Item | Value |
---|---|
geneid | 8907 |
ensemblid | ENSG00000072958.9 |
hgncid | 13667 |
symbol | AP1M1 |
name | adaptor related protein complex 1 subunit mu 1 |
refseq_nuc | NM_032493.4 |
refseq_prot | NP_115882.1 |
ensembl_nuc | ENST00000291439.8 |
ensembl_prot | ENSP00000291439.2 |
mane_status | MANE Select |
chr | chr19 |
start | 16197911 |
end | 16245906 |
strand | + |
ver | v1.2 |
region | chr19:16197911-16245906 |
region5000 | chr19:16192911-16250906 |
regionname0 | AP1M1_chr19_16197911_16245906 |
regionname5000 | AP1M1_chr19_16192911_16250906 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1269 | 207 | 75 | 32 | 73 | 2 | 23 | AP1M1_chr19_16192911_16250906 | AP1M1 | ATGTC others(1264): Show |
chr19 | 16192911 | 16250906 | ||
a0001c0002 | 0/0 | 1269 | 98 | 10 | 29 | 38 | 6 | 15 | AP1M1_chr19_16192911_16250906 | AP1M1 | ATGTC others(1264): Show |
chr19 | 16192911 | 16250906 | ||
a0001c0003 | 0/0 | 1269 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | ATGTC others(1264): Show |
chr19 | 16192911 | 16250906 | ||
a0001c0004 | 0/0 | 1269 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | ATGTC others(1264): Show |
chr19 | 16192911 | 16250906 | ||
a0001c0005 | 0/0 | 1269 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | ATGTC others(1264): Show |
chr19 | 16192911 | 16250906 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 0/0 | 12862 | 28 | 1 | 9 | 14 | 0 | 4 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12857): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0003 | 1/0 | 12859 | 11 | 1 | 2 | 2 | 0 | 5 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12854): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0005 | 0/0 | 12887 | 10 | 0 | 1 | 9 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12882): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0006 | 0/0 | 12862 | 6 | 0 | 2 | 1 | 0 | 3 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12857): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0007 | 0/0 | 12867 | 6 | 6 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12862): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0008 | 0/0 | 12890 | 5 | 0 | 0 | 5 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12885): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0009 | 0/0 | 12867 | 5 | 5 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12862): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0013 | 0/0 | 12859 | 4 | 4 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12854): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0014 | 0/0 | 12861 | 4 | 0 | 1 | 3 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12856): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0016 | 0/0 | 12861 | 3 | 3 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12856): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0017 | 0/0 | 12888 | 3 | 0 | 1 | 2 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12883): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0018 | 0/0 | 12887 | 3 | 3 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12882): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0019 | 0/0 | 12863 | 3 | 0 | 0 | 3 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12858): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0020 | 0/0 | 12863 | 3 | 0 | 1 | 2 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12858): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0026 | 0/0 | 12849 | 2 | 2 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12844): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0027 | 0/0 | 12864 | 2 | 2 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12859): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0028 | 0/0 | 12860 | 2 | 0 | 0 | 0 | 0 | 2 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12855): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0029 | 0/0 | 12867 | 2 | 1 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12862): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0030 | 0/0 | 12870 | 2 | 2 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12865): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0031 | 0/0 | 12882 | 2 | 1 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12877): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0032 | 0/0 | 12883 | 2 | 1 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12878): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0033 | 0/0 | 12890 | 2 | 0 | 1 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12885): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0034 | 0/0 | 12891 | 2 | 0 | 0 | 2 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12886): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0035 | 0/0 | 12886 | 2 | 0 | 2 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12881): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0036 | 0/0 | 12894 | 2 | 0 | 0 | 2 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12889): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0037 | 0/0 | 12895 | 2 | 2 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12890): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0038 | 0/0 | 12862 | 2 | 2 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12857): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0039 | 0/0 | 12857 | 2 | 2 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12852): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0040 | 0/0 | 12860 | 2 | 2 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12855): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0041 | 0/0 | 12857 | 2 | 2 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12852): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0042 | 0/0 | 12869 | 2 | 1 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12864): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0043 | 0/0 | 12875 | 2 | 2 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12870): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0044 | 0/0 | 12844 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12839): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0045 | 0/0 | 12853 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12848): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0078 | 0/0 | 12861 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12856): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0079 | 0/0 | 12840 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12835): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0080 | 0/0 | 12858 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12853): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0081 | 0/0 | 12858 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12853): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0082 | 0/0 | 12859 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12854): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0083 | 0/0 | 12859 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12854): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0084 | 0/1 | 12863 | 1 | 0 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12858): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0085 | 0/0 | 12861 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12856): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0086 | 0/0 | 12867 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12862): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0087 | 0/0 | 12860 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12855): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0089 | 0/0 | 12863 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12858): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0090 | 0/0 | 12861 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12856): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0091 | 0/0 | 12863 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12858): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0092 | 0/0 | 12859 | 1 | 0 | 0 | 0 | 1 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12854): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0093 | 0/0 | 12860 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12855): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0094 | 0/0 | 12849 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12844): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0095 | 0/0 | 12859 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12854): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0096 | 0/0 | 12846 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12841): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0097 | 0/0 | 12867 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12862): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0098 | 0/0 | 12853 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12848): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0100 | 0/0 | 12859 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12854): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0101 | 0/0 | 12865 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12860): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0102 | 0/0 | 12867 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12862): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0103 | 0/0 | 12887 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12882): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0104 | 0/0 | 12896 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12891): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0105 | 0/0 | 12871 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12866): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0106 | 0/0 | 12886 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12881): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0108 | 0/0 | 12890 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12885): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0109 | 0/0 | 12889 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12884): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0110 | 0/0 | 12894 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12889): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0111 | 0/0 | 12860 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12855): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0112 | 0/0 | 12885 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12880): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0113 | 0/0 | 12887 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12882): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0114 | 0/0 | 12888 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12883): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0115 | 0/0 | 12890 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12885): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0116 | 0/0 | 12889 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12884): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0117 | 0/0 | 12890 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12885): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0118 | 0/0 | 12889 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12884): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0119 | 0/0 | 12888 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12883): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0120 | 0/0 | 12887 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12882): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0121 | 0/0 | 12889 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12884): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0122 | 0/0 | 12893 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12888): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0123 | 0/0 | 12896 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12891): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0124 | 0/0 | 12888 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12883): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0125 | 0/0 | 12889 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12884): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0126 | 0/0 | 12889 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12884): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0127 | 0/0 | 12886 | 1 | 0 | 0 | 0 | 1 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12881): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0128 | 0/0 | 12861 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12856): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0129 | 0/0 | 12887 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12882): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0130 | 0/0 | 12889 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12884): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0131 | 0/0 | 12864 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12859): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0132 | 0/0 | 12865 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12860): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0133 | 0/0 | 12869 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12864): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0134 | 0/0 | 12863 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12858): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0135 | 0/0 | 12864 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12859): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0136 | 0/0 | 12864 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12859): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0137 | 0/0 | 12868 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12863): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0138 | 0/0 | 12867 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12862): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0139 | 0/0 | 12862 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12857): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0140 | 0/0 | 12867 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12862): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0141 | 0/0 | 12869 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12864): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0142 | 0/0 | 12866 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12861): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0143 | 0/0 | 12864 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12859): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0144 | 0/0 | 12866 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12861): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0145 | 0/0 | 12872 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12867): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0146 | 0/0 | 12867 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12862): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0147 | 0/0 | 12870 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12865): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0148 | 0/0 | 12869 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12864): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0149 | 0/0 | 12868 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12863): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0150 | 0/0 | 12863 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12858): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0151 | 0/0 | 12869 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12864): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0152 | 0/0 | 12872 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12867): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0153 | 0/0 | 12870 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12865): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0154 | 0/0 | 12873 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12868): Show |
chr19 | 16192911 | 16250906 |
a0001c0001t0155 | 0/0 | 12892 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12887): Show |
chr19 | 16192911 | 16250906 |
a0001c0002t0001 | 0/0 | 12860 | 31 | 3 | 8 | 13 | 3 | 4 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12855): Show |
chr19 | 16192911 | 16250906 |
a0001c0002t0004 | 0/0 | 12861 | 10 | 0 | 6 | 1 | 1 | 2 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12856): Show |
chr19 | 16192911 | 16250906 |
a0001c0002t0010 | 0/0 | 12859 | 4 | 0 | 1 | 3 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12854): Show |
chr19 | 16192911 | 16250906 |
a0001c0002t0011 | 0/0 | 12863 | 4 | 0 | 0 | 4 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12858): Show |
chr19 | 16192911 | 16250906 |
a0001c0002t0012 | 0/0 | 12862 | 4 | 0 | 2 | 1 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12857): Show |
chr19 | 16192911 | 16250906 |
a0001c0002t0015 | 0/0 | 12860 | 3 | 0 | 0 | 3 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12855): Show |
chr19 | 16192911 | 16250906 |
a0001c0002t0021 | 0/0 | 12863 | 2 | 0 | 0 | 0 | 0 | 2 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12858): Show |
chr19 | 16192911 | 16250906 |
a0001c0002t0022 | 0/0 | 12861 | 2 | 0 | 2 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12856): Show |
chr19 | 16192911 | 16250906 |
a0001c0002t0023 | 0/0 | 12858 | 2 | 1 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12853): Show |
chr19 | 16192911 | 16250906 |
a0001c0002t0024 | 0/0 | 12863 | 2 | 2 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12858): Show |
chr19 | 16192911 | 16250906 |
a0001c0002t0025 | 0/0 | 12866 | 2 | 0 | 1 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12861): Show |
chr19 | 16192911 | 16250906 |
a0001c0002t0046 | 0/0 | 12848 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12843): Show |
chr19 | 16192911 | 16250906 |
a0001c0002t0047 | 0/0 | 12864 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12859): Show |
chr19 | 16192911 | 16250906 |
a0001c0002t0048 | 0/0 | 12860 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12855): Show |
chr19 | 16192911 | 16250906 |
a0001c0002t0049 | 0/0 | 12859 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12854): Show |
chr19 | 16192911 | 16250906 |
a0001c0002t0050 | 0/0 | 12860 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12855): Show |
chr19 | 16192911 | 16250906 |
a0001c0002t0051 | 0/0 | 12861 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12856): Show |
chr19 | 16192911 | 16250906 |
a0001c0002t0052 | 0/0 | 12861 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12856): Show |
chr19 | 16192911 | 16250906 |
a0001c0002t0053 | 0/0 | 12837 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12832): Show |
chr19 | 16192911 | 16250906 |
a0001c0002t0054 | 0/0 | 12846 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12841): Show |
chr19 | 16192911 | 16250906 |
a0001c0002t0055 | 0/0 | 12847 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12842): Show |
chr19 | 16192911 | 16250906 |
a0001c0002t0056 | 0/0 | 12850 | 1 | 0 | 0 | 0 | 1 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12845): Show |
chr19 | 16192911 | 16250906 |
a0001c0002t0057 | 0/0 | 12848 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12843): Show |
chr19 | 16192911 | 16250906 |
a0001c0002t0058 | 0/0 | 12857 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12852): Show |
chr19 | 16192911 | 16250906 |
a0001c0002t0059 | 0/0 | 12853 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12848): Show |
chr19 | 16192911 | 16250906 |
a0001c0002t0060 | 0/0 | 12862 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12857): Show |
chr19 | 16192911 | 16250906 |
a0001c0002t0061 | 0/0 | 12862 | 1 | 0 | 0 | 0 | 1 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12857): Show |
chr19 | 16192911 | 16250906 |
a0001c0002t0062 | 0/0 | 12854 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12849): Show |
chr19 | 16192911 | 16250906 |
a0001c0002t0063 | 0/0 | 12857 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12852): Show |
chr19 | 16192911 | 16250906 |
a0001c0002t0064 | 0/0 | 12861 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12856): Show |
chr19 | 16192911 | 16250906 |
a0001c0002t0065 | 0/0 | 12864 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12859): Show |
chr19 | 16192911 | 16250906 |
a0001c0002t0066 | 0/0 | 12862 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12857): Show |
chr19 | 16192911 | 16250906 |
a0001c0002t0067 | 0/0 | 12840 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12835): Show |
chr19 | 16192911 | 16250906 |
a0001c0002t0068 | 0/0 | 12858 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12853): Show |
chr19 | 16192911 | 16250906 |
a0001c0002t0069 | 0/0 | 12865 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12860): Show |
chr19 | 16192911 | 16250906 |
a0001c0002t0070 | 0/0 | 12859 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12854): Show |
chr19 | 16192911 | 16250906 |
a0001c0002t0071 | 0/0 | 12862 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12857): Show |
chr19 | 16192911 | 16250906 |
a0001c0002t0073 | 0/0 | 12869 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12864): Show |
chr19 | 16192911 | 16250906 |
a0001c0002t0074 | 0/0 | 12846 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12841): Show |
chr19 | 16192911 | 16250906 |
a0001c0002t0075 | 0/0 | 12857 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12852): Show |
chr19 | 16192911 | 16250906 |
a0001c0002t0076 | 0/0 | 12862 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12857): Show |
chr19 | 16192911 | 16250906 |
a0001c0002t0077 | 0/0 | 12864 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12859): Show |
chr19 | 16192911 | 16250906 |
a0001c0002t0099 | 0/0 | 12847 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12842): Show |
chr19 | 16192911 | 16250906 |
a0001c0003t0088 | 0/0 | 12860 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12855): Show |
chr19 | 16192911 | 16250906 |
a0001c0004t0107 | 0/0 | 12888 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12883): Show |
chr19 | 16192911 | 16250906 |
a0001c0005t0072 | 0/0 | 12866 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | GGAAG others(12861): Show |
chr19 | 16192911 | 16250906 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0001 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0002g0003 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0002g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0003g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0003g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0003g0199 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0005g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0005g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0005g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0005g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0005g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0005g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0005g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0005g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0005g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0005g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0006g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0006g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0006g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0006g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0006g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0007g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0007g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0008g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0008g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0008g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0008g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0008g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0009g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0009g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0009g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0009g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0013g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0013g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0013g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0013g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0014g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0014g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0014g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0014g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0016g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0016g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0016g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0017g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0017g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0017g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0018g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0018g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0018g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0019g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0019g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0019g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0020g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0020g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0020g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0026g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0026g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0027g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0027g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0028g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0028g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0029g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0029g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0030g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0030g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0031g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0031g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0032g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0032g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0033g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0033g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0034g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0034g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0035g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0035g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0036g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0036g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0037g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0037g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0038g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0038g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0039g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0039g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0040g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0040g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0041g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0042g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0042g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0043g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0043g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0044g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0045g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0078g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0079g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0080g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0081g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0082g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0083g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0084g0195 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0085g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0086g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0087g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0089g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0090g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0091g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0092g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0093g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0094g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0095g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0096g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0097g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0098g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0100g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0101g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0102g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0103g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0104g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0105g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0106g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0108g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0109g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0110g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0111g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0112g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0113g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0114g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0115g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0116g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0117g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0118g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0119g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0120g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0121g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0122g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0123g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0124g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0125g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0126g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0127g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0128g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0129g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0130g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0131g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0132g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0133g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0134g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0135g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0136g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0137g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0138g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0139g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0140g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0141g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0142g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0143g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0144g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0145g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0146g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0147g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0148g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0149g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0150g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0151g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0152g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0153g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0154g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0155g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0004g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0004g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0004g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0004g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0004g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0004g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0004g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0004g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0004g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0004g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0010g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0010g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0010g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0010g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0011g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0011g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0011g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0011g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0012g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0012g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0012g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0012g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0015g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0015g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0015g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0021g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0021g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0022g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0022g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0023g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0023g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0024g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0024g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0025g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0025g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0046g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0047g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0048g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0049g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0050g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0051g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0052g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0053g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0054g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0055g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0056g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0057g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0058g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0059g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0060g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0061g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0062g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0063g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0064g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0065g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0066g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0067g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0068g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0069g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0070g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0071g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0073g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0074g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0075g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0076g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0077g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0099g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0003t0088g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0004t0107g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0005t0072g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0001 | g0012 | EUR | GBR | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG00099 | hp2 | a0001 | c0001 | t0127 | g0221 | EUR | GBR | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG00140 | hp1 | a0001 | c0002 | t0056 | g0130 | EUR | GBR | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG00140 | hp2 | a0001 | c0002 | t0061 | g0012 | EUR | GBR | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG00423 | hp1 | a0001 | c0001 | t0019 | g0069 | EAS | CHS | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG00423 | hp2 | a0001 | c0001 | t0005 | g0231 | EAS | CHS | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG00438 | hp1 | a0001 | c0001 | t0136 | g0061 | EAS | CHS | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG00438 | hp2 | a0001 | c0001 | t0005 | g0225 | EAS | CHS | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG00544 | hp1 | a0001 | c0001 | t0103 | g0241 | EAS | CHS | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG00544 | hp2 | a0001 | c0001 | t0091 | g0201 | EAS | CHS | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG00558 | hp1 | a0001 | c0001 | t0017 | g0235 | EAS | CHS | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | CHS | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG00597 | hp2 | a0001 | c0002 | t0001 | g0167 | EAS | CHS | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG00609 | hp1 | a0001 | c0001 | t0005 | g0227 | EAS | CHS | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG00609 | hp2 | a0001 | c0002 | t0011 | g0113 | EAS | CHS | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG00673 | hp1 | a0001 | c0002 | t0011 | g0146 | EAS | CHS | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG00673 | hp2 | a0001 | c0001 | t0005 | g0219 | EAS | CHS | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG00735 | hp1 | a0001 | c0001 | t0032 | g0027 | AMR | PUR | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG00735 | hp2 | a0001 | c0001 | t0020 | g0083 | AMR | PUR | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0173 | AMR | PUR | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG00738 | hp2 | a0001 | c0002 | t0001 | g0101 | AMR | PUR | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01069 | hp1 | a0001 | c0001 | t0005 | g0216 | AMR | PUR | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01069 | hp2 | a0001 | c0001 | t0014 | g0010 | AMR | PUR | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01071 | hp1 | a0001 | c0002 | t0059 | g0099 | AMR | PUR | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01074 | hp1 | a0001 | c0002 | t0001 | g0135 | AMR | PUR | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01074 | hp2 | a0001 | c0002 | t0001 | g0136 | AMR | PUR | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01081 | hp1 | a0001 | c0001 | t0079 | g0177 | AMR | PUR | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01099 | hp1 | a0001 | c0002 | t0022 | g0162 | AMR | PUR | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01099 | hp2 | a0001 | c0001 | t0083 | g0176 | AMR | PUR | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01109 | hp1 | a0001 | c0001 | t0031 | g0024 | AMR | PUR | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01109 | hp2 | a0001 | c0001 | t0121 | g0257 | AMR | PUR | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01167 | hp1 | a0001 | c0001 | t0149 | g0037 | AMR | PUR | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01167 | hp2 | a0001 | c0002 | t0058 | g0126 | AMR | PUR | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01169 | hp1 | a0001 | c0002 | t0066 | g0159 | AMR | PUR | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01169 | hp2 | a0001 | c0001 | t0151 | g0055 | AMR | PUR | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01192 | hp1 | a0001 | c0002 | t0004 | g0134 | AMR | PUR | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01243 | hp1 | a0001 | c0001 | t0035 | g0256 | AMR | PUR | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01243 | hp2 | a0001 | c0002 | t0012 | g0125 | AMR | PUR | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01255 | hp1 | a0001 | c0002 | t0012 | g0093 | AMR | CLM | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01256 | hp1 | a0001 | c0002 | t0001 | g0089 | AMR | CLM | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01256 | hp2 | a0001 | c0001 | t0081 | g0193 | AMR | CLM | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01257 | hp1 | a0001 | c0002 | t0001 | g0128 | AMR | CLM | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01257 | hp2 | a0001 | c0001 | t0006 | g0185 | AMR | CLM | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01258 | hp1 | a0001 | c0001 | t0006 | g0186 | AMR | CLM | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01258 | hp2 | a0001 | c0001 | t0003 | g0194 | AMR | CLM | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01261 | hp1 | a0001 | c0002 | t0001 | g0150 | AMR | CLM | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0062 | AMR | CLM | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01346 | hp1 | a0001 | c0005 | t0072 | g0004 | AMR | CLM | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01346 | hp2 | a0001 | c0001 | t0101 | g0064 | AMR | CLM | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01358 | hp1 | a0001 | c0001 | t0033 | g0233 | AMR | CLM | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01358 | hp2 | a0001 | c0002 | t0001 | g0110 | AMR | CLM | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01361 | hp1 | a0001 | c0001 | t0147 | g0213 | AMR | CLM | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01361 | hp2 | a0001 | c0002 | t0047 | g0096 | AMR | CLM | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01433 | hp1 | a0001 | c0002 | t0050 | g0166 | AMR | CLM | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01433 | hp2 | a0001 | c0002 | t0063 | g0155 | AMR | CLM | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01496 | hp1 | a0001 | c0002 | t0064 | g0161 | AMR | CLM | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0075 | AMR | CLM | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01884 | hp1 | a0001 | c0001 | t0131 | g0007 | AFR | ACB | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01884 | hp2 | a0001 | c0001 | t0031 | g0025 | AFR | ACB | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01891 | hp1 | a0001 | c0003 | t0088 | g0187 | AFR | ACB | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01891 | hp2 | a0001 | c0001 | t0106 | g0260 | AFR | ACB | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01928 | hp1 | a0001 | c0002 | t0004 | g0091 | AMR | PEL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01928 | hp2 | a0001 | c0001 | t0017 | g0232 | AMR | PEL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01934 | hp1 | a0001 | c0001 | t0029 | g0183 | AMR | PEL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01934 | hp2 | a0001 | c0002 | t0004 | g0102 | AMR | PEL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0068 | AMR | PEL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01975 | hp2 | a0001 | c0002 | t0001 | g0090 | AMR | PEL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01978 | hp1 | a0001 | c0002 | t0004 | g0011 | AMR | PEL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01978 | hp2 | a0001 | c0001 | t0035 | g0255 | AMR | PEL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01993 | hp1 | a0001 | c0002 | t0010 | g0157 | AMR | PEL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01993 | hp2 | a0001 | c0002 | t0051 | g0127 | AMR | PEL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02015 | hp1 | a0001 | c0001 | t0005 | g0247 | EAS | KHV | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02015 | hp2 | a0001 | c0001 | t0003 | g0188 | EAS | KHV | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02055 | hp1 | a0001 | c0001 | t0030 | g0005 | AFR | ACB | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02055 | hp2 | a0001 | c0001 | t0130 | g0076 | AFR | ACB | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | KHV | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02080 | hp2 | a0001 | c0001 | t0126 | g0244 | EAS | KHV | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | KHV | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02083 | hp2 | a0001 | c0002 | t0048 | g0119 | EAS | KHV | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02132 | hp1 | a0001 | c0001 | t0034 | g0273 | EAS | KHV | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02135 | hp1 | a0001 | c0002 | t0073 | g0114 | EAS | KHV | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | KHV | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02145 | hp1 | a0001 | c0001 | t0007 | g0006 | AFR | ACB | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02145 | hp2 | a0001 | c0001 | t0105 | g0272 | AFR | ACB | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02155 | hp1 | a0001 | c0001 | t0132 | g0063 | EAS | CDX | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02155 | hp2 | a0001 | c0002 | t0060 | g0158 | EAS | CDX | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02165 | hp1 | a0001 | c0002 | t0001 | g0148 | EAS | CDX | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | CDX | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02257 | hp1 | a0001 | c0001 | t0152 | g0077 | AFR | ACB | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02257 | hp2 | a0001 | c0001 | t0045 | g0023 | AFR | ACB | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02258 | hp1 | a0001 | c0001 | t0039 | g0051 | AFR | ACB | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02258 | hp2 | a0001 | c0001 | t0150 | g0009 | AFR | ACB | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0071 | AMR | PEL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02273 | hp2 | a0001 | c0002 | t0004 | g0103 | AMR | PEL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02280 | hp1 | a0001 | c0001 | t0013 | g0014 | AFR | ACB | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02280 | hp2 | a0001 | c0001 | t0018 | g0268 | AFR | ACB | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02293 | hp2 | a0001 | c0002 | t0022 | g0151 | AMR | PEL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02300 | hp1 | a0001 | c0002 | t0049 | g0143 | AMR | PEL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02300 | hp2 | a0001 | c0002 | t0004 | g0104 | AMR | PEL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02451 | hp1 | a0001 | c0002 | t0075 | g0168 | AFR | ACB | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02451 | hp2 | a0001 | c0001 | t0097 | g0179 | AFR | ACB | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | KHV | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02523 | hp2 | a0001 | c0001 | t0148 | g0058 | EAS | KHV | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02572 | hp1 | a0001 | c0001 | t0043 | g0009 | AFR | GWD | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02572 | hp2 | a0001 | c0001 | t0110 | g0261 | AFR | GWD | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02602 | hp1 | a0001 | c0002 | t0001 | g0034 | SAS | PJL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02602 | hp2 | a0001 | c0001 | t0153 | g0080 | SAS | PJL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02615 | hp1 | a0001 | c0001 | t0038 | g0223 | AFR | GWD | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02615 | hp2 | a0001 | c0001 | t0009 | g0017 | AFR | GWD | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02630 | hp1 | a0001 | c0001 | t0013 | g0005 | AFR | GWD | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02630 | hp2 | a0001 | c0001 | t0039 | g0053 | AFR | GWD | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02647 | hp1 | a0001 | c0001 | t0026 | g0279 | AFR | GWD | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02647 | hp2 | a0001 | c0001 | t0018 | g0270 | AFR | GWD | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02683 | hp1 | a0001 | c0002 | t0054 | g0095 | SAS | PJL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02683 | hp2 | a0001 | c0001 | t0003 | g0015 | SAS | PJL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02717 | hp1 | a0001 | c0002 | t0024 | g0118 | AFR | GWD | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02717 | hp2 | a0001 | c0001 | t0041 | g0008 | AFR | GWD | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02723 | hp1 | a0001 | c0001 | t0138 | g0211 | AFR | GWD | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02723 | hp2 | a0001 | c0001 | t0128 | g0022 | AFR | GWD | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02735 | hp1 | a0001 | c0002 | t0021 | g0094 | SAS | PJL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02735 | hp2 | a0001 | c0002 | t0021 | g0098 | SAS | PJL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02738 | hp1 | a0001 | c0001 | t0085 | g0203 | SAS | PJL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02738 | hp2 | a0001 | c0002 | t0099 | g0142 | SAS | PJL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0046 | AFR | GWD | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02809 | hp2 | a0001 | c0001 | t0032 | g0026 | AFR | GWD | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02818 | hp1 | a0001 | c0001 | t0027 | g0029 | AFR | GWD | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02818 | hp2 | a0001 | c0002 | t0071 | g0106 | AFR | GWD | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02886 | hp1 | a0001 | c0001 | t0003 | g0032 | AFR | GWD | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02886 | hp2 | a0001 | c0001 | t0030 | g0178 | AFR | GWD | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02895 | hp1 | a0001 | c0001 | t0016 | g0018 | AFR | GWD | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02895 | hp2 | a0001 | c0001 | t0038 | g0224 | AFR | GWD | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02896 | hp1 | a0001 | c0001 | t0094 | g0277 | AFR | GWD | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02896 | hp2 | a0001 | c0001 | t0009 | g0207 | AFR | GWD | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02897 | hp1 | a0001 | c0001 | t0009 | g0206 | AFR | GWD | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02897 | hp2 | a0001 | c0001 | t0111 | g0020 | AFR | GWD | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02922 | hp1 | a0001 | c0001 | t0027 | g0028 | AFR | ESN | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02922 | hp2 | a0001 | c0001 | t0143 | g0007 | AFR | ESN | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02965 | hp1 | a0001 | c0002 | t0001 | g0111 | AFR | ESN | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02965 | hp2 | a0001 | c0001 | t0098 | g0182 | AFR | ESN | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02976 | hp1 | a0001 | c0002 | t0024 | g0088 | AFR | ESN | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02976 | hp2 | a0001 | c0001 | t0007 | g0002 | AFR | ESN | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03098 | hp1 | a0001 | c0001 | t0013 | g0184 | AFR | MSL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03098 | hp2 | a0001 | c0001 | t0102 | g0214 | AFR | MSL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03130 | hp1 | a0001 | c0001 | t0007 | g0002 | AFR | ESN | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03130 | hp2 | a0001 | c0001 | t0037 | g0271 | AFR | ESN | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03139 | hp1 | a0001 | c0002 | t0062 | g0170 | AFR | ESN | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03139 | hp2 | a0001 | c0001 | t0009 | g0209 | AFR | ESN | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03195 | hp1 | a0001 | c0001 | t0043 | g0059 | AFR | ESN | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03195 | hp2 | a0001 | c0001 | t0007 | g0002 | AFR | ESN | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03209 | hp1 | a0001 | c0001 | t0026 | g0280 | AFR | MSL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03209 | hp2 | a0001 | c0001 | t0141 | g0283 | AFR | MSL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03239 | hp1 | a0001 | c0002 | t0025 | g0274 | SAS | PJL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03239 | hp2 | a0001 | c0001 | t0087 | g0013 | SAS | PJL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03453 | hp1 | a0001 | c0001 | t0086 | g0281 | AFR | MSL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03453 | hp2 | a0001 | c0001 | t0016 | g0019 | AFR | MSL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03486 | hp1 | a0001 | c0001 | t0137 | g0212 | AFR | MSL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03486 | hp2 | a0001 | c0001 | t0016 | g0021 | AFR | MSL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03490 | hp1 | a0001 | c0001 | t0006 | g0015 | SAS | PJL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03490 | hp2 | a0001 | c0001 | t0006 | g0016 | SAS | PJL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03491 | hp1 | a0001 | c0001 | t0080 | g0189 | SAS | PJL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03491 | hp2 | a0001 | c0002 | t0001 | g0122 | SAS | PJL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03492 | hp1 | a0001 | c0001 | t0006 | g0016 | SAS | PJL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03492 | hp2 | a0001 | c0001 | t0082 | g0192 | SAS | PJL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03516 | hp1 | a0001 | c0001 | t0018 | g0269 | AFR | ESN | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03516 | hp2 | a0001 | c0001 | t0146 | g0210 | AFR | ESN | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03540 | hp1 | a0001 | c0001 | t0133 | g0057 | AFR | GWD | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03540 | hp2 | a0001 | c0002 | t0053 | g0165 | AFR | GWD | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03579 | hp1 | a0001 | c0001 | t0013 | g0180 | AFR | MSL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03579 | hp2 | a0001 | c0002 | t0001 | g0275 | AFR | MSL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0045 | SAS | PJL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03669 | hp2 | a0001 | c0001 | t0028 | g0197 | SAS | PJL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0047 | SAS | STU | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03688 | hp2 | a0001 | c0002 | t0012 | g0141 | SAS | STU | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03710 | hp1 | a0001 | c0002 | t0023 | g0169 | SAS | PJL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03710 | hp2 | a0001 | c0001 | t0003 | g0175 | SAS | PJL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03831 | hp1 | a0001 | c0001 | t0003 | g0196 | SAS | BEB | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03831 | hp2 | a0001 | c0001 | t0139 | g0048 | SAS | BEB | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0072 | SAS | BEB | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03834 | hp2 | a0001 | c0002 | t0004 | g0116 | SAS | BEB | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03927 | hp1 | a0001 | c0001 | t0003 | g0205 | SAS | BEB | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03927 | hp2 | a0001 | c0002 | t0004 | g0153 | SAS | BEB | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03942 | hp1 | a0001 | c0001 | t0134 | g0050 | SAS | BEB | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03942 | hp2 | a0001 | c0001 | t0042 | g0081 | SAS | BEB | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG04115 | hp1 | a0001 | c0002 | t0057 | g0117 | SAS | STU | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG04115 | hp2 | a0001 | c0002 | t0055 | g0132 | SAS | STU | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG04184 | hp1 | a0001 | c0001 | t0028 | g0190 | SAS | BEB | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0067 | SAS | BEB | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG04204 | hp1 | a0001 | c0001 | t0093 | g0013 | SAS | STU | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG04204 | hp2 | a0001 | c0002 | t0001 | g0121 | SAS | STU | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18522 | hp1 | a0001 | c0001 | t0040 | g0052 | AFR | YRI | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18522 | hp2 | a0001 | c0001 | t0040 | g0035 | AFR | YRI | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18906 | hp1 | a0001 | c0001 | t0095 | g0181 | AFR | YRI | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18906 | hp2 | a0001 | c0001 | t0009 | g0017 | AFR | YRI | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18939 | hp1 | a0001 | c0002 | t0070 | g0171 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18939 | hp2 | a0001 | c0001 | t0117 | g0240 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18943 | hp1 | a0001 | c0002 | t0011 | g0152 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18943 | hp2 | a0001 | c0001 | t0036 | g0266 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18944 | hp1 | a0001 | c0002 | t0015 | g0087 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18944 | hp2 | a0001 | c0001 | t0119 | g0236 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18945 | hp1 | a0001 | c0001 | t0005 | g0229 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18945 | hp2 | a0001 | c0002 | t0067 | g0112 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18947 | hp1 | a0001 | c0001 | t0008 | g0250 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18947 | hp2 | a0001 | c0002 | t0001 | g0163 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18948 | hp1 | a0001 | c0002 | t0001 | g0124 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18948 | hp2 | a0001 | c0001 | t0014 | g0039 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18949 | hp1 | a0001 | c0002 | t0074 | g0011 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18949 | hp2 | a0001 | c0001 | t0114 | g0215 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18951 | hp1 | a0001 | c0002 | t0046 | g0137 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18951 | hp2 | a0001 | c0001 | t0008 | g0252 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18954 | hp1 | a0001 | c0001 | t0003 | g0191 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18954 | hp2 | a0001 | c0001 | t0104 | g0234 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18957 | hp1 | a0001 | c0002 | t0001 | g0107 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18957 | hp2 | a0001 | c0001 | t0112 | g0228 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18962 | hp1 | a0001 | c0001 | t0135 | g0282 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18962 | hp2 | a0001 | c0001 | t0113 | g0220 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18964 | hp1 | a0001 | c0002 | t0015 | g0085 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18964 | hp2 | a0001 | c0001 | t0005 | g0246 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18965 | hp1 | a0001 | c0001 | t0019 | g0041 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18965 | hp2 | a0001 | c0002 | t0001 | g0131 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18968 | hp1 | a0001 | c0002 | t0001 | g0120 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18968 | hp2 | a0001 | c0001 | t0116 | g0263 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18969 | hp1 | a0001 | c0001 | t0008 | g0253 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18969 | hp2 | a0001 | c0001 | t0014 | g0038 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18971 | hp1 | a0001 | c0001 | t0115 | g0226 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18971 | hp2 | a0001 | c0001 | t0008 | g0251 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18978 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18981 | hp2 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18982 | hp1 | a0001 | c0002 | t0010 | g0139 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18982 | hp2 | a0001 | c0001 | t0100 | g0174 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18983 | hp1 | a0001 | c0001 | t0033 | g0222 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18983 | hp2 | a0001 | c0001 | t0122 | g0259 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18984 | hp1 | a0001 | c0001 | t0014 | g0042 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18984 | hp2 | a0001 | c0004 | t0107 | g0239 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18985 | hp1 | a0001 | c0001 | t0108 | g0264 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18985 | hp2 | a0001 | c0001 | t0020 | g0065 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18986 | hp1 | a0001 | c0002 | t0065 | g0129 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18986 | hp2 | a0001 | c0001 | t0034 | g0262 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18988 | hp1 | a0001 | c0001 | t0118 | g0237 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18988 | hp2 | a0001 | c0002 | t0012 | g0160 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18997 | hp1 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18997 | hp2 | a0001 | c0001 | t0125 | g0230 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA19002 | hp1 | a0001 | c0001 | t0044 | g0238 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA19002 | hp2 | a0001 | c0002 | t0015 | g0086 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA19007 | hp1 | a0001 | c0001 | t0089 | g0202 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA19007 | hp2 | a0001 | c0002 | t0001 | g0149 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA19011 | hp1 | a0001 | c0001 | t0019 | g0078 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA19011 | hp2 | a0001 | c0002 | t0001 | g0156 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA19054 | hp1 | a0001 | c0002 | t0076 | g0115 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA19056 | hp1 | a0001 | c0002 | t0010 | g0092 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA19056 | hp2 | a0001 | c0001 | t0008 | g0218 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA19058 | hp2 | a0001 | c0001 | t0129 | g0217 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA19064 | hp1 | a0001 | c0001 | t0090 | g0200 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA19079 | hp1 | a0001 | c0002 | t0004 | g0133 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA19079 | hp2 | a0001 | c0001 | t0005 | g0242 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA19080 | hp1 | a0001 | c0002 | t0001 | g0138 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA19080 | hp2 | a0001 | c0001 | t0109 | g0249 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA19082 | hp1 | a0001 | c0002 | t0077 | g0004 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA19082 | hp2 | a0001 | c0001 | t0006 | g0198 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA19084 | hp2 | a0001 | c0002 | t0011 | g0123 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA19086 | hp1 | a0001 | c0002 | t0052 | g0144 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA19086 | hp2 | a0001 | c0001 | t0120 | g0265 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA19088 | hp1 | a0001 | c0001 | t0036 | g0254 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA19088 | hp2 | a0001 | c0001 | t0124 | g0245 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA19089 | hp1 | a0001 | c0002 | t0010 | g0140 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA19089 | hp2 | a0001 | c0001 | t0020 | g0049 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA19090 | hp1 | a0001 | c0002 | t0069 | g0145 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA19090 | hp2 | a0001 | c0001 | t0017 | g0248 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA19240 | hp1 | a0001 | c0001 | t0123 | g0258 | AFR | YRI | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA19240 | hp2 | a0001 | c0001 | t0041 | g0008 | AFR | YRI | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA20129 | hp1 | a0001 | c0001 | t0140 | g0054 | AFR | ASW | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA20129 | hp2 | a0001 | c0001 | t0007 | g0006 | AFR | ASW | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA20752 | hp1 | a0001 | c0002 | t0001 | g0147 | EUR | TSI | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA20752 | hp2 | a0001 | c0002 | t0001 | g0109 | EUR | TSI | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA20805 | hp1 | a0001 | c0001 | t0092 | g0172 | EUR | TSI | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA20805 | hp2 | a0001 | c0002 | t0004 | g0004 | EUR | TSI | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA20905 | hp1 | a0001 | c0001 | t0003 | g0204 | SAS | GIH | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA20905 | hp2 | a0001 | c0002 | t0001 | g0031 | SAS | GIH | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01123 | hp1 | a0001 | c0002 | t0025 | g0105 | AMR | CLM | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01123 | hp2 | a0001 | c0001 | t0142 | g0036 | AMR | CLM | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02486 | hp1 | a0001 | c0001 | t0144 | g0276 | AFR | ACB | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02486 | hp2 | a0001 | c0001 | t0145 | g0030 | AFR | ACB | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02559 | hp1 | a0001 | c0001 | t0042 | g0044 | AFR | ACB | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02559 | hp2 | a0001 | c0001 | t0037 | g0267 | AFR | ACB | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03471 | hp1 | a0001 | c0001 | t0029 | g0014 | AFR | MSL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03471 | hp2 | a0001 | c0002 | t0023 | g0164 | AFR | MSL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG06807 | hp1 | a0001 | c0001 | t0154 | g0056 | AFR | USA | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG06807 | hp2 | a0001 | c0002 | t0001 | g0108 | AFR | USA | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18955 | hp1 | a0001 | c0001 | t0005 | g0243 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18955 | hp2 | a0001 | c0002 | t0068 | g0154 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA20300 | hp1 | a0001 | c0001 | t0007 | g0002 | AFR | USA | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA20300 | hp2 | a0001 | c0001 | t0155 | g0208 | AFR | USA | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA21309 | hp1 | a0001 | c0001 | t0096 | g0005 | AFR | LWK | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA21309 | hp2 | a0001 | c0001 | t0078 | g0278 | AFR | LWK | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
homoSapiens | chm13v2 | a0001 | c0001 | t0084 | g0195 | REF | REF | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0199 | REF | REF | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:16209087 | C | T | 1 | a0001c0005 | 1 | HG01346.hp1 | synonymous_variant | LOW | c.456C>T | p.Thr152Thr | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/12 | 572/12859 | 456/1272 | 152/423 | chr19 | 16209087 | |||
chr19:16227648 | C | A | 1 | a0001c0003 | 1 | HG01891.hp1 | synonymous_variant | LOW | c.774C>A | p.Pro258Pro | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 7/12 | 890/12859 | 774/1272 | 258/423 | chr19 | 16227648 | |||
chr19:16228904 | C | T | 2 | a0001c0002 a0001c0005 |
99 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(96): Show |
synonymous_variant | LOW | c.1023C>T | p.Ile341Ile | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/12 | 1139/12859 | 1023/1272 | 341/423 | chr19 | 16228904 | |||
chr19:16233609 | C | T | 1 | a0001c0004 | 1 | NA18984.hp2 | synonymous_variant | LOW | c.1164C>T | p.Ser388Ser | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 10/12 | 1280/12859 | 1164/1272 | 388/423 | chr19 | 16233609 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:16197975 | T | TCGCTGCC others(18): Show |
77 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0007 others(74): Show |
152 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(149): Show |
5_prime_UTR_variant | MODIFIER | c.-43_-19dupCCGCCACC others(17): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/12 | 18 | INFO_REALIGN_3_PRIME | chr19 | 16197975 | |||||
chr19:16197975 | T | TCGCTGCC others(43): Show |
1 | a0001c0001t0155 | 1 | NA20300.hp2 | 5_prime_UTR_variant | MODIFIER | c.-19_-18insCCGCCACC others(42): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/12 | 18 | INFO_REALIGN_3_PRIME | chr19 | 16197975 | |||||
chr19:16198008 | G | GCCGCCAC others(18): Show |
1 | a0001c0001t0101 | 1 | HG01346.hp2 | 5_prime_UTR_variant | MODIFIER | c.-19_-18insCCGCCACC others(17): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/12 | 18 | chr19 | 16198008 | ||||||
chr19:16234653 | G | A | 1 | a0001c0001t0102 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*218G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 218 | chr19 | 16234653 | ||||||
chr19:16234702 | C | T | 1 | a0001c0001t0100 | 1 | NA18982.hp2 | 3_prime_UTR_variant | MODIFIER | c.*267C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 267 | chr19 | 16234702 | ||||||
chr19:16234822 | G | A | 1 | a0001c0001t0044 | 1 | NA19002.hp1 | 3_prime_UTR_variant | MODIFIER | c.*387G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 387 | chr19 | 16234822 | ||||||
chr19:16234837 | C | T | 9 | a0001c0001t0042 a0001c0001t0043 a0001c0001t0148 others(6): Show |
11 | HG01167.hp1 HG01169.hp2 HG02257.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*402C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 402 | chr19 | 16234837 | ||||||
chr19:16234934 | C | G | 1 | a0001c0002t0099 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*499C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 499 | chr19 | 16234934 | ||||||
chr19:16234972 | T | C | 1 | a0001c0001t0148 | 1 | HG02523.hp2 | 3_prime_UTR_variant | MODIFIER | c.*537T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 537 | chr19 | 16234972 | ||||||
chr19:16235011 | G | A | 83 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0016 others(80): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
3_prime_UTR_variant | MODIFIER | c.*576G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 576 | chr19 | 16235011 | ||||||
chr19:16235013 | C | T | 1 | a0001c0001t0041 | 2 | HG02717.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*578C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 578 | chr19 | 16235013 | ||||||
chr19:16235020 | C | T | 1 | a0001c0001t0129 | 1 | NA19058.hp2 | 3_prime_UTR_variant | MODIFIER | c.*585C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 585 | chr19 | 16235020 | ||||||
chr19:16235021 | G | T | 9 | a0001c0001t0013 a0001c0001t0029 a0001c0001t0030 others(6): Show |
14 | HG01361.hp1 HG01934.hp1 HG02055.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*586G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 586 | chr19 | 16235021 | ||||||
chr19:16235039 | G | A | 1 | a0001c0001t0095 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*604G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 604 | chr19 | 16235039 | ||||||
chr19:16235058 | G | A | 1 | a0001c0001t0045 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*623G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 623 | chr19 | 16235058 | ||||||
chr19:16235073 | T | A | 1 | a0001c0002t0046 | 1 | NA18951.hp1 | 3_prime_UTR_variant | MODIFIER | c.*638T>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 638 | chr19 | 16235073 | ||||||
chr19:16235079 | G | A | 1 | a0001c0001t0130 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*644G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 644 | chr19 | 16235079 | ||||||
chr19:16235092 | C | G | 1 | a0001c0001t0094 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*657C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 657 | chr19 | 16235092 | ||||||
chr19:16235118 | G | A | 2 | a0001c0001t0102 a0001c0001t0131 |
2 | HG01884.hp1 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*683G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 683 | chr19 | 16235118 | ||||||
chr19:16235365 | A | G | 91 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0016 others(88): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
3_prime_UTR_variant | MODIFIER | c.*930A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 930 | chr19 | 16235365 | ||||||
chr19:16235494 | G | A | 1 | a0001c0001t0132 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1059G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 1059 | chr19 | 16235494 | ||||||
chr19:16235561 | G | T | 1 | a0001c0001t0044 | 1 | NA19002.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1126G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 1126 | chr19 | 16235561 | ||||||
chr19:16235680 | T | A | 1 | a0001c0002t0047 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1245T>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 1245 | chr19 | 16235680 | ||||||
chr19:16235824 | C | T | 1 | a0001c0001t0093 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1389C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 1389 | chr19 | 16235824 | ||||||
chr19:16235940 | C | T | 33 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0014 others(30): Show |
76 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*1505C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 1505 | chr19 | 16235940 | ||||||
chr19:16235965 | C | T | 1 | a0001c0001t0092 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1530C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 1530 | chr19 | 16235965 | ||||||
chr19:16235992 | C | T | 10 | a0001c0001t0042 a0001c0001t0043 a0001c0001t0133 others(7): Show |
12 | HG01167.hp1 HG01169.hp2 HG02257.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1557C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 1557 | chr19 | 16235992 | ||||||
chr19:16235998 | C | T | 3 | a0001c0001t0089 a0001c0001t0090 a0001c0001t0091 |
3 | HG00544.hp2 NA19007.hp1 NA19064.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1563C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 1563 | chr19 | 16235998 | ||||||
chr19:16236036 | G | T | 1 | a0001c0001t0128 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1601G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 1601 | chr19 | 16236036 | ||||||
chr19:16236101 | TATC | T | 32 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0009 others(29): Show |
80 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*1668_*1670delTCA | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 1668 | INFO_REALIGN_3_PRIME | chr19 | 16236101 | |||||
chr19:16236103 | T | G | 1 | a0001c0001t0142 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1668T>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 1668 | chr19 | 16236103 | ||||||
chr19:16236204 | C | T | 1 | a0001c0001t0127 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1769C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 1769 | chr19 | 16236204 | ||||||
chr19:16236421 | T | G | 1 | a0001c0001t0078 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1986T>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 1986 | chr19 | 16236421 | ||||||
chr19:16236426 | G | A | 1 | a0001c0001t0103 | 1 | HG00544.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1991G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 1991 | chr19 | 16236426 | ||||||
chr19:16236428 | G | A | 1 | a0001c0001t0102 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1993G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 1993 | chr19 | 16236428 | ||||||
chr19:16236438 | G | A | 46 | a0001c0001t0031 a0001c0001t0032 a0001c0002t0001 others(43): Show |
103 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*2003G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 2003 | chr19 | 16236438 | ||||||
chr19:16236474 | C | T | 1 | a0001c0001t0038 | 2 | HG02615.hp1 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2039C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 2039 | chr19 | 16236474 | ||||||
chr19:16236546 | T | A | 1 | a0001c0002t0048 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2111T>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 2111 | chr19 | 16236546 | ||||||
chr19:16236607 | T | C | 1 | a0001c0001t0007 | 6 | HG02145.hp1 HG02976.hp2 HG03130.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2172T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 2172 | chr19 | 16236607 | ||||||
chr19:16236772 | A | G | 1 | a0001c0001t0007 | 6 | HG02145.hp1 HG02976.hp2 HG03130.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2337A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 2337 | chr19 | 16236772 | ||||||
chr19:16236789 | C | T | 1 | a0001c0003t0088 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2354C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 2354 | chr19 | 16236789 | ||||||
chr19:16236901 | CG | C | 39 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0009 others(36): Show |
87 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*2467delG | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 2467 | chr19 | 16236901 | ||||||
chr19:16236902 | GAACTTCA others(29): Show |
G | 1 | a0001c0002t0077 | 1 | NA19082.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2469_*2504delACTT others(32): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 2469 | INFO_REALIGN_3_PRIME | chr19 | 16236902 | |||||
chr19:16237197 | G | T | 12 | a0001c0001t0042 a0001c0001t0043 a0001c0001t0133 others(9): Show |
14 | HG01167.hp1 HG01169.hp2 HG02257.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2762G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 2762 | chr19 | 16237197 | ||||||
chr19:16237231 | C | T | 1 | a0001c0001t0145 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2796C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 2796 | chr19 | 16237231 | ||||||
chr19:16237316 | C | T | 1 | a0001c0001t0144 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2881C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 2881 | chr19 | 16237316 | ||||||
chr19:16237376 | G | T | 3 | a0001c0001t0102 a0001c0001t0131 a0001c0001t0143 |
3 | HG01884.hp1 HG02922.hp2 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2941G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 2941 | chr19 | 16237376 | ||||||
chr19:16237388 | A | T | 1 | a0001c0001t0044 | 1 | NA19002.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2953A>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 2953 | chr19 | 16237388 | ||||||
chr19:16237458 | C | T | 1 | a0001c0001t0126 | 1 | HG02080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3023C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 3023 | chr19 | 16237458 | ||||||
chr19:16237602 | G | A | 1 | a0001c0001t0045 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3167G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 3167 | chr19 | 16237602 | ||||||
chr19:16237771 | C | G | 84 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0009 others(81): Show |
187 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(184): Show |
3_prime_UTR_variant | MODIFIER | c.*3336C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 3336 | chr19 | 16237771 | ||||||
chr19:16237796 | ACCAAGAC others(18): Show |
A | 1 | a0001c0001t0044 | 1 | NA19002.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3362_*3386delCCAA others(21): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 3362 | chr19 | 16237796 | ||||||
chr19:16237842 | A | C | 1 | a0001c0001t0139 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3407A>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 3407 | chr19 | 16237842 | ||||||
chr19:16237849 | T | A | 7 | a0001c0001t0031 a0001c0001t0032 a0001c0001t0092 others(4): Show |
9 | HG00735.hp1 HG01109.hp1 HG01884.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3414T>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 3414 | chr19 | 16237849 | ||||||
chr19:16237926 | C | G | 3 | a0001c0001t0102 a0001c0001t0131 a0001c0001t0143 |
3 | HG01884.hp1 HG02922.hp2 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3491C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 3491 | chr19 | 16237926 | ||||||
chr19:16237927 | G | A | 1 | a0001c0001t0130 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3492G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 3492 | chr19 | 16237927 | ||||||
chr19:16238039 | C | T | 45 | a0001c0001t0078 a0001c0002t0001 a0001c0002t0004 others(42): Show |
100 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*3604C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 3604 | chr19 | 16238039 | ||||||
chr19:16238119 | C | T | 1 | a0001c0001t0144 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3684C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 3684 | chr19 | 16238119 | ||||||
chr19:16238135 | A | C | 39 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0009 others(36): Show |
87 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*3700A>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 3700 | chr19 | 16238135 | ||||||
chr19:16238137 | G | A | 1 | a0001c0001t0133 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3702G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 3702 | chr19 | 16238137 | ||||||
chr19:16238255 | C | G | 5 | a0001c0001t0009 a0001c0001t0138 a0001c0001t0146 others(2): Show |
9 | HG01361.hp1 HG02615.hp2 HG02723.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3820C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 3820 | chr19 | 16238255 | ||||||
chr19:16238308 | T | TA | 45 | a0001c0001t0078 a0001c0002t0001 a0001c0002t0004 others(42): Show |
100 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*3874dupA | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 3875 | INFO_REALIGN_3_PRIME | chr19 | 16238308 | |||||
chr19:16238382 | T | C | 39 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0009 others(36): Show |
87 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*3947T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 3947 | chr19 | 16238382 | ||||||
chr19:16238440 | T | C | 45 | a0001c0001t0078 a0001c0002t0001 a0001c0002t0004 others(42): Show |
100 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*4005T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4005 | chr19 | 16238440 | ||||||
chr19:16238475 | A | G | 45 | a0001c0001t0078 a0001c0002t0001 a0001c0002t0004 others(42): Show |
100 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*4040A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4040 | chr19 | 16238475 | ||||||
chr19:16238519 | G | A | 3 | a0001c0002t0049 a0001c0002t0050 a0001c0002t0051 |
3 | HG01433.hp1 HG01993.hp2 HG02300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4084G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4084 | chr19 | 16238519 | ||||||
chr19:16238542 | G | A | 6 | a0001c0001t0013 a0001c0001t0029 a0001c0001t0030 others(3): Show |
11 | HG01934.hp1 HG02055.hp1 HG02280.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4107G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4107 | chr19 | 16238542 | ||||||
chr19:16238722 | C | CT | 18 | a0001c0001t0002 a0001c0001t0014 a0001c0001t0019 others(15): Show |
52 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*4304dupT | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4305 | INFO_REALIGN_3_PRIME | chr19 | 16238722 | |||||
chr19:16238722 | C | CTT | 27 | a0001c0001t0009 a0001c0001t0020 a0001c0001t0039 others(24): Show |
38 | HG00438.hp1 HG00735.hp2 HG01123.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*4303_*4304dupTT | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4305 | INFO_REALIGN_3_PRIME | chr19 | 16238722 | |||||
chr19:16238722 | C | CTTT | 3 | a0001c0001t0007 a0001c0001t0144 a0001c0001t0154 |
8 | HG02145.hp1 HG02486.hp1 HG02976.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4302_*4304dupTTT | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4305 | INFO_REALIGN_3_PRIME | chr19 | 16238722 | |||||
chr19:16238722 | CT | C | 51 | a0001c0001t0008 a0001c0001t0078 a0001c0001t0104 others(48): Show |
110 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*4304delT | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4304 | INFO_REALIGN_3_PRIME | chr19 | 16238722 | |||||
chr19:16238789 | G | A | 2 | a0001c0001t0035 a0001c0001t0121 |
3 | HG01109.hp2 HG01243.hp1 HG01978.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4354G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4354 | chr19 | 16238789 | ||||||
chr19:16238789 | G | GGCTCACT others(5): Show |
1 | a0001c0001t0104 | 1 | NA18954.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4355_*4366dupGCTC others(8): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4367 | INFO_REALIGN_3_PRIME | chr19 | 16238789 | |||||
chr19:16238930 | G | T | 1 | a0001c0002t0077 | 1 | NA19082.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4495G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4495 | chr19 | 16238930 | ||||||
chr19:16239239 | C | CT | 15 | a0001c0001t0008 a0001c0001t0017 a0001c0001t0028 others(12): Show |
25 | HG00558.hp1 HG01243.hp1 HG01891.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*4844dupT | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4845 | INFO_REALIGN_3_PRIME | chr19 | 16239239 | |||||
chr19:16239239 | C | CTTTTTTT others(1): Show |
5 | a0001c0001t0029 a0001c0001t0037 a0001c0001t0086 others(2): Show |
7 | HG01934.hp1 HG02451.hp2 HG02559.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4837_*4844dupTTTT others(4): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4845 | INFO_REALIGN_3_PRIME | chr19 | 16239239 | |||||
chr19:16239239 | C | CTTTTTTT others(4): Show |
1 | a0001c0001t0030 | 2 | HG02055.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4834_*4844dupTTTT others(7): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4845 | INFO_REALIGN_3_PRIME | chr19 | 16239239 | |||||
chr19:16239239 | CT | C | 5 | a0001c0001t0031 a0001c0001t0080 a0001c0001t0081 others(2): Show |
6 | HG00099.hp2 HG01109.hp1 HG01256.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4844delT | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4844 | INFO_REALIGN_3_PRIME | chr19 | 16239239 | |||||
chr19:16239239 | CTTTTT | C | 10 | a0001c0002t0004 a0001c0002t0012 a0001c0002t0023 others(7): Show |
23 | HG01192.hp1 HG01243.hp2 HG01255.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*4840_*4844delTTTT others(1): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4840 | INFO_REALIGN_3_PRIME | chr19 | 16239239 | |||||
chr19:16239239 | CTTTTTT | C | 13 | a0001c0001t0098 a0001c0002t0001 a0001c0002t0011 others(10): Show |
49 | HG00099.hp1 HG00597.hp2 HG00609.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*4839_*4844delTTTT others(2): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4839 | INFO_REALIGN_3_PRIME | chr19 | 16239239 | |||||
chr19:16239239 | CTTTTTTT | C | 9 | a0001c0002t0010 a0001c0002t0021 a0001c0002t0049 others(6): Show |
13 | HG00140.hp2 HG01071.hp1 HG01167.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*4838_*4844delTTTT others(3): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4838 | INFO_REALIGN_3_PRIME | chr19 | 16239239 | |||||
chr19:16239239 | CTTTTTTT others(4): Show |
C | 5 | a0001c0001t0026 a0001c0001t0094 a0001c0001t0102 others(2): Show |
6 | HG01884.hp1 HG02647.hp1 HG02896.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4834_*4844delTTTT others(7): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4834 | INFO_REALIGN_3_PRIME | chr19 | 16239239 | |||||
chr19:16239239 | CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0096 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4832_*4844delTTTT others(9): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4832 | INFO_REALIGN_3_PRIME | chr19 | 16239239 | |||||
chr19:16239239 | CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0137 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4831_*4844delTTTT others(10): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4831 | INFO_REALIGN_3_PRIME | chr19 | 16239239 | |||||
chr19:16239239 | CTTTTTTT others(8): Show |
C | 13 | a0001c0001t0009 a0001c0001t0019 a0001c0001t0045 others(10): Show |
19 | HG00423.hp1 HG00438.hp1 HG01361.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*4830_*4844delTTTT others(11): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4830 | INFO_REALIGN_3_PRIME | chr19 | 16239239 | |||||
chr19:16239239 | CTTTTTTT others(9): Show |
C | 20 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0020 others(17): Show |
59 | HG00558.hp2 HG00597.hp1 HG00735.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*4829_*4844delTTTT others(12): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4829 | INFO_REALIGN_3_PRIME | chr19 | 16239239 | |||||
chr19:16239239 | CTTTTTTT others(10): Show |
C | 3 | a0001c0001t0014 a0001c0001t0144 a0001c0001t0149 |
6 | HG01069.hp2 HG01167.hp1 HG02486.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4828_*4844delTTTT others(13): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4828 | INFO_REALIGN_3_PRIME | chr19 | 16239239 | |||||
chr19:16239239 | CTTTTTTT others(11): Show |
C | 2 | a0001c0002t0046 a0001c0002t0057 |
2 | HG04115.hp1 NA18951.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4827_*4844delTTTT others(14): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4827 | INFO_REALIGN_3_PRIME | chr19 | 16239239 | |||||
chr19:16239239 | CTTTTTTT others(12): Show |
C | 8 | a0001c0001t0016 a0001c0001t0038 a0001c0001t0079 others(5): Show |
11 | HG00140.hp1 HG01081.hp1 HG02615.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4826_*4844delTTTT others(15): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4826 | INFO_REALIGN_3_PRIME | chr19 | 16239239 | |||||
chr19:16239239 | CTTTTTTT others(13): Show |
C | 1 | a0001c0002t0054 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4825_*4844delTTTT others(16): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4825 | INFO_REALIGN_3_PRIME | chr19 | 16239239 | |||||
chr19:16239239 | CTTTTTTT others(19): Show |
C | 1 | a0001c0002t0053 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4819_*4844delTTTT others(22): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4819 | INFO_REALIGN_3_PRIME | chr19 | 16239239 | |||||
chr19:16239245 | T | C | 1 | a0001c0002t0073 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4810T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4810 | chr19 | 16239245 | ||||||
chr19:16239246 | T | C | 1 | a0001c0002t0052 | 1 | NA19086.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4811T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4811 | chr19 | 16239246 | ||||||
chr19:16239273 | T | G | 5 | a0001c0001t0009 a0001c0001t0138 a0001c0001t0146 others(2): Show |
9 | HG01361.hp1 HG02615.hp2 HG02723.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4838T>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4838 | chr19 | 16239273 | ||||||
chr19:16239341 | G | A | 2 | a0001c0001t0131 a0001c0001t0143 |
2 | HG01884.hp1 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4906G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4906 | chr19 | 16239341 | ||||||
chr19:16239419 | C | A | 39 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0009 others(36): Show |
87 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*4984C>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4984 | chr19 | 16239419 | ||||||
chr19:16239429 | C | G | 6 | a0001c0001t0009 a0001c0001t0137 a0001c0001t0138 others(3): Show |
10 | HG01361.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4994C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4994 | chr19 | 16239429 | ||||||
chr19:16239562 | C | G | 1 | a0001c0001t0038 | 2 | HG02615.hp1 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5127C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5127 | chr19 | 16239562 | ||||||
chr19:16239666 | T | C | 1 | a0001c0001t0142 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5231T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5231 | chr19 | 16239666 | ||||||
chr19:16239671 | G | A | 6 | a0001c0001t0009 a0001c0001t0137 a0001c0001t0138 others(3): Show |
10 | HG01361.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*5236G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5236 | chr19 | 16239671 | ||||||
chr19:16239809 | T | C | 84 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0009 others(81): Show |
187 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(184): Show |
3_prime_UTR_variant | MODIFIER | c.*5374T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5374 | chr19 | 16239809 | ||||||
chr19:16239819 | T | G | 1 | a0001c0001t0121 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5384T>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5384 | chr19 | 16239819 | ||||||
chr19:16239825 | A | G | 45 | a0001c0001t0078 a0001c0002t0001 a0001c0002t0004 others(42): Show |
100 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*5390A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5390 | chr19 | 16239825 | ||||||
chr19:16239861 | G | A | 1 | a0001c0002t0049 | 1 | HG02300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5426G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5426 | chr19 | 16239861 | ||||||
chr19:16239978 | A | G | 126 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0007 others(123): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
3_prime_UTR_variant | MODIFIER | c.*5543A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5543 | chr19 | 16239978 | ||||||
chr19:16239997 | A | AG | 2 | a0001c0001t0026 a0001c0001t0094 |
3 | HG02647.hp1 HG02896.hp1 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5562_*5563insG | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5563 | chr19 | 16239997 | ||||||
chr19:16240041 | G | T | 39 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0009 others(36): Show |
87 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*5606G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5606 | chr19 | 16240041 | ||||||
chr19:16240059 | A | C | 3 | a0001c0001t0078 a0001c0002t0062 a0001c0002t0075 |
3 | HG02451.hp1 HG03139.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5624A>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5624 | chr19 | 16240059 | ||||||
chr19:16240109 | A | G | 1 | a0001c0001t0007 | 6 | HG02145.hp1 HG02976.hp2 HG03130.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5674A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5674 | chr19 | 16240109 | ||||||
chr19:16240199 | G | A | 1 | a0001c0001t0145 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5764G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5764 | chr19 | 16240199 | ||||||
chr19:16240240 | CTCTGTGT others(13): Show |
C | 2 | a0001c0002t0067 a0001c0002t0074 |
2 | NA18945.hp2 NA18949.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5807_*5826delCTGT others(16): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5807 | INFO_REALIGN_3_PRIME | chr19 | 16240240 | |||||
chr19:16240242 | C | CTG | 12 | a0001c0001t0003 a0001c0001t0013 a0001c0001t0016 others(9): Show |
15 | HG01891.hp1 HG01934.hp1 HG02055.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*5837_*5838dupGT | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5839 | INFO_REALIGN_3_PRIME | chr19 | 16240242 | |||||
chr19:16240242 | C | CTGTG | 3 | a0001c0001t0013 a0001c0001t0027 a0001c0001t0128 |
4 | HG02723.hp2 HG02818.hp1 HG02922.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5835_*5838dupGTGT | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5839 | INFO_REALIGN_3_PRIME | chr19 | 16240242 | |||||
chr19:16240248 | GTGTGTGT others(19): Show |
G | 3 | a0001c0001t0078 a0001c0002t0062 a0001c0002t0075 |
3 | HG02451.hp1 HG03139.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5839_*5864delATGT others(22): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5839 | INFO_REALIGN_3_PRIME | chr19 | 16240248 | |||||
chr19:16240250 | GTGTGTGT others(17): Show |
G | 3 | a0001c0002t0001 a0001c0002t0024 a0001c0002t0059 |
3 | HG01071.hp1 HG02965.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5839_*5862delATGT others(20): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5839 | INFO_REALIGN_3_PRIME | chr19 | 16240250 | |||||
chr19:16240252 | GTGTGTGT others(15): Show |
G | 2 | a0001c0002t0024 a0001c0002t0071 |
2 | HG02717.hp1 HG02818.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5839_*5860delATGT others(18): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5839 | INFO_REALIGN_3_PRIME | chr19 | 16240252 | |||||
chr19:16240254 | GTGTGTGT others(13): Show |
G | 30 | a0001c0001t0100 a0001c0002t0001 a0001c0002t0004 others(27): Show |
64 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*5839_*5858delATGT others(16): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5839 | INFO_REALIGN_3_PRIME | chr19 | 16240254 | |||||
chr19:16240256 | GTGTGTGT others(11): Show |
G | 10 | a0001c0001t0006 a0001c0002t0001 a0001c0002t0011 others(7): Show |
17 | HG00673.hp1 HG01074.hp1 HG01358.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*5839_*5856delATGT others(14): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5839 | INFO_REALIGN_3_PRIME | chr19 | 16240256 | |||||
chr19:16240258 | G | C | 36 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0009 others(33): Show |
84 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*5823G>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5823 | chr19 | 16240258 | ||||||
chr19:16240258 | GTGTGTGT others(9): Show |
G | 4 | a0001c0002t0001 a0001c0002t0004 a0001c0002t0025 others(1): Show |
11 | HG00738.hp2 HG01074.hp2 HG01123.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*5839_*5854delATGT others(12): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5839 | INFO_REALIGN_3_PRIME | chr19 | 16240258 | |||||
chr19:16240260 | GTGTGTGT others(7): Show |
G | 1 | a0001c0002t0077 | 1 | NA19082.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5839_*5852delATGT others(10): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5839 | INFO_REALIGN_3_PRIME | chr19 | 16240260 | |||||
chr19:16240266 | GTGTGTGT others(1): Show |
G | 2 | a0001c0001t0038 a0001c0001t0102 |
3 | HG02615.hp1 HG02895.hp2 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5839_*5846delATGT others(4): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5839 | INFO_REALIGN_3_PRIME | chr19 | 16240266 | |||||
chr19:16240267 | TGTGTGTA others(34): Show |
T | 36 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0009 others(33): Show |
84 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*5839_*5879delATGT others(37): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5839 | INFO_REALIGN_3_PRIME | chr19 | 16240267 | |||||
chr19:16240268 | GTGTGTA | G | 3 | a0001c0001t0016 a0001c0001t0111 a0001c0001t0143 |
3 | HG02895.hp1 HG02897.hp2 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5839_*5844delATGT others(2): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5839 | INFO_REALIGN_3_PRIME | chr19 | 16240268 | |||||
chr19:16240270 | GTGTA | G | 3 | a0001c0001t0105 a0001c0001t0106 a0001c0001t0131 |
3 | HG01884.hp1 HG01891.hp2 HG02145.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5839_*5842delATGT | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5839 | INFO_REALIGN_3_PRIME | chr19 | 16240270 | |||||
chr19:16240272 | G | A | 1 | a0001c0001t0026 | 2 | HG02647.hp1 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5837G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5837 | chr19 | 16240272 | ||||||
chr19:16240272 | GTA | G | 21 | a0001c0001t0005 a0001c0001t0017 a0001c0001t0018 others(18): Show |
33 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*5839_*5840delAT | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5839 | INFO_REALIGN_3_PRIME | chr19 | 16240272 | |||||
chr19:16240274 | A | G | 26 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0013 others(23): Show |
36 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*5839A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5839 | chr19 | 16240274 | ||||||
chr19:16240276 | G | A | 3 | a0001c0001t0031 a0001c0001t0032 a0001c0001t0038 |
6 | HG00735.hp1 HG01109.hp1 HG01884.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5841G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5841 | chr19 | 16240276 | ||||||
chr19:16240278 | G | A | 3 | a0001c0001t0045 a0001c0001t0103 a0001c0001t0113 |
3 | HG00544.hp1 HG02257.hp2 NA18962.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5843G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5843 | chr19 | 16240278 | ||||||
chr19:16240280 | G | A | 23 | a0001c0001t0005 a0001c0001t0017 a0001c0001t0018 others(20): Show |
40 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*5845G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5845 | chr19 | 16240280 | ||||||
chr19:16240280 | G | GTA | 7 | a0001c0001t0008 a0001c0001t0034 a0001c0001t0109 others(4): Show |
12 | HG02080.hp2 HG02132.hp1 NA18939.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*5846_*5847insAT | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5847 | INFO_REALIGN_3_PRIME | chr19 | 16240280 | |||||
chr19:16240598 | C | T | 1 | a0001c0002t0061 | 1 | HG00140.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6163C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 6163 | chr19 | 16240598 | ||||||
chr19:16240699 | T | C | 1 | a0001c0001t0144 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6264T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 6264 | chr19 | 16240699 | ||||||
chr19:16240707 | C | G | 1 | a0001c0001t0104 | 1 | NA18954.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6272C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 6272 | chr19 | 16240707 | ||||||
chr19:16240916 | T | C | 39 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0009 others(36): Show |
87 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*6481T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 6481 | chr19 | 16240916 | ||||||
chr19:16241010 | A | T | 39 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0009 others(36): Show |
87 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*6575A>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 6575 | chr19 | 16241010 | ||||||
chr19:16241023 | T | C | 1 | a0001c0001t0045 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6588T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 6588 | chr19 | 16241023 | ||||||
chr19:16241033 | A | G | 1 | a0001c0002t0077 | 1 | NA19082.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6598A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 6598 | chr19 | 16241033 | ||||||
chr19:16241054 | C | G | 1 | a0001c0003t0088 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6619C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 6619 | chr19 | 16241054 | ||||||
chr19:16241059 | G | A | 2 | a0001c0001t0131 a0001c0001t0143 |
2 | HG01884.hp1 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6624G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 6624 | chr19 | 16241059 | ||||||
chr19:16241067 | T | G | 1 | a0001c0001t0045 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6632T>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 6632 | chr19 | 16241067 | ||||||
chr19:16241186 | C | T | 1 | a0001c0001t0007 | 6 | HG02145.hp1 HG02976.hp2 HG03130.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*6751C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 6751 | chr19 | 16241186 | ||||||
chr19:16241253 | C | T | 1 | a0001c0001t0115 | 1 | NA18971.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6818C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 6818 | chr19 | 16241253 | ||||||
chr19:16241269 | C | T | 11 | a0001c0001t0042 a0001c0001t0043 a0001c0001t0133 others(8): Show |
13 | HG01167.hp1 HG01169.hp2 HG02257.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*6834C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 6834 | chr19 | 16241269 | ||||||
chr19:16241309 | C | CAA | 43 | a0001c0001t0078 a0001c0002t0001 a0001c0002t0004 others(40): Show |
98 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*6886_*6887dupAA | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 6888 | INFO_REALIGN_3_PRIME | chr19 | 16241309 | |||||
chr19:16241309 | CA | C | 7 | a0001c0001t0031 a0001c0001t0032 a0001c0001t0090 others(4): Show |
9 | HG00735.hp1 HG01109.hp1 HG01884.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*6887delA | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 6887 | INFO_REALIGN_3_PRIME | chr19 | 16241309 | |||||
chr19:16241592 | C | T | 84 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0009 others(81): Show |
187 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(184): Show |
3_prime_UTR_variant | MODIFIER | c.*7157C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 7157 | chr19 | 16241592 | ||||||
chr19:16241621 | C | A | 1 | a0001c0001t0144 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7186C>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 7186 | chr19 | 16241621 | ||||||
chr19:16241655 | CT | C | 50 | a0001c0001t0078 a0001c0001t0102 a0001c0001t0130 others(47): Show |
105 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*7224delT | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 7224 | INFO_REALIGN_3_PRIME | chr19 | 16241655 | |||||
chr19:16241673 | G | A | 45 | a0001c0001t0078 a0001c0002t0001 a0001c0002t0004 others(42): Show |
100 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*7238G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 7238 | chr19 | 16241673 | ||||||
chr19:16241716 | T | C | 84 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0009 others(81): Show |
187 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(184): Show |
3_prime_UTR_variant | MODIFIER | c.*7281T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 7281 | chr19 | 16241716 | ||||||
chr19:16241792 | C | A | 45 | a0001c0001t0078 a0001c0002t0001 a0001c0002t0004 others(42): Show |
100 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*7357C>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 7357 | chr19 | 16241792 | ||||||
chr19:16241949 | C | T | 45 | a0001c0001t0078 a0001c0002t0001 a0001c0002t0004 others(42): Show |
100 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*7514C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 7514 | chr19 | 16241949 | ||||||
chr19:16242309 | CA | C | 73 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0007 others(70): Show |
146 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(143): Show |
3_prime_UTR_variant | MODIFIER | c.*7886delA | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 7886 | INFO_REALIGN_3_PRIME | chr19 | 16242309 | |||||
chr19:16242309 | CAA | C | 45 | a0001c0001t0078 a0001c0001t0104 a0001c0002t0001 others(42): Show |
100 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*7885_*7886delAA | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 7885 | INFO_REALIGN_3_PRIME | chr19 | 16242309 | |||||
chr19:16242608 | T | C | 2 | a0001c0001t0080 a0001c0001t0082 |
2 | HG03491.hp1 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8173T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 8173 | chr19 | 16242608 | ||||||
chr19:16242688 | G | T | 3 | a0001c0001t0102 a0001c0001t0131 a0001c0001t0143 |
3 | HG01884.hp1 HG02922.hp2 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8253G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 8253 | chr19 | 16242688 | ||||||
chr19:16242827 | T | C | 45 | a0001c0001t0078 a0001c0002t0001 a0001c0002t0004 others(42): Show |
100 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*8392T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 8392 | chr19 | 16242827 | ||||||
chr19:16242846 | C | T | 1 | a0001c0001t0145 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8411C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 8411 | chr19 | 16242846 | ||||||
chr19:16242979 | C | T | 2 | a0001c0001t0080 a0001c0001t0082 |
2 | HG03491.hp1 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8544C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 8544 | chr19 | 16242979 | ||||||
chr19:16243246 | TTTTTTG | T | 118 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0007 others(115): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
3_prime_UTR_variant | MODIFIER | c.*8846_*8851delTGTT others(2): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 8846 | INFO_REALIGN_3_PRIME | chr19 | 16243246 | |||||
chr19:16243246 | TTTTTTGT others(5): Show |
T | 5 | a0001c0001t0039 a0001c0001t0040 a0001c0001t0041 others(2): Show |
8 | HG01884.hp1 HG02258.hp1 HG02630.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*8840_*8851delTGTT others(8): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 8840 | INFO_REALIGN_3_PRIME | chr19 | 16243246 | |||||
chr19:16243432 | C | CTT | 33 | a0001c0002t0001 a0001c0002t0004 a0001c0002t0010 others(30): Show |
83 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*8998_*8999insTT | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 8999 | INFO_REALIGN_3_PRIME | chr19 | 16243432 | |||||
chr19:16243432 | C | CTTT | 10 | a0001c0001t0078 a0001c0002t0012 a0001c0002t0021 others(7): Show |
14 | HG01169.hp1 HG01243.hp2 HG01255.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*8998_*8999insTTT | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 8999 | INFO_REALIGN_3_PRIME | chr19 | 16243432 | |||||
chr19:16243434 | A | AT | 12 | a0001c0001t0008 a0001c0001t0034 a0001c0001t0085 others(9): Show |
17 | HG02055.hp2 HG02080.hp2 HG02132.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*9015dupT | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 9016 | INFO_REALIGN_3_PRIME | chr19 | 16243434 | |||||
chr19:16243434 | A | T | 45 | a0001c0001t0078 a0001c0002t0001 a0001c0002t0004 others(42): Show |
100 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*8999A>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 8999 | chr19 | 16243434 | ||||||
chr19:16243434 | ATT | A | 33 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0009 others(30): Show |
81 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*9014_*9015delTT | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 9014 | INFO_REALIGN_3_PRIME | chr19 | 16243434 | |||||
chr19:16243445 | T | G | 33 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0009 others(30): Show |
81 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*9010T>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 9010 | chr19 | 16243445 | ||||||
chr19:16243447 | T | G | 33 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0009 others(30): Show |
81 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*9012T>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 9012 | chr19 | 16243447 | ||||||
chr19:16243449 | T | G | 33 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0009 others(30): Show |
81 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*9014T>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 9014 | chr19 | 16243449 | ||||||
chr19:16243453 | A | G | 33 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0009 others(30): Show |
81 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*9018A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 9018 | chr19 | 16243453 | ||||||
chr19:16243775 | C | T | 1 | a0001c0001t0138 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9340C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 9340 | chr19 | 16243775 | ||||||
chr19:16243898 | G | A | 1 | a0001c0001t0035 | 2 | HG01243.hp1 HG01978.hp2 |
3_prime_UTR_variant | MODIFIER | c.*9463G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 9463 | chr19 | 16243898 | ||||||
chr19:16243945 | A | G | 1 | a0001c0002t0015 | 3 | NA18944.hp1 NA18964.hp1 NA19002.hp2 |
3_prime_UTR_variant | MODIFIER | c.*9510A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 9510 | chr19 | 16243945 | ||||||
chr19:16244324 | A | G | 47 | a0001c0001t0078 a0001c0001t0130 a0001c0001t0145 others(44): Show |
102 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*9889A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 9889 | chr19 | 16244324 | ||||||
chr19:16244342 | C | G | 1 | a0001c0001t0134 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9907C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 9907 | chr19 | 16244342 | ||||||
chr19:16244627 | G | A | 33 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0009 others(30): Show |
81 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*10192G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10192 | chr19 | 16244627 | ||||||
chr19:16244647 | G | A | 45 | a0001c0001t0078 a0001c0002t0001 a0001c0002t0004 others(42): Show |
100 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*10212G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10212 | chr19 | 16244647 | ||||||
chr19:16244687 | G | A | 2 | a0001c0001t0031 a0001c0001t0032 |
4 | HG00735.hp1 HG01109.hp1 HG01884.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*10252G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10252 | chr19 | 16244687 | ||||||
chr19:16244703 | G | A | 48 | a0001c0001t0078 a0001c0001t0102 a0001c0001t0131 others(45): Show |
103 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*10268G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10268 | chr19 | 16244703 | ||||||
chr19:16244755 | G | A | 48 | a0001c0001t0078 a0001c0001t0102 a0001c0001t0131 others(45): Show |
103 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*10320G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10320 | chr19 | 16244755 | ||||||
chr19:16244792 | TGCAGTCC | T | 3 | a0001c0001t0102 a0001c0001t0131 a0001c0001t0143 |
3 | HG01884.hp1 HG02922.hp2 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*10366_*10372delCA others(5): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10366 | INFO_REALIGN_3_PRIME | chr19 | 16244792 | |||||
chr19:16244803 | G | C | 3 | a0001c0001t0102 a0001c0001t0131 a0001c0001t0143 |
3 | HG01884.hp1 HG02922.hp2 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*10368G>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10368 | chr19 | 16244803 | ||||||
chr19:16244807 | G | A | 3 | a0001c0001t0102 a0001c0001t0131 a0001c0001t0143 |
3 | HG01884.hp1 HG02922.hp2 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*10372G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10372 | chr19 | 16244807 | ||||||
chr19:16244837 | A | AAAAT | 34 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0017 others(31): Show |
55 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*10425_*10428dupAT others(2): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10429 | INFO_REALIGN_3_PRIME | chr19 | 16244837 | |||||
chr19:16244837 | A | AAAATAAA others(1): Show |
4 | a0001c0001t0036 a0001c0001t0102 a0001c0001t0122 others(1): Show |
5 | HG03098.hp2 NA18943.hp2 NA18983.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*10421_*10428dupAT others(6): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10429 | INFO_REALIGN_3_PRIME | chr19 | 16244837 | |||||
chr19:16244841 | T | A | 75 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0009 others(72): Show |
178 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(175): Show |
3_prime_UTR_variant | MODIFIER | c.*10406T>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10406 | chr19 | 16244841 | ||||||
chr19:16244845 | T | A | 1 | a0001c0001t0140 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10410T>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10410 | chr19 | 16244845 | ||||||
chr19:16244881 | G | GTTT | 4 | a0001c0001t0016 a0001c0001t0111 a0001c0001t0128 others(1): Show |
6 | HG02486.hp1 HG02723.hp2 HG02895.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*10447_*10449dupTT others(1): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10450 | INFO_REALIGN_3_PRIME | chr19 | 16244881 | |||||
chr19:16244881 | G | T | 25 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0017 others(22): Show |
42 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*10446G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10446 | chr19 | 16244881 | ||||||
chr19:16244882 | T | TTTG | 4 | a0001c0001t0006 a0001c0001t0089 a0001c0001t0090 others(1): Show |
9 | HG00544.hp2 HG01257.hp2 HG01258.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*10478_*10480dupTT others(1): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10481 | INFO_REALIGN_3_PRIME | chr19 | 16244882 | |||||
chr19:16244882 | T | TTTGTTG | 22 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0017 others(19): Show |
38 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*10475_*10480dupTT others(4): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10481 | INFO_REALIGN_3_PRIME | chr19 | 16244882 | |||||
chr19:16244882 | T | TTTGTTGT others(2): Show |
4 | a0001c0001t0033 a0001c0001t0108 a0001c0001t0115 others(1): Show |
5 | HG01358.hp1 NA18955.hp2 NA18971.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*10472_*10480dupTT others(7): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10481 | INFO_REALIGN_3_PRIME | chr19 | 16244882 | |||||
chr19:16244882 | T | TTTGTTGT others(5): Show |
1 | a0001c0001t0140 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10469_*10480dupTT others(10): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10481 | INFO_REALIGN_3_PRIME | chr19 | 16244882 | |||||
chr19:16244882 | T | TTTTTTG | 24 | a0001c0001t0002 a0001c0001t0014 a0001c0001t0018 others(21): Show |
63 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*10449_*10450insTT others(4): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10450 | INFO_REALIGN_3_PRIME | chr19 | 16244882 | |||||
chr19:16244882 | T | TTTTTTGT others(2): Show |
16 | a0001c0001t0007 a0001c0001t0009 a0001c0001t0040 others(13): Show |
28 | HG01346.hp2 HG01433.hp2 HG02145.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*10449_*10450insTT others(7): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10450 | INFO_REALIGN_3_PRIME | chr19 | 16244882 | |||||
chr19:16244882 | T | TTTTTTGT others(5): Show |
34 | a0001c0001t0038 a0001c0001t0042 a0001c0001t0130 others(31): Show |
84 | HG00099.hp1 HG00597.hp2 HG00738.hp2 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*10449_*10450insTT others(10): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10450 | INFO_REALIGN_3_PRIME | chr19 | 16244882 | |||||
chr19:16244882 | T | TTTTTTGT others(8): Show |
13 | a0001c0001t0152 a0001c0001t0154 a0001c0002t0011 others(10): Show |
18 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*10449_*10450insTT others(13): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10450 | INFO_REALIGN_3_PRIME | chr19 | 16244882 | |||||
chr19:16244882 | T | TTTTTTGT others(11): Show |
1 | a0001c0001t0043 | 2 | HG02572.hp1 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*10449_*10450insTT others(16): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10450 | INFO_REALIGN_3_PRIME | chr19 | 16244882 | |||||
chr19:16244882 | T | TTTTTTTG | 5 | a0001c0001t0027 a0001c0001t0035 a0001c0001t0036 others(2): Show |
8 | HG01109.hp2 HG01243.hp1 HG01978.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*10449_*10450insTT others(5): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10450 | INFO_REALIGN_3_PRIME | chr19 | 16244882 | |||||
chr19:16244882 | T | TTTTTTTG others(3): Show |
1 | a0001c0001t0123 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10449_*10450insTT others(8): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10450 | INFO_REALIGN_3_PRIME | chr19 | 16244882 | |||||
chr19:16244885 | G | T | 12 | a0001c0001t0013 a0001c0001t0026 a0001c0001t0029 others(9): Show |
20 | HG00735.hp1 HG01109.hp1 HG01884.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*10450G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10450 | chr19 | 16244885 | ||||||
chr19:16244888 | G | T | 1 | a0001c0001t0097 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10453G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10453 | chr19 | 16244888 | ||||||
chr19:16245011 | C | T | 1 | a0001c0005t0072 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10576C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10576 | chr19 | 16245011 | ||||||
chr19:16245143 | G | A | 45 | a0001c0001t0078 a0001c0002t0001 a0001c0002t0004 others(42): Show |
100 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*10708G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10708 | chr19 | 16245143 | ||||||
chr19:16245148 | G | A | 45 | a0001c0001t0078 a0001c0002t0001 a0001c0002t0004 others(42): Show |
100 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*10713G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10713 | chr19 | 16245148 | ||||||
chr19:16245170 | A | G | 2 | a0001c0001t0130 a0001c0001t0145 |
2 | HG02055.hp2 HG02486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*10735A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10735 | chr19 | 16245170 | ||||||
chr19:16245245 | C | T | 1 | a0001c0001t0140 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10810C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10810 | chr19 | 16245245 | ||||||
chr19:16245275 | C | T | 83 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0009 others(80): Show |
186 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(183): Show |
3_prime_UTR_variant | MODIFIER | c.*10840C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10840 | chr19 | 16245275 | ||||||
chr19:16245364 | C | T | 2 | a0001c0001t0116 a0001c0001t0119 |
2 | NA18944.hp2 NA18968.hp2 |
3_prime_UTR_variant | MODIFIER | c.*10929C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10929 | chr19 | 16245364 | ||||||
chr19:16245414 | C | T | 83 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0009 others(80): Show |
186 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(183): Show |
3_prime_UTR_variant | MODIFIER | c.*10979C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10979 | chr19 | 16245414 | ||||||
chr19:16245682 | C | G | 1 | a0001c0001t0141 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11247C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 11247 | chr19 | 16245682 | ||||||
chr19:16245710 | T | C | 1 | a0001c0001t0083 | 1 | HG01099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11275T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 11275 | chr19 | 16245710 | ||||||
chr19:16245720 | G | A | 33 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0009 others(30): Show |
81 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*11285G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 11285 | chr19 | 16245720 | ||||||
chr19:16245739 | G | A | 83 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0009 others(80): Show |
186 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(183): Show |
3_prime_UTR_variant | MODIFIER | c.*11304G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 11304 | chr19 | 16245739 | ||||||
chr19:16245795 | G | A | 83 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0009 others(80): Show |
186 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(183): Show |
3_prime_UTR_variant | MODIFIER | c.*11360G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 11360 | chr19 | 16245795 | ||||||
chr19:16245874 | G | T | 3 | a0001c0001t0130 a0001c0001t0141 a0001c0001t0145 |
3 | HG02055.hp2 HG02486.hp2 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*11439G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 11439 | chr19 | 16245874 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:16198079 | C | T | 1 | a0001c0001t0141g0283 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.42+11C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16198079 | |||||||
chr19:16198211 | C | T | 1 | a0001c0001t0135g0282 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.42+143C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16198211 | |||||||
chr19:16198237 | C | CG | 10 | a0001c0001t0016g0018 a0001c0001t0016g0019 a0001c0001t0016g0021 others(7): Show |
10 | HG00735.hp1 HG01109.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.42+174dupG | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr19 | 16198237 | ||||||
chr19:16198260 | C | T | 5 | a0001c0001t0026g0279 a0001c0001t0026g0280 a0001c0001t0078g0278 others(2): Show |
5 | HG02647.hp1 HG02896.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.42+192C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16198260 | |||||||
chr19:16198330 | T | C | 1 | a0001c0001t0027g0028 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+262T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16198330 | |||||||
chr19:16198339 | G | C | 1 | a0001c0001t0027g0029 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.42+271G>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16198339 | |||||||
chr19:16198350 | G | A | 1 | a0001c0001t0145g0030 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.42+282G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16198350 | |||||||
chr19:16198438 | G | A | 2 | a0001c0001t0007g0002 a0001c0001t0007g0006 |
6 | HG02145.hp1 HG02976.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.42+370G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16198438 | |||||||
chr19:16198546 | C | G | 1 | a0001c0001t0144g0276 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.42+478C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16198546 | |||||||
chr19:16198668 | A | G | 1 | a0001c0002t0001g0275 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.42+600A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16198668 | |||||||
chr19:16198699 | C | T | 1 | a0001c0002t0025g0274 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.42+631C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16198699 | |||||||
chr19:16198738 | G | A | 1 | a0001c0002t0001g0031 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.42+670G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16198738 | |||||||
chr19:16198805 | C | CT | 72 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(69): Show |
72 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.42+746dupT | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr19 | 16198805 | ||||||
chr19:16198871 | A | T | 9 | a0001c0001t0009g0017 a0001c0001t0009g0206 a0001c0001t0009g0207 others(6): Show |
10 | HG01361.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.42+803A>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16198871 | |||||||
chr19:16198901 | G | C | 1 | a0001c0001t0003g0032 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.42+833G>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16198901 | |||||||
chr19:16199039 | C | T | 1 | a0001c0001t0034g0273 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.42+971C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16199039 | |||||||
chr19:16199087 | T | C | 245 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0010 others(242): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.42+1019T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16199087 | |||||||
chr19:16199112 | A | G | 71 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(68): Show |
71 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.42+1044A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16199112 | |||||||
chr19:16199427 | G | A | 1 | a0001c0002t0001g0033 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.42+1359G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16199427 | |||||||
chr19:16199516 | G | A | 1 | a0001c0002t0001g0275 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.42+1448G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16199516 | |||||||
chr19:16199558 | G | C | 1 | a0001c0002t0001g0034 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.42+1490G>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16199558 | |||||||
chr19:16199814 | C | T | 170 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(167): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.42+1746C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16199814 | |||||||
chr19:16200055 | T | C | 1 | a0001c0001t0040g0035 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.42+1987T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16200055 | |||||||
chr19:16200259 | G | A | 69 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(66): Show |
69 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.42+2191G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16200259 | |||||||
chr19:16200341 | G | C | 1 | a0001c0001t0144g0276 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.42+2273G>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16200341 | |||||||
chr19:16200600 | C | T | 1 | a0001c0002t0070g0171 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.42+2532C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16200600 | |||||||
chr19:16200648 | G | A | 1 | a0001c0001t0142g0036 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.42+2580G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16200648 | |||||||
chr19:16200661 | G | A | 5 | a0001c0001t0016g0018 a0001c0001t0016g0019 a0001c0001t0016g0021 others(2): Show |
5 | HG02723.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.42+2593G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16200661 | |||||||
chr19:16201137 | G | A | 3 | a0001c0002t0015g0085 a0001c0002t0015g0086 a0001c0002t0015g0087 |
3 | NA18944.hp1 NA18964.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.43-2322G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16201137 | |||||||
chr19:16201290 | G | T | 1 | a0001c0002t0062g0170 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.43-2169G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16201290 | |||||||
chr19:16201388 | C | CT | 7 | a0001c0001t0003g0204 a0001c0001t0003g0205 a0001c0001t0085g0203 others(4): Show |
7 | HG00597.hp2 HG02451.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.43-2043dupT | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr19 | 16201388 | ||||||
chr19:16201388 | CT | C | 119 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0010 others(116): Show |
131 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.43-2043delT | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr19 | 16201388 | ||||||
chr19:16201388 | CTT | C | 17 | a0001c0001t0002g0040 a0001c0001t0002g0043 a0001c0001t0005g0216 others(14): Show |
17 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.43-2044_43-2043del others(2): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr19 | 16201388 | ||||||
chr19:16201388 | CTTTTTTT others(9): Show |
C | 2 | a0001c0001t0131g0007 a0001c0001t0143g0007 |
2 | HG01884.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.43-2058_43-2043del others(16): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr19 | 16201388 | ||||||
chr19:16201439 | G | C | 173 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(170): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.43-2020G>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16201439 | |||||||
chr19:16201456 | TGGCACAA others(4): Show |
T | 173 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(170): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.43-1999_43-1989del others(11): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr19 | 16201456 | ||||||
chr19:16201641 | G | A | 2 | a0001c0001t0042g0044 a0001c0001t0152g0077 |
2 | HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.43-1818G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16201641 | |||||||
chr19:16201846 | C | T | 1 | a0001c0001t0137g0212 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.43-1613C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16201846 | |||||||
chr19:16201868 | G | A | 1 | a0001c0001t0002g0045 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.43-1591G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16201868 | |||||||
chr19:16201908 | T | C | 173 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(170): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.43-1551T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16201908 | |||||||
chr19:16201940 | G | A | 2 | a0001c0001t0007g0002 a0001c0001t0007g0006 |
6 | HG02145.hp1 HG02976.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.43-1519G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16201940 | |||||||
chr19:16201986 | G | A | 2 | a0001c0001t0038g0223 a0001c0001t0038g0224 |
2 | HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.43-1473G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16201986 | |||||||
chr19:16202041 | G | A | 2 | a0001c0002t0024g0088 a0001c0002t0059g0099 |
2 | HG01071.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.43-1418G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16202041 | |||||||
chr19:16202064 | G | A | 3 | a0001c0001t0102g0214 a0001c0001t0131g0007 a0001c0001t0143g0007 |
3 | HG01884.hp1 HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.43-1395G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16202064 | |||||||
chr19:16202121 | C | T | 1 | a0001c0001t0002g0043 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.43-1338C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16202121 | |||||||
chr19:16202141 | G | A | 1 | a0001c0001t0002g0046 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.43-1318G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16202141 | |||||||
chr19:16202172 | G | A | 1 | a0001c0001t0002g0047 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.43-1287G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16202172 | |||||||
chr19:16202249 | A | G | 173 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(170): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.43-1210A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16202249 | |||||||
chr19:16202311 | C | T | 1 | a0001c0001t0002g0075 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.43-1148C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16202311 | |||||||
chr19:16202395 | T | A | 1 | a0001c0002t0001g0100 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.43-1064T>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16202395 | |||||||
chr19:16202417 | C | T | 1 | a0001c0002t0021g0098 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.43-1042C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16202417 | |||||||
chr19:16202796 | G | T | 2 | a0001c0001t0038g0223 a0001c0001t0038g0224 |
2 | HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.43-663G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16202796 | |||||||
chr19:16203113 | C | T | 99 | a0001c0002t0001g0012 a0001c0002t0001g0031 a0001c0002t0001g0033 others(96): Show |
99 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.43-346C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16203113 | |||||||
chr19:16203313 | G | A | 1 | a0001c0001t0079g0177 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.43-146G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16203313 | |||||||
chr19:16203728 | C | T | 3 | a0001c0001t0002g0073 a0001c0001t0002g0074 a0001c0001t0014g0042 |
3 | HG02523.hp1 NA18981.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.199+113C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | chr19 | 16203728 | |||||||
chr19:16203891 | C | G | 5 | a0001c0001t0102g0214 a0001c0001t0130g0076 a0001c0001t0131g0007 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.199+276C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | chr19 | 16203891 | |||||||
chr19:16203966 | A | G | 168 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.199+351A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | chr19 | 16203966 | |||||||
chr19:16203997 | C | T | 1 | a0001c0002t0050g0166 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.199+382C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | chr19 | 16203997 | |||||||
chr19:16203998 | G | A | 2 | a0001c0001t0042g0044 a0001c0001t0152g0077 |
2 | HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.199+383G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | chr19 | 16203998 | |||||||
chr19:16204133 | C | A | 42 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(39): Show |
42 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(39): Show |
intron_variant | MODIFIER | c.199+518C>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | chr19 | 16204133 | |||||||
chr19:16204140 | G | T | 3 | a0001c0002t0023g0164 a0001c0002t0023g0169 a0001c0002t0053g0165 |
3 | HG03471.hp2 HG03540.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.199+525G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | chr19 | 16204140 | |||||||
chr19:16204184 | G | A | 1 | a0001c0001t0139g0048 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.199+569G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | chr19 | 16204184 | |||||||
chr19:16204334 | C | G | 1 | a0001c0001t0144g0276 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.199+719C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | chr19 | 16204334 | |||||||
chr19:16204353 | C | T | 4 | a0001c0001t0031g0024 a0001c0001t0031g0025 a0001c0001t0032g0026 others(1): Show |
4 | HG00735.hp1 HG01109.hp1 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.199+738C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | chr19 | 16204353 | |||||||
chr19:16204412 | C | T | 168 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.199+797C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | chr19 | 16204412 | |||||||
chr19:16204428 | C | T | 1 | a0001c0002t0001g0163 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.199+813C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | chr19 | 16204428 | |||||||
chr19:16204578 | C | T | 5 | a0001c0001t0102g0214 a0001c0001t0130g0076 a0001c0001t0131g0007 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.199+963C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | chr19 | 16204578 | |||||||
chr19:16204712 | G | A | 99 | a0001c0002t0001g0012 a0001c0002t0001g0031 a0001c0002t0001g0033 others(96): Show |
99 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.199+1097G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | chr19 | 16204712 | |||||||
chr19:16204714 | C | A | 6 | a0001c0002t0001g0089 a0001c0002t0001g0101 a0001c0002t0004g0102 others(3): Show |
6 | HG00738.hp2 HG01123.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.199+1099C>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | chr19 | 16204714 | |||||||
chr19:16204833 | C | CT | 36 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0010 others(33): Show |
42 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.199+1233dupT | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 16204833 | ||||||
chr19:16204833 | CT | C | 154 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(151): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.199+1233delT | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 16204833 | ||||||
chr19:16204894 | C | G | 168 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.199+1279C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | chr19 | 16204894 | |||||||
chr19:16204916 | C | T | 69 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(66): Show |
69 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.199+1301C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | chr19 | 16204916 | |||||||
chr19:16204944 | C | T | 14 | a0001c0001t0042g0044 a0001c0001t0042g0081 a0001c0001t0043g0009 others(11): Show |
14 | HG01167.hp1 HG01169.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.199+1329C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | chr19 | 16204944 | |||||||
chr19:16204950 | C | A | 9 | a0001c0001t0009g0017 a0001c0001t0009g0206 a0001c0001t0009g0207 others(6): Show |
10 | HG01361.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.199+1335C>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | chr19 | 16204950 | |||||||
chr19:16204955 | C | CGA | 99 | a0001c0002t0001g0012 a0001c0002t0001g0031 a0001c0002t0001g0033 others(96): Show |
99 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.199+1342_199+1343d others(4): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 16204955 | ||||||
chr19:16205122 | C | T | 5 | a0001c0001t0102g0214 a0001c0001t0130g0076 a0001c0001t0131g0007 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.200-1219C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | chr19 | 16205122 | |||||||
chr19:16205129 | G | A | 1 | a0001c0001t0036g0254 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.200-1212G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | chr19 | 16205129 | |||||||
chr19:16205205 | G | A | 2 | a0001c0001t0009g0206 a0001c0001t0009g0207 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.200-1136G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | chr19 | 16205205 | |||||||
chr19:16205341 | A | G | 1 | a0001c0002t0062g0170 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.200-1000A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | chr19 | 16205341 | |||||||
chr19:16205357 | G | A | 1 | a0001c0002t0071g0106 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.200-984G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | chr19 | 16205357 | |||||||
chr19:16205436 | A | G | 1 | a0001c0001t0045g0023 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.200-905A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | chr19 | 16205436 | |||||||
chr19:16205563 | C | A | 1 | a0001c0002t0059g0099 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.200-778C>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | chr19 | 16205563 | |||||||
chr19:16205587 | C | T | 1 | a0001c0001t0008g0253 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.200-754C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | chr19 | 16205587 | |||||||
chr19:16205669 | A | G | 2 | a0001c0001t0002g0074 a0001c0001t0014g0042 |
2 | NA18981.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.200-672A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | chr19 | 16205669 | |||||||
chr19:16205969 | G | A | 12 | a0001c0001t0013g0005 a0001c0001t0013g0014 a0001c0001t0013g0180 others(9): Show |
12 | HG01934.hp1 HG02055.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.200-372G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | chr19 | 16205969 | |||||||
chr19:16206063 | G | A | 37 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0010 others(34): Show |
43 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.200-278G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | chr19 | 16206063 | |||||||
chr19:16206608 | T | TG | 98 | a0001c0002t0001g0012 a0001c0002t0001g0031 a0001c0002t0001g0033 others(95): Show |
98 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.267+204dupG | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 16206608 | ||||||
chr19:16206668 | T | C | 9 | a0001c0001t0009g0017 a0001c0001t0009g0206 a0001c0001t0009g0207 others(6): Show |
10 | HG01361.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.267+260T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 3/11 | chr19 | 16206668 | |||||||
chr19:16206965 | G | A | 99 | a0001c0002t0001g0012 a0001c0002t0001g0031 a0001c0002t0001g0033 others(96): Show |
99 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.267+557G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 3/11 | chr19 | 16206965 | |||||||
chr19:16206984 | G | A | 1 | a0001c0002t0001g0108 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.267+576G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 3/11 | chr19 | 16206984 | |||||||
chr19:16207063 | G | A | 99 | a0001c0002t0001g0012 a0001c0002t0001g0031 a0001c0002t0001g0033 others(96): Show |
99 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.267+655G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 3/11 | chr19 | 16207063 | |||||||
chr19:16207143 | G | T | 2 | a0001c0001t0042g0081 a0001c0001t0153g0080 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.267+735G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 3/11 | chr19 | 16207143 | |||||||
chr19:16207345 | T | C | 1 | a0001c0001t0016g0019 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.268-674T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 3/11 | chr19 | 16207345 | |||||||
chr19:16207435 | G | A | 1 | a0001c0001t0142g0036 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.268-584G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 3/11 | chr19 | 16207435 | |||||||
chr19:16207470 | G | A | 9 | a0001c0002t0001g0089 a0001c0002t0001g0090 a0001c0002t0001g0101 others(6): Show |
9 | HG00738.hp2 HG01123.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.268-549G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 3/11 | chr19 | 16207470 | |||||||
chr19:16207522 | G | A | 168 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.268-497G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 3/11 | chr19 | 16207522 | |||||||
chr19:16207523 | A | G | 69 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(66): Show |
69 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.268-496A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 3/11 | chr19 | 16207523 | |||||||
chr19:16207533 | C | T | 1 | a0001c0001t0039g0053 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.268-486C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 3/11 | chr19 | 16207533 | |||||||
chr19:16207584 | G | A | 3 | a0001c0001t0102g0214 a0001c0001t0131g0007 a0001c0001t0143g0007 |
3 | HG01884.hp1 HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.268-435G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 3/11 | chr19 | 16207584 | |||||||
chr19:16207610 | C | A | 1 | a0001c0001t0027g0029 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.268-409C>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 3/11 | chr19 | 16207610 | |||||||
chr19:16207689 | C | G | 1 | a0001c0002t0066g0159 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.268-330C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 3/11 | chr19 | 16207689 | |||||||
chr19:16207775 | C | T | 1 | a0001c0001t0032g0027 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.268-244C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 3/11 | chr19 | 16207775 | |||||||
chr19:16207796 | G | A | 2 | a0001c0001t0006g0185 a0001c0001t0006g0186 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.268-223G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 3/11 | chr19 | 16207796 | |||||||
chr19:16207846 | C | G | 1 | a0001c0001t0006g0016 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.268-173C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 3/11 | chr19 | 16207846 | |||||||
chr19:16207885 | C | T | 1 | a0001c0001t0002g0072 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.268-134C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 3/11 | chr19 | 16207885 | |||||||
chr19:16207886 | A | G | 169 | a0001c0001t0002g0072 a0001c0001t0005g0216 a0001c0001t0005g0219 others(166): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.268-133A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 3/11 | chr19 | 16207886 | |||||||
chr19:16207938 | G | A | 1 | a0001c0001t0002g0060 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.268-81G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 3/11 | chr19 | 16207938 | |||||||
chr19:16207970 | C | T | 70 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(67): Show |
70 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.268-49C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 3/11 | chr19 | 16207970 | |||||||
chr19:16208001 | C | A | 12 | a0001c0001t0013g0005 a0001c0001t0013g0014 a0001c0001t0013g0180 others(9): Show |
12 | HG01934.hp1 HG02055.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.268-18C>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 3/11 | chr19 | 16208001 | |||||||
chr19:16208334 | G | A | 5 | a0001c0001t0102g0214 a0001c0001t0130g0076 a0001c0001t0131g0007 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.398+185G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 4/11 | chr19 | 16208334 | |||||||
chr19:16208516 | C | T | 1 | a0001c0001t0002g0071 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.398+367C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 4/11 | chr19 | 16208516 | |||||||
chr19:16208691 | G | A | 7 | a0001c0001t0035g0255 a0001c0001t0035g0256 a0001c0001t0036g0254 others(4): Show |
7 | HG01109.hp2 HG01243.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.399-339G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 4/11 | chr19 | 16208691 | |||||||
chr19:16208732 | C | T | 3 | a0001c0001t0036g0254 a0001c0001t0036g0266 a0001c0001t0122g0259 |
3 | NA18943.hp2 NA18983.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.399-298C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 4/11 | chr19 | 16208732 | |||||||
chr19:16208814 | A | ATTGGCTT others(18): Show |
1 | a0001c0002t0004g0091 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.399-213_399-189dup others(25): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 16208814 | ||||||
chr19:16208943 | C | G | 2 | a0001c0001t0007g0002 a0001c0001t0007g0006 |
6 | HG02145.hp1 HG02976.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.399-87C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 4/11 | chr19 | 16208943 | |||||||
chr19:16209198 | T | C | 3 | a0001c0001t0036g0254 a0001c0001t0036g0266 a0001c0001t0122g0259 |
3 | NA18943.hp2 NA18983.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.546+21T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16209198 | |||||||
chr19:16209264 | C | G | 99 | a0001c0002t0001g0012 a0001c0002t0001g0031 a0001c0002t0001g0033 others(96): Show |
99 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.546+87C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16209264 | |||||||
chr19:16209340 | T | C | 2 | a0001c0001t0035g0255 a0001c0001t0035g0256 |
2 | HG01243.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.546+163T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16209340 | |||||||
chr19:16209370 | G | A | 1 | a0001c0001t0140g0054 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.546+193G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16209370 | |||||||
chr19:16209487 | C | T | 1 | a0001c0002t0060g0158 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.546+310C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16209487 | |||||||
chr19:16209578 | G | C | 1 | a0001c0003t0088g0187 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.546+401G>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16209578 | |||||||
chr19:16209619 | GA | G | 98 | a0001c0002t0001g0012 a0001c0002t0001g0031 a0001c0002t0001g0033 others(95): Show |
98 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.546+454delA | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16209619 | ||||||
chr19:16209683 | C | T | 4 | a0001c0001t0008g0250 a0001c0001t0008g0251 a0001c0001t0008g0252 others(1): Show |
4 | NA18947.hp1 NA18951.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.546+506C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16209683 | |||||||
chr19:16209706 | C | G | 1 | a0001c0002t0010g0157 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.546+529C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16209706 | |||||||
chr19:16209726 | G | C | 3 | a0001c0001t0102g0214 a0001c0001t0131g0007 a0001c0001t0143g0007 |
3 | HG01884.hp1 HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.546+549G>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16209726 | |||||||
chr19:16209744 | A | AGATCATA others(39): Show |
1 | a0001c0002t0015g0085 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.546+568_546+613dup others(46): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16209744 | ||||||
chr19:16209895 | G | A | 1 | a0001c0001t0140g0054 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.546+718G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16209895 | |||||||
chr19:16209942 | C | T | 168 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.546+765C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16209942 | |||||||
chr19:16209962 | G | A | 2 | a0001c0001t0038g0223 a0001c0001t0038g0224 |
2 | HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.546+785G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16209962 | |||||||
chr19:16209979 | T | C | 168 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.546+802T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16209979 | |||||||
chr19:16210163 | T | G | 1 | a0001c0002t0001g0111 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.546+986T>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16210163 | |||||||
chr19:16210173 | T | A | 1 | a0001c0001t0145g0030 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.546+996T>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16210173 | |||||||
chr19:16210236 | T | C | 168 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.546+1059T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16210236 | |||||||
chr19:16210262 | A | G | 69 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(66): Show |
69 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.546+1085A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16210262 | |||||||
chr19:16210268 | G | T | 1 | a0001c0002t0001g0156 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.546+1091G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16210268 | |||||||
chr19:16210269 | T | G | 1 | a0001c0002t0001g0156 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.546+1092T>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16210269 | |||||||
chr19:16210382 | G | A | 2 | a0001c0001t0002g0010 a0001c0001t0014g0010 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.546+1205G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16210382 | |||||||
chr19:16210543 | C | T | 2 | a0001c0001t0038g0223 a0001c0001t0038g0224 |
2 | HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.546+1366C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16210543 | |||||||
chr19:16211100 | T | TG | 152 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(149): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.546+1924dupG | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16211100 | ||||||
chr19:16211101 | G | GGT | 15 | a0001c0001t0017g0248 a0001c0001t0032g0027 a0001c0001t0123g0258 others(12): Show |
15 | HG00735.hp1 HG01099.hp1 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.546+1924_546+1925i others(4): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16211101 | |||||||
chr19:16211101 | G | GT | 9 | a0001c0001t0002g0046 a0001c0001t0040g0052 a0001c0001t0102g0214 others(6): Show |
9 | HG01433.hp2 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.546+1936dupT | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16211101 | ||||||
chr19:16211159 | G | GAT | 289 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0010 others(286): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.546+1982_546+1983i others(4): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16211159 | |||||||
chr19:16211309 | G | A | 1 | a0001c0001t0123g0258 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.546+2132G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16211309 | |||||||
chr19:16211373 | C | T | 4 | a0001c0001t0003g0175 a0001c0001t0083g0176 a0001c0001t0087g0013 others(1): Show |
4 | HG01099.hp2 HG03239.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.546+2196C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16211373 | |||||||
chr19:16211556 | A | T | 168 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.546+2379A>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16211556 | |||||||
chr19:16211611 | G | A | 12 | a0001c0001t0005g0216 a0001c0001t0005g0225 a0001c0001t0005g0227 others(9): Show |
12 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(9): Show |
intron_variant | MODIFIER | c.546+2434G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16211611 | |||||||
chr19:16211614 | G | T | 1 | a0001c0001t0142g0036 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.546+2437G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16211614 | |||||||
chr19:16211622 | C | T | 1 | a0001c0002t0053g0165 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.546+2445C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16211622 | |||||||
chr19:16211881 | A | C | 2 | a0001c0001t0018g0270 a0001c0001t0037g0271 |
2 | HG02647.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.546+2704A>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16211881 | |||||||
chr19:16212136 | C | T | 9 | a0001c0001t0009g0017 a0001c0001t0009g0206 a0001c0001t0009g0207 others(6): Show |
10 | HG01361.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.546+2959C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16212136 | |||||||
chr19:16212248 | T | G | 1 | a0001c0002t0067g0112 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.546+3071T>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16212248 | |||||||
chr19:16212412 | G | A | 1 | a0001c0002t0011g0113 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.546+3235G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16212412 | |||||||
chr19:16212484 | T | C | 1 | a0001c0001t0008g0218 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.546+3307T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16212484 | |||||||
chr19:16212485 | C | T | 1 | a0001c0001t0008g0218 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.546+3308C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16212485 | |||||||
chr19:16212486 | T | G | 1 | a0001c0001t0008g0218 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.546+3309T>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16212486 | |||||||
chr19:16212515 | C | T | 2 | a0001c0001t0003g0204 a0001c0001t0003g0205 |
2 | HG03927.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.546+3338C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16212515 | |||||||
chr19:16212646 | A | G | 3 | a0001c0001t0005g0246 a0001c0001t0005g0247 a0001c0001t0124g0245 |
3 | HG02015.hp1 NA18964.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.546+3469A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16212646 | |||||||
chr19:16212653 | G | A | 1 | a0001c0001t0144g0276 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.546+3476G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16212653 | |||||||
chr19:16212731 | T | G | 3 | a0001c0001t0102g0214 a0001c0001t0131g0007 a0001c0001t0143g0007 |
3 | HG01884.hp1 HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.546+3554T>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16212731 | |||||||
chr19:16212762 | C | T | 243 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0010 others(240): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.546+3585C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16212762 | |||||||
chr19:16212767 | C | T | 4 | a0001c0001t0031g0024 a0001c0001t0031g0025 a0001c0001t0032g0026 others(1): Show |
4 | HG00735.hp1 HG01109.hp1 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.546+3590C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16212767 | |||||||
chr19:16212782 | C | G | 2 | a0001c0001t0130g0076 a0001c0001t0145g0030 |
2 | HG02055.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.546+3605C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16212782 | |||||||
chr19:16212855 | CA | C | 3 | a0001c0001t0008g0218 a0001c0001t0120g0265 a0001c0002t0015g0085 |
3 | NA18964.hp1 NA19056.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.546+3682delA | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16212855 | ||||||
chr19:16212910 | T | C | 168 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.546+3733T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16212910 | |||||||
chr19:16213126 | T | A | 3 | a0001c0002t0023g0164 a0001c0002t0023g0169 a0001c0002t0053g0165 |
3 | HG03471.hp2 HG03540.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.546+3949T>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16213126 | |||||||
chr19:16213265 | G | C | 1 | a0001c0001t0105g0272 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.546+4088G>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16213265 | |||||||
chr19:16213271 | T | C | 168 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.546+4094T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16213271 | |||||||
chr19:16213352 | CT | C | 3 | a0001c0002t0012g0160 a0001c0002t0015g0085 a0001c0002t0015g0086 |
3 | NA18964.hp1 NA18988.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.546+4182delT | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16213352 | ||||||
chr19:16213401 | T | C | 168 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.546+4224T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16213401 | |||||||
chr19:16213428 | A | G | 1 | a0001c0001t0144g0276 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.546+4251A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16213428 | |||||||
chr19:16213506 | T | C | 13 | a0001c0001t0042g0044 a0001c0001t0042g0081 a0001c0001t0043g0009 others(10): Show |
13 | HG01167.hp1 HG01169.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.546+4329T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16213506 | |||||||
chr19:16213603 | T | C | 5 | a0001c0001t0016g0018 a0001c0001t0016g0019 a0001c0001t0016g0021 others(2): Show |
5 | HG02723.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.546+4426T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16213603 | |||||||
chr19:16213718 | C | T | 9 | a0001c0001t0009g0017 a0001c0001t0009g0206 a0001c0001t0009g0207 others(6): Show |
10 | HG01361.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.546+4541C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16213718 | |||||||
chr19:16213955 | A | T | 1 | a0001c0001t0028g0197 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.546+4778A>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16213955 | |||||||
chr19:16213959 | T | C | 2 | a0001c0001t0008g0218 a0001c0001t0034g0273 |
2 | HG02132.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.546+4782T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16213959 | |||||||
chr19:16214044 | T | C | 1 | a0001c0001t0031g0024 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.546+4867T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16214044 | |||||||
chr19:16214046 | C | T | 1 | a0001c0001t0031g0024 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.546+4869C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16214046 | |||||||
chr19:16214052 | C | CTTT | 127 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(124): Show |
127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.546+4887_546+4889d others(5): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16214052 | ||||||
chr19:16214052 | C | CTTTT | 37 | a0001c0001t0005g0231 a0001c0001t0005g0242 a0001c0001t0005g0243 others(34): Show |
37 | HG00423.hp2 HG00673.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.546+4886_546+4889d others(6): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16214052 | ||||||
chr19:16214052 | C | T | 1 | a0001c0001t0031g0024 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.546+4875C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16214052 | |||||||
chr19:16214081 | C | T | 2 | a0001c0001t0002g0046 a0001c0001t0040g0052 |
2 | HG02809.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.546+4904C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16214081 | |||||||
chr19:16214178 | A | G | 5 | a0001c0001t0026g0279 a0001c0001t0026g0280 a0001c0001t0078g0278 others(2): Show |
5 | HG02647.hp1 HG02896.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.546+5001A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16214178 | |||||||
chr19:16214213 | T | A | 1 | a0001c0001t0039g0051 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.546+5036T>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16214213 | |||||||
chr19:16214293 | G | A | 4 | a0001c0002t0004g0116 a0001c0002t0004g0153 a0001c0002t0025g0274 others(1): Show |
4 | HG03239.hp1 HG03834.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.546+5116G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16214293 | |||||||
chr19:16214316 | C | G | 1 | a0001c0001t0141g0283 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.546+5139C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16214316 | |||||||
chr19:16214353 | G | A | 1 | a0001c0001t0140g0054 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.546+5176G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16214353 | |||||||
chr19:16214356 | C | CT | 8 | a0001c0001t0002g0070 a0001c0001t0003g0196 a0001c0001t0085g0203 others(5): Show |
8 | HG01928.hp1 HG02486.hp2 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.546+5192dupT | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16214356 | ||||||
chr19:16214356 | C | CTT | 146 | a0001c0001t0005g0219 a0001c0001t0005g0225 a0001c0001t0005g0227 others(143): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.546+5191_546+5192d others(4): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16214356 | ||||||
chr19:16214356 | C | CTTT | 17 | a0001c0001t0005g0216 a0001c0001t0016g0021 a0001c0001t0018g0269 others(14): Show |
17 | HG00544.hp1 HG01069.hp1 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.546+5190_546+5192d others(5): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16214356 | ||||||
chr19:16214356 | C | T | 1 | a0001c0002t0011g0152 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.546+5179C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16214356 | |||||||
chr19:16214512 | C | T | 167 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(164): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.546+5335C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16214512 | |||||||
chr19:16214691 | C | A | 174 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(171): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.546+5514C>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16214691 | |||||||
chr19:16214729 | C | T | 1 | a0001c0001t0005g0216 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.546+5552C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16214729 | |||||||
chr19:16214744 | C | A | 3 | a0001c0001t0102g0214 a0001c0001t0131g0007 a0001c0001t0143g0007 |
3 | HG01884.hp1 HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.546+5567C>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16214744 | |||||||
chr19:16214759 | T | G | 5 | a0001c0001t0102g0214 a0001c0001t0130g0076 a0001c0001t0131g0007 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.546+5582T>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16214759 | |||||||
chr19:16214810 | A | T | 3 | a0001c0001t0102g0214 a0001c0001t0131g0007 a0001c0001t0143g0007 |
3 | HG01884.hp1 HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.546+5633A>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16214810 | |||||||
chr19:16214910 | G | T | 1 | a0001c0001t0144g0276 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.546+5733G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16214910 | |||||||
chr19:16214950 | T | C | 1 | a0001c0001t0006g0198 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.546+5773T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16214950 | |||||||
chr19:16215053 | A | G | 38 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0010 others(35): Show |
44 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.546+5876A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215053 | |||||||
chr19:16215087 | G | T | 168 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.546+5910G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215087 | |||||||
chr19:16215190 | A | G | 168 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.546+6013A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215190 | |||||||
chr19:16215191 | A | AGGCAGG | 12 | a0001c0001t0109g0249 a0001c0001t0124g0245 a0001c0002t0001g0107 others(9): Show |
12 | HG01074.hp1 HG01074.hp2 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.546+6017_546+6018i others(8): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16215191 | ||||||
chr19:16215194 | C | CAGGGGCG | 8 | a0001c0001t0127g0221 a0001c0002t0001g0097 a0001c0002t0001g0138 others(5): Show |
8 | HG00099.hp2 HG01099.hp1 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.546+6017_546+6018i others(9): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215194 | |||||||
chr19:16215194 | C | CAGGGGCG others(1): Show |
9 | a0001c0001t0005g0246 a0001c0001t0008g0250 a0001c0001t0115g0226 others(6): Show |
9 | HG01169.hp1 HG01433.hp2 HG03688.hp2 others(6): Show |
intron_variant | MODIFIER | c.546+6017_546+6018i others(10): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215194 | |||||||
chr19:16215194 | C | CAGGGGCG others(2): Show |
4 | a0001c0001t0008g0251 a0001c0002t0001g0149 a0001c0002t0001g0156 others(1): Show |
4 | NA18971.hp2 NA19002.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.546+6017_546+6018i others(11): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215194 | |||||||
chr19:16215194 | C | CAGGGGCG others(3): Show |
7 | a0001c0001t0005g0231 a0001c0001t0005g0247 a0001c0001t0008g0252 others(4): Show |
7 | HG00423.hp2 HG01361.hp2 HG02015.hp1 others(4): Show |
intron_variant | MODIFIER | c.546+6017_546+6018i others(12): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215194 | |||||||
chr19:16215194 | C | CAGGGGCG others(4): Show |
4 | a0001c0001t0117g0240 a0001c0001t0120g0265 a0001c0002t0001g0163 others(1): Show |
4 | HG03710.hp1 NA18939.hp2 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.546+6017_546+6018i others(13): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215194 | |||||||
chr19:16215194 | C | CAGGGGCG others(5): Show |
1 | a0001c0002t0054g0095 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.546+6017_546+6018i others(14): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215194 | |||||||
chr19:16215194 | C | CAGGGGCG others(7): Show |
1 | a0001c0002t0004g0091 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.546+6017_546+6018i others(16): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215194 | |||||||
chr19:16215194 | C | CAGGGGCG others(6): Show |
2 | a0001c0001t0033g0222 a0001c0001t0038g0224 |
2 | HG02895.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.546+6017_546+6018i others(15): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215194 | |||||||
chr19:16215194 | C | CAGGGGCG others(7): Show |
6 | a0001c0001t0005g0227 a0001c0001t0017g0232 a0001c0001t0017g0248 others(3): Show |
6 | HG00609.hp1 HG01358.hp1 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.546+6017_546+6018i others(16): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215194 | |||||||
chr19:16215194 | C | CAGGGGCG others(8): Show |
7 | a0001c0001t0005g0216 a0001c0001t0008g0218 a0001c0001t0008g0253 others(4): Show |
7 | HG01069.hp1 HG02080.hp2 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.546+6017_546+6018i others(17): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215194 | |||||||
chr19:16215194 | C | CAGGGGCG others(9): Show |
1 | a0001c0001t0034g0273 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.546+6017_546+6018i others(18): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215194 | |||||||
chr19:16215194 | C | CAGGGGCG others(10): Show |
3 | a0001c0001t0005g0229 a0001c0001t0114g0215 a0001c0001t0125g0230 |
3 | NA18945.hp1 NA18949.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.546+6017_546+6018i others(19): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215194 | |||||||
chr19:16215194 | C | CAGGGGCG others(11): Show |
1 | a0001c0001t0129g0217 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.546+6017_546+6018i others(20): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215194 | |||||||
chr19:16215194 | C | CAGGGGCG others(13): Show |
1 | a0001c0002t0012g0160 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.546+6017_546+6018i others(22): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215194 | |||||||
chr19:16215194 | C | CAGGGGCG others(14): Show |
1 | a0001c0001t0005g0243 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.546+6017_546+6018i others(23): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215194 | |||||||
chr19:16215194 | C | CAGGGGGC others(3): Show |
1 | a0001c0002t0068g0154 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.546+6017_546+6018i others(12): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215194 | |||||||
chr19:16215195 | G | A | 96 | a0001c0001t0002g0075 a0001c0001t0005g0219 a0001c0001t0005g0225 others(93): Show |
96 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.546+6018G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215195 | |||||||
chr19:16215200 | C | CG | 29 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 others(26): Show |
30 | HG00544.hp2 HG01258.hp2 HG01361.hp1 others(27): Show |
intron_variant | MODIFIER | c.546+6034dupG | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16215200 | ||||||
chr19:16215200 | C | CGG | 20 | a0001c0001t0003g0173 a0001c0001t0018g0268 a0001c0001t0026g0279 others(17): Show |
20 | HG00738.hp1 HG01257.hp1 HG01358.hp2 others(17): Show |
intron_variant | MODIFIER | c.546+6033_546+6034d others(4): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16215200 | ||||||
chr19:16215200 | C | CGGG | 17 | a0001c0001t0018g0269 a0001c0001t0019g0069 a0001c0001t0042g0081 others(14): Show |
17 | HG00140.hp1 HG00423.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.546+6032_546+6034d others(5): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16215200 | ||||||
chr19:16215200 | C | G | 74 | a0001c0001t0005g0216 a0001c0001t0005g0227 a0001c0001t0005g0229 others(71): Show |
74 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(71): Show |
intron_variant | MODIFIER | c.546+6023C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215200 | |||||||
chr19:16215200 | CG | C | 31 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0043 others(28): Show |
33 | HG00558.hp2 HG01069.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.546+6034delG | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16215200 | ||||||
chr19:16215206 | G | A | 1 | a0001c0001t0005g0225 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.546+6029G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215206 | |||||||
chr19:16215207 | G | GGGGGGGG others(5): Show |
1 | a0001c0001t0005g0242 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.546+6034_546+6035i others(14): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16215207 | ||||||
chr19:16215207 | GGGGGAGA others(7): Show |
G | 1 | a0001c0001t0005g0225 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.546+6035_546+6048d others(16): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16215207 | ||||||
chr19:16215209 | G | GGGGGGGG others(21): Show |
1 | a0001c0001t0104g0234 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.546+6034_546+6035i others(30): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16215209 | ||||||
chr19:16215210 | G | A | 1 | a0001c0001t0145g0030 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.546+6033G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215210 | |||||||
chr19:16215210 | G | GGGGGGGG others(13): Show |
1 | a0001c0001t0113g0220 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.546+6034_546+6035i others(22): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16215210 | ||||||
chr19:16215210 | G | GGGGGGGG others(14): Show |
1 | a0001c0001t0103g0241 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.546+6034_546+6035i others(23): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16215210 | ||||||
chr19:16215210 | GGAGAGGG others(11): Show |
G | 1 | a0001c0001t0044g0238 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.546+6035_546+6052d others(20): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16215210 | ||||||
chr19:16215211 | GA | G | 3 | a0001c0001t0140g0054 a0001c0002t0001g0089 a0001c0002t0025g0105 |
3 | HG01123.hp1 HG01256.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.546+6035delA | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215211 | |||||||
chr19:16215212 | A | G | 153 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0227 others(150): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.546+6035A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215212 | |||||||
chr19:16215213 | G | A | 1 | a0001c0001t0102g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.546+6036G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215213 | |||||||
chr19:16215214 | A | G | 158 | a0001c0001t0002g0073 a0001c0001t0005g0216 a0001c0001t0005g0219 others(155): Show |
158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.546+6037A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215214 | |||||||
chr19:16215214 | AG | A | 6 | a0001c0001t0009g0207 a0001c0001t0009g0209 a0001c0001t0137g0212 others(3): Show |
6 | HG01361.hp1 HG02723.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.546+6043delG | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16215214 | ||||||
chr19:16215216 | G | GGGGGGGG others(5): Show |
1 | a0001c0001t0032g0026 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.546+6043_546+6044i others(14): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16215216 | ||||||
chr19:16215216 | G | GGGGGGGG others(6): Show |
1 | a0001c0001t0038g0223 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.546+6043_546+6044i others(15): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16215216 | ||||||
chr19:16215216 | G | GGGGGGGG others(9): Show |
1 | a0001c0001t0031g0024 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.546+6043_546+6044i others(18): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16215216 | ||||||
chr19:16215219 | G | GGGGGGGG others(4): Show |
1 | a0001c0002t0011g0146 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.546+6043_546+6044i others(13): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16215219 | ||||||
chr19:16215220 | G | A | 3 | a0001c0001t0002g0073 a0001c0001t0009g0017 a0001c0001t0009g0206 |
4 | HG02523.hp1 HG02615.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.546+6043G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215220 | |||||||
chr19:16215220 | G | GGGGGGGG others(7): Show |
1 | a0001c0001t0045g0023 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.546+6043_546+6044i others(16): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215220 | |||||||
chr19:16215220 | G | GGGGGGGG others(5): Show |
1 | a0001c0002t0070g0171 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.546+6043_546+6044i others(14): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215220 | |||||||
chr19:16215220 | G | GGGGGGGG others(11): Show |
1 | a0001c0001t0032g0027 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.546+6043_546+6044i others(20): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215220 | |||||||
chr19:16215220 | G | GGGGGGGG others(9): Show |
1 | a0001c0002t0001g0100 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.546+6043_546+6044i others(18): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215220 | |||||||
chr19:16215221 | A | G | 30 | a0001c0001t0002g0073 a0001c0001t0005g0243 a0001c0001t0009g0017 others(27): Show |
31 | HG00673.hp1 HG00735.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.546+6044A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215221 | |||||||
chr19:16215221 | A | T | 1 | a0001c0002t0070g0171 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.546+6044A>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215221 | |||||||
chr19:16215222 | G | C | 1 | a0001c0002t0048g0119 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.546+6045G>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215222 | |||||||
chr19:16215223 | G | GGGGGGGG others(14): Show |
1 | a0001c0002t0062g0170 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.546+6050_546+6051i others(23): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16215223 | ||||||
chr19:16215233 | A | G | 1 | a0001c0001t0044g0238 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.546+6056A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215233 | |||||||
chr19:16215237 | G | GA | 3 | a0001c0001t0102g0214 a0001c0001t0131g0007 a0001c0001t0143g0007 |
3 | HG01884.hp1 HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.546+6061dupA | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16215237 | ||||||
chr19:16215284 | A | C | 1 | a0001c0001t0120g0265 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.546+6107A>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215284 | |||||||
chr19:16215333 | T | C | 1 | a0001c0001t0031g0024 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.546+6156T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215333 | |||||||
chr19:16215334 | G | T | 1 | a0001c0001t0031g0024 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.546+6157G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215334 | |||||||
chr19:16215335 | C | G | 1 | a0001c0001t0031g0024 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.546+6158C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215335 | |||||||
chr19:16215391 | G | C | 1 | a0001c0001t0031g0024 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.546+6214G>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215391 | |||||||
chr19:16215392 | C | G | 1 | a0001c0001t0031g0024 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.546+6215C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215392 | |||||||
chr19:16215392 | C | T | 12 | a0001c0001t0042g0044 a0001c0001t0042g0081 a0001c0001t0043g0009 others(9): Show |
12 | HG01167.hp1 HG01169.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.546+6215C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215392 | |||||||
chr19:16215400 | G | A | 99 | a0001c0002t0001g0012 a0001c0002t0001g0031 a0001c0002t0001g0033 others(96): Show |
99 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.546+6223G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215400 | |||||||
chr19:16215463 | C | CA | 25 | a0001c0001t0002g0040 a0001c0001t0005g0219 a0001c0001t0006g0198 others(22): Show |
25 | HG00597.hp2 HG00673.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.546+6315dupA | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16215463 | ||||||
chr19:16215463 | C | CAA | 6 | a0001c0001t0141g0283 a0001c0002t0001g0033 a0001c0002t0001g0156 others(3): Show |
6 | HG03209.hp2 NA18947.hp2 NA18955.hp2 others(3): Show |
intron_variant | MODIFIER | c.546+6314_546+6315d others(4): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16215463 | ||||||
chr19:16215463 | CA | C | 124 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0010 others(121): Show |
134 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.546+6315delA | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16215463 | ||||||
chr19:16215463 | CAA | C | 35 | a0001c0001t0002g0068 a0001c0001t0005g0216 a0001c0001t0008g0218 others(32): Show |
36 | HG01069.hp1 HG01109.hp1 HG01256.hp2 others(33): Show |
intron_variant | MODIFIER | c.546+6314_546+6315d others(4): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16215463 | ||||||
chr19:16215463 | CAAAAAAA others(1): Show |
C | 10 | a0001c0001t0005g0231 a0001c0001t0009g0017 a0001c0001t0009g0206 others(7): Show |
11 | HG00423.hp2 HG01361.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.546+6308_546+6315d others(10): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16215463 | ||||||
chr19:16215463 | CAAAAAAA others(7): Show |
C | 2 | a0001c0001t0038g0223 a0001c0001t0038g0224 |
2 | HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.546+6302_546+6315d others(16): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16215463 | ||||||
chr19:16215467 | A | T | 1 | a0001c0002t0071g0106 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.546+6290A>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215467 | |||||||
chr19:16215496 | T | TGTTTAAT others(3): Show |
1 | a0001c0001t0032g0027 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.546+6321_546+6330d others(12): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16215496 | ||||||
chr19:16215622 | T | C | 5 | a0001c0001t0102g0214 a0001c0001t0130g0076 a0001c0001t0131g0007 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.546+6445T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215622 | |||||||
chr19:16215855 | G | A | 7 | a0001c0001t0035g0255 a0001c0001t0035g0256 a0001c0001t0036g0254 others(4): Show |
7 | HG01109.hp2 HG01243.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.546+6678G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215855 | |||||||
chr19:16215869 | G | A | 1 | a0001c0001t0140g0054 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.546+6692G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215869 | |||||||
chr19:16216005 | T | C | 2 | a0001c0001t0006g0185 a0001c0001t0006g0186 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.546+6828T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16216005 | |||||||
chr19:16216077 | T | TATGATTC others(3): Show |
1 | a0001c0002t0001g0131 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.546+6902_546+6903i others(12): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16216077 | ||||||
chr19:16216080 | A | G | 219 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0010 others(216): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.546+6903A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16216080 | |||||||
chr19:16216080 | A | T | 1 | a0001c0001t0002g0072 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.546+6903A>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16216080 | |||||||
chr19:16216211 | C | T | 1 | a0001c0001t0029g0183 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.546+7034C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16216211 | |||||||
chr19:16216212 | A | G | 1 | a0001c0001t0029g0183 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.546+7035A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16216212 | |||||||
chr19:16216220 | C | T | 69 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(66): Show |
69 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.546+7043C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16216220 | |||||||
chr19:16216272 | C | A | 1 | a0001c0002t0001g0121 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.546+7095C>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16216272 | |||||||
chr19:16216348 | G | A | 1 | a0001c0001t0090g0200 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.546+7171G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16216348 | |||||||
chr19:16216355 | G | C | 1 | a0001c0001t0079g0177 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.546+7178G>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16216355 | |||||||
chr19:16216404 | C | A | 1 | a0001c0001t0008g0218 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.546+7227C>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16216404 | |||||||
chr19:16216405 | A | C | 1 | a0001c0001t0008g0218 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.546+7228A>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16216405 | |||||||
chr19:16216444 | C | CA | 6 | a0001c0001t0038g0223 a0001c0001t0120g0265 a0001c0001t0140g0054 others(3): Show |
6 | HG02135.hp1 HG02615.hp1 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.546+7281dupA | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16216444 | ||||||
chr19:16216444 | CA | C | 8 | a0001c0001t0008g0218 a0001c0001t0037g0271 a0001c0001t0098g0182 others(5): Show |
8 | HG01167.hp2 HG01257.hp1 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.546+7281delA | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16216444 | ||||||
chr19:16216478 | A | G | 38 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0010 others(35): Show |
44 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.546+7301A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16216478 | |||||||
chr19:16216505 | C | G | 1 | a0001c0001t0026g0280 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.546+7328C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16216505 | |||||||
chr19:16216507 | G | T | 1 | a0001c0001t0008g0218 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.546+7330G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16216507 | |||||||
chr19:16216531 | T | G | 1 | a0001c0002t0099g0142 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.546+7354T>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16216531 | |||||||
chr19:16216570 | T | C | 167 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(164): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.546+7393T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16216570 | |||||||
chr19:16216788 | G | T | 1 | a0001c0001t0008g0218 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.546+7611G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16216788 | |||||||
chr19:16216944 | T | C | 168 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.546+7767T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16216944 | |||||||
chr19:16216972 | G | T | 1 | a0001c0002t0012g0160 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.546+7795G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16216972 | |||||||
chr19:16217051 | G | A | 1 | a0001c0001t0137g0212 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.546+7874G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16217051 | |||||||
chr19:16217118 | G | A | 9 | a0001c0001t0009g0017 a0001c0001t0009g0206 a0001c0001t0009g0207 others(6): Show |
10 | HG01361.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.546+7941G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16217118 | |||||||
chr19:16217234 | A | C | 245 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0010 others(242): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.546+8057A>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16217234 | |||||||
chr19:16217263 | A | G | 1 | a0001c0001t0146g0210 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.546+8086A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16217263 | |||||||
chr19:16217421 | A | T | 1 | a0001c0001t0008g0218 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.546+8244A>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16217421 | |||||||
chr19:16217466 | A | G | 1 | a0001c0002t0023g0164 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.546+8289A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16217466 | |||||||
chr19:16217516 | G | C | 1 | a0001c0002t0076g0115 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.546+8339G>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16217516 | |||||||
chr19:16217520 | G | A | 5 | a0001c0001t0102g0214 a0001c0001t0130g0076 a0001c0001t0131g0007 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.546+8343G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16217520 | |||||||
chr19:16217546 | G | A | 13 | a0001c0001t0042g0044 a0001c0001t0042g0081 a0001c0001t0043g0009 others(10): Show |
13 | HG01167.hp1 HG01169.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.546+8369G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16217546 | |||||||
chr19:16217577 | C | T | 69 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(66): Show |
69 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.546+8400C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16217577 | |||||||
chr19:16217632 | C | G | 1 | a0001c0002t0001g0156 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.546+8455C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16217632 | |||||||
chr19:16217753 | C | T | 42 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0010 others(39): Show |
49 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(46): Show |
intron_variant | MODIFIER | c.546+8576C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16217753 | |||||||
chr19:16217871 | C | T | 69 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(66): Show |
69 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.547-8550C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16217871 | |||||||
chr19:16218157 | C | T | 1 | a0001c0002t0001g0121 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.547-8264C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16218157 | |||||||
chr19:16218180 | G | A | 69 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(66): Show |
69 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.547-8241G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16218180 | |||||||
chr19:16218242 | A | C | 42 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(39): Show |
42 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(39): Show |
intron_variant | MODIFIER | c.547-8179A>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16218242 | |||||||
chr19:16218288 | A | G | 1 | a0001c0002t0001g0100 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.547-8133A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16218288 | |||||||
chr19:16218487 | T | C | 173 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(170): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.547-7934T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16218487 | |||||||
chr19:16218557 | G | A | 168 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.547-7864G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16218557 | |||||||
chr19:16218571 | C | G | 1 | a0001c0002t0001g0109 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.547-7850C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16218571 | |||||||
chr19:16218825 | C | T | 1 | a0001c0002t0004g0091 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.547-7596C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16218825 | |||||||
chr19:16218826 | T | C | 1 | a0001c0002t0004g0091 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.547-7595T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16218826 | |||||||
chr19:16219064 | G | GT | 68 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0010 others(65): Show |
80 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.547-7342dupT | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16219064 | ||||||
chr19:16219064 | GT | G | 87 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(84): Show |
87 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.547-7342delT | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16219064 | ||||||
chr19:16219068 | T | G | 1 | a0001c0003t0088g0187 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.547-7353T>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16219068 | |||||||
chr19:16219086 | G | T | 1 | a0001c0001t0006g0016 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.547-7335G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16219086 | |||||||
chr19:16219126 | A | G | 168 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.547-7295A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16219126 | |||||||
chr19:16219232 | A | G | 168 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.547-7189A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16219232 | |||||||
chr19:16219363 | C | A | 1 | a0001c0001t0034g0262 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.547-7058C>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16219363 | |||||||
chr19:16219397 | TG | T | 150 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(147): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.547-7023delG | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16219397 | |||||||
chr19:16219398 | G | GT | 6 | a0001c0001t0002g0045 a0001c0001t0002g0067 a0001c0001t0003g0205 others(3): Show |
6 | HG00544.hp2 HG02630.hp2 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.547-7007dupT | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16219398 | ||||||
chr19:16219398 | G | T | 15 | a0001c0001t0016g0019 a0001c0001t0031g0024 a0001c0001t0032g0027 others(12): Show |
15 | HG00735.hp1 HG01109.hp1 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.547-7023G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16219398 | |||||||
chr19:16219400 | T | G | 9 | a0001c0001t0016g0019 a0001c0001t0031g0024 a0001c0001t0045g0023 others(6): Show |
9 | HG01109.hp1 HG01361.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.547-7021T>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16219400 | |||||||
chr19:16219401 | T | G | 156 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(153): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.547-7020T>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16219401 | |||||||
chr19:16219402 | T | G | 1 | a0001c0002t0001g0121 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.547-7019T>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16219402 | |||||||
chr19:16219406 | T | G | 1 | a0001c0001t0002g0066 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.547-7015T>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16219406 | |||||||
chr19:16219407 | T | C | 1 | a0001c0002t0075g0168 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.547-7014T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16219407 | |||||||
chr19:16219428 | G | A | 2 | a0001c0001t0002g0067 a0001c0001t0002g0072 |
2 | HG03834.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.547-6993G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16219428 | |||||||
chr19:16219544 | C | T | 69 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(66): Show |
69 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.547-6877C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16219544 | |||||||
chr19:16219558 | C | T | 2 | a0001c0002t0068g0154 a0001c0003t0088g0187 |
2 | HG01891.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.547-6863C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16219558 | |||||||
chr19:16219607 | A | C | 9 | a0001c0001t0009g0017 a0001c0001t0009g0206 a0001c0001t0009g0207 others(6): Show |
10 | HG01361.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.547-6814A>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16219607 | |||||||
chr19:16219734 | T | C | 173 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(170): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.547-6687T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16219734 | |||||||
chr19:16220005 | G | A | 44 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0010 others(41): Show |
51 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.547-6416G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16220005 | |||||||
chr19:16220013 | T | C | 1 | a0001c0001t0083g0176 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.547-6408T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16220013 | |||||||
chr19:16220037 | G | A | 168 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.547-6384G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16220037 | |||||||
chr19:16220204 | C | A | 1 | a0001c0001t0144g0276 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.547-6217C>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16220204 | |||||||
chr19:16220266 | G | A | 1 | a0001c0002t0073g0114 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.547-6155G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16220266 | |||||||
chr19:16220324 | G | A | 1 | a0001c0002t0001g0122 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.547-6097G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16220324 | |||||||
chr19:16220372 | C | T | 1 | a0001c0001t0121g0257 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.547-6049C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16220372 | |||||||
chr19:16220375 | CTTTTGGG others(4): Show |
C | 1 | a0001c0002t0064g0161 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.547-6040_547-6030d others(13): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16220375 | ||||||
chr19:16220383 | G | GT | 5 | a0001c0001t0007g0006 a0001c0001t0045g0023 a0001c0002t0001g0167 others(2): Show |
5 | HG00597.hp2 HG01928.hp1 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.547-6031dupT | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16220383 | ||||||
chr19:16220436 | G | C | 1 | a0001c0001t0032g0027 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.547-5985G>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16220436 | |||||||
chr19:16220437 | C | G | 1 | a0001c0001t0032g0027 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.547-5984C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16220437 | |||||||
chr19:16220452 | G | A | 1 | a0001c0001t0028g0190 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.547-5969G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16220452 | |||||||
chr19:16220542 | C | T | 168 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.547-5879C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16220542 | |||||||
chr19:16220633 | T | C | 168 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.547-5788T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16220633 | |||||||
chr19:16220832 | G | A | 5 | a0001c0001t0102g0214 a0001c0001t0130g0076 a0001c0001t0131g0007 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.547-5589G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16220832 | |||||||
chr19:16220885 | T | C | 1 | a0001c0002t0012g0160 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.547-5536T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16220885 | |||||||
chr19:16221085 | G | A | 1 | a0001c0001t0042g0081 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.547-5336G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16221085 | |||||||
chr19:16221132 | T | C | 5 | a0001c0001t0102g0214 a0001c0001t0130g0076 a0001c0001t0131g0007 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.547-5289T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16221132 | |||||||
chr19:16221196 | T | C | 173 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(170): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.547-5225T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16221196 | |||||||
chr19:16221275 | C | T | 168 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.547-5146C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16221275 | |||||||
chr19:16221394 | G | T | 1 | a0001c0002t0048g0119 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.547-5027G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16221394 | |||||||
chr19:16221523 | A | G | 168 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.547-4898A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16221523 | |||||||
chr19:16221683 | C | T | 1 | a0001c0001t0133g0057 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.547-4738C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16221683 | |||||||
chr19:16221689 | A | C | 3 | a0001c0001t0102g0214 a0001c0001t0131g0007 a0001c0001t0143g0007 |
3 | HG01884.hp1 HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.547-4732A>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16221689 | |||||||
chr19:16221738 | C | T | 1 | a0001c0002t0048g0119 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.547-4683C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16221738 | |||||||
chr19:16221975 | C | T | 1 | a0001c0001t0101g0064 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.547-4446C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16221975 | |||||||
chr19:16222188 | TTATTATT others(2): Show |
T | 152 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(149): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.547-4224_547-4216d others(11): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16222188 | ||||||
chr19:16222197 | C | T | 21 | a0001c0001t0016g0018 a0001c0001t0031g0024 a0001c0001t0031g0025 others(18): Show |
21 | HG00735.hp1 HG01109.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.547-4224C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16222197 | |||||||
chr19:16222199 | A | T | 1 | a0001c0001t0130g0076 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.547-4222A>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16222199 | |||||||
chr19:16222200 | TTATTATT others(1): Show |
T | 5 | a0001c0002t0004g0134 a0001c0002t0024g0088 a0001c0002t0060g0158 others(2): Show |
5 | HG01192.hp1 HG02155.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.547-4219_547-4212d others(10): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16222200 | ||||||
chr19:16222201 | TATTATTA others(3): Show |
T | 5 | a0001c0001t0016g0018 a0001c0001t0038g0223 a0001c0001t0038g0224 others(2): Show |
5 | HG02615.hp1 HG02895.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.547-4219_547-4210d others(12): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16222201 | |||||||
chr19:16222202 | A | T | 1 | a0001c0001t0130g0076 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.547-4219A>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16222202 | |||||||
chr19:16222202 | ATTATTAT others(3): Show |
A | 5 | a0001c0001t0031g0024 a0001c0001t0031g0025 a0001c0001t0032g0026 others(2): Show |
5 | HG00735.hp1 HG01109.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.547-4216_547-4207d others(12): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16222202 | ||||||
chr19:16222205 | A | T | 3 | a0001c0001t0102g0214 a0001c0001t0130g0076 a0001c0001t0145g0030 |
3 | HG02055.hp2 HG02486.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.547-4216A>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16222205 | |||||||
chr19:16222206 | TTA | T | 5 | a0001c0001t0002g0003 a0001c0001t0002g0046 a0001c0001t0002g0068 others(2): Show |
6 | HG01123.hp2 HG01255.hp2 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.547-4213_547-4212d others(4): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16222206 | ||||||
chr19:16222207 | TA | T | 33 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0010 others(30): Show |
37 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.547-4213delA | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16222207 | |||||||
chr19:16222208 | A | AT | 14 | a0001c0001t0009g0017 a0001c0001t0009g0209 a0001c0001t0042g0044 others(11): Show |
14 | HG01167.hp1 HG01169.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.547-4211dupT | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16222208 | ||||||
chr19:16222208 | A | T | 13 | a0001c0001t0102g0214 a0001c0001t0130g0076 a0001c0001t0131g0007 others(10): Show |
13 | HG00597.hp2 HG01074.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.547-4213A>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16222208 | |||||||
chr19:16222211 | A | AT | 11 | a0001c0001t0007g0002 a0001c0001t0007g0006 a0001c0001t0009g0017 others(8): Show |
15 | HG01361.hp1 HG02145.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.547-4196dupT | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16222211 | ||||||
chr19:16222211 | A | T | 151 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0010 others(148): Show |
157 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.547-4210A>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16222211 | |||||||
chr19:16222214 | T | A | 3 | a0001c0001t0003g0173 a0001c0001t0027g0028 a0001c0001t0037g0271 |
3 | HG00738.hp1 HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.547-4207T>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16222214 | |||||||
chr19:16222223 | T | G | 1 | a0001c0001t0044g0238 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.547-4198T>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16222223 | |||||||
chr19:16222283 | C | T | 5 | a0001c0001t0102g0214 a0001c0001t0130g0076 a0001c0001t0131g0007 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.547-4138C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16222283 | |||||||
chr19:16222379 | TA | T | 7 | a0001c0001t0008g0218 a0001c0001t0037g0271 a0001c0001t0040g0052 others(4): Show |
7 | HG01256.hp2 HG03130.hp2 NA18522.hp1 others(4): Show |
intron_variant | MODIFIER | c.547-4033delA | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16222379 | ||||||
chr19:16222405 | G | A | 1 | a0001c0001t0140g0054 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.547-4016G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16222405 | |||||||
chr19:16222411 | T | G | 168 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.547-4010T>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16222411 | |||||||
chr19:16222559 | C | T | 1 | a0001c0001t0040g0052 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.547-3862C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16222559 | |||||||
chr19:16222595 | T | TTTTG | 173 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(170): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.547-3818_547-3815d others(6): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16222595 | ||||||
chr19:16222755 | G | C | 1 | a0001c0001t0019g0069 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.547-3666G>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16222755 | |||||||
chr19:16222998 | C | G | 1 | a0001c0001t0137g0212 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.547-3423C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16222998 | |||||||
chr19:16223023 | G | A | 1 | a0001c0001t0019g0069 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.547-3398G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16223023 | |||||||
chr19:16223109 | T | C | 69 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(66): Show |
69 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.547-3312T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16223109 | |||||||
chr19:16223139 | A | G | 1 | a0001c0002t0051g0127 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.547-3282A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16223139 | |||||||
chr19:16223187 | G | A | 47 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0010 others(44): Show |
58 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.547-3234G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16223187 | |||||||
chr19:16223193 | C | T | 1 | a0001c0001t0144g0276 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.547-3228C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16223193 | |||||||
chr19:16223203 | T | G | 176 | a0001c0001t0002g0082 a0001c0001t0003g0191 a0001c0001t0005g0216 others(173): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.547-3218T>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16223203 | |||||||
chr19:16223213 | G | A | 71 | a0001c0001t0003g0191 a0001c0001t0005g0216 a0001c0001t0005g0219 others(68): Show |
71 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.547-3208G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16223213 | |||||||
chr19:16223223 | C | A | 1 | a0001c0001t0002g0066 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.547-3198C>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16223223 | |||||||
chr19:16223272 | G | T | 1 | a0001c0002t0058g0126 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.547-3149G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16223272 | |||||||
chr19:16223312 | C | G | 168 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.547-3109C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16223312 | |||||||
chr19:16223520 | C | T | 1 | a0001c0002t0001g0128 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.547-2901C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16223520 | |||||||
chr19:16223589 | G | A | 2 | a0001c0001t0038g0223 a0001c0001t0038g0224 |
2 | HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.547-2832G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16223589 | |||||||
chr19:16223753 | G | A | 1 | a0001c0002t0062g0170 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.547-2668G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16223753 | |||||||
chr19:16223791 | C | T | 2 | a0001c0001t0080g0189 a0001c0001t0082g0192 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.547-2630C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16223791 | |||||||
chr19:16223846 | A | G | 5 | a0001c0001t0026g0279 a0001c0001t0026g0280 a0001c0001t0078g0278 others(2): Show |
5 | HG02647.hp1 HG02896.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.547-2575A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16223846 | |||||||
chr19:16223897 | C | T | 1 | a0001c0001t0112g0228 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.547-2524C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16223897 | |||||||
chr19:16223944 | A | G | 1 | a0001c0001t0008g0253 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.547-2477A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16223944 | |||||||
chr19:16224007 | C | T | 168 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.547-2414C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16224007 | |||||||
chr19:16224128 | G | A | 168 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.547-2293G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16224128 | |||||||
chr19:16224166 | G | A | 168 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.547-2255G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16224166 | |||||||
chr19:16224238 | C | T | 1 | a0001c0001t0033g0222 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.547-2183C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16224238 | |||||||
chr19:16224349 | C | T | 69 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(66): Show |
69 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.547-2072C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16224349 | |||||||
chr19:16224371 | C | T | 1 | a0001c0001t0108g0264 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.547-2050C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16224371 | |||||||
chr19:16224452 | G | A | 2 | a0001c0001t0035g0255 a0001c0001t0035g0256 |
2 | HG01243.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.547-1969G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16224452 | |||||||
chr19:16224482 | G | A | 1 | a0001c0002t0001g0108 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.547-1939G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16224482 | |||||||
chr19:16224559 | C | T | 46 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0010 others(43): Show |
57 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.547-1862C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16224559 | |||||||
chr19:16224679 | C | T | 1 | a0001c0002t0067g0112 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.547-1742C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16224679 | |||||||
chr19:16224774 | C | T | 1 | a0001c0001t0123g0258 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.547-1647C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16224774 | |||||||
chr19:16224796 | C | G | 4 | a0001c0001t0039g0051 a0001c0001t0039g0053 a0001c0001t0040g0035 others(1): Show |
5 | HG02258.hp1 HG02630.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.547-1625C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16224796 | |||||||
chr19:16224800 | G | A | 1 | a0001c0001t0144g0276 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.547-1621G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16224800 | |||||||
chr19:16224929 | C | T | 168 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.547-1492C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16224929 | |||||||
chr19:16224965 | G | GGA | 71 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(68): Show |
72 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.547-1441_547-1440d others(4): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16224965 | ||||||
chr19:16225031 | C | T | 2 | a0001c0001t0038g0223 a0001c0001t0038g0224 |
2 | HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.547-1390C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16225031 | |||||||
chr19:16225034 | T | G | 1 | a0001c0001t0002g0062 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.547-1387T>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16225034 | |||||||
chr19:16225038 | G | A | 1 | a0001c0001t0115g0226 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.547-1383G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16225038 | |||||||
chr19:16225051 | G | A | 1 | a0001c0001t0028g0197 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.547-1370G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16225051 | |||||||
chr19:16225088 | A | T | 168 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.547-1333A>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16225088 | |||||||
chr19:16225383 | A | G | 168 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.547-1038A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16225383 | |||||||
chr19:16225403 | AG | A | 168 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.547-1015delG | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16225403 | ||||||
chr19:16225419 | C | T | 1 | a0001c0001t0003g0205 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.547-1002C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16225419 | |||||||
chr19:16225432 | A | T | 168 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.547-989A>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16225432 | |||||||
chr19:16225478 | C | T | 1 | a0001c0004t0107g0239 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.547-943C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16225478 | |||||||
chr19:16225480 | TCA | T | 7 | a0001c0001t0035g0255 a0001c0001t0035g0256 a0001c0001t0036g0254 others(4): Show |
7 | HG01109.hp2 HG01243.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.547-939_547-938del others(2): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16225480 | ||||||
chr19:16225529 | G | A | 2 | a0001c0001t0002g0046 a0001c0001t0040g0052 |
2 | HG02809.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.547-892G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16225529 | |||||||
chr19:16225564 | G | A | 1 | a0001c0002t0001g0089 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.547-857G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16225564 | |||||||
chr19:16225830 | G | C | 99 | a0001c0002t0001g0012 a0001c0002t0001g0031 a0001c0002t0001g0033 others(96): Show |
99 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.547-591G>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16225830 | |||||||
chr19:16225891 | G | A | 1 | a0001c0001t0017g0235 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.547-530G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16225891 | |||||||
chr19:16225900 | G | T | 42 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(39): Show |
42 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(39): Show |
intron_variant | MODIFIER | c.547-521G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16225900 | |||||||
chr19:16226137 | TA | T | 168 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.547-283delA | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16226137 | |||||||
chr19:16226140 | AG | A | 168 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.547-278delG | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16226140 | ||||||
chr19:16226409 | C | T | 1 | a0001c0001t0029g0183 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.547-12C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16226409 | |||||||
chr19:16226612 | T | C | 173 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(170): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.673+65T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 6/11 | chr19 | 16226612 | |||||||
chr19:16226745 | T | C | 5 | a0001c0001t0016g0018 a0001c0001t0016g0019 a0001c0001t0016g0021 others(2): Show |
5 | HG02723.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.673+198T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 6/11 | chr19 | 16226745 | |||||||
chr19:16226777 | C | T | 169 | a0001c0001t0003g0173 a0001c0001t0005g0216 a0001c0001t0005g0219 others(166): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.673+230C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 6/11 | chr19 | 16226777 | |||||||
chr19:16226848 | C | T | 168 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.673+301C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 6/11 | chr19 | 16226848 | |||||||
chr19:16226936 | G | A | 168 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.673+389G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 6/11 | chr19 | 16226936 | |||||||
chr19:16226970 | G | A | 1 | a0001c0002t0057g0117 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.673+423G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 6/11 | chr19 | 16226970 | |||||||
chr19:16227237 | C | T | 2 | a0001c0001t0038g0223 a0001c0001t0038g0224 |
2 | HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.674-311C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 6/11 | chr19 | 16227237 | |||||||
chr19:16227313 | TG | T | 99 | a0001c0002t0001g0012 a0001c0002t0001g0031 a0001c0002t0001g0033 others(96): Show |
99 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.674-231delG | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr19 | 16227313 | ||||||
chr19:16227401 | A | G | 1 | a0001c0002t0012g0093 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.674-147A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 6/11 | chr19 | 16227401 | |||||||
chr19:16227463 | C | T | 69 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(66): Show |
69 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.674-85C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 6/11 | chr19 | 16227463 | |||||||
chr19:16227721 | G | A | 168 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.816+31G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 7/11 | chr19 | 16227721 | |||||||
chr19:16227884 | C | T | 4 | a0001c0001t0031g0024 a0001c0001t0031g0025 a0001c0001t0032g0026 others(1): Show |
4 | HG00735.hp1 HG01109.hp1 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+194C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 7/11 | chr19 | 16227884 | |||||||
chr19:16228219 | C | T | 1 | a0001c0002t0001g0108 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.888+11C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 8/11 | chr19 | 16228219 | |||||||
chr19:16228258 | G | A | 99 | a0001c0002t0001g0012 a0001c0002t0001g0031 a0001c0002t0001g0033 others(96): Show |
99 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.888+50G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 8/11 | chr19 | 16228258 | |||||||
chr19:16228336 | A | T | 1 | a0001c0001t0140g0054 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.888+128A>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 8/11 | chr19 | 16228336 | |||||||
chr19:16228537 | G | T | 2 | a0001c0002t0001g0163 a0001c0002t0001g0167 |
2 | HG00597.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.889-233G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 8/11 | chr19 | 16228537 | |||||||
chr19:16228547 | C | T | 8 | a0001c0001t0009g0017 a0001c0001t0009g0206 a0001c0001t0009g0207 others(5): Show |
9 | HG01361.hp1 HG02615.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.889-223C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 8/11 | chr19 | 16228547 | |||||||
chr19:16228620 | G | A | 1 | a0001c0002t0001g0109 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.889-150G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 8/11 | chr19 | 16228620 | |||||||
chr19:16228751 | G | A | 10 | a0001c0001t0013g0005 a0001c0001t0013g0014 a0001c0001t0013g0180 others(7): Show |
10 | HG01934.hp1 HG02055.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.889-19G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 8/11 | chr19 | 16228751 | |||||||
chr19:16229063 | A | G | 168 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.1047+135A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16229063 | |||||||
chr19:16229066 | G | A | 1 | a0001c0001t0002g0045 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1047+138G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16229066 | |||||||
chr19:16229075 | G | T | 168 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.1047+147G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16229075 | |||||||
chr19:16229076 | A | T | 168 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.1047+148A>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16229076 | |||||||
chr19:16229110 | A | C | 1 | a0001c0001t0045g0023 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1047+182A>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16229110 | |||||||
chr19:16229114 | G | A | 99 | a0001c0002t0001g0012 a0001c0002t0001g0031 a0001c0002t0001g0033 others(96): Show |
99 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.1047+186G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16229114 | |||||||
chr19:16229162 | G | C | 1 | a0001c0001t0017g0235 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1047+234G>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16229162 | |||||||
chr19:16229319 | A | G | 198 | a0001c0001t0002g0046 a0001c0001t0005g0216 a0001c0001t0005g0219 others(195): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.1047+391A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16229319 | |||||||
chr19:16229368 | G | A | 1 | a0001c0001t0140g0054 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1047+440G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16229368 | |||||||
chr19:16229469 | A | G | 161 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(158): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.1047+541A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16229469 | |||||||
chr19:16229601 | G | A | 2 | a0001c0002t0024g0118 a0001c0002t0071g0106 |
2 | HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1047+673G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16229601 | |||||||
chr19:16229820 | T | C | 1 | a0001c0001t0153g0080 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1047+892T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16229820 | |||||||
chr19:16229873 | G | A | 1 | a0001c0002t0046g0137 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1047+945G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16229873 | |||||||
chr19:16229877 | C | T | 2 | a0001c0001t0043g0059 a0001c0001t0154g0056 |
2 | HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1047+949C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16229877 | |||||||
chr19:16229935 | G | A | 3 | a0001c0001t0002g0046 a0001c0001t0040g0052 a0001c0002t0001g0034 |
3 | HG02602.hp1 HG02809.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1047+1007G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16229935 | |||||||
chr19:16229982 | G | T | 1 | a0001c0001t0134g0050 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1047+1054G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16229982 | |||||||
chr19:16230027 | T | A | 1 | a0001c0001t0034g0262 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1047+1099T>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16230027 | |||||||
chr19:16230044 | G | A | 1 | a0001c0001t0005g0231 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1047+1116G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16230044 | |||||||
chr19:16230245 | G | T | 49 | a0001c0002t0001g0031 a0001c0002t0001g0033 a0001c0002t0001g0089 others(46): Show |
49 | HG00609.hp2 HG00738.hp2 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.1047+1317G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16230245 | |||||||
chr19:16230404 | C | CTT | 160 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(157): Show |
160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.1047+1489_1047+149 others(6): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr19 | 16230404 | ||||||
chr19:16230404 | C | CTTT | 6 | a0001c0001t0005g0246 a0001c0001t0016g0018 a0001c0001t0016g0019 others(3): Show |
6 | HG02723.hp2 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1047+1488_1047+149 others(7): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr19 | 16230404 | ||||||
chr19:16230404 | CT | C | 64 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0010 others(61): Show |
75 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.1047+1490delT | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr19 | 16230404 | ||||||
chr19:16230404 | CTT | C | 9 | a0001c0001t0009g0017 a0001c0001t0009g0206 a0001c0001t0009g0207 others(6): Show |
10 | HG01361.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1047+1489_1047+149 others(6): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr19 | 16230404 | ||||||
chr19:16230423 | C | T | 1 | a0001c0001t0144g0276 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1047+1495C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16230423 | |||||||
chr19:16230471 | G | A | 3 | a0001c0001t0026g0279 a0001c0001t0026g0280 a0001c0001t0094g0277 |
3 | HG02647.hp1 HG02896.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1047+1543G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16230471 | |||||||
chr19:16230485 | G | C | 168 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.1047+1557G>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16230485 | |||||||
chr19:16230521 | G | A | 3 | a0001c0001t0102g0214 a0001c0001t0131g0007 a0001c0001t0143g0007 |
3 | HG01884.hp1 HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1047+1593G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16230521 | |||||||
chr19:16230828 | C | T | 173 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(170): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.1047+1900C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16230828 | |||||||
chr19:16230938 | G | A | 3 | a0001c0001t0102g0214 a0001c0001t0131g0007 a0001c0001t0143g0007 |
3 | HG01884.hp1 HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1047+2010G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16230938 | |||||||
chr19:16231054 | T | C | 289 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0010 others(286): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.1047+2126T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16231054 | |||||||
chr19:16231063 | C | T | 1 | a0001c0002t0050g0166 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1047+2135C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16231063 | |||||||
chr19:16231116 | G | A | 2 | a0001c0001t0097g0179 a0001c0002t0001g0275 |
2 | HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1047+2188G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16231116 | |||||||
chr19:16231157 | G | A | 7 | a0001c0001t0043g0009 a0001c0001t0043g0059 a0001c0001t0133g0057 others(4): Show |
7 | HG01167.hp1 HG01169.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1047+2229G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16231157 | |||||||
chr19:16231218 | G | A | 1 | a0001c0001t0144g0276 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1048-2275G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16231218 | |||||||
chr19:16231220 | G | A | 1 | a0001c0001t0145g0030 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1048-2273G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16231220 | |||||||
chr19:16231236 | C | T | 4 | a0001c0001t0031g0024 a0001c0001t0031g0025 a0001c0001t0032g0026 others(1): Show |
4 | HG00735.hp1 HG01109.hp1 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.1048-2257C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16231236 | |||||||
chr19:16231237 | A | G | 173 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(170): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.1048-2256A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16231237 | |||||||
chr19:16231287 | C | CA | 8 | a0001c0001t0003g0032 a0001c0001t0003g0196 a0001c0001t0006g0198 others(5): Show |
8 | HG00735.hp1 HG01081.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1048-2183dupA | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr19 | 16231287 | ||||||
chr19:16231287 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0003g0188 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1048-2193_1048-218 others(15): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr19 | 16231287 | ||||||
chr19:16231297 | AAAAAAAA others(9): Show |
A | 1 | a0001c0002t0010g0140 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1048-2194_1048-217 others(20): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr19 | 16231297 | ||||||
chr19:16231298 | AAAAAAAA others(8): Show |
A | 97 | a0001c0002t0001g0012 a0001c0002t0001g0031 a0001c0002t0001g0033 others(94): Show |
97 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.1048-2193_1048-217 others(19): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr19 | 16231298 | ||||||
chr19:16231299 | AAAAAAAA others(7): Show |
A | 1 | a0001c0002t0059g0099 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1048-2192_1048-217 others(18): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr19 | 16231299 | ||||||
chr19:16231309 | A | AC | 54 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0010 others(51): Show |
61 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.1048-2184_1048-218 others(5): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16231309 | |||||||
chr19:16231309 | A | C | 5 | a0001c0001t0014g0010 a0001c0001t0014g0042 a0001c0001t0020g0049 others(2): Show |
5 | HG01069.hp2 HG01167.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.1048-2184A>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16231309 | |||||||
chr19:16231310 | AC | A | 48 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(45): Show |
48 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.1048-2182delC | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16231310 | |||||||
chr19:16231311 | C | A | 13 | a0001c0001t0017g0232 a0001c0001t0017g0235 a0001c0001t0018g0270 others(10): Show |
13 | HG00558.hp1 HG00735.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1048-2182C>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16231311 | |||||||
chr19:16231313 | C | CAG | 14 | a0001c0001t0002g0001 a0001c0001t0002g0067 a0001c0001t0007g0002 others(11): Show |
18 | HG00423.hp1 HG00735.hp2 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.1048-2172_1048-217 others(6): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr19 | 16231313 | ||||||
chr19:16231313 | C | G | 62 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0010 others(59): Show |
69 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.1048-2180C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16231313 | |||||||
chr19:16231313 | CAG | C | 8 | a0001c0001t0016g0018 a0001c0001t0016g0019 a0001c0001t0016g0021 others(5): Show |
8 | HG02723.hp2 HG02895.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.1048-2172_1048-217 others(6): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr19 | 16231313 | ||||||
chr19:16231315 | G | C | 160 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(157): Show |
160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.1048-2178G>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16231315 | |||||||
chr19:16231332 | C | T | 2 | a0001c0001t0130g0076 a0001c0001t0145g0030 |
2 | HG02055.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1048-2161C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16231332 | |||||||
chr19:16231333 | A | G | 99 | a0001c0002t0001g0012 a0001c0002t0001g0031 a0001c0002t0001g0033 others(96): Show |
99 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.1048-2160A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16231333 | |||||||
chr19:16231335 | A | G | 1 | a0001c0001t0144g0276 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1048-2158A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16231335 | |||||||
chr19:16231403 | T | A | 1 | a0001c0001t0144g0276 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1048-2090T>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16231403 | |||||||
chr19:16231501 | G | C | 168 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.1048-1992G>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16231501 | |||||||
chr19:16231533 | G | A | 67 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(64): Show |
67 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.1048-1960G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16231533 | |||||||
chr19:16231630 | AT | A | 168 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.1048-1861delT | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr19 | 16231630 | ||||||
chr19:16231646 | G | T | 2 | a0001c0001t0005g0225 a0001c0001t0005g0227 |
2 | HG00438.hp2 HG00609.hp1 |
intron_variant | MODIFIER | c.1048-1847G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16231646 | |||||||
chr19:16231692 | C | T | 99 | a0001c0002t0001g0012 a0001c0002t0001g0031 a0001c0002t0001g0033 others(96): Show |
99 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.1048-1801C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16231692 | |||||||
chr19:16231746 | G | A | 2 | a0001c0001t0003g0194 a0001c0001t0081g0193 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1048-1747G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16231746 | |||||||
chr19:16231781 | T | A | 168 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.1048-1712T>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16231781 | |||||||
chr19:16231860 | G | A | 3 | a0001c0001t0102g0214 a0001c0001t0131g0007 a0001c0001t0143g0007 |
3 | HG01884.hp1 HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1048-1633G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16231860 | |||||||
chr19:16231883 | A | G | 3 | a0001c0001t0102g0214 a0001c0001t0131g0007 a0001c0001t0143g0007 |
3 | HG01884.hp1 HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1048-1610A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16231883 | |||||||
chr19:16232129 | G | A | 1 | a0001c0001t0140g0054 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1048-1364G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16232129 | |||||||
chr19:16232282 | G | T | 1 | a0001c0002t0004g0116 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1048-1211G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16232282 | |||||||
chr19:16232288 | G | T | 1 | a0001c0001t0002g0066 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1048-1205G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16232288 | |||||||
chr19:16232307 | C | T | 3 | a0001c0001t0102g0214 a0001c0001t0131g0007 a0001c0001t0143g0007 |
3 | HG01884.hp1 HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1048-1186C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16232307 | |||||||
chr19:16232401 | G | A | 1 | a0001c0002t0004g0102 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1048-1092G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16232401 | |||||||
chr19:16232425 | T | C | 2 | a0001c0001t0149g0037 a0001c0001t0151g0055 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1048-1068T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16232425 | |||||||
chr19:16232519 | C | T | 4 | a0001c0001t0031g0024 a0001c0001t0031g0025 a0001c0001t0032g0026 others(1): Show |
4 | HG00735.hp1 HG01109.hp1 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.1048-974C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16232519 | |||||||
chr19:16232600 | G | A | 1 | a0001c0002t0001g0108 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1048-893G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16232600 | |||||||
chr19:16232610 | G | A | 5 | a0001c0001t0026g0279 a0001c0001t0026g0280 a0001c0001t0078g0278 others(2): Show |
5 | HG02647.hp1 HG02896.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1048-883G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16232610 | |||||||
chr19:16232660 | G | A | 9 | a0001c0001t0009g0017 a0001c0001t0009g0206 a0001c0001t0009g0207 others(6): Show |
10 | HG01361.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1048-833G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16232660 | |||||||
chr19:16232685 | C | A | 1 | a0001c0002t0001g0136 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1048-808C>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16232685 | |||||||
chr19:16232755 | G | A | 1 | a0001c0001t0100g0174 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1048-738G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16232755 | |||||||
chr19:16233003 | G | A | 60 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(57): Show |
60 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.1048-490G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16233003 | |||||||
chr19:16233036 | T | A | 99 | a0001c0002t0001g0012 a0001c0002t0001g0031 a0001c0002t0001g0033 others(96): Show |
99 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.1048-457T>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16233036 | |||||||
chr19:16233107 | G | A | 1 | a0001c0001t0003g0204 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1048-386G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16233107 | |||||||
chr19:16233146 | A | G | 168 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.1048-347A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16233146 | |||||||
chr19:16233154 | A | G | 6 | a0001c0001t0013g0014 a0001c0001t0013g0180 a0001c0001t0013g0184 others(3): Show |
6 | HG02280.hp1 HG02451.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1048-339A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16233154 | |||||||
chr19:16233169 | T | C | 2 | a0001c0001t0103g0241 a0001c0001t0113g0220 |
2 | HG00544.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.1048-324T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16233169 | |||||||
chr19:16233268 | C | T | 44 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0010 others(41): Show |
51 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.1048-225C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16233268 | |||||||
chr19:16233372 | C | T | 1 | a0001c0001t0028g0190 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1048-121C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16233372 | |||||||
chr19:16233480 | G | A | 2 | a0001c0001t0007g0002 a0001c0001t0007g0006 |
6 | HG02145.hp1 HG02976.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1048-13G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16233480 | |||||||
chr19:16233640 | G | A | 1 | a0001c0001t0044g0238 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1173+22G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 10/11 | chr19 | 16233640 | |||||||
chr19:16233702 | G | T | 7 | a0001c0001t0035g0255 a0001c0001t0035g0256 a0001c0001t0036g0254 others(4): Show |
7 | HG01109.hp2 HG01243.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.1173+84G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 10/11 | chr19 | 16233702 | |||||||
chr19:16233717 | C | G | 170 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(167): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.1173+99C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 10/11 | chr19 | 16233717 | |||||||
chr19:16233788 | A | C | 8 | a0001c0001t0009g0017 a0001c0001t0009g0206 a0001c0001t0009g0207 others(5): Show |
9 | HG01361.hp1 HG02615.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1173+170A>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 10/11 | chr19 | 16233788 | |||||||
chr19:16233817 | C | T | 37 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0010 others(34): Show |
43 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.1173+199C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 10/11 | chr19 | 16233817 | |||||||
chr19:16233836 | A | G | 173 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(170): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.1173+218A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 10/11 | chr19 | 16233836 | |||||||
chr19:16233871 | AC | A | 42 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(39): Show |
42 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(39): Show |
intron_variant | MODIFIER | c.1173+255delC | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr19 | 16233871 | ||||||
chr19:16233948 | G | A | 3 | a0001c0001t0006g0016 a0001c0001t0006g0185 a0001c0001t0006g0186 |
4 | HG01257.hp2 HG01258.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.1174-251G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 10/11 | chr19 | 16233948 | |||||||
chr19:16233974 | G | A | 1 | a0001c0001t0141g0283 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1174-225G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 10/11 | chr19 | 16233974 | |||||||
chr19:16234095 | A | C | 1 | a0001c0002t0062g0170 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1174-104A>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 10/11 | chr19 | 16234095 | |||||||
chr19:16234157 | C | T | 1 | a0001c0001t0097g0179 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1174-42C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 10/11 | chr19 | 16234157 | |||||||
chr19:16234282 | A | G | 1 | a0001c0001t0044g0238 | 1 | NA19002.hp1 | splice_region_variant&intron_variant | LOW | c.1249+8A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 11/11 | chr19 | 16234282 | |||||||
chr19:16234283 | G | A | 1 | a0001c0001t0044g0238 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1249+9G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 11/11 | chr19 | 16234283 | |||||||
chr19:16234288 | T | C | 171 | a0001c0001t0005g0216 a0001c0001t0005g0219 a0001c0001t0005g0225 others(168): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.1249+14T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 11/11 | chr19 | 16234288 | |||||||
chr19:16234292 | C | T | 1 | a0001c0001t0141g0283 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1249+18C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 11/11 | chr19 | 16234292 | |||||||
chr19:16234298 | G | C | 1 | a0001c0001t0038g0223 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1249+24G>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 11/11 | chr19 | 16234298 | |||||||
chr19:16234379 | G | A | 1 | a0001c0001t0145g0030 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1250-34G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 11/11 | chr19 | 16234379 |