Item | Value |
---|---|
geneid | 3841 |
ensemblid | ENSG00000196911.12 |
hgncid | 6398 |
symbol | KPNA5 |
name | karyopherin subunit alpha 5 |
refseq_nuc | NM_001366306.2 |
refseq_prot | NP_001353235.1 |
ensembl_nuc | ENST00000368564.7 |
ensembl_prot | ENSP00000357552.1 |
mane_status | MANE Select |
chr | chr6 |
start | 116681211 |
end | 116741867 |
strand | + |
ver | v1.2 |
region | chr6:116681211-116741867 |
region5000 | chr6:116676211-116746867 |
regionname0 | KPNA5_chr6_116681211_116741867 |
regionname5000 | KPNA5_chr6_116676211_116746867 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 539 | 338 | 89 | 48 | 143 | 16 | 40 | 117 | KPNA5_chr6_116676211_116746867 | KPNA5 | MDAMA others(534): Show |
chr6 | 116676211 | 116746867 |
a0002 | 0/0 | 539 | 4 | 0 | 2 | 0 | 0 | 2 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | MDAMA others(534): Show |
chr6 | 116676211 | 116746867 |
a0003 | 0/0 | 539 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | MDAMA others(534): Show |
chr6 | 116676211 | 116746867 |
a0004 | 0/0 | 539 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | KPNA5_chr6_116676211_116746867 | KPNA5 | MDAMA others(534): Show |
chr6 | 116676211 | 116746867 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1617 | 330 | 84 | 45 | 143 | 16 | 40 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATGGA others(1612): Show |
chr6 | 116676211 | 116746867 | ||
a0001c0002 | 0/0 | 1617 | 7 | 5 | 2 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATGGA others(1612): Show |
chr6 | 116676211 | 116746867 | ||
a0001c0004 | 0/0 | 1617 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATGGA others(1612): Show |
chr6 | 116676211 | 116746867 | ||
a0002c0003 | 0/0 | 1617 | 4 | 0 | 2 | 0 | 0 | 2 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATGGA others(1612): Show |
chr6 | 116676211 | 116746867 | ||
a0003c0006 | 0/0 | 1617 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATGGA others(1612): Show |
chr6 | 116676211 | 116746867 | ||
a0004c0005 | 0/0 | 1617 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATGGA others(1612): Show |
chr6 | 116676211 | 116746867 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 11288 | 99 | 12 | 22 | 47 | 5 | 12 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11283): Show |
chr6 | 116676211 | 116746867 |
a0001c0001t0002 | 0/0 | 11282 | 63 | 0 | 4 | 48 | 4 | 7 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11277): Show |
chr6 | 116676211 | 116746867 |
a0001c0001t0003 | 0/0 | 11290 | 34 | 11 | 2 | 14 | 2 | 5 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11285): Show |
chr6 | 116676211 | 116746867 |
a0001c0001t0004 | 0/0 | 11288 | 17 | 3 | 1 | 12 | 0 | 1 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11283): Show |
chr6 | 116676211 | 116746867 |
a0001c0001t0005 | 0/0 | 11290 | 7 | 6 | 1 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11285): Show |
chr6 | 116676211 | 116746867 |
a0001c0001t0006 | 0/0 | 11290 | 7 | 2 | 0 | 1 | 0 | 4 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11285): Show |
chr6 | 116676211 | 116746867 |
a0001c0001t0007 | 0/0 | 11282 | 7 | 0 | 4 | 0 | 3 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11277): Show |
chr6 | 116676211 | 116746867 |
a0001c0001t0009 | 0/0 | 11290 | 6 | 6 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11285): Show |
chr6 | 116676211 | 116746867 |
a0001c0001t0010 | 0/0 | 11284 | 6 | 5 | 0 | 0 | 0 | 1 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11279): Show |
chr6 | 116676211 | 116746867 |
a0001c0001t0011 | 0/0 | 11289 | 5 | 5 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11284): Show |
chr6 | 116676211 | 116746867 |
a0001c0001t0012 | 0/0 | 11288 | 4 | 3 | 0 | 0 | 1 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11283): Show |
chr6 | 116676211 | 116746867 |
a0001c0001t0013 | 0/0 | 11288 | 4 | 0 | 0 | 4 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11283): Show |
chr6 | 116676211 | 116746867 |
a0001c0001t0014 | 0/0 | 11290 | 3 | 2 | 1 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11285): Show |
chr6 | 116676211 | 116746867 |
a0001c0001t0015 | 0/1 | 11290 | 3 | 0 | 0 | 0 | 1 | 1 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11285): Show |
chr6 | 116676211 | 116746867 |
a0001c0001t0016 | 0/0 | 11288 | 3 | 3 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11283): Show |
chr6 | 116676211 | 116746867 |
a0001c0001t0017 | 0/0 | 11288 | 3 | 3 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11283): Show |
chr6 | 116676211 | 116746867 |
a0001c0001t0019 | 0/0 | 11282 | 3 | 0 | 0 | 3 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11277): Show |
chr6 | 116676211 | 116746867 |
a0001c0001t0020 | 0/0 | 11290 | 3 | 0 | 0 | 3 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11285): Show |
chr6 | 116676211 | 116746867 |
a0001c0001t0021 | 0/0 | 11285 | 3 | 3 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11280): Show |
chr6 | 116676211 | 116746867 |
a0001c0001t0022 | 0/0 | 11288 | 2 | 0 | 0 | 2 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11283): Show |
chr6 | 116676211 | 116746867 |
a0001c0001t0023 | 0/0 | 11290 | 2 | 0 | 1 | 0 | 0 | 1 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11285): Show |
chr6 | 116676211 | 116746867 |
a0001c0001t0024 | 0/0 | 11288 | 2 | 2 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11283): Show |
chr6 | 116676211 | 116746867 |
a0001c0001t0025 | 0/0 | 11291 | 2 | 2 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11286): Show |
chr6 | 116676211 | 116746867 |
a0001c0001t0026 | 0/0 | 11290 | 2 | 2 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11285): Show |
chr6 | 116676211 | 116746867 |
a0001c0001t0027 | 0/0 | 11290 | 2 | 2 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11285): Show |
chr6 | 116676211 | 116746867 |
a0001c0001t0029 | 0/0 | 11290 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11285): Show |
chr6 | 116676211 | 116746867 |
a0001c0001t0030 | 0/0 | 11291 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11286): Show |
chr6 | 116676211 | 116746867 |
a0001c0001t0031 | 0/0 | 11291 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11286): Show |
chr6 | 116676211 | 116746867 |
a0001c0001t0032 | 0/0 | 11288 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11283): Show |
chr6 | 116676211 | 116746867 |
a0001c0001t0033 | 0/0 | 11290 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11285): Show |
chr6 | 116676211 | 116746867 |
a0001c0001t0034 | 0/0 | 11288 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11283): Show |
chr6 | 116676211 | 116746867 |
a0001c0001t0035 | 0/0 | 11288 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11283): Show |
chr6 | 116676211 | 116746867 |
a0001c0001t0036 | 0/0 | 11288 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11283): Show |
chr6 | 116676211 | 116746867 |
a0001c0001t0037 | 0/0 | 11288 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11283): Show |
chr6 | 116676211 | 116746867 |
a0001c0001t0038 | 0/0 | 11288 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11283): Show |
chr6 | 116676211 | 116746867 |
a0001c0001t0039 | 0/0 | 11288 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11283): Show |
chr6 | 116676211 | 116746867 |
a0001c0001t0040 | 0/0 | 11288 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11283): Show |
chr6 | 116676211 | 116746867 |
a0001c0001t0041 | 0/0 | 11288 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11283): Show |
chr6 | 116676211 | 116746867 |
a0001c0001t0042 | 0/0 | 11288 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11283): Show |
chr6 | 116676211 | 116746867 |
a0001c0001t0043 | 0/0 | 11287 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11282): Show |
chr6 | 116676211 | 116746867 |
a0001c0001t0044 | 0/0 | 11288 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11283): Show |
chr6 | 116676211 | 116746867 |
a0001c0001t0046 | 0/0 | 11288 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11283): Show |
chr6 | 116676211 | 116746867 |
a0001c0001t0047 | 0/0 | 11290 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11285): Show |
chr6 | 116676211 | 116746867 |
a0001c0001t0048 | 0/0 | 11290 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11285): Show |
chr6 | 116676211 | 116746867 |
a0001c0001t0049 | 0/0 | 11290 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11285): Show |
chr6 | 116676211 | 116746867 |
a0001c0001t0050 | 0/0 | 11290 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11285): Show |
chr6 | 116676211 | 116746867 |
a0001c0001t0051 | 0/0 | 11290 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11285): Show |
chr6 | 116676211 | 116746867 |
a0001c0001t0052 | 0/0 | 11288 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11283): Show |
chr6 | 116676211 | 116746867 |
a0001c0001t0053 | 0/0 | 11288 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11283): Show |
chr6 | 116676211 | 116746867 |
a0001c0001t0055 | 0/0 | 11291 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11286): Show |
chr6 | 116676211 | 116746867 |
a0001c0001t0056 | 0/0 | 11290 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11285): Show |
chr6 | 116676211 | 116746867 |
a0001c0001t0057 | 0/0 | 11290 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11285): Show |
chr6 | 116676211 | 116746867 |
a0001c0001t0058 | 0/0 | 11288 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11283): Show |
chr6 | 116676211 | 116746867 |
a0001c0001t0060 | 0/0 | 11284 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11279): Show |
chr6 | 116676211 | 116746867 |
a0001c0001t0061 | 0/0 | 11281 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11276): Show |
chr6 | 116676211 | 116746867 |
a0001c0001t0062 | 0/0 | 11282 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11277): Show |
chr6 | 116676211 | 116746867 |
a0001c0001t0063 | 0/0 | 11282 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11277): Show |
chr6 | 116676211 | 116746867 |
a0001c0001t0064 | 0/0 | 11282 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11277): Show |
chr6 | 116676211 | 116746867 |
a0001c0001t0065 | 0/0 | 11282 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11277): Show |
chr6 | 116676211 | 116746867 |
a0001c0001t0066 | 0/0 | 11282 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11277): Show |
chr6 | 116676211 | 116746867 |
a0001c0001t0067 | 0/0 | 11282 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11277): Show |
chr6 | 116676211 | 116746867 |
a0001c0001t0068 | 0/0 | 11290 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11285): Show |
chr6 | 116676211 | 116746867 |
a0001c0001t0069 | 0/0 | 11286 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11281): Show |
chr6 | 116676211 | 116746867 |
a0001c0002t0008 | 0/0 | 11287 | 6 | 5 | 1 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11282): Show |
chr6 | 116676211 | 116746867 |
a0001c0002t0028 | 0/0 | 11288 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11283): Show |
chr6 | 116676211 | 116746867 |
a0001c0004t0003 | 0/0 | 11290 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11285): Show |
chr6 | 116676211 | 116746867 |
a0002c0003t0018 | 0/0 | 11290 | 3 | 0 | 2 | 0 | 0 | 1 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11285): Show |
chr6 | 116676211 | 116746867 |
a0002c0003t0054 | 0/0 | 11290 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11285): Show |
chr6 | 116676211 | 116746867 |
a0003c0006t0045 | 0/0 | 11288 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11283): Show |
chr6 | 116676211 | 116746867 |
a0004c0005t0059 | 0/0 | 11282 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | ATCTT others(11277): Show |
chr6 | 116676211 | 116746867 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0235 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0002g0012 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0003g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0003g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0003g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0003g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0004g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0004g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0004g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0004g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0004g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0004g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0004g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0004g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0004g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0004g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0004g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0004g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0005g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0005g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0005g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0005g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0005g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0005g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0005g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0006g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0006g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0006g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0006g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0006g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0006g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0006g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0007g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0007g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0007g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0007g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0007g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0007g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0007g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0009g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0009g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0009g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0009g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0009g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0009g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0010g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0010g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0010g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0010g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0010g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0010g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0011g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0011g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0011g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0011g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0011g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0012g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0012g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0012g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0012g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0013g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0013g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0013g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0014g0007 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0014g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0015g0179 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0015g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0015g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0016g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0016g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0016g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0017g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0017g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0017g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0019g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0019g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0019g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0020g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0020g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0020g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0021g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0021g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0021g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0022g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0022g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0023g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0023g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0024g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0024g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0025g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0025g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0026g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0026g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0027g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0027g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0029g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0030g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0031g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0032g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0033g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0034g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0035g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0036g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0037g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0038g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0039g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0040g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0041g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0042g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0043g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0044g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0046g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0047g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0048g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0049g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0050g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0051g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0052g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0053g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0055g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0056g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0057g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0058g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0060g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0061g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0062g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0063g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0064g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0065g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0066g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0067g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0068g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0001t0069g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0002t0008g0020 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0002t0008g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0002t0008g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0002t0008g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0002t0008g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0002t0028g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0001c0004t0003g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0002c0003t0018g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0002c0003t0018g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0002c0003t0054g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0003c0006t0045g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
a0004c0005t0059g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0186 | EUR | GBR | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0087 | EUR | GBR | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG00280 | hp1 | a0001 | c0001 | t0015 | g0180 | EUR | FIN | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG00280 | hp2 | a0001 | c0001 | t0007 | g0058 | EUR | FIN | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0066 | EUR | FIN | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG00323 | hp2 | a0001 | c0001 | t0003 | g0199 | EUR | FIN | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG00544 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | CHS | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | CHS | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG00558 | hp1 | a0001 | c0001 | t0013 | g0204 | EAS | CHS | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | CHS | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | CHS | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | CHS | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG00639 | hp1 | a0001 | c0001 | t0043 | g0016 | AMR | PUR | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG00639 | hp2 | a0001 | c0002 | t0008 | g0020 | AMR | PUR | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG00642 | hp1 | a0001 | c0001 | t0003 | g0238 | AMR | PUR | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG00673 | hp1 | a0001 | c0001 | t0003 | g0223 | EAS | CHS | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | CHS | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG00738 | hp2 | a0001 | c0004 | t0003 | g0222 | AMR | PUR | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0298 | AMR | PUR | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG00741 | hp2 | a0001 | c0001 | t0014 | g0007 | AMR | PUR | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0030 | AMR | PUR | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG01071 | hp2 | a0001 | c0001 | t0034 | g0264 | AMR | PUR | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG01074 | hp2 | a0001 | c0002 | t0028 | g0168 | AMR | PUR | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG01081 | hp2 | a0001 | c0001 | t0064 | g0103 | AMR | PUR | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG01106 | hp2 | a0001 | c0001 | t0004 | g0286 | AMR | PUR | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG01167 | hp1 | a0001 | c0001 | t0007 | g0068 | AMR | PUR | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG01167 | hp2 | a0001 | c0001 | t0040 | g0187 | AMR | PUR | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG01169 | hp1 | a0001 | c0001 | t0023 | g0202 | AMR | PUR | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG01169 | hp2 | a0001 | c0001 | t0007 | g0055 | AMR | PUR | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG01243 | hp1 | a0001 | c0001 | t0042 | g0003 | AMR | PUR | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG01243 | hp2 | a0001 | c0001 | t0005 | g0279 | AMR | PUR | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG01258 | hp1 | a0002 | c0003 | t0018 | g0019 | AMR | CLM | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | CLM | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG01261 | hp1 | a0001 | c0001 | t0007 | g0093 | AMR | CLM | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | CLM | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG01358 | hp1 | a0001 | c0001 | t0007 | g0092 | AMR | CLM | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG01361 | hp1 | a0001 | c0001 | t0037 | g0138 | AMR | CLM | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | CLM | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0073 | AMR | CLM | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG01433 | hp2 | a0001 | c0001 | t0003 | g0196 | AMR | CLM | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG01496 | hp2 | a0001 | c0001 | t0061 | g0069 | AMR | CLM | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0193 | EUR | IBS | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG01515 | hp2 | a0001 | c0001 | t0007 | g0057 | EUR | IBS | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0080 | EUR | IBS | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0234 | EUR | IBS | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG01517 | hp1 | a0001 | c0001 | t0007 | g0091 | EUR | IBS | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0192 | EUR | IBS | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG01884 | hp1 | a0001 | c0001 | t0012 | g0153 | AFR | ACB | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG01884 | hp2 | a0001 | c0001 | t0069 | g0165 | AFR | ACB | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | PEL | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | KHV | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02027 | hp2 | a0001 | c0001 | t0003 | g0253 | EAS | KHV | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | KHV | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02055 | hp1 | a0001 | c0001 | t0029 | g0161 | AFR | ACB | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02055 | hp2 | a0001 | c0001 | t0011 | g0149 | AFR | ACB | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02056 | hp2 | a0001 | c0001 | t0003 | g0245 | EAS | KHV | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | KHV | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02129 | hp2 | a0001 | c0001 | t0006 | g0104 | EAS | KHV | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02132 | hp1 | a0001 | c0001 | t0004 | g0027 | EAS | KHV | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | KHV | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02145 | hp1 | a0001 | c0001 | t0010 | g0033 | AFR | ACB | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | ACB | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02148 | hp1 | a0002 | c0003 | t0018 | g0019 | AMR | PEL | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0099 | AMR | PEL | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02165 | hp1 | a0001 | c0001 | t0003 | g0201 | EAS | CDX | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | CDX | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02257 | hp1 | a0001 | c0001 | t0024 | g0134 | AFR | ACB | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0241 | AFR | ACB | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02258 | hp1 | a0001 | c0001 | t0017 | g0296 | AFR | ACB | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02258 | hp2 | a0001 | c0001 | t0003 | g0240 | AFR | ACB | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02273 | hp1 | a0001 | c0001 | t0032 | g0206 | AMR | PEL | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02280 | hp1 | a0001 | c0002 | t0008 | g0256 | AFR | ACB | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02280 | hp2 | a0001 | c0001 | t0060 | g0034 | AFR | ACB | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02300 | hp2 | a0001 | c0001 | t0065 | g0074 | AMR | PEL | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02451 | hp2 | a0001 | c0001 | t0056 | g0281 | AFR | ACB | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02572 | hp1 | a0001 | c0001 | t0026 | g0109 | AFR | GWD | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02572 | hp2 | a0001 | c0001 | t0011 | g0141 | AFR | GWD | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02602 | hp1 | a0001 | c0001 | t0004 | g0287 | SAS | PJL | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02615 | hp1 | a0001 | c0001 | t0003 | g0175 | AFR | GWD | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02615 | hp2 | a0001 | c0001 | t0005 | g0282 | AFR | GWD | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02630 | hp1 | a0001 | c0001 | t0009 | g0143 | AFR | GWD | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02630 | hp2 | a0001 | c0001 | t0009 | g0262 | AFR | GWD | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02647 | hp1 | a0001 | c0001 | t0006 | g0260 | AFR | GWD | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02647 | hp2 | a0001 | c0001 | t0005 | g0219 | AFR | GWD | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02683 | hp2 | a0001 | c0001 | t0003 | g0178 | SAS | PJL | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0010 | SAS | PJL | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0251 | SAS | PJL | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02717 | hp1 | a0001 | c0001 | t0025 | g0144 | AFR | GWD | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02717 | hp2 | a0001 | c0001 | t0003 | g0146 | AFR | GWD | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02723 | hp1 | a0001 | c0001 | t0055 | g0278 | AFR | GWD | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02723 | hp2 | a0001 | c0001 | t0009 | g0171 | AFR | GWD | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02735 | hp2 | a0002 | c0003 | t0054 | g0162 | SAS | PJL | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02809 | hp1 | a0001 | c0001 | t0004 | g0288 | AFR | GWD | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02809 | hp2 | a0001 | c0001 | t0038 | g0018 | AFR | GWD | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02818 | hp1 | a0001 | c0001 | t0068 | g0137 | AFR | GWD | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02818 | hp2 | a0001 | c0001 | t0016 | g0152 | AFR | GWD | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02886 | hp1 | a0001 | c0001 | t0027 | g0107 | AFR | GWD | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02886 | hp2 | a0001 | c0001 | t0005 | g0276 | AFR | GWD | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02895 | hp2 | a0001 | c0001 | t0021 | g0166 | AFR | GWD | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02896 | hp1 | a0001 | c0001 | t0003 | g0026 | AFR | GWD | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02896 | hp2 | a0001 | c0001 | t0016 | g0148 | AFR | GWD | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02897 | hp1 | a0001 | c0001 | t0021 | g0170 | AFR | GWD | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02897 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | GWD | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02922 | hp1 | a0001 | c0001 | t0003 | g0211 | AFR | ESN | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02922 | hp2 | a0001 | c0002 | t0008 | g0020 | AFR | ESN | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02965 | hp1 | a0001 | c0001 | t0017 | g0293 | AFR | ESN | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02965 | hp2 | a0001 | c0001 | t0005 | g0280 | AFR | ESN | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02970 | hp1 | a0003 | c0006 | t0045 | g0017 | AFR | ESN | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02970 | hp2 | a0001 | c0001 | t0051 | g0247 | AFR | ESN | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02976 | hp1 | a0001 | c0002 | t0008 | g0169 | AFR | ESN | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02976 | hp2 | a0001 | c0001 | t0021 | g0164 | AFR | ESN | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG03017 | hp1 | a0001 | c0001 | t0003 | g0173 | SAS | PJL | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG03017 | hp2 | a0001 | c0001 | t0006 | g0105 | SAS | PJL | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG03041 | hp1 | a0001 | c0001 | t0004 | g0289 | AFR | GWD | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG03041 | hp2 | a0001 | c0001 | t0010 | g0032 | AFR | GWD | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | MSL | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG03098 | hp2 | a0001 | c0001 | t0016 | g0147 | AFR | MSL | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG03130 | hp1 | a0001 | c0001 | t0026 | g0110 | AFR | ESN | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ESN | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG03139 | hp1 | a0001 | c0001 | t0011 | g0114 | AFR | ESN | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | ESN | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG03195 | hp1 | a0001 | c0001 | t0012 | g0017 | AFR | ESN | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG03195 | hp2 | a0001 | c0001 | t0014 | g0026 | AFR | ESN | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | MSL | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG03209 | hp2 | a0001 | c0002 | t0008 | g0167 | AFR | MSL | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG03225 | hp1 | a0001 | c0001 | t0009 | g0172 | AFR | MSL | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG03225 | hp2 | a0001 | c0001 | t0053 | g0182 | AFR | MSL | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG03239 | hp1 | a0001 | c0001 | t0062 | g0096 | SAS | PJL | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0075 | SAS | PJL | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG03453 | hp1 | a0001 | c0001 | t0009 | g0220 | AFR | MSL | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG03453 | hp2 | a0001 | c0001 | t0012 | g0154 | AFR | MSL | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG03486 | hp1 | a0001 | c0001 | t0027 | g0108 | AFR | MSL | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG03486 | hp2 | a0001 | c0002 | t0008 | g0257 | AFR | MSL | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG03490 | hp2 | a0001 | c0001 | t0003 | g0023 | SAS | PJL | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0249 | SAS | PJL | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0040 | SAS | PJL | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG03492 | hp1 | a0001 | c0001 | t0003 | g0023 | SAS | PJL | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0039 | SAS | PJL | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG03516 | hp1 | a0001 | c0001 | t0058 | g0140 | AFR | ESN | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG03516 | hp2 | a0001 | c0001 | t0030 | g0255 | AFR | ESN | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG03540 | hp1 | a0001 | c0001 | t0017 | g0292 | AFR | GWD | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG03540 | hp2 | a0001 | c0001 | t0025 | g0106 | AFR | GWD | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG03654 | hp2 | a0001 | c0001 | t0006 | g0136 | SAS | PJL | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG03669 | hp1 | a0001 | c0001 | t0044 | g0002 | SAS | PJL | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG03669 | hp2 | a0001 | c0001 | t0041 | g0102 | SAS | PJL | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG03688 | hp1 | a0002 | c0003 | t0018 | g0163 | SAS | STU | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | STU | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG03831 | hp1 | a0001 | c0001 | t0006 | g0122 | SAS | BEB | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG03831 | hp2 | a0001 | c0001 | t0046 | g0002 | SAS | BEB | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | BEB | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0098 | SAS | BEB | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG03927 | hp1 | a0001 | c0001 | t0006 | g0121 | SAS | BEB | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0083 | SAS | BEB | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0085 | SAS | BEB | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG03942 | hp2 | a0001 | c0001 | t0031 | g0221 | SAS | BEB | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0228 | SAS | BEB | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG04184 | hp2 | a0001 | c0001 | t0047 | g0024 | SAS | BEB | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG04199 | hp1 | a0001 | c0001 | t0023 | g0246 | SAS | STU | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG04199 | hp2 | a0001 | c0001 | t0052 | g0117 | SAS | STU | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG04204 | hp1 | a0001 | c0001 | t0010 | g0101 | SAS | STU | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | STU | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG04228 | hp1 | a0001 | c0001 | t0036 | g0232 | SAS | STU | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | STU | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18612 | hp1 | a0001 | c0001 | t0039 | g0263 | EAS | CHB | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18612 | hp2 | a0001 | c0001 | t0004 | g0027 | EAS | CHB | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | CHB | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | YRI | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18906 | hp2 | a0001 | c0001 | t0011 | g0113 | AFR | YRI | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18942 | hp2 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18943 | hp1 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18944 | hp1 | a0001 | c0001 | t0013 | g0001 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18944 | hp2 | a0001 | c0001 | t0004 | g0291 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18949 | hp2 | a0001 | c0001 | t0067 | g0077 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18951 | hp1 | a0001 | c0001 | t0033 | g0214 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18954 | hp2 | a0001 | c0001 | t0003 | g0243 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18961 | hp2 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18964 | hp1 | a0001 | c0001 | t0003 | g0210 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18964 | hp2 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18966 | hp2 | a0001 | c0001 | t0020 | g0025 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18970 | hp1 | a0001 | c0001 | t0020 | g0200 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18973 | hp1 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18977 | hp1 | a0001 | c0001 | t0022 | g0003 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18977 | hp2 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18983 | hp2 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18985 | hp1 | a0001 | c0001 | t0050 | g0198 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18990 | hp1 | a0001 | c0001 | t0004 | g0294 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18993 | hp2 | a0001 | c0001 | t0003 | g0224 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18997 | hp1 | a0001 | c0001 | t0019 | g0095 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18997 | hp2 | a0001 | c0001 | t0020 | g0248 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18999 | hp2 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA19000 | hp2 | a0001 | c0001 | t0004 | g0295 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA19006 | hp1 | a0001 | c0001 | t0035 | g0001 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA19006 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA19010 | hp2 | a0001 | c0001 | t0049 | g0242 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA19012 | hp2 | a0001 | c0001 | t0019 | g0088 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA19030 | hp1 | a0001 | c0001 | t0011 | g0142 | AFR | LWK | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA19030 | hp2 | a0001 | c0001 | t0003 | g0212 | AFR | LWK | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA19043 | hp1 | a0001 | c0001 | t0057 | g0111 | AFR | LWK | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | LWK | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA19057 | hp2 | a0001 | c0001 | t0013 | g0001 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA19059 | hp1 | a0001 | c0001 | t0022 | g0236 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA19059 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA19068 | hp2 | a0001 | c0001 | t0003 | g0176 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA19074 | hp1 | a0001 | c0001 | t0063 | g0045 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA19075 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA19075 | hp2 | a0001 | c0001 | t0003 | g0274 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA19078 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA19078 | hp2 | a0001 | c0001 | t0003 | g0273 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA19083 | hp2 | a0001 | c0001 | t0003 | g0266 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA19085 | hp1 | a0001 | c0001 | t0019 | g0063 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA19087 | hp1 | a0004 | c0005 | t0059 | g0060 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA19087 | hp2 | a0001 | c0001 | t0004 | g0297 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA19091 | hp1 | a0001 | c0001 | t0013 | g0203 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA19091 | hp2 | a0001 | c0001 | t0066 | g0079 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA19240 | hp1 | a0001 | c0001 | t0010 | g0031 | AFR | YRI | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA19240 | hp2 | a0001 | c0001 | t0024 | g0135 | AFR | YRI | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA20129 | hp1 | a0001 | c0001 | t0003 | g0239 | AFR | ASW | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | ASW | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA20752 | hp1 | a0001 | c0001 | t0003 | g0237 | EUR | TSI | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0012 | EUR | TSI | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA20805 | hp1 | a0001 | c0001 | t0012 | g0155 | EUR | TSI | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0184 | EUR | TSI | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | GIH | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA20905 | hp2 | a0001 | c0001 | t0015 | g0181 | SAS | GIH | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | CLM | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02109 | hp1 | a0001 | c0001 | t0005 | g0283 | AFR | ACB | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02559 | hp1 | a0001 | c0001 | t0009 | g0275 | AFR | ACB | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG02559 | hp2 | a0001 | c0001 | t0003 | g0218 | AFR | ACB | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG03471 | hp1 | a0001 | c0001 | t0006 | g0299 | AFR | MSL | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG03471 | hp2 | a0001 | c0001 | t0010 | g0084 | AFR | MSL | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG06807 | hp1 | a0001 | c0001 | t0004 | g0290 | AFR | USA | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
HG06807 | hp2 | a0001 | c0001 | t0005 | g0277 | AFR | USA | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18955 | hp1 | a0001 | c0001 | t0048 | g0213 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA20300 | hp1 | a0001 | c0001 | t0014 | g0007 | AFR | USA | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | USA | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA21309 | hp1 | a0001 | c0001 | t0003 | g0197 | AFR | LWK | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
NA21309 | hp2 | a0001 | c0001 | t0010 | g0071 | AFR | LWK | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
homoSapiens | chm13v2 | a0001 | c0001 | t0015 | g0179 | REF | REF | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0235 | REF | REF | KPNA5_chr6_116676211_116746867 | KPNA5 | chr6 | 116676211 | 116746867 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:116689362 | G | A | 1 | a0002 | 4 | HG01258.hp1 HG02148.hp1 HG02735.hp2 others(1): Show |
missense_variant | MODERATE | c.47G>A | p.Ser16Asn | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 2/14 | 171/11288 | 47/1620 | 16/539 | chr6 | 116689362 | |||
chr6:116689371 | A | C | 1 | a0003 | 1 | HG02970.hp1 | missense_variant | MODERATE | c.56A>C | p.Asn19Thr | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 2/14 | 180/11288 | 56/1620 | 19/539 | chr6 | 116689371 | |||
chr6:116726595 | C | T | 1 | a0004 | 1 | NA19087.hp1 | missense_variant | MODERATE | c.1226C>T | p.Thr409Ile | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 12/14 | 1350/11288 | 1226/1620 | 409/539 | chr6 | 116726595 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:116689432 | A | G | 2 | a0001c0002 a0002c0003 |
11 | HG00639.hp2 HG01074.hp2 HG01258.hp1 others(8): Show |
synonymous_variant | LOW | c.117A>G | p.Arg39Arg | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 2/14 | 241/11288 | 117/1620 | 39/539 | chr6 | 116689432 | |||
chr6:116724328 | T | C | 1 | a0001c0004 | 1 | HG00738.hp2 | synonymous_variant | LOW | c.952T>C | p.Leu318Leu | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 10/14 | 1076/11288 | 952/1620 | 318/539 | chr6 | 116724328 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:116732939 | G | A | 2 | a0001c0002t0008 a0001c0002t0028 |
7 | HG00639.hp2 HG01074.hp2 HG02280.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*616G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 616 | chr6 | 116732939 | ||||||
chr6:116733055 | A | G | 2 | a0001c0001t0021 a0001c0001t0069 |
4 | HG01884.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*732A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 732 | chr6 | 116733055 | ||||||
chr6:116733065 | G | T | 1 | a0001c0001t0068 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*742G>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 742 | chr6 | 116733065 | ||||||
chr6:116733144 | C | T | 1 | a0001c0001t0020 | 3 | NA18966.hp2 NA18970.hp1 NA18997.hp2 |
3_prime_UTR_variant | MODIFIER | c.*821C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 821 | chr6 | 116733144 | ||||||
chr6:116733276 | TAAGTAC | T | 13 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0010 others(10): Show |
88 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*964_*969delACAAGT | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 964 | INFO_REALIGN_3_PRIME | chr6 | 116733276 | |||||
chr6:116733350 | G | T | 1 | a0001c0001t0058 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1027G>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 1027 | chr6 | 116733350 | ||||||
chr6:116733554 | G | T | 28 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(25): Show |
127 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*1231G>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 1231 | chr6 | 116733554 | ||||||
chr6:116733753 | A | C | 1 | a0001c0001t0067 | 1 | NA18949.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1430A>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 1430 | chr6 | 116733753 | ||||||
chr6:116733878 | C | A | 1 | a0001c0001t0025 | 2 | HG02717.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1555C>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 1555 | chr6 | 116733878 | ||||||
chr6:116733964 | A | G | 1 | a0001c0001t0017 | 3 | HG02258.hp1 HG02965.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1641A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 1641 | chr6 | 116733964 | ||||||
chr6:116734069 | C | T | 1 | a0001c0001t0024 | 2 | HG02257.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1746C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 1746 | chr6 | 116734069 | ||||||
chr6:116734147 | G | A | 2 | a0002c0003t0018 a0002c0003t0054 |
4 | HG01258.hp1 HG02148.hp1 HG02735.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1824G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 1824 | chr6 | 116734147 | ||||||
chr6:116734558 | G | T | 1 | a0001c0001t0057 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2235G>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 2235 | chr6 | 116734558 | ||||||
chr6:116734570 | TCTTGG | T | 2 | a0001c0001t0021 a0001c0001t0069 |
4 | HG01884.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2266_*2270delGGCT others(1): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 2266 | INFO_REALIGN_3_PRIME | chr6 | 116734570 | |||||
chr6:116734601 | A | T | 28 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(25): Show |
127 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*2278A>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 2278 | chr6 | 116734601 | ||||||
chr6:116734676 | A | G | 1 | a0001c0001t0068 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2353A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 2353 | chr6 | 116734676 | ||||||
chr6:116734716 | G | GA | 6 | a0001c0001t0011 a0001c0001t0025 a0001c0001t0030 others(3): Show |
11 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2408dupA | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 2409 | INFO_REALIGN_3_PRIME | chr6 | 116734716 | |||||
chr6:116734716 | G | GAA | 2 | a0001c0001t0009 a0001c0001t0029 |
7 | HG02055.hp1 HG02559.hp1 HG02630.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2407_*2408dupAA | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 2409 | INFO_REALIGN_3_PRIME | chr6 | 116734716 | |||||
chr6:116734728 | A | G | 1 | a0001c0001t0053 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2405A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 2405 | chr6 | 116734728 | ||||||
chr6:116734869 | T | C | 1 | a0001c0001t0032 | 1 | HG02273.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2546T>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 2546 | chr6 | 116734869 | ||||||
chr6:116735242 | T | C | 1 | a0001c0001t0019 | 3 | NA18997.hp1 NA19012.hp2 NA19085.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2919T>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 2919 | chr6 | 116735242 | ||||||
chr6:116735822 | T | C | 2 | a0001c0001t0026 a0001c0001t0057 |
3 | HG02572.hp1 HG03130.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3499T>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 3499 | chr6 | 116735822 | ||||||
chr6:116736026 | G | A | 1 | a0004c0005t0059 | 1 | NA19087.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3703G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 3703 | chr6 | 116736026 | ||||||
chr6:116736040 | C | T | 1 | a0001c0001t0066 | 1 | NA19091.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3717C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 3717 | chr6 | 116736040 | ||||||
chr6:116736053 | A | G | 2 | a0001c0001t0065 a0002c0003t0018 |
4 | HG01258.hp1 HG02148.hp1 HG02300.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3730A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 3730 | chr6 | 116736053 | ||||||
chr6:116736056 | A | G | 1 | a0001c0001t0027 | 2 | HG02886.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3733A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 3733 | chr6 | 116736056 | ||||||
chr6:116736185 | A | C | 1 | a0001c0001t0064 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3862A>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 3862 | chr6 | 116736185 | ||||||
chr6:116736253 | T | C | 1 | a0001c0001t0033 | 1 | NA18951.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3930T>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 3930 | chr6 | 116736253 | ||||||
chr6:116736296 | A | G | 1 | a0001c0001t0052 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3973A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 3973 | chr6 | 116736296 | ||||||
chr6:116736444 | G | C | 1 | a0001c0001t0029 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4121G>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 4121 | chr6 | 116736444 | ||||||
chr6:116736624 | A | G | 1 | a0001c0001t0051 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4301A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 4301 | chr6 | 116736624 | ||||||
chr6:116737373 | A | G | 2 | a0001c0001t0026 a0001c0001t0057 |
3 | HG02572.hp1 HG03130.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5050A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 5050 | chr6 | 116737373 | ||||||
chr6:116737419 | T | G | 1 | a0001c0001t0019 | 3 | NA18997.hp1 NA19012.hp2 NA19085.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5096T>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 5096 | chr6 | 116737419 | ||||||
chr6:116737435 | G | A | 1 | a0001c0001t0025 | 2 | HG02717.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5112G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 5112 | chr6 | 116737435 | ||||||
chr6:116737518 | C | T | 1 | a0001c0001t0016 | 3 | HG02818.hp2 HG02896.hp2 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5195C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 5195 | chr6 | 116737518 | ||||||
chr6:116737529 | T | C | 1 | a0001c0001t0056 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5206T>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 5206 | chr6 | 116737529 | ||||||
chr6:116737609 | T | G | 1 | a0001c0001t0060 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5286T>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 5286 | chr6 | 116737609 | ||||||
chr6:116737879 | G | C | 1 | a0001c0001t0034 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5556G>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 5556 | chr6 | 116737879 | ||||||
chr6:116737879 | G | T | 15 | a0001c0001t0003 a0001c0001t0014 a0001c0001t0015 others(12): Show |
54 | HG00280.hp1 HG00323.hp2 HG00642.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*5556G>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 5556 | chr6 | 116737879 | ||||||
chr6:116738127 | G | A | 3 | a0001c0001t0010 a0001c0001t0025 a0001c0001t0060 |
9 | HG02145.hp1 HG02280.hp2 HG02717.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*5804G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 5804 | chr6 | 116738127 | ||||||
chr6:116738178 | G | A | 1 | a0001c0001t0055 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5855G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 5855 | chr6 | 116738178 | ||||||
chr6:116738183 | C | G | 1 | a0001c0001t0068 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5860C>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 5860 | chr6 | 116738183 | ||||||
chr6:116738271 | G | C | 1 | a0001c0001t0047 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5948G>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 5948 | chr6 | 116738271 | ||||||
chr6:116738362 | G | C | 1 | a0001c0001t0035 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6039G>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 6039 | chr6 | 116738362 | ||||||
chr6:116738371 | C | A | 1 | a0001c0001t0048 | 1 | NA18955.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6048C>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 6048 | chr6 | 116738371 | ||||||
chr6:116738404 | T | C | 29 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0006 others(26): Show |
92 | HG00280.hp1 HG00323.hp2 HG00642.hp1 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*6081T>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 6081 | chr6 | 116738404 | ||||||
chr6:116738437 | A | G | 15 | a0001c0001t0003 a0001c0001t0014 a0001c0001t0015 others(12): Show |
54 | HG00280.hp1 HG00323.hp2 HG00642.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*6114A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 6114 | chr6 | 116738437 | ||||||
chr6:116738499 | C | A | 1 | a0001c0001t0036 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6176C>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 6176 | chr6 | 116738499 | ||||||
chr6:116738619 | G | A | 1 | a0001c0001t0037 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6296G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 6296 | chr6 | 116738619 | ||||||
chr6:116738683 | A | T | 29 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0006 others(26): Show |
92 | HG00280.hp1 HG00323.hp2 HG00642.hp1 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*6360A>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 6360 | chr6 | 116738683 | ||||||
chr6:116738766 | C | T | 1 | a0001c0001t0015 | 2 | HG00280.hp1 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6443C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 6443 | chr6 | 116738766 | ||||||
chr6:116738845 | C | T | 1 | a0001c0001t0013 | 4 | HG00558.hp1 NA18944.hp1 NA19057.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6522C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 6522 | chr6 | 116738845 | ||||||
chr6:116738984 | G | T | 1 | a0001c0001t0046 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6661G>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 6661 | chr6 | 116738984 | ||||||
chr6:116739031 | G | A | 7 | a0001c0001t0005 a0001c0001t0021 a0001c0001t0055 others(4): Show |
17 | HG01243.hp2 HG01258.hp1 HG01884.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*6708G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 6708 | chr6 | 116739031 | ||||||
chr6:116739032 | T | C | 7 | a0001c0001t0005 a0001c0001t0021 a0001c0001t0055 others(4): Show |
17 | HG01243.hp2 HG01258.hp1 HG01884.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*6709T>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 6709 | chr6 | 116739032 | ||||||
chr6:116739054 | A | G | 1 | a0001c0001t0063 | 1 | NA19074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6731A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 6731 | chr6 | 116739054 | ||||||
chr6:116739090 | T | C | 1 | a0001c0001t0038 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6767T>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 6767 | chr6 | 116739090 | ||||||
chr6:116739099 | A | T | 2 | a0001c0001t0004 a0001c0001t0017 |
20 | HG00544.hp1 HG01106.hp2 HG02132.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*6776A>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 6776 | chr6 | 116739099 | ||||||
chr6:116739149 | C | G | 1 | a0003c0006t0045 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6826C>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 6826 | chr6 | 116739149 | ||||||
chr6:116739214 | A | C | 2 | a0002c0003t0018 a0002c0003t0054 |
4 | HG01258.hp1 HG02148.hp1 HG02735.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6891A>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 6891 | chr6 | 116739214 | ||||||
chr6:116739215 | A | C | 2 | a0001c0001t0021 a0001c0001t0069 |
4 | HG01884.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6892A>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 6892 | chr6 | 116739215 | ||||||
chr6:116739369 | A | C | 1 | a0001c0001t0031 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7046A>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 7046 | chr6 | 116739369 | ||||||
chr6:116739381 | C | T | 2 | a0002c0003t0018 a0002c0003t0054 |
4 | HG01258.hp1 HG02148.hp1 HG02735.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*7058C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 7058 | chr6 | 116739381 | ||||||
chr6:116739403 | C | T | 1 | a0001c0001t0051 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7080C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 7080 | chr6 | 116739403 | ||||||
chr6:116739437 | A | G | 5 | a0001c0001t0005 a0001c0001t0055 a0001c0001t0056 others(2): Show |
13 | HG01243.hp2 HG01258.hp1 HG02109.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*7114A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 7114 | chr6 | 116739437 | ||||||
chr6:116739530 | C | T | 2 | a0002c0003t0018 a0002c0003t0054 |
4 | HG01258.hp1 HG02148.hp1 HG02735.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*7207C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 7207 | chr6 | 116739530 | ||||||
chr6:116739610 | G | A | 1 | a0001c0001t0014 | 3 | HG00741.hp2 HG03195.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7287G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 7287 | chr6 | 116739610 | ||||||
chr6:116739694 | A | G | 3 | a0001c0001t0010 a0001c0001t0025 a0001c0001t0060 |
9 | HG02145.hp1 HG02280.hp2 HG02717.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*7371A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 7371 | chr6 | 116739694 | ||||||
chr6:116739737 | G | C | 2 | a0001c0001t0012 a0003c0006t0045 |
5 | HG01884.hp1 HG02970.hp1 HG03195.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*7414G>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 7414 | chr6 | 116739737 | ||||||
chr6:116739754 | C | T | 1 | a0001c0001t0050 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7431C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 7431 | chr6 | 116739754 | ||||||
chr6:116739757 | T | C | 1 | a0001c0001t0049 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7434T>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 7434 | chr6 | 116739757 | ||||||
chr6:116739792 | A | C | 1 | a0001c0001t0007 | 7 | HG00280.hp2 HG01167.hp1 HG01169.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*7469A>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 7469 | chr6 | 116739792 | ||||||
chr6:116739792 | A | G | 1 | a0001c0001t0062 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7469A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 7469 | chr6 | 116739792 | ||||||
chr6:116739813 | T | G | 29 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0006 others(26): Show |
92 | HG00280.hp1 HG00323.hp2 HG00642.hp1 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*7490T>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 7490 | chr6 | 116739813 | ||||||
chr6:116739870 | A | G | 1 | a0001c0001t0044 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7547A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 7547 | chr6 | 116739870 | ||||||
chr6:116739932 | G | C | 29 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0006 others(26): Show |
92 | HG00280.hp1 HG00323.hp2 HG00642.hp1 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*7609G>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 7609 | chr6 | 116739932 | ||||||
chr6:116740040 | T | G | 2 | a0001c0001t0021 a0001c0001t0069 |
4 | HG01884.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*7717T>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 7717 | chr6 | 116740040 | ||||||
chr6:116740250 | C | T | 2 | a0001c0001t0026 a0001c0001t0057 |
3 | HG02572.hp1 HG03130.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7927C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 7927 | chr6 | 116740250 | ||||||
chr6:116740312 | C | T | 2 | a0002c0003t0018 a0002c0003t0054 |
4 | HG01258.hp1 HG02148.hp1 HG02735.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*7989C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 7989 | chr6 | 116740312 | ||||||
chr6:116740558 | A | G | 1 | a0001c0001t0022 | 2 | NA18977.hp1 NA19059.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8235A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 8235 | chr6 | 116740558 | ||||||
chr6:116740607 | A | T | 1 | a0001c0001t0023 | 2 | HG01169.hp1 HG04199.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8284A>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 8284 | chr6 | 116740607 | ||||||
chr6:116740638 | T | C | 1 | a0001c0001t0039 | 1 | NA18612.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8315T>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 8315 | chr6 | 116740638 | ||||||
chr6:116740746 | A | G | 2 | a0002c0003t0018 a0002c0003t0054 |
4 | HG01258.hp1 HG02148.hp1 HG02735.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*8423A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 8423 | chr6 | 116740746 | ||||||
chr6:116740757 | T | C | 1 | a0001c0001t0040 | 1 | HG01167.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8434T>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 8434 | chr6 | 116740757 | ||||||
chr6:116740994 | TA | T | 3 | a0001c0001t0043 a0001c0001t0061 a0001c0002t0008 |
8 | HG00639.hp1 HG00639.hp2 HG01496.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*8681delA | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 8681 | INFO_REALIGN_3_PRIME | chr6 | 116740994 | |||||
chr6:116741036 | A | ATAT | 29 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0006 others(26): Show |
92 | HG00280.hp1 HG00323.hp2 HG00642.hp1 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*8714_*8716dupTAT | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 8717 | INFO_REALIGN_3_PRIME | chr6 | 116741036 | |||||
chr6:116741195 | T | G | 1 | a0001c0001t0041 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8872T>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 8872 | chr6 | 116741195 | ||||||
chr6:116741356 | CT | C | 29 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0006 others(26): Show |
92 | HG00280.hp1 HG00323.hp2 HG00642.hp1 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*9042delT | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 9042 | INFO_REALIGN_3_PRIME | chr6 | 116741356 | |||||
chr6:116741435 | C | G | 1 | a0001c0001t0042 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9112C>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 14/14 | 9112 | chr6 | 116741435 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:116681617 | C | T | 1 | a0001c0001t0006g0299 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.4+279C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | chr6 | 116681617 | |||||||
chr6:116681796 | C | T | 1 | a0001c0001t0001g0298 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.4+458C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | chr6 | 116681796 | |||||||
chr6:116682035 | G | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
2 | HG00597.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.4+697G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | chr6 | 116682035 | |||||||
chr6:116682062 | C | G | 15 | a0001c0001t0004g0008 a0001c0001t0004g0009 a0001c0001t0004g0027 others(12): Show |
20 | HG00544.hp1 HG01106.hp2 HG02132.hp1 others(17): Show |
intron_variant | MODIFIER | c.4+724C>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | chr6 | 116682062 | |||||||
chr6:116682233 | G | A | 1 | a0001c0001t0002g0030 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.4+895G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | chr6 | 116682233 | |||||||
chr6:116682365 | TTGA | T | 80 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(77): Show |
86 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.4+1028_4+1030delTG others(1): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | chr6 | 116682365 | |||||||
chr6:116682458 | A | T | 2 | a0001c0001t0001g0284 a0001c0001t0001g0285 |
2 | NA19004.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.4+1120A>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | chr6 | 116682458 | |||||||
chr6:116682925 | G | C | 45 | a0001c0001t0001g0016 a0001c0001t0001g0112 a0001c0001t0001g0115 others(42): Show |
45 | HG00639.hp1 HG00741.hp1 HG01123.hp1 others(42): Show |
intron_variant | MODIFIER | c.4+1587G>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | chr6 | 116682925 | |||||||
chr6:116682988 | A | T | 1 | a0001c0001t0004g0297 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.4+1650A>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | chr6 | 116682988 | |||||||
chr6:116683077 | T | C | 80 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(77): Show |
86 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.4+1739T>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | chr6 | 116683077 | |||||||
chr6:116683091 | G | C | 1 | a0001c0001t0001g0145 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.4+1753G>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | chr6 | 116683091 | |||||||
chr6:116683227 | A | G | 8 | a0001c0001t0005g0276 a0001c0001t0005g0277 a0001c0001t0005g0279 others(5): Show |
8 | HG01243.hp2 HG02109.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.4+1889A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | chr6 | 116683227 | |||||||
chr6:116683290 | C | T | 4 | a0001c0001t0003g0007 a0001c0001t0003g0026 a0001c0001t0014g0007 others(1): Show |
5 | HG00741.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.4+1952C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | chr6 | 116683290 | |||||||
chr6:116683602 | T | C | 1 | a0001c0001t0003g0146 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.4+2264T>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | chr6 | 116683602 | |||||||
chr6:116683666 | G | A | 1 | a0001c0001t0010g0031 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.4+2328G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | chr6 | 116683666 | |||||||
chr6:116683818 | C | T | 1 | a0001c0001t0009g0275 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.4+2480C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | chr6 | 116683818 | |||||||
chr6:116683896 | C | CT | 15 | a0001c0001t0001g0265 a0001c0001t0001g0267 a0001c0001t0001g0268 others(12): Show |
16 | HG00741.hp2 HG01071.hp2 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.4+2592dupT | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr6 | 116683896 | ||||||
chr6:116683896 | C | CTT | 7 | a0001c0001t0001g0004 a0001c0001t0001g0145 a0001c0001t0001g0270 others(4): Show |
10 | HG00544.hp2 HG00642.hp2 NA18942.hp1 others(7): Show |
intron_variant | MODIFIER | c.4+2591_4+2592dupTT | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr6 | 116683896 | ||||||
chr6:116683896 | CT | C | 102 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0021 others(99): Show |
119 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.4+2592delT | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr6 | 116683896 | ||||||
chr6:116683896 | CTTTT | C | 23 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(20): Show |
24 | HG00639.hp2 HG01074.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.4+2589_4+2592delTT others(2): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr6 | 116683896 | ||||||
chr6:116683896 | CTTTTT | C | 27 | a0001c0001t0001g0016 a0001c0001t0001g0112 a0001c0001t0001g0115 others(24): Show |
27 | HG00639.hp1 HG00741.hp1 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.4+2588_4+2592delTT others(3): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr6 | 116683896 | ||||||
chr6:116683896 | CTTTTTT | C | 10 | a0001c0001t0006g0104 a0001c0001t0006g0105 a0001c0001t0025g0106 others(7): Show |
11 | HG01258.hp1 HG02129.hp2 HG02148.hp1 others(8): Show |
intron_variant | MODIFIER | c.4+2587_4+2592delTT others(4): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr6 | 116683896 | ||||||
chr6:116683896 | CTTTTTTT others(5): Show |
C | 2 | a0001c0001t0004g0286 a0001c0001t0004g0287 |
2 | HG01106.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.4+2581_4+2592delTT others(10): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr6 | 116683896 | ||||||
chr6:116683896 | CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0029g0161 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.4+2580_4+2592delTT others(11): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr6 | 116683896 | ||||||
chr6:116683896 | CTTTTTTT others(10): Show |
C | 4 | a0001c0001t0010g0031 a0001c0001t0010g0032 a0001c0001t0010g0033 others(1): Show |
4 | HG02145.hp1 HG02280.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.4+2576_4+2592delTT others(15): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr6 | 116683896 | ||||||
chr6:116683896 | CTTTTTTT others(14): Show |
C | 18 | a0001c0001t0001g0018 a0001c0001t0001g0150 a0001c0001t0001g0151 others(15): Show |
18 | HG01884.hp1 HG02055.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.4+2572_4+2592delTT others(19): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr6 | 116683896 | ||||||
chr6:116683986 | C | T | 1 | a0001c0001t0004g0287 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.4+2648C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | chr6 | 116683986 | |||||||
chr6:116684126 | C | T | 2 | a0001c0001t0001g0005 a0001c0001t0001g0261 |
4 | NA18968.hp2 NA19007.hp2 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.4+2788C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | chr6 | 116684126 | |||||||
chr6:116684154 | C | T | 2 | a0001c0001t0001g0124 a0001c0001t0058g0140 |
2 | HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.4+2816C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | chr6 | 116684154 | |||||||
chr6:116684155 | G | A | 80 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(77): Show |
86 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.4+2817G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | chr6 | 116684155 | |||||||
chr6:116684215 | A | G | 4 | a0001c0001t0021g0164 a0001c0001t0021g0166 a0001c0001t0021g0170 others(1): Show |
4 | HG01884.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.4+2877A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | chr6 | 116684215 | |||||||
chr6:116684622 | C | T | 3 | a0001c0001t0026g0109 a0001c0001t0026g0110 a0001c0001t0057g0111 |
3 | HG02572.hp1 HG03130.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.4+3284C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | chr6 | 116684622 | |||||||
chr6:116684712 | A | G | 1 | a0001c0001t0058g0140 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4+3374A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | chr6 | 116684712 | |||||||
chr6:116684834 | T | C | 1 | a0001c0001t0016g0147 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4+3496T>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | chr6 | 116684834 | |||||||
chr6:116685112 | CA | C | 4 | a0001c0001t0001g0123 a0001c0001t0001g0139 a0001c0001t0001g0298 others(1): Show |
4 | HG00741.hp1 HG01255.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.4+3779delA | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr6 | 116685112 | ||||||
chr6:116685272 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.4+3934G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | chr6 | 116685272 | |||||||
chr6:116685300 | C | T | 1 | a0001c0001t0027g0108 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.4+3962C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | chr6 | 116685300 | |||||||
chr6:116685310 | C | T | 2 | a0001c0001t0021g0166 a0001c0001t0021g0170 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.4+3972C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | chr6 | 116685310 | |||||||
chr6:116685322 | T | C | 1 | a0001c0001t0003g0218 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.4+3984T>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | chr6 | 116685322 | |||||||
chr6:116685347 | C | T | 2 | a0001c0001t0001g0016 a0001c0001t0043g0016 |
2 | HG00639.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.5-3973C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | chr6 | 116685347 | |||||||
chr6:116685518 | A | G | 3 | a0002c0003t0018g0019 a0002c0003t0018g0163 a0002c0003t0054g0162 |
4 | HG01258.hp1 HG02148.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.5-3802A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | chr6 | 116685518 | |||||||
chr6:116685532 | G | A | 29 | a0001c0001t0001g0018 a0001c0001t0001g0150 a0001c0001t0001g0151 others(26): Show |
30 | HG01243.hp2 HG01258.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.5-3788G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | chr6 | 116685532 | |||||||
chr6:116685773 | A | C | 2 | a0001c0001t0027g0107 a0001c0001t0027g0108 |
2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.5-3547A>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | chr6 | 116685773 | |||||||
chr6:116685905 | G | A | 9 | a0001c0001t0005g0219 a0001c0001t0005g0276 a0001c0001t0005g0277 others(6): Show |
9 | HG01243.hp2 HG02109.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.5-3415G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | chr6 | 116685905 | |||||||
chr6:116685949 | C | T | 1 | a0001c0001t0006g0260 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.5-3371C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | chr6 | 116685949 | |||||||
chr6:116685981 | A | C | 12 | a0001c0001t0005g0219 a0001c0001t0005g0276 a0001c0001t0005g0277 others(9): Show |
13 | HG01243.hp2 HG01258.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.5-3339A>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | chr6 | 116685981 | |||||||
chr6:116686020 | T | C | 36 | a0001c0001t0001g0016 a0001c0001t0001g0112 a0001c0001t0001g0115 others(33): Show |
36 | HG00639.hp1 HG01123.hp1 HG01255.hp1 others(33): Show |
intron_variant | MODIFIER | c.5-3300T>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | chr6 | 116686020 | |||||||
chr6:116686021 | C | T | 30 | a0001c0001t0001g0016 a0001c0001t0001g0112 a0001c0001t0001g0115 others(27): Show |
30 | HG00639.hp1 HG01123.hp1 HG01255.hp1 others(27): Show |
intron_variant | MODIFIER | c.5-3299C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | chr6 | 116686021 | |||||||
chr6:116686034 | A | G | 2 | a0001c0001t0025g0106 a0001c0001t0025g0144 |
2 | HG02717.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.5-3286A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | chr6 | 116686034 | |||||||
chr6:116686158 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.5-3162G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | chr6 | 116686158 | |||||||
chr6:116686196 | G | A | 1 | a0001c0001t0011g0141 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.5-3124G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | chr6 | 116686196 | |||||||
chr6:116686236 | A | G | 12 | a0001c0001t0001g0018 a0001c0001t0001g0156 a0001c0001t0001g0157 others(9): Show |
12 | HG01884.hp1 HG02109.hp2 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.5-3084A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | chr6 | 116686236 | |||||||
chr6:116686314 | CT | C | 12 | a0001c0001t0005g0219 a0001c0001t0005g0276 a0001c0001t0005g0277 others(9): Show |
13 | HG01243.hp2 HG01258.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.5-2999delT | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr6 | 116686314 | ||||||
chr6:116686373 | C | T | 84 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(81): Show |
90 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.5-2947C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | chr6 | 116686373 | |||||||
chr6:116686691 | C | A | 2 | a0001c0001t0003g0173 a0001c0001t0031g0221 |
2 | HG03017.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.5-2629C>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | chr6 | 116686691 | |||||||
chr6:116686715 | G | A | 12 | a0001c0001t0005g0219 a0001c0001t0005g0276 a0001c0001t0005g0277 others(9): Show |
13 | HG01243.hp2 HG01258.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.5-2605G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | chr6 | 116686715 | |||||||
chr6:116686725 | G | T | 2 | a0001c0001t0001g0258 a0001c0001t0001g0269 |
2 | HG01081.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.5-2595G>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | chr6 | 116686725 | |||||||
chr6:116686879 | A | G | 1 | a0001c0001t0002g0100 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.5-2441A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | chr6 | 116686879 | |||||||
chr6:116686994 | G | A | 2 | a0001c0001t0025g0106 a0001c0001t0025g0144 |
2 | HG02717.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.5-2326G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | chr6 | 116686994 | |||||||
chr6:116687233 | A | G | 1 | a0001c0001t0033g0214 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.5-2087A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | chr6 | 116687233 | |||||||
chr6:116687414 | G | A | 1 | a0001c0004t0003g0222 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.5-1906G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | chr6 | 116687414 | |||||||
chr6:116687599 | T | G | 1 | a0001c0001t0010g0031 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.5-1721T>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | chr6 | 116687599 | |||||||
chr6:116687745 | T | C | 11 | a0001c0001t0006g0104 a0001c0001t0006g0105 a0001c0001t0006g0121 others(8): Show |
11 | HG02129.hp2 HG02572.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.5-1575T>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | chr6 | 116687745 | |||||||
chr6:116687750 | C | T | 1 | a0001c0001t0001g0268 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.5-1570C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | chr6 | 116687750 | |||||||
chr6:116687765 | A | T | 1 | a0002c0003t0018g0163 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.5-1555A>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | chr6 | 116687765 | |||||||
chr6:116687856 | A | G | 1 | a0001c0001t0001g0160 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.5-1464A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | chr6 | 116687856 | |||||||
chr6:116687874 | T | C | 12 | a0001c0001t0006g0104 a0001c0001t0006g0105 a0001c0001t0006g0121 others(9): Show |
12 | HG02129.hp2 HG02572.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.5-1446T>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | chr6 | 116687874 | |||||||
chr6:116688116 | C | A | 1 | a0001c0001t0001g0174 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.5-1204C>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | chr6 | 116688116 | |||||||
chr6:116688172 | G | T | 1 | a0001c0001t0068g0137 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.5-1148G>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | chr6 | 116688172 | |||||||
chr6:116688230 | G | A | 2 | a0001c0001t0003g0146 a0001c0001t0003g0175 |
2 | HG02615.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.5-1090G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | chr6 | 116688230 | |||||||
chr6:116688286 | T | C | 31 | a0001c0001t0001g0016 a0001c0001t0001g0112 a0001c0001t0001g0115 others(28): Show |
31 | HG00639.hp1 HG00741.hp1 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.5-1034T>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | chr6 | 116688286 | |||||||
chr6:116688504 | T | C | 1 | a0001c0001t0006g0260 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.5-816T>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | chr6 | 116688504 | |||||||
chr6:116688844 | A | G | 3 | a0001c0001t0001g0133 a0001c0001t0024g0134 a0001c0001t0024g0135 |
3 | HG02257.hp1 NA19240.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.5-476A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | chr6 | 116688844 | |||||||
chr6:116688845 | T | C | 1 | a0001c0001t0003g0176 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.5-475T>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | chr6 | 116688845 | |||||||
chr6:116688953 | C | CT | 120 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(117): Show |
128 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.5-358dupT | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr6 | 116688953 | ||||||
chr6:116689176 | A | G | 3 | a0002c0003t0018g0019 a0002c0003t0018g0163 a0002c0003t0054g0162 |
4 | HG01258.hp1 HG02148.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.5-144A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | chr6 | 116689176 | |||||||
chr6:116689247 | C | T | 3 | a0002c0003t0018g0019 a0002c0003t0018g0163 a0002c0003t0054g0162 |
4 | HG01258.hp1 HG02148.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.5-73C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 1/13 | chr6 | 116689247 | |||||||
chr6:116689984 | A | G | 1 | a0001c0001t0002g0099 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.138+531A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 2/13 | chr6 | 116689984 | |||||||
chr6:116690021 | G | A | 120 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(117): Show |
128 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.138+568G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 2/13 | chr6 | 116690021 | |||||||
chr6:116690082 | C | CTTCTATT others(8): Show |
113 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(110): Show |
120 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.138+644_138+658dup others(15): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr6 | 116690082 | ||||||
chr6:116690082 | C | CTTCTATT others(23): Show |
6 | a0001c0002t0008g0020 a0001c0002t0008g0167 a0001c0002t0008g0169 others(3): Show |
7 | HG00639.hp2 HG01074.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.138+658_138+659ins others(30): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr6 | 116690082 | ||||||
chr6:116690217 | G | C | 98 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(95): Show |
104 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.138+764G>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 2/13 | chr6 | 116690217 | |||||||
chr6:116690307 | G | C | 9 | a0001c0001t0005g0219 a0001c0001t0005g0276 a0001c0001t0005g0277 others(6): Show |
9 | HG01243.hp2 HG02109.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.138+854G>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 2/13 | chr6 | 116690307 | |||||||
chr6:116690510 | G | C | 8 | a0001c0001t0005g0219 a0001c0001t0005g0276 a0001c0001t0005g0277 others(5): Show |
8 | HG01243.hp2 HG02109.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.138+1057G>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 2/13 | chr6 | 116690510 | |||||||
chr6:116690513 | G | A | 1 | a0001c0001t0056g0281 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.138+1060G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 2/13 | chr6 | 116690513 | |||||||
chr6:116690526 | C | G | 4 | a0001c0002t0008g0169 a0001c0002t0008g0256 a0001c0002t0008g0257 others(1): Show |
4 | HG01074.hp2 HG02280.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.138+1073C>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 2/13 | chr6 | 116690526 | |||||||
chr6:116690591 | C | T | 84 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(81): Show |
90 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.138+1138C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 2/13 | chr6 | 116690591 | |||||||
chr6:116690630 | A | T | 22 | a0001c0001t0005g0219 a0001c0001t0005g0276 a0001c0001t0005g0277 others(19): Show |
24 | HG00639.hp2 HG01074.hp2 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.138+1177A>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 2/13 | chr6 | 116690630 | |||||||
chr6:116690642 | C | CA | 12 | a0001c0001t0005g0219 a0001c0001t0005g0276 a0001c0001t0005g0277 others(9): Show |
13 | HG01243.hp2 HG01258.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.138+1206dupA | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr6 | 116690642 | ||||||
chr6:116690642 | CA | C | 8 | a0001c0001t0001g0120 a0001c0001t0002g0070 a0001c0001t0002g0098 others(5): Show |
8 | HG01167.hp1 HG01496.hp2 HG03834.hp2 others(5): Show |
intron_variant | MODIFIER | c.138+1206delA | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr6 | 116690642 | ||||||
chr6:116690877 | T | C | 1 | a0001c0001t0001g0177 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.139-1178T>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 2/13 | chr6 | 116690877 | |||||||
chr6:116691046 | T | C | 1 | a0001c0001t0003g0223 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.139-1009T>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 2/13 | chr6 | 116691046 | |||||||
chr6:116691098 | G | A | 1 | a0001c0001t0003g0178 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.139-957G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 2/13 | chr6 | 116691098 | |||||||
chr6:116691101 | C | T | 1 | a0001c0001t0001g0160 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.139-954C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 2/13 | chr6 | 116691101 | |||||||
chr6:116691146 | T | A | 1 | a0001c0001t0003g0146 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.139-909T>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 2/13 | chr6 | 116691146 | |||||||
chr6:116691258 | T | C | 3 | a0001c0001t0004g0288 a0001c0001t0004g0289 a0001c0001t0004g0290 |
3 | HG02809.hp1 HG03041.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.139-797T>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 2/13 | chr6 | 116691258 | |||||||
chr6:116691393 | A | G | 1 | a0001c0001t0006g0260 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.139-662A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 2/13 | chr6 | 116691393 | |||||||
chr6:116691905 | A | G | 4 | a0001c0001t0003g0211 a0001c0001t0003g0212 a0001c0001t0003g0218 others(1): Show |
4 | HG02559.hp2 HG02922.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.139-150A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 2/13 | chr6 | 116691905 | |||||||
chr6:116692037 | G | A | 1 | a0001c0001t0003g0178 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.139-18G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 2/13 | chr6 | 116692037 | |||||||
chr6:116692284 | G | A | 11 | a0001c0001t0006g0104 a0001c0001t0006g0105 a0001c0001t0006g0121 others(8): Show |
11 | HG02129.hp2 HG02572.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.241-9G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 3/13 | chr6 | 116692284 | |||||||
chr6:116692458 | G | GT | 13 | a0001c0001t0005g0219 a0001c0001t0005g0276 a0001c0001t0005g0277 others(10): Show |
13 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.340+75dupT | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr6 | 116692458 | ||||||
chr6:116692521 | T | C | 8 | a0001c0001t0005g0219 a0001c0001t0005g0276 a0001c0001t0005g0277 others(5): Show |
8 | HG01243.hp2 HG02109.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.340+129T>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | chr6 | 116692521 | |||||||
chr6:116692718 | T | A | 1 | a0001c0001t0001g0269 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.340+326T>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | chr6 | 116692718 | |||||||
chr6:116692850 | A | G | 1 | a0001c0001t0068g0137 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.340+458A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | chr6 | 116692850 | |||||||
chr6:116692874 | A | G | 1 | a0001c0001t0001g0254 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.340+482A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | chr6 | 116692874 | |||||||
chr6:116692893 | A | T | 7 | a0001c0001t0001g0119 a0001c0001t0001g0123 a0001c0001t0001g0131 others(4): Show |
7 | HG00741.hp1 HG01255.hp1 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.340+501A>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | chr6 | 116692893 | |||||||
chr6:116693023 | A | G | 1 | a0001c0001t0002g0097 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.340+631A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | chr6 | 116693023 | |||||||
chr6:116693057 | A | G | 2 | a0001c0001t0003g0210 a0001c0001t0003g0253 |
2 | HG02027.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.340+665A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | chr6 | 116693057 | |||||||
chr6:116693190 | G | A | 120 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(117): Show |
128 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.340+798G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | chr6 | 116693190 | |||||||
chr6:116693197 | C | T | 1 | a0001c0001t0002g0067 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.340+805C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | chr6 | 116693197 | |||||||
chr6:116693217 | G | A | 1 | a0001c0001t0003g0224 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.340+825G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | chr6 | 116693217 | |||||||
chr6:116693572 | T | C | 3 | a0002c0003t0018g0019 a0002c0003t0018g0163 a0002c0003t0054g0162 |
4 | HG01258.hp1 HG02148.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.340+1180T>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | chr6 | 116693572 | |||||||
chr6:116693668 | T | C | 5 | a0001c0001t0012g0017 a0001c0001t0012g0153 a0001c0001t0012g0154 others(2): Show |
5 | HG01884.hp1 HG02970.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.340+1276T>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | chr6 | 116693668 | |||||||
chr6:116693677 | T | G | 120 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(117): Show |
128 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.340+1285T>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | chr6 | 116693677 | |||||||
chr6:116693706 | C | A | 1 | a0001c0001t0001g0225 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.340+1314C>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | chr6 | 116693706 | |||||||
chr6:116693707 | G | A | 13 | a0001c0001t0001g0226 a0001c0001t0006g0104 a0001c0001t0006g0105 others(10): Show |
13 | HG02129.hp2 HG02572.hp1 HG02818.hp1 others(10): Show |
intron_variant | MODIFIER | c.340+1315G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | chr6 | 116693707 | |||||||
chr6:116693738 | T | C | 1 | a0001c0001t0001g0133 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.340+1346T>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | chr6 | 116693738 | |||||||
chr6:116693787 | T | A | 6 | a0001c0002t0008g0020 a0001c0002t0008g0167 a0001c0002t0008g0169 others(3): Show |
7 | HG00639.hp2 HG01074.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.340+1395T>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | chr6 | 116693787 | |||||||
chr6:116693818 | A | G | 18 | a0001c0001t0001g0018 a0001c0001t0001g0150 a0001c0001t0001g0151 others(15): Show |
18 | HG01884.hp1 HG02055.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.340+1426A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | chr6 | 116693818 | |||||||
chr6:116693869 | G | T | 31 | a0001c0001t0001g0016 a0001c0001t0001g0112 a0001c0001t0001g0115 others(28): Show |
31 | HG00639.hp1 HG00741.hp1 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.340+1477G>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | chr6 | 116693869 | |||||||
chr6:116693872 | C | T | 1 | a0001c0001t0006g0122 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.340+1480C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | chr6 | 116693872 | |||||||
chr6:116694002 | C | T | 190 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0112 others(187): Show |
203 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.340+1610C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | chr6 | 116694002 | |||||||
chr6:116694031 | A | G | 9 | a0001c0001t0005g0219 a0001c0001t0005g0276 a0001c0001t0005g0277 others(6): Show |
9 | HG01243.hp2 HG02109.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.340+1639A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | chr6 | 116694031 | |||||||
chr6:116694052 | C | A | 5 | a0001c0001t0010g0031 a0001c0001t0010g0032 a0001c0001t0010g0033 others(2): Show |
5 | HG02145.hp1 HG02280.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.340+1660C>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | chr6 | 116694052 | |||||||
chr6:116694316 | A | G | 3 | a0001c0001t0009g0143 a0001c0001t0011g0141 a0001c0001t0011g0142 |
3 | HG02572.hp2 HG02630.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.340+1924A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | chr6 | 116694316 | |||||||
chr6:116694333 | A | G | 120 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(117): Show |
128 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.340+1941A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | chr6 | 116694333 | |||||||
chr6:116694489 | C | G | 1 | a0001c0001t0062g0096 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.340+2097C>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | chr6 | 116694489 | |||||||
chr6:116694644 | C | T | 6 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 others(3): Show |
6 | HG00738.hp1 HG01074.hp1 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.340+2252C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | chr6 | 116694644 | |||||||
chr6:116694645 | G | A | 83 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(80): Show |
89 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.340+2253G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | chr6 | 116694645 | |||||||
chr6:116694663 | T | C | 6 | a0001c0001t0009g0171 a0001c0001t0009g0172 a0001c0001t0009g0220 others(3): Show |
6 | HG02055.hp1 HG02559.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.340+2271T>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | chr6 | 116694663 | |||||||
chr6:116694735 | T | TA | 3 | a0001c0001t0003g0223 a0001c0001t0015g0180 a0001c0001t0015g0181 |
3 | HG00280.hp1 HG00673.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.340+2347dupA | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr6 | 116694735 | ||||||
chr6:116694867 | A | G | 3 | a0002c0003t0018g0019 a0002c0003t0018g0163 a0002c0003t0054g0162 |
4 | HG01258.hp1 HG02148.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.340+2475A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | chr6 | 116694867 | |||||||
chr6:116694875 | C | T | 2 | a0001c0001t0001g0118 a0001c0001t0001g0130 |
2 | HG03654.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.340+2483C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | chr6 | 116694875 | |||||||
chr6:116694891 | G | A | 190 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0112 others(187): Show |
203 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.340+2499G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | chr6 | 116694891 | |||||||
chr6:116695124 | G | C | 14 | a0001c0001t0006g0104 a0001c0001t0006g0105 a0001c0001t0006g0121 others(11): Show |
14 | HG02129.hp2 HG02572.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.340+2732G>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | chr6 | 116695124 | |||||||
chr6:116695135 | G | T | 1 | a0001c0001t0002g0066 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.340+2743G>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | chr6 | 116695135 | |||||||
chr6:116695166 | C | A | 1 | a0001c0001t0003g0210 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.340+2774C>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | chr6 | 116695166 | |||||||
chr6:116695398 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.340+3006T>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | chr6 | 116695398 | |||||||
chr6:116695455 | G | A | 2 | a0001c0001t0001g0156 a0001c0001t0001g0157 |
2 | HG03130.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.340+3063G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | chr6 | 116695455 | |||||||
chr6:116695506 | C | T | 6 | a0001c0002t0008g0020 a0001c0002t0008g0167 a0001c0002t0008g0169 others(3): Show |
7 | HG00639.hp2 HG01074.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.340+3114C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | chr6 | 116695506 | |||||||
chr6:116695533 | C | T | 1 | a0001c0001t0003g0178 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.340+3141C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | chr6 | 116695533 | |||||||
chr6:116695602 | C | T | 1 | a0001c0002t0008g0167 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.341-3102C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | chr6 | 116695602 | |||||||
chr6:116695908 | T | A | 1 | a0001c0001t0053g0182 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.341-2796T>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | chr6 | 116695908 | |||||||
chr6:116695988 | T | C | 9 | a0001c0001t0005g0219 a0001c0001t0005g0276 a0001c0001t0005g0277 others(6): Show |
9 | HG01243.hp2 HG02109.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.341-2716T>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | chr6 | 116695988 | |||||||
chr6:116696088 | C | T | 1 | a0001c0001t0006g0299 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.341-2616C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | chr6 | 116696088 | |||||||
chr6:116696268 | A | G | 15 | a0001c0001t0004g0008 a0001c0001t0004g0009 a0001c0001t0004g0027 others(12): Show |
20 | HG00544.hp1 HG01106.hp2 HG02132.hp1 others(17): Show |
intron_variant | MODIFIER | c.341-2436A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | chr6 | 116696268 | |||||||
chr6:116696341 | CA | C | 3 | a0002c0003t0018g0019 a0002c0003t0018g0163 a0002c0003t0054g0162 |
4 | HG01258.hp1 HG02148.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.341-2360delA | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr6 | 116696341 | ||||||
chr6:116696404 | A | T | 5 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(2): Show |
5 | HG01106.hp1 HG01109.hp2 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.341-2300A>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | chr6 | 116696404 | |||||||
chr6:116696491 | G | T | 2 | a0001c0001t0025g0106 a0001c0001t0025g0144 |
2 | HG02717.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.341-2213G>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | chr6 | 116696491 | |||||||
chr6:116696910 | C | T | 6 | a0001c0001t0009g0171 a0001c0001t0009g0172 a0001c0001t0009g0220 others(3): Show |
6 | HG02055.hp1 HG02559.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.341-1794C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | chr6 | 116696910 | |||||||
chr6:116696947 | T | G | 1 | a0001c0001t0001g0158 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.341-1757T>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | chr6 | 116696947 | |||||||
chr6:116696949 | G | T | 11 | a0001c0001t0006g0104 a0001c0001t0006g0105 a0001c0001t0006g0121 others(8): Show |
11 | HG02129.hp2 HG02572.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.341-1755G>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | chr6 | 116696949 | |||||||
chr6:116697040 | A | G | 13 | a0001c0001t0005g0219 a0001c0001t0005g0276 a0001c0001t0005g0277 others(10): Show |
13 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.341-1664A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | chr6 | 116697040 | |||||||
chr6:116697110 | C | T | 1 | a0001c0001t0057g0111 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.341-1594C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | chr6 | 116697110 | |||||||
chr6:116697440 | G | A | 9 | a0001c0001t0005g0219 a0001c0001t0005g0276 a0001c0001t0005g0277 others(6): Show |
9 | HG01243.hp2 HG02109.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.341-1264G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | chr6 | 116697440 | |||||||
chr6:116697592 | C | T | 1 | a0001c0001t0032g0206 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.341-1112C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | chr6 | 116697592 | |||||||
chr6:116697757 | A | T | 1 | a0001c0001t0001g0133 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.341-947A>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | chr6 | 116697757 | |||||||
chr6:116697764 | G | T | 2 | a0001c0001t0026g0110 a0001c0001t0057g0111 |
2 | HG03130.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.341-940G>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | chr6 | 116697764 | |||||||
chr6:116697965 | T | G | 12 | a0001c0001t0005g0219 a0001c0001t0005g0276 a0001c0001t0005g0277 others(9): Show |
13 | HG01243.hp2 HG01258.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.341-739T>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | chr6 | 116697965 | |||||||
chr6:116698123 | A | G | 1 | a0001c0001t0020g0248 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.341-581A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | chr6 | 116698123 | |||||||
chr6:116698237 | C | T | 18 | a0001c0001t0001g0018 a0001c0001t0001g0150 a0001c0001t0001g0151 others(15): Show |
18 | HG01884.hp1 HG02055.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.341-467C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | chr6 | 116698237 | |||||||
chr6:116698309 | G | C | 7 | a0001c0001t0006g0104 a0001c0001t0006g0105 a0001c0001t0006g0121 others(4): Show |
7 | HG02129.hp2 HG02886.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.341-395G>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | chr6 | 116698309 | |||||||
chr6:116698370 | C | T | 3 | a0002c0003t0018g0019 a0002c0003t0018g0163 a0002c0003t0054g0162 |
4 | HG01258.hp1 HG02148.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.341-334C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | chr6 | 116698370 | |||||||
chr6:116698393 | G | C | 83 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(80): Show |
89 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.341-311G>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | chr6 | 116698393 | |||||||
chr6:116698444 | A | G | 120 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(117): Show |
128 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.341-260A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | chr6 | 116698444 | |||||||
chr6:116698576 | A | G | 3 | a0001c0001t0026g0109 a0001c0001t0026g0110 a0001c0001t0057g0111 |
3 | HG02572.hp1 HG03130.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.341-128A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | chr6 | 116698576 | |||||||
chr6:116698652 | A | G | 1 | a0001c0001t0068g0137 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.341-52A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | chr6 | 116698652 | |||||||
chr6:116698683 | G | T | 120 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(117): Show |
128 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.341-21G>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 4/13 | chr6 | 116698683 | |||||||
chr6:116699534 | A | G | 1 | a0001c0001t0010g0071 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.435+736A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 5/13 | chr6 | 116699534 | |||||||
chr6:116699596 | T | C | 2 | a0001c0001t0001g0183 a0001c0001t0001g0227 |
2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.435+798T>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 5/13 | chr6 | 116699596 | |||||||
chr6:116699601 | T | G | 1 | a0001c0001t0001g0184 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.435+803T>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 5/13 | chr6 | 116699601 | |||||||
chr6:116699652 | A | G | 1 | a0001c0001t0069g0165 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.435+854A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 5/13 | chr6 | 116699652 | |||||||
chr6:116699655 | A | C | 1 | a0001c0001t0053g0182 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.435+857A>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 5/13 | chr6 | 116699655 | |||||||
chr6:116699718 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.435+920G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 5/13 | chr6 | 116699718 | |||||||
chr6:116699853 | G | C | 12 | a0001c0001t0001g0018 a0001c0001t0001g0156 a0001c0001t0001g0157 others(9): Show |
12 | HG01884.hp1 HG02109.hp2 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.435+1055G>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 5/13 | chr6 | 116699853 | |||||||
chr6:116700065 | A | G | 83 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(80): Show |
89 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.435+1267A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 5/13 | chr6 | 116700065 | |||||||
chr6:116700112 | G | A | 37 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0013 others(34): Show |
42 | HG00323.hp1 HG00609.hp1 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.435+1314G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 5/13 | chr6 | 116700112 | |||||||
chr6:116700161 | G | A | 12 | a0001c0001t0005g0219 a0001c0001t0005g0276 a0001c0001t0005g0277 others(9): Show |
13 | HG01243.hp2 HG01258.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.435+1363G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 5/13 | chr6 | 116700161 | |||||||
chr6:116700207 | C | T | 1 | a0001c0001t0002g0080 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.435+1409C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 5/13 | chr6 | 116700207 | |||||||
chr6:116700307 | C | CA | 120 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(117): Show |
128 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.435+1516dupA | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 116700307 | ||||||
chr6:116700365 | G | A | 1 | a0001c0001t0003g0176 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.435+1567G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 5/13 | chr6 | 116700365 | |||||||
chr6:116700384 | A | G | 3 | a0001c0001t0002g0015 a0001c0001t0002g0078 a0001c0001t0066g0079 |
4 | NA18951.hp2 NA19003.hp2 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.435+1586A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 5/13 | chr6 | 116700384 | |||||||
chr6:116700393 | C | T | 1 | a0001c0001t0002g0098 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.435+1595C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 5/13 | chr6 | 116700393 | |||||||
chr6:116700399 | G | A | 1 | a0001c0001t0004g0291 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.435+1601G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 5/13 | chr6 | 116700399 | |||||||
chr6:116700425 | A | G | 120 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(117): Show |
128 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.436-1594A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 5/13 | chr6 | 116700425 | |||||||
chr6:116700435 | A | G | 83 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(80): Show |
89 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.436-1584A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 5/13 | chr6 | 116700435 | |||||||
chr6:116700465 | T | C | 1 | a0001c0001t0003g0228 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.436-1554T>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 5/13 | chr6 | 116700465 | |||||||
chr6:116700465 | TAAAC | T | 84 | a0001c0001t0001g0285 a0001c0001t0002g0010 a0001c0001t0002g0011 others(81): Show |
90 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.436-1536_436-1533d others(6): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr6 | 116700465 | ||||||
chr6:116700483 | A | C | 1 | a0001c0001t0051g0247 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.436-1536A>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 5/13 | chr6 | 116700483 | |||||||
chr6:116700496 | T | A | 1 | a0001c0002t0008g0256 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.436-1523T>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 5/13 | chr6 | 116700496 | |||||||
chr6:116700623 | G | C | 2 | a0001c0001t0025g0106 a0001c0001t0025g0144 |
2 | HG02717.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.436-1396G>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 5/13 | chr6 | 116700623 | |||||||
chr6:116700637 | G | A | 4 | a0001c0001t0003g0211 a0001c0001t0003g0212 a0001c0001t0003g0218 others(1): Show |
4 | HG02559.hp2 HG02922.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.436-1382G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 5/13 | chr6 | 116700637 | |||||||
chr6:116700712 | T | A | 120 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(117): Show |
128 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.436-1307T>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 5/13 | chr6 | 116700712 | |||||||
chr6:116701063 | A | G | 1 | a0001c0001t0052g0117 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.436-956A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 5/13 | chr6 | 116701063 | |||||||
chr6:116701137 | T | C | 1 | a0001c0001t0001g0156 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.436-882T>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 5/13 | chr6 | 116701137 | |||||||
chr6:116701148 | A | G | 120 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(117): Show |
128 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.436-871A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 5/13 | chr6 | 116701148 | |||||||
chr6:116701306 | G | A | 4 | a0001c0001t0001g0018 a0001c0001t0001g0159 a0001c0001t0001g0160 others(1): Show |
4 | HG02109.hp2 HG02809.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.436-713G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 5/13 | chr6 | 116701306 | |||||||
chr6:116701344 | C | T | 9 | a0001c0001t0005g0219 a0001c0001t0005g0276 a0001c0001t0005g0277 others(6): Show |
9 | HG01243.hp2 HG02109.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.436-675C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 5/13 | chr6 | 116701344 | |||||||
chr6:116701422 | G | A | 190 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0112 others(187): Show |
203 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.436-597G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 5/13 | chr6 | 116701422 | |||||||
chr6:116701847 | A | G | 2 | a0001c0001t0025g0106 a0001c0001t0025g0144 |
2 | HG02717.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.436-172A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 5/13 | chr6 | 116701847 | |||||||
chr6:116702325 | T | G | 3 | a0001c0001t0002g0051 a0001c0001t0002g0081 a0001c0001t0002g0082 |
3 | HG00597.hp1 NA19011.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.567+175T>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 6/13 | chr6 | 116702325 | |||||||
chr6:116702407 | G | C | 120 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(117): Show |
128 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.567+257G>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 6/13 | chr6 | 116702407 | |||||||
chr6:116702470 | G | A | 1 | a0001c0001t0006g0260 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.567+320G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 6/13 | chr6 | 116702470 | |||||||
chr6:116702607 | T | C | 1 | a0001c0001t0025g0144 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.567+457T>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 6/13 | chr6 | 116702607 | |||||||
chr6:116702648 | G | A | 1 | a0001c0001t0068g0137 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.567+498G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 6/13 | chr6 | 116702648 | |||||||
chr6:116702656 | G | A | 22 | a0001c0001t0005g0219 a0001c0001t0005g0276 a0001c0001t0005g0277 others(19): Show |
24 | HG00639.hp2 HG01074.hp2 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.567+506G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 6/13 | chr6 | 116702656 | |||||||
chr6:116702667 | C | A | 1 | a0001c0002t0008g0256 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.567+517C>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 6/13 | chr6 | 116702667 | |||||||
chr6:116702730 | A | G | 15 | a0001c0001t0004g0008 a0001c0001t0004g0009 a0001c0001t0004g0027 others(12): Show |
20 | HG00544.hp1 HG01106.hp2 HG02132.hp1 others(17): Show |
intron_variant | MODIFIER | c.567+580A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 6/13 | chr6 | 116702730 | |||||||
chr6:116702816 | C | T | 6 | a0001c0002t0008g0020 a0001c0002t0008g0167 a0001c0002t0008g0169 others(3): Show |
7 | HG00639.hp2 HG01074.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.567+666C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 6/13 | chr6 | 116702816 | |||||||
chr6:116703064 | A | G | 5 | a0001c0001t0006g0104 a0001c0001t0006g0105 a0001c0001t0006g0121 others(2): Show |
5 | HG02129.hp2 HG03017.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.567+914A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 6/13 | chr6 | 116703064 | |||||||
chr6:116703263 | A | AT | 6 | a0001c0001t0003g0274 a0001c0001t0006g0104 a0001c0001t0006g0105 others(3): Show |
6 | HG02129.hp2 HG03017.hp2 HG03654.hp2 others(3): Show |
intron_variant | MODIFIER | c.567+1129dupT | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr6 | 116703263 | ||||||
chr6:116703263 | AT | A | 10 | a0001c0001t0002g0035 a0001c0001t0002g0052 a0001c0001t0002g0215 others(7): Show |
10 | HG01243.hp2 HG02109.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.567+1129delT | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr6 | 116703263 | ||||||
chr6:116703345 | T | C | 190 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0112 others(187): Show |
203 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.567+1195T>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 6/13 | chr6 | 116703345 | |||||||
chr6:116703379 | C | G | 3 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0070 |
3 | NA18966.hp1 NA19006.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.567+1229C>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 6/13 | chr6 | 116703379 | |||||||
chr6:116703423 | C | T | 1 | a0001c0001t0001g0205 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.567+1273C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 6/13 | chr6 | 116703423 | |||||||
chr6:116703498 | G | A | 37 | a0001c0001t0001g0016 a0001c0001t0001g0112 a0001c0001t0001g0115 others(34): Show |
37 | HG00639.hp1 HG00741.hp1 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.567+1348G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 6/13 | chr6 | 116703498 | |||||||
chr6:116703558 | C | T | 83 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(80): Show |
89 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.567+1408C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 6/13 | chr6 | 116703558 | |||||||
chr6:116703559 | G | A | 8 | a0001c0001t0005g0219 a0001c0001t0005g0276 a0001c0001t0005g0277 others(5): Show |
8 | HG01243.hp2 HG02109.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.567+1409G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 6/13 | chr6 | 116703559 | |||||||
chr6:116703834 | GAATAA | G | 4 | a0001c0001t0003g0007 a0001c0001t0003g0026 a0001c0001t0014g0007 others(1): Show |
5 | HG00741.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.568-1229_568-1225d others(7): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr6 | 116703834 | ||||||
chr6:116704070 | C | T | 2 | a0001c0001t0005g0279 a0001c0001t0005g0280 |
2 | HG01243.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.568-1002C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 6/13 | chr6 | 116704070 | |||||||
chr6:116704418 | T | C | 15 | a0001c0001t0004g0008 a0001c0001t0004g0009 a0001c0001t0004g0027 others(12): Show |
20 | HG00544.hp1 HG01106.hp2 HG02132.hp1 others(17): Show |
intron_variant | MODIFIER | c.568-654T>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 6/13 | chr6 | 116704418 | |||||||
chr6:116704457 | C | T | 120 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(117): Show |
128 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.568-615C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 6/13 | chr6 | 116704457 | |||||||
chr6:116704670 | G | C | 2 | a0001c0001t0025g0106 a0001c0001t0025g0144 |
2 | HG02717.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.568-402G>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 6/13 | chr6 | 116704670 | |||||||
chr6:116705250 | T | C | 4 | a0001c0001t0021g0164 a0001c0001t0021g0166 a0001c0001t0021g0170 others(1): Show |
4 | HG01884.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.656+90T>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116705250 | |||||||
chr6:116705351 | C | T | 1 | a0001c0001t0006g0260 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.656+191C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116705351 | |||||||
chr6:116705356 | G | A | 1 | a0001c0001t0006g0260 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.656+196G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116705356 | |||||||
chr6:116705380 | A | T | 2 | a0001c0001t0013g0203 a0001c0001t0013g0204 |
2 | HG00558.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.656+220A>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116705380 | |||||||
chr6:116705411 | A | G | 84 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(81): Show |
90 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.656+251A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116705411 | |||||||
chr6:116705660 | C | T | 26 | a0001c0001t0001g0016 a0001c0001t0001g0112 a0001c0001t0001g0115 others(23): Show |
26 | HG00639.hp1 HG00741.hp1 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.656+500C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116705660 | |||||||
chr6:116705752 | G | A | 1 | a0001c0001t0001g0120 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.656+592G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116705752 | |||||||
chr6:116705788 | C | T | 241 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0112 others(238): Show |
256 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(253): Show |
intron_variant | MODIFIER | c.656+628C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116705788 | |||||||
chr6:116705838 | T | C | 3 | a0002c0003t0018g0019 a0002c0003t0018g0163 a0002c0003t0054g0162 |
4 | HG01258.hp1 HG02148.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.656+678T>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116705838 | |||||||
chr6:116705871 | A | G | 18 | a0001c0001t0001g0018 a0001c0001t0001g0150 a0001c0001t0001g0151 others(15): Show |
18 | HG01884.hp1 HG02055.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.656+711A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116705871 | |||||||
chr6:116705958 | A | G | 1 | a0001c0001t0003g0176 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.656+798A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116705958 | |||||||
chr6:116706051 | A | G | 1 | a0001c0001t0002g0050 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.656+891A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116706051 | |||||||
chr6:116706262 | T | C | 3 | a0001c0001t0021g0164 a0001c0001t0021g0166 a0001c0001t0021g0170 |
3 | HG02895.hp2 HG02897.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.656+1102T>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116706262 | |||||||
chr6:116706275 | A | G | 1 | a0001c0002t0008g0256 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.656+1115A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116706275 | |||||||
chr6:116706393 | A | T | 1 | a0001c0001t0002g0052 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.656+1233A>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116706393 | |||||||
chr6:116706394 | T | A | 1 | a0001c0001t0002g0052 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.656+1234T>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116706394 | |||||||
chr6:116706407 | A | C | 1 | a0001c0001t0068g0137 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.656+1247A>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116706407 | |||||||
chr6:116706518 | C | T | 4 | a0001c0002t0008g0169 a0001c0002t0008g0256 a0001c0002t0008g0257 others(1): Show |
4 | HG01074.hp2 HG02280.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.656+1358C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116706518 | |||||||
chr6:116706562 | G | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
2 | HG00597.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.656+1402G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116706562 | |||||||
chr6:116706668 | A | G | 1 | a0001c0001t0003g0023 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.656+1508A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116706668 | |||||||
chr6:116706715 | G | A | 14 | a0001c0001t0006g0104 a0001c0001t0006g0105 a0001c0001t0006g0121 others(11): Show |
14 | HG02129.hp2 HG02572.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.656+1555G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116706715 | |||||||
chr6:116706842 | G | A | 5 | a0001c0001t0009g0171 a0001c0001t0009g0172 a0001c0001t0009g0220 others(2): Show |
5 | HG02055.hp1 HG02559.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.656+1682G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116706842 | |||||||
chr6:116706927 | G | A | 1 | a0001c0001t0002g0083 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.656+1767G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116706927 | |||||||
chr6:116706991 | G | C | 241 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0112 others(238): Show |
256 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(253): Show |
intron_variant | MODIFIER | c.656+1831G>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116706991 | |||||||
chr6:116707032 | C | T | 2 | a0001c0001t0006g0105 a0001c0001t0006g0122 |
2 | HG03017.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.656+1872C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116707032 | |||||||
chr6:116707056 | C | T | 15 | a0001c0001t0004g0008 a0001c0001t0004g0009 a0001c0001t0004g0027 others(12): Show |
20 | HG00544.hp1 HG01106.hp2 HG02132.hp1 others(17): Show |
intron_variant | MODIFIER | c.656+1896C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116707056 | |||||||
chr6:116707086 | C | T | 5 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0120 others(2): Show |
5 | NA18957.hp2 NA18998.hp1 NA19066.hp1 others(2): Show |
intron_variant | MODIFIER | c.656+1926C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116707086 | |||||||
chr6:116707218 | G | A | 37 | a0001c0001t0001g0016 a0001c0001t0001g0112 a0001c0001t0001g0115 others(34): Show |
37 | HG00639.hp1 HG00741.hp1 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.656+2058G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116707218 | |||||||
chr6:116707503 | T | G | 2 | a0001c0001t0003g0237 a0001c0001t0003g0238 |
2 | HG00642.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.656+2343T>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116707503 | |||||||
chr6:116707737 | C | T | 15 | a0001c0001t0004g0008 a0001c0001t0004g0009 a0001c0001t0004g0027 others(12): Show |
20 | HG00544.hp1 HG01106.hp2 HG02132.hp1 others(17): Show |
intron_variant | MODIFIER | c.656+2577C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116707737 | |||||||
chr6:116707851 | G | A | 115 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(112): Show |
123 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.656+2691G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116707851 | |||||||
chr6:116707940 | C | G | 26 | a0001c0001t0001g0244 a0001c0001t0003g0024 a0001c0001t0003g0025 others(23): Show |
26 | HG00323.hp2 HG00673.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.656+2780C>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116707940 | |||||||
chr6:116708016 | C | T | 2 | a0001c0001t0025g0106 a0001c0001t0025g0144 |
2 | HG02717.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.656+2856C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116708016 | |||||||
chr6:116708077 | T | A | 84 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(81): Show |
90 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.656+2917T>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116708077 | |||||||
chr6:116708085 | T | C | 120 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(117): Show |
128 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.656+2925T>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116708085 | |||||||
chr6:116708232 | C | T | 4 | a0001c0001t0021g0164 a0001c0001t0021g0166 a0001c0001t0021g0170 others(1): Show |
4 | HG01884.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.656+3072C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116708232 | |||||||
chr6:116708630 | T | C | 14 | a0001c0001t0006g0104 a0001c0001t0006g0105 a0001c0001t0006g0121 others(11): Show |
14 | HG02129.hp2 HG02572.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.656+3470T>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116708630 | |||||||
chr6:116708680 | C | T | 1 | a0001c0001t0009g0262 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.656+3520C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116708680 | |||||||
chr6:116708747 | A | G | 9 | a0001c0001t0001g0018 a0001c0001t0001g0159 a0001c0001t0001g0160 others(6): Show |
9 | HG01884.hp1 HG02109.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.656+3587A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116708747 | |||||||
chr6:116708958 | G | A | 1 | a0001c0001t0001g0229 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.656+3798G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116708958 | |||||||
chr6:116708975 | G | A | 1 | a0001c0001t0006g0104 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.656+3815G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116708975 | |||||||
chr6:116709177 | C | T | 2 | a0001c0001t0001g0284 a0001c0001t0001g0285 |
2 | NA19004.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.656+4017C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116709177 | |||||||
chr6:116709224 | C | T | 2 | a0001c0001t0002g0081 a0001c0001t0002g0082 |
2 | HG00597.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.656+4064C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116709224 | |||||||
chr6:116709233 | A | T | 2 | a0001c0001t0001g0284 a0001c0001t0001g0285 |
2 | NA19004.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.656+4073A>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116709233 | |||||||
chr6:116709284 | C | A | 1 | a0001c0001t0026g0110 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.656+4124C>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116709284 | |||||||
chr6:116709298 | G | A | 2 | a0001c0001t0005g0279 a0001c0001t0005g0280 |
2 | HG01243.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.656+4138G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116709298 | |||||||
chr6:116709300 | G | A | 37 | a0001c0001t0001g0016 a0001c0001t0001g0112 a0001c0001t0001g0115 others(34): Show |
37 | HG00639.hp1 HG00741.hp1 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.656+4140G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116709300 | |||||||
chr6:116709408 | G | A | 1 | a0001c0001t0001g0160 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.656+4248G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116709408 | |||||||
chr6:116709409 | G | T | 6 | a0001c0001t0001g0003 a0001c0001t0001g0225 a0001c0001t0001g0265 others(3): Show |
7 | HG01243.hp1 HG01952.hp2 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.656+4249G>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116709409 | |||||||
chr6:116709513 | G | A | 7 | a0001c0001t0006g0104 a0001c0001t0006g0105 a0001c0001t0006g0121 others(4): Show |
7 | HG02129.hp2 HG02886.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.656+4353G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116709513 | |||||||
chr6:116709535 | T | A | 270 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(267): Show |
292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.656+4375T>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116709535 | |||||||
chr6:116709625 | A | G | 6 | a0001c0001t0009g0171 a0001c0001t0009g0172 a0001c0001t0009g0220 others(3): Show |
6 | HG02055.hp1 HG02559.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.656+4465A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116709625 | |||||||
chr6:116709635 | G | C | 1 | a0001c0001t0068g0137 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.656+4475G>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116709635 | |||||||
chr6:116709645 | A | C | 1 | a0001c0001t0001g0127 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.656+4485A>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116709645 | |||||||
chr6:116709647 | A | G | 1 | a0001c0001t0004g0287 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.656+4487A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116709647 | |||||||
chr6:116709770 | C | CT | 20 | a0001c0001t0006g0104 a0001c0001t0006g0105 a0001c0001t0006g0121 others(17): Show |
21 | HG00639.hp2 HG00738.hp2 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.656+4622dupT | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 116709770 | ||||||
chr6:116709789 | G | A | 1 | a0001c0001t0026g0109 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.656+4629G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116709789 | |||||||
chr6:116709994 | C | T | 1 | a0001c0001t0023g0246 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.656+4834C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116709994 | |||||||
chr6:116710001 | C | T | 1 | a0001c0001t0068g0137 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.656+4841C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116710001 | |||||||
chr6:116710020 | A | G | 11 | a0001c0001t0006g0104 a0001c0001t0006g0105 a0001c0001t0006g0121 others(8): Show |
11 | HG02129.hp2 HG02572.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.656+4860A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116710020 | |||||||
chr6:116710136 | T | A | 3 | a0002c0003t0018g0019 a0002c0003t0018g0163 a0002c0003t0054g0162 |
4 | HG01258.hp1 HG02148.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.656+4976T>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116710136 | |||||||
chr6:116710216 | C | A | 2 | a0001c0001t0002g0036 a0001c0001t0002g0072 |
2 | NA18999.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.656+5056C>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116710216 | |||||||
chr6:116710446 | C | T | 1 | a0001c0001t0068g0137 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.656+5286C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116710446 | |||||||
chr6:116710483 | C | G | 1 | a0001c0001t0001g0191 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.656+5323C>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116710483 | |||||||
chr6:116710807 | AT | A | 8 | a0001c0001t0010g0031 a0001c0001t0010g0032 a0001c0001t0010g0033 others(5): Show |
8 | HG02145.hp1 HG02280.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.657-5403delT | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 116710807 | ||||||
chr6:116710841 | C | G | 1 | a0001c0001t0001g0205 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.657-5378C>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116710841 | |||||||
chr6:116710859 | G | T | 1 | a0001c0001t0003g0245 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.657-5360G>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116710859 | |||||||
chr6:116710873 | T | A | 95 | a0001c0001t0002g0010 a0001c0001t0002g0012 a0001c0001t0002g0013 others(92): Show |
101 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.657-5346T>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116710873 | |||||||
chr6:116710873 | T | TATATATA others(8): Show |
1 | a0001c0001t0002g0011 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.657-5346_657-5345i others(17): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116710873 | |||||||
chr6:116710873 | T | TTA | 8 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0021 others(5): Show |
13 | HG00140.hp1 HG00544.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.657-5326_657-5325d others(4): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 116710873 | ||||||
chr6:116710873 | T | TTATA | 4 | a0001c0001t0001g0132 a0001c0001t0001g0191 a0001c0001t0001g0230 others(1): Show |
4 | HG01175.hp1 HG01358.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.657-5328_657-5325d others(6): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 116710873 | ||||||
chr6:116710875 | A | T | 1 | a0001c0001t0003g0190 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.657-5344A>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116710875 | |||||||
chr6:116710891 | A | AT | 3 | a0001c0001t0003g0197 a0001c0001t0003g0223 a0001c0001t0003g0238 |
3 | HG00642.hp1 HG00673.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.657-5327dupT | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 116710891 | ||||||
chr6:116710891 | ATATTTTT others(6): Show |
A | 1 | a0001c0001t0061g0069 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.657-5326_657-5314d others(15): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 116710891 | ||||||
chr6:116710892 | TA | T | 12 | a0001c0001t0001g0244 a0001c0001t0003g0025 a0001c0001t0003g0201 others(9): Show |
12 | HG01169.hp1 HG02027.hp2 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.657-5326delA | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116710892 | |||||||
chr6:116710893 | A | T | 27 | a0001c0001t0003g0023 a0001c0001t0003g0024 a0001c0001t0003g0173 others(24): Show |
29 | HG00642.hp1 HG00673.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.657-5326A>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116710893 | |||||||
chr6:116710893 | AT | A | 8 | a0001c0001t0001g0188 a0001c0001t0001g0194 a0001c0001t0001g0195 others(5): Show |
8 | HG01258.hp2 HG02273.hp1 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.657-5307delT | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 116710893 | ||||||
chr6:116710893 | ATTT | A | 13 | a0001c0001t0002g0030 a0001c0001t0004g0008 a0001c0001t0004g0009 others(10): Show |
18 | HG00544.hp1 HG01071.hp1 HG02129.hp2 others(15): Show |
intron_variant | MODIFIER | c.657-5309_657-5307d others(5): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 116710893 | ||||||
chr6:116710893 | ATTTTT | A | 15 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(12): Show |
16 | HG00639.hp2 HG01884.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.657-5311_657-5307d others(7): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 116710893 | ||||||
chr6:116710893 | ATTTTTTT others(4): Show |
A | 1 | a0001c0001t0006g0260 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.657-5317_657-5307d others(13): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 116710893 | ||||||
chr6:116710893 | ATTTTTTT others(6): Show |
A | 8 | a0001c0001t0005g0219 a0001c0001t0005g0276 a0001c0001t0005g0277 others(5): Show |
8 | HG01243.hp2 HG02109.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.657-5319_657-5307d others(15): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 116710893 | ||||||
chr6:116710894 | T | TA | 14 | a0001c0001t0001g0254 a0001c0001t0002g0011 a0001c0001t0002g0048 others(11): Show |
16 | HG01074.hp2 HG01109.hp2 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.657-5325_657-5324i others(3): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116710894 | |||||||
chr6:116710894 | T | TATA | 22 | a0001c0001t0001g0115 a0001c0001t0001g0118 a0001c0001t0001g0119 others(19): Show |
22 | HG00741.hp1 HG01255.hp1 HG01361.hp1 others(19): Show |
intron_variant | MODIFIER | c.657-5325_657-5324i others(5): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116710894 | |||||||
chr6:116710894 | T | TATATA | 15 | a0001c0001t0001g0016 a0001c0001t0001g0112 a0001c0001t0001g0116 others(12): Show |
15 | HG00639.hp1 HG01123.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.657-5325_657-5324i others(7): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116710894 | |||||||
chr6:116710894 | T | TATATATA | 7 | a0001c0001t0006g0136 a0001c0001t0009g0171 a0001c0001t0021g0164 others(4): Show |
7 | HG02280.hp1 HG02723.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.657-5325_657-5324i others(9): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116710894 | |||||||
chr6:116710894 | T | TATATATA others(2): Show |
6 | a0001c0001t0002g0015 a0001c0001t0002g0047 a0001c0001t0002g0076 others(3): Show |
7 | HG02129.hp1 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.657-5325_657-5324i others(11): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116710894 | |||||||
chr6:116710894 | T | TATATATA others(4): Show |
4 | a0001c0001t0002g0014 a0001c0001t0002g0046 a0001c0001t0002g0065 others(1): Show |
5 | HG03041.hp2 NA18965.hp2 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.657-5325_657-5324i others(13): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116710894 | |||||||
chr6:116710894 | T | TATATATA others(6): Show |
12 | a0001c0001t0002g0044 a0001c0001t0002g0050 a0001c0001t0002g0061 others(9): Show |
12 | HG02040.hp2 HG02818.hp1 HG03239.hp1 others(9): Show |
intron_variant | MODIFIER | c.657-5325_657-5324i others(15): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116710894 | |||||||
chr6:116710894 | T | TATATATA others(8): Show |
21 | a0001c0001t0002g0013 a0001c0001t0002g0035 a0001c0001t0002g0043 others(18): Show |
22 | HG00280.hp2 HG00323.hp1 HG00673.hp2 others(19): Show |
intron_variant | MODIFIER | c.657-5325_657-5324i others(17): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116710894 | |||||||
chr6:116710894 | T | TATATATA others(10): Show |
11 | a0001c0001t0002g0042 a0001c0001t0002g0056 a0001c0001t0002g0064 others(8): Show |
11 | HG00609.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.657-5325_657-5324i others(19): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116710894 | |||||||
chr6:116710894 | T | TATATATA others(12): Show |
11 | a0001c0001t0002g0010 a0001c0001t0002g0012 a0001c0001t0002g0041 others(8): Show |
13 | HG00140.hp2 HG01175.hp2 HG01516.hp1 others(10): Show |
intron_variant | MODIFIER | c.657-5325_657-5324i others(21): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116710894 | |||||||
chr6:116710894 | T | TATATATA others(14): Show |
8 | a0001c0001t0002g0039 a0001c0001t0002g0040 a0001c0001t0002g0051 others(5): Show |
8 | HG01081.hp2 HG01433.hp1 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.657-5325_657-5324i others(23): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116710894 | |||||||
chr6:116710894 | T | TATATATA others(16): Show |
1 | a0001c0001t0002g0038 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.657-5325_657-5324i others(25): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116710894 | |||||||
chr6:116710894 | T | TATATATA others(18): Show |
4 | a0001c0001t0002g0036 a0001c0001t0002g0081 a0001c0001t0002g0082 others(1): Show |
4 | HG00597.hp1 HG03669.hp2 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.657-5325_657-5324i others(27): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116710894 | |||||||
chr6:116710894 | T | TATATATA others(20): Show |
1 | a0001c0001t0002g0037 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.657-5325_657-5324i others(29): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116710894 | |||||||
chr6:116710895 | T | A | 57 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(54): Show |
74 | HG00140.hp1 HG00544.hp2 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.657-5324T>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116710895 | |||||||
chr6:116710896 | T | A | 134 | a0001c0001t0001g0016 a0001c0001t0001g0112 a0001c0001t0001g0115 others(131): Show |
141 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.657-5323T>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116710896 | |||||||
chr6:116710897 | T | A | 19 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0126 others(16): Show |
20 | HG00140.hp1 HG01106.hp1 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.657-5322T>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116710897 | |||||||
chr6:116710898 | T | A | 117 | a0001c0001t0001g0016 a0001c0001t0001g0115 a0001c0001t0001g0131 others(114): Show |
124 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.657-5321T>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116710898 | |||||||
chr6:116710900 | T | A | 111 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(108): Show |
119 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.657-5319T>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116710900 | |||||||
chr6:116710902 | T | A | 109 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(106): Show |
117 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.657-5317T>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116710902 | |||||||
chr6:116710904 | T | A | 110 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(107): Show |
118 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.657-5315T>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116710904 | |||||||
chr6:116710906 | T | A | 14 | a0001c0001t0021g0164 a0001c0001t0021g0166 a0001c0001t0021g0170 others(11): Show |
16 | HG00639.hp2 HG01074.hp2 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.657-5313T>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116710906 | |||||||
chr6:116710906 | T | G | 98 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(95): Show |
104 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.657-5313T>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116710906 | |||||||
chr6:116710908 | T | A | 120 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(117): Show |
128 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.657-5311T>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116710908 | |||||||
chr6:116710971 | G | T | 120 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(117): Show |
128 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.657-5248G>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116710971 | |||||||
chr6:116710988 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.657-5231G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116710988 | |||||||
chr6:116711012 | C | T | 2 | a0001c0001t0002g0081 a0001c0001t0002g0082 |
2 | HG00597.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.657-5207C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116711012 | |||||||
chr6:116711106 | C | T | 1 | a0001c0001t0002g0065 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.657-5113C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116711106 | |||||||
chr6:116711153 | T | C | 1 | a0001c0001t0017g0293 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.657-5066T>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116711153 | |||||||
chr6:116711154 | G | A | 1 | a0001c0001t0057g0111 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.657-5065G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116711154 | |||||||
chr6:116711183 | C | T | 2 | a0001c0001t0011g0113 a0001c0001t0011g0114 |
2 | HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.657-5036C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116711183 | |||||||
chr6:116711255 | AT | A | 61 | a0001c0001t0001g0016 a0001c0001t0001g0112 a0001c0001t0001g0115 others(58): Show |
63 | HG00639.hp1 HG00639.hp2 HG00741.hp1 others(60): Show |
intron_variant | MODIFIER | c.657-4949delT | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 116711255 | ||||||
chr6:116711255 | ATT | A | 94 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(91): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.657-4950_657-4949d others(4): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 116711255 | ||||||
chr6:116711270 | T | G | 9 | a0001c0001t0004g0295 a0001c0001t0006g0104 a0001c0001t0006g0105 others(6): Show |
9 | HG02129.hp2 HG03017.hp2 HG03654.hp2 others(6): Show |
intron_variant | MODIFIER | c.657-4949T>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116711270 | |||||||
chr6:116711347 | C | A | 2 | a0001c0001t0001g0016 a0001c0001t0043g0016 |
2 | HG00639.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.657-4872C>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116711347 | |||||||
chr6:116711500 | TG | T | 6 | a0001c0001t0009g0171 a0001c0001t0009g0172 a0001c0001t0009g0220 others(3): Show |
6 | HG02055.hp1 HG02559.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.657-4718delG | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116711500 | |||||||
chr6:116711538 | A | ATG | 29 | a0001c0001t0001g0016 a0001c0001t0001g0112 a0001c0001t0001g0115 others(26): Show |
29 | HG00639.hp1 HG00741.hp1 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.657-4655_657-4654d others(4): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 116711538 | ||||||
chr6:116711538 | A | ATGTG | 4 | a0001c0001t0001g0120 a0001c0001t0001g0129 a0001c0001t0005g0219 others(1): Show |
4 | HG02572.hp1 HG02647.hp2 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.657-4657_657-4654d others(6): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 116711538 | ||||||
chr6:116711538 | A | ATGTGTG | 92 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(89): Show |
99 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.657-4659_657-4654d others(8): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 116711538 | ||||||
chr6:116711538 | A | ATGTGTGT others(1): Show |
10 | a0001c0001t0002g0085 a0001c0001t0002g0090 a0001c0001t0002g0094 others(7): Show |
10 | HG01074.hp2 HG01496.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.657-4661_657-4654d others(10): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 116711538 | ||||||
chr6:116711538 | A | ATGTGTGT others(3): Show |
6 | a0001c0001t0005g0276 a0001c0001t0005g0279 a0001c0001t0005g0280 others(3): Show |
6 | HG01243.hp2 HG02451.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.657-4663_657-4654d others(12): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 116711538 | ||||||
chr6:116711538 | A | ATGTGTGT others(5): Show |
4 | a0001c0001t0021g0164 a0002c0003t0018g0019 a0002c0003t0018g0163 others(1): Show |
5 | HG01258.hp1 HG02148.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.657-4665_657-4654d others(14): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 116711538 | ||||||
chr6:116711538 | A | ATGTGTGT others(7): Show |
1 | a0001c0001t0069g0165 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.657-4667_657-4654d others(16): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 116711538 | ||||||
chr6:116711538 | A | ATGTGTGT others(13): Show |
2 | a0001c0001t0021g0166 a0001c0001t0021g0170 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.657-4673_657-4654d others(22): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 116711538 | ||||||
chr6:116711538 | ATG | A | 3 | a0001c0001t0003g0212 a0001c0001t0003g0240 a0001c0001t0003g0241 |
3 | HG02257.hp2 HG02258.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.657-4655_657-4654d others(4): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 116711538 | ||||||
chr6:116711538 | ATGTGTG | A | 7 | a0001c0001t0009g0171 a0001c0001t0009g0172 a0001c0001t0009g0220 others(4): Show |
7 | HG02055.hp1 HG02559.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.657-4659_657-4654d others(8): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 116711538 | ||||||
chr6:116711632 | CTGTATTT others(9): Show |
C | 1 | a0001c0001t0001g0265 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.657-4585_657-4570d others(18): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 116711632 | ||||||
chr6:116711660 | T | G | 15 | a0001c0001t0004g0008 a0001c0001t0004g0009 a0001c0001t0004g0027 others(12): Show |
20 | HG00544.hp1 HG01106.hp2 HG02132.hp1 others(17): Show |
intron_variant | MODIFIER | c.657-4559T>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116711660 | |||||||
chr6:116711674 | T | G | 1 | a0001c0001t0001g0194 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.657-4545T>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116711674 | |||||||
chr6:116711740 | G | A | 1 | a0001c0001t0001g0118 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.657-4479G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116711740 | |||||||
chr6:116711831 | C | T | 1 | a0001c0001t0001g0271 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.657-4388C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116711831 | |||||||
chr6:116711912 | C | T | 6 | a0001c0002t0008g0020 a0001c0002t0008g0167 a0001c0002t0008g0169 others(3): Show |
7 | HG00639.hp2 HG01074.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.657-4307C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116711912 | |||||||
chr6:116711913 | G | T | 2 | a0001c0001t0001g0188 a0001c0001t0036g0232 |
2 | HG03688.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.657-4306G>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116711913 | |||||||
chr6:116712136 | T | C | 1 | a0001c0001t0001g0188 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.657-4083T>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116712136 | |||||||
chr6:116712193 | A | G | 120 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(117): Show |
128 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.657-4026A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116712193 | |||||||
chr6:116712355 | G | A | 2 | a0001c0001t0025g0106 a0001c0001t0025g0144 |
2 | HG02717.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.657-3864G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116712355 | |||||||
chr6:116712404 | A | G | 1 | a0001c0001t0068g0137 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.657-3815A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116712404 | |||||||
chr6:116712501 | C | T | 2 | a0001c0001t0023g0202 a0001c0001t0023g0246 |
2 | HG01169.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.657-3718C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116712501 | |||||||
chr6:116712799 | T | A | 106 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(103): Show |
114 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.657-3420T>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116712799 | |||||||
chr6:116713164 | T | G | 1 | a0001c0001t0001g0250 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.657-3055T>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116713164 | |||||||
chr6:116713456 | G | A | 1 | a0001c0001t0001g0254 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.657-2763G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116713456 | |||||||
chr6:116713522 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.657-2697G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116713522 | |||||||
chr6:116713876 | G | A | 1 | a0001c0001t0001g0021 | 2 | NA18975.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.657-2343G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116713876 | |||||||
chr6:116713914 | T | C | 1 | a0001c0001t0006g0260 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.657-2305T>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116713914 | |||||||
chr6:116713979 | T | A | 5 | a0001c0001t0006g0104 a0001c0001t0006g0105 a0001c0001t0006g0121 others(2): Show |
5 | HG02129.hp2 HG03017.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.657-2240T>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116713979 | |||||||
chr6:116714121 | T | C | 9 | a0001c0001t0005g0219 a0001c0001t0005g0276 a0001c0001t0005g0277 others(6): Show |
9 | HG01243.hp2 HG02109.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.657-2098T>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116714121 | |||||||
chr6:116714177 | TTCTCC | T | 3 | a0001c0001t0009g0143 a0001c0001t0011g0141 a0001c0001t0011g0142 |
3 | HG02572.hp2 HG02630.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.657-2035_657-2031d others(7): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 116714177 | ||||||
chr6:116714366 | A | G | 2 | a0001c0001t0002g0039 a0001c0001t0002g0040 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.657-1853A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116714366 | |||||||
chr6:116714512 | G | A | 3 | a0002c0003t0018g0019 a0002c0003t0018g0163 a0002c0003t0054g0162 |
4 | HG01258.hp1 HG02148.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.657-1707G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116714512 | |||||||
chr6:116714522 | T | C | 1 | a0001c0001t0051g0247 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.657-1697T>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116714522 | |||||||
chr6:116714563 | A | G | 1 | a0001c0001t0001g0158 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.657-1656A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116714563 | |||||||
chr6:116714701 | C | T | 4 | a0001c0001t0021g0164 a0001c0001t0021g0166 a0001c0001t0021g0170 others(1): Show |
4 | HG01884.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.657-1518C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116714701 | |||||||
chr6:116714722 | A | C | 1 | a0001c0001t0003g0201 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.657-1497A>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116714722 | |||||||
chr6:116714963 | G | A | 5 | a0001c0001t0002g0038 a0001c0001t0002g0043 a0001c0001t0002g0215 others(2): Show |
5 | NA18943.hp2 NA18960.hp2 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.657-1256G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116714963 | |||||||
chr6:116715240 | A | G | 31 | a0001c0001t0001g0016 a0001c0001t0001g0112 a0001c0001t0001g0115 others(28): Show |
31 | HG00639.hp1 HG00741.hp1 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.657-979A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116715240 | |||||||
chr6:116715249 | T | C | 6 | a0001c0002t0008g0020 a0001c0002t0008g0167 a0001c0002t0008g0169 others(3): Show |
7 | HG00639.hp2 HG01074.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.657-970T>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116715249 | |||||||
chr6:116715578 | A | T | 2 | a0001c0001t0025g0106 a0001c0001t0025g0144 |
2 | HG02717.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.657-641A>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116715578 | |||||||
chr6:116715609 | T | C | 3 | a0002c0003t0018g0019 a0002c0003t0018g0163 a0002c0003t0054g0162 |
4 | HG01258.hp1 HG02148.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.657-610T>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116715609 | |||||||
chr6:116715680 | G | A | 1 | a0001c0001t0003g0196 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.657-539G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116715680 | |||||||
chr6:116715788 | C | T | 6 | a0001c0001t0005g0219 a0001c0001t0005g0279 a0001c0001t0005g0280 others(3): Show |
6 | HG01243.hp2 HG02109.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.657-431C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116715788 | |||||||
chr6:116715819 | G | A | 4 | a0001c0001t0021g0164 a0001c0001t0021g0166 a0001c0001t0021g0170 others(1): Show |
4 | HG01884.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.657-400G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116715819 | |||||||
chr6:116715845 | G | C | 1 | a0001c0001t0016g0147 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.657-374G>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116715845 | |||||||
chr6:116715870 | G | A | 5 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0217 others(2): Show |
5 | HG01109.hp1 HG01167.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.657-349G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116715870 | |||||||
chr6:116715914 | C | CA | 7 | a0001c0001t0009g0171 a0001c0001t0009g0172 a0001c0001t0009g0220 others(4): Show |
7 | HG02055.hp1 HG02559.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.657-294dupA | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr6 | 116715914 | ||||||
chr6:116716094 | C | G | 1 | a0001c0001t0069g0165 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.657-125C>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 7/13 | chr6 | 116716094 | |||||||
chr6:116716453 | A | G | 50 | a0001c0001t0001g0244 a0001c0001t0003g0007 a0001c0001t0003g0023 others(47): Show |
52 | HG00280.hp1 HG00323.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.756+135A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 8/13 | chr6 | 116716453 | |||||||
chr6:116716525 | G | A | 1 | a0001c0001t0003g0237 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.756+207G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 8/13 | chr6 | 116716525 | |||||||
chr6:116716737 | A | G | 3 | a0001c0001t0016g0147 a0001c0001t0016g0148 a0001c0001t0016g0152 |
3 | HG02818.hp2 HG02896.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.756+419A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 8/13 | chr6 | 116716737 | |||||||
chr6:116716955 | T | C | 5 | a0001c0001t0009g0143 a0001c0001t0011g0113 a0001c0001t0011g0114 others(2): Show |
5 | HG02572.hp2 HG02630.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.756+637T>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 8/13 | chr6 | 116716955 | |||||||
chr6:116717063 | C | A | 16 | a0001c0001t0005g0219 a0001c0001t0005g0276 a0001c0001t0005g0277 others(13): Show |
17 | HG01243.hp2 HG01258.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.756+745C>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 8/13 | chr6 | 116717063 | |||||||
chr6:116717113 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.756+795C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 8/13 | chr6 | 116717113 | |||||||
chr6:116717160 | G | A | 3 | a0002c0003t0018g0019 a0002c0003t0018g0163 a0002c0003t0054g0162 |
4 | HG01258.hp1 HG02148.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.756+842G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 8/13 | chr6 | 116717160 | |||||||
chr6:116717174 | C | T | 1 | a0001c0001t0001g0157 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.756+856C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 8/13 | chr6 | 116717174 | |||||||
chr6:116717239 | G | A | 3 | a0002c0003t0018g0019 a0002c0003t0018g0163 a0002c0003t0054g0162 |
4 | HG01258.hp1 HG02148.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.756+921G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 8/13 | chr6 | 116717239 | |||||||
chr6:116717241 | C | T | 1 | a0001c0001t0003g0176 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.756+923C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 8/13 | chr6 | 116717241 | |||||||
chr6:116717753 | T | C | 7 | a0001c0001t0006g0104 a0001c0001t0006g0105 a0001c0001t0006g0121 others(4): Show |
7 | HG02129.hp2 HG02886.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.756+1435T>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 8/13 | chr6 | 116717753 | |||||||
chr6:116717836 | A | C | 83 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(80): Show |
89 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.756+1518A>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 8/13 | chr6 | 116717836 | |||||||
chr6:116717885 | GC | G | 18 | a0001c0001t0001g0018 a0001c0001t0001g0150 a0001c0001t0001g0151 others(15): Show |
18 | HG01884.hp1 HG02055.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.756+1575delC | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr6 | 116717885 | ||||||
chr6:116718060 | T | C | 190 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0112 others(187): Show |
203 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.756+1742T>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 8/13 | chr6 | 116718060 | |||||||
chr6:116718266 | CT | C | 7 | a0001c0001t0003g0218 a0001c0002t0008g0020 a0001c0002t0008g0167 others(4): Show |
8 | HG00639.hp2 HG01074.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.756+1962delT | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr6 | 116718266 | ||||||
chr6:116718294 | G | A | 15 | a0001c0001t0004g0008 a0001c0001t0004g0009 a0001c0001t0004g0027 others(12): Show |
20 | HG00544.hp1 HG01106.hp2 HG02132.hp1 others(17): Show |
intron_variant | MODIFIER | c.756+1976G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 8/13 | chr6 | 116718294 | |||||||
chr6:116718355 | C | T | 49 | a0001c0001t0001g0244 a0001c0001t0003g0007 a0001c0001t0003g0023 others(46): Show |
51 | HG00280.hp1 HG00323.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.756+2037C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 8/13 | chr6 | 116718355 | |||||||
chr6:116718408 | G | A | 3 | a0001c0001t0004g0288 a0001c0001t0004g0289 a0001c0001t0004g0290 |
3 | HG02809.hp1 HG03041.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.756+2090G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 8/13 | chr6 | 116718408 | |||||||
chr6:116718483 | G | A | 3 | a0001c0001t0026g0109 a0001c0001t0026g0110 a0001c0001t0057g0111 |
3 | HG02572.hp1 HG03130.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.756+2165G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 8/13 | chr6 | 116718483 | |||||||
chr6:116718503 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.756+2185G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 8/13 | chr6 | 116718503 | |||||||
chr6:116718764 | C | T | 12 | a0001c0001t0006g0104 a0001c0001t0006g0105 a0001c0001t0006g0121 others(9): Show |
12 | HG02129.hp2 HG02717.hp1 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.756+2446C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 8/13 | chr6 | 116718764 | |||||||
chr6:116718774 | T | C | 84 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(81): Show |
90 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.756+2456T>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 8/13 | chr6 | 116718774 | |||||||
chr6:116718806 | C | T | 6 | a0001c0002t0008g0020 a0001c0002t0008g0167 a0001c0002t0008g0169 others(3): Show |
7 | HG00639.hp2 HG01074.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.756+2488C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 8/13 | chr6 | 116718806 | |||||||
chr6:116718808 | C | A | 22 | a0001c0001t0005g0219 a0001c0001t0005g0276 a0001c0001t0005g0277 others(19): Show |
24 | HG00639.hp2 HG01074.hp2 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.756+2490C>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 8/13 | chr6 | 116718808 | |||||||
chr6:116718830 | C | T | 6 | a0001c0002t0008g0020 a0001c0002t0008g0167 a0001c0002t0008g0169 others(3): Show |
7 | HG00639.hp2 HG01074.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.756+2512C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 8/13 | chr6 | 116718830 | |||||||
chr6:116718872 | A | T | 83 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(80): Show |
89 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.756+2554A>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 8/13 | chr6 | 116718872 | |||||||
chr6:116718955 | C | T | 6 | a0001c0002t0008g0020 a0001c0002t0008g0167 a0001c0002t0008g0169 others(3): Show |
7 | HG00639.hp2 HG01074.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.756+2637C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 8/13 | chr6 | 116718955 | |||||||
chr6:116719083 | C | T | 6 | a0001c0001t0009g0171 a0001c0001t0009g0172 a0001c0001t0009g0220 others(3): Show |
6 | HG02055.hp1 HG02559.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.756+2765C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 8/13 | chr6 | 116719083 | |||||||
chr6:116719100 | A | G | 9 | a0001c0001t0001g0186 a0001c0001t0001g0191 a0001c0001t0001g0230 others(6): Show |
10 | HG00140.hp1 HG00639.hp2 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.756+2782A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 8/13 | chr6 | 116719100 | |||||||
chr6:116719186 | A | G | 2 | a0001c0001t0006g0105 a0001c0001t0006g0122 |
2 | HG03017.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.756+2868A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 8/13 | chr6 | 116719186 | |||||||
chr6:116719203 | A | G | 1 | a0001c0001t0010g0033 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.756+2885A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 8/13 | chr6 | 116719203 | |||||||
chr6:116719329 | T | C | 120 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(117): Show |
128 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.757-2797T>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 8/13 | chr6 | 116719329 | |||||||
chr6:116719487 | T | G | 6 | a0001c0001t0009g0171 a0001c0001t0009g0172 a0001c0001t0009g0220 others(3): Show |
6 | HG02055.hp1 HG02559.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.757-2639T>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 8/13 | chr6 | 116719487 | |||||||
chr6:116719702 | A | G | 1 | a0001c0001t0006g0260 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.757-2424A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 8/13 | chr6 | 116719702 | |||||||
chr6:116719866 | AAAT | A | 120 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(117): Show |
128 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.757-2254_757-2252d others(5): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr6 | 116719866 | ||||||
chr6:116720086 | A | G | 6 | a0001c0002t0008g0020 a0001c0002t0008g0167 a0001c0002t0008g0169 others(3): Show |
7 | HG00639.hp2 HG01074.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.757-2040A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 8/13 | chr6 | 116720086 | |||||||
chr6:116720163 | G | A | 1 | a0001c0001t0001g0251 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.757-1963G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 8/13 | chr6 | 116720163 | |||||||
chr6:116720261 | C | T | 1 | a0001c0001t0002g0073 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.757-1865C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 8/13 | chr6 | 116720261 | |||||||
chr6:116720413 | TC | T | 15 | a0001c0001t0004g0008 a0001c0001t0004g0009 a0001c0001t0004g0027 others(12): Show |
20 | HG00544.hp1 HG01106.hp2 HG02132.hp1 others(17): Show |
intron_variant | MODIFIER | c.757-1711delC | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr6 | 116720413 | ||||||
chr6:116720598 | T | C | 15 | a0001c0001t0004g0008 a0001c0001t0004g0009 a0001c0001t0004g0027 others(12): Show |
20 | HG00544.hp1 HG01106.hp2 HG02132.hp1 others(17): Show |
intron_variant | MODIFIER | c.757-1528T>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 8/13 | chr6 | 116720598 | |||||||
chr6:116721017 | G | C | 6 | a0001c0002t0008g0020 a0001c0002t0008g0167 a0001c0002t0008g0169 others(3): Show |
7 | HG00639.hp2 HG01074.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.757-1109G>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 8/13 | chr6 | 116721017 | |||||||
chr6:116721086 | G | A | 6 | a0001c0002t0008g0020 a0001c0002t0008g0167 a0001c0002t0008g0169 others(3): Show |
7 | HG00639.hp2 HG01074.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.757-1040G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 8/13 | chr6 | 116721086 | |||||||
chr6:116721399 | C | T | 98 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(95): Show |
104 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.757-727C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 8/13 | chr6 | 116721399 | |||||||
chr6:116721460 | C | G | 120 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(117): Show |
128 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.757-666C>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 8/13 | chr6 | 116721460 | |||||||
chr6:116721518 | G | A | 120 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(117): Show |
128 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.757-608G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 8/13 | chr6 | 116721518 | |||||||
chr6:116721644 | A | G | 1 | a0001c0001t0001g0209 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.757-482A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 8/13 | chr6 | 116721644 | |||||||
chr6:116721949 | A | C | 31 | a0001c0001t0001g0016 a0001c0001t0001g0112 a0001c0001t0001g0115 others(28): Show |
31 | HG00639.hp1 HG00741.hp1 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.757-177A>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 8/13 | chr6 | 116721949 | |||||||
chr6:116721970 | A | C | 12 | a0001c0001t0005g0219 a0001c0001t0005g0276 a0001c0001t0005g0277 others(9): Show |
13 | HG01243.hp2 HG01258.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.757-156A>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 8/13 | chr6 | 116721970 | |||||||
chr6:116722000 | CAA | C | 6 | a0001c0002t0008g0020 a0001c0002t0008g0167 a0001c0002t0008g0169 others(3): Show |
7 | HG00639.hp2 HG01074.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.757-125_757-124del others(2): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 8/13 | chr6 | 116722000 | |||||||
chr6:116722309 | G | A | 3 | a0002c0003t0018g0019 a0002c0003t0018g0163 a0002c0003t0054g0162 |
4 | HG01258.hp1 HG02148.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.920+20G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 9/13 | chr6 | 116722309 | |||||||
chr6:116722330 | G | A | 3 | a0001c0002t0008g0256 a0001c0002t0008g0257 a0001c0002t0028g0168 |
3 | HG01074.hp2 HG02280.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.920+41G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 9/13 | chr6 | 116722330 | |||||||
chr6:116722453 | C | T | 2 | a0001c0001t0025g0106 a0001c0001t0025g0144 |
2 | HG02717.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.920+164C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 9/13 | chr6 | 116722453 | |||||||
chr6:116722482 | G | A | 1 | a0001c0001t0006g0299 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.920+193G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 9/13 | chr6 | 116722482 | |||||||
chr6:116722659 | A | C | 11 | a0001c0001t0006g0104 a0001c0001t0006g0105 a0001c0001t0006g0121 others(8): Show |
11 | HG02129.hp2 HG02572.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.920+370A>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 9/13 | chr6 | 116722659 | |||||||
chr6:116722874 | A | C | 1 | a0001c0001t0010g0084 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.920+585A>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 9/13 | chr6 | 116722874 | |||||||
chr6:116722942 | AC | A | 8 | a0001c0001t0005g0219 a0001c0001t0005g0276 a0001c0001t0005g0277 others(5): Show |
8 | HG01243.hp2 HG02109.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.920+654delC | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 9/13 | chr6 | 116722942 | |||||||
chr6:116722984 | G | T | 6 | a0001c0002t0008g0020 a0001c0002t0008g0167 a0001c0002t0008g0169 others(3): Show |
7 | HG00639.hp2 HG01074.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.920+695G>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 9/13 | chr6 | 116722984 | |||||||
chr6:116723625 | T | C | 6 | a0001c0002t0008g0020 a0001c0002t0008g0167 a0001c0002t0008g0169 others(3): Show |
7 | HG00639.hp2 HG01074.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.921-672T>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 9/13 | chr6 | 116723625 | |||||||
chr6:116723682 | ATAGTAT | A | 12 | a0001c0001t0006g0104 a0001c0001t0006g0105 a0001c0001t0006g0121 others(9): Show |
12 | HG02129.hp2 HG02572.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.921-611_921-606del others(6): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr6 | 116723682 | ||||||
chr6:116723972 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.921-325G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 9/13 | chr6 | 116723972 | |||||||
chr6:116724132 | C | T | 9 | a0001c0001t0005g0219 a0001c0001t0005g0276 a0001c0001t0005g0277 others(6): Show |
9 | HG01243.hp2 HG02109.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.921-165C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 9/13 | chr6 | 116724132 | |||||||
chr6:116724146 | A | T | 3 | a0002c0003t0018g0019 a0002c0003t0018g0163 a0002c0003t0054g0162 |
4 | HG01258.hp1 HG02148.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.921-151A>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 9/13 | chr6 | 116724146 | |||||||
chr6:116724214 | C | G | 2 | a0001c0001t0012g0017 a0003c0006t0045g0017 |
2 | HG02970.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.921-83C>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 9/13 | chr6 | 116724214 | |||||||
chr6:116724527 | C | T | 14 | a0001c0001t0003g0240 a0001c0001t0003g0241 a0001c0001t0006g0104 others(11): Show |
14 | HG02129.hp2 HG02257.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.999+152C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 10/13 | chr6 | 116724527 | |||||||
chr6:116724579 | TTTTA | T | 82 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(79): Show |
88 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.999+213_999+216del others(4): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr6 | 116724579 | ||||||
chr6:116724774 | AATTT | A | 2 | a0001c0002t0008g0020 a0001c0002t0008g0167 |
3 | HG00639.hp2 HG02922.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.999+416_999+419del others(4): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr6 | 116724774 | ||||||
chr6:116724954 | G | A | 9 | a0001c0001t0005g0219 a0001c0001t0005g0276 a0001c0001t0005g0277 others(6): Show |
9 | HG01243.hp2 HG02109.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.999+579G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 10/13 | chr6 | 116724954 | |||||||
chr6:116725342 | C | T | 3 | a0002c0003t0018g0019 a0002c0003t0018g0163 a0002c0003t0054g0162 |
4 | HG01258.hp1 HG02148.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.1000-409C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 10/13 | chr6 | 116725342 | |||||||
chr6:116725701 | A | T | 1 | a0001c0001t0003g0176 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1000-50A>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 10/13 | chr6 | 116725701 | |||||||
chr6:116726048 | G | A | 3 | a0001c0001t0026g0109 a0001c0001t0026g0110 a0001c0001t0057g0111 |
3 | HG02572.hp1 HG03130.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1125+172G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 11/13 | chr6 | 116726048 | |||||||
chr6:116726059 | C | CGTGTGTG others(7): Show |
6 | a0001c0002t0008g0020 a0001c0002t0008g0167 a0001c0002t0008g0169 others(3): Show |
7 | HG00639.hp2 HG01074.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1125+183_1125+184i others(16): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 11/13 | chr6 | 116726059 | |||||||
chr6:116726060 | A | G | 6 | a0001c0002t0008g0020 a0001c0002t0008g0167 a0001c0002t0008g0169 others(3): Show |
7 | HG00639.hp2 HG01074.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1125+184A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 11/13 | chr6 | 116726060 | |||||||
chr6:116726061 | A | AGT | 10 | a0001c0001t0001g0126 a0001c0001t0001g0157 a0001c0001t0001g0186 others(7): Show |
10 | HG00140.hp1 HG01175.hp1 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.1125+206_1125+207d others(4): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr6 | 116726061 | ||||||
chr6:116726061 | A | AGTGTGTG others(1): Show |
9 | a0001c0001t0002g0039 a0001c0001t0002g0040 a0001c0001t0006g0121 others(6): Show |
9 | HG02647.hp1 HG02818.hp1 HG03130.hp1 others(6): Show |
intron_variant | MODIFIER | c.1125+200_1125+207d others(10): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr6 | 116726061 | ||||||
chr6:116726061 | A | AGTGTGTG others(3): Show |
8 | a0001c0001t0006g0104 a0001c0001t0006g0105 a0001c0001t0006g0122 others(5): Show |
8 | HG01884.hp2 HG02129.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1125+198_1125+207d others(12): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr6 | 116726061 | ||||||
chr6:116726061 | A | AGTGTGTG others(5): Show |
83 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(80): Show |
89 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.1125+196_1125+207d others(14): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr6 | 116726061 | ||||||
chr6:116726061 | A | AGTGTGTG others(7): Show |
4 | a0001c0001t0002g0070 a0001c0001t0025g0106 a0001c0001t0025g0144 others(1): Show |
4 | HG02717.hp1 HG03540.hp2 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.1125+194_1125+207d others(16): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr6 | 116726061 | ||||||
chr6:116726061 | A | AGTGTGTG others(9): Show |
6 | a0001c0001t0005g0219 a0001c0001t0005g0279 a0001c0001t0005g0280 others(3): Show |
6 | HG01243.hp2 HG02109.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1125+192_1125+207d others(18): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr6 | 116726061 | ||||||
chr6:116726061 | A | AGTGTGTG others(11): Show |
1 | a0001c0001t0056g0281 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1125+190_1125+207d others(20): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr6 | 116726061 | ||||||
chr6:116726061 | A | AGTGTGTG others(13): Show |
5 | a0001c0001t0004g0286 a0001c0001t0004g0287 a0001c0001t0017g0292 others(2): Show |
5 | HG01106.hp2 HG02258.hp1 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.1125+188_1125+207d others(22): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr6 | 116726061 | ||||||
chr6:116726061 | A | AGTGTGTG others(17): Show |
8 | a0001c0001t0004g0008 a0001c0001t0004g0009 a0001c0001t0004g0027 others(5): Show |
13 | HG00544.hp1 HG02132.hp1 HG06807.hp1 others(10): Show |
intron_variant | MODIFIER | c.1125+207_1125+208i others(26): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr6 | 116726061 | ||||||
chr6:116726061 | A | AGTGTGTG others(19): Show |
5 | a0001c0001t0004g0288 a0001c0001t0004g0289 a0002c0003t0018g0019 others(2): Show |
6 | HG01258.hp1 HG02148.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.1125+207_1125+208i others(28): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr6 | 116726061 | ||||||
chr6:116726061 | A | T | 6 | a0001c0002t0008g0020 a0001c0002t0008g0167 a0001c0002t0008g0169 others(3): Show |
7 | HG00639.hp2 HG01074.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1125+185A>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 11/13 | chr6 | 116726061 | |||||||
chr6:116726082 | G | A | 6 | a0001c0001t0009g0171 a0001c0001t0009g0172 a0001c0001t0009g0220 others(3): Show |
6 | HG02055.hp1 HG02559.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1125+206G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 11/13 | chr6 | 116726082 | |||||||
chr6:116726084 | C | G | 2 | a0001c0001t0006g0260 a0001c0001t0053g0182 |
2 | HG02647.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1125+208C>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 11/13 | chr6 | 116726084 | |||||||
chr6:116726311 | A | T | 1 | a0001c0001t0026g0109 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1126-184A>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 11/13 | chr6 | 116726311 | |||||||
chr6:116726757 | TATATC | T | 9 | a0001c0001t0005g0219 a0001c0001t0005g0276 a0001c0001t0005g0277 others(6): Show |
9 | HG01243.hp2 HG02109.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1253+137_1253+141d others(7): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr6 | 116726757 | ||||||
chr6:116726778 | AT | A | 19 | a0001c0001t0001g0018 a0001c0001t0001g0150 a0001c0001t0001g0151 others(16): Show |
19 | HG01071.hp2 HG01884.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1253+165delT | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr6 | 116726778 | ||||||
chr6:116726901 | T | C | 1 | a0001c0001t0012g0154 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1253+279T>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 12/13 | chr6 | 116726901 | |||||||
chr6:116726973 | C | T | 1 | a0001c0001t0003g0223 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1253+351C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 12/13 | chr6 | 116726973 | |||||||
chr6:116727182 | G | C | 3 | a0001c0001t0021g0164 a0001c0001t0021g0166 a0001c0001t0021g0170 |
3 | HG02895.hp2 HG02897.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1253+560G>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 12/13 | chr6 | 116727182 | |||||||
chr6:116727947 | AAAAC | A | 3 | a0001c0001t0021g0164 a0001c0001t0021g0166 a0001c0001t0021g0170 |
3 | HG02895.hp2 HG02897.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1253+1328_1253+133 others(8): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr6 | 116727947 | ||||||
chr6:116728415 | T | C | 1 | a0001c0001t0002g0043 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1254-1148T>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 12/13 | chr6 | 116728415 | |||||||
chr6:116728500 | T | C | 2 | a0001c0001t0025g0106 a0001c0001t0025g0144 |
2 | HG02717.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1254-1063T>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 12/13 | chr6 | 116728500 | |||||||
chr6:116728551 | C | A | 1 | a0001c0001t0002g0081 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1254-1012C>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 12/13 | chr6 | 116728551 | |||||||
chr6:116728553 | C | T | 1 | a0001c0001t0002g0081 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1254-1010C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 12/13 | chr6 | 116728553 | |||||||
chr6:116728605 | A | G | 1 | a0001c0001t0003g0243 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1254-958A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 12/13 | chr6 | 116728605 | |||||||
chr6:116728608 | G | A | 6 | a0001c0002t0008g0020 a0001c0002t0008g0167 a0001c0002t0008g0169 others(3): Show |
7 | HG00639.hp2 HG01074.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1254-955G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 12/13 | chr6 | 116728608 | |||||||
chr6:116728619 | A | G | 1 | a0001c0001t0069g0165 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1254-944A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 12/13 | chr6 | 116728619 | |||||||
chr6:116728661 | A | G | 2 | a0001c0001t0001g0124 a0001c0001t0058g0140 |
2 | HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1254-902A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 12/13 | chr6 | 116728661 | |||||||
chr6:116728690 | T | C | 1 | a0001c0002t0008g0167 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1254-873T>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 12/13 | chr6 | 116728690 | |||||||
chr6:116728817 | G | A | 6 | a0001c0002t0008g0020 a0001c0002t0008g0167 a0001c0002t0008g0169 others(3): Show |
7 | HG00639.hp2 HG01074.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1254-746G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 12/13 | chr6 | 116728817 | |||||||
chr6:116728947 | T | C | 119 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(116): Show |
127 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.1254-616T>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 12/13 | chr6 | 116728947 | |||||||
chr6:116728950 | A | T | 1 | a0001c0001t0062g0096 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1254-613A>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 12/13 | chr6 | 116728950 | |||||||
chr6:116729094 | T | C | 1 | a0001c0001t0020g0248 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1254-469T>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 12/13 | chr6 | 116729094 | |||||||
chr6:116729147 | C | T | 1 | a0001c0001t0002g0062 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1254-416C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 12/13 | chr6 | 116729147 | |||||||
chr6:116729158 | C | CGT | 57 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(54): Show |
70 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.1254-364_1254-363d others(4): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr6 | 116729158 | ||||||
chr6:116729158 | C | CGTGT | 36 | a0001c0001t0001g0119 a0001c0001t0001g0124 a0001c0001t0001g0127 others(33): Show |
41 | HG00280.hp2 HG00544.hp1 HG01167.hp1 others(38): Show |
intron_variant | MODIFIER | c.1254-366_1254-363d others(6): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr6 | 116729158 | ||||||
chr6:116729158 | C | CGTGTGT | 32 | a0001c0001t0001g0016 a0001c0001t0001g0112 a0001c0001t0001g0115 others(29): Show |
34 | HG00140.hp2 HG00639.hp1 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.1254-368_1254-363d others(8): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr6 | 116729158 | ||||||
chr6:116729158 | C | CGTGTGTG others(1): Show |
43 | a0001c0001t0001g0118 a0001c0001t0001g0123 a0001c0001t0001g0126 others(40): Show |
45 | HG00323.hp1 HG00609.hp1 HG01243.hp2 others(42): Show |
intron_variant | MODIFIER | c.1254-370_1254-363d others(10): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr6 | 116729158 | ||||||
chr6:116729158 | C | CGTGTGTG others(3): Show |
16 | a0001c0001t0001g0133 a0001c0001t0002g0012 a0001c0001t0002g0039 others(13): Show |
17 | HG00597.hp1 HG01175.hp2 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.1254-372_1254-363d others(12): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr6 | 116729158 | ||||||
chr6:116729158 | C | CGTGTGTG others(5): Show |
3 | a0001c0001t0001g0125 a0001c0001t0002g0030 a0001c0001t0002g0064 |
3 | HG01071.hp1 HG04204.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.1254-374_1254-363d others(14): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr6 | 116729158 | ||||||
chr6:116729158 | C | CGTGTGTG others(7): Show |
1 | a0001c0001t0002g0051 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1254-376_1254-363d others(16): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr6 | 116729158 | ||||||
chr6:116729158 | CGT | C | 16 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0193 others(13): Show |
21 | HG00738.hp2 HG01074.hp1 HG01515.hp1 others(18): Show |
intron_variant | MODIFIER | c.1254-364_1254-363d others(4): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr6 | 116729158 | ||||||
chr6:116729158 | CGTGT | C | 28 | a0001c0001t0003g0007 a0001c0001t0003g0023 a0001c0001t0003g0026 others(25): Show |
30 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.1254-366_1254-363d others(6): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr6 | 116729158 | ||||||
chr6:116729158 | CGTGTGT | C | 35 | a0001c0001t0001g0018 a0001c0001t0001g0156 a0001c0001t0001g0157 others(32): Show |
36 | HG00673.hp1 HG01258.hp1 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.1254-368_1254-363d others(8): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr6 | 116729158 | ||||||
chr6:116729158 | CGTGTGTG others(1): Show |
C | 13 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0011g0149 others(10): Show |
14 | HG00639.hp2 HG01074.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.1254-370_1254-363d others(10): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr6 | 116729158 | ||||||
chr6:116729158 | CGTGTGTG others(3): Show |
C | 1 | a0001c0001t0002g0100 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1254-372_1254-363d others(12): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr6 | 116729158 | ||||||
chr6:116729158 | CGTGTGTG others(7): Show |
C | 3 | a0001c0001t0026g0109 a0001c0001t0026g0110 a0001c0001t0057g0111 |
3 | HG02572.hp1 HG03130.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1254-376_1254-363d others(16): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr6 | 116729158 | ||||||
chr6:116729158 | CGTGTGTG others(9): Show |
C | 1 | a0001c0001t0006g0299 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1254-378_1254-363d others(18): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr6 | 116729158 | ||||||
chr6:116729199 | G | GTGTGTGT others(4): Show |
1 | a0001c0001t0052g0117 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1254-363_1254-362i others(13): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr6 | 116729199 | ||||||
chr6:116729220 | T | TA | 26 | a0001c0001t0002g0040 a0001c0001t0002g0047 a0001c0001t0002g0215 others(23): Show |
28 | HG00639.hp2 HG01074.hp2 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.1254-328dupA | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr6 | 116729220 | ||||||
chr6:116729220 | T | TAA | 88 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(85): Show |
94 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.1254-329_1254-328d others(4): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr6 | 116729220 | ||||||
chr6:116729220 | TA | T | 16 | a0001c0001t0001g0126 a0001c0001t0004g0008 a0001c0001t0004g0009 others(13): Show |
21 | HG00544.hp1 HG01106.hp2 HG02132.hp1 others(18): Show |
intron_variant | MODIFIER | c.1254-328delA | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr6 | 116729220 | ||||||
chr6:116729490 | A | G | 2 | a0001c0001t0027g0107 a0001c0001t0027g0108 |
2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1254-73A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 12/13 | chr6 | 116729490 | |||||||
chr6:116729871 | G | A | 1 | a0001c0001t0002g0094 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1432+130G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | chr6 | 116729871 | |||||||
chr6:116729883 | C | A | 2 | a0001c0001t0025g0106 a0001c0001t0025g0144 |
2 | HG02717.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1432+142C>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | chr6 | 116729883 | |||||||
chr6:116729895 | ATTTT | A | 31 | a0001c0001t0001g0016 a0001c0001t0001g0112 a0001c0001t0001g0115 others(28): Show |
31 | HG00639.hp1 HG00741.hp1 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.1432+156_1432+159d others(6): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr6 | 116729895 | ||||||
chr6:116730065 | A | C | 3 | a0001c0001t0002g0215 a0001c0001t0002g0216 a0001c0001t0002g0259 |
3 | NA18943.hp2 NA18970.hp2 NA19059.hp2 |
intron_variant | MODIFIER | c.1432+324A>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | chr6 | 116730065 | |||||||
chr6:116730084 | A | AT | 105 | a0001c0001t0001g0022 a0001c0001t0001g0174 a0001c0001t0001g0177 others(102): Show |
113 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.1432+363dupT | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr6 | 116730084 | ||||||
chr6:116730084 | AT | A | 21 | a0001c0001t0001g0003 a0001c0001t0001g0112 a0001c0001t0001g0225 others(18): Show |
22 | HG01243.hp1 HG01243.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.1432+363delT | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr6 | 116730084 | ||||||
chr6:116730128 | C | T | 9 | a0001c0001t0005g0219 a0001c0001t0005g0276 a0001c0001t0005g0277 others(6): Show |
9 | HG01243.hp2 HG02109.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1432+387C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | chr6 | 116730128 | |||||||
chr6:116730152 | T | TCTTGGCT others(8): Show |
1 | a0001c0001t0001g0126 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1432+413_1432+427d others(17): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr6 | 116730152 | ||||||
chr6:116730171 | C | G | 1 | a0001c0001t0062g0096 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1432+430C>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | chr6 | 116730171 | |||||||
chr6:116730363 | A | G | 9 | a0001c0001t0005g0219 a0001c0001t0005g0276 a0001c0001t0005g0277 others(6): Show |
9 | HG01243.hp2 HG02109.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1432+622A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | chr6 | 116730363 | |||||||
chr6:116730432 | T | C | 2 | a0001c0001t0049g0242 a0001c0001t0050g0198 |
2 | NA18985.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.1432+691T>C | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | chr6 | 116730432 | |||||||
chr6:116730523 | T | G | 1 | a0001c0001t0001g0254 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1432+782T>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | chr6 | 116730523 | |||||||
chr6:116730599 | A | G | 7 | a0001c0001t0006g0104 a0001c0001t0006g0105 a0001c0001t0006g0121 others(4): Show |
7 | HG02129.hp2 HG02886.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.1432+858A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | chr6 | 116730599 | |||||||
chr6:116730771 | A | G | 82 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(79): Show |
88 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.1432+1030A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | chr6 | 116730771 | |||||||
chr6:116731199 | G | T | 1 | a0001c0001t0002g0078 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1433-937G>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | chr6 | 116731199 | |||||||
chr6:116731201 | A | G | 5 | a0001c0001t0009g0143 a0001c0001t0011g0113 a0001c0001t0011g0114 others(2): Show |
5 | HG02572.hp2 HG02630.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1433-935A>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | chr6 | 116731201 | |||||||
chr6:116731470 | G | A | 7 | a0001c0001t0006g0104 a0001c0001t0006g0105 a0001c0001t0006g0121 others(4): Show |
7 | HG02129.hp2 HG02886.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.1433-666G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | chr6 | 116731470 | |||||||
chr6:116731518 | C | T | 1 | a0001c0001t0001g0251 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1433-618C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | chr6 | 116731518 | |||||||
chr6:116731550 | C | T | 2 | a0001c0001t0002g0073 a0001c0001t0065g0074 |
2 | HG01433.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1433-586C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | chr6 | 116731550 | |||||||
chr6:116731637 | CAT | C | 4 | a0001c0001t0006g0299 a0001c0001t0026g0109 a0001c0001t0026g0110 others(1): Show |
4 | HG02572.hp1 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1433-496_1433-495d others(4): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr6 | 116731637 | ||||||
chr6:116731747 | C | T | 3 | a0001c0001t0026g0109 a0001c0001t0026g0110 a0001c0001t0057g0111 |
3 | HG02572.hp1 HG03130.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1433-389C>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | chr6 | 116731747 | |||||||
chr6:116731756 | C | G | 1 | a0001c0001t0002g0087 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1433-380C>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | chr6 | 116731756 | |||||||
chr6:116731893 | C | G | 1 | a0001c0001t0003g0245 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1433-243C>G | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | chr6 | 116731893 | |||||||
chr6:116731908 | G | A | 190 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0112 others(187): Show |
203 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.1433-228G>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | chr6 | 116731908 | |||||||
chr6:116731997 | G | T | 7 | a0001c0001t0006g0104 a0001c0001t0006g0105 a0001c0001t0006g0121 others(4): Show |
7 | HG02129.hp2 HG02886.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.1433-139G>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | chr6 | 116731997 | |||||||
chr6:116732072 | G | GTT | 3 | a0001c0001t0001g0159 a0001c0001t0005g0276 a0001c0001t0005g0279 |
3 | HG01243.hp2 HG02886.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1433-62_1433-61dup others(2): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr6 | 116732072 | ||||||
chr6:116732074 | T | A | 1 | a0001c0001t0001g0126 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1433-62T>A | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | chr6 | 116732074 | |||||||
chr6:116732074 | T | TTA | 12 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0022 others(9): Show |
14 | HG01074.hp1 HG01175.hp1 HG01515.hp1 others(11): Show |
intron_variant | MODIFIER | c.1433-15_1433-14dup others(2): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr6 | 116732074 | ||||||
chr6:116732074 | T | TTATA | 11 | a0001c0001t0001g0002 a0001c0001t0001g0189 a0001c0001t0001g0205 others(8): Show |
11 | HG00558.hp1 HG00609.hp2 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.1433-17_1433-14dup others(4): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr6 | 116732074 | ||||||
chr6:116732074 | T | TTATATA | 7 | a0001c0001t0001g0005 a0001c0001t0001g0183 a0001c0001t0001g0284 others(4): Show |
7 | HG00323.hp2 HG01071.hp2 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.1433-19_1433-14dup others(6): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr6 | 116732074 | ||||||
chr6:116732074 | T | TTATATAT others(1): Show |
12 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0022 others(9): Show |
12 | HG00140.hp1 HG00738.hp1 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.1433-21_1433-14dup others(8): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr6 | 116732074 | ||||||
chr6:116732074 | T | TTATATAT others(3): Show |
15 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0028 others(12): Show |
15 | HG00544.hp2 HG00642.hp1 HG00642.hp2 others(12): Show |
intron_variant | MODIFIER | c.1433-23_1433-14dup others(10): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr6 | 116732074 | ||||||
chr6:116732074 | T | TTATATAT others(5): Show |
13 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(10): Show |
13 | HG01255.hp2 HG01361.hp2 HG01516.hp2 others(10): Show |
intron_variant | MODIFIER | c.1433-25_1433-14dup others(12): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr6 | 116732074 | ||||||
chr6:116732074 | T | TTATATAT others(7): Show |
8 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(5): Show |
9 | HG02717.hp2 HG03688.hp2 NA18612.hp1 others(6): Show |
intron_variant | MODIFIER | c.1433-27_1433-14dup others(14): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr6 | 116732074 | ||||||
chr6:116732074 | T | TTATATAT others(9): Show |
3 | a0001c0001t0003g0223 a0001c0001t0004g0008 a0001c0001t0017g0293 |
3 | HG00673.hp1 HG02965.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.1433-29_1433-14dup others(16): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr6 | 116732074 | ||||||
chr6:116732074 | T | TTATATAT others(11): Show |
1 | a0001c0001t0001g0261 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1433-31_1433-14dup others(18): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr6 | 116732074 | ||||||
chr6:116732074 | T | TTTATATA others(10): Show |
1 | a0001c0001t0014g0007 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1433-61_1433-60ins others(17): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr6 | 116732074 | ||||||
chr6:116732074 | T | TTTTA | 3 | a0001c0001t0001g0208 a0001c0001t0003g0253 a0001c0001t0005g0277 |
3 | HG02027.hp2 HG02735.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1433-61_1433-60ins others(4): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr6 | 116732074 | ||||||
chr6:116732074 | T | TTTTATA | 4 | a0001c0001t0001g0156 a0001c0001t0001g0254 a0001c0001t0003g0210 others(1): Show |
4 | HG01109.hp2 HG02647.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1433-61_1433-60ins others(6): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr6 | 116732074 | ||||||
chr6:116732074 | T | TTTTATAT others(1): Show |
4 | a0001c0001t0001g0207 a0001c0001t0001g0209 a0001c0001t0003g0025 others(1): Show |
4 | HG01106.hp1 HG01123.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1433-61_1433-60ins others(8): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr6 | 116732074 | ||||||
chr6:116732074 | T | TTTTATAT others(3): Show |
7 | a0001c0001t0001g0158 a0001c0001t0001g0160 a0001c0001t0003g0007 others(4): Show |
7 | HG02109.hp1 HG02895.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1433-61_1433-60ins others(10): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr6 | 116732074 | ||||||
chr6:116732074 | T | TTTTATAT others(5): Show |
6 | a0001c0001t0001g0249 a0001c0001t0003g0173 a0001c0001t0003g0201 others(3): Show |
6 | HG02165.hp1 HG02257.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1433-61_1433-60ins others(12): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr6 | 116732074 | ||||||
chr6:116732074 | T | TTTTATAT others(7): Show |
3 | a0001c0001t0001g0018 a0001c0001t0026g0110 a0001c0001t0033g0214 |
3 | HG02109.hp2 HG03130.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.1433-61_1433-60ins others(14): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr6 | 116732074 | ||||||
chr6:116732074 | T | TTTTATAT others(9): Show |
7 | a0001c0001t0003g0023 a0001c0001t0003g0024 a0001c0001t0003g0176 others(4): Show |
8 | HG02559.hp2 HG03490.hp2 HG03492.hp1 others(5): Show |
intron_variant | MODIFIER | c.1433-61_1433-60ins others(16): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr6 | 116732074 | ||||||
chr6:116732074 | T | TTTTATAT others(11): Show |
4 | a0001c0001t0004g0288 a0001c0001t0014g0007 a0001c0001t0014g0026 others(1): Show |
4 | HG00741.hp2 HG02809.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1433-61_1433-60ins others(18): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr6 | 116732074 | ||||||
chr6:116732074 | T | TTTTATAT others(15): Show |
2 | a0001c0001t0003g0266 a0001c0001t0031g0221 |
2 | HG03942.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.1433-61_1433-60ins others(22): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr6 | 116732074 | ||||||
chr6:116732074 | T | TTTTATAT others(17): Show |
1 | a0001c0001t0003g0274 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1433-61_1433-60ins others(24): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr6 | 116732074 | ||||||
chr6:116732074 | TTA | T | 7 | a0001c0001t0001g0151 a0001c0001t0003g0237 a0001c0001t0003g0243 others(4): Show |
7 | HG02970.hp2 HG03209.hp1 HG03669.hp2 others(4): Show |
intron_variant | MODIFIER | c.1433-15_1433-14del others(2): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr6 | 116732074 | ||||||
chr6:116732074 | TTATA | T | 4 | a0001c0001t0001g0029 a0001c0001t0007g0055 a0001c0001t0007g0068 others(1): Show |
4 | HG00597.hp2 HG01167.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.1433-17_1433-14del others(4): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr6 | 116732074 | ||||||
chr6:116732074 | TTATATA | T | 9 | a0001c0001t0001g0112 a0001c0001t0001g0150 a0001c0001t0003g0196 others(6): Show |
9 | HG00280.hp2 HG00738.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.1433-19_1433-14del others(6): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr6 | 116732074 | ||||||
chr6:116732074 | TTATATAT others(1): Show |
T | 12 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0119 others(9): Show |
13 | HG01358.hp1 HG01515.hp2 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.1433-21_1433-14del others(8): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr6 | 116732074 | ||||||
chr6:116732074 | TTATATAT others(3): Show |
T | 13 | a0001c0001t0001g0016 a0001c0001t0001g0120 a0001c0001t0001g0130 others(10): Show |
14 | HG00639.hp2 HG01074.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.1433-23_1433-14del others(10): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr6 | 116732074 | ||||||
chr6:116732074 | TTATATAT others(5): Show |
T | 12 | a0001c0001t0001g0115 a0001c0001t0001g0118 a0001c0001t0001g0123 others(9): Show |
12 | HG00639.hp1 HG01496.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1433-25_1433-14del others(12): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr6 | 116732074 | ||||||
chr6:116732074 | TTATATAT others(7): Show |
T | 14 | a0001c0001t0001g0116 a0001c0001t0001g0127 a0001c0001t0001g0128 others(11): Show |
15 | HG00609.hp1 HG00741.hp1 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.1433-27_1433-14del others(14): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr6 | 116732074 | ||||||
chr6:116732074 | TTATATAT others(9): Show |
T | 16 | a0001c0001t0001g0231 a0001c0001t0002g0014 a0001c0001t0002g0035 others(13): Show |
17 | HG01433.hp1 HG01884.hp2 HG02027.hp1 others(14): Show |
intron_variant | MODIFIER | c.1433-29_1433-14del others(16): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr6 | 116732074 | ||||||
chr6:116732074 | TTATATAT others(11): Show |
T | 17 | a0001c0001t0001g0251 a0001c0001t0002g0041 a0001c0001t0002g0051 others(14): Show |
17 | HG00597.hp1 HG02300.hp2 HG02698.hp2 others(14): Show |
intron_variant | MODIFIER | c.1433-31_1433-14del others(18): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr6 | 116732074 | ||||||
chr6:116732074 | TTATATAT others(13): Show |
T | 66 | a0001c0001t0001g0217 a0001c0001t0002g0010 a0001c0001t0002g0011 others(63): Show |
72 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.1433-33_1433-14del others(20): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr6 | 116732074 | ||||||
chr6:116732074 | TTATATAT others(15): Show |
T | 3 | a0001c0001t0001g0194 a0001c0001t0006g0260 a0001c0001t0013g0001 |
4 | HG01258.hp2 HG02647.hp1 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.1433-35_1433-14del others(22): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr6 | 116732074 | ||||||
chr6:116732074 | TTATATAT others(17): Show |
T | 1 | a0001c0001t0006g0104 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1433-37_1433-14del others(24): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr6 | 116732074 | ||||||
chr6:116732074 | TTATATAT others(19): Show |
T | 7 | a0001c0001t0003g0197 a0001c0001t0006g0105 a0001c0001t0006g0121 others(4): Show |
7 | HG02886.hp1 HG03017.hp2 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1433-39_1433-14del others(26): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr6 | 116732074 | ||||||
chr6:116732074 | TTATATAT others(21): Show |
T | 1 | a0001c0001t0040g0187 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1433-41_1433-14del others(28): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr6 | 116732074 | ||||||
chr6:116732074 | TTATATAT others(23): Show |
T | 7 | a0001c0001t0001g0124 a0001c0001t0009g0171 a0001c0001t0009g0172 others(4): Show |
7 | HG02055.hp1 HG02559.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1433-43_1433-14del others(30): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr6 | 116732074 | ||||||
chr6:116732075 | TATATATA others(4): Show |
T | 1 | a0001c0001t0001g0126 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1433-60_1433-50del others(11): Show |
KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | chr6 | 116732075 | |||||||
chr6:116732076 | A | T | 3 | a0001c0001t0003g0245 a0001c0001t0005g0280 a0001c0001t0056g0281 |
3 | HG02056.hp2 HG02451.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1433-60A>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | chr6 | 116732076 | |||||||
chr6:116732078 | A | T | 6 | a0001c0001t0001g0151 a0001c0001t0003g0237 a0001c0001t0003g0243 others(3): Show |
6 | HG02970.hp2 HG03209.hp1 HG03669.hp2 others(3): Show |
intron_variant | MODIFIER | c.1433-58A>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | chr6 | 116732078 | |||||||
chr6:116732080 | A | T | 3 | a0001c0001t0007g0055 a0001c0001t0007g0068 a0001c0001t0011g0149 |
3 | HG01167.hp1 HG01169.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.1433-56A>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | chr6 | 116732080 | |||||||
chr6:116732082 | A | T | 6 | a0001c0001t0001g0150 a0001c0001t0003g0196 a0001c0001t0003g0212 others(3): Show |
6 | HG00738.hp2 HG01261.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.1433-54A>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | chr6 | 116732082 | |||||||
chr6:116732084 | A | T | 7 | a0001c0001t0003g0239 a0001c0001t0007g0057 a0001c0001t0007g0091 others(4): Show |
7 | HG01358.hp1 HG01515.hp2 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.1433-52A>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | chr6 | 116732084 | |||||||
chr6:116732086 | A | T | 6 | a0001c0001t0003g0178 a0001c0001t0023g0202 a0001c0001t0023g0246 others(3): Show |
7 | HG00639.hp2 HG01074.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.1433-50A>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | chr6 | 116732086 | |||||||
chr6:116732088 | A | T | 6 | a0001c0001t0003g0224 a0001c0001t0021g0166 a0001c0001t0021g0170 others(3): Show |
6 | HG02280.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1433-48A>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | chr6 | 116732088 | |||||||
chr6:116732090 | A | T | 3 | a0001c0001t0002g0042 a0001c0001t0026g0109 a0002c0003t0018g0019 |
4 | HG00609.hp1 HG01258.hp1 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.1433-46A>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | chr6 | 116732090 | |||||||
chr6:116732092 | A | T | 14 | a0001c0001t0002g0014 a0001c0001t0002g0035 a0001c0001t0002g0046 others(11): Show |
15 | HG01433.hp1 HG01884.hp2 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.1433-44A>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | chr6 | 116732092 | |||||||
chr6:116732094 | A | T | 13 | a0001c0001t0002g0041 a0001c0001t0002g0051 a0001c0001t0002g0062 others(10): Show |
13 | HG00597.hp1 HG02300.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.1433-42A>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | chr6 | 116732094 | |||||||
chr6:116732096 | A | T | 59 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(56): Show |
64 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.1433-40A>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | chr6 | 116732096 | |||||||
chr6:116732102 | A | T | 1 | a0001c0001t0003g0197 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1433-34A>T | KPNA5 | ENSG00000196911.12 | transcript | ENST00000368564.7 | protein_coding | 13/13 | chr6 | 116732102 |