geneid | 2742 |
---|---|
ensemblid | ENSG00000101958.14 |
hgncid | 4327 |
symbol | GLRA2 |
name | glycine receptor alpha 2 |
refseq_nuc | NM_002063.4 |
refseq_prot | NP_002054.1 |
ensembl_nuc | ENST00000218075.9 |
ensembl_prot | ENSP00000218075.4 |
mane_status | MANE Select |
chr | chrX |
start | 14529536 |
end | 14731812 |
strand | + |
ver | v1.2 |
region | chrX:14529536-14731812 |
region5000 | chrX:14524536-14736812 |
regionname0 | GLRA2_chrX_14529536_14731812 |
regionname5000 | GLRA2_chrX_14524536_14736812 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 452 | 231 | 69 | 47 | 80 | 11 | 22 | 59 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
a0002 | 0/0 | 452 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1359 | 182 | 42 | 33 | 79 | 7 | 19 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
c0002 | 0/0 | 1359 | 37 | 18 | 11 | 1 | 4 | 3 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
c0003 | 0/0 | 1359 | 8 | 7 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
c0004 | 0/0 | 1359 | 2 | 1 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
c0005 | 0/0 | 1359 | 2 | 1 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
c0006 | 0/0 | 1359 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 1838 | 39 | 2 | 6 | 23 | 3 | 5 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
t0002 | 0/0 | 1840 | 30 | 3 | 7 | 19 | 0 | 1 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
t0003 | 0/1 | 1830 | 22 | 1 | 6 | 8 | 3 | 3 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
t0004 | 0/0 | 1836 | 17 | 3 | 4 | 9 | 0 | 1 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
t0005 | 0/0 | 1838 | 13 | 4 | 4 | 0 | 3 | 2 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
t0006 | 0/0 | 1842 | 13 | 1 | 4 | 6 | 0 | 2 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
t0007 | 0/0 | 1840 | 12 | 4 | 7 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
t0008 | 0/0 | 1834 | 11 | 5 | 0 | 3 | 0 | 3 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
t0009 | 0/0 | 1820 | 5 | 3 | 2 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
t0010 | 0/0 | 1822 | 5 | 4 | 0 | 0 | 0 | 1 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
t0011 | 0/0 | 1842 | 4 | 2 | 0 | 0 | 1 | 1 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
t0012 | 0/0 | 1854 | 4 | 3 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
t0013 | 0/0 | 1830 | 3 | 2 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
t0014 | 0/0 | 1836 | 3 | 3 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
t0015 | 0/0 | 1841 | 3 | 1 | 0 | 2 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
t0016 | 0/0 | 1844 | 3 | 0 | 0 | 3 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
t0017 | 0/0 | 1848 | 3 | 2 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
t0018 | 0/0 | 1818 | 2 | 2 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
t0019 | 0/0 | 1828 | 2 | 0 | 0 | 1 | 0 | 1 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
t0020 | 0/0 | 1832 | 2 | 0 | 1 | 0 | 1 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
t0021 | 0/0 | 1834 | 2 | 2 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
t0022 | 0/0 | 1842 | 2 | 0 | 0 | 2 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
t0023 | 0/0 | 1850 | 2 | 1 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
t0024 | 0/0 | 1822 | 2 | 2 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
t0025 | 0/0 | 1834 | 2 | 2 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
t0026 | 0/0 | 1840 | 2 | 1 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
t0027 | 0/0 | 1842 | 2 | 2 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
t0028 | 0/0 | 1838 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
t0029 | 0/0 | 1838 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
t0030 | 0/0 | 1834 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
t0031 | 0/0 | 1834 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
t0032 | 0/0 | 1836 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
t0033 | 0/0 | 1838 | 1 | 0 | 0 | 0 | 0 | 1 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
t0034 | 0/0 | 1840 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
t0035 | 0/0 | 1839 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
t0036 | 0/0 | 1844 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
t0037 | 0/0 | 1843 | 1 | 0 | 0 | 0 | 0 | 1 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
t0038 | 0/0 | 1847 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
t0039 | 0/0 | 1848 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
t0040 | 1/0 | 1850 | 1 | 0 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
t0041 | 0/0 | 1858 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
t0042 | 0/0 | 1840 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
t0043 | 0/0 | 1834 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
t0044 | 0/0 | 1848 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
t0045 | 0/0 | 1838 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
t0046 | 0/0 | 1832 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
t0047 | 0/0 | 1846 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
t0048 | 0/0 | 1846 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
t0049 | 0/0 | 1830 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0047 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0082 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1359 | 182 | 42 | 33 | 79 | 7 | 19 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
a0001c0002 | 0/0 | 1359 | 37 | 18 | 11 | 1 | 4 | 3 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
a0001c0003 | 0/0 | 1359 | 8 | 7 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
a0001c0004 | 0/0 | 1359 | 2 | 1 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
a0001c0005 | 0/0 | 1359 | 2 | 1 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
a0002c0006 | 0/0 | 1359 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3196 | 39 | 2 | 6 | 23 | 3 | 5 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
a0001c0001t0002 | 0/0 | 3198 | 29 | 2 | 7 | 19 | 0 | 1 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
a0001c0001t0003 | 0/1 | 3188 | 21 | 1 | 5 | 8 | 3 | 3 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
a0001c0001t0004 | 0/0 | 3194 | 17 | 3 | 4 | 9 | 0 | 1 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
a0001c0001t0005 | 0/0 | 3196 | 4 | 1 | 2 | 0 | 0 | 1 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
a0001c0001t0006 | 0/0 | 3200 | 11 | 0 | 3 | 6 | 0 | 2 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
a0001c0001t0007 | 0/0 | 3198 | 2 | 2 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
a0001c0001t0008 | 0/0 | 3192 | 11 | 5 | 0 | 3 | 0 | 3 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
a0001c0001t0009 | 0/0 | 3178 | 5 | 3 | 2 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
a0001c0001t0010 | 0/0 | 3180 | 4 | 3 | 0 | 0 | 0 | 1 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
a0001c0001t0011 | 0/0 | 3200 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
a0001c0001t0012 | 0/0 | 3212 | 4 | 3 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
a0001c0001t0013 | 0/0 | 3188 | 3 | 2 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
a0001c0001t0014 | 0/0 | 3194 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
a0001c0001t0015 | 0/0 | 3199 | 3 | 1 | 0 | 2 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
a0001c0001t0016 | 0/0 | 3202 | 3 | 0 | 0 | 3 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
a0001c0001t0017 | 0/0 | 3206 | 3 | 2 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
a0001c0001t0018 | 0/0 | 3176 | 2 | 2 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
a0001c0001t0019 | 0/0 | 3186 | 2 | 0 | 0 | 1 | 0 | 1 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
a0001c0001t0020 | 0/0 | 3190 | 2 | 0 | 1 | 0 | 1 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
a0001c0001t0021 | 0/0 | 3192 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
a0001c0001t0022 | 0/0 | 3200 | 2 | 0 | 0 | 2 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
a0001c0001t0029 | 0/0 | 3196 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
a0001c0001t0031 | 0/0 | 3192 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
a0001c0001t0033 | 0/0 | 3196 | 1 | 0 | 0 | 0 | 0 | 1 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
a0001c0001t0034 | 0/0 | 3198 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
a0001c0001t0035 | 0/0 | 3197 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
a0001c0001t0038 | 0/0 | 3205 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
a0001c0001t0040 | 1/0 | 3208 | 1 | 0 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
a0001c0001t0041 | 0/0 | 3216 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
a0001c0001t0042 | 0/0 | 3198 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
a0001c0001t0044 | 0/0 | 3206 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
a0001c0001t0048 | 0/0 | 3204 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
a0001c0001t0049 | 0/0 | 3188 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
a0001c0002t0003 | 0/0 | 3188 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
a0001c0002t0005 | 0/0 | 3196 | 9 | 3 | 2 | 0 | 3 | 1 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
a0001c0002t0007 | 0/0 | 3198 | 8 | 1 | 6 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
a0001c0002t0010 | 0/0 | 3180 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
a0001c0002t0011 | 0/0 | 3200 | 3 | 1 | 0 | 0 | 1 | 1 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
a0001c0002t0014 | 0/0 | 3194 | 2 | 2 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
a0001c0002t0021 | 0/0 | 3192 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
a0001c0002t0023 | 0/0 | 3208 | 2 | 1 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
a0001c0002t0024 | 0/0 | 3180 | 2 | 2 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
a0001c0002t0028 | 0/0 | 3196 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
a0001c0002t0036 | 0/0 | 3202 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
a0001c0002t0037 | 0/0 | 3201 | 1 | 0 | 0 | 0 | 0 | 1 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
a0001c0002t0039 | 0/0 | 3206 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
a0001c0002t0043 | 0/0 | 3192 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
a0001c0002t0045 | 0/0 | 3196 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
a0001c0002t0046 | 0/0 | 3190 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
a0001c0002t0047 | 0/0 | 3204 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
a0001c0003t0007 | 0/0 | 3198 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
a0001c0003t0025 | 0/0 | 3192 | 2 | 2 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
a0001c0003t0026 | 0/0 | 3198 | 2 | 1 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
a0001c0003t0027 | 0/0 | 3200 | 2 | 2 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
a0001c0003t0030 | 0/0 | 3192 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
a0001c0004t0007 | 0/0 | 3198 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
a0001c0004t0032 | 0/0 | 3194 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
a0001c0005t0006 | 0/0 | 3200 | 2 | 1 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
a0002c0006t0002 | 0/0 | 3198 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | copy fasta | chrX | 14524536 | 14736812 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0003g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0003g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0003g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0003g0047 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0003g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0004g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0004g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0004g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0004g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0004g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0004g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0004g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0004g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0004g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0004g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0004g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0004g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0004g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0004g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0004g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0005g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0005g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0005g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0005g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0006g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0006g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0006g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0006g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0006g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0006g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0006g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0006g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0006g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0006g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0006g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0007g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0007g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0008g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0008g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0008g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0008g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0008g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0008g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0008g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0008g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0008g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0008g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0008g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0009g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0009g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0009g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0009g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0009g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0010g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0010g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0010g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0010g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0011g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0012g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0012g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0012g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0012g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0013g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0013g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0013g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0014g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0015g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0015g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0015g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0016g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0016g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0016g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0017g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0017g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0017g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0018g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0018g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0019g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0019g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0020g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0020g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0021g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0022g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0022g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0029g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0031g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0033g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0034g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0035g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0038g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0040g0082 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0041g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0042g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0044g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0048g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0001t0049g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0002t0003g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0002t0005g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0002t0005g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0002t0005g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0002t0005g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0002t0005g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0002t0005g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0002t0005g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0002t0005g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0002t0005g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0002t0007g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0002t0007g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0002t0007g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0002t0007g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0002t0007g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0002t0007g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0002t0007g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0002t0007g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0002t0010g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0002t0011g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0002t0011g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0002t0011g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0002t0014g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0002t0014g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0002t0021g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0002t0023g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0002t0023g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0002t0024g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0002t0024g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0002t0028g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0002t0036g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0002t0037g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0002t0039g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0002t0043g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0002t0045g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0002t0046g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0002t0047g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0003t0007g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0003t0025g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0003t0025g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0003t0026g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0003t0026g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0003t0027g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0003t0027g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0003t0030g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0004t0007g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0004t0032g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0005t0006g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0001c0005t0006g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
a0002c0006t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0002 | t0011 | g0217 | EUR | GBR | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG00280 | hp1 | a0001 | c0002 | t0005 | g0214 | EUR | FIN | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG00323 | hp1 | a0001 | c0001 | t0020 | g0207 | EUR | FIN | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0113 | EUR | FIN | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG00558 | hp2 | a0001 | c0001 | t0003 | g0049 | EAS | CHS | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG00609 | hp1 | a0001 | c0001 | t0003 | g0139 | EAS | CHS | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | CHS | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG00639 | hp1 | a0001 | c0001 | t0003 | g0046 | AMR | PUR | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0157 | AMR | PUR | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG00642 | hp1 | a0001 | c0001 | t0006 | g0092 | AMR | PUR | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | CHS | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG00733 | hp1 | a0001 | c0001 | t0005 | g0108 | AMR | PUR | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG00733 | hp2 | a0001 | c0002 | t0007 | g0192 | AMR | PUR | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG00738 | hp1 | a0001 | c0001 | t0042 | g0132 | AMR | PUR | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG00741 | hp2 | a0001 | c0002 | t0007 | g0208 | AMR | PUR | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG01069 | hp1 | a0001 | c0002 | t0007 | g0023 | AMR | PUR | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG01070 | hp1 | a0001 | c0001 | t0004 | g0220 | AMR | PUR | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG01070 | hp2 | a0001 | c0001 | t0009 | g0225 | AMR | PUR | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG01071 | hp1 | a0001 | c0002 | t0007 | g0022 | AMR | PUR | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG01071 | hp2 | a0001 | c0001 | t0009 | g0224 | AMR | PUR | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG01074 | hp1 | a0001 | c0003 | t0026 | g0176 | AMR | PUR | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0166 | AMR | PUR | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG01081 | hp2 | a0001 | c0001 | t0003 | g0206 | AMR | PUR | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0163 | AMR | PUR | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG01106 | hp1 | a0001 | c0001 | t0012 | g0104 | AMR | PUR | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG01109 | hp1 | a0001 | c0002 | t0023 | g0186 | AMR | PUR | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG01243 | hp1 | a0001 | c0001 | t0013 | g0073 | AMR | PUR | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG01255 | hp1 | a0001 | c0001 | t0006 | g0130 | AMR | CLM | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG01256 | hp1 | a0001 | c0002 | t0007 | g0209 | AMR | CLM | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG01257 | hp1 | a0001 | c0001 | t0003 | g0044 | AMR | CLM | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG01258 | hp1 | a0001 | c0001 | t0003 | g0045 | AMR | CLM | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG01261 | hp1 | a0001 | c0002 | t0005 | g0205 | AMR | CLM | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG01358 | hp1 | a0001 | c0002 | t0003 | g0145 | AMR | CLM | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG01361 | hp1 | a0001 | c0001 | t0005 | g0057 | AMR | CLM | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG01361 | hp2 | a0001 | c0005 | t0006 | g0095 | AMR | CLM | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG01433 | hp1 | a0001 | c0002 | t0007 | g0210 | AMR | CLM | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG01496 | hp1 | a0001 | c0001 | t0003 | g0039 | AMR | CLM | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0143 | AMR | CLM | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG01515 | hp1 | a0001 | c0001 | t0003 | g0226 | EUR | IBS | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG01516 | hp1 | a0001 | c0002 | t0005 | g0213 | EUR | IBS | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0043 | EUR | IBS | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG01517 | hp1 | a0001 | c0001 | t0003 | g0221 | EUR | IBS | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG01517 | hp2 | a0001 | c0002 | t0005 | g0215 | EUR | IBS | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG01891 | hp1 | a0001 | c0001 | t0012 | g0154 | AFR | ACB | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG01891 | hp2 | a0001 | c0003 | t0007 | g0067 | AFR | ACB | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG01928 | hp1 | a0001 | c0001 | t0004 | g0159 | AMR | PEL | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0168 | AMR | PEL | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG01952 | hp1 | a0001 | c0001 | t0004 | g0021 | AMR | PEL | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0165 | AMR | PEL | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG01981 | hp2 | a0001 | c0001 | t0020 | g0048 | AMR | PEL | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG02004 | hp1 | a0001 | c0001 | t0004 | g0156 | AMR | PEL | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG02004 | hp2 | a0001 | c0001 | t0006 | g0218 | AMR | PEL | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG02015 | hp1 | a0001 | c0002 | t0007 | g0114 | EAS | KHV | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | KHV | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG02056 | hp1 | a0001 | c0001 | t0004 | g0081 | EAS | KHV | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | KHV | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | KHV | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG02080 | hp2 | a0001 | c0001 | t0004 | g0162 | EAS | KHV | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG02083 | hp1 | a0001 | c0001 | t0019 | g0131 | EAS | KHV | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG02145 | hp1 | a0001 | c0001 | t0007 | g0079 | AFR | ACB | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG02257 | hp1 | a0001 | c0001 | t0009 | g0064 | AFR | ACB | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG02257 | hp2 | a0001 | c0002 | t0036 | g0063 | AFR | ACB | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG02258 | hp1 | a0001 | c0002 | t0028 | g0062 | AFR | ACB | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG02280 | hp1 | a0001 | c0001 | t0049 | g0075 | AFR | ACB | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG02280 | hp2 | a0001 | c0001 | t0012 | g0174 | AFR | ACB | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG02293 | hp1 | a0001 | c0004 | t0007 | g0094 | AMR | PEL | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG02293 | hp2 | a0001 | c0002 | t0046 | g0179 | AMR | PEL | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0096 | AMR | PEL | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG02451 | hp1 | a0001 | c0001 | t0008 | g0196 | AFR | ACB | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG02451 | hp2 | a0001 | c0001 | t0017 | g0078 | AFR | ACB | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | KHV | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG02572 | hp1 | a0001 | c0003 | t0025 | g0175 | AFR | GWD | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG02602 | hp1 | a0001 | c0002 | t0037 | g0028 | SAS | PJL | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG02615 | hp1 | a0001 | c0003 | t0027 | g0178 | AFR | GWD | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0194 | AFR | GWD | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG02622 | hp1 | a0001 | c0003 | t0026 | g0180 | AFR | GWD | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG02622 | hp2 | a0001 | c0001 | t0013 | g0199 | AFR | GWD | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG02630 | hp1 | a0001 | c0001 | t0014 | g0228 | AFR | GWD | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG02630 | hp2 | a0001 | c0001 | t0031 | g0060 | AFR | GWD | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG02647 | hp1 | a0001 | c0002 | t0045 | g0177 | AFR | GWD | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG02683 | hp1 | a0001 | c0001 | t0008 | g0227 | SAS | PJL | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG02698 | hp1 | a0001 | c0001 | t0019 | g0142 | SAS | PJL | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG02717 | hp1 | a0001 | c0002 | t0014 | g0026 | AFR | GWD | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG02735 | hp1 | a0001 | c0001 | t0005 | g0216 | SAS | PJL | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG02738 | hp1 | a0001 | c0001 | t0004 | g0150 | SAS | PJL | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG02809 | hp1 | a0001 | c0001 | t0010 | g0070 | AFR | GWD | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG02809 | hp2 | a0001 | c0002 | t0021 | g0024 | AFR | GWD | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG02886 | hp1 | a0001 | c0001 | t0008 | g0231 | AFR | GWD | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG02886 | hp2 | a0001 | c0002 | t0043 | g0191 | AFR | GWD | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG02895 | hp1 | a0001 | c0001 | t0010 | g0074 | AFR | GWD | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG02897 | hp1 | a0001 | c0003 | t0027 | g0182 | AFR | GWD | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG02897 | hp2 | a0001 | c0001 | t0010 | g0071 | AFR | GWD | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG02922 | hp1 | a0001 | c0001 | t0021 | g0190 | AFR | ESN | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG02922 | hp2 | a0001 | c0003 | t0025 | g0181 | AFR | ESN | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG02965 | hp1 | a0001 | c0001 | t0044 | g0193 | AFR | ESN | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG02970 | hp1 | a0001 | c0001 | t0018 | g0033 | AFR | ESN | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG02970 | hp2 | a0001 | c0001 | t0008 | g0195 | AFR | ESN | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG02976 | hp1 | a0001 | c0002 | t0047 | g0183 | AFR | ESN | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG02976 | hp2 | a0001 | c0001 | t0012 | g0099 | AFR | ESN | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG03017 | hp1 | a0001 | c0001 | t0003 | g0037 | SAS | PJL | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG03041 | hp1 | a0001 | c0001 | t0004 | g0027 | AFR | GWD | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG03041 | hp2 | a0001 | c0001 | t0011 | g0188 | AFR | GWD | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG03098 | hp1 | a0001 | c0004 | t0032 | g0005 | AFR | MSL | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG03130 | hp1 | a0001 | c0001 | t0007 | g0077 | AFR | ESN | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG03139 | hp1 | a0001 | c0002 | t0005 | g0014 | AFR | ESN | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG03195 | hp1 | a0001 | c0002 | t0024 | g0017 | AFR | ESN | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG03195 | hp2 | a0001 | c0001 | t0018 | g0080 | AFR | ESN | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG03209 | hp1 | a0001 | c0002 | t0005 | g0002 | AFR | MSL | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG03225 | hp1 | a0001 | c0001 | t0005 | g0006 | AFR | MSL | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG03239 | hp2 | a0001 | c0001 | t0033 | g0040 | SAS | PJL | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG03453 | hp1 | a0001 | c0001 | t0038 | g0030 | AFR | MSL | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG03453 | hp2 | a0001 | c0001 | t0008 | g0007 | AFR | MSL | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG03486 | hp1 | a0001 | c0002 | t0023 | g0065 | AFR | MSL | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG03486 | hp2 | a0001 | c0001 | t0013 | g0185 | AFR | MSL | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG03490 | hp1 | a0001 | c0001 | t0010 | g0085 | SAS | PJL | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG03516 | hp1 | a0001 | c0001 | t0015 | g0103 | AFR | ESN | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG03516 | hp2 | a0001 | c0002 | t0007 | g0013 | AFR | ESN | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG03540 | hp1 | a0001 | c0001 | t0041 | g0153 | AFR | GWD | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG03540 | hp2 | a0001 | c0002 | t0005 | g0015 | AFR | GWD | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG03579 | hp1 | a0001 | c0001 | t0009 | g0223 | AFR | MSL | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG03654 | hp1 | a0001 | c0001 | t0008 | g0128 | SAS | PJL | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG03688 | hp1 | a0001 | c0002 | t0005 | g0056 | SAS | STU | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG03710 | hp1 | a0001 | c0001 | t0006 | g0134 | SAS | PJL | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG03942 | hp1 | a0001 | c0001 | t0003 | g0041 | SAS | BEB | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | STU | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0035 | SAS | BEB | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0098 | SAS | BEB | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG04199 | hp1 | a0001 | c0002 | t0011 | g0086 | SAS | STU | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG04204 | hp1 | a0001 | c0001 | t0008 | g0141 | SAS | STU | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | STU | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA18522 | hp1 | a0001 | c0001 | t0004 | g0197 | AFR | YRI | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | CHB | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA18747 | hp1 | a0001 | c0001 | t0004 | g0155 | EAS | CHB | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA18906 | hp1 | a0001 | c0003 | t0030 | g0198 | AFR | YRI | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA18906 | hp2 | a0001 | c0002 | t0024 | g0016 | AFR | YRI | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA18943 | hp1 | a0001 | c0001 | t0034 | g0167 | EAS | JPT | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA18944 | hp1 | a0001 | c0001 | t0008 | g0140 | EAS | JPT | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA18945 | hp1 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA18950 | hp1 | a0001 | c0001 | t0035 | g0172 | EAS | JPT | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA18950 | hp2 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA18957 | hp1 | a0001 | c0001 | t0004 | g0203 | EAS | JPT | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA18957 | hp2 | a0001 | c0001 | t0006 | g0200 | EAS | JPT | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA18962 | hp1 | a0001 | c0001 | t0008 | g0201 | EAS | JPT | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA18965 | hp1 | a0001 | c0001 | t0017 | g0118 | EAS | JPT | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA18966 | hp1 | a0001 | c0001 | t0004 | g0119 | EAS | JPT | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA18967 | hp1 | a0001 | c0001 | t0004 | g0202 | EAS | JPT | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA18970 | hp1 | a0001 | c0001 | t0004 | g0126 | EAS | JPT | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA18979 | hp1 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA18984 | hp1 | a0001 | c0001 | t0006 | g0053 | EAS | JPT | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA18986 | hp1 | a0001 | c0001 | t0022 | g0059 | EAS | JPT | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA18989 | hp1 | a0001 | c0001 | t0016 | g0116 | EAS | JPT | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA18994 | hp1 | a0001 | c0001 | t0006 | g0122 | EAS | JPT | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA19004 | hp1 | a0001 | c0001 | t0022 | g0058 | EAS | JPT | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA19006 | hp1 | a0001 | c0001 | t0015 | g0068 | EAS | JPT | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA19007 | hp1 | a0001 | c0001 | t0006 | g0117 | EAS | JPT | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA19012 | hp1 | a0001 | c0001 | t0003 | g0229 | EAS | JPT | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA19030 | hp1 | a0001 | c0002 | t0010 | g0031 | AFR | LWK | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA19030 | hp2 | a0001 | c0001 | t0008 | g0230 | AFR | LWK | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA19043 | hp1 | a0001 | c0005 | t0006 | g0144 | AFR | LWK | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA19058 | hp1 | a0001 | c0001 | t0004 | g0204 | EAS | JPT | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA19060 | hp1 | a0001 | c0001 | t0016 | g0091 | EAS | JPT | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA19062 | hp1 | a0001 | c0001 | t0003 | g0136 | EAS | JPT | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA19063 | hp1 | a0001 | c0001 | t0004 | g0164 | EAS | JPT | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA19072 | hp1 | a0001 | c0001 | t0008 | g0009 | EAS | JPT | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA19075 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA19076 | hp1 | a0001 | c0001 | t0006 | g0004 | EAS | JPT | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA19085 | hp1 | a0001 | c0001 | t0015 | g0112 | EAS | JPT | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA19088 | hp1 | a0001 | c0001 | t0006 | g0087 | EAS | JPT | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA19091 | hp1 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | YRI | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA19240 | hp2 | a0001 | c0002 | t0014 | g0025 | AFR | YRI | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA20129 | hp1 | a0001 | c0001 | t0009 | g0032 | AFR | ASW | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA20129 | hp2 | a0001 | c0002 | t0011 | g0076 | AFR | ASW | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0109 | EUR | TSI | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0110 | EUR | TSI | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA20905 | hp1 | a0001 | c0001 | t0006 | g0100 | SAS | GIH | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG01123 | hp1 | a0001 | c0002 | t0005 | g0010 | AMR | CLM | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG02109 | hp1 | a0001 | c0001 | t0017 | g0169 | AFR | ACB | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG02109 | hp2 | a0001 | c0002 | t0039 | g0184 | AFR | ACB | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG02486 | hp1 | a0001 | c0001 | t0048 | g0018 | AFR | ACB | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | MSL | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG06807 | hp1 | a0001 | c0001 | t0029 | g0012 | AFR | USA | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
HG06807 | hp2 | a0001 | c0001 | t0004 | g0069 | AFR | USA | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA18955 | hp1 | a0001 | c0001 | t0016 | g0148 | EAS | JPT | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA20300 | hp1 | a0001 | c0001 | t0003 | g0052 | AFR | USA | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
NA20300 | hp2 | a0002 | c0006 | t0002 | g0189 | AFR | USA | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0047 | REF | REF | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0040 | g0082 | REF | REF | GLRA2_chrX_14524536_14736812 | GLRA2 | chrX | 14524536 | 14736812 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:14730319
|
C | T | 1 | a0002 | 1 | NA20300.hp2 | missense_variant | MODERATE | c.1193C>T | p.Pro398Leu | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 9/9 | 1715/3208 | 1193/1359 | 398/452 | chrX | 14730319 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:14604327
|
C | T | 1 | a0001c0005 | 2 | HG01361.hp2 NA19043.hp1 |
synonymous_variant | LOW | c.507C>T | p.Thr169Thr | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 5/9 | 1029/3208 | 507/1359 | 169/452 | chrX | 14604327 | ||
chrX:14609022
|
T | C | 3 | a0001c0002a0001c0003a0002c0006 | 46 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(43): Show |
synonymous_variant | LOW | c.747T>C | p.His249His | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/9 | 1269/3208 | 747/1359 | 249/452 | chrX | 14609022 | ||
chrX:14730215
|
C | T | 2 | a0001c0003a0001c0004 | 10 | HG01074.hp1 HG01891.hp2 HG02293.hp1 others(7): Show |
synonymous_variant | LOW | c.1089C>T | p.Asp363Asp | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 9/9 | 1611/3208 | 1089/1359 | 363/452 | chrX | 14730215 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:14529555
|
A | G | 1 | a0001c0001t0049 | 1 | HG02280.hp1 | 5_prime_UTR_variant | MODIFIER | c.-503A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 1/9 | 503 | chrX | 14529555 | |||||
chrX:14529819
|
A | G | 8 | a0001c0001t0048a0001c0002t0024a0001c0002t0045others(5): Show | 12 | HG01074.hp1 HG02293.hp2 HG02486.hp1 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-239A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 1/9 | 239 | chrX | 14529819 | |||||
chrX:14529911
|
A | T | 8 | a0001c0001t0048a0001c0002t0024a0001c0002t0045others(5): Show | 12 | HG01074.hp1 HG02293.hp2 HG02486.hp1 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-147A>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 1/9 | 147 | chrX | 14529911 | |||||
chrX:14529920
|
A | G | 1 | a0001c0001t0044 | 1 | HG02965.hp1 | 5_prime_UTR_variant | MODIFIER | c.-138A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 1/9 | 138 | chrX | 14529920 | |||||
chrX:14730743
|
C | T | 1 | a0001c0002t0043 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*258C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 9/9 | 258 | chrX | 14730743 | |||||
chrX:14730884
|
T | C | 2 | a0001c0002t0028a0001c0002t0045 | 2 | HG02258.hp1 HG02647.hp1 |
3_prime_UTR_variant | MODIFIER | c.*399T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 9/9 | 399 | chrX | 14730884 | |||||
chrX:14730889
|
TATACACA others(5): Show |
T | 1 | a0001c0001t0029 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*406_*417delTACACA others(6): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 9/9 | 406 | INFO_REALIGN_3_PRIME | chrX | 14730889 | ||||
chrX:14730891
|
T | TACAC | 1 | a0001c0001t0012 | 4 | HG01106.hp1 HG01891.hp1 HG02280.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*462_*465dupCACA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 9/9 | 466 | INFO_REALIGN_3_PRIME | chrX | 14730891 | ||||
chrX:14730891
|
T | TACACACA others(1): Show |
1 | a0001c0001t0041 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*458_*465dupCACACA others(2): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 9/9 | 466 | INFO_REALIGN_3_PRIME | chrX | 14730891 | ||||
chrX:14730891
|
TAC | T | 3 | a0001c0001t0017a0001c0001t0044a0001c0002t0039 | 5 | HG02109.hp1 HG02109.hp2 HG02451.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*464_*465delCA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 9/9 | 464 | INFO_REALIGN_3_PRIME | chrX | 14730891 | ||||
chrX:14730891
|
TACAC | T | 3 | a0001c0001t0038a0001c0001t0048a0001c0002t0047 | 3 | HG02486.hp1 HG02976.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*462_*465delCACA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 9/9 | 462 | INFO_REALIGN_3_PRIME | chrX | 14730891 | ||||
chrX:14730891
|
TACACAC | T | 2 | a0001c0001t0016a0001c0002t0036 | 4 | HG02257.hp2 NA18955.hp1 NA18989.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*460_*465delCACACA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 9/9 | 460 | INFO_REALIGN_3_PRIME | chrX | 14730891 | ||||
chrX:14730891
|
TACACACA others(1): Show |
T | 5 | a0001c0001t0006a0001c0001t0011a0001c0002t0011others(2): Show | 19 | HG00140.hp1 HG00642.hp1 HG01255.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*458_*465delCACACA others(2): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 9/9 | 458 | INFO_REALIGN_3_PRIME | chrX | 14730891 | ||||
chrX:14730891
|
TACACACA others(3): Show |
T | 8 | a0001c0001t0002a0001c0001t0007a0001c0001t0034others(5): Show | 45 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*456_*465delCACACA others(4): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 9/9 | 456 | INFO_REALIGN_3_PRIME | chrX | 14730891 | ||||
chrX:14730891
|
TACACACA others(5): Show |
T | 7 | a0001c0001t0001a0001c0001t0005a0001c0001t0022others(4): Show | 57 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*454_*465delCACACA others(6): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 9/9 | 454 | INFO_REALIGN_3_PRIME | chrX | 14730891 | ||||
chrX:14730891
|
TACACACA others(7): Show |
T | 4 | a0001c0001t0004a0001c0001t0014a0001c0002t0014others(1): Show | 21 | HG01070.hp1 HG01928.hp1 HG01952.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*452_*465delCACACA others(8): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 9/9 | 452 | INFO_REALIGN_3_PRIME | chrX | 14730891 | ||||
chrX:14730891
|
TACACACA others(9): Show |
T | 7 | a0001c0001t0008a0001c0001t0021a0001c0001t0031others(4): Show | 18 | HG02451.hp1 HG02572.hp1 HG02630.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*450_*465delCACACA others(10): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 9/9 | 450 | INFO_REALIGN_3_PRIME | chrX | 14730891 | ||||
chrX:14730891
|
TACACACA others(11): Show |
T | 2 | a0001c0001t0020a0001c0002t0046 | 3 | HG00323.hp1 HG01981.hp2 HG02293.hp2 |
3_prime_UTR_variant | MODIFIER | c.*448_*465delCACACA others(12): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 9/9 | 448 | INFO_REALIGN_3_PRIME | chrX | 14730891 | ||||
chrX:14730891
|
TACACACA others(13): Show |
T | 4 | a0001c0001t0003a0001c0001t0013a0001c0001t0049others(1): Show | 26 | HG00558.hp2 HG00609.hp1 HG00639.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*446_*465delCACACA others(14): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 9/9 | 446 | INFO_REALIGN_3_PRIME | chrX | 14730891 | ||||
chrX:14730891
|
TACACACA others(15): Show |
T | 1 | a0001c0001t0019 | 2 | HG02083.hp1 HG02698.hp1 |
3_prime_UTR_variant | MODIFIER | c.*444_*465delCACACA others(16): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 9/9 | 444 | INFO_REALIGN_3_PRIME | chrX | 14730891 | ||||
chrX:14730891
|
TACACACA others(21): Show |
T | 3 | a0001c0001t0010a0001c0002t0010a0001c0002t0024 | 7 | HG02809.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*438_*465delCACACA others(22): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 9/9 | 438 | INFO_REALIGN_3_PRIME | chrX | 14730891 | ||||
chrX:14730891
|
TACACACA others(23): Show |
T | 1 | a0001c0001t0009 | 5 | HG01070.hp2 HG01071.hp2 HG02257.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*436_*465delCACACA others(24): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 9/9 | 436 | INFO_REALIGN_3_PRIME | chrX | 14730891 | ||||
chrX:14730891
|
TACACACA others(25): Show |
T | 1 | a0001c0001t0018 | 2 | HG02970.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*434_*465delCACACA others(26): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 9/9 | 434 | INFO_REALIGN_3_PRIME | chrX | 14730891 | ||||
chrX:14730939
|
CACACACA others(4): Show |
C | 1 | a0001c0001t0035 | 1 | NA18950.hp1 | 3_prime_UTR_variant | MODIFIER | c.*456_*466delCACACA others(5): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 9/9 | 456 | INFO_REALIGN_3_PRIME | chrX | 14730939 | ||||
chrX:14730941
|
CACACACA others(2): Show |
C | 1 | a0001c0001t0015 | 3 | HG03516.hp1 NA19006.hp1 NA19085.hp1 |
3_prime_UTR_variant | MODIFIER | c.*458_*466delCACACA others(3): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 9/9 | 458 | INFO_REALIGN_3_PRIME | chrX | 14730941 | ||||
chrX:14730941
|
CACACACA others(3): Show |
C | 1 | a0001c0001t0042 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*459_*468delACACAC others(4): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 9/9 | 459 | INFO_REALIGN_3_PRIME | chrX | 14730941 | ||||
chrX:14730943
|
CACACACA | C | 1 | a0001c0002t0037 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*460_*466delCACACA others(1): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 9/9 | 460 | INFO_REALIGN_3_PRIME | chrX | 14730943 | ||||
chrX:14731075
|
G | T | 4 | a0001c0001t0013a0001c0001t0031a0001c0001t0049others(1): Show | 6 | HG01243.hp1 HG02280.hp1 HG02622.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*590G>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 9/9 | 590 | chrX | 14731075 | |||||
chrX:14731219
|
T | C | 28 | a0001c0001t0003a0001c0001t0005a0001c0001t0007others(25): Show | 75 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*734T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 9/9 | 734 | chrX | 14731219 | |||||
chrX:14731262
|
G | GTAAT | 1 | a0001c0001t0022 | 2 | NA18986.hp1 NA19004.hp1 |
3_prime_UTR_variant | MODIFIER | c.*783_*786dupAATT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 9/9 | 787 | INFO_REALIGN_3_PRIME | chrX | 14731262 | ||||
chrX:14731482
|
T | C | 17 | a0001c0001t0005a0001c0001t0007a0001c0001t0011others(14): Show | 42 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*997T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 9/9 | 997 | chrX | 14731482 | |||||
chrX:14731674
|
G | GA | 1 | a0001c0001t0038 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1198dupA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 9/9 | 1199 | INFO_REALIGN_3_PRIME | chrX | 14731674 | ||||
chrX:14731716
|
C | A | 1 | a0001c0001t0034 | 1 | NA18943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1231C>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 9/9 | 1231 | chrX | 14731716 | |||||
chrX:14731758
|
G | C | 1 | a0001c0003t0030 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1273G>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 9/9 | 1273 | chrX | 14731758 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:14530724
|
T | C | 1 | a0001c0002t0005g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.68+599T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 1/8 | chrX | 14530724 | ||||||
chrX:14530901
|
G | A | 1 | a0001c0001t0001g0003 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.68+776G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 1/8 | chrX | 14530901 | ||||||
chrX:14530969
|
C | T | 2 | a0001c0001t0008g0230a0001c0001t0008g0231 | 2 | HG02886.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.68+844C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 1/8 | chrX | 14530969 | ||||||
chrX:14531176
|
A | G | 1 | a0001c0001t0003g0229 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.68+1051A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 1/8 | chrX | 14531176 | ||||||
chrX:14531330
|
T | C | 1 | a0001c0001t0006g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.69-909T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 1/8 | chrX | 14531330 | ||||||
chrX:14531385
|
A | C | 1 | a0001c0001t0014g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.69-854A>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 1/8 | chrX | 14531385 | ||||||
chrX:14531483
|
T | C | 2 | a0001c0001t0005g0006a0001c0004t0032g0005 | 2 | HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.69-756T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 1/8 | chrX | 14531483 | ||||||
chrX:14531842
|
G | A | 1 | a0001c0001t0008g0007 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.69-397G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 1/8 | chrX | 14531842 | ||||||
chrX:14532195
|
G | A | 2 | a0001c0001t0001g0001a0001c0001t0001g0008 | 3 | NA18971.hp1 NA19079.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.69-44G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 1/8 | chrX | 14532195 | ||||||
chrX:14532755
|
T | C | 1 | a0001c0001t0008g0009 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.202+383T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14532755 | ||||||
chrX:14532916
|
TCAA | T | 1 | a0001c0002t0005g0010 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.202+548_202+550del others(3): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14532916 | |||||
chrX:14532994
|
A | G | 1 | a0001c0001t0008g0227 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.202+622A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14532994 | ||||||
chrX:14533219
|
T | C | 1 | a0001c0001t0001g0011 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.202+847T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14533219 | ||||||
chrX:14533237
|
G | A | 3 | a0001c0001t0029g0012a0001c0002t0005g0014a0001c0002t0007g0013 | 3 | HG03139.hp1 HG03516.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.202+865G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14533237 | ||||||
chrX:14533427
|
A | G | 2 | a0001c0002t0005g0014a0001c0002t0007g0013 | 2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.202+1055A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14533427 | ||||||
chrX:14533523
|
G | GA | 12 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0004g0021others(9): Show | 12 | HG01069.hp1 HG01071.hp1 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.202+1164dupA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14533523 | |||||
chrX:14533523
|
G | GAA | 1 | a0001c0002t0005g0015 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.202+1163_202+1164d others(4): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14533523 | |||||
chrX:14533523
|
GA | G | 8 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0002g0222others(5): Show | 9 | HG01070.hp1 HG01070.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.202+1164delA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14533523 | |||||
chrX:14533523
|
GAA | G | 1 | a0001c0001t0003g0226 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.202+1163_202+1164d others(4): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14533523 | |||||
chrX:14533627
|
A | G | 1 | a0001c0001t0001g0219 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.202+1255A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14533627 | ||||||
chrX:14533842
|
A | T | 15 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0003g0206others(12): Show | 15 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.202+1470A>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14533842 | ||||||
chrX:14534213
|
G | GT | 6 | a0001c0001t0004g0202a0001c0001t0004g0203a0001c0001t0004g0204others(3): Show | 6 | HG02683.hp1 HG03453.hp2 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.202+1856dupT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14534213 | |||||
chrX:14534213
|
GT | G | 10 | a0001c0001t0001g0029a0001c0001t0002g0034a0001c0001t0004g0220others(7): Show | 10 | HG01070.hp1 HG02602.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.202+1856delT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14534213 | |||||
chrX:14534213
|
GTT | G | 1 | a0001c0001t0004g0027 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.202+1855_202+1856d others(4): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14534213 | |||||
chrX:14534213
|
GTTT | G | 15 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0003g0206others(12): Show | 15 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.202+1854_202+1856d others(5): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14534213 | |||||
chrX:14534244
|
TTAAAGTC | T | 1 | a0001c0001t0006g0200 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.202+1876_202+1882d others(9): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14534244 | |||||
chrX:14534300
|
T | C | 53 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(50): Show | 53 | HG00558.hp2 HG00639.hp1 HG01123.hp2 others(50): Show |
intron_variant | MODIFIER | c.202+1928T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14534300 | ||||||
chrX:14534510
|
T | C | 26 | a0001c0001t0001g0036a0001c0001t0001g0042a0001c0001t0001g0050others(23): Show | 26 | HG00558.hp2 HG00639.hp1 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.202+2138T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14534510 | ||||||
chrX:14534538
|
G | C | 2 | a0001c0002t0024g0016a0001c0002t0024g0017 | 2 | HG03195.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.202+2166G>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14534538 | ||||||
chrX:14534647
|
T | C | 1 | a0001c0002t0005g0205 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.202+2275T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14534647 | ||||||
chrX:14534951
|
C | T | 113 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(110): Show | 113 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.202+2579C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14534951 | ||||||
chrX:14534953
|
A | C | 1 | a0001c0001t0012g0174 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.202+2581A>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14534953 | ||||||
chrX:14535390
|
T | C | 1 | a0001c0001t0031g0060 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.202+3018T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14535390 | ||||||
chrX:14535432
|
C | A | 1 | a0001c0001t0004g0081 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.202+3060C>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14535432 | ||||||
chrX:14535588
|
A | G | 1 | a0001c0001t0002g0034 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.202+3216A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14535588 | ||||||
chrX:14535642
|
A | G | 1 | a0001c0001t0006g0200 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.202+3270A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14535642 | ||||||
chrX:14536129
|
G | A | 15 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0003g0206others(12): Show | 15 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.202+3757G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14536129 | ||||||
chrX:14536144
|
A | C | 3 | a0001c0001t0009g0032a0001c0001t0018g0033a0001c0002t0010g0031 | 3 | HG02970.hp1 NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.202+3772A>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14536144 | ||||||
chrX:14536356
|
C | G | 230 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(227): Show | 231 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.202+3984C>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14536356 | ||||||
chrX:14536763
|
G | GA | 1 | a0001c0001t0001g0083 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.202+4398dupA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14536763 | |||||
chrX:14536873
|
CAG | C | 2 | a0001c0002t0014g0025a0001c0002t0014g0026 | 2 | HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.202+4504_202+4505d others(4): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14536873 | |||||
chrX:14536932
|
A | G | 1 | a0001c0001t0006g0218 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.202+4560A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14536932 | ||||||
chrX:14537881
|
G | C | 1 | a0001c0001t0001g0084 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.202+5509G>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14537881 | ||||||
chrX:14537970
|
GC | G | 1 | a0001c0001t0014g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.202+5599delC | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14537970 | ||||||
chrX:14538034
|
C | A | 1 | a0001c0001t0029g0012 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.202+5662C>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14538034 | ||||||
chrX:14538983
|
T | TAA | 1 | a0001c0001t0010g0085 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.202+6612_202+6613d others(4): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14538983 | |||||
chrX:14539002
|
A | T | 1 | a0001c0001t0013g0199 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.202+6630A>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14539002 | ||||||
chrX:14539174
|
G | A | 1 | a0001c0001t0006g0218 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.202+6802G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14539174 | ||||||
chrX:14539921
|
AG | A | 1 | a0001c0001t0002g0222 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.202+7552delG | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14539921 | |||||
chrX:14540274
|
C | T | 2 | a0001c0001t0001g0173a0001c0001t0035g0172 | 2 | NA18948.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.202+7902C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14540274 | ||||||
chrX:14540344
|
A | C | 1 | a0001c0002t0011g0217 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.202+7972A>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14540344 | ||||||
chrX:14540363
|
G | T | 1 | a0001c0001t0001g0171 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.202+7991G>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14540363 | ||||||
chrX:14540616
|
C | T | 1 | a0001c0001t0005g0057 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.202+8244C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14540616 | ||||||
chrX:14540838
|
C | T | 1 | a0001c0001t0018g0080 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.202+8466C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14540838 | ||||||
chrX:14540915
|
G | A | 1 | a0001c0002t0011g0086 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.202+8543G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14540915 | ||||||
chrX:14540922
|
G | C | 1 | a0001c0001t0008g0230 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.202+8550G>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14540922 | ||||||
chrX:14541096
|
C | T | 1 | a0001c0002t0005g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.202+8724C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14541096 | ||||||
chrX:14541272
|
A | AG | 1 | a0001c0001t0002g0061 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.202+8904dupG | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14541272 | |||||
chrX:14541904
|
A | G | 17 | a0001c0001t0001g0170a0001c0001t0001g0211a0001c0001t0001g0212others(14): Show | 17 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(14): Show |
intron_variant | MODIFIER | c.202+9532A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14541904 | ||||||
chrX:14542329
|
G | A | 5 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0090others(2): Show | 5 | NA18612.hp1 NA19009.hp1 NA19060.hp1 others(2): Show |
intron_variant | MODIFIER | c.202+9957G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14542329 | ||||||
chrX:14542410
|
G | A | 1 | a0001c0001t0006g0092 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.202+10038G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14542410 | ||||||
chrX:14542464
|
G | A | 1 | a0001c0002t0028g0062 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.202+10092G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14542464 | ||||||
chrX:14542607
|
T | TC | 1 | a0001c0001t0002g0222 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.202+10237dupC | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14542607 | |||||
chrX:14542629
|
G | GA | 2 | a0001c0001t0002g0093a0001c0001t0008g0230 | 2 | NA19030.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.202+10269dupA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14542629 | |||||
chrX:14542785
|
T | G | 1 | a0001c0001t0001g0170 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.202+10413T>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14542785 | ||||||
chrX:14542820
|
C | T | 1 | a0001c0001t0017g0169 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.202+10448C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14542820 | ||||||
chrX:14542834
|
A | AG | 1 | a0001c0001t0002g0222 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.202+10464dupG | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14542834 | |||||
chrX:14542881
|
C | T | 13 | a0001c0001t0001g0083a0001c0001t0002g0088a0001c0001t0002g0089others(10): Show | 13 | HG01081.hp1 HG01099.hp1 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.202+10509C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14542881 | ||||||
chrX:14542924
|
G | GC | 1 | a0001c0001t0002g0222 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.202+10555dupC | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14542924 | |||||
chrX:14543020
|
AT | A | 1 | a0001c0001t0002g0222 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.202+10653delT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14543020 | |||||
chrX:14543039
|
A | C | 1 | a0001c0001t0002g0222 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.202+10667A>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14543039 | ||||||
chrX:14543075
|
TC | T | 1 | a0001c0001t0002g0222 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.202+10705delC | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14543075 | |||||
chrX:14543099
|
G | A | 16 | a0001c0001t0001g0170a0001c0001t0001g0211a0001c0001t0001g0212others(13): Show | 16 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(13): Show |
intron_variant | MODIFIER | c.202+10727G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14543099 | ||||||
chrX:14543236
|
C | CA | 39 | a0001c0001t0001g0066a0001c0001t0001g0083a0001c0001t0001g0097others(36): Show | 39 | HG00323.hp1 HG00621.hp1 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.202+10889dupA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14543236 | |||||
chrX:14543236
|
C | CAA | 7 | a0001c0002t0024g0016a0001c0002t0024g0017a0001c0002t0045g0177others(4): Show | 7 | HG01074.hp1 HG02293.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.202+10888_202+1088 others(6): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14543236 | |||||
chrX:14543236
|
C | CAAA | 1 | a0001c0003t0025g0175 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.202+10887_202+1088 others(7): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14543236 | |||||
chrX:14543236
|
C | CAAAA | 1 | a0001c0001t0048g0018 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.202+10886_202+1088 others(8): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14543236 | |||||
chrX:14543236
|
CAAA | C | 2 | a0001c0001t0002g0194a0001c0001t0008g0231 | 2 | HG02615.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.202+10887_202+1088 others(7): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14543236 | |||||
chrX:14543236
|
CAAAA | C | 6 | a0001c0001t0004g0197a0001c0001t0007g0079a0001c0001t0008g0195others(3): Show | 6 | HG02145.hp1 HG02451.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.202+10886_202+1088 others(8): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14543236 | |||||
chrX:14543289
|
T | C | 3 | a0001c0001t0001g0187a0001c0001t0002g0034a0001c0001t0038g0030 | 3 | HG03453.hp1 HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.202+10917T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14543289 | ||||||
chrX:14543393
|
A | G | 17 | a0001c0001t0001g0170a0001c0001t0001g0211a0001c0001t0001g0212others(14): Show | 17 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(14): Show |
intron_variant | MODIFIER | c.202+11021A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14543393 | ||||||
chrX:14543405
|
T | A | 1 | a0001c0001t0001g0036 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.202+11033T>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14543405 | ||||||
chrX:14543560
|
T | G | 1 | a0001c0003t0007g0067 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.202+11188T>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14543560 | ||||||
chrX:14543629
|
C | G | 17 | a0001c0001t0001g0170a0001c0001t0001g0211a0001c0001t0001g0212others(14): Show | 17 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(14): Show |
intron_variant | MODIFIER | c.202+11257C>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14543629 | ||||||
chrX:14543721
|
T | C | 1 | a0001c0002t0036g0063 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.202+11349T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14543721 | ||||||
chrX:14543958
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.202+11586C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14543958 | ||||||
chrX:14543993
|
G | GA | 1 | a0001c0001t0002g0222 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.202+11623dupA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14543993 | |||||
chrX:14544054
|
A | AG | 1 | a0001c0001t0002g0222 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.202+11685dupG | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14544054 | |||||
chrX:14544090
|
A | G | 4 | a0001c0001t0007g0077a0001c0001t0007g0079a0001c0001t0017g0078others(1): Show | 4 | HG02145.hp1 HG02451.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.202+11718A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14544090 | ||||||
chrX:14544188
|
T | C | 1 | a0001c0003t0026g0176 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.202+11816T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14544188 | ||||||
chrX:14544192
|
TAAAC | T | 2 | a0001c0001t0009g0224a0001c0001t0009g0225 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.202+11826_202+1182 others(8): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14544192 | |||||
chrX:14544437
|
CA | C | 17 | a0001c0001t0001g0170a0001c0001t0001g0211a0001c0001t0001g0212others(14): Show | 17 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(14): Show |
intron_variant | MODIFIER | c.202+12071delA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14544437 | |||||
chrX:14544465
|
C | A | 9 | a0001c0001t0001g0187a0001c0001t0002g0034a0001c0001t0004g0027others(6): Show | 9 | HG01070.hp1 HG02630.hp1 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.202+12093C>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14544465 | ||||||
chrX:14544929
|
C | T | 7 | a0001c0001t0001g0187a0001c0001t0002g0034a0001c0001t0004g0027others(4): Show | 7 | HG02970.hp1 HG03041.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.202+12557C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14544929 | ||||||
chrX:14545111
|
T | C | 17 | a0001c0001t0001g0170a0001c0001t0001g0211a0001c0001t0001g0212others(14): Show | 17 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(14): Show |
intron_variant | MODIFIER | c.202+12739T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14545111 | ||||||
chrX:14545354
|
A | T | 1 | a0001c0001t0002g0161 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.202+12982A>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14545354 | ||||||
chrX:14545449
|
C | T | 1 | a0001c0001t0004g0027 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.202+13077C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14545449 | ||||||
chrX:14545759
|
G | A | 1 | a0001c0001t0005g0006 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.202+13387G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14545759 | ||||||
chrX:14545759
|
G | C | 9 | a0001c0001t0001g0187a0001c0001t0002g0034a0001c0001t0004g0027others(6): Show | 9 | HG01070.hp1 HG02630.hp1 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.202+13387G>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14545759 | ||||||
chrX:14545895
|
G | C | 17 | a0001c0001t0001g0170a0001c0001t0001g0211a0001c0001t0001g0212others(14): Show | 17 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(14): Show |
intron_variant | MODIFIER | c.202+13523G>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14545895 | ||||||
chrX:14546062
|
A | G | 1 | a0001c0001t0044g0193 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.202+13690A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14546062 | ||||||
chrX:14546470
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.202+14098T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14546470 | ||||||
chrX:14546475
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.202+14103C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14546475 | ||||||
chrX:14546494
|
T | TA | 1 | a0001c0001t0001g0107 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.202+14130dupA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14546494 | |||||
chrX:14546566
|
C | A | 2 | a0001c0001t0004g0220a0001c0001t0014g0228 | 2 | HG01070.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.202+14194C>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14546566 | ||||||
chrX:14546599
|
A | AT | 3 | a0001c0001t0001g0105a0001c0001t0002g0222a0001c0001t0004g0220 | 3 | HG00621.hp1 HG01070.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.202+14240dupT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14546599 | |||||
chrX:14546599
|
ATT | A | 16 | a0001c0001t0001g0170a0001c0001t0001g0211a0001c0001t0001g0212others(13): Show | 16 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(13): Show |
intron_variant | MODIFIER | c.202+14239_202+1424 others(6): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14546599 | |||||
chrX:14546706
|
G | T | 16 | a0001c0001t0001g0170a0001c0001t0001g0211a0001c0001t0001g0212others(13): Show | 16 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(13): Show |
intron_variant | MODIFIER | c.202+14334G>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14546706 | ||||||
chrX:14546747
|
T | C | 1 | a0001c0002t0005g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.202+14375T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14546747 | ||||||
chrX:14547148
|
A | G | 16 | a0001c0001t0001g0170a0001c0001t0001g0211a0001c0001t0001g0212others(13): Show | 16 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(13): Show |
intron_variant | MODIFIER | c.202+14776A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14547148 | ||||||
chrX:14547526
|
TATAAG | T | 1 | a0001c0001t0012g0174 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.202+15156_202+1516 others(9): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14547526 | |||||
chrX:14548222
|
A | G | 1 | a0001c0001t0002g0168 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.202+15850A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14548222 | ||||||
chrX:14548330
|
A | G | 9 | a0001c0001t0001g0187a0001c0001t0002g0034a0001c0001t0004g0027others(6): Show | 9 | HG01070.hp1 HG02630.hp1 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.202+15958A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14548330 | ||||||
chrX:14548404
|
TTATC | T | 1 | a0001c0001t0008g0230 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.202+16035_202+1603 others(8): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14548404 | |||||
chrX:14548497
|
G | A | 2 | a0001c0001t0005g0108a0001c0004t0007g0094 | 2 | HG00733.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.202+16125G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14548497 | ||||||
chrX:14548590
|
C | T | 16 | a0001c0001t0001g0170a0001c0001t0001g0211a0001c0001t0001g0212others(13): Show | 16 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(13): Show |
intron_variant | MODIFIER | c.202+16218C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14548590 | ||||||
chrX:14548675
|
C | T | 2 | a0001c0001t0003g0054a0001c0001t0003g0055 | 2 | NA18945.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.202+16303C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14548675 | ||||||
chrX:14548729
|
G | A | 16 | a0001c0001t0001g0170a0001c0001t0001g0211a0001c0001t0001g0212others(13): Show | 16 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(13): Show |
intron_variant | MODIFIER | c.202+16357G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14548729 | ||||||
chrX:14548935
|
T | TGAA | 110 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(107): Show | 110 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.202+16565_202+1656 others(7): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14548935 | |||||
chrX:14549221
|
T | C | 1 | a0001c0001t0015g0112 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.202+16849T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14549221 | ||||||
chrX:14549333
|
A | G | 54 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(51): Show | 54 | HG00558.hp2 HG00639.hp1 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.202+16961A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14549333 | ||||||
chrX:14549455
|
C | T | 1 | a0001c0001t0016g0091 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.202+17083C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14549455 | ||||||
chrX:14549463
|
G | A | 3 | a0001c0001t0011g0188a0001c0001t0021g0190a0002c0006t0002g0189 | 3 | HG02922.hp1 HG03041.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.202+17091G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14549463 | ||||||
chrX:14550189
|
C | T | 15 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0003g0206others(12): Show | 15 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.202+17817C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14550189 | ||||||
chrX:14550260
|
GT | G | 2 | a0001c0001t0004g0164a0001c0002t0005g0014 | 2 | HG03139.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.202+17901delT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14550260 | |||||
chrX:14550274
|
A | T | 7 | a0001c0001t0001g0160a0001c0001t0002g0090a0001c0001t0004g0202others(4): Show | 7 | HG01109.hp1 HG03239.hp1 NA18957.hp1 others(4): Show |
intron_variant | MODIFIER | c.202+17902A>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14550274 | ||||||
chrX:14550446
|
C | T | 2 | a0001c0001t0004g0220a0001c0001t0014g0228 | 2 | HG01070.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.202+18074C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14550446 | ||||||
chrX:14550548
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.202+18176G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14550548 | ||||||
chrX:14550767
|
T | G | 1 | a0001c0001t0044g0193 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.202+18395T>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14550767 | ||||||
chrX:14550798
|
C | A | 2 | a0001c0001t0002g0019a0001c0001t0002g0020 | 2 | NA18977.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.202+18426C>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14550798 | ||||||
chrX:14550819
|
C | G | 7 | a0001c0001t0002g0194a0001c0001t0004g0197a0001c0001t0008g0195others(4): Show | 7 | HG02451.hp1 HG02615.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.202+18447C>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14550819 | ||||||
chrX:14550903
|
TC | T | 1 | a0001c0001t0002g0222 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.202+18533delC | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14550903 | |||||
chrX:14550921
|
G | A | 19 | a0001c0001t0001g0113a0001c0001t0001g0211a0001c0001t0001g0212others(16): Show | 19 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(16): Show |
intron_variant | MODIFIER | c.202+18549G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14550921 | ||||||
chrX:14550932
|
AC | A | 1 | a0001c0001t0002g0222 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.202+18562delC | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14550932 | |||||
chrX:14550980
|
G | GT | 1 | a0001c0001t0002g0222 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.202+18611dupT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14550980 | |||||
chrX:14551089
|
C | T | 19 | a0001c0001t0001g0113a0001c0001t0001g0211a0001c0001t0001g0212others(16): Show | 19 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(16): Show |
intron_variant | MODIFIER | c.202+18717C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14551089 | ||||||
chrX:14551124
|
T | C | 2 | a0001c0001t0003g0035a0001c0001t0003g0037 | 2 | HG03017.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.202+18752T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14551124 | ||||||
chrX:14551215
|
A | AT | 1 | a0001c0001t0002g0093 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.202+18844dupT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14551215 | |||||
chrX:14551386
|
GA | G | 1 | a0001c0001t0002g0222 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.202+19016delA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14551386 | |||||
chrX:14551404
|
G | A | 20 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0097others(17): Show | 21 | HG02080.hp1 HG02523.hp1 HG04184.hp2 others(18): Show |
intron_variant | MODIFIER | c.202+19032G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14551404 | ||||||
chrX:14551443
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.202+19071C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14551443 | ||||||
chrX:14551474
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.202+19102G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14551474 | ||||||
chrX:14551484
|
G | A | 1 | a0001c0002t0011g0076 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.202+19112G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14551484 | ||||||
chrX:14551548
|
G | A | 1 | a0001c0002t0005g0014 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.202+19176G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14551548 | ||||||
chrX:14551566
|
C | T | 10 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0158others(7): Show | 10 | HG00639.hp2 HG01928.hp1 HG01952.hp1 others(7): Show |
intron_variant | MODIFIER | c.202+19194C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14551566 | ||||||
chrX:14551703
|
C | A | 9 | a0001c0001t0001g0187a0001c0001t0002g0034a0001c0001t0004g0027others(6): Show | 9 | HG01070.hp1 HG02630.hp1 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.202+19331C>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14551703 | ||||||
chrX:14551895
|
T | TG | 1 | a0001c0001t0002g0222 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.202+19528dupG | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14551895 | |||||
chrX:14551904
|
C | CT | 1 | a0001c0001t0002g0222 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.202+19534dupT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14551904 | |||||
chrX:14552284
|
G | A | 7 | a0001c0001t0002g0194a0001c0001t0004g0197a0001c0001t0008g0195others(4): Show | 7 | HG02451.hp1 HG02615.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.202+19912G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14552284 | ||||||
chrX:14552312
|
G | C | 1 | a0001c0001t0003g0206 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.202+19940G>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14552312 | ||||||
chrX:14552338
|
A | T | 1 | a0001c0001t0003g0055 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.202+19966A>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14552338 | ||||||
chrX:14552662
|
T | G | 4 | a0001c0001t0008g0195a0001c0001t0008g0196a0001c0001t0008g0230others(1): Show | 4 | HG02451.hp1 HG02886.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.202+20290T>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14552662 | ||||||
chrX:14552755
|
T | A | 1 | a0001c0002t0010g0031 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.202+20383T>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14552755 | ||||||
chrX:14553001
|
T | TG | 1 | a0001c0001t0002g0222 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.202+20632dupG | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14553001 | |||||
chrX:14553044
|
A | G | 1 | a0001c0001t0003g0054 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.202+20672A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14553044 | ||||||
chrX:14553095
|
T | C | 1 | a0001c0001t0003g0038 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.202+20723T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14553095 | ||||||
chrX:14553172
|
G | GT | 1 | a0001c0001t0002g0222 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.202+20803dupT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14553172 | |||||
chrX:14553656
|
G | A | 2 | a0001c0001t0004g0126a0001c0001t0044g0193 | 2 | HG02965.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.203-20677G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14553656 | ||||||
chrX:14553712
|
TA | T | 1 | a0001c0001t0002g0222 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.203-20618delA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14553712 | |||||
chrX:14553820
|
C | A | 9 | a0001c0002t0045g0177a0001c0002t0046g0179a0001c0002t0047g0183others(6): Show | 9 | HG01074.hp1 HG02293.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.203-20513C>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14553820 | ||||||
chrX:14554012
|
C | T | 1 | a0001c0004t0032g0005 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.203-20321C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14554012 | ||||||
chrX:14554298
|
TC | T | 1 | a0001c0001t0002g0222 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.203-20033delC | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14554298 | |||||
chrX:14554413
|
CT | C | 1 | a0001c0001t0002g0222 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.203-19918delT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14554413 | |||||
chrX:14554988
|
G | A | 1 | a0001c0001t0004g0027 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.203-19345G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14554988 | ||||||
chrX:14555366
|
A | G | 3 | a0001c0001t0011g0188a0001c0001t0021g0190a0002c0006t0002g0189 | 3 | HG02922.hp1 HG03041.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.203-18967A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14555366 | ||||||
chrX:14555427
|
AC | A | 1 | a0001c0001t0002g0093 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.203-18903delC | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14555427 | |||||
chrX:14555764
|
G | A | 1 | a0001c0001t0002g0127 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.203-18569G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14555764 | ||||||
chrX:14555933
|
C | CG | 1 | a0001c0001t0004g0202 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.203-18397dupG | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14555933 | |||||
chrX:14555972
|
G | T | 3 | a0001c0001t0001g0066a0001c0001t0018g0080a0001c0001t0031g0060 | 3 | HG02055.hp1 HG02630.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.203-18361G>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14555972 | ||||||
chrX:14556211
|
A | C | 10 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0158others(7): Show | 10 | HG00639.hp2 HG01928.hp1 HG01952.hp1 others(7): Show |
intron_variant | MODIFIER | c.203-18122A>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14556211 | ||||||
chrX:14556883
|
A | AC | 7 | a0001c0001t0012g0104a0001c0001t0012g0154a0001c0001t0012g0174others(4): Show | 7 | HG01106.hp1 HG01891.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.203-17448dupC | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14556883 | |||||
chrX:14556922
|
AT | A | 4 | a0001c0002t0045g0177a0001c0003t0025g0175a0001c0003t0025g0181others(1): Show | 4 | HG02572.hp1 HG02615.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.203-17410delT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14556922 | ||||||
chrX:14557030
|
G | A | 115 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(112): Show | 115 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.203-17303G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14557030 | ||||||
chrX:14557102
|
C | CT | 4 | a0001c0001t0004g0202a0001c0002t0005g0015a0001c0003t0025g0181others(1): Show | 4 | HG02622.hp1 HG02922.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.203-17200dupT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14557102 | |||||
chrX:14557102
|
C | CTT | 1 | a0001c0002t0005g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.203-17201_203-1720 others(6): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14557102 | |||||
chrX:14557102
|
C | CTTTTT | 1 | a0001c0002t0005g0014 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.203-17204_203-1720 others(9): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14557102 | |||||
chrX:14557102
|
C | CTTTTTT | 1 | a0001c0002t0007g0013 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.203-17205_203-1720 others(10): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14557102 | |||||
chrX:14557102
|
CT | C | 100 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0083others(97): Show | 101 | HG00323.hp2 HG00558.hp1 HG00609.hp1 others(98): Show |
intron_variant | MODIFIER | c.203-17200delT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14557102 | |||||
chrX:14557102
|
CTT | C | 24 | a0001c0001t0001g0066a0001c0001t0001g0111a0001c0001t0002g0194others(21): Show | 24 | HG00741.hp1 HG01070.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.203-17201_203-1720 others(6): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14557102 | |||||
chrX:14557102
|
CTTT | C | 21 | a0001c0001t0001g0036a0001c0001t0001g0042a0001c0001t0001g0050others(18): Show | 21 | HG00558.hp2 HG00639.hp1 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.203-17202_203-1720 others(7): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14557102 | |||||
chrX:14557102
|
CTTTT | C | 1 | a0001c0001t0003g0226 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.203-17203_203-1720 others(8): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14557102 | |||||
chrX:14557102
|
CTTTTTTT | C | 1 | a0001c0003t0025g0175 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.203-17206_203-1720 others(11): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14557102 | |||||
chrX:14557102
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0002t0005g0056 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.203-17212_203-1720 others(17): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14557102 | |||||
chrX:14557102
|
CTTTTTTT others(7): Show |
C | 15 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0003g0206others(12): Show | 15 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.203-17213_203-1720 others(18): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14557102 | |||||
chrX:14557102
|
CTTTTTTT others(10): Show |
C | 16 | a0001c0001t0001g0029a0001c0001t0001g0072a0001c0001t0004g0069others(13): Show | 16 | HG01243.hp1 HG02132.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.203-17216_203-1720 others(21): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14557102 | |||||
chrX:14557194
|
T | C | 116 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(113): Show | 116 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.203-17139T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14557194 | ||||||
chrX:14557202
|
G | T | 99 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(96): Show | 99 | HG00558.hp2 HG00639.hp1 HG00733.hp2 others(96): Show |
intron_variant | MODIFIER | c.203-17131G>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14557202 | ||||||
chrX:14557208
|
T | C | 115 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(112): Show | 115 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.203-17125T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14557208 | ||||||
chrX:14557230
|
C | T | 115 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(112): Show | 115 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.203-17103C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14557230 | ||||||
chrX:14557240
|
C | A | 1 | a0001c0001t0001g0105 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.203-17093C>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14557240 | ||||||
chrX:14557265
|
A | G | 1 | a0001c0003t0007g0067 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.203-17068A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14557265 | ||||||
chrX:14557317
|
A | G | 1 | a0001c0001t0041g0153 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.203-17016A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14557317 | ||||||
chrX:14557329
|
G | A | 3 | a0001c0001t0013g0185a0001c0002t0023g0186a0001c0002t0039g0184 | 3 | HG01109.hp1 HG02109.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.203-17004G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14557329 | ||||||
chrX:14557395
|
A | G | 3 | a0001c0001t0011g0188a0001c0001t0021g0190a0002c0006t0002g0189 | 3 | HG02922.hp1 HG03041.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.203-16938A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14557395 | ||||||
chrX:14557397
|
A | G | 3 | a0001c0001t0011g0188a0001c0001t0021g0190a0002c0006t0002g0189 | 3 | HG02922.hp1 HG03041.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.203-16936A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14557397 | ||||||
chrX:14557404
|
T | C | 3 | a0001c0001t0011g0188a0001c0001t0021g0190a0002c0006t0002g0189 | 3 | HG02922.hp1 HG03041.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.203-16929T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14557404 | ||||||
chrX:14557410
|
C | T | 1 | a0001c0001t0006g0053 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.203-16923C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14557410 | ||||||
chrX:14557478
|
T | C | 16 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0003g0206others(13): Show | 16 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(13): Show |
intron_variant | MODIFIER | c.203-16855T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14557478 | ||||||
chrX:14557576
|
T | C | 1 | a0001c0001t0003g0206 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.203-16757T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14557576 | ||||||
chrX:14557718
|
CAG | C | 1 | a0001c0001t0004g0204 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.203-16614_203-1661 others(6): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14557718 | ||||||
chrX:14557725
|
T | C | 1 | a0001c0001t0008g0230 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.203-16608T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14557725 | ||||||
chrX:14557758
|
G | A | 1 | a0001c0002t0037g0028 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.203-16575G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14557758 | ||||||
chrX:14557869
|
TA | T | 1 | a0001c0001t0002g0093 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.203-16457delA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14557869 | |||||
chrX:14558130
|
C | T | 3 | a0001c0001t0011g0188a0001c0001t0021g0190a0002c0006t0002g0189 | 3 | HG02922.hp1 HG03041.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.203-16203C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14558130 | ||||||
chrX:14558302
|
T | C | 1 | a0001c0001t0002g0194 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.203-16031T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14558302 | ||||||
chrX:14558802
|
G | A | 1 | a0001c0001t0005g0108 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.203-15531G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14558802 | ||||||
chrX:14558825
|
AT | A | 1 | a0001c0001t0016g0148 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.203-15493delT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14558825 | |||||
chrX:14558932
|
C | G | 1 | a0001c0002t0011g0217 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.203-15401C>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14558932 | ||||||
chrX:14559031
|
A | G | 15 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0003g0206others(12): Show | 15 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.203-15302A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14559031 | ||||||
chrX:14559078
|
G | GCC | 1 | a0001c0001t0002g0093 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.203-15254_203-1525 others(6): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14559078 | |||||
chrX:14559153
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.203-15180C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14559153 | ||||||
chrX:14559419
|
C | CT | 24 | a0001c0001t0001g0106a0001c0001t0001g0111a0001c0001t0001g0121others(21): Show | 24 | HG00642.hp1 HG00741.hp1 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.203-14884dupT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14559419 | |||||
chrX:14559419
|
C | CTT | 2 | a0001c0001t0001g0158a0001c0001t0008g0009 | 2 | HG02129.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.203-14885_203-1488 others(6): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14559419 | |||||
chrX:14559419
|
C | CTTT | 1 | a0001c0001t0001g0152 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.203-14886_203-1488 others(7): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14559419 | |||||
chrX:14559419
|
CT | C | 33 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0129others(30): Show | 33 | HG01167.hp1 HG01496.hp1 HG02055.hp1 others(30): Show |
intron_variant | MODIFIER | c.203-14884delT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14559419 | |||||
chrX:14559419
|
CTT | C | 4 | a0001c0001t0006g0200a0001c0001t0008g0230a0001c0001t0008g0231others(1): Show | 4 | HG02886.hp1 HG03041.hp2 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.203-14885_203-1488 others(6): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14559419 | |||||
chrX:14559419
|
CTTT | C | 5 | a0001c0001t0002g0194a0001c0001t0004g0197a0001c0001t0008g0195others(2): Show | 5 | HG02451.hp1 HG02615.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.203-14886_203-1488 others(7): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14559419 | |||||
chrX:14559419
|
CTTTTTTT others(5): Show |
C | 15 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0003g0206others(12): Show | 15 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.203-14895_203-1488 others(16): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14559419 | |||||
chrX:14559569
|
AC | A | 1 | a0001c0001t0002g0093 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.203-14762delC | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14559569 | |||||
chrX:14559573
|
C | T | 1 | a0001c0002t0028g0062 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.203-14760C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14559573 | ||||||
chrX:14559811
|
C | T | 15 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0003g0206others(12): Show | 15 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.203-14522C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14559811 | ||||||
chrX:14559822
|
TG | T | 1 | a0001c0001t0002g0093 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.203-14507delG | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14559822 | |||||
chrX:14559999
|
G | A | 1 | a0001c0001t0006g0100 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.203-14334G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14559999 | ||||||
chrX:14560074
|
C | T | 2 | a0001c0001t0008g0195a0001c0001t0008g0196 | 2 | HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.203-14259C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14560074 | ||||||
chrX:14560149
|
CT | C | 1 | a0001c0001t0002g0061 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.203-14179delT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14560149 | |||||
chrX:14560189
|
GC | G | 1 | a0001c0001t0002g0093 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.203-14141delC | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14560189 | |||||
chrX:14560327
|
A | AT | 1 | a0001c0001t0002g0093 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.203-14005dupT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14560327 | |||||
chrX:14560471
|
TC | T | 1 | a0001c0001t0002g0093 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.203-13859delC | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14560471 | |||||
chrX:14560513
|
CA | C | 1 | a0001c0001t0002g0093 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.203-13814delA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14560513 | |||||
chrX:14560639
|
C | T | 1 | a0001c0001t0002g0149 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.203-13694C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14560639 | ||||||
chrX:14560797
|
C | CA | 12 | a0001c0001t0001g0029a0001c0001t0002g0093a0001c0001t0002g0115others(9): Show | 12 | HG02056.hp1 HG02622.hp1 HG02738.hp1 others(9): Show |
intron_variant | MODIFIER | c.203-13511dupA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14560797 | |||||
chrX:14560797
|
C | CAA | 1 | a0001c0002t0046g0179 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.203-13512_203-1351 others(6): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14560797 | |||||
chrX:14560797
|
CA | C | 20 | a0001c0001t0001g0011a0001c0001t0001g0146a0001c0001t0001g0173others(17): Show | 20 | HG00558.hp1 HG00741.hp2 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.203-13511delA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14560797 | |||||
chrX:14560797
|
CAA | C | 15 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0003g0206others(12): Show | 15 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.203-13512_203-1351 others(6): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14560797 | |||||
chrX:14560797
|
CAAA | C | 1 | a0001c0001t0005g0216 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.203-13513_203-1351 others(7): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14560797 | |||||
chrX:14560797
|
CAAAAA | C | 2 | a0001c0001t0001g0036a0001c0001t0003g0044 | 2 | HG01257.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.203-13515_203-1351 others(9): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14560797 | |||||
chrX:14560797
|
CAAAAAAA | C | 21 | a0001c0001t0001g0050a0001c0001t0001g0109a0001c0001t0001g0110others(18): Show | 21 | HG00558.hp2 HG00639.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.203-13517_203-1351 others(11): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14560797 | |||||
chrX:14560797
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0008g0007 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.203-13521_203-1351 others(15): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14560797 | |||||
chrX:14560825
|
A | G | 4 | a0001c0001t0048g0018a0001c0002t0005g0002a0001c0002t0024g0016others(1): Show | 4 | HG02486.hp1 HG03195.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.203-13508A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14560825 | ||||||
chrX:14560889
|
TACAC | T | 1 | a0001c0001t0014g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.203-13438_203-1343 others(8): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14560889 | |||||
chrX:14561569
|
C | A | 1 | a0001c0001t0002g0061 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.203-12764C>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14561569 | ||||||
chrX:14561648
|
GT | G | 1 | a0001c0001t0002g0093 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.203-12683delT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14561648 | |||||
chrX:14561831
|
C | T | 3 | a0001c0001t0001g0066a0001c0001t0018g0080a0001c0001t0031g0060 | 3 | HG02055.hp1 HG02630.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.203-12502C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14561831 | ||||||
chrX:14561847
|
TA | T | 1 | a0001c0001t0002g0061 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.203-12485delA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14561847 | ||||||
chrX:14561850
|
A | G | 2 | a0001c0002t0005g0014a0001c0002t0007g0013 | 2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.203-12483A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14561850 | ||||||
chrX:14562037
|
A | G | 1 | a0001c0001t0029g0012 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.203-12296A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14562037 | ||||||
chrX:14562167
|
G | A | 21 | a0001c0001t0048g0018a0001c0002t0005g0002a0001c0002t0005g0015others(18): Show | 21 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.203-12166G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14562167 | ||||||
chrX:14562405
|
G | GC | 1 | a0001c0001t0002g0093 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.203-11925dupC | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14562405 | |||||
chrX:14562562
|
G | GT | 1 | a0001c0001t0001g0083 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.203-11768dupT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14562562 | |||||
chrX:14562562
|
GT | G | 1 | a0001c0001t0002g0061 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.203-11768delT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14562562 | |||||
chrX:14562830
|
T | C | 1 | a0001c0002t0043g0191 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.203-11503T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14562830 | ||||||
chrX:14563082
|
G | A | 1 | a0001c0001t0003g0229 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.203-11251G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14563082 | ||||||
chrX:14563085
|
C | T | 4 | a0001c0002t0007g0022a0001c0002t0007g0023a0001c0002t0007g0192others(1): Show | 4 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.203-11248C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14563085 | ||||||
chrX:14563296
|
T | C | 7 | a0001c0001t0001g0187a0001c0001t0002g0034a0001c0001t0004g0027others(4): Show | 7 | HG02970.hp1 HG03041.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.203-11037T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14563296 | ||||||
chrX:14563299
|
C | G | 1 | a0001c0001t0008g0007 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.203-11034C>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14563299 | ||||||
chrX:14563505
|
T | G | 11 | a0001c0001t0001g0160a0001c0001t0002g0101a0001c0001t0002g0151others(8): Show | 11 | HG00738.hp1 HG01255.hp1 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.203-10828T>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14563505 | ||||||
chrX:14563771
|
A | C | 2 | a0001c0001t0001g0083a0001c0001t0004g0162 | 2 | HG02080.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.203-10562A>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14563771 | ||||||
chrX:14564028
|
G | A | 1 | a0001c0001t0044g0193 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.203-10305G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14564028 | ||||||
chrX:14564060
|
C | A | 3 | a0001c0001t0011g0188a0001c0001t0021g0190a0002c0006t0002g0189 | 3 | HG02922.hp1 HG03041.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.203-10273C>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14564060 | ||||||
chrX:14564120
|
A | G | 1 | a0001c0001t0001g0050 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.203-10213A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14564120 | ||||||
chrX:14564209
|
A | G | 1 | a0001c0001t0034g0167 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.203-10124A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14564209 | ||||||
chrX:14564223
|
T | C | 1 | a0001c0002t0005g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.203-10110T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14564223 | ||||||
chrX:14564224
|
C | T | 1 | a0001c0001t0017g0169 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.203-10109C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14564224 | ||||||
chrX:14564283
|
G | C | 1 | a0001c0001t0014g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.203-10050G>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14564283 | ||||||
chrX:14564324
|
G | GA | 10 | a0001c0001t0004g0069a0001c0001t0007g0079a0001c0001t0009g0064others(7): Show | 10 | HG01243.hp1 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.203-9998dupA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14564324 | |||||
chrX:14564324
|
GA | G | 1 | a0001c0001t0002g0061 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.203-9998delA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14564324 | |||||
chrX:14564357
|
C | CA | 1 | a0001c0001t0002g0061 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.203-9975dupA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14564357 | |||||
chrX:14564360
|
C | CA | 1 | a0001c0001t0002g0061 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.203-9969dupA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14564360 | |||||
chrX:14564437
|
TG | T | 1 | a0001c0001t0002g0061 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.203-9894delG | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14564437 | |||||
chrX:14564468
|
C | T | 1 | a0001c0003t0030g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.203-9865C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14564468 | ||||||
chrX:14564469
|
A | T | 1 | a0001c0003t0030g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.203-9864A>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14564469 | ||||||
chrX:14564471
|
G | T | 1 | a0001c0003t0030g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.203-9862G>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14564471 | ||||||
chrX:14564472
|
C | G | 1 | a0001c0003t0030g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.203-9861C>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14564472 | ||||||
chrX:14564474
|
G | T | 1 | a0001c0003t0030g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.203-9859G>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14564474 | ||||||
chrX:14564474
|
GA | G | 1 | a0001c0001t0002g0061 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.203-9856delA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14564474 | |||||
chrX:14564475
|
A | T | 1 | a0001c0003t0030g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.203-9858A>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14564475 | ||||||
chrX:14564476
|
A | AGC | 1 | a0001c0003t0030g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.203-9857_203-9856i others(4): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14564476 | ||||||
chrX:14564607
|
C | T | 1 | a0001c0001t0044g0193 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.203-9726C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14564607 | ||||||
chrX:14564700
|
G | GGA | 1 | a0001c0001t0002g0061 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.203-9626_203-9625d others(4): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14564700 | |||||
chrX:14564839
|
G | GT | 1 | a0001c0001t0002g0061 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.203-9492dupT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14564839 | |||||
chrX:14564919
|
AAAAGAAA others(63): Show |
A | 2 | a0001c0002t0024g0016a0001c0002t0024g0017 | 2 | HG03195.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.203-9343_203-9274d others(72): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14564919 | |||||
chrX:14564951
|
A | C | 29 | a0001c0001t0001g0036a0001c0001t0001g0042a0001c0001t0001g0050others(26): Show | 29 | HG00558.hp2 HG00639.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.203-9382A>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14564951 | ||||||
chrX:14565265
|
C | CT | 1 | a0001c0001t0002g0061 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.203-9068_203-9067i others(3): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14565265 | ||||||
chrX:14565281
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.203-9052G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14565281 | ||||||
chrX:14565363
|
TAAAAG | T | 1 | a0001c0001t0002g0149 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.203-8968_203-8964d others(7): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14565363 | |||||
chrX:14565489
|
G | T | 111 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(108): Show | 111 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.203-8844G>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14565489 | ||||||
chrX:14565520
|
CTGTT | C | 86 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(83): Show | 86 | HG00558.hp2 HG00639.hp1 HG00733.hp2 others(83): Show |
intron_variant | MODIFIER | c.203-8810_203-8807d others(6): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14565520 | |||||
chrX:14565583
|
T | TA | 1 | a0001c0001t0002g0061 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.203-8748dupA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14565583 | |||||
chrX:14565620
|
T | TA | 1 | a0001c0001t0002g0222 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.203-8711dupA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14565620 | |||||
chrX:14565735
|
G | A | 111 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(108): Show | 111 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.203-8598G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14565735 | ||||||
chrX:14566083
|
GA | G | 1 | a0001c0001t0002g0222 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.203-8243delA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14566083 | |||||
chrX:14566397
|
T | TC | 1 | a0001c0001t0002g0222 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.203-7935dupC | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14566397 | |||||
chrX:14566483
|
G | A | 111 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(108): Show | 111 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.203-7850G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14566483 | ||||||
chrX:14566568
|
TAA | T | 1 | a0001c0002t0043g0191 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.203-7764_203-7763d others(4): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14566568 | ||||||
chrX:14566637
|
AC | A | 1 | a0001c0001t0002g0061 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.203-7694delC | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14566637 | |||||
chrX:14566690
|
G | C | 1 | a0001c0001t0018g0080 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.203-7643G>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14566690 | ||||||
chrX:14566798
|
G | A | 113 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(110): Show | 113 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.203-7535G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14566798 | ||||||
chrX:14566827
|
GC | G | 1 | a0001c0001t0002g0061 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.203-7500delC | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14566827 | |||||
chrX:14566882
|
C | T | 1 | a0001c0001t0004g0204 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.203-7451C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14566882 | ||||||
chrX:14567011
|
C | T | 111 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(108): Show | 111 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.203-7322C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14567011 | ||||||
chrX:14567093
|
G | A | 1 | a0001c0001t0002g0165 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.203-7240G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14567093 | ||||||
chrX:14567294
|
TA | T | 1 | a0001c0001t0002g0222 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.203-7037delA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14567294 | |||||
chrX:14567399
|
CT | C | 1 | a0001c0001t0002g0061 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.203-6931delT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14567399 | |||||
chrX:14567423
|
A | G | 13 | a0001c0001t0048g0018a0001c0002t0024g0016a0001c0002t0024g0017others(10): Show | 13 | HG01074.hp1 HG01891.hp2 HG02293.hp2 others(10): Show |
intron_variant | MODIFIER | c.203-6910A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14567423 | ||||||
chrX:14567432
|
GA | G | 1 | a0001c0001t0038g0030 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.203-6898delA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14567432 | |||||
chrX:14567691
|
CT | C | 1 | a0001c0001t0002g0061 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.203-6639delT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14567691 | |||||
chrX:14567735
|
G | T | 1 | a0001c0001t0001g0072 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.203-6598G>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14567735 | ||||||
chrX:14567903
|
A | T | 1 | a0001c0001t0004g0203 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.203-6430A>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14567903 | ||||||
chrX:14568075
|
C | A | 1 | a0001c0001t0009g0064 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.203-6258C>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14568075 | ||||||
chrX:14568081
|
C | G | 6 | a0001c0001t0002g0194a0001c0001t0004g0197a0001c0001t0008g0195others(3): Show | 6 | HG02451.hp1 HG02615.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.203-6252C>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14568081 | ||||||
chrX:14568100
|
CT | C | 1 | a0001c0001t0002g0061 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.203-6227delT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14568100 | |||||
chrX:14568110
|
A | T | 1 | a0001c0001t0014g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.203-6223A>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14568110 | ||||||
chrX:14568113
|
A | G | 1 | a0001c0001t0014g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.203-6220A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14568113 | ||||||
chrX:14568197
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.203-6136G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14568197 | ||||||
chrX:14568348
|
C | T | 113 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(110): Show | 113 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.203-5985C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14568348 | ||||||
chrX:14568372
|
AG | A | 1 | a0001c0001t0002g0061 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.203-5959delG | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14568372 | |||||
chrX:14568383
|
G | GT | 1 | a0001c0001t0002g0061 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.203-5949dupT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14568383 | |||||
chrX:14568414
|
CG | C | 1 | a0001c0001t0002g0222 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.203-5916delG | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14568414 | |||||
chrX:14568463
|
T | C | 114 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(111): Show | 114 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.203-5870T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14568463 | ||||||
chrX:14568549
|
CG | C | 1 | a0001c0001t0002g0222 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.203-5781delG | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14568549 | |||||
chrX:14568550
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.203-5783G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14568550 | ||||||
chrX:14568574
|
TC | T | 1 | a0001c0001t0002g0222 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.203-5756delC | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14568574 | |||||
chrX:14568575
|
C | T | 1 | a0001c0001t0002g0124 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.203-5758C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14568575 | ||||||
chrX:14568585
|
CG | C | 1 | a0001c0001t0002g0222 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.203-5742delG | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14568585 | |||||
chrX:14568692
|
CA | C | 1 | a0001c0001t0002g0165 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.203-5624delA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14568692 | |||||
chrX:14568709
|
A | G | 112 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(109): Show | 112 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.203-5624A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14568709 | ||||||
chrX:14568710
|
G | A | 112 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(109): Show | 112 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.203-5623G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14568710 | ||||||
chrX:14568714
|
A | AAG | 2 | a0001c0001t0017g0078a0001c0001t0044g0193 | 2 | HG02451.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.203-5619_203-5618i others(4): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14568714 | ||||||
chrX:14568715
|
G | A | 2 | a0001c0001t0017g0078a0001c0001t0044g0193 | 2 | HG02451.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.203-5618G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14568715 | ||||||
chrX:14568715
|
G | GA | 112 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(109): Show | 112 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.203-5610dupA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14568715 | |||||
chrX:14568834
|
G | A | 1 | a0001c0001t0002g0124 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.203-5499G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14568834 | ||||||
chrX:14569084
|
G | GC | 1 | a0001c0001t0002g0222 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.203-5245dupC | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14569084 | |||||
chrX:14569245
|
AC | A | 1 | a0001c0001t0002g0061 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.203-5084delC | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14569245 | |||||
chrX:14569301
|
CT | C | 1 | a0001c0001t0002g0061 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.203-5028delT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14569301 | |||||
chrX:14569443
|
T | C | 7 | a0001c0001t0001g0187a0001c0001t0002g0034a0001c0001t0004g0027others(4): Show | 7 | HG02970.hp1 HG03041.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.203-4890T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14569443 | ||||||
chrX:14569491
|
G | A | 1 | a0001c0001t0001g0084 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.203-4842G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14569491 | ||||||
chrX:14569563
|
T | C | 16 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0003g0206others(13): Show | 16 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(13): Show |
intron_variant | MODIFIER | c.203-4770T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14569563 | ||||||
chrX:14569597
|
T | TA | 114 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(111): Show | 114 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.203-4731dupA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14569597 | |||||
chrX:14569603
|
TG | T | 1 | a0001c0001t0002g0061 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.203-4728delG | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14569603 | |||||
chrX:14569924
|
GA | G | 1 | a0001c0001t0002g0061 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.203-4406delA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14569924 | |||||
chrX:14570269
|
TAC | T | 1 | a0001c0002t0005g0056 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.203-4056_203-4055d others(4): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14570269 | |||||
chrX:14570333
|
C | A | 1 | a0001c0003t0026g0180 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.203-4000C>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14570333 | ||||||
chrX:14570357
|
C | T | 2 | a0001c0001t0002g0019a0001c0001t0002g0020 | 2 | NA18977.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.203-3976C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14570357 | ||||||
chrX:14570691
|
A | G | 3 | a0001c0001t0011g0188a0001c0001t0021g0190a0002c0006t0002g0189 | 3 | HG02922.hp1 HG03041.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.203-3642A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14570691 | ||||||
chrX:14570820
|
TC | T | 1 | a0001c0002t0043g0191 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.203-3512delC | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14570820 | ||||||
chrX:14570833
|
T | C | 1 | a0001c0002t0007g0209 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.203-3500T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14570833 | ||||||
chrX:14570855
|
A | G | 3 | a0001c0001t0012g0104a0001c0001t0012g0174a0001c0001t0041g0153 | 3 | HG01106.hp1 HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.203-3478A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14570855 | ||||||
chrX:14570991
|
C | T | 114 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(111): Show | 114 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.203-3342C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14570991 | ||||||
chrX:14571110
|
G | C | 2 | a0001c0001t0001g0125a0001c0001t0001g0133 | 2 | HG02135.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.203-3223G>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14571110 | ||||||
chrX:14571124
|
A | G | 1 | a0001c0001t0044g0193 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.203-3209A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14571124 | ||||||
chrX:14571144
|
A | G | 1 | a0001c0001t0006g0218 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.203-3189A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14571144 | ||||||
chrX:14571185
|
T | C | 1 | a0001c0001t0044g0193 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.203-3148T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14571185 | ||||||
chrX:14571240
|
A | G | 116 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(113): Show | 116 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.203-3093A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14571240 | ||||||
chrX:14571298
|
G | A | 1 | a0001c0002t0005g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.203-3035G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14571298 | ||||||
chrX:14571533
|
A | C | 1 | a0001c0001t0004g0220 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.203-2800A>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14571533 | ||||||
chrX:14571768
|
A | AG | 116 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(113): Show | 116 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.203-2565_203-2564i others(3): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14571768 | ||||||
chrX:14571770
|
C | A | 116 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(113): Show | 116 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.203-2563C>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14571770 | ||||||
chrX:14571779
|
G | A | 116 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(113): Show | 116 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.203-2554G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14571779 | ||||||
chrX:14571908
|
A | C | 1 | a0001c0001t0004g0220 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.203-2425A>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14571908 | ||||||
chrX:14572010
|
T | C | 116 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(113): Show | 116 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.203-2323T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14572010 | ||||||
chrX:14572344
|
A | G | 1 | a0001c0001t0001g0011 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.203-1989A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14572344 | ||||||
chrX:14572524
|
C | T | 119 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(116): Show | 119 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.203-1809C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14572524 | ||||||
chrX:14573250
|
C | G | 117 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(114): Show | 117 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.203-1083C>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14573250 | ||||||
chrX:14573254
|
C | A | 100 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(97): Show | 100 | HG00323.hp1 HG00558.hp2 HG00639.hp1 others(97): Show |
intron_variant | MODIFIER | c.203-1079C>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14573254 | ||||||
chrX:14573321
|
C | T | 1 | a0001c0001t0006g0218 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.203-1012C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14573321 | ||||||
chrX:14573407
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.203-926G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14573407 | ||||||
chrX:14573520
|
A | C | 1 | a0001c0001t0002g0090 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.203-813A>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14573520 | ||||||
chrX:14573777
|
G | A | 99 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(96): Show | 99 | HG00323.hp1 HG00558.hp2 HG00639.hp1 others(96): Show |
intron_variant | MODIFIER | c.203-556G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14573777 | ||||||
chrX:14574078
|
G | A | 16 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0005g0216others(13): Show | 16 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.203-255G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14574078 | ||||||
chrX:14574209
|
CT | C | 1 | a0001c0001t0014g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.203-115delT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 14574209 | |||||
chrX:14574214
|
T | A | 1 | a0001c0001t0014g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.203-119T>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14574214 | ||||||
chrX:14574323
|
C | T | 1 | a0001c0001t0012g0099 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.203-10C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 2/8 | chrX | 14574323 | ||||||
chrX:14574734
|
A | G | 1 | a0001c0002t0036g0063 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.270+334A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | chrX | 14574734 | ||||||
chrX:14574746
|
G | A | 3 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0090 | 3 | NA18612.hp1 NA19009.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.270+346G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | chrX | 14574746 | ||||||
chrX:14574811
|
G | T | 16 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0005g0216others(13): Show | 16 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.270+411G>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | chrX | 14574811 | ||||||
chrX:14574909
|
C | T | 115 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(112): Show | 115 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.270+509C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | chrX | 14574909 | ||||||
chrX:14575011
|
T | TAC | 1 | a0001c0002t0005g0015 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.270+625_270+626dup others(2): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 14575011 | |||||
chrX:14575023
|
C | T | 2 | a0001c0001t0003g0206a0001c0001t0020g0207 | 2 | HG00323.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.270+623C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | chrX | 14575023 | ||||||
chrX:14575039
|
A | C | 1 | a0001c0001t0008g0227 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.270+639A>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | chrX | 14575039 | ||||||
chrX:14575061
|
TA | T | 1 | a0001c0001t0008g0009 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.270+663delA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 14575061 | |||||
chrX:14575090
|
C | CA | 2 | a0001c0001t0001g0125a0001c0001t0038g0030 | 2 | HG02135.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.270+701dupA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 14575090 | |||||
chrX:14575090
|
CA | C | 2 | a0001c0001t0008g0007a0001c0001t0011g0188 | 2 | HG03041.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.270+701delA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 14575090 | |||||
chrX:14575164
|
C | G | 115 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(112): Show | 115 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.270+764C>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | chrX | 14575164 | ||||||
chrX:14575202
|
A | AT | 3 | a0001c0001t0003g0035a0001c0001t0004g0021a0001c0001t0006g0087 | 3 | HG01952.hp1 HG04184.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.270+818dupT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 14575202 | |||||
chrX:14575202
|
AT | A | 77 | a0001c0001t0001g0029a0001c0001t0001g0066a0001c0001t0001g0072others(74): Show | 77 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(74): Show |
intron_variant | MODIFIER | c.270+818delT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 14575202 | |||||
chrX:14575202
|
ATT | A | 5 | a0001c0001t0001g0187a0001c0001t0002g0034a0001c0001t0004g0027others(2): Show | 5 | HG02970.hp1 HG03041.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.270+817_270+818del others(2): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 14575202 | |||||
chrX:14575292
|
C | T | 98 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(95): Show | 98 | HG00323.hp1 HG00558.hp2 HG00639.hp1 others(95): Show |
intron_variant | MODIFIER | c.270+892C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | chrX | 14575292 | ||||||
chrX:14575458
|
C | A | 98 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(95): Show | 98 | HG00323.hp1 HG00558.hp2 HG00639.hp1 others(95): Show |
intron_variant | MODIFIER | c.270+1058C>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | chrX | 14575458 | ||||||
chrX:14575460
|
A | G | 1 | a0001c0001t0016g0148 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.270+1060A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | chrX | 14575460 | ||||||
chrX:14575557
|
G | A | 2 | a0001c0001t0003g0206a0001c0001t0020g0207 | 2 | HG00323.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.270+1157G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | chrX | 14575557 | ||||||
chrX:14575565
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.270+1165G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | chrX | 14575565 | ||||||
chrX:14575630
|
T | TA | 115 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(112): Show | 115 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.270+1239dupA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 14575630 | |||||
chrX:14575678
|
C | T | 1 | a0001c0001t0029g0012 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.270+1278C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | chrX | 14575678 | ||||||
chrX:14575731
|
C | A | 2 | a0001c0001t0003g0041a0001c0001t0033g0040 | 2 | HG03239.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.270+1331C>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | chrX | 14575731 | ||||||
chrX:14575898
|
T | C | 6 | a0001c0001t0001g0187a0001c0001t0002g0034a0001c0001t0004g0027others(3): Show | 6 | HG02970.hp1 HG03041.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.270+1498T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | chrX | 14575898 | ||||||
chrX:14576064
|
T | TA | 18 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0005g0216others(15): Show | 18 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.270+1680dupA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 14576064 | |||||
chrX:14576064
|
TA | T | 3 | a0001c0001t0001g0050a0001c0001t0008g0009a0001c0005t0006g0144 | 3 | NA18983.hp1 NA19043.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.270+1680delA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 14576064 | |||||
chrX:14576164
|
G | A | 57 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(54): Show | 57 | HG00323.hp1 HG00558.hp2 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.270+1764G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | chrX | 14576164 | ||||||
chrX:14576302
|
G | A | 16 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0005g0216others(13): Show | 16 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.270+1902G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | chrX | 14576302 | ||||||
chrX:14576376
|
C | T | 115 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(112): Show | 115 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.270+1976C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | chrX | 14576376 | ||||||
chrX:14576449
|
G | GA | 1 | a0001c0002t0007g0209 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.270+2050dupA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 14576449 | |||||
chrX:14576538
|
T | C | 1 | a0001c0001t0044g0193 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.270+2138T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | chrX | 14576538 | ||||||
chrX:14576734
|
G | A | 1 | a0001c0002t0014g0025 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.270+2334G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | chrX | 14576734 | ||||||
chrX:14577072
|
T | C | 7 | a0001c0001t0012g0099a0001c0001t0012g0104a0001c0001t0012g0154others(4): Show | 7 | HG01106.hp1 HG01891.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.270+2672T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | chrX | 14577072 | ||||||
chrX:14577115
|
A | G | 1 | a0001c0002t0005g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.270+2715A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | chrX | 14577115 | ||||||
chrX:14577200
|
G | A | 97 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(94): Show | 97 | HG00323.hp1 HG00558.hp2 HG00639.hp1 others(94): Show |
intron_variant | MODIFIER | c.270+2800G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | chrX | 14577200 | ||||||
chrX:14577381
|
G | A | 1 | a0001c0004t0007g0094 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.270+2981G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | chrX | 14577381 | ||||||
chrX:14577417
|
A | T | 18 | a0001c0001t0001g0129a0001c0001t0001g0211a0001c0001t0001g0212others(15): Show | 18 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.270+3017A>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | chrX | 14577417 | ||||||
chrX:14577516
|
C | G | 115 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(112): Show | 115 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.270+3116C>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | chrX | 14577516 | ||||||
chrX:14577542
|
G | C | 1 | a0001c0001t0013g0199 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.270+3142G>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | chrX | 14577542 | ||||||
chrX:14577570
|
A | C | 2 | a0001c0001t0009g0032a0001c0001t0018g0033 | 2 | HG02970.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.270+3170A>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | chrX | 14577570 | ||||||
chrX:14577613
|
TGACTTCC others(5): Show |
T | 1 | a0001c0001t0013g0185 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.270+3214_270+3225d others(14): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | chrX | 14577613 | ||||||
chrX:14577633
|
G | A | 1 | a0001c0002t0005g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.270+3233G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | chrX | 14577633 | ||||||
chrX:14577934
|
C | T | 1 | a0001c0002t0007g0209 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.271-3249C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | chrX | 14577934 | ||||||
chrX:14577979
|
G | A | 18 | a0001c0001t0001g0129a0001c0001t0001g0211a0001c0001t0001g0212others(15): Show | 18 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.271-3204G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | chrX | 14577979 | ||||||
chrX:14577980
|
C | T | 18 | a0001c0001t0001g0129a0001c0001t0001g0211a0001c0001t0001g0212others(15): Show | 18 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.271-3203C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | chrX | 14577980 | ||||||
chrX:14578037
|
T | A | 17 | a0001c0001t0001g0129a0001c0001t0001g0211a0001c0001t0001g0212others(14): Show | 17 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.271-3146T>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | chrX | 14578037 | ||||||
chrX:14578235
|
G | A | 97 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(94): Show | 97 | HG00323.hp1 HG00558.hp2 HG00639.hp1 others(94): Show |
intron_variant | MODIFIER | c.271-2948G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | chrX | 14578235 | ||||||
chrX:14578309
|
G | A | 1 | a0001c0002t0007g0210 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.271-2874G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | chrX | 14578309 | ||||||
chrX:14579008
|
C | T | 1 | a0001c0001t0002g0194 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.271-2175C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | chrX | 14579008 | ||||||
chrX:14579281
|
C | T | 1 | a0001c0001t0014g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.271-1902C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | chrX | 14579281 | ||||||
chrX:14579335
|
C | CT | 1 | a0001c0001t0006g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.271-1834dupT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 14579335 | |||||
chrX:14579335
|
CT | C | 2 | a0001c0001t0001g0146a0001c0002t0011g0086 | 2 | HG00558.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.271-1834delT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 14579335 | |||||
chrX:14579349
|
T | A | 97 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(94): Show | 97 | HG00323.hp1 HG00558.hp2 HG00639.hp1 others(94): Show |
intron_variant | MODIFIER | c.271-1834T>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | chrX | 14579349 | ||||||
chrX:14579349
|
T | TA | 18 | a0001c0001t0001g0129a0001c0001t0001g0211a0001c0001t0001g0212others(15): Show | 18 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.271-1832dupA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 14579349 | |||||
chrX:14579382
|
T | C | 1 | a0001c0002t0024g0016 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.271-1801T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | chrX | 14579382 | ||||||
chrX:14579608
|
G | C | 97 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(94): Show | 97 | HG00323.hp1 HG00558.hp2 HG00639.hp1 others(94): Show |
intron_variant | MODIFIER | c.271-1575G>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | chrX | 14579608 | ||||||
chrX:14579839
|
G | A | 1 | a0001c0001t0002g0165 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.271-1344G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | chrX | 14579839 | ||||||
chrX:14579934
|
G | A | 1 | a0001c0002t0005g0010 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.271-1249G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | chrX | 14579934 | ||||||
chrX:14580274
|
A | G | 1 | a0001c0001t0048g0018 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.271-909A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | chrX | 14580274 | ||||||
chrX:14580525
|
C | A | 1 | a0001c0001t0001g0084 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.271-658C>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | chrX | 14580525 | ||||||
chrX:14580611
|
T | G | 1 | a0001c0001t0004g0150 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.271-572T>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | chrX | 14580611 | ||||||
chrX:14580732
|
C | T | 1 | a0001c0001t0017g0078 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.271-451C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | chrX | 14580732 | ||||||
chrX:14580856
|
G | A | 118 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(115): Show | 118 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.271-327G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | chrX | 14580856 | ||||||
chrX:14580905
|
T | C | 118 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(115): Show | 118 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.271-278T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | chrX | 14580905 | ||||||
chrX:14580974
|
G | A | 1 | a0001c0001t0004g0069 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.271-209G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | chrX | 14580974 | ||||||
chrX:14581019
|
C | G | 118 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(115): Show | 118 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.271-164C>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | chrX | 14581019 | ||||||
chrX:14581078
|
C | T | 1 | a0001c0001t0016g0148 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.271-105C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | chrX | 14581078 | ||||||
chrX:14581108
|
A | G | 118 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(115): Show | 118 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.271-75A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 3/8 | chrX | 14581108 | ||||||
chrX:14581450
|
A | G | 118 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(115): Show | 118 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.494+44A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14581450 | ||||||
chrX:14581672
|
T | C | 118 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(115): Show | 118 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.494+266T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14581672 | ||||||
chrX:14581766
|
G | GCA | 32 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(29): Show | 33 | HG00558.hp2 HG00639.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.494+399_494+400dup others(2): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14581766 | |||||
chrX:14581766
|
G | GCACA | 17 | a0001c0001t0001g0029a0001c0001t0001g0133a0001c0001t0002g0098others(14): Show | 17 | HG00323.hp1 HG01081.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.494+397_494+400dup others(4): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14581766 | |||||
chrX:14581766
|
G | GCACACA | 6 | a0001c0001t0008g0195a0001c0001t0008g0231a0001c0001t0013g0199others(3): Show | 6 | HG02622.hp2 HG02630.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.494+395_494+400dup others(6): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14581766 | |||||
chrX:14581766
|
G | GCACACAC others(1): Show |
10 | a0001c0001t0001g0072a0001c0001t0004g0197a0001c0001t0004g0220others(7): Show | 10 | HG01070.hp1 HG02132.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.494+393_494+400dup others(8): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14581766 | |||||
chrX:14581766
|
G | GCACACAC others(3): Show |
1 | a0001c0001t0002g0194 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.494+391_494+400dup others(10): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14581766 | |||||
chrX:14581766
|
G | GCACACAC others(5): Show |
1 | a0001c0001t0001g0066 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.494+389_494+400dup others(12): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14581766 | |||||
chrX:14581766
|
GCA | G | 20 | a0001c0001t0001g0121a0001c0001t0001g0152a0001c0001t0002g0088others(17): Show | 20 | HG00733.hp1 HG01081.hp1 HG01943.hp1 others(17): Show |
intron_variant | MODIFIER | c.494+399_494+400del others(2): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14581766 | |||||
chrX:14581766
|
GCACA | G | 41 | a0001c0001t0001g0129a0001c0001t0001g0211a0001c0001t0001g0212others(38): Show | 41 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.494+397_494+400del others(4): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14581766 | |||||
chrX:14581766
|
GCACACA | G | 1 | a0001c0001t0001g0083 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.494+395_494+400del others(6): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14581766 | |||||
chrX:14581766
|
GCACACAC others(1): Show |
G | 1 | a0001c0001t0016g0091 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.494+393_494+400del others(8): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14581766 | |||||
chrX:14581766
|
GCACACAC others(7): Show |
G | 1 | a0001c0001t0010g0071 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.494+387_494+400del others(14): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14581766 | |||||
chrX:14581766
|
GCACACAC others(9): Show |
G | 9 | a0001c0001t0004g0069a0001c0001t0007g0079a0001c0001t0009g0064others(6): Show | 9 | HG01243.hp1 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.494+385_494+400del others(16): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14581766 | |||||
chrX:14581805
|
CA | C | 1 | a0001c0001t0018g0033 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.494+402delA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14581805 | |||||
chrX:14581805
|
CAA | C | 1 | a0001c0001t0013g0185 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.494+401_494+402del others(2): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14581805 | |||||
chrX:14581806
|
A | AC | 1 | a0001c0001t0001g0036 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.494+400_494+401ins others(1): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14581806 | ||||||
chrX:14581817
|
C | T | 118 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(115): Show | 118 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.494+411C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14581817 | ||||||
chrX:14582045
|
A | T | 118 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(115): Show | 118 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.494+639A>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14582045 | ||||||
chrX:14582046
|
T | A | 118 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(115): Show | 118 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.494+640T>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14582046 | ||||||
chrX:14582057
|
C | CT | 119 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(116): Show | 119 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.494+662dupT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14582057 | |||||
chrX:14582057
|
CT | C | 1 | a0001c0001t0041g0153 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.494+662delT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14582057 | |||||
chrX:14582073
|
A | AT | 118 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(115): Show | 118 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.494+674dupT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14582073 | |||||
chrX:14582116
|
G | C | 1 | a0001c0001t0013g0073 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.494+710G>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14582116 | ||||||
chrX:14582184
|
T | C | 118 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(115): Show | 118 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.494+778T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14582184 | ||||||
chrX:14582189
|
G | C | 2 | a0001c0001t0002g0096a0001c0005t0006g0095 | 2 | HG01361.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.494+783G>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14582189 | ||||||
chrX:14582212
|
T | TC | 63 | a0001c0001t0001g0072a0001c0001t0001g0129a0001c0001t0001g0211others(60): Show | 63 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.494+811dupC | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14582212 | |||||
chrX:14582213
|
C | CT | 1 | a0001c0002t0043g0191 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.494+807_494+808ins others(1): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14582213 | ||||||
chrX:14582217
|
C | CCT | 35 | a0001c0001t0001g0029a0001c0001t0001g0066a0001c0001t0001g0187others(32): Show | 35 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(32): Show |
intron_variant | MODIFIER | c.494+811_494+812ins others(2): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14582217 | ||||||
chrX:14582218
|
T | C | 54 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(51): Show | 54 | HG00323.hp1 HG00639.hp1 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.494+812T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14582218 | ||||||
chrX:14582219
|
C | CT | 1 | a0001c0001t0003g0055 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.494+813_494+814ins others(1): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14582219 | ||||||
chrX:14582219
|
C | T | 18 | a0001c0001t0001g0036a0001c0001t0001g0042a0001c0001t0001g0050others(15): Show | 18 | HG00323.hp1 HG00639.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.494+813C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14582219 | ||||||
chrX:14582223
|
A | C | 118 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(115): Show | 118 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.494+817A>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14582223 | ||||||
chrX:14582224
|
C | A | 18 | a0001c0001t0001g0129a0001c0001t0001g0211a0001c0001t0001g0212others(15): Show | 18 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.494+818C>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14582224 | ||||||
chrX:14582225
|
C | A | 1 | a0001c0001t0017g0078 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.494+819C>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14582225 | ||||||
chrX:14582388
|
A | C | 118 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(115): Show | 118 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.494+982A>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14582388 | ||||||
chrX:14582567
|
T | C | 118 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(115): Show | 118 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.494+1161T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14582567 | ||||||
chrX:14582632
|
G | C | 118 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(115): Show | 118 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.494+1226G>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14582632 | ||||||
chrX:14582666
|
G | A | 118 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(115): Show | 118 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.494+1260G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14582666 | ||||||
chrX:14582859
|
A | G | 118 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(115): Show | 118 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.494+1453A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14582859 | ||||||
chrX:14582878
|
C | T | 118 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(115): Show | 118 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.494+1472C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14582878 | ||||||
chrX:14583523
|
G | C | 1 | a0001c0001t0001g0129 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.494+2117G>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14583523 | ||||||
chrX:14583568
|
C | G | 117 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(114): Show | 117 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.494+2162C>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14583568 | ||||||
chrX:14583670
|
C | T | 1 | a0001c0001t0003g0055 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.494+2264C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14583670 | ||||||
chrX:14583736
|
G | C | 117 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(114): Show | 117 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.494+2330G>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14583736 | ||||||
chrX:14583936
|
C | T | 15 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0005g0216others(12): Show | 15 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.494+2530C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14583936 | ||||||
chrX:14584208
|
G | A | 3 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0102 | 3 | NA18977.hp1 NA19005.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.494+2802G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14584208 | ||||||
chrX:14584213
|
G | A | 1 | a0001c0002t0007g0114 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.494+2807G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14584213 | ||||||
chrX:14584263
|
A | G | 1 | a0001c0001t0002g0161 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.494+2857A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14584263 | ||||||
chrX:14584451
|
C | T | 117 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(114): Show | 117 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.494+3045C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14584451 | ||||||
chrX:14584488
|
G | A | 117 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(114): Show | 117 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.494+3082G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14584488 | ||||||
chrX:14585008
|
G | A | 117 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(114): Show | 117 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.494+3602G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14585008 | ||||||
chrX:14585054
|
G | A | 117 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(114): Show | 117 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.494+3648G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14585054 | ||||||
chrX:14585198
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.494+3792G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14585198 | ||||||
chrX:14585610
|
A | G | 1 | a0001c0001t0008g0140 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.494+4204A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14585610 | ||||||
chrX:14585889
|
C | G | 118 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(115): Show | 118 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.494+4483C>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14585889 | ||||||
chrX:14586031
|
A | C | 1 | a0001c0001t0004g0156 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.494+4625A>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14586031 | ||||||
chrX:14586037
|
G | A | 132 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(129): Show | 132 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.494+4631G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14586037 | ||||||
chrX:14586080
|
G | GA | 1 | a0001c0001t0006g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.494+4677dupA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14586080 | |||||
chrX:14586164
|
TA | T | 1 | a0001c0001t0001g0121 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.494+4767delA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14586164 | |||||
chrX:14587326
|
T | G | 118 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(115): Show | 118 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.494+5920T>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14587326 | ||||||
chrX:14587460
|
G | A | 1 | a0001c0001t0008g0007 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.494+6054G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14587460 | ||||||
chrX:14587468
|
G | T | 1 | a0001c0001t0001g0106 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.494+6062G>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14587468 | ||||||
chrX:14587518
|
T | C | 2 | a0001c0001t0001g0083a0001c0001t0004g0162 | 2 | HG02080.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.494+6112T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14587518 | ||||||
chrX:14587543
|
T | C | 19 | a0001c0001t0001g0129a0001c0001t0001g0211a0001c0001t0001g0212others(16): Show | 19 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.494+6137T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14587543 | ||||||
chrX:14587639
|
G | GT | 1 | a0001c0001t0006g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.494+6239dupT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14587639 | |||||
chrX:14587905
|
A | AT | 4 | a0001c0001t0003g0035a0001c0001t0006g0004a0001c0001t0029g0012others(1): Show | 4 | HG02886.hp2 HG04184.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.494+6514dupT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14587905 | |||||
chrX:14587905
|
AT | A | 6 | a0001c0001t0003g0229a0001c0001t0008g0007a0001c0001t0011g0188others(3): Show | 6 | HG02622.hp2 HG02922.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.494+6514delT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14587905 | |||||
chrX:14587925
|
T | C | 1 | a0001c0001t0001g0083 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.494+6519T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14587925 | ||||||
chrX:14588283
|
G | T | 99 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(96): Show | 99 | HG00323.hp1 HG00558.hp2 HG00639.hp1 others(96): Show |
intron_variant | MODIFIER | c.494+6877G>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14588283 | ||||||
chrX:14588343
|
T | G | 18 | a0001c0001t0001g0129a0001c0001t0001g0211a0001c0001t0001g0212others(15): Show | 18 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.494+6937T>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14588343 | ||||||
chrX:14588509
|
T | C | 1 | a0001c0001t0017g0169 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.494+7103T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14588509 | ||||||
chrX:14588567
|
G | GT | 1 | a0001c0002t0003g0145 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.494+7167dupT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14588567 | |||||
chrX:14588597
|
GT | G | 1 | a0001c0001t0020g0048 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.494+7200delT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14588597 | |||||
chrX:14588723
|
T | A | 1 | a0001c0001t0042g0132 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.494+7317T>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14588723 | ||||||
chrX:14589079
|
G | A | 7 | a0001c0002t0005g0015a0001c0002t0007g0022a0001c0002t0007g0023others(4): Show | 7 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.494+7673G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14589079 | ||||||
chrX:14589441
|
T | C | 18 | a0001c0001t0001g0129a0001c0001t0001g0211a0001c0001t0001g0212others(15): Show | 18 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.494+8035T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14589441 | ||||||
chrX:14589495
|
T | TA | 1 | a0001c0001t0001g0152 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.494+8106dupA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14589495 | |||||
chrX:14589495
|
TA | T | 105 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(102): Show | 105 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.494+8106delA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14589495 | |||||
chrX:14589495
|
TAA | T | 1 | a0001c0001t0004g0220 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.494+8105_494+8106d others(4): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14589495 | |||||
chrX:14589634
|
G | A | 18 | a0001c0001t0001g0129a0001c0001t0001g0211a0001c0001t0001g0212others(15): Show | 18 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.494+8228G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14589634 | ||||||
chrX:14589670
|
C | CAA | 18 | a0001c0001t0001g0129a0001c0001t0001g0211a0001c0001t0001g0212others(15): Show | 18 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.494+8270_494+8271d others(4): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14589670 | |||||
chrX:14589678
|
T | A | 116 | a0001c0001t0001g0029a0001c0001t0001g0050a0001c0001t0001g0066others(113): Show | 116 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.494+8272T>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14589678 | ||||||
chrX:14589680
|
T | A | 3 | a0001c0002t0005g0002a0001c0002t0011g0217a0001c0002t0043g0191 | 3 | HG00140.hp1 HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.494+8274T>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14589680 | ||||||
chrX:14589706
|
A | ATATACAC others(11): Show |
115 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(112): Show | 115 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.494+8308_494+8309i others(20): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14589706 | |||||
chrX:14589711
|
C | CACATATA others(9): Show |
2 | a0001c0001t0009g0032a0001c0001t0018g0033 | 2 | HG02970.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.494+8308_494+8309i others(18): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14589711 | |||||
chrX:14589717
|
T | C | 2 | a0001c0001t0009g0032a0001c0001t0018g0033 | 2 | HG02970.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.494+8311T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14589717 | ||||||
chrX:14590070
|
C | T | 100 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(97): Show | 100 | HG00323.hp1 HG00558.hp2 HG00639.hp1 others(97): Show |
intron_variant | MODIFIER | c.494+8664C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14590070 | ||||||
chrX:14590136
|
A | G | 2 | a0001c0001t0001g0105a0001c0001t0001g0137 | 2 | HG00621.hp1 HG00673.hp1 |
intron_variant | MODIFIER | c.494+8730A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14590136 | ||||||
chrX:14590275
|
T | C | 15 | a0001c0001t0048g0018a0001c0002t0010g0031a0001c0002t0024g0016others(12): Show | 15 | HG01074.hp1 HG01891.hp2 HG02293.hp2 others(12): Show |
intron_variant | MODIFIER | c.494+8869T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14590275 | ||||||
chrX:14590443
|
A | G | 100 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(97): Show | 100 | HG00323.hp1 HG00558.hp2 HG00639.hp1 others(97): Show |
intron_variant | MODIFIER | c.494+9037A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14590443 | ||||||
chrX:14590678
|
C | A | 1 | a0001c0002t0023g0065 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.494+9272C>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14590678 | ||||||
chrX:14590816
|
G | A | 1 | a0001c0001t0005g0108 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.494+9410G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14590816 | ||||||
chrX:14591042
|
C | T | 2 | a0001c0001t0001g0129a0001c0002t0003g0145 | 2 | HG01167.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.494+9636C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14591042 | ||||||
chrX:14591071
|
T | C | 1 | a0001c0002t0043g0191 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.494+9665T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14591071 | ||||||
chrX:14591438
|
G | A | 118 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(115): Show | 118 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.494+10032G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14591438 | ||||||
chrX:14591476
|
A | C | 18 | a0001c0001t0001g0129a0001c0001t0001g0211a0001c0001t0001g0212others(15): Show | 18 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.494+10070A>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14591476 | ||||||
chrX:14591596
|
T | C | 3 | a0001c0003t0025g0175a0001c0003t0025g0181a0001c0003t0030g0198 | 3 | HG02572.hp1 HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.494+10190T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14591596 | ||||||
chrX:14591819
|
G | A | 118 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(115): Show | 118 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.494+10413G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14591819 | ||||||
chrX:14591881
|
A | G | 100 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(97): Show | 100 | HG00323.hp1 HG00558.hp2 HG00639.hp1 others(97): Show |
intron_variant | MODIFIER | c.494+10475A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14591881 | ||||||
chrX:14591911
|
A | G | 17 | a0001c0001t0001g0129a0001c0001t0001g0211a0001c0001t0001g0212others(14): Show | 17 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.494+10505A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14591911 | ||||||
chrX:14592135
|
C | T | 4 | a0001c0001t0011g0188a0001c0001t0013g0199a0001c0001t0021g0190others(1): Show | 4 | HG02622.hp2 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.494+10729C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14592135 | ||||||
chrX:14592168
|
C | G | 1 | a0001c0001t0014g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.494+10762C>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14592168 | ||||||
chrX:14592217
|
C | A | 1 | a0001c0001t0022g0058 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.494+10811C>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14592217 | ||||||
chrX:14592541
|
G | A | 100 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(97): Show | 100 | HG00323.hp1 HG00558.hp2 HG00639.hp1 others(97): Show |
intron_variant | MODIFIER | c.494+11135G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14592541 | ||||||
chrX:14592592
|
A | G | 2 | a0001c0001t0009g0032a0001c0001t0018g0033 | 2 | HG02970.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.494+11186A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14592592 | ||||||
chrX:14593207
|
G | A | 1 | a0001c0002t0045g0177 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.495-11108G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14593207 | ||||||
chrX:14593247
|
C | G | 16 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0005g0216others(13): Show | 16 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.495-11068C>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14593247 | ||||||
chrX:14593267
|
TGTG | T | 15 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0005g0216others(12): Show | 15 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.495-11044_495-1104 others(7): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14593267 | |||||
chrX:14593354
|
G | C | 1 | a0001c0001t0004g0027 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.495-10961G>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14593354 | ||||||
chrX:14593386
|
G | A | 1 | a0001c0001t0013g0073 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.495-10929G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14593386 | ||||||
chrX:14593390
|
T | C | 16 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0005g0216others(13): Show | 16 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.495-10925T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14593390 | ||||||
chrX:14593511
|
G | C | 16 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0005g0216others(13): Show | 16 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.495-10804G>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14593511 | ||||||
chrX:14593712
|
TA | T | 102 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(99): Show | 102 | HG00323.hp1 HG00558.hp2 HG00639.hp1 others(99): Show |
intron_variant | MODIFIER | c.495-10601delA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14593712 | |||||
chrX:14593759
|
G | A | 1 | a0001c0001t0004g0156 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.495-10556G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14593759 | ||||||
chrX:14593920
|
A | T | 1 | a0001c0002t0043g0191 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.495-10395A>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14593920 | ||||||
chrX:14594077
|
C | G | 1 | a0001c0002t0010g0031 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.495-10238C>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14594077 | ||||||
chrX:14594254
|
TC | T | 1 | a0001c0001t0001g0212 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.495-10056delC | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14594254 | |||||
chrX:14594258
|
C | CT | 1 | a0001c0002t0043g0191 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.495-10057_495-1005 others(5): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14594258 | ||||||
chrX:14594259
|
C | T | 106 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(103): Show | 106 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.495-10056C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14594259 | ||||||
chrX:14594297
|
A | G | 114 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(111): Show | 114 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.495-10018A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14594297 | ||||||
chrX:14594443
|
T | G | 96 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(93): Show | 96 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.495-9872T>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14594443 | ||||||
chrX:14594465
|
A | AAATGACT others(3): Show |
1 | a0001c0001t0008g0009 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.495-9847_495-9838d others(12): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14594465 | |||||
chrX:14594523
|
CT | C | 1 | a0001c0001t0008g0009 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.495-9789delT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14594523 | |||||
chrX:14594593
|
AT | A | 1 | a0001c0001t0008g0009 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.495-9718delT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14594593 | |||||
chrX:14594940
|
G | GA | 6 | a0001c0001t0001g0152a0001c0001t0002g0098a0001c0001t0002g0120others(3): Show | 6 | HG01928.hp1 HG02080.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.495-9355dupA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14594940 | |||||
chrX:14594940
|
GA | G | 29 | a0001c0001t0001g0066a0001c0001t0001g0107a0001c0001t0001g0121others(26): Show | 29 | HG01106.hp1 HG01192.hp1 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.495-9355delA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14594940 | |||||
chrX:14594940
|
GAA | G | 12 | a0001c0001t0004g0027a0001c0001t0004g0197a0001c0001t0009g0032others(9): Show | 12 | HG01243.hp1 HG02622.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.495-9356_495-9355d others(4): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14594940 | |||||
chrX:14594940
|
GAAA | G | 19 | a0001c0001t0002g0194a0001c0001t0004g0220a0001c0001t0049g0075others(16): Show | 19 | HG01070.hp1 HG01074.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.495-9357_495-9355d others(5): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14594940 | |||||
chrX:14594940
|
GAAAA | G | 50 | a0001c0001t0001g0036a0001c0001t0001g0042a0001c0001t0001g0109others(47): Show | 50 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.495-9358_495-9355d others(6): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14594940 | |||||
chrX:14594940
|
GAAAAA | G | 16 | a0001c0001t0002g0034a0001c0001t0003g0043a0001c0001t0008g0231others(13): Show | 16 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.495-9359_495-9355d others(7): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14594940 | |||||
chrX:14595738
|
C | T | 13 | a0001c0002t0007g0022a0001c0002t0007g0023a0001c0002t0007g0192others(10): Show | 13 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.495-8577C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14595738 | ||||||
chrX:14595767
|
G | C | 1 | a0001c0005t0006g0144 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.495-8548G>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14595767 | ||||||
chrX:14596009
|
C | A | 3 | a0001c0001t0004g0027a0001c0001t0004g0069a0001c0001t0004g0197 | 3 | HG03041.hp1 HG06807.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.495-8306C>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14596009 | ||||||
chrX:14596059
|
A | G | 6 | a0001c0001t0001g0029a0001c0001t0001g0066a0001c0001t0001g0072others(3): Show | 6 | HG02055.hp1 HG02132.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.495-8256A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14596059 | ||||||
chrX:14596132
|
A | G | 35 | a0001c0001t0001g0036a0001c0001t0001g0042a0001c0001t0001g0109others(32): Show | 35 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.495-8183A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14596132 | ||||||
chrX:14596225
|
G | A | 1 | a0001c0001t0004g0220 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.495-8090G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14596225 | ||||||
chrX:14596451
|
G | T | 28 | a0001c0001t0002g0120a0001c0001t0002g0194a0001c0001t0004g0021others(25): Show | 28 | HG01070.hp1 HG01074.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.495-7864G>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14596451 | ||||||
chrX:14596464
|
AC | A | 1 | a0001c0001t0008g0009 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.495-7846delC | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14596464 | |||||
chrX:14596536
|
T | C | 4 | a0001c0002t0023g0065a0001c0002t0023g0186a0001c0002t0039g0184others(1): Show | 4 | HG01109.hp1 HG02109.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.495-7779T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14596536 | ||||||
chrX:14596540
|
G | A | 3 | a0001c0001t0001g0029a0001c0001t0001g0072a0001c0001t0008g0227 | 3 | HG02132.hp1 HG02683.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.495-7775G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14596540 | ||||||
chrX:14596654
|
AAAT | A | 34 | a0001c0002t0005g0002a0001c0002t0005g0010a0001c0002t0005g0014others(31): Show | 34 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.495-7650_495-7648d others(5): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14596654 | |||||
chrX:14596803
|
TC | T | 1 | a0001c0001t0008g0009 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.495-7510delC | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14596803 | |||||
chrX:14596884
|
C | T | 1 | a0001c0001t0003g0229 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.495-7431C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14596884 | ||||||
chrX:14596886
|
A | G | 2 | a0001c0001t0001g0147a0001c0001t0002g0143 | 2 | HG01496.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.495-7429A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14596886 | ||||||
chrX:14596899
|
C | A | 2 | a0001c0002t0014g0025a0001c0002t0014g0026 | 2 | HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.495-7416C>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14596899 | ||||||
chrX:14597047
|
GC | G | 1 | a0001c0001t0008g0009 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.495-7263delC | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14597047 | |||||
chrX:14597072
|
T | A | 21 | a0001c0002t0005g0002a0001c0002t0005g0010a0001c0002t0005g0014others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.495-7243T>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14597072 | ||||||
chrX:14597132
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.495-7183G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14597132 | ||||||
chrX:14597213
|
GCCTT | G | 1 | a0001c0002t0003g0145 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.495-7097_495-7094d others(6): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14597213 | |||||
chrX:14597345
|
T | C | 1 | a0001c0001t0006g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.495-6970T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14597345 | ||||||
chrX:14597469
|
TG | T | 1 | a0001c0001t0008g0009 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.495-6841delG | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14597469 | |||||
chrX:14597562
|
G | C | 6 | a0001c0001t0001g0029a0001c0001t0001g0066a0001c0001t0001g0072others(3): Show | 6 | HG02055.hp1 HG02132.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.495-6753G>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14597562 | ||||||
chrX:14597591
|
G | A | 41 | a0001c0001t0001g0029a0001c0001t0001g0066a0001c0001t0001g0072others(38): Show | 41 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.495-6724G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14597591 | ||||||
chrX:14597829
|
TG | T | 1 | a0001c0001t0008g0009 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.495-6483delG | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14597829 | |||||
chrX:14597874
|
C | A | 40 | a0001c0001t0001g0029a0001c0001t0001g0066a0001c0001t0001g0072others(37): Show | 40 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.495-6441C>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14597874 | ||||||
chrX:14598235
|
T | TG | 1 | a0001c0001t0008g0009 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.495-6080_495-6079i others(3): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14598235 | ||||||
chrX:14598579
|
T | C | 3 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0047 | 3 | HG03017.hp1 HG04184.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.495-5736T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14598579 | ||||||
chrX:14598641
|
T | G | 1 | a0002c0006t0002g0189 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.495-5674T>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14598641 | ||||||
chrX:14598701
|
TC | T | 1 | a0001c0001t0008g0009 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.495-5611delC | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14598701 | |||||
chrX:14598772
|
A | G | 46 | a0001c0001t0048g0018a0001c0002t0003g0145a0001c0002t0005g0002others(43): Show | 46 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.495-5543A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14598772 | ||||||
chrX:14599305
|
A | G | 1 | a0001c0001t0013g0185 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.495-5010A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14599305 | ||||||
chrX:14599409
|
C | T | 6 | a0001c0001t0001g0029a0001c0001t0001g0066a0001c0001t0001g0072others(3): Show | 6 | HG02055.hp1 HG02132.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.495-4906C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14599409 | ||||||
chrX:14599466
|
A | T | 1 | a0001c0001t0001g0137 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.495-4849A>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14599466 | ||||||
chrX:14599634
|
CT | C | 1 | a0001c0001t0008g0009 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.495-4677delT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14599634 | |||||
chrX:14599675
|
G | A | 22 | a0001c0002t0003g0145a0001c0002t0005g0002a0001c0002t0005g0010others(19): Show | 22 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.495-4640G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14599675 | ||||||
chrX:14599794
|
T | G | 1 | a0001c0001t0013g0185 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.495-4521T>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14599794 | ||||||
chrX:14600096
|
T | C | 17 | a0001c0001t0002g0120a0001c0001t0002g0194a0001c0001t0004g0021others(14): Show | 17 | HG01070.hp1 HG01928.hp1 HG01952.hp1 others(14): Show |
intron_variant | MODIFIER | c.495-4219T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14600096 | ||||||
chrX:14600122
|
C | T | 1 | a0001c0001t0016g0116 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.495-4193C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14600122 | ||||||
chrX:14600332
|
A | G | 6 | a0001c0001t0001g0029a0001c0001t0001g0066a0001c0001t0001g0072others(3): Show | 6 | HG02055.hp1 HG02132.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.495-3983A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14600332 | ||||||
chrX:14600422
|
C | G | 1 | a0001c0002t0043g0191 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.495-3893C>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14600422 | ||||||
chrX:14600507
|
T | A | 5 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0090others(2): Show | 5 | NA18612.hp1 NA19009.hp1 NA19060.hp1 others(2): Show |
intron_variant | MODIFIER | c.495-3808T>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14600507 | ||||||
chrX:14600672
|
A | AT | 1 | a0001c0001t0001g0152 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.495-3636dupT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14600672 | |||||
chrX:14600727
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.495-3588C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14600727 | ||||||
chrX:14600746
|
A | G | 36 | a0001c0001t0048g0018a0001c0002t0003g0145a0001c0002t0005g0002others(33): Show | 36 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.495-3569A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14600746 | ||||||
chrX:14601001
|
G | GT | 4 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0004g0150others(1): Show | 4 | HG00733.hp1 HG02738.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.495-3303dupT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14601001 | |||||
chrX:14601001
|
GT | G | 3 | a0001c0001t0001g0138a0001c0001t0014g0228a0001c0001t0044g0193 | 3 | HG02630.hp1 HG02965.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.495-3303delT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14601001 | |||||
chrX:14601001
|
GTTT | G | 2 | a0001c0001t0003g0047a0001c0002t0003g0145 | 2 | HG01358.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.495-3305_495-3303d others(5): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14601001 | |||||
chrX:14601009
|
T | G | 14 | a0001c0001t0048g0018a0001c0002t0007g0022a0001c0002t0007g0023others(11): Show | 14 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.495-3306T>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14601009 | ||||||
chrX:14601009
|
T | TG | 102 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(99): Show | 102 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.495-3306_495-3305i others(3): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14601009 | ||||||
chrX:14601113
|
C | A | 22 | a0001c0002t0003g0145a0001c0002t0005g0002a0001c0002t0005g0010others(19): Show | 22 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.495-3202C>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14601113 | ||||||
chrX:14601134
|
C | T | 36 | a0001c0001t0048g0018a0001c0002t0003g0145a0001c0002t0005g0002others(33): Show | 36 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.495-3181C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14601134 | ||||||
chrX:14601186
|
A | T | 1 | a0001c0004t0032g0005 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.495-3129A>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14601186 | ||||||
chrX:14601761
|
T | C | 1 | a0001c0001t0038g0030 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.495-2554T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14601761 | ||||||
chrX:14601816
|
G | A | 1 | a0001c0001t0031g0060 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.495-2499G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14601816 | ||||||
chrX:14601931
|
T | C | 3 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0047 | 3 | HG03017.hp1 HG04184.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.495-2384T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14601931 | ||||||
chrX:14602070
|
A | C | 1 | a0001c0001t0002g0115 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.495-2245A>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14602070 | ||||||
chrX:14602152
|
G | GA | 1 | a0001c0001t0002g0061 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.495-2158dupA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14602152 | |||||
chrX:14602274
|
C | CA | 1 | a0001c0002t0011g0086 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.495-2035dupA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14602274 | |||||
chrX:14602322
|
G | A | 1 | a0001c0001t0008g0141 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.495-1993G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14602322 | ||||||
chrX:14602352
|
G | GTTGT | 11 | a0001c0001t0002g0143a0001c0001t0005g0006a0001c0001t0005g0108others(8): Show | 11 | HG00642.hp1 HG00733.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.495-1928_495-1925d others(6): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14602352 | |||||
chrX:14602352
|
G | GTTGTTTG others(1): Show |
4 | a0001c0001t0001g0113a0001c0001t0001g0129a0001c0005t0006g0095others(1): Show | 4 | HG00323.hp2 HG01167.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.495-1932_495-1925d others(10): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14602352 | |||||
chrX:14602352
|
GTTGT | G | 87 | a0001c0001t0001g0036a0001c0001t0001g0042a0001c0001t0001g0066others(84): Show | 87 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.495-1928_495-1925d others(6): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14602352 | |||||
chrX:14602352
|
GTTGTTTG others(1): Show |
G | 1 | a0001c0001t0003g0049 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.495-1932_495-1925d others(10): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14602352 | |||||
chrX:14602352
|
GTTGTTTG others(5): Show |
G | 2 | a0001c0001t0001g0187a0001c0001t0014g0228 | 2 | HG02630.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.495-1936_495-1925d others(14): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14602352 | |||||
chrX:14602448
|
G | C | 4 | a0001c0001t0008g0195a0001c0001t0008g0196a0001c0001t0008g0230others(1): Show | 4 | HG02451.hp1 HG02886.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.495-1867G>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14602448 | ||||||
chrX:14602534
|
C | A | 3 | a0001c0001t0004g0202a0001c0001t0004g0203a0001c0001t0004g0204 | 3 | NA18957.hp1 NA18967.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.495-1781C>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14602534 | ||||||
chrX:14602610
|
C | G | 1 | a0001c0001t0001g0121 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.495-1705C>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14602610 | ||||||
chrX:14603081
|
A | AT | 54 | a0001c0001t0001g0036a0001c0001t0001g0042a0001c0001t0001g0107others(51): Show | 54 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.495-1220dupT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14603081 | |||||
chrX:14603081
|
A | ATT | 1 | a0001c0001t0031g0060 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.495-1221_495-1220d others(4): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14603081 | |||||
chrX:14603081
|
A | ATTT | 1 | a0001c0002t0005g0056 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.495-1222_495-1220d others(5): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14603081 | |||||
chrX:14603081
|
AT | A | 4 | a0001c0001t0001g0187a0001c0001t0004g0164a0001c0001t0006g0134others(1): Show | 4 | HG01516.hp1 HG03710.hp1 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.495-1220delT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14603081 | |||||
chrX:14603096
|
G | T | 3 | a0001c0002t0010g0031a0001c0002t0024g0016a0001c0002t0024g0017 | 3 | HG03195.hp1 NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.495-1219G>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14603096 | ||||||
chrX:14603422
|
A | G | 2 | a0001c0001t0004g0119a0001c0001t0004g0126 | 2 | NA18966.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.495-893A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14603422 | ||||||
chrX:14604177
|
CT | C | 13 | a0001c0002t0007g0022a0001c0002t0007g0023a0001c0002t0007g0192others(10): Show | 13 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.495-137delT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | chrX | 14604177 | ||||||
chrX:14604294
|
A | AT | 1 | a0001c0001t0001g0152 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.495-11dupT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 14604294 | |||||
chrX:14604543
|
A | AGT | 45 | a0001c0001t0001g0011a0001c0001t0001g0097a0001c0001t0001g0121others(42): Show | 45 | HG00558.hp1 HG00639.hp2 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.577+195_577+196dup others(2): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 14604543 | |||||
chrX:14604543
|
A | AGTGT | 11 | a0001c0001t0001g0170a0001c0001t0001g0173a0001c0001t0002g0020others(8): Show | 11 | HG01255.hp1 HG01981.hp1 HG02683.hp2 others(8): Show |
intron_variant | MODIFIER | c.577+193_577+196dup others(4): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 14604543 | |||||
chrX:14604543
|
A | AGTGTGT | 1 | a0001c0001t0006g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.577+191_577+196dup others(6): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 14604543 | |||||
chrX:14604543
|
AGT | A | 22 | a0001c0001t0001g0113a0001c0001t0001g0125a0001c0001t0001g0138others(19): Show | 22 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.577+195_577+196del others(2): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 14604543 | |||||
chrX:14604543
|
AGTGT | A | 49 | a0001c0001t0001g0036a0001c0001t0001g0042a0001c0001t0001g0109others(46): Show | 49 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.577+193_577+196del others(4): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 14604543 | |||||
chrX:14604543
|
AGTGTGT | A | 28 | a0001c0001t0001g0105a0001c0001t0003g0035a0001c0001t0003g0037others(25): Show | 28 | HG00621.hp1 HG00733.hp2 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.577+191_577+196del others(6): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 14604543 | |||||
chrX:14604543
|
AGTGTGTG others(1): Show |
A | 23 | a0001c0001t0002g0120a0001c0001t0004g0027a0001c0001t0004g0069others(20): Show | 23 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.577+189_577+196del others(8): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 14604543 | |||||
chrX:14604543
|
AGTGTGTG others(3): Show |
A | 3 | a0001c0001t0002g0222a0001c0001t0011g0188a0001c0001t0021g0190 | 3 | HG02922.hp1 HG03041.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.577+187_577+196del others(10): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 14604543 | |||||
chrX:14604543
|
AGTGTGTG others(5): Show |
A | 7 | a0001c0001t0001g0029a0001c0001t0001g0066a0001c0001t0001g0072others(4): Show | 7 | HG02055.hp1 HG02132.hp1 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.577+185_577+196del others(12): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 14604543 | |||||
chrX:14604543
|
AGTGTGTG others(7): Show |
A | 3 | a0001c0001t0014g0228a0001c0001t0017g0078a0001c0001t0018g0080 | 3 | HG02451.hp2 HG02630.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.577+183_577+196del others(14): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 14604543 | |||||
chrX:14604543
|
AGTGTGTG others(9): Show |
A | 1 | a0001c0001t0001g0147 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.577+181_577+196del others(16): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 14604543 | |||||
chrX:14604543
|
AGTGTGTG others(15): Show |
A | 2 | a0001c0001t0009g0032a0001c0001t0018g0033 | 2 | HG02970.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.577+175_577+196del others(22): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 14604543 | |||||
chrX:14604562
|
G | T | 1 | a0001c0001t0008g0195 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.577+165G>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 5/8 | chrX | 14604562 | ||||||
chrX:14604671
|
G | A | 3 | a0001c0002t0010g0031a0001c0002t0024g0016a0001c0002t0024g0017 | 3 | HG03195.hp1 NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.577+274G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 5/8 | chrX | 14604671 | ||||||
chrX:14605113
|
T | C | 31 | a0001c0001t0002g0120a0001c0001t0002g0194a0001c0001t0004g0021others(28): Show | 31 | HG01070.hp1 HG01074.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.577+716T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 5/8 | chrX | 14605113 | ||||||
chrX:14605338
|
T | C | 1 | a0001c0001t0005g0006 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.577+941T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 5/8 | chrX | 14605338 | ||||||
chrX:14605510
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.577+1113C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 5/8 | chrX | 14605510 | ||||||
chrX:14605732
|
A | AT | 1 | a0001c0001t0041g0153 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.577+1342dupT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 14605732 | |||||
chrX:14606015
|
A | AT | 3 | a0001c0001t0001g0146a0001c0001t0004g0069a0001c0001t0012g0174 | 3 | HG00558.hp1 HG02280.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.578-1103dupT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 14606015 | |||||
chrX:14606015
|
AT | A | 53 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(50): Show | 53 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.578-1103delT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 14606015 | |||||
chrX:14606015
|
ATT | A | 2 | a0001c0001t0002g0061a0001c0001t0008g0227 | 2 | HG02683.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.578-1104_578-1103d others(4): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 14606015 | |||||
chrX:14606015
|
ATTT | A | 13 | a0001c0002t0007g0022a0001c0002t0007g0023a0001c0002t0007g0192others(10): Show | 13 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.578-1105_578-1103d others(5): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 14606015 | |||||
chrX:14606047
|
T | C | 10 | a0001c0002t0023g0065a0001c0002t0023g0186a0001c0002t0039g0184others(7): Show | 10 | HG01074.hp1 HG01109.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.578-1084T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 5/8 | chrX | 14606047 | ||||||
chrX:14606120
|
A | G | 43 | a0001c0001t0001g0036a0001c0001t0001g0042a0001c0001t0001g0109others(40): Show | 43 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.578-1011A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 5/8 | chrX | 14606120 | ||||||
chrX:14606155
|
T | TA | 17 | a0001c0001t0002g0120a0001c0001t0002g0123a0001c0001t0002g0194others(14): Show | 17 | HG01928.hp1 HG01952.hp1 HG02004.hp1 others(14): Show |
intron_variant | MODIFIER | c.578-958dupA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 14606155 | |||||
chrX:14606155
|
TA | T | 9 | a0001c0001t0001g0029a0001c0001t0001g0066a0001c0001t0001g0072others(6): Show | 9 | HG02055.hp1 HG02132.hp1 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.578-958delA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 14606155 | |||||
chrX:14606155
|
TAA | T | 35 | a0001c0002t0005g0002a0001c0002t0005g0010a0001c0002t0005g0014others(32): Show | 35 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.578-959_578-958del others(2): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 14606155 | |||||
chrX:14606212
|
A | G | 13 | a0001c0002t0007g0022a0001c0002t0007g0023a0001c0002t0007g0192others(10): Show | 13 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.578-919A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 5/8 | chrX | 14606212 | ||||||
chrX:14606270
|
G | T | 1 | a0001c0001t0001g0029 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.578-861G>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 5/8 | chrX | 14606270 | ||||||
chrX:14606542
|
A | G | 1 | a0001c0001t0001g0125 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.578-589A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 5/8 | chrX | 14606542 | ||||||
chrX:14607277
|
C | CT | 101 | a0001c0001t0001g0036a0001c0001t0002g0061a0001c0001t0002g0120others(98): Show | 101 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.715+24dupT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 14607277 | |||||
chrX:14607277
|
C | CTT | 12 | a0001c0001t0001g0042a0001c0001t0001g0109a0001c0001t0001g0110others(9): Show | 12 | HG00741.hp1 HG01123.hp2 HG01515.hp1 others(9): Show |
intron_variant | MODIFIER | c.715+23_715+24dupTT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 14607277 | |||||
chrX:14607277
|
CT | C | 1 | a0001c0001t0004g0164 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.715+24delT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 14607277 | |||||
chrX:14607805
|
A | G | 4 | a0001c0001t0002g0061a0001c0001t0003g0049a0001c0001t0003g0139others(1): Show | 4 | HG00558.hp2 HG00609.hp1 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.715+537A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 6/8 | chrX | 14607805 | ||||||
chrX:14607900
|
G | A | 5 | a0001c0002t0028g0062a0001c0002t0045g0177a0001c0003t0025g0175others(2): Show | 5 | HG02258.hp1 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.715+632G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 6/8 | chrX | 14607900 | ||||||
chrX:14608015
|
T | C | 1 | a0001c0002t0005g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.715+747T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 6/8 | chrX | 14608015 | ||||||
chrX:14608182
|
T | C | 1 | a0001c0002t0005g0205 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.716-809T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 6/8 | chrX | 14608182 | ||||||
chrX:14608557
|
TTATATGC others(7): Show |
T | 2 | a0001c0001t0003g0035a0001c0001t0003g0037 | 2 | HG03017.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.716-423_716-410del others(14): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 14608557 | |||||
chrX:14608706
|
C | T | 1 | a0001c0002t0007g0210 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.716-285C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 6/8 | chrX | 14608706 | ||||||
chrX:14608900
|
C | CT | 8 | a0001c0001t0001g0036a0001c0001t0001g0042a0001c0001t0001g0109others(5): Show | 8 | HG00741.hp1 HG01123.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.716-73dupT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 14608900 | |||||
chrX:14608900
|
CT | C | 32 | a0001c0001t0001g0029a0001c0001t0001g0066a0001c0001t0001g0072others(29): Show | 32 | HG00323.hp1 HG00558.hp2 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.716-73delT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 14608900 | |||||
chrX:14609415
|
T | C | 1 | a0001c0001t0003g0136 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.930+210T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14609415 | ||||||
chrX:14609946
|
AAAG | A | 3 | a0001c0001t0002g0034a0001c0001t0038g0030a0001c0001t0044g0193 | 3 | HG02965.hp1 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.930+745_930+747del others(3): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14609946 | |||||
chrX:14609950
|
A | C | 116 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(113): Show | 116 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.930+745A>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14609950 | ||||||
chrX:14610238
|
A | G | 1 | a0001c0001t0001g0137 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.930+1033A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14610238 | ||||||
chrX:14610671
|
A | G | 4 | a0001c0001t0003g0044a0001c0001t0003g0045a0001c0001t0003g0046others(1): Show | 4 | HG00639.hp1 HG01257.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.930+1466A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14610671 | ||||||
chrX:14610864
|
T | C | 1 | a0001c0001t0002g0120 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.930+1659T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14610864 | ||||||
chrX:14610941
|
T | A | 1 | a0001c0001t0007g0079 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.930+1736T>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14610941 | ||||||
chrX:14610962
|
CA | C | 1 | a0001c0001t0017g0118 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.930+1762delA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14610962 | |||||
chrX:14610986
|
T | C | 4 | a0001c0002t0023g0065a0001c0002t0023g0186a0001c0002t0039g0184others(1): Show | 4 | HG01109.hp1 HG02109.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.930+1781T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14610986 | ||||||
chrX:14611013
|
AC | A | 1 | a0001c0001t0017g0118 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.930+1810delC | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14611013 | |||||
chrX:14611268
|
A | G | 47 | a0001c0001t0001g0036a0001c0001t0001g0042a0001c0001t0001g0109others(44): Show | 47 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.930+2063A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14611268 | ||||||
chrX:14611288
|
G | A | 7 | a0001c0001t0010g0070a0001c0001t0010g0071a0001c0001t0010g0074others(4): Show | 7 | HG01243.hp1 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.930+2083G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14611288 | ||||||
chrX:14611483
|
G | A | 35 | a0001c0002t0003g0145a0001c0002t0005g0002a0001c0002t0005g0010others(32): Show | 35 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.930+2278G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14611483 | ||||||
chrX:14611614
|
A | AT | 1 | a0001c0001t0017g0118 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.930+2414dupT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14611614 | |||||
chrX:14611792
|
TA | T | 1 | a0001c0001t0017g0118 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.930+2590delA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14611792 | |||||
chrX:14611886
|
C | CT | 1 | a0001c0001t0017g0118 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.930+2685dupT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14611886 | |||||
chrX:14611891
|
G | C | 1 | a0001c0002t0037g0028 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.930+2686G>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14611891 | ||||||
chrX:14611930
|
A | AC | 1 | a0001c0001t0017g0118 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.930+2727dupC | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14611930 | |||||
chrX:14611956
|
C | A | 1 | a0001c0001t0008g0140 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.930+2751C>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14611956 | ||||||
chrX:14612149
|
CA | C | 1 | a0001c0001t0002g0061 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.930+2950delA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14612149 | |||||
chrX:14612155
|
A | G | 47 | a0001c0001t0048g0018a0001c0002t0003g0145a0001c0002t0005g0002others(44): Show | 47 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.930+2950A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14612155 | ||||||
chrX:14612167
|
C | A | 1 | a0001c0001t0001g0072 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.930+2962C>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14612167 | ||||||
chrX:14612259
|
CA | C | 1 | a0001c0001t0017g0118 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.930+3058delA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14612259 | |||||
chrX:14612457
|
A | T | 33 | a0001c0002t0003g0145a0001c0002t0005g0002a0001c0002t0005g0010others(30): Show | 33 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.930+3252A>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14612457 | ||||||
chrX:14612464
|
T | C | 46 | a0001c0002t0003g0145a0001c0002t0005g0002a0001c0002t0005g0010others(43): Show | 46 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.930+3259T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14612464 | ||||||
chrX:14612483
|
CA | C | 1 | a0001c0001t0017g0118 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.930+3281delA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14612483 | |||||
chrX:14612637
|
T | C | 1 | a0001c0001t0008g0007 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.930+3432T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14612637 | ||||||
chrX:14612692
|
GA | G | 1 | a0001c0001t0002g0061 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.930+3490delA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14612692 | |||||
chrX:14612829
|
T | TG | 1 | a0001c0001t0017g0118 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.930+3631dupG | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14612829 | |||||
chrX:14612939
|
T | C | 120 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0042others(117): Show | 120 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.930+3734T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14612939 | ||||||
chrX:14613152
|
GT | G | 1 | a0001c0001t0017g0118 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.930+3950delT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14613152 | |||||
chrX:14613490
|
TA | T | 13 | a0001c0002t0007g0022a0001c0002t0007g0023a0001c0002t0007g0192others(10): Show | 13 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.930+4293delA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14613490 | |||||
chrX:14613500
|
A | G | 2 | a0001c0002t0024g0016a0001c0002t0024g0017 | 2 | HG03195.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.930+4295A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14613500 | ||||||
chrX:14613578
|
A | T | 1 | a0001c0001t0019g0131 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.930+4373A>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14613578 | ||||||
chrX:14613617
|
AT | A | 1 | a0001c0001t0017g0118 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.930+4415delT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14613617 | |||||
chrX:14613653
|
G | A | 2 | a0001c0001t0004g0081a0001c0001t0004g0155 | 2 | HG02056.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.930+4448G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14613653 | ||||||
chrX:14613663
|
A | G | 6 | a0001c0001t0001g0029a0001c0001t0001g0066a0001c0001t0001g0072others(3): Show | 6 | HG02055.hp1 HG02132.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.930+4458A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14613663 | ||||||
chrX:14613733
|
G | GT | 1 | a0001c0001t0008g0128 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.930+4536dupT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14613733 | |||||
chrX:14613734
|
T | TA | 1 | a0001c0001t0017g0118 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.930+4529_930+4530i others(3): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14613734 | ||||||
chrX:14613761
|
G | T | 1 | a0001c0001t0014g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.930+4556G>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14613761 | ||||||
chrX:14614054
|
TC | T | 1 | a0001c0001t0008g0201 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.930+4852delC | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14614054 | |||||
chrX:14614093
|
A | AC | 1 | a0001c0001t0017g0118 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.930+4888_930+4889i others(3): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14614093 | ||||||
chrX:14614798
|
T | TA | 1 | a0001c0001t0017g0118 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.930+5593_930+5594i others(3): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14614798 | ||||||
chrX:14615019
|
T | G | 1 | a0001c0001t0001g0211 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.930+5814T>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14615019 | ||||||
chrX:14615051
|
G | A | 14 | a0001c0002t0005g0002a0001c0002t0005g0010a0001c0002t0005g0205others(11): Show | 14 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.930+5846G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14615051 | ||||||
chrX:14615143
|
A | G | 2 | a0001c0001t0007g0077a0001c0001t0007g0079 | 2 | HG02145.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.930+5938A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14615143 | ||||||
chrX:14615496
|
GC | G | 1 | a0001c0001t0001g0133 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.930+6293delC | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14615496 | |||||
chrX:14615840
|
C | T | 21 | a0001c0002t0005g0002a0001c0002t0005g0010a0001c0002t0005g0014others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.930+6635C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14615840 | ||||||
chrX:14616177
|
A | G | 1 | a0001c0001t0014g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.930+6972A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14616177 | ||||||
chrX:14616624
|
C | T | 34 | a0001c0001t0001g0036a0001c0001t0001g0042a0001c0001t0001g0109others(31): Show | 34 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.930+7419C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14616624 | ||||||
chrX:14616743
|
C | T | 35 | a0001c0002t0005g0002a0001c0002t0005g0010a0001c0002t0005g0014others(32): Show | 35 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.930+7538C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14616743 | ||||||
chrX:14616744
|
G | A | 45 | a0001c0001t0001g0036a0001c0001t0001g0042a0001c0001t0001g0109others(42): Show | 45 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.930+7539G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14616744 | ||||||
chrX:14616808
|
T | C | 14 | a0001c0001t0048g0018a0001c0002t0007g0022a0001c0002t0007g0023others(11): Show | 14 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.930+7603T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14616808 | ||||||
chrX:14616900
|
G | A | 7 | a0001c0001t0010g0070a0001c0001t0010g0071a0001c0001t0010g0074others(4): Show | 7 | HG01243.hp1 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.930+7695G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14616900 | ||||||
chrX:14617635
|
A | G | 2 | a0001c0002t0005g0213a0001c0002t0005g0215 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.930+8430A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14617635 | ||||||
chrX:14617743
|
C | T | 22 | a0001c0002t0005g0002a0001c0002t0005g0010a0001c0002t0005g0014others(19): Show | 22 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.930+8538C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14617743 | ||||||
chrX:14618107
|
T | C | 2 | a0001c0003t0026g0176a0001c0003t0027g0182 | 2 | HG01074.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.930+8902T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14618107 | ||||||
chrX:14618400
|
TGTA | T | 1 | a0001c0001t0029g0012 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.930+9198_930+9200d others(5): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14618400 | |||||
chrX:14618443
|
G | T | 108 | a0001c0001t0001g0036a0001c0001t0001g0042a0001c0001t0001g0109others(105): Show | 108 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.930+9238G>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14618443 | ||||||
chrX:14618472
|
C | G | 74 | a0001c0001t0001g0036a0001c0001t0001g0042a0001c0001t0001g0109others(71): Show | 74 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.930+9267C>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14618472 | ||||||
chrX:14618657
|
G | C | 1 | a0001c0001t0014g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.930+9452G>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14618657 | ||||||
chrX:14618681
|
G | GTT | 3 | a0001c0001t0009g0032a0001c0001t0018g0033a0001c0001t0018g0080 | 3 | HG02970.hp1 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.930+9477_930+9478i others(4): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14618681 | |||||
chrX:14619074
|
T | C | 13 | a0001c0001t0009g0032a0001c0001t0018g0033a0001c0001t0018g0080others(10): Show | 13 | HG01074.hp1 HG01109.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.930+9869T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14619074 | ||||||
chrX:14619221
|
A | G | 1 | a0001c0001t0029g0012 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.930+10016A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14619221 | ||||||
chrX:14619566
|
ACTACCTT others(2): Show |
A | 30 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0038others(27): Show | 30 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.930+10374_930+1038 others(13): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14619566 | |||||
chrX:14619701
|
G | A | 18 | a0001c0001t0009g0032a0001c0001t0018g0033a0001c0001t0018g0080others(15): Show | 18 | HG01074.hp1 HG01109.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.930+10496G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14619701 | ||||||
chrX:14619826
|
C | T | 7 | a0001c0002t0007g0022a0001c0002t0007g0023a0001c0002t0007g0192others(4): Show | 7 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.930+10621C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14619826 | ||||||
chrX:14620002
|
C | CCG | 1 | a0001c0002t0021g0024 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.930+10797_930+1079 others(6): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14620002 | ||||||
chrX:14620003
|
G | A | 1 | a0001c0002t0005g0015 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.930+10798G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14620003 | ||||||
chrX:14620003
|
G | C | 19 | a0001c0001t0009g0032a0001c0001t0014g0228a0001c0001t0018g0033others(16): Show | 19 | HG01074.hp1 HG01109.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.930+10798G>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14620003 | ||||||
chrX:14620003
|
G | GT | 41 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0038others(38): Show | 41 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.930+10809dupT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14620003 | |||||
chrX:14620003
|
G | GTT | 2 | a0001c0001t0003g0055a0001c0001t0015g0068 | 2 | NA19006.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.930+10808_930+1080 others(6): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14620003 | |||||
chrX:14620003
|
G | T | 1 | a0001c0002t0021g0024 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.930+10798G>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14620003 | ||||||
chrX:14620092
|
C | T | 1 | a0001c0001t0010g0070 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.930+10887C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14620092 | ||||||
chrX:14620144
|
T | C | 3 | a0001c0001t0009g0032a0001c0001t0018g0033a0001c0001t0018g0080 | 3 | HG02970.hp1 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.930+10939T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14620144 | ||||||
chrX:14620153
|
GTAATC | G | 1 | a0001c0001t0011g0188 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.930+10954_930+1095 others(9): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14620153 | |||||
chrX:14620312
|
C | T | 6 | a0001c0001t0012g0099a0001c0001t0012g0104a0001c0001t0012g0154others(3): Show | 6 | HG01106.hp1 HG01891.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.930+11107C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14620312 | ||||||
chrX:14620631
|
T | C | 1 | a0001c0001t0015g0068 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.930+11426T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14620631 | ||||||
chrX:14621026
|
A | C | 5 | a0001c0001t0007g0079a0001c0001t0013g0073a0001c0001t0013g0185others(2): Show | 5 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.930+11821A>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14621026 | ||||||
chrX:14621095
|
C | A | 1 | a0001c0001t0001g0171 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.930+11890C>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14621095 | ||||||
chrX:14621327
|
AT | A | 1 | a0001c0001t0008g0009 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.930+12132delT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14621327 | |||||
chrX:14621337
|
TA | T | 1 | a0001c0002t0043g0191 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.930+12136delA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14621337 | |||||
chrX:14621338
|
A | T | 91 | a0001c0001t0001g0029a0001c0001t0001g0066a0001c0001t0001g0072others(88): Show | 91 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.930+12133A>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14621338 | ||||||
chrX:14621349
|
T | C | 8 | a0001c0001t0048g0018a0001c0002t0007g0022a0001c0002t0007g0023others(5): Show | 8 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.930+12144T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14621349 | ||||||
chrX:14621368
|
C | CTT | 8 | a0001c0001t0048g0018a0001c0002t0007g0022a0001c0002t0007g0023others(5): Show | 8 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.930+12172_930+1217 others(6): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14621368 | |||||
chrX:14621458
|
C | T | 11 | a0001c0002t0028g0062a0001c0002t0045g0177a0001c0002t0046g0179others(8): Show | 11 | HG01074.hp1 HG01891.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.930+12253C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14621458 | ||||||
chrX:14621795
|
G | C | 26 | a0001c0001t0002g0061a0001c0001t0003g0035a0001c0001t0003g0037others(23): Show | 26 | HG00558.hp2 HG00609.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.930+12590G>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14621795 | ||||||
chrX:14621821
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.930+12616C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14621821 | ||||||
chrX:14621918
|
A | T | 1 | a0001c0001t0008g0230 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.930+12713A>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14621918 | ||||||
chrX:14621932
|
G | A | 17 | a0001c0001t0002g0120a0001c0001t0002g0194a0001c0001t0004g0021others(14): Show | 17 | HG01070.hp1 HG01928.hp1 HG01952.hp1 others(14): Show |
intron_variant | MODIFIER | c.930+12727G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14621932 | ||||||
chrX:14621934
|
C | CA | 1 | a0001c0001t0001g0113 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.930+12730dupA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14621934 | |||||
chrX:14622128
|
T | C | 1 | a0001c0001t0002g0194 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.930+12923T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14622128 | ||||||
chrX:14622188
|
G | A | 1 | a0001c0001t0002g0124 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.930+12983G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14622188 | ||||||
chrX:14622255
|
T | G | 4 | a0001c0001t0002g0101a0001c0001t0002g0151a0001c0001t0004g0164others(1): Show | 4 | HG02027.hp1 HG02074.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.930+13050T>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14622255 | ||||||
chrX:14622417
|
T | C | 1 | a0001c0001t0020g0207 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.930+13212T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14622417 | ||||||
chrX:14622419
|
A | G | 1 | a0001c0001t0020g0207 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.930+13214A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14622419 | ||||||
chrX:14622521
|
G | A | 27 | a0001c0001t0009g0032a0001c0001t0014g0228a0001c0001t0018g0033others(24): Show | 27 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.930+13316G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14622521 | ||||||
chrX:14622631
|
T | C | 1 | a0001c0002t0043g0191 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.930+13426T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14622631 | ||||||
chrX:14622804
|
C | T | 69 | a0001c0001t0002g0061a0001c0001t0003g0035a0001c0001t0003g0037others(66): Show | 69 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.930+13599C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14622804 | ||||||
chrX:14622904
|
A | G | 1 | a0001c0001t0029g0012 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.930+13699A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14622904 | ||||||
chrX:14622925
|
T | C | 42 | a0001c0001t0002g0061a0001c0001t0003g0035a0001c0001t0003g0037others(39): Show | 42 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.930+13720T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14622925 | ||||||
chrX:14623023
|
G | A | 1 | a0001c0001t0014g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.930+13818G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14623023 | ||||||
chrX:14623063
|
G | A | 19 | a0001c0001t0001g0029a0001c0001t0009g0032a0001c0001t0018g0033others(16): Show | 19 | HG01074.hp1 HG01109.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.930+13858G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14623063 | ||||||
chrX:14623252
|
G | A | 8 | a0001c0001t0048g0018a0001c0002t0007g0022a0001c0002t0007g0023others(5): Show | 8 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.930+14047G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14623252 | ||||||
chrX:14623258
|
A | G | 8 | a0001c0001t0048g0018a0001c0002t0007g0022a0001c0002t0007g0023others(5): Show | 8 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.930+14053A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14623258 | ||||||
chrX:14623292
|
C | T | 1 | a0001c0001t0004g0155 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.930+14087C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14623292 | ||||||
chrX:14623505
|
T | C | 3 | a0001c0002t0005g0014a0001c0002t0007g0013a0001c0002t0011g0076 | 3 | HG03139.hp1 HG03516.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.930+14300T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14623505 | ||||||
chrX:14623514
|
A | G | 70 | a0001c0001t0002g0061a0001c0001t0003g0035a0001c0001t0003g0037others(67): Show | 70 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.930+14309A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14623514 | ||||||
chrX:14623518
|
C | T | 3 | a0001c0003t0025g0175a0001c0003t0025g0181a0001c0003t0030g0198 | 3 | HG02572.hp1 HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.930+14313C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14623518 | ||||||
chrX:14623582
|
G | A | 3 | a0001c0001t0009g0032a0001c0001t0018g0033a0001c0001t0018g0080 | 3 | HG02970.hp1 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.930+14377G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14623582 | ||||||
chrX:14623654
|
T | G | 18 | a0001c0001t0009g0032a0001c0001t0018g0033a0001c0001t0018g0080others(15): Show | 18 | HG01074.hp1 HG01109.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.930+14449T>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14623654 | ||||||
chrX:14623667
|
G | A | 18 | a0001c0001t0009g0032a0001c0001t0018g0033a0001c0001t0018g0080others(15): Show | 18 | HG01074.hp1 HG01109.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.930+14462G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14623667 | ||||||
chrX:14623744
|
A | G | 1 | a0001c0001t0003g0049 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.930+14539A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14623744 | ||||||
chrX:14623745
|
G | T | 1 | a0001c0001t0003g0049 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.930+14540G>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14623745 | ||||||
chrX:14623777
|
C | T | 7 | a0001c0002t0007g0022a0001c0002t0007g0023a0001c0002t0007g0192others(4): Show | 7 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.930+14572C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14623777 | ||||||
chrX:14623779
|
A | C | 1 | a0001c0001t0014g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.930+14574A>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14623779 | ||||||
chrX:14623907
|
G | T | 18 | a0001c0001t0009g0032a0001c0001t0018g0033a0001c0001t0018g0080others(15): Show | 18 | HG01074.hp1 HG01109.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.930+14702G>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14623907 | ||||||
chrX:14623957
|
C | T | 3 | a0001c0001t0002g0034a0001c0001t0038g0030a0001c0001t0044g0193 | 3 | HG02965.hp1 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.930+14752C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14623957 | ||||||
chrX:14623981
|
G | C | 7 | a0001c0002t0007g0022a0001c0002t0007g0023a0001c0002t0007g0192others(4): Show | 7 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.930+14776G>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14623981 | ||||||
chrX:14624209
|
T | C | 10 | a0001c0001t0001g0050a0001c0001t0001g0084a0001c0001t0001g0146others(7): Show | 10 | HG00558.hp1 HG02080.hp1 NA18944.hp1 others(7): Show |
intron_variant | MODIFIER | c.930+15004T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14624209 | ||||||
chrX:14624285
|
CT | C | 1 | a0001c0001t0002g0061 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.930+15084delT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14624285 | |||||
chrX:14624301
|
C | T | 1 | a0001c0001t0004g0069 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.930+15096C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14624301 | ||||||
chrX:14624544
|
C | T | 2 | a0001c0001t0003g0041a0001c0001t0033g0040 | 2 | HG03239.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.930+15339C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14624544 | ||||||
chrX:14624695
|
A | G | 20 | a0001c0001t0002g0120a0001c0001t0002g0194a0001c0001t0004g0021others(17): Show | 20 | HG01070.hp1 HG01928.hp1 HG01952.hp1 others(17): Show |
intron_variant | MODIFIER | c.930+15490A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14624695 | ||||||
chrX:14624760
|
T | C | 8 | a0001c0001t0048g0018a0001c0002t0007g0022a0001c0002t0007g0023others(5): Show | 8 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.930+15555T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14624760 | ||||||
chrX:14624773
|
T | C | 1 | a0001c0002t0005g0010 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.930+15568T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14624773 | ||||||
chrX:14624774
|
G | T | 1 | a0001c0002t0005g0010 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.930+15569G>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14624774 | ||||||
chrX:14624859
|
A | G | 2 | a0001c0001t0012g0154a0001c0001t0015g0103 | 2 | HG01891.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.930+15654A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14624859 | ||||||
chrX:14625100
|
A | AATG | 1 | a0001c0001t0008g0009 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.930+15896_930+1589 others(7): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14625100 | |||||
chrX:14625154
|
A | T | 6 | a0001c0001t0001g0029a0001c0001t0001g0066a0001c0001t0001g0072others(3): Show | 6 | HG02055.hp1 HG02132.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.930+15949A>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14625154 | ||||||
chrX:14625168
|
AC | A | 1 | a0001c0001t0008g0009 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.930+15967delC | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14625168 | |||||
chrX:14625177
|
T | G | 3 | a0001c0001t0022g0058a0001c0001t0022g0059a0001c0001t0034g0167 | 3 | NA18943.hp1 NA18986.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.930+15972T>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14625177 | ||||||
chrX:14625196
|
CT | C | 1 | a0001c0001t0008g0009 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.930+15993delT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14625196 | |||||
chrX:14625233
|
AT | A | 1 | a0001c0001t0008g0009 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.930+16029delT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14625233 | ||||||
chrX:14625330
|
G | A | 19 | a0001c0002t0005g0002a0001c0002t0005g0010a0001c0002t0005g0014others(16): Show | 19 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.930+16125G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14625330 | ||||||
chrX:14625340
|
T | C | 27 | a0001c0001t0009g0032a0001c0001t0014g0228a0001c0001t0018g0033others(24): Show | 27 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.930+16135T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14625340 | ||||||
chrX:14625348
|
T | C | 1 | a0001c0001t0002g0061 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.930+16143T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14625348 | ||||||
chrX:14625414
|
C | T | 6 | a0001c0001t0001g0029a0001c0001t0001g0066a0001c0001t0001g0072others(3): Show | 6 | HG02055.hp1 HG02132.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.930+16209C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14625414 | ||||||
chrX:14625446
|
T | C | 4 | a0001c0001t0002g0163a0001c0001t0002g0165a0001c0001t0002g0166others(1): Show | 4 | HG01081.hp1 HG01099.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.930+16241T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14625446 | ||||||
chrX:14625471
|
T | C | 8 | a0001c0001t0048g0018a0001c0002t0007g0022a0001c0002t0007g0023others(5): Show | 8 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.930+16266T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14625471 | ||||||
chrX:14625546
|
G | T | 1 | a0001c0001t0031g0060 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.930+16341G>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14625546 | ||||||
chrX:14625564
|
A | C | 2 | a0001c0001t0003g0221a0001c0001t0003g0226 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.930+16359A>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14625564 | ||||||
chrX:14625610
|
G | GC | 1 | a0001c0001t0015g0068 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.930+16406dupC | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14625610 | |||||
chrX:14625881
|
T | C | 6 | a0001c0001t0001g0029a0001c0001t0001g0066a0001c0001t0001g0072others(3): Show | 6 | HG02055.hp1 HG02132.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.930+16676T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14625881 | ||||||
chrX:14625919
|
AG | A | 1 | a0001c0001t0015g0068 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.930+16717delG | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14625919 | |||||
chrX:14626041
|
G | C | 1 | a0001c0002t0047g0183 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.930+16836G>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14626041 | ||||||
chrX:14626132
|
A | AT | 1 | a0001c0001t0015g0068 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.930+16931dupT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14626132 | |||||
chrX:14626211
|
A | C | 38 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0038others(35): Show | 38 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.930+17006A>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14626211 | ||||||
chrX:14626243
|
A | G | 2 | a0001c0001t0003g0035a0001c0001t0003g0037 | 2 | HG03017.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.930+17038A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14626243 | ||||||
chrX:14626302
|
A | G | 2 | a0001c0001t0003g0054a0001c0001t0003g0055 | 2 | NA18945.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.930+17097A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14626302 | ||||||
chrX:14626312
|
T | C | 1 | a0001c0001t0014g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.930+17107T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14626312 | ||||||
chrX:14626484
|
C | A | 41 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0038others(38): Show | 41 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.930+17279C>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14626484 | ||||||
chrX:14626614
|
A | G | 19 | a0001c0001t0009g0032a0001c0001t0014g0228a0001c0001t0018g0033others(16): Show | 19 | HG01074.hp1 HG01109.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.930+17409A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14626614 | ||||||
chrX:14626690
|
TG | T | 1 | a0001c0001t0015g0068 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.930+17487delG | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14626690 | |||||
chrX:14626951
|
AT | A | 1 | a0001c0001t0015g0068 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.930+17748delT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14626951 | |||||
chrX:14626967
|
GA | G | 1 | a0001c0001t0015g0068 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.930+17765delA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14626967 | |||||
chrX:14627072
|
G | A | 1 | a0001c0001t0004g0162 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.930+17867G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14627072 | ||||||
chrX:14627243
|
AT | A | 1 | a0001c0001t0015g0068 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.930+18041delT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14627243 | |||||
chrX:14627276
|
A | G | 19 | a0001c0001t0009g0032a0001c0001t0014g0228a0001c0001t0018g0033others(16): Show | 19 | HG01074.hp1 HG01109.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.930+18071A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14627276 | ||||||
chrX:14627291
|
T | C | 1 | a0001c0001t0003g0051 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.930+18086T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14627291 | ||||||
chrX:14627380
|
CA | C | 1 | a0001c0001t0015g0068 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.930+18178delA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14627380 | |||||
chrX:14627489
|
T | C | 18 | a0001c0001t0009g0032a0001c0001t0018g0033a0001c0001t0018g0080others(15): Show | 18 | HG01074.hp1 HG01109.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.930+18284T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14627489 | ||||||
chrX:14628366
|
G | A | 19 | a0001c0002t0005g0002a0001c0002t0005g0010a0001c0002t0005g0014others(16): Show | 19 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.930+19161G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14628366 | ||||||
chrX:14628485
|
A | T | 7 | a0001c0002t0007g0022a0001c0002t0007g0023a0001c0002t0007g0192others(4): Show | 7 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.930+19280A>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14628485 | ||||||
chrX:14628494
|
T | C | 1 | a0001c0001t0001g0133 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.930+19289T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14628494 | ||||||
chrX:14628513
|
C | T | 7 | a0001c0001t0010g0070a0001c0001t0010g0071a0001c0001t0010g0074others(4): Show | 7 | HG01243.hp1 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.930+19308C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14628513 | ||||||
chrX:14628668
|
A | G | 19 | a0001c0001t0009g0032a0001c0001t0014g0228a0001c0001t0018g0033others(16): Show | 19 | HG01074.hp1 HG01109.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.930+19463A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14628668 | ||||||
chrX:14629176
|
G | A | 2 | a0001c0002t0007g0209a0001c0002t0011g0086 | 2 | HG01256.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.930+19971G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14629176 | ||||||
chrX:14629184
|
A | G | 3 | a0001c0001t0004g0150a0001c0001t0008g0128a0001c0001t0008g0141 | 3 | HG02738.hp1 HG03654.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.930+19979A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14629184 | ||||||
chrX:14629222
|
G | A | 68 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0038others(65): Show | 68 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.930+20017G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14629222 | ||||||
chrX:14629253
|
T | C | 1 | a0001c0001t0003g0038 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.930+20048T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14629253 | ||||||
chrX:14629833
|
T | C | 1 | a0001c0002t0011g0217 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.930+20628T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14629833 | ||||||
chrX:14629889
|
A | G | 8 | a0001c0001t0048g0018a0001c0002t0007g0022a0001c0002t0007g0023others(5): Show | 8 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.930+20684A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14629889 | ||||||
chrX:14629994
|
G | A | 1 | a0001c0002t0043g0191 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.930+20789G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14629994 | ||||||
chrX:14630097
|
G | T | 27 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0038others(24): Show | 27 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.930+20892G>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14630097 | ||||||
chrX:14630296
|
C | T | 1 | a0001c0001t0031g0060 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.930+21091C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14630296 | ||||||
chrX:14630344
|
T | C | 18 | a0001c0001t0009g0032a0001c0001t0018g0033a0001c0001t0018g0080others(15): Show | 18 | HG01074.hp1 HG01109.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.930+21139T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14630344 | ||||||
chrX:14630470
|
A | G | 1 | a0001c0001t0001g0083 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.930+21265A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14630470 | ||||||
chrX:14630803
|
C | CT | 2 | a0001c0001t0001g0083a0001c0001t0001g0212 | 2 | NA18960.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.930+21616dupT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14630803 | |||||
chrX:14630803
|
CT | C | 51 | a0001c0001t0001g0003a0001c0001t0001g0029a0001c0001t0001g0066others(48): Show | 51 | HG00733.hp2 HG01069.hp1 HG01070.hp1 others(48): Show |
intron_variant | MODIFIER | c.930+21616delT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14630803 | |||||
chrX:14630803
|
CTT | C | 19 | a0001c0002t0005g0002a0001c0002t0005g0010a0001c0002t0005g0014others(16): Show | 19 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.930+21615_930+2161 others(6): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14630803 | |||||
chrX:14631105
|
A | G | 1 | a0001c0001t0004g0220 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.930+21900A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14631105 | ||||||
chrX:14631226
|
C | G | 1 | a0001c0001t0001g0187 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.930+22021C>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14631226 | ||||||
chrX:14631396
|
G | GC | 1 | a0001c0001t0001g0083 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.930+22191_930+2219 others(5): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14631396 | ||||||
chrX:14631550
|
A | AT | 4 | a0001c0002t0007g0022a0001c0002t0007g0023a0001c0002t0007g0192others(1): Show | 4 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.930+22354dupT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14631550 | |||||
chrX:14631637
|
T | TC | 1 | a0001c0001t0001g0083 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.930+22434dupC | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14631637 | |||||
chrX:14631771
|
G | A | 1 | a0001c0001t0008g0140 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.930+22566G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14631771 | ||||||
chrX:14631814
|
A | G | 1 | a0001c0001t0014g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.930+22609A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14631814 | ||||||
chrX:14631860
|
TTG | T | 19 | a0001c0002t0005g0002a0001c0002t0005g0010a0001c0002t0005g0014others(16): Show | 19 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.930+22663_930+2266 others(6): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14631860 | |||||
chrX:14631883
|
C | CAT | 6 | a0001c0001t0001g0029a0001c0001t0001g0066a0001c0001t0001g0072others(3): Show | 6 | HG02055.hp1 HG02132.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.930+22680_930+2268 others(6): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14631883 | |||||
chrX:14631915
|
C | CATATGTA others(255): Show |
1 | a0001c0001t0004g0202 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.930+22728_930+2272 others(266): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14631915 | |||||
chrX:14631915
|
C | CATATGTA others(379): Show |
3 | a0001c0002t0014g0025a0001c0002t0014g0026a0001c0002t0021g0024 | 3 | HG02717.hp1 HG02809.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.930+22728_930+2272 others(390): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14631915 | |||||
chrX:14631915
|
C | CATATGTA others(353): Show |
27 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0038others(24): Show | 27 | HG00558.hp2 HG00609.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.930+22728_930+2272 others(364): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14631915 | |||||
chrX:14631915
|
C | CATATGTA others(405): Show |
4 | a0001c0001t0010g0070a0001c0001t0013g0073a0001c0001t0013g0185others(1): Show | 4 | HG01243.hp1 HG02280.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.930+22728_930+2272 others(416): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14631915 | |||||
chrX:14631915
|
C | CATATGTA others(379): Show |
3 | a0001c0001t0010g0071a0001c0001t0010g0074a0001c0001t0020g0207 | 3 | HG00323.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.930+22728_930+2272 others(390): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14631915 | |||||
chrX:14631915
|
C | CATATGTA others(431): Show |
1 | a0001c0001t0013g0199 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.930+22728_930+2272 others(442): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14631915 | |||||
chrX:14631915
|
C | CATATGTA others(309): Show |
3 | a0001c0001t0009g0032a0001c0001t0018g0033a0001c0001t0018g0080 | 3 | HG02970.hp1 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.930+22728_930+2272 others(320): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14631915 | |||||
chrX:14631915
|
C | CATATGTA others(285): Show |
1 | a0001c0001t0048g0018 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.930+22728_930+2272 others(296): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14631915 | |||||
chrX:14631915
|
C | CATATGTA others(335): Show |
1 | a0001c0003t0026g0180 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.930+22728_930+2272 others(346): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14631915 | |||||
chrX:14631915
|
C | CATATGTA others(405): Show |
1 | a0001c0001t0007g0079 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.930+22728_930+2272 others(416): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14631915 | |||||
chrX:14631915
|
C | CATATGTA others(309): Show |
10 | a0001c0002t0028g0062a0001c0002t0045g0177a0001c0002t0046g0179others(7): Show | 10 | HG01074.hp1 HG01891.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.930+22728_930+2272 others(320): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14631915 | |||||
chrX:14631915
|
C | CATATGTA others(359): Show |
2 | a0001c0001t0003g0041a0001c0001t0033g0040 | 2 | HG03239.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.930+22728_930+2272 others(370): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14631915 | |||||
chrX:14631915
|
C | CATATGTA others(351): Show |
1 | a0001c0001t0021g0190 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.930+22728_930+2272 others(362): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14631915 | |||||
chrX:14631915
|
C | CATATGTA others(255): Show |
1 | a0001c0001t0014g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.930+22728_930+2272 others(266): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14631915 | |||||
chrX:14631915
|
C | CATATGTA others(283): Show |
1 | a0001c0001t0034g0167 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.930+22728_930+2272 others(294): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14631915 | |||||
chrX:14631915
|
C | CATATGTA others(257): Show |
13 | a0001c0002t0005g0002a0001c0002t0005g0010a0001c0002t0005g0205others(10): Show | 13 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.930+22728_930+2272 others(268): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14631915 | |||||
chrX:14631915
|
C | CATATGTA others(257): Show |
129 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(126): Show | 130 | HG00323.hp2 HG00558.hp1 HG00621.hp1 others(127): Show |
intron_variant | MODIFIER | c.930+22728_930+2272 others(268): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14631915 | |||||
chrX:14631915
|
C | CATATGTA others(257): Show |
1 | a0001c0001t0001g0138 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.930+22728_930+2272 others(268): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14631915 | |||||
chrX:14631915
|
C | CATATGTA others(257): Show |
1 | a0001c0001t0006g0134 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.930+22728_930+2272 others(268): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14631915 | |||||
chrX:14631915
|
C | CATATGTA others(257): Show |
5 | a0001c0001t0001g0029a0001c0001t0001g0066a0001c0001t0001g0072others(2): Show | 5 | HG02055.hp1 HG02132.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.930+22728_930+2272 others(268): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14631915 | |||||
chrX:14631915
|
C | CATATGTA others(231): Show |
1 | a0001c0002t0005g0014 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.930+22728_930+2272 others(242): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14631915 | |||||
chrX:14631915
|
C | CATATGTA others(231): Show |
1 | a0001c0001t0002g0135 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.930+22728_930+2272 others(242): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14631915 | |||||
chrX:14631915
|
C | CATATGTA others(231): Show |
4 | a0001c0002t0005g0015a0001c0002t0007g0013a0001c0002t0007g0209others(1): Show | 4 | HG01256.hp1 HG03516.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.930+22728_930+2272 others(242): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14631915 | |||||
chrX:14631915
|
C | CATATGTA others(283): Show |
1 | a0001c0001t0017g0078 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.930+22728_930+2272 others(294): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14631915 | |||||
chrX:14631915
|
C | CATATGTA others(353): Show |
1 | a0001c0002t0005g0056 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.930+22728_930+2272 others(364): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14631915 | |||||
chrX:14631915
|
C | CATATGTA others(255): Show |
6 | a0001c0002t0007g0022a0001c0002t0007g0023a0001c0002t0007g0192others(3): Show | 6 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.930+22728_930+2272 others(266): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14631915 | |||||
chrX:14631915
|
C | CATATGTA others(233): Show |
1 | a0001c0001t0008g0007 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.930+22728_930+2272 others(244): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14631915 | |||||
chrX:14631915
|
C | CATATGTA others(257): Show |
1 | a0001c0002t0043g0191 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.930+22722_930+2272 others(268): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14631915 | |||||
chrX:14631915
|
C | CATATGTA others(309): Show |
4 | a0001c0002t0023g0065a0001c0002t0023g0186a0001c0002t0039g0184others(1): Show | 4 | HG01109.hp1 HG02109.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.930+22722_930+2272 others(320): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14631915 | |||||
chrX:14631916
|
A | ATATGTAT others(255): Show |
1 | a0002c0006t0002g0189 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.930+22728_930+2272 others(266): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14631916 | |||||
chrX:14632118
|
A | G | 8 | a0001c0001t0048g0018a0001c0002t0007g0022a0001c0002t0007g0023others(5): Show | 8 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.930+22913A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14632118 | ||||||
chrX:14632259
|
G | A | 20 | a0001c0002t0005g0002a0001c0002t0005g0010a0001c0002t0005g0014others(17): Show | 20 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.930+23054G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14632259 | ||||||
chrX:14632374
|
C | A | 8 | a0001c0001t0048g0018a0001c0002t0007g0022a0001c0002t0007g0023others(5): Show | 8 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.930+23169C>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14632374 | ||||||
chrX:14632522
|
G | A | 1 | a0001c0001t0002g0149 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.930+23317G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14632522 | ||||||
chrX:14632612
|
C | T | 43 | a0001c0001t0001g0137a0001c0001t0003g0035a0001c0001t0003g0037others(40): Show | 43 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.930+23407C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14632612 | ||||||
chrX:14632765
|
C | T | 1 | a0001c0001t0008g0007 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.930+23560C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14632765 | ||||||
chrX:14632894
|
A | C | 18 | a0001c0001t0009g0032a0001c0001t0018g0033a0001c0001t0018g0080others(15): Show | 18 | HG01074.hp1 HG01109.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.930+23689A>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14632894 | ||||||
chrX:14633185
|
T | A | 1 | a0001c0002t0007g0013 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.930+23980T>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14633185 | ||||||
chrX:14633193
|
G | A | 3 | a0001c0001t0011g0188a0001c0001t0021g0190a0001c0002t0021g0024 | 3 | HG02809.hp2 HG02922.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.930+23988G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14633193 | ||||||
chrX:14633233
|
C | T | 6 | a0001c0001t0001g0029a0001c0001t0001g0066a0001c0001t0001g0072others(3): Show | 6 | HG02055.hp1 HG02132.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.930+24028C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14633233 | ||||||
chrX:14633234
|
G | A | 18 | a0001c0001t0009g0032a0001c0001t0018g0033a0001c0001t0018g0080others(15): Show | 18 | HG01074.hp1 HG01109.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.930+24029G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14633234 | ||||||
chrX:14633345
|
AT | A | 1 | a0001c0001t0001g0083 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.930+24142delT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14633345 | |||||
chrX:14633391
|
A | AC | 1 | a0001c0001t0001g0083 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.930+24186_930+2418 others(5): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14633391 | ||||||
chrX:14633497
|
A | AAAC | 1 | a0001c0001t0014g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.930+24313_930+2431 others(7): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14633497 | |||||
chrX:14633608
|
A | AT | 1 | a0001c0001t0001g0083 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.930+24407dupT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14633608 | |||||
chrX:14633655
|
AG | A | 1 | a0001c0001t0014g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.930+24451delG | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14633655 | ||||||
chrX:14633659
|
A | T | 1 | a0001c0001t0003g0049 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.930+24454A>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14633659 | ||||||
chrX:14633726
|
A | AG | 1 | a0001c0001t0001g0083 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.930+24525dupG | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14633726 | |||||
chrX:14633787
|
G | A | 1 | a0001c0001t0044g0193 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.930+24582G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14633787 | ||||||
chrX:14633826
|
CACTT | C | 19 | a0001c0002t0005g0002a0001c0002t0005g0010a0001c0002t0005g0014others(16): Show | 19 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.930+24625_930+2462 others(8): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14633826 | |||||
chrX:14633876
|
A | AC | 1 | a0001c0001t0001g0083 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.930+24673dupC | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14633876 | |||||
chrX:14633935
|
A | G | 15 | a0001c0002t0023g0065a0001c0002t0023g0186a0001c0002t0028g0062others(12): Show | 15 | HG01074.hp1 HG01109.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.930+24730A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14633935 | ||||||
chrX:14633988
|
G | A | 1 | a0001c0001t0031g0060 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.930+24783G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14633988 | ||||||
chrX:14634044
|
G | GT | 1 | a0001c0001t0001g0083 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.930+24841dupT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14634044 | |||||
chrX:14634094
|
AC | A | 1 | a0001c0001t0001g0083 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.930+24892delC | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14634094 | |||||
chrX:14634106
|
GC | G | 1 | a0001c0001t0001g0083 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.930+24904delC | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14634106 | |||||
chrX:14634178
|
A | AC | 1 | a0001c0001t0001g0083 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.930+24975dupC | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14634178 | |||||
chrX:14634229
|
G | A | 7 | a0001c0002t0007g0022a0001c0002t0007g0023a0001c0002t0007g0192others(4): Show | 7 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.930+25024G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14634229 | ||||||
chrX:14634241
|
A | AC | 1 | a0001c0001t0001g0083 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.930+25038dupC | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14634241 | |||||
chrX:14634338
|
A | AT | 1 | a0001c0001t0001g0083 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.930+25137dupT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14634338 | |||||
chrX:14634419
|
A | T | 1 | a0001c0002t0043g0191 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.930+25214A>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14634419 | ||||||
chrX:14634559
|
T | TC | 1 | a0001c0001t0001g0083 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.930+25355dupC | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14634559 | |||||
chrX:14634722
|
T | TACAGA | 1 | a0001c0001t0001g0083 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.930+25519_930+2552 others(9): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14634722 | |||||
chrX:14634859
|
A | T | 1 | a0001c0001t0004g0162 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.930+25654A>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14634859 | ||||||
chrX:14635121
|
T | C | 1 | a0001c0001t0014g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.930+25916T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14635121 | ||||||
chrX:14635344
|
T | G | 2 | a0001c0001t0008g0195a0001c0001t0008g0196 | 2 | HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.930+26139T>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14635344 | ||||||
chrX:14635610
|
G | A | 3 | a0001c0002t0046g0179a0001c0003t0026g0176a0001c0003t0027g0182 | 3 | HG01074.hp1 HG02293.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.930+26405G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14635610 | ||||||
chrX:14636192
|
A | C | 1 | a0001c0001t0001g0158 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.930+26987A>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14636192 | ||||||
chrX:14636324
|
C | T | 1 | a0001c0001t0038g0030 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.930+27119C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14636324 | ||||||
chrX:14636327
|
A | T | 43 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0038others(40): Show | 43 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.930+27122A>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14636327 | ||||||
chrX:14636392
|
C | T | 42 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0038others(39): Show | 42 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.930+27187C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14636392 | ||||||
chrX:14636605
|
A | G | 70 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0038others(67): Show | 70 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.930+27400A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14636605 | ||||||
chrX:14636664
|
A | G | 1 | a0001c0001t0017g0078 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.930+27459A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14636664 | ||||||
chrX:14636885
|
A | T | 3 | a0001c0001t0004g0150a0001c0001t0008g0128a0001c0001t0008g0141 | 3 | HG02738.hp1 HG03654.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.930+27680A>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14636885 | ||||||
chrX:14637046
|
A | G | 5 | a0001c0001t0011g0188a0001c0001t0021g0190a0001c0002t0014g0025others(2): Show | 5 | HG02717.hp1 HG02809.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.930+27841A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14637046 | ||||||
chrX:14637516
|
CCA | C | 1 | a0001c0001t0008g0007 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.930+28315_930+2831 others(6): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14637516 | |||||
chrX:14637520
|
AC | A | 3 | a0001c0001t0001g0029a0001c0001t0001g0072a0001c0001t0008g0227 | 3 | HG02132.hp1 HG02683.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.930+28316delC | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14637520 | ||||||
chrX:14637722
|
T | C | 3 | a0001c0001t0009g0032a0001c0001t0018g0033a0001c0001t0018g0080 | 3 | HG02970.hp1 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.930+28517T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14637722 | ||||||
chrX:14638229
|
G | T | 1 | a0001c0001t0001g0158 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.930+29024G>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14638229 | ||||||
chrX:14638941
|
A | G | 1 | a0001c0001t0014g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.930+29736A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14638941 | ||||||
chrX:14638950
|
T | C | 4 | a0001c0001t0002g0163a0001c0001t0002g0165a0001c0001t0002g0166others(1): Show | 4 | HG01081.hp1 HG01099.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.930+29745T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14638950 | ||||||
chrX:14639048
|
G | T | 5 | a0001c0001t0011g0188a0001c0001t0021g0190a0001c0002t0014g0025others(2): Show | 5 | HG02717.hp1 HG02809.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.930+29843G>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14639048 | ||||||
chrX:14639359
|
T | C | 1 | a0001c0001t0008g0227 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.930+30154T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14639359 | ||||||
chrX:14639413
|
A | G | 20 | a0001c0001t0002g0120a0001c0001t0002g0194a0001c0001t0004g0021others(17): Show | 20 | HG01070.hp1 HG01928.hp1 HG01952.hp1 others(17): Show |
intron_variant | MODIFIER | c.930+30208A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14639413 | ||||||
chrX:14639644
|
A | G | 1 | a0001c0001t0002g0101 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.930+30439A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14639644 | ||||||
chrX:14639755
|
ACT | A | 3 | a0001c0001t0009g0032a0001c0001t0018g0033a0001c0001t0018g0080 | 3 | HG02970.hp1 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.930+30554_930+3055 others(6): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14639755 | |||||
chrX:14639791
|
C | T | 230 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(227): Show | 231 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.930+30586C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14639791 | ||||||
chrX:14639897
|
A | C | 18 | a0001c0001t0009g0032a0001c0001t0018g0033a0001c0001t0018g0080others(15): Show | 18 | HG01074.hp1 HG01109.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.930+30692A>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14639897 | ||||||
chrX:14640151
|
A | AT | 1 | a0001c0001t0014g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.930+30956dupT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14640151 | |||||
chrX:14640269
|
C | G | 4 | a0001c0001t0009g0032a0001c0001t0014g0228a0001c0001t0018g0033others(1): Show | 4 | HG02630.hp1 HG02970.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.930+31064C>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14640269 | ||||||
chrX:14640281
|
G | T | 1 | a0001c0001t0014g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.930+31076G>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14640281 | ||||||
chrX:14640481
|
G | A | 13 | a0001c0001t0002g0120a0001c0001t0002g0194a0001c0001t0004g0021others(10): Show | 13 | HG01070.hp1 HG01928.hp1 HG01952.hp1 others(10): Show |
intron_variant | MODIFIER | c.930+31276G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14640481 | ||||||
chrX:14641149
|
A | T | 1 | a0001c0001t0011g0188 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.930+31944A>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14641149 | ||||||
chrX:14641514
|
A | G | 17 | a0001c0001t0002g0120a0001c0001t0002g0194a0001c0001t0004g0021others(14): Show | 17 | HG01070.hp1 HG01928.hp1 HG01952.hp1 others(14): Show |
intron_variant | MODIFIER | c.930+32309A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14641514 | ||||||
chrX:14641945
|
C | T | 5 | a0001c0002t0028g0062a0001c0002t0045g0177a0001c0003t0025g0175others(2): Show | 5 | HG02258.hp1 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.930+32740C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14641945 | ||||||
chrX:14642489
|
T | C | 1 | a0001c0001t0001g0125 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.930+33284T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14642489 | ||||||
chrX:14642595
|
A | AT | 8 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0004g0119others(5): Show | 8 | HG00741.hp1 HG02293.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.930+33403dupT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14642595 | |||||
chrX:14642595
|
A | T | 3 | a0001c0001t0011g0188a0001c0001t0021g0190a0001c0002t0021g0024 | 3 | HG02809.hp2 HG02922.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.930+33390A>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14642595 | ||||||
chrX:14642595
|
AT | A | 1 | a0001c0001t0003g0046 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.930+33403delT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14642595 | |||||
chrX:14642630
|
A | G | 1 | a0001c0001t0014g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.930+33425A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14642630 | ||||||
chrX:14642799
|
G | C | 34 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0038others(31): Show | 34 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.930+33594G>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14642799 | ||||||
chrX:14642803
|
G | C | 1 | a0001c0001t0015g0068 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.930+33598G>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14642803 | ||||||
chrX:14643053
|
G | A | 1 | a0001c0001t0016g0091 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.930+33848G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14643053 | ||||||
chrX:14643237
|
T | C | 1 | a0001c0001t0038g0030 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.930+34032T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14643237 | ||||||
chrX:14643466
|
G | A | 7 | a0001c0002t0007g0022a0001c0002t0007g0023a0001c0002t0007g0192others(4): Show | 7 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.930+34261G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14643466 | ||||||
chrX:14643718
|
C | T | 1 | a0001c0001t0012g0104 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.930+34513C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14643718 | ||||||
chrX:14643970
|
G | A | 1 | a0001c0001t0001g0097 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.930+34765G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14643970 | ||||||
chrX:14644028
|
A | G | 3 | a0001c0001t0002g0034a0001c0001t0038g0030a0001c0001t0044g0193 | 3 | HG02965.hp1 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.930+34823A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14644028 | ||||||
chrX:14644135
|
G | T | 1 | a0001c0001t0020g0207 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.930+34930G>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14644135 | ||||||
chrX:14644559
|
A | G | 2 | a0001c0001t0001g0173a0001c0001t0035g0172 | 2 | NA18948.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.930+35354A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14644559 | ||||||
chrX:14644670
|
C | CT | 1 | a0001c0001t0014g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.930+35472dupT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14644670 | |||||
chrX:14644725
|
A | G | 1 | a0001c0001t0029g0012 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.930+35520A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14644725 | ||||||
chrX:14645180
|
T | C | 3 | a0001c0001t0009g0032a0001c0001t0018g0033a0001c0001t0018g0080 | 3 | HG02970.hp1 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.930+35975T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14645180 | ||||||
chrX:14645387
|
G | T | 1 | a0001c0001t0006g0218 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.930+36182G>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14645387 | ||||||
chrX:14645604
|
A | C | 37 | a0001c0001t0031g0060a0001c0002t0003g0145a0001c0002t0005g0002others(34): Show | 37 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.930+36399A>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14645604 | ||||||
chrX:14646105
|
G | A | 1 | a0001c0001t0014g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.930+36900G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14646105 | ||||||
chrX:14646309
|
A | C | 18 | a0001c0001t0009g0032a0001c0001t0018g0033a0001c0001t0018g0080others(15): Show | 18 | HG01074.hp1 HG01109.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.930+37104A>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14646309 | ||||||
chrX:14646379
|
T | G | 40 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0038others(37): Show | 40 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.930+37174T>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14646379 | ||||||
chrX:14646398
|
CTAATT | C | 2 | a0001c0001t0001g0113a0001c0001t0001g0129 | 2 | HG00323.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.930+37198_930+3720 others(9): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14646398 | |||||
chrX:14646491
|
T | C | 1 | a0001c0002t0014g0026 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.930+37286T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14646491 | ||||||
chrX:14646709
|
G | A | 1 | a0001c0002t0007g0208 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.930+37504G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14646709 | ||||||
chrX:14646921
|
G | A | 3 | a0001c0001t0009g0032a0001c0001t0018g0033a0001c0001t0018g0080 | 3 | HG02970.hp1 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.930+37716G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14646921 | ||||||
chrX:14647204
|
G | T | 3 | a0001c0001t0009g0032a0001c0001t0018g0033a0001c0001t0018g0080 | 3 | HG02970.hp1 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.930+37999G>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14647204 | ||||||
chrX:14647430
|
T | C | 4 | a0001c0001t0009g0032a0001c0001t0014g0228a0001c0001t0018g0033others(1): Show | 4 | HG02630.hp1 HG02970.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.930+38225T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14647430 | ||||||
chrX:14648239
|
C | T | 3 | a0001c0001t0009g0032a0001c0001t0018g0033a0001c0001t0018g0080 | 3 | HG02970.hp1 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.930+39034C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14648239 | ||||||
chrX:14648745
|
A | G | 8 | a0001c0001t0048g0018a0001c0002t0007g0022a0001c0002t0007g0023others(5): Show | 8 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.930+39540A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14648745 | ||||||
chrX:14648995
|
C | A | 1 | a0001c0001t0002g0120 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.930+39790C>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14648995 | ||||||
chrX:14649085
|
G | A | 1 | a0001c0001t0004g0027 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.930+39880G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14649085 | ||||||
chrX:14649214
|
T | TA | 1 | a0001c0001t0014g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.930+40023dupA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14649214 | |||||
chrX:14649214
|
TA | T | 8 | a0001c0001t0001g0036a0001c0001t0001g0113a0001c0001t0002g0089others(5): Show | 8 | HG00323.hp2 HG01257.hp2 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.930+40023delA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14649214 | |||||
chrX:14649215
|
A | T | 6 | a0001c0001t0001g0029a0001c0001t0001g0066a0001c0001t0001g0072others(3): Show | 6 | HG02055.hp1 HG02132.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.930+40010A>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14649215 | ||||||
chrX:14649574
|
T | C | 112 | a0001c0001t0001g0029a0001c0001t0001g0066a0001c0001t0001g0072others(109): Show | 112 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.930+40369T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14649574 | ||||||
chrX:14650032
|
A | G | 1 | a0001c0001t0005g0108 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.931-40678A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14650032 | ||||||
chrX:14650095
|
T | C | 8 | a0001c0001t0007g0079a0001c0001t0010g0070a0001c0001t0010g0071others(5): Show | 8 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.931-40615T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14650095 | ||||||
chrX:14650325
|
C | T | 36 | a0001c0001t0031g0060a0001c0002t0005g0002a0001c0002t0005g0010others(33): Show | 36 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.931-40385C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14650325 | ||||||
chrX:14650341
|
A | G | 37 | a0001c0001t0031g0060a0001c0002t0003g0145a0001c0002t0005g0002others(34): Show | 37 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.931-40369A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14650341 | ||||||
chrX:14650367
|
G | GA | 1 | a0001c0002t0043g0191 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.931-40332dupA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14650367 | |||||
chrX:14650367
|
GA | G | 1 | a0001c0001t0001g0133 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.931-40332delA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14650367 | |||||
chrX:14650618
|
C | CA | 1 | a0001c0001t0017g0169 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.931-40084dupA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14650618 | |||||
chrX:14651138
|
G | T | 2 | a0001c0001t0001g0173a0001c0001t0035g0172 | 2 | NA18948.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.931-39572G>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14651138 | ||||||
chrX:14651451
|
C | T | 41 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0038others(38): Show | 41 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.931-39259C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14651451 | ||||||
chrX:14652039
|
A | T | 1 | a0001c0001t0001g0029 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.931-38671A>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14652039 | ||||||
chrX:14652401
|
C | T | 1 | a0001c0001t0014g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.931-38309C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14652401 | ||||||
chrX:14652465
|
G | A | 3 | a0001c0001t0011g0188a0001c0001t0021g0190a0001c0002t0021g0024 | 3 | HG02809.hp2 HG02922.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.931-38245G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14652465 | ||||||
chrX:14653049
|
G | GA | 1 | a0001c0001t0029g0012 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.931-37650dupA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14653049 | |||||
chrX:14653143
|
A | AT | 1 | a0001c0001t0001g0133 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.931-37558dupT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14653143 | |||||
chrX:14653600
|
C | G | 230 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(227): Show | 231 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.931-37110C>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14653600 | ||||||
chrX:14653632
|
T | C | 1 | a0001c0001t0014g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.931-37078T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14653632 | ||||||
chrX:14654030
|
C | G | 1 | a0001c0001t0001g0133 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.931-36680C>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14654030 | ||||||
chrX:14654050
|
A | G | 37 | a0001c0001t0031g0060a0001c0002t0003g0145a0001c0002t0005g0002others(34): Show | 37 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.931-36660A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14654050 | ||||||
chrX:14654384
|
CTA | C | 1 | a0001c0001t0006g0053 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.931-36324_931-3632 others(6): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14654384 | |||||
chrX:14654527
|
C | G | 1 | a0001c0001t0014g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.931-36183C>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14654527 | ||||||
chrX:14654816
|
A | T | 1 | a0001c0002t0005g0056 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.931-35894A>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14654816 | ||||||
chrX:14655132
|
AAAT | A | 1 | a0001c0001t0014g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.931-35566_931-3556 others(7): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14655132 | |||||
chrX:14655167
|
T | C | 35 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0038others(32): Show | 35 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.931-35543T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14655167 | ||||||
chrX:14655206
|
T | C | 5 | a0001c0001t0001g0029a0001c0001t0001g0072a0001c0001t0001g0187others(2): Show | 5 | HG02132.hp1 HG02683.hp1 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.931-35504T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14655206 | ||||||
chrX:14655393
|
T | TC | 1 | a0001c0001t0004g0202 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.931-35313dupC | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14655393 | |||||
chrX:14655463
|
T | A | 5 | a0001c0001t0001g0029a0001c0001t0001g0072a0001c0001t0001g0187others(2): Show | 5 | HG02132.hp1 HG02683.hp1 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.931-35247T>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14655463 | ||||||
chrX:14655736
|
C | T | 1 | a0001c0001t0008g0230 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.931-34974C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14655736 | ||||||
chrX:14655759
|
CT | C | 34 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0038others(31): Show | 34 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.931-34950delT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14655759 | ||||||
chrX:14655816
|
T | C | 1 | a0001c0001t0001g0187 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.931-34894T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14655816 | ||||||
chrX:14655990
|
T | C | 3 | a0001c0001t0009g0032a0001c0001t0018g0033a0001c0001t0018g0080 | 3 | HG02970.hp1 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.931-34720T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14655990 | ||||||
chrX:14656877
|
C | T | 1 | a0001c0001t0029g0012 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.931-33833C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14656877 | ||||||
chrX:14657236
|
TG | T | 3 | a0001c0001t0009g0032a0001c0001t0018g0033a0001c0001t0018g0080 | 3 | HG02970.hp1 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.931-33470delG | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14657236 | |||||
chrX:14657303
|
A | G | 1 | a0001c0001t0014g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.931-33407A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14657303 | ||||||
chrX:14657468
|
T | G | 3 | a0001c0001t0009g0032a0001c0001t0018g0033a0001c0001t0018g0080 | 3 | HG02970.hp1 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.931-33242T>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14657468 | ||||||
chrX:14657506
|
G | A | 1 | a0001c0001t0008g0227 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.931-33204G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14657506 | ||||||
chrX:14657772
|
G | T | 1 | a0001c0002t0005g0015 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.931-32938G>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14657772 | ||||||
chrX:14658641
|
T | C | 54 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0038others(51): Show | 54 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.931-32069T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14658641 | ||||||
chrX:14658934
|
G | A | 37 | a0001c0001t0031g0060a0001c0002t0003g0145a0001c0002t0005g0002others(34): Show | 37 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.931-31776G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14658934 | ||||||
chrX:14659433
|
T | C | 17 | a0001c0001t0002g0120a0001c0001t0002g0194a0001c0001t0004g0021others(14): Show | 17 | HG01070.hp1 HG01928.hp1 HG01952.hp1 others(14): Show |
intron_variant | MODIFIER | c.931-31277T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14659433 | ||||||
chrX:14659470
|
G | C | 37 | a0001c0001t0031g0060a0001c0002t0003g0145a0001c0002t0005g0002others(34): Show | 37 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.931-31240G>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14659470 | ||||||
chrX:14659471
|
C | CCAA | 37 | a0001c0001t0031g0060a0001c0002t0003g0145a0001c0002t0005g0002others(34): Show | 37 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.931-31239_931-3123 others(7): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14659471 | ||||||
chrX:14659473
|
T | G | 37 | a0001c0001t0031g0060a0001c0002t0003g0145a0001c0002t0005g0002others(34): Show | 37 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.931-31237T>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14659473 | ||||||
chrX:14659676
|
G | A | 7 | a0001c0002t0007g0022a0001c0002t0007g0023a0001c0002t0007g0192others(4): Show | 7 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.931-31034G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14659676 | ||||||
chrX:14659770
|
T | C | 1 | a0001c0001t0003g0046 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.931-30940T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14659770 | ||||||
chrX:14659859
|
A | G | 1 | a0001c0001t0001g0066 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.931-30851A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14659859 | ||||||
chrX:14659895
|
T | C | 3 | a0001c0002t0007g0022a0001c0002t0007g0023a0001c0002t0007g0192 | 3 | HG00733.hp2 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.931-30815T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14659895 | ||||||
chrX:14659964
|
G | A | 1 | a0001c0001t0002g0061 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.931-30746G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14659964 | ||||||
chrX:14660358
|
T | G | 1 | a0001c0005t0006g0095 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.931-30352T>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14660358 | ||||||
chrX:14660373
|
A | C | 36 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0038others(33): Show | 36 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.931-30337A>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14660373 | ||||||
chrX:14660649
|
G | A | 3 | a0001c0001t0009g0032a0001c0001t0018g0033a0001c0001t0018g0080 | 3 | HG02970.hp1 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.931-30061G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14660649 | ||||||
chrX:14660769
|
G | A | 6 | a0001c0001t0001g0029a0001c0001t0001g0066a0001c0001t0001g0072others(3): Show | 6 | HG02055.hp1 HG02132.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.931-29941G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14660769 | ||||||
chrX:14661083
|
G | A | 17 | a0001c0001t0002g0120a0001c0001t0002g0194a0001c0001t0004g0021others(14): Show | 17 | HG01070.hp1 HG01928.hp1 HG01952.hp1 others(14): Show |
intron_variant | MODIFIER | c.931-29627G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14661083 | ||||||
chrX:14661097
|
C | CATGA | 5 | a0001c0001t0002g0194a0001c0001t0004g0164a0001c0001t0004g0220others(2): Show | 5 | HG01070.hp1 HG02615.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.931-29583_931-2958 others(8): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14661097 | |||||
chrX:14661097
|
CATGA | C | 70 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0038others(67): Show | 70 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.931-29583_931-2958 others(8): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14661097 | |||||
chrX:14661492
|
G | GA | 1 | a0001c0001t0014g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.931-29209dupA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14661492 | |||||
chrX:14661506
|
T | C | 1 | a0001c0001t0014g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.931-29204T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14661506 | ||||||
chrX:14661864
|
C | G | 42 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0038others(39): Show | 42 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.931-28846C>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14661864 | ||||||
chrX:14661874
|
G | GA | 86 | a0001c0001t0001g0029a0001c0001t0001g0066a0001c0001t0001g0072others(83): Show | 86 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.931-28818dupA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14661874 | |||||
chrX:14661874
|
GA | G | 4 | a0001c0001t0002g0034a0001c0001t0004g0204a0001c0001t0038g0030others(1): Show | 4 | HG02965.hp1 HG03453.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.931-28818delA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14661874 | |||||
chrX:14662243
|
G | A | 1 | a0001c0001t0029g0012 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.931-28467G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14662243 | ||||||
chrX:14662249
|
A | AACAC | 8 | a0001c0001t0048g0018a0001c0002t0007g0022a0001c0002t0007g0023others(5): Show | 8 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.931-28446_931-2844 others(8): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14662249 | |||||
chrX:14662249
|
AACACAC | A | 2 | a0001c0001t0009g0224a0001c0001t0009g0225 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.931-28448_931-2844 others(10): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14662249 | |||||
chrX:14662671
|
T | C | 2 | a0001c0001t0031g0060a0001c0002t0043g0191 | 2 | HG02630.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.931-28039T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14662671 | ||||||
chrX:14662692
|
C | T | 2 | a0001c0002t0005g0010a0001c0002t0036g0063 | 2 | HG01123.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.931-28018C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14662692 | ||||||
chrX:14662881
|
TTATTA | T | 7 | a0001c0001t0010g0070a0001c0001t0010g0071a0001c0001t0010g0074others(4): Show | 7 | HG01243.hp1 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.931-27827_931-2782 others(9): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14662881 | |||||
chrX:14663006
|
T | C | 7 | a0001c0001t0001g0029a0001c0001t0001g0066a0001c0001t0001g0072others(4): Show | 7 | HG02055.hp1 HG02132.hp1 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.931-27704T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14663006 | ||||||
chrX:14663098
|
T | A | 1 | a0001c0001t0006g0218 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.931-27612T>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14663098 | ||||||
chrX:14663133
|
T | C | 1 | a0001c0001t0001g0187 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.931-27577T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14663133 | ||||||
chrX:14663411
|
G | C | 9 | a0001c0001t0041g0153a0001c0001t0048g0018a0001c0002t0007g0022others(6): Show | 9 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.931-27299G>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14663411 | ||||||
chrX:14663445
|
T | C | 5 | a0001c0001t0044g0193a0001c0002t0023g0065a0001c0002t0023g0186others(2): Show | 5 | HG01109.hp1 HG02109.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.931-27265T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14663445 | ||||||
chrX:14663514
|
A | G | 4 | a0001c0001t0009g0032a0001c0001t0014g0228a0001c0001t0018g0033others(1): Show | 4 | HG02630.hp1 HG02970.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.931-27196A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14663514 | ||||||
chrX:14663516
|
T | TAC | 45 | a0001c0001t0001g0187a0001c0001t0009g0032a0001c0001t0018g0033others(42): Show | 45 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.931-27170_931-2716 others(6): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14663516 | |||||
chrX:14663516
|
T | TACAC | 2 | a0001c0001t0002g0143a0001c0001t0014g0228 | 2 | HG01496.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.931-27172_931-2716 others(8): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14663516 | |||||
chrX:14663689
|
TA | T | 1 | a0001c0001t0002g0194 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.931-27017delA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14663689 | |||||
chrX:14663750
|
T | C | 3 | a0001c0001t0009g0032a0001c0001t0018g0033a0001c0001t0018g0080 | 3 | HG02970.hp1 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.931-26960T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14663750 | ||||||
chrX:14663790
|
G | C | 4 | a0001c0001t0009g0032a0001c0001t0014g0228a0001c0001t0018g0033others(1): Show | 4 | HG02630.hp1 HG02970.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.931-26920G>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14663790 | ||||||
chrX:14664101
|
A | G | 1 | a0001c0001t0001g0105 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.931-26609A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14664101 | ||||||
chrX:14664559
|
T | C | 3 | a0001c0001t0009g0032a0001c0001t0018g0033a0001c0001t0018g0080 | 3 | HG02970.hp1 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.931-26151T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14664559 | ||||||
chrX:14664952
|
A | G | 4 | a0001c0001t0002g0163a0001c0001t0002g0165a0001c0001t0002g0166others(1): Show | 4 | HG01081.hp1 HG01099.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.931-25758A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14664952 | ||||||
chrX:14664981
|
A | C | 7 | a0001c0001t0010g0070a0001c0001t0010g0071a0001c0001t0010g0074others(4): Show | 7 | HG01243.hp1 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.931-25729A>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14664981 | ||||||
chrX:14665444
|
G | A | 6 | a0001c0001t0001g0029a0001c0001t0001g0066a0001c0001t0001g0072others(3): Show | 6 | HG02055.hp1 HG02132.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.931-25266G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14665444 | ||||||
chrX:14665469
|
A | AATT | 3 | a0001c0001t0005g0006a0001c0001t0007g0077a0001c0001t0007g0079 | 3 | HG02145.hp1 HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.931-25237_931-2523 others(7): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14665469 | |||||
chrX:14666056
|
C | CATAATA | 51 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0038others(48): Show | 51 | HG00323.hp1 HG00558.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.931-24651_931-2464 others(10): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14666056 | |||||
chrX:14666090
|
G | A | 3 | a0001c0001t0009g0032a0001c0001t0018g0033a0001c0001t0018g0080 | 3 | HG02970.hp1 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.931-24620G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14666090 | ||||||
chrX:14666796
|
G | A | 1 | a0001c0001t0016g0116 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.931-23914G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14666796 | ||||||
chrX:14666908
|
A | G | 36 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0038others(33): Show | 36 | HG00323.hp1 HG00558.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.931-23802A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14666908 | ||||||
chrX:14667007
|
T | C | 3 | a0001c0001t0009g0032a0001c0001t0018g0033a0001c0001t0018g0080 | 3 | HG02970.hp1 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.931-23703T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14667007 | ||||||
chrX:14667051
|
G | A | 4 | a0001c0001t0009g0032a0001c0001t0014g0228a0001c0001t0018g0033others(1): Show | 4 | HG02630.hp1 HG02970.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.931-23659G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14667051 | ||||||
chrX:14667238
|
A | C | 1 | a0001c0001t0006g0122 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.931-23472A>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14667238 | ||||||
chrX:14667444
|
T | C | 1 | a0001c0001t0014g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.931-23266T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14667444 | ||||||
chrX:14668112
|
T | C | 4 | a0001c0002t0007g0022a0001c0002t0007g0023a0001c0002t0007g0192others(1): Show | 4 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.931-22598T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14668112 | ||||||
chrX:14668778
|
C | T | 18 | a0001c0001t0002g0120a0001c0001t0002g0127a0001c0001t0002g0194others(15): Show | 18 | HG01070.hp1 HG01928.hp1 HG01952.hp1 others(15): Show |
intron_variant | MODIFIER | c.931-21932C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14668778 | ||||||
chrX:14669124
|
A | G | 40 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0038others(37): Show | 40 | HG00323.hp1 HG00558.hp2 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.931-21586A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14669124 | ||||||
chrX:14669176
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.931-21534C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14669176 | ||||||
chrX:14669562
|
TCTTGA | T | 3 | a0001c0001t0009g0032a0001c0001t0018g0033a0001c0001t0018g0080 | 3 | HG02970.hp1 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.931-21144_931-2114 others(9): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14669562 | |||||
chrX:14669593
|
C | G | 8 | a0001c0001t0048g0018a0001c0002t0007g0022a0001c0002t0007g0023others(5): Show | 8 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.931-21117C>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14669593 | ||||||
chrX:14669706
|
C | T | 7 | a0001c0002t0007g0022a0001c0002t0007g0023a0001c0002t0007g0192others(4): Show | 7 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.931-21004C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14669706 | ||||||
chrX:14669996
|
C | T | 1 | a0001c0002t0014g0026 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.931-20714C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14669996 | ||||||
chrX:14670125
|
G | C | 4 | a0001c0001t0009g0032a0001c0001t0014g0228a0001c0001t0018g0033others(1): Show | 4 | HG02630.hp1 HG02970.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.931-20585G>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14670125 | ||||||
chrX:14670177
|
T | C | 1 | a0001c0002t0028g0062 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.931-20533T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14670177 | ||||||
chrX:14670345
|
G | C | 4 | a0001c0001t0009g0032a0001c0001t0014g0228a0001c0001t0018g0033others(1): Show | 4 | HG02630.hp1 HG02970.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.931-20365G>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14670345 | ||||||
chrX:14670371
|
A | C | 1 | a0001c0001t0020g0048 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.931-20339A>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14670371 | ||||||
chrX:14670373
|
C | A | 4 | a0001c0002t0007g0022a0001c0002t0007g0023a0001c0002t0007g0192others(1): Show | 4 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.931-20337C>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14670373 | ||||||
chrX:14670447
|
T | C | 1 | a0001c0001t0002g0101 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.931-20263T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14670447 | ||||||
chrX:14670566
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.931-20144G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14670566 | ||||||
chrX:14670622
|
T | A | 36 | a0001c0001t0014g0228a0001c0002t0003g0145a0001c0002t0005g0002others(33): Show | 36 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.931-20088T>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14670622 | ||||||
chrX:14670740
|
G | A | 1 | a0001c0001t0004g0162 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.931-19970G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14670740 | ||||||
chrX:14670817
|
C | T | 7 | a0001c0002t0007g0022a0001c0002t0007g0023a0001c0002t0007g0192others(4): Show | 7 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.931-19893C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14670817 | ||||||
chrX:14671122
|
C | T | 1 | a0001c0001t0001g0152 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.931-19588C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14671122 | ||||||
chrX:14671321
|
T | C | 1 | a0001c0001t0044g0193 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.931-19389T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14671321 | ||||||
chrX:14671364
|
G | C | 1 | a0001c0001t0006g0218 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.931-19346G>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14671364 | ||||||
chrX:14671447
|
T | A | 1 | a0001c0003t0030g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.931-19263T>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14671447 | ||||||
chrX:14671448
|
A | T | 1 | a0001c0003t0030g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.931-19262A>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14671448 | ||||||
chrX:14671528
|
A | AC | 44 | a0001c0001t0005g0006a0001c0001t0007g0077a0001c0001t0007g0079others(41): Show | 44 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.931-19182_931-1918 others(5): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14671528 | ||||||
chrX:14671626
|
G | T | 15 | a0001c0001t0005g0006a0001c0001t0007g0077a0001c0001t0007g0079others(12): Show | 15 | HG01074.hp1 HG01891.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.931-19084G>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14671626 | ||||||
chrX:14671702
|
G | A | 6 | a0001c0001t0001g0029a0001c0001t0001g0066a0001c0001t0001g0072others(3): Show | 6 | HG02055.hp1 HG02132.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.931-19008G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14671702 | ||||||
chrX:14671751
|
A | G | 5 | a0001c0001t0011g0188a0001c0001t0021g0190a0001c0002t0014g0025others(2): Show | 5 | HG02717.hp1 HG02809.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.931-18959A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14671751 | ||||||
chrX:14671753
|
C | T | 1 | a0001c0001t0002g0151 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.931-18957C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14671753 | ||||||
chrX:14671764
|
A | G | 8 | a0001c0001t0048g0018a0001c0002t0007g0022a0001c0002t0007g0023others(5): Show | 8 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.931-18946A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14671764 | ||||||
chrX:14671989
|
T | C | 92 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0038others(89): Show | 92 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.931-18721T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14671989 | ||||||
chrX:14671993
|
G | T | 1 | a0001c0001t0001g0137 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.931-18717G>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14671993 | ||||||
chrX:14672570
|
G | GT | 44 | a0001c0001t0005g0006a0001c0001t0007g0077a0001c0001t0007g0079others(41): Show | 44 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.931-18133dupT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14672570 | |||||
chrX:14672583
|
A | G | 52 | a0001c0001t0005g0006a0001c0001t0007g0077a0001c0001t0007g0079others(49): Show | 52 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.931-18127A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14672583 | ||||||
chrX:14672789
|
C | T | 1 | a0001c0001t0008g0007 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.931-17921C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14672789 | ||||||
chrX:14672790
|
G | A | 42 | a0001c0001t0005g0006a0001c0001t0007g0077a0001c0001t0009g0032others(39): Show | 42 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.931-17920G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14672790 | ||||||
chrX:14673113
|
A | G | 118 | a0001c0001t0001g0029a0001c0001t0001g0066a0001c0001t0001g0072others(115): Show | 118 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.931-17597A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14673113 | ||||||
chrX:14673369
|
C | T | 1 | a0001c0001t0013g0073 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.931-17341C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14673369 | ||||||
chrX:14673416
|
C | T | 1 | a0001c0002t0005g0015 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.931-17294C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14673416 | ||||||
chrX:14673428
|
T | C | 1 | a0001c0001t0008g0007 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.931-17282T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14673428 | ||||||
chrX:14673634
|
C | T | 4 | a0001c0002t0023g0065a0001c0002t0023g0186a0001c0002t0039g0184others(1): Show | 4 | HG01109.hp1 HG02109.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.931-17076C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14673634 | ||||||
chrX:14673745
|
G | C | 38 | a0001c0001t0005g0006a0001c0001t0007g0077a0001c0001t0007g0079others(35): Show | 38 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.931-16965G>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14673745 | ||||||
chrX:14673814
|
G | A | 1 | a0001c0001t0013g0185 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.931-16896G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14673814 | ||||||
chrX:14673902
|
G | A | 1 | a0001c0001t0031g0060 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.931-16808G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14673902 | ||||||
chrX:14674083
|
T | C | 92 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0038others(89): Show | 92 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.931-16627T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14674083 | ||||||
chrX:14674129
|
C | T | 115 | a0001c0001t0001g0029a0001c0001t0001g0066a0001c0001t0001g0072others(112): Show | 115 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.931-16581C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14674129 | ||||||
chrX:14674138
|
C | G | 43 | a0001c0001t0005g0006a0001c0001t0007g0077a0001c0001t0007g0079others(40): Show | 43 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.931-16572C>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14674138 | ||||||
chrX:14674325
|
A | G | 6 | a0001c0001t0001g0029a0001c0001t0001g0066a0001c0001t0001g0072others(3): Show | 6 | HG02055.hp1 HG02132.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.931-16385A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14674325 | ||||||
chrX:14674350
|
G | C | 3 | a0001c0001t0012g0104a0001c0001t0012g0174a0001c0001t0041g0153 | 3 | HG01106.hp1 HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.931-16360G>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14674350 | ||||||
chrX:14674404
|
G | A | 40 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0038others(37): Show | 40 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.931-16306G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14674404 | ||||||
chrX:14674431
|
T | C | 3 | a0001c0001t0009g0032a0001c0001t0018g0033a0001c0001t0018g0080 | 3 | HG02970.hp1 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.931-16279T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14674431 | ||||||
chrX:14674744
|
CTCTT | C | 1 | a0001c0001t0001g0042 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.931-15958_931-1595 others(8): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14674744 | |||||
chrX:14674760
|
T | TTC | 1 | a0001c0001t0003g0052 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.931-15937_931-1593 others(6): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14674760 | |||||
chrX:14674956
|
T | C | 39 | a0001c0001t0005g0006a0001c0001t0007g0077a0001c0001t0007g0079others(36): Show | 39 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.931-15754T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14674956 | ||||||
chrX:14675094
|
A | G | 19 | a0001c0002t0005g0002a0001c0002t0005g0010a0001c0002t0005g0014others(16): Show | 19 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.931-15616A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14675094 | ||||||
chrX:14675225
|
C | T | 2 | a0001c0001t0001g0001a0001c0001t0001g0008 | 3 | NA18971.hp1 NA19079.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.931-15485C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14675225 | ||||||
chrX:14675563
|
A | T | 12 | a0001c0002t0028g0062a0001c0002t0045g0177a0001c0002t0046g0179others(9): Show | 12 | HG01074.hp1 HG01891.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.931-15147A>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14675563 | ||||||
chrX:14675808
|
C | T | 2 | a0001c0001t0003g0221a0001c0001t0003g0226 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.931-14902C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14675808 | ||||||
chrX:14675912
|
C | T | 2 | a0001c0001t0001g0146a0001c0001t0006g0200 | 2 | HG00558.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.931-14798C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14675912 | ||||||
chrX:14676007
|
T | A | 1 | a0001c0001t0014g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.931-14703T>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14676007 | ||||||
chrX:14676334
|
TAAAG | T | 1 | a0001c0001t0001g0129 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.931-14373_931-1437 others(8): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14676334 | |||||
chrX:14676483
|
C | T | 1 | a0001c0001t0003g0047 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.931-14227C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14676483 | ||||||
chrX:14676990
|
C | T | 1 | a0001c0001t0002g0194 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.931-13720C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14676990 | ||||||
chrX:14677464
|
C | T | 1 | a0001c0001t0029g0012 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.931-13246C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14677464 | ||||||
chrX:14677875
|
GTTTGTT | G | 1 | a0001c0002t0005g0010 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.931-12824_931-1281 others(10): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14677875 | |||||
chrX:14678037
|
G | T | 3 | a0001c0001t0020g0048a0001c0001t0020g0207a0001c0002t0003g0145 | 3 | HG00323.hp1 HG01358.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.931-12673G>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14678037 | ||||||
chrX:14678066
|
G | A | 1 | a0001c0002t0036g0063 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.931-12644G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14678066 | ||||||
chrX:14678250
|
G | A | 3 | a0001c0001t0009g0032a0001c0001t0018g0033a0001c0001t0018g0080 | 3 | HG02970.hp1 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.931-12460G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14678250 | ||||||
chrX:14678705
|
G | C | 1 | a0001c0001t0001g0113 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.931-12005G>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14678705 | ||||||
chrX:14678709
|
G | C | 17 | a0001c0001t0002g0120a0001c0001t0002g0194a0001c0001t0004g0021others(14): Show | 17 | HG01070.hp1 HG01928.hp1 HG01952.hp1 others(14): Show |
intron_variant | MODIFIER | c.931-12001G>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14678709 | ||||||
chrX:14678848
|
G | A | 1 | a0001c0001t0008g0196 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.931-11862G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14678848 | ||||||
chrX:14678930
|
G | A | 3 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0102 | 3 | NA18977.hp1 NA19005.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.931-11780G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14678930 | ||||||
chrX:14679100
|
A | ACAC | 1 | a0001c0001t0003g0039 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.931-11584_931-1158 others(7): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14679100 | |||||
chrX:14679340
|
C | T | 3 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0047 | 3 | HG03017.hp1 HG04184.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.931-11370C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14679340 | ||||||
chrX:14679427
|
T | TA | 41 | a0001c0001t0002g0127a0001c0001t0004g0202a0001c0001t0005g0006others(38): Show | 41 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.931-11272dupA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14679427 | |||||
chrX:14679427
|
TA | T | 1 | a0001c0001t0003g0044 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.931-11272delA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14679427 | |||||
chrX:14679446
|
A | AAAAG | 44 | a0001c0001t0005g0006a0001c0001t0007g0077a0001c0001t0007g0079others(41): Show | 44 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.931-11262_931-1125 others(8): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14679446 | |||||
chrX:14679583
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.931-11127C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14679583 | ||||||
chrX:14679614
|
T | C | 1 | a0001c0001t0003g0051 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.931-11096T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14679614 | ||||||
chrX:14679649
|
C | T | 1 | a0001c0002t0007g0208 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.931-11061C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14679649 | ||||||
chrX:14680209
|
C | G | 1 | a0001c0001t0001g0129 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.931-10501C>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14680209 | ||||||
chrX:14680345
|
G | C | 1 | a0001c0001t0002g0061 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.931-10365G>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14680345 | ||||||
chrX:14680370
|
ATATGC | A | 114 | a0001c0001t0001g0029a0001c0001t0001g0066a0001c0001t0001g0072others(111): Show | 114 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.931-10334_931-1033 others(9): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14680370 | |||||
chrX:14680782
|
G | T | 6 | a0001c0001t0001g0029a0001c0001t0001g0066a0001c0001t0001g0072others(3): Show | 6 | HG02055.hp1 HG02132.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.931-9928G>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14680782 | ||||||
chrX:14680801
|
G | A | 117 | a0001c0001t0001g0029a0001c0001t0001g0066a0001c0001t0001g0072others(114): Show | 117 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.931-9909G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14680801 | ||||||
chrX:14680802
|
A | T | 44 | a0001c0001t0005g0006a0001c0001t0007g0077a0001c0001t0007g0079others(41): Show | 44 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.931-9908A>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14680802 | ||||||
chrX:14680861
|
T | C | 90 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0038others(87): Show | 90 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.931-9849T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14680861 | ||||||
chrX:14680869
|
T | C | 1 | a0001c0002t0043g0191 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.931-9841T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14680869 | ||||||
chrX:14681352
|
GCTTT | G | 1 | a0001c0002t0023g0065 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.931-9354_931-9351d others(6): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14681352 | |||||
chrX:14681381
|
AATTC | A | 1 | a0001c0001t0004g0204 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.931-9315_931-9312d others(6): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14681381 | |||||
chrX:14681457
|
T | C | 40 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0038others(37): Show | 40 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.931-9253T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14681457 | ||||||
chrX:14681547
|
G | T | 12 | a0001c0002t0028g0062a0001c0002t0045g0177a0001c0002t0046g0179others(9): Show | 12 | HG01074.hp1 HG01891.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.931-9163G>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14681547 | ||||||
chrX:14681612
|
C | T | 1 | a0001c0001t0029g0012 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.931-9098C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14681612 | ||||||
chrX:14681613
|
G | A | 1 | a0001c0001t0014g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.931-9097G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14681613 | ||||||
chrX:14681866
|
TG | T | 1 | a0001c0001t0002g0093 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.931-8841delG | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14681866 | |||||
chrX:14681891
|
C | CA | 6 | a0001c0001t0001g0084a0001c0001t0002g0096a0001c0001t0004g0119others(3): Show | 6 | HG02300.hp1 NA18944.hp1 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.931-8799dupA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14681891 | |||||
chrX:14681891
|
C | CAA | 1 | a0001c0001t0019g0131 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.931-8800_931-8799d others(4): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14681891 | |||||
chrX:14681891
|
CA | C | 18 | a0001c0001t0001g0011a0001c0001t0001g0187a0001c0001t0002g0222others(15): Show | 18 | HG00733.hp1 HG00733.hp2 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.931-8799delA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14681891 | |||||
chrX:14681891
|
CAA | C | 5 | a0001c0001t0001g0029a0001c0001t0001g0066a0001c0001t0008g0007others(2): Show | 5 | HG02055.hp1 HG02109.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.931-8800_931-8799d others(4): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14681891 | |||||
chrX:14681904
|
A | AT | 2 | a0001c0001t0008g0230a0001c0001t0008g0231 | 2 | HG02886.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.931-8806_931-8805i others(3): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14681904 | ||||||
chrX:14681904
|
A | ATAT | 2 | a0001c0001t0008g0195a0001c0001t0008g0196 | 2 | HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.931-8806_931-8805i others(5): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14681904 | ||||||
chrX:14681904
|
A | ATATATAT others(4): Show |
4 | a0001c0002t0005g0014a0001c0002t0005g0015a0001c0002t0007g0013others(1): Show | 4 | HG03139.hp1 HG03516.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.931-8806_931-8805i others(13): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14681904 | ||||||
chrX:14681904
|
A | ATATATAT others(30): Show |
1 | a0001c0001t0003g0229 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.931-8806_931-8805i others(39): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14681904 | ||||||
chrX:14681904
|
A | T | 1 | a0001c0001t0004g0197 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.931-8806A>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14681904 | ||||||
chrX:14681906
|
A | AATATATA others(1): Show |
1 | a0001c0002t0014g0026 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.931-8803_931-8802i others(10): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14681906 | |||||
chrX:14681906
|
A | AATATATA others(17): Show |
1 | a0001c0001t0020g0207 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.931-8803_931-8802i others(26): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14681906 | |||||
chrX:14681906
|
A | AT | 4 | a0001c0001t0002g0034a0001c0001t0002g0194a0001c0001t0003g0041others(1): Show | 4 | HG02615.hp2 HG03239.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.931-8804_931-8803i others(3): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14681906 | ||||||
chrX:14681906
|
A | ATATATAT | 1 | a0001c0002t0014g0025 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.931-8804_931-8803i others(9): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14681906 | ||||||
chrX:14681906
|
A | ATATATAT others(8): Show |
1 | a0001c0004t0007g0094 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.931-8804_931-8803i others(17): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14681906 | ||||||
chrX:14681906
|
A | ATATATAT others(12): Show |
3 | a0001c0001t0003g0035a0001c0001t0003g0039a0001c0001t0003g0049 | 3 | HG00558.hp2 HG01496.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.931-8804_931-8803i others(21): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14681906 | ||||||
chrX:14681906
|
A | ATATATAT others(18): Show |
1 | a0001c0001t0003g0051 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.931-8804_931-8803i others(27): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14681906 | ||||||
chrX:14681906
|
A | ATATATAT others(20): Show |
1 | a0001c0001t0003g0052 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.931-8804_931-8803i others(29): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14681906 | ||||||
chrX:14681906
|
A | ATATATAT others(24): Show |
2 | a0001c0001t0003g0221a0001c0001t0003g0226 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.931-8804_931-8803i others(33): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14681906 | ||||||
chrX:14681906
|
A | T | 12 | a0001c0001t0003g0229a0001c0001t0004g0027a0001c0001t0004g0069others(9): Show | 12 | HG02451.hp1 HG02886.hp1 HG02970.hp2 others(9): Show |
intron_variant | MODIFIER | c.931-8804A>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14681906 | ||||||
chrX:14681908
|
A | AATATATA others(7): Show |
2 | a0001c0001t0003g0043a0001c0001t0005g0057 | 2 | HG01361.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.931-8801_931-8800i others(16): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14681908 | |||||
chrX:14681908
|
A | AATATATA others(9): Show |
2 | a0001c0001t0003g0044a0001c0001t0003g0045 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.931-8801_931-8800i others(18): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14681908 | |||||
chrX:14681908
|
A | AT | 2 | a0001c0001t0038g0030a0001c0001t0044g0193 | 2 | HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.931-8802_931-8801i others(3): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14681908 | ||||||
chrX:14681908
|
A | ATATATAT | 3 | a0001c0001t0011g0188a0001c0001t0021g0190a0001c0002t0021g0024 | 3 | HG02809.hp2 HG02922.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.931-8802_931-8801i others(9): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14681908 | ||||||
chrX:14681908
|
A | ATATATAT others(8): Show |
2 | a0001c0001t0003g0046a0001c0001t0003g0206 | 2 | HG00639.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.931-8802_931-8801i others(17): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14681908 | ||||||
chrX:14681908
|
A | ATATATAT others(12): Show |
2 | a0001c0001t0003g0037a0001c0001t0003g0047 | 2 | HG03017.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.931-8802_931-8801i others(21): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14681908 | ||||||
chrX:14681908
|
A | ATATATAT others(16): Show |
1 | a0001c0002t0003g0145 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.931-8802_931-8801i others(25): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14681908 | ||||||
chrX:14681908
|
A | ATATATAT others(18): Show |
3 | a0001c0001t0003g0055a0001c0001t0003g0139a0001c0001t0020g0048 | 3 | HG00609.hp1 HG01981.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.931-8802_931-8801i others(27): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14681908 | ||||||
chrX:14681908
|
A | ATATATAT others(24): Show |
1 | a0001c0001t0003g0054 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.931-8802_931-8801i others(33): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14681908 | ||||||
chrX:14681908
|
A | ATATATAT others(26): Show |
1 | a0001c0001t0003g0136 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.931-8802_931-8801i others(35): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14681908 | ||||||
chrX:14681908
|
A | T | 37 | a0001c0001t0002g0034a0001c0001t0002g0120a0001c0001t0002g0194others(34): Show | 37 | HG00323.hp1 HG00558.hp2 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.931-8802A>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14681908 | ||||||
chrX:14681910
|
A | AAAAAAAA others(20): Show |
1 | a0001c0002t0028g0062 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.931-8799_931-8798i others(29): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14681910 | |||||
chrX:14681910
|
A | AAAAAAAA others(21): Show |
6 | a0001c0002t0046g0179a0001c0003t0026g0176a0001c0003t0026g0180others(3): Show | 6 | HG01074.hp1 HG02293.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.931-8799_931-8798i others(30): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14681910 | |||||
chrX:14681910
|
A | AAAAAAAA others(25): Show |
1 | a0001c0002t0023g0186 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.931-8799_931-8798i others(34): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14681910 | |||||
chrX:14681910
|
A | AAAAAAAA others(20): Show |
5 | a0001c0001t0005g0006a0001c0001t0007g0077a0001c0002t0045g0177others(2): Show | 5 | HG02572.hp1 HG02647.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.931-8799_931-8798i others(29): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14681910 | |||||
chrX:14681910
|
A | AAAAAAAA others(19): Show |
1 | a0001c0004t0032g0005 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.931-8799_931-8798i others(28): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14681910 | |||||
chrX:14681910
|
A | AAAAAAAA others(21): Show |
1 | a0001c0002t0047g0183 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.931-8799_931-8798i others(30): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14681910 | |||||
chrX:14681910
|
A | AAAAAAAA others(25): Show |
1 | a0001c0002t0007g0208 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.931-8799_931-8798i others(34): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14681910 | |||||
chrX:14681910
|
A | AAAAAAAA others(20): Show |
1 | a0001c0002t0023g0065 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.931-8799_931-8798i others(29): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14681910 | |||||
chrX:14681910
|
A | AAAAAAAA others(22): Show |
1 | a0001c0002t0005g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.931-8799_931-8798i others(31): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14681910 | |||||
chrX:14681910
|
A | AAAAAAAA others(24): Show |
6 | a0001c0002t0005g0010a0001c0002t0005g0213a0001c0002t0007g0114others(3): Show | 6 | HG01123.hp1 HG01433.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.931-8799_931-8798i others(33): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14681910 | |||||
chrX:14681910
|
A | AAAAAAAA others(23): Show |
1 | a0001c0002t0005g0215 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.931-8799_931-8798i others(32): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14681910 | |||||
chrX:14681910
|
A | AAAAAAAT others(4): Show |
2 | a0001c0001t0009g0032a0001c0001t0018g0033 | 2 | HG02970.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.931-8799_931-8798i others(13): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14681910 | |||||
chrX:14681910
|
A | AAAAAAAT others(12): Show |
1 | a0001c0001t0031g0060 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.931-8799_931-8798i others(21): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14681910 | |||||
chrX:14681910
|
A | AAAAAAAT others(24): Show |
5 | a0001c0002t0005g0056a0001c0002t0005g0205a0001c0002t0005g0214others(2): Show | 5 | HG00280.hp1 HG01256.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.931-8799_931-8798i others(33): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14681910 | |||||
chrX:14681910
|
A | AAAAAATA others(5): Show |
1 | a0001c0001t0018g0080 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.931-8799_931-8798i others(14): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14681910 | |||||
chrX:14681910
|
A | AAAAAATA others(25): Show |
1 | a0001c0002t0011g0217 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.931-8799_931-8798i others(34): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14681910 | |||||
chrX:14681910
|
A | AAAAATAT others(4): Show |
2 | a0001c0001t0010g0071a0001c0001t0010g0074 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.931-8799_931-8798i others(13): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14681910 | |||||
chrX:14681910
|
A | AAAAATAT others(8): Show |
1 | a0001c0001t0049g0075 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.931-8799_931-8798i others(17): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14681910 | |||||
chrX:14681910
|
A | AAAAATAT others(10): Show |
1 | a0001c0001t0013g0185 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.931-8799_931-8798i others(19): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14681910 | |||||
chrX:14681910
|
A | AAAATATA others(5): Show |
1 | a0001c0001t0010g0070 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.931-8799_931-8798i others(14): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14681910 | |||||
chrX:14681910
|
A | AAAATATA others(17): Show |
1 | a0001c0002t0043g0191 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.931-8799_931-8798i others(26): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14681910 | |||||
chrX:14681910
|
A | AAATATAT others(8): Show |
1 | a0001c0001t0013g0199 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.931-8799_931-8798i others(17): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14681910 | |||||
chrX:14681910
|
A | AAATATAT others(10): Show |
1 | a0001c0001t0007g0079 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.931-8799_931-8798i others(19): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14681910 | |||||
chrX:14681910
|
A | AAATATAT others(12): Show |
1 | a0001c0001t0013g0073 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.931-8799_931-8798i others(21): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14681910 | |||||
chrX:14681910
|
A | AAT | 1 | a0001c0001t0001g0158 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.931-8781_931-8780d others(4): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14681910 | |||||
chrX:14681910
|
A | AT | 4 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0105others(1): Show | 5 | HG00621.hp1 NA18971.hp1 NA19079.hp1 others(2): Show |
intron_variant | MODIFIER | c.931-8800_931-8799i others(3): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14681910 | ||||||
chrX:14681910
|
A | ATATATAT others(18): Show |
1 | a0001c0001t0015g0068 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.931-8800_931-8799i others(27): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14681910 | ||||||
chrX:14681910
|
A | ATATATAT others(28): Show |
1 | a0001c0001t0003g0038 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.931-8800_931-8799i others(37): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14681910 | ||||||
chrX:14681910
|
A | T | 71 | a0001c0001t0001g0066a0001c0001t0001g0146a0001c0001t0001g0170others(68): Show | 71 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.931-8800A>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14681910 | ||||||
chrX:14681910
|
AAT | A | 2 | a0001c0001t0001g0072a0001c0001t0048g0018 | 2 | HG02132.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.931-8781_931-8780d others(4): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14681910 | |||||
chrX:14681911
|
A | AAAAAAAA others(46): Show |
1 | a0001c0001t0014g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.931-8799_931-8798i others(55): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14681911 | ||||||
chrX:14681911
|
A | AAAAAAAA others(23): Show |
1 | a0001c0002t0039g0184 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.931-8799_931-8798i others(32): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14681911 | ||||||
chrX:14681911
|
A | AAAAAAAA others(21): Show |
1 | a0001c0003t0007g0067 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.931-8799_931-8798i others(30): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14681911 | ||||||
chrX:14681912
|
T | A | 11 | a0001c0001t0001g0173a0001c0001t0006g0092a0001c0001t0006g0134others(8): Show | 11 | HG00642.hp1 HG00738.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.931-8798T>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14681912 | ||||||
chrX:14681913
|
A | G | 35 | a0001c0001t0005g0006a0001c0001t0007g0077a0001c0002t0005g0002others(32): Show | 35 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.931-8797A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14681913 | ||||||
chrX:14681913
|
AT | A | 1 | a0001c0001t0002g0093 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.931-8796delT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14681913 | ||||||
chrX:14681914
|
T | A | 3 | a0001c0001t0012g0104a0001c0001t0012g0174a0001c0001t0041g0153 | 3 | HG01106.hp1 HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.931-8796T>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14681914 | ||||||
chrX:14681935
|
A | G | 36 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0038others(33): Show | 36 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.931-8775A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14681935 | ||||||
chrX:14681939
|
ATG | A | 1 | a0001c0001t0002g0093 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.931-8761_931-8760d others(4): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14681939 | |||||
chrX:14681945
|
G | C | 1 | a0001c0001t0002g0149 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.931-8765G>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14681945 | ||||||
chrX:14681993
|
G | GTA | 14 | a0001c0001t0005g0006a0001c0001t0007g0077a0001c0002t0028g0062others(11): Show | 14 | HG01074.hp1 HG01891.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.931-8715_931-8714d others(4): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14681993 | |||||
chrX:14681995
|
A | ATG | 42 | a0001c0001t0004g0220a0001c0001t0006g0117a0001c0001t0007g0079others(39): Show | 42 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.931-8699_931-8698d others(4): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14681995 | |||||
chrX:14681995
|
ATG | A | 10 | a0001c0001t0001g0029a0001c0001t0001g0072a0001c0001t0001g0187others(7): Show | 10 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.931-8699_931-8698d others(4): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14681995 | |||||
chrX:14682021
|
A | G | 1 | a0001c0002t0005g0056 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.931-8689A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14682021 | ||||||
chrX:14682105
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.931-8605T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14682105 | ||||||
chrX:14682154
|
G | A | 1 | a0001c0002t0028g0062 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.931-8556G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14682154 | ||||||
chrX:14682209
|
A | G | 1 | a0001c0001t0014g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.931-8501A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14682209 | ||||||
chrX:14682263
|
G | C | 1 | a0001c0001t0029g0012 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.931-8447G>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14682263 | ||||||
chrX:14682334
|
T | C | 97 | a0001c0001t0001g0029a0001c0001t0001g0066a0001c0001t0001g0072others(94): Show | 97 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.931-8376T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14682334 | ||||||
chrX:14682373
|
C | T | 28 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0038others(25): Show | 28 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.931-8337C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14682373 | ||||||
chrX:14682551
|
CT | C | 1 | a0001c0001t0002g0034 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.931-8148delT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14682551 | |||||
chrX:14682583
|
G | T | 15 | a0001c0002t0005g0002a0001c0002t0005g0010a0001c0002t0005g0056others(12): Show | 15 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.931-8127G>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14682583 | ||||||
chrX:14682701
|
T | TC | 1 | a0001c0001t0002g0163 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.931-8003dupC | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14682701 | |||||
chrX:14682754
|
A | G | 20 | a0001c0001t0002g0120a0001c0001t0002g0194a0001c0001t0004g0021others(17): Show | 20 | HG01070.hp1 HG01928.hp1 HG01952.hp1 others(17): Show |
intron_variant | MODIFIER | c.931-7956A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14682754 | ||||||
chrX:14682855
|
G | C | 90 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0038others(87): Show | 90 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.931-7855G>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14682855 | ||||||
chrX:14682949
|
A | G | 1 | a0001c0001t0029g0012 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.931-7761A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14682949 | ||||||
chrX:14682953
|
A | T | 1 | a0001c0001t0029g0012 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.931-7757A>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14682953 | ||||||
chrX:14682963
|
G | A | 1 | a0001c0001t0029g0012 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.931-7747G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14682963 | ||||||
chrX:14682964
|
A | G | 1 | a0001c0001t0029g0012 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.931-7746A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14682964 | ||||||
chrX:14682968
|
G | C | 1 | a0001c0001t0029g0012 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.931-7742G>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14682968 | ||||||
chrX:14683179
|
T | C | 40 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0038others(37): Show | 40 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.931-7531T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14683179 | ||||||
chrX:14683181
|
T | C | 1 | a0001c0002t0010g0031 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.931-7529T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14683181 | ||||||
chrX:14683314
|
G | T | 88 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0038others(85): Show | 88 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.931-7396G>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14683314 | ||||||
chrX:14683341
|
A | G | 5 | a0001c0001t0009g0032a0001c0001t0018g0033a0001c0001t0018g0080others(2): Show | 5 | HG02630.hp2 HG02886.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.931-7369A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14683341 | ||||||
chrX:14683359
|
G | C | 4 | a0001c0001t0002g0157a0001c0001t0006g0092a0001c0001t0006g0130others(1): Show | 4 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(1): Show |
intron_variant | MODIFIER | c.931-7351G>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14683359 | ||||||
chrX:14683363
|
C | A | 1 | a0001c0001t0002g0098 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.931-7347C>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14683363 | ||||||
chrX:14683364
|
T | G | 1 | a0001c0001t0002g0098 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.931-7346T>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14683364 | ||||||
chrX:14683438
|
TG | T | 1 | a0001c0001t0002g0093 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.931-7270delG | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14683438 | |||||
chrX:14683664
|
G | T | 7 | a0001c0001t0010g0070a0001c0001t0010g0071a0001c0001t0010g0074others(4): Show | 7 | HG01243.hp1 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.931-7046G>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14683664 | ||||||
chrX:14684014
|
GA | G | 1 | a0001c0001t0002g0093 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.931-6694delA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14684014 | |||||
chrX:14684068
|
G | A | 91 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0038others(88): Show | 91 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.931-6642G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14684068 | ||||||
chrX:14684092
|
T | C | 1 | a0001c0001t0009g0223 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.931-6618T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14684092 | ||||||
chrX:14684153
|
C | T | 4 | a0001c0002t0005g0205a0001c0002t0005g0213a0001c0002t0005g0214others(1): Show | 4 | HG00280.hp1 HG01261.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.931-6557C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14684153 | ||||||
chrX:14684203
|
GT | G | 1 | a0001c0001t0002g0093 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.931-6503delT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14684203 | |||||
chrX:14684234
|
T | C | 125 | a0001c0001t0001g0029a0001c0001t0001g0066a0001c0001t0001g0072others(122): Show | 125 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.931-6476T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14684234 | ||||||
chrX:14684252
|
T | C | 26 | a0001c0001t0002g0120a0001c0001t0002g0194a0001c0001t0004g0021others(23): Show | 26 | HG01070.hp1 HG01106.hp1 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.931-6458T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14684252 | ||||||
chrX:14684276
|
T | A | 1 | a0001c0001t0004g0164 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.931-6434T>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14684276 | ||||||
chrX:14684376
|
G | T | 2 | a0001c0001t0001g0147a0001c0001t0002g0143 | 2 | HG01496.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.931-6334G>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14684376 | ||||||
chrX:14684393
|
TA | T | 1 | a0001c0001t0002g0093 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.931-6314delA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14684393 | |||||
chrX:14684407
|
C | A | 3 | a0001c0001t0004g0150a0001c0001t0008g0128a0001c0001t0008g0141 | 3 | HG02738.hp1 HG03654.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.931-6303C>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14684407 | ||||||
chrX:14684452
|
TG | T | 1 | a0001c0001t0002g0093 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.931-6256delG | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14684452 | |||||
chrX:14684703
|
A | G | 4 | a0001c0002t0005g0014a0001c0002t0005g0015a0001c0002t0007g0013others(1): Show | 4 | HG03139.hp1 HG03516.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.931-6007A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14684703 | ||||||
chrX:14684713
|
T | G | 118 | a0001c0001t0001g0029a0001c0001t0001g0066a0001c0001t0001g0072others(115): Show | 118 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.931-5997T>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14684713 | ||||||
chrX:14684754
|
T | C | 4 | a0001c0001t0009g0064a0001c0001t0009g0223a0001c0001t0009g0224others(1): Show | 4 | HG01070.hp2 HG01071.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.931-5956T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14684754 | ||||||
chrX:14684924
|
C | T | 4 | a0001c0002t0007g0022a0001c0002t0007g0023a0001c0002t0007g0192others(1): Show | 4 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.931-5786C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14684924 | ||||||
chrX:14684936
|
G | T | 1 | a0001c0001t0001g0171 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.931-5774G>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14684936 | ||||||
chrX:14684950
|
GT | G | 1 | a0001c0001t0002g0093 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.931-5757delT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14684950 | |||||
chrX:14684986
|
TC | T | 1 | a0001c0001t0002g0093 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.931-5721delC | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14684986 | |||||
chrX:14685001
|
AT | A | 1 | a0001c0001t0002g0093 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.931-5706delT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14685001 | |||||
chrX:14685043
|
CA | C | 1 | a0001c0001t0002g0093 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.931-5664delA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14685043 | |||||
chrX:14685105
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.931-5605C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14685105 | ||||||
chrX:14685160
|
T | G | 1 | a0001c0001t0004g0220 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.931-5550T>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14685160 | ||||||
chrX:14685183
|
G | A | 1 | a0001c0002t0007g0209 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.931-5527G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14685183 | ||||||
chrX:14685228
|
T | C | 36 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0038others(33): Show | 36 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.931-5482T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14685228 | ||||||
chrX:14685245
|
G | A | 12 | a0001c0001t0009g0032a0001c0001t0018g0033a0001c0001t0018g0080others(9): Show | 12 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.931-5465G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14685245 | ||||||
chrX:14685277
|
CT | C | 1 | a0001c0001t0002g0093 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.931-5426delT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14685277 | |||||
chrX:14685316
|
C | T | 43 | a0001c0001t0005g0006a0001c0001t0007g0077a0001c0001t0007g0079others(40): Show | 43 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.931-5394C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14685316 | ||||||
chrX:14685411
|
C | T | 2 | a0001c0001t0031g0060a0001c0002t0043g0191 | 2 | HG02630.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.931-5299C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14685411 | ||||||
chrX:14685615
|
T | C | 1 | a0001c0001t0002g0194 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.931-5095T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14685615 | ||||||
chrX:14685652
|
C | T | 1 | a0001c0001t0004g0220 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.931-5058C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14685652 | ||||||
chrX:14685671
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.931-5039G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14685671 | ||||||
chrX:14685776
|
T | C | 41 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0038others(38): Show | 41 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.931-4934T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14685776 | ||||||
chrX:14685779
|
AT | A | 1 | a0001c0001t0002g0093 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.931-4925delT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14685779 | |||||
chrX:14685800
|
G | A | 1 | a0001c0001t0008g0140 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.931-4910G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14685800 | ||||||
chrX:14685908
|
T | G | 1 | a0001c0001t0003g0051 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.931-4802T>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14685908 | ||||||
chrX:14686023
|
A | G | 38 | a0001c0001t0005g0006a0001c0001t0007g0077a0001c0001t0007g0079others(35): Show | 38 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.931-4687A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14686023 | ||||||
chrX:14686061
|
C | T | 1 | a0001c0001t0014g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.931-4649C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14686061 | ||||||
chrX:14686141
|
C | T | 1 | a0001c0001t0031g0060 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.931-4569C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14686141 | ||||||
chrX:14686267
|
G | C | 1 | a0001c0001t0002g0143 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.931-4443G>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14686267 | ||||||
chrX:14686667
|
C | G | 2 | a0001c0001t0008g0195a0001c0001t0008g0196 | 2 | HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.931-4043C>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14686667 | ||||||
chrX:14686833
|
C | T | 49 | a0001c0001t0005g0006a0001c0001t0007g0077a0001c0001t0009g0032others(46): Show | 49 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.931-3877C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14686833 | ||||||
chrX:14686857
|
T | C | 37 | a0001c0001t0005g0006a0001c0001t0007g0077a0001c0001t0007g0079others(34): Show | 37 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.931-3853T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14686857 | ||||||
chrX:14686883
|
G | A | 3 | a0001c0001t0009g0032a0001c0001t0018g0033a0001c0001t0018g0080 | 3 | HG02970.hp1 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.931-3827G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14686883 | ||||||
chrX:14687093
|
GT | G | 1 | a0001c0001t0002g0093 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.931-3615delT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14687093 | |||||
chrX:14687176
|
G | T | 7 | a0001c0002t0007g0022a0001c0002t0007g0023a0001c0002t0007g0192others(4): Show | 7 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.931-3534G>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14687176 | ||||||
chrX:14687258
|
T | C | 2 | a0001c0001t0020g0048a0001c0001t0020g0207 | 2 | HG00323.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.931-3452T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14687258 | ||||||
chrX:14687322
|
C | T | 25 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0038others(22): Show | 25 | HG00558.hp2 HG00609.hp1 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.931-3388C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14687322 | ||||||
chrX:14687591
|
C | T | 7 | a0001c0002t0007g0022a0001c0002t0007g0023a0001c0002t0007g0192others(4): Show | 7 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.931-3119C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14687591 | ||||||
chrX:14688235
|
C | T | 38 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0038others(35): Show | 38 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.931-2475C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14688235 | ||||||
chrX:14688334
|
A | G | 1 | a0001c0001t0019g0131 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.931-2376A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14688334 | ||||||
chrX:14688383
|
T | C | 12 | a0001c0001t0001g0097a0001c0001t0002g0019a0001c0001t0002g0020others(9): Show | 12 | HG04184.hp2 NA18955.hp1 NA18965.hp1 others(9): Show |
intron_variant | MODIFIER | c.931-2327T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14688383 | ||||||
chrX:14688468
|
C | T | 41 | a0001c0001t0009g0032a0001c0001t0014g0228a0001c0001t0018g0033others(38): Show | 41 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.931-2242C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14688468 | ||||||
chrX:14688775
|
C | T | 48 | a0001c0001t0009g0032a0001c0001t0014g0228a0001c0001t0018g0033others(45): Show | 48 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.931-1935C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14688775 | ||||||
chrX:14688776
|
C | T | 36 | a0001c0001t0014g0228a0001c0002t0005g0002a0001c0002t0005g0010others(33): Show | 36 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.931-1934C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14688776 | ||||||
chrX:14688788
|
G | T | 1 | a0001c0002t0043g0191 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.931-1922G>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14688788 | ||||||
chrX:14688887
|
G | A | 1 | a0001c0001t0010g0085 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.931-1823G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14688887 | ||||||
chrX:14688890
|
G | A | 1 | a0001c0001t0014g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.931-1820G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14688890 | ||||||
chrX:14689040
|
G | A | 94 | a0001c0001t0001g0029a0001c0001t0001g0066a0001c0001t0001g0072others(91): Show | 94 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.931-1670G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14689040 | ||||||
chrX:14689166
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.931-1544G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14689166 | ||||||
chrX:14689959
|
T | C | 4 | a0001c0001t0002g0163a0001c0001t0002g0165a0001c0001t0002g0166others(1): Show | 4 | HG01081.hp1 HG01099.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.931-751T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14689959 | ||||||
chrX:14690096
|
A | T | 5 | a0001c0001t0009g0032a0001c0001t0018g0033a0001c0001t0018g0080others(2): Show | 5 | HG02630.hp2 HG02886.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.931-614A>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14690096 | ||||||
chrX:14690373
|
G | A | 1 | a0001c0001t0003g0051 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.931-337G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14690373 | ||||||
chrX:14690498
|
G | A | 114 | a0001c0001t0001g0029a0001c0001t0001g0066a0001c0001t0001g0072others(111): Show | 114 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.931-212G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14690498 | ||||||
chrX:14690516
|
T | C | 5 | a0001c0001t0009g0032a0001c0001t0018g0033a0001c0001t0018g0080others(2): Show | 5 | HG02630.hp2 HG02886.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.931-194T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14690516 | ||||||
chrX:14690649
|
T | C | 1 | a0001c0001t0014g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.931-61T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14690649 | ||||||
chrX:14690677
|
C | CTG | 8 | a0001c0001t0012g0099a0001c0001t0012g0104a0001c0001t0012g0154others(5): Show | 8 | HG01106.hp1 HG01891.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.931-19_931-18dupGT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chrX | 14690677 | |||||
chrX:14690677
|
C | G | 3 | a0001c0001t0009g0032a0001c0001t0018g0033a0001c0001t0018g0080 | 3 | HG02970.hp1 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.931-33C>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14690677 | ||||||
chrX:14690679
|
G | C | 4 | a0001c0002t0005g0014a0001c0002t0005g0015a0001c0002t0007g0013others(1): Show | 4 | HG03139.hp1 HG03516.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.931-31G>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14690679 | ||||||
chrX:14690691
|
G | C | 7 | a0001c0001t0010g0070a0001c0001t0010g0071a0001c0001t0010g0074others(4): Show | 7 | HG01243.hp1 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.931-19G>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 7/8 | chrX | 14690691 | ||||||
chrX:14691271
|
C | CTG | 8 | a0001c0001t0003g0039a0001c0001t0003g0043a0001c0001t0003g0044others(5): Show | 8 | HG00639.hp1 HG01070.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1080+465_1080+466d others(4): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14691271 | |||||
chrX:14691271
|
CTG | C | 23 | a0001c0001t0001g0050a0001c0001t0001g0146a0001c0001t0001g0147others(20): Show | 23 | HG00558.hp1 HG01081.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.1080+465_1080+466d others(4): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14691271 | |||||
chrX:14691271
|
CTGTG | C | 60 | a0001c0001t0001g0011a0001c0001t0001g0083a0001c0001t0001g0106others(57): Show | 60 | HG00323.hp2 HG00609.hp1 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.1080+463_1080+466d others(6): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14691271 | |||||
chrX:14691271
|
CTGTGTG | C | 24 | a0001c0001t0001g0036a0001c0001t0001g0042a0001c0001t0001g0097others(21): Show | 24 | HG00323.hp1 HG00558.hp2 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.1080+461_1080+466d others(8): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14691271 | |||||
chrX:14691271
|
CTGTGTGT others(1): Show |
C | 28 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(25): Show | 29 | HG00741.hp1 HG01358.hp1 HG01981.hp2 others(26): Show |
intron_variant | MODIFIER | c.1080+459_1080+466d others(10): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14691271 | |||||
chrX:14691271
|
CTGTGTGT others(3): Show |
C | 22 | a0001c0001t0001g0107a0001c0001t0001g0121a0001c0001t0001g0137others(19): Show | 22 | HG00673.hp1 HG00733.hp2 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.1080+457_1080+466d others(12): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14691271 | |||||
chrX:14691271
|
CTGTGTGT others(5): Show |
C | 8 | a0001c0001t0004g0027a0001c0001t0004g0069a0001c0001t0004g0197others(5): Show | 8 | HG02602.hp1 HG02630.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1080+455_1080+466d others(14): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14691271 | |||||
chrX:14691271
|
CTGTGTGT others(7): Show |
C | 19 | a0001c0002t0005g0002a0001c0002t0005g0010a0001c0002t0005g0015others(16): Show | 19 | HG00140.hp1 HG00280.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1080+453_1080+466d others(16): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14691271 | |||||
chrX:14691271
|
CTGTGTGT others(9): Show |
C | 8 | a0001c0002t0005g0213a0001c0002t0005g0215a0001c0002t0046g0179others(5): Show | 8 | HG01074.hp1 HG01516.hp1 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.1080+451_1080+466d others(18): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14691271 | |||||
chrX:14691271
|
CTGTGTGT others(11): Show |
C | 4 | a0001c0002t0005g0014a0001c0002t0007g0013a0001c0002t0007g0208others(1): Show | 4 | HG00741.hp2 HG03139.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1080+449_1080+466d others(20): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14691271 | |||||
chrX:14691271
|
CTGTGTGT others(19): Show |
C | 1 | a0001c0001t0003g0055 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1080+441_1080+466d others(28): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14691271 | |||||
chrX:14691271
|
CTGTGTGT others(23): Show |
C | 1 | a0001c0002t0036g0063 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1080+437_1080+466d others(32): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14691271 | |||||
chrX:14691272
|
T | A | 1 | a0001c0001t0031g0060 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1080+413T>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14691272 | ||||||
chrX:14691276
|
T | A | 1 | a0001c0002t0043g0191 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1080+417T>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14691276 | ||||||
chrX:14691282
|
T | A | 2 | a0001c0001t0009g0032a0001c0001t0018g0033 | 2 | HG02970.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1080+423T>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14691282 | ||||||
chrX:14691284
|
T | A | 4 | a0001c0001t0014g0228a0001c0001t0018g0080a0001c0002t0037g0028others(1): Show | 4 | HG02602.hp1 HG02630.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1080+425T>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14691284 | ||||||
chrX:14691286
|
T | A | 19 | a0001c0002t0005g0002a0001c0002t0005g0010a0001c0002t0005g0015others(16): Show | 19 | HG00140.hp1 HG00280.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1080+427T>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14691286 | ||||||
chrX:14691288
|
T | A | 6 | a0001c0002t0046g0179a0001c0003t0007g0067a0001c0003t0026g0176others(3): Show | 6 | HG01074.hp1 HG01891.hp2 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.1080+429T>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14691288 | ||||||
chrX:14691290
|
T | A | 4 | a0001c0002t0005g0014a0001c0002t0007g0013a0001c0002t0007g0208others(1): Show | 4 | HG00741.hp2 HG03139.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1080+431T>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14691290 | ||||||
chrX:14691302
|
T | A | 1 | a0001c0002t0036g0063 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1080+443T>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14691302 | ||||||
chrX:14691310
|
TGTGTGTG others(9): Show |
T | 1 | a0001c0001t0001g0072 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1080+453_1080+468d others(18): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14691310 | |||||
chrX:14691312
|
TGTGTGTG others(7): Show |
T | 3 | a0001c0001t0001g0029a0001c0001t0001g0066a0001c0001t0008g0227 | 3 | HG02055.hp1 HG02683.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1080+455_1080+468d others(16): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14691312 | |||||
chrX:14691314
|
TGTGTGTG others(5): Show |
T | 3 | a0001c0001t0001g0187a0001c0001t0008g0007a0001c0001t0038g0030 | 3 | HG03453.hp1 HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1080+457_1080+468d others(14): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14691314 | |||||
chrX:14691316
|
TGTGTGTG others(3): Show |
T | 1 | a0001c0001t0029g0012 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1080+459_1080+468d others(12): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14691316 | |||||
chrX:14691318
|
TGTGTGTG others(1): Show |
T | 3 | a0001c0001t0001g0171a0001c0001t0002g0034a0001c0001t0044g0193 | 3 | HG02965.hp1 HG03471.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1080+461_1080+468d others(10): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14691318 | |||||
chrX:14691320
|
T | C | 2 | a0001c0001t0031g0060a0001c0002t0043g0191 | 2 | HG02630.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1080+461T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14691320 | ||||||
chrX:14691320
|
TGTGTGC | T | 1 | a0001c0001t0015g0068 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1080+463_1080+468d others(8): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14691320 | |||||
chrX:14691322
|
T | C | 3 | a0001c0001t0014g0228a0001c0001t0031g0060a0001c0002t0043g0191 | 3 | HG02630.hp1 HG02630.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1080+463T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14691322 | ||||||
chrX:14691324
|
T | C | 6 | a0001c0001t0001g0097a0001c0001t0001g0158a0001c0001t0003g0054others(3): Show | 6 | HG02129.hp1 HG02630.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1080+465T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14691324 | ||||||
chrX:14691328
|
C | T | 35 | a0001c0001t0014g0228a0001c0002t0005g0002a0001c0002t0005g0010others(32): Show | 35 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.1080+469C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14691328 | ||||||
chrX:14691332
|
T | C | 94 | a0001c0001t0001g0029a0001c0001t0001g0066a0001c0001t0001g0072others(91): Show | 94 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.1080+473T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14691332 | ||||||
chrX:14691354
|
C | T | 40 | a0001c0001t0009g0032a0001c0001t0014g0228a0001c0001t0018g0033others(37): Show | 40 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.1080+495C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14691354 | ||||||
chrX:14691676
|
G | C | 2 | a0001c0001t0031g0060a0001c0002t0043g0191 | 2 | HG02630.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1080+817G>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14691676 | ||||||
chrX:14692575
|
A | C | 8 | a0001c0001t0048g0018a0001c0002t0007g0022a0001c0002t0007g0023others(5): Show | 8 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1080+1716A>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14692575 | ||||||
chrX:14692689
|
A | G | 1 | a0001c0002t0007g0210 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1080+1830A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14692689 | ||||||
chrX:14693045
|
CA | C | 7 | a0001c0002t0007g0022a0001c0002t0007g0023a0001c0002t0007g0192others(4): Show | 7 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1080+2198delA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14693045 | |||||
chrX:14693054
|
AAAAG | A | 35 | a0001c0001t0014g0228a0001c0002t0005g0002a0001c0002t0005g0010others(32): Show | 35 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.1080+2201_1080+220 others(8): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14693054 | |||||
chrX:14693060
|
AAG | A | 3 | a0001c0001t0004g0027a0001c0001t0004g0069a0001c0001t0004g0197 | 3 | HG03041.hp1 HG06807.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1080+2204_1080+220 others(6): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14693060 | |||||
chrX:14693129
|
A | G | 8 | a0001c0001t0003g0039a0001c0001t0003g0043a0001c0001t0003g0044others(5): Show | 8 | HG00639.hp1 HG01081.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1080+2270A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14693129 | ||||||
chrX:14693246
|
T | C | 1 | a0001c0002t0005g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1080+2387T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14693246 | ||||||
chrX:14693307
|
C | A | 3 | a0001c0001t0002g0034a0001c0001t0038g0030a0001c0001t0044g0193 | 3 | HG02965.hp1 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1080+2448C>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14693307 | ||||||
chrX:14693439
|
C | A | 93 | a0001c0001t0001g0029a0001c0001t0001g0066a0001c0001t0001g0072others(90): Show | 93 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.1080+2580C>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14693439 | ||||||
chrX:14693552
|
GATAGA | G | 1 | a0001c0001t0002g0222 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1080+2695_1080+269 others(9): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14693552 | |||||
chrX:14693743
|
G | T | 111 | a0001c0001t0001g0029a0001c0001t0001g0066a0001c0001t0001g0072others(108): Show | 111 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.1080+2884G>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14693743 | ||||||
chrX:14693791
|
T | G | 5 | a0001c0001t0009g0032a0001c0001t0018g0033a0001c0001t0018g0080others(2): Show | 5 | HG02630.hp2 HG02886.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1080+2932T>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14693791 | ||||||
chrX:14693958
|
A | G | 29 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0038others(26): Show | 29 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.1080+3099A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14693958 | ||||||
chrX:14694258
|
G | A | 3 | a0001c0002t0005g0014a0001c0002t0007g0013a0001c0002t0011g0076 | 3 | HG03139.hp1 HG03516.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1080+3399G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14694258 | ||||||
chrX:14694500
|
T | TC | 1 | a0001c0001t0002g0222 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1080+3643dupC | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14694500 | |||||
chrX:14694666
|
G | GA | 1 | a0001c0001t0002g0222 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1080+3808dupA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14694666 | |||||
chrX:14694767
|
C | T | 1 | a0001c0001t0004g0159 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1080+3908C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14694767 | ||||||
chrX:14694918
|
A | G | 1 | a0001c0001t0019g0131 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1080+4059A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14694918 | ||||||
chrX:14695159
|
C | CA | 39 | a0001c0001t0005g0006a0001c0001t0007g0077a0001c0001t0007g0079others(36): Show | 39 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.1080+4310dupA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14695159 | |||||
chrX:14695291
|
G | T | 4 | a0001c0001t0002g0163a0001c0001t0002g0165a0001c0001t0002g0166others(1): Show | 4 | HG01081.hp1 HG01099.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.1080+4432G>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14695291 | ||||||
chrX:14695341
|
A | AT | 1 | a0001c0001t0002g0222 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1080+4488dupT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14695341 | |||||
chrX:14695561
|
C | T | 2 | a0001c0001t0001g0173a0001c0001t0035g0172 | 2 | NA18948.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.1080+4702C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14695561 | ||||||
chrX:14696118
|
GA | G | 1 | a0001c0001t0002g0222 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1080+5261delA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14696118 | |||||
chrX:14696211
|
G | GGA | 1 | a0001c0001t0002g0222 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1080+5356_1080+535 others(6): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14696211 | |||||
chrX:14696219
|
C | CGAGG | 2 | a0001c0001t0001g0146a0001c0001t0006g0200 | 2 | HG00558.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.1080+5379_1080+538 others(8): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14696219 | |||||
chrX:14696274
|
T | G | 3 | a0001c0002t0005g0014a0001c0002t0007g0013a0001c0002t0011g0076 | 3 | HG03139.hp1 HG03516.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1080+5415T>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14696274 | ||||||
chrX:14696324
|
A | G | 1 | a0001c0001t0009g0223 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1080+5465A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14696324 | ||||||
chrX:14696366
|
C | CA | 1 | a0001c0001t0002g0222 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1080+5511dupA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14696366 | |||||
chrX:14696533
|
A | G | 1 | a0001c0001t0006g0134 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1080+5674A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14696533 | ||||||
chrX:14696696
|
C | T | 1 | a0001c0001t0004g0220 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1080+5837C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14696696 | ||||||
chrX:14696763
|
G | T | 35 | a0001c0001t0014g0228a0001c0002t0005g0002a0001c0002t0005g0010others(32): Show | 35 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.1080+5904G>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14696763 | ||||||
chrX:14696809
|
C | G | 3 | a0001c0003t0025g0175a0001c0003t0025g0181a0001c0003t0030g0198 | 3 | HG02572.hp1 HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1080+5950C>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14696809 | ||||||
chrX:14696899
|
G | GT | 1 | a0001c0001t0002g0222 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1080+6044dupT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14696899 | |||||
chrX:14696924
|
G | T | 1 | a0001c0001t0003g0136 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1080+6065G>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14696924 | ||||||
chrX:14696990
|
TG | T | 1 | a0001c0001t0002g0222 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1080+6133delG | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14696990 | |||||
chrX:14697091
|
G | GA | 9 | a0001c0001t0011g0188a0001c0001t0048g0018a0001c0002t0007g0022others(6): Show | 9 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.1080+6243dupA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14697091 | |||||
chrX:14697091
|
G | GAA | 24 | a0001c0001t0014g0228a0001c0002t0005g0002a0001c0002t0005g0010others(21): Show | 24 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.1080+6242_1080+624 others(6): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14697091 | |||||
chrX:14697091
|
G | GAAA | 15 | a0001c0001t0005g0006a0001c0001t0007g0077a0001c0001t0007g0079others(12): Show | 15 | HG01074.hp1 HG01891.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.1080+6241_1080+624 others(7): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14697091 | |||||
chrX:14697362
|
T | C | 5 | a0001c0001t0009g0032a0001c0001t0018g0033a0001c0001t0018g0080others(2): Show | 5 | HG02630.hp2 HG02886.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1080+6503T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14697362 | ||||||
chrX:14697466
|
G | A | 1 | a0001c0001t0016g0148 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1080+6607G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14697466 | ||||||
chrX:14697479
|
TAATC | T | 6 | a0001c0001t0001g0029a0001c0001t0001g0066a0001c0001t0001g0072others(3): Show | 6 | HG02055.hp1 HG02132.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.1080+6622_1080+662 others(8): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14697479 | |||||
chrX:14697480
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1080+6621A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14697480 | ||||||
chrX:14697562
|
G | A | 2 | a0001c0001t0001g0173a0001c0001t0035g0172 | 2 | NA18948.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.1080+6703G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14697562 | ||||||
chrX:14698051
|
A | G | 40 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0038others(37): Show | 40 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.1080+7192A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14698051 | ||||||
chrX:14698181
|
A | AT | 1 | a0001c0001t0001g0171 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1080+7328dupT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14698181 | |||||
chrX:14698370
|
T | A | 7 | a0001c0002t0007g0022a0001c0002t0007g0023a0001c0002t0007g0192others(4): Show | 7 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1080+7511T>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14698370 | ||||||
chrX:14698681
|
C | CA | 16 | a0001c0001t0001g0152a0001c0001t0001g0212a0001c0001t0002g0061others(13): Show | 16 | HG00558.hp2 HG00609.hp1 HG02080.hp2 others(13): Show |
intron_variant | MODIFIER | c.1080+7850dupA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14698681 | |||||
chrX:14698681
|
C | CAA | 2 | a0001c0001t0002g0101a0001c0002t0014g0025 | 2 | HG02027.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1080+7849_1080+785 others(6): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14698681 | |||||
chrX:14698681
|
C | CAAA | 1 | a0001c0001t0001g0105 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1080+7848_1080+785 others(7): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14698681 | |||||
chrX:14698681
|
CA | C | 48 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0129others(45): Show | 48 | HG00140.hp1 HG00323.hp1 HG00741.hp2 others(45): Show |
intron_variant | MODIFIER | c.1080+7850delA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14698681 | |||||
chrX:14698681
|
CAA | C | 6 | a0001c0002t0005g0214a0001c0002t0043g0191a0001c0003t0025g0175others(3): Show | 6 | HG00280.hp1 HG02572.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1080+7849_1080+785 others(6): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14698681 | |||||
chrX:14698681
|
CAAAA | C | 7 | a0001c0002t0007g0022a0001c0002t0007g0023a0001c0002t0007g0192others(4): Show | 7 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1080+7847_1080+785 others(8): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14698681 | |||||
chrX:14698681
|
CAAAAAA | C | 1 | a0001c0001t0005g0216 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1080+7845_1080+785 others(10): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14698681 | |||||
chrX:14698681
|
CAAAAAAA others(1): Show |
C | 1 | a0001c0001t0009g0032 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1080+7843_1080+785 others(12): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14698681 | |||||
chrX:14698843
|
G | A | 1 | a0001c0002t0007g0209 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1080+7984G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14698843 | ||||||
chrX:14698986
|
C | G | 2 | a0001c0001t0009g0032a0001c0001t0018g0033 | 2 | HG02970.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1080+8127C>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14698986 | ||||||
chrX:14699198
|
A | G | 1 | a0001c0005t0006g0144 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1080+8339A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14699198 | ||||||
chrX:14699299
|
A | G | 41 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0038others(38): Show | 41 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.1080+8440A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14699299 | ||||||
chrX:14699380
|
G | C | 6 | a0001c0002t0046g0179a0001c0003t0007g0067a0001c0003t0026g0176others(3): Show | 6 | HG01074.hp1 HG01891.hp2 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.1080+8521G>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14699380 | ||||||
chrX:14699636
|
A | AC | 1 | a0001c0001t0002g0222 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1080+8780dupC | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14699636 | |||||
chrX:14699651
|
A | G | 1 | a0001c0001t0029g0012 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1080+8792A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14699651 | ||||||
chrX:14699776
|
A | T | 1 | a0001c0002t0005g0056 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1080+8917A>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14699776 | ||||||
chrX:14699820
|
CCTTTGCA others(43): Show |
C | 1 | a0001c0001t0003g0229 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1080+8962_1080+901 others(54): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14699820 | ||||||
chrX:14699961
|
A | AC | 1 | a0001c0001t0002g0222 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1080+9103dupC | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14699961 | |||||
chrX:14700116
|
G | C | 1 | a0001c0002t0005g0205 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1080+9257G>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14700116 | ||||||
chrX:14700141
|
C | T | 3 | a0001c0001t0010g0070a0001c0001t0010g0071a0001c0001t0010g0074 | 3 | HG02809.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1080+9282C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14700141 | ||||||
chrX:14700146
|
T | TC | 1 | a0001c0001t0002g0222 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1080+9289dupC | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14700146 | |||||
chrX:14700325
|
C | T | 1 | a0001c0001t0002g0034 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1080+9466C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14700325 | ||||||
chrX:14700340
|
G | A | 3 | a0001c0001t0009g0032a0001c0001t0018g0033a0001c0001t0018g0080 | 3 | HG02970.hp1 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1080+9481G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14700340 | ||||||
chrX:14700456
|
G | C | 1 | a0001c0001t0002g0120 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1080+9597G>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14700456 | ||||||
chrX:14700477
|
G | A | 1 | a0001c0001t0017g0169 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1080+9618G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14700477 | ||||||
chrX:14700690
|
T | C | 1 | a0001c0001t0016g0116 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1080+9831T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14700690 | ||||||
chrX:14700741
|
G | GA | 1 | a0001c0001t0002g0222 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1080+9884dupA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14700741 | |||||
chrX:14700771
|
AT | A | 1 | a0001c0001t0002g0222 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1080+9919delT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14700771 | |||||
chrX:14700813
|
G | GT | 1 | a0001c0004t0007g0094 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1080+9962dupT | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14700813 | |||||
chrX:14701181
|
GA | G | 1 | a0001c0001t0002g0222 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1080+10325delA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14701181 | |||||
chrX:14701287
|
AG | A | 1 | a0001c0001t0002g0222 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1080+10430delG | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14701287 | |||||
chrX:14701313
|
T | A | 34 | a0001c0001t0002g0061a0001c0001t0003g0035a0001c0001t0003g0037others(31): Show | 34 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.1080+10454T>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14701313 | ||||||
chrX:14701362
|
G | A | 42 | a0001c0001t0014g0228a0001c0001t0048g0018a0001c0002t0005g0002others(39): Show | 42 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.1080+10503G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14701362 | ||||||
chrX:14701473
|
G | A | 3 | a0001c0001t0009g0032a0001c0001t0018g0033a0001c0001t0018g0080 | 3 | HG02970.hp1 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1080+10614G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14701473 | ||||||
chrX:14701589
|
G | T | 85 | a0001c0001t0002g0061a0001c0001t0003g0035a0001c0001t0003g0037others(82): Show | 85 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.1080+10730G>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14701589 | ||||||
chrX:14701744
|
A | T | 1 | a0001c0001t0012g0174 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1080+10885A>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14701744 | ||||||
chrX:14701990
|
A | C | 1 | a0001c0001t0012g0154 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1080+11131A>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14701990 | ||||||
chrX:14702162
|
T | G | 3 | a0001c0001t0009g0032a0001c0001t0018g0033a0001c0001t0018g0080 | 3 | HG02970.hp1 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1080+11303T>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14702162 | ||||||
chrX:14702417
|
TC | T | 1 | a0001c0001t0002g0222 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1080+11561delC | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14702417 | |||||
chrX:14702502
|
A | G | 29 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0038others(26): Show | 29 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.1080+11643A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14702502 | ||||||
chrX:14702539
|
T | G | 26 | a0001c0001t0002g0120a0001c0001t0002g0194a0001c0001t0004g0021others(23): Show | 26 | HG01070.hp1 HG01106.hp1 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.1080+11680T>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14702539 | ||||||
chrX:14702564
|
C | A | 6 | a0001c0001t0013g0073a0001c0001t0013g0185a0001c0001t0013g0199others(3): Show | 6 | HG01243.hp1 HG02280.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1080+11705C>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14702564 | ||||||
chrX:14702830
|
C | T | 3 | a0001c0001t0009g0032a0001c0001t0018g0033a0001c0001t0018g0080 | 3 | HG02970.hp1 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1080+11971C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14702830 | ||||||
chrX:14702913
|
G | T | 1 | a0001c0001t0029g0012 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1080+12054G>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14702913 | ||||||
chrX:14702938
|
AG | A | 1 | a0001c0001t0002g0143 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1080+12084delG | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14702938 | |||||
chrX:14702974
|
C | T | 1 | a0001c0001t0006g0087 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1080+12115C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14702974 | ||||||
chrX:14703069
|
C | T | 103 | a0001c0001t0002g0120a0001c0001t0002g0194a0001c0001t0003g0035others(100): Show | 103 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.1080+12210C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14703069 | ||||||
chrX:14703771
|
A | G | 37 | a0001c0001t0002g0120a0001c0001t0002g0194a0001c0001t0004g0021others(34): Show | 37 | HG01070.hp1 HG01106.hp1 HG01891.hp1 others(34): Show |
intron_variant | MODIFIER | c.1080+12912A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14703771 | ||||||
chrX:14703782
|
CCCTTGGT others(4): Show |
C | 1 | a0001c0002t0007g0114 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1080+12925_1080+12 others(17): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14703782 | |||||
chrX:14703797
|
G | T | 2 | a0001c0001t0001g0173a0001c0001t0035g0172 | 2 | NA18948.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.1080+12938G>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14703797 | ||||||
chrX:14703838
|
GGTCACCT others(6): Show |
G | 1 | a0001c0002t0037g0028 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1080+12980_1080+12 others(19): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14703838 | ||||||
chrX:14703989
|
A | G | 37 | a0001c0001t0002g0120a0001c0001t0002g0194a0001c0001t0004g0021others(34): Show | 37 | HG01070.hp1 HG01106.hp1 HG01891.hp1 others(34): Show |
intron_variant | MODIFIER | c.1080+13130A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14703989 | ||||||
chrX:14704105
|
T | A | 1 | a0001c0003t0026g0180 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1080+13246T>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14704105 | ||||||
chrX:14704462
|
C | A | 3 | a0001c0001t0009g0032a0001c0001t0018g0033a0001c0001t0018g0080 | 3 | HG02970.hp1 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1080+13603C>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14704462 | ||||||
chrX:14704652
|
G | A | 4 | a0001c0001t0001g0029a0001c0001t0001g0072a0001c0001t0001g0187others(1): Show | 4 | HG02132.hp1 HG02683.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1080+13793G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14704652 | ||||||
chrX:14704696
|
A | C | 1 | a0001c0001t0001g0003 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1080+13837A>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14704696 | ||||||
chrX:14704702
|
C | T | 2 | a0001c0001t0017g0078a0001c0001t0017g0169 | 2 | HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1080+13843C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14704702 | ||||||
chrX:14705271
|
G | A | 33 | a0001c0001t0002g0120a0001c0001t0002g0194a0001c0001t0004g0021others(30): Show | 33 | HG01070.hp1 HG01106.hp1 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.1080+14412G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14705271 | ||||||
chrX:14705949
|
C | A | 6 | a0001c0001t0013g0073a0001c0001t0013g0185a0001c0001t0013g0199others(3): Show | 6 | HG01243.hp1 HG02280.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1080+15090C>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14705949 | ||||||
chrX:14706054
|
TGCCCAGA others(40): Show |
T | 78 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0038others(75): Show | 78 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.1080+15204_1080+15 others(53): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14706054 | |||||
chrX:14706203
|
C | T | 4 | a0001c0001t0021g0190a0001c0002t0014g0025a0001c0002t0014g0026others(1): Show | 4 | HG02717.hp1 HG02809.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1080+15344C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14706203 | ||||||
chrX:14706269
|
A | ACATGCTT others(1): Show |
3 | a0001c0001t0009g0032a0001c0001t0018g0033a0001c0001t0018g0080 | 3 | HG02970.hp1 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1080+15410_1080+15 others(14): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14706269 | ||||||
chrX:14706398
|
C | T | 34 | a0001c0001t0002g0120a0001c0001t0002g0194a0001c0001t0004g0021others(31): Show | 34 | HG01070.hp1 HG01106.hp1 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.1080+15539C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14706398 | ||||||
chrX:14706427
|
C | T | 2 | a0001c0001t0021g0190a0001c0002t0021g0024 | 2 | HG02809.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1080+15568C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14706427 | ||||||
chrX:14706957
|
G | A | 6 | a0001c0001t0013g0073a0001c0001t0013g0185a0001c0001t0013g0199others(3): Show | 6 | HG01243.hp1 HG02280.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1080+16098G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14706957 | ||||||
chrX:14707036
|
C | CA | 39 | a0001c0001t0005g0006a0001c0001t0005g0057a0001c0001t0005g0216others(36): Show | 39 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.1080+16182dupA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14707036 | |||||
chrX:14707043
|
AC | A | 1 | a0001c0001t0004g0021 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1080+16186delC | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14707043 | |||||
chrX:14707100
|
T | C | 5 | a0001c0001t0001g0105a0001c0001t0001g0158a0001c0001t0002g0157others(2): Show | 5 | HG00621.hp1 HG00639.hp2 HG00642.hp1 others(2): Show |
intron_variant | MODIFIER | c.1080+16241T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14707100 | ||||||
chrX:14707382
|
A | C | 1 | a0001c0001t0002g0135 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1080+16523A>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14707382 | ||||||
chrX:14707496
|
T | A | 1 | a0001c0002t0007g0114 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1080+16637T>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14707496 | ||||||
chrX:14707556
|
A | G | 7 | a0001c0002t0007g0022a0001c0002t0007g0023a0001c0002t0007g0192others(4): Show | 7 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1080+16697A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14707556 | ||||||
chrX:14707757
|
G | GGT | 76 | a0001c0001t0001g0138a0001c0001t0003g0035a0001c0001t0003g0037others(73): Show | 76 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.1080+16914_1080+16 others(8): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14707757 | |||||
chrX:14707757
|
G | GGTGT | 4 | a0001c0001t0008g0195a0001c0001t0008g0196a0001c0001t0008g0230others(1): Show | 4 | HG02451.hp1 HG02886.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1080+16912_1080+16 others(10): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14707757 | |||||
chrX:14707757
|
G | GGTGTGT | 2 | a0001c0001t0031g0060a0001c0002t0043g0191 | 2 | HG02630.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1080+16910_1080+16 others(12): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14707757 | |||||
chrX:14707757
|
G | GGTGTGTG others(1): Show |
14 | a0001c0001t0012g0099a0001c0001t0012g0104a0001c0001t0012g0154others(11): Show | 14 | HG01106.hp1 HG01243.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.1080+16908_1080+16 others(14): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14707757 | |||||
chrX:14707757
|
G | GGTGTGTG others(3): Show |
19 | a0001c0001t0002g0120a0001c0001t0002g0194a0001c0001t0004g0021others(16): Show | 19 | HG01070.hp1 HG01928.hp1 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.1080+16906_1080+16 others(16): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14707757 | |||||
chrX:14707757
|
G | GGTGTGTG others(5): Show |
1 | a0001c0001t0029g0012 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1080+16904_1080+16 others(18): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14707757 | |||||
chrX:14707757
|
GGT | G | 7 | a0001c0002t0007g0022a0001c0002t0007g0023a0001c0002t0007g0192others(4): Show | 7 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1080+16914_1080+16 others(8): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14707757 | |||||
chrX:14707778
|
G | A | 3 | a0001c0001t0009g0032a0001c0001t0018g0033a0001c0001t0018g0080 | 3 | HG02970.hp1 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1080+16919G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14707778 | ||||||
chrX:14707784
|
G | A | 19 | a0001c0001t0005g0057a0001c0001t0005g0216a0001c0002t0005g0002others(16): Show | 19 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.1080+16925G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14707784 | ||||||
chrX:14707843
|
G | A | 5 | a0001c0001t0002g0163a0001c0001t0002g0165a0001c0001t0002g0166others(2): Show | 5 | HG00738.hp1 HG01081.hp1 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.1080+16984G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14707843 | ||||||
chrX:14707885
|
A | C | 3 | a0001c0001t0009g0032a0001c0001t0018g0033a0001c0001t0018g0080 | 3 | HG02970.hp1 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1080+17026A>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14707885 | ||||||
chrX:14708259
|
C | T | 67 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0038others(64): Show | 67 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.1080+17400C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14708259 | ||||||
chrX:14708262
|
C | T | 3 | a0001c0001t0009g0032a0001c0001t0018g0033a0001c0001t0018g0080 | 3 | HG02970.hp1 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1080+17403C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14708262 | ||||||
chrX:14708477
|
G | A | 19 | a0001c0001t0005g0057a0001c0001t0005g0216a0001c0002t0005g0002others(16): Show | 19 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.1080+17618G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14708477 | ||||||
chrX:14708638
|
A | G | 3 | a0001c0001t0009g0032a0001c0001t0018g0033a0001c0001t0018g0080 | 3 | HG02970.hp1 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1080+17779A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14708638 | ||||||
chrX:14708663
|
G | A | 1 | a0001c0002t0036g0063 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1080+17804G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14708663 | ||||||
chrX:14708956
|
AAGAG | A | 6 | a0001c0001t0013g0073a0001c0001t0013g0185a0001c0001t0013g0199others(3): Show | 6 | HG01243.hp1 HG02280.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1080+18105_1080+18 others(10): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14708956 | |||||
chrX:14709430
|
C | CAAGT | 1 | a0001c0001t0004g0220 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1080+18572_1080+18 others(10): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14709430 | |||||
chrX:14709781
|
A | G | 6 | a0001c0001t0013g0073a0001c0001t0013g0185a0001c0001t0013g0199others(3): Show | 6 | HG01243.hp1 HG02280.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1080+18922A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14709781 | ||||||
chrX:14709909
|
A | G | 1 | a0001c0001t0011g0188 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1080+19050A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14709909 | ||||||
chrX:14709933
|
T | C | 2 | a0001c0002t0014g0025a0001c0002t0014g0026 | 2 | HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1080+19074T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14709933 | ||||||
chrX:14710169
|
A | G | 2 | a0001c0001t0003g0041a0001c0001t0033g0040 | 2 | HG03239.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1080+19310A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14710169 | ||||||
chrX:14710316
|
G | A | 1 | a0001c0001t0005g0108 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1080+19457G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14710316 | ||||||
chrX:14710426
|
C | G | 7 | a0001c0002t0007g0022a0001c0002t0007g0023a0001c0002t0007g0192others(4): Show | 7 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1080+19567C>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14710426 | ||||||
chrX:14710625
|
T | C | 9 | a0001c0001t0012g0099a0001c0001t0012g0104a0001c0001t0012g0154others(6): Show | 9 | HG01106.hp1 HG01891.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1081-19582T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14710625 | ||||||
chrX:14710648
|
C | G | 4 | a0001c0001t0001g0029a0001c0001t0001g0072a0001c0001t0002g0061others(1): Show | 4 | HG02132.hp1 HG02683.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1081-19559C>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14710648 | ||||||
chrX:14710662
|
C | T | 67 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(64): Show | 68 | HG00558.hp1 HG00673.hp1 HG00738.hp1 others(65): Show |
intron_variant | MODIFIER | c.1081-19545C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14710662 | ||||||
chrX:14710768
|
C | T | 70 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0038others(67): Show | 70 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.1081-19439C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14710768 | ||||||
chrX:14711072
|
T | C | 1 | a0001c0001t0017g0078 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1081-19135T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14711072 | ||||||
chrX:14711516
|
G | A | 2 | a0001c0002t0014g0025a0001c0002t0014g0026 | 2 | HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1081-18691G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14711516 | ||||||
chrX:14711912
|
T | C | 132 | a0001c0001t0001g0029a0001c0001t0001g0066a0001c0001t0001g0072others(129): Show | 132 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.1081-18295T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14711912 | ||||||
chrX:14711968
|
G | A | 1 | a0001c0001t0006g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1081-18239G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14711968 | ||||||
chrX:14712408
|
T | C | 122 | a0001c0001t0002g0120a0001c0001t0002g0194a0001c0001t0003g0035others(119): Show | 122 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.1081-17799T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14712408 | ||||||
chrX:14712408
|
T | G | 1 | a0001c0001t0002g0124 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1081-17799T>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14712408 | ||||||
chrX:14712413
|
A | T | 1 | a0001c0001t0003g0038 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1081-17794A>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14712413 | ||||||
chrX:14712506
|
G | GA | 2 | a0001c0001t0001g0147a0001c0001t0002g0143 | 2 | HG01496.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.1081-17689dupA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14712506 | |||||
chrX:14712506
|
GA | G | 7 | a0001c0001t0015g0068a0001c0001t0021g0190a0001c0002t0021g0024others(4): Show | 7 | HG01109.hp1 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1081-17689delA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14712506 | |||||
chrX:14712683
|
T | TG | 1 | a0001c0001t0001g0083 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1081-17517dupG | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14712683 | |||||
chrX:14713091
|
T | G | 3 | a0001c0001t0009g0032a0001c0001t0018g0033a0001c0001t0018g0080 | 3 | HG02970.hp1 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1081-17116T>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14713091 | ||||||
chrX:14713093
|
G | T | 7 | a0001c0001t0014g0228a0001c0001t0021g0190a0001c0001t0031g0060others(4): Show | 7 | HG02630.hp1 HG02630.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1081-17114G>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14713093 | ||||||
chrX:14713141
|
A | G | 116 | a0001c0001t0002g0120a0001c0001t0002g0194a0001c0001t0003g0035others(113): Show | 116 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.1081-17066A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14713141 | ||||||
chrX:14713534
|
T | C | 1 | a0001c0001t0014g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1081-16673T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14713534 | ||||||
chrX:14713723
|
T | A | 116 | a0001c0001t0002g0120a0001c0001t0002g0194a0001c0001t0003g0035others(113): Show | 116 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.1081-16484T>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14713723 | ||||||
chrX:14713800
|
A | C | 2 | a0001c0001t0001g0097a0001c0001t0006g0200 | 2 | NA18957.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.1081-16407A>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14713800 | ||||||
chrX:14713831
|
A | C | 2 | a0001c0001t0003g0054a0001c0001t0003g0055 | 2 | NA18945.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1081-16376A>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14713831 | ||||||
chrX:14714228
|
C | A | 1 | a0001c0001t0004g0150 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1081-15979C>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14714228 | ||||||
chrX:14714616
|
A | G | 8 | a0001c0001t0011g0188a0001c0002t0007g0022a0001c0002t0007g0023others(5): Show | 8 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1081-15591A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14714616 | ||||||
chrX:14714634
|
T | TG | 1 | a0001c0001t0006g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1081-15568dupG | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14714634 | |||||
chrX:14714669
|
T | TG | 1 | a0001c0001t0006g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1081-15536dupG | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14714669 | |||||
chrX:14714994
|
G | C | 2 | a0001c0002t0014g0025a0001c0002t0014g0026 | 2 | HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1081-15213G>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14714994 | ||||||
chrX:14715256
|
T | C | 1 | a0001c0001t0001g0066 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1081-14951T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14715256 | ||||||
chrX:14715283
|
G | GC | 1 | a0001c0001t0006g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1081-14921dupC | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14715283 | |||||
chrX:14715447
|
T | A | 15 | a0001c0001t0005g0057a0001c0001t0005g0216a0001c0002t0005g0002others(12): Show | 15 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.1081-14760T>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14715447 | ||||||
chrX:14716018
|
A | AG | 1 | a0001c0001t0006g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1081-14187dupG | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14716018 | |||||
chrX:14716101
|
G | A | 74 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0038others(71): Show | 74 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.1081-14106G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14716101 | ||||||
chrX:14716201
|
G | GA | 1 | a0001c0001t0006g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1081-14006_1081-14 others(7): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14716201 | ||||||
chrX:14716561
|
G | A | 6 | a0001c0001t0013g0073a0001c0001t0013g0185a0001c0001t0013g0199others(3): Show | 6 | HG01243.hp1 HG02280.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1081-13646G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14716561 | ||||||
chrX:14716681
|
T | C | 1 | a0001c0001t0006g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1081-13526T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14716681 | ||||||
chrX:14716682
|
C | T | 1 | a0001c0001t0006g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1081-13525C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14716682 | ||||||
chrX:14716690
|
C | A | 3 | a0001c0001t0010g0070a0001c0001t0010g0071a0001c0001t0010g0074 | 3 | HG02809.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1081-13517C>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14716690 | ||||||
chrX:14716798
|
TA | T | 1 | a0001c0001t0006g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1081-13404delA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14716798 | |||||
chrX:14716807
|
A | C | 1 | a0001c0001t0008g0007 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1081-13400A>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14716807 | ||||||
chrX:14716822
|
C | T | 1 | a0001c0001t0008g0128 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1081-13385C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14716822 | ||||||
chrX:14716905
|
A | ATT | 1 | a0001c0001t0006g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1081-13302_1081-13 others(8): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14716905 | ||||||
chrX:14717220
|
G | GC | 1 | a0001c0001t0006g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1081-12985dupC | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14717220 | |||||
chrX:14717253
|
A | G | 2 | a0001c0001t0004g0027a0001c0001t0004g0197 | 2 | HG03041.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1081-12954A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14717253 | ||||||
chrX:14717345
|
T | TA | 59 | a0001c0001t0002g0120a0001c0001t0002g0194a0001c0001t0003g0035others(56): Show | 59 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.1081-12846dupA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14717345 | |||||
chrX:14717345
|
TA | T | 2 | a0001c0001t0002g0166a0001c0001t0018g0080 | 2 | HG01081.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1081-12846delA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14717345 | |||||
chrX:14717429
|
T | C | 34 | a0001c0001t0002g0120a0001c0001t0002g0194a0001c0001t0004g0021others(31): Show | 34 | HG01070.hp1 HG01106.hp1 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.1081-12778T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14717429 | ||||||
chrX:14717580
|
A | AAGTTTAT others(27): Show |
34 | a0001c0001t0002g0120a0001c0001t0002g0194a0001c0001t0004g0021others(31): Show | 34 | HG01070.hp1 HG01106.hp1 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.1081-12623_1081-12 others(40): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14717580 | |||||
chrX:14717661
|
T | TA | 1 | a0001c0001t0006g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1081-12545dupA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14717661 | |||||
chrX:14717740
|
T | TA | 37 | a0001c0001t0002g0061a0001c0001t0002g0089a0001c0001t0002g0096others(34): Show | 37 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.1081-12450dupA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14717740 | |||||
chrX:14717740
|
T | TAA | 2 | a0001c0001t0003g0041a0001c0001t0038g0030 | 2 | HG03453.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1081-12451_1081-12 others(8): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14717740 | |||||
chrX:14717740
|
TA | T | 11 | a0001c0001t0001g0011a0001c0001t0001g0147a0001c0001t0002g0143others(8): Show | 11 | HG01496.hp2 HG01934.hp1 HG02602.hp1 others(8): Show |
intron_variant | MODIFIER | c.1081-12450delA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14717740 | |||||
chrX:14717740
|
TAA | T | 2 | a0001c0001t0001g0133a0001c0001t0004g0220 | 2 | HG01070.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.1081-12451_1081-12 others(8): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14717740 | |||||
chrX:14717785
|
CA | C | 1 | a0001c0001t0006g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1081-12420delA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14717785 | |||||
chrX:14717947
|
G | A | 1 | a0001c0002t0043g0191 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1081-12260G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14717947 | ||||||
chrX:14717987
|
A | G | 3 | a0001c0001t0004g0027a0001c0001t0004g0069a0001c0001t0004g0197 | 3 | HG03041.hp1 HG06807.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1081-12220A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14717987 | ||||||
chrX:14718130
|
G | GAT | 1 | a0001c0001t0006g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1081-12077_1081-12 others(8): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14718130 | ||||||
chrX:14718276
|
A | G | 1 | a0001c0001t0001g0211 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1081-11931A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14718276 | ||||||
chrX:14718557
|
GAT | G | 1 | a0001c0001t0022g0059 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1081-11649_1081-11 others(8): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14718557 | ||||||
chrX:14718617
|
C | T | 117 | a0001c0001t0002g0120a0001c0001t0002g0194a0001c0001t0003g0035others(114): Show | 117 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.1081-11590C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14718617 | ||||||
chrX:14718725
|
G | C | 12 | a0001c0001t0012g0099a0001c0001t0012g0104a0001c0001t0012g0154others(9): Show | 12 | HG01106.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1081-11482G>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14718725 | ||||||
chrX:14718916
|
A | AG | 1 | a0001c0001t0006g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1081-11288dupG | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14718916 | |||||
chrX:14719164
|
GTTTTA | G | 2 | a0001c0001t0021g0190a0001c0002t0021g0024 | 2 | HG02809.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1081-11033_1081-11 others(11): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14719164 | |||||
chrX:14719386
|
G | GA | 1 | a0001c0001t0004g0202 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1081-10816dupA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14719386 | |||||
chrX:14719514
|
C | A | 2 | a0001c0001t0001g0113a0001c0001t0001g0129 | 2 | HG00323.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.1081-10693C>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14719514 | ||||||
chrX:14719747
|
C | T | 1 | a0001c0002t0003g0145 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1081-10460C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14719747 | ||||||
chrX:14720450
|
G | T | 3 | a0001c0001t0009g0032a0001c0001t0018g0033a0001c0001t0018g0080 | 3 | HG02970.hp1 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1081-9757G>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14720450 | ||||||
chrX:14720496
|
G | A | 74 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0038others(71): Show | 74 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.1081-9711G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14720496 | ||||||
chrX:14720699
|
A | G | 1 | a0001c0001t0003g0139 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1081-9508A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14720699 | ||||||
chrX:14720792
|
T | C | 1 | a0001c0001t0004g0021 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1081-9415T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14720792 | ||||||
chrX:14721111
|
A | T | 4 | a0001c0001t0006g0117a0001c0001t0016g0116a0001c0001t0016g0148others(1): Show | 4 | NA18955.hp1 NA18965.hp1 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.1081-9096A>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14721111 | ||||||
chrX:14721120
|
C | CA | 11 | a0001c0001t0001g0106a0001c0001t0001g0111a0001c0001t0002g0151others(8): Show | 11 | HG00741.hp1 HG01243.hp1 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1081-9068dupA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14721120 | |||||
chrX:14721120
|
CA | C | 18 | a0001c0001t0001g0011a0001c0001t0001g0029a0001c0001t0001g0072others(15): Show | 18 | HG02132.hp1 HG02280.hp2 HG03453.hp1 others(15): Show |
intron_variant | MODIFIER | c.1081-9068delA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14721120 | |||||
chrX:14721120
|
CAA | C | 71 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0038others(68): Show | 71 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.1081-9069_1081-906 others(6): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14721120 | |||||
chrX:14721120
|
CAAA | C | 6 | a0001c0001t0014g0228a0001c0002t0028g0062a0001c0002t0045g0177others(3): Show | 6 | HG01891.hp2 HG02258.hp1 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.1081-9070_1081-906 others(7): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14721120 | |||||
chrX:14721336
|
C | CA | 117 | a0001c0001t0002g0120a0001c0001t0002g0194a0001c0001t0003g0035others(114): Show | 117 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.1081-8865dupA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14721336 | |||||
chrX:14721512
|
C | T | 13 | a0001c0001t0002g0120a0001c0001t0004g0021a0001c0001t0004g0081others(10): Show | 13 | HG01928.hp1 HG01952.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.1081-8695C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14721512 | ||||||
chrX:14721842
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1081-8365C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14721842 | ||||||
chrX:14722243
|
C | G | 4 | a0001c0002t0005g0014a0001c0002t0005g0015a0001c0002t0007g0013others(1): Show | 4 | HG03139.hp1 HG03516.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1081-7964C>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14722243 | ||||||
chrX:14722748
|
A | G | 4 | a0001c0002t0023g0065a0001c0002t0023g0186a0001c0002t0039g0184others(1): Show | 4 | HG01109.hp1 HG02109.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1081-7459A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14722748 | ||||||
chrX:14722898
|
A | G | 1 | a0001c0001t0006g0053 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1081-7309A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14722898 | ||||||
chrX:14723415
|
A | G | 3 | a0001c0001t0009g0032a0001c0001t0018g0033a0001c0001t0018g0080 | 3 | HG02970.hp1 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1081-6792A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14723415 | ||||||
chrX:14723826
|
C | T | 74 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0038others(71): Show | 74 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.1081-6381C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14723826 | ||||||
chrX:14724009
|
C | A | 1 | a0001c0002t0024g0016 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1081-6198C>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14724009 | ||||||
chrX:14724038
|
A | G | 3 | a0001c0002t0010g0031a0001c0002t0024g0016a0001c0002t0024g0017 | 3 | HG03195.hp1 NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1081-6169A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14724038 | ||||||
chrX:14724171
|
T | C | 3 | a0001c0001t0004g0027a0001c0001t0004g0069a0001c0001t0004g0197 | 3 | HG03041.hp1 HG06807.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1081-6036T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14724171 | ||||||
chrX:14724192
|
G | A | 1 | a0001c0001t0002g0061 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1081-6015G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14724192 | ||||||
chrX:14724409
|
G | A | 12 | a0001c0001t0012g0099a0001c0001t0012g0104a0001c0001t0012g0154others(9): Show | 12 | HG01106.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1081-5798G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14724409 | ||||||
chrX:14724607
|
C | T | 1 | a0001c0002t0010g0031 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1081-5600C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14724607 | ||||||
chrX:14724626
|
C | CA | 15 | a0001c0001t0001g0029a0001c0001t0001g0072a0001c0001t0001g0125others(12): Show | 15 | HG02027.hp1 HG02132.hp1 HG02135.hp1 others(12): Show |
intron_variant | MODIFIER | c.1081-5555dupA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14724626 | |||||
chrX:14724626
|
C | CAA | 4 | a0001c0001t0002g0020a0001c0001t0002g0034a0001c0001t0002g0102others(1): Show | 4 | HG03471.hp1 NA18977.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.1081-5556_1081-555 others(6): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14724626 | |||||
chrX:14724626
|
C | CAAA | 2 | a0001c0001t0002g0019a0001c0001t0002g0090 | 2 | NA19005.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.1081-5557_1081-555 others(7): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14724626 | |||||
chrX:14724626
|
C | CAAAAAAA others(2): Show |
1 | a0001c0001t0018g0080 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1081-5563_1081-555 others(13): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14724626 | |||||
chrX:14724626
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0018g0033 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1081-5564_1081-555 others(14): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14724626 | |||||
chrX:14724626
|
C | CAAAAAAA others(4): Show |
13 | a0001c0001t0004g0021a0001c0001t0004g0027a0001c0001t0004g0126others(10): Show | 13 | HG01070.hp1 HG01928.hp1 HG01952.hp1 others(10): Show |
intron_variant | MODIFIER | c.1081-5565_1081-555 others(15): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14724626 | |||||
chrX:14724626
|
C | CAAAAAAA others(5): Show |
9 | a0001c0001t0002g0120a0001c0001t0002g0194a0001c0001t0004g0069others(6): Show | 9 | HG02004.hp1 HG02523.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1081-5566_1081-555 others(16): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14724626 | |||||
chrX:14724626
|
C | CAAAAAAA others(6): Show |
1 | a0001c0001t0004g0081 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1081-5567_1081-555 others(17): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14724626 | |||||
chrX:14724626
|
CA | C | 5 | a0001c0001t0004g0150a0001c0001t0009g0064a0001c0001t0009g0223others(2): Show | 5 | HG01070.hp2 HG01071.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1081-5555delA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14724626 | |||||
chrX:14724626
|
CAA | C | 6 | a0001c0001t0013g0073a0001c0001t0013g0185a0001c0001t0013g0199others(3): Show | 6 | HG01243.hp1 HG02280.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1081-5556_1081-555 others(6): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14724626 | |||||
chrX:14724626
|
CAAA | C | 3 | a0001c0001t0017g0169a0001c0001t0044g0193a0001c0001t0048g0018 | 3 | HG02109.hp1 HG02486.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1081-5557_1081-555 others(7): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14724626 | |||||
chrX:14724626
|
CAAAA | C | 8 | a0001c0001t0012g0099a0001c0001t0012g0104a0001c0001t0012g0154others(5): Show | 8 | HG01106.hp1 HG01891.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1081-5558_1081-555 others(8): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14724626 | |||||
chrX:14724626
|
CAAAAA | C | 2 | a0001c0001t0029g0012a0001c0002t0010g0031 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1081-5559_1081-555 others(9): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14724626 | |||||
chrX:14724626
|
CAAAAAAA | C | 3 | a0001c0002t0005g0214a0001c0002t0024g0016a0001c0002t0024g0017 | 3 | HG00280.hp1 HG03195.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1081-5561_1081-555 others(11): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14724626 | |||||
chrX:14724626
|
CAAAAAAA others(1): Show |
C | 70 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0038others(67): Show | 70 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.1081-5562_1081-555 others(12): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14724626 | |||||
chrX:14724648
|
A | AC | 1 | a0001c0001t0001g0146 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1081-5559_1081-555 others(5): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14724648 | ||||||
chrX:14724648
|
A | C | 2 | a0001c0001t0001g0097a0001c0001t0006g0200 | 2 | NA18957.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.1081-5559A>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14724648 | ||||||
chrX:14724671
|
T | C | 3 | a0001c0002t0010g0031a0001c0002t0024g0016a0001c0002t0024g0017 | 3 | HG03195.hp1 NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1081-5536T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14724671 | ||||||
chrX:14724926
|
GAATGGAA others(17): Show |
G | 1 | a0001c0001t0005g0108 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1081-5255_1081-523 others(28): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14724926 | |||||
chrX:14725241
|
A | G | 118 | a0001c0001t0002g0120a0001c0001t0002g0194a0001c0001t0003g0035others(115): Show | 118 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.1081-4966A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14725241 | ||||||
chrX:14725315
|
C | T | 26 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0038others(23): Show | 26 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.1081-4892C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14725315 | ||||||
chrX:14725462
|
C | G | 1 | a0001c0001t0004g0197 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1081-4745C>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14725462 | ||||||
chrX:14725879
|
G | A | 3 | a0001c0002t0010g0031a0001c0002t0024g0016a0001c0002t0024g0017 | 3 | HG03195.hp1 NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1081-4328G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14725879 | ||||||
chrX:14726153
|
A | G | 7 | a0001c0001t0013g0073a0001c0001t0013g0185a0001c0001t0013g0199others(4): Show | 7 | HG01243.hp1 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1081-4054A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14726153 | ||||||
chrX:14726160
|
T | C | 1 | a0001c0001t0004g0150 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1081-4047T>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14726160 | ||||||
chrX:14726769
|
C | G | 1 | a0001c0001t0005g0006 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1081-3438C>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14726769 | ||||||
chrX:14726974
|
T | TA | 11 | a0001c0001t0012g0099a0001c0001t0012g0104a0001c0001t0012g0154others(8): Show | 11 | HG01106.hp1 HG01891.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1081-3232dupA | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14726974 | |||||
chrX:14727124
|
A | G | 3 | a0001c0001t0010g0070a0001c0001t0010g0071a0001c0001t0010g0074 | 3 | HG02809.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1081-3083A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14727124 | ||||||
chrX:14727245
|
T | TAA | 2 | a0001c0001t0004g0081a0001c0001t0004g0155 | 2 | HG02056.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.1081-2959_1081-295 others(6): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14727245 | |||||
chrX:14727869
|
A | G | 4 | a0001c0002t0023g0065a0001c0002t0023g0186a0001c0002t0039g0184others(1): Show | 4 | HG01109.hp1 HG02109.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1081-2338A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14727869 | ||||||
chrX:14727926
|
C | A | 1 | a0001c0001t0002g0101 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1081-2281C>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14727926 | ||||||
chrX:14727941
|
A | G | 1 | a0001c0001t0001g0173 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1081-2266A>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14727941 | ||||||
chrX:14728380
|
G | A | 1 | a0001c0002t0005g0056 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1081-1827G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14728380 | ||||||
chrX:14728515
|
G | A | 3 | a0001c0001t0009g0032a0001c0001t0018g0033a0001c0001t0018g0080 | 3 | HG02970.hp1 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1081-1692G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14728515 | ||||||
chrX:14728518
|
C | G | 4 | a0001c0001t0009g0064a0001c0001t0009g0223a0001c0001t0009g0224others(1): Show | 4 | HG01070.hp2 HG01071.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1081-1689C>G | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14728518 | ||||||
chrX:14728676
|
C | T | 1 | a0001c0001t0015g0068 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1081-1531C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14728676 | ||||||
chrX:14728930
|
C | T | 6 | a0001c0001t0021g0190a0001c0002t0014g0025a0001c0002t0014g0026others(3): Show | 6 | HG02258.hp1 HG02647.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1081-1277C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14728930 | ||||||
chrX:14729351
|
C | T | 1 | a0001c0001t0001g0029 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1081-856C>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14729351 | ||||||
chrX:14729535
|
T | A | 1 | a0001c0001t0008g0007 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1081-672T>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14729535 | ||||||
chrX:14729724
|
TGGG | T | 1 | a0001c0002t0005g0214 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1081-480_1081-478d others(5): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14729724 | |||||
chrX:14729788
|
A | C | 3 | a0001c0001t0009g0032a0001c0001t0018g0033a0001c0001t0018g0080 | 3 | HG02970.hp1 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1081-419A>C | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14729788 | ||||||
chrX:14729789
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G | A | 85 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0038others(82): Show | 85 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.1081-418G>A | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14729789 | ||||||
chrX:14729806
|
C | CTGAA | 1 | a0001c0001t0001g0105 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1081-378_1081-375d others(6): Show |
GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 14729806 | |||||
chrX:14729865
|
G | T | 22 | a0001c0001t0002g0120a0001c0001t0002g0194a0001c0001t0004g0021others(19): Show | 22 | HG01070.hp1 HG01928.hp1 HG01952.hp1 others(19): Show |
intron_variant | MODIFIER | c.1081-342G>T | GLRA2 | ENSG00000101958.14 | transcript | ENST00000218075.9 | protein_coding | 8/8 | chrX | 14729865 |