Item | Value |
---|---|
geneid | 3840 |
ensemblid | ENSG00000186432.10 |
hgncid | 6397 |
symbol | KPNA4 |
name | karyopherin subunit alpha 4 |
refseq_nuc | NM_002268.5 |
refseq_prot | NP_002259.1 |
ensembl_nuc | ENST00000334256.9 |
ensembl_prot | ENSP00000334373.4 |
mane_status | MANE Select |
chr | chr3 |
start | 160495007 |
end | 160565571 |
strand | - |
ver | v1.2 |
region | chr3:160495007-160565571 |
region5000 | chr3:160490007-160570571 |
regionname0 | KPNA4_chr3_160495007_160565571 |
regionname5000 | KPNA4_chr3_160490007_160570571 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 521 | 307 | 92 | 60 | 110 | 12 | 31 | 84 | KPNA4_chr3_160490007_160570571 | KPNA4 | MADNE others(516): Show |
chr3 | 160490007 | 160570571 |
a0002 | 0/0 | 521 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | MADNE others(516): Show |
chr3 | 160490007 | 160570571 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1563 | 275 | 73 | 59 | 102 | 11 | 28 | KPNA4_chr3_160490007_160570571 | KPNA4 | ATGGC others(1558): Show |
chr3 | 160490007 | 160570571 | ||
a0001c0002 | 0/0 | 1563 | 17 | 16 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | ATGGC others(1558): Show |
chr3 | 160490007 | 160570571 | ||
a0001c0003 | 0/0 | 1563 | 9 | 3 | 0 | 2 | 1 | 3 | KPNA4_chr3_160490007_160570571 | KPNA4 | ATGGC others(1558): Show |
chr3 | 160490007 | 160570571 | ||
a0001c0004 | 0/0 | 1563 | 6 | 0 | 0 | 6 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | ATGGC others(1558): Show |
chr3 | 160490007 | 160570571 | ||
a0002c0005 | 0/0 | 1563 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA4_chr3_160490007_160570571 | KPNA4 | ATGGC others(1558): Show |
chr3 | 160490007 | 160570571 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 8952 | 118 | 21 | 22 | 56 | 4 | 13 | KPNA4_chr3_160490007_160570571 | KPNA4 | AGATC others(8947): Show |
chr3 | 160490007 | 160570571 |
a0001c0001t0002 | 0/0 | 8954 | 60 | 9 | 16 | 28 | 1 | 6 | KPNA4_chr3_160490007_160570571 | KPNA4 | AGATC others(8949): Show |
chr3 | 160490007 | 160570571 |
a0001c0001t0003 | 0/0 | 8953 | 17 | 0 | 6 | 0 | 3 | 8 | KPNA4_chr3_160490007_160570571 | KPNA4 | AGATC others(8948): Show |
chr3 | 160490007 | 160570571 |
a0001c0001t0005 | 0/0 | 8955 | 8 | 7 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | AGATC others(8950): Show |
chr3 | 160490007 | 160570571 |
a0001c0001t0006 | 0/0 | 8954 | 6 | 0 | 0 | 6 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | AGATC others(8949): Show |
chr3 | 160490007 | 160570571 |
a0001c0001t0007 | 0/0 | 8955 | 6 | 4 | 2 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | AGATC others(8950): Show |
chr3 | 160490007 | 160570571 |
a0001c0001t0008 | 0/0 | 8954 | 6 | 6 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | AGATT others(8949): Show |
chr3 | 160490007 | 160570571 |
a0001c0001t0011 | 0/0 | 8953 | 5 | 5 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | AGATC others(8948): Show |
chr3 | 160490007 | 160570571 |
a0001c0001t0012 | 0/0 | 8955 | 5 | 4 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | AGATC others(8950): Show |
chr3 | 160490007 | 160570571 |
a0001c0001t0015 | 0/0 | 8953 | 3 | 1 | 0 | 1 | 0 | 1 | KPNA4_chr3_160490007_160570571 | KPNA4 | AGATC others(8948): Show |
chr3 | 160490007 | 160570571 |
a0001c0001t0016 | 0/0 | 8952 | 3 | 0 | 0 | 3 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | AGATC others(8947): Show |
chr3 | 160490007 | 160570571 |
a0001c0001t0017 | 0/0 | 8954 | 3 | 0 | 0 | 3 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | AGATC others(8949): Show |
chr3 | 160490007 | 160570571 |
a0001c0001t0018 | 0/0 | 8953 | 3 | 3 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | AGATC others(8948): Show |
chr3 | 160490007 | 160570571 |
a0001c0001t0019 | 0/0 | 8953 | 2 | 0 | 2 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | AGATC others(8948): Show |
chr3 | 160490007 | 160570571 |
a0001c0001t0020 | 0/0 | 8955 | 2 | 0 | 1 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | AGATC others(8950): Show |
chr3 | 160490007 | 160570571 |
a0001c0001t0021 | 0/0 | 8952 | 2 | 0 | 1 | 0 | 1 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | AGATC others(8947): Show |
chr3 | 160490007 | 160570571 |
a0001c0001t0022 | 0/0 | 8955 | 2 | 2 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | AGATC others(8950): Show |
chr3 | 160490007 | 160570571 |
a0001c0001t0023 | 0/0 | 8951 | 2 | 1 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | AGATC others(8946): Show |
chr3 | 160490007 | 160570571 |
a0001c0001t0024 | 0/0 | 8952 | 2 | 2 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | AGATC others(8947): Show |
chr3 | 160490007 | 160570571 |
a0001c0001t0028 | 0/0 | 8953 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | AGATC others(8948): Show |
chr3 | 160490007 | 160570571 |
a0001c0001t0029 | 0/0 | 8953 | 1 | 0 | 0 | 0 | 1 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | AGATC others(8948): Show |
chr3 | 160490007 | 160570571 |
a0001c0001t0030 | 0/0 | 8954 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | AGATC others(8949): Show |
chr3 | 160490007 | 160570571 |
a0001c0001t0031 | 0/0 | 8956 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | AGATC others(8951): Show |
chr3 | 160490007 | 160570571 |
a0001c0001t0032 | 0/0 | 8955 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | AGATC others(8950): Show |
chr3 | 160490007 | 160570571 |
a0001c0001t0033 | 0/0 | 8953 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | AGATC others(8948): Show |
chr3 | 160490007 | 160570571 |
a0001c0001t0034 | 0/0 | 8956 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | AGATC others(8951): Show |
chr3 | 160490007 | 160570571 |
a0001c0001t0039 | 0/0 | 8955 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | AGATC others(8950): Show |
chr3 | 160490007 | 160570571 |
a0001c0001t0040 | 0/0 | 8954 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | AGATC others(8949): Show |
chr3 | 160490007 | 160570571 |
a0001c0001t0041 | 0/0 | 8955 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | AGATC others(8950): Show |
chr3 | 160490007 | 160570571 |
a0001c0001t0043 | 0/0 | 8952 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | AGATC others(8947): Show |
chr3 | 160490007 | 160570571 |
a0001c0001t0044 | 0/0 | 8952 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | AGATC others(8947): Show |
chr3 | 160490007 | 160570571 |
a0001c0001t0045 | 0/0 | 8952 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | AGATC others(8947): Show |
chr3 | 160490007 | 160570571 |
a0001c0001t0046 | 0/0 | 8952 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | AGATC others(8947): Show |
chr3 | 160490007 | 160570571 |
a0001c0001t0047 | 0/0 | 8952 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | AGATC others(8947): Show |
chr3 | 160490007 | 160570571 |
a0001c0001t0048 | 0/0 | 8954 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | AGATC others(8949): Show |
chr3 | 160490007 | 160570571 |
a0001c0001t0049 | 0/0 | 8952 | 1 | 0 | 0 | 0 | 1 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | AGATC others(8947): Show |
chr3 | 160490007 | 160570571 |
a0001c0001t0050 | 0/0 | 8957 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | AGATC others(8952): Show |
chr3 | 160490007 | 160570571 |
a0001c0001t0051 | 0/0 | 8956 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | AGATC others(8951): Show |
chr3 | 160490007 | 160570571 |
a0001c0001t0052 | 0/0 | 8952 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | AGATC others(8947): Show |
chr3 | 160490007 | 160570571 |
a0001c0002t0009 | 0/0 | 8954 | 5 | 5 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | AGATC others(8949): Show |
chr3 | 160490007 | 160570571 |
a0001c0002t0010 | 0/0 | 8953 | 5 | 5 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | AGATC others(8948): Show |
chr3 | 160490007 | 160570571 |
a0001c0002t0014 | 0/0 | 8953 | 3 | 3 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | AGATC others(8948): Show |
chr3 | 160490007 | 160570571 |
a0001c0002t0025 | 0/0 | 8953 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | AGATC others(8948): Show |
chr3 | 160490007 | 160570571 |
a0001c0002t0026 | 0/0 | 8953 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | AGATC others(8948): Show |
chr3 | 160490007 | 160570571 |
a0001c0002t0027 | 0/0 | 8953 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | AGATC others(8948): Show |
chr3 | 160490007 | 160570571 |
a0001c0002t0042 | 0/0 | 8954 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | AGATC others(8949): Show |
chr3 | 160490007 | 160570571 |
a0001c0003t0004 | 0/0 | 8964 | 7 | 2 | 0 | 2 | 0 | 3 | KPNA4_chr3_160490007_160570571 | KPNA4 | AGATC others(8959): Show |
chr3 | 160490007 | 160570571 |
a0001c0003t0035 | 0/0 | 8954 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | AGATC others(8949): Show |
chr3 | 160490007 | 160570571 |
a0001c0003t0036 | 0/0 | 8964 | 1 | 0 | 0 | 0 | 1 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | AGATC others(8959): Show |
chr3 | 160490007 | 160570571 |
a0001c0004t0013 | 0/0 | 8956 | 4 | 0 | 0 | 4 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | AGATC others(8951): Show |
chr3 | 160490007 | 160570571 |
a0001c0004t0037 | 0/0 | 8956 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | AGATC others(8951): Show |
chr3 | 160490007 | 160570571 |
a0001c0004t0038 | 0/0 | 8955 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | AGATC others(8950): Show |
chr3 | 160490007 | 160570571 |
a0002c0005t0004 | 0/0 | 8964 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA4_chr3_160490007_160570571 | KPNA4 | AGATC others(8959): Show |
chr3 | 160490007 | 160570571 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0008 | 1/0 | 2 | 0 | 0 | 0 | 1 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0009 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0011 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0263 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0002g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0003g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0003g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0003g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0003g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0003g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0003g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0003g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0003g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0003g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0003g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0005g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0005g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0005g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0005g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0005g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0005g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0005g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0005g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0006g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0006g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0006g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0007g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0007g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0007g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0007g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0007g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0008g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0008g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0008g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0008g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0008g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0008g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0011g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0011g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0011g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0011g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0011g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0012g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0012g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0012g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0012g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0012g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0015g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0015g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0015g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0016g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0016g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0016g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0017g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0017g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0017g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0018g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0018g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0018g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0019g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0019g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0020g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0020g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0021g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0021g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0022g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0022g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0023g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0023g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0024g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0024g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0028g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0029g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0030g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0031g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0032g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0033g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0034g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0039g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0040g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0041g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0043g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0044g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0045g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0046g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0047g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0048g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0049g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0050g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0051g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0001t0052g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0002t0009g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0002t0009g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0002t0009g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0002t0009g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0002t0009g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0002t0010g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0002t0010g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0002t0010g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0002t0010g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0002t0010g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0002t0014g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0002t0014g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0002t0014g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0002t0025g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0002t0026g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0002t0027g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0002t0042g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0003t0004g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0003t0004g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0003t0004g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0003t0004g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0003t0004g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0003t0004g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0003t0004g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0003t0035g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0003t0036g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0004t0013g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0004t0013g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0004t0013g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0004t0013g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0004t0037g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0001c0004t0038g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
a0002c0005t0004g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0021 | g0036 | EUR | GBR | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG00099 | hp2 | a0001 | c0003 | t0036 | g0106 | EUR | GBR | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0255 | EUR | GBR | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG00140 | hp2 | a0001 | c0001 | t0003 | g0021 | EUR | GBR | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG00280 | hp1 | a0001 | c0001 | t0049 | g0207 | EUR | FIN | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG00280 | hp2 | a0001 | c0001 | t0003 | g0020 | EUR | FIN | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0200 | EUR | FIN | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG00323 | hp2 | a0001 | c0001 | t0029 | g0037 | EUR | FIN | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | CHS | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG00423 | hp2 | a0001 | c0001 | t0006 | g0002 | EAS | CHS | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG00544 | hp1 | a0001 | c0001 | t0016 | g0224 | EAS | CHS | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | CHS | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG00558 | hp1 | a0001 | c0001 | t0032 | g0018 | EAS | CHS | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | CHS | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | CHS | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | CHS | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | CHS | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0086 | AMR | PUR | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG00642 | hp2 | a0001 | c0001 | t0052 | g0211 | AMR | PUR | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | CHS | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0076 | AMR | PUR | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG00735 | hp2 | a0001 | c0001 | t0003 | g0025 | AMR | PUR | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG00738 | hp1 | a0001 | c0001 | t0019 | g0118 | AMR | PUR | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0061 | AMR | PUR | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG00741 | hp1 | a0001 | c0001 | t0047 | g0209 | AMR | PUR | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG00741 | hp2 | a0001 | c0001 | t0041 | g0023 | AMR | PUR | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG01069 | hp2 | a0001 | c0001 | t0012 | g0110 | AMR | PUR | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0062 | AMR | PUR | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0084 | AMR | PUR | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG01106 | hp2 | a0001 | c0001 | t0003 | g0024 | AMR | PUR | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0090 | AMR | PUR | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG01167 | hp1 | a0001 | c0001 | t0007 | g0094 | AMR | PUR | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG01167 | hp2 | a0001 | c0001 | t0019 | g0119 | AMR | PUR | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG01168 | hp2 | a0001 | c0001 | t0003 | g0022 | AMR | PUR | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG01169 | hp1 | a0001 | c0001 | t0021 | g0026 | AMR | PUR | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG01169 | hp2 | a0001 | c0001 | t0007 | g0006 | AMR | PUR | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0089 | AMR | PUR | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG01243 | hp2 | a0001 | c0002 | t0025 | g0135 | AMR | PUR | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG01255 | hp1 | a0001 | c0001 | t0043 | g0186 | AMR | CLM | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG01255 | hp2 | a0001 | c0001 | t0005 | g0102 | AMR | CLM | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | CLM | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0082 | AMR | CLM | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | CLM | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | CLM | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG01261 | hp2 | a0001 | c0001 | t0033 | g0117 | AMR | CLM | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | CLM | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG01358 | hp1 | a0001 | c0001 | t0003 | g0028 | AMR | CLM | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | CLM | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG01361 | hp2 | a0001 | c0001 | t0003 | g0029 | AMR | CLM | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG01433 | hp1 | a0001 | c0001 | t0048 | g0275 | AMR | CLM | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0073 | AMR | CLM | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | CLM | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG01516 | hp1 | a0001 | c0001 | t0003 | g0033 | EUR | IBS | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0088 | AFR | ACB | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG01891 | hp2 | a0001 | c0001 | t0011 | g0122 | AFR | ACB | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0071 | AMR | PEL | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0087 | AMR | PEL | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | PEL | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0053 | AMR | PEL | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG01993 | hp1 | a0001 | c0001 | t0030 | g0085 | AMR | PEL | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0074 | AFR | ACB | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02055 | hp2 | a0001 | c0001 | t0005 | g0099 | AFR | ACB | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02056 | hp1 | a0001 | c0001 | t0017 | g0267 | EAS | KHV | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02056 | hp2 | a0001 | c0001 | t0017 | g0262 | EAS | KHV | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02074 | hp1 | a0001 | c0001 | t0020 | g0064 | EAS | KHV | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | KHV | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | KHV | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | KHV | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02145 | hp1 | a0001 | c0002 | t0009 | g0145 | AFR | ACB | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | ACB | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PEL | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02148 | hp2 | a0001 | c0001 | t0020 | g0051 | AMR | PEL | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | CDX | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | CDX | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02257 | hp2 | a0001 | c0001 | t0008 | g0286 | AFR | ACB | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0042 | AFR | ACB | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | PEL | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | PEL | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02280 | hp1 | a0001 | c0001 | t0005 | g0100 | AFR | ACB | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0060 | AFR | ACB | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02451 | hp1 | a0001 | c0002 | t0009 | g0139 | AFR | ACB | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02451 | hp2 | a0001 | c0001 | t0005 | g0096 | AFR | ACB | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | KHV | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0035 | SAS | PJL | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02615 | hp1 | a0001 | c0001 | t0022 | g0127 | AFR | GWD | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02615 | hp2 | a0001 | c0001 | t0008 | g0289 | AFR | GWD | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02622 | hp1 | a0001 | c0001 | t0018 | g0284 | AFR | GWD | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0128 | AFR | GWD | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02630 | hp2 | a0001 | c0001 | t0011 | g0124 | AFR | GWD | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02647 | hp1 | a0001 | c0002 | t0027 | g0143 | AFR | GWD | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02647 | hp2 | a0001 | c0001 | t0011 | g0123 | AFR | GWD | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0264 | SAS | PJL | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0056 | SAS | PJL | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02717 | hp1 | a0001 | c0001 | t0005 | g0097 | AFR | GWD | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02717 | hp2 | a0001 | c0001 | t0039 | g0111 | AFR | GWD | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02723 | hp1 | a0001 | c0003 | t0035 | g0104 | AFR | GWD | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02723 | hp2 | a0001 | c0002 | t0010 | g0136 | AFR | GWD | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0079 | SAS | PJL | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02738 | hp1 | a0001 | c0003 | t0004 | g0108 | SAS | PJL | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02738 | hp2 | a0001 | c0001 | t0015 | g0258 | SAS | PJL | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02809 | hp1 | a0001 | c0001 | t0024 | g0170 | AFR | GWD | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02818 | hp2 | a0001 | c0001 | t0018 | g0282 | AFR | GWD | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02886 | hp1 | a0001 | c0001 | t0012 | g0112 | AFR | GWD | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02886 | hp2 | a0001 | c0002 | t0010 | g0134 | AFR | GWD | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02895 | hp1 | a0001 | c0001 | t0024 | g0204 | AFR | GWD | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02895 | hp2 | a0001 | c0002 | t0014 | g0133 | AFR | GWD | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02896 | hp1 | a0001 | c0001 | t0023 | g0253 | AFR | GWD | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02896 | hp2 | a0001 | c0001 | t0008 | g0290 | AFR | GWD | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02897 | hp1 | a0001 | c0001 | t0008 | g0285 | AFR | GWD | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02897 | hp2 | a0001 | c0002 | t0014 | g0132 | AFR | GWD | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02922 | hp1 | a0001 | c0002 | t0042 | g0142 | AFR | ESN | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0055 | AFR | ESN | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02965 | hp1 | a0001 | c0001 | t0012 | g0115 | AFR | ESN | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0041 | AFR | ESN | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02970 | hp1 | a0001 | c0001 | t0005 | g0101 | AFR | ESN | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02970 | hp2 | a0001 | c0002 | t0009 | g0138 | AFR | ESN | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02976 | hp1 | a0001 | c0003 | t0004 | g0105 | AFR | ESN | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02976 | hp2 | a0001 | c0001 | t0034 | g0146 | AFR | ESN | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG03041 | hp2 | a0001 | c0001 | t0007 | g0091 | AFR | GWD | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG03098 | hp1 | a0001 | c0002 | t0009 | g0129 | AFR | MSL | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG03098 | hp2 | a0001 | c0001 | t0008 | g0287 | AFR | MSL | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | ESN | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ESN | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG03139 | hp2 | a0001 | c0002 | t0010 | g0140 | AFR | ESN | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG03195 | hp1 | a0001 | c0001 | t0031 | g0103 | AFR | ESN | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ESN | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG03209 | hp1 | a0001 | c0002 | t0026 | g0141 | AFR | MSL | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | MSL | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG03225 | hp1 | a0001 | c0001 | t0012 | g0114 | AFR | MSL | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG03225 | hp2 | a0001 | c0002 | t0010 | g0137 | AFR | MSL | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0083 | SAS | PJL | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG03239 | hp2 | a0001 | c0001 | t0003 | g0030 | SAS | PJL | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG03453 | hp1 | a0001 | c0001 | t0005 | g0098 | AFR | MSL | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | MSL | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | MSL | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | MSL | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG03490 | hp2 | a0001 | c0001 | t0003 | g0034 | SAS | PJL | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG03540 | hp1 | a0001 | c0001 | t0011 | g0121 | AFR | GWD | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG03579 | hp1 | a0001 | c0001 | t0028 | g0116 | AFR | MSL | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG03579 | hp2 | a0001 | c0001 | t0018 | g0283 | AFR | MSL | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG03669 | hp2 | a0002 | c0005 | t0004 | g0156 | SAS | PJL | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG03688 | hp1 | a0001 | c0001 | t0003 | g0016 | SAS | STU | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0248 | SAS | STU | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0015 | SAS | PJL | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0075 | SAS | PJL | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | BEB | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0080 | SAS | BEB | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | BEB | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG03834 | hp2 | a0001 | c0003 | t0004 | g0107 | SAS | BEB | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG03942 | hp1 | a0001 | c0001 | t0003 | g0017 | SAS | BEB | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0261 | SAS | BEB | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | STU | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG04115 | hp2 | a0001 | c0003 | t0004 | g0155 | SAS | STU | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0014 | SAS | BEB | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0256 | SAS | BEB | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0063 | SAS | STU | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | STU | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA18522 | hp1 | a0001 | c0001 | t0044 | g0202 | AFR | YRI | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA18522 | hp2 | a0001 | c0001 | t0011 | g0120 | AFR | YRI | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | CHB | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA18612 | hp2 | a0001 | c0001 | t0046 | g0185 | EAS | CHB | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA18747 | hp1 | a0001 | c0001 | t0045 | g0243 | EAS | CHB | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | CHB | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA18906 | hp1 | a0001 | c0001 | t0022 | g0126 | AFR | YRI | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | YRI | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA18939 | hp1 | a0001 | c0001 | t0023 | g0218 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA18939 | hp2 | a0001 | c0004 | t0038 | g0151 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA18942 | hp1 | a0001 | c0001 | t0006 | g0002 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA18942 | hp2 | a0001 | c0001 | t0015 | g0178 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA18944 | hp1 | a0001 | c0003 | t0004 | g0157 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA18945 | hp1 | a0001 | c0001 | t0016 | g0240 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA18951 | hp2 | a0001 | c0001 | t0006 | g0019 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA18959 | hp2 | a0001 | c0004 | t0037 | g0150 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA18960 | hp2 | a0001 | c0004 | t0013 | g0152 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA18968 | hp2 | a0001 | c0001 | t0006 | g0002 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA18971 | hp2 | a0001 | c0003 | t0004 | g0158 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA18990 | hp1 | a0001 | c0004 | t0013 | g0153 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA18993 | hp2 | a0001 | c0001 | t0017 | g0176 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA19002 | hp1 | a0001 | c0001 | t0006 | g0002 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA19011 | hp1 | a0001 | c0001 | t0016 | g0252 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | LWK | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA19030 | hp2 | a0001 | c0001 | t0007 | g0095 | AFR | LWK | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA19043 | hp1 | a0001 | c0002 | t0014 | g0144 | AFR | LWK | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA19043 | hp2 | a0001 | c0001 | t0005 | g0093 | AFR | LWK | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA19064 | hp2 | a0001 | c0001 | t0006 | g0031 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA19084 | hp1 | a0001 | c0004 | t0013 | g0148 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA19088 | hp1 | a0001 | c0004 | t0013 | g0149 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA19240 | hp2 | a0001 | c0003 | t0004 | g0109 | AFR | YRI | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA20129 | hp1 | a0001 | c0001 | t0008 | g0288 | AFR | ASW | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA20129 | hp2 | a0001 | c0002 | t0010 | g0131 | AFR | ASW | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0188 | EUR | TSI | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0068 | EUR | TSI | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0244 | SAS | GIH | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA20905 | hp2 | a0001 | c0001 | t0003 | g0032 | SAS | GIH | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG01123 | hp1 | a0001 | c0001 | t0003 | g0027 | AMR | CLM | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0059 | AMR | CLM | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02486 | hp1 | a0001 | c0002 | t0009 | g0130 | AFR | ACB | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02486 | hp2 | a0001 | c0001 | t0040 | g0125 | AFR | ACB | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02559 | hp1 | a0001 | c0001 | t0015 | g0216 | AFR | ACB | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG03471 | hp1 | a0001 | c0001 | t0012 | g0113 | AFR | MSL | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG03471 | hp2 | a0001 | c0001 | t0050 | g0163 | AFR | MSL | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG06807 | hp1 | a0001 | c0001 | t0007 | g0092 | AFR | USA | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | USA | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | USA | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA20300 | hp2 | a0001 | c0001 | t0007 | g0006 | AFR | USA | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0039 | AFR | LWK | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
NA21309 | hp2 | a0001 | c0001 | t0051 | g0274 | AFR | LWK | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0263 | REF | REF | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0008 | REF | REF | KPNA4_chr3_160490007_160570571 | KPNA4 | chr3 | 160490007 | 160570571 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:160535896 | T | C | 1 | a0002 | 1 | HG03669.hp2 | missense_variant&splice_region_variant | MODERATE | c.116A>G | p.Asn39Ser | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 3/17 | 405/8952 | 116/1566 | 39/521 | chr3 | 160535896 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:160509818 | A | G | 2 | a0001c0003 a0002c0005 |
10 | HG00099.hp2 HG02723.hp1 HG02738.hp1 others(7): Show |
synonymous_variant | LOW | c.1191T>C | p.Ile397Ile | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 14/17 | 1480/8952 | 1191/1566 | 397/521 | chr3 | 160509818 | |||
chr3:160514149 | T | C | 1 | a0001c0002 | 17 | HG01243.hp2 HG02145.hp1 HG02451.hp1 others(14): Show |
synonymous_variant | LOW | c.1065A>G | p.Ala355Ala | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 13/17 | 1354/8952 | 1065/1566 | 355/521 | chr3 | 160514149 | |||
chr3:160525977 | G | A | 1 | a0001c0004 | 6 | NA18939.hp2 NA18959.hp2 NA18960.hp2 others(3): Show |
synonymous_variant | LOW | c.687C>T | p.Arg229Arg | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 9/17 | 976/8952 | 687/1566 | 229/521 | chr3 | 160525977 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:160495088 | C | T | 1 | a0001c0001t0045 | 1 | NA18747.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7016G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 17/17 | 7016 | chr3 | 160495088 | ||||||
chr3:160495093 | C | G | 1 | a0001c0002t0026 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7011G>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 17/17 | 7011 | chr3 | 160495093 | ||||||
chr3:160495314 | G | A | 38 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(35): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
3_prime_UTR_variant | MODIFIER | c.*6790C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 17/17 | 6790 | chr3 | 160495314 | ||||||
chr3:160495426 | T | A | 11 | a0001c0002t0009 a0001c0002t0010 a0001c0002t0014 others(8): Show |
27 | HG00099.hp2 HG01243.hp2 HG02145.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*6678A>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 17/17 | 6678 | chr3 | 160495426 | ||||||
chr3:160495498 | C | T | 4 | a0001c0001t0002 a0001c0001t0020 a0001c0001t0029 others(1): Show |
64 | HG00323.hp2 HG00423.hp1 HG00642.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*6606G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 17/17 | 6606 | chr3 | 160495498 | ||||||
chr3:160495505 | A | C | 1 | a0001c0001t0022 | 2 | HG02615.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6599T>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 17/17 | 6599 | chr3 | 160495505 | ||||||
chr3:160495523 | G | GGAA | 40 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(37): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(167): Show |
3_prime_UTR_variant | MODIFIER | c.*6578_*6580dupTTC | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 17/17 | 6580 | chr3 | 160495523 | ||||||
chr3:160495879 | C | T | 6 | a0001c0001t0008 a0001c0001t0022 a0001c0001t0040 others(3): Show |
12 | HG01433.hp1 HG02257.hp2 HG02486.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*6225G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 17/17 | 6225 | chr3 | 160495879 | ||||||
chr3:160495916 | C | CT | 9 | a0001c0001t0015 a0001c0001t0020 a0001c0001t0031 others(6): Show |
24 | HG02074.hp1 HG02145.hp1 HG02148.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*6187dupA | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 17/17 | 6187 | chr3 | 160495916 | ||||||
chr3:160495916 | CT | C | 11 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0018 others(8): Show |
35 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*6187delA | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 17/17 | 6187 | chr3 | 160495916 | ||||||
chr3:160495916 | CTT | C | 5 | a0001c0001t0011 a0001c0001t0019 a0001c0001t0021 others(2): Show |
11 | HG00099.hp1 HG00738.hp1 HG01167.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*6186_*6187delAA | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 17/17 | 6186 | chr3 | 160495916 | ||||||
chr3:160496214 | G | T | 2 | a0001c0001t0011 a0001c0001t0028 |
6 | HG01891.hp2 HG02630.hp2 HG02647.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5890C>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 17/17 | 5890 | chr3 | 160496214 | ||||||
chr3:160496216 | A | T | 7 | a0001c0002t0009 a0001c0002t0010 a0001c0002t0014 others(4): Show |
17 | HG01243.hp2 HG02145.hp1 HG02451.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*5888T>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 17/17 | 5888 | chr3 | 160496216 | ||||||
chr3:160496350 | G | A | 2 | a0001c0004t0037 a0001c0004t0038 |
2 | NA18939.hp2 NA18959.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5754C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 17/17 | 5754 | chr3 | 160496350 | ||||||
chr3:160496436 | C | T | 4 | a0001c0001t0011 a0001c0001t0019 a0001c0001t0028 others(1): Show |
9 | HG00738.hp1 HG01167.hp2 HG01261.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*5668G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 17/17 | 5668 | chr3 | 160496436 | ||||||
chr3:160496636 | G | A | 7 | a0001c0002t0009 a0001c0002t0010 a0001c0002t0014 others(4): Show |
17 | HG01243.hp2 HG02145.hp1 HG02451.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*5468C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 17/17 | 5468 | chr3 | 160496636 | ||||||
chr3:160496661 | C | G | 1 | a0001c0001t0046 | 1 | NA18612.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5443G>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 17/17 | 5443 | chr3 | 160496661 | ||||||
chr3:160496681 | G | A | 10 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(7): Show |
94 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*5423C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 17/17 | 5423 | chr3 | 160496681 | ||||||
chr3:160496728 | T | C | 1 | a0001c0001t0016 | 3 | HG00544.hp1 NA18945.hp1 NA19011.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5376A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 17/17 | 5376 | chr3 | 160496728 | ||||||
chr3:160497153 | G | A | 1 | a0001c0001t0024 | 2 | HG02809.hp1 HG02895.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4951C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 17/17 | 4951 | chr3 | 160497153 | ||||||
chr3:160497284 | G | A | 4 | a0001c0003t0004 a0001c0003t0035 a0001c0003t0036 others(1): Show |
10 | HG00099.hp2 HG02723.hp1 HG02738.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4820C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 17/17 | 4820 | chr3 | 160497284 | ||||||
chr3:160497325 | T | C | 1 | a0001c0001t0030 | 1 | HG01993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4779A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 17/17 | 4779 | chr3 | 160497325 | ||||||
chr3:160497402 | A | G | 1 | a0001c0001t0031 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4702T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 17/17 | 4702 | chr3 | 160497402 | ||||||
chr3:160497409 | C | T | 1 | a0001c0003t0035 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4695G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 17/17 | 4695 | chr3 | 160497409 | ||||||
chr3:160497654 | T | C | 4 | a0001c0001t0011 a0001c0001t0019 a0001c0001t0028 others(1): Show |
9 | HG00738.hp1 HG01167.hp2 HG01261.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4450A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 17/17 | 4450 | chr3 | 160497654 | ||||||
chr3:160497754 | C | T | 1 | a0001c0001t0011 | 5 | HG01891.hp2 HG02630.hp2 HG02647.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4350G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 17/17 | 4350 | chr3 | 160497754 | ||||||
chr3:160497760 | T | C | 36 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(33): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
3_prime_UTR_variant | MODIFIER | c.*4344A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 17/17 | 4344 | chr3 | 160497760 | ||||||
chr3:160497814 | G | A | 4 | a0001c0001t0034 a0001c0004t0013 a0001c0004t0037 others(1): Show |
7 | HG02976.hp2 NA18939.hp2 NA18959.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4290C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 17/17 | 4290 | chr3 | 160497814 | ||||||
chr3:160498097 | T | C | 7 | a0001c0002t0009 a0001c0002t0010 a0001c0002t0014 others(4): Show |
17 | HG01243.hp2 HG02145.hp1 HG02451.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*4007A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 17/17 | 4007 | chr3 | 160498097 | ||||||
chr3:160498473 | T | C | 4 | a0001c0003t0004 a0001c0003t0035 a0001c0003t0036 others(1): Show |
10 | HG00099.hp2 HG02723.hp1 HG02738.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3631A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 17/17 | 3631 | chr3 | 160498473 | ||||||
chr3:160498923 | A | C | 5 | a0001c0001t0008 a0001c0001t0040 a0001c0001t0048 others(2): Show |
10 | HG01433.hp1 HG02257.hp2 HG02486.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3181T>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 17/17 | 3181 | chr3 | 160498923 | ||||||
chr3:160499053 | C | A | 1 | a0001c0001t0028 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3051G>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 17/17 | 3051 | chr3 | 160499053 | ||||||
chr3:160499104 | C | T | 1 | a0001c0001t0044 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3000G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 17/17 | 3000 | chr3 | 160499104 | ||||||
chr3:160499307 | T | C | 1 | a0001c0001t0046 | 1 | NA18612.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2797A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 17/17 | 2797 | chr3 | 160499307 | ||||||
chr3:160499483 | TA | T | 10 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(7): Show |
96 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*2620delT | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 17/17 | 2620 | chr3 | 160499483 | ||||||
chr3:160499484 | A | T | 1 | a0001c0001t0001 | 1 | NA18612.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2620T>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 17/17 | 2620 | chr3 | 160499484 | ||||||
chr3:160499517 | G | A | 1 | a0001c0001t0047 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2587C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 17/17 | 2587 | chr3 | 160499517 | ||||||
chr3:160499695 | G | A | 40 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(37): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(167): Show |
3_prime_UTR_variant | MODIFIER | c.*2409C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 17/17 | 2409 | chr3 | 160499695 | ||||||
chr3:160499969 | C | G | 1 | a0001c0002t0025 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2135G>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 17/17 | 2135 | chr3 | 160499969 | ||||||
chr3:160500045 | C | CATAATAA others(1): Show |
3 | a0001c0003t0004 a0001c0003t0036 a0002c0005t0004 |
9 | HG00099.hp2 HG02738.hp1 HG02976.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2058_*2059insCTTA others(4): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 17/17 | 2058 | chr3 | 160500045 | ||||||
chr3:160500115 | T | A | 1 | a0001c0002t0027 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1989A>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 17/17 | 1989 | chr3 | 160500115 | ||||||
chr3:160500125 | T | TA | 4 | a0001c0003t0036 a0001c0004t0013 a0001c0004t0037 others(1): Show |
7 | HG00099.hp2 NA18939.hp2 NA18959.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1978dupT | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 17/17 | 1978 | chr3 | 160500125 | ||||||
chr3:160500148 | C | A | 1 | a0001c0001t0043 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1956G>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 17/17 | 1956 | chr3 | 160500148 | ||||||
chr3:160500149 | A | C | 1 | a0001c0001t0043 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1955T>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 17/17 | 1955 | chr3 | 160500149 | ||||||
chr3:160501295 | A | C | 1 | a0001c0001t0028 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*809T>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 17/17 | 809 | chr3 | 160501295 | ||||||
chr3:160501587 | A | G | 1 | a0001c0001t0019 | 2 | HG00738.hp1 HG01167.hp2 |
3_prime_UTR_variant | MODIFIER | c.*517T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 17/17 | 517 | chr3 | 160501587 | ||||||
chr3:160501603 | T | C | 2 | a0001c0001t0012 a0001c0001t0039 |
6 | HG01069.hp2 HG02717.hp2 HG02886.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*501A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 17/17 | 501 | chr3 | 160501603 | ||||||
chr3:160501762 | T | C | 1 | a0001c0001t0040 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*342A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 17/17 | 342 | chr3 | 160501762 | ||||||
chr3:160501896 | G | A | 1 | a0001c0001t0049 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*208C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 17/17 | 208 | chr3 | 160501896 | ||||||
chr3:160502022 | G | GTA | 4 | a0001c0001t0017 a0001c0001t0041 a0001c0001t0050 others(1): Show |
6 | HG00741.hp2 HG02056.hp1 HG02056.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*80_*81dupTA | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 17/17 | 81 | chr3 | 160502022 | ||||||
chr3:160502022 | GTA | G | 7 | a0001c0002t0009 a0001c0002t0010 a0001c0002t0014 others(4): Show |
17 | HG01243.hp2 HG02145.hp1 HG02451.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*80_*81delTA | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 17/17 | 80 | chr3 | 160502022 | ||||||
chr3:160502051 | T | C | 2 | a0001c0001t0052 a0001c0002t0042 |
2 | HG00642.hp2 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*53A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 17/17 | 53 | chr3 | 160502051 | ||||||
chr3:160565338 | A | C | 36 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(33): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(158): Show |
5_prime_UTR_variant | MODIFIER | c.-56T>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/17 | 56 | chr3 | 160565338 | ||||||
chr3:160565507 | G | A | 1 | a0001c0001t0018 | 3 | HG02622.hp1 HG02818.hp2 HG03579.hp2 |
5_prime_UTR_variant | MODIFIER | c.-225C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/17 | 225 | chr3 | 160565507 | ||||||
chr3:160565567 | G | A | 1 | a0001c0001t0008 | 6 | HG02257.hp2 HG02615.hp2 HG02896.hp2 others(3): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-285C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/17 | chr3 | 160565567 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:160502370 | T | C | 12 | a0001c0001t0012g0110 a0001c0001t0012g0112 a0001c0001t0012g0113 others(9): Show |
12 | HG01069.hp2 HG02717.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.1468-168A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 16/16 | chr3 | 160502370 | |||||||
chr3:160502374 | C | T | 1 | a0002c0005t0004g0156 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1468-172G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 16/16 | chr3 | 160502374 | |||||||
chr3:160502404 | T | C | 9 | a0001c0003t0004g0105 a0001c0003t0004g0107 a0001c0003t0004g0108 others(6): Show |
9 | HG00099.hp2 HG02738.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.1468-202A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 16/16 | chr3 | 160502404 | |||||||
chr3:160502412 | C | A | 1 | a0001c0001t0040g0125 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1468-210G>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 16/16 | chr3 | 160502412 | |||||||
chr3:160502528 | G | A | 1 | a0001c0001t0028g0116 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1468-326C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 16/16 | chr3 | 160502528 | |||||||
chr3:160502553 | T | C | 1 | a0001c0002t0027g0143 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1468-351A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 16/16 | chr3 | 160502553 | |||||||
chr3:160502671 | A | T | 1 | a0001c0001t0049g0207 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1468-469T>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 16/16 | chr3 | 160502671 | |||||||
chr3:160502707 | A | G | 1 | a0001c0001t0012g0110 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1468-505T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 16/16 | chr3 | 160502707 | |||||||
chr3:160502837 | G | A | 1 | a0001c0001t0044g0202 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1468-635C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 16/16 | chr3 | 160502837 | |||||||
chr3:160502897 | G | C | 1 | a0001c0001t0002g0039 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1468-695C>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 16/16 | chr3 | 160502897 | |||||||
chr3:160502928 | T | C | 27 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0016 others(24): Show |
30 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(27): Show |
intron_variant | MODIFIER | c.1468-726A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 16/16 | chr3 | 160502928 | |||||||
chr3:160503010 | T | C | 17 | a0001c0002t0009g0129 a0001c0002t0009g0130 a0001c0002t0009g0138 others(14): Show |
17 | HG01243.hp2 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.1468-808A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 16/16 | chr3 | 160503010 | |||||||
chr3:160503051 | C | CT | 12 | a0001c0001t0008g0285 a0001c0001t0008g0286 a0001c0001t0008g0287 others(9): Show |
12 | HG01433.hp1 HG02257.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.1468-850_1468-849i others(3): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 16/16 | chr3 | 160503051 | |||||||
chr3:160503110 | C | CAAACA | 10 | a0001c0001t0008g0285 a0001c0001t0008g0286 a0001c0001t0008g0287 others(7): Show |
10 | HG01433.hp1 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1468-913_1468-909d others(7): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 16/16 | chr3 | 160503110 | |||||||
chr3:160503184 | T | TA | 10 | a0001c0001t0001g0257 a0001c0001t0011g0120 a0001c0001t0011g0121 others(7): Show |
10 | HG00738.hp1 HG01167.hp2 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.1468-983dupT | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 16/16 | chr3 | 160503184 | |||||||
chr3:160503378 | C | T | 1 | a0001c0001t0001g0244 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1468-1176G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 16/16 | chr3 | 160503378 | |||||||
chr3:160503541 | T | A | 3 | a0001c0001t0019g0118 a0001c0001t0019g0119 a0001c0001t0033g0117 |
3 | HG00738.hp1 HG01167.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.1468-1339A>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 16/16 | chr3 | 160503541 | |||||||
chr3:160503589 | T | C | 1 | a0001c0001t0007g0091 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1467+1369A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 16/16 | chr3 | 160503589 | |||||||
chr3:160503845 | G | A | 1 | a0001c0001t0031g0103 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1467+1113C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 16/16 | chr3 | 160503845 | |||||||
chr3:160503933 | A | G | 2 | a0001c0001t0001g0213 a0001c0001t0001g0215 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1467+1025T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 16/16 | chr3 | 160503933 | |||||||
chr3:160503954 | A | T | 163 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(160): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.1467+1004T>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 16/16 | chr3 | 160503954 | |||||||
chr3:160504028 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1467+930C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 16/16 | chr3 | 160504028 | |||||||
chr3:160504414 | G | C | 1 | a0001c0001t0011g0122 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1467+544C>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 16/16 | chr3 | 160504414 | |||||||
chr3:160504590 | G | A | 1 | a0001c0001t0001g0184 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1467+368C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 16/16 | chr3 | 160504590 | |||||||
chr3:160504616 | A | T | 9 | a0001c0003t0004g0105 a0001c0003t0004g0107 a0001c0003t0004g0108 others(6): Show |
9 | HG00099.hp2 HG02738.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.1467+342T>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 16/16 | chr3 | 160504616 | |||||||
chr3:160504942 | C | T | 3 | a0001c0001t0012g0112 a0001c0001t0012g0113 a0001c0001t0012g0114 |
3 | HG02886.hp1 HG03225.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1467+16G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 16/16 | chr3 | 160504942 | |||||||
chr3:160505091 | T | G | 1 | a0001c0001t0001g0184 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1373-39A>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 15/16 | chr3 | 160505091 | |||||||
chr3:160505244 | C | T | 180 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 others(177): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.1373-192G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 15/16 | chr3 | 160505244 | |||||||
chr3:160505257 | G | A | 1 | a0001c0002t0027g0143 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1373-205C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 15/16 | chr3 | 160505257 | |||||||
chr3:160505384 | G | A | 163 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(160): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.1373-332C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 15/16 | chr3 | 160505384 | |||||||
chr3:160505614 | A | C | 2 | a0001c0001t0002g0004 a0001c0001t0002g0072 |
3 | NA18943.hp2 NA19012.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1373-562T>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 15/16 | chr3 | 160505614 | |||||||
chr3:160505806 | G | C | 17 | a0001c0002t0009g0129 a0001c0002t0009g0130 a0001c0002t0009g0138 others(14): Show |
17 | HG01243.hp2 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.1373-754C>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 15/16 | chr3 | 160505806 | |||||||
chr3:160506108 | C | T | 4 | a0001c0001t0007g0006 a0001c0001t0007g0092 a0001c0001t0007g0094 others(1): Show |
5 | HG01167.hp1 HG01169.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1373-1056G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 15/16 | chr3 | 160506108 | |||||||
chr3:160506178 | A | T | 151 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(148): Show |
158 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.1373-1126T>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 15/16 | chr3 | 160506178 | |||||||
chr3:160506309 | C | T | 1 | a0001c0001t0001g0245 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1373-1257G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 15/16 | chr3 | 160506309 | |||||||
chr3:160506326 | A | G | 148 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(145): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.1373-1274T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 15/16 | chr3 | 160506326 | |||||||
chr3:160506358 | C | T | 1 | a0001c0001t0001g0174 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1373-1306G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 15/16 | chr3 | 160506358 | |||||||
chr3:160506372 | G | A | 2 | a0001c0001t0002g0004 a0001c0001t0002g0072 |
3 | NA18943.hp2 NA19012.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1373-1320C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 15/16 | chr3 | 160506372 | |||||||
chr3:160506626 | T | C | 1 | a0001c0001t0049g0207 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1372+1481A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 15/16 | chr3 | 160506626 | |||||||
chr3:160506915 | A | G | 6 | a0001c0001t0001g0003 a0001c0001t0001g0169 a0001c0001t0001g0177 others(3): Show |
8 | HG02258.hp2 HG02622.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1372+1192T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 15/16 | chr3 | 160506915 | |||||||
chr3:160507077 | T | A | 9 | a0001c0001t0001g0164 a0001c0001t0001g0205 a0001c0001t0001g0206 others(6): Show |
9 | HG01243.hp1 HG02145.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1372+1030A>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 15/16 | chr3 | 160507077 | |||||||
chr3:160507080 | A | AT | 9 | a0001c0001t0001g0164 a0001c0001t0001g0205 a0001c0001t0001g0206 others(6): Show |
9 | HG01243.hp1 HG02145.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1372+1026dupA | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 15/16 | chr3 | 160507080 | |||||||
chr3:160507256 | T | C | 1 | a0001c0001t0008g0289 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1372+851A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 15/16 | chr3 | 160507256 | |||||||
chr3:160507347 | A | G | 2 | a0001c0001t0024g0170 a0001c0001t0024g0204 |
2 | HG02809.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1372+760T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 15/16 | chr3 | 160507347 | |||||||
chr3:160507461 | T | C | 2 | a0001c0001t0002g0040 a0001c0001t0002g0041 |
2 | HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1372+646A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 15/16 | chr3 | 160507461 | |||||||
chr3:160507499 | C | CA | 28 | a0001c0001t0001g0171 a0001c0001t0001g0173 a0001c0001t0001g0197 others(25): Show |
28 | HG00280.hp2 HG00673.hp1 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.1372+607dupT | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 15/16 | chr3 | 160507499 | |||||||
chr3:160507499 | CA | C | 38 | a0001c0001t0002g0067 a0001c0001t0012g0110 a0001c0001t0012g0112 others(35): Show |
38 | HG01069.hp2 HG01243.hp2 HG01993.hp1 others(35): Show |
intron_variant | MODIFIER | c.1372+607delT | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 15/16 | chr3 | 160507499 | |||||||
chr3:160507534 | A | C | 1 | a0001c0001t0001g0227 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1372+573T>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 15/16 | chr3 | 160507534 | |||||||
chr3:160507636 | C | T | 1 | a0001c0001t0001g0242 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1372+471G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 15/16 | chr3 | 160507636 | |||||||
chr3:160507794 | G | T | 1 | a0001c0001t0005g0093 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1372+313C>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 15/16 | chr3 | 160507794 | |||||||
chr3:160508381 | A | C | 1 | a0001c0001t0005g0099 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1210-112T>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 14/16 | chr3 | 160508381 | |||||||
chr3:160508473 | C | T | 1 | a0001c0003t0004g0105 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1210-204G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 14/16 | chr3 | 160508473 | |||||||
chr3:160508519 | C | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0271 |
3 | HG01981.hp1 HG03490.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1210-250G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 14/16 | chr3 | 160508519 | |||||||
chr3:160508587 | AGGAGGCT others(6): Show |
A | 7 | a0001c0003t0004g0107 a0001c0003t0004g0108 a0001c0003t0004g0155 others(4): Show |
7 | HG00099.hp2 HG02738.hp1 HG03669.hp2 others(4): Show |
intron_variant | MODIFIER | c.1210-331_1210-319d others(15): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 14/16 | chr3 | 160508587 | |||||||
chr3:160508678 | GATTT | G | 5 | a0001c0001t0011g0120 a0001c0001t0011g0121 a0001c0001t0011g0122 others(2): Show |
5 | HG01891.hp2 HG02630.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1210-413_1210-410d others(6): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 14/16 | chr3 | 160508678 | |||||||
chr3:160508787 | T | C | 97 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(94): Show |
103 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.1210-518A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 14/16 | chr3 | 160508787 | |||||||
chr3:160508951 | G | C | 1 | a0001c0001t0015g0258 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1210-682C>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 14/16 | chr3 | 160508951 | |||||||
chr3:160509078 | G | A | 6 | a0001c0001t0001g0003 a0001c0001t0001g0169 a0001c0001t0001g0177 others(3): Show |
8 | HG02258.hp2 HG02622.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1209+722C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 14/16 | chr3 | 160509078 | |||||||
chr3:160509170 | C | T | 6 | a0001c0001t0011g0120 a0001c0001t0011g0121 a0001c0001t0011g0122 others(3): Show |
6 | HG01891.hp2 HG02630.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1209+630G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 14/16 | chr3 | 160509170 | |||||||
chr3:160509339 | A | C | 2 | a0001c0001t0022g0126 a0001c0001t0022g0127 |
2 | HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1209+461T>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 14/16 | chr3 | 160509339 | |||||||
chr3:160509432 | T | C | 24 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0016 others(21): Show |
27 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(24): Show |
intron_variant | MODIFIER | c.1209+368A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 14/16 | chr3 | 160509432 | |||||||
chr3:160509660 | G | A | 3 | a0001c0001t0019g0118 a0001c0001t0019g0119 a0001c0001t0033g0117 |
3 | HG00738.hp1 HG01167.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.1209+140C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 14/16 | chr3 | 160509660 | |||||||
chr3:160509690 | C | G | 9 | a0001c0001t0005g0093 a0001c0001t0005g0096 a0001c0001t0005g0097 others(6): Show |
9 | HG01255.hp2 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1209+110G>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 14/16 | chr3 | 160509690 | |||||||
chr3:160509919 | A | C | 12 | a0001c0001t0012g0110 a0001c0001t0012g0112 a0001c0001t0012g0113 others(9): Show |
12 | HG01069.hp2 HG02717.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.1138-48T>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 13/16 | chr3 | 160509919 | |||||||
chr3:160509939 | T | G | 1 | a0001c0002t0009g0130 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1138-68A>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 13/16 | chr3 | 160509939 | |||||||
chr3:160510104 | T | C | 61 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(58): Show |
64 | HG00323.hp2 HG00423.hp1 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.1138-233A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 13/16 | chr3 | 160510104 | |||||||
chr3:160510186 | C | T | 1 | a0001c0001t0001g0260 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1138-315G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 13/16 | chr3 | 160510186 | |||||||
chr3:160510256 | T | C | 6 | a0001c0004t0013g0148 a0001c0004t0013g0149 a0001c0004t0013g0152 others(3): Show |
6 | NA18939.hp2 NA18959.hp2 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.1138-385A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 13/16 | chr3 | 160510256 | |||||||
chr3:160510352 | CATA | C | 88 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(85): Show |
94 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.1138-484_1138-482d others(5): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 13/16 | chr3 | 160510352 | |||||||
chr3:160510421 | G | A | 1 | a0001c0001t0001g0226 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1138-550C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 13/16 | chr3 | 160510421 | |||||||
chr3:160510702 | C | A | 12 | a0001c0001t0012g0110 a0001c0001t0012g0112 a0001c0001t0012g0113 others(9): Show |
12 | HG01069.hp2 HG02717.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.1138-831G>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 13/16 | chr3 | 160510702 | |||||||
chr3:160510763 | C | T | 1 | a0001c0001t0011g0121 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1138-892G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 13/16 | chr3 | 160510763 | |||||||
chr3:160510849 | G | A | 1 | a0001c0001t0003g0021 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1138-978C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 13/16 | chr3 | 160510849 | |||||||
chr3:160510939 | C | T | 61 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(58): Show |
64 | HG00323.hp2 HG00423.hp1 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.1138-1068G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 13/16 | chr3 | 160510939 | |||||||
chr3:160511067 | C | T | 1 | a0001c0001t0001g0232 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1138-1196G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 13/16 | chr3 | 160511067 | |||||||
chr3:160511228 | C | G | 1 | a0001c0001t0052g0211 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1138-1357G>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 13/16 | chr3 | 160511228 | |||||||
chr3:160511329 | T | G | 4 | a0001c0001t0007g0006 a0001c0001t0007g0092 a0001c0001t0007g0094 others(1): Show |
5 | HG01167.hp1 HG01169.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1138-1458A>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 13/16 | chr3 | 160511329 | |||||||
chr3:160511432 | C | A | 1 | a0001c0001t0032g0018 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1138-1561G>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 13/16 | chr3 | 160511432 | |||||||
chr3:160511714 | T | TTATA | 61 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(58): Show |
64 | HG00323.hp2 HG00423.hp1 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.1138-1847_1138-184 others(8): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 13/16 | chr3 | 160511714 | |||||||
chr3:160511714 | T | TTATATA | 53 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0016 others(50): Show |
56 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(53): Show |
intron_variant | MODIFIER | c.1138-1849_1138-184 others(10): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 13/16 | chr3 | 160511714 | |||||||
chr3:160511714 | T | TTATATAT others(1): Show |
6 | a0001c0001t0011g0120 a0001c0001t0011g0121 a0001c0001t0011g0122 others(3): Show |
6 | HG01891.hp2 HG02630.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1138-1851_1138-184 others(12): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 13/16 | chr3 | 160511714 | |||||||
chr3:160511714 | T | TTATATAT others(3): Show |
1 | a0001c0003t0035g0104 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1138-1853_1138-184 others(14): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 13/16 | chr3 | 160511714 | |||||||
chr3:160511720 | A | G | 1 | a0001c0001t0005g0096 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1138-1849T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 13/16 | chr3 | 160511720 | |||||||
chr3:160511729 | T | TATATAA | 3 | a0001c0001t0019g0118 a0001c0001t0019g0119 a0001c0001t0033g0117 |
3 | HG00738.hp1 HG01167.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.1138-1859_1138-185 others(10): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 13/16 | chr3 | 160511729 | |||||||
chr3:160511802 | C | T | 1 | a0001c0002t0010g0134 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1138-1931G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 13/16 | chr3 | 160511802 | |||||||
chr3:160512046 | A | G | 1 | a0002c0005t0004g0156 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1137+2031T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 13/16 | chr3 | 160512046 | |||||||
chr3:160512120 | T | G | 10 | a0001c0001t0008g0285 a0001c0001t0008g0286 a0001c0001t0008g0287 others(7): Show |
10 | HG01433.hp1 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1137+1957A>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 13/16 | chr3 | 160512120 | |||||||
chr3:160512488 | T | A | 8 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0192 others(5): Show |
8 | HG00544.hp2 HG00621.hp1 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.1137+1589A>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 13/16 | chr3 | 160512488 | |||||||
chr3:160512587 | G | A | 27 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0016 others(24): Show |
30 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(27): Show |
intron_variant | MODIFIER | c.1137+1490C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 13/16 | chr3 | 160512587 | |||||||
chr3:160512637 | G | C | 9 | a0001c0003t0004g0105 a0001c0003t0004g0107 a0001c0003t0004g0108 others(6): Show |
9 | HG00099.hp2 HG02738.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.1137+1440C>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 13/16 | chr3 | 160512637 | |||||||
chr3:160512757 | G | A | 1 | a0001c0001t0016g0224 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1137+1320C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 13/16 | chr3 | 160512757 | |||||||
chr3:160512826 | T | TA | 9 | a0001c0003t0004g0105 a0001c0003t0004g0107 a0001c0003t0004g0108 others(6): Show |
9 | HG00099.hp2 HG02738.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.1137+1250dupT | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 13/16 | chr3 | 160512826 | |||||||
chr3:160512876 | C | G | 17 | a0001c0002t0009g0129 a0001c0002t0009g0130 a0001c0002t0009g0138 others(14): Show |
17 | HG01243.hp2 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.1137+1201G>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 13/16 | chr3 | 160512876 | |||||||
chr3:160513106 | G | A | 3 | a0001c0001t0002g0005 a0001c0001t0002g0049 a0001c0001t0002g0058 |
4 | NA18962.hp2 NA19007.hp1 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.1137+971C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 13/16 | chr3 | 160513106 | |||||||
chr3:160513193 | T | C | 10 | a0001c0003t0004g0105 a0001c0003t0004g0107 a0001c0003t0004g0108 others(7): Show |
10 | HG00099.hp2 HG02723.hp1 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.1137+884A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 13/16 | chr3 | 160513193 | |||||||
chr3:160513210 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1137+867A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 13/16 | chr3 | 160513210 | |||||||
chr3:160513249 | G | GT | 62 | a0001c0001t0001g0159 a0001c0001t0001g0167 a0001c0001t0001g0181 others(59): Show |
65 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.1137+827dupA | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 13/16 | chr3 | 160513249 | |||||||
chr3:160513249 | G | GTT | 56 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(53): Show |
59 | HG00323.hp2 HG00423.hp1 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.1137+826_1137+827d others(4): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 13/16 | chr3 | 160513249 | |||||||
chr3:160513249 | G | GTTT | 11 | a0001c0001t0002g0044 a0001c0001t0002g0049 a0001c0001t0002g0050 others(8): Show |
11 | HG01123.hp2 HG01257.hp2 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.1137+825_1137+827d others(5): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 13/16 | chr3 | 160513249 | |||||||
chr3:160513249 | GT | G | 8 | a0001c0001t0001g0192 a0001c0001t0012g0110 a0001c0002t0014g0132 others(5): Show |
8 | HG01069.hp2 HG02897.hp2 NA18939.hp2 others(5): Show |
intron_variant | MODIFIER | c.1137+827delA | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 13/16 | chr3 | 160513249 | |||||||
chr3:160513415 | CA | C | 10 | a0001c0003t0004g0105 a0001c0003t0004g0107 a0001c0003t0004g0108 others(7): Show |
10 | HG00099.hp2 HG02723.hp1 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.1137+661delT | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 13/16 | chr3 | 160513415 | |||||||
chr3:160513453 | T | G | 1 | a0001c0001t0001g0210 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1137+624A>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 13/16 | chr3 | 160513453 | |||||||
chr3:160513580 | G | A | 7 | a0001c0003t0004g0107 a0001c0003t0004g0108 a0001c0003t0004g0155 others(4): Show |
7 | HG00099.hp2 HG02738.hp1 HG03669.hp2 others(4): Show |
intron_variant | MODIFIER | c.1137+497C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 13/16 | chr3 | 160513580 | |||||||
chr3:160513621 | T | C | 3 | a0001c0001t0002g0040 a0001c0001t0002g0041 a0001c0003t0035g0104 |
3 | HG02723.hp1 HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1137+456A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 13/16 | chr3 | 160513621 | |||||||
chr3:160513651 | C | T | 3 | a0001c0001t0018g0282 a0001c0001t0018g0283 a0001c0001t0018g0284 |
3 | HG02622.hp1 HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1137+426G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 13/16 | chr3 | 160513651 | |||||||
chr3:160513945 | T | C | 17 | a0001c0002t0009g0129 a0001c0002t0009g0130 a0001c0002t0009g0138 others(14): Show |
17 | HG01243.hp2 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.1137+132A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 13/16 | chr3 | 160513945 | |||||||
chr3:160514041 | A | G | 9 | a0001c0001t0005g0093 a0001c0001t0005g0096 a0001c0001t0005g0097 others(6): Show |
9 | HG01255.hp2 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1137+36T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 13/16 | chr3 | 160514041 | |||||||
chr3:160514452 | G | A | 61 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(58): Show |
64 | HG00323.hp2 HG00423.hp1 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.1033-271C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 12/16 | chr3 | 160514452 | |||||||
chr3:160514476 | T | C | 1 | a0001c0001t0003g0028 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1033-295A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 12/16 | chr3 | 160514476 | |||||||
chr3:160514513 | T | C | 1 | a0001c0001t0023g0253 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1033-332A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 12/16 | chr3 | 160514513 | |||||||
chr3:160514644 | C | T | 140 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(137): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.1033-463G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 12/16 | chr3 | 160514644 | |||||||
chr3:160514906 | T | C | 1 | a0001c0001t0048g0275 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1032+546A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 12/16 | chr3 | 160514906 | |||||||
chr3:160515006 | T | C | 1 | a0001c0001t0015g0178 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1032+446A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 12/16 | chr3 | 160515006 | |||||||
chr3:160515366 | C | T | 27 | a0001c0002t0009g0129 a0001c0002t0009g0130 a0001c0002t0009g0138 others(24): Show |
27 | HG00099.hp2 HG01243.hp2 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.1032+86G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 12/16 | chr3 | 160515366 | |||||||
chr3:160515616 | T | A | 6 | a0001c0001t0008g0285 a0001c0001t0008g0286 a0001c0001t0008g0287 others(3): Show |
6 | HG02257.hp2 HG02615.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.904-36A>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160515616 | |||||||
chr3:160515618 | C | CT | 13 | a0001c0001t0001g0190 a0001c0001t0001g0244 a0001c0001t0001g0270 others(10): Show |
13 | HG00544.hp2 HG00735.hp2 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.904-39dupA | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160515618 | |||||||
chr3:160515776 | G | A | 2 | a0001c0001t0005g0101 a0001c0001t0005g0102 |
2 | HG01255.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.904-196C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160515776 | |||||||
chr3:160515796 | G | A | 3 | a0001c0001t0003g0021 a0001c0001t0003g0024 a0001c0001t0003g0033 |
3 | HG00140.hp2 HG01106.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.904-216C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160515796 | |||||||
chr3:160515890 | T | C | 1 | a0001c0001t0001g0160 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.904-310A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160515890 | |||||||
chr3:160515897 | G | A | 1 | a0001c0001t0001g0254 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.904-317C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160515897 | |||||||
chr3:160515967 | T | C | 10 | a0001c0001t0002g0004 a0001c0001t0002g0013 a0001c0001t0002g0050 others(7): Show |
11 | HG01433.hp2 HG01952.hp1 HG01981.hp2 others(8): Show |
intron_variant | MODIFIER | c.904-387A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160515967 | |||||||
chr3:160516074 | C | T | 1 | a0001c0001t0005g0093 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.904-494G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160516074 | |||||||
chr3:160516133 | C | T | 18 | a0001c0001t0001g0277 a0001c0002t0009g0129 a0001c0002t0009g0130 others(15): Show |
18 | HG01243.hp2 HG02145.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.904-553G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160516133 | |||||||
chr3:160516255 | G | T | 9 | a0001c0001t0005g0093 a0001c0001t0005g0096 a0001c0001t0005g0097 others(6): Show |
9 | HG01255.hp2 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.904-675C>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160516255 | |||||||
chr3:160516272 | A | G | 1 | a0001c0001t0031g0103 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.904-692T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160516272 | |||||||
chr3:160516281 | T | C | 1 | a0001c0001t0031g0103 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.904-701A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160516281 | |||||||
chr3:160516284 | A | G | 1 | a0001c0001t0031g0103 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.904-704T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160516284 | |||||||
chr3:160516288 | T | G | 1 | a0001c0001t0031g0103 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.904-708A>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160516288 | |||||||
chr3:160516290 | CTCCAAGA others(1570): Show |
C | 1 | a0001c0001t0031g0103 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.904-2287_904-711de others(1): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160516290 | |||||||
chr3:160516442 | T | TA | 63 | a0001c0001t0002g0048 a0001c0001t0002g0066 a0001c0001t0003g0014 others(60): Show |
66 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.904-863dupT | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160516442 | |||||||
chr3:160516442 | T | TAA | 85 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(82): Show |
88 | HG00323.hp2 HG00423.hp1 HG00642.hp1 others(85): Show |
intron_variant | MODIFIER | c.904-864_904-863dup others(2): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160516442 | |||||||
chr3:160516642 | C | T | 2 | a0001c0001t0001g0226 a0001c0001t0001g0229 |
2 | NA19060.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.904-1062G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160516642 | |||||||
chr3:160516699 | G | C | 1 | a0001c0002t0010g0131 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.904-1119C>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160516699 | |||||||
chr3:160516747 | G | A | 1 | a0001c0001t0023g0253 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.904-1167C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160516747 | |||||||
chr3:160516960 | T | G | 148 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(145): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.904-1380A>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160516960 | |||||||
chr3:160517036 | TCA | T | 3 | a0001c0001t0019g0118 a0001c0001t0019g0119 a0001c0001t0033g0117 |
3 | HG00738.hp1 HG01167.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.904-1458_904-1457d others(4): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160517036 | |||||||
chr3:160517287 | A | G | 2 | a0001c0004t0037g0150 a0001c0004t0038g0151 |
2 | NA18939.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.904-1707T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160517287 | |||||||
chr3:160517312 | C | T | 1 | a0001c0001t0023g0253 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.904-1732G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160517312 | |||||||
chr3:160517354 | A | G | 4 | a0001c0004t0013g0148 a0001c0004t0013g0149 a0001c0004t0037g0150 others(1): Show |
4 | NA18939.hp2 NA18959.hp2 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.904-1774T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160517354 | |||||||
chr3:160517471 | T | C | 1 | a0001c0001t0043g0186 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.904-1891A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160517471 | |||||||
chr3:160517506 | T | C | 6 | a0001c0001t0012g0110 a0001c0001t0012g0112 a0001c0001t0012g0113 others(3): Show |
6 | HG01069.hp2 HG02717.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.904-1926A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160517506 | |||||||
chr3:160517608 | A | G | 1 | a0001c0001t0001g0194 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.904-2028T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160517608 | |||||||
chr3:160517646 | T | C | 1 | a0001c0001t0045g0243 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.904-2066A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160517646 | |||||||
chr3:160517769 | C | G | 27 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0016 others(24): Show |
30 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(27): Show |
intron_variant | MODIFIER | c.904-2189G>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160517769 | |||||||
chr3:160517868 | T | C | 1 | a0001c0001t0031g0103 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.904-2288A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160517868 | |||||||
chr3:160517980 | G | A | 1 | a0001c0001t0002g0070 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.904-2400C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160517980 | |||||||
chr3:160518129 | G | GT | 23 | a0001c0001t0001g0190 a0001c0001t0002g0058 a0001c0001t0002g0077 others(20): Show |
23 | HG00544.hp1 HG00544.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.904-2550dupA | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160518129 | |||||||
chr3:160518292 | C | T | 1 | a0001c0001t0002g0128 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.904-2712G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160518292 | |||||||
chr3:160518386 | C | T | 1 | a0001c0001t0046g0185 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.904-2806G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160518386 | |||||||
chr3:160518424 | C | T | 2 | a0001c0001t0002g0040 a0001c0001t0002g0041 |
2 | HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.904-2844G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160518424 | |||||||
chr3:160518585 | C | T | 1 | a0001c0001t0049g0207 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.904-3005G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160518585 | |||||||
chr3:160518724 | G | A | 1 | a0001c0001t0001g0237 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.903+3055C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160518724 | |||||||
chr3:160518868 | C | A | 3 | a0001c0001t0018g0282 a0001c0001t0018g0283 a0001c0001t0018g0284 |
3 | HG02622.hp1 HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.903+2911G>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160518868 | |||||||
chr3:160518870 | A | C | 25 | a0001c0001t0001g0003 a0001c0001t0001g0169 a0001c0001t0001g0177 others(22): Show |
27 | HG01243.hp2 HG01993.hp2 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.903+2909T>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160518870 | |||||||
chr3:160519075 | G | T | 1 | a0001c0001t0040g0125 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.903+2704C>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160519075 | |||||||
chr3:160519084 | ATC | A | 24 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0016 others(21): Show |
27 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(24): Show |
intron_variant | MODIFIER | c.903+2693_903+2694d others(4): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160519084 | |||||||
chr3:160519199 | A | G | 1 | a0001c0002t0027g0143 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.903+2580T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160519199 | |||||||
chr3:160519309 | G | T | 2 | a0001c0001t0022g0126 a0001c0001t0022g0127 |
2 | HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.903+2470C>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160519309 | |||||||
chr3:160519401 | T | C | 1 | a0001c0001t0006g0031 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.903+2378A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160519401 | |||||||
chr3:160519560 | T | C | 154 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(151): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.903+2219A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160519560 | |||||||
chr3:160519598 | T | C | 2 | a0001c0001t0001g0213 a0001c0001t0001g0215 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.903+2181A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160519598 | |||||||
chr3:160519621 | C | T | 1 | a0001c0002t0042g0142 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.903+2158G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160519621 | |||||||
chr3:160519652 | G | A | 1 | a0001c0001t0001g0248 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.903+2127C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160519652 | |||||||
chr3:160519657 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.903+2122G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160519657 | |||||||
chr3:160519663 | T | C | 139 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(136): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.903+2116A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160519663 | |||||||
chr3:160519672 | G | A | 1 | a0001c0001t0017g0267 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.903+2107C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160519672 | |||||||
chr3:160519712 | G | A | 1 | a0001c0001t0002g0038 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.903+2067C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160519712 | |||||||
chr3:160519749 | T | G | 1 | a0001c0001t0022g0127 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.903+2030A>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160519749 | |||||||
chr3:160519801 | C | CA | 22 | a0001c0001t0001g0164 a0001c0001t0001g0172 a0001c0001t0001g0180 others(19): Show |
22 | HG00609.hp2 HG01981.hp1 HG02056.hp1 others(19): Show |
intron_variant | MODIFIER | c.903+1977dupT | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160519801 | |||||||
chr3:160519801 | C | CAAAAAA | 7 | a0001c0001t0012g0112 a0001c0001t0012g0113 a0001c0004t0013g0149 others(4): Show |
7 | HG02886.hp1 HG03471.hp1 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.903+1972_903+1977d others(8): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160519801 | |||||||
chr3:160519801 | C | CAAAAAAA others(6): Show |
1 | a0001c0001t0031g0103 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.903+1965_903+1977d others(15): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160519801 | |||||||
chr3:160519801 | C | CAAAAAAA others(7): Show |
2 | a0001c0003t0004g0107 a0001c0003t0036g0106 |
2 | HG00099.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.903+1964_903+1977d others(16): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160519801 | |||||||
chr3:160519801 | C | CAAAAAAA others(8): Show |
3 | a0001c0003t0004g0105 a0001c0003t0004g0108 a0001c0003t0004g0109 |
3 | HG02738.hp1 HG02976.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.903+1963_903+1977d others(17): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160519801 | |||||||
chr3:160519801 | C | CAAAAAAA others(13): Show |
1 | a0001c0003t0004g0157 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.903+1958_903+1977d others(22): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160519801 | |||||||
chr3:160519801 | C | CAAAAAAA others(15): Show |
1 | a0001c0003t0004g0155 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.903+1956_903+1977d others(24): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160519801 | |||||||
chr3:160519801 | C | CAAAAAAA others(18): Show |
1 | a0001c0003t0004g0158 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.903+1953_903+1977d others(27): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160519801 | |||||||
chr3:160519801 | CAA | C | 8 | a0001c0001t0005g0093 a0001c0001t0005g0096 a0001c0001t0005g0097 others(5): Show |
8 | HG01255.hp2 HG01891.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.903+1976_903+1977d others(4): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160519801 | |||||||
chr3:160519801 | CAAA | C | 36 | a0001c0001t0002g0042 a0001c0001t0002g0061 a0001c0001t0002g0077 others(33): Show |
36 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(33): Show |
intron_variant | MODIFIER | c.903+1975_903+1977d others(5): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160519801 | |||||||
chr3:160519801 | CAAAA | C | 60 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(57): Show |
66 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.903+1974_903+1977d others(6): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160519801 | |||||||
chr3:160519801 | CAAAAA | C | 17 | a0001c0001t0002g0128 a0001c0002t0009g0129 a0001c0002t0009g0130 others(14): Show |
17 | HG01243.hp2 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.903+1973_903+1977d others(7): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160519801 | |||||||
chr3:160519864 | A | G | 1 | a0001c0001t0002g0039 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.903+1915T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160519864 | |||||||
chr3:160520253 | T | G | 12 | a0001c0001t0012g0110 a0001c0001t0012g0112 a0001c0001t0012g0113 others(9): Show |
12 | HG01069.hp2 HG02717.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.903+1526A>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160520253 | |||||||
chr3:160520256 | C | CT | 7 | a0001c0003t0004g0107 a0001c0003t0004g0108 a0001c0003t0004g0155 others(4): Show |
7 | HG00099.hp2 HG02738.hp1 HG03669.hp2 others(4): Show |
intron_variant | MODIFIER | c.903+1522dupA | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160520256 | |||||||
chr3:160520418 | A | AT | 11 | a0001c0001t0001g0193 a0001c0001t0001g0195 a0001c0001t0003g0014 others(8): Show |
11 | HG00621.hp1 HG01891.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.903+1360dupA | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160520418 | |||||||
chr3:160520549 | C | T | 12 | a0001c0001t0001g0165 a0001c0001t0001g0173 a0001c0001t0001g0174 others(9): Show |
12 | HG00609.hp2 HG00673.hp2 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.903+1230G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160520549 | |||||||
chr3:160520622 | AG | A | 57 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(54): Show |
60 | HG00323.hp2 HG00423.hp1 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.903+1156delC | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160520622 | |||||||
chr3:160520776 | C | A | 6 | a0001c0001t0011g0120 a0001c0001t0011g0121 a0001c0001t0011g0122 others(3): Show |
6 | HG01891.hp2 HG02630.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.903+1003G>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160520776 | |||||||
chr3:160521590 | G | C | 1 | a0001c0002t0010g0136 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.903+189C>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160521590 | |||||||
chr3:160521755 | T | A | 1 | a0001c0001t0017g0267 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.903+24A>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 11/16 | chr3 | 160521755 | |||||||
chr3:160521997 | C | T | 1 | a0001c0001t0002g0079 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.772-87G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 10/16 | chr3 | 160521997 | |||||||
chr3:160522050 | C | T | 1 | a0001c0001t0002g0043 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.772-140G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 10/16 | chr3 | 160522050 | |||||||
chr3:160522055 | C | T | 1 | a0001c0001t0002g0007 | 2 | HG01346.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.772-145G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 10/16 | chr3 | 160522055 | |||||||
chr3:160522067 | T | C | 3 | a0001c0001t0018g0282 a0001c0001t0018g0283 a0001c0001t0018g0284 |
3 | HG02622.hp1 HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.772-157A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 10/16 | chr3 | 160522067 | |||||||
chr3:160522068 | C | T | 1 | a0001c0001t0002g0062 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.772-158G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 10/16 | chr3 | 160522068 | |||||||
chr3:160522296 | G | A | 6 | a0001c0001t0012g0110 a0001c0001t0012g0112 a0001c0001t0012g0113 others(3): Show |
6 | HG01069.hp2 HG02717.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.772-386C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 10/16 | chr3 | 160522296 | |||||||
chr3:160522527 | G | A | 2 | a0001c0001t0022g0126 a0001c0001t0022g0127 |
2 | HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.772-617C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 10/16 | chr3 | 160522527 | |||||||
chr3:160522579 | T | C | 6 | a0001c0001t0012g0110 a0001c0001t0012g0112 a0001c0001t0012g0113 others(3): Show |
6 | HG01069.hp2 HG02717.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.772-669A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 10/16 | chr3 | 160522579 | |||||||
chr3:160522709 | C | T | 2 | a0001c0001t0001g0193 a0001c0001t0001g0196 |
2 | NA18945.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.772-799G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 10/16 | chr3 | 160522709 | |||||||
chr3:160522710 | G | A | 6 | a0001c0001t0002g0062 a0001c0001t0002g0063 a0001c0001t0002g0068 others(3): Show |
6 | HG00735.hp1 HG01070.hp1 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.772-800C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 10/16 | chr3 | 160522710 | |||||||
chr3:160522746 | C | T | 7 | a0001c0003t0004g0107 a0001c0003t0004g0108 a0001c0003t0004g0155 others(4): Show |
7 | HG00099.hp2 HG02738.hp1 HG03669.hp2 others(4): Show |
intron_variant | MODIFIER | c.772-836G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 10/16 | chr3 | 160522746 | |||||||
chr3:160522883 | G | GA | 147 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(144): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.772-974dupT | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 10/16 | chr3 | 160522883 | |||||||
chr3:160522883 | G | GAA | 8 | a0001c0001t0002g0083 a0001c0001t0003g0029 a0001c0001t0012g0110 others(5): Show |
8 | HG01069.hp2 HG01361.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.772-975_772-974dup others(2): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 10/16 | chr3 | 160522883 | |||||||
chr3:160523160 | A | G | 1 | a0001c0002t0027g0143 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.772-1250T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 10/16 | chr3 | 160523160 | |||||||
chr3:160523300 | G | A | 27 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0016 others(24): Show |
30 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(27): Show |
intron_variant | MODIFIER | c.772-1390C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 10/16 | chr3 | 160523300 | |||||||
chr3:160523542 | G | T | 1 | a0001c0001t0031g0103 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.772-1632C>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 10/16 | chr3 | 160523542 | |||||||
chr3:160523562 | C | T | 12 | a0001c0001t0012g0110 a0001c0001t0012g0112 a0001c0001t0012g0113 others(9): Show |
12 | HG01069.hp2 HG02717.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.772-1652G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 10/16 | chr3 | 160523562 | |||||||
chr3:160523658 | G | T | 61 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(58): Show |
64 | HG00323.hp2 HG00423.hp1 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.772-1748C>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 10/16 | chr3 | 160523658 | |||||||
chr3:160523787 | G | A | 5 | a0001c0001t0011g0120 a0001c0001t0011g0121 a0001c0001t0011g0122 others(2): Show |
5 | HG01891.hp2 HG02630.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.772-1877C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 10/16 | chr3 | 160523787 | |||||||
chr3:160523869 | A | G | 149 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(146): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.771+1931T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 10/16 | chr3 | 160523869 | |||||||
chr3:160523886 | G | C | 124 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(121): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.771+1914C>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 10/16 | chr3 | 160523886 | |||||||
chr3:160523906 | A | T | 2 | a0001c0001t0001g0195 a0001c0001t0046g0185 |
2 | HG00621.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.771+1894T>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 10/16 | chr3 | 160523906 | |||||||
chr3:160524132 | T | C | 10 | a0001c0003t0004g0105 a0001c0003t0004g0107 a0001c0003t0004g0108 others(7): Show |
10 | HG00099.hp2 HG02723.hp1 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.771+1668A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 10/16 | chr3 | 160524132 | |||||||
chr3:160524704 | T | C | 1 | a0001c0001t0001g0173 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.771+1096A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 10/16 | chr3 | 160524704 | |||||||
chr3:160524753 | C | T | 1 | a0001c0001t0001g0276 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.771+1047G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 10/16 | chr3 | 160524753 | |||||||
chr3:160524755 | A | T | 1 | a0001c0001t0001g0276 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.771+1045T>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 10/16 | chr3 | 160524755 | |||||||
chr3:160524848 | T | A | 4 | a0001c0001t0001g0219 a0001c0001t0001g0234 a0001c0001t0001g0235 others(1): Show |
4 | HG01361.hp1 HG02148.hp1 NA18940.hp2 others(1): Show |
intron_variant | MODIFIER | c.771+952A>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 10/16 | chr3 | 160524848 | |||||||
chr3:160525386 | TTG | T | 107 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(104): Show |
113 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.771+412_771+413del others(2): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 10/16 | chr3 | 160525386 | |||||||
chr3:160525396 | T | C | 1 | a0001c0001t0040g0125 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.771+404A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 10/16 | chr3 | 160525396 | |||||||
chr3:160525414 | C | T | 1 | a0001c0001t0001g0255 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.771+386G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 10/16 | chr3 | 160525414 | |||||||
chr3:160525537 | A | G | 3 | a0001c0001t0003g0021 a0001c0001t0003g0024 a0001c0001t0003g0033 |
3 | HG00140.hp2 HG01106.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.771+263T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 10/16 | chr3 | 160525537 | |||||||
chr3:160525590 | G | A | 2 | a0001c0001t0002g0076 a0001c0001t0002g0090 |
2 | HG00735.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.771+210C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 10/16 | chr3 | 160525590 | |||||||
chr3:160525893 | T | C | 1 | a0001c0001t0002g0079 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.726+45A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 9/16 | chr3 | 160525893 | |||||||
chr3:160525921 | T | G | 1 | a0001c0001t0001g0255 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.726+17A>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 9/16 | chr3 | 160525921 | |||||||
chr3:160526166 | A | G | 2 | a0001c0001t0003g0029 a0001c0001t0003g0030 |
2 | HG01361.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.557-59T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 8/16 | chr3 | 160526166 | |||||||
chr3:160526184 | A | T | 1 | a0001c0001t0001g0219 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.557-77T>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 8/16 | chr3 | 160526184 | |||||||
chr3:160526199 | G | C | 2 | a0001c0001t0001g0190 a0001c0001t0001g0191 |
2 | HG00544.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.557-92C>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 8/16 | chr3 | 160526199 | |||||||
chr3:160526201 | A | T | 2 | a0001c0001t0001g0190 a0001c0001t0001g0191 |
2 | HG00544.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.557-94T>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 8/16 | chr3 | 160526201 | |||||||
chr3:160526285 | A | G | 285 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(282): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.557-178T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 8/16 | chr3 | 160526285 | |||||||
chr3:160526299 | C | T | 2 | a0001c0001t0022g0126 a0001c0001t0022g0127 |
2 | HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.557-192G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 8/16 | chr3 | 160526299 | |||||||
chr3:160526316 | C | T | 1 | a0001c0001t0018g0283 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.557-209G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 8/16 | chr3 | 160526316 | |||||||
chr3:160526585 | C | T | 3 | a0001c0001t0019g0118 a0001c0001t0019g0119 a0001c0001t0033g0117 |
3 | HG00738.hp1 HG01167.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.557-478G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 8/16 | chr3 | 160526585 | |||||||
chr3:160526765 | A | T | 4 | a0001c0001t0007g0006 a0001c0001t0007g0092 a0001c0001t0007g0094 others(1): Show |
5 | HG01167.hp1 HG01169.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.557-658T>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 8/16 | chr3 | 160526765 | |||||||
chr3:160526950 | T | C | 1 | a0001c0001t0002g0005 | 2 | NA18962.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.557-843A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 8/16 | chr3 | 160526950 | |||||||
chr3:160526954 | A | G | 1 | a0001c0001t0040g0125 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.557-847T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 8/16 | chr3 | 160526954 | |||||||
chr3:160527004 | C | T | 24 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0016 others(21): Show |
27 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(24): Show |
intron_variant | MODIFIER | c.557-897G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 8/16 | chr3 | 160527004 | |||||||
chr3:160527174 | A | G | 1 | a0001c0003t0004g0107 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.556+779T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 8/16 | chr3 | 160527174 | |||||||
chr3:160527552 | G | A | 1 | a0001c0001t0001g0248 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.556+401C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 8/16 | chr3 | 160527552 | |||||||
chr3:160527621 | T | C | 2 | a0001c0001t0008g0285 a0001c0001t0008g0290 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.556+332A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 8/16 | chr3 | 160527621 | |||||||
chr3:160527765 | A | G | 8 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0192 others(5): Show |
8 | HG00544.hp2 HG00621.hp1 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.556+188T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 8/16 | chr3 | 160527765 | |||||||
chr3:160527944 | T | A | 1 | a0001c0001t0001g0255 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.556+9A>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 8/16 | chr3 | 160527944 | |||||||
chr3:160528057 | A | G | 9 | a0001c0001t0011g0120 a0001c0001t0011g0121 a0001c0001t0011g0122 others(6): Show |
9 | HG00738.hp1 HG01167.hp2 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.470-18T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 7/16 | chr3 | 160528057 | |||||||
chr3:160528160 | A | G | 154 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(151): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.470-121T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 7/16 | chr3 | 160528160 | |||||||
chr3:160528186 | T | G | 1 | a0001c0001t0031g0103 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.470-147A>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 7/16 | chr3 | 160528186 | |||||||
chr3:160528192 | C | T | 122 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(119): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.470-153G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 7/16 | chr3 | 160528192 | |||||||
chr3:160528334 | G | A | 149 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(146): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.470-295C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 7/16 | chr3 | 160528334 | |||||||
chr3:160528353 | A | G | 1 | a0001c0001t0052g0211 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.470-314T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 7/16 | chr3 | 160528353 | |||||||
chr3:160528376 | G | GT | 5 | a0001c0001t0001g0266 a0001c0001t0016g0224 a0001c0001t0016g0240 others(2): Show |
5 | HG00544.hp1 HG02056.hp2 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.470-338dupA | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 7/16 | chr3 | 160528376 | |||||||
chr3:160528417 | G | A | 1 | a0001c0001t0002g0071 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.470-378C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 7/16 | chr3 | 160528417 | |||||||
chr3:160528651 | C | T | 2 | a0001c0001t0006g0031 a0001c0001t0032g0018 |
2 | HG00558.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.470-612G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 7/16 | chr3 | 160528651 | |||||||
chr3:160529053 | T | A | 3 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0168 |
3 | HG02559.hp2 HG02818.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.470-1014A>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 7/16 | chr3 | 160529053 | |||||||
chr3:160529334 | A | G | 1 | a0001c0001t0040g0125 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.470-1295T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 7/16 | chr3 | 160529334 | |||||||
chr3:160529346 | G | T | 2 | a0001c0001t0001g0171 a0001c0001t0001g0172 |
2 | HG02257.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.470-1307C>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 7/16 | chr3 | 160529346 | |||||||
chr3:160529419 | C | T | 6 | a0001c0001t0001g0003 a0001c0001t0001g0169 a0001c0001t0001g0177 others(3): Show |
8 | HG02258.hp2 HG02622.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.470-1380G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 7/16 | chr3 | 160529419 | |||||||
chr3:160529515 | G | A | 2 | a0001c0003t0004g0155 a0002c0005t0004g0156 |
2 | HG03669.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.469+1340C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 7/16 | chr3 | 160529515 | |||||||
chr3:160529563 | AATTAGTG others(2): Show |
A | 10 | a0001c0003t0004g0105 a0001c0003t0004g0107 a0001c0003t0004g0108 others(7): Show |
10 | HG00099.hp2 HG02723.hp1 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.469+1283_469+1291d others(11): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 7/16 | chr3 | 160529563 | |||||||
chr3:160529722 | A | G | 1 | a0001c0001t0001g0200 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.469+1133T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 7/16 | chr3 | 160529722 | |||||||
chr3:160529778 | G | GA | 9 | a0001c0001t0005g0093 a0001c0001t0005g0096 a0001c0001t0005g0097 others(6): Show |
9 | HG01255.hp2 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.469+1076dupT | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 7/16 | chr3 | 160529778 | |||||||
chr3:160529851 | C | T | 5 | a0001c0001t0011g0120 a0001c0001t0011g0121 a0001c0001t0011g0122 others(2): Show |
5 | HG01891.hp2 HG02630.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.469+1004G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 7/16 | chr3 | 160529851 | |||||||
chr3:160529896 | G | A | 1 | a0001c0001t0052g0211 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.469+959C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 7/16 | chr3 | 160529896 | |||||||
chr3:160529951 | C | T | 3 | a0001c0001t0019g0118 a0001c0001t0019g0119 a0001c0001t0033g0117 |
3 | HG00738.hp1 HG01167.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.469+904G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 7/16 | chr3 | 160529951 | |||||||
chr3:160530034 | C | T | 11 | a0001c0001t0001g0223 a0001c0003t0004g0105 a0001c0003t0004g0107 others(8): Show |
11 | HG00099.hp2 HG01069.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.469+821G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 7/16 | chr3 | 160530034 | |||||||
chr3:160530134 | C | CA | 31 | a0001c0001t0001g0167 a0001c0001t0001g0177 a0001c0001t0001g0180 others(28): Show |
32 | HG00609.hp1 HG00609.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.469+720dupT | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 7/16 | chr3 | 160530134 | |||||||
chr3:160530134 | CA | C | 11 | a0001c0001t0001g0187 a0001c0001t0001g0213 a0001c0001t0001g0231 others(8): Show |
11 | HG00099.hp2 HG01257.hp1 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.469+720delT | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 7/16 | chr3 | 160530134 | |||||||
chr3:160530134 | CAAAAAAA others(8): Show |
C | 9 | a0001c0001t0001g0164 a0001c0001t0001g0205 a0001c0001t0001g0206 others(6): Show |
9 | HG01243.hp1 HG02145.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.469+706_469+720del others(15): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 7/16 | chr3 | 160530134 | |||||||
chr3:160530507 | C | G | 1 | a0001c0001t0049g0207 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.469+348G>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 7/16 | chr3 | 160530507 | |||||||
chr3:160530694 | T | G | 1 | a0001c0001t0002g0084 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.469+161A>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 7/16 | chr3 | 160530694 | |||||||
chr3:160530738 | C | G | 2 | a0001c0002t0009g0138 a0001c0002t0009g0139 |
2 | HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.469+117G>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 7/16 | chr3 | 160530738 | |||||||
chr3:160530769 | T | G | 2 | a0001c0001t0003g0014 a0001c0001t0003g0016 |
2 | HG03688.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.469+86A>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 7/16 | chr3 | 160530769 | |||||||
chr3:160530815 | T | TA | 4 | a0001c0001t0007g0006 a0001c0001t0007g0092 a0001c0001t0007g0094 others(1): Show |
5 | HG01167.hp1 HG01169.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.469+39dupT | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 7/16 | chr3 | 160530815 | |||||||
chr3:160531442 | A | T | 2 | a0001c0001t0001g0266 a0001c0001t0002g0074 |
2 | HG02055.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.383+20T>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 6/16 | chr3 | 160531442 | |||||||
chr3:160531443 | A | T | 9 | a0001c0003t0004g0105 a0001c0003t0004g0107 a0001c0003t0004g0108 others(6): Show |
9 | HG00099.hp2 HG02738.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.383+19T>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 6/16 | chr3 | 160531443 | |||||||
chr3:160531637 | A | G | 6 | a0001c0001t0011g0120 a0001c0001t0011g0121 a0001c0001t0011g0122 others(3): Show |
6 | HG01891.hp2 HG02630.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.288-80T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 5/16 | chr3 | 160531637 | |||||||
chr3:160531664 | A | G | 2 | a0001c0001t0019g0118 a0001c0001t0019g0119 |
2 | HG00738.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.288-107T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 5/16 | chr3 | 160531664 | |||||||
chr3:160531722 | A | G | 3 | a0001c0001t0018g0282 a0001c0001t0018g0283 a0001c0001t0018g0284 |
3 | HG02622.hp1 HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.288-165T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 5/16 | chr3 | 160531722 | |||||||
chr3:160531744 | T | C | 1 | a0001c0001t0028g0116 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.288-187A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 5/16 | chr3 | 160531744 | |||||||
chr3:160531941 | C | A | 1 | a0001c0001t0001g0168 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.288-384G>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 5/16 | chr3 | 160531941 | |||||||
chr3:160532087 | T | C | 6 | a0001c0001t0001g0003 a0001c0001t0001g0169 a0001c0001t0001g0177 others(3): Show |
8 | HG02258.hp2 HG02622.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.288-530A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 5/16 | chr3 | 160532087 | |||||||
chr3:160532229 | G | T | 1 | a0001c0001t0001g0245 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.288-672C>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 5/16 | chr3 | 160532229 | |||||||
chr3:160532349 | A | G | 12 | a0001c0001t0012g0110 a0001c0001t0012g0112 a0001c0001t0012g0113 others(9): Show |
12 | HG01069.hp2 HG02717.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.288-792T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 5/16 | chr3 | 160532349 | |||||||
chr3:160532460 | T | C | 1 | a0001c0001t0001g0244 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.288-903A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 5/16 | chr3 | 160532460 | |||||||
chr3:160532656 | C | T | 1 | a0001c0001t0001g0273 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.288-1099G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 5/16 | chr3 | 160532656 | |||||||
chr3:160532772 | C | A | 2 | a0001c0001t0002g0076 a0001c0001t0002g0090 |
2 | HG00735.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.288-1215G>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 5/16 | chr3 | 160532772 | |||||||
chr3:160532773 | T | A | 2 | a0001c0001t0002g0076 a0001c0001t0002g0090 |
2 | HG00735.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.288-1216A>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 5/16 | chr3 | 160532773 | |||||||
chr3:160532892 | C | G | 12 | a0001c0001t0012g0110 a0001c0001t0012g0112 a0001c0001t0012g0113 others(9): Show |
12 | HG01069.hp2 HG02717.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.288-1335G>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 5/16 | chr3 | 160532892 | |||||||
chr3:160532908 | C | T | 3 | a0001c0001t0019g0118 a0001c0001t0019g0119 a0001c0001t0033g0117 |
3 | HG00738.hp1 HG01167.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.288-1351G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 5/16 | chr3 | 160532908 | |||||||
chr3:160533082 | G | C | 1 | a0001c0001t0015g0178 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.288-1525C>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 5/16 | chr3 | 160533082 | |||||||
chr3:160533092 | T | C | 124 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(121): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.288-1535A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 5/16 | chr3 | 160533092 | |||||||
chr3:160533103 | A | G | 12 | a0001c0001t0012g0110 a0001c0001t0012g0112 a0001c0001t0012g0113 others(9): Show |
12 | HG01069.hp2 HG02717.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.288-1546T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 5/16 | chr3 | 160533103 | |||||||
chr3:160533166 | G | A | 2 | a0001c0001t0022g0126 a0001c0001t0022g0127 |
2 | HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.288-1609C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 5/16 | chr3 | 160533166 | |||||||
chr3:160533228 | C | T | 4 | a0001c0001t0007g0006 a0001c0001t0007g0092 a0001c0001t0007g0094 others(1): Show |
5 | HG01167.hp1 HG01169.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.288-1671G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 5/16 | chr3 | 160533228 | |||||||
chr3:160533276 | C | T | 1 | a0001c0001t0017g0267 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.288-1719G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 5/16 | chr3 | 160533276 | |||||||
chr3:160533359 | A | T | 1 | a0001c0001t0002g0070 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.288-1802T>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 5/16 | chr3 | 160533359 | |||||||
chr3:160533448 | T | A | 87 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(84): Show |
93 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.288-1891A>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 5/16 | chr3 | 160533448 | |||||||
chr3:160533542 | T | A | 6 | a0001c0001t0001g0003 a0001c0001t0001g0169 a0001c0001t0001g0177 others(3): Show |
8 | HG02258.hp2 HG02622.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.287+1971A>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 5/16 | chr3 | 160533542 | |||||||
chr3:160533563 | G | A | 1 | a0001c0001t0001g0238 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.287+1950C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 5/16 | chr3 | 160533563 | |||||||
chr3:160533749 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.287+1764C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 5/16 | chr3 | 160533749 | |||||||
chr3:160534457 | C | T | 1 | a0001c0001t0001g0245 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.287+1056G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 5/16 | chr3 | 160534457 | |||||||
chr3:160534674 | G | A | 1 | a0001c0001t0001g0248 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.287+839C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 5/16 | chr3 | 160534674 | |||||||
chr3:160534695 | C | T | 2 | a0001c0001t0006g0019 a0001c0001t0020g0064 |
2 | HG02074.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.287+818G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 5/16 | chr3 | 160534695 | |||||||
chr3:160534714 | C | T | 1 | a0001c0001t0001g0266 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.287+799G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 5/16 | chr3 | 160534714 | |||||||
chr3:160534718 | G | GAAAAAAA others(3): Show |
21 | a0001c0001t0012g0110 a0001c0001t0012g0114 a0001c0001t0012g0115 others(18): Show |
21 | HG01069.hp2 HG01243.hp2 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.287+785_287+794dup others(10): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 5/16 | chr3 | 160534718 | |||||||
chr3:160534718 | G | GAAAAAAA others(4): Show |
69 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(66): Show |
72 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.287+784_287+794dup others(11): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 5/16 | chr3 | 160534718 | |||||||
chr3:160534718 | G | GAAAAAAA others(5): Show |
13 | a0001c0001t0002g0042 a0001c0001t0002g0046 a0001c0001t0002g0048 others(10): Show |
13 | HG00738.hp1 HG01109.hp1 HG01978.hp2 others(10): Show |
intron_variant | MODIFIER | c.287+783_287+794dup others(12): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 5/16 | chr3 | 160534718 | |||||||
chr3:160534718 | G | GAAAAAAA others(6): Show |
14 | a0001c0001t0003g0020 a0001c0001t0003g0032 a0001c0001t0003g0033 others(11): Show |
17 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(14): Show |
intron_variant | MODIFIER | c.287+782_287+794dup others(13): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 5/16 | chr3 | 160534718 | |||||||
chr3:160534718 | G | GAAAAAAA others(7): Show |
16 | a0001c0001t0003g0014 a0001c0001t0003g0016 a0001c0001t0003g0017 others(13): Show |
16 | HG00140.hp2 HG00741.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.287+781_287+794dup others(14): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 5/16 | chr3 | 160534718 | |||||||
chr3:160534718 | G | GAAAAAAA others(8): Show |
6 | a0001c0001t0003g0015 a0001c0001t0003g0025 a0001c0001t0003g0028 others(3): Show |
6 | HG00735.hp2 HG01169.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.287+780_287+794dup others(15): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 5/16 | chr3 | 160534718 | |||||||
chr3:160534718 | G | GAAAAAAA others(9): Show |
1 | a0001c0001t0003g0027 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.287+779_287+794dup others(16): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 5/16 | chr3 | 160534718 | |||||||
chr3:160534776 | A | T | 1 | a0001c0001t0001g0222 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.287+737T>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 5/16 | chr3 | 160534776 | |||||||
chr3:160534973 | C | T | 1 | a0001c0002t0009g0130 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.287+540G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 5/16 | chr3 | 160534973 | |||||||
chr3:160534979 | C | T | 1 | a0001c0001t0031g0103 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.287+534G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 5/16 | chr3 | 160534979 | |||||||
chr3:160534982 | A | G | 1 | a0001c0001t0040g0125 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.287+531T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 5/16 | chr3 | 160534982 | |||||||
chr3:160535206 | A | G | 1 | a0001c0001t0001g0231 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.287+307T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 5/16 | chr3 | 160535206 | |||||||
chr3:160535475 | G | A | 9 | a0001c0003t0004g0105 a0001c0003t0004g0107 a0001c0003t0004g0108 others(6): Show |
9 | HG00099.hp2 HG02738.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.287+38C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 5/16 | chr3 | 160535475 | |||||||
chr3:160535605 | G | A | 1 | a0001c0004t0013g0153 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.235-40C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 4/16 | chr3 | 160535605 | |||||||
chr3:160535693 | G | A | 1 | a0001c0001t0040g0125 | 1 | HG02486.hp2 | splice_region_variant&intron_variant | LOW | c.205-3C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 3/16 | chr3 | 160535693 | |||||||
chr3:160535900 | T | TA | 115 | a0001c0001t0001g0173 a0001c0001t0001g0177 a0001c0001t0001g0179 others(112): Show |
121 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(118): Show |
splice_region_variant&intron_variant | LOW | c.115-4dupT | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 2/16 | chr3 | 160535900 | |||||||
chr3:160535900 | T | TAA | 28 | a0001c0001t0001g0011 a0001c0001t0001g0271 a0001c0001t0002g0042 others(25): Show |
29 | HG00738.hp1 HG01069.hp2 HG01109.hp1 others(26): Show |
splice_region_variant&intron_variant | LOW | c.115-5_115-4dupTT | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 2/16 | chr3 | 160535900 | |||||||
chr3:160535900 | T | TAAA | 17 | a0001c0001t0011g0120 a0001c0001t0011g0121 a0001c0001t0011g0122 others(14): Show |
17 | HG01891.hp2 HG02451.hp1 HG02630.hp2 others(14): Show |
splice_region_variant&intron_variant | LOW | c.115-6_115-4dupTTT | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 2/16 | chr3 | 160535900 | |||||||
chr3:160535900 | TA | T | 12 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0001g0270 others(9): Show |
12 | HG01167.hp1 HG02615.hp1 HG02809.hp1 others(9): Show |
splice_region_variant&intron_variant | LOW | c.115-4delT | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 2/16 | chr3 | 160535900 | |||||||
chr3:160535941 | G | A | 24 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0016 others(21): Show |
27 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(24): Show |
intron_variant | MODIFIER | c.115-44C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 2/16 | chr3 | 160535941 | |||||||
chr3:160536076 | G | T | 1 | a0001c0001t0002g0078 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.115-179C>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 2/16 | chr3 | 160536076 | |||||||
chr3:160536161 | A | C | 4 | a0001c0001t0001g0221 a0001c0001t0001g0239 a0001c0001t0001g0250 others(1): Show |
4 | NA18947.hp2 NA18969.hp2 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.115-264T>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 2/16 | chr3 | 160536161 | |||||||
chr3:160536494 | G | A | 1 | a0001c0001t0002g0070 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.114+302C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 2/16 | chr3 | 160536494 | |||||||
chr3:160536537 | G | C | 1 | a0001c0001t0001g0273 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.114+259C>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 2/16 | chr3 | 160536537 | |||||||
chr3:160537156 | CCCTCATA others(45): Show |
C | 1 | a0001c0001t0033g0117 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.70-368_70-317delTA others(50): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160537156 | |||||||
chr3:160537172 | T | C | 1 | a0001c0001t0040g0125 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.70-332A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160537172 | |||||||
chr3:160537427 | C | T | 1 | a0001c0001t0040g0125 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.70-587G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160537427 | |||||||
chr3:160537679 | A | G | 3 | a0001c0001t0001g0230 a0001c0001t0001g0259 a0001c0001t0001g0260 |
3 | NA18943.hp1 NA18971.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.70-839T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160537679 | |||||||
chr3:160537685 | G | A | 1 | a0001c0001t0002g0039 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.70-845C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160537685 | |||||||
chr3:160537742 | G | A | 5 | a0001c0001t0011g0120 a0001c0001t0011g0121 a0001c0001t0011g0122 others(2): Show |
5 | HG01891.hp2 HG02630.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.70-902C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160537742 | |||||||
chr3:160537917 | T | C | 149 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(146): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.70-1077A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160537917 | |||||||
chr3:160537982 | T | A | 24 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(21): Show |
24 | HG00544.hp2 HG00558.hp2 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.70-1142A>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160537982 | |||||||
chr3:160537995 | A | G | 1 | a0001c0001t0002g0039 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.70-1155T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160537995 | |||||||
chr3:160538009 | G | C | 1 | a0001c0001t0048g0275 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.70-1169C>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160538009 | |||||||
chr3:160538133 | G | A | 1 | a0001c0001t0033g0117 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.70-1293C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160538133 | |||||||
chr3:160538133 | GTATGTAT others(11): Show |
G | 1 | a0001c0001t0002g0043 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.70-1311_70-1294del others(18): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160538133 | |||||||
chr3:160538147 | A | ATG | 5 | a0001c0001t0011g0120 a0001c0001t0011g0121 a0001c0001t0011g0122 others(2): Show |
5 | HG01891.hp2 HG02630.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.70-1308_70-1307ins others(2): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160538147 | |||||||
chr3:160538386 | A | G | 15 | a0001c0001t0012g0110 a0001c0001t0012g0112 a0001c0001t0012g0113 others(12): Show |
15 | HG01069.hp2 HG02486.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.70-1546T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160538386 | |||||||
chr3:160538389 | G | A | 1 | a0001c0001t0002g0073 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.70-1549C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160538389 | |||||||
chr3:160538425 | T | C | 1 | a0001c0001t0002g0067 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.70-1585A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160538425 | |||||||
chr3:160538531 | G | A | 1 | a0001c0001t0001g0184 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.70-1691C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160538531 | |||||||
chr3:160538557 | T | C | 1 | a0001c0001t0001g0261 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.70-1717A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160538557 | |||||||
chr3:160538592 | T | C | 1 | a0001c0001t0015g0178 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.70-1752A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160538592 | |||||||
chr3:160538616 | C | A | 1 | a0001c0001t0002g0075 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.70-1776G>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160538616 | |||||||
chr3:160539000 | C | T | 10 | a0001c0002t0009g0129 a0001c0002t0009g0130 a0001c0002t0009g0138 others(7): Show |
10 | HG02145.hp1 HG02451.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.70-2160G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160539000 | |||||||
chr3:160539598 | G | C | 124 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(121): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.70-2758C>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160539598 | |||||||
chr3:160539657 | AG | A | 3 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0200 |
3 | HG00323.hp1 HG03669.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.70-2818delC | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160539657 | |||||||
chr3:160539686 | G | A | 1 | a0001c0002t0026g0141 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.70-2846C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160539686 | |||||||
chr3:160539807 | T | A | 1 | a0001c0001t0012g0114 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.70-2967A>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160539807 | |||||||
chr3:160539837 | C | T | 1 | a0001c0001t0002g0005 | 2 | NA18962.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.70-2997G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160539837 | |||||||
chr3:160539998 | C | CT | 113 | a0001c0001t0001g0159 a0001c0001t0001g0173 a0001c0001t0002g0004 others(110): Show |
119 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.70-3159dupA | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160539998 | |||||||
chr3:160539998 | CT | C | 15 | a0001c0001t0012g0110 a0001c0001t0012g0112 a0001c0001t0012g0113 others(12): Show |
15 | HG01069.hp2 HG02486.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.70-3159delA | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160539998 | |||||||
chr3:160540081 | C | T | 4 | a0001c0001t0007g0006 a0001c0001t0007g0092 a0001c0001t0007g0094 others(1): Show |
5 | HG01167.hp1 HG01169.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.70-3241G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160540081 | |||||||
chr3:160540130 | G | A | 9 | a0001c0001t0005g0093 a0001c0001t0005g0096 a0001c0001t0005g0097 others(6): Show |
9 | HG01255.hp2 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.70-3290C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160540130 | |||||||
chr3:160540157 | G | A | 1 | a0001c0001t0052g0211 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.70-3317C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160540157 | |||||||
chr3:160540247 | C | A | 9 | a0001c0001t0008g0285 a0001c0001t0008g0286 a0001c0001t0008g0287 others(6): Show |
9 | HG01433.hp1 HG02257.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.70-3407G>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160540247 | |||||||
chr3:160540370 | T | C | 4 | a0001c0001t0007g0006 a0001c0001t0007g0092 a0001c0001t0007g0094 others(1): Show |
5 | HG01167.hp1 HG01169.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.70-3530A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160540370 | |||||||
chr3:160540493 | G | A | 140 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(137): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.70-3653C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160540493 | |||||||
chr3:160540531 | T | A | 3 | a0001c0001t0019g0118 a0001c0001t0019g0119 a0001c0001t0033g0117 |
3 | HG00738.hp1 HG01167.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.70-3691A>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160540531 | |||||||
chr3:160540607 | C | T | 12 | a0001c0001t0001g0165 a0001c0001t0001g0173 a0001c0001t0001g0174 others(9): Show |
12 | HG00609.hp2 HG00673.hp2 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.70-3767G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160540607 | |||||||
chr3:160540669 | T | C | 1 | a0001c0001t0001g0248 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.70-3829A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160540669 | |||||||
chr3:160540890 | T | G | 6 | a0001c0001t0011g0120 a0001c0001t0011g0121 a0001c0001t0011g0122 others(3): Show |
6 | HG01891.hp2 HG02630.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.70-4050A>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160540890 | |||||||
chr3:160541005 | A | G | 1 | a0001c0001t0001g0220 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.70-4165T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160541005 | |||||||
chr3:160541081 | A | T | 129 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(126): Show |
135 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.70-4241T>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160541081 | |||||||
chr3:160541360 | G | T | 3 | a0001c0001t0018g0282 a0001c0001t0018g0283 a0001c0001t0018g0284 |
3 | HG02622.hp1 HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.70-4520C>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160541360 | |||||||
chr3:160541375 | G | A | 1 | a0001c0001t0001g0238 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.70-4535C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160541375 | |||||||
chr3:160541408 | T | C | 1 | a0001c0001t0001g0270 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.70-4568A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160541408 | |||||||
chr3:160541576 | T | C | 1 | a0001c0001t0040g0125 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.70-4736A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160541576 | |||||||
chr3:160541579 | T | C | 61 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(58): Show |
64 | HG00323.hp2 HG00423.hp1 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.70-4739A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160541579 | |||||||
chr3:160541626 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.70-4786G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160541626 | |||||||
chr3:160541645 | A | ACG | 5 | a0001c0001t0001g0179 a0001c0001t0005g0100 a0001c0001t0011g0120 others(2): Show |
5 | HG02280.hp1 HG02630.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.70-4807_70-4806dup others(2): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160541645 | |||||||
chr3:160541647 | G | GCA | 35 | a0001c0001t0001g0212 a0001c0001t0001g0247 a0001c0001t0003g0014 others(32): Show |
38 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(35): Show |
intron_variant | MODIFIER | c.70-4808_70-4807ins others(2): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160541647 | |||||||
chr3:160541647 | G | GCACA | 4 | a0001c0002t0027g0143 a0001c0003t0004g0107 a0001c0003t0004g0108 others(1): Show |
4 | HG00099.hp2 HG02647.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.70-4808_70-4807ins others(4): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160541647 | |||||||
chr3:160541649 | G | A | 45 | a0001c0001t0001g0212 a0001c0001t0001g0247 a0001c0001t0003g0014 others(42): Show |
48 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(45): Show |
intron_variant | MODIFIER | c.70-4809C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160541649 | |||||||
chr3:160541649 | G | GCA | 48 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0159 others(45): Show |
52 | HG00609.hp2 HG00673.hp2 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.70-4811_70-4810dup others(2): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160541649 | |||||||
chr3:160541649 | G | GCACA | 23 | a0001c0001t0001g0011 a0001c0001t0001g0164 a0001c0001t0001g0181 others(20): Show |
24 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.70-4813_70-4810dup others(4): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160541649 | |||||||
chr3:160541649 | G | GCACACA | 9 | a0001c0001t0001g0183 a0001c0001t0001g0197 a0001c0001t0001g0198 others(6): Show |
9 | HG01257.hp1 HG01258.hp1 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.70-4815_70-4810dup others(6): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160541649 | |||||||
chr3:160541649 | G | GCGCA | 3 | a0001c0001t0011g0122 a0001c0001t0012g0110 a0001c0001t0012g0115 |
3 | HG01069.hp2 HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.70-4810_70-4809ins others(4): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160541649 | |||||||
chr3:160541649 | G | GCGCACA | 5 | a0001c0001t0012g0112 a0001c0001t0031g0103 a0001c0001t0039g0111 others(2): Show |
5 | HG02717.hp2 HG02886.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.70-4810_70-4809ins others(6): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160541649 | |||||||
chr3:160541649 | G | GCGCACAC others(1): Show |
6 | a0001c0001t0012g0113 a0001c0001t0012g0114 a0001c0004t0013g0148 others(3): Show |
6 | HG03225.hp1 HG03471.hp1 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.70-4810_70-4809ins others(8): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160541649 | |||||||
chr3:160541649 | GCA | G | 25 | a0001c0001t0001g0219 a0001c0001t0001g0249 a0001c0001t0002g0007 others(22): Show |
26 | HG00323.hp2 HG00735.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.70-4811_70-4810del others(2): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160541649 | |||||||
chr3:160541649 | GCACA | G | 24 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0013 others(21): Show |
26 | HG00423.hp1 HG01433.hp2 HG01952.hp1 others(23): Show |
intron_variant | MODIFIER | c.70-4813_70-4810del others(4): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160541649 | |||||||
chr3:160541649 | GCACACAC others(5): Show |
G | 1 | a0001c0001t0011g0123 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.70-4821_70-4810del others(12): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160541649 | |||||||
chr3:160541651 | A | G | 22 | a0001c0001t0001g0217 a0001c0001t0002g0039 a0001c0001t0002g0040 others(19): Show |
22 | HG00642.hp1 HG01099.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.70-4811T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160541651 | |||||||
chr3:160541653 | A | G | 23 | a0001c0001t0002g0007 a0001c0001t0002g0055 a0001c0001t0002g0056 others(20): Show |
24 | HG00323.hp2 HG00735.hp1 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.70-4813T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160541653 | |||||||
chr3:160541655 | A | G | 24 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0013 others(21): Show |
26 | HG00423.hp1 HG01433.hp2 HG01952.hp1 others(23): Show |
intron_variant | MODIFIER | c.70-4815T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160541655 | |||||||
chr3:160541663 | A | G | 1 | a0001c0001t0011g0123 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.70-4823T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160541663 | |||||||
chr3:160542636 | A | G | 1 | a0001c0001t0015g0216 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.70-5796T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160542636 | |||||||
chr3:160542691 | G | T | 3 | a0001c0001t0018g0282 a0001c0001t0018g0283 a0001c0001t0018g0284 |
3 | HG02622.hp1 HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.70-5851C>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160542691 | |||||||
chr3:160542747 | C | A | 1 | a0001c0001t0040g0125 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.70-5907G>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160542747 | |||||||
chr3:160542778 | T | TAA | 15 | a0001c0001t0012g0110 a0001c0001t0012g0112 a0001c0001t0012g0113 others(12): Show |
15 | HG01069.hp2 HG02486.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.70-5939_70-5938ins others(2): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160542778 | |||||||
chr3:160543096 | GA | G | 107 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(104): Show |
113 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.70-6257delT | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160543096 | |||||||
chr3:160543316 | T | G | 1 | a0001c0003t0035g0104 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.70-6476A>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160543316 | |||||||
chr3:160543394 | G | A | 2 | a0001c0001t0011g0123 a0001c0001t0011g0124 |
2 | HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.70-6554C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160543394 | |||||||
chr3:160543736 | A | G | 2 | a0001c0004t0013g0148 a0001c0004t0013g0149 |
2 | NA19084.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.70-6896T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160543736 | |||||||
chr3:160543782 | T | C | 1 | a0001c0001t0002g0039 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.70-6942A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160543782 | |||||||
chr3:160543871 | T | C | 1 | a0001c0001t0015g0178 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.70-7031A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160543871 | |||||||
chr3:160543956 | C | G | 88 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(85): Show |
94 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.70-7116G>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160543956 | |||||||
chr3:160543962 | A | G | 6 | a0001c0001t0012g0110 a0001c0001t0012g0112 a0001c0001t0012g0113 others(3): Show |
6 | HG01069.hp2 HG02717.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.70-7122T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160543962 | |||||||
chr3:160544014 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.70-7174G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160544014 | |||||||
chr3:160544173 | T | C | 1 | a0001c0001t0001g0181 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.70-7333A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160544173 | |||||||
chr3:160544206 | CTG | C | 88 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(85): Show |
94 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.70-7368_70-7367del others(2): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160544206 | |||||||
chr3:160544361 | T | C | 1 | a0001c0001t0001g0242 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.70-7521A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160544361 | |||||||
chr3:160544408 | A | T | 4 | a0001c0001t0007g0006 a0001c0001t0007g0092 a0001c0001t0007g0094 others(1): Show |
5 | HG01167.hp1 HG01169.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.70-7568T>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160544408 | |||||||
chr3:160544553 | G | T | 1 | a0001c0001t0001g0248 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.70-7713C>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160544553 | |||||||
chr3:160544592 | A | G | 1 | a0001c0001t0003g0017 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.70-7752T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160544592 | |||||||
chr3:160544615 | T | C | 1 | a0001c0001t0003g0030 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.70-7775A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160544615 | |||||||
chr3:160544661 | A | G | 211 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0164 others(208): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.70-7821T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160544661 | |||||||
chr3:160544679 | G | A | 3 | a0001c0001t0019g0118 a0001c0001t0019g0119 a0001c0001t0033g0117 |
3 | HG00738.hp1 HG01167.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.70-7839C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160544679 | |||||||
chr3:160544756 | A | C | 1 | a0001c0001t0002g0039 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.70-7916T>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160544756 | |||||||
chr3:160544802 | G | GT | 10 | a0001c0001t0002g0077 a0001c0001t0012g0110 a0001c0001t0012g0112 others(7): Show |
10 | HG00738.hp1 HG01069.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.70-7963dupA | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160544802 | |||||||
chr3:160544802 | GT | G | 10 | a0001c0003t0004g0105 a0001c0003t0004g0107 a0001c0003t0004g0108 others(7): Show |
10 | HG00099.hp2 HG02723.hp1 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.70-7963delA | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160544802 | |||||||
chr3:160544844 | C | T | 2 | a0001c0002t0014g0132 a0001c0002t0014g0133 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.70-8004G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160544844 | |||||||
chr3:160544844 | CA | C | 3 | a0001c0001t0018g0282 a0001c0001t0018g0283 a0001c0001t0018g0284 |
3 | HG02622.hp1 HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.70-8005delT | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160544844 | |||||||
chr3:160545015 | C | T | 57 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(54): Show |
60 | HG00323.hp2 HG00423.hp1 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.70-8175G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160545015 | |||||||
chr3:160545241 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.70-8401C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160545241 | |||||||
chr3:160545301 | T | C | 9 | a0001c0003t0004g0105 a0001c0003t0004g0107 a0001c0003t0004g0108 others(6): Show |
9 | HG00099.hp2 HG02738.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.70-8461A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160545301 | |||||||
chr3:160545406 | ATC | A | 61 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(58): Show |
64 | HG00323.hp2 HG00423.hp1 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.70-8568_70-8567del others(2): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160545406 | |||||||
chr3:160545447 | A | G | 1 | a0001c0001t0002g0147 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.70-8607T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160545447 | |||||||
chr3:160545516 | C | A | 2 | a0001c0001t0022g0126 a0001c0001t0022g0127 |
2 | HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.70-8676G>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160545516 | |||||||
chr3:160545596 | T | A | 107 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(104): Show |
113 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.70-8756A>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160545596 | |||||||
chr3:160545684 | T | C | 1 | a0001c0001t0007g0091 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.70-8844A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160545684 | |||||||
chr3:160545705 | T | C | 1 | a0001c0001t0045g0243 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.70-8865A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160545705 | |||||||
chr3:160545848 | TAACA | T | 24 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0016 others(21): Show |
27 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(24): Show |
intron_variant | MODIFIER | c.70-9012_70-9009del others(4): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160545848 | |||||||
chr3:160545850 | A | G | 2 | a0001c0002t0014g0132 a0001c0002t0014g0133 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.70-9010T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160545850 | |||||||
chr3:160545885 | T | C | 1 | a0001c0001t0001g0181 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.70-9045A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160545885 | |||||||
chr3:160545894 | G | A | 19 | a0001c0001t0011g0120 a0001c0001t0011g0121 a0001c0001t0011g0122 others(16): Show |
19 | HG00099.hp2 HG00738.hp1 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.70-9054C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160545894 | |||||||
chr3:160546344 | C | A | 2 | a0001c0001t0022g0126 a0001c0001t0022g0127 |
2 | HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.70-9504G>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160546344 | |||||||
chr3:160546446 | C | T | 3 | a0001c0001t0019g0118 a0001c0001t0019g0119 a0001c0001t0033g0117 |
3 | HG00738.hp1 HG01167.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.70-9606G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160546446 | |||||||
chr3:160546478 | A | G | 61 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(58): Show |
64 | HG00323.hp2 HG00423.hp1 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.70-9638T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160546478 | |||||||
chr3:160546521 | A | C | 2 | a0001c0001t0001g0279 a0001c0001t0001g0280 |
2 | NA18944.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.70-9681T>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160546521 | |||||||
chr3:160546526 | A | G | 2 | a0001c0001t0001g0279 a0001c0001t0001g0280 |
2 | NA18944.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.70-9686T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160546526 | |||||||
chr3:160546722 | C | T | 3 | a0001c0002t0014g0132 a0001c0002t0014g0133 a0001c0002t0014g0144 |
3 | HG02895.hp2 HG02897.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.70-9882G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160546722 | |||||||
chr3:160546730 | T | C | 1 | a0001c0001t0002g0069 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.70-9890A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160546730 | |||||||
chr3:160546751 | A | AT | 139 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(136): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.70-9912dupA | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160546751 | |||||||
chr3:160546767 | C | T | 1 | a0001c0001t0040g0125 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.70-9927G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160546767 | |||||||
chr3:160546777 | A | C | 1 | a0001c0001t0002g0076 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.70-9937T>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160546777 | |||||||
chr3:160546816 | C | T | 17 | a0001c0002t0009g0129 a0001c0002t0009g0130 a0001c0002t0009g0138 others(14): Show |
17 | HG01243.hp2 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.70-9976G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160546816 | |||||||
chr3:160546854 | T | C | 2 | a0001c0001t0008g0285 a0001c0001t0008g0290 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.70-10014A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160546854 | |||||||
chr3:160546871 | A | G | 1 | a0001c0001t0002g0056 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.70-10031T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160546871 | |||||||
chr3:160546933 | G | A | 4 | a0001c0001t0007g0006 a0001c0001t0007g0092 a0001c0001t0007g0094 others(1): Show |
5 | HG01167.hp1 HG01169.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.70-10093C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160546933 | |||||||
chr3:160548029 | T | C | 53 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(50): Show |
56 | HG00323.hp2 HG00423.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.70-11189A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160548029 | |||||||
chr3:160548103 | G | A | 1 | a0001c0002t0027g0143 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.70-11263C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160548103 | |||||||
chr3:160548146 | T | C | 4 | a0001c0001t0007g0006 a0001c0001t0007g0092 a0001c0001t0007g0094 others(1): Show |
5 | HG01167.hp1 HG01169.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.70-11306A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160548146 | |||||||
chr3:160548207 | T | G | 1 | a0001c0001t0012g0115 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.70-11367A>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160548207 | |||||||
chr3:160548223 | T | G | 2 | a0001c0001t0001g0244 a0001c0003t0035g0104 |
2 | HG02723.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.70-11383A>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160548223 | |||||||
chr3:160548246 | A | G | 10 | a0001c0001t0002g0004 a0001c0001t0002g0013 a0001c0001t0002g0050 others(7): Show |
11 | HG01433.hp2 HG01952.hp1 HG01981.hp2 others(8): Show |
intron_variant | MODIFIER | c.70-11406T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160548246 | |||||||
chr3:160548422 | A | G | 17 | a0001c0002t0009g0129 a0001c0002t0009g0130 a0001c0002t0009g0138 others(14): Show |
17 | HG01243.hp2 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.70-11582T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160548422 | |||||||
chr3:160548491 | C | G | 12 | a0001c0001t0012g0110 a0001c0001t0012g0112 a0001c0001t0012g0113 others(9): Show |
12 | HG01069.hp2 HG02717.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.70-11651G>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160548491 | |||||||
chr3:160548492 | C | T | 1 | a0001c0001t0002g0154 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.70-11652G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160548492 | |||||||
chr3:160548555 | T | C | 2 | a0001c0001t0001g0179 a0001c0001t0001g0180 |
2 | HG00609.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.70-11715A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160548555 | |||||||
chr3:160548559 | T | G | 10 | a0001c0003t0004g0105 a0001c0003t0004g0107 a0001c0003t0004g0108 others(7): Show |
10 | HG00099.hp2 HG02723.hp1 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.70-11719A>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160548559 | |||||||
chr3:160548741 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.70-11901C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160548741 | |||||||
chr3:160549097 | T | C | 1 | a0001c0001t0031g0103 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.70-12257A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160549097 | |||||||
chr3:160549602 | G | A | 1 | a0001c0001t0002g0070 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.70-12762C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160549602 | |||||||
chr3:160549792 | A | G | 1 | a0001c0001t0001g0194 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.70-12952T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160549792 | |||||||
chr3:160550014 | C | T | 9 | a0001c0003t0004g0105 a0001c0003t0004g0107 a0001c0003t0004g0108 others(6): Show |
9 | HG00099.hp2 HG02738.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.70-13174G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160550014 | |||||||
chr3:160550070 | C | T | 140 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(137): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.70-13230G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160550070 | |||||||
chr3:160550233 | A | G | 36 | a0001c0001t0011g0120 a0001c0001t0011g0121 a0001c0001t0011g0122 others(33): Show |
36 | HG00099.hp2 HG00738.hp1 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.70-13393T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160550233 | |||||||
chr3:160550452 | A | T | 1 | a0001c0001t0002g0040 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.70-13612T>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160550452 | |||||||
chr3:160550522 | C | T | 1 | a0001c0001t0051g0274 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.70-13682G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160550522 | |||||||
chr3:160550752 | C | T | 1 | a0001c0001t0007g0091 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.70-13912G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160550752 | |||||||
chr3:160550784 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.70-13944G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160550784 | |||||||
chr3:160550921 | G | C | 6 | a0001c0001t0012g0110 a0001c0001t0012g0112 a0001c0001t0012g0113 others(3): Show |
6 | HG01069.hp2 HG02717.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.70-14081C>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160550921 | |||||||
chr3:160551060 | G | C | 3 | a0001c0001t0019g0118 a0001c0001t0019g0119 a0001c0001t0033g0117 |
3 | HG00738.hp1 HG01167.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.69+14154C>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160551060 | |||||||
chr3:160551071 | A | ATTC | 140 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(137): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.69+14140_69+14142d others(5): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160551071 | |||||||
chr3:160551133 | G | C | 1 | a0001c0001t0001g0245 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.69+14081C>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160551133 | |||||||
chr3:160551415 | T | G | 2 | a0001c0001t0003g0029 a0001c0001t0003g0030 |
2 | HG01361.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.69+13799A>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160551415 | |||||||
chr3:160551524 | A | G | 1 | a0001c0001t0002g0049 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.69+13690T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160551524 | |||||||
chr3:160551533 | T | C | 1 | a0001c0002t0042g0142 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.69+13681A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160551533 | |||||||
chr3:160551635 | AG | A | 24 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0016 others(21): Show |
27 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(24): Show |
intron_variant | MODIFIER | c.69+13578delC | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160551635 | |||||||
chr3:160551760 | C | CTTA | 3 | a0001c0001t0019g0118 a0001c0001t0019g0119 a0001c0001t0033g0117 |
3 | HG00738.hp1 HG01167.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.69+13453_69+13454i others(5): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160551760 | |||||||
chr3:160551762 | G | T | 3 | a0001c0001t0019g0118 a0001c0001t0019g0119 a0001c0001t0033g0117 |
3 | HG00738.hp1 HG01167.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.69+13452C>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160551762 | |||||||
chr3:160551764 | G | A | 3 | a0001c0001t0019g0118 a0001c0001t0019g0119 a0001c0001t0033g0117 |
3 | HG00738.hp1 HG01167.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.69+13450C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160551764 | |||||||
chr3:160551765 | C | G | 3 | a0001c0001t0019g0118 a0001c0001t0019g0119 a0001c0001t0033g0117 |
3 | HG00738.hp1 HG01167.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.69+13449G>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160551765 | |||||||
chr3:160551766 | C | CTTAATTA | 3 | a0001c0001t0019g0118 a0001c0001t0019g0119 a0001c0001t0033g0117 |
3 | HG00738.hp1 HG01167.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.69+13447_69+13448i others(9): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160551766 | |||||||
chr3:160551849 | TA | T | 4 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0016 others(1): Show |
4 | HG03688.hp1 HG03710.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.69+13364delT | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160551849 | |||||||
chr3:160551939 | T | TG | 50 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0160 others(47): Show |
53 | HG00140.hp1 HG00621.hp1 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.69+13274dupC | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160551939 | |||||||
chr3:160551939 | TG | T | 49 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0168 others(46): Show |
50 | HG00099.hp2 HG00323.hp1 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.69+13274delC | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160551939 | |||||||
chr3:160551939 | TGG | T | 23 | a0001c0001t0005g0093 a0001c0001t0005g0096 a0001c0001t0005g0097 others(20): Show |
23 | HG01069.hp2 HG01255.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.69+13273_69+13274d others(4): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160551939 | |||||||
chr3:160551940 | G | T | 1 | a0001c0001t0001g0198 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.69+13274C>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160551940 | |||||||
chr3:160551941 | G | T | 1 | a0001c0001t0001g0197 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.69+13273C>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160551941 | |||||||
chr3:160551945 | G | C | 1 | a0001c0001t0017g0262 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.69+13269C>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160551945 | |||||||
chr3:160551950 | G | C | 9 | a0001c0001t0005g0093 a0001c0001t0005g0096 a0001c0001t0005g0097 others(6): Show |
9 | HG01255.hp2 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.69+13264C>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160551950 | |||||||
chr3:160552333 | T | C | 107 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(104): Show |
113 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.69+12881A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160552333 | |||||||
chr3:160552351 | T | C | 1 | a0001c0001t0012g0115 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.69+12863A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160552351 | |||||||
chr3:160552638 | T | C | 2 | a0001c0001t0001g0264 a0001c0001t0001g0265 |
2 | HG02602.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.69+12576A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160552638 | |||||||
chr3:160552876 | A | G | 36 | a0001c0001t0011g0120 a0001c0001t0011g0121 a0001c0001t0011g0122 others(33): Show |
36 | HG00099.hp2 HG00738.hp1 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.69+12338T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160552876 | |||||||
chr3:160552976 | G | T | 6 | a0001c0001t0012g0110 a0001c0001t0012g0112 a0001c0001t0012g0113 others(3): Show |
6 | HG01069.hp2 HG02717.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.69+12238C>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160552976 | |||||||
chr3:160553062 | C | T | 17 | a0001c0002t0009g0129 a0001c0002t0009g0130 a0001c0002t0009g0138 others(14): Show |
17 | HG01243.hp2 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.69+12152G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160553062 | |||||||
chr3:160553079 | C | T | 1 | a0001c0001t0002g0039 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.69+12135G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160553079 | |||||||
chr3:160553202 | C | T | 1 | a0001c0001t0046g0185 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.69+12012G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160553202 | |||||||
chr3:160553400 | T | A | 9 | a0001c0001t0011g0120 a0001c0001t0011g0121 a0001c0001t0011g0122 others(6): Show |
9 | HG00738.hp1 HG01167.hp2 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.69+11814A>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160553400 | |||||||
chr3:160553460 | A | G | 17 | a0001c0002t0009g0129 a0001c0002t0009g0130 a0001c0002t0009g0138 others(14): Show |
17 | HG01243.hp2 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.69+11754T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160553460 | |||||||
chr3:160553593 | T | C | 2 | a0001c0001t0008g0288 a0001c0001t0008g0289 |
2 | HG02615.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.69+11621A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160553593 | |||||||
chr3:160553641 | T | C | 1 | a0001c0001t0018g0284 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.69+11573A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160553641 | |||||||
chr3:160554007 | C | T | 9 | a0001c0001t0011g0120 a0001c0001t0011g0121 a0001c0001t0011g0122 others(6): Show |
9 | HG00738.hp1 HG01167.hp2 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.69+11207G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160554007 | |||||||
chr3:160554030 | G | C | 1 | a0001c0002t0027g0143 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.69+11184C>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160554030 | |||||||
chr3:160554340 | G | T | 3 | a0001c0001t0022g0126 a0001c0001t0022g0127 a0001c0001t0040g0125 |
3 | HG02486.hp2 HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.69+10874C>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160554340 | |||||||
chr3:160554416 | T | G | 1 | a0001c0001t0028g0116 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.69+10798A>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160554416 | |||||||
chr3:160554566 | G | A | 1 | a0001c0001t0050g0163 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.69+10648C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160554566 | |||||||
chr3:160554568 | G | C | 2 | a0001c0001t0002g0081 a0001c0001t0002g0154 |
2 | NA18747.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.69+10646C>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160554568 | |||||||
chr3:160554600 | A | T | 97 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(94): Show |
103 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.69+10614T>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160554600 | |||||||
chr3:160554660 | T | A | 1 | a0001c0001t0001g0266 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.69+10554A>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160554660 | |||||||
chr3:160554685 | GTTAAGCT others(13): Show |
G | 1 | a0001c0001t0001g0196 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.69+10509_69+10528d others(22): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160554685 | |||||||
chr3:160554876 | T | C | 1 | a0001c0001t0001g0195 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.69+10338A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160554876 | |||||||
chr3:160555055 | G | A | 1 | a0001c0003t0004g0109 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.69+10159C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160555055 | |||||||
chr3:160555251 | G | C | 1 | a0001c0001t0017g0267 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.69+9963C>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160555251 | |||||||
chr3:160555371 | G | C | 1 | a0001c0001t0001g0268 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.69+9843C>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160555371 | |||||||
chr3:160555473 | T | C | 1 | a0001c0001t0031g0103 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.69+9741A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160555473 | |||||||
chr3:160555513 | T | C | 2 | a0001c0001t0022g0126 a0001c0001t0022g0127 |
2 | HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.69+9701A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160555513 | |||||||
chr3:160555589 | G | A | 2 | a0001c0001t0008g0285 a0001c0001t0008g0290 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.69+9625C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160555589 | |||||||
chr3:160555749 | C | T | 163 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(160): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.69+9465G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160555749 | |||||||
chr3:160555803 | CTTTTA | C | 3 | a0001c0001t0011g0120 a0001c0001t0011g0121 a0001c0001t0011g0122 |
3 | HG01891.hp2 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.69+9406_69+9410del others(5): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160555803 | |||||||
chr3:160555923 | C | T | 6 | a0001c0001t0012g0110 a0001c0001t0012g0112 a0001c0001t0012g0113 others(3): Show |
6 | HG01069.hp2 HG02717.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.69+9291G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160555923 | |||||||
chr3:160555970 | C | T | 154 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(151): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.69+9244G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160555970 | |||||||
chr3:160555991 | C | T | 1 | a0001c0002t0010g0131 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.69+9223G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160555991 | |||||||
chr3:160556020 | G | A | 8 | a0001c0001t0002g0082 a0001c0001t0002g0083 a0001c0001t0002g0084 others(5): Show |
8 | HG00642.hp1 HG01099.hp2 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.69+9194C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160556020 | |||||||
chr3:160556039 | A | T | 1 | a0001c0001t0001g0196 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.69+9175T>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160556039 | |||||||
chr3:160556043 | C | G | 1 | a0001c0001t0001g0196 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.69+9171G>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160556043 | |||||||
chr3:160556044 | T | A | 1 | a0001c0001t0001g0196 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.69+9170A>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160556044 | |||||||
chr3:160556045 | G | A | 1 | a0001c0001t0001g0196 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.69+9169C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160556045 | |||||||
chr3:160556047 | T | G | 1 | a0001c0001t0001g0196 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.69+9167A>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160556047 | |||||||
chr3:160556048 | T | A | 1 | a0001c0001t0001g0196 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.69+9166A>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160556048 | |||||||
chr3:160556050 | C | A | 1 | a0001c0001t0001g0196 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.69+9164G>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160556050 | |||||||
chr3:160556051 | C | A | 1 | a0001c0001t0001g0196 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.69+9163G>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160556051 | |||||||
chr3:160556052 | C | G | 1 | a0001c0001t0001g0196 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.69+9162G>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160556052 | |||||||
chr3:160556055 | C | A | 1 | a0001c0001t0001g0196 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.69+9159G>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160556055 | |||||||
chr3:160556057 | C | G | 1 | a0001c0001t0001g0196 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.69+9157G>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160556057 | |||||||
chr3:160556058 | C | G | 1 | a0001c0001t0001g0196 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.69+9156G>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160556058 | |||||||
chr3:160556059 | C | T | 1 | a0001c0001t0001g0196 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.69+9155G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160556059 | |||||||
chr3:160556062 | C | T | 1 | a0001c0001t0001g0196 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.69+9152G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160556062 | |||||||
chr3:160556063 | C | T | 1 | a0001c0001t0001g0196 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.69+9151G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160556063 | |||||||
chr3:160556065 | C | G | 1 | a0001c0001t0001g0196 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.69+9149G>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160556065 | |||||||
chr3:160556067 | G | T | 1 | a0001c0001t0001g0196 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.69+9147C>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160556067 | |||||||
chr3:160556069 | T | G | 1 | a0001c0001t0001g0196 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.69+9145A>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160556069 | |||||||
chr3:160556074 | C | T | 24 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0016 others(21): Show |
27 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(24): Show |
intron_variant | MODIFIER | c.69+9140G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160556074 | |||||||
chr3:160556234 | A | C | 1 | a0001c0001t0001g0196 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.69+8980T>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160556234 | |||||||
chr3:160556282 | G | C | 1 | a0001c0001t0001g0196 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.69+8932C>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160556282 | |||||||
chr3:160556283 | A | T | 1 | a0001c0001t0001g0196 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.69+8931T>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160556283 | |||||||
chr3:160556287 | A | T | 1 | a0001c0001t0001g0196 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.69+8927T>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160556287 | |||||||
chr3:160556288 | C | G | 1 | a0001c0001t0001g0196 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.69+8926G>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160556288 | |||||||
chr3:160556341 | G | GT | 9 | a0001c0001t0008g0285 a0001c0001t0008g0286 a0001c0001t0008g0287 others(6): Show |
9 | HG01433.hp1 HG02257.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.69+8872dupA | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160556341 | |||||||
chr3:160556347 | G | T | 1 | a0001c0001t0001g0196 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.69+8867C>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160556347 | |||||||
chr3:160556348 | G | T | 1 | a0001c0001t0001g0196 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.69+8866C>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160556348 | |||||||
chr3:160556385 | T | TTTTCTCA others(11): Show |
1 | a0001c0001t0001g0196 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.69+8828_69+8829ins others(18): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160556385 | |||||||
chr3:160556400 | C | A | 6 | a0001c0001t0011g0120 a0001c0001t0011g0121 a0001c0001t0011g0122 others(3): Show |
6 | HG01891.hp2 HG02630.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.69+8814G>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160556400 | |||||||
chr3:160556473 | G | A | 3 | a0001c0001t0019g0118 a0001c0001t0019g0119 a0001c0001t0033g0117 |
3 | HG00738.hp1 HG01167.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.69+8741C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160556473 | |||||||
chr3:160556611 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.69+8603C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160556611 | |||||||
chr3:160556646 | C | T | 27 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0016 others(24): Show |
30 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(27): Show |
intron_variant | MODIFIER | c.69+8568G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160556646 | |||||||
chr3:160556826 | T | A | 1 | a0001c0002t0014g0144 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.69+8388A>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160556826 | |||||||
chr3:160557161 | T | C | 1 | a0001c0001t0001g0270 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.69+8053A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160557161 | |||||||
chr3:160557229 | C | A | 2 | a0001c0002t0009g0129 a0001c0002t0009g0130 |
2 | HG02486.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.69+7985G>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160557229 | |||||||
chr3:160557243 | G | A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0271 |
3 | HG01981.hp1 HG03490.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.69+7971C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160557243 | |||||||
chr3:160557413 | G | C | 1 | a0001c0001t0003g0032 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.69+7801C>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160557413 | |||||||
chr3:160557558 | G | A | 140 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(137): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.69+7656C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160557558 | |||||||
chr3:160557724 | G | C | 1 | a0001c0001t0001g0272 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.69+7490C>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160557724 | |||||||
chr3:160558107 | G | C | 154 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(151): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.69+7107C>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160558107 | |||||||
chr3:160558279 | A | C | 139 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(136): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.69+6935T>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160558279 | |||||||
chr3:160558336 | A | G | 8 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0192 others(5): Show |
8 | HG00544.hp2 HG00621.hp1 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.69+6878T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160558336 | |||||||
chr3:160558472 | G | A | 2 | a0001c0003t0004g0157 a0001c0003t0004g0158 |
2 | NA18944.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.69+6742C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160558472 | |||||||
chr3:160558571 | T | C | 2 | a0001c0001t0022g0126 a0001c0001t0022g0127 |
2 | HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.69+6643A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160558571 | |||||||
chr3:160558751 | CT | C | 10 | a0001c0001t0001g0184 a0001c0001t0001g0189 a0001c0001t0001g0281 others(7): Show |
10 | HG00558.hp2 HG02602.hp1 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.69+6462delA | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160558751 | |||||||
chr3:160558757 | T | A | 2 | a0001c0001t0034g0146 a0001c0001t0040g0125 |
2 | HG02486.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.69+6457A>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160558757 | |||||||
chr3:160558758 | T | A | 260 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(257): Show |
275 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.69+6456A>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160558758 | |||||||
chr3:160559195 | T | C | 1 | a0001c0001t0031g0103 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.69+6019A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160559195 | |||||||
chr3:160559314 | T | C | 5 | a0001c0001t0011g0120 a0001c0001t0011g0121 a0001c0001t0011g0122 others(2): Show |
5 | HG01891.hp2 HG02630.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.69+5900A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160559314 | |||||||
chr3:160559316 | G | C | 1 | a0001c0002t0009g0145 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.69+5898C>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160559316 | |||||||
chr3:160559495 | C | T | 1 | a0001c0001t0003g0014 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.69+5719G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160559495 | |||||||
chr3:160559588 | A | G | 1 | a0001c0001t0007g0092 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.69+5626T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160559588 | |||||||
chr3:160559638 | C | G | 2 | a0001c0001t0001g0165 a0001c0001t0001g0281 |
2 | NA18946.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.69+5576G>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160559638 | |||||||
chr3:160559794 | A | C | 1 | a0001c0001t0046g0185 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.69+5420T>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160559794 | |||||||
chr3:160559881 | T | C | 1 | a0001c0001t0003g0033 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.69+5333A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160559881 | |||||||
chr3:160559897 | C | A | 1 | a0001c0001t0001g0273 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.69+5317G>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160559897 | |||||||
chr3:160560007 | G | C | 1 | a0001c0001t0031g0103 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.69+5207C>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160560007 | |||||||
chr3:160560053 | A | C | 1 | a0001c0001t0007g0091 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.69+5161T>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160560053 | |||||||
chr3:160560205 | G | C | 9 | a0001c0001t0011g0120 a0001c0001t0011g0121 a0001c0001t0011g0122 others(6): Show |
9 | HG00738.hp1 HG01167.hp2 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.69+5009C>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160560205 | |||||||
chr3:160560372 | G | A | 139 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(136): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.69+4842C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160560372 | |||||||
chr3:160560386 | G | A | 1 | a0001c0001t0040g0125 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.69+4828C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160560386 | |||||||
chr3:160560690 | C | T | 186 | a0001c0001t0001g0003 a0001c0001t0001g0165 a0001c0001t0001g0166 others(183): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.69+4524G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160560690 | |||||||
chr3:160561030 | T | C | 2 | a0001c0001t0022g0126 a0001c0001t0022g0127 |
2 | HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.69+4184A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160561030 | |||||||
chr3:160561157 | AGTT | A | 3 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0021g0036 |
3 | HG00099.hp1 HG02602.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.69+4054_69+4056del others(3): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160561157 | |||||||
chr3:160561518 | T | C | 1 | a0001c0001t0002g0090 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.69+3696A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160561518 | |||||||
chr3:160561586 | A | G | 2 | a0001c0002t0009g0129 a0001c0002t0009g0130 |
2 | HG02486.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.69+3628T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160561586 | |||||||
chr3:160561623 | G | A | 27 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0016 others(24): Show |
30 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(27): Show |
intron_variant | MODIFIER | c.69+3591C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160561623 | |||||||
chr3:160561629 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.69+3585G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160561629 | |||||||
chr3:160562091 | T | A | 163 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(160): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.69+3123A>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160562091 | |||||||
chr3:160562111 | T | C | 1 | a0001c0001t0021g0036 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.69+3103A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160562111 | |||||||
chr3:160562701 | G | C | 1 | a0001c0001t0001g0276 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.69+2513C>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160562701 | |||||||
chr3:160563095 | C | G | 1 | a0001c0001t0002g0038 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.69+2119G>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160563095 | |||||||
chr3:160563179 | TGGATCAT others(10): Show |
T | 61 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(58): Show |
64 | HG00323.hp2 HG00423.hp1 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.69+2018_69+2034del others(17): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160563179 | |||||||
chr3:160563218 | T | C | 19 | a0001c0001t0002g0007 a0001c0001t0002g0128 a0001c0002t0009g0129 others(16): Show |
20 | HG01243.hp2 HG01346.hp2 HG01496.hp2 others(17): Show |
intron_variant | MODIFIER | c.69+1996A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160563218 | |||||||
chr3:160563221 | A | G | 1 | a0001c0001t0050g0163 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.69+1993T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160563221 | |||||||
chr3:160563446 | T | C | 1 | a0001c0001t0001g0277 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.69+1768A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160563446 | |||||||
chr3:160563506 | T | C | 1 | a0001c0001t0034g0146 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.69+1708A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160563506 | |||||||
chr3:160563509 | T | C | 1 | a0001c0001t0002g0147 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.69+1705A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160563509 | |||||||
chr3:160563562 | T | C | 1 | a0001c0001t0001g0012 | 2 | HG01070.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.69+1652A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160563562 | |||||||
chr3:160563663 | T | C | 1 | a0001c0001t0001g0278 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.69+1551A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160563663 | |||||||
chr3:160563728 | A | T | 1 | a0001c0001t0029g0037 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.69+1486T>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160563728 | |||||||
chr3:160563759 | T | C | 6 | a0001c0004t0013g0148 a0001c0004t0013g0149 a0001c0004t0013g0152 others(3): Show |
6 | NA18939.hp2 NA18959.hp2 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.69+1455A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160563759 | |||||||
chr3:160563776 | T | C | 1 | a0001c0001t0001g0280 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.69+1438A>G | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160563776 | |||||||
chr3:160563979 | TCA | T | 24 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0016 others(21): Show |
27 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(24): Show |
intron_variant | MODIFIER | c.69+1233_69+1234del others(2): Show |
KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160563979 | |||||||
chr3:160564179 | A | G | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG01109.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.69+1035T>C | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160564179 | |||||||
chr3:160564678 | G | A | 2 | a0001c0001t0001g0279 a0001c0001t0001g0280 |
2 | NA18944.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.69+536C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160564678 | |||||||
chr3:160564925 | C | T | 1 | a0001c0001t0002g0013 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.69+289G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160564925 | |||||||
chr3:160564926 | C | A | 1 | a0001c0001t0002g0154 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.69+288G>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160564926 | |||||||
chr3:160565016 | G | A | 1 | a0001c0001t0001g0281 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.69+198C>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160565016 | |||||||
chr3:160565136 | T | A | 4 | a0001c0003t0004g0155 a0001c0003t0004g0157 a0001c0003t0004g0158 others(1): Show |
4 | HG03669.hp2 HG04115.hp2 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.69+78A>T | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160565136 | |||||||
chr3:160565142 | C | T | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG01952.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.69+72G>A | KPNA4 | ENSG00000186432.10 | transcript | ENST00000334256.9 | protein_coding | 1/16 | chr3 | 160565142 |