geneid | 8487 |
---|---|
ensemblid | ENSG00000092208.19 |
hgncid | 10884 |
symbol | GEMIN2 |
name | gem nuclear organelle associated protein 2 |
refseq_nuc | NM_003616.3 |
refseq_prot | NP_003607.2 |
ensembl_nuc | ENST00000308317.12 |
ensembl_prot | ENSP00000308533.7 |
mane_status | MANE Select |
chr | chr14 |
start | 39114323 |
end | 39136973 |
strand | + |
ver | v1.2 |
region | chr14:39114323-39136973 |
region5000 | chr14:39109323-39141973 |
regionname0 | GEMIN2_chr14_39114323_39136973 |
regionname5000 | GEMIN2_chr14_39109323_39141973 |
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 | 269 | 422 | 91 | 76 | 195 | 16 | 42 | 153 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | copy fasta | chr14 | 39109323 | 39141973 |
a0002 | 0/0 | 269 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | copy fasta | chr14 | 39109323 | 39141973 |
a0003 | 0/0 | 269 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | copy fasta | chr14 | 39109323 | 39141973 |
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 | 810 | 422 | 91 | 76 | 195 | 16 | 42 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | copy fasta | chr14 | 39109323 | 39141973 |
c0002 | 0/0 | 810 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | copy fasta | chr14 | 39109323 | 39141973 |
c0003 | 0/0 | 810 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | copy fasta | chr14 | 39109323 | 39141973 |
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 | 1/1 | 511 | 419 | 91 | 75 | 193 | 16 | 42 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | copy fasta | chr14 | 39109323 | 39141973 |
t0002 | 0/0 | 511 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | copy fasta | chr14 | 39109323 | 39141973 |
t0003 | 0/0 | 511 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | copy fasta | chr14 | 39109323 | 39141973 |
t0004 | 0/0 | 511 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | copy fasta | chr14 | 39109323 | 39141973 |
t0005 | 0/0 | 511 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | copy fasta | chr14 | 39109323 | 39141973 |
t0006 | 0/0 | 511 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | copy fasta | chr14 | 39109323 | 39141973 |
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 | 7 | 0 | 4 | 3 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0002 | 0/0 | 6 | 0 | 0 | 3 | 0 | 3 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0004 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0005 | 0/0 | 4 | 3 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0009 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0010 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0011 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0012 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0020 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0021 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0022 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0023 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0031 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0032 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0104 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0336 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
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 | 810 | 422 | 91 | 76 | 195 | 16 | 42 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | copy fasta | chr14 | 39109323 | 39141973 |
a0002c0003 | 0/0 | 810 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | copy fasta | chr14 | 39109323 | 39141973 |
a0003c0002 | 0/0 | 810 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | copy fasta | chr14 | 39109323 | 39141973 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 1320 | 418 | 90 | 75 | 193 | 16 | 42 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | copy fasta | chr14 | 39109323 | 39141973 |
a0001c0001t0002 | 0/0 | 1320 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | copy fasta | chr14 | 39109323 | 39141973 |
a0001c0001t0003 | 0/0 | 1320 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | copy fasta | chr14 | 39109323 | 39141973 |
a0001c0001t0004 | 0/0 | 1320 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | copy fasta | chr14 | 39109323 | 39141973 |
a0001c0001t0006 | 0/0 | 1320 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | copy fasta | chr14 | 39109323 | 39141973 |
a0002c0003t0001 | 0/0 | 1320 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | copy fasta | chr14 | 39109323 | 39141973 |
a0003c0002t0005 | 0/0 | 1320 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | copy fasta | chr14 | 39109323 | 39141973 |
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 | 7 | 0 | 4 | 3 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0002 | 0/0 | 5 | 0 | 0 | 2 | 0 | 3 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0004 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0005 | 0/0 | 4 | 3 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0023 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0104 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0004g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0006g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0002c0003t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0003c0002t0005g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0195 | EUR | GBR | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | GBR | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0191 | EUR | GBR | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0101 | EUR | GBR | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | FIN | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0188 | EUR | FIN | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | CHS | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | CHS | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | CHS | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | CHS | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | CHS | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | CHS | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0333 | EAS | CHS | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | CHS | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | CHS | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0341 | AMR | PUR | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | CHS | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0293 | AMR | PUR | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0319 | AMR | PUR | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0328 | AMR | PUR | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0352 | AMR | PUR | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0326 | AMR | PUR | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0350 | AMR | PUR | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0337 | AMR | PUR | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0290 | AMR | PUR | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0338 | AMR | PUR | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0342 | AMR | CLM | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | CLM | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0354 | AMR | CLM | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | CLM | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | CLM | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | CLM | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0301 | AMR | CLM | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | CLM | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0298 | AMR | CLM | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | CLM | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0022 | EUR | IBS | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0040 | EUR | IBS | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0235 | EUR | IBS | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0161 | EUR | IBS | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0022 | EUR | IBS | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0231 | EUR | IBS | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | ACB | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0344 | AFR | ACB | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | ACB | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PEL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0325 | AMR | PEL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | PEL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0307 | AMR | PEL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02004 | hp1 | a0001 | c0001 | t0006 | g0020 | AMR | PEL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | KHV | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | ACB | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | KHV | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | KHV | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | KHV | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0357 | EAS | KHV | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PEL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PEL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | CDX | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | CDX | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0348 | AFR | ACB | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0329 | AMR | PEL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PEL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | ACB | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0331 | EAS | KHV | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | KHV | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | GWD | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0285 | SAS | PJL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0286 | SAS | PJL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0311 | SAS | PJL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0356 | SAS | PJL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | GWD | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | GWD | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | GWD | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0351 | AFR | ESN | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | ESN | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ESN | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | ESN | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0347 | AFR | ESN | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | ESN | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0345 | AFR | ESN | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | GWD | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | MSL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03098 | hp2 | a0002 | c0003 | t0001 | g0339 | AFR | MSL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | ESN | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0360 | AFR | ESN | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0340 | AFR | MSL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | MSL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | MSL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0257 | SAS | PJL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | MSL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | MSL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | MSL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | MSL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0317 | SAS | PJL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0318 | SAS | PJL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ESN | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | ESN | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | STU | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | STU | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0316 | SAS | PJL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0291 | SAS | BEB | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | BEB | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0320 | SAS | BEB | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | BEB | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0323 | SAS | BEB | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0353 | SAS | BEB | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | BEB | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0315 | SAS | STU | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0343 | SAS | STU | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0355 | SAS | STU | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0274 | SAS | STU | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0283 | SAS | STU | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | STU | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | YRI | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | YRI | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | CHB | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | CHB | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0359 | AFR | YRI | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0358 | AFR | YRI | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0365 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18945 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0366 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0362 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0363 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0364 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19011 | hp2 | a0003 | c0002 | t0005 | g0171 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | LWK | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0349 | AFR | LWK | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19043 | hp1 | a0001 | c0001 | t0003 | g0038 | AFR | LWK | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | LWK | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | YRI | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | YRI | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ASW | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ASW | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0284 | EUR | TSI | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0336 | EUR | TSI | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0273 | EUR | TSI | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0187 | EUR | TSI | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0313 | SAS | GIH | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | GIH | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | CLM | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | ACB | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0346 | AFR | ACB | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | ACB | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | MSL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | USA | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | USA | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | USA | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0361 | AFR | USA | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | LWK | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | LWK | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0104 | REF | REF | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0023 | REF | REF | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:39114384
|
C | G | 1 | a0002 | 1 | HG03098.hp2 | missense_variant | MODERATE | c.46C>G | p.Arg16Gly | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 1/10 | 62/1320 | 46/810 | 16/269 | chr14 | 39114384 | ||
chr14:39132061
|
T | G | 1 | a0003 | 1 | NA19011.hp2 | missense_variant | MODERATE | c.704T>G | p.Leu235Arg | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 8/10 | 720/1320 | 704/810 | 235/269 | chr14 | 39132061 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:39136481
|
G | T | 1 | a0001c0001t0006 | 1 | HG02004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2G>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 10/10 | 2 | chr14 | 39136481 | |||||
chr14:39136532
|
C | G | 1 | a0003c0002t0005 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*53C>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 10/10 | 53 | chr14 | 39136532 | |||||
chr14:39136533
|
T | C | 1 | a0003c0002t0005 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*54T>C | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 10/10 | 54 | chr14 | 39136533 | |||||
chr14:39136537
|
G | A | 1 | a0003c0002t0005 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*58G>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 10/10 | 58 | chr14 | 39136537 | |||||
chr14:39136578
|
A | T | 1 | a0003c0002t0005 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*99A>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 10/10 | 99 | chr14 | 39136578 | |||||
chr14:39136621
|
T | C | 1 | a0001c0001t0002 | 1 | NA19065.hp1 | 3_prime_UTR_variant | MODIFIER | c.*142T>C | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 10/10 | 142 | chr14 | 39136621 | |||||
chr14:39136754
|
A | G | 1 | a0001c0001t0004 | 1 | NA18945.hp1 | 3_prime_UTR_variant | MODIFIER | c.*275A>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 10/10 | 275 | chr14 | 39136754 | |||||
chr14:39136890
|
G | C | 1 | a0001c0001t0003 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*411G>C | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 10/10 | 411 | chr14 | 39136890 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:39114517
|
C | T | 4 | a0001c0001t0001g0034a0001c0001t0001g0364a0001c0001t0001g0365others(1): Show | 5 | NA18941.hp2 NA18954.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.137+42C>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 1/9 | chr14 | 39114517 | ||||||
chr14:39114527
|
G | T | 21 | a0001c0001t0001g0033a0001c0001t0001g0344a0001c0001t0001g0345others(18): Show | 22 | HG00738.hp2 HG01070.hp1 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.137+52G>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 1/9 | chr14 | 39114527 | ||||||
chr14:39114598
|
A | G | 3 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343 | 3 | HG00642.hp1 HG01257.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.137+123A>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 1/9 | chr14 | 39114598 | ||||||
chr14:39114671
|
T | G | 5 | a0001c0001t0001g0344a0001c0001t0001g0345a0001c0001t0001g0346others(2): Show | 5 | HG01891.hp1 HG02109.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.138-158T>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 1/9 | chr14 | 39114671 | ||||||
chr14:39114672
|
C | G | 1 | a0001c0001t0001g0340 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.138-157C>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 1/9 | chr14 | 39114672 | ||||||
chr14:39114772
|
A | G | 1 | a0002c0003t0001g0339 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.138-57A>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 1/9 | chr14 | 39114772 | ||||||
chr14:39114793
|
G | T | 3 | a0001c0001t0001g0032a0001c0001t0001g0337a0001c0001t0001g0338 | 4 | HG00733.hp1 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.138-36G>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 1/9 | chr14 | 39114793 | ||||||
chr14:39115064
|
A | G | 1 | a0001c0001t0001g0336 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.222+151A>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 2/9 | chr14 | 39115064 | ||||||
chr14:39115111
|
C | A | 5 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(2): Show | 5 | HG02280.hp2 HG03130.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.222+198C>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 2/9 | chr14 | 39115111 | ||||||
chr14:39115217
|
G | GTT | 72 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0031others(69): Show | 77 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.222+306_222+307dup others(2): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr14 | 39115217 | |||||
chr14:39115260
|
C | T | 77 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0031others(74): Show | 82 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.222+347C>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 2/9 | chr14 | 39115260 | ||||||
chr14:39115282
|
C | T | 77 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0031others(74): Show | 82 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.222+369C>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 2/9 | chr14 | 39115282 | ||||||
chr14:39115372
|
G | T | 2 | a0001c0001t0001g0362a0001c0001t0001g0363 | 2 | NA18954.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.222+459G>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 2/9 | chr14 | 39115372 | ||||||
chr14:39115456
|
C | CT | 26 | a0001c0001t0001g0008a0001c0001t0001g0121a0001c0001t0001g0122others(23): Show | 28 | HG01109.hp1 HG01109.hp2 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.222+562dupT | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr14 | 39115456 | |||||
chr14:39115456
|
C | CTT | 191 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(188): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.222+561_222+562dup others(2): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr14 | 39115456 | |||||
chr14:39115456
|
C | CTTT | 50 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(47): Show | 58 | HG00597.hp2 HG00673.hp1 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.222+560_222+562dup others(3): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr14 | 39115456 | |||||
chr14:39115554
|
T | G | 1 | a0001c0001t0001g0121 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.222+641T>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 2/9 | chr14 | 39115554 | ||||||
chr14:39115601
|
C | T | 2 | a0001c0001t0001g0120a0001c0001t0001g0142 | 2 | HG02965.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.222+688C>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 2/9 | chr14 | 39115601 | ||||||
chr14:39115622
|
A | G | 6 | a0001c0001t0001g0024a0001c0001t0001g0118a0001c0001t0001g0119others(3): Show | 7 | HG02647.hp2 HG02809.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.222+709A>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 2/9 | chr14 | 39115622 | ||||||
chr14:39115638
|
G | T | 1 | a0001c0001t0001g0239 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.222+725G>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 2/9 | chr14 | 39115638 | ||||||
chr14:39115713
|
C | T | 1 | a0001c0001t0001g0238 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.222+800C>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 2/9 | chr14 | 39115713 | ||||||
chr14:39115754
|
C | T | 7 | a0001c0001t0001g0012a0001c0001t0001g0315a0001c0001t0001g0316others(4): Show | 9 | HG00735.hp2 HG02683.hp2 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.222+841C>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 2/9 | chr14 | 39115754 | ||||||
chr14:39115890
|
T | C | 1 | a0001c0001t0001g0143 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.222+977T>C | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 2/9 | chr14 | 39115890 | ||||||
chr14:39116015
|
G | A | 7 | a0001c0001t0001g0122a0001c0001t0001g0144a0001c0001t0001g0145others(4): Show | 7 | HG01243.hp1 HG02451.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.222+1102G>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 2/9 | chr14 | 39116015 | ||||||
chr14:39116073
|
T | C | 1 | a0001c0001t0001g0271 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.222+1160T>C | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 2/9 | chr14 | 39116073 | ||||||
chr14:39116075
|
G | A | 30 | a0001c0001t0001g0033a0001c0001t0001g0122a0001c0001t0001g0143others(27): Show | 31 | HG00738.hp2 HG01070.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.222+1162G>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 2/9 | chr14 | 39116075 | ||||||
chr14:39116116
|
A | G | 1 | a0001c0001t0001g0117 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.222+1203A>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 2/9 | chr14 | 39116116 | ||||||
chr14:39116229
|
T | C | 1 | a0001c0001t0001g0121 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.222+1316T>C | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 2/9 | chr14 | 39116229 | ||||||
chr14:39116385
|
G | A | 1 | a0001c0001t0001g0272 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.222+1472G>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 2/9 | chr14 | 39116385 | ||||||
chr14:39116410
|
CT | C | 96 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(93): Show | 114 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.222+1513delT | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr14 | 39116410 | |||||
chr14:39116444
|
T | A | 77 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0031others(74): Show | 82 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.222+1531T>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 2/9 | chr14 | 39116444 | ||||||
chr14:39116625
|
T | TCTAA | 362 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(359): Show | 417 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(414): Show |
intron_variant | MODIFIER | c.223-1372_223-1371i others(6): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr14 | 39116625 | |||||
chr14:39116748
|
G | GGATT | 3 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0141 | 3 | HG01243.hp2 HG01255.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.223-1232_223-1229d others(6): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr14 | 39116748 | |||||
chr14:39116772
|
A | C | 72 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0031others(69): Show | 77 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.223-1227A>C | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 2/9 | chr14 | 39116772 | ||||||
chr14:39116782
|
G | A | 23 | a0001c0001t0001g0008a0001c0001t0001g0035a0001c0001t0001g0036others(20): Show | 25 | HG01109.hp1 HG01261.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.223-1217G>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 2/9 | chr14 | 39116782 | ||||||
chr14:39116982
|
C | T | 22 | a0001c0001t0001g0033a0001c0001t0001g0344a0001c0001t0001g0345others(19): Show | 23 | HG00738.hp2 HG01070.hp1 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.223-1017C>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 2/9 | chr14 | 39116982 | ||||||
chr14:39117047
|
C | T | 1 | a0001c0001t0001g0314 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.223-952C>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 2/9 | chr14 | 39117047 | ||||||
chr14:39117082
|
G | A | 1 | a0001c0001t0001g0207 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.223-917G>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 2/9 | chr14 | 39117082 | ||||||
chr14:39117129
|
G | A | 1 | a0001c0001t0001g0046 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.223-870G>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 2/9 | chr14 | 39117129 | ||||||
chr14:39117137
|
T | C | 1 | a0001c0001t0001g0321 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.223-862T>C | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 2/9 | chr14 | 39117137 | ||||||
chr14:39117218
|
G | T | 1 | a0001c0001t0001g0045 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.223-781G>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 2/9 | chr14 | 39117218 | ||||||
chr14:39117242
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.223-757C>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 2/9 | chr14 | 39117242 | ||||||
chr14:39117270
|
C | CA | 279 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(276): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.223-714dupA | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr14 | 39117270 | |||||
chr14:39117270
|
CA | C | 22 | a0001c0001t0001g0033a0001c0001t0001g0344a0001c0001t0001g0345others(19): Show | 23 | HG00738.hp2 HG01070.hp1 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.223-714delA | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr14 | 39117270 | |||||
chr14:39117317
|
G | A | 4 | a0001c0001t0001g0024a0001c0001t0001g0118a0001c0001t0001g0119others(1): Show | 5 | HG01934.hp1 HG02647.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.223-682G>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 2/9 | chr14 | 39117317 | ||||||
chr14:39117336
|
C | T | 29 | a0001c0001t0001g0033a0001c0001t0001g0122a0001c0001t0001g0144others(26): Show | 30 | HG00738.hp2 HG01070.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.223-663C>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 2/9 | chr14 | 39117336 | ||||||
chr14:39117401
|
G | T | 98 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(95): Show | 116 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.223-598G>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 2/9 | chr14 | 39117401 | ||||||
chr14:39117461
|
A | G | 7 | a0001c0001t0001g0122a0001c0001t0001g0144a0001c0001t0001g0145others(4): Show | 7 | HG01243.hp1 HG02451.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.223-538A>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 2/9 | chr14 | 39117461 | ||||||
chr14:39117538
|
C | A | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | HG02258.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.223-461C>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 2/9 | chr14 | 39117538 | ||||||
chr14:39117587
|
A | G | 40 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(37): Show | 49 | HG00099.hp2 HG00438.hp1 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.223-412A>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 2/9 | chr14 | 39117587 | ||||||
chr14:39117601
|
T | C | 6 | a0001c0001t0001g0024a0001c0001t0001g0118a0001c0001t0001g0119others(3): Show | 7 | HG02647.hp2 HG02809.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.223-398T>C | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 2/9 | chr14 | 39117601 | ||||||
chr14:39117619
|
C | G | 1 | a0001c0001t0001g0239 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.223-380C>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 2/9 | chr14 | 39117619 | ||||||
chr14:39117804
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.223-195C>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 2/9 | chr14 | 39117804 | ||||||
chr14:39117885
|
A | G | 1 | a0001c0001t0001g0109 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.223-114A>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 2/9 | chr14 | 39117885 | ||||||
chr14:39117908
|
T | C | 1 | a0001c0001t0001g0092 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.223-91T>C | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 2/9 | chr14 | 39117908 | ||||||
chr14:39118144
|
A | G | 77 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0031others(74): Show | 82 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.312+56A>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 3/9 | chr14 | 39118144 | ||||||
chr14:39118186
|
G | T | 1 | a0001c0001t0001g0236 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.312+98G>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 3/9 | chr14 | 39118186 | ||||||
chr14:39118234
|
G | A | 311 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(308): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.312+146G>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 3/9 | chr14 | 39118234 | ||||||
chr14:39118331
|
A | G | 1 | a0001c0001t0001g0313 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.313-209A>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 3/9 | chr14 | 39118331 | ||||||
chr14:39118334
|
A | T | 4 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(1): Show | 4 | HG02280.hp2 HG03130.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.313-206A>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 3/9 | chr14 | 39118334 | ||||||
chr14:39118406
|
G | C | 7 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(4): Show | 7 | HG02129.hp1 NA18612.hp2 NA18983.hp1 others(4): Show |
intron_variant | MODIFIER | c.313-134G>C | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 3/9 | chr14 | 39118406 | ||||||
chr14:39118412
|
T | C | 1 | a0001c0001t0001g0114 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.313-128T>C | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 3/9 | chr14 | 39118412 | ||||||
chr14:39118668
|
G | C | 1 | a0001c0001t0001g0140 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.372+69G>C | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 4/9 | chr14 | 39118668 | ||||||
chr14:39118780
|
A | AT | 38 | a0001c0001t0001g0033a0001c0001t0001g0037a0001c0001t0001g0089others(35): Show | 39 | HG00423.hp2 HG00597.hp1 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.372+201dupT | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr14 | 39118780 | |||||
chr14:39118780
|
A | ATT | 6 | a0001c0001t0001g0347a0001c0001t0001g0349a0001c0001t0001g0358others(3): Show | 6 | HG02970.hp1 HG03195.hp1 NA18906.hp1 others(3): Show |
intron_variant | MODIFIER | c.372+200_372+201dup others(2): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr14 | 39118780 | |||||
chr14:39119036
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.372+437C>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 4/9 | chr14 | 39119036 | ||||||
chr14:39119098
|
A | G | 1 | a0001c0001t0001g0199 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.372+499A>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 4/9 | chr14 | 39119098 | ||||||
chr14:39119117
|
A | T | 1 | a0001c0001t0001g0036 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.372+518A>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 4/9 | chr14 | 39119117 | ||||||
chr14:39119187
|
C | T | 2 | a0001c0001t0001g0256a0001c0001t0001g0257 | 2 | HG03239.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.372+588C>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 4/9 | chr14 | 39119187 | ||||||
chr14:39119480
|
G | C | 1 | a0001c0001t0001g0208 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.372+881G>C | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 4/9 | chr14 | 39119480 | ||||||
chr14:39119532
|
A | T | 2 | a0001c0001t0001g0362a0001c0001t0001g0363 | 2 | NA18954.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.372+933A>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 4/9 | chr14 | 39119532 | ||||||
chr14:39119541
|
A | G | 18 | a0001c0001t0001g0008a0001c0001t0001g0035a0001c0001t0001g0036others(15): Show | 20 | HG01109.hp1 HG01261.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.372+942A>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 4/9 | chr14 | 39119541 | ||||||
chr14:39119556
|
GA | G | 66 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0014others(63): Show | 75 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.372+965delA | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr14 | 39119556 | |||||
chr14:39119987
|
A | T | 5 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0307others(2): Show | 5 | HG01981.hp2 NA18963.hp2 NA18980.hp2 others(2): Show |
intron_variant | MODIFIER | c.372+1388A>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 4/9 | chr14 | 39119987 | ||||||
chr14:39120073
|
C | A | 7 | a0001c0001t0001g0122a0001c0001t0001g0144a0001c0001t0001g0145others(4): Show | 7 | HG01243.hp1 HG02451.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.372+1474C>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 4/9 | chr14 | 39120073 | ||||||
chr14:39120080
|
A | T | 1 | a0001c0001t0001g0087 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.372+1481A>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 4/9 | chr14 | 39120080 | ||||||
chr14:39120154
|
C | A | 1 | a0001c0001t0001g0200 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.372+1555C>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 4/9 | chr14 | 39120154 | ||||||
chr14:39120219
|
A | T | 3 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0198 | 3 | NA18948.hp1 NA18953.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.372+1620A>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 4/9 | chr14 | 39120219 | ||||||
chr14:39120419
|
T | C | 1 | a0001c0001t0001g0322 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.372+1820T>C | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 4/9 | chr14 | 39120419 | ||||||
chr14:39120464
|
A | T | 66 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0014others(63): Show | 75 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.372+1865A>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 4/9 | chr14 | 39120464 | ||||||
chr14:39120607
|
G | A | 98 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(95): Show | 116 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.373-1823G>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 4/9 | chr14 | 39120607 | ||||||
chr14:39120608
|
GTTTTA | G | 340 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(337): Show | 385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.373-1798_373-1794d others(7): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr14 | 39120608 | |||||
chr14:39120732
|
A | G | 1 | a0001c0001t0001g0121 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.373-1698A>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 4/9 | chr14 | 39120732 | ||||||
chr14:39120847
|
G | A | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | HG02258.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.373-1583G>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 4/9 | chr14 | 39120847 | ||||||
chr14:39121026
|
T | C | 1 | a0001c0001t0001g0239 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.373-1404T>C | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 4/9 | chr14 | 39121026 | ||||||
chr14:39121090
|
T | C | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | HG02258.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.373-1340T>C | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 4/9 | chr14 | 39121090 | ||||||
chr14:39121150
|
AT | A | 21 | a0001c0001t0001g0033a0001c0001t0001g0344a0001c0001t0001g0345others(18): Show | 22 | HG00738.hp2 HG01070.hp1 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.373-1274delT | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr14 | 39121150 | |||||
chr14:39121451
|
T | A | 1 | a0001c0001t0001g0209 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.373-979T>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 4/9 | chr14 | 39121451 | ||||||
chr14:39121708
|
TTTTG | T | 3 | a0001c0001t0001g0240a0001c0001t0001g0263a0001c0001t0001g0264 | 3 | HG02809.hp2 HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.373-706_373-703del others(4): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr14 | 39121708 | |||||
chr14:39121750
|
G | A | 1 | a0001c0001t0001g0273 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.373-680G>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 4/9 | chr14 | 39121750 | ||||||
chr14:39121813
|
G | A | 3 | a0001c0001t0001g0239a0001c0001t0001g0274a0002c0003t0001g0339 | 3 | HG02622.hp1 HG03098.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.373-617G>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 4/9 | chr14 | 39121813 | ||||||
chr14:39121877
|
T | TG | 71 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0031others(68): Show | 76 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.373-553_373-552ins others(1): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 4/9 | chr14 | 39121877 | ||||||
chr14:39121878
|
A | G | 6 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0267others(3): Show | 6 | HG01981.hp1 HG02630.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.373-552A>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 4/9 | chr14 | 39121878 | ||||||
chr14:39121879
|
A | AT | 8 | a0001c0001t0001g0024a0001c0001t0001g0086a0001c0001t0001g0118others(5): Show | 9 | HG02647.hp2 HG02809.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.373-537dupT | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr14 | 39121879 | |||||
chr14:39121879
|
A | T | 71 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0031others(68): Show | 76 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.373-551A>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 4/9 | chr14 | 39121879 | ||||||
chr14:39121903
|
G | T | 98 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(95): Show | 116 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.373-527G>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 4/9 | chr14 | 39121903 | ||||||
chr14:39121999
|
G | A | 2 | a0001c0001t0001g0013a0001c0001t0001g0047 | 3 | HG02015.hp1 NA19004.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.373-431G>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 4/9 | chr14 | 39121999 | ||||||
chr14:39122088
|
C | T | 1 | a0001c0001t0001g0340 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.373-342C>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 4/9 | chr14 | 39122088 | ||||||
chr14:39122331
|
C | T | 6 | a0001c0001t0001g0024a0001c0001t0001g0118a0001c0001t0001g0119others(3): Show | 7 | HG02647.hp2 HG02809.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.373-99C>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 4/9 | chr14 | 39122331 | ||||||
chr14:39122361
|
C | CT | 98 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(95): Show | 116 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.373-60dupT | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr14 | 39122361 | |||||
chr14:39122392
|
T | C | 1 | a0001c0001t0001g0210 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.373-38T>C | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 4/9 | chr14 | 39122392 | ||||||
chr14:39122409
|
G | GT | 102 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(99): Show | 121 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(118): Show |
splice_region_variant&intron_variant | LOW | c.373-8dupT | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr14 | 39122409 | |||||
chr14:39122913
|
G | C | 1 | a0001c0001t0003g0038 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.486+370G>C | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | chr14 | 39122913 | ||||||
chr14:39122946
|
A | G | 1 | a0001c0001t0003g0038 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.486+403A>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | chr14 | 39122946 | ||||||
chr14:39123006
|
A | G | 341 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(338): Show | 386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.486+463A>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | chr14 | 39123006 | ||||||
chr14:39123036
|
C | T | 40 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(37): Show | 49 | HG00099.hp2 HG00438.hp1 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.486+493C>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | chr14 | 39123036 | ||||||
chr14:39123443
|
G | A | 1 | a0001c0001t0001g0276 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.486+900G>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | chr14 | 39123443 | ||||||
chr14:39123474
|
T | C | 2 | a0001c0001t0001g0157a0001c0001t0001g0200 | 2 | HG02572.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.486+931T>C | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | chr14 | 39123474 | ||||||
chr14:39123603
|
G | C | 18 | a0001c0001t0001g0008a0001c0001t0001g0035a0001c0001t0001g0036others(15): Show | 20 | HG01109.hp1 HG01261.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.486+1060G>C | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | chr14 | 39123603 | ||||||
chr14:39123620
|
C | T | 24 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0047others(21): Show | 25 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.486+1077C>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | chr14 | 39123620 | ||||||
chr14:39123686
|
C | A | 2 | a0001c0001t0001g0024a0001c0001t0001g0118 | 3 | HG02647.hp2 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.486+1143C>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | chr14 | 39123686 | ||||||
chr14:39123686
|
C | CTATA | 5 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0270others(2): Show | 5 | HG01109.hp2 HG02280.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.486+1163_486+1166d others(6): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 39123686 | |||||
chr14:39123686
|
C | CTATATAT others(3): Show |
3 | a0001c0001t0001g0300a0001c0001t0001g0301a0001c0001t0001g0330 | 3 | HG01361.hp1 HG02040.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.486+1157_486+1166d others(12): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 39123686 | |||||
chr14:39123686
|
C | CTATATAT others(5): Show |
23 | a0001c0001t0001g0011a0001c0001t0001g0031a0001c0001t0001g0273others(20): Show | 26 | HG00323.hp1 HG00597.hp2 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.486+1155_486+1166d others(14): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 39123686 | |||||
chr14:39123686
|
C | CTATATAT others(7): Show |
3 | a0001c0001t0001g0275a0001c0001t0001g0290a0001c0001t0001g0324 | 3 | HG01169.hp1 HG01981.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.486+1153_486+1166d others(16): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 39123686 | |||||
chr14:39123686
|
C | CTATATAT others(9): Show |
3 | a0001c0001t0001g0271a0001c0001t0001g0284a0001c0001t0001g0321 | 3 | HG01123.hp2 NA19009.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.486+1151_486+1166d others(18): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 39123686 | |||||
chr14:39123686
|
C | CTATATAT others(11): Show |
2 | a0001c0001t0001g0282a0001c0001t0001g0335 | 2 | NA18974.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.486+1149_486+1166d others(20): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 39123686 | |||||
chr14:39123686
|
C | T | 4 | a0001c0001t0001g0119a0001c0001t0001g0240a0001c0001t0001g0263others(1): Show | 4 | HG02809.hp2 HG02922.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.486+1143C>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | chr14 | 39123686 | ||||||
chr14:39123686
|
CTA | C | 7 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0154others(4): Show | 7 | HG02738.hp2 NA18946.hp2 NA18948.hp2 others(4): Show |
intron_variant | MODIFIER | c.486+1165_486+1166d others(4): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 39123686 | |||||
chr14:39123686
|
CTATA | C | 50 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0026others(47): Show | 63 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.486+1163_486+1166d others(6): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 39123686 | |||||
chr14:39123703
|
TATATA | T | 4 | a0001c0001t0001g0043a0001c0001t0001g0194a0001c0001t0001g0337others(1): Show | 4 | HG01168.hp1 HG01169.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.486+1161_486+1165d others(7): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | chr14 | 39123703 | ||||||
chr14:39123704
|
ATATAT | A | 18 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0124others(15): Show | 22 | HG00438.hp2 HG00609.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.486+1163_486+1167d others(7): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 39123704 | |||||
chr14:39123705
|
TATA | T | 7 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0255others(4): Show | 7 | HG01175.hp1 HG01346.hp2 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.486+1163_486+1165d others(5): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | chr14 | 39123705 | ||||||
chr14:39123706
|
A | T | 2 | a0001c0001t0001g0341a0001c0001t0001g0342 | 2 | HG00642.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.486+1163A>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | chr14 | 39123706 | ||||||
chr14:39123706
|
ATAT | A | 18 | a0001c0001t0001g0033a0001c0001t0001g0162a0001c0001t0001g0198others(15): Show | 19 | HG00738.hp2 HG01255.hp1 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.486+1165_486+1167d others(5): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 39123706 | |||||
chr14:39123706
|
ATATT | A | 9 | a0001c0001t0001g0030a0001c0001t0001g0151a0001c0001t0001g0152others(6): Show | 10 | HG01070.hp1 HG01516.hp2 NA18944.hp1 others(7): Show |
intron_variant | MODIFIER | c.486+1165_486+1168d others(6): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 39123706 | |||||
chr14:39123706
|
ATATTTTT others(1): Show |
A | 38 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0016others(35): Show | 45 | HG00408.hp1 HG00558.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.486+1165_486+1172d others(10): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 39123706 | |||||
chr14:39123708
|
A | AT | 6 | a0001c0001t0001g0105a0001c0001t0001g0108a0001c0001t0001g0116others(3): Show | 6 | HG01934.hp2 HG02970.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.486+1195dupT | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 39123708 | |||||
chr14:39123708
|
A | ATATATAT others(4): Show |
1 | a0001c0001t0001g0319 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.486+1166_486+1167i others(13): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 39123708 | |||||
chr14:39123708
|
A | ATATATAT others(18): Show |
1 | a0001c0001t0001g0278 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.486+1166_486+1167i others(27): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 39123708 | |||||
chr14:39123708
|
A | ATATATAT others(20): Show |
1 | a0001c0001t0001g0310 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.486+1166_486+1167i others(29): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 39123708 | |||||
chr14:39123708
|
A | ATATATAT others(24): Show |
1 | a0001c0001t0001g0277 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.486+1166_486+1167i others(33): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 39123708 | |||||
chr14:39123708
|
A | ATATATAT others(19): Show |
2 | a0001c0001t0001g0279a0001c0001t0001g0280 | 2 | NA19002.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.486+1166_486+1167i others(28): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 39123708 | |||||
chr14:39123708
|
A | ATATATAT others(21): Show |
1 | a0001c0001t0001g0157 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.486+1166_486+1167i others(30): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 39123708 | |||||
chr14:39123708
|
A | ATATATAT others(23): Show |
1 | a0001c0001t0001g0343 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.486+1166_486+1167i others(32): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 39123708 | |||||
chr14:39123708
|
A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0314 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.486+1166_486+1167i others(26): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 39123708 | |||||
chr14:39123708
|
A | ATATATAT others(18): Show |
2 | a0001c0001t0001g0272a0001c0001t0001g0281 | 2 | NA18612.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.486+1166_486+1167i others(27): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 39123708 | |||||
chr14:39123708
|
A | ATATATAT others(15): Show |
1 | a0001c0001t0001g0311 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.486+1166_486+1167i others(24): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 39123708 | |||||
chr14:39123708
|
A | ATATATAT others(16): Show |
3 | a0001c0001t0001g0283a0001c0001t0001g0305a0001c0001t0001g0306 | 3 | HG04228.hp1 NA19001.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.486+1166_486+1167i others(25): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 39123708 | |||||
chr14:39123708
|
A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0200 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.486+1166_486+1167i others(26): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 39123708 | |||||
chr14:39123708
|
A | ATATATAT others(19): Show |
3 | a0001c0001t0001g0265a0001c0001t0001g0267a0001c0001t0001g0323 | 3 | HG02630.hp1 HG02886.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.486+1166_486+1167i others(28): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 39123708 | |||||
chr14:39123708
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0285 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.486+1166_486+1167i others(23): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 39123708 | |||||
chr14:39123708
|
A | ATATATAT others(15): Show |
2 | a0001c0001t0001g0286a0001c0001t0001g0307 | 2 | HG01981.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.486+1166_486+1167i others(24): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 39123708 | |||||
chr14:39123708
|
A | ATATATAT others(16): Show |
1 | a0001c0001t0001g0308 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.486+1166_486+1167i others(25): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 39123708 | |||||
chr14:39123708
|
A | ATATATAT others(17): Show |
2 | a0001c0001t0001g0287a0001c0001t0001g0309 | 2 | NA18963.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.486+1166_486+1167i others(26): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 39123708 | |||||
chr14:39123708
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0291 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.486+1166_486+1167i others(23): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 39123708 | |||||
chr14:39123708
|
A | ATATATAT others(15): Show |
1 | a0001c0001t0001g0292 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.486+1166_486+1167i others(24): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 39123708 | |||||
chr14:39123708
|
A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0268 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.486+1166_486+1167i others(26): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 39123708 | |||||
chr14:39123708
|
A | ATATATAT others(18): Show |
1 | a0001c0001t0001g0269 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.486+1166_486+1167i others(27): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 39123708 | |||||
chr14:39123708
|
A | ATATATAT others(12): Show |
2 | a0001c0001t0001g0144a0001c0001t0001g0145 | 2 | HG01243.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.486+1166_486+1167i others(21): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 39123708 | |||||
chr14:39123708
|
A | ATATATAT others(9): Show |
1 | a0001c0001t0001g0122 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.486+1166_486+1167i others(18): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 39123708 | |||||
chr14:39123708
|
A | ATATATAT others(10): Show |
2 | a0001c0001t0001g0146a0001c0001t0001g0266 | 2 | HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.486+1166_486+1167i others(19): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 39123708 | |||||
chr14:39123708
|
A | ATATATAT others(11): Show |
1 | a0001c0001t0001g0147 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.486+1166_486+1167i others(20): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 39123708 | |||||
chr14:39123708
|
A | ATATATAT others(5): Show |
3 | a0001c0001t0001g0012a0001c0001t0001g0207a0001c0001t0001g0320 | 5 | HG02683.hp2 HG02698.hp2 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.486+1166_486+1167i others(14): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 39123708 | |||||
chr14:39123708
|
A | ATATATAT others(9): Show |
1 | a0001c0001t0001g0148 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.486+1166_486+1167i others(18): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 39123708 | |||||
chr14:39123708
|
A | ATATATAT others(13): Show |
1 | a0001c0001t0001g0239 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.486+1166_486+1167i others(22): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 39123708 | |||||
chr14:39123708
|
A | ATATATAT others(10): Show |
1 | a0001c0001t0001g0241 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.486+1166_486+1167i others(19): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 39123708 | |||||
chr14:39123708
|
A | T | 10 | a0001c0001t0001g0032a0001c0001t0001g0044a0001c0001t0001g0107others(7): Show | 11 | HG00099.hp1 HG00642.hp1 HG00733.hp1 others(8): Show |
intron_variant | MODIFIER | c.486+1165A>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | chr14 | 39123708 | ||||||
chr14:39123708
|
AT | A | 17 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0028others(14): Show | 22 | HG00438.hp1 HG00639.hp2 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.486+1195delT | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 39123708 | |||||
chr14:39123708
|
ATT | A | 23 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0029others(20): Show | 29 | HG00099.hp2 HG00609.hp2 HG01496.hp2 others(26): Show |
intron_variant | MODIFIER | c.486+1194_486+1195d others(4): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 39123708 | |||||
chr14:39123708
|
ATTTTTTT others(1): Show |
A | 14 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0070others(11): Show | 14 | HG00558.hp1 HG00621.hp1 HG02071.hp2 others(11): Show |
intron_variant | MODIFIER | c.486+1188_486+1195d others(10): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 39123708 | |||||
chr14:39123709
|
T | TATATATA others(4): Show |
2 | a0001c0001t0001g0293a0001c0001t0001g0312 | 2 | HG00733.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.486+1166_486+1167i others(13): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | chr14 | 39123709 | ||||||
chr14:39123709
|
T | TATATATA others(6): Show |
5 | a0001c0001t0001g0041a0001c0001t0001g0276a0001c0001t0001g0313others(2): Show | 5 | HG02071.hp1 HG02258.hp2 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.486+1166_486+1167i others(15): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | chr14 | 39123709 | ||||||
chr14:39123709
|
T | TATATATA others(12): Show |
1 | a0001c0001t0001g0143 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.486+1166_486+1167i others(21): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | chr14 | 39123709 | ||||||
chr14:39123709
|
T | TATATATA others(14): Show |
1 | a0001c0001t0001g0315 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.486+1166_486+1167i others(23): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | chr14 | 39123709 | ||||||
chr14:39123710
|
T | A | 37 | a0001c0001t0001g0011a0001c0001t0001g0031a0001c0001t0001g0035others(34): Show | 40 | HG00323.hp1 HG00597.hp2 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.486+1167T>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | chr14 | 39123710 | ||||||
chr14:39123711
|
T | A | 19 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0041others(16): Show | 22 | HG00438.hp1 HG00639.hp2 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.486+1168T>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | chr14 | 39123711 | ||||||
chr14:39123712
|
T | A | 29 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0029others(26): Show | 35 | HG00099.hp2 HG00609.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.486+1169T>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | chr14 | 39123712 | ||||||
chr14:39123713
|
T | A | 19 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0041others(16): Show | 22 | HG00438.hp1 HG00639.hp2 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.486+1170T>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | chr14 | 39123713 | ||||||
chr14:39123714
|
T | A | 20 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0029others(17): Show | 26 | HG00099.hp2 HG00609.hp2 HG01496.hp2 others(23): Show |
intron_variant | MODIFIER | c.486+1171T>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | chr14 | 39123714 | ||||||
chr14:39123715
|
T | A | 12 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0137others(9): Show | 15 | HG00438.hp1 HG00639.hp2 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.486+1172T>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | chr14 | 39123715 | ||||||
chr14:39123716
|
T | A | 6 | a0001c0001t0001g0009a0001c0001t0001g0069a0001c0001t0001g0136others(3): Show | 8 | HG00099.hp2 HG00609.hp2 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.486+1173T>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | chr14 | 39123716 | ||||||
chr14:39123738
|
T | G | 1 | a0001c0001t0001g0313 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.486+1195T>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | chr14 | 39123738 | ||||||
chr14:39123786
|
T | A | 1 | a0001c0001t0001g0202 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.487-1206T>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | chr14 | 39123786 | ||||||
chr14:39123828
|
C | T | 4 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(1): Show | 4 | HG02280.hp2 HG03130.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.487-1164C>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | chr14 | 39123828 | ||||||
chr14:39123999
|
TC | T | 40 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(37): Show | 49 | HG00099.hp2 HG00438.hp1 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.487-991delC | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 39123999 | |||||
chr14:39124152
|
G | A | 31 | a0001c0001t0001g0033a0001c0001t0001g0122a0001c0001t0001g0143others(28): Show | 32 | HG00738.hp2 HG01070.hp1 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.487-840G>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | chr14 | 39124152 | ||||||
chr14:39124356
|
A | G | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(94): Show | 115 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.487-636A>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | chr14 | 39124356 | ||||||
chr14:39124420
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.487-572G>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | chr14 | 39124420 | ||||||
chr14:39124421
|
TA | T | 11 | a0001c0001t0001g0027a0001c0001t0001g0186a0001c0001t0001g0187others(8): Show | 12 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(9): Show |
intron_variant | MODIFIER | c.487-565delA | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 39124421 | |||||
chr14:39124461
|
A | G | 1 | a0001c0001t0001g0217 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.487-531A>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | chr14 | 39124461 | ||||||
chr14:39124616
|
C | CA | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(94): Show | 115 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.487-369dupA | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 39124616 | |||||
chr14:39124634
|
G | A | 1 | a0001c0001t0001g0239 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.487-358G>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | chr14 | 39124634 | ||||||
chr14:39124666
|
G | A | 67 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(64): Show | 83 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.487-326G>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | chr14 | 39124666 | ||||||
chr14:39124684
|
C | T | 7 | a0001c0001t0001g0122a0001c0001t0001g0144a0001c0001t0001g0145others(4): Show | 7 | HG01243.hp1 HG02451.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.487-308C>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | chr14 | 39124684 | ||||||
chr14:39124727
|
C | G | 1 | a0001c0001t0001g0132 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.487-265C>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | chr14 | 39124727 | ||||||
chr14:39124776
|
A | G | 6 | a0001c0001t0001g0024a0001c0001t0001g0118a0001c0001t0001g0119others(3): Show | 7 | HG02647.hp2 HG02809.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.487-216A>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | chr14 | 39124776 | ||||||
chr14:39124804
|
G | A | 7 | a0001c0001t0001g0122a0001c0001t0001g0144a0001c0001t0001g0145others(4): Show | 7 | HG01243.hp1 HG02451.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.487-188G>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | chr14 | 39124804 | ||||||
chr14:39124816
|
C | T | 7 | a0001c0001t0001g0122a0001c0001t0001g0144a0001c0001t0001g0145others(4): Show | 7 | HG01243.hp1 HG02451.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.487-176C>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | chr14 | 39124816 | ||||||
chr14:39124868
|
A | C | 6 | a0001c0001t0001g0122a0001c0001t0001g0145a0001c0001t0001g0146others(3): Show | 6 | HG01243.hp1 HG02451.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.487-124A>C | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 5/9 | chr14 | 39124868 | ||||||
chr14:39125083
|
T | C | 3 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0239 | 3 | HG02622.hp1 NA18980.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.531+47T>C | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 6/9 | chr14 | 39125083 | ||||||
chr14:39125174
|
T | G | 65 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0014others(62): Show | 74 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.531+138T>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 6/9 | chr14 | 39125174 | ||||||
chr14:39125199
|
A | G | 1 | a0001c0001t0001g0068 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.531+163A>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 6/9 | chr14 | 39125199 | ||||||
chr14:39125291
|
G | C | 4 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(1): Show | 4 | HG02280.hp2 HG03130.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.531+255G>C | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 6/9 | chr14 | 39125291 | ||||||
chr14:39125345
|
T | C | 7 | a0001c0001t0001g0122a0001c0001t0001g0144a0001c0001t0001g0145others(4): Show | 7 | HG01243.hp1 HG02451.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.531+309T>C | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 6/9 | chr14 | 39125345 | ||||||
chr14:39125515
|
C | T | 1 | a0001c0001t0001g0264 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.531+479C>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 6/9 | chr14 | 39125515 | ||||||
chr14:39125649
|
C | A | 1 | a0001c0001t0001g0358 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.531+613C>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 6/9 | chr14 | 39125649 | ||||||
chr14:39125738
|
T | C | 1 | a0001c0001t0001g0070 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.531+702T>C | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 6/9 | chr14 | 39125738 | ||||||
chr14:39125759
|
T | C | 22 | a0001c0001t0001g0008a0001c0001t0001g0035a0001c0001t0001g0036others(19): Show | 24 | HG01109.hp1 HG01261.hp1 HG02258.hp1 others(21): Show |
intron_variant | MODIFIER | c.531+723T>C | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 6/9 | chr14 | 39125759 | ||||||
chr14:39125772
|
G | A | 110 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(107): Show | 128 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.531+736G>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 6/9 | chr14 | 39125772 | ||||||
chr14:39125910
|
T | C | 6 | a0001c0001t0001g0024a0001c0001t0001g0118a0001c0001t0001g0119others(3): Show | 7 | HG02647.hp2 HG02809.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.531+874T>C | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 6/9 | chr14 | 39125910 | ||||||
chr14:39125975
|
G | A | 3 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045 | 3 | HG02809.hp1 HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.531+939G>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 6/9 | chr14 | 39125975 | ||||||
chr14:39126019
|
C | CA | 7 | a0001c0001t0001g0027a0001c0001t0001g0186a0001c0001t0001g0187others(4): Show | 8 | HG00099.hp1 HG01074.hp1 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.531+997dupA | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr14 | 39126019 | |||||
chr14:39126048
|
T | C | 5 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0267others(2): Show | 5 | HG02630.hp1 HG02886.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.531+1012T>C | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 6/9 | chr14 | 39126048 | ||||||
chr14:39126083
|
GT | G | 64 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0014others(61): Show | 73 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.531+1050delT | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr14 | 39126083 | |||||
chr14:39126116
|
C | G | 98 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(95): Show | 116 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.531+1080C>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 6/9 | chr14 | 39126116 | ||||||
chr14:39126184
|
C | CT | 14 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(11): Show | 14 | HG00597.hp2 HG01361.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.531+1163dupT | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr14 | 39126184 | |||||
chr14:39126204
|
G | C | 1 | a0001c0001t0001g0246 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.531+1168G>C | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 6/9 | chr14 | 39126204 | ||||||
chr14:39126244
|
A | C | 1 | a0001c0001t0001g0116 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.531+1208A>C | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 6/9 | chr14 | 39126244 | ||||||
chr14:39126387
|
C | G | 1 | a0001c0001t0001g0121 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.531+1351C>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 6/9 | chr14 | 39126387 | ||||||
chr14:39126410
|
G | C | 1 | a0001c0001t0001g0227 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.531+1374G>C | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 6/9 | chr14 | 39126410 | ||||||
chr14:39126530
|
C | T | 77 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0031others(74): Show | 82 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.531+1494C>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 6/9 | chr14 | 39126530 | ||||||
chr14:39126573
|
A | G | 1 | a0001c0001t0001g0116 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.531+1537A>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 6/9 | chr14 | 39126573 | ||||||
chr14:39126575
|
T | A | 12 | a0001c0001t0001g0008a0001c0001t0001g0126a0001c0001t0001g0127others(9): Show | 14 | HG01109.hp1 HG01261.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.531+1539T>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 6/9 | chr14 | 39126575 | ||||||
chr14:39126589
|
G | T | 18 | a0001c0001t0001g0008a0001c0001t0001g0035a0001c0001t0001g0036others(15): Show | 20 | HG01109.hp1 HG01261.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.531+1553G>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 6/9 | chr14 | 39126589 | ||||||
chr14:39126671
|
T | C | 40 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(37): Show | 49 | HG00099.hp2 HG00438.hp1 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.532-1609T>C | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 6/9 | chr14 | 39126671 | ||||||
chr14:39126712
|
G | C | 1 | a0001c0001t0001g0116 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.532-1568G>C | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 6/9 | chr14 | 39126712 | ||||||
chr14:39126753
|
TTTTTGTT others(3): Show |
T | 77 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0031others(74): Show | 82 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.532-1507_532-1498d others(12): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr14 | 39126753 | |||||
chr14:39127015
|
A | G | 341 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(338): Show | 386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.532-1265A>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 6/9 | chr14 | 39127015 | ||||||
chr14:39127044
|
T | C | 1 | a0001c0001t0001g0143 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.532-1236T>C | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 6/9 | chr14 | 39127044 | ||||||
chr14:39127055
|
C | T | 1 | a0002c0003t0001g0339 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.532-1225C>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 6/9 | chr14 | 39127055 | ||||||
chr14:39127090
|
C | CT | 108 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0024others(105): Show | 115 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(112): Show |
intron_variant | MODIFIER | c.532-1171dupT | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr14 | 39127090 | |||||
chr14:39127090
|
C | CTT | 8 | a0001c0001t0001g0269a0001c0001t0001g0304a0001c0001t0001g0311others(5): Show | 8 | HG00673.hp1 HG00738.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.532-1172_532-1171d others(4): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr14 | 39127090 | |||||
chr14:39127091
|
T | C | 39 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(36): Show | 48 | HG00099.hp2 HG00438.hp1 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.532-1189T>C | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 6/9 | chr14 | 39127091 | ||||||
chr14:39127145
|
A | AAGCGGCA others(14): Show |
1 | a0001c0001t0001g0239 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.532-1134_532-1114d others(23): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr14 | 39127145 | |||||
chr14:39127215
|
C | T | 7 | a0001c0001t0001g0122a0001c0001t0001g0144a0001c0001t0001g0145others(4): Show | 7 | HG01243.hp1 HG02451.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.532-1065C>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 6/9 | chr14 | 39127215 | ||||||
chr14:39127216
|
G | A | 6 | a0001c0001t0001g0024a0001c0001t0001g0118a0001c0001t0001g0119others(3): Show | 7 | HG02647.hp2 HG02809.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.532-1064G>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 6/9 | chr14 | 39127216 | ||||||
chr14:39127252
|
G | C | 2 | a0001c0001t0001g0035a0001c0001t0001g0037 | 2 | HG02280.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.532-1028G>C | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 6/9 | chr14 | 39127252 | ||||||
chr14:39127290
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.532-990G>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 6/9 | chr14 | 39127290 | ||||||
chr14:39127336
|
G | GT | 98 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0033others(95): Show | 103 | HG00323.hp1 HG00423.hp2 HG00642.hp1 others(100): Show |
intron_variant | MODIFIER | c.532-920dupT | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr14 | 39127336 | |||||
chr14:39127336
|
G | GTT | 77 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0014others(74): Show | 87 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.532-921_532-920dup others(2): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr14 | 39127336 | |||||
chr14:39127336
|
G | GTTT | 17 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(14): Show | 17 | HG00558.hp2 HG00621.hp1 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.532-922_532-920dup others(3): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr14 | 39127336 | |||||
chr14:39127336
|
GT | G | 6 | a0001c0001t0001g0101a0001c0001t0001g0107a0001c0001t0001g0121others(3): Show | 6 | HG00140.hp2 HG01516.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.532-920delT | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr14 | 39127336 | |||||
chr14:39127401
|
G | A | 77 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0031others(74): Show | 82 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.532-879G>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 6/9 | chr14 | 39127401 | ||||||
chr14:39127410
|
C | T | 6 | a0001c0001t0001g0024a0001c0001t0001g0118a0001c0001t0001g0119others(3): Show | 7 | HG02647.hp2 HG02809.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.532-870C>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 6/9 | chr14 | 39127410 | ||||||
chr14:39127461
|
G | T | 5 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0267others(2): Show | 5 | HG02630.hp1 HG02886.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.532-819G>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 6/9 | chr14 | 39127461 | ||||||
chr14:39127571
|
A | C | 6 | a0001c0001t0001g0024a0001c0001t0001g0118a0001c0001t0001g0119others(3): Show | 7 | HG02647.hp2 HG02809.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.532-709A>C | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 6/9 | chr14 | 39127571 | ||||||
chr14:39127592
|
G | C | 1 | a0001c0001t0001g0173 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.532-688G>C | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 6/9 | chr14 | 39127592 | ||||||
chr14:39127712
|
T | G | 1 | a0001c0001t0001g0045 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.532-568T>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 6/9 | chr14 | 39127712 | ||||||
chr14:39127716
|
TCCTAGGA others(6): Show |
T | 23 | a0001c0001t0001g0272a0001c0001t0001g0277a0001c0001t0001g0278others(20): Show | 23 | HG00423.hp2 HG00642.hp1 HG01257.hp2 others(20): Show |
intron_variant | MODIFIER | c.532-561_532-549del others(13): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr14 | 39127716 | |||||
chr14:39127797
|
C | T | 40 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(37): Show | 49 | HG00099.hp2 HG00438.hp1 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.532-483C>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 6/9 | chr14 | 39127797 | ||||||
chr14:39127929
|
G | A | 5 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0267others(2): Show | 5 | HG02630.hp1 HG02886.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.532-351G>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 6/9 | chr14 | 39127929 | ||||||
chr14:39127993
|
G | A | 1 | a0001c0001t0001g0207 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.532-287G>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 6/9 | chr14 | 39127993 | ||||||
chr14:39127999
|
C | T | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | HG02258.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.532-281C>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 6/9 | chr14 | 39127999 | ||||||
chr14:39128000
|
G | A | 40 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(37): Show | 49 | HG00099.hp2 HG00438.hp1 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.532-280G>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 6/9 | chr14 | 39128000 | ||||||
chr14:39128062
|
T | C | 340 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(337): Show | 385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.532-218T>C | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 6/9 | chr14 | 39128062 | ||||||
chr14:39128067
|
C | CA | 86 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0025others(83): Show | 92 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.532-187dupA | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr14 | 39128067 | |||||
chr14:39128067
|
C | CAA | 8 | a0001c0001t0001g0048a0001c0001t0001g0054a0001c0001t0001g0068others(5): Show | 8 | HG01258.hp1 HG01884.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.532-188_532-187dup others(2): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr14 | 39128067 | |||||
chr14:39128067
|
CA | C | 14 | a0001c0001t0001g0077a0001c0001t0001g0087a0001c0001t0001g0100others(11): Show | 14 | HG01256.hp2 HG02886.hp1 HG02897.hp2 others(11): Show |
intron_variant | MODIFIER | c.532-187delA | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr14 | 39128067 | |||||
chr14:39128094
|
G | C | 65 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0014others(62): Show | 74 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.532-186G>C | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 6/9 | chr14 | 39128094 | ||||||
chr14:39128132
|
T | C | 4 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(1): Show | 4 | HG02809.hp1 HG03486.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.532-148T>C | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 6/9 | chr14 | 39128132 | ||||||
chr14:39128425
|
A | G | 1 | a0001c0001t0001g0079 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.600+77A>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | chr14 | 39128425 | ||||||
chr14:39128480
|
C | A | 1 | a0001c0001t0001g0366 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.600+132C>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | chr14 | 39128480 | ||||||
chr14:39128484
|
T | C | 1 | a0001c0001t0001g0139 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.600+136T>C | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | chr14 | 39128484 | ||||||
chr14:39128485
|
C | CT | 249 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(246): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.600+160dupT | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr14 | 39128485 | |||||
chr14:39128485
|
C | CTT | 79 | a0001c0001t0001g0024a0001c0001t0001g0033a0001c0001t0001g0035others(76): Show | 81 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.600+159_600+160dup others(2): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr14 | 39128485 | |||||
chr14:39128485
|
C | T | 1 | a0001c0001t0001g0139 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.600+137C>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | chr14 | 39128485 | ||||||
chr14:39128490
|
T | TC | 2 | a0001c0001t0001g0007a0001c0001t0001g0046 | 4 | HG02135.hp2 NA18961.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.600+142_600+143ins others(1): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | chr14 | 39128490 | ||||||
chr14:39128522
|
G | A | 3 | a0001c0001t0001g0186a0001c0001t0001g0192a0001c0001t0001g0195 | 3 | HG00099.hp1 HG01074.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.600+174G>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | chr14 | 39128522 | ||||||
chr14:39128584
|
C | T | 41 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(38): Show | 50 | HG00099.hp2 HG00438.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.600+236C>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | chr14 | 39128584 | ||||||
chr14:39128609
|
A | G | 1 | a0001c0001t0003g0038 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.600+261A>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | chr14 | 39128609 | ||||||
chr14:39128636
|
G | A | 6 | a0001c0001t0001g0024a0001c0001t0001g0118a0001c0001t0001g0119others(3): Show | 7 | HG02647.hp2 HG02809.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.600+288G>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | chr14 | 39128636 | ||||||
chr14:39128647
|
C | T | 13 | a0001c0001t0001g0024a0001c0001t0001g0118a0001c0001t0001g0119others(10): Show | 14 | HG01243.hp1 HG02451.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.600+299C>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | chr14 | 39128647 | ||||||
chr14:39128757
|
C | A | 22 | a0001c0001t0001g0033a0001c0001t0001g0344a0001c0001t0001g0345others(19): Show | 23 | HG00738.hp2 HG01070.hp1 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.600+409C>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | chr14 | 39128757 | ||||||
chr14:39128763
|
A | G | 1 | a0001c0001t0001g0207 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.600+415A>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | chr14 | 39128763 | ||||||
chr14:39128794
|
T | C | 5 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0267others(2): Show | 5 | HG02630.hp1 HG02886.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.600+446T>C | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | chr14 | 39128794 | ||||||
chr14:39128797
|
G | T | 22 | a0001c0001t0001g0033a0001c0001t0001g0344a0001c0001t0001g0345others(19): Show | 23 | HG00738.hp2 HG01070.hp1 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.600+449G>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | chr14 | 39128797 | ||||||
chr14:39128828
|
G | T | 1 | a0001c0001t0001g0064 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.600+480G>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | chr14 | 39128828 | ||||||
chr14:39128967
|
C | G | 13 | a0001c0001t0001g0024a0001c0001t0001g0118a0001c0001t0001g0119others(10): Show | 14 | HG01243.hp1 HG02451.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.600+619C>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | chr14 | 39128967 | ||||||
chr14:39129125
|
G | A | 13 | a0001c0001t0001g0024a0001c0001t0001g0118a0001c0001t0001g0119others(10): Show | 14 | HG01243.hp1 HG02451.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.600+777G>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | chr14 | 39129125 | ||||||
chr14:39129236
|
G | A | 1 | a0001c0001t0003g0038 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.600+888G>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | chr14 | 39129236 | ||||||
chr14:39129355
|
C | T | 2 | a0001c0001t0001g0166a0001c0001t0001g0169 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.600+1007C>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | chr14 | 39129355 | ||||||
chr14:39129397
|
G | A | 2 | a0001c0001t0001g0189a0001c0001t0001g0233 | 2 | HG03490.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.600+1049G>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | chr14 | 39129397 | ||||||
chr14:39129412
|
T | A | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(94): Show | 115 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.600+1064T>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | chr14 | 39129412 | ||||||
chr14:39129469
|
A | G | 77 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0031others(74): Show | 82 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.600+1121A>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | chr14 | 39129469 | ||||||
chr14:39129474
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.600+1126C>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | chr14 | 39129474 | ||||||
chr14:39129722
|
A | G | 1 | a0001c0001t0001g0239 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.600+1374A>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | chr14 | 39129722 | ||||||
chr14:39129732
|
A | G | 13 | a0001c0001t0001g0024a0001c0001t0001g0118a0001c0001t0001g0119others(10): Show | 14 | HG01243.hp1 HG02451.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.600+1384A>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | chr14 | 39129732 | ||||||
chr14:39129734
|
ATTTG | A | 13 | a0001c0001t0001g0024a0001c0001t0001g0118a0001c0001t0001g0119others(10): Show | 14 | HG01243.hp1 HG02451.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.600+1388_600+1391d others(6): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr14 | 39129734 | |||||
chr14:39129742
|
A | G | 31 | a0001c0001t0001g0008a0001c0001t0001g0024a0001c0001t0001g0035others(28): Show | 34 | HG01109.hp1 HG01243.hp1 HG01261.hp1 others(31): Show |
intron_variant | MODIFIER | c.600+1394A>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | chr14 | 39129742 | ||||||
chr14:39129756
|
G | A | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 131 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.600+1408G>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | chr14 | 39129756 | ||||||
chr14:39129763
|
C | T | 341 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(338): Show | 386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.600+1415C>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | chr14 | 39129763 | ||||||
chr14:39129919
|
A | G | 15 | a0001c0001t0001g0024a0001c0001t0001g0118a0001c0001t0001g0119others(12): Show | 16 | HG01243.hp1 HG02451.hp2 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.600+1571A>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | chr14 | 39129919 | ||||||
chr14:39129920
|
T | C | 2 | a0001c0001t0001g0222a0001c0001t0001g0225 | 2 | HG01496.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.600+1572T>C | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | chr14 | 39129920 | ||||||
chr14:39129927
|
C | T | 22 | a0001c0001t0001g0033a0001c0001t0001g0344a0001c0001t0001g0345others(19): Show | 23 | HG00738.hp2 HG01070.hp1 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.600+1579C>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | chr14 | 39129927 | ||||||
chr14:39129933
|
T | TG | 14 | a0001c0001t0001g0033a0001c0001t0001g0207a0001c0001t0001g0349others(11): Show | 15 | HG01070.hp1 HG01255.hp1 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.600+1586dupG | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr14 | 39129933 | |||||
chr14:39129934
|
G | GGT | 6 | a0001c0001t0001g0345a0001c0001t0001g0346a0001c0001t0001g0347others(3): Show | 6 | HG00738.hp2 HG02109.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.600+1586_600+1587i others(4): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | chr14 | 39129934 | ||||||
chr14:39129934
|
G | GGTT | 3 | a0001c0001t0001g0143a0001c0001t0001g0344a0001c0001t0001g0348 | 3 | HG01891.hp1 HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.600+1586_600+1587i others(5): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | chr14 | 39129934 | ||||||
chr14:39129934
|
G | GT | 44 | a0001c0001t0001g0024a0001c0001t0001g0045a0001c0001t0001g0046others(41): Show | 45 | HG00609.hp1 HG00609.hp2 HG01109.hp1 others(42): Show |
intron_variant | MODIFIER | c.600+1610dupT | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr14 | 39129934 | |||||
chr14:39129934
|
G | GTT | 49 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016others(46): Show | 55 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.600+1609_600+1610d others(4): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr14 | 39129934 | |||||
chr14:39129934
|
G | GTTT | 18 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0051others(15): Show | 21 | HG00423.hp1 HG01433.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.600+1608_600+1610d others(5): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr14 | 39129934 | |||||
chr14:39129934
|
GT | G | 65 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0021others(62): Show | 71 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.600+1610delT | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr14 | 39129934 | |||||
chr14:39129934
|
GTTTTTTT others(7): Show |
G | 4 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(1): Show | 4 | HG02280.hp2 HG03130.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.600+1597_600+1610d others(16): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr14 | 39129934 | |||||
chr14:39129935
|
T | G | 1 | a0001c0001t0001g0360 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.600+1587T>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | chr14 | 39129935 | ||||||
chr14:39129949
|
T | G | 1 | a0001c0001t0001g0211 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.600+1601T>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | chr14 | 39129949 | ||||||
chr14:39129977
|
G | C | 5 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0307others(2): Show | 5 | HG01981.hp2 NA18963.hp2 NA18980.hp2 others(2): Show |
intron_variant | MODIFIER | c.600+1629G>C | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | chr14 | 39129977 | ||||||
chr14:39129985
|
G | T | 7 | a0001c0001t0001g0122a0001c0001t0001g0144a0001c0001t0001g0145others(4): Show | 7 | HG01243.hp1 HG02451.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.600+1637G>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | chr14 | 39129985 | ||||||
chr14:39130088
|
GAATATTT others(11): Show |
G | 14 | a0001c0001t0001g0024a0001c0001t0001g0118a0001c0001t0001g0119others(11): Show | 15 | HG00438.hp1 HG01243.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.600+1757_600+1774d others(20): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr14 | 39130088 | |||||
chr14:39130456
|
C | T | 13 | a0001c0001t0001g0024a0001c0001t0001g0118a0001c0001t0001g0119others(10): Show | 14 | HG01243.hp1 HG02451.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.601-1502C>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | chr14 | 39130456 | ||||||
chr14:39130485
|
A | C | 1 | a0001c0001t0001g0206 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.601-1473A>C | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | chr14 | 39130485 | ||||||
chr14:39130577
|
C | A | 1 | a0001c0001t0001g0239 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.601-1381C>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | chr14 | 39130577 | ||||||
chr14:39130586
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.601-1372G>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | chr14 | 39130586 | ||||||
chr14:39130629
|
C | A | 1 | a0001c0001t0001g0089 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.601-1329C>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | chr14 | 39130629 | ||||||
chr14:39130660
|
G | A | 1 | a0001c0001t0001g0058 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.601-1298G>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | chr14 | 39130660 | ||||||
chr14:39130763
|
C | T | 3 | a0001c0001t0001g0240a0001c0001t0001g0263a0001c0001t0001g0264 | 3 | HG02809.hp2 HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.601-1195C>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | chr14 | 39130763 | ||||||
chr14:39130888
|
C | G | 5 | a0001c0001t0001g0019a0001c0001t0001g0057a0001c0001t0001g0066others(2): Show | 6 | HG00408.hp1 HG00558.hp2 NA18951.hp1 others(3): Show |
intron_variant | MODIFIER | c.601-1070C>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | chr14 | 39130888 | ||||||
chr14:39130937
|
T | G | 6 | a0001c0001t0001g0024a0001c0001t0001g0118a0001c0001t0001g0119others(3): Show | 7 | HG02647.hp2 HG02809.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.601-1021T>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | chr14 | 39130937 | ||||||
chr14:39131008
|
G | A | 242 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(239): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.601-950G>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | chr14 | 39131008 | ||||||
chr14:39131030
|
G | A | 1 | a0002c0003t0001g0339 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.601-928G>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | chr14 | 39131030 | ||||||
chr14:39131033
|
C | T | 1 | a0001c0001t0001g0029 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.601-925C>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | chr14 | 39131033 | ||||||
chr14:39131035
|
C | T | 2 | a0001c0001t0001g0179a0001c0001t0001g0251 | 2 | NA19003.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.601-923C>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | chr14 | 39131035 | ||||||
chr14:39131036
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.601-922G>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | chr14 | 39131036 | ||||||
chr14:39131126
|
G | C | 8 | a0001c0001t0001g0349a0001c0001t0001g0351a0001c0001t0001g0352others(5): Show | 8 | HG00738.hp2 HG01261.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.601-832G>C | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | chr14 | 39131126 | ||||||
chr14:39131187
|
C | T | 1 | a0002c0003t0001g0339 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.601-771C>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | chr14 | 39131187 | ||||||
chr14:39131229
|
A | G | 13 | a0001c0001t0001g0024a0001c0001t0001g0118a0001c0001t0001g0119others(10): Show | 14 | HG01243.hp1 HG02451.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.601-729A>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | chr14 | 39131229 | ||||||
chr14:39131253
|
C | T | 6 | a0001c0001t0001g0024a0001c0001t0001g0118a0001c0001t0001g0119others(3): Show | 7 | HG02647.hp2 HG02809.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.601-705C>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | chr14 | 39131253 | ||||||
chr14:39131326
|
A | G | 1 | a0001c0001t0001g0184 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.601-632A>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | chr14 | 39131326 | ||||||
chr14:39131487
|
T | C | 1 | a0001c0001t0001g0051 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.601-471T>C | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | chr14 | 39131487 | ||||||
chr14:39131499
|
A | T | 13 | a0001c0001t0001g0024a0001c0001t0001g0118a0001c0001t0001g0119others(10): Show | 14 | HG01243.hp1 HG02451.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.601-459A>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | chr14 | 39131499 | ||||||
chr14:39131544
|
T | C | 7 | a0001c0001t0001g0122a0001c0001t0001g0144a0001c0001t0001g0145others(4): Show | 7 | HG01243.hp1 HG02451.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.601-414T>C | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | chr14 | 39131544 | ||||||
chr14:39131596
|
A | G | 8 | a0001c0001t0001g0033a0001c0001t0001g0350a0001c0001t0001g0353others(5): Show | 9 | HG01070.hp1 HG01255.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.601-362A>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | chr14 | 39131596 | ||||||
chr14:39131794
|
C | G | 5 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(2): Show | 5 | HG02280.hp2 HG03130.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.601-164C>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | chr14 | 39131794 | ||||||
chr14:39131896
|
T | G | 13 | a0001c0001t0001g0024a0001c0001t0001g0118a0001c0001t0001g0119others(10): Show | 14 | HG01243.hp1 HG02451.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.601-62T>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | chr14 | 39131896 | ||||||
chr14:39131918
|
A | C | 6 | a0001c0001t0001g0024a0001c0001t0001g0118a0001c0001t0001g0119others(3): Show | 7 | HG02647.hp2 HG02809.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.601-40A>C | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | chr14 | 39131918 | ||||||
chr14:39131946
|
A | AT | 7 | a0001c0001t0001g0122a0001c0001t0001g0144a0001c0001t0001g0145others(4): Show | 7 | HG01243.hp1 HG02451.hp2 HG02572.hp2 others(4): Show |
splice_acceptor_variant&intron_variant | HIGH | c.601-3dupT | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr14 | 39131946 | |||||
chr14:39132351
|
T | A | 1 | a0003c0002t0005g0171 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.711+283T>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 8/9 | chr14 | 39132351 | ||||||
chr14:39132373
|
A | C | 1 | a0001c0001t0001g0143 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.711+305A>C | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 8/9 | chr14 | 39132373 | ||||||
chr14:39132432
|
G | A | 41 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(38): Show | 50 | HG00099.hp2 HG00438.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.711+364G>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 8/9 | chr14 | 39132432 | ||||||
chr14:39132454
|
C | T | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(94): Show | 115 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.711+386C>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 8/9 | chr14 | 39132454 | ||||||
chr14:39132465
|
A | G | 1 | a0003c0002t0005g0171 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.711+397A>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 8/9 | chr14 | 39132465 | ||||||
chr14:39132466
|
G | A | 1 | a0003c0002t0005g0171 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.711+398G>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 8/9 | chr14 | 39132466 | ||||||
chr14:39132468
|
T | G | 1 | a0003c0002t0005g0171 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.711+400T>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 8/9 | chr14 | 39132468 | ||||||
chr14:39132551
|
A | G | 1 | a0001c0001t0001g0220 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.711+483A>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 8/9 | chr14 | 39132551 | ||||||
chr14:39132664
|
C | CT | 62 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0031others(59): Show | 67 | HG00323.hp1 HG00642.hp1 HG00673.hp1 others(64): Show |
intron_variant | MODIFIER | c.711+618dupT | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 39132664 | |||||
chr14:39132664
|
C | CTT | 25 | a0001c0001t0001g0102a0001c0001t0001g0266a0001c0001t0001g0267others(22): Show | 25 | HG00423.hp2 HG00597.hp2 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.711+617_711+618dup others(2): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 39132664 | |||||
chr14:39132666
|
T | C | 41 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(38): Show | 50 | HG00099.hp2 HG00438.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.711+598T>C | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 8/9 | chr14 | 39132666 | ||||||
chr14:39132675
|
TTTTTTTT others(5): Show |
T | 1 | a0001c0001t0001g0301 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.711+612_711+623del others(12): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 39132675 | |||||
chr14:39132684
|
TTTC | T | 16 | a0001c0001t0001g0024a0001c0001t0001g0040a0001c0001t0001g0118others(13): Show | 17 | HG01515.hp2 HG02451.hp2 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.711+619_711+621del others(3): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 39132684 | |||||
chr14:39132685
|
TTC | T | 102 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(99): Show | 121 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.711+619_711+620del others(2): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 39132685 | |||||
chr14:39132686
|
TC | T | 111 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(108): Show | 130 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.711+619delC | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 8/9 | chr14 | 39132686 | ||||||
chr14:39132687
|
C | T | 132 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0011others(129): Show | 148 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.711+619C>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 8/9 | chr14 | 39132687 | ||||||
chr14:39132701
|
T | C | 1 | a0001c0001t0001g0214 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.711+633T>C | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 8/9 | chr14 | 39132701 | ||||||
chr14:39132720
|
C | T | 24 | a0001c0001t0001g0033a0001c0001t0001g0143a0001c0001t0001g0207others(21): Show | 25 | HG00738.hp2 HG01070.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.711+652C>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 8/9 | chr14 | 39132720 | ||||||
chr14:39132747
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.711+679C>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 8/9 | chr14 | 39132747 | ||||||
chr14:39132824
|
G | A | 1 | a0001c0001t0003g0038 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.711+756G>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 8/9 | chr14 | 39132824 | ||||||
chr14:39132827
|
C | T | 3 | a0001c0001t0001g0302a0001c0001t0001g0303a0001c0001t0001g0304 | 3 | NA18960.hp1 NA18998.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.711+759C>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 8/9 | chr14 | 39132827 | ||||||
chr14:39132975
|
G | GGT | 8 | a0001c0001t0001g0024a0001c0001t0001g0048a0001c0001t0001g0070others(5): Show | 9 | HG00558.hp1 HG00639.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.712-661_712-660dup others(2): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 39132975 | |||||
chr14:39132975
|
GGT | G | 116 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(113): Show | 136 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.712-661_712-660del others(2): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 39132975 | |||||
chr14:39132980
|
GTGTGTGT others(21): Show |
G | 21 | a0001c0001t0001g0033a0001c0001t0001g0344a0001c0001t0001g0345others(18): Show | 22 | HG01070.hp1 HG01255.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.712-661_712-634del others(28): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 39132980 | |||||
chr14:39132983
|
T | A | 1 | a0003c0002t0005g0171 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.712-678T>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 8/9 | chr14 | 39132983 | ||||||
chr14:39132984
|
GTGTGTGT others(17): Show |
G | 7 | a0001c0001t0001g0122a0001c0001t0001g0145a0001c0001t0001g0146others(4): Show | 7 | HG01243.hp1 HG02451.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.712-659_712-636del others(24): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 39132984 | |||||
chr14:39132986
|
GTGTGTGT others(15): Show |
G | 1 | a0001c0001t0001g0144 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.712-659_712-638del others(22): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 39132986 | |||||
chr14:39132998
|
GTGTA | G | 3 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045 | 3 | HG02809.hp1 HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.712-661_712-658del others(4): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 39132998 | |||||
chr14:39133000
|
G | A | 74 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0019others(71): Show | 80 | HG00323.hp1 HG00597.hp2 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.712-661G>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 8/9 | chr14 | 39133000 | ||||||
chr14:39133000
|
GTATATAT others(21): Show |
G | 1 | a0001c0001t0001g0352 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.712-651_712-624del others(28): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 39133000 | |||||
chr14:39133002
|
A | G | 6 | a0001c0001t0001g0024a0001c0001t0001g0055a0001c0001t0001g0118others(3): Show | 7 | HG02647.hp2 HG02809.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.712-659A>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 8/9 | chr14 | 39133002 | ||||||
chr14:39133004
|
A | G | 5 | a0001c0001t0001g0024a0001c0001t0001g0118a0001c0001t0001g0119others(2): Show | 6 | HG02647.hp2 HG02809.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.712-657A>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 8/9 | chr14 | 39133004 | ||||||
chr14:39133006
|
A | G | 5 | a0001c0001t0001g0024a0001c0001t0001g0118a0001c0001t0001g0119others(2): Show | 6 | HG02647.hp2 HG02809.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.712-655A>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 8/9 | chr14 | 39133006 | ||||||
chr14:39133008
|
A | G | 73 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0031others(70): Show | 78 | HG00323.hp1 HG00597.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.712-653A>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 8/9 | chr14 | 39133008 | ||||||
chr14:39133008
|
ATG | A | 2 | a0001c0001t0001g0022a0001c0001t0001g0103 | 3 | HG01515.hp1 HG01517.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.712-635_712-634del others(2): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 39133008 | |||||
chr14:39133010
|
G | A | 8 | a0001c0001t0001g0024a0001c0001t0001g0043a0001c0001t0001g0044others(5): Show | 9 | HG02647.hp2 HG02809.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.712-651G>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 8/9 | chr14 | 39133010 | ||||||
chr14:39133024
|
G | T | 1 | a0003c0002t0005g0171 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.712-637G>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 8/9 | chr14 | 39133024 | ||||||
chr14:39133025
|
T | A | 1 | a0003c0002t0005g0171 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.712-636T>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 8/9 | chr14 | 39133025 | ||||||
chr14:39133026
|
G | A | 75 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0031others(72): Show | 80 | HG00323.hp1 HG00597.hp2 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.712-635G>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 8/9 | chr14 | 39133026 | ||||||
chr14:39133026
|
GTA | G | 5 | a0001c0001t0001g0017a0001c0001t0001g0061a0001c0001t0001g0088others(2): Show | 6 | HG01081.hp2 HG01358.hp1 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.712-623_712-622del others(2): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 39133026 | |||||
chr14:39133028
|
A | G | 77 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0014others(74): Show | 86 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.712-633A>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 8/9 | chr14 | 39133028 | ||||||
chr14:39133030
|
A | G | 2 | a0001c0001t0001g0013a0001c0001t0001g0232 | 3 | HG03710.hp2 NA19004.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.712-631A>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 8/9 | chr14 | 39133030 | ||||||
chr14:39133030
|
ATATATAT others(4): Show |
A | 1 | a0003c0002t0005g0171 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.712-629_712-619del others(11): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 39133030 | |||||
chr14:39133030
|
ATATATAT others(5): Show |
A | 1 | a0001c0001t0001g0279 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.712-621_712-610del others(12): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 39133030 | |||||
chr14:39133052
|
A | C | 13 | a0001c0001t0001g0024a0001c0001t0001g0118a0001c0001t0001g0119others(10): Show | 14 | HG01243.hp1 HG02451.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.712-609A>C | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 8/9 | chr14 | 39133052 | ||||||
chr14:39133053
|
T | TTA | 13 | a0001c0001t0001g0024a0001c0001t0001g0118a0001c0001t0001g0119others(10): Show | 14 | HG01243.hp1 HG02451.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.712-608_712-607ins others(2): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 8/9 | chr14 | 39133053 | ||||||
chr14:39133054
|
C | A | 13 | a0001c0001t0001g0024a0001c0001t0001g0118a0001c0001t0001g0119others(10): Show | 14 | HG01243.hp1 HG02451.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.712-607C>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 8/9 | chr14 | 39133054 | ||||||
chr14:39133056
|
T | A | 13 | a0001c0001t0001g0024a0001c0001t0001g0118a0001c0001t0001g0119others(10): Show | 14 | HG01243.hp1 HG02451.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.712-605T>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 8/9 | chr14 | 39133056 | ||||||
chr14:39133090
|
G | A | 341 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(338): Show | 386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.712-571G>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 8/9 | chr14 | 39133090 | ||||||
chr14:39133099
|
CTG | C | 98 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(95): Show | 116 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.712-558_712-557del others(2): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 39133099 | |||||
chr14:39133187
|
T | TAG | 316 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(313): Show | 358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.712-471_712-470dup others(2): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 39133187 | |||||
chr14:39133196
|
A | C | 72 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0031others(69): Show | 77 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.712-465A>C | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 8/9 | chr14 | 39133196 | ||||||
chr14:39133197
|
A | G | 1 | a0001c0001t0001g0316 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.712-464A>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 8/9 | chr14 | 39133197 | ||||||
chr14:39133310
|
T | TAC | 341 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(338): Show | 386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.712-350_712-349ins others(2): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 39133310 | |||||
chr14:39133318
|
A | AAT | 14 | a0001c0001t0001g0008a0001c0001t0001g0062a0001c0001t0001g0126others(11): Show | 16 | HG01109.hp1 HG01261.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.712-328_712-327dup others(2): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 39133318 | |||||
chr14:39133337
|
A | T | 1 | a0003c0002t0005g0171 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.712-324A>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 8/9 | chr14 | 39133337 | ||||||
chr14:39133338
|
T | A | 1 | a0003c0002t0005g0171 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.712-323T>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 8/9 | chr14 | 39133338 | ||||||
chr14:39133432
|
T | A | 1 | a0003c0002t0005g0171 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.712-229T>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 8/9 | chr14 | 39133432 | ||||||
chr14:39133451
|
A | C | 6 | a0001c0001t0001g0024a0001c0001t0001g0118a0001c0001t0001g0119others(3): Show | 7 | HG02647.hp2 HG02809.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.712-210A>C | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 8/9 | chr14 | 39133451 | ||||||
chr14:39133536
|
T | G | 1 | a0003c0002t0005g0171 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.712-125T>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 8/9 | chr14 | 39133536 | ||||||
chr14:39133541
|
C | T | 6 | a0001c0001t0001g0024a0001c0001t0001g0118a0001c0001t0001g0119others(3): Show | 7 | HG02647.hp2 HG02809.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.712-120C>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 8/9 | chr14 | 39133541 | ||||||
chr14:39133766
|
G | A | 4 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(1): Show | 4 | HG02280.hp2 HG03130.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.770+47G>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 9/9 | chr14 | 39133766 | ||||||
chr14:39133855
|
G | A | 1 | a0001c0001t0001g0040 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.770+136G>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 9/9 | chr14 | 39133855 | ||||||
chr14:39133873
|
A | G | 6 | a0001c0001t0001g0024a0001c0001t0001g0118a0001c0001t0001g0119others(3): Show | 7 | HG02647.hp2 HG02809.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.770+154A>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 9/9 | chr14 | 39133873 | ||||||
chr14:39133889
|
G | C | 66 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0014others(63): Show | 75 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.770+170G>C | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 9/9 | chr14 | 39133889 | ||||||
chr14:39133941
|
G | A | 1 | a0003c0002t0005g0171 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.770+222G>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 9/9 | chr14 | 39133941 | ||||||
chr14:39133944
|
C | G | 1 | a0003c0002t0005g0171 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.770+225C>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 9/9 | chr14 | 39133944 | ||||||
chr14:39133952
|
C | T | 77 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0031others(74): Show | 82 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.770+233C>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 9/9 | chr14 | 39133952 | ||||||
chr14:39133996
|
A | G | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(94): Show | 115 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.770+277A>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 9/9 | chr14 | 39133996 | ||||||
chr14:39134077
|
G | A | 1 | a0001c0001t0001g0045 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.770+358G>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 9/9 | chr14 | 39134077 | ||||||
chr14:39134173
|
T | C | 1 | a0001c0001t0001g0279 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.770+454T>C | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 9/9 | chr14 | 39134173 | ||||||
chr14:39134319
|
A | G | 1 | a0001c0001t0001g0239 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.770+600A>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 9/9 | chr14 | 39134319 | ||||||
chr14:39134332
|
C | T | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(94): Show | 115 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.770+613C>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 9/9 | chr14 | 39134332 | ||||||
chr14:39134355
|
C | A | 341 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(338): Show | 386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.770+636C>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 9/9 | chr14 | 39134355 | ||||||
chr14:39134365
|
C | T | 13 | a0001c0001t0001g0024a0001c0001t0001g0118a0001c0001t0001g0119others(10): Show | 14 | HG01243.hp1 HG02451.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.770+646C>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 9/9 | chr14 | 39134365 | ||||||
chr14:39134513
|
T | C | 1 | a0001c0001t0001g0176 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.770+794T>C | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 9/9 | chr14 | 39134513 | ||||||
chr14:39134673
|
G | A | 1 | a0001c0001t0001g0076 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.770+954G>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 9/9 | chr14 | 39134673 | ||||||
chr14:39134822
|
C | T | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(94): Show | 115 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.770+1103C>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 9/9 | chr14 | 39134822 | ||||||
chr14:39134831
|
A | G | 341 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(338): Show | 386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.770+1112A>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 9/9 | chr14 | 39134831 | ||||||
chr14:39134876
|
C | A | 21 | a0001c0001t0001g0033a0001c0001t0001g0344a0001c0001t0001g0345others(18): Show | 22 | HG00738.hp2 HG01070.hp1 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.770+1157C>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 9/9 | chr14 | 39134876 | ||||||
chr14:39134968
|
G | A | 1 | a0001c0001t0001g0278 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.770+1249G>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 9/9 | chr14 | 39134968 | ||||||
chr14:39134996
|
A | AT | 5 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0267others(2): Show | 5 | HG02630.hp1 HG02886.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.770+1283dupT | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 39134996 | |||||
chr14:39135009
|
A | G | 1 | a0001c0001t0001g0084 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.770+1290A>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 9/9 | chr14 | 39135009 | ||||||
chr14:39135055
|
A | G | 1 | a0001c0001t0001g0143 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.770+1336A>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 9/9 | chr14 | 39135055 | ||||||
chr14:39135124
|
TCTGA | T | 59 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0014others(56): Show | 68 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.771-1312_771-1309d others(6): Show |
GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 39135124 | |||||
chr14:39135131
|
G | A | 72 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0031others(69): Show | 77 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.771-1309G>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 9/9 | chr14 | 39135131 | ||||||
chr14:39135265
|
A | T | 1 | a0001c0001t0001g0121 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.771-1175A>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 9/9 | chr14 | 39135265 | ||||||
chr14:39135307
|
C | T | 3 | a0001c0001t0001g0124a0001c0001t0001g0177a0001c0001t0001g0182 | 3 | NA18947.hp1 NA19006.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.771-1133C>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 9/9 | chr14 | 39135307 | ||||||
chr14:39135370
|
T | G | 13 | a0001c0001t0001g0024a0001c0001t0001g0118a0001c0001t0001g0119others(10): Show | 14 | HG01243.hp1 HG02451.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.771-1070T>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 9/9 | chr14 | 39135370 | ||||||
chr14:39135415
|
G | C | 2 | a0001c0001t0001g0126a0001c0001t0001g0128 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.771-1025G>C | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 9/9 | chr14 | 39135415 | ||||||
chr14:39135540
|
C | T | 1 | a0001c0001t0001g0107 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.771-900C>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 9/9 | chr14 | 39135540 | ||||||
chr14:39135630
|
G | A | 66 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0014others(63): Show | 75 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.771-810G>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 9/9 | chr14 | 39135630 | ||||||
chr14:39135654
|
G | A | 3 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343 | 3 | HG00642.hp1 HG01257.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.771-786G>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 9/9 | chr14 | 39135654 | ||||||
chr14:39135712
|
G | C | 1 | a0003c0002t0005g0171 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.771-728G>C | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 9/9 | chr14 | 39135712 | ||||||
chr14:39135713
|
C | G | 1 | a0003c0002t0005g0171 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.771-727C>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 9/9 | chr14 | 39135713 | ||||||
chr14:39135725
|
C | T | 341 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(338): Show | 386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.771-715C>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 9/9 | chr14 | 39135725 | ||||||
chr14:39135889
|
A | G | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | HG02258.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.771-551A>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 9/9 | chr14 | 39135889 | ||||||
chr14:39135932
|
A | G | 1 | a0001c0001t0001g0191 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.771-508A>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 9/9 | chr14 | 39135932 | ||||||
chr14:39135958
|
A | T | 13 | a0001c0001t0001g0024a0001c0001t0001g0118a0001c0001t0001g0119others(10): Show | 14 | HG01243.hp1 HG02451.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.771-482A>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 9/9 | chr14 | 39135958 | ||||||
chr14:39136195
|
T | C | 65 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0014others(62): Show | 74 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.771-245T>C | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 9/9 | chr14 | 39136195 | ||||||
chr14:39136273
|
C | T | 1 | a0001c0001t0001g0239 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.771-167C>T | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 9/9 | chr14 | 39136273 | ||||||
chr14:39136338
|
T | C | 319 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(316): Show | 362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.771-102T>C | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 9/9 | chr14 | 39136338 | ||||||
chr14:39136367
|
T | A | 1 | a0003c0002t0005g0171 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.771-73T>A | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 9/9 | chr14 | 39136367 | ||||||
chr14:39136381
|
T | G | 4 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(1): Show | 4 | HG02280.hp2 HG03130.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.771-59T>G | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 9/9 | chr14 | 39136381 | ||||||
chr14:39136418
|
T | TTG | 13 | a0001c0001t0001g0024a0001c0001t0001g0118a0001c0001t0001g0119others(10): Show | 14 | HG01243.hp1 HG02451.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.771-21_771-20insGT | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 39136418 |