Item | Value |
---|---|
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 | 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 | MAWVP others(264): Show |
chr14 | 39109323 | 39141973 |
a0002 | 0/0 | 269 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | MAWVP others(264): Show |
chr14 | 39109323 | 39141973 |
a0003 | 0/0 | 269 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | MAWVP others(264): Show |
chr14 | 39109323 | 39141973 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 807 | 422 | 91 | 76 | 195 | 16 | 42 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | ATGGC others(802): Show |
chr14 | 39109323 | 39141973 | ||
a0002c0003 | 0/0 | 807 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | ATGGC others(802): Show |
chr14 | 39109323 | 39141973 | ||
a0003c0002 | 0/0 | 807 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | ATGGC others(802): Show |
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 | GGCTG others(1315): Show |
chr14 | 39109323 | 39141973 |
a0001c0001t0002 | 0/0 | 1320 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | GGCTG others(1315): Show |
chr14 | 39109323 | 39141973 |
a0001c0001t0003 | 0/0 | 1320 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | GGCTG others(1315): Show |
chr14 | 39109323 | 39141973 |
a0001c0001t0004 | 0/0 | 1320 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | GGCTG others(1315): Show |
chr14 | 39109323 | 39141973 |
a0001c0001t0006 | 0/0 | 1320 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | GGCTG others(1315): Show |
chr14 | 39109323 | 39141973 |
a0002c0003t0001 | 0/0 | 1320 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | GGCTG others(1315): Show |
chr14 | 39109323 | 39141973 |
a0003c0002t0005 | 0/0 | 1320 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | GGCTG others(1315): Show |
chr14 | 39109323 | 39141973 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 11 | 0 | 6 | 3 | 2 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0002 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0003 | 0/0 | 6 | 0 | 3 | 2 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0004 | 0/0 | 5 | 0 | 0 | 2 | 0 | 3 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0007 | 0/0 | 4 | 3 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0009 | 0/0 | 4 | 0 | 0 | 0 | 0 | 4 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0010 | 0/0 | 4 | 1 | 2 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | 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 | 3 | 0 | 0 | 3 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0018 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0020 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 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 | 0 | 1 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0028 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | 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 | 0 | 2 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0037 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0045 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0046 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0047 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 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 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 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 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 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 | 1 | 0 | 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 | 0 | 1 | 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 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0100 | 0/1 | 1 | 0 | 0 | 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 | 0/0 | 1 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 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 | 0 | 1 | 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 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 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 | 1 | 0 | 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 | 0 | 0 | 1 | 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 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 1 | 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 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 1 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 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 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 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 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 | 0 | 0 | 1 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 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 |
a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0004g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0001c0001t0006g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0002c0003t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
a0003c0002t0005g0161 | 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 | g0035 | EUR | GBR | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | GBR | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0184 | 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 | g0020 | EUR | FIN | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0181 | EUR | FIN | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | CHS | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | CHS | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | CHS | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | CHS | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | CHS | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | CHS | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | CHS | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | CHS | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | CHS | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0261 | 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 | g0201 | AMR | PUR | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0307 | 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 | g0294 | 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 | g0047 | AMR | PUR | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0288 | AMR | PUR | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0295 | AMR | PUR | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0317 | AMR | PUR | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0303 | AMR | PUR | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0304 | AMR | PUR | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0238 | 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 | g0010 | 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 | g0105 | AMR | CLM | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0308 | AMR | CLM | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | CLM | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0319 | AMR | CLM | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | CLM | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0069 | 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 | g0267 | AMR | CLM | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | CLM | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | CLM | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0053 | EUR | IBS | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0222 | EUR | IBS | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0164 | EUR | IBS | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0218 | EUR | IBS | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0310 | AFR | ACB | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | ACB | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0192 | 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 | g0001 | AMR | PEL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0019 | 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 | g0018 | AMR | PEL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PEL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PEL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | PEL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PEL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02004 | hp1 | a0001 | c0001 | t0006 | g0013 | AMR | PEL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0026 | 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 | g0266 | EAS | KHV | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | ACB | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | KHV | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | KHV | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | KHV | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0179 | 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 | g0223 | EAS | CDX | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0046 | 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 | g0314 | AFR | ACB | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0049 | 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 | g0298 | AMR | PEL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0195 | 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 | g0045 | EAS | KHV | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | KHV | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | GWD | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | GWD | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0077 | 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 | g0009 | SAS | PJL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0273 | SAS | PJL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0067 | 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 | g0016 | AFR | GWD | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0271 | SAS | PJL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0281 | SAS | PJL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0321 | SAS | PJL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | GWD | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0070 | 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 | g0246 | AFR | GWD | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0074 | 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 | g0221 | 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 | g0316 | AFR | ESN | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0227 | 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 | g0207 | AFR | ESN | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0313 | AFR | ESN | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ESN | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | ESN | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0311 | AFR | ESN | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0248 | 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 | g0305 | AFR | MSL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | ESN | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ESN | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0325 | AFR | ESN | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0306 | 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 | g0007 | 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 | g0040 | SAS | PJL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0243 | 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 | g0059 | AFR | MSL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | MSL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0285 | SAS | PJL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0286 | 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 | g0242 | AFR | ESN | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | MSL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0003 | 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 | g0009 | SAS | STU | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | STU | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0284 | SAS | PJL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | BEB | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | BEB | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0009 | 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 | g0297 | SAS | BEB | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0318 | SAS | BEB | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | BEB | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0287 | SAS | STU | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0309 | SAS | STU | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0320 | SAS | STU | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0254 | SAS | STU | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0275 | SAS | STU | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | STU | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | YRI | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | YRI | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | CHB | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | CHB | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0323 | AFR | YRI | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0322 | AFR | YRI | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18945 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0276 | 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 | g0003 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0301 | 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 | g0283 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0004 | 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 | g0096 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19011 | hp2 | a0003 | c0002 | t0005 | g0161 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | LWK | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0315 | AFR | LWK | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19043 | hp1 | a0001 | c0001 | t0003 | g0052 | 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 | g0011 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0270 | 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 | g0005 | 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 | g0084 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0063 | 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 | g0014 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | YRI | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | YRI | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ASW | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ASW | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0258 | EUR | TSI | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0302 | EUR | TSI | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0253 | EUR | TSI | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0180 | EUR | TSI | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0282 | 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 | g0034 | AMR | CLM | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | CLM | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0312 | 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 | g0217 | AFR | ACB | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0056 | 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 | g0198 | AFR | USA | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | USA | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0324 | AFR | USA | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | LWK | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | LWK | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0100 | REF | REF | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0028 | REF | REF | GEMIN2_chr14_39109323_39141973 | GEMIN2 | chr14 | 39109323 | 39141973 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
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 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
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 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:39114517 | C | T | 4 | a0001c0001t0001g0048 a0001c0001t0001g0328 a0001c0001t0001g0329 others(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 | 19 | a0001c0001t0001g0010 a0001c0001t0001g0310 a0001c0001t0001g0311 others(16): 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 | a0001c0001t0001g0307 a0001c0001t0001g0308 a0001c0001t0001g0309 |
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 | a0001c0001t0001g0310 a0001c0001t0001g0311 a0001c0001t0001g0312 others(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 | a0001c0001t0001g0306 | 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 | a0002c0003t0001g0305 | 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 | a0001c0001t0001g0047 a0001c0001t0001g0303 a0001c0001t0001g0304 |
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 | a0001c0001t0001g0302 | 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 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(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 | 64 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0021 others(61): 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 | 69 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0021 others(66): 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 | 69 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0021 others(66): 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 | a0001c0001t0001g0326 a0001c0001t0001g0327 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0121 a0001c0001t0001g0122 others(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 | 174 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(171): 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 | 44 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0039 others(41): 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 | a0001c0001t0001g0120 a0001c0001t0001g0142 |
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 | a0001c0001t0001g0029 a0001c0001t0001g0118 a0001c0001t0001g0119 others(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 | a0001c0001t0001g0226 | 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 | a0001c0001t0001g0225 | 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 | 6 | a0001c0001t0001g0009 a0001c0001t0001g0284 a0001c0001t0001g0285 others(3): 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 | a0001c0001t0001g0122 a0001c0001t0001g0144 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0251 | 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 | 28 | a0001c0001t0001g0010 a0001c0001t0001g0122 a0001c0001t0001g0143 others(25): 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 | a0001c0001t0001g0252 | 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 | 84 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(81): 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 | 69 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0021 others(66): 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 | 326 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(323): Show |
416 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(413): 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 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0141 |
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 | 64 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0021 others(61): 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 | a0001c0001t0001g0016 a0001c0001t0001g0049 a0001c0001t0001g0050 others(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 | 20 | a0001c0001t0001g0010 a0001c0001t0001g0310 a0001c0001t0001g0311 others(17): 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 | a0001c0001t0001g0283 | 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 | a0001c0001t0001g0196 | 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 | a0001c0001t0001g0060 | 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 | a0001c0001t0001g0289 | 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 | a0001c0001t0001g0059 | 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 | 249 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(246): 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 | 20 | a0001c0001t0001g0010 a0001c0001t0001g0310 a0001c0001t0001g0311 others(17): 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 | a0001c0001t0001g0029 a0001c0001t0001g0118 a0001c0001t0001g0119 others(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 | 27 | a0001c0001t0001g0010 a0001c0001t0001g0122 a0001c0001t0001g0144 others(24): 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 | 86 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(83): 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 | a0001c0001t0001g0122 a0001c0001t0001g0144 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0055 a0001c0001t0001g0056 |
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 | 39 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0019 others(36): 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 | a0001c0001t0001g0029 a0001c0001t0001g0118 a0001c0001t0001g0119 others(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 | a0001c0001t0001g0226 | 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 | a0001c0001t0001g0094 | 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 | 69 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0021 others(66): 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 | a0001c0001t0001g0223 | 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 | 281 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(278): 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 | a0001c0001t0001g0282 | 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 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(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 | 5 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0150 others(2): 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 | 36 | a0001c0001t0001g0010 a0001c0001t0001g0051 a0001c0001t0001g0091 others(33): 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 | a0001c0001t0001g0313 a0001c0001t0001g0315 a0001c0001t0001g0322 others(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 | a0001c0001t0001g0090 | 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 | a0001c0001t0001g0188 | 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 | a0001c0001t0001g0050 | 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 | 1 | a0001c0001t0001g0040 | 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 | a0001c0001t0001g0197 | 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 | a0001c0001t0001g0326 a0001c0001t0001g0327 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0049 a0001c0001t0001g0050 others(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 | 57 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(54): 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 | 3 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0278 |
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 | a0001c0001t0001g0122 a0001c0001t0001g0144 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0089 | 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 | a0001c0001t0001g0189 | 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 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 |
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 | a0001c0001t0001g0290 | 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 | 57 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(54): 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 | 86 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(83): 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 | 308 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(305): 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 | a0001c0001t0001g0055 a0001c0001t0001g0056 |
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 | a0001c0001t0001g0226 | 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 | a0001c0001t0001g0055 a0001c0001t0001g0056 |
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 | 19 | a0001c0001t0001g0010 a0001c0001t0001g0310 a0001c0001t0001g0311 others(16): 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 | a0001c0001t0001g0198 | 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 | a0001c0001t0001g0227 a0001c0001t0001g0243 a0001c0001t0001g0244 |
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 | a0001c0001t0001g0253 | 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 | a0001c0001t0001g0226 a0001c0001t0001g0254 a0002c0003t0001g0305 |
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 | 63 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0021 others(60): 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 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0247 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0088 a0001c0001t0001g0118 others(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 | 63 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0021 others(60): 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 | 86 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(83): 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 | a0001c0001t0001g0022 a0001c0001t0001g0061 |
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 | a0001c0001t0001g0306 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0118 a0001c0001t0001g0119 others(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 | 86 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(83): 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 | a0001c0001t0001g0199 | 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 | 90 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(87): 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 | a0001c0001t0003g0052 | 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 | a0001c0001t0003g0052 | 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 | 309 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(306): 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 | 39 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0019 others(36): 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 | a0001c0001t0001g0256 | 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 | a0001c0001t0001g0153 a0001c0001t0001g0189 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0049 a0001c0001t0001g0050 others(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 | 19 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0022 others(16): 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 | a0001c0001t0001g0029 a0001c0001t0001g0118 |
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 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0250 others(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 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0296 |
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 |
21 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0045 others(18): 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 | a0001c0001t0001g0255 a0001c0001t0001g0259 a0001c0001t0001g0291 |
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 | a0001c0001t0001g0251 a0001c0001t0001g0258 a0001c0001t0001g0289 |
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 | a0001c0001t0001g0257 a0001c0001t0001g0301 |
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 | a0001c0001t0001g0119 a0001c0001t0001g0227 a0001c0001t0001g0243 others(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 | 6 | a0001c0001t0001g0032 a0001c0001t0001g0106 a0001c0001t0001g0107 others(3): 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 | 46 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0033 others(43): 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 | a0001c0001t0001g0003 a0001c0001t0001g0057 a0001c0001t0001g0303 others(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 | 16 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0017 others(13): 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 | a0001c0001t0001g0010 a0001c0001t0001g0165 a0001c0001t0001g0166 others(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 | a0001c0001t0001g0307 a0001c0001t0001g0308 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0187 others(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 | 8 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0030 others(5): 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 | 36 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0012 others(33): 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 | a0001c0001t0001g0001 a0001c0001t0001g0108 a0001c0001t0001g0116 others(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 | a0001c0001t0001g0288 | 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 | a0001c0001t0001g0270 | 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 | a0001c0001t0001g0280 | 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 | a0001c0001t0001g0042 | 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 | a0001c0001t0001g0269 a0001c0001t0001g0274 |
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 | a0001c0001t0001g0153 | 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 | a0001c0001t0001g0309 | 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 | a0001c0001t0001g0283 | 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 | a0001c0001t0001g0021 a0001c0001t0001g0252 |
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 | a0001c0001t0001g0281 | 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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0275 |
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 | a0001c0001t0001g0189 | 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 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0297 |
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 | a0001c0001t0001g0273 | 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 | a0001c0001t0001g0271 a0001c0001t0001g0278 |
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 | a0001c0001t0001g0043 | 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 | a0001c0001t0001g0021 a0001c0001t0001g0044 |
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 | a0001c0001t0001g0042 | 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 | a0001c0001t0001g0021 | 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 | a0001c0001t0001g0248 | 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 | a0001c0001t0001g0249 | 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 | a0001c0001t0001g0144 a0001c0001t0001g0145 |
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 | a0001c0001t0001g0147 a0001c0001t0001g0245 |
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 | a0001c0001t0001g0146 | 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 |
2 | a0001c0001t0001g0009 a0001c0001t0001g0196 |
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 | a0001c0001t0001g0226 | 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 | a0001c0001t0001g0228 | 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 | a0001c0001t0001g0035 a0001c0001t0001g0047 a0001c0001t0001g0058 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0037 others(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 | 13 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0025 others(10): 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 | a0001c0001t0001g0268 a0001c0001t0001g0279 |
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 | a0001c0001t0001g0055 a0001c0001t0001g0256 a0001c0001t0001g0282 others(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 | a0001c0001t0001g0287 | 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 | 36 | a0001c0001t0001g0020 a0001c0001t0001g0037 a0001c0001t0001g0041 others(33): 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 | a0001c0001t0001g0018 a0001c0001t0001g0036 a0001c0001t0001g0055 others(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 | 28 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0037 others(25): 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 | a0001c0001t0001g0018 a0001c0001t0001g0036 a0001c0001t0001g0055 others(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 | 19 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0037 others(16): 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 | a0001c0001t0001g0018 a0001c0001t0001g0036 a0001c0001t0001g0136 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0079 a0001c0001t0001g0137 others(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 | a0001c0001t0001g0282 | 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 | a0001c0001t0001g0190 | 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 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(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 | 39 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0019 others(36): 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 | 29 | a0001c0001t0001g0010 a0001c0001t0001g0122 a0001c0001t0001g0143 others(26): 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 | 85 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(82): 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 | a0001c0001t0001g0050 | 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 | 10 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0165 others(7): 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 | a0001c0001t0001g0205 | 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 | 85 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(82): 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 | a0001c0001t0001g0226 | 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 | 58 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(55): 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 | a0001c0001t0001g0122 a0001c0001t0001g0144 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0134 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0118 a0001c0001t0001g0119 others(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 | a0001c0001t0001g0122 a0001c0001t0001g0144 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0122 a0001c0001t0001g0144 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0122 a0001c0001t0001g0145 a0001c0001t0001g0146 others(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 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0226 |
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 | 56 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(53): 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 | a0001c0001t0001g0078 | 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 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(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 | a0001c0001t0001g0122 a0001c0001t0001g0144 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0244 | 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 | a0001c0001t0001g0322 | 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 | a0001c0001t0001g0080 | 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 | a0001c0001t0001g0016 a0001c0001t0001g0049 a0001c0001t0001g0050 others(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 | 100 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(97): 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 | a0001c0001t0001g0029 a0001c0001t0001g0118 a0001c0001t0001g0119 others(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 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 |
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 | 6 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0165 others(3): 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 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0247 others(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 | 55 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(52): 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 | 86 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(83): 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 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(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 | a0001c0001t0001g0232 | 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 | a0001c0001t0001g0206 | 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 | 69 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0021 others(66): 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 | a0001c0001t0001g0016 a0001c0001t0001g0126 a0001c0001t0001g0127 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0049 a0001c0001t0001g0050 others(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 | 39 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0019 others(36): 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 | 69 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0021 others(66): 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 | 309 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(306): 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 | a0002c0003t0001g0305 | 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 | 97 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 others(94): 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 | a0001c0001t0001g0249 a0001c0001t0001g0277 a0001c0001t0001g0281 others(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 | 38 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0019 others(35): 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 | a0001c0001t0001g0226 | 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 | a0001c0001t0001g0122 a0001c0001t0001g0144 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0118 a0001c0001t0001g0119 others(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 | a0001c0001t0001g0049 a0001c0001t0001g0051 |
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 | a0001c0001t0001g0181 | 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 | 88 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 others(85): Show |
102 | HG00323.hp1 HG00423.hp2 HG00642.hp1 others(99): 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 | 66 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(63): 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 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0071 others(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 | a0001c0001t0001g0101 a0001c0001t0001g0106 a0001c0001t0001g0121 others(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 | 69 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0021 others(66): 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 | a0001c0001t0001g0029 a0001c0001t0001g0118 a0001c0001t0001g0119 others(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 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0247 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0118 a0001c0001t0001g0119 others(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 | a0001c0001t0001g0167 | 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 | a0001c0001t0001g0059 | 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 | 18 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0043 others(15): 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 | 39 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0019 others(36): 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 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0247 others(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 | a0001c0001t0001g0196 | 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 | a0001c0001t0001g0055 a0001c0001t0001g0056 |
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 | 39 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0019 others(36): 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 | 309 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(306): 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 | 78 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0017 others(75): 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 | a0001c0001t0001g0064 a0001c0001t0001g0076 a0001c0001t0001g0078 others(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 | 13 | a0001c0001t0001g0041 a0001c0001t0001g0085 a0001c0001t0001g0089 others(10): 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 | 56 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(53): 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 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(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 | a0001c0001t0001g0087 | 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 | a0001c0001t0001g0330 | 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 | 230 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(227): 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 | 77 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(74): 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 | a0001c0001t0001g0015 a0001c0001t0001g0060 |
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 | 2 | a0001c0001t0001g0035 a0001c0001t0001g0165 |
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 | 40 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0019 others(37): 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 | a0001c0001t0003g0052 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0118 a0001c0001t0001g0119 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0118 a0001c0001t0001g0119 others(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 | 20 | a0001c0001t0001g0010 a0001c0001t0001g0310 a0001c0001t0001g0311 others(17): 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 | a0001c0001t0001g0196 | 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 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0247 others(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 | 20 | a0001c0001t0001g0010 a0001c0001t0001g0310 a0001c0001t0001g0311 others(17): 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 | a0001c0001t0001g0072 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0118 a0001c0001t0001g0119 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0118 a0001c0001t0001g0119 others(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 | a0001c0001t0003g0052 | 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 | a0001c0001t0001g0155 a0001c0001t0001g0158 |
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 | a0001c0001t0001g0182 a0001c0001t0001g0220 |
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 | 85 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(82): 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 | 69 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0021 others(66): 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 | a0001c0001t0001g0226 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0118 a0001c0001t0001g0119 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0118 a0001c0001t0001g0119 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0029 a0001c0001t0001g0049 others(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 | 100 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(97): 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 | 309 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(306): 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 | a0001c0001t0001g0029 a0001c0001t0001g0118 a0001c0001t0001g0119 others(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 | a0001c0001t0001g0212 a0001c0001t0001g0214 |
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 | 20 | a0001c0001t0001g0010 a0001c0001t0001g0310 a0001c0001t0001g0311 others(17): 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 | 12 | a0001c0001t0001g0010 a0001c0001t0001g0196 a0001c0001t0001g0315 others(9): 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 | a0001c0001t0001g0311 a0001c0001t0001g0312 a0001c0001t0001g0313 others(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 | a0001c0001t0001g0143 a0001c0001t0001g0310 a0001c0001t0001g0314 |
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 | 43 | a0001c0001t0001g0029 a0001c0001t0001g0037 a0001c0001t0001g0059 others(40): 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 | 43 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0013 others(40): 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 | 15 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0014 others(12): 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 | 58 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0021 others(55): 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 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(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 | a0001c0001t0001g0325 | 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 | a0001c0001t0001g0209 | 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 | 3 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0278 |
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 | a0001c0001t0001g0122 a0001c0001t0001g0144 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0118 a0001c0001t0001g0119 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0118 a0001c0001t0001g0119 others(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 | a0001c0001t0001g0195 | 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 | a0001c0001t0001g0226 | 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 | a0001c0001t0001g0092 | 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 | a0001c0001t0001g0066 | 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 | a0001c0001t0001g0227 a0001c0001t0001g0243 a0001c0001t0001g0244 |
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 | a0001c0001t0001g0024 a0001c0001t0001g0065 a0001c0001t0001g0075 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0118 a0001c0001t0001g0119 others(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 | 218 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(215): 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 | a0002c0003t0001g0305 | 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 | a0001c0001t0001g0038 | 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 | a0001c0001t0001g0173 a0001c0001t0001g0236 |
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 | a0001c0001t0001g0167 | 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 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0317 others(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 | a0002c0003t0001g0305 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0118 a0001c0001t0001g0119 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0118 a0001c0001t0001g0119 others(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 | a0001c0001t0001g0178 | 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 | a0001c0001t0001g0068 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0118 a0001c0001t0001g0119 others(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 | a0001c0001t0001g0122 a0001c0001t0001g0144 a0001c0001t0001g0145 others(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 | 6 | a0001c0001t0001g0010 a0001c0001t0001g0318 a0001c0001t0001g0320 others(3): 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 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0118 a0001c0001t0001g0119 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0118 a0001c0001t0001g0119 others(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 | a0001c0001t0001g0122 a0001c0001t0001g0144 a0001c0001t0001g0145 others(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 | a0003c0002t0005g0161 | 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 | 40 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0019 others(37): 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 | 85 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(82): 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 | a0003c0002t0005g0161 | 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 | a0003c0002t0005g0161 | 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 | a0003c0002t0005g0161 | 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 | a0001c0001t0001g0211 | 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 | 56 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0021 others(53): 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 | 23 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0102 others(20): 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 | 40 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0019 others(37): 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 | a0001c0001t0001g0267 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0053 others(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 | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(91): 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 | 102 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(99): Show |
129 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.711+619delC | GEMIN2 | ENSG00000092208.19 | transcript | ENST00000308317.12 | protein_coding | 8/9 | chr14 | 39132686 | |||||||
chr14:39132687 | C | T | 119 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(116): 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 | a0001c0001t0001g0202 | 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 | 22 | a0001c0001t0001g0010 a0001c0001t0001g0143 a0001c0001t0001g0196 others(19): 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 | a0001c0001t0001g0157 | 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 | a0001c0001t0003g0052 | 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 | a0001c0001t0001g0272 a0001c0001t0001g0276 a0001c0001t0001g0277 |
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 | a0001c0001t0001g0029 a0001c0001t0001g0076 a0001c0001t0001g0080 others(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 | 102 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(99): 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 | 19 | a0001c0001t0001g0010 a0001c0001t0001g0310 a0001c0001t0001g0311 others(16): 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 | a0003c0002t0005g0161 | 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 | a0001c0001t0001g0122 a0001c0001t0001g0145 a0001c0001t0001g0146 others(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 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 |
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 | 68 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0021 others(65): 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 | a0001c0001t0001g0317 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0118 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0118 a0001c0001t0001g0119 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0118 a0001c0001t0001g0119 others(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 | 67 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0021 others(64): 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 | a0001c0001t0001g0001 a0001c0001t0001g0103 |
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 | a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0058 others(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 | a0003c0002t0005g0161 | 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 | a0003c0002t0005g0161 | 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 | 67 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0021 others(64): 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 | a0001c0001t0001g0023 a0001c0001t0001g0069 a0001c0001t0001g0090 others(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 | 68 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(65): 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 | a0001c0001t0001g0022 a0001c0001t0001g0219 |
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 | a0003c0002t0005g0161 | 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 | a0001c0001t0001g0269 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0118 a0001c0001t0001g0119 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0118 a0001c0001t0001g0119 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0118 a0001c0001t0001g0119 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0118 a0001c0001t0001g0119 others(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 | 309 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(306): 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 | 86 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(83): 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 | 284 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(281): 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 | 64 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0021 others(61): 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 | a0001c0001t0001g0284 | 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 | 309 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(306): 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 | a0001c0001t0001g0016 a0001c0001t0001g0070 a0001c0001t0001g0126 others(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 | a0003c0002t0005g0161 | 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 | a0003c0002t0005g0161 | 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 | a0003c0002t0005g0161 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0118 a0001c0001t0001g0119 others(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 | a0003c0002t0005g0161 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0118 a0001c0001t0001g0119 others(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 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(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 | a0001c0001t0001g0053 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0118 a0001c0001t0001g0119 others(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 | 57 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(54): 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 | a0003c0002t0005g0161 | 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 | a0003c0002t0005g0161 | 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 | 69 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0021 others(66): 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 | 85 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(82): 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 | a0001c0001t0001g0059 | 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 | a0001c0001t0001g0269 | 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 | a0001c0001t0001g0226 | 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 | 85 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(82): 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 | 309 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(306): 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 | a0001c0001t0001g0029 a0001c0001t0001g0118 a0001c0001t0001g0119 others(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 | a0001c0001t0001g0170 | 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 | a0001c0001t0001g0084 | 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 | 85 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(82): 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 | 309 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(306): 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 | 19 | a0001c0001t0001g0010 a0001c0001t0001g0310 a0001c0001t0001g0311 others(16): 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 | a0001c0001t0001g0270 | 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 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0247 others(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 | a0001c0001t0001g0083 | 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 | 50 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(47): 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 | 64 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0021 others(61): 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 | a0001c0001t0001g0124 a0001c0001t0001g0171 a0001c0001t0001g0175 |
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 | a0001c0001t0001g0029 a0001c0001t0001g0118 a0001c0001t0001g0119 others(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 | a0001c0001t0001g0126 a0001c0001t0001g0128 |
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 | a0001c0001t0001g0106 | 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 | 57 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(54): 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 | a0001c0001t0001g0307 a0001c0001t0001g0308 a0001c0001t0001g0309 |
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 | a0003c0002t0005g0161 | 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 | a0003c0002t0005g0161 | 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 | 309 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(306): 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 | a0001c0001t0001g0055 a0001c0001t0001g0056 |
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 | a0001c0001t0001g0184 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0118 a0001c0001t0001g0119 others(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 | 56 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(53): 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 | a0001c0001t0001g0226 | 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 | 287 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(284): 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 | a0003c0002t0005g0161 | 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 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0118 a0001c0001t0001g0119 others(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 |