76): Show |
79 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.466-170G>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48404564 | |||||||
| chr19:48404634 | G | A | 1 | a0001c0001t0001g0163 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.466-100G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48404634 | |||||||
| chr19:48404692 | C | T | 3 | a0001c0007t0004g0309 a0001c0007t0007g0310 a0001c0012t0014g0302 |
3 | HG00733.hp1 HG01433.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.466-42C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48404692 | |||||||
| chr19:48405374 | AG | A | 130 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(127): Show |
130 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(127): Show |
intron_variant | MODIFIER | c.1085+25delG | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 48405374 | ||||||
| chr19:48405614 | G | A | 8 | a0001c0001t0001g0225 a0001c0001t0002g0180 a0001c0001t0002g0222 others(5): Show |
8 | HG01884.hp2 HG02622.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1085+261G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48405614 | |||||||
| chr19:48405632 | G | A | 13 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0163 others(10): Show |
13 | HG00408.hp2 HG00621.hp1 HG02155.hp2 others(10): Show |
intron_variant | MODIFIER | c.1085+279G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48405632 | |||||||
| chr19:48406086 | T | C | 138 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(135): Show |
138 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(135): Show |
intron_variant | MODIFIER | c.1085+733T>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48406086 | |||||||
| chr19:48406154 | C | T | 1 | a0001c0002t0002g0178 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1085+801C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48406154 | |||||||
| chr19:48406176 | G | A | 42 | a0001c0001t0001g0340 a0001c0001t0001g0342 a0001c0001t0001g0344 others(39): Show |
43 | HG00423.hp1 HG00597.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.1085+823G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48406176 | |||||||
| chr19:48406290 | G | A | 1 | a0001c0001t0002g0061 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1085+937G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48406290 | |||||||
| chr19:48406346 | A | G | 6 | a0001c0001t0001g0303 a0001c0002t0002g0077 a0001c0002t0002g0304 others(3): Show |
6 | HG01884.hp1 HG02886.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1085+993A>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48406346 | |||||||
| chr19:48406357 | A | G | 1 | a0001c0008t0001g0043 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1085+1004A>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48406357 | |||||||
| chr19:48406357 | A | T | 8 | a0001c0001t0001g0225 a0001c0001t0002g0180 a0001c0001t0002g0222 others(5): Show |
8 | HG01884.hp2 HG02622.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1085+1004A>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48406357 | |||||||
| chr19:48406385 | G | A | 4 | a0001c0001t0001g0164 a0001c0001t0001g0166 a0001c0001t0001g0172 others(1): Show |
4 | HG01346.hp1 HG03041.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.1085+1032G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48406385 | |||||||
| chr19:48406414 | G | A | 138 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(135): Show |
138 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(135): Show |
intron_variant | MODIFIER | c.1085+1061G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48406414 | |||||||
| chr19:48406579 | C | A | 3 | a0001c0007t0004g0309 a0001c0007t0007g0310 a0001c0012t0014g0302 |
3 | HG00733.hp1 HG01433.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1085+1226C>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48406579 | |||||||
| chr19:48406685 | G | T | 1 | a0001c0001t0001g0018 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1085+1332G>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48406685 | |||||||
| chr19:48406714 | G | A | 2 | a0001c0002t0002g0102 a0001c0004t0002g0099 |
2 | HG01261.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1085+1361G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48406714 | |||||||
| chr19:48406805 | T | C | 1 | a0001c0002t0002g0301 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1085+1452T>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48406805 | |||||||
| chr19:48406816 | A | G | 1 | a0001c0002t0002g0074 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1085+1463A>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48406816 | |||||||
| chr19:48406821 | G | A | 137 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(134): Show |
137 | HG00099.hp2 HG00609.hp1 HG00621.hp2 others(134): Show |
intron_variant | MODIFIER | c.1085+1468G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48406821 | |||||||
| chr19:48406960 | TTTTC | T | 3 | a0001c0002t0002g0316 a0001c0002t0002g0319 a0001c0002t0003g0007 |
3 | HG01243.hp1 HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1085+1619_1085+162 others(8): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 48406960 | ||||||
| chr19:48406985 | C | CT | 131 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(128): Show |
131 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.1085+1643dupT | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 48406985 | ||||||
| chr19:48406985 | C | CTT | 8 | a0001c0002t0002g0013 a0001c0002t0002g0314 a0001c0002t0002g0316 others(5): Show |
8 | HG00733.hp1 HG01243.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.1085+1642_1085+164 others(6): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 48406985 | ||||||
| chr19:48407060 | C | T | 2 | a0001c0002t0002g0247 a0001c0002t0002g0292 |
2 | NA18962.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.1085+1707C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48407060 | |||||||
| chr19:48407087 | C | T | 1 | a0001c0001t0001g0032 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1085+1734C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48407087 | |||||||
| chr19:48407153 | G | T | 2 | a0001c0001t0002g0179 a0001c0002t0002g0284 |
2 | HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1085+1800G>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48407153 | |||||||
| chr19:48407192 | C | T | 1 | a0001c0001t0001g0177 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1085+1839C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48407192 | |||||||
| chr19:48407241 | G | A | 3 | a0001c0007t0004g0309 a0001c0007t0007g0310 a0001c0012t0014g0302 |
3 | HG00733.hp1 HG01433.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1085+1888G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48407241 | |||||||
| chr19:48407555 | G | A | 3 | a0001c0002t0002g0135 a0001c0002t0002g0141 a0001c0002t0002g0142 |
3 | HG01891.hp2 HG02572.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1085+2202G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48407555 | |||||||
| chr19:48407626 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1085+2273C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48407626 | |||||||
| chr19:48407662 | G | A | 1 | a0001c0001t0002g0179 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1085+2309G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48407662 | |||||||
| chr19:48408079 | A | G | 1 | a0001c0002t0002g0301 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1085+2726A>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48408079 | |||||||
| chr19:48408106 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1085+2753G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48408106 | |||||||
| chr19:48408108 | G | A | 1 | a0001c0007t0007g0310 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1085+2755G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48408108 | |||||||
| chr19:48408109 | C | T | 7 | a0001c0003t0002g0345 a0001c0003t0002g0347 a0001c0003t0002g0348 others(4): Show |
7 | HG01928.hp2 HG01952.hp1 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.1085+2756C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48408109 | |||||||
| chr19:48408161 | T | C | 1 | a0001c0001t0001g0151 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1085+2808T>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48408161 | |||||||
| chr19:48408207 | G | A | 1 | a0001c0002t0002g0282 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1085+2854G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48408207 | |||||||
| chr19:48408258 | C | T | 2 | a0001c0001t0002g0179 a0001c0002t0002g0284 |
2 | HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1085+2905C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48408258 | |||||||
| chr19:48408330 | T | A | 6 | a0001c0001t0001g0303 a0001c0002t0002g0077 a0001c0002t0002g0304 others(3): Show |
6 | HG01884.hp1 HG02886.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1085+2977T>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48408330 | |||||||
| chr19:48408333 | C | CA | 17 | a0001c0001t0001g0081 a0001c0001t0001g0133 a0001c0001t0001g0155 others(14): Show |
17 | HG01884.hp2 HG01978.hp1 HG02056.hp2 others(14): Show |
intron_variant | MODIFIER | c.1085+2999dupA | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 48408333 | ||||||
| chr19:48408333 | CA | C | 118 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(115): Show |
118 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(115): Show |
intron_variant | MODIFIER | c.1085+2999delA | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 48408333 | ||||||
| chr19:48408363 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1085+3010G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48408363 | |||||||
| chr19:48408420 | G | T | 1 | a0001c0001t0001g0154 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1085+3067G>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48408420 | |||||||
| chr19:48408492 | C | T | 1 | a0001c0002t0002g0293 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1085+3139C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48408492 | |||||||
| chr19:48408554 | C | T | 6 | a0001c0001t0001g0303 a0001c0002t0002g0077 a0001c0002t0002g0304 others(3): Show |
6 | HG01884.hp1 HG02886.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1085+3201C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48408554 | |||||||
| chr19:48408769 | G | A | 1 | a0001c0008t0001g0143 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1085+3416G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48408769 | |||||||
| chr19:48408819 | TA | T | 245 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(242): Show |
246 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.1085+3481delA | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 48408819 | ||||||
| chr19:48408839 | G | A | 122 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(119): Show |
123 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.1085+3486G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48408839 | |||||||
| chr19:48409018 | G | A | 1 | a0001c0002t0002g0273 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1085+3665G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48409018 | |||||||
| chr19:48409057 | G | A | 6 | a0001c0002t0002g0013 a0001c0002t0002g0207 a0001c0002t0002g0208 others(3): Show |
6 | HG02486.hp2 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1085+3704G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48409057 | |||||||
| chr19:48409064 | G | A | 3 | a0001c0001t0001g0279 a0001c0004t0002g0280 a0001c0004t0002g0281 |
3 | HG01891.hp1 HG02145.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1085+3711G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48409064 | |||||||
| chr19:48409126 | G | A | 5 | a0001c0002t0002g0207 a0001c0002t0002g0208 a0001c0002t0002g0211 others(2): Show |
5 | HG02486.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1085+3773G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48409126 | |||||||
| chr19:48409131 | G | A | 1 | a0001c0001t0002g0271 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1085+3778G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48409131 | |||||||
| chr19:48409132 | A | G | 140 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(137): Show |
140 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(137): Show |
intron_variant | MODIFIER | c.1085+3779A>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48409132 | |||||||
| chr19:48409170 | T | C | 6 | a0001c0001t0001g0303 a0001c0002t0002g0077 a0001c0002t0002g0304 others(3): Show |
6 | HG01884.hp1 HG02886.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1085+3817T>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48409170 | |||||||
| chr19:48409224 | T | G | 8 | a0001c0001t0001g0225 a0001c0001t0002g0180 a0001c0001t0002g0222 others(5): Show |
8 | HG01884.hp2 HG02622.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1085+3871T>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48409224 | |||||||
| chr19:48409229 | C | A | 6 | a0001c0001t0001g0225 a0001c0001t0002g0180 a0001c0001t0002g0222 others(3): Show |
6 | HG01884.hp2 HG02818.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1085+3876C>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48409229 | |||||||
| chr19:48409274 | C | CT | 30 | a0001c0001t0001g0081 a0001c0001t0001g0100 a0001c0001t0001g0111 others(27): Show |
30 | HG00673.hp2 HG01070.hp2 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.1085+3943dupT | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 48409274 | ||||||
| chr19:48409274 | CT | C | 104 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0014 others(101): Show |
104 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(101): Show |
intron_variant | MODIFIER | c.1085+3943delT | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 48409274 | ||||||
| chr19:48409274 | CTT | C | 26 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0087 others(23): Show |
26 | HG00558.hp1 HG00639.hp1 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.1085+3942_1085+394 others(6): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 48409274 | ||||||
| chr19:48409280 | T | C | 1 | a0001c0002t0003g0007 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1085+3927T>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48409280 | |||||||
| chr19:48409381 | C | T | 3 | a0001c0001t0001g0050 a0001c0001t0010g0322 a0001c0001t0011g0323 |
3 | HG02257.hp1 NA18906.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.1085+4028C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48409381 | |||||||
| chr19:48409402 | C | T | 2 | a0001c0001t0002g0179 a0001c0002t0002g0301 |
2 | HG02109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1085+4049C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48409402 | |||||||
| chr19:48409556 | C | T | 11 | a0001c0001t0001g0294 a0001c0001t0002g0029 a0001c0001t0002g0295 others(8): Show |
11 | HG00140.hp1 HG02258.hp2 HG02683.hp2 others(8): Show |
intron_variant | MODIFIER | c.1085+4203C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48409556 | |||||||
| chr19:48409607 | A | G | 82 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(79): Show |
82 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.1085+4254A>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48409607 | |||||||
| chr19:48409664 | G | A | 2 | a0001c0011t0002g0299 a0001c0011t0002g0300 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1085+4311G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48409664 | |||||||
| chr19:48409702 | T | C | 6 | a0001c0001t0001g0164 a0001c0001t0001g0166 a0001c0001t0002g0167 others(3): Show |
6 | HG01346.hp1 HG02809.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1086-4289T>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48409702 | |||||||
| chr19:48409931 | C | G | 3 | a0001c0001t0001g0342 a0001c0002t0002g0339 a0001c0002t0002g0341 |
3 | HG01109.hp1 HG02738.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.1086-4060C>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48409931 | |||||||
| chr19:48409936 | C | T | 2 | a0001c0001t0002g0029 a0001c0002t0002g0028 |
2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1086-4055C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48409936 | |||||||
| chr19:48410046 | A | C | 1 | a0001c0002t0002g0013 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1086-3945A>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48410046 | |||||||
| chr19:48410058 | T | C | 3 | a0001c0003t0002g0328 a0001c0003t0002g0331 a0001c0003t0002g0343 |
3 | HG00673.hp1 HG02083.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1086-3933T>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48410058 | |||||||
| chr19:48410076 | C | T | 2 | a0001c0001t0001g0160 a0001c0001t0001g0161 |
2 | HG02451.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.1086-3915C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48410076 | |||||||
| chr19:48410077 | G | C | 5 | a0001c0001t0001g0015 a0001c0001t0002g0042 a0001c0001t0013g0017 others(2): Show |
5 | HG00408.hp1 NA18952.hp1 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.1086-3914G>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48410077 | |||||||
| chr19:48410118 | C | T | 3 | a0001c0007t0004g0309 a0001c0007t0007g0310 a0001c0012t0014g0302 |
3 | HG00733.hp1 HG01433.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1086-3873C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48410118 | |||||||
| chr19:48410402 | C | T | 2 | a0001c0001t0002g0179 a0001c0002t0002g0284 |
2 | HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1086-3589C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48410402 | |||||||
| chr19:48410464 | G | C | 6 | a0001c0001t0001g0303 a0001c0002t0002g0077 a0001c0002t0002g0304 others(3): Show |
6 | HG01884.hp1 HG02886.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1086-3527G>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48410464 | |||||||
| chr19:48410483 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1086-3508G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48410483 | |||||||
| chr19:48410527 | C | CA | 14 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0117 others(11): Show |
14 | HG00558.hp1 HG01169.hp2 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.1086-3440dupA | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 48410527 | ||||||
| chr19:48410527 | C | CAA | 83 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(80): Show |
84 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.1086-3441_1086-344 others(6): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 48410527 | ||||||
| chr19:48410527 | C | CAAA | 35 | a0001c0001t0001g0110 a0001c0001t0001g0133 a0001c0001t0001g0196 others(32): Show |
35 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.1086-3442_1086-344 others(7): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 48410527 | ||||||
| chr19:48410527 | C | CAAAA | 25 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0032 others(22): Show |
25 | HG00639.hp1 HG00642.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.1086-3443_1086-344 others(8): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 48410527 | ||||||
| chr19:48410527 | C | CAAAAA | 72 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0018 others(69): Show |
72 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.1086-3444_1086-344 others(9): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 48410527 | ||||||
| chr19:48410527 | C | CAAAAAA | 44 | a0001c0001t0001g0011 a0001c0001t0001g0034 a0001c0001t0001g0044 others(41): Show |
44 | HG00609.hp1 HG00621.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1086-3445_1086-344 others(10): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 48410527 | ||||||
| chr19:48410527 | CAAAAAAA others(1): Show |
C | 6 | a0001c0001t0001g0303 a0001c0002t0002g0077 a0001c0002t0002g0304 others(3): Show |
6 | HG01884.hp1 HG02886.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1086-3447_1086-344 others(12): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 48410527 | ||||||
| chr19:48410554 | A | C | 20 | a0001c0001t0001g0054 a0001c0001t0001g0175 a0001c0001t0001g0176 others(17): Show |
20 | HG00609.hp1 HG02015.hp1 HG02132.hp1 others(17): Show |
intron_variant | MODIFIER | c.1086-3437A>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48410554 | |||||||
| chr19:48410571 | C | T | 4 | a0001c0001t0001g0279 a0001c0002t0002g0178 a0001c0004t0002g0280 others(1): Show |
4 | HG01891.hp1 HG02145.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1086-3420C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48410571 | |||||||
| chr19:48410688 | C | T | 1 | a0001c0001t0002g0080 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1086-3303C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48410688 | |||||||
| chr19:48410921 | G | C | 105 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0014 others(102): Show |
105 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.1086-3070G>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48410921 | |||||||
| chr19:48410981 | G | A | 2 | a0001c0001t0001g0110 a0001c0001t0001g0245 |
2 | HG00741.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.1086-3010G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48410981 | |||||||
| chr19:48411225 | T | C | 4 | a0001c0001t0001g0279 a0001c0002t0002g0178 a0001c0004t0002g0280 others(1): Show |
4 | HG01891.hp1 HG02145.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1086-2766T>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48411225 | |||||||
| chr19:48411326 | A | AAAT | 35 | a0001c0001t0001g0113 a0001c0001t0001g0152 a0001c0001t0001g0156 others(32): Show |
35 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.1086-2624_1086-262 others(7): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 48411326 | ||||||
| chr19:48411326 | A | AAATAAT | 27 | a0001c0001t0001g0048 a0001c0001t0001g0124 a0001c0001t0001g0128 others(24): Show |
27 | HG00735.hp1 HG01099.hp1 HG01361.hp2 others(24): Show |
intron_variant | MODIFIER | c.1086-2627_1086-262 others(10): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 48411326 | ||||||
| chr19:48411326 | AAAT | A | 30 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0033 others(27): Show |
30 | HG00639.hp1 HG01169.hp2 HG01346.hp1 others(27): Show |
intron_variant | MODIFIER | c.1086-2624_1086-262 others(7): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 48411326 | ||||||
| chr19:48411326 | AAATAAT | A | 72 | a0001c0001t0001g0069 a0001c0001t0001g0110 a0001c0001t0001g0133 others(69): Show |
72 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.1086-2627_1086-262 others(10): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 48411326 | ||||||
| chr19:48411326 | AAATAATA others(2): Show |
A | 99 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(96): Show |
99 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(96): Show |
intron_variant | MODIFIER | c.1086-2630_1086-262 others(13): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 48411326 | ||||||
| chr19:48411326 | AAATAATA others(5): Show |
A | 1 | a0001c0020t0002g0206 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1086-2633_1086-262 others(16): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 48411326 | ||||||
| chr19:48411326 | AAATAATA others(8): Show |
A | 7 | a0001c0001t0001g0303 a0001c0002t0002g0077 a0001c0002t0002g0301 others(4): Show |
7 | HG01884.hp1 HG02109.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1086-2636_1086-262 others(19): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 48411326 | ||||||
| chr19:48411371 | G | T | 1 | a0001c0002t0002g0301 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1086-2620G>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48411371 | |||||||
| chr19:48411374 | G | A | 1 | a0001c0003t0015g0362 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1086-2617G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48411374 | |||||||
| chr19:48411417 | C | T | 35 | a0001c0001t0001g0342 a0001c0001t0001g0364 a0001c0002t0002g0339 others(32): Show |
36 | HG00597.hp1 HG00609.hp2 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.1086-2574C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48411417 | |||||||
| chr19:48411511 | C | T | 4 | a0001c0001t0001g0134 a0001c0002t0002g0135 a0001c0002t0002g0141 others(1): Show |
4 | HG00280.hp1 HG01891.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1086-2480C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48411511 | |||||||
| chr19:48411785 | A | C | 271 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(268): Show |
272 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(269): Show |
intron_variant | MODIFIER | c.1086-2206A>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48411785 | |||||||
| chr19:48411946 | A | G | 1 | a0001c0002t0002g0288 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1086-2045A>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48411946 | |||||||
| chr19:48412143 | G | A | 35 | a0001c0001t0001g0342 a0001c0001t0001g0364 a0001c0002t0002g0339 others(32): Show |
36 | HG00597.hp1 HG00609.hp2 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.1086-1848G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48412143 | |||||||
| chr19:48412288 | C | A | 1 | a0001c0004t0002g0280 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1086-1703C>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48412288 | |||||||
| chr19:48412348 | C | A | 246 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(243): Show |
247 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.1086-1643C>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48412348 | |||||||
| chr19:48412386 | AGAAAG | A | 9 | a0001c0001t0001g0225 a0001c0001t0002g0180 a0001c0001t0002g0222 others(6): Show |
9 | HG01884.hp2 HG02257.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1086-1604_1086-160 others(9): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48412386 | |||||||
| chr19:48412393 | G | T | 1 | a0001c0001t0001g0111 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1086-1598G>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48412393 | |||||||
| chr19:48412421 | A | AAAAG | 69 | a0001c0001t0001g0023 a0001c0001t0001g0032 a0001c0001t0001g0034 others(66): Show |
69 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.1086-1512_1086-150 others(8): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 48412421 | ||||||
| chr19:48412421 | A | AAAAGAAA others(1): Show |
29 | a0001c0001t0001g0069 a0001c0001t0001g0095 a0001c0001t0001g0098 others(26): Show |
29 | HG00408.hp1 HG00673.hp2 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.1086-1516_1086-150 others(12): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 48412421 | ||||||
| chr19:48412421 | A | AAAAGAAA others(5): Show |
8 | a0001c0001t0001g0158 a0001c0001t0001g0257 a0001c0001t0001g0286 others(5): Show |
8 | HG00423.hp1 HG00597.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1086-1520_1086-150 others(16): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 48412421 | ||||||
| chr19:48412421 | A | AAAAGAAA others(9): Show |
3 | a0001c0001t0001g0269 a0001c0001t0001g0340 a0001c0002t0002g0074 |
3 | HG04204.hp1 NA19056.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.1086-1524_1086-150 others(20): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 48412421 | ||||||
| chr19:48412421 | A | AAAAGAAA others(20): Show |
1 | a0001c0015t0002g0318 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1086-1553_1086-155 others(31): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 48412421 | ||||||
| chr19:48412421 | A | AAAG | 3 | a0001c0001t0001g0189 a0001c0003t0002g0349 a0001c0003t0015g0362 |
3 | NA18965.hp2 NA19084.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.1086-1568_1086-156 others(7): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 48412421 | ||||||
| chr19:48412421 | A | AAAGAAAG others(8): Show |
1 | a0001c0004t0002g0107 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1086-1568_1086-156 others(19): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 48412421 | ||||||
| chr19:48412421 | AAAAG | A | 61 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0031 others(58): Show |
61 | HG00280.hp2 HG00558.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.1086-1512_1086-150 others(8): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 48412421 | ||||||
| chr19:48412421 | AAAAGAAA others(1): Show |
A | 40 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0036 others(37): Show |
40 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.1086-1516_1086-150 others(12): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 48412421 | ||||||
| chr19:48412421 | AAAAGAAA others(5): Show |
A | 20 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(17): Show |
20 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.1086-1520_1086-150 others(16): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 48412421 | ||||||
| chr19:48412421 | AAAAGAAA others(9): Show |
A | 13 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0289 others(10): Show |
13 | HG02109.hp2 HG02280.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.1086-1524_1086-150 others(20): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 48412421 | ||||||
| chr19:48412479 | A | G | 1 | a0001c0001t0002g0180 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1086-1512A>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48412479 | |||||||
| chr19:48412514 | G | A | 6 | a0001c0001t0001g0303 a0001c0002t0002g0077 a0001c0002t0002g0304 others(3): Show |
6 | HG01884.hp1 HG02886.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1086-1477G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48412514 | |||||||
| chr19:48412661 | C | T | 1 | a0001c0002t0002g0301 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1086-1330C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48412661 | |||||||
| chr19:48412682 | G | C | 246 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(243): Show |
247 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.1086-1309G>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48412682 | |||||||
| chr19:48412713 | C | T | 6 | a0001c0001t0001g0303 a0001c0002t0002g0077 a0001c0002t0002g0304 others(3): Show |
6 | HG01884.hp1 HG02886.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1086-1278C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48412713 | |||||||
| chr19:48412720 | C | T | 10 | a0001c0001t0001g0225 a0001c0001t0002g0180 a0001c0001t0002g0222 others(7): Show |
10 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1086-1271C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48412720 | |||||||
| chr19:48412827 | TA | T | 15 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0048 others(12): Show |
15 | HG01074.hp2 HG01167.hp1 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.1086-1148delA | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 48412827 | ||||||
| chr19:48412850 | GGAGGGCA others(337): Show |
G | 3 | a0001c0001t0001g0150 a0001c0002t0002g0301 a0001c0003t0002g0332 |
3 | HG02109.hp2 NA18963.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1086-944_1086-601d others(2): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 48412850 | ||||||
| chr19:48412875 | A | G | 1 | a0001c0002t0002g0319 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1086-1116A>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48412875 | |||||||
| chr19:48412907 | G | A | 6 | a0001c0002t0002g0091 a0001c0002t0002g0207 a0001c0002t0002g0208 others(3): Show |
6 | HG02280.hp2 HG02486.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1086-1084G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48412907 | |||||||
| chr19:48413017 | T | G | 8 | a0001c0001t0001g0279 a0001c0001t0002g0179 a0001c0002t0002g0013 others(5): Show |
8 | HG01891.hp1 HG02145.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1086-974T>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48413017 | |||||||
| chr19:48413077 | A | G | 14 | a0001c0001t0001g0225 a0001c0001t0001g0279 a0001c0001t0002g0180 others(11): Show |
14 | HG01884.hp2 HG01891.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1086-914A>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48413077 | |||||||
| chr19:48413175 | T | TA | 40 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0081 others(37): Show |
40 | HG00609.hp1 HG01884.hp2 HG01891.hp1 others(37): Show |
intron_variant | MODIFIER | c.1086-801dupA | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 48413175 | ||||||
| chr19:48413175 | TA | T | 44 | a0001c0001t0001g0032 a0001c0001t0001g0076 a0001c0001t0001g0157 others(41): Show |
45 | HG00099.hp2 HG00597.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.1086-801delA | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 48413175 | ||||||
| chr19:48413191 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1086-800G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48413191 | |||||||
| chr19:48413217 | G | T | 13 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0087 others(10): Show |
13 | HG00639.hp1 HG01346.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1086-774G>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48413217 | |||||||
| chr19:48413226 | A | G | 1 | a0001c0002t0002g0301 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1086-765A>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48413226 | |||||||
| chr19:48413299 | G | A | 15 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0087 others(12): Show |
15 | HG00639.hp1 HG01167.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1086-692G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48413299 | |||||||
| chr19:48413428 | A | C | 1 | a0001c0001t0001g0150 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1086-563A>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48413428 | |||||||
| chr19:48413655 | C | G | 1 | a0001c0002t0002g0273 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1086-336C>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48413655 | |||||||
| chr19:48413657 | G | C | 1 | a0001c0002t0002g0273 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1086-334G>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48413657 | |||||||
| chr19:48413660 | T | A | 1 | a0001c0002t0002g0273 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1086-331T>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48413660 | |||||||
| chr19:48413661 | C | A | 1 | a0001c0002t0002g0273 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1086-330C>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48413661 | |||||||
| chr19:48413661 | C | CA | 231 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(228): Show |
232 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.1086-309dupA | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 48413661 | ||||||
| chr19:48413661 | C | CAA | 33 | a0001c0001t0001g0021 a0001c0001t0001g0051 a0001c0001t0001g0058 others(30): Show |
33 | HG00558.hp1 HG00642.hp1 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.1086-310_1086-309d others(4): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 48413661 | ||||||
| chr19:48413693 | G | A | 2 | a0001c0011t0002g0299 a0001c0011t0002g0300 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1086-298G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48413693 | |||||||
| chr19:48414160 | T | C | 1 | a0001c0002t0002g0013 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1200+55T>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 5/13 | chr19 | 48414160 | |||||||
| chr19:48414649 | G | C | 9 | a0001c0001t0001g0294 a0001c0001t0002g0295 a0001c0001t0002g0296 others(6): Show |
9 | HG00140.hp1 HG02683.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.1412+65G>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 6/13 | chr19 | 48414649 | |||||||
| chr19:48414659 | C | T | 2 | a0001c0002t0002g0316 a0001c0002t0003g0007 |
2 | HG01243.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1412+75C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 6/13 | chr19 | 48414659 | |||||||
| chr19:48414794 | A | G | 11 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(8): Show |
11 | HG02055.hp2 HG02257.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.1413-70A>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 6/13 | chr19 | 48414794 | |||||||
| chr19:48415255 | C | A | 3 | a0001c0007t0004g0309 a0001c0007t0007g0310 a0001c0012t0014g0302 |
3 | HG00733.hp1 HG01433.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1581+223C>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 7/13 | chr19 | 48415255 | |||||||
| chr19:48415357 | G | A | 3 | a0001c0004t0002g0213 a0001c0004t0002g0214 a0001c0004t0002g0274 |
3 | HG01070.hp2 HG01071.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1581+325G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 7/13 | chr19 | 48415357 | |||||||
| chr19:48415365 | G | T | 1 | a0001c0003t0002g0078 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1581+333G>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 7/13 | chr19 | 48415365 | |||||||
| chr19:48415366 | T | C | 1 | a0001c0003t0002g0078 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1581+334T>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 7/13 | chr19 | 48415366 | |||||||
| chr19:48415368 | T | A | 1 | a0001c0003t0002g0078 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1581+336T>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 7/13 | chr19 | 48415368 | |||||||
| chr19:48415369 | C | CGGCACGG others(434): Show |
1 | a0001c0003t0002g0078 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1581+337_1581+338i others(443): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 7/13 | chr19 | 48415369 | |||||||
| chr19:48415425 | A | G | 1 | a0001c0001t0001g0255 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1581+393A>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 7/13 | chr19 | 48415425 | |||||||
| chr19:48415426 | T | C | 41 | a0001c0003t0002g0002 a0001c0003t0002g0019 a0001c0003t0002g0057 others(38): Show |
42 | HG00099.hp2 HG00597.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.1581+394T>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 7/13 | chr19 | 48415426 | |||||||
| chr19:48415542 | AGGAGGCG others(64): Show |
A | 2 | a0001c0001t0001g0144 a0003c0019t0001g0118 |
2 | HG01358.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1582-417_1582-347d others(73): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr19 | 48415542 | ||||||
| chr19:48415585 | A | AGGGCTGG others(64): Show |
2 | a0001c0004t0002g0213 a0001c0004t0002g0214 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1582-394_1582-324d others(73): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr19 | 48415585 | ||||||
| chr19:48415716 | G | A | 1 | a0001c0001t0002g0179 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1582-286G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 7/13 | chr19 | 48415716 | |||||||
| chr19:48416170 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1735+15T>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 8/13 | chr19 | 48416170 | |||||||
| chr19:48416212 | C | T | 1 | a0001c0002t0002g0288 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1735+57C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 8/13 | chr19 | 48416212 | |||||||
| chr19:48416213 | G | A | 9 | a0001c0001t0001g0294 a0001c0001t0002g0295 a0001c0001t0002g0296 others(6): Show |
9 | HG00140.hp1 HG02683.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.1735+58G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 8/13 | chr19 | 48416213 | |||||||
| chr19:48416244 | C | G | 1 | a0001c0001t0001g0004 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1735+89C>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 8/13 | chr19 | 48416244 | |||||||
| chr19:48416555 | G | A | 5 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0189 others(2): Show |
5 | HG00609.hp1 HG02132.hp1 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.1735+400G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 8/13 | chr19 | 48416555 | |||||||
| chr19:48416682 | A | G | 261 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(258): Show |
262 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.1735+527A>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 8/13 | chr19 | 48416682 | |||||||
| chr19:48416745 | C | CTT | 200 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(197): Show |
201 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.1735+602_1735+603d others(4): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 48416745 | ||||||
| chr19:48416745 | C | CTTT | 47 | a0001c0001t0001g0036 a0001c0001t0001g0069 a0001c0001t0001g0081 others(44): Show |
47 | HG00423.hp2 HG00558.hp1 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.1735+601_1735+603d others(5): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 48416745 | ||||||
| chr19:48416801 | C | T | 4 | a0001c0001t0001g0048 a0001c0001t0001g0124 a0001c0001t0001g0128 others(1): Show |
4 | HG00735.hp1 HG01099.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.1735+646C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 8/13 | chr19 | 48416801 | |||||||
| chr19:48416891 | T | C | 279 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(276): Show |
280 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.1735+736T>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 8/13 | chr19 | 48416891 | |||||||
| chr19:48416937 | G | A | 1 | a0001c0004t0002g0083 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1735+782G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 8/13 | chr19 | 48416937 | |||||||
| chr19:48417024 | C | T | 3 | a0001c0007t0004g0309 a0001c0007t0007g0310 a0001c0012t0014g0302 |
3 | HG00733.hp1 HG01433.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1735+869C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 8/13 | chr19 | 48417024 | |||||||
| chr19:48417041 | G | A | 9 | a0001c0001t0001g0225 a0001c0001t0002g0180 a0001c0001t0002g0222 others(6): Show |
9 | HG01884.hp2 HG02257.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1735+886G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 8/13 | chr19 | 48417041 | |||||||
| chr19:48417104 | T | C | 1 | a0001c0001t0001g0134 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1735+949T>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 8/13 | chr19 | 48417104 | |||||||
| chr19:48417116 | T | G | 2 | a0001c0002t0002g0282 a0001c0002t0002g0283 |
2 | HG02723.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1735+961T>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 8/13 | chr19 | 48417116 | |||||||
| chr19:48417709 | C | T | 4 | a0001c0002t0002g0319 a0001c0007t0004g0309 a0001c0007t0007g0310 others(1): Show |
4 | HG00733.hp1 HG01433.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1736-1525C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 8/13 | chr19 | 48417709 | |||||||
| chr19:48417795 | C | T | 2 | a0001c0011t0002g0299 a0001c0011t0002g0300 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1736-1439C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 8/13 | chr19 | 48417795 | |||||||
| chr19:48417877 | T | C | 1 | a0001c0002t0002g0193 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1736-1357T>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 8/13 | chr19 | 48417877 | |||||||
| chr19:48417934 | T | C | 1 | a0001c0002t0002g0178 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1736-1300T>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 8/13 | chr19 | 48417934 | |||||||
| chr19:48418027 | C | T | 4 | a0001c0001t0002g0030 a0001c0001t0002g0066 a0001c0002t0002g0067 others(1): Show |
4 | NA18965.hp1 NA18979.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.1736-1207C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 8/13 | chr19 | 48418027 | |||||||
| chr19:48418033 | C | CT | 22 | a0001c0001t0001g0009 a0001c0001t0001g0060 a0001c0001t0001g0076 others(19): Show |
22 | HG00140.hp1 HG00558.hp2 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.1736-1183dupT | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 48418033 | ||||||
| chr19:48418033 | CT | C | 21 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0087 others(18): Show |
21 | HG00639.hp1 HG01074.hp1 HG01346.hp1 others(18): Show |
intron_variant | MODIFIER | c.1736-1183delT | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 48418033 | ||||||
| chr19:48418110 | T | G | 1 | a0001c0001t0002g0079 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1736-1124T>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 8/13 | chr19 | 48418110 | |||||||
| chr19:48418222 | G | A | 1 | a0001c0004t0002g0274 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1736-1012G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 8/13 | chr19 | 48418222 | |||||||
| chr19:48418232 | C | T | 1 | a0001c0001t0001g0005 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1736-1002C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 8/13 | chr19 | 48418232 | |||||||
| chr19:48418235 | G | A | 1 | a0001c0001t0002g0119 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1736-999G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 8/13 | chr19 | 48418235 | |||||||
| chr19:48418313 | G | A | 3 | a0001c0001t0001g0279 a0001c0004t0002g0280 a0001c0004t0002g0281 |
3 | HG01891.hp1 HG02145.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1736-921G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 8/13 | chr19 | 48418313 | |||||||
| chr19:48418602 | A | G | 1 | a0001c0001t0009g0070 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1736-632A>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 8/13 | chr19 | 48418602 | |||||||
| chr19:48418664 | A | G | 268 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(265): Show |
269 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.1736-570A>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 8/13 | chr19 | 48418664 | |||||||
| chr19:48418701 | C | T | 3 | a0001c0007t0004g0309 a0001c0007t0007g0310 a0001c0012t0014g0302 |
3 | HG00733.hp1 HG01433.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1736-533C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 8/13 | chr19 | 48418701 | |||||||
| chr19:48418887 | G | A | 1 | a0001c0003t0002g0330 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1736-347G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 8/13 | chr19 | 48418887 | |||||||
| chr19:48418957 | CAG | C | 3 | a0001c0007t0004g0309 a0001c0007t0007g0310 a0001c0012t0014g0302 |
3 | HG00733.hp1 HG01433.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1736-273_1736-272d others(4): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 48418957 | ||||||
| chr19:48419052 | C | CT | 11 | a0001c0001t0001g0071 a0001c0001t0001g0257 a0001c0001t0001g0294 others(8): Show |
11 | HG00597.hp2 HG01346.hp2 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.1736-170dupT | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 48419052 | ||||||
| chr19:48419081 | C | G | 11 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0087 others(8): Show |
11 | HG00639.hp1 HG01074.hp1 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.1736-153C>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 8/13 | chr19 | 48419081 | |||||||
| chr19:48419092 | T | A | 2 | a0001c0001t0001g0133 a0001c0002t0002g0121 |
2 | HG02056.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.1736-142T>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 8/13 | chr19 | 48419092 | |||||||
| chr19:48419438 | T | G | 32 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0031 others(29): Show |
32 | HG00621.hp1 HG00621.hp2 HG01257.hp2 others(29): Show |
intron_variant | MODIFIER | c.1861+79T>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 9/13 | chr19 | 48419438 | |||||||
| chr19:48419443 | G | C | 1 | a0001c0001t0001g0149 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1861+84G>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 9/13 | chr19 | 48419443 | |||||||
| chr19:48419443 | G | T | 7 | a0001c0002t0002g0013 a0001c0002t0002g0091 a0001c0002t0002g0207 others(4): Show |
7 | HG02280.hp2 HG02486.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1861+84G>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 9/13 | chr19 | 48419443 | |||||||
| chr19:48419448 | G | T | 1 | a0001c0001t0001g0087 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1861+89G>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 9/13 | chr19 | 48419448 | |||||||
| chr19:48419515 | CT | C | 240 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(237): Show |
241 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.1862-57delT | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr19 | 48419515 | ||||||
| chr19:48419528 | T | C | 1 | a0001c0001t0002g0179 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1862-57T>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 9/13 | chr19 | 48419528 | |||||||
| chr19:48419844 | C | A | 176 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(173): Show |
176 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.2091+30C>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 10/13 | chr19 | 48419844 | |||||||
| chr19:48419895 | G | T | 1 | a0001c0002t0002g0301 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2091+81G>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 10/13 | chr19 | 48419895 | |||||||
| chr19:48419904 | G | C | 7 | a0001c0001t0002g0119 a0001c0001t0002g0120 a0001c0001t0002g0277 others(4): Show |
7 | HG03834.hp1 NA18942.hp1 NA18962.hp2 others(4): Show |
intron_variant | MODIFIER | c.2091+90G>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 10/13 | chr19 | 48419904 | |||||||
| chr19:48420203 | C | T | 1 | a0001c0002t0002g0297 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2091+389C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 10/13 | chr19 | 48420203 | |||||||
| chr19:48420274 | T | A | 276 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(273): Show |
277 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.2091+460T>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 10/13 | chr19 | 48420274 | |||||||
| chr19:48420405 | G | A | 41 | a0001c0003t0002g0002 a0001c0003t0002g0019 a0001c0003t0002g0057 others(38): Show |
42 | HG00099.hp2 HG00597.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.2091+591G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 10/13 | chr19 | 48420405 | |||||||
| chr19:48420408 | A | G | 1 | a0001c0002t0002g0135 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2091+594A>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 10/13 | chr19 | 48420408 | |||||||
| chr19:48420564 | G | A | 4 | a0001c0002t0002g0013 a0001c0007t0004g0309 a0001c0007t0007g0310 others(1): Show |
4 | HG00733.hp1 HG01433.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2091+750G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 10/13 | chr19 | 48420564 | |||||||
| chr19:48420564 | G | C | 2 | a0001c0002t0002g0316 a0001c0002t0003g0007 |
2 | HG01243.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.2091+750G>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 10/13 | chr19 | 48420564 | |||||||
| chr19:48420634 | T | C | 1 | a0001c0001t0008g0220 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2091+820T>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 10/13 | chr19 | 48420634 | |||||||
| chr19:48420672 | A | G | 9 | a0001c0001t0001g0225 a0001c0001t0002g0180 a0001c0001t0002g0222 others(6): Show |
9 | HG01884.hp2 HG02257.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.2091+858A>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 10/13 | chr19 | 48420672 | |||||||
| chr19:48420687 | G | A | 1 | a0001c0001t0001g0344 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2091+873G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 10/13 | chr19 | 48420687 | |||||||
| chr19:48420718 | T | C | 276 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(273): Show |
277 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.2091+904T>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 10/13 | chr19 | 48420718 | |||||||
| chr19:48420741 | G | A | 13 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0087 others(10): Show |
13 | HG00639.hp1 HG01074.hp1 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.2091+927G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 10/13 | chr19 | 48420741 | |||||||
| chr19:48420780 | T | G | 1 | a0001c0001t0002g0179 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2091+966T>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 10/13 | chr19 | 48420780 | |||||||
| chr19:48421148 | T | G | 260 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(257): Show |
261 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.2092-637T>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 10/13 | chr19 | 48421148 | |||||||
| chr19:48421155 | G | A | 1 | a0001c0002t0002g0093 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2092-630G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 10/13 | chr19 | 48421155 | |||||||
| chr19:48421204 | G | A | 1 | a0001c0001t0001g0248 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2092-581G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 10/13 | chr19 | 48421204 | |||||||
| chr19:48421255 | C | T | 1 | a0001c0002t0002g0319 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2092-530C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 10/13 | chr19 | 48421255 | |||||||
| chr19:48421282 | G | A | 1 | a0001c0001t0001g0098 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2092-503G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 10/13 | chr19 | 48421282 | |||||||
| chr19:48421325 | G | A | 13 | a0001c0001t0001g0303 a0001c0002t0002g0013 a0001c0002t0002g0077 others(10): Show |
13 | HG01884.hp1 HG02280.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.2092-460G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 10/13 | chr19 | 48421325 | |||||||
| chr19:48421345 | T | C | 1 | a0001c0001t0001g0344 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2092-440T>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 10/13 | chr19 | 48421345 | |||||||
| chr19:48421424 | G | A | 2 | a0001c0011t0002g0299 a0001c0011t0002g0300 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.2092-361G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 10/13 | chr19 | 48421424 | |||||||
| chr19:48421427 | T | TA | 277 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(274): Show |
278 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.2092-346dupA | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 48421427 | ||||||
| chr19:48421506 | T | C | 276 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(273): Show |
277 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.2092-279T>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 10/13 | chr19 | 48421506 | |||||||
| chr19:48421520 | G | T | 2 | a0001c0001t0001g0129 a0001c0002t0002g0284 |
2 | HG00738.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2092-265G>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 10/13 | chr19 | 48421520 | |||||||
| chr19:48421653 | C | A | 10 | a0001c0001t0001g0023 a0001c0001t0002g0024 a0001c0001t0002g0055 others(7): Show |
10 | HG00280.hp2 HG00735.hp2 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.2092-132C>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 10/13 | chr19 | 48421653 | |||||||
| chr19:48421669 | T | C | 13 | a0001c0001t0001g0294 a0001c0001t0002g0295 a0001c0001t0002g0296 others(10): Show |
13 | HG00140.hp1 HG00733.hp1 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.2092-116T>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 10/13 | chr19 | 48421669 | |||||||
| chr19:48421706 | G | A | 173 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(170): Show |
173 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.2092-79G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 10/13 | chr19 | 48421706 | |||||||
| chr19:48422165 | G | A | 1 | a0001c0001t0002g0313 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2252+220G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48422165 | |||||||
| chr19:48422246 | C | T | 5 | a0001c0003t0002g0312 a0001c0003t0002g0327 a0001c0003t0002g0329 others(2): Show |
5 | HG00609.hp2 HG02074.hp2 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.2252+301C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48422246 | |||||||
| chr19:48422341 | G | A | 2 | a0001c0001t0001g0069 a0001c0001t0001g0215 |
2 | HG03831.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.2252+396G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48422341 | |||||||
| chr19:48422382 | G | A | 1 | a0001c0001t0001g0354 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2252+437G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48422382 | |||||||
| chr19:48422428 | T | C | 1 | a0001c0003t0002g0073 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2252+483T>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48422428 | |||||||
| chr19:48422481 | C | A | 1 | a0001c0001t0001g0350 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2252+536C>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48422481 | |||||||
| chr19:48422560 | G | A | 3 | a0001c0003t0002g0345 a0001c0003t0002g0347 a0001c0003t0002g0348 |
3 | NA18951.hp2 NA18971.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.2252+615G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48422560 | |||||||
| chr19:48422609 | C | CA | 8 | a0001c0001t0001g0054 a0001c0001t0001g0278 a0001c0001t0001g0279 others(5): Show |
8 | HG01243.hp1 HG01891.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.2252+678dupA | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48422609 | ||||||
| chr19:48422609 | CA | C | 46 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(43): Show |
46 | HG00140.hp1 HG00639.hp1 HG01070.hp2 others(43): Show |
intron_variant | MODIFIER | c.2252+678delA | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48422609 | ||||||
| chr19:48422639 | G | A | 30 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0087 others(27): Show |
30 | HG00639.hp1 HG00733.hp1 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.2252+694G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48422639 | |||||||
| chr19:48422679 | C | G | 1 | a0001c0003t0002g0327 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2252+734C>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48422679 | |||||||
| chr19:48422679 | C | T | 228 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(225): Show |
229 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.2252+734C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48422679 | |||||||
| chr19:48422981 | C | T | 9 | a0001c0001t0001g0225 a0001c0001t0002g0180 a0001c0001t0002g0222 others(6): Show |
9 | HG01884.hp2 HG02257.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.2252+1036C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48422981 | |||||||
| chr19:48423079 | C | T | 5 | a0001c0001t0002g0029 a0001c0002t0002g0028 a0001c0004t0002g0213 others(2): Show |
5 | HG01070.hp2 HG01071.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.2252+1134C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48423079 | |||||||
| chr19:48423253 | G | A | 1 | a0001c0002t0002g0093 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2252+1308G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48423253 | |||||||
| chr19:48423308 | T | C | 194 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(191): Show |
194 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(191): Show |
intron_variant | MODIFIER | c.2252+1363T>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48423308 | |||||||
| chr19:48423324 | G | A | 1 | a0001c0003t0002g0324 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2252+1379G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48423324 | |||||||
| chr19:48423330 | A | G | 1 | a0001c0001t0001g0230 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2252+1385A>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48423330 | |||||||
| chr19:48423349 | G | C | 30 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0087 others(27): Show |
30 | HG00639.hp1 HG00733.hp1 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.2252+1404G>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48423349 | |||||||
| chr19:48423352 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2252+1407C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48423352 | |||||||
| chr19:48423359 | C | G | 1 | a0001c0002t0002g0284 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2252+1414C>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48423359 | |||||||
| chr19:48423361 | G | C | 6 | a0001c0002t0002g0091 a0001c0002t0002g0207 a0001c0002t0002g0208 others(3): Show |
6 | HG02280.hp2 HG02486.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.2252+1416G>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48423361 | |||||||
| chr19:48423466 | C | T | 6 | a0001c0001t0001g0164 a0001c0001t0001g0166 a0001c0001t0002g0167 others(3): Show |
6 | HG01346.hp1 HG02809.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.2252+1521C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48423466 | |||||||
| chr19:48423593 | C | G | 3 | a0001c0001t0001g0279 a0001c0004t0002g0280 a0001c0004t0002g0281 |
3 | HG01891.hp1 HG02145.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2252+1648C>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48423593 | |||||||
| chr19:48423688 | C | T | 1 | a0001c0001t0001g0189 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2252+1743C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48423688 | |||||||
| chr19:48423738 | C | A | 1 | a0001c0001t0002g0147 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2252+1793C>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48423738 | |||||||
| chr19:48423763 | G | A | 32 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0087 others(29): Show |
32 | HG00639.hp1 HG00733.hp1 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.2252+1818G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48423763 | |||||||
| chr19:48423794 | G | A | 3 | a0001c0002t0002g0178 a0001c0002t0002g0316 a0001c0002t0003g0007 |
3 | HG01243.hp1 HG02630.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.2252+1849G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48423794 | |||||||
| chr19:48424094 | G | A | 4 | a0001c0001t0001g0048 a0001c0001t0001g0124 a0001c0001t0001g0128 others(1): Show |
4 | HG00735.hp1 HG01099.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.2252+2149G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48424094 | |||||||
| chr19:48424185 | G | A | 1 | a0001c0001t0002g0137 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2252+2240G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48424185 | |||||||
| chr19:48424242 | C | A | 2 | a0001c0002t0002g0204 a0001c0002t0002g0205 |
2 | HG00140.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.2252+2297C>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48424242 | |||||||
| chr19:48424243 | C | T | 2 | a0001c0002t0002g0204 a0001c0002t0002g0205 |
2 | HG00140.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.2252+2298C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48424243 | |||||||
| chr19:48424265 | A | AT | 80 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(77): Show |
80 | HG00423.hp1 HG00423.hp2 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.2252+2343dupT | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48424265 | ||||||
| chr19:48424265 | A | ATT | 7 | a0001c0001t0001g0272 a0001c0001t0001g0286 a0001c0001t0002g0358 others(4): Show |
7 | HG00558.hp1 HG01169.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2252+2342_2252+234 others(6): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48424265 | ||||||
| chr19:48424265 | A | ATTTTTTT others(2828): Show |
1 | a0001c0004t0002g0213 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.2252+2342_2252+234 others(2839): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48424265 | ||||||
| chr19:48424265 | A | ATTTTTTT others(2826): Show |
1 | a0001c0004t0002g0214 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.2252+2342_2252+234 others(2837): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48424265 | ||||||
| chr19:48424265 | A | ATTTTTTT others(2828): Show |
2 | a0001c0002t0002g0306 a0001c0002t0002g0307 |
2 | HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2252+2342_2252+234 others(2839): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48424265 | ||||||
| chr19:48424265 | A | ATTTTTTT others(2826): Show |
1 | a0001c0002t0002g0319 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2252+2342_2252+234 others(2837): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48424265 | ||||||
| chr19:48424265 | A | ATTTTTTT others(2827): Show |
1 | a0001c0012t0014g0302 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2252+2342_2252+234 others(2838): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48424265 | ||||||
| chr19:48424265 | A | ATTTTTTT others(2829): Show |
1 | a0001c0002t0002g0211 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2252+2342_2252+234 others(2840): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48424265 | ||||||
| chr19:48424266 | T | TTTTTTTT others(2827): Show |
1 | a0001c0002t0002g0207 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2252+2341_2252+234 others(2838): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48424266 | ||||||
| chr19:48424266 | T | TTTTTTTT others(2827): Show |
1 | a0001c0004t0002g0274 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2252+2342_2252+234 others(2838): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48424266 | ||||||
| chr19:48424266 | T | TTTTTTTT others(2827): Show |
3 | a0001c0002t0002g0077 a0001c0002t0002g0304 a0001c0002t0002g0305 |
3 | HG01884.hp1 HG02886.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2252+2342_2252+234 others(2838): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48424266 | ||||||
| chr19:48424266 | T | TTTTTTTT others(2829): Show |
1 | a0001c0001t0002g0179 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2252+2342_2252+234 others(2840): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48424266 | ||||||
| chr19:48424266 | T | TTTTTTTT others(2826): Show |
2 | a0001c0002t0002g0288 a0001c0007t0004g0309 |
2 | HG00733.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.2252+2342_2252+234 others(2837): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48424266 | ||||||
| chr19:48424266 | T | TTTTTTTT others(2823): Show |
2 | a0001c0001t0002g0029 a0001c0002t0002g0028 |
2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2252+2342_2252+234 others(2834): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48424266 | ||||||
| chr19:48424266 | T | TTTTTTTT others(2828): Show |
2 | a0001c0002t0002g0091 a0001c0010t0002g0210 |
2 | HG02280.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.2252+2342_2252+234 others(2839): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48424266 | ||||||
| chr19:48424266 | T | TTTTTTTT others(2827): Show |
1 | a0001c0010t0002g0209 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.2252+2342_2252+234 others(2838): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48424266 | ||||||
| chr19:48424266 | T | TTTTTTTT others(2826): Show |
1 | a0001c0007t0007g0310 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2252+2342_2252+234 others(2837): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48424266 | ||||||
| chr19:48424266 | T | TTTTTTTT others(2828): Show |
1 | a0001c0001t0001g0303 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2252+2347_2252+234 others(2839): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48424266 | ||||||
| chr19:48424266 | T | TTTTTTTT others(2829): Show |
1 | a0001c0002t0002g0208 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2252+2347_2252+234 others(2840): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48424266 | ||||||
| chr19:48424267 | T | TTTTTTTT others(2827): Show |
1 | a0001c0002t0002g0013 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2252+2342_2252+234 others(2838): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48424267 | ||||||
| chr19:48424267 | T | TTTTTTTT others(2821): Show |
6 | a0001c0001t0001g0294 a0001c0001t0002g0295 a0001c0001t0002g0296 others(3): Show |
6 | HG02683.hp2 HG03239.hp2 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.2252+2342_2252+234 others(2832): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48424267 | ||||||
| chr19:48424267 | T | TTTTTTTT others(2830): Show |
1 | a0001c0002t0002g0109 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2252+2347_2252+234 others(2841): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48424267 | ||||||
| chr19:48424267 | T | TTTTTTTT others(2830): Show |
1 | a0001c0002t0002g0311 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2252+2347_2252+234 others(2841): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48424267 | ||||||
| chr19:48424267 | T | TTTTTTTT others(2829): Show |
7 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0154 others(4): Show |
7 | HG01074.hp1 HG01346.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.2252+2347_2252+234 others(2840): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48424267 | ||||||
| chr19:48424267 | T | TTTTTTTT others(2828): Show |
1 | a0001c0002t0002g0165 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2252+2347_2252+234 others(2839): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48424267 | ||||||
| chr19:48424267 | T | TTTTTTTT others(2822): Show |
1 | a0001c0002t0002g0314 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2252+2347_2252+234 others(2833): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48424267 | ||||||
| chr19:48424267 | T | TTTTTTTT others(2831): Show |
1 | a0001c0001t0001g0087 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2252+2343_2252+234 others(2842): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48424267 | ||||||
| chr19:48424267 | T | TTTTTTTT others(2830): Show |
1 | a0001c0002t0002g0284 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2252+2343_2252+234 others(2841): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48424267 | ||||||
| chr19:48424294 | A | G | 43 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0087 others(40): Show |
43 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.2252+2349A>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48424294 | |||||||
| chr19:48424357 | G | A | 2 | a0001c0001t0002g0277 a0001c0002t0002g0311 |
2 | HG03471.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.2252+2412G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48424357 | |||||||
| chr19:48424364 | G | A | 1 | a0001c0002t0002g0194 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2252+2419G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48424364 | |||||||
| chr19:48424416 | G | A | 1 | a0001c0004t0002g0107 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2252+2471G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48424416 | |||||||
| chr19:48424420 | A | G | 1 | a0001c0018t0002g0049 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.2252+2475A>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48424420 | |||||||
| chr19:48424432 | A | G | 1 | a0001c0018t0002g0049 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.2252+2487A>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48424432 | |||||||
| chr19:48424654 | C | A | 1 | a0001c0001t0002g0271 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2252+2709C>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48424654 | |||||||
| chr19:48424758 | C | T | 2 | a0001c0001t0002g0295 a0001c0001t0002g0296 |
2 | HG03239.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2252+2813C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48424758 | |||||||
| chr19:48424826 | A | G | 1 | a0001c0002t0002g0266 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2252+2881A>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48424826 | |||||||
| chr19:48424858 | C | T | 5 | a0001c0001t0001g0032 a0001c0001t0001g0088 a0001c0001t0001g0089 others(2): Show |
5 | HG02257.hp2 HG02717.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2252+2913C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48424858 | |||||||
| chr19:48424865 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2252+2920C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48424865 | |||||||
| chr19:48424948 | C | A | 10 | a0001c0001t0002g0030 a0001c0001t0002g0066 a0001c0002t0002g0067 others(7): Show |
10 | NA18612.hp2 NA18747.hp2 NA18952.hp2 others(7): Show |
intron_variant | MODIFIER | c.2252+3003C>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48424948 | |||||||
| chr19:48424964 | G | A | 1 | a0001c0002t0002g0284 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2252+3019G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48424964 | |||||||
| chr19:48425022 | TTC | T | 20 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0050 others(17): Show |
20 | HG00639.hp1 HG01074.hp1 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.2252+3098_2252+309 others(6): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48425022 | ||||||
| chr19:48425022 | TTCTC | T | 27 | a0001c0001t0001g0294 a0001c0001t0002g0029 a0001c0001t0002g0179 others(24): Show |
27 | HG00733.hp1 HG01070.hp2 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.2252+3096_2252+309 others(8): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48425022 | ||||||
| chr19:48425031 | T | C | 6 | a0001c0001t0001g0303 a0001c0002t0002g0077 a0001c0002t0002g0304 others(3): Show |
6 | HG01884.hp1 HG02886.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.2252+3086T>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48425031 | |||||||
| chr19:48425043 | T | A | 3 | a0001c0004t0002g0351 a0001c0004t0002g0353 a0001c0022t0002g0334 |
3 | HG01975.hp2 HG02015.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.2252+3098T>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48425043 | |||||||
| chr19:48425067 | A | G | 1 | a0001c0002t0002g0284 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2252+3122A>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48425067 | |||||||
| chr19:48425128 | A | T | 1 | a0001c0008t0001g0043 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2252+3183A>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48425128 | |||||||
| chr19:48425190 | C | T | 2 | a0001c0001t0001g0255 a0001c0001t0001g0342 |
2 | HG01081.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.2252+3245C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48425190 | |||||||
| chr19:48425220 | T | C | 10 | a0001c0001t0001g0279 a0001c0002t0002g0178 a0001c0002t0002g0282 others(7): Show |
10 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.2252+3275T>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48425220 | |||||||
| chr19:48425239 | G | A | 1 | a0001c0002t0002g0284 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2252+3294G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48425239 | |||||||
| chr19:48425307 | T | C | 12 | a0001c0001t0001g0011 a0001c0001t0001g0023 a0001c0001t0001g0096 others(9): Show |
12 | HG02145.hp1 HG02280.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.2252+3362T>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48425307 | |||||||
| chr19:48425339 | T | A | 15 | a0001c0001t0002g0030 a0001c0001t0002g0066 a0001c0002t0002g0067 others(12): Show |
16 | HG02083.hp1 NA18612.hp2 NA18747.hp2 others(13): Show |
intron_variant | MODIFIER | c.2252+3394T>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48425339 | |||||||
| chr19:48425449 | T | C | 98 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0018 others(95): Show |
98 | HG00280.hp2 HG00621.hp1 HG00621.hp2 others(95): Show |
intron_variant | MODIFIER | c.2252+3504T>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48425449 | |||||||
| chr19:48425756 | C | T | 3 | a0001c0001t0001g0279 a0001c0004t0002g0280 a0001c0004t0002g0281 |
3 | HG01891.hp1 HG02145.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2252+3811C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48425756 | |||||||
| chr19:48425805 | A | G | 1 | a0001c0001t0001g0239 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2252+3860A>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48425805 | |||||||
| chr19:48425840 | G | A | 25 | a0001c0001t0001g0294 a0001c0001t0002g0029 a0001c0001t0002g0179 others(22): Show |
25 | HG00733.hp1 HG01070.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.2252+3895G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48425840 | |||||||
| chr19:48425909 | C | T | 8 | a0001c0001t0001g0279 a0001c0002t0002g0178 a0001c0002t0002g0282 others(5): Show |
8 | HG01243.hp1 HG01891.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.2252+3964C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48425909 | |||||||
| chr19:48425926 | C | T | 3 | a0001c0001t0001g0285 a0001c0001t0002g0256 a0001c0023t0002g0270 |
3 | HG00140.hp2 HG03239.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2252+3981C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48425926 | |||||||
| chr19:48425934 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2252+3989G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48425934 | |||||||
| chr19:48426221 | T | TTTTTTTT others(7): Show |
1 | a0001c0002t0002g0109 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2252+4278_2252+427 others(18): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48426221 | ||||||
| chr19:48426222 | T | TTTTTTTT others(6): Show |
8 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0154 others(5): Show |
8 | HG01074.hp1 HG01346.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.2252+4278_2252+427 others(17): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48426222 | ||||||
| chr19:48426223 | T | TTTTTTTT others(5): Show |
1 | a0001c0002t0002g0165 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2252+4278_2252+427 others(16): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48426223 | |||||||
| chr19:48426224 | C | CT | 6 | a0001c0001t0001g0060 a0001c0001t0001g0215 a0001c0001t0001g0285 others(3): Show |
6 | HG00140.hp2 HG03239.hp1 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.2252+4296dupT | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48426224 | ||||||
| chr19:48426224 | C | CTTTCTTT others(16): Show |
1 | a0001c0002t0002g0207 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2252+4282_2252+428 others(27): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48426224 | ||||||
| chr19:48426224 | C | CTTTCTTT others(17): Show |
2 | a0001c0002t0002g0091 a0001c0002t0002g0211 |
2 | HG02280.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.2252+4282_2252+428 others(28): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48426224 | ||||||
| chr19:48426224 | C | CTTTCTTT others(18): Show |
1 | a0001c0002t0002g0208 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2252+4282_2252+428 others(29): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48426224 | ||||||
| chr19:48426224 | C | CTTTCTTT others(20): Show |
2 | a0001c0010t0002g0209 a0001c0010t0002g0210 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2252+4282_2252+428 others(31): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48426224 | ||||||
| chr19:48426224 | C | CTTTCTTT others(11): Show |
2 | a0001c0007t0007g0310 a0001c0012t0014g0302 |
2 | HG01433.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2252+4282_2252+428 others(22): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48426224 | ||||||
| chr19:48426224 | C | CTTTCTTT others(12): Show |
2 | a0001c0002t0002g0288 a0001c0007t0004g0309 |
2 | HG00733.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.2252+4282_2252+428 others(23): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48426224 | ||||||
| chr19:48426224 | C | CTTTTTTT | 6 | a0001c0001t0001g0272 a0001c0002t0002g0135 a0001c0002t0002g0141 others(3): Show |
6 | HG01169.hp2 HG01891.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.2252+4290_2252+429 others(11): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48426224 | ||||||
| chr19:48426224 | C | CTTTTTTT others(4): Show |
2 | a0001c0001t0002g0029 a0001c0002t0002g0028 |
2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2252+4286_2252+429 others(15): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48426224 | ||||||
| chr19:48426224 | C | CTTTTTTT others(10): Show |
6 | a0001c0001t0001g0294 a0001c0001t0002g0295 a0001c0002t0002g0297 others(3): Show |
6 | HG02683.hp2 HG03239.hp2 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.2252+4293_2252+429 others(21): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48426224 | ||||||
| chr19:48426224 | C | T | 11 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0087 others(8): Show |
11 | HG00639.hp1 HG01074.hp1 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.2252+4279C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48426224 | |||||||
| chr19:48426224 | CT | C | 12 | a0001c0001t0001g0033 a0001c0001t0001g0161 a0001c0001t0001g0203 others(9): Show |
12 | HG01070.hp1 HG01099.hp2 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.2252+4296delT | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48426224 | ||||||
| chr19:48426226 | T | TTTTTTTT others(7): Show |
1 | a0001c0001t0001g0087 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2252+4290_2252+429 others(18): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48426226 | ||||||
| chr19:48426227 | T | TTTTTTTT others(9): Show |
1 | a0001c0001t0002g0179 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2252+4293_2252+429 others(20): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48426227 | ||||||
| chr19:48426274 | G | A | 2 | a0001c0011t0002g0299 a0001c0011t0002g0300 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.2252+4329G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48426274 | |||||||
| chr19:48426297 | C | G | 10 | a0001c0001t0001g0225 a0001c0001t0002g0180 a0001c0001t0002g0222 others(7): Show |
10 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.2252+4352C>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48426297 | |||||||
| chr19:48426353 | G | A | 4 | a0001c0001t0001g0272 a0001c0001t0001g0286 a0001c0001t0011g0323 others(1): Show |
4 | HG02055.hp1 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.2252+4408G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48426353 | |||||||
| chr19:48426400 | A | G | 1 | a0001c0001t0001g0034 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2252+4455A>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48426400 | |||||||
| chr19:48426413 | A | G | 1 | a0001c0001t0001g0236 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.2252+4468A>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48426413 | |||||||
| chr19:48426473 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2252+4528G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48426473 | |||||||
| chr19:48426534 | T | C | 44 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0087 others(41): Show |
44 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.2252+4589T>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48426534 | |||||||
| chr19:48426865 | G | A | 35 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0087 others(32): Show |
35 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.2252+4920G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48426865 | |||||||
| chr19:48426987 | T | C | 1 | a0001c0001t0001g0176 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2252+5042T>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48426987 | |||||||
| chr19:48427037 | CAGTT | C | 17 | a0001c0001t0002g0029 a0001c0002t0002g0013 a0001c0002t0002g0028 others(14): Show |
17 | HG00733.hp1 HG01070.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.2252+5095_2252+509 others(8): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48427037 | ||||||
| chr19:48427102 | T | C | 35 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0087 others(32): Show |
35 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.2252+5157T>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48427102 | |||||||
| chr19:48427122 | C | T | 2 | a0001c0002t0002g0316 a0001c0002t0003g0007 |
2 | HG01243.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.2252+5177C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48427122 | |||||||
| chr19:48427210 | A | G | 1 | a0001c0002t0002g0284 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2252+5265A>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48427210 | |||||||
| chr19:48427256 | G | A | 1 | a0001c0002t0002g0301 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2252+5311G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48427256 | |||||||
| chr19:48427298 | C | G | 35 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0087 others(32): Show |
35 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.2252+5353C>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48427298 | |||||||
| chr19:48427388 | A | AT | 236 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(233): Show |
237 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.2252+5444dupT | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48427388 | ||||||
| chr19:48427410 | A | G | 35 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0087 others(32): Show |
35 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.2252+5465A>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48427410 | |||||||
| chr19:48427472 | C | CT | 16 | a0001c0001t0001g0001 a0001c0001t0001g0111 a0001c0001t0001g0112 others(13): Show |
17 | HG00609.hp1 HG00735.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.2252+5552dupT | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48427472 | ||||||
| chr19:48427472 | CT | C | 35 | a0001c0001t0001g0048 a0001c0001t0001g0125 a0001c0001t0001g0157 others(32): Show |
35 | HG01169.hp2 HG01256.hp1 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.2252+5552delT | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48427472 | ||||||
| chr19:48427472 | CTTT | C | 28 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0087 others(25): Show |
28 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.2252+5550_2252+555 others(7): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48427472 | ||||||
| chr19:48427479 | T | C | 2 | a0001c0002t0002g0109 a0001c0002t0002g0314 |
2 | HG03139.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.2252+5534T>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48427479 | |||||||
| chr19:48427480 | T | C | 16 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0087 others(13): Show |
16 | HG00639.hp1 HG01074.hp1 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.2252+5535T>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48427480 | |||||||
| chr19:48427639 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2252+5694C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48427639 | |||||||
| chr19:48427641 | GGTAATTT others(25): Show |
G | 1 | a0001c0002t0002g0284 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2252+5697_2252+572 others(36): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48427641 | |||||||
| chr19:48427674 | T | C | 1 | a0001c0002t0002g0284 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2252+5729T>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48427674 | |||||||
| chr19:48427716 | TGTGATCC others(37): Show |
T | 1 | a0001c0002t0002g0314 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2252+5776_2252+581 others(48): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48427716 | ||||||
| chr19:48427724 | G | A | 44 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0087 others(41): Show |
44 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.2252+5779G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48427724 | |||||||
| chr19:48427732 | C | T | 34 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0087 others(31): Show |
34 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.2252+5787C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48427732 | |||||||
| chr19:48427964 | G | C | 35 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0087 others(32): Show |
35 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.2252+6019G>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48427964 | |||||||
| chr19:48427965 | C | T | 35 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0087 others(32): Show |
35 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.2252+6020C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48427965 | |||||||
| chr19:48427985 | C | G | 35 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0087 others(32): Show |
35 | HG00639.hp1 HG00733.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.2252+6040C>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48427985 | |||||||
| chr19:48428029 | C | CTCTGTGG | 4 | a0001c0001t0001g0272 a0001c0001t0001g0286 a0001c0001t0011g0323 others(1): Show |
4 | HG02055.hp1 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.2252+6085_2252+609 others(11): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48428029 | ||||||
| chr19:48428044 | C | CT | 27 | a0001c0001t0001g0004 a0001c0001t0001g0089 a0001c0001t0001g0168 others(24): Show |
27 | HG01169.hp2 HG01891.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.2252+6117dupT | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48428044 | ||||||
| chr19:48428044 | CT | C | 29 | a0001c0001t0001g0036 a0001c0001t0001g0140 a0001c0001t0001g0294 others(26): Show |
29 | HG00733.hp1 HG01070.hp2 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.2252+6117delT | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48428044 | ||||||
| chr19:48428052 | T | G | 2 | a0001c0001t0002g0029 a0001c0002t0002g0028 |
2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2252+6107T>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48428052 | |||||||
| chr19:48428091 | C | T | 1 | a0001c0001t0001g0275 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2252+6146C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48428091 | |||||||
| chr19:48428263 | C | G | 1 | a0001c0004t0002g0351 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2252+6318C>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48428263 | |||||||
| chr19:48428391 | A | G | 6 | a0001c0002t0002g0091 a0001c0002t0002g0207 a0001c0002t0002g0208 others(3): Show |
6 | HG02280.hp2 HG02486.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.2252+6446A>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48428391 | |||||||
| chr19:48428404 | C | T | 1 | a0001c0001t0001g0364 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2252+6459C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48428404 | |||||||
| chr19:48428454 | G | A | 37 | a0001c0001t0001g0069 a0001c0001t0001g0110 a0001c0001t0001g0195 others(34): Show |
37 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.2252+6509G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48428454 | |||||||
| chr19:48428770 | C | G | 1 | a0001c0002t0002g0194 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2252+6825C>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48428770 | |||||||
| chr19:48428816 | T | G | 306 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(303): Show |
307 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.2252+6871T>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48428816 | |||||||
| chr19:48428822 | A | C | 11 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0087 others(8): Show |
11 | HG00639.hp1 HG01074.hp1 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.2252+6877A>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48428822 | |||||||
| chr19:48428962 | C | T | 1 | a0001c0001t0002g0024 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2252+7017C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48428962 | |||||||
| chr19:48429042 | A | G | 1 | a0001c0001t0002g0313 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2252+7097A>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48429042 | |||||||
| chr19:48429080 | T | C | 306 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(303): Show |
307 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.2252+7135T>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48429080 | |||||||
| chr19:48429288 | T | C | 306 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(303): Show |
307 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.2252+7343T>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48429288 | |||||||
| chr19:48429715 | A | ATG | 85 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0021 others(82): Show |
85 | HG00621.hp1 HG00621.hp2 HG00733.hp2 others(82): Show |
intron_variant | MODIFIER | c.2252+7794_2252+779 others(6): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48429715 | ||||||
| chr19:48429715 | A | ATGTG | 14 | a0001c0001t0001g0014 a0001c0001t0001g0303 a0001c0001t0002g0061 others(11): Show |
14 | HG00280.hp2 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.2252+7792_2252+779 others(8): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48429715 | ||||||
| chr19:48429715 | A | ATGTGTG | 8 | a0001c0001t0001g0279 a0001c0001t0001g0294 a0001c0001t0002g0295 others(5): Show |
8 | HG01891.hp1 HG02683.hp2 HG03239.hp2 others(5): Show |
intron_variant | MODIFIER | c.2252+7790_2252+779 others(10): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48429715 | ||||||
| chr19:48429715 | A | ATGTGTGT others(3): Show |
4 | a0001c0001t0002g0029 a0001c0002t0002g0013 a0001c0002t0002g0028 others(1): Show |
4 | HG02258.hp2 HG02965.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.2252+7786_2252+779 others(14): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48429715 | ||||||
| chr19:48429965 | T | C | 2 | a0001c0002t0002g0282 a0001c0002t0002g0283 |
2 | HG02723.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2252+8020T>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48429965 | |||||||
| chr19:48430084 | T | C | 1 | a0001c0001t0001g0279 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2252+8139T>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48430084 | |||||||
| chr19:48430429 | CCTCAAGT others(109): Show |
C | 5 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0040 others(2): Show |
5 | HG02615.hp2 HG02622.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.2252+8491_2252+860 others(4): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48430429 | ||||||
| chr19:48430663 | T | A | 2 | a0001c0001t0002g0029 a0001c0002t0002g0028 |
2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2252+8718T>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48430663 | |||||||
| chr19:48430714 | A | G | 6 | a0001c0002t0002g0091 a0001c0002t0002g0207 a0001c0002t0002g0208 others(3): Show |
6 | HG02280.hp2 HG02486.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.2252+8769A>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48430714 | |||||||
| chr19:48430803 | ATTTCTTT | A | 13 | a0001c0002t0002g0091 a0001c0002t0002g0207 a0001c0002t0002g0208 others(10): Show |
13 | HG01070.hp2 HG01071.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.2252+8876_2252+888 others(11): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48430803 | ||||||
| chr19:48430821 | C | CT | 19 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0087 others(16): Show |
19 | HG00558.hp2 HG00639.hp1 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.2252+8892dupT | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48430821 | ||||||
| chr19:48430821 | CT | C | 9 | a0001c0001t0001g0048 a0001c0001t0001g0065 a0001c0001t0001g0140 others(6): Show |
9 | HG01243.hp1 HG01256.hp1 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.2252+8892delT | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48430821 | ||||||
| chr19:48430888 | T | G | 2 | a0001c0001t0001g0279 a0001c0002t0002g0284 |
2 | HG01891.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2252+8943T>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48430888 | |||||||
| chr19:48431015 | C | T | 2 | a0001c0001t0001g0001 a0001c0001t0001g0112 |
3 | NA18955.hp2 NA18990.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.2252+9070C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48431015 | |||||||
| chr19:48431069 | T | C | 3 | a0001c0004t0002g0351 a0001c0004t0002g0353 a0001c0022t0002g0334 |
3 | HG01975.hp2 HG02015.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.2252+9124T>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48431069 | |||||||
| chr19:48431449 | G | C | 1 | a0001c0002t0002g0178 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2252+9504G>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48431449 | |||||||
| chr19:48431477 | G | A | 6 | a0001c0002t0002g0091 a0001c0002t0002g0207 a0001c0002t0002g0208 others(3): Show |
6 | HG02280.hp2 HG02486.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.2252+9532G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48431477 | |||||||
| chr19:48431585 | C | CT | 21 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0031 others(18): Show |
21 | HG00621.hp2 HG01070.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.2252+9656dupT | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48431585 | ||||||
| chr19:48431648 | G | A | 1 | a0001c0001t0002g0131 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2252+9703G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48431648 | |||||||
| chr19:48431859 | A | G | 1 | a0001c0002t0002g0178 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2253-9910A>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48431859 | |||||||
| chr19:48431877 | G | A | 1 | a0001c0001t0002g0179 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2253-9892G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48431877 | |||||||
| chr19:48431913 | C | CTTTATTT | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(98): Show |
101 | HG00280.hp2 HG00621.hp1 HG00621.hp2 others(98): Show |
intron_variant | MODIFIER | c.2253-9845_2253-983 others(11): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48431913 | ||||||
| chr19:48432025 | G | T | 8 | a0001c0002t0002g0091 a0001c0002t0002g0207 a0001c0002t0002g0208 others(5): Show |
8 | HG02280.hp2 HG02486.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.2253-9744G>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48432025 | |||||||
| chr19:48432214 | TTTTC | T | 10 | a0001c0001t0001g0272 a0001c0001t0001g0286 a0001c0001t0011g0323 others(7): Show |
10 | HG00733.hp1 HG01169.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.2253-9547_2253-954 others(8): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48432214 | ||||||
| chr19:48432222 | CT | C | 6 | a0001c0001t0001g0065 a0001c0001t0001g0101 a0001c0001t0001g0187 others(3): Show |
6 | HG01256.hp2 HG01257.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.2253-9532delT | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48432222 | ||||||
| chr19:48432226 | T | C | 2 | a0001c0001t0002g0276 a0001c0013t0001g0246 |
2 | NA18956.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.2253-9543T>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48432226 | |||||||
| chr19:48432392 | C | T | 6 | a0001c0001t0001g0279 a0001c0001t0002g0029 a0001c0002t0002g0013 others(3): Show |
6 | HG01891.hp1 HG02258.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.2253-9377C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48432392 | |||||||
| chr19:48432396 | T | C | 63 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0018 others(60): Show |
63 | HG00280.hp2 HG00621.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.2253-9373T>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48432396 | |||||||
| chr19:48432525 | C | G | 1 | a0001c0004t0002g0099 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2253-9244C>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48432525 | |||||||
| chr19:48432691 | T | C | 2 | a0001c0002t0002g0229 a0001c0002t0002g0237 |
2 | HG02738.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.2253-9078T>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48432691 | |||||||
| chr19:48432697 | G | A | 2 | a0001c0001t0001g0279 a0001c0002t0002g0284 |
2 | HG01891.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2253-9072G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48432697 | |||||||
| chr19:48432773 | CT | C | 7 | a0001c0001t0001g0031 a0001c0001t0001g0060 a0001c0001t0001g0268 others(4): Show |
7 | HG00140.hp1 HG01943.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.2253-8981delT | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48432773 | ||||||
| chr19:48432788 | T | A | 23 | a0001c0001t0001g0248 a0001c0001t0001g0279 a0001c0001t0002g0029 others(20): Show |
23 | HG00438.hp2 HG01070.hp2 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.2253-8981T>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48432788 | |||||||
| chr19:48432936 | G | A | 1 | a0001c0002t0002g0194 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2253-8833G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48432936 | |||||||
| chr19:48432952 | A | G | 3 | a0001c0004t0002g0213 a0001c0004t0002g0214 a0001c0004t0002g0274 |
3 | HG01070.hp2 HG01071.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2253-8817A>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48432952 | |||||||
| chr19:48433549 | C | T | 11 | a0001c0001t0001g0272 a0001c0001t0001g0286 a0001c0001t0011g0323 others(8): Show |
11 | HG00733.hp1 HG01169.hp2 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.2253-8220C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48433549 | |||||||
| chr19:48433580 | A | G | 4 | a0001c0002t0002g0284 a0001c0004t0002g0213 a0001c0004t0002g0214 others(1): Show |
4 | HG01070.hp2 HG01071.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.2253-8189A>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48433580 | |||||||
| chr19:48433653 | A | G | 3 | a0001c0001t0002g0167 a0001c0002t0002g0093 a0001c0002t0002g0311 |
3 | HG02809.hp2 HG03225.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2253-8116A>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48433653 | |||||||
| chr19:48433685 | A | T | 4 | a0001c0001t0002g0167 a0001c0002t0002g0093 a0001c0002t0002g0109 others(1): Show |
4 | HG02809.hp2 HG03139.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2253-8084A>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48433685 | |||||||
| chr19:48433777 | C | G | 2 | a0001c0002t0002g0141 a0001c0002t0002g0287 |
2 | HG02615.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2253-7992C>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48433777 | |||||||
| chr19:48433800 | A | G | 1 | a0001c0002t0002g0293 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2253-7969A>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48433800 | |||||||
| chr19:48433829 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2253-7940C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48433829 | |||||||
| chr19:48433891 | C | G | 1 | a0001c0003t0002g0361 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2253-7878C>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48433891 | |||||||
| chr19:48433902 | A | G | 14 | a0001c0001t0002g0042 a0001c0001t0002g0249 a0001c0001t0002g0252 others(11): Show |
14 | HG00438.hp1 HG01167.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.2253-7867A>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48433902 | |||||||
| chr19:48433904 | G | A | 5 | a0001c0001t0002g0137 a0001c0001t0002g0146 a0001c0001t0002g0147 others(2): Show |
5 | HG00733.hp2 HG01074.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.2253-7865G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48433904 | |||||||
| chr19:48433951 | C | CT | 10 | a0001c0001t0001g0272 a0001c0001t0001g0286 a0001c0002t0002g0142 others(7): Show |
10 | HG00733.hp1 HG01169.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.2253-7803dupT | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48433951 | ||||||
| chr19:48433957 | T | C | 1 | a0001c0002t0002g0319 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2253-7812T>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48433957 | |||||||
| chr19:48433971 | T | C | 1 | a0001c0002t0002g0028 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2253-7798T>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48433971 | |||||||
| chr19:48434030 | G | A | 2 | a0001c0001t0002g0167 a0001c0001t0002g0179 |
2 | HG02809.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2253-7739G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48434030 | |||||||
| chr19:48434099 | C | T | 2 | a0001c0002t0002g0316 a0001c0002t0003g0007 |
2 | HG01243.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.2253-7670C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48434099 | |||||||
| chr19:48434230 | A | G | 332 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(329): Show |
333 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.2253-7539A>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48434230 | |||||||
| chr19:48434232 | A | G | 322 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(319): Show |
323 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.2253-7537A>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48434232 | |||||||
| chr19:48434584 | CT | C | 3 | a0001c0001t0009g0070 a0001c0002t0002g0231 a0001c0003t0002g0349 |
3 | HG01169.hp2 NA18955.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.2253-7179delT | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48434584 | ||||||
| chr19:48434609 | T | C | 17 | a0001c0001t0002g0029 a0001c0001t0002g0035 a0001c0001t0002g0167 others(14): Show |
17 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.2253-7160T>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48434609 | |||||||
| chr19:48434618 | T | C | 1 | a0001c0005t0001g0022 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2253-7151T>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48434618 | |||||||
| chr19:48434645 | G | A | 204 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(201): Show |
205 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.2253-7124G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48434645 | |||||||
| chr19:48434830 | C | T | 18 | a0001c0002t0002g0028 a0001c0002t0002g0039 a0001c0002t0002g0091 others(15): Show |
18 | HG01975.hp2 HG02015.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2253-6939C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48434830 | |||||||
| chr19:48434899 | A | T | 1 | a0001c0002t0002g0077 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2253-6870A>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48434899 | |||||||
| chr19:48434919 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2253-6850G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48434919 | |||||||
| chr19:48434962 | T | A | 1 | a0001c0002t0002g0247 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2253-6807T>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48434962 | |||||||
| chr19:48435125 | G | C | 3 | a0001c0002t0002g0304 a0001c0002t0002g0307 a0001c0002t0003g0008 |
3 | HG01884.hp1 HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2253-6644G>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48435125 | |||||||
| chr19:48435296 | G | GT | 337 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(334): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.2253-6454dupT | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48435296 | ||||||
| chr19:48435296 | G | GTT | 15 | a0001c0001t0001g0098 a0001c0001t0001g0164 a0001c0001t0001g0286 others(12): Show |
15 | HG00438.hp1 HG02055.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.2253-6455_2253-645 others(6): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48435296 | ||||||
| chr19:48435296 | G | T | 2 | a0001c0002t0002g0141 a0001c0002t0002g0287 |
2 | HG02615.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2253-6473G>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48435296 | |||||||
| chr19:48435340 | A | G | 288 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(285): Show |
289 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.2253-6429A>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48435340 | |||||||
| chr19:48435482 | G | A | 205 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(202): Show |
206 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.2253-6287G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48435482 | |||||||
| chr19:48435585 | C | T | 1 | a0001c0003t0002g0312 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2253-6184C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48435585 | |||||||
| chr19:48435606 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2253-6163G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48435606 | |||||||
| chr19:48435682 | A | T | 1 | a0001c0001t0002g0276 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2253-6087A>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48435682 | |||||||
| chr19:48435689 | T | C | 245 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(242): Show |
246 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.2253-6080T>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48435689 | |||||||
| chr19:48435695 | G | T | 1 | a0001c0003t0002g0104 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.2253-6074G>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48435695 | |||||||
| chr19:48435719 | T | A | 3 | a0001c0001t0001g0071 a0001c0001t0001g0075 a0001c0001t0001g0076 |
3 | HG01069.hp1 HG01071.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.2253-6050T>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48435719 | |||||||
| chr19:48436010 | C | T | 2 | a0001c0004t0002g0188 a0001c0022t0002g0334 |
2 | HG02015.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.2253-5759C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48436010 | |||||||
| chr19:48436231 | C | T | 1 | a0001c0001t0002g0226 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2253-5538C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48436231 | |||||||
| chr19:48436291 | C | T | 288 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(285): Show |
289 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.2253-5478C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48436291 | |||||||
| chr19:48436300 | T | C | 2 | a0001c0003t0002g0361 a0001c0003t0015g0362 |
2 | HG01069.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.2253-5469T>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48436300 | |||||||
| chr19:48436336 | T | C | 4 | a0001c0002t0002g0028 a0001c0002t0002g0039 a0001c0002t0002g0208 others(1): Show |
4 | HG02486.hp2 HG02723.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2253-5433T>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48436336 | |||||||
| chr19:48436453 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2253-5316C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48436453 | |||||||
| chr19:48436580 | G | A | 1 | a0001c0002t0002g0242 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.2253-5189G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48436580 | |||||||
| chr19:48436758 | G | A | 1 | a0001c0002t0002g0293 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2253-5011G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48436758 | |||||||
| chr19:48436792 | T | C | 2 | a0001c0002t0002g0293 a0001c0003t0002g0260 |
2 | HG00673.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.2253-4977T>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48436792 | |||||||
| chr19:48436858 | G | A | 1 | a0001c0001t0001g0064 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2253-4911G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48436858 | |||||||
| chr19:48436890 | G | A | 3 | a0001c0004t0002g0213 a0001c0004t0002g0214 a0001c0004t0002g0274 |
3 | HG01070.hp2 HG01071.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2253-4879G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48436890 | |||||||
| chr19:48437045 | C | T | 5 | a0001c0001t0002g0137 a0001c0001t0002g0146 a0001c0001t0002g0147 others(2): Show |
5 | HG00733.hp2 HG01074.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.2253-4724C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48437045 | |||||||
| chr19:48437582 | G | A | 2 | a0001c0001t0001g0275 a0001c0001t0001g0278 |
2 | NA18747.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.2253-4187G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48437582 | |||||||
| chr19:48437650 | C | G | 51 | a0001c0001t0002g0020 a0001c0001t0002g0024 a0001c0001t0002g0042 others(48): Show |
51 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(48): Show |
intron_variant | MODIFIER | c.2253-4119C>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48437650 | |||||||
| chr19:48437748 | C | T | 1 | a0001c0001t0013g0017 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2253-4021C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48437748 | |||||||
| chr19:48438000 | A | C | 9 | a0001c0002t0002g0038 a0001c0002t0002g0077 a0001c0002t0002g0142 others(6): Show |
9 | HG01884.hp1 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.2253-3769A>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48438000 | |||||||
| chr19:48438015 | T | TAG | 305 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(302): Show |
306 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.2253-3750_2253-374 others(6): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48438015 | ||||||
| chr19:48438287 | C | CT | 18 | a0001c0002t0002g0053 a0001c0002t0002g0093 a0001c0002t0002g0109 others(15): Show |
18 | HG00597.hp1 HG01109.hp1 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.2253-3453dupT | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48438287 | ||||||
| chr19:48438287 | C | CTTTTTTT | 15 | a0001c0001t0002g0020 a0001c0001t0002g0052 a0001c0001t0002g0055 others(12): Show |
15 | HG00280.hp2 HG00738.hp2 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.2253-3459_2253-345 others(11): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48438287 | ||||||
| chr19:48438287 | C | CTTTTTTT others(1): Show |
19 | a0001c0001t0002g0047 a0001c0001t0002g0056 a0001c0001t0002g0080 others(16): Show |
19 | HG00140.hp2 HG00735.hp2 HG01975.hp2 others(16): Show |
intron_variant | MODIFIER | c.2253-3460_2253-345 others(12): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48438287 | ||||||
| chr19:48438287 | C | CTTTTTTT others(2): Show |
8 | a0001c0001t0002g0042 a0001c0001t0002g0249 a0001c0001t0002g0258 others(5): Show |
8 | HG00408.hp2 HG00438.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.2253-3461_2253-345 others(13): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48438287 | ||||||
| chr19:48438287 | C | CTTTTTTT others(3): Show |
4 | a0001c0001t0002g0024 a0001c0001t0002g0256 a0001c0001t0002g0296 others(1): Show |
4 | HG03471.hp1 HG03942.hp2 NA20805.hp2 others(1): Show |
intron_variant | MODIFIER | c.2253-3462_2253-345 others(14): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48438287 | ||||||
| chr19:48438287 | C | CTTTTTTT others(4): Show |
4 | a0001c0004t0002g0213 a0001c0004t0002g0214 a0001c0004t0002g0274 others(1): Show |
4 | HG01070.hp2 HG01071.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.2253-3463_2253-345 others(15): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48438287 | ||||||
| chr19:48438287 | C | CTTTTTTT others(5): Show |
4 | a0001c0001t0002g0167 a0001c0002t0002g0304 a0001c0002t0002g0307 others(1): Show |
4 | HG01884.hp1 HG02809.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2253-3464_2253-345 others(16): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48438287 | ||||||
| chr19:48438287 | C | CTTTTTTT others(6): Show |
8 | a0001c0001t0002g0179 a0001c0002t0002g0038 a0001c0002t0002g0077 others(5): Show |
8 | HG02572.hp1 HG02723.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.2253-3465_2253-345 others(17): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48438287 | ||||||
| chr19:48438287 | CTT | C | 8 | a0001c0001t0001g0018 a0001c0001t0001g0069 a0001c0001t0001g0110 others(5): Show |
8 | HG00741.hp2 HG01109.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.2253-3454_2253-345 others(6): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48438287 | ||||||
| chr19:48438287 | CTTT | C | 77 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0021 others(74): Show |
77 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.2253-3455_2253-345 others(7): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48438287 | ||||||
| chr19:48438287 | CTTTT | C | 122 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(119): Show |
123 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.2253-3456_2253-345 others(8): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48438287 | ||||||
| chr19:48438287 | CTTTTTTT others(1): Show |
C | 8 | a0001c0001t0002g0276 a0001c0002t0002g0039 a0001c0002t0002g0091 others(5): Show |
8 | HG01261.hp1 HG02280.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.2253-3460_2253-345 others(12): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48438287 | ||||||
| chr19:48438287 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0002g0146 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2253-3462_2253-345 others(14): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48438287 | ||||||
| chr19:48438288 | T | TTTTTTTT others(7): Show |
1 | a0001c0002t0002g0288 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2253-3472_2253-347 others(18): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48438288 | ||||||
| chr19:48438523 | C | T | 1 | a0001c0001t0002g0296 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2253-3246C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48438523 | |||||||
| chr19:48438593 | C | T | 2 | a0001c0004t0002g0213 a0001c0004t0002g0214 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.2253-3176C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48438593 | |||||||
| chr19:48438594 | G | A | 3 | a0001c0001t0001g0101 a0001c0009t0001g0116 a0001c0009t0001g0223 |
3 | HG02109.hp1 HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2253-3175G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48438594 | |||||||
| chr19:48438891 | C | T | 15 | a0001c0001t0002g0029 a0001c0001t0002g0035 a0001c0001t0002g0180 others(12): Show |
15 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.2253-2878C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48438891 | |||||||
| chr19:48439158 | G | A | 9 | a0001c0002t0002g0028 a0001c0002t0002g0039 a0001c0002t0002g0091 others(6): Show |
9 | HG01261.hp1 HG02280.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.2253-2611G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48439158 | |||||||
| chr19:48439857 | C | T | 84 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0048 others(81): Show |
85 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.2253-1912C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48439857 | |||||||
| chr19:48439858 | G | A | 2 | a0001c0001t0001g0015 a0005c0016t0001g0016 |
2 | NA18971.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.2253-1911G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48439858 | |||||||
| chr19:48439898 | G | A | 6 | a0001c0002t0002g0013 a0001c0002t0002g0165 a0001c0002t0002g0316 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.2253-1871G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48439898 | |||||||
| chr19:48440054 | A | G | 1 | a0001c0002t0002g0284 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2253-1715A>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48440054 | |||||||
| chr19:48440117 | A | G | 4 | a0001c0001t0001g0048 a0001c0001t0001g0124 a0001c0001t0001g0128 others(1): Show |
4 | HG00735.hp1 HG01099.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.2253-1652A>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48440117 | |||||||
| chr19:48440221 | A | T | 59 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0032 others(56): Show |
59 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.2253-1548A>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48440221 | |||||||
| chr19:48440225 | T | A | 3 | a0001c0001t0001g0354 a0001c0002t0002g0053 a0001c0002t0003g0007 |
3 | HG01243.hp1 HG04204.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.2253-1544T>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48440225 | |||||||
| chr19:48440565 | C | T | 1 | a0001c0001t0002g0066 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.2253-1204C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48440565 | |||||||
| chr19:48440664 | T | C | 272 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(269): Show |
273 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.2253-1105T>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48440664 | |||||||
| chr19:48440678 | C | CCCCATTT others(11): Show |
285 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(282): Show |
286 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.2253-1089_2253-108 others(22): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48440678 | ||||||
| chr19:48440812 | G | A | 1 | a0001c0001t0008g0220 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2253-957G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48440812 | |||||||
| chr19:48440843 | C | T | 1 | a0001c0002t0002g0242 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.2253-926C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48440843 | |||||||
| chr19:48440988 | C | A | 1 | a0001c0001t0001g0113 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2253-781C>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48440988 | |||||||
| chr19:48441033 | G | A | 8 | a0001c0002t0002g0038 a0001c0002t0002g0077 a0001c0002t0002g0142 others(5): Show |
8 | HG01884.hp1 HG02572.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.2253-736G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48441033 | |||||||
| chr19:48441092 | C | T | 3 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0315 |
3 | NA18948.hp1 NA18983.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.2253-677C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48441092 | |||||||
| chr19:48441132 | AGACAGGT others(10): Show |
A | 9 | a0001c0002t0002g0028 a0001c0002t0002g0039 a0001c0002t0002g0091 others(6): Show |
9 | HG01261.hp1 HG02280.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.2253-630_2253-614d others(19): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48441132 | ||||||
| chr19:48441249 | G | A | 2 | a0001c0001t0001g0001 a0001c0001t0001g0112 |
3 | NA18955.hp2 NA18990.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.2253-520G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48441249 | |||||||
| chr19:48441294 | C | T | 1 | a0001c0018t0002g0049 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.2253-475C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48441294 | |||||||
| chr19:48441362 | C | CA | 15 | a0001c0002t0002g0093 a0001c0002t0002g0102 a0001c0002t0002g0109 others(12): Show |
15 | HG01261.hp1 HG01433.hp2 HG02040.hp1 others(12): Show |
intron_variant | MODIFIER | c.2253-384dupA | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48441362 | ||||||
| chr19:48441362 | CA | C | 23 | a0001c0001t0001g0076 a0001c0001t0001g0153 a0001c0001t0001g0173 others(20): Show |
23 | HG00408.hp2 HG00438.hp1 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.2253-384delA | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48441362 | ||||||
| chr19:48441378 | A | G | 1 | a0001c0001t0002g0258 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2253-391A>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48441378 | |||||||
| chr19:48441382 | A | AG | 8 | a0001c0001t0001g0081 a0001c0001t0001g0112 a0001c0001t0001g0150 others(5): Show |
8 | HG03017.hp1 HG03710.hp2 NA18906.hp1 others(5): Show |
intron_variant | MODIFIER | c.2253-387_2253-386i others(3): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48441382 | |||||||
| chr19:48441382 | A | G | 235 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(232): Show |
236 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.2253-387A>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48441382 | |||||||
| chr19:48441493 | G | T | 13 | a0001c0001t0002g0042 a0001c0001t0002g0249 a0001c0001t0002g0252 others(10): Show |
13 | HG00408.hp2 HG00438.hp1 HG01975.hp2 others(10): Show |
intron_variant | MODIFIER | c.2253-276G>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48441493 | |||||||
| chr19:48441756 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2253-13C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48441756 | |||||||
| chr19:48441979 | C | T | 3 | a0001c0001t0001g0071 a0001c0001t0001g0075 a0001c0001t0001g0076 |
3 | HG01069.hp1 HG01071.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.2440+23C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 12/13 | chr19 | 48441979 | |||||||
| chr19:48442082 | T | TC | 48 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0018 others(45): Show |
48 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.2441-65dupC | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr19 | 48442082 | ||||||
| chr19:48442100 | G | A | 1 | a0001c0001t0002g0052 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2441-50G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 12/13 | chr19 | 48442100 | |||||||
| chr19:48442100 | G | C | 1 | a0001c0001t0001g0238 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2441-50G>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 12/13 | chr19 | 48442100 | |||||||
| chr19:48442415 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.2673+33G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 13/13 | chr19 | 48442415 | |||||||
| chr19:48442430 | G | A | 2 | a0001c0001t0002g0167 a0001c0001t0002g0179 |
2 | HG02809.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2673+48G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 13/13 | chr19 | 48442430 | |||||||
| chr19:48442469 | C | G | 3 | a0001c0004t0002g0213 a0001c0004t0002g0214 a0001c0004t0002g0274 |
3 | HG01070.hp2 HG01071.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2673+87C>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 13/13 | chr19 | 48442469 | |||||||
| chr19:48442486 | G | T | 15 | a0001c0002t0002g0013 a0001c0002t0002g0028 a0001c0002t0002g0039 others(12): Show |
15 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.2673+104G>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 13/13 | chr19 | 48442486 |