Item | Value |
---|---|
geneid | 4673 |
ensemblid | ENSG00000187109.15 |
hgncid | 7637 |
symbol | NAP1L1 |
name | nucleosome assembly protein 1 like 1 |
refseq_nuc | NM_004537.7 |
refseq_prot | NP_004528.1 |
ensembl_nuc | ENST00000618691.5 |
ensembl_prot | ENSP00000477538.1 |
mane_status | MANE Select |
chr | chr12 |
start | 76036585 |
end | 76084685 |
strand | - |
ver | v1.2 |
region | chr12:76036585-76084685 |
region5000 | chr12:76031585-76089685 |
regionname0 | NAP1L1_chr12_76036585_76084685 |
regionname5000 | NAP1L1_chr12_76031585_76089685 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 391 | 355 | 95 | 70 | 140 | 14 | 34 | 104 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | MADID others(386): Show |
chr12 | 76031585 | 76089685 |
a0002 | 0/0 | 391 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | MADID others(386): Show |
chr12 | 76031585 | 76089685 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1173 | 230 | 28 | 38 | 137 | 6 | 20 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | ATGGC others(1168): Show |
chr12 | 76031585 | 76089685 | ||
a0001c0002 | 0/0 | 1173 | 93 | 61 | 16 | 3 | 5 | 8 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | ATGGC others(1168): Show |
chr12 | 76031585 | 76089685 | ||
a0001c0003 | 1/0 | 1173 | 32 | 6 | 16 | 0 | 3 | 6 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | ATGGC others(1168): Show |
chr12 | 76031585 | 76089685 | ||
a0002c0004 | 0/0 | 1173 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | ATGGC others(1168): Show |
chr12 | 76031585 | 76089685 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 13160 | 66 | 0 | 8 | 50 | 0 | 8 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13155): Show |
chr12 | 76031585 | 76089685 |
a0001c0001t0002 | 0/0 | 13161 | 45 | 5 | 12 | 17 | 5 | 6 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13156): Show |
chr12 | 76031585 | 76089685 |
a0001c0001t0003 | 0/0 | 13161 | 24 | 0 | 1 | 23 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13156): Show |
chr12 | 76031585 | 76089685 |
a0001c0001t0006 | 0/0 | 13161 | 16 | 2 | 7 | 6 | 1 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13156): Show |
chr12 | 76031585 | 76089685 |
a0001c0001t0007 | 0/0 | 13161 | 8 | 8 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13156): Show |
chr12 | 76031585 | 76089685 |
a0001c0001t0008 | 0/0 | 13161 | 6 | 0 | 4 | 2 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13156): Show |
chr12 | 76031585 | 76089685 |
a0001c0001t0011 | 0/0 | 13163 | 4 | 0 | 0 | 4 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13158): Show |
chr12 | 76031585 | 76089685 |
a0001c0001t0012 | 0/0 | 13162 | 4 | 2 | 0 | 0 | 0 | 2 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13157): Show |
chr12 | 76031585 | 76089685 |
a0001c0001t0013 | 0/0 | 13160 | 4 | 3 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13155): Show |
chr12 | 76031585 | 76089685 |
a0001c0001t0030 | 0/0 | 13161 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13156): Show |
chr12 | 76031585 | 76089685 |
a0001c0001t0032 | 0/0 | 13159 | 2 | 0 | 0 | 1 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13154): Show |
chr12 | 76031585 | 76089685 |
a0001c0001t0033 | 0/0 | 13160 | 2 | 0 | 0 | 2 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13155): Show |
chr12 | 76031585 | 76089685 |
a0001c0001t0034 | 0/0 | 13161 | 2 | 0 | 0 | 2 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13156): Show |
chr12 | 76031585 | 76089685 |
a0001c0001t0035 | 0/0 | 13160 | 2 | 0 | 0 | 2 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13155): Show |
chr12 | 76031585 | 76089685 |
a0001c0001t0036 | 0/0 | 13162 | 2 | 0 | 2 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13157): Show |
chr12 | 76031585 | 76089685 |
a0001c0001t0037 | 0/0 | 13160 | 2 | 1 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13155): Show |
chr12 | 76031585 | 76089685 |
a0001c0001t0038 | 0/0 | 13161 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13156): Show |
chr12 | 76031585 | 76089685 |
a0001c0001t0042 | 0/0 | 13161 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13156): Show |
chr12 | 76031585 | 76089685 |
a0001c0001t0043 | 0/0 | 13161 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13156): Show |
chr12 | 76031585 | 76089685 |
a0001c0001t0047 | 0/0 | 13161 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13156): Show |
chr12 | 76031585 | 76089685 |
a0001c0001t0048 | 0/0 | 13162 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13157): Show |
chr12 | 76031585 | 76089685 |
a0001c0001t0049 | 0/0 | 13162 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13157): Show |
chr12 | 76031585 | 76089685 |
a0001c0001t0050 | 0/0 | 13162 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13157): Show |
chr12 | 76031585 | 76089685 |
a0001c0001t0057 | 0/0 | 13160 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13155): Show |
chr12 | 76031585 | 76089685 |
a0001c0001t0068 | 0/0 | 13160 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13155): Show |
chr12 | 76031585 | 76089685 |
a0001c0001t0069 | 0/0 | 13162 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13157): Show |
chr12 | 76031585 | 76089685 |
a0001c0001t0070 | 0/0 | 13161 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13156): Show |
chr12 | 76031585 | 76089685 |
a0001c0001t0071 | 0/0 | 13148 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13143): Show |
chr12 | 76031585 | 76089685 |
a0001c0001t0072 | 0/1 | 13161 | 1 | 0 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13156): Show |
chr12 | 76031585 | 76089685 |
a0001c0001t0073 | 0/0 | 13161 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13156): Show |
chr12 | 76031585 | 76089685 |
a0001c0001t0075 | 0/0 | 13147 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13142): Show |
chr12 | 76031585 | 76089685 |
a0001c0001t0076 | 0/0 | 13147 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13142): Show |
chr12 | 76031585 | 76089685 |
a0001c0001t0077 | 0/0 | 13161 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13156): Show |
chr12 | 76031585 | 76089685 |
a0001c0001t0078 | 0/0 | 13160 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13155): Show |
chr12 | 76031585 | 76089685 |
a0001c0001t0079 | 0/0 | 13160 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13155): Show |
chr12 | 76031585 | 76089685 |
a0001c0001t0080 | 0/0 | 13162 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13157): Show |
chr12 | 76031585 | 76089685 |
a0001c0001t0081 | 0/0 | 13162 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13157): Show |
chr12 | 76031585 | 76089685 |
a0001c0001t0082 | 0/0 | 13160 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13155): Show |
chr12 | 76031585 | 76089685 |
a0001c0001t0083 | 0/0 | 13161 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13156): Show |
chr12 | 76031585 | 76089685 |
a0001c0001t0084 | 0/0 | 13162 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13157): Show |
chr12 | 76031585 | 76089685 |
a0001c0001t0085 | 0/0 | 13163 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13158): Show |
chr12 | 76031585 | 76089685 |
a0001c0001t0086 | 0/0 | 13162 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13157): Show |
chr12 | 76031585 | 76089685 |
a0001c0001t0087 | 0/0 | 13161 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13156): Show |
chr12 | 76031585 | 76089685 |
a0001c0001t0089 | 0/0 | 13161 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13156): Show |
chr12 | 76031585 | 76089685 |
a0001c0001t0090 | 0/0 | 13162 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13157): Show |
chr12 | 76031585 | 76089685 |
a0001c0001t0091 | 0/0 | 13161 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13156): Show |
chr12 | 76031585 | 76089685 |
a0001c0001t0092 | 0/0 | 13163 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13158): Show |
chr12 | 76031585 | 76089685 |
a0001c0001t0093 | 0/0 | 13160 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13155): Show |
chr12 | 76031585 | 76089685 |
a0001c0001t0094 | 0/0 | 13160 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13155): Show |
chr12 | 76031585 | 76089685 |
a0001c0001t0095 | 0/0 | 13161 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13156): Show |
chr12 | 76031585 | 76089685 |
a0001c0001t0096 | 0/0 | 13161 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13156): Show |
chr12 | 76031585 | 76089685 |
a0001c0001t0097 | 0/0 | 13159 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13154): Show |
chr12 | 76031585 | 76089685 |
a0001c0001t0098 | 0/0 | 13160 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13155): Show |
chr12 | 76031585 | 76089685 |
a0001c0001t0101 | 0/0 | 13162 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13157): Show |
chr12 | 76031585 | 76089685 |
a0001c0002t0004 | 0/0 | 13162 | 23 | 2 | 9 | 3 | 2 | 7 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13157): Show |
chr12 | 76031585 | 76089685 |
a0001c0002t0005 | 0/0 | 13159 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13154): Show |
chr12 | 76031585 | 76089685 |
a0001c0002t0009 | 0/0 | 13162 | 4 | 4 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13157): Show |
chr12 | 76031585 | 76089685 |
a0001c0002t0014 | 0/0 | 13149 | 3 | 3 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13144): Show |
chr12 | 76031585 | 76089685 |
a0001c0002t0015 | 0/0 | 13144 | 4 | 3 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13139): Show |
chr12 | 76031585 | 76089685 |
a0001c0002t0016 | 0/0 | 13160 | 3 | 3 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13155): Show |
chr12 | 76031585 | 76089685 |
a0001c0002t0018 | 0/0 | 13161 | 3 | 2 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13156): Show |
chr12 | 76031585 | 76089685 |
a0001c0002t0019 | 0/0 | 13158 | 3 | 3 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13153): Show |
chr12 | 76031585 | 76089685 |
a0001c0002t0020 | 0/0 | 13163 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13158): Show |
chr12 | 76031585 | 76089685 |
a0001c0002t0021 | 0/0 | 13163 | 2 | 0 | 0 | 0 | 1 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13158): Show |
chr12 | 76031585 | 76089685 |
a0001c0002t0022 | 0/0 | 13161 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13156): Show |
chr12 | 76031585 | 76089685 |
a0001c0002t0023 | 0/0 | 13160 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13155): Show |
chr12 | 76031585 | 76089685 |
a0001c0002t0024 | 0/0 | 13161 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13156): Show |
chr12 | 76031585 | 76089685 |
a0001c0002t0025 | 0/0 | 13161 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13156): Show |
chr12 | 76031585 | 76089685 |
a0001c0002t0027 | 0/0 | 13161 | 2 | 0 | 1 | 0 | 1 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13156): Show |
chr12 | 76031585 | 76089685 |
a0001c0002t0028 | 0/0 | 13162 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13157): Show |
chr12 | 76031585 | 76089685 |
a0001c0002t0029 | 0/0 | 13163 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13158): Show |
chr12 | 76031585 | 76089685 |
a0001c0002t0031 | 0/0 | 13162 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13157): Show |
chr12 | 76031585 | 76089685 |
a0001c0002t0039 | 0/0 | 13160 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13155): Show |
chr12 | 76031585 | 76089685 |
a0001c0002t0040 | 0/0 | 13161 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13156): Show |
chr12 | 76031585 | 76089685 |
a0001c0002t0041 | 0/0 | 13149 | 2 | 1 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13144): Show |
chr12 | 76031585 | 76089685 |
a0001c0002t0044 | 0/0 | 13161 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13156): Show |
chr12 | 76031585 | 76089685 |
a0001c0002t0045 | 0/0 | 13163 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13158): Show |
chr12 | 76031585 | 76089685 |
a0001c0002t0046 | 0/0 | 13143 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13138): Show |
chr12 | 76031585 | 76089685 |
a0001c0002t0051 | 0/0 | 13161 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13156): Show |
chr12 | 76031585 | 76089685 |
a0001c0002t0052 | 0/0 | 13160 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13155): Show |
chr12 | 76031585 | 76089685 |
a0001c0002t0053 | 0/0 | 13161 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13156): Show |
chr12 | 76031585 | 76089685 |
a0001c0002t0054 | 0/0 | 13162 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13157): Show |
chr12 | 76031585 | 76089685 |
a0001c0002t0055 | 0/0 | 13162 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13157): Show |
chr12 | 76031585 | 76089685 |
a0001c0002t0056 | 0/0 | 13159 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13154): Show |
chr12 | 76031585 | 76089685 |
a0001c0002t0058 | 0/0 | 13159 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13154): Show |
chr12 | 76031585 | 76089685 |
a0001c0002t0061 | 0/0 | 13161 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13156): Show |
chr12 | 76031585 | 76089685 |
a0001c0002t0062 | 0/0 | 13159 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13154): Show |
chr12 | 76031585 | 76089685 |
a0001c0002t0063 | 0/0 | 13160 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13155): Show |
chr12 | 76031585 | 76089685 |
a0001c0002t0064 | 0/0 | 13159 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13154): Show |
chr12 | 76031585 | 76089685 |
a0001c0002t0065 | 0/0 | 13116 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13111): Show |
chr12 | 76031585 | 76089685 |
a0001c0002t0067 | 0/0 | 13160 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13155): Show |
chr12 | 76031585 | 76089685 |
a0001c0002t0074 | 0/0 | 13163 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13158): Show |
chr12 | 76031585 | 76089685 |
a0001c0002t0088 | 0/0 | 13162 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13157): Show |
chr12 | 76031585 | 76089685 |
a0001c0002t0099 | 0/0 | 13162 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13157): Show |
chr12 | 76031585 | 76089685 |
a0001c0002t0100 | 0/0 | 13163 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13158): Show |
chr12 | 76031585 | 76089685 |
a0001c0002t0102 | 0/0 | 13160 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13155): Show |
chr12 | 76031585 | 76089685 |
a0001c0002t0103 | 0/0 | 13145 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13140): Show |
chr12 | 76031585 | 76089685 |
a0001c0002t0104 | 0/0 | 13162 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13157): Show |
chr12 | 76031585 | 76089685 |
a0001c0003t0005 | 1/0 | 13159 | 20 | 5 | 8 | 0 | 1 | 5 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13154): Show |
chr12 | 76031585 | 76089685 |
a0001c0003t0010 | 0/0 | 13159 | 4 | 0 | 1 | 0 | 2 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13154): Show |
chr12 | 76031585 | 76089685 |
a0001c0003t0017 | 0/0 | 13158 | 3 | 0 | 3 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13153): Show |
chr12 | 76031585 | 76089685 |
a0001c0003t0026 | 0/0 | 13160 | 2 | 0 | 2 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13155): Show |
chr12 | 76031585 | 76089685 |
a0001c0003t0059 | 0/0 | 13159 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13154): Show |
chr12 | 76031585 | 76089685 |
a0001c0003t0060 | 0/0 | 13159 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13154): Show |
chr12 | 76031585 | 76089685 |
a0001c0003t0066 | 0/0 | 13157 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13152): Show |
chr12 | 76031585 | 76089685 |
a0002c0004t0014 | 0/0 | 13149 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | CTTTT others(13144): Show |
chr12 | 76031585 | 76089685 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0004 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0013 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0021 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0023 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0003g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0003g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0003g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0003g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0006g0003 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0006g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0006g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0006g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0006g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0006g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0006g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0006g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0006g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0006g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0006g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0006g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0007g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0007g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0007g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0007g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0007g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0007g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0007g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0008g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0008g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0008g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0008g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0008g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0008g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0011g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0011g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0011g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0011g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0012g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0012g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0012g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0012g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0013g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0013g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0013g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0030g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0032g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0032g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0033g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0033g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0034g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0034g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0035g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0035g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0036g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0037g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0037g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0038g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0038g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0042g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0043g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0047g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0048g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0049g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0050g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0057g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0068g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0069g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0070g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0071g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0072g0206 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0073g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0075g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0076g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0077g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0078g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0079g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0080g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0081g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0082g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0083g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0084g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0085g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0086g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0087g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0089g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0090g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0091g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0092g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0093g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0094g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0095g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0096g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0097g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0098g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0101g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0004g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0004g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0004g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0004g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0004g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0004g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0004g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0004g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0004g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0004g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0004g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0004g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0004g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0004g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0004g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0004g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0004g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0004g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0004g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0004g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0004g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0004g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0004g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0005g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0009g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0009g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0009g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0014g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0014g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0015g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0015g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0015g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0016g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0016g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0016g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0018g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0018g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0018g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0019g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0019g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0019g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0020g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0020g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0021g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0021g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0022g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0022g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0023g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0023g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0024g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0024g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0025g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0025g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0027g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0027g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0028g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0028g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0029g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0029g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0031g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0031g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0039g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0039g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0040g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0040g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0041g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0041g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0044g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0045g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0046g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0051g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0052g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0053g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0054g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0055g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0056g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0058g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0061g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0062g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0063g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0064g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0065g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0067g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0074g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0088g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0099g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0100g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0102g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0103g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0104g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0003t0005g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0003t0005g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0003t0005g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0003t0005g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0003t0005g0239 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0003t0005g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0003t0005g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0003t0005g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0003t0005g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0003t0005g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0003t0005g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0003t0005g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0003t0005g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0003t0005g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0003t0005g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0003t0005g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0003t0005g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0003t0005g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0003t0010g0007 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0003t0010g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0003t0017g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0003t0017g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0003t0026g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0003t0026g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0003t0059g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0003t0060g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0003t0066g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0002c0004t0014g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0002 | t0004 | g0307 | EUR | GBR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0023 | EUR | GBR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG00323 | hp1 | a0001 | c0001 | t0006 | g0092 | EUR | FIN | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG00323 | hp2 | a0001 | c0003 | t0005 | g0242 | EUR | FIN | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG00423 | hp1 | a0001 | c0001 | t0003 | g0128 | EAS | CHS | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | CHS | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | CHS | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | CHS | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | CHS | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | CHS | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG00558 | hp2 | a0001 | c0001 | t0006 | g0043 | EAS | CHS | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | CHS | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG00642 | hp1 | a0001 | c0003 | t0010 | g0007 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG00733 | hp1 | a0001 | c0002 | t0104 | g0316 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG00735 | hp1 | a0001 | c0001 | t0003 | g0095 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG00738 | hp1 | a0001 | c0002 | t0004 | g0314 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG00738 | hp2 | a0001 | c0003 | t0026 | g0236 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG00741 | hp1 | a0001 | c0002 | t0004 | g0287 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG00741 | hp2 | a0001 | c0003 | t0005 | g0234 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01069 | hp1 | a0001 | c0002 | t0053 | g0301 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01069 | hp2 | a0001 | c0003 | t0066 | g0240 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0042 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01071 | hp2 | a0001 | c0003 | t0017 | g0029 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01074 | hp1 | a0001 | c0003 | t0060 | g0249 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01081 | hp1 | a0001 | c0002 | t0004 | g0302 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01081 | hp2 | a0001 | c0002 | t0061 | g0279 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01099 | hp1 | a0001 | c0002 | t0018 | g0308 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0120 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01106 | hp2 | a0001 | c0001 | t0070 | g0205 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01109 | hp2 | a0001 | c0002 | t0041 | g0150 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01167 | hp1 | a0001 | c0003 | t0005 | g0028 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0059 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01169 | hp2 | a0001 | c0003 | t0017 | g0235 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01175 | hp1 | a0001 | c0003 | t0026 | g0270 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0183 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01192 | hp1 | a0001 | c0003 | t0005 | g0027 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01192 | hp2 | a0001 | c0002 | t0004 | g0281 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01243 | hp1 | a0001 | c0001 | t0013 | g0014 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01243 | hp2 | a0001 | c0003 | t0005 | g0247 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01255 | hp1 | a0001 | c0001 | t0006 | g0009 | AMR | CLM | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01255 | hp2 | a0001 | c0003 | t0005 | g0028 | AMR | CLM | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01256 | hp1 | a0001 | c0001 | t0006 | g0008 | AMR | CLM | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01256 | hp2 | a0001 | c0003 | t0005 | g0244 | AMR | CLM | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01258 | hp1 | a0001 | c0001 | t0006 | g0008 | AMR | CLM | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0023 | AMR | CLM | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01261 | hp1 | a0001 | c0002 | t0015 | g0154 | AMR | CLM | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01261 | hp2 | a0001 | c0001 | t0036 | g0010 | AMR | CLM | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01358 | hp1 | a0001 | c0001 | t0036 | g0010 | AMR | CLM | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01358 | hp2 | a0001 | c0003 | t0005 | g0027 | AMR | CLM | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01361 | hp1 | a0001 | c0003 | t0017 | g0029 | AMR | CLM | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01361 | hp2 | a0001 | c0002 | t0004 | g0291 | AMR | CLM | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | CLM | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01433 | hp2 | a0001 | c0002 | t0004 | g0290 | AMR | CLM | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0021 | EUR | IBS | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01515 | hp2 | a0001 | c0003 | t0010 | g0007 | EUR | IBS | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0122 | EUR | IBS | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01516 | hp2 | a0001 | c0002 | t0027 | g0277 | EUR | IBS | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01517 | hp1 | a0001 | c0002 | t0067 | g0278 | EUR | IBS | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01517 | hp2 | a0001 | c0003 | t0010 | g0007 | EUR | IBS | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01884 | hp1 | a0001 | c0003 | t0005 | g0246 | AFR | ACB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01884 | hp2 | a0001 | c0002 | t0102 | g0226 | AFR | ACB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01891 | hp1 | a0001 | c0001 | t0007 | g0020 | AFR | ACB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01891 | hp2 | a0001 | c0003 | t0059 | g0237 | AFR | ACB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01928 | hp1 | a0001 | c0001 | t0006 | g0009 | AMR | PEL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01928 | hp2 | a0001 | c0001 | t0008 | g0258 | AMR | PEL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01934 | hp2 | a0001 | c0001 | t0084 | g0132 | AMR | PEL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01975 | hp1 | a0001 | c0001 | t0006 | g0033 | AMR | PEL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01975 | hp2 | a0001 | c0001 | t0008 | g0133 | AMR | PEL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01978 | hp1 | a0001 | c0002 | t0004 | g0286 | AMR | PEL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01978 | hp2 | a0001 | c0002 | t0004 | g0288 | AMR | PEL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01981 | hp1 | a0001 | c0001 | t0006 | g0051 | AMR | PEL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02015 | hp2 | a0001 | c0001 | t0049 | g0065 | EAS | KHV | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02040 | hp1 | a0001 | c0001 | t0079 | g0179 | EAS | KHV | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02040 | hp2 | a0001 | c0001 | t0003 | g0098 | EAS | KHV | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02055 | hp1 | a0001 | c0002 | t0063 | g0214 | AFR | ACB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02055 | hp2 | a0001 | c0002 | t0014 | g0152 | AFR | ACB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | KHV | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02074 | hp1 | a0001 | c0001 | t0006 | g0125 | EAS | KHV | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02074 | hp2 | a0001 | c0001 | t0003 | g0046 | EAS | KHV | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02080 | hp2 | a0001 | c0001 | t0069 | g0080 | EAS | KHV | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02129 | hp2 | a0001 | c0001 | t0006 | g0061 | EAS | KHV | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02132 | hp1 | a0001 | c0001 | t0094 | g0111 | EAS | KHV | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02145 | hp1 | a0001 | c0002 | t0103 | g0233 | AFR | ACB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02145 | hp2 | a0001 | c0001 | t0101 | g0159 | AFR | ACB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02148 | hp1 | a0001 | c0001 | t0006 | g0123 | AMR | PEL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02155 | hp1 | a0001 | c0001 | t0095 | g0104 | EAS | CDX | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | CDX | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02165 | hp1 | a0001 | c0001 | t0032 | g0145 | EAS | CDX | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02165 | hp2 | a0001 | c0001 | t0006 | g0003 | EAS | CDX | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02257 | hp1 | a0001 | c0002 | t0022 | g0267 | AFR | ACB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02257 | hp2 | a0001 | c0002 | t0009 | g0149 | AFR | ACB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02258 | hp1 | a0001 | c0002 | t0020 | g0218 | AFR | ACB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02258 | hp2 | a0001 | c0003 | t0005 | g0243 | AFR | ACB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | PEL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02273 | hp2 | a0001 | c0002 | t0004 | g0289 | AMR | PEL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02280 | hp1 | a0001 | c0001 | t0007 | g0165 | AFR | ACB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02280 | hp2 | a0001 | c0002 | t0023 | g0224 | AFR | ACB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PEL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02293 | hp2 | a0001 | c0001 | t0008 | g0129 | AMR | PEL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02300 | hp1 | a0001 | c0003 | t0005 | g0251 | AMR | PEL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02300 | hp2 | a0001 | c0001 | t0078 | g0208 | AMR | PEL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02451 | hp1 | a0001 | c0001 | t0007 | g0160 | AFR | ACB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02451 | hp2 | a0001 | c0001 | t0012 | g0077 | AFR | ACB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02523 | hp1 | a0001 | c0001 | t0071 | g0081 | EAS | KHV | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02523 | hp2 | a0001 | c0001 | t0035 | g0113 | EAS | KHV | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02572 | hp1 | a0001 | c0001 | t0013 | g0014 | AFR | GWD | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02572 | hp2 | a0001 | c0002 | t0031 | g0273 | AFR | GWD | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02602 | hp1 | a0001 | c0002 | t0004 | g0296 | SAS | PJL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02602 | hp2 | a0001 | c0003 | t0005 | g0241 | SAS | PJL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02615 | hp1 | a0001 | c0002 | t0023 | g0225 | AFR | GWD | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02615 | hp2 | a0001 | c0001 | t0007 | g0162 | AFR | GWD | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02622 | hp1 | a0001 | c0002 | t0074 | g0274 | AFR | GWD | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02622 | hp2 | a0001 | c0002 | t0039 | g0155 | AFR | GWD | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0086 | AFR | GWD | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02630 | hp2 | a0001 | c0002 | t0028 | g0147 | AFR | GWD | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02647 | hp1 | a0001 | c0001 | t0038 | g0072 | AFR | GWD | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02647 | hp2 | a0001 | c0002 | t0004 | g0313 | AFR | GWD | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02698 | hp2 | a0001 | c0001 | t0037 | g0057 | SAS | PJL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02717 | hp1 | a0001 | c0002 | t0025 | g0275 | AFR | GWD | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02717 | hp2 | a0002 | c0004 | t0014 | g0151 | AFR | GWD | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02723 | hp1 | a0001 | c0002 | t0005 | g0254 | AFR | GWD | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02723 | hp2 | a0001 | c0002 | t0029 | g0139 | AFR | GWD | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02809 | hp1 | a0001 | c0002 | t0019 | g0141 | AFR | GWD | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02809 | hp2 | a0001 | c0001 | t0007 | g0161 | AFR | GWD | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0060 | AFR | GWD | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02818 | hp2 | a0001 | c0001 | t0057 | g0087 | AFR | GWD | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02886 | hp1 | a0001 | c0002 | t0016 | g0269 | AFR | GWD | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02886 | hp2 | a0001 | c0002 | t0019 | g0143 | AFR | GWD | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02895 | hp1 | a0001 | c0002 | t0025 | g0276 | AFR | GWD | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02895 | hp2 | a0001 | c0002 | t0056 | g0268 | AFR | GWD | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02896 | hp1 | a0001 | c0001 | t0007 | g0137 | AFR | GWD | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02896 | hp2 | a0001 | c0002 | t0052 | g0312 | AFR | GWD | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02897 | hp1 | a0001 | c0002 | t0024 | g0310 | AFR | GWD | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02897 | hp2 | a0001 | c0002 | t0064 | g0228 | AFR | GWD | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02922 | hp1 | a0001 | c0002 | t0018 | g0294 | AFR | ESN | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02922 | hp2 | a0001 | c0002 | t0065 | g0284 | AFR | ESN | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02965 | hp1 | a0001 | c0001 | t0037 | g0073 | AFR | ESN | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02965 | hp2 | a0001 | c0001 | t0007 | g0020 | AFR | ESN | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02970 | hp1 | a0001 | c0003 | t0005 | g0248 | AFR | ESN | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02970 | hp2 | a0001 | c0001 | t0007 | g0158 | AFR | ESN | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02976 | hp1 | a0001 | c0002 | t0088 | g0138 | AFR | ESN | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02976 | hp2 | a0001 | c0002 | t0040 | g0210 | AFR | ESN | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03017 | hp1 | a0001 | c0003 | t0005 | g0238 | SAS | PJL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0066 | SAS | PJL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03041 | hp1 | a0001 | c0002 | t0009 | g0017 | AFR | GWD | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0047 | AFR | GWD | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03098 | hp1 | a0001 | c0002 | t0046 | g0220 | AFR | MSL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03098 | hp2 | a0001 | c0002 | t0004 | g0304 | AFR | MSL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03130 | hp1 | a0001 | c0001 | t0030 | g0011 | AFR | ESN | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03130 | hp2 | a0001 | c0002 | t0014 | g0018 | AFR | ESN | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03139 | hp1 | a0001 | c0002 | t0015 | g0019 | AFR | ESN | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03139 | hp2 | a0001 | c0002 | t0040 | g0157 | AFR | ESN | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03195 | hp1 | a0001 | c0002 | t0016 | g0227 | AFR | ESN | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03195 | hp2 | a0001 | c0002 | t0051 | g0223 | AFR | ESN | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03209 | hp1 | a0001 | c0002 | t0039 | g0156 | AFR | MSL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03209 | hp2 | a0001 | c0002 | t0009 | g0017 | AFR | MSL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03225 | hp1 | a0001 | c0002 | t0015 | g0019 | AFR | MSL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03225 | hp2 | a0001 | c0001 | t0013 | g0088 | AFR | MSL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03239 | hp1 | a0001 | c0001 | t0093 | g0052 | SAS | PJL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03239 | hp2 | a0001 | c0003 | t0005 | g0245 | SAS | PJL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03453 | hp1 | a0001 | c0001 | t0030 | g0011 | AFR | MSL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03453 | hp2 | a0001 | c0002 | t0055 | g0280 | AFR | MSL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03486 | hp1 | a0001 | c0002 | t0031 | g0265 | AFR | MSL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03486 | hp2 | a0001 | c0002 | t0099 | g0212 | AFR | MSL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0256 | SAS | PJL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03490 | hp2 | a0001 | c0001 | t0068 | g0303 | SAS | PJL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03491 | hp1 | a0001 | c0002 | t0004 | g0283 | SAS | PJL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03491 | hp2 | a0001 | c0001 | t0032 | g0032 | SAS | PJL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03540 | hp1 | a0001 | c0002 | t0045 | g0217 | AFR | GWD | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03540 | hp2 | a0001 | c0001 | t0013 | g0085 | AFR | GWD | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03654 | hp1 | a0001 | c0002 | t0004 | g0282 | SAS | PJL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03704 | hp1 | a0001 | c0002 | t0021 | g0297 | SAS | PJL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0013 | SAS | PJL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03710 | hp2 | a0001 | c0002 | t0004 | g0309 | SAS | PJL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0257 | SAS | BEB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03831 | hp2 | a0001 | c0003 | t0005 | g0250 | SAS | BEB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03834 | hp1 | a0001 | c0002 | t0004 | g0299 | SAS | BEB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03927 | hp1 | a0001 | c0003 | t0010 | g0271 | SAS | BEB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03927 | hp2 | a0001 | c0002 | t0004 | g0292 | SAS | BEB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG04115 | hp1 | a0001 | c0001 | t0012 | g0034 | SAS | STU | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG04115 | hp2 | a0001 | c0001 | t0012 | g0036 | SAS | STU | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0049 | SAS | BEB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | BEB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG04199 | hp1 | a0001 | c0003 | t0005 | g0272 | SAS | STU | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG04199 | hp2 | a0001 | c0002 | t0004 | g0315 | SAS | STU | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0076 | SAS | STU | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | STU | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18522 | hp1 | a0001 | c0002 | t0015 | g0153 | AFR | YRI | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18522 | hp2 | a0001 | c0002 | t0028 | g0146 | AFR | YRI | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | CHB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | CHB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18747 | hp1 | a0001 | c0001 | t0047 | g0067 | EAS | CHB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | CHB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0090 | AFR | YRI | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18906 | hp2 | a0001 | c0002 | t0022 | g0266 | AFR | YRI | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18939 | hp2 | a0001 | c0001 | t0098 | g0101 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18941 | hp1 | a0001 | c0001 | t0091 | g0103 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18944 | hp1 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18948 | hp1 | a0001 | c0001 | t0082 | g0195 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18948 | hp2 | a0001 | c0001 | t0011 | g0039 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18949 | hp2 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18951 | hp2 | a0001 | c0001 | t0003 | g0117 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18954 | hp2 | a0001 | c0001 | t0097 | g0055 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18956 | hp2 | a0001 | c0001 | t0096 | g0094 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18957 | hp2 | a0001 | c0001 | t0087 | g0107 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18962 | hp1 | a0001 | c0001 | t0035 | g0114 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18963 | hp2 | a0001 | c0001 | t0089 | g0099 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18965 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18969 | hp1 | a0001 | c0001 | t0080 | g0038 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18971 | hp1 | a0001 | c0001 | t0086 | g0126 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18972 | hp1 | a0001 | c0001 | t0003 | g0116 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18972 | hp2 | a0001 | c0001 | t0081 | g0196 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18974 | hp1 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18975 | hp2 | a0001 | c0001 | t0003 | g0115 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18977 | hp1 | a0001 | c0001 | t0090 | g0068 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18979 | hp1 | a0001 | c0001 | t0073 | g0130 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18979 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18980 | hp1 | a0001 | c0002 | t0004 | g0285 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18981 | hp1 | a0001 | c0001 | t0050 | g0194 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18981 | hp2 | a0001 | c0001 | t0092 | g0097 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18982 | hp1 | a0001 | c0001 | t0003 | g0127 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18982 | hp2 | a0001 | c0001 | t0006 | g0048 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18983 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18988 | hp1 | a0001 | c0001 | t0008 | g0262 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18991 | hp1 | a0001 | c0001 | t0033 | g0064 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18991 | hp2 | a0001 | c0001 | t0011 | g0121 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18992 | hp1 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18993 | hp2 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18998 | hp1 | a0001 | c0001 | t0011 | g0041 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18999 | hp1 | a0001 | c0002 | t0004 | g0306 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19001 | hp2 | a0001 | c0002 | t0004 | g0305 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19002 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19002 | hp2 | a0001 | c0001 | t0034 | g0187 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19003 | hp1 | a0001 | c0001 | t0085 | g0040 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19004 | hp1 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19005 | hp2 | a0001 | c0001 | t0011 | g0037 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19006 | hp1 | a0001 | c0001 | t0048 | g0062 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19006 | hp2 | a0001 | c0001 | t0076 | g0201 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19007 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19009 | hp2 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19010 | hp1 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19011 | hp1 | a0001 | c0001 | t0083 | g0075 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19011 | hp2 | a0001 | c0001 | t0075 | g0168 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19012 | hp1 | a0001 | c0001 | t0006 | g0003 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19030 | hp1 | a0001 | c0002 | t0009 | g0231 | AFR | LWK | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19030 | hp2 | a0001 | c0002 | t0024 | g0311 | AFR | LWK | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19043 | hp1 | a0001 | c0002 | t0058 | g0148 | AFR | LWK | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19043 | hp2 | a0001 | c0001 | t0038 | g0058 | AFR | LWK | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19054 | hp1 | a0001 | c0001 | t0033 | g0079 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19057 | hp2 | a0001 | c0001 | t0008 | g0261 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19060 | hp1 | a0001 | c0001 | t0043 | g0035 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19065 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19065 | hp2 | a0001 | c0001 | t0034 | g0199 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19079 | hp2 | a0001 | c0001 | t0003 | g0119 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19085 | hp1 | a0001 | c0001 | t0003 | g0105 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19240 | hp1 | a0001 | c0002 | t0020 | g0219 | AFR | YRI | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19240 | hp2 | a0001 | c0002 | t0054 | g0295 | AFR | YRI | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA20129 | hp1 | a0001 | c0001 | t0006 | g0053 | AFR | ASW | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA20129 | hp2 | a0001 | c0003 | t0005 | g0252 | AFR | ASW | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0071 | EUR | TSI | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA20752 | hp2 | a0001 | c0002 | t0004 | g0298 | EUR | TSI | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0135 | EUR | TSI | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA20805 | hp2 | a0001 | c0002 | t0021 | g0300 | EUR | TSI | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | GIH | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0063 | SAS | GIH | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01123 | hp1 | a0001 | c0001 | t0008 | g0131 | AMR | CLM | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01123 | hp2 | a0001 | c0002 | t0027 | g0222 | AMR | CLM | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02109 | hp1 | a0001 | c0002 | t0100 | g0164 | AFR | ACB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02109 | hp2 | a0001 | c0002 | t0044 | g0221 | AFR | ACB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02486 | hp1 | a0001 | c0002 | t0062 | g0230 | AFR | ACB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02486 | hp2 | a0001 | c0002 | t0029 | g0140 | AFR | ACB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02559 | hp1 | a0001 | c0002 | t0019 | g0142 | AFR | ACB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02559 | hp2 | a0001 | c0002 | t0014 | g0018 | AFR | ACB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03471 | hp1 | a0001 | c0002 | t0041 | g0232 | AFR | MSL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0091 | AFR | MSL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG06807 | hp1 | a0001 | c0003 | t0005 | g0253 | AFR | USA | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG06807 | hp2 | a0001 | c0001 | t0012 | g0044 | AFR | USA | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18955 | hp1 | a0001 | c0001 | t0077 | g0083 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA20300 | hp1 | a0001 | c0001 | t0006 | g0003 | AFR | USA | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA20300 | hp2 | a0001 | c0002 | t0016 | g0229 | AFR | USA | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA21309 | hp1 | a0001 | c0001 | t0042 | g0202 | AFR | LWK | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA21309 | hp2 | a0001 | c0002 | t0018 | g0293 | AFR | LWK | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
homoSapiens | chm13v2 | a0001 | c0001 | t0072 | g0206 | REF | REF | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
homoSapiens | grch38p0 | a0001 | c0003 | t0005 | g0239 | REF | REF | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:76060272 | T | C | 1 | a0002 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.214A>G | p.Arg72Gly | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 5/15 | 353/13159 | 214/1176 | 72/391 | chr12 | 76060272 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:76056120 | T | C | 3 | a0001c0001 a0001c0002 a0002c0004 |
323 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(320): Show |
synonymous_variant | LOW | c.471A>G | p.Lys157Lys | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 7/15 | 610/13159 | 471/1176 | 157/391 | chr12 | 76056120 | |||
chr12:76060186 | G | A | 1 | a0001c0001 | 229 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(226): Show |
synonymous_variant | LOW | c.300C>T | p.His100His | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 5/15 | 439/13159 | 300/1176 | 100/391 | chr12 | 76060186 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:76036610 | CATA | C | 2 | a0001c0002t0015 a0001c0002t0103 |
5 | HG01261.hp1 HG02145.hp1 HG03139.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*11816_*11818delTA others(1): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 11816 | chr12 | 76036610 | ||||||
chr12:76036612 | T | C | 1 | a0001c0001t0002 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11817A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 11817 | chr12 | 76036612 | ||||||
chr12:76036728 | G | A | 1 | a0001c0002t0023 | 2 | HG02280.hp2 HG02615.hp1 |
3_prime_UTR_variant | MODIFIER | c.*11701C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 11701 | chr12 | 76036728 | ||||||
chr12:76036734 | G | A | 64 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(61): Show |
253 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(250): Show |
3_prime_UTR_variant | MODIFIER | c.*11695C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 11695 | chr12 | 76036734 | ||||||
chr12:76036918 | C | CA | 17 | a0001c0001t0034 a0001c0001t0077 a0001c0001t0086 others(14): Show |
26 | HG01261.hp1 HG01891.hp2 HG02109.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*11510dupT | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 11510 | chr12 | 76036918 | ||||||
chr12:76036941 | G | A | 1 | a0001c0001t0078 | 1 | HG02300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11488C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 11488 | chr12 | 76036941 | ||||||
chr12:76036981 | T | C | 4 | a0001c0002t0014 a0001c0002t0028 a0001c0002t0041 others(1): Show |
8 | HG01109.hp2 HG02055.hp2 HG02559.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*11448A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 11448 | chr12 | 76036981 | ||||||
chr12:76037016 | C | G | 1 | a0001c0003t0060 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11413G>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 11413 | chr12 | 76037016 | ||||||
chr12:76037236 | T | C | 1 | a0001c0001t0091 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11193A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 11193 | chr12 | 76037236 | ||||||
chr12:76037285 | A | G | 1 | a0001c0002t0009 | 4 | HG02257.hp2 HG03041.hp1 HG03209.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*11144T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 11144 | chr12 | 76037285 | ||||||
chr12:76037358 | T | C | 54 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(51): Show |
231 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(228): Show |
3_prime_UTR_variant | MODIFIER | c.*11071A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 11071 | chr12 | 76037358 | ||||||
chr12:76037572 | C | T | 8 | a0001c0002t0009 a0001c0002t0014 a0001c0002t0028 others(5): Show |
17 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*10857G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 10857 | chr12 | 76037572 | ||||||
chr12:76037585 | GACAA | G | 1 | a0001c0002t0019 | 3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*10840_*10843delTT others(2): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 10840 | chr12 | 76037585 | ||||||
chr12:76037848 | G | A | 1 | a0001c0002t0009 | 4 | HG02257.hp2 HG03041.hp1 HG03209.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*10581C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 10581 | chr12 | 76037848 | ||||||
chr12:76037879 | T | C | 1 | a0001c0001t0079 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10550A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 10550 | chr12 | 76037879 | ||||||
chr12:76038053 | G | C | 1 | a0001c0002t0061 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10376C>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 10376 | chr12 | 76038053 | ||||||
chr12:76038062 | G | C | 1 | a0001c0002t0045 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10367C>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 10367 | chr12 | 76038062 | ||||||
chr12:76038148 | T | C | 2 | a0001c0001t0047 a0001c0001t0049 |
2 | HG02015.hp2 NA18747.hp1 |
3_prime_UTR_variant | MODIFIER | c.*10281A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 10281 | chr12 | 76038148 | ||||||
chr12:76038322 | T | G | 1 | a0001c0002t0046 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10107A>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 10107 | chr12 | 76038322 | ||||||
chr12:76038594 | A | G | 1 | a0001c0001t0089 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9835T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 9835 | chr12 | 76038594 | ||||||
chr12:76038726 | A | T | 1 | a0001c0003t0010 | 4 | HG00642.hp1 HG01515.hp2 HG01517.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*9703T>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 9703 | chr12 | 76038726 | ||||||
chr12:76038932 | T | C | 1 | a0001c0002t0019 | 3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*9497A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 9497 | chr12 | 76038932 | ||||||
chr12:76039021 | G | A | 3 | a0001c0001t0011 a0001c0001t0080 a0001c0001t0085 |
6 | NA18948.hp2 NA18969.hp1 NA18991.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*9408C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 9408 | chr12 | 76039021 | ||||||
chr12:76039052 | G | C | 4 | a0001c0002t0025 a0001c0002t0027 a0001c0002t0061 others(1): Show |
6 | HG01081.hp2 HG01123.hp2 HG01516.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*9377C>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 9377 | chr12 | 76039052 | ||||||
chr12:76039199 | T | C | 1 | a0001c0002t0055 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9230A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 9230 | chr12 | 76039199 | ||||||
chr12:76039350 | A | C | 2 | a0001c0002t0015 a0001c0002t0103 |
5 | HG01261.hp1 HG02145.hp1 HG03139.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*9079T>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 9079 | chr12 | 76039350 | ||||||
chr12:76039441 | C | T | 10 | a0001c0002t0009 a0001c0002t0014 a0001c0002t0020 others(7): Show |
20 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*8988G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 8988 | chr12 | 76039441 | ||||||
chr12:76039456 | T | C | 16 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0032 others(13): Show |
89 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*8973A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 8973 | chr12 | 76039456 | ||||||
chr12:76039922 | G | A | 1 | a0001c0001t0101 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8507C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 8507 | chr12 | 76039922 | ||||||
chr12:76040068 | T | C | 2 | a0001c0002t0015 a0001c0002t0103 |
5 | HG01261.hp1 HG02145.hp1 HG03139.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*8361A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 8361 | chr12 | 76040068 | ||||||
chr12:76040110 | T | G | 1 | a0001c0002t0019 | 3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8319A>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 8319 | chr12 | 76040110 | ||||||
chr12:76040347 | T | C | 10 | a0001c0002t0009 a0001c0002t0014 a0001c0002t0020 others(7): Show |
20 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*8082A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 8082 | chr12 | 76040347 | ||||||
chr12:76040369 | A | G | 2 | a0001c0002t0015 a0001c0002t0103 |
5 | HG01261.hp1 HG02145.hp1 HG03139.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*8060T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 8060 | chr12 | 76040369 | ||||||
chr12:76040518 | T | TAC | 4 | a0001c0001t0011 a0001c0001t0080 a0001c0001t0081 others(1): Show |
7 | NA18948.hp2 NA18969.hp1 NA18972.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*7909_*7910dupGT | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 7910 | chr12 | 76040518 | ||||||
chr12:76040518 | TAC | T | 2 | a0001c0002t0015 a0001c0002t0103 |
5 | HG01261.hp1 HG02145.hp1 HG03139.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*7909_*7910delGT | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 7909 | chr12 | 76040518 | ||||||
chr12:76040584 | CGGCTCAC others(37): Show |
C | 1 | a0001c0002t0065 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7801_*7844delCACA others(40): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 7801 | chr12 | 76040584 | ||||||
chr12:76040710 | C | T | 3 | a0001c0002t0044 a0001c0002t0046 a0001c0002t0102 |
3 | HG01884.hp2 HG02109.hp2 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7719G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 7719 | chr12 | 76040710 | ||||||
chr12:76041461 | A | G | 1 | a0001c0002t0051 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6968T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 6968 | chr12 | 76041461 | ||||||
chr12:76041541 | C | G | 1 | a0001c0001t0085 | 1 | NA19003.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6888G>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 6888 | chr12 | 76041541 | ||||||
chr12:76041631 | T | C | 1 | a0001c0002t0058 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6798A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 6798 | chr12 | 76041631 | ||||||
chr12:76041651 | G | A | 2 | a0001c0002t0009 a0001c0002t0039 |
6 | HG02257.hp2 HG02622.hp2 HG03041.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*6778C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 6778 | chr12 | 76041651 | ||||||
chr12:76041678 | T | TA | 4 | a0001c0002t0025 a0001c0002t0027 a0001c0002t0061 others(1): Show |
6 | HG01081.hp2 HG01123.hp2 HG01516.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*6750dupT | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 6750 | chr12 | 76041678 | ||||||
chr12:76041694 | C | A | 4 | a0001c0002t0025 a0001c0002t0027 a0001c0002t0061 others(1): Show |
6 | HG01081.hp2 HG01123.hp2 HG01516.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*6735G>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 6735 | chr12 | 76041694 | ||||||
chr12:76041793 | T | C | 1 | a0001c0002t0019 | 3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6636A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 6636 | chr12 | 76041793 | ||||||
chr12:76041801 | C | T | 1 | a0001c0002t0025 | 2 | HG02717.hp1 HG02895.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6628G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 6628 | chr12 | 76041801 | ||||||
chr12:76041895 | A | G | 1 | a0001c0001t0075 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6534T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 6534 | chr12 | 76041895 | ||||||
chr12:76041912 | C | T | 1 | a0001c0002t0054 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6517G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 6517 | chr12 | 76041912 | ||||||
chr12:76041929 | G | C | 1 | a0001c0002t0019 | 3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6500C>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 6500 | chr12 | 76041929 | ||||||
chr12:76041959 | G | A | 1 | a0001c0001t0082 | 1 | NA18948.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6470C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 6470 | chr12 | 76041959 | ||||||
chr12:76041980 | A | T | 1 | a0001c0002t0019 | 3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6449T>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 6449 | chr12 | 76041980 | ||||||
chr12:76042054 | A | AT | 10 | a0001c0001t0036 a0001c0001t0084 a0001c0001t0101 others(7): Show |
17 | HG00642.hp1 HG01261.hp2 HG01358.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*6374dupA | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 6374 | chr12 | 76042054 | ||||||
chr12:76042313 | T | G | 3 | a0001c0002t0014 a0001c0002t0041 a0002c0004t0014 |
6 | HG01109.hp2 HG02055.hp2 HG02559.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*6116A>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 6116 | chr12 | 76042313 | ||||||
chr12:76042405 | TAAAGACA others(6): Show |
T | 2 | a0001c0001t0075 a0001c0001t0076 |
2 | NA19006.hp2 NA19011.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6011_*6023delGGGT others(9): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 6011 | chr12 | 76042405 | ||||||
chr12:76042413 | C | G | 2 | a0001c0002t0015 a0001c0002t0103 |
5 | HG01261.hp1 HG02145.hp1 HG03139.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6016G>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 6016 | chr12 | 76042413 | ||||||
chr12:76042509 | G | A | 1 | a0001c0002t0051 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5920C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 5920 | chr12 | 76042509 | ||||||
chr12:76042602 | T | C | 1 | a0001c0002t0058 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5827A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 5827 | chr12 | 76042602 | ||||||
chr12:76042734 | T | C | 1 | a0001c0002t0019 | 3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5695A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 5695 | chr12 | 76042734 | ||||||
chr12:76043031 | T | A | 3 | a0001c0002t0024 a0001c0002t0052 a0001c0002t0065 |
4 | HG02896.hp2 HG02897.hp1 HG02922.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5398A>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 5398 | chr12 | 76043031 | ||||||
chr12:76043065 | T | A | 1 | a0001c0001t0087 | 1 | NA18957.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5364A>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 5364 | chr12 | 76043065 | ||||||
chr12:76043098 | C | T | 2 | a0001c0002t0056 a0001c0002t0064 |
2 | HG02895.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5331G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 5331 | chr12 | 76043098 | ||||||
chr12:76043127 | T | C | 2 | a0001c0002t0056 a0001c0002t0064 |
2 | HG02895.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5302A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 5302 | chr12 | 76043127 | ||||||
chr12:76043153 | T | C | 1 | a0001c0002t0019 | 3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5276A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 5276 | chr12 | 76043153 | ||||||
chr12:76043301 | G | A | 2 | a0001c0002t0029 a0001c0002t0088 |
3 | HG02486.hp2 HG02723.hp2 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5128C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 5128 | chr12 | 76043301 | ||||||
chr12:76043358 | T | G | 9 | a0001c0001t0003 a0001c0001t0035 a0001c0001t0043 others(6): Show |
33 | HG00423.hp1 HG00735.hp1 HG02040.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*5071A>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 5071 | chr12 | 76043358 | ||||||
chr12:76043385 | C | T | 3 | a0001c0002t0014 a0001c0002t0041 a0002c0004t0014 |
6 | HG01109.hp2 HG02055.hp2 HG02559.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5044G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 5044 | chr12 | 76043385 | ||||||
chr12:76043395 | C | T | 1 | a0001c0001t0083 | 1 | NA19011.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5034G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 5034 | chr12 | 76043395 | ||||||
chr12:76043477 | G | GA | 53 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(50): Show |
174 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(171): Show |
3_prime_UTR_variant | MODIFIER | c.*4951dupT | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 4951 | chr12 | 76043477 | ||||||
chr12:76043477 | G | GAA | 13 | a0001c0001t0012 a0001c0001t0068 a0001c0001t0092 others(10): Show |
42 | HG00140.hp1 HG00733.hp1 HG00738.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*4950_*4951dupTT | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 4951 | chr12 | 76043477 | ||||||
chr12:76043477 | GA | G | 6 | a0001c0001t0032 a0001c0002t0056 a0001c0003t0010 others(3): Show |
12 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*4951delT | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 4951 | chr12 | 76043477 | ||||||
chr12:76043536 | A | G | 4 | a0001c0001t0007 a0001c0001t0101 a0001c0002t0015 others(1): Show |
14 | HG01261.hp1 HG01891.hp1 HG02145.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*4893T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 4893 | chr12 | 76043536 | ||||||
chr12:76043839 | T | G | 1 | a0001c0002t0062 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4590A>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 4590 | chr12 | 76043839 | ||||||
chr12:76043911 | G | C | 3 | a0001c0001t0006 a0001c0001t0036 a0001c0001t0093 |
19 | HG00323.hp1 HG00558.hp2 HG01255.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*4518C>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 4518 | chr12 | 76043911 | ||||||
chr12:76043937 | C | G | 1 | a0001c0002t0065 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4492G>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 4492 | chr12 | 76043937 | ||||||
chr12:76043993 | G | A | 65 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(62): Show |
256 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(253): Show |
3_prime_UTR_variant | MODIFIER | c.*4436C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 4436 | chr12 | 76043993 | ||||||
chr12:76044040 | TTTTGAGA others(9): Show |
T | 1 | a0001c0002t0046 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4373_*4388delGTGC others(12): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 4373 | chr12 | 76044040 | ||||||
chr12:76044225 | C | T | 5 | a0001c0001t0007 a0001c0001t0042 a0001c0001t0101 others(2): Show |
15 | HG01261.hp1 HG01891.hp1 HG02145.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*4204G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 4204 | chr12 | 76044225 | ||||||
chr12:76044481 | T | C | 2 | a0001c0001t0037 a0001c0001t0038 |
4 | HG02647.hp1 HG02698.hp2 HG02965.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3948A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 3948 | chr12 | 76044481 | ||||||
chr12:76044483 | T | C | 3 | a0001c0002t0014 a0001c0002t0041 a0002c0004t0014 |
6 | HG01109.hp2 HG02055.hp2 HG02559.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3946A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 3946 | chr12 | 76044483 | ||||||
chr12:76045085 | T | A | 2 | a0001c0001t0094 a0001c0001t0095 |
2 | HG02132.hp1 HG02155.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3344A>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 3344 | chr12 | 76045085 | ||||||
chr12:76045201 | A | G | 1 | a0001c0001t0073 | 1 | NA18979.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3228T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 3228 | chr12 | 76045201 | ||||||
chr12:76045369 | G | A | 5 | a0001c0001t0007 a0001c0001t0042 a0001c0001t0101 others(2): Show |
15 | HG01261.hp1 HG01891.hp1 HG02145.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3060C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 3060 | chr12 | 76045369 | ||||||
chr12:76045471 | A | G | 1 | a0001c0001t0070 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2958T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 2958 | chr12 | 76045471 | ||||||
chr12:76045604 | C | T | 1 | a0001c0002t0058 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2825G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 2825 | chr12 | 76045604 | ||||||
chr12:76045682 | C | A | 1 | a0001c0002t0102 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2747G>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 2747 | chr12 | 76045682 | ||||||
chr12:76045698 | T | C | 2 | a0001c0002t0009 a0001c0002t0039 |
6 | HG02257.hp2 HG02622.hp2 HG03041.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2731A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 2731 | chr12 | 76045698 | ||||||
chr12:76045724 | C | T | 1 | a0001c0001t0030 | 2 | HG03130.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2705G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 2705 | chr12 | 76045724 | ||||||
chr12:76045879 | A | G | 70 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(67): Show |
263 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(260): Show |
3_prime_UTR_variant | MODIFIER | c.*2550T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 2550 | chr12 | 76045879 | ||||||
chr12:76045941 | TCAGAATA others(6): Show |
T | 6 | a0001c0001t0071 a0001c0002t0014 a0001c0002t0015 others(3): Show |
12 | HG01109.hp2 HG01261.hp1 HG02055.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2475_*2487delGGTT others(9): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 2475 | chr12 | 76045941 | ||||||
chr12:76045954 | C | T | 81 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(78): Show |
294 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(291): Show |
3_prime_UTR_variant | MODIFIER | c.*2475G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 2475 | chr12 | 76045954 | ||||||
chr12:76046206 | A | T | 1 | a0001c0001t0070 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2223T>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 2223 | chr12 | 76046206 | ||||||
chr12:76046275 | A | T | 1 | a0001c0002t0044 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2154T>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 2154 | chr12 | 76046275 | ||||||
chr12:76046429 | T | C | 1 | a0001c0002t0019 | 3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2000A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 2000 | chr12 | 76046429 | ||||||
chr12:76046740 | T | C | 1 | a0001c0002t0063 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1689A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 1689 | chr12 | 76046740 | ||||||
chr12:76046762 | C | T | 3 | a0001c0002t0016 a0001c0002t0056 a0001c0002t0064 |
5 | HG02886.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1667G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 1667 | chr12 | 76046762 | ||||||
chr12:76046842 | A | T | 1 | a0001c0002t0028 | 2 | HG02630.hp2 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1587T>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 1587 | chr12 | 76046842 | ||||||
chr12:76046868 | T | A | 1 | a0001c0001t0096 | 1 | NA18956.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1561A>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 1561 | chr12 | 76046868 | ||||||
chr12:76047162 | T | C | 1 | a0001c0002t0019 | 3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1267A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 1267 | chr12 | 76047162 | ||||||
chr12:76047371 | A | AT | 15 | a0001c0002t0004 a0001c0002t0020 a0001c0002t0021 others(12): Show |
42 | HG00140.hp1 HG00733.hp1 HG00738.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*1057dupA | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 1057 | chr12 | 76047371 | ||||||
chr12:76047371 | AT | A | 6 | a0001c0001t0068 a0001c0002t0046 a0001c0002t0064 others(3): Show |
6 | HG01069.hp2 HG01517.hp1 HG02897.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1057delA | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 1057 | chr12 | 76047371 | ||||||
chr12:76047374 | T | TTA | 6 | a0001c0001t0069 a0001c0002t0014 a0001c0002t0028 others(3): Show |
11 | HG01109.hp2 HG02055.hp2 HG02080.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1054_*1055insTA | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 1054 | chr12 | 76047374 | ||||||
chr12:76047375 | T | TA | 58 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(55): Show |
242 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(239): Show |
3_prime_UTR_variant | MODIFIER | c.*1053_*1054insT | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 1053 | chr12 | 76047375 | ||||||
chr12:76047376 | T | A | 3 | a0001c0001t0013 a0001c0001t0097 a0001c0001t0098 |
6 | HG01243.hp1 HG02572.hp1 HG03225.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1053A>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 1053 | chr12 | 76047376 | ||||||
chr12:76047379 | T | A | 1 | a0001c0002t0041 | 2 | HG01109.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1050A>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 1050 | chr12 | 76047379 | ||||||
chr12:76047380 | T | A | 1 | a0001c0002t0009 | 4 | HG02257.hp2 HG03041.hp1 HG03209.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1049A>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 1049 | chr12 | 76047380 | ||||||
chr12:76047388 | T | A | 5 | a0001c0001t0007 a0001c0001t0101 a0001c0002t0040 others(2): Show |
13 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1041A>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 1041 | chr12 | 76047388 | ||||||
chr12:76047427 | C | CT | 10 | a0001c0001t0047 a0001c0001t0048 a0001c0001t0049 others(7): Show |
15 | HG02015.hp2 HG02109.hp2 HG02257.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1001dupA | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 1001 | chr12 | 76047427 | ||||||
chr12:76047632 | A | G | 1 | a0001c0002t0009 | 4 | HG02257.hp2 HG03041.hp1 HG03209.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*797T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 797 | chr12 | 76047632 | ||||||
chr12:76047673 | T | C | 1 | a0001c0002t0102 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*756A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 756 | chr12 | 76047673 | ||||||
chr12:76047808 | C | T | 1 | a0001c0001t0043 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*621G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 621 | chr12 | 76047808 | ||||||
chr12:76048031 | A | G | 1 | a0001c0001t0042 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*398T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 398 | chr12 | 76048031 | ||||||
chr12:76048133 | T | A | 5 | a0001c0002t0014 a0001c0002t0015 a0001c0002t0041 others(2): Show |
11 | HG01109.hp2 HG01261.hp1 HG02055.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*296A>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 296 | chr12 | 76048133 | ||||||
chr12:76084660 | G | A | 1 | a0001c0002t0104 | 1 | HG00733.hp1 | 5_prime_UTR_variant | MODIFIER | c.-114C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/15 | 10441 | chr12 | 76084660 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:76048619 | T | C | 1 | a0001c0001t0057g0087 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1141-155A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 14/14 | chr12 | 76048619 | |||||||
chr12:76049110 | C | CT | 3 | a0001c0002t0019g0141 a0001c0002t0019g0142 a0001c0002t0019g0143 |
3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1140+89dupA | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 14/14 | chr12 | 76049110 | |||||||
chr12:76049127 | T | C | 78 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(75): Show |
92 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.1140+73A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 14/14 | chr12 | 76049127 | |||||||
chr12:76049137 | A | G | 3 | a0001c0002t0019g0141 a0001c0002t0019g0142 a0001c0002t0019g0143 |
3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1140+63T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 14/14 | chr12 | 76049137 | |||||||
chr12:76049406 | A | G | 1 | a0001c0002t0046g0220 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1090-156T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 13/14 | chr12 | 76049406 | |||||||
chr12:76049476 | C | T | 1 | a0001c0002t0028g0146 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1090-226G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 13/14 | chr12 | 76049476 | |||||||
chr12:76049676 | C | T | 3 | a0001c0002t0044g0221 a0001c0002t0046g0220 a0001c0002t0102g0226 |
3 | HG01884.hp2 HG02109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1089+80G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 13/14 | chr12 | 76049676 | |||||||
chr12:76049687 | A | G | 6 | a0001c0002t0025g0275 a0001c0002t0025g0276 a0001c0002t0027g0222 others(3): Show |
6 | HG01081.hp2 HG01123.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1089+69T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 13/14 | chr12 | 76049687 | |||||||
chr12:76049712 | T | C | 1 | a0001c0001t0043g0035 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1089+44A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 13/14 | chr12 | 76049712 | |||||||
chr12:76049804 | G | C | 2 | a0001c0001t0001g0030 a0001c0001t0008g0261 |
3 | NA18971.hp2 NA19054.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.1060-19C>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 12/14 | chr12 | 76049804 | |||||||
chr12:76049813 | T | C | 1 | a0001c0001t0070g0205 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1060-28A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 12/14 | chr12 | 76049813 | |||||||
chr12:76049910 | G | T | 3 | a0001c0002t0024g0310 a0001c0002t0024g0311 a0001c0002t0052g0312 |
3 | HG02896.hp2 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1060-125C>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 12/14 | chr12 | 76049910 | |||||||
chr12:76049997 | G | A | 1 | a0001c0001t0002g0118 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1060-212C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 12/14 | chr12 | 76049997 | |||||||
chr12:76050103 | G | A | 3 | a0001c0002t0031g0265 a0001c0002t0031g0273 a0001c0002t0074g0274 |
3 | HG02572.hp2 HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1060-318C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 12/14 | chr12 | 76050103 | |||||||
chr12:76050106 | G | A | 1 | a0001c0002t0021g0300 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1060-321C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 12/14 | chr12 | 76050106 | |||||||
chr12:76050237 | C | T | 3 | a0001c0002t0019g0141 a0001c0002t0019g0142 a0001c0002t0019g0143 |
3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1059+294G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 12/14 | chr12 | 76050237 | |||||||
chr12:76050272 | T | C | 5 | a0001c0002t0009g0017 a0001c0002t0009g0149 a0001c0002t0009g0231 others(2): Show |
6 | HG02257.hp2 HG02622.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1059+259A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 12/14 | chr12 | 76050272 | |||||||
chr12:76050351 | A | G | 72 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(69): Show |
86 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.1059+180T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 12/14 | chr12 | 76050351 | |||||||
chr12:76050436 | A | G | 3 | a0001c0002t0019g0141 a0001c0002t0019g0142 a0001c0002t0019g0143 |
3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1059+95T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 12/14 | chr12 | 76050436 | |||||||
chr12:76050730 | G | A | 196 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(193): Show |
228 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(225): Show |
intron_variant | MODIFIER | c.937-77C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 11/14 | chr12 | 76050730 | |||||||
chr12:76050753 | A | G | 1 | a0001c0002t0062g0230 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.937-100T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 11/14 | chr12 | 76050753 | |||||||
chr12:76050802 | C | T | 1 | a0001c0001t0037g0073 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.937-149G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 11/14 | chr12 | 76050802 | |||||||
chr12:76050905 | G | A | 1 | a0001c0001t0006g0061 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.937-252C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 11/14 | chr12 | 76050905 | |||||||
chr12:76051002 | G | GA | 48 | a0001c0001t0001g0172 a0001c0001t0001g0185 a0001c0001t0003g0046 others(45): Show |
48 | HG00140.hp1 HG00733.hp1 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.937-350dupT | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 11/14 | chr12 | 76051002 | |||||||
chr12:76051002 | G | GAA | 17 | a0001c0002t0004g0304 a0001c0002t0009g0017 a0001c0002t0009g0149 others(14): Show |
19 | HG01109.hp2 HG02257.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.937-351_937-350dup others(2): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 11/14 | chr12 | 76051002 | |||||||
chr12:76051030 | T | C | 4 | a0001c0001t0001g0022 a0001c0001t0001g0176 a0001c0001t0075g0168 others(1): Show |
5 | NA18955.hp2 NA18999.hp2 NA19006.hp2 others(2): Show |
intron_variant | MODIFIER | c.937-377A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 11/14 | chr12 | 76051030 | |||||||
chr12:76051330 | T | A | 1 | a0001c0001t0002g0070 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.937-677A>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 11/14 | chr12 | 76051330 | |||||||
chr12:76051330 | T | TA | 110 | a0001c0001t0001g0182 a0001c0001t0002g0002 a0001c0001t0002g0004 others(107): Show |
127 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.937-678dupT | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 11/14 | chr12 | 76051330 | |||||||
chr12:76051341 | A | C | 1 | a0001c0002t0051g0223 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.937-688T>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 11/14 | chr12 | 76051341 | |||||||
chr12:76051617 | C | T | 1 | a0001c0001t0002g0021 | 2 | HG01109.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.937-964G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 11/14 | chr12 | 76051617 | |||||||
chr12:76051633 | G | A | 1 | a0001c0001t0001g0264 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.937-980C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 11/14 | chr12 | 76051633 | |||||||
chr12:76051634 | G | C | 1 | a0001c0001t0001g0264 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.937-981C>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 11/14 | chr12 | 76051634 | |||||||
chr12:76051637 | C | T | 200 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(197): Show |
232 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(229): Show |
intron_variant | MODIFIER | c.937-984G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 11/14 | chr12 | 76051637 | |||||||
chr12:76051826 | C | T | 1 | a0001c0002t0065g0284 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.937-1173G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 11/14 | chr12 | 76051826 | |||||||
chr12:76052024 | T | A | 1 | a0001c0002t0004g0313 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.936+1067A>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 11/14 | chr12 | 76052024 | |||||||
chr12:76052266 | C | A | 6 | a0001c0002t0020g0218 a0001c0002t0020g0219 a0001c0002t0029g0139 others(3): Show |
6 | HG02258.hp1 HG02486.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.936+825G>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 11/14 | chr12 | 76052266 | |||||||
chr12:76052270 | A | C | 1 | a0001c0001t0008g0262 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.936+821T>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 11/14 | chr12 | 76052270 | |||||||
chr12:76052276 | C | T | 5 | a0001c0002t0014g0018 a0001c0002t0014g0152 a0001c0002t0041g0150 others(2): Show |
6 | HG01109.hp2 HG02055.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.936+815G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 11/14 | chr12 | 76052276 | |||||||
chr12:76052312 | A | G | 3 | a0001c0002t0019g0141 a0001c0002t0019g0142 a0001c0002t0019g0143 |
3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.936+779T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 11/14 | chr12 | 76052312 | |||||||
chr12:76052315 | T | C | 49 | a0001c0001t0068g0303 a0001c0002t0004g0281 a0001c0002t0004g0282 others(46): Show |
50 | HG00140.hp1 HG00733.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.936+776A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 11/14 | chr12 | 76052315 | |||||||
chr12:76052528 | T | G | 200 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(197): Show |
232 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(229): Show |
intron_variant | MODIFIER | c.936+563A>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 11/14 | chr12 | 76052528 | |||||||
chr12:76052712 | T | C | 1 | a0001c0002t0004g0309 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.936+379A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 11/14 | chr12 | 76052712 | |||||||
chr12:76053144 | A | G | 6 | a0001c0002t0025g0275 a0001c0002t0025g0276 a0001c0002t0027g0222 others(3): Show |
6 | HG01081.hp2 HG01123.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.917-34T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 10/14 | chr12 | 76053144 | |||||||
chr12:76053575 | T | A | 1 | a0001c0001t0008g0258 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.770+195A>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 9/14 | chr12 | 76053575 | |||||||
chr12:76053610 | G | C | 38 | a0001c0001t0068g0303 a0001c0002t0004g0281 a0001c0002t0004g0282 others(35): Show |
38 | HG00140.hp1 HG00733.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.770+160C>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 9/14 | chr12 | 76053610 | |||||||
chr12:76053731 | A | T | 1 | a0001c0001t0002g0042 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.770+39T>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 9/14 | chr12 | 76053731 | |||||||
chr12:76053733 | A | T | 1 | a0001c0001t0002g0042 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.770+37T>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 9/14 | chr12 | 76053733 | |||||||
chr12:76053734 | A | T | 1 | a0001c0001t0002g0042 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.770+36T>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 9/14 | chr12 | 76053734 | |||||||
chr12:76053736 | A | C | 1 | a0001c0001t0002g0042 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.770+34T>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 9/14 | chr12 | 76053736 | |||||||
chr12:76053737 | A | T | 1 | a0001c0001t0002g0042 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.770+33T>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 9/14 | chr12 | 76053737 | |||||||
chr12:76053740 | A | C | 1 | a0001c0001t0002g0042 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.770+30T>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 9/14 | chr12 | 76053740 | |||||||
chr12:76054012 | A | T | 1 | a0001c0003t0005g0242 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.631-103T>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 8/14 | chr12 | 76054012 | |||||||
chr12:76054012 | AT | A | 271 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(268): Show |
306 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(303): Show |
intron_variant | MODIFIER | c.631-104delA | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 8/14 | chr12 | 76054012 | |||||||
chr12:76054111 | C | G | 1 | a0001c0002t0022g0266 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.631-202G>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 8/14 | chr12 | 76054111 | |||||||
chr12:76054144 | G | A | 1 | a0001c0002t0058g0148 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.631-235C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 8/14 | chr12 | 76054144 | |||||||
chr12:76054180 | C | T | 1 | a0001c0001t0002g0122 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.631-271G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 8/14 | chr12 | 76054180 | |||||||
chr12:76054277 | ACCTCGG | A | 72 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(69): Show |
86 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.631-374_631-369del others(6): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 8/14 | chr12 | 76054277 | |||||||
chr12:76054305 | C | T | 2 | a0001c0002t0019g0141 a0001c0002t0019g0143 |
2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.631-396G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 8/14 | chr12 | 76054305 | |||||||
chr12:76054804 | T | A | 200 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(197): Show |
232 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(229): Show |
intron_variant | MODIFIER | c.630+215A>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 8/14 | chr12 | 76054804 | |||||||
chr12:76054912 | A | G | 1 | a0001c0001t0001g0260 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.630+107T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 8/14 | chr12 | 76054912 | |||||||
chr12:76055003 | T | C | 5 | a0001c0002t0009g0017 a0001c0002t0009g0149 a0001c0002t0009g0231 others(2): Show |
6 | HG02257.hp2 HG02622.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.630+16A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 8/14 | chr12 | 76055003 | |||||||
chr12:76055433 | G | A | 2 | a0001c0002t0016g0229 a0001c0002t0016g0269 |
2 | HG02886.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.559-343C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 7/14 | chr12 | 76055433 | |||||||
chr12:76055727 | G | C | 1 | a0001c0001t0006g0053 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.558+306C>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 7/14 | chr12 | 76055727 | |||||||
chr12:76055817 | T | C | 1 | a0001c0002t0022g0267 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.558+216A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 7/14 | chr12 | 76055817 | |||||||
chr12:76056240 | AAGCACAG others(2): Show |
A | 4 | a0001c0002t0015g0019 a0001c0002t0015g0153 a0001c0002t0015g0154 others(1): Show |
5 | HG01261.hp1 HG02145.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.430-88_430-80delGA others(7): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76056240 | |||||||
chr12:76056356 | A | G | 5 | a0001c0002t0009g0017 a0001c0002t0009g0149 a0001c0002t0009g0231 others(2): Show |
6 | HG02257.hp2 HG02622.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.430-195T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76056356 | |||||||
chr12:76056378 | T | C | 1 | a0001c0002t0102g0226 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.430-217A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76056378 | |||||||
chr12:76056398 | T | TA | 15 | a0001c0001t0003g0105 a0001c0001t0003g0106 a0001c0002t0014g0018 others(12): Show |
16 | HG01109.hp2 HG02055.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.430-238dupT | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76056398 | |||||||
chr12:76056398 | T | TAA | 5 | a0001c0002t0009g0017 a0001c0002t0009g0149 a0001c0002t0009g0231 others(2): Show |
6 | HG02257.hp2 HG02622.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.430-239_430-238dup others(2): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76056398 | |||||||
chr12:76056652 | A | G | 1 | a0001c0002t0046g0220 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.430-491T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76056652 | |||||||
chr12:76057079 | T | C | 2 | a0001c0001t0047g0067 a0001c0001t0049g0065 |
2 | HG02015.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.430-918A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76057079 | |||||||
chr12:76057636 | T | C | 6 | a0001c0002t0020g0218 a0001c0002t0020g0219 a0001c0002t0029g0139 others(3): Show |
6 | HG02258.hp1 HG02486.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.430-1475A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76057636 | |||||||
chr12:76057657 | AAT | A | 8 | a0001c0002t0020g0218 a0001c0002t0020g0219 a0001c0002t0028g0146 others(5): Show |
8 | HG02258.hp1 HG02486.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.430-1498_430-1497d others(4): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76057657 | |||||||
chr12:76057688 | G | C | 1 | a0001c0001t0001g0173 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.430-1527C>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76057688 | |||||||
chr12:76057867 | C | T | 1 | a0001c0001t0036g0010 | 2 | HG01261.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.430-1706G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76057867 | |||||||
chr12:76057916 | T | C | 236 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(233): Show |
268 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.430-1755A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76057916 | |||||||
chr12:76057919 | G | C | 6 | a0001c0002t0020g0218 a0001c0002t0020g0219 a0001c0002t0029g0139 others(3): Show |
6 | HG02258.hp1 HG02486.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.430-1758C>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76057919 | |||||||
chr12:76057986 | A | G | 1 | a0001c0001t0001g0264 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.429+1812T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76057986 | |||||||
chr12:76058095 | G | A | 6 | a0001c0002t0020g0218 a0001c0002t0020g0219 a0001c0002t0029g0139 others(3): Show |
6 | HG02258.hp1 HG02486.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.429+1703C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058095 | |||||||
chr12:76058150 | T | C | 1 | a0001c0001t0001g0185 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.429+1648A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058150 | |||||||
chr12:76058159 | C | A | 3 | a0001c0002t0009g0017 a0001c0002t0009g0149 a0001c0002t0009g0231 |
4 | HG02257.hp2 HG03041.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.429+1639G>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058159 | |||||||
chr12:76058166 | T | C | 5 | a0001c0001t0002g0086 a0001c0001t0013g0014 a0001c0001t0013g0085 others(2): Show |
6 | HG01243.hp1 HG02572.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.429+1632A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058166 | |||||||
chr12:76058191 | C | CTTCA | 6 | a0001c0001t0003g0098 a0001c0002t0015g0019 a0001c0002t0015g0153 others(3): Show |
7 | HG01261.hp1 HG02040.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.429+1606_429+1607i others(6): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058191 | |||||||
chr12:76058191 | C | CTTCATAT others(3): Show |
5 | a0001c0002t0019g0141 a0001c0002t0019g0142 a0001c0002t0019g0143 others(2): Show |
5 | HG02559.hp1 HG02622.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.429+1606_429+1607i others(12): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058191 | |||||||
chr12:76058191 | C | CTTCATAT others(11): Show |
1 | a0001c0001t0007g0161 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.429+1606_429+1607i others(20): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058191 | |||||||
chr12:76058191 | C | CTTCATAT others(15): Show |
2 | a0001c0001t0007g0165 a0001c0001t0042g0202 |
2 | HG02280.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.429+1606_429+1607i others(24): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058191 | |||||||
chr12:76058191 | C | CTTCATAT others(17): Show |
1 | a0001c0001t0007g0020 | 2 | HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.429+1606_429+1607i others(26): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058191 | |||||||
chr12:76058191 | C | CTTCATAT others(19): Show |
2 | a0001c0001t0007g0137 a0001c0001t0007g0160 |
2 | HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.429+1606_429+1607i others(28): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058191 | |||||||
chr12:76058191 | C | CTTCATAT others(23): Show |
1 | a0001c0001t0101g0159 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.429+1606_429+1607i others(32): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058191 | |||||||
chr12:76058191 | C | CTTCATAT others(35): Show |
1 | a0001c0001t0007g0162 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.429+1606_429+1607i others(44): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058191 | |||||||
chr12:76058192 | T | TTC | 7 | a0001c0001t0002g0102 a0001c0001t0003g0015 a0001c0001t0035g0113 others(4): Show |
8 | HG02258.hp1 HG02523.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.429+1605_429+1606i others(4): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058192 | |||||||
chr12:76058193 | A | T | 198 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(195): Show |
230 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(227): Show |
intron_variant | MODIFIER | c.429+1605T>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058193 | |||||||
chr12:76058194 | C | CAT | 4 | a0001c0002t0004g0287 a0001c0002t0004g0290 a0001c0002t0025g0275 others(1): Show |
4 | HG00741.hp1 HG01433.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.429+1602_429+1603d others(4): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058194 | |||||||
chr12:76058194 | C | CATAT | 4 | a0001c0002t0004g0304 a0001c0002t0027g0277 a0001c0002t0061g0279 others(1): Show |
4 | HG01081.hp2 HG01516.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.429+1600_429+1603d others(6): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058194 | |||||||
chr12:76058194 | C | CATATATA others(1): Show |
4 | a0001c0002t0023g0225 a0001c0002t0027g0222 a0001c0002t0044g0221 others(1): Show |
4 | HG01123.hp2 HG02109.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.429+1596_429+1603d others(10): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058194 | |||||||
chr12:76058194 | C | CATATATA others(3): Show |
1 | a0001c0002t0023g0224 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.429+1594_429+1603d others(12): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058194 | |||||||
chr12:76058194 | C | CATATATA others(11): Show |
1 | a0001c0002t0021g0300 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.429+1586_429+1603d others(20): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058194 | |||||||
chr12:76058194 | C | CATATATA others(13): Show |
1 | a0001c0002t0065g0284 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.429+1584_429+1603d others(22): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058194 | |||||||
chr12:76058194 | C | T | 26 | a0001c0001t0002g0102 a0001c0001t0003g0015 a0001c0001t0003g0098 others(23): Show |
29 | HG01261.hp1 HG01891.hp1 HG02040.hp2 others(26): Show |
intron_variant | MODIFIER | c.429+1604G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058194 | |||||||
chr12:76058194 | CAT | C | 66 | a0001c0001t0002g0047 a0001c0001t0002g0050 a0001c0001t0002g0109 others(63): Show |
74 | HG00558.hp2 HG00597.hp2 HG00735.hp1 others(71): Show |
intron_variant | MODIFIER | c.429+1602_429+1603d others(4): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058194 | |||||||
chr12:76058194 | CATAT | C | 40 | a0001c0001t0002g0060 a0001c0001t0030g0011 a0001c0001t0037g0057 others(37): Show |
46 | HG00323.hp2 HG00642.hp1 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.429+1600_429+1603d others(6): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058194 | |||||||
chr12:76058194 | CATATAT | C | 44 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0012 others(41): Show |
51 | HG00438.hp2 HG00544.hp2 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.429+1598_429+1603d others(8): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058194 | |||||||
chr12:76058194 | CATATATA others(7): Show |
C | 81 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(78): Show |
95 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.429+1590_429+1603d others(16): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058194 | |||||||
chr12:76058284 | A | G | 3 | a0001c0002t0019g0141 a0001c0002t0019g0142 a0001c0002t0019g0143 |
3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.429+1514T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058284 | |||||||
chr12:76058311 | T | C | 22 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0042 others(19): Show |
24 | HG00544.hp2 HG01070.hp1 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.429+1487A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058311 | |||||||
chr12:76058387 | C | CT | 10 | a0001c0002t0004g0309 a0001c0002t0014g0018 a0001c0002t0014g0152 others(7): Show |
11 | HG01109.hp2 HG01175.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.429+1410dupA | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058387 | |||||||
chr12:76058387 | CT | C | 111 | a0001c0001t0001g0174 a0001c0001t0002g0002 a0001c0001t0002g0004 others(108): Show |
128 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.429+1410delA | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058387 | |||||||
chr12:76058543 | C | T | 7 | a0001c0003t0005g0241 a0001c0003t0005g0245 a0001c0003t0010g0007 others(4): Show |
10 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.429+1255G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058543 | |||||||
chr12:76058699 | CTTTT | C | 3 | a0001c0002t0019g0141 a0001c0002t0019g0142 a0001c0002t0019g0143 |
3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.429+1095_429+1098d others(6): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058699 | |||||||
chr12:76058724 | A | T | 1 | a0001c0001t0012g0034 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.429+1074T>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058724 | |||||||
chr12:76058810 | C | G | 199 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(196): Show |
231 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.429+988G>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058810 | |||||||
chr12:76058818 | A | T | 1 | a0001c0001t0012g0034 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.429+980T>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058818 | |||||||
chr12:76058864 | T | C | 1 | a0001c0001t0001g0188 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.429+934A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058864 | |||||||
chr12:76059008 | A | G | 18 | a0001c0002t0009g0017 a0001c0002t0009g0149 a0001c0002t0009g0231 others(15): Show |
20 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.429+790T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76059008 | |||||||
chr12:76059026 | C | T | 1 | a0001c0002t0062g0230 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.429+772G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76059026 | |||||||
chr12:76059136 | A | G | 2 | a0001c0002t0027g0277 a0001c0002t0067g0278 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.429+662T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76059136 | |||||||
chr12:76059258 | T | C | 3 | a0001c0002t0019g0141 a0001c0002t0019g0142 a0001c0002t0019g0143 |
3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.429+540A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76059258 | |||||||
chr12:76059522 | T | C | 110 | a0001c0001t0001g0177 a0001c0001t0002g0002 a0001c0001t0002g0004 others(107): Show |
127 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.429+276A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76059522 | |||||||
chr12:76059647 | T | C | 1 | a0001c0001t0001g0216 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.429+151A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76059647 | |||||||
chr12:76059656 | G | A | 1 | a0001c0002t0004g0288 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.429+142C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76059656 | |||||||
chr12:76059668 | C | T | 2 | a0001c0002t0004g0309 a0001c0002t0021g0297 |
2 | HG03704.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.429+130G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76059668 | |||||||
chr12:76060057 | T | C | 3 | a0001c0002t0019g0141 a0001c0002t0019g0142 a0001c0002t0019g0143 |
3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.348+81A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 5/14 | chr12 | 76060057 | |||||||
chr12:76060081 | G | A | 271 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(268): Show |
306 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(303): Show |
intron_variant | MODIFIER | c.348+57C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 5/14 | chr12 | 76060081 | |||||||
chr12:76060093 | C | T | 199 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(196): Show |
231 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.348+45G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 5/14 | chr12 | 76060093 | |||||||
chr12:76060117 | CAAAGTAG others(3): Show |
C | 3 | a0001c0002t0004g0281 a0001c0002t0004g0304 a0001c0002t0054g0295 |
3 | HG01192.hp2 HG03098.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.348+11_348+20delCT others(8): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 5/14 | chr12 | 76060117 | |||||||
chr12:76060461 | C | T | 1 | a0001c0002t0029g0139 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.207-182G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76060461 | |||||||
chr12:76060582 | T | C | 9 | a0001c0002t0016g0227 a0001c0002t0016g0229 a0001c0002t0016g0269 others(6): Show |
9 | HG02109.hp1 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.207-303A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76060582 | |||||||
chr12:76060668 | A | G | 224 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(221): Show |
259 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(256): Show |
intron_variant | MODIFIER | c.207-389T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76060668 | |||||||
chr12:76060826 | C | T | 7 | a0001c0003t0005g0027 a0001c0003t0005g0028 a0001c0003t0005g0242 others(4): Show |
9 | HG00323.hp2 HG00738.hp2 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.207-547G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76060826 | |||||||
chr12:76060939 | A | T | 10 | a0001c0002t0009g0017 a0001c0002t0009g0149 a0001c0002t0009g0231 others(7): Show |
11 | HG02257.hp2 HG02486.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.207-660T>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76060939 | |||||||
chr12:76060980 | C | A | 5 | a0001c0002t0028g0146 a0001c0002t0028g0147 a0001c0002t0029g0139 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.207-701G>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76060980 | |||||||
chr12:76061032 | G | C | 9 | a0001c0002t0014g0018 a0001c0002t0014g0152 a0001c0002t0015g0019 others(6): Show |
11 | HG01109.hp2 HG01261.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.207-753C>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76061032 | |||||||
chr12:76061076 | C | G | 1 | a0001c0001t0001g0176 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.207-797G>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76061076 | |||||||
chr12:76061103 | A | G | 3 | a0001c0002t0024g0310 a0001c0002t0024g0311 a0001c0002t0052g0312 |
3 | HG02896.hp2 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.207-824T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76061103 | |||||||
chr12:76061234 | T | G | 1 | a0001c0002t0058g0148 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.207-955A>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76061234 | |||||||
chr12:76061313 | T | C | 9 | a0001c0002t0014g0018 a0001c0002t0014g0152 a0001c0002t0015g0019 others(6): Show |
11 | HG01109.hp2 HG01261.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.207-1034A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76061313 | |||||||
chr12:76061377 | G | A | 1 | a0001c0001t0003g0095 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.207-1098C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76061377 | |||||||
chr12:76061487 | C | T | 1 | a0001c0001t0002g0059 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.207-1208G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76061487 | |||||||
chr12:76061640 | A | C | 1 | a0001c0001t0002g0086 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.207-1361T>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76061640 | |||||||
chr12:76061822 | T | C | 6 | a0001c0002t0020g0218 a0001c0002t0020g0219 a0001c0002t0029g0139 others(3): Show |
6 | HG02258.hp1 HG02486.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.207-1543A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76061822 | |||||||
chr12:76061934 | T | C | 271 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(268): Show |
306 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(303): Show |
intron_variant | MODIFIER | c.207-1655A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76061934 | |||||||
chr12:76062037 | C | T | 225 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(222): Show |
260 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(257): Show |
intron_variant | MODIFIER | c.207-1758G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76062037 | |||||||
chr12:76062155 | G | A | 1 | a0001c0002t0004g0315 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.207-1876C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76062155 | |||||||
chr12:76062176 | G | A | 1 | a0001c0002t0044g0221 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.207-1897C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76062176 | |||||||
chr12:76062228 | C | G | 3 | a0001c0002t0019g0141 a0001c0002t0019g0142 a0001c0002t0019g0143 |
3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.207-1949G>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76062228 | |||||||
chr12:76062341 | C | T | 3 | a0001c0002t0009g0017 a0001c0002t0009g0149 a0001c0002t0009g0231 |
4 | HG02257.hp2 HG03041.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.207-2062G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76062341 | |||||||
chr12:76062412 | T | C | 1 | a0001c0001t0003g0093 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.207-2133A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76062412 | |||||||
chr12:76062447 | G | A | 1 | a0001c0001t0002g0078 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.207-2168C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76062447 | |||||||
chr12:76062777 | C | T | 1 | a0001c0001t0008g0258 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.207-2498G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76062777 | |||||||
chr12:76062936 | G | GA | 3 | a0001c0002t0019g0141 a0001c0002t0019g0142 a0001c0002t0019g0143 |
3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.207-2658dupT | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76062936 | |||||||
chr12:76062994 | T | C | 9 | a0001c0002t0014g0018 a0001c0002t0014g0152 a0001c0002t0015g0019 others(6): Show |
11 | HG01109.hp2 HG01261.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.207-2715A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76062994 | |||||||
chr12:76063006 | A | G | 4 | a0001c0002t0027g0222 a0001c0002t0027g0277 a0001c0002t0061g0279 others(1): Show |
4 | HG01081.hp2 HG01123.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.207-2727T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76063006 | |||||||
chr12:76063067 | A | G | 2 | a0001c0002t0022g0266 a0001c0002t0022g0267 |
2 | HG02257.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.207-2788T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76063067 | |||||||
chr12:76063076 | A | G | 6 | a0001c0002t0020g0218 a0001c0002t0020g0219 a0001c0002t0029g0139 others(3): Show |
6 | HG02258.hp1 HG02486.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.207-2797T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76063076 | |||||||
chr12:76063342 | A | G | 9 | a0001c0002t0014g0018 a0001c0002t0014g0152 a0001c0002t0015g0019 others(6): Show |
11 | HG01109.hp2 HG01261.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.207-3063T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76063342 | |||||||
chr12:76063421 | A | C | 1 | a0001c0001t0013g0088 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.207-3142T>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76063421 | |||||||
chr12:76063538 | C | G | 1 | a0001c0001t0002g0102 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.207-3259G>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76063538 | |||||||
chr12:76063588 | G | A | 1 | a0001c0001t0079g0179 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.207-3309C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76063588 | |||||||
chr12:76063712 | A | G | 3 | a0001c0002t0019g0141 a0001c0002t0019g0142 a0001c0002t0019g0143 |
3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.207-3433T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76063712 | |||||||
chr12:76063824 | T | A | 13 | a0001c0001t0007g0020 a0001c0001t0007g0137 a0001c0001t0007g0158 others(10): Show |
14 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.207-3545A>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76063824 | |||||||
chr12:76063861 | G | C | 1 | a0001c0002t0065g0284 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.206+3510C>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76063861 | |||||||
chr12:76063880 | T | TAAA | 7 | a0001c0002t0014g0018 a0001c0002t0014g0152 a0001c0002t0015g0019 others(4): Show |
9 | HG01109.hp2 HG01261.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.206+3490_206+3491i others(5): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76063880 | |||||||
chr12:76063881 | T | A | 9 | a0001c0002t0014g0018 a0001c0002t0014g0152 a0001c0002t0015g0019 others(6): Show |
11 | HG01109.hp2 HG01261.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.206+3490A>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76063881 | |||||||
chr12:76063881 | T | TA | 34 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0163 others(31): Show |
35 | HG00738.hp1 HG01069.hp1 HG01361.hp2 others(32): Show |
intron_variant | MODIFIER | c.206+3489dupT | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76063881 | |||||||
chr12:76063881 | T | TAA | 91 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(88): Show |
105 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.206+3488_206+3489d others(4): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76063881 | |||||||
chr12:76063881 | TAAAA | T | 11 | a0001c0002t0009g0017 a0001c0002t0009g0149 a0001c0002t0009g0231 others(8): Show |
12 | HG02257.hp2 HG02258.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.206+3486_206+3489d others(6): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76063881 | |||||||
chr12:76063881 | TAAAAAAA others(2): Show |
T | 108 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0012 others(105): Show |
125 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.206+3481_206+3489d others(11): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76063881 | |||||||
chr12:76064031 | G | A | 3 | a0001c0002t0019g0141 a0001c0002t0019g0142 a0001c0002t0019g0143 |
3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.206+3340C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76064031 | |||||||
chr12:76064194 | C | T | 1 | a0001c0002t0029g0140 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.206+3177G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76064194 | |||||||
chr12:76064443 | T | A | 1 | a0001c0001t0001g0185 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.206+2928A>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76064443 | |||||||
chr12:76064926 | G | A | 3 | a0001c0002t0019g0141 a0001c0002t0019g0142 a0001c0002t0019g0143 |
3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.206+2445C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76064926 | |||||||
chr12:76065065 | A | G | 1 | a0001c0002t0004g0296 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.206+2306T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76065065 | |||||||
chr12:76065093 | A | G | 1 | a0001c0002t0088g0138 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.206+2278T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76065093 | |||||||
chr12:76065106 | T | C | 1 | a0001c0001t0001g0197 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.206+2265A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76065106 | |||||||
chr12:76065124 | T | C | 1 | a0001c0001t0006g0125 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.206+2247A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76065124 | |||||||
chr12:76065303 | G | T | 3 | a0001c0002t0029g0139 a0001c0002t0029g0140 a0001c0002t0088g0138 |
3 | HG02486.hp2 HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.206+2068C>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76065303 | |||||||
chr12:76065345 | A | C | 2 | a0001c0002t0023g0224 a0001c0002t0023g0225 |
2 | HG02280.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.206+2026T>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76065345 | |||||||
chr12:76065363 | A | G | 2 | a0001c0002t0004g0292 a0001c0002t0004g0296 |
2 | HG02602.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.206+2008T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76065363 | |||||||
chr12:76065467 | T | C | 1 | a0001c0002t0062g0230 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.206+1904A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76065467 | |||||||
chr12:76065532 | TA | T | 305 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(302): Show |
344 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(341): Show |
intron_variant | MODIFIER | c.206+1838delT | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76065532 | |||||||
chr12:76065546 | A | G | 1 | a0001c0002t0004g0283 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.206+1825T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76065546 | |||||||
chr12:76066053 | TA | T | 6 | a0001c0002t0019g0141 a0001c0002t0019g0142 a0001c0002t0019g0143 others(3): Show |
6 | HG01069.hp2 HG02559.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.206+1317delT | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76066053 | |||||||
chr12:76066097 | AAAAT | A | 3 | a0001c0002t0023g0225 a0001c0002t0027g0222 a0001c0003t0060g0249 |
3 | HG01074.hp1 HG01123.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.206+1270_206+1273d others(6): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76066097 | |||||||
chr12:76066097 | AAAATAAA others(1): Show |
A | 17 | a0001c0002t0025g0275 a0001c0002t0025g0276 a0001c0002t0044g0221 others(14): Show |
19 | HG00323.hp2 HG00738.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.206+1266_206+1273d others(10): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76066097 | |||||||
chr12:76066097 | AAAATAAA others(5): Show |
A | 4 | a0001c0002t0027g0277 a0001c0002t0058g0148 a0001c0002t0063g0214 others(1): Show |
4 | HG01516.hp2 HG01517.hp1 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.206+1262_206+1273d others(14): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76066097 | |||||||
chr12:76066121 | TAAATAAA others(13): Show |
T | 1 | a0001c0002t0029g0139 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.206+1230_206+1249d others(22): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76066121 | |||||||
chr12:76066125 | TAAATAAA others(9): Show |
T | 10 | a0001c0001t0001g0198 a0001c0002t0016g0227 a0001c0002t0019g0141 others(7): Show |
10 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.206+1230_206+1245d others(18): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76066125 | |||||||
chr12:76066125 | TAAATAAA others(13): Show |
T | 1 | a0001c0001t0003g0108 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.206+1226_206+1245d others(22): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76066125 | |||||||
chr12:76066129 | TAAATAAA others(5): Show |
T | 13 | a0001c0001t0007g0137 a0001c0002t0004g0290 a0001c0002t0014g0018 others(10): Show |
14 | HG00733.hp1 HG01109.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.206+1230_206+1241d others(14): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76066129 | |||||||
chr12:76066129 | TAAATAAA others(9): Show |
T | 73 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(70): Show |
85 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.206+1226_206+1241d others(18): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76066129 | |||||||
chr12:76066133 | T | C | 1 | a0001c0003t0005g0238 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.206+1238A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76066133 | |||||||
chr12:76066133 | TAAATAAA others(1): Show |
T | 11 | a0001c0002t0005g0254 a0001c0002t0016g0229 a0001c0002t0016g0269 others(8): Show |
11 | HG01175.hp1 HG01358.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.206+1230_206+1237d others(10): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76066133 | |||||||
chr12:76066133 | TAAATAAA others(5): Show |
T | 137 | a0001c0001t0001g0171 a0001c0001t0001g0173 a0001c0001t0001g0264 others(134): Show |
156 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.206+1226_206+1237d others(14): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76066133 | |||||||
chr12:76066137 | T | C | 5 | a0001c0002t0023g0224 a0001c0002t0023g0225 a0001c0003t0005g0238 others(2): Show |
5 | HG01256.hp2 HG01891.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.206+1234A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76066137 | |||||||
chr12:76066137 | TAAAC | T | 5 | a0001c0002t0004g0314 a0001c0002t0004g0315 a0001c0002t0018g0308 others(2): Show |
5 | HG00738.hp1 HG01099.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.206+1230_206+1233d others(6): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76066137 | |||||||
chr12:76066137 | TAAACAAA others(1): Show |
T | 29 | a0001c0001t0002g0023 a0001c0001t0002g0071 a0001c0001t0002g0183 others(26): Show |
30 | HG00140.hp2 HG00741.hp1 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.206+1226_206+1233d others(10): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76066137 | |||||||
chr12:76066141 | C | T | 2 | a0001c0001t0002g0021 a0001c0003t0005g0252 |
3 | HG01109.hp1 HG01515.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.206+1230G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76066141 | |||||||
chr12:76066145 | C | T | 3 | a0001c0002t0004g0314 a0001c0002t0004g0315 a0001c0002t0018g0308 |
3 | HG00738.hp1 HG01099.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.206+1226G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76066145 | |||||||
chr12:76066202 | C | T | 3 | a0001c0002t0009g0017 a0001c0002t0009g0149 a0001c0002t0009g0231 |
4 | HG02257.hp2 HG03041.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.206+1169G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76066202 | |||||||
chr12:76066215 | C | A | 1 | a0001c0001t0001g0180 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.206+1156G>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76066215 | |||||||
chr12:76066396 | G | T | 1 | a0001c0001t0002g0050 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.206+975C>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76066396 | |||||||
chr12:76066452 | A | G | 1 | a0001c0002t0004g0292 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.206+919T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76066452 | |||||||
chr12:76066527 | C | T | 15 | a0001c0002t0009g0017 a0001c0002t0009g0149 a0001c0002t0009g0231 others(12): Show |
17 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.206+844G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76066527 | |||||||
chr12:76066605 | C | T | 3 | a0001c0002t0019g0141 a0001c0002t0019g0142 a0001c0002t0019g0143 |
3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.206+766G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76066605 | |||||||
chr12:76066692 | A | G | 1 | a0001c0001t0002g0047 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.206+679T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76066692 | |||||||
chr12:76066834 | G | A | 1 | a0001c0002t0065g0284 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.206+537C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76066834 | |||||||
chr12:76066841 | G | C | 1 | a0001c0001t0001g0184 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.206+530C>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76066841 | |||||||
chr12:76066912 | G | A | 1 | a0001c0001t0002g0071 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.206+459C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76066912 | |||||||
chr12:76066987 | G | C | 200 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(197): Show |
232 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(229): Show |
intron_variant | MODIFIER | c.206+384C>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76066987 | |||||||
chr12:76067000 | CAA | C | 4 | a0001c0002t0015g0019 a0001c0002t0015g0153 a0001c0002t0015g0154 others(1): Show |
5 | HG01261.hp1 HG02145.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.206+369_206+370del others(2): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76067000 | |||||||
chr12:76067153 | C | T | 222 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(219): Show |
257 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(254): Show |
intron_variant | MODIFIER | c.206+218G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76067153 | |||||||
chr12:76067259 | A | C | 1 | a0001c0001t0013g0085 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.206+112T>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76067259 | |||||||
chr12:76067266 | A | G | 36 | a0001c0001t0068g0303 a0001c0002t0004g0281 a0001c0002t0004g0282 others(33): Show |
36 | HG00140.hp1 HG00733.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.206+105T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76067266 | |||||||
chr12:76067319 | G | T | 10 | a0001c0002t0014g0018 a0001c0002t0014g0152 a0001c0002t0028g0146 others(7): Show |
11 | HG01109.hp2 HG02055.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.206+52C>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76067319 | |||||||
chr12:76067357 | T | C | 203 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(200): Show |
235 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.206+14A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76067357 | |||||||
chr12:76067365 | C | T | 262 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(259): Show |
297 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(294): Show |
splice_region_variant&intron_variant | LOW | c.206+6G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76067365 | |||||||
chr12:76067477 | T | TA | 112 | a0001c0001t0001g0171 a0001c0001t0002g0002 a0001c0001t0002g0004 others(109): Show |
129 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(126): Show |
splice_region_variant&intron_variant | LOW | c.104-5dupT | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76067477 | |||||||
chr12:76067574 | T | G | 1 | a0001c0001t0008g0129 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.104-101A>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76067574 | |||||||
chr12:76067604 | C | T | 1 | a0001c0001t0002g0066 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.104-131G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76067604 | |||||||
chr12:76067826 | G | T | 1 | a0001c0002t0004g0283 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.104-353C>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76067826 | |||||||
chr12:76067934 | T | C | 1 | a0001c0002t0046g0220 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.104-461A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76067934 | |||||||
chr12:76068095 | T | G | 1 | a0001c0001t0087g0107 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.104-622A>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76068095 | |||||||
chr12:76068152 | C | T | 1 | a0001c0002t0004g0299 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.104-679G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76068152 | |||||||
chr12:76068352 | C | T | 1 | a0001c0001t0042g0202 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.103+557G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76068352 | |||||||
chr12:76068410 | C | T | 1 | a0001c0001t0001g0175 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.103+499G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76068410 | |||||||
chr12:76068641 | G | A | 2 | a0001c0001t0002g0069 a0001c0001t0002g0070 |
2 | NA18957.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.103+268C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76068641 | |||||||
chr12:76068722 | C | A | 1 | a0001c0001t0001g0185 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.103+187G>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76068722 | |||||||
chr12:76068728 | C | T | 1 | a0001c0001t0007g0137 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.103+181G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76068728 | |||||||
chr12:76068729 | G | A | 3 | a0001c0002t0019g0141 a0001c0002t0019g0142 a0001c0002t0019g0143 |
3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.103+180C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76068729 | |||||||
chr12:76068735 | T | TAC | 34 | a0001c0001t0001g0030 a0001c0001t0001g0134 a0001c0001t0001g0191 others(31): Show |
35 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.103+172_103+173dup others(2): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76068735 | |||||||
chr12:76068735 | T | TACAC | 41 | a0001c0001t0001g0166 a0001c0001t0001g0175 a0001c0001t0001g0176 others(38): Show |
44 | HG00140.hp2 HG00741.hp1 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.103+170_103+173dup others(4): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76068735 | |||||||
chr12:76068735 | T | TACACAC | 66 | a0001c0001t0001g0006 a0001c0001t0001g0025 a0001c0001t0001g0031 others(63): Show |
77 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.103+168_103+173dup others(6): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76068735 | |||||||
chr12:76068735 | T | TACACACA others(1): Show |
43 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0144 others(40): Show |
48 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.103+166_103+173dup others(8): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76068735 | |||||||
chr12:76068735 | T | TACACACA others(3): Show |
29 | a0001c0001t0001g0001 a0001c0001t0001g0186 a0001c0001t0001g0188 others(26): Show |
35 | HG00544.hp2 HG00733.hp2 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.103+164_103+173dup others(10): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76068735 | |||||||
chr12:76068735 | T | TACACACA others(5): Show |
19 | a0001c0001t0001g0189 a0001c0001t0001g0200 a0001c0001t0002g0013 others(16): Show |
21 | HG00544.hp1 HG00558.hp2 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.103+162_103+173dup others(12): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76068735 | |||||||
chr12:76068735 | T | TACACACA others(7): Show |
14 | a0001c0001t0001g0136 a0001c0001t0001g0190 a0001c0001t0001g0203 others(11): Show |
17 | HG01069.hp1 HG01081.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.103+160_103+173dup others(14): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76068735 | |||||||
chr12:76068735 | T | TACACACA others(9): Show |
6 | a0001c0001t0006g0053 a0001c0001t0006g0092 a0001c0001t0093g0052 others(3): Show |
7 | HG00323.hp1 HG01081.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.103+158_103+173dup others(16): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76068735 | |||||||
chr12:76068735 | T | TACACACA others(11): Show |
1 | a0001c0002t0039g0156 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.103+156_103+173dup others(18): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76068735 | |||||||
chr12:76068735 | T | TACACACA others(13): Show |
2 | a0001c0001t0002g0071 a0001c0002t0009g0149 |
2 | HG02257.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.103+154_103+173dup others(20): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76068735 | |||||||
chr12:76068735 | T | TACACACA others(19): Show |
1 | a0001c0002t0029g0140 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.103+148_103+173dup others(26): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76068735 | |||||||
chr12:76068735 | TAC | T | 6 | a0001c0001t0001g0174 a0001c0002t0023g0224 a0001c0002t0065g0284 others(3): Show |
6 | HG00738.hp2 HG01884.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.103+172_103+173del others(2): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76068735 | |||||||
chr12:76068735 | TACAC | T | 7 | a0001c0001t0037g0057 a0001c0002t0004g0282 a0001c0002t0063g0214 others(4): Show |
7 | HG00741.hp2 HG01074.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.103+170_103+173del others(4): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76068735 | |||||||
chr12:76068735 | TACACACA others(3): Show |
T | 2 | a0001c0001t0002g0090 a0001c0001t0002g0091 |
2 | HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.103+164_103+173del others(10): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76068735 | |||||||
chr12:76068735 | TACACACA others(5): Show |
T | 2 | a0001c0002t0028g0146 a0001c0002t0028g0147 |
2 | HG02630.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.103+162_103+173del others(12): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76068735 | |||||||
chr12:76068735 | TACACACA others(9): Show |
T | 5 | a0001c0002t0014g0018 a0001c0002t0014g0152 a0001c0002t0041g0150 others(2): Show |
6 | HG01109.hp2 HG02055.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.103+158_103+173del others(16): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76068735 | |||||||
chr12:76068735 | TACACACA others(13): Show |
T | 2 | a0001c0001t0037g0073 a0001c0001t0038g0072 |
2 | HG02647.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.103+154_103+173del others(20): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76068735 | |||||||
chr12:76068777 | C | T | 1 | a0001c0002t0004g0313 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.103+132G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76068777 | |||||||
chr12:76068780 | T | A | 5 | a0001c0002t0009g0017 a0001c0002t0009g0149 a0001c0002t0009g0231 others(2): Show |
6 | HG02257.hp2 HG02622.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.103+129A>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76068780 | |||||||
chr12:76068832 | T | C | 200 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(197): Show |
232 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(229): Show |
intron_variant | MODIFIER | c.103+77A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76068832 | |||||||
chr12:76069062 | TA | T | 3 | a0001c0002t0019g0141 a0001c0002t0019g0142 a0001c0002t0019g0143 |
3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.18-69delT | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76069062 | |||||||
chr12:76069289 | A | G | 1 | a0001c0001t0001g0173 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.18-295T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76069289 | |||||||
chr12:76069361 | T | C | 2 | a0001c0001t0075g0168 a0001c0001t0076g0201 |
2 | NA19006.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.18-367A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76069361 | |||||||
chr12:76069444 | G | C | 1 | a0001c0002t0102g0226 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.18-450C>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76069444 | |||||||
chr12:76069695 | C | T | 1 | a0001c0002t0004g0291 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.18-701G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76069695 | |||||||
chr12:76069824 | TA | T | 7 | a0001c0001t0006g0008 a0001c0002t0015g0019 a0001c0002t0015g0153 others(4): Show |
9 | HG01169.hp2 HG01256.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.18-831delT | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76069824 | |||||||
chr12:76070054 | G | GA | 6 | a0001c0002t0025g0275 a0001c0002t0025g0276 a0001c0002t0027g0222 others(3): Show |
6 | HG01081.hp2 HG01123.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.18-1061dupT | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76070054 | |||||||
chr12:76070122 | CT | C | 201 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(198): Show |
234 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(231): Show |
intron_variant | MODIFIER | c.18-1129delA | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76070122 | |||||||
chr12:76070122 | CTT | C | 17 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0031 others(14): Show |
19 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(16): Show |
intron_variant | MODIFIER | c.18-1130_18-1129del others(2): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76070122 | |||||||
chr12:76070134 | T | G | 9 | a0001c0001t0007g0020 a0001c0001t0007g0137 a0001c0001t0007g0158 others(6): Show |
10 | HG01891.hp1 HG02145.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.18-1140A>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76070134 | |||||||
chr12:76070196 | C | G | 1 | a0001c0001t0001g0172 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.18-1202G>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76070196 | |||||||
chr12:76070214 | C | G | 1 | a0001c0002t0046g0220 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.18-1220G>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76070214 | |||||||
chr12:76070269 | T | C | 1 | a0001c0001t0006g0125 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.18-1275A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76070269 | |||||||
chr12:76070288 | A | G | 3 | a0001c0002t0019g0141 a0001c0002t0019g0142 a0001c0002t0019g0143 |
3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.18-1294T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76070288 | |||||||
chr12:76070370 | A | T | 1 | a0001c0001t0002g0090 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.18-1376T>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76070370 | |||||||
chr12:76070431 | A | C | 1 | a0001c0002t0004g0307 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.18-1437T>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76070431 | |||||||
chr12:76070520 | T | C | 1 | a0001c0001t0035g0113 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.18-1526A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76070520 | |||||||
chr12:76070827 | T | C | 78 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(75): Show |
92 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.18-1833A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76070827 | |||||||
chr12:76070857 | A | G | 264 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(261): Show |
299 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.18-1863T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76070857 | |||||||
chr12:76070982 | T | C | 3 | a0001c0002t0019g0141 a0001c0002t0019g0142 a0001c0002t0019g0143 |
3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.18-1988A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76070982 | |||||||
chr12:76070991 | A | G | 7 | a0001c0002t0020g0218 a0001c0002t0020g0219 a0001c0002t0044g0221 others(4): Show |
7 | HG01884.hp2 HG02109.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.18-1997T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76070991 | |||||||
chr12:76071153 | A | T | 1 | a0001c0001t0012g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.18-2159T>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76071153 | |||||||
chr12:76071267 | A | G | 5 | a0001c0002t0020g0218 a0001c0002t0020g0219 a0001c0002t0044g0221 others(2): Show |
5 | HG02109.hp2 HG02258.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.18-2273T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76071267 | |||||||
chr12:76071465 | G | C | 109 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0012 others(106): Show |
126 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.18-2471C>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76071465 | |||||||
chr12:76071784 | G | A | 3 | a0001c0002t0029g0139 a0001c0002t0029g0140 a0001c0002t0088g0138 |
3 | HG02486.hp2 HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.17+2419C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76071784 | |||||||
chr12:76071960 | GA | G | 279 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(276): Show |
314 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(311): Show |
intron_variant | MODIFIER | c.17+2242delT | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76071960 | |||||||
chr12:76071974 | T | A | 3 | a0001c0003t0005g0246 a0001c0003t0005g0247 a0001c0003t0005g0248 |
3 | HG01243.hp2 HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.17+2229A>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76071974 | |||||||
chr12:76072206 | A | G | 3 | a0001c0002t0019g0141 a0001c0002t0019g0142 a0001c0002t0019g0143 |
3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.17+1997T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76072206 | |||||||
chr12:76072231 | A | G | 1 | a0001c0001t0002g0045 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.17+1972T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76072231 | |||||||
chr12:76072282 | CAAG | C | 4 | a0001c0003t0005g0234 a0001c0003t0005g0250 a0001c0003t0005g0251 others(1): Show |
4 | HG00741.hp2 HG01074.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.17+1918_17+1920del others(3): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76072282 | |||||||
chr12:76072300 | T | TA | 10 | a0001c0002t0004g0285 a0001c0002t0024g0310 a0001c0002t0024g0311 others(7): Show |
10 | HG01081.hp2 HG01123.hp2 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.17+1902dupT | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76072300 | |||||||
chr12:76072316 | C | A | 9 | a0001c0002t0014g0018 a0001c0002t0014g0152 a0001c0002t0015g0019 others(6): Show |
11 | HG01109.hp2 HG01261.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.17+1887G>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76072316 | |||||||
chr12:76072450 | G | A | 218 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(215): Show |
253 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(250): Show |
intron_variant | MODIFIER | c.17+1753C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76072450 | |||||||
chr12:76072535 | A | C | 5 | a0001c0002t0014g0018 a0001c0002t0014g0152 a0001c0002t0041g0150 others(2): Show |
6 | HG01109.hp2 HG02055.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.17+1668T>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76072535 | |||||||
chr12:76072680 | G | A | 1 | a0001c0001t0068g0303 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.17+1523C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76072680 | |||||||
chr12:76072853 | G | A | 5 | a0001c0001t0034g0199 a0001c0002t0015g0019 a0001c0002t0015g0153 others(2): Show |
6 | HG01261.hp1 HG02145.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.17+1350C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76072853 | |||||||
chr12:76072903 | C | A | 1 | a0001c0001t0001g0200 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.17+1300G>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76072903 | |||||||
chr12:76072923 | G | A | 5 | a0001c0002t0009g0017 a0001c0002t0009g0149 a0001c0002t0009g0231 others(2): Show |
6 | HG02257.hp2 HG02622.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.17+1280C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76072923 | |||||||
chr12:76073013 | G | T | 2 | a0001c0001t0003g0096 a0001c0001t0092g0097 |
2 | NA18981.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.17+1190C>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76073013 | |||||||
chr12:76073079 | C | G | 1 | a0001c0002t0024g0311 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.17+1124G>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76073079 | |||||||
chr12:76073136 | A | G | 1 | a0001c0002t0039g0155 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.17+1067T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76073136 | |||||||
chr12:76073146 | T | A | 40 | a0001c0001t0068g0303 a0001c0002t0004g0281 a0001c0002t0004g0282 others(37): Show |
40 | HG00140.hp1 HG00733.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.17+1057A>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76073146 | |||||||
chr12:76073158 | T | G | 1 | a0001c0001t0070g0205 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.17+1045A>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76073158 | |||||||
chr12:76073485 | C | T | 3 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0171 |
3 | HG02056.hp2 HG02129.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.17+718G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76073485 | |||||||
chr12:76073501 | CT | C | 257 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(254): Show |
292 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.17+701delA | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76073501 | |||||||
chr12:76073562 | T | A | 2 | a0001c0001t0077g0083 a0001c0001t0097g0055 |
2 | NA18954.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.17+641A>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76073562 | |||||||
chr12:76073734 | C | T | 3 | a0001c0002t0019g0141 a0001c0002t0019g0142 a0001c0002t0019g0143 |
3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.17+469G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76073734 | |||||||
chr12:76073830 | A | C | 2 | a0001c0001t0075g0168 a0001c0001t0076g0201 |
2 | NA19006.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.17+373T>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76073830 | |||||||
chr12:76074010 | A | T | 4 | a0001c0002t0027g0222 a0001c0002t0027g0277 a0001c0002t0061g0279 others(1): Show |
4 | HG01081.hp2 HG01123.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.17+193T>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76074010 | |||||||
chr12:76074058 | T | G | 2 | a0001c0002t0028g0146 a0001c0002t0028g0147 |
2 | HG02630.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.17+145A>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76074058 | |||||||
chr12:76074129 | T | C | 3 | a0001c0002t0024g0310 a0001c0002t0024g0311 a0001c0002t0052g0312 |
3 | HG02896.hp2 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.17+74A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76074129 | |||||||
chr12:76074327 | A | G | 3 | a0001c0002t0019g0141 a0001c0002t0019g0142 a0001c0002t0019g0143 |
3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-20-88T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76074327 | |||||||
chr12:76074407 | A | G | 3 | a0001c0002t0019g0141 a0001c0002t0019g0142 a0001c0002t0019g0143 |
3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-20-168T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76074407 | |||||||
chr12:76074784 | T | G | 1 | a0001c0002t0022g0267 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-20-545A>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76074784 | |||||||
chr12:76074794 | G | A | 3 | a0001c0002t0019g0141 a0001c0002t0019g0142 a0001c0002t0019g0143 |
3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-20-555C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76074794 | |||||||
chr12:76074810 | C | T | 3 | a0001c0002t0019g0141 a0001c0002t0019g0142 a0001c0002t0019g0143 |
3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-20-571G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76074810 | |||||||
chr12:76075068 | G | A | 18 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0054 others(15): Show |
22 | HG00438.hp2 HG00735.hp2 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.-20-829C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76075068 | |||||||
chr12:76075269 | G | A | 40 | a0001c0001t0068g0303 a0001c0002t0004g0281 a0001c0002t0004g0282 others(37): Show |
40 | HG00140.hp1 HG00733.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.-20-1030C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76075269 | |||||||
chr12:76075330 | T | A | 1 | a0001c0001t0002g0084 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-20-1091A>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76075330 | |||||||
chr12:76075345 | T | C | 2 | a0001c0001t0003g0116 a0001c0001t0035g0114 |
2 | NA18962.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.-20-1106A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76075345 | |||||||
chr12:76075396 | G | A | 1 | a0001c0002t0065g0284 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-20-1157C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76075396 | |||||||
chr12:76075413 | C | T | 5 | a0001c0002t0009g0017 a0001c0002t0009g0149 a0001c0002t0009g0231 others(2): Show |
6 | HG02257.hp2 HG02622.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20-1174G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76075413 | |||||||
chr12:76075454 | C | T | 1 | a0001c0002t0051g0223 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-20-1215G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76075454 | |||||||
chr12:76075611 | GA | G | 3 | a0001c0002t0019g0141 a0001c0002t0019g0142 a0001c0002t0019g0143 |
3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-20-1373delT | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76075611 | |||||||
chr12:76075734 | G | A | 3 | a0001c0002t0019g0141 a0001c0002t0019g0142 a0001c0002t0019g0143 |
3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-20-1495C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76075734 | |||||||
chr12:76075775 | G | T | 2 | a0001c0002t0028g0146 a0001c0002t0028g0147 |
2 | HG02630.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-20-1536C>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76075775 | |||||||
chr12:76075788 | C | T | 1 | a0001c0002t0029g0140 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-20-1549G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76075788 | |||||||
chr12:76075848 | T | C | 1 | a0001c0002t0051g0223 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-20-1609A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76075848 | |||||||
chr12:76075892 | C | T | 1 | a0001c0001t0001g0167 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-20-1653G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76075892 | |||||||
chr12:76075944 | G | A | 5 | a0001c0001t0002g0086 a0001c0001t0013g0014 a0001c0001t0013g0085 others(2): Show |
6 | HG01243.hp1 HG02572.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20-1705C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76075944 | |||||||
chr12:76075953 | C | A | 1 | a0001c0001t0001g0207 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-20-1714G>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76075953 | |||||||
chr12:76076064 | C | T | 1 | a0001c0002t0044g0221 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-20-1825G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076064 | |||||||
chr12:76076181 | C | T | 1 | a0001c0002t0004g0290 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-20-1942G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076181 | |||||||
chr12:76076496 | G | T | 3 | a0001c0002t0029g0139 a0001c0002t0029g0140 a0001c0002t0088g0138 |
3 | HG02486.hp2 HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-20-2257C>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076496 | |||||||
chr12:76076544 | A | G | 1 | a0001c0002t0044g0221 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-20-2305T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076544 | |||||||
chr12:76076547 | GAAATATA others(3): Show |
G | 1 | a0001c0002t0025g0276 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-20-2318_-20-2309d others(12): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076547 | |||||||
chr12:76076547 | GAAATATA others(11): Show |
G | 1 | a0001c0001t0002g0056 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-20-2326_-20-2309d others(20): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076547 | |||||||
chr12:76076549 | A | AAT | 9 | a0001c0002t0004g0289 a0001c0002t0004g0304 a0001c0002t0019g0141 others(6): Show |
9 | HG00741.hp2 HG01074.hp1 HG02273.hp2 others(6): Show |
intron_variant | MODIFIER | c.-20-2312_-20-2311d others(4): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076549 | |||||||
chr12:76076549 | A | AATAT | 5 | a0001c0002t0004g0282 a0001c0002t0019g0142 a0001c0003t0005g0250 others(2): Show |
5 | HG02559.hp1 HG02717.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.-20-2314_-20-2311d others(6): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076549 | |||||||
chr12:76076549 | A | AATATATA others(1): Show |
5 | a0001c0002t0004g0299 a0001c0002t0028g0146 a0001c0002t0028g0147 others(2): Show |
5 | HG01256.hp2 HG01884.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20-2318_-20-2311d others(10): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076549 | |||||||
chr12:76076549 | A | AATATATA others(3): Show |
4 | a0001c0002t0004g0281 a0001c0003t0005g0028 a0001c0003t0005g0241 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20-2320_-20-2311d others(12): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076549 | |||||||
chr12:76076549 | A | AATATATA others(5): Show |
5 | a0001c0002t0004g0305 a0001c0002t0018g0294 a0001c0003t0005g0245 others(2): Show |
5 | HG01891.hp2 HG02922.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20-2322_-20-2311d others(14): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076549 | |||||||
chr12:76076549 | A | AATATATA others(7): Show |
3 | a0001c0002t0004g0313 a0001c0003t0005g0242 a0001c0003t0005g0253 |
3 | HG00323.hp2 HG02647.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-20-2324_-20-2311d others(16): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076549 | |||||||
chr12:76076549 | A | AATATATA others(9): Show |
4 | a0001c0002t0004g0291 a0001c0003t0005g0027 a0001c0003t0005g0248 others(1): Show |
4 | HG01175.hp1 HG01358.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20-2326_-20-2311d others(18): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076549 | |||||||
chr12:76076549 | A | AATATATA others(11): Show |
6 | a0001c0002t0004g0285 a0001c0002t0004g0307 a0001c0002t0004g0315 others(3): Show |
6 | HG00140.hp1 HG01884.hp1 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20-2328_-20-2311d others(20): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076549 | |||||||
chr12:76076549 | A | AATATATA others(13): Show |
5 | a0001c0002t0004g0309 a0001c0002t0004g0314 a0001c0003t0005g0027 others(2): Show |
6 | HG00738.hp1 HG01192.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20-2330_-20-2311d others(22): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076549 | |||||||
chr12:76076549 | A | AATATATA others(15): Show |
1 | a0001c0003t0005g0028 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-20-2332_-20-2311d others(24): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076549 | |||||||
chr12:76076549 | A | AATATATA others(17): Show |
2 | a0001c0002t0004g0298 a0001c0003t0010g0271 |
2 | HG03927.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-20-2334_-20-2311d others(26): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076549 | |||||||
chr12:76076549 | A | AATATATA others(21): Show |
1 | a0001c0003t0026g0236 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-20-2338_-20-2311d others(30): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076549 | |||||||
chr12:76076549 | AAT | A | 4 | a0001c0001t0068g0303 a0001c0002t0023g0224 a0001c0002t0041g0232 others(1): Show |
4 | HG02280.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20-2312_-20-2311d others(4): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076549 | |||||||
chr12:76076549 | AATAT | A | 7 | a0001c0002t0004g0292 a0001c0002t0009g0017 a0001c0002t0009g0149 others(4): Show |
8 | HG01109.hp2 HG02109.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.-20-2314_-20-2311d others(6): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076549 | |||||||
chr12:76076549 | AATATATA others(1): Show |
A | 7 | a0001c0002t0016g0227 a0001c0002t0016g0229 a0001c0002t0016g0269 others(4): Show |
7 | HG00642.hp1 HG01243.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-20-2318_-20-2311d others(10): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076549 | |||||||
chr12:76076549 | AATATATA others(3): Show |
A | 2 | a0001c0002t0040g0157 a0001c0002t0046g0220 |
2 | HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-20-2320_-20-2311d others(12): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076549 | |||||||
chr12:76076549 | AATATATA others(5): Show |
A | 5 | a0001c0002t0025g0275 a0001c0002t0027g0222 a0001c0002t0027g0277 others(2): Show |
5 | HG01081.hp2 HG01123.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20-2322_-20-2311d others(14): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076549 | |||||||
chr12:76076549 | AATATATA others(7): Show |
A | 11 | a0001c0001t0001g0030 a0001c0001t0001g0134 a0001c0001t0007g0020 others(8): Show |
12 | HG01891.hp1 HG01928.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.-20-2324_-20-2311d others(16): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076549 | |||||||
chr12:76076549 | AATATATA others(9): Show |
A | 20 | a0001c0001t0001g0030 a0001c0001t0001g0255 a0001c0001t0001g0259 others(17): Show |
20 | HG00323.hp1 HG00642.hp2 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.-20-2326_-20-2311d others(18): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076549 | |||||||
chr12:76076549 | AATATATA others(11): Show |
A | 27 | a0001c0001t0001g0024 a0001c0001t0001g0175 a0001c0001t0001g0177 others(24): Show |
28 | HG01261.hp1 HG01516.hp1 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.-20-2328_-20-2311d others(20): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076549 | |||||||
chr12:76076549 | AATATATA others(13): Show |
A | 164 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(161): Show |
193 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(190): Show |
intron_variant | MODIFIER | c.-20-2330_-20-2311d others(22): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076549 | |||||||
chr12:76076549 | AATATATA others(15): Show |
A | 1 | a0001c0001t0001g0260 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-20-2332_-20-2311d others(24): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076549 | |||||||
chr12:76076549 | AATATATA others(19): Show |
A | 1 | a0001c0002t0051g0223 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-20-2336_-20-2311d others(28): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076549 | |||||||
chr12:76076549 | AATATATA others(21): Show |
A | 3 | a0001c0002t0005g0254 a0001c0002t0022g0266 a0001c0002t0022g0267 |
3 | HG02257.hp1 HG02723.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-20-2338_-20-2311d others(30): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076549 | |||||||
chr12:76076549 | AATATATA others(23): Show |
A | 4 | a0001c0002t0004g0290 a0001c0002t0104g0316 a0001c0003t0017g0029 others(1): Show |
4 | HG00733.hp1 HG01069.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20-2340_-20-2311d others(32): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076549 | |||||||
chr12:76076590 | A | C | 2 | a0001c0002t0009g0017 a0001c0002t0009g0149 |
3 | HG02257.hp2 HG03041.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-20-2351T>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076590 | |||||||
chr12:76076592 | A | ATATATAT others(9): Show |
1 | a0001c0002t0018g0308 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-20-2354_-20-2353i others(18): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076592 | |||||||
chr12:76076592 | A | C | 4 | a0001c0002t0015g0019 a0001c0002t0015g0153 a0001c0002t0015g0154 others(1): Show |
5 | HG01261.hp1 HG02145.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-20-2353T>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076592 | |||||||
chr12:76076618 | T | A | 1 | a0001c0001t0086g0126 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-20-2379A>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076618 | |||||||
chr12:76076826 | C | T | 3 | a0001c0002t0024g0310 a0001c0002t0024g0311 a0001c0002t0052g0312 |
3 | HG02896.hp2 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-20-2587G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076826 | |||||||
chr12:76077254 | T | G | 1 | a0001c0002t0019g0143 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-20-3015A>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76077254 | |||||||
chr12:76077658 | C | T | 1 | a0001c0002t0063g0214 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-20-3419G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76077658 | |||||||
chr12:76077929 | G | A | 3 | a0001c0002t0019g0141 a0001c0002t0019g0142 a0001c0002t0019g0143 |
3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-20-3690C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76077929 | |||||||
chr12:76077980 | C | CA | 144 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(141): Show |
168 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.-20-3742dupT | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76077980 | |||||||
chr12:76077980 | C | CAA | 73 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0256 others(70): Show |
83 | HG00438.hp2 HG00544.hp2 HG00735.hp2 others(80): Show |
intron_variant | MODIFIER | c.-20-3743_-20-3742d others(4): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76077980 | |||||||
chr12:76077980 | C | CAAA | 6 | a0001c0001t0001g0207 a0001c0001t0003g0089 a0001c0001t0008g0133 others(3): Show |
6 | HG01975.hp2 HG02015.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.-20-3744_-20-3742d others(5): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76077980 | |||||||
chr12:76077980 | CA | C | 5 | a0001c0002t0004g0289 a0001c0002t0009g0017 a0001c0002t0009g0149 others(2): Show |
6 | HG02257.hp2 HG02273.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20-3742delT | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76077980 | |||||||
chr12:76077981 | A | G | 1 | a0001c0002t0044g0221 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-20-3742T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76077981 | |||||||
chr12:76078000 | A | G | 11 | a0001c0002t0009g0017 a0001c0002t0009g0149 a0001c0002t0009g0231 others(8): Show |
12 | HG02257.hp2 HG02258.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.-20-3761T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76078000 | |||||||
chr12:76078003 | G | A | 275 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(272): Show |
310 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(307): Show |
intron_variant | MODIFIER | c.-20-3764C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76078003 | |||||||
chr12:76078025 | G | GT | 5 | a0001c0002t0009g0017 a0001c0002t0009g0149 a0001c0002t0009g0231 others(2): Show |
6 | HG02257.hp2 HG02622.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20-3787dupA | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76078025 | |||||||
chr12:76078028 | T | C | 2 | a0001c0001t0002g0090 a0001c0001t0002g0091 |
2 | HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-20-3789A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76078028 | |||||||
chr12:76078177 | A | C | 5 | a0001c0002t0020g0218 a0001c0002t0020g0219 a0001c0002t0028g0146 others(2): Show |
5 | HG02258.hp1 HG02630.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.-20-3938T>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76078177 | |||||||
chr12:76078324 | T | C | 2 | a0001c0002t0028g0146 a0001c0002t0028g0147 |
2 | HG02630.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-20-4085A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76078324 | |||||||
chr12:76078392 | G | A | 1 | a0001c0001t0078g0208 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-20-4153C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76078392 | |||||||
chr12:76078603 | G | A | 1 | a0001c0002t0022g0267 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-20-4364C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76078603 | |||||||
chr12:76078662 | T | C | 1 | a0001c0002t0004g0307 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-20-4423A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76078662 | |||||||
chr12:76078753 | T | C | 1 | a0001c0001t0006g0092 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-20-4514A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76078753 | |||||||
chr12:76078798 | G | A | 2 | a0001c0002t0004g0314 a0001c0002t0004g0315 |
2 | HG00738.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.-20-4559C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76078798 | |||||||
chr12:76078813 | G | C | 1 | a0001c0001t0001g0209 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-20-4574C>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76078813 | |||||||
chr12:76078836 | A | G | 3 | a0001c0002t0019g0141 a0001c0002t0019g0142 a0001c0002t0019g0143 |
3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-20-4597T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76078836 | |||||||
chr12:76078910 | C | T | 1 | a0001c0001t0002g0021 | 2 | HG01109.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.-20-4671G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76078910 | |||||||
chr12:76078958 | A | T | 1 | a0001c0001t0003g0127 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-20-4719T>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76078958 | |||||||
chr12:76078982 | C | CAT | 5 | a0001c0001t0002g0122 a0001c0001t0003g0093 a0001c0001t0003g0095 others(2): Show |
5 | HG00735.hp1 HG01516.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20-4745_-20-4744d others(4): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76078982 | |||||||
chr12:76078994 | T | C | 3 | a0001c0002t0005g0254 a0001c0002t0039g0155 a0001c0002t0039g0156 |
3 | HG02622.hp2 HG02723.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-20-4755A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76078994 | |||||||
chr12:76078994 | T | TAC | 13 | a0001c0002t0019g0141 a0001c0002t0019g0142 a0001c0002t0019g0143 others(10): Show |
13 | HG01109.hp2 HG02258.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.-20-4757_-20-4756d others(4): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76078994 | |||||||
chr12:76078994 | T | TACAC | 7 | a0001c0002t0014g0018 a0001c0002t0014g0152 a0001c0002t0027g0222 others(4): Show |
8 | HG01081.hp2 HG01123.hp2 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.-20-4759_-20-4756d others(6): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76078994 | |||||||
chr12:76078996 | C | T | 193 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(190): Show |
225 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(222): Show |
intron_variant | MODIFIER | c.-20-4757G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76078996 | |||||||
chr12:76079014 | T | C | 1 | a0001c0002t0102g0226 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-20-4775A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76079014 | |||||||
chr12:76079144 | A | G | 3 | a0001c0002t0019g0141 a0001c0002t0019g0142 a0001c0002t0019g0143 |
3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-20-4905T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76079144 | |||||||
chr12:76079215 | A | C | 13 | a0001c0002t0014g0018 a0001c0002t0014g0152 a0001c0002t0020g0218 others(10): Show |
14 | HG01109.hp2 HG02055.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.-20-4976T>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76079215 | |||||||
chr12:76079241 | T | C | 3 | a0001c0002t0009g0017 a0001c0002t0009g0149 a0001c0002t0009g0231 |
4 | HG02257.hp2 HG03041.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20-5002A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76079241 | |||||||
chr12:76079249 | T | C | 1 | a0001c0002t0041g0232 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-20-5010A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76079249 | |||||||
chr12:76079305 | C | T | 3 | a0001c0002t0019g0141 a0001c0002t0019g0142 a0001c0002t0019g0143 |
3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-20-5066G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76079305 | |||||||
chr12:76079494 | T | C | 40 | a0001c0001t0002g0045 a0001c0001t0002g0102 a0001c0001t0002g0109 others(37): Show |
44 | HG00423.hp1 HG00597.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.-21+5073A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76079494 | |||||||
chr12:76079684 | A | AT | 55 | a0001c0001t0001g0163 a0001c0001t0001g0215 a0001c0001t0001g0255 others(52): Show |
56 | HG00140.hp1 HG00558.hp2 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.-21+4882dupA | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76079684 | |||||||
chr12:76079684 | A | ATT | 6 | a0001c0002t0004g0286 a0001c0002t0004g0287 a0001c0002t0004g0288 others(3): Show |
6 | HG00741.hp1 HG01978.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.-21+4881_-21+4882d others(4): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76079684 | |||||||
chr12:76079941 | A | C | 271 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(268): Show |
306 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(303): Show |
intron_variant | MODIFIER | c.-21+4626T>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76079941 | |||||||
chr12:76080050 | G | A | 1 | a0001c0001t0001g0213 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-21+4517C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76080050 | |||||||
chr12:76080077 | T | C | 1 | a0001c0002t0004g0309 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-21+4490A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76080077 | |||||||
chr12:76080106 | A | G | 2 | a0001c0002t0044g0221 a0001c0002t0046g0220 |
2 | HG02109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-21+4461T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76080106 | |||||||
chr12:76080158 | A | G | 225 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(222): Show |
260 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(257): Show |
intron_variant | MODIFIER | c.-21+4409T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76080158 | |||||||
chr12:76080248 | T | C | 1 | a0001c0002t0103g0233 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-21+4319A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76080248 | |||||||
chr12:76080540 | C | G | 1 | a0001c0002t0045g0217 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-21+4027G>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76080540 | |||||||
chr12:76080678 | G | A | 1 | a0001c0002t0063g0214 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-21+3889C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76080678 | |||||||
chr12:76080832 | CAT | C | 3 | a0001c0002t0019g0141 a0001c0002t0019g0142 a0001c0002t0019g0143 |
3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-21+3733_-21+3734d others(4): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76080832 | |||||||
chr12:76080976 | T | C | 225 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(222): Show |
260 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(257): Show |
intron_variant | MODIFIER | c.-21+3591A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76080976 | |||||||
chr12:76081035 | C | G | 200 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(197): Show |
232 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(229): Show |
intron_variant | MODIFIER | c.-21+3532G>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081035 | |||||||
chr12:76081078 | C | CT | 258 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(255): Show |
291 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(288): Show |
intron_variant | MODIFIER | c.-21+3488dupA | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081078 | |||||||
chr12:76081078 | C | CTT | 19 | a0001c0002t0004g0285 a0001c0002t0009g0017 a0001c0002t0009g0149 others(16): Show |
21 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.-21+3487_-21+3488d others(4): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081078 | |||||||
chr12:76081082 | T | TC | 3 | a0001c0002t0031g0265 a0001c0002t0031g0273 a0001c0002t0074g0274 |
3 | HG02572.hp2 HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-21+3484_-21+3485i others(3): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081082 | |||||||
chr12:76081115 | T | C | 200 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(197): Show |
232 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(229): Show |
intron_variant | MODIFIER | c.-21+3452A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081115 | |||||||
chr12:76081209 | A | G | 200 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(197): Show |
232 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(229): Show |
intron_variant | MODIFIER | c.-21+3358T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081209 | |||||||
chr12:76081232 | G | C | 1 | a0001c0001t0003g0119 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-21+3335C>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081232 | |||||||
chr12:76081244 | G | C | 1 | a0001c0001t0001g0031 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-21+3323C>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081244 | |||||||
chr12:76081307 | TAAGTA | T | 1 | a0001c0001t0002g0002 | 3 | HG00735.hp2 HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-21+3255_-21+3259d others(7): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081307 | |||||||
chr12:76081313 | A | T | 1 | a0001c0001t0002g0042 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-21+3254T>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081313 | |||||||
chr12:76081475 | C | T | 1 | a0001c0002t0040g0157 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-21+3092G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081475 | |||||||
chr12:76081509 | A | G | 3 | a0001c0002t0019g0141 a0001c0002t0019g0142 a0001c0002t0019g0143 |
3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-21+3058T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081509 | |||||||
chr12:76081654 | G | C | 1 | a0001c0001t0001g0215 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-21+2913C>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081654 | |||||||
chr12:76081656 | A | T | 1 | a0001c0001t0001g0215 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-21+2911T>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081656 | |||||||
chr12:76081685 | A | T | 6 | a0001c0001t0011g0037 a0001c0001t0011g0039 a0001c0001t0011g0041 others(3): Show |
6 | NA18948.hp2 NA18969.hp1 NA18991.hp2 others(3): Show |
intron_variant | MODIFIER | c.-21+2882T>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081685 | |||||||
chr12:76081738 | T | A | 1 | a0001c0001t0001g0215 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-21+2829A>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081738 | |||||||
chr12:76081780 | T | G | 1 | a0001c0001t0001g0215 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-21+2787A>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081780 | |||||||
chr12:76081797 | T | C | 1 | a0001c0001t0001g0215 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-21+2770A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081797 | |||||||
chr12:76081807 | T | C | 1 | a0001c0001t0001g0215 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-21+2760A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081807 | |||||||
chr12:76081809 | T | C | 1 | a0001c0001t0001g0215 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-21+2758A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081809 | |||||||
chr12:76081810 | G | C | 1 | a0001c0001t0001g0215 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-21+2757C>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081810 | |||||||
chr12:76081811 | C | A | 1 | a0001c0001t0001g0215 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-21+2756G>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081811 | |||||||
chr12:76081814 | A | T | 1 | a0001c0001t0001g0215 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-21+2753T>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081814 | |||||||
chr12:76081817 | A | C | 1 | a0001c0001t0001g0215 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-21+2750T>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081817 | |||||||
chr12:76081818 | A | C | 1 | a0001c0001t0001g0215 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-21+2749T>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081818 | |||||||
chr12:76081820 | T | C | 1 | a0001c0001t0001g0215 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-21+2747A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081820 | |||||||
chr12:76081825 | T | C | 1 | a0001c0001t0001g0215 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-21+2742A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081825 | |||||||
chr12:76081828 | A | C | 1 | a0001c0001t0001g0215 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-21+2739T>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081828 | |||||||
chr12:76081829 | T | A | 1 | a0001c0001t0001g0215 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-21+2738A>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081829 | |||||||
chr12:76081830 | G | A | 1 | a0001c0001t0001g0215 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-21+2737C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081830 | |||||||
chr12:76081837 | G | T | 1 | a0001c0001t0001g0215 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-21+2730C>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081837 | |||||||
chr12:76081840 | T | A | 1 | a0001c0001t0001g0215 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-21+2727A>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081840 | |||||||
chr12:76081970 | C | A | 33 | a0001c0001t0068g0303 a0001c0002t0004g0281 a0001c0002t0004g0282 others(30): Show |
33 | HG00140.hp1 HG00733.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.-21+2597G>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081970 | |||||||
chr12:76082004 | T | C | 6 | a0001c0001t0001g0216 a0001c0001t0008g0129 a0001c0001t0008g0131 others(3): Show |
6 | HG01123.hp1 HG01934.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.-21+2563A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76082004 | |||||||
chr12:76082051 | C | CAAGT | 3 | a0001c0002t0019g0141 a0001c0002t0019g0142 a0001c0002t0019g0143 |
3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-21+2515_-21+2516i others(6): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76082051 | |||||||
chr12:76082272 | G | C | 5 | a0001c0002t0009g0017 a0001c0002t0009g0149 a0001c0002t0009g0231 others(2): Show |
6 | HG02257.hp2 HG02622.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.-21+2295C>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76082272 | |||||||
chr12:76082349 | T | C | 9 | a0001c0002t0014g0018 a0001c0002t0014g0152 a0001c0002t0015g0019 others(6): Show |
11 | HG01109.hp2 HG01261.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-21+2218A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76082349 | |||||||
chr12:76082391 | G | A | 1 | a0001c0002t0029g0140 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-21+2176C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76082391 | |||||||
chr12:76082642 | A | G | 1 | a0001c0001t0012g0036 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-21+1925T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76082642 | |||||||
chr12:76082822 | A | G | 1 | a0001c0001t0043g0035 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-21+1745T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76082822 | |||||||
chr12:76082857 | A | C | 204 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(201): Show |
236 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(233): Show |
intron_variant | MODIFIER | c.-21+1710T>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76082857 | |||||||
chr12:76083176 | A | G | 287 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(284): Show |
322 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(319): Show |
intron_variant | MODIFIER | c.-21+1391T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76083176 | |||||||
chr12:76083299 | G | T | 2 | a0001c0001t0002g0120 a0001c0001t0012g0034 |
2 | HG01099.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-21+1268C>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76083299 | |||||||
chr12:76083356 | A | T | 2 | a0001c0002t0039g0155 a0001c0002t0039g0156 |
2 | HG02622.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-21+1211T>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76083356 | |||||||
chr12:76083471 | T | TTC | 29 | a0001c0001t0068g0303 a0001c0002t0004g0285 a0001c0002t0004g0286 others(26): Show |
29 | HG00140.hp1 HG00733.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.-21+1095_-21+1096i others(4): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76083471 | |||||||
chr12:76083472 | C | T | 2 | a0001c0002t0004g0281 a0001c0002t0055g0280 |
2 | HG01192.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-21+1095G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76083472 | |||||||
chr12:76083473 | C | A | 29 | a0001c0001t0068g0303 a0001c0002t0004g0285 a0001c0002t0004g0286 others(26): Show |
29 | HG00140.hp1 HG00733.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.-21+1094G>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76083473 | |||||||
chr12:76083473 | C | CA | 25 | a0001c0001t0001g0030 a0001c0001t0001g0134 a0001c0001t0001g0136 others(22): Show |
26 | HG00423.hp2 HG00642.hp2 HG01175.hp1 others(23): Show |
intron_variant | MODIFIER | c.-21+1093dupT | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76083473 | |||||||
chr12:76083473 | C | CAA | 7 | a0001c0002t0025g0275 a0001c0002t0025g0276 a0001c0002t0027g0277 others(4): Show |
7 | HG01081.hp2 HG01516.hp2 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.-21+1092_-21+1093d others(4): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76083473 | |||||||
chr12:76083473 | CA | C | 119 | a0001c0001t0001g0144 a0001c0001t0002g0002 a0001c0001t0002g0004 others(116): Show |
139 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(136): Show |
intron_variant | MODIFIER | c.-21+1093delT | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76083473 | |||||||
chr12:76083553 | G | C | 37 | a0001c0001t0068g0303 a0001c0002t0004g0281 a0001c0002t0004g0282 others(34): Show |
37 | HG00140.hp1 HG00733.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.-21+1014C>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76083553 | |||||||
chr12:76083581 | G | T | 3 | a0001c0002t0019g0141 a0001c0002t0019g0142 a0001c0002t0019g0143 |
3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-21+986C>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76083581 | |||||||
chr12:76083616 | A | G | 3 | a0001c0002t0029g0139 a0001c0002t0029g0140 a0001c0002t0088g0138 |
3 | HG02486.hp2 HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-21+951T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76083616 | |||||||
chr12:76083766 | A | G | 1 | a0001c0001t0007g0137 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-21+801T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76083766 | |||||||
chr12:76083938 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-21+629G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76083938 | |||||||
chr12:76083947 | C | G | 1 | a0001c0001t0006g0033 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-21+620G>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76083947 | |||||||
chr12:76083995 | G | A | 1 | a0001c0001t0002g0135 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-21+572C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76083995 | |||||||
chr12:76084161 | A | C | 116 | a0001c0001t0001g0134 a0001c0001t0002g0002 a0001c0001t0002g0004 others(113): Show |
133 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.-21+406T>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76084161 | |||||||
chr12:76084262 | T | G | 2 | a0001c0002t0004g0314 a0001c0002t0004g0315 |
2 | HG00738.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.-21+305A>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76084262 | |||||||
chr12:76084379 | C | T | 1 | a0001c0001t0032g0032 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-21+188G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76084379 | |||||||
chr12:76084433 | A | G | 1 | a0001c0001t0001g0031 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-21+134T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76084433 |