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 | copy fasta | chr19 | 48388668 | 48449931 |
a0002 | 0/0 | 1336 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
a0003 | 0/0 | 1336 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
a0004 | 0/0 | 1330 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
a0005 | 0/0 | 1336 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 4011 | 227 | 51 | 50 | 89 | 7 | 29 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
c0002 | 1/0 | 4011 | 61 | 30 | 4 | 17 | 1 | 8 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
c0003 | 0/0 | 4011 | 36 | 0 | 3 | 31 | 1 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
c0004 | 0/0 | 4011 | 12 | 4 | 4 | 4 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
c0005 | 0/0 | 4011 | 5 | 0 | 4 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
c0006 | 0/0 | 4011 | 3 | 1 | 2 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
c0007 | 0/0 | 4011 | 2 | 1 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
c0008 | 0/0 | 4011 | 2 | 0 | 2 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
c0009 | 0/0 | 4011 | 2 | 2 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
c0010 | 0/0 | 4011 | 2 | 2 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
c0011 | 0/0 | 4011 | 2 | 0 | 2 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
c0012 | 0/0 | 4011 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
c0013 | 0/0 | 4011 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
c0014 | 0/0 | 4011 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
c0015 | 0/0 | 4011 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
c0016 | 0/0 | 3993 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
c0017 | 0/0 | 4011 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
c0018 | 0/0 | 4011 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
c0019 | 0/0 | 4011 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
c0020 | 0/0 | 4011 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
c0021 | 0/0 | 4011 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
c0022 | 0/0 | 4011 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
c0023 | 0/0 | 4011 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 1501 | 176 | 37 | 50 | 66 | 4 | 18 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
t0002 | 1/0 | 1501 | 175 | 49 | 20 | 77 | 6 | 22 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
t0003 | 0/0 | 1501 | 2 | 1 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
t0004 | 0/0 | 1501 | 2 | 1 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
t0005 | 0/0 | 1501 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
t0006 | 0/0 | 1501 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
t0007 | 0/0 | 1501 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
t0008 | 0/0 | 1501 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
t0009 | 0/0 | 1501 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
t0010 | 0/0 | 1501 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
t0011 | 0/0 | 1501 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
t0012 | 0/0 | 1501 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
t0013 | 0/0 | 1501 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
t0014 | 0/0 | 1501 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
t0015 | 0/0 | 1547 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0147 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0262 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0357 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 4011 | 227 | 51 | 50 | 89 | 7 | 29 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
a0001c0002 | 1/0 | 4011 | 61 | 30 | 4 | 17 | 1 | 8 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
a0001c0003 | 0/0 | 4011 | 36 | 0 | 3 | 31 | 1 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
a0001c0004 | 0/0 | 4011 | 12 | 4 | 4 | 4 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
a0001c0005 | 0/0 | 4011 | 5 | 0 | 4 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
a0001c0006 | 0/0 | 4011 | 3 | 1 | 2 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
a0001c0007 | 0/0 | 4011 | 2 | 1 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
a0001c0008 | 0/0 | 4011 | 2 | 0 | 2 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
a0001c0009 | 0/0 | 4011 | 2 | 2 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
a0001c0010 | 0/0 | 4011 | 2 | 2 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
a0001c0011 | 0/0 | 4011 | 2 | 0 | 2 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
a0001c0012 | 0/0 | 4011 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
a0001c0013 | 0/0 | 4011 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
a0001c0015 | 0/0 | 4011 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
a0001c0018 | 0/0 | 4011 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
a0001c0020 | 0/0 | 4011 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
a0001c0021 | 0/0 | 4011 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
a0001c0022 | 0/0 | 4011 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
a0001c0023 | 0/0 | 4011 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
a0002c0014 | 0/0 | 4011 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
a0003c0017 | 0/0 | 4011 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
a0004c0016 | 0/0 | 3993 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
a0005c0019 | 0/0 | 4011 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | 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 | copy fasta | chr19 | 48388668 | 48449931 |
a0001c0001t0002 | 0/0 | 5511 | 60 | 14 | 7 | 24 | 3 | 12 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
a0001c0001t0004 | 0/0 | 5511 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
a0001c0001t0005 | 0/0 | 5511 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
a0001c0001t0006 | 0/0 | 5511 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
a0001c0001t0008 | 0/0 | 5511 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
a0001c0001t0009 | 0/0 | 5511 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
a0001c0001t0010 | 0/0 | 5511 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
a0001c0001t0011 | 0/0 | 5511 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
a0001c0001t0013 | 0/0 | 5511 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
a0001c0002t0002 | 1/0 | 5511 | 58 | 29 | 3 | 16 | 1 | 8 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
a0001c0002t0003 | 0/0 | 5511 | 2 | 1 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
a0001c0002t0012 | 0/0 | 5511 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
a0001c0003t0002 | 0/0 | 5511 | 35 | 0 | 3 | 30 | 1 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
a0001c0003t0015 | 0/0 | 5557 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
a0001c0004t0002 | 0/0 | 5511 | 12 | 4 | 4 | 4 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
a0001c0005t0001 | 0/0 | 5511 | 5 | 0 | 4 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
a0001c0006t0001 | 0/0 | 5511 | 2 | 1 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
a0001c0006t0002 | 0/0 | 5511 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
a0001c0007t0004 | 0/0 | 5511 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
a0001c0007t0007 | 0/0 | 5511 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
a0001c0008t0001 | 0/0 | 5511 | 2 | 0 | 2 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
a0001c0009t0001 | 0/0 | 5511 | 2 | 2 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
a0001c0010t0002 | 0/0 | 5511 | 2 | 2 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
a0001c0011t0002 | 0/0 | 5511 | 2 | 0 | 2 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
a0001c0012t0014 | 0/0 | 5511 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
a0001c0013t0001 | 0/0 | 5511 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
a0001c0015t0002 | 0/0 | 5511 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
a0001c0018t0002 | 0/0 | 5511 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
a0001c0020t0002 | 0/0 | 5511 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
a0001c0021t0001 | 0/0 | 5511 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
a0001c0022t0002 | 0/0 | 5511 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
a0001c0023t0002 | 0/0 | 5511 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
a0002c0014t0001 | 0/0 | 5511 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
a0003c0017t0001 | 0/0 | 5511 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
a0004c0016t0001 | 0/0 | 5493 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
a0005c0019t0001 | 0/0 | 5511 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | copy fasta | chr19 | 48388668 | 48449931 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0001t0001g0008 | 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 | 0 | 0 | 1 | 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 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 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 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 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 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 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 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0001t0001g0224 | 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 |
a0001c0001t0001g0253 | 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 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0001t0001g0258 | 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 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0001t0001g0287 | 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 |
a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0001t0001g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0001t0001g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 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 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
a0001c0001t0002g0106 | 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 |
a0001c0001t0002g0148 | 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 |
a0001c0001t0002g0225 | 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 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0001t0002g0259 | 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 |
a0001c0001t0002g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0001t0002g0361 | 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 |
a0001c0001t0005g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0001t0006g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0001t0008g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0001t0009g0068 | 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 |
a0001c0001t0013g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0002t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0002t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0002t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0002t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0002t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0002t0002g0089 | 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 |
a0001c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0002t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0002t0002g0107 | 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 |
a0001c0002t0002g0147 | 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 |
a0001c0002t0002g0285 | 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 |
a0001c0002t0003g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0002t0003g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0002t0012g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0003t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0003t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0003t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0003t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0003t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0003t0002g0083 | 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 |
a0001c0003t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0003t0002g0254 | 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 |
a0001c0003t0002g0346 | 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 |
a0001c0003t0002g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0003t0002g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0003t0002g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0003t0002g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0003t0002g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0003t0002g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0003t0002g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0003t0002g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0003t0015g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0004t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0004t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0004t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0004t0002g0105 | 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 |
a0001c0004t0002g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0004t0002g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0005t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0005t0001g0070 | 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 |
a0001c0005t0001g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0006t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0006t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0001c0006t0002g0025 | 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 |
a0001c0008t0001g0041 | 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 |
a0001c0018t0002g0047 | 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 |
a0001c0021t0001g0356 | 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 |
a0003c0017t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0004c0016t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
a0005c0019t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 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 | g0071 | 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 | g0059 | 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 | g0111 | EAS | CHS | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
HG00597 | hp1 | a0001 | c0003 | t0002 | g0365 | EAS | CHS | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0256 | 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 | g0032 | EAS | CHS | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0085 | 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 | g0023 | 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 | g0054 | 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 | g0053 | AMR | PUR | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
HG00741 | hp1 | a0001 | c0021 | t0001 | g0356 | AMR | PUR | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
HG01069 | hp2 | a0001 | c0003 | t0002 | g0363 | 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 | g0073 | 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 | g0020 | 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 | g0055 | 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 | g0005 | AMR | PUR | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0080 | 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 | g0063 | 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 | g0049 | AMR | CLM | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0061 | 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 | g0100 | AMR | CLM | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0220 | 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 | g0069 | 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 | g0041 | 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 | g0025 | AMR | CLM | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
HG01496 | hp2 | a0001 | c0005 | t0001 | g0070 | 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 | g0225 | 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 | g0348 | AMR | PEL | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0029 | 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 | g0355 | 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 | g0012 | EAS | KHV | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | ACB | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
HG02056 | hp1 | a0001 | c0002 | t0012 | g0090 | 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 | g0253 | 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 | g0345 | 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 | g0018 | 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 | g0098 | 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 | g0016 | 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 | g0132 | 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 | g0088 | AFR | ACB | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0027 | 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 | g0354 | 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 | g0089 | AFR | ACB | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
HG02293 | hp1 | a0001 | c0001 | t0008 | g0221 | AMR | PEL | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
HG02293 | hp2 | a0001 | c0004 | t0002 | g0353 | AMR | PEL | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
HG02300 | hp1 | a0001 | c0003 | t0002 | g0358 | 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 | g0265 | AFR | ACB | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
HG02523 | hp1 | a0001 | c0001 | t0005 | g0057 | 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 | g0288 | AFR | GWD | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0035 | 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 | g0038 | 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 | g0087 | AFR | GWD | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
HG02723 | hp1 | a0001 | c0002 | t0002 | g0037 | AFR | GWD | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
HG02723 | hp2 | a0001 | c0002 | t0002 | g0284 | 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 | g0258 | 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 | g0097 | AFR | GWD | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
HG02886 | hp2 | a0001 | c0002 | t0002 | g0075 | 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 | g0030 | 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 | g0026 | 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 | g0264 | AFR | ESN | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | ESN | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
HG02976 | hp2 | a0001 | c0002 | t0002 | g0283 | 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 | g0306 | 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 | g0094 | 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 | g0009 | 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 | g0107 | AFR | ESN | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
HG03209 | hp1 | a0001 | c0001 | t0006 | g0004 | AFR | MSL | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
HG03209 | hp2 | a0001 | c0002 | t0002 | g0305 | AFR | MSL | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
HG03225 | hp1 | a0001 | c0002 | t0003 | g0006 | AFR | MSL | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
HG03225 | hp2 | a0001 | c0002 | t0002 | g0091 | AFR | MSL | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0286 | 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 | g0021 | AFR | MSL | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
HG03453 | hp2 | a0001 | c0002 | t0002 | g0036 | 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 | g0259 | 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 | g0046 | SAS | PJL | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
HG03710 | hp1 | a0003 | 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 | g0056 | 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 | g0078 | 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 | g0067 | 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 | g0002 | 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 | g0093 | SAS | STU | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0050 | 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 | g0051 | SAS | STU | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0224 | 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 | g0076 | 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 | g0096 | AFR | YRI | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
NA18941 | hp1 | a0001 | c0003 | t0002 | g0102 | 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 | g0337 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
NA18942 | hp2 | a0001 | c0002 | t0002 | g0039 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0361 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
NA18945 | hp1 | a0001 | c0018 | t0002 | g0047 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
NA18945 | hp2 | a0001 | c0003 | t0002 | g0332 | 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 | g0048 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
NA18951 | hp2 | a0001 | c0003 | t0002 | g0350 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
NA18952 | hp2 | a0001 | c0003 | t0002 | g0017 | 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 | g0083 | 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 | g0336 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
NA18963 | hp1 | a0001 | c0003 | t0002 | g0333 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0131 | 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 | g0028 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
NA18965 | hp2 | a0001 | c0003 | t0015 | g0364 | 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 | g0044 | 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 | g0347 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0013 | 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 | g0360 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
NA18977 | hp1 | a0001 | c0004 | t0002 | g0105 | 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 | g0058 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
NA18979 | hp2 | a0001 | c0002 | t0002 | g0092 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0052 | 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 | g0359 | 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 | g0112 | 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 | g0042 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0079 | 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 | g0104 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0352 | 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 | g0060 | 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 | g0106 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
NA19009 | hp1 | a0001 | c0004 | t0002 | g0081 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
NA19009 | hp2 | a0001 | c0002 | t0002 | g0065 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0366 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0176 | 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 | g0346 | 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 | g0072 | 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 | g0043 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
NA19059 | hp1 | a0001 | c0003 | t0002 | g0084 | 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 | g0019 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
NA19065 | hp2 | a0004 | c0016 | t0001 | g0015 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
NA19066 | hp2 | a0001 | c0003 | t0002 | g0254 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
NA19068 | hp2 | a0001 | c0001 | t0013 | g0014 | 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 | g0362 | 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 | g0082 | 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 | g0349 | 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 | g0066 | 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 | g0064 | 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 | g0351 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0103 | 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 | g0086 | 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 | g0034 | 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 | g0148 | EUR | TSI | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0357 | EUR | TSI | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0257 | EUR | TSI | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0045 | 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 | g0099 | 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 | g0282 | 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 | a0005 | 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 | g0022 | 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 | g0011 | AFR | USA | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
NA18955 | hp1 | a0001 | c0001 | t0009 | g0068 | EAS | JPT | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0110 | 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 | g0285 | AFR | USA | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
NA21309 | hp2 | a0001 | c0006 | t0001 | g0024 | AFR | LWK | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0262 | REF | REF | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0002 | g0147 | REF | REF | GRIN2D_chr19_48388668_48449931 | GRIN2D | chr19 | 48388668 | 48449931 |
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 | a0005 | 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 | a0004 | 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 | a0003 | 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 |
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 | a0001c0007a0001c0012 | 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 | a0001c0003a0001c0005a0001c0022 | 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 | a0001c0001a0001c0004a0001c0005others(13): Show | 262 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(259): 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 | a0001c0001a0001c0005a0001c0006others(11): Show | 249 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(246): 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 | a0001c0001a0001c0005a0001c0006others(11): Show | 249 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(246): 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 |
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 | a0001c0001t0004a0001c0007t0004a0001c0012t0014 | 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 | a0001c0001t0006a0001c0002t0003 | 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 | a0001c0001t0010a0001c0001t0011 | 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 | a0001c0001t0004a0001c0007t0004a0001c0007t0007others(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 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(16): Show | 184 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(181): 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 |
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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0002g0101a0001c0001t0002g0103a0001c0001t0002g0106others(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 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(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 | 295 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(292): Show | 295 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(292): 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 | a0001c0001t0001g0176 | 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 | a0001c0001t0001g0175a0001c0001t0001g0366a0001c0001t0002g0360others(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 | a0001c0001t0001g0177 | 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 | a0001c0001t0001g0176 | 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 | a0001c0003t0002g0358a0001c0003t0002g0359 | 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | 124 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0175others(121): Show | 124 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(121): 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 | a0001c0001t0001g0294a0001c0001t0002g0295a0001c0001t0002g0296others(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 | a0001c0001t0001g0176a0001c0001t0001g0303a0001c0001t0002g0179others(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 | 139 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(136): 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 | a0001c0001t0001g0093 | 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 | a0001c0001t0001g0173a0001c0001t0001g0286a0001c0001t0001g0287others(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 | 185 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(182): 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 | a0001c0003t0002g0363 | 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 | a0001c0001t0001g0294a0001c0001t0002g0027a0001c0001t0002g0295others(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 | a0001c0001t0002g0028 | 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 | a0001c0003t0015g0364 | 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 | a0001c0002t0002g0301a0001c0011t0002g0299a0001c0011t0002g0300 | 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 | a0001c0001t0001g0294a0001c0001t0002g0295a0001c0001t0002g0296others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(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 | a0001c0002t0002g0282 | 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 | a0001c0002t0002g0301a0001c0011t0002g0299a0001c0011t0002g0300 | 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 | a0001c0002t0002g0283a0001c0002t0002g0284 | 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 | a0001c0001t0002g0028 | 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 | a0001c0001t0001g0352a0001c0001t0001g0354a0001c0004t0002g0353others(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 | a0001c0001t0001g0294a0001c0001t0002g0027a0001c0001t0002g0295others(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 | a0001c0001t0002g0027a0001c0002t0002g0026 | 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 | 37 | a0001c0001t0001g0340a0001c0001t0001g0342a0001c0001t0001g0344others(34): 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 | a0001c0001t0002g0101a0001c0001t0002g0103a0001c0001t0002g0106others(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 | a0001c0002t0012g0090 | 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 | a0005c0019t0001g0118 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0085others(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 | a0001c0001t0001g0021a0001c0001t0002g0022 | 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 | a0001c0001t0001g0003 | 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 | a0001c0004t0002g0213a0001c0004t0002g0214 | 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 | a0001c0001t0001g0279a0001c0004t0002g0280a0001c0004t0002g0281 | 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 | a0001c0001t0001g0294a0001c0001t0002g0027a0001c0001t0002g0295others(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 | a0001c0001t0002g0179a0001c0002t0002g0285 | 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 | a0001c0004t0002g0213a0001c0004t0002g0214 | 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 | 281 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(278): Show | 281 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(278): 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 | a0001c0002t0002g0011 | 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 | a0001c0002t0002g0301a0001c0011t0002g0299a0001c0011t0002g0300 | 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 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0315 | 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 | a0001c0002t0002g0285 | 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 | a0001c0003t0002g0082a0001c0003t0002g0083a0001c0003t0002g0084others(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 | a0001c0001t0001g0195a0001c0001t0001g0218a0001c0001t0001g0219others(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 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0224others(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 | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(228): Show | 231 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(228): 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | 276 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(273): Show | 276 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.465+2407G>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 3/13 | chr19 | 48401264 | ||||||
chr19:48401265
|
G | A | 278 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(275): Show | 278 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(275): 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 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0002g0167others(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 | a0001c0001t0001g0117a0001c0001t0001g0168a0001c0001t0001g0169others(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 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(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 | 77 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(74): Show | 77 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(74): 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 | a0001c0002t0002g0301a0001c0011t0002g0299a0001c0011t0002g0300 | 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 | a0001c0001t0001g0294a0001c0001t0002g0027a0001c0001t0002g0295others(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 | 37 | a0001c0001t0001g0232a0001c0001t0001g0303a0001c0001t0001g0340others(34): 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 | a0001c0001t0001g0303a0001c0002t0002g0304a0001c0002t0002g0305others(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 | a0001c0001t0001g0294a0001c0001t0002g0295a0001c0001t0002g0296others(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 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0002g0167others(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 | 20 | a0001c0001t0001g0013a0001c0001t0001g0110a0001c0001t0001g0111others(17): 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 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(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 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0125others(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 | a0001c0002t0002g0284 | 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 | a0001c0001t0001g0166a0001c0001t0002g0167a0001c0002t0002g0107 | 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 | a0001c0002t0002g0283 | 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 | a0001c0002t0002g0089 | 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 | a0001c0001t0001g0012a0001c0001t0001g0038a0001c0001t0001g0073others(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 | 143 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(140): Show | 143 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(140): 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 | a0001c0001t0011g0323a0001c0002t0002g0316a0001c0002t0002g0319 | 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 | a0001c0001t0001g0366 | 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 | a0001c0001t0001g0123a0001c0001t0001g0163a0001c0001t0001g0236 | 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 | a0001c0001t0001g0294a0001c0001t0002g0295a0001c0001t0002g0296others(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 | a0001c0001t0001g0352a0001c0002t0002g0229a0001c0002t0002g0237others(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 | 131 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(128): Show | 131 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(128): 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 | a0001c0001t0011g0323a0001c0002t0002g0316a0001c0002t0002g0319 | 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 | a0001c0001t0001g0366 | 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 | a0001c0001t0001g0095 | 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 | a0001c0002t0002g0285a0001c0011t0002g0299 | 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 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0016others(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 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0094 | 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 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0048others(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 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0029others(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 | a0001c0001t0001g0019a0001c0001t0001g0031a0001c0001t0001g0032others(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 | 192 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(189): Show | 192 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(189): 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 | a0001c0002t0012g0090 | 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 | a0001c0001t0001g0049a0001c0001t0001g0294a0001c0001t0002g0027others(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 | a0001c0001t0001g0134a0001c0002t0002g0135a0001c0002t0002g0141others(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 | 71 | a0001c0001t0001g0110a0001c0001t0001g0117a0001c0001t0001g0124others(68): Show | 71 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(68): 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 | a0001c0001t0001g0079a0001c0001t0001g0136a0001c0001t0001g0168others(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 | a0001c0001t0001g0294a0001c0001t0002g0027a0001c0001t0002g0295others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(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 | 45 | a0001c0001t0001g0289a0001c0001t0001g0340a0001c0001t0001g0342others(42): 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 | a0001c0001t0001g0013a0001c0001t0001g0056a0001c0001t0001g0073others(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 | a0001c0001t0001g0016a0001c0001t0001g0042a0001c0001t0001g0096others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(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 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0029others(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 | a0001c0001t0001g0032a0001c0001t0001g0048a0001c0001t0001g0052others(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 | a0001c0001t0001g0030a0001c0001t0001g0062a0001c0001t0001g0063others(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 | a0001c0001t0001g0069a0001c0001t0001g0085a0001c0001t0002g0054others(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 | a0001c0001t0001g0175a0001c0001t0002g0033a0001c0004t0002g0281 | 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 | a0001c0001t0001g0134a0001c0001t0001g0164a0001c0001t0001g0166others(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 | 19 | a0001c0001t0001g0129a0001c0001t0001g0144a0001c0001t0001g0200others(16): 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0079others(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 | 73 | a0001c0001t0001g0008a0001c0001t0001g0176a0001c0001t0001g0195others(70): Show | 73 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(70): 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 | a0001c0001t0001g0099a0001c0001t0001g0275a0001c0001t0001g0278others(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 | a0001c0001t0001g0294a0001c0001t0002g0027a0001c0001t0002g0295others(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 | a0001c0002t0002g0039 | 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 | a0001c0001t0001g0272a0001c0001t0001g0287a0001c0001t0010g0322others(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 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0243others(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 | a0001c0001t0001g0110a0001c0001t0001g0128a0001c0001t0001g0130others(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 | a0001c0001t0001g0079a0001c0001t0001g0166a0001c0001t0001g0196others(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 | 119 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(116): Show | 119 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(116): 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 | a0001c0001t0001g0245a0001c0001t0001g0269a0001c0001t0001g0279others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(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 | 272 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(269): Show | 272 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(269): 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 | a0001c0001t0001g0294a0001c0001t0002g0295a0001c0001t0002g0296others(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 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0289 | 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 | a0001c0003t0002g0359 | 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 | 79 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(76): Show | 79 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(76): 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 | a0001c0001t0001g0145a0001c0001t0001g0153a0001c0001t0001g0154others(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 | a0001c0003t0002g0076 | 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 | a0001c0001t0001g0099 | 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 | a0001c0001t0002g0295a0001c0001t0002g0296 | 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 | 131 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(128): Show | 131 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(128): 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 | a0001c0002t0002g0316a0001c0002t0002g0319 | 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 | a0001c0001t0001g0224a0001c0001t0002g0180a0001c0001t0002g0222others(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 | a0001c0001t0001g0340a0001c0001t0001g0342a0001c0002t0002g0339others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(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 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0217others(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 | 121 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(118): Show | 121 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(118): 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 | a0001c0002t0002g0229a0001c0002t0002g0237 | 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 | a0003c0017t0001g0115 | 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 | 80 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(77): Show | 80 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(77): 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 | a0001c0007t0004g0309a0001c0007t0007g0310a0001c0012t0014g0302 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(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 | a0001c0001t0001g0224a0001c0001t0002g0180a0001c0001t0002g0222others(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 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0163others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(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 | 43 | a0001c0001t0001g0340a0001c0001t0001g0342a0001c0001t0001g0344others(40): 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 | a0001c0001t0002g0059 | 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 | a0001c0001t0001g0303a0001c0002t0002g0075a0001c0002t0002g0304others(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 | a0001c0008t0001g0041 | 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 | a0001c0001t0001g0224a0001c0001t0002g0180a0001c0001t0002g0222others(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 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0172others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(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 | a0001c0007t0004g0309a0001c0007t0007g0310a0001c0012t0014g0302 | 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 | a0001c0001t0001g0016 | 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 | a0001c0002t0002g0100a0001c0004t0002g0097 | 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 | a0001c0002t0002g0072 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(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 | a0001c0002t0002g0316a0001c0002t0002g0319a0001c0002t0003g0005 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(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 | a0001c0002t0002g0011a0001c0002t0002g0314a0001c0002t0002g0316others(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 | a0001c0002t0002g0247a0001c0002t0002g0292 | 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 | a0001c0001t0001g0030 | 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 | a0001c0001t0002g0179a0001c0002t0002g0285 | 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 | a0001c0001t0001g0176 | 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 | a0001c0007t0004g0309a0001c0007t0007g0310a0001c0012t0014g0302 | 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 | a0001c0002t0002g0135a0001c0002t0002g0141a0001c0002t0002g0142 | 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 | a0001c0001t0001g0085 | 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 | a0001c0003t0002g0347a0001c0003t0002g0349a0001c0003t0002g0350others(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 | ||||||
chr19:48408202
|
C | T | 1 | a0001c0001t0001g0262 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1085+2849C>T | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 4/13 | chr19 | 48408202 | ||||||
chr19:48408207
|
G | A | 1 | a0001c0002t0002g0283 | 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 | a0001c0001t0002g0179a0001c0002t0002g0285 | 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 | a0001c0001t0001g0303a0001c0002t0002g0075a0001c0002t0002g0304others(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 | a0001c0001t0001g0079a0001c0001t0001g0133a0001c0001t0001g0155others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(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 | a0001c0001t0001g0303a0001c0002t0002g0075a0001c0002t0002g0304others(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 | 247 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(244): Show | 247 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(244): 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 | 124 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(121): Show | 124 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(121): 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 | a0001c0002t0002g0011a0001c0002t0002g0207a0001c0002t0002g0208others(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 | a0001c0001t0001g0279a0001c0004t0002g0280a0001c0004t0002g0281 | 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 | a0001c0002t0002g0207a0001c0002t0002g0208a0001c0002t0002g0211others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(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 | a0001c0001t0001g0303a0001c0002t0002g0075a0001c0002t0002g0304others(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 | a0001c0001t0001g0224a0001c0001t0002g0180a0001c0001t0002g0222others(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 | a0001c0001t0001g0224a0001c0001t0002g0180a0001c0001t0002g0222others(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 | a0001c0001t0001g0079a0001c0001t0001g0098a0001c0001t0001g0109others(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 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0085others(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 | a0001c0002t0003g0005 | 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 | a0001c0001t0001g0048a0001c0001t0010g0322a0001c0001t0011g0323 | 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 | a0001c0001t0002g0179a0001c0002t0002g0301 | 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 | a0001c0001t0001g0294a0001c0001t0002g0027a0001c0001t0002g0295others(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 | 83 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(80): Show | 83 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(80): 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 | a0001c0011t0002g0299a0001c0011t0002g0300 | 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 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0002g0167others(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 | a0001c0001t0001g0342a0001c0002t0002g0339a0001c0002t0002g0341 | 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 | a0001c0001t0002g0027a0001c0002t0002g0026 | 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 | a0001c0002t0002g0011 | 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 | a0001c0003t0002g0328a0001c0003t0002g0331a0001c0003t0002g0343 | 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 | a0001c0001t0001g0160a0001c0001t0001g0161 | 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 | a0001c0001t0001g0013a0001c0001t0002g0040a0001c0001t0013g0014others(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 | a0001c0007t0004g0309a0001c0007t0007g0310a0001c0012t0014g0302 | 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 | a0001c0001t0002g0179a0001c0002t0002g0285 | 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 | a0001c0001t0001g0303a0001c0002t0002g0075a0001c0002t0002g0304others(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 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0117others(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 | 85 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(82): Show | 85 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(82): 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 | a0001c0001t0001g0108a0001c0001t0001g0133a0001c0001t0001g0196others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0030others(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 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0016others(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 | a0001c0001t0001g0009a0001c0001t0001g0032a0001c0001t0001g0042others(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 | a0001c0001t0001g0303a0001c0002t0002g0075a0001c0002t0002g0304others(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 | a0001c0001t0001g0052a0001c0001t0001g0175a0001c0001t0001g0177others(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 | a0001c0001t0001g0279a0001c0002t0002g0178a0001c0004t0002g0280others(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 | a0001c0001t0002g0078 | 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 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(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 | 3 | a0001c0001t0001g0108a0001c0001t0001g0245a0001c0001t0001g0262 | 3 | HG00741.hp2 HG01167.hp1 homoSapiens_chm13v2.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 | a0001c0001t0001g0279a0001c0002t0002g0178a0001c0004t0002g0280others(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 | a0001c0001t0001g0111a0001c0001t0001g0152a0001c0001t0001g0156others(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 | a0001c0001t0001g0046a0001c0001t0001g0124a0001c0001t0001g0128others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0031others(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 | 73 | a0001c0001t0001g0067a0001c0001t0001g0108a0001c0001t0001g0133others(70): Show | 73 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(70): 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0001g0303a0001c0002t0002g0075a0001c0002t0002g0301others(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 | a0001c0003t0015g0364 | 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 | 36 | a0001c0001t0001g0342a0001c0001t0001g0366a0001c0002t0002g0339others(33): 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 | a0001c0001t0001g0134a0001c0002t0002g0135a0001c0002t0002g0141others(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 | 273 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(270): Show | 273 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(270): 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 | a0001c0002t0002g0282 | 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 | 36 | a0001c0001t0001g0342a0001c0001t0001g0366a0001c0002t0002g0339others(33): 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 | 248 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(245): Show | 248 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(245): 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 | a0001c0001t0001g0224a0001c0001t0002g0180a0001c0001t0002g0222others(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 | a0001c0001t0001g0109 | 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 | a0001c0001t0001g0021a0001c0001t0001g0030a0001c0001t0001g0032others(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 | a0001c0001t0001g0067a0001c0001t0001g0093a0001c0001t0001g0096others(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 | a0001c0001t0001g0158a0001c0001t0001g0256a0001c0001t0001g0287others(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 | a0001c0001t0001g0269a0001c0001t0001g0340a0001c0002t0002g0072 | 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 | a0001c0001t0001g0189a0001c0003t0002g0351a0001c0003t0015g0364 | 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 | a0001c0004t0002g0105 | 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 | a0001c0001t0001g0012a0001c0001t0001g0029a0001c0001t0001g0043others(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 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0034others(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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0289others(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 | a0001c0001t0001g0303a0001c0002t0002g0075a0001c0002t0002g0304others(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 | 248 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(245): Show | 248 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(245): 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 | a0001c0001t0001g0303a0001c0002t0002g0075a0001c0002t0002g0304others(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 | a0001c0001t0001g0224a0001c0001t0002g0180a0001c0001t0002g0222others(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 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0046others(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 | a0001c0001t0001g0150a0001c0002t0002g0301a0001c0003t0002g0333 | 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 | a0001c0002t0002g0089a0001c0002t0002g0207a0001c0002t0002g0208others(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 | a0001c0001t0001g0279a0001c0001t0002g0179a0001c0002t0002g0011others(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 | a0001c0001t0001g0224a0001c0001t0001g0279a0001c0001t0002g0180others(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 | a0001c0001t0001g0052a0001c0001t0001g0060a0001c0001t0001g0079others(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 | 45 | a0001c0001t0001g0030a0001c0001t0001g0074a0001c0001t0001g0157others(42): 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0085others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0085others(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 | 232 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(229): 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 | a0001c0001t0001g0019a0001c0001t0001g0049a0001c0001t0001g0056others(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 | a0001c0011t0002g0299a0001c0011t0002g0300 | 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 | a0001c0002t0002g0011 | 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 | a0001c0001t0001g0294a0001c0001t0002g0295a0001c0001t0002g0296others(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 | a0001c0002t0002g0316a0001c0002t0003g0005 | 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 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(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 | a0001c0007t0004g0309a0001c0007t0007g0310a0001c0012t0014g0302 | 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 | a0001c0004t0002g0213a0001c0004t0002g0214a0001c0004t0002g0274 | 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 | a0001c0003t0002g0076 | 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 | a0001c0003t0002g0076 | 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 | a0001c0003t0002g0076 | 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 | a0001c0003t0002g0076 | 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 | 42 | a0001c0003t0002g0017a0001c0003t0002g0055a0001c0003t0002g0071others(39): 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 | a0001c0001t0001g0144a0005c0019t0001g0118 | 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 | a0001c0004t0002g0213a0001c0004t0002g0214 | 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 | a0001c0002t0002g0282 | 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 | a0001c0001t0001g0294a0001c0001t0002g0295a0001c0001t0002g0296others(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 | a0001c0001t0001g0002 | 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 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0189others(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 | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(260): Show | 263 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.1735+527A>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 8/13 | chr19 | 48416682 | ||||||
chr19:48416745
|
C | CTT | 201 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(198): 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 | a0001c0001t0001g0034a0001c0001t0001g0067a0001c0001t0001g0079others(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 | a0001c0001t0001g0046a0001c0001t0001g0124a0001c0001t0001g0128others(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 | 281 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(278): Show | 281 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(278): 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 | a0001c0004t0002g0081 | 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 | a0001c0007t0004g0309a0001c0007t0007g0310a0001c0012t0014g0302 | 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 | a0001c0001t0001g0224a0001c0001t0002g0180a0001c0001t0002g0222others(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 | a0001c0002t0002g0283a0001c0002t0002g0284 | 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 | a0001c0002t0002g0319a0001c0007t0004g0309a0001c0007t0007g0310others(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 | a0001c0011t0002g0299a0001c0011t0002g0300 | 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 | a0001c0001t0002g0028a0001c0001t0002g0064a0001c0002t0002g0065others(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 | a0001c0001t0001g0007a0001c0001t0001g0058a0001c0001t0001g0074others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0085others(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 | a0001c0001t0002g0077 | 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 | a0001c0001t0001g0003 | 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 | a0001c0001t0001g0279a0001c0004t0002g0280a0001c0004t0002g0281 | 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 | a0001c0001t0009g0068 | 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 | 270 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(267): Show | 270 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(267): 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 | a0001c0007t0004g0309a0001c0007t0007g0310a0001c0012t0014g0302 | 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 | a0001c0007t0004g0309a0001c0007t0007g0310a0001c0012t0014g0302 | 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 | a0001c0001t0001g0069a0001c0001t0001g0256a0001c0001t0001g0294others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0085others(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 | a0001c0001t0001g0133a0001c0002t0002g0121 | 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 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0029others(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 | a0001c0002t0002g0011a0001c0002t0002g0089a0001c0002t0002g0207others(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 | a0001c0001t0001g0085 | 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 | 242 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(239): Show | 242 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(239): 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 | 177 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(174): Show | 177 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(174): 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 | a0001c0001t0002g0119a0001c0001t0002g0120a0001c0001t0002g0277others(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 | 278 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(275): Show | 278 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.2091+460T>A | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 10/13 | chr19 | 48420274 | ||||||
chr19:48420405
|
G | A | 42 | a0001c0003t0002g0017a0001c0003t0002g0055a0001c0003t0002g0071others(39): 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 | a0001c0002t0002g0011a0001c0007t0004g0309a0001c0007t0007g0310others(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 | a0001c0002t0002g0316a0001c0002t0003g0005 | 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 | a0001c0001t0008g0221 | 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 | a0001c0001t0001g0224a0001c0001t0002g0180a0001c0001t0002g0222others(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 | 278 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(275): Show | 278 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(275): 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0085others(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 | 262 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(259): Show | 262 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(259): 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 | a0001c0002t0002g0091 | 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 | a0001c0001t0001g0096 | 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 | a0001c0001t0001g0303a0001c0002t0002g0011a0001c0002t0002g0075others(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 | a0001c0011t0002g0299a0001c0011t0002g0300 | 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 | 279 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(276): Show | 279 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(276): 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 | 278 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(275): Show | 278 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(275): 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 | a0001c0001t0001g0129a0001c0002t0002g0285 | 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 | a0001c0001t0001g0021a0001c0001t0002g0022a0001c0001t0002g0053others(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 | a0001c0001t0001g0294a0001c0001t0002g0295a0001c0001t0002g0296others(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 | 174 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(171): Show | 174 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(171): 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 | a0001c0003t0002g0312a0001c0003t0002g0327a0001c0003t0002g0329others(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 | a0001c0001t0001g0067a0001c0001t0001g0215 | 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 | a0001c0001t0001g0357 | 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 | a0001c0003t0002g0071 | 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 | a0001c0001t0001g0352 | 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 | a0001c0003t0002g0347a0001c0003t0002g0349a0001c0003t0002g0350 | 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 | a0001c0001t0001g0052a0001c0001t0001g0278a0001c0001t0001g0279others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0048others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0085others(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 | 230 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(227): Show | 230 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(227): 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 | a0001c0001t0001g0224a0001c0001t0002g0180a0001c0001t0002g0222others(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 | a0001c0001t0002g0027a0001c0002t0002g0026a0001c0004t0002g0213others(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 | a0001c0002t0002g0091 | 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 | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 195 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(192): 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0085others(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 | a0001c0002t0002g0285 | 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 | a0001c0002t0002g0089a0001c0002t0002g0207a0001c0002t0002g0208others(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 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0002g0167others(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 | a0001c0001t0001g0279a0001c0004t0002g0280a0001c0004t0002g0281 | 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 | a0001c0001t0002g0148 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0085others(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 | a0001c0002t0002g0178a0001c0002t0002g0316a0001c0002t0003g0005 | 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 | a0001c0001t0001g0046a0001c0001t0001g0124a0001c0001t0001g0128others(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 | a0001c0002t0002g0204a0001c0002t0002g0205 | 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 | a0001c0002t0002g0204a0001c0002t0002g0205 | 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 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0038others(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 | a0001c0001t0001g0272a0001c0001t0001g0287a0001c0001t0002g0360others(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 | a0001c0002t0002g0305a0001c0002t0002g0307 | 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 | a0001c0002t0002g0075a0001c0002t0002g0304a0001c0002t0002g0306 | 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 | a0001c0002t0002g0282a0001c0007t0004g0309 | 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 | a0001c0001t0002g0027a0001c0002t0002g0026 | 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 | a0001c0002t0002g0089a0001c0010t0002g0210 | 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 | a0001c0002t0002g0011 | 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 | a0001c0001t0001g0294a0001c0001t0002g0295a0001c0001t0002g0296others(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 | a0001c0002t0002g0107 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0154others(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 | a0001c0001t0001g0085 | 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 | a0001c0002t0002g0285 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0085others(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 | a0001c0001t0002g0277a0001c0002t0002g0311 | 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 | a0001c0004t0002g0105 | 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 | a0001c0018t0002g0047 | 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 | a0001c0018t0002g0047 | 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 | a0001c0001t0002g0295a0001c0001t0002g0296 | 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 | a0001c0001t0001g0030a0001c0001t0001g0086a0001c0001t0001g0087others(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 | a0001c0001t0002g0028a0001c0001t0002g0064a0001c0002t0002g0065others(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 | a0001c0002t0002g0285 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0048others(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 | a0001c0001t0001g0294a0001c0001t0002g0027a0001c0001t0002g0179others(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 | a0001c0001t0001g0303a0001c0002t0002g0075a0001c0002t0002g0304others(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 | a0001c0004t0002g0353a0001c0004t0002g0355a0001c0022t0002g0334 | 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 | a0001c0002t0002g0285 | 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 | a0001c0008t0001g0041 | 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 | a0001c0001t0001g0255a0001c0001t0001g0342 | 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 | a0001c0001t0001g0279a0001c0002t0002g0178a0001c0002t0002g0283others(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 | a0001c0002t0002g0285 | 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 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0094others(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 | 16 | a0001c0001t0002g0028a0001c0001t0002g0064a0001c0002t0002g0065others(13): 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 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0016others(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 | a0001c0001t0001g0279a0001c0004t0002g0280a0001c0004t0002g0281 | 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 | a0001c0001t0001g0294a0001c0001t0002g0027a0001c0001t0002g0179others(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 | a0001c0001t0001g0279a0001c0002t0002g0178a0001c0002t0002g0283others(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 | a0001c0001t0001g0286a0001c0001t0002g0257a0001c0023t0002g0270 | 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 | a0001c0002t0002g0107 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0154others(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 | a0001c0001t0001g0058a0001c0001t0001g0215a0001c0001t0001g0286others(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 | a0001c0002t0002g0089a0001c0002t0002g0211 | 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 | a0001c0010t0002g0209a0001c0010t0002g0210 | 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 | a0001c0007t0007g0310a0001c0012t0014g0302 | 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 | a0001c0002t0002g0282a0001c0007t0004g0309 | 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 | a0001c0001t0001g0272a0001c0002t0002g0135a0001c0002t0002g0141others(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 | a0001c0001t0002g0027a0001c0002t0002g0026 | 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 | a0001c0001t0001g0294a0001c0001t0002g0295a0001c0002t0002g0297others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0085others(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 | a0001c0001t0001g0031a0001c0001t0001g0161a0001c0001t0001g0203others(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 | a0001c0001t0001g0085 | 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 | a0001c0011t0002g0299a0001c0011t0002g0300 | 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 | a0001c0001t0001g0224a0001c0001t0002g0180a0001c0001t0002g0222others(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 | a0001c0001t0001g0272a0001c0001t0001g0287a0001c0001t0011g0323others(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 | a0001c0001t0001g0032 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0085others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0085others(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 | a0001c0001t0001g0177 | 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 | a0001c0001t0002g0027a0001c0002t0002g0011a0001c0002t0002g0026others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0085others(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 | a0001c0002t0002g0316a0001c0002t0003g0005 | 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 | a0001c0002t0002g0285 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0085others(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 | 238 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(235): Show | 238 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(235): 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0085others(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 | 17 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0112others(14): 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 | a0001c0001t0001g0046a0001c0001t0001g0125a0001c0001t0001g0157others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0085others(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 | a0001c0002t0002g0107a0001c0002t0002g0314 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0085others(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 | a0001c0002t0002g0285 | 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 | a0001c0002t0002g0285 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0085others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0085others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0085others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0085others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0085others(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 | a0001c0001t0001g0272a0001c0001t0001g0287a0001c0001t0011g0323others(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 | a0001c0001t0001g0002a0001c0001t0001g0087a0001c0001t0001g0168others(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 | a0001c0001t0001g0034a0001c0001t0001g0140a0001c0001t0001g0294others(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 | a0001c0001t0002g0027a0001c0002t0002g0026 | 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 | a0001c0004t0002g0353 | 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 | a0001c0002t0002g0089a0001c0002t0002g0207a0001c0002t0002g0208others(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 | a0001c0001t0001g0366 | 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 | 38 | a0001c0001t0001g0067a0001c0001t0001g0108a0001c0001t0001g0195others(35): Show | 38 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(35): 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 | 308 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(305): Show | 308 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(305): 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0085others(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 | a0001c0001t0002g0022 | 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 | 308 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(305): Show | 308 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.2252+7135T>C | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48429080 | ||||||
chr19:48429288
|
T | C | 308 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(305): Show | 308 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(305): 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 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0019others(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 | a0001c0001t0001g0012a0001c0001t0001g0303a0001c0001t0002g0059others(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 | a0001c0001t0001g0279a0001c0001t0001g0294a0001c0001t0002g0295others(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 | a0001c0001t0002g0027a0001c0002t0002g0011a0001c0002t0002g0026others(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 | a0001c0002t0002g0283a0001c0002t0002g0284 | 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 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0038others(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 | a0001c0001t0002g0027a0001c0002t0002g0026 | 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 | a0001c0002t0002g0089a0001c0002t0002g0207a0001c0002t0002g0208others(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 | a0001c0002t0002g0089a0001c0002t0002g0207a0001c0002t0002g0208others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0085others(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 | a0001c0001t0001g0046a0001c0001t0001g0063a0001c0001t0001g0140others(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 | a0001c0001t0001g0279a0001c0002t0002g0285 | 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 | 3 | a0001c0001t0001g0110a0001c0001t0001g0112a0001c0001t0001g0113 | 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 | a0001c0004t0002g0353a0001c0004t0002g0355a0001c0022t0002g0334 | 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 | a0001c0002t0002g0089a0001c0002t0002g0207a0001c0002t0002g0208others(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 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0029others(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 | a0001c0001t0002g0132 | 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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(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 | a0001c0002t0002g0089a0001c0002t0002g0207a0001c0002t0002g0208others(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 | ||||||
chr19:48432045
|
T | TG | 365 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(362): Show | 365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.2253-9722dupG | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 48432045 | |||||
chr19:48432214
|
TTTTC | T | 10 | a0001c0001t0001g0272a0001c0001t0001g0287a0001c0001t0011g0323others(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 | a0001c0001t0001g0063a0001c0001t0001g0099a0001c0001t0001g0187others(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 | a0001c0001t0002g0276a0001c0013t0001g0246 | 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 | a0001c0001t0001g0279a0001c0001t0002g0027a0001c0002t0002g0011others(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 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0016others(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 | a0001c0004t0002g0097 | 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 | a0001c0002t0002g0229a0001c0002t0002g0237 | 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 | a0001c0001t0001g0279a0001c0002t0002g0285 | 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 | a0001c0001t0001g0029a0001c0001t0001g0058a0001c0001t0001g0268others(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 | a0001c0001t0001g0248a0001c0001t0001g0279a0001c0001t0002g0027others(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 | a0001c0004t0002g0213a0001c0004t0002g0214a0001c0004t0002g0274 | 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 | ||||||
chr19:48433074
|
A | AGC | 365 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(362): Show | 365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.2253-8695_2253-869 others(6): Show |
GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48433074 | ||||||
chr19:48433549
|
C | T | 11 | a0001c0001t0001g0272a0001c0001t0001g0287a0001c0001t0011g0323others(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 | a0001c0002t0002g0285a0001c0004t0002g0213a0001c0004t0002g0214others(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 | a0001c0001t0002g0167a0001c0002t0002g0091a0001c0002t0002g0311 | 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 | a0001c0001t0002g0167a0001c0002t0002g0091a0001c0002t0002g0107others(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 | a0001c0002t0002g0141a0001c0002t0002g0288 | 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 | a0001c0003t0002g0363 | 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 | a0001c0001t0002g0040a0001c0001t0002g0249a0001c0001t0002g0252others(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 | a0001c0001t0002g0137a0001c0001t0002g0146a0001c0001t0002g0148others(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 | a0001c0001t0001g0272a0001c0001t0001g0287a0001c0002t0002g0142others(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 | a0001c0002t0002g0026 | 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 | a0001c0001t0002g0167a0001c0001t0002g0179 | 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 | a0001c0002t0002g0316a0001c0002t0003g0005 | 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 | 334 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(331): Show | 334 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.2253-7539A>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48434230 | ||||||
chr19:48434232
|
A | G | 324 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(321): Show | 324 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(321): 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 | a0001c0001t0009g0068a0001c0002t0002g0231a0001c0003t0002g0351 | 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 | a0001c0001t0002g0027a0001c0001t0002g0033a0001c0001t0002g0167others(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 | a0001c0005t0001g0020 | 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 | 206 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(203): Show | 206 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(203): 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 | a0001c0002t0002g0026a0001c0002t0002g0037a0001c0002t0002g0089others(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 | a0001c0002t0002g0075 | 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 | a0001c0001t0001g0095 | 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 | a0001c0002t0002g0304a0001c0002t0002g0307a0001c0002t0003g0006 | 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 | 340 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(337): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): 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 | a0001c0001t0001g0096a0001c0001t0001g0164a0001c0001t0001g0287others(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 | a0001c0002t0002g0141a0001c0002t0002g0288 | 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 | 290 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(287): Show | 290 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.2253-6429A>G | GRIN2D | ENSG00000105464.4 | transcript | ENST00000263269.4 | protein_coding | 11/13 | chr19 | 48435340 | ||||||
chr19:48435482
|
G | A | 207 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(204): Show | 207 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(204): 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 | 247 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(244): Show | 247 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(244): 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 | a0001c0003t0002g0102 | 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 | a0001c0001t0001g0069a0001c0001t0001g0073a0001c0001t0001g0074 | 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 | a0001c0004t0002g0188a0001c0022t0002g0334 | 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 | 290 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(287): Show | 290 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(287): 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 | a0001c0003t0002g0363a0001c0003t0015g0364 | 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 | a0001c0002t0002g0026a0001c0002t0002g0037a0001c0002t0002g0208others(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 | a0001c0001t0001g0099 | 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 | a0001c0002t0002g0293a0001c0003t0002g0260 | 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 | a0001c0001t0001g0062 | 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 | a0001c0004t0002g0213a0001c0004t0002g0214a0001c0004t0002g0274 | 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 | a0001c0001t0002g0137a0001c0001t0002g0146a0001c0001t0002g0148others(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 | a0001c0001t0001g0275a0001c0001t0001g0278 | 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 | a0001c0001t0002g0018a0001c0001t0002g0022a0001c0001t0002g0040others(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 | a0001c0001t0013g0014 | 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 | a0001c0002t0002g0036a0001c0002t0002g0075a0001c0002t0002g0142others(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 | 307 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(304): Show | 307 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(304): 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 | a0001c0002t0002g0051a0001c0002t0002g0091a0001c0002t0002g0107others(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 | a0001c0001t0002g0018a0001c0001t0002g0050a0001c0001t0002g0053others(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 | a0001c0001t0002g0045a0001c0001t0002g0054a0001c0001t0002g0078others(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 | a0001c0001t0002g0040a0001c0001t0002g0249a0001c0001t0002g0259others(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 | a0001c0001t0002g0022a0001c0001t0002g0257a0001c0001t0002g0296others(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 | a0001c0004t0002g0213a0001c0004t0002g0214a0001c0004t0002g0274others(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 | a0001c0001t0002g0167a0001c0002t0002g0304a0001c0002t0002g0307others(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 | a0001c0001t0002g0179a0001c0002t0002g0036a0001c0002t0002g0075others(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 | a0001c0001t0001g0016a0001c0001t0001g0067a0001c0001t0001g0108others(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 | 78 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0019others(75): Show | 78 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(75): 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 | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): 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 | a0001c0001t0002g0276a0001c0002t0002g0037a0001c0002t0002g0089others(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 | a0001c0002t0002g0282 | 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 | a0001c0004t0002g0213a0001c0004t0002g0214 | 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 | a0001c0001t0001g0099a0001c0009t0001g0116a0001c0009t0001g0223 | 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 | a0001c0001t0002g0027a0001c0001t0002g0033a0001c0001t0002g0180others(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 | a0001c0002t0002g0026a0001c0002t0002g0037a0001c0002t0002g0089others(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 | 85 | a0001c0001t0001g0010a0001c0001t0001g0046a0001c0001t0001g0058others(82): 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 | a0001c0001t0001g0013a0004c0016t0001g0015 | 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 | a0001c0002t0002g0011a0001c0002t0002g0165a0001c0002t0002g0316others(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 | a0001c0002t0002g0285 | 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 | a0001c0001t0001g0046a0001c0001t0001g0124a0001c0001t0001g0128others(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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0030others(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 | a0001c0001t0001g0357a0001c0002t0002g0051a0001c0002t0003g0005 | 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 | a0001c0001t0002g0064 | 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 | 274 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(271): Show | 274 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(271): 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 |
287 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(284): Show | 287 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(284): 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 | a0001c0001t0008g0221 | 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 | a0001c0001t0001g0111 | 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 | a0001c0002t0002g0036a0001c0002t0002g0075a0001c0002t0002g0142others(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 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0315 | 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 | a0001c0002t0002g0026a0001c0002t0002g0037a0001c0002t0002g0089others(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 | 3 | a0001c0001t0001g0110a0001c0001t0001g0112a0001c0001t0001g0113 | 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 | a0001c0018t0002g0047 | 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 | a0001c0002t0002g0091a0001c0002t0002g0100a0001c0002t0002g0107others(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 | a0001c0001t0001g0074a0001c0001t0001g0153a0001c0001t0001g0173others(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 | a0001c0001t0002g0259 | 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 | a0001c0001t0001g0079a0001c0001t0001g0110a0001c0001t0001g0150others(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 | 237 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(234): Show | 237 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(234): 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 | a0001c0001t0002g0040a0001c0001t0002g0249a0001c0001t0002g0252others(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 | a0001c0001t0001g0069a0001c0001t0001g0073a0001c0001t0001g0074 | 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 | 49 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0016others(46): Show | 49 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(46): 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 | a0001c0001t0002g0050 | 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 | a0001c0001t0002g0167a0001c0001t0002g0179 | 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 | a0001c0004t0002g0213a0001c0004t0002g0214a0001c0004t0002g0274 | 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 | a0001c0002t0002g0011a0001c0002t0002g0026a0001c0002t0002g0037others(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 |