Item | Value |
---|---|
geneid | 1176 |
ensemblid | ENSG00000177879.17 |
hgncid | 2013 |
symbol | AP3S1 |
name | adaptor related protein complex 3 subunit sigma 1 |
refseq_nuc | NM_001284.4 |
refseq_prot | NP_001275.1 |
ensembl_nuc | ENST00000316788.12 |
ensembl_prot | ENSP00000325369.7 |
mane_status | MANE Select |
chr | chr5 |
start | 115841935 |
end | 115914081 |
strand | + |
ver | v1.2 |
region | chr5:115841935-115914081 |
region5000 | chr5:115836935-115919081 |
regionname0 | AP3S1_chr5_115841935_115914081 |
regionname5000 | AP3S1_chr5_115836935_115919081 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 193 | 376 | 88 | 72 | 158 | 14 | 42 | 124 | AP3S1_chr5_115836935_115919081 | AP3S1 | MIKAI others(188): Show |
chr5 | 115836935 | 115919081 |
a0002 | 0/0 | 193 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | MIKAI others(188): Show |
chr5 | 115836935 | 115919081 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 579 | 376 | 88 | 72 | 158 | 14 | 42 | AP3S1_chr5_115836935_115919081 | AP3S1 | ATGAT others(574): Show |
chr5 | 115836935 | 115919081 | ||
a0002c0002 | 0/0 | 579 | 2 | 2 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | ATGAT others(574): Show |
chr5 | 115836935 | 115919081 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 1276 | 357 | 73 | 70 | 158 | 14 | 40 | AP3S1_chr5_115836935_115919081 | AP3S1 | AGGGG others(1271): Show |
chr5 | 115836935 | 115919081 |
a0001c0001t0002 | 0/0 | 1276 | 8 | 8 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | AGGGG others(1271): Show |
chr5 | 115836935 | 115919081 |
a0001c0001t0003 | 0/0 | 1276 | 5 | 1 | 2 | 0 | 0 | 2 | AP3S1_chr5_115836935_115919081 | AP3S1 | AGGGG others(1271): Show |
chr5 | 115836935 | 115919081 |
a0001c0001t0004 | 0/0 | 1276 | 3 | 3 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | AGGGG others(1271): Show |
chr5 | 115836935 | 115919081 |
a0001c0001t0005 | 0/0 | 1277 | 3 | 3 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | AGGGG others(1272): Show |
chr5 | 115836935 | 115919081 |
a0002c0002t0001 | 0/0 | 1276 | 2 | 2 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | AGGGG others(1271): Show |
chr5 | 115836935 | 115919081 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0002 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0011 | 1/0 | 2 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0047 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0002g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0002g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0002g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0002g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0002g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0002g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0003g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0003g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0004g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0004g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0005g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0005g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0001c0001t0005g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0002c0002t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
a0002c0002t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0127 | EUR | GBR | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0303 | EUR | GBR | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0155 | EUR | GBR | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0263 | EUR | GBR | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | FIN | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0264 | EUR | FIN | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | CHS | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | CHS | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | CHS | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | CHS | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | CHS | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | PUR | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0325 | AMR | PUR | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0296 | AMR | PUR | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0323 | AMR | PUR | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0322 | AMR | PUR | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0316 | AMR | PUR | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | CLM | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG01256 | hp1 | a0001 | c0001 | t0003 | g0023 | AMR | CLM | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | CLM | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG01258 | hp2 | a0001 | c0001 | t0003 | g0021 | AMR | CLM | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0298 | AMR | CLM | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | CLM | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0326 | AMR | CLM | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | CLM | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | CLM | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0331 | AMR | CLM | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | CLM | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0024 | EUR | IBS | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0063 | EUR | IBS | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0268 | EUR | IBS | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0025 | EUR | IBS | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | ACB | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | ACB | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0300 | AMR | PEL | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0306 | AMR | PEL | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0311 | AMR | PEL | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | PEL | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | PEL | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PEL | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PEL | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0309 | AMR | PEL | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02055 | hp2 | a0001 | c0001 | t0005 | g0059 | AFR | ACB | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | KHV | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | KHV | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | KHV | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | KHV | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | KHV | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02145 | hp1 | a0001 | c0001 | t0003 | g0022 | AFR | ACB | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0305 | AMR | PEL | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | CDX | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | CDX | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0339 | AFR | ACB | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | ACB | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | PEL | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PEL | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0314 | AFR | ACB | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | PEL | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PEL | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0286 | AMR | PEL | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02451 | hp1 | a0001 | c0001 | t0004 | g0201 | AFR | ACB | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0318 | AFR | ACB | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | KHV | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0344 | AFR | GWD | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02622 | hp2 | a0001 | c0001 | t0005 | g0095 | AFR | GWD | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0334 | AFR | GWD | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0345 | AFR | GWD | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0270 | SAS | PJL | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0320 | SAS | PJL | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0337 | AFR | GWD | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0289 | SAS | PJL | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02809 | hp1 | a0001 | c0001 | t0004 | g0350 | AFR | GWD | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0329 | AFR | GWD | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | GWD | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0340 | AFR | ESN | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0232 | AFR | ESN | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | ESN | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ESN | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0335 | AFR | ESN | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0250 | SAS | PJL | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG03041 | hp1 | a0001 | c0001 | t0005 | g0215 | AFR | GWD | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0349 | AFR | MSL | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | MSL | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG03130 | hp1 | a0002 | c0002 | t0001 | g0228 | AFR | ESN | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0336 | AFR | ESN | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | ESN | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | MSL | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0347 | AFR | MSL | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | MSL | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | MSL | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | MSL | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | MSL | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0341 | AFR | MSL | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0346 | AFR | MSL | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0330 | SAS | PJL | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG03490 | hp2 | a0001 | c0001 | t0003 | g0156 | SAS | PJL | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0276 | SAS | PJL | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0091 | SAS | PJL | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | ESN | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0338 | AFR | ESN | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0343 | AFR | GWD | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | MSL | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0274 | SAS | PJL | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0324 | SAS | PJL | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0275 | SAS | PJL | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | STU | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | STU | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0321 | SAS | PJL | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | BEB | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | BEB | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0252 | SAS | BEB | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0191 | SAS | BEB | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0327 | SAS | STU | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | STU | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | STU | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0317 | SAS | STU | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | STU | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0262 | SAS | STU | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | STU | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | STU | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0328 | AFR | YRI | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | YRI | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18906 | hp1 | a0002 | c0002 | t0001 | g0229 | AFR | YRI | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | YRI | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0352 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0332 | AFR | LWK | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0094 | AFR | LWK | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | YRI | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0315 | AFR | YRI | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0351 | AFR | ASW | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ASW | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0093 | EUR | TSI | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0267 | EUR | TSI | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0166 | EUR | TSI | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0140 | EUR | TSI | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | GIH | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0287 | SAS | GIH | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | ACB | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02486 | hp2 | a0001 | c0001 | t0004 | g0196 | AFR | ACB | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0342 | AFR | ACB | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | ACB | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | MSL | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0348 | AFR | MSL | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | USA | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | USA | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0299 | AFR | USA | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | USA | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0333 | AFR | LWK | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | LWK | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0047 | REF | REF | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0011 | REF | REF | AP3S1_chr5_115836935_115919081 | AP3S1 | chr5 | 115836935 | 115919081 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:115913362 | G | A | 1 | a0002 | 2 | HG03130.hp1 NA18906.hp1 |
missense_variant&splice_region_variant | MODERATE | c.454G>A | p.Ala152Thr | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 6/6 | 557/1276 | 454/582 | 152/193 | chr5 | 115913362 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:115842024 | G | C | 1 | a0001c0001t0003 | 5 | HG01256.hp1 HG01258.hp2 HG02145.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-14G>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/6 | 14 | chr5 | 115842024 | ||||||
chr5:115913723 | T | A | 1 | a0001c0001t0004 | 3 | HG02451.hp1 HG02486.hp2 HG02809.hp1 |
3_prime_UTR_variant | MODIFIER | c.*233T>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 6/6 | 233 | chr5 | 115913723 | ||||||
chr5:115913852 | G | A | 1 | a0001c0001t0005 | 3 | HG02055.hp2 HG02622.hp2 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*362G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 6/6 | 362 | chr5 | 115913852 | ||||||
chr5:115913980 | C | CT | 1 | a0001c0001t0005 | 3 | HG02055.hp2 HG02622.hp2 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*491dupT | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 6/6 | 492 | INFO_REALIGN_3_PRIME | chr5 | 115913980 | |||||
chr5:115913982 | A | T | 1 | a0001c0001t0005 | 3 | HG02055.hp2 HG02622.hp2 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*492A>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 6/6 | 492 | chr5 | 115913982 | ||||||
chr5:115914036 | C | G | 1 | a0001c0001t0002 | 8 | HG02615.hp2 HG02630.hp2 HG02809.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*546C>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 6/6 | 546 | chr5 | 115914036 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:115842260 | G | T | 1 | a0001c0001t0001g0352 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.69+154G>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115842260 | |||||||
chr5:115842372 | AGGCCCTG others(17): Show |
A | 1 | a0001c0001t0001g0019 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.69+273_69+296delGG others(22): Show |
AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 115842372 | ||||||
chr5:115842451 | A | C | 20 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(17): Show |
20 | HG02257.hp1 HG02559.hp1 HG02615.hp2 others(17): Show |
intron_variant | MODIFIER | c.69+345A>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115842451 | |||||||
chr5:115842470 | C | T | 1 | a0001c0001t0001g0351 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.69+364C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115842470 | |||||||
chr5:115842507 | GCCCGGGA others(19): Show |
G | 1 | a0001c0001t0004g0350 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.69+403_69+428delCC others(24): Show |
AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 115842507 | ||||||
chr5:115842551 | C | G | 1 | a0001c0001t0001g0331 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.69+445C>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115842551 | |||||||
chr5:115842636 | T | C | 1 | a0001c0001t0001g0020 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.69+530T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115842636 | |||||||
chr5:115842670 | C | G | 1 | a0001c0001t0001g0330 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.69+564C>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115842670 | |||||||
chr5:115842698 | C | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(151): Show |
168 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.69+592C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115842698 | |||||||
chr5:115842746 | C | G | 2 | a0001c0001t0002g0328 a0001c0001t0002g0329 |
2 | HG02809.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.69+640C>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115842746 | |||||||
chr5:115842790 | G | A | 3 | a0001c0001t0003g0021 a0001c0001t0003g0022 a0001c0001t0003g0023 |
3 | HG01256.hp1 HG01258.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.69+684G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115842790 | |||||||
chr5:115842836 | C | T | 3 | a0001c0001t0001g0348 a0001c0001t0001g0349 a0001c0001t0001g0351 |
3 | HG03098.hp1 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.69+730C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115842836 | |||||||
chr5:115842963 | A | AATAGTAG others(1): Show |
11 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0210 others(8): Show |
11 | HG01496.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.69+860_69+867dupAG others(6): Show |
AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 115842963 | ||||||
chr5:115842992 | A | AG | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(151): Show |
168 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.69+886_69+887insG | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115842992 | |||||||
chr5:115843166 | A | G | 20 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(17): Show |
20 | HG02257.hp1 HG02559.hp1 HG02615.hp2 others(17): Show |
intron_variant | MODIFIER | c.69+1060A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115843166 | |||||||
chr5:115843236 | G | T | 2 | a0001c0001t0001g0216 a0001c0001t0001g0217 |
2 | HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.69+1130G>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115843236 | |||||||
chr5:115843457 | T | C | 5 | a0001c0001t0001g0332 a0001c0001t0001g0348 a0001c0001t0001g0349 others(2): Show |
5 | HG02809.hp1 HG03098.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.69+1351T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115843457 | |||||||
chr5:115843527 | A | G | 1 | a0001c0001t0001g0330 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.69+1421A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115843527 | |||||||
chr5:115843543 | A | G | 11 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0210 others(8): Show |
11 | HG01496.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.69+1437A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115843543 | |||||||
chr5:115843646 | A | G | 1 | a0001c0001t0001g0207 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.69+1540A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115843646 | |||||||
chr5:115843649 | A | G | 2 | a0001c0001t0001g0205 a0001c0001t0001g0206 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.69+1543A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115843649 | |||||||
chr5:115843762 | T | C | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.69+1656T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115843762 | |||||||
chr5:115843995 | T | C | 7 | a0001c0001t0001g0002 a0001c0001t0001g0218 a0001c0001t0001g0219 others(4): Show |
10 | HG01255.hp2 HG01981.hp2 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.69+1889T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115843995 | |||||||
chr5:115844023 | C | T | 1 | a0001c0001t0001g0204 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.69+1917C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115844023 | |||||||
chr5:115844026 | T | G | 20 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(17): Show |
20 | HG02257.hp1 HG02559.hp1 HG02615.hp2 others(17): Show |
intron_variant | MODIFIER | c.69+1920T>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115844026 | |||||||
chr5:115844090 | T | A | 1 | a0001c0001t0001g0026 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.69+1984T>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115844090 | |||||||
chr5:115844100 | T | A | 1 | a0001c0001t0001g0224 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.69+1994T>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115844100 | |||||||
chr5:115844177 | A | G | 1 | a0001c0001t0001g0330 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.69+2071A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115844177 | |||||||
chr5:115844449 | G | A | 3 | a0001c0001t0001g0020 a0001c0001t0001g0225 a0001c0001t0001g0226 |
3 | HG02717.hp1 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.69+2343G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115844449 | |||||||
chr5:115844523 | A | G | 1 | a0001c0001t0001g0013 | 2 | HG02615.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.69+2417A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115844523 | |||||||
chr5:115844628 | G | A | 2 | a0001c0001t0001g0027 a0001c0001t0001g0028 |
2 | HG03704.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.69+2522G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115844628 | |||||||
chr5:115844709 | C | G | 1 | a0001c0001t0001g0203 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.69+2603C>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115844709 | |||||||
chr5:115844719 | G | A | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(113): Show |
130 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.69+2613G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115844719 | |||||||
chr5:115844732 | A | G | 11 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0210 others(8): Show |
11 | HG01496.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.69+2626A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115844732 | |||||||
chr5:115844861 | A | G | 2 | a0001c0001t0001g0322 a0001c0001t0001g0323 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.69+2755A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115844861 | |||||||
chr5:115844949 | CTAACTCT others(14): Show |
C | 11 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0210 others(8): Show |
11 | HG01496.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.69+2846_69+2866del others(21): Show |
AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 115844949 | ||||||
chr5:115845141 | C | A | 11 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0210 others(8): Show |
11 | HG01496.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.69+3035C>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115845141 | |||||||
chr5:115845210 | T | G | 1 | a0001c0001t0001g0331 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.69+3104T>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115845210 | |||||||
chr5:115845353 | T | C | 1 | a0001c0001t0001g0227 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.69+3247T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115845353 | |||||||
chr5:115845362 | A | T | 1 | a0001c0001t0001g0321 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.69+3256A>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115845362 | |||||||
chr5:115845441 | G | C | 1 | a0001c0001t0001g0208 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.69+3335G>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115845441 | |||||||
chr5:115845462 | T | C | 1 | a0001c0001t0004g0350 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.69+3356T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115845462 | |||||||
chr5:115845491 | T | C | 1 | a0001c0001t0001g0324 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.69+3385T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115845491 | |||||||
chr5:115845697 | G | T | 1 | a0001c0001t0001g0330 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.69+3591G>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115845697 | |||||||
chr5:115845836 | C | CA | 80 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(77): Show |
87 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.69+3768dupA | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 115845836 | ||||||
chr5:115845836 | C | CAA | 10 | a0001c0001t0001g0006 a0001c0001t0001g0043 a0001c0001t0001g0044 others(7): Show |
11 | HG00423.hp2 HG01081.hp1 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.69+3767_69+3768dup others(2): Show |
AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 115845836 | ||||||
chr5:115845836 | C | CAAA | 13 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0032 others(10): Show |
13 | HG00423.hp1 HG00738.hp1 HG01256.hp2 others(10): Show |
intron_variant | MODIFIER | c.69+3766_69+3768dup others(3): Show |
AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 115845836 | ||||||
chr5:115845836 | C | CAAAAAAA others(5): Show |
3 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0002c0002t0001g0229 |
3 | HG01243.hp2 HG03139.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.69+3757_69+3768dup others(12): Show |
AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 115845836 | ||||||
chr5:115845836 | C | CAAAAAAA others(6): Show |
1 | a0002c0002t0001g0228 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.69+3756_69+3768dup others(13): Show |
AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 115845836 | ||||||
chr5:115845836 | C | CAAAAAAA others(8): Show |
1 | a0001c0001t0001g0029 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.69+3754_69+3768dup others(15): Show |
AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 115845836 | ||||||
chr5:115845836 | CA | C | 9 | a0001c0001t0001g0025 a0001c0001t0001g0188 a0001c0001t0001g0189 others(6): Show |
9 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.69+3768delA | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 115845836 | ||||||
chr5:115845836 | CAAAA | C | 6 | a0001c0001t0001g0225 a0001c0001t0001g0234 a0001c0001t0001g0235 others(3): Show |
6 | HG02886.hp2 HG03490.hp1 HG03704.hp2 others(3): Show |
intron_variant | MODIFIER | c.69+3765_69+3768del others(4): Show |
AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 115845836 | ||||||
chr5:115845836 | CAAAAA | C | 29 | a0001c0001t0001g0208 a0001c0001t0001g0217 a0001c0001t0001g0219 others(26): Show |
29 | HG00738.hp2 HG01071.hp2 HG01175.hp2 others(26): Show |
intron_variant | MODIFIER | c.69+3764_69+3768del others(5): Show |
AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 115845836 | ||||||
chr5:115845836 | CAAAAAA | C | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(77): Show |
94 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.69+3763_69+3768del others(6): Show |
AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 115845836 | ||||||
chr5:115845836 | CAAAAAAA others(3): Show |
C | 4 | a0001c0001t0001g0195 a0001c0001t0001g0326 a0001c0001t0001g0327 others(1): Show |
4 | HG01358.hp1 HG04115.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.69+3759_69+3768del others(10): Show |
AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 115845836 | ||||||
chr5:115845836 | CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0004g0196 a0001c0001t0004g0350 |
2 | HG02486.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.69+3758_69+3768del others(11): Show |
AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 115845836 | ||||||
chr5:115845836 | CAAAAAAA others(5): Show |
C | 3 | a0001c0001t0001g0013 a0001c0001t0001g0197 a0001c0001t0001g0198 |
4 | HG02615.hp1 HG02738.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.69+3757_69+3768del others(12): Show |
AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 115845836 | ||||||
chr5:115845836 | CAAAAAAA others(6): Show |
C | 2 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
2 | HG02735.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.69+3756_69+3768del others(13): Show |
AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 115845836 | ||||||
chr5:115845836 | CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0004g0201 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.69+3755_69+3768del others(14): Show |
AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 115845836 | ||||||
chr5:115845836 | CAAAAAAA others(9): Show |
C | 15 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0335 others(12): Show |
15 | HG02257.hp1 HG02559.hp1 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.69+3753_69+3768del others(16): Show |
AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 115845836 | ||||||
chr5:115845836 | CAAAAAAA others(10): Show |
C | 1 | a0001c0001t0001g0226 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.69+3752_69+3768del others(17): Show |
AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 115845836 | ||||||
chr5:115845836 | CAAAAAAA others(16): Show |
C | 1 | a0001c0001t0001g0202 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.69+3746_69+3768del others(23): Show |
AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 115845836 | ||||||
chr5:115845885 | G | A | 1 | a0001c0001t0001g0324 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.69+3779G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115845885 | |||||||
chr5:115846038 | C | T | 4 | a0001c0001t0001g0233 a0001c0001t0002g0232 a0002c0002t0001g0228 others(1): Show |
4 | HG02258.hp2 HG02922.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.69+3932C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115846038 | |||||||
chr5:115846071 | G | T | 1 | a0001c0001t0001g0347 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.69+3965G>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115846071 | |||||||
chr5:115846123 | A | T | 4 | a0001c0001t0001g0233 a0001c0001t0002g0232 a0002c0002t0001g0228 others(1): Show |
4 | HG02258.hp2 HG02922.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.69+4017A>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115846123 | |||||||
chr5:115846130 | C | G | 36 | a0001c0001t0001g0195 a0001c0001t0001g0208 a0001c0001t0001g0209 others(33): Show |
36 | HG00735.hp1 HG01358.hp1 HG01496.hp1 others(33): Show |
intron_variant | MODIFIER | c.69+4024C>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115846130 | |||||||
chr5:115846247 | A | G | 1 | a0001c0001t0001g0324 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.69+4141A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115846247 | |||||||
chr5:115846388 | T | A | 1 | a0001c0001t0001g0123 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.69+4282T>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115846388 | |||||||
chr5:115846446 | A | T | 23 | a0001c0001t0001g0195 a0001c0001t0001g0325 a0001c0001t0001g0326 others(20): Show |
23 | HG00735.hp1 HG01358.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.69+4340A>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115846446 | |||||||
chr5:115846555 | GT | G | 11 | a0001c0001t0001g0010 a0001c0001t0001g0043 a0001c0001t0001g0053 others(8): Show |
12 | HG01167.hp2 HG01928.hp2 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.69+4466delT | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 115846555 | ||||||
chr5:115846565 | T | C | 2 | a0001c0001t0001g0348 a0001c0001t0001g0349 |
2 | HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.69+4459T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115846565 | |||||||
chr5:115846573 | A | T | 1 | a0001c0001t0001g0217 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.69+4467A>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115846573 | |||||||
chr5:115846758 | G | A | 11 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0335 others(8): Show |
11 | HG02257.hp1 HG02559.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.69+4652G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115846758 | |||||||
chr5:115846775 | C | T | 3 | a0001c0001t0001g0340 a0001c0001t0001g0341 a0001c0001t0001g0342 |
3 | HG02559.hp1 HG02922.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.69+4669C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115846775 | |||||||
chr5:115846824 | C | T | 1 | a0001c0001t0001g0187 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.69+4718C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115846824 | |||||||
chr5:115846829 | T | C | 1 | a0001c0001t0001g0324 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.69+4723T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115846829 | |||||||
chr5:115846909 | A | G | 5 | a0001c0001t0001g0195 a0001c0001t0001g0325 a0001c0001t0001g0326 others(2): Show |
5 | HG00735.hp1 HG01358.hp1 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.69+4803A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115846909 | |||||||
chr5:115846951 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.69+4845G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115846951 | |||||||
chr5:115847112 | A | G | 2 | a0001c0001t0001g0348 a0001c0001t0001g0349 |
2 | HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.69+5006A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115847112 | |||||||
chr5:115847116 | C | G | 1 | a0001c0001t0001g0257 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.69+5010C>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115847116 | |||||||
chr5:115847268 | A | T | 1 | a0001c0001t0001g0320 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.69+5162A>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115847268 | |||||||
chr5:115847433 | C | T | 1 | a0001c0001t0001g0319 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.69+5327C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115847433 | |||||||
chr5:115847536 | C | CT | 15 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0335 others(12): Show |
15 | HG02257.hp1 HG02559.hp1 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.69+5431dupT | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 115847536 | ||||||
chr5:115847545 | G | A | 1 | a0001c0001t0001g0259 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.69+5439G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115847545 | |||||||
chr5:115847586 | T | A | 6 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(3): Show |
6 | HG02055.hp2 HG02572.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.69+5480T>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115847586 | |||||||
chr5:115847601 | A | G | 2 | a0001c0001t0002g0328 a0001c0001t0002g0329 |
2 | HG02809.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.69+5495A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115847601 | |||||||
chr5:115847638 | T | C | 1 | a0001c0001t0001g0237 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.69+5532T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115847638 | |||||||
chr5:115847657 | A | G | 1 | a0001c0001t0001g0186 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.69+5551A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115847657 | |||||||
chr5:115847909 | A | G | 1 | a0001c0001t0002g0329 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.69+5803A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115847909 | |||||||
chr5:115847959 | A | G | 1 | a0001c0001t0001g0018 | 2 | HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.69+5853A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115847959 | |||||||
chr5:115847979 | T | C | 1 | a0001c0001t0001g0260 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.69+5873T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115847979 | |||||||
chr5:115848152 | C | CTTTAGCA others(18): Show |
15 | a0001c0001t0001g0195 a0001c0001t0001g0208 a0001c0001t0001g0209 others(12): Show |
15 | HG00735.hp1 HG01358.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.69+6047_69+6071dup others(25): Show |
AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 115848152 | ||||||
chr5:115848473 | A | G | 1 | a0001c0001t0001g0256 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.69+6367A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115848473 | |||||||
chr5:115848562 | G | T | 1 | a0001c0001t0001g0185 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.69+6456G>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115848562 | |||||||
chr5:115848632 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.69+6526C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115848632 | |||||||
chr5:115848717 | C | G | 3 | a0001c0001t0001g0348 a0001c0001t0001g0349 a0001c0001t0001g0351 |
3 | HG03098.hp1 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.69+6611C>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115848717 | |||||||
chr5:115848753 | T | C | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(109): Show |
126 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.69+6647T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115848753 | |||||||
chr5:115848790 | T | C | 21 | a0001c0001t0001g0324 a0001c0001t0001g0332 a0001c0001t0001g0333 others(18): Show |
21 | HG02257.hp1 HG02559.hp1 HG02615.hp2 others(18): Show |
intron_variant | MODIFIER | c.69+6684T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115848790 | |||||||
chr5:115848823 | C | G | 3 | a0001c0001t0001g0017 a0001c0001t0001g0257 a0001c0001t0001g0318 |
4 | HG01884.hp2 HG02451.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.69+6717C>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115848823 | |||||||
chr5:115849025 | TCTTTCTG others(4): Show |
T | 1 | a0001c0001t0001g0333 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.69+6927_69+6937del others(11): Show |
AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 115849025 | ||||||
chr5:115849173 | T | G | 1 | a0001c0001t0001g0324 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.69+7067T>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115849173 | |||||||
chr5:115849185 | T | G | 1 | a0001c0001t0001g0332 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.69+7079T>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115849185 | |||||||
chr5:115849513 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.69+7407G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115849513 | |||||||
chr5:115849617 | C | T | 1 | a0001c0001t0001g0121 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.69+7511C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115849617 | |||||||
chr5:115849641 | C | T | 1 | a0001c0001t0001g0324 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.69+7535C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115849641 | |||||||
chr5:115849714 | A | G | 1 | a0001c0001t0001g0029 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.69+7608A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115849714 | |||||||
chr5:115849867 | G | A | 2 | a0001c0001t0002g0328 a0001c0001t0002g0329 |
2 | HG02809.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.69+7761G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115849867 | |||||||
chr5:115849874 | A | G | 1 | a0001c0001t0004g0350 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.69+7768A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115849874 | |||||||
chr5:115849984 | C | T | 1 | a0001c0001t0001g0120 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.69+7878C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115849984 | |||||||
chr5:115850092 | C | A | 1 | a0001c0001t0001g0330 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.69+7986C>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115850092 | |||||||
chr5:115850292 | C | CCTG | 3 | a0001c0001t0001g0324 a0001c0001t0001g0332 a0001c0001t0004g0350 |
3 | HG02809.hp1 HG03654.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.69+8188_69+8189ins others(3): Show |
AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 115850292 | ||||||
chr5:115850493 | C | T | 2 | a0001c0001t0001g0332 a0001c0001t0004g0350 |
2 | HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.69+8387C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115850493 | |||||||
chr5:115850702 | T | G | 2 | a0001c0001t0001g0332 a0001c0001t0004g0350 |
2 | HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.69+8596T>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115850702 | |||||||
chr5:115850820 | T | C | 1 | a0001c0001t0001g0122 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.69+8714T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115850820 | |||||||
chr5:115850910 | T | G | 1 | a0001c0001t0001g0334 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.69+8804T>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115850910 | |||||||
chr5:115851131 | T | C | 14 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0335 others(11): Show |
14 | HG02257.hp1 HG02559.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.69+9025T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115851131 | |||||||
chr5:115851202 | T | C | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(142): Show |
157 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.69+9096T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115851202 | |||||||
chr5:115851297 | A | G | 1 | a0001c0001t0001g0339 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.69+9191A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115851297 | |||||||
chr5:115851551 | G | T | 1 | a0001c0001t0001g0313 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.69+9445G>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115851551 | |||||||
chr5:115851851 | T | G | 1 | a0001c0001t0001g0019 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.69+9745T>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115851851 | |||||||
chr5:115851983 | GAGATTA | G | 15 | a0001c0001t0001g0195 a0001c0001t0001g0208 a0001c0001t0001g0209 others(12): Show |
15 | HG00735.hp1 HG01358.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.69+9879_69+9884del others(6): Show |
AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 115851983 | ||||||
chr5:115852081 | C | G | 1 | a0001c0001t0001g0332 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.69+9975C>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115852081 | |||||||
chr5:115852098 | A | T | 1 | a0001c0001t0001g0332 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.69+9992A>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115852098 | |||||||
chr5:115852114 | T | C | 1 | a0001c0001t0001g0032 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.69+10008T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115852114 | |||||||
chr5:115852245 | A | C | 1 | a0001c0001t0001g0324 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.69+10139A>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115852245 | |||||||
chr5:115852332 | C | T | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(88): Show |
103 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(100): Show |
intron_variant | MODIFIER | c.69+10226C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115852332 | |||||||
chr5:115852570 | T | A | 126 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(123): Show |
138 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.69+10464T>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115852570 | |||||||
chr5:115852617 | T | C | 143 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(140): Show |
155 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.69+10511T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115852617 | |||||||
chr5:115852841 | A | G | 14 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0335 others(11): Show |
14 | HG02257.hp1 HG02559.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.69+10735A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115852841 | |||||||
chr5:115852880 | G | A | 1 | a0001c0001t0001g0330 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.69+10774G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115852880 | |||||||
chr5:115852963 | A | G | 143 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(140): Show |
155 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.69+10857A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115852963 | |||||||
chr5:115852987 | A | C | 1 | a0001c0001t0001g0332 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.69+10881A>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115852987 | |||||||
chr5:115853039 | A | G | 1 | a0001c0001t0001g0332 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.69+10933A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115853039 | |||||||
chr5:115853218 | A | G | 14 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0335 others(11): Show |
14 | HG02257.hp1 HG02559.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.69+11112A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115853218 | |||||||
chr5:115853260 | A | G | 1 | a0001c0001t0001g0332 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.69+11154A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115853260 | |||||||
chr5:115853666 | T | G | 1 | a0001c0001t0001g0324 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.69+11560T>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115853666 | |||||||
chr5:115853803 | A | G | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(241): Show |
261 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.69+11697A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115853803 | |||||||
chr5:115853823 | A | T | 1 | a0001c0001t0001g0324 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.69+11717A>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115853823 | |||||||
chr5:115853912 | A | G | 1 | a0001c0001t0001g0324 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.69+11806A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115853912 | |||||||
chr5:115854038 | G | T | 4 | a0001c0001t0001g0020 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG02717.hp1 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.69+11932G>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115854038 | |||||||
chr5:115854050 | C | A | 1 | a0001c0001t0001g0100 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.69+11944C>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115854050 | |||||||
chr5:115854492 | C | G | 1 | a0001c0001t0001g0119 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.70-12178C>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115854492 | |||||||
chr5:115854679 | C | CT | 6 | a0001c0001t0001g0019 a0001c0001t0001g0251 a0001c0001t0001g0324 others(3): Show |
6 | HG02280.hp1 HG02809.hp2 HG03654.hp2 others(3): Show |
intron_variant | MODIFIER | c.70-11978dupT | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 115854679 | ||||||
chr5:115854679 | C | CTT | 14 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0335 others(11): Show |
14 | HG02257.hp1 HG02559.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.70-11979_70-11978d others(4): Show |
AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 115854679 | ||||||
chr5:115854679 | CT | C | 5 | a0001c0001t0001g0017 a0001c0001t0001g0161 a0001c0001t0001g0257 others(2): Show |
6 | HG01884.hp2 HG02451.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.70-11978delT | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 115854679 | ||||||
chr5:115854681 | T | C | 1 | a0001c0001t0001g0261 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.70-11989T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115854681 | |||||||
chr5:115854931 | T | G | 1 | a0001c0001t0001g0224 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.70-11739T>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115854931 | |||||||
chr5:115854966 | T | C | 1 | a0001c0001t0001g0262 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.70-11704T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115854966 | |||||||
chr5:115854967 | A | G | 14 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0335 others(11): Show |
14 | HG02257.hp1 HG02559.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.70-11703A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115854967 | |||||||
chr5:115854992 | ATG | A | 8 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0210 others(5): Show |
8 | HG01891.hp1 HG02486.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.70-11666_70-11665d others(4): Show |
AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 115854992 | ||||||
chr5:115855019 | A | ATATC | 82 | a0001c0001t0001g0013 a0001c0001t0001g0028 a0001c0001t0001g0030 others(79): Show |
83 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.70-11609_70-11606d others(6): Show |
AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 115855019 | ||||||
chr5:115855019 | A | ATATCTAT others(1): Show |
18 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0027 others(15): Show |
20 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(17): Show |
intron_variant | MODIFIER | c.70-11613_70-11606d others(10): Show |
AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 115855019 | ||||||
chr5:115855019 | A | ATATCTAT others(5): Show |
2 | a0001c0001t0001g0056 a0001c0001t0001g0101 |
2 | HG03540.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.70-11617_70-11606d others(14): Show |
AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 115855019 | ||||||
chr5:115855019 | ATATC | A | 31 | a0001c0001t0001g0020 a0001c0001t0001g0042 a0001c0001t0001g0048 others(28): Show |
31 | HG00438.hp1 HG00741.hp1 HG01496.hp1 others(28): Show |
intron_variant | MODIFIER | c.70-11609_70-11606d others(6): Show |
AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 115855019 | ||||||
chr5:115855019 | ATATCTAT others(9): Show |
A | 1 | a0001c0001t0004g0350 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.70-11621_70-11606d others(18): Show |
AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 115855019 | ||||||
chr5:115855139 | C | T | 1 | a0001c0001t0001g0108 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.70-11531C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115855139 | |||||||
chr5:115855155 | G | A | 1 | a0001c0001t0001g0282 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.70-11515G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115855155 | |||||||
chr5:115855287 | C | T | 1 | a0001c0001t0001g0324 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.70-11383C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115855287 | |||||||
chr5:115855310 | A | G | 2 | a0001c0001t0001g0348 a0001c0001t0001g0349 |
2 | HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.70-11360A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115855310 | |||||||
chr5:115855370 | C | T | 1 | a0001c0001t0001g0332 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.70-11300C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115855370 | |||||||
chr5:115855407 | C | T | 1 | a0001c0001t0001g0330 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.70-11263C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115855407 | |||||||
chr5:115855421 | C | T | 1 | a0001c0001t0003g0022 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.70-11249C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115855421 | |||||||
chr5:115855472 | T | G | 12 | a0001c0001t0001g0007 a0001c0001t0001g0026 a0001c0001t0001g0048 others(9): Show |
13 | HG00597.hp2 HG02080.hp2 HG02083.hp2 others(10): Show |
intron_variant | MODIFIER | c.70-11198T>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115855472 | |||||||
chr5:115855505 | A | G | 1 | a0001c0001t0001g0318 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.70-11165A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115855505 | |||||||
chr5:115855588 | C | T | 1 | a0001c0001t0001g0019 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.70-11082C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115855588 | |||||||
chr5:115855654 | C | T | 9 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0210 others(6): Show |
9 | HG01496.hp1 HG01891.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.70-11016C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115855654 | |||||||
chr5:115855770 | T | A | 4 | a0001c0001t0001g0020 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG02717.hp1 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.70-10900T>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115855770 | |||||||
chr5:115855926 | A | G | 1 | a0001c0001t0001g0158 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.70-10744A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115855926 | |||||||
chr5:115856145 | A | G | 8 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(5): Show |
8 | HG01070.hp2 HG01071.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.70-10525A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115856145 | |||||||
chr5:115856336 | A | G | 1 | a0001c0001t0001g0051 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.70-10334A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115856336 | |||||||
chr5:115856367 | G | A | 1 | a0001c0001t0001g0351 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.70-10303G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115856367 | |||||||
chr5:115856432 | CT | C | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(137): Show |
152 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.70-10223delT | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 115856432 | ||||||
chr5:115856572 | C | T | 1 | a0001c0001t0005g0215 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.70-10098C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115856572 | |||||||
chr5:115856642 | C | CATT | 142 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(139): Show |
154 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.70-10028_70-10027i others(5): Show |
AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115856642 | |||||||
chr5:115856643 | G | T | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(138): Show |
153 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.70-10027G>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115856643 | |||||||
chr5:115856846 | T | G | 1 | a0001c0001t0001g0332 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.70-9824T>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115856846 | |||||||
chr5:115856893 | A | G | 1 | a0001c0001t0001g0182 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.70-9777A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115856893 | |||||||
chr5:115856933 | G | A | 125 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(122): Show |
137 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(134): Show |
intron_variant | MODIFIER | c.70-9737G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115856933 | |||||||
chr5:115856989 | C | T | 79 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(76): Show |
91 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.70-9681C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115856989 | |||||||
chr5:115857122 | G | A | 8 | a0001c0001t0001g0036 a0001c0001t0001g0049 a0001c0001t0001g0050 others(5): Show |
8 | HG00738.hp1 HG01081.hp1 HG02015.hp1 others(5): Show |
intron_variant | MODIFIER | c.70-9548G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115857122 | |||||||
chr5:115857258 | T | A | 1 | a0001c0001t0001g0138 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.70-9412T>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115857258 | |||||||
chr5:115857324 | G | A | 2 | a0001c0001t0001g0049 a0001c0001t0001g0330 |
2 | HG02056.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.70-9346G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115857324 | |||||||
chr5:115857364 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.70-9306C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115857364 | |||||||
chr5:115857394 | C | T | 15 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0335 others(12): Show |
15 | HG02257.hp1 HG02559.hp1 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.70-9276C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115857394 | |||||||
chr5:115857669 | C | T | 1 | a0001c0001t0001g0332 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.70-9001C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115857669 | |||||||
chr5:115857867 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.70-8803G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115857867 | |||||||
chr5:115858282 | C | T | 7 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0068 others(4): Show |
7 | HG01243.hp2 HG02055.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.70-8388C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115858282 | |||||||
chr5:115858411 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.70-8259G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115858411 | |||||||
chr5:115858602 | T | C | 1 | a0001c0001t0001g0320 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.70-8068T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115858602 | |||||||
chr5:115858672 | G | A | 2 | a0001c0001t0001g0283 a0001c0001t0001g0284 |
2 | NA18965.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.70-7998G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115858672 | |||||||
chr5:115858824 | A | T | 4 | a0001c0001t0002g0343 a0001c0001t0002g0344 a0001c0001t0002g0345 others(1): Show |
4 | HG02615.hp2 HG02630.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.70-7846A>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115858824 | |||||||
chr5:115858844 | A | G | 1 | a0001c0001t0001g0332 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.70-7826A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115858844 | |||||||
chr5:115858885 | T | C | 59 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0024 others(56): Show |
61 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.70-7785T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115858885 | |||||||
chr5:115858930 | A | G | 4 | a0001c0001t0001g0020 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG02717.hp1 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.70-7740A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115858930 | |||||||
chr5:115859020 | A | C | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(148): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.70-7650A>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115859020 | |||||||
chr5:115859071 | A | G | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(83): Show |
97 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(94): Show |
intron_variant | MODIFIER | c.70-7599A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115859071 | |||||||
chr5:115859281 | C | G | 1 | a0001c0001t0001g0330 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.70-7389C>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115859281 | |||||||
chr5:115859631 | C | A | 1 | a0001c0001t0001g0351 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.70-7039C>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115859631 | |||||||
chr5:115859708 | G | A | 2 | a0001c0001t0001g0216 a0001c0001t0001g0217 |
2 | HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.70-6962G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115859708 | |||||||
chr5:115860078 | T | C | 1 | a0001c0001t0001g0332 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.70-6592T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115860078 | |||||||
chr5:115860418 | C | G | 1 | a0001c0001t0001g0324 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.70-6252C>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115860418 | |||||||
chr5:115860467 | T | C | 2 | a0001c0001t0001g0088 a0001c0001t0001g0125 |
2 | HG01099.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.70-6203T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115860467 | |||||||
chr5:115860493 | G | C | 1 | a0001c0001t0001g0168 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.70-6177G>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115860493 | |||||||
chr5:115860531 | A | G | 1 | a0001c0001t0001g0324 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.70-6139A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115860531 | |||||||
chr5:115860588 | A | T | 1 | a0001c0001t0001g0324 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.70-6082A>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115860588 | |||||||
chr5:115860682 | T | C | 1 | a0001c0001t0002g0094 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.70-5988T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115860682 | |||||||
chr5:115860712 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.70-5958G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115860712 | |||||||
chr5:115860726 | C | T | 1 | a0001c0001t0001g0019 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.70-5944C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115860726 | |||||||
chr5:115860897 | A | G | 4 | a0001c0001t0001g0101 a0001c0001t0001g0270 a0001c0001t0001g0274 others(1): Show |
4 | HG02683.hp2 HG03654.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.70-5773A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115860897 | |||||||
chr5:115860940 | T | C | 20 | a0001c0001t0001g0061 a0001c0001t0001g0224 a0001c0001t0001g0238 others(17): Show |
20 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.70-5730T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115860940 | |||||||
chr5:115860990 | C | T | 1 | a0001c0001t0001g0249 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.70-5680C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115860990 | |||||||
chr5:115861054 | C | T | 1 | a0001c0001t0001g0281 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.70-5616C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115861054 | |||||||
chr5:115861095 | A | G | 20 | a0001c0001t0001g0061 a0001c0001t0001g0224 a0001c0001t0001g0238 others(17): Show |
20 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.70-5575A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115861095 | |||||||
chr5:115861181 | G | C | 1 | a0001c0001t0001g0050 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.70-5489G>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115861181 | |||||||
chr5:115861291 | T | C | 1 | a0001c0001t0001g0019 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.70-5379T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115861291 | |||||||
chr5:115861437 | AT | A | 3 | a0001c0001t0001g0013 a0001c0001t0001g0198 a0001c0001t0004g0196 |
4 | HG02486.hp2 HG02615.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.70-5232delT | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115861437 | |||||||
chr5:115861571 | T | C | 1 | a0001c0001t0001g0122 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.70-5099T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115861571 | |||||||
chr5:115861642 | C | T | 13 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0336 others(10): Show |
13 | HG02257.hp1 HG02559.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.70-5028C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115861642 | |||||||
chr5:115861850 | A | T | 1 | a0001c0001t0001g0339 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.70-4820A>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115861850 | |||||||
chr5:115861856 | T | C | 1 | a0001c0001t0001g0330 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.70-4814T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115861856 | |||||||
chr5:115861860 | C | CT | 50 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0088 others(47): Show |
52 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.70-4806dupT | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 115861860 | ||||||
chr5:115861860 | C | CTT | 4 | a0001c0001t0001g0217 a0001c0001t0001g0309 a0001c0001t0001g0351 others(1): Show |
4 | HG01891.hp1 HG02004.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.70-4807_70-4806dup others(2): Show |
AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 115861860 | ||||||
chr5:115861860 | CTTTTCTT others(4): Show |
C | 2 | a0001c0001t0001g0341 a0001c0001t0001g0342 |
2 | HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.70-4805_70-4795del others(11): Show |
AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 115861860 | ||||||
chr5:115861864 | TC | T | 4 | a0001c0001t0001g0248 a0001c0001t0001g0310 a0001c0001t0001g0311 others(1): Show |
4 | HG01975.hp1 NA18939.hp2 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.70-4805delC | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115861864 | |||||||
chr5:115861865 | C | CT | 13 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(10): Show |
13 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.70-4786dupT | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 115861865 | ||||||
chr5:115861865 | C | T | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(132): Show |
149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.70-4805C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115861865 | |||||||
chr5:115861865 | CT | C | 10 | a0001c0001t0001g0008 a0001c0001t0001g0057 a0001c0001t0001g0136 others(7): Show |
10 | HG01168.hp1 HG01168.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.70-4786delT | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 115861865 | ||||||
chr5:115861870 | T | C | 4 | a0001c0001t0001g0033 a0001c0001t0001g0065 a0001c0001t0001g0169 others(1): Show |
4 | HG00438.hp2 HG01081.hp2 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.70-4800T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115861870 | |||||||
chr5:115862106 | T | C | 1 | a0001c0001t0001g0271 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.70-4564T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115862106 | |||||||
chr5:115862334 | A | T | 13 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0336 others(10): Show |
13 | HG02257.hp1 HG02559.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.70-4336A>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115862334 | |||||||
chr5:115862451 | T | G | 1 | a0001c0001t0001g0048 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.70-4219T>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115862451 | |||||||
chr5:115862494 | C | G | 1 | a0001c0001t0002g0346 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.70-4176C>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115862494 | |||||||
chr5:115862494 | C | T | 1 | a0001c0001t0001g0269 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.70-4176C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115862494 | |||||||
chr5:115862653 | A | G | 1 | a0001c0001t0001g0216 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.70-4017A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115862653 | |||||||
chr5:115862847 | G | A | 1 | a0001c0001t0001g0029 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.70-3823G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115862847 | |||||||
chr5:115862881 | G | A | 14 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0336 others(11): Show |
14 | HG02257.hp1 HG02559.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.70-3789G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115862881 | |||||||
chr5:115863105 | G | A | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(137): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.70-3565G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115863105 | |||||||
chr5:115863126 | G | A | 5 | a0001c0001t0001g0020 a0001c0001t0001g0225 a0001c0001t0001g0226 others(2): Show |
5 | HG02717.hp1 HG02809.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.70-3544G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115863126 | |||||||
chr5:115863189 | G | A | 1 | a0001c0001t0001g0324 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.70-3481G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115863189 | |||||||
chr5:115863237 | A | C | 6 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(3): Show |
6 | HG01070.hp2 HG01071.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.70-3433A>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115863237 | |||||||
chr5:115863269 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.70-3401C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115863269 | |||||||
chr5:115863398 | A | T | 1 | a0001c0001t0001g0213 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.70-3272A>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115863398 | |||||||
chr5:115863442 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.70-3228G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115863442 | |||||||
chr5:115863467 | G | T | 1 | a0001c0001t0001g0257 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.70-3203G>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115863467 | |||||||
chr5:115863663 | T | C | 5 | a0001c0001t0001g0020 a0001c0001t0001g0225 a0001c0001t0001g0226 others(2): Show |
5 | HG02717.hp1 HG02809.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.70-3007T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115863663 | |||||||
chr5:115863669 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.70-3001C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115863669 | |||||||
chr5:115863670 | G | A | 9 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0231 others(6): Show |
11 | HG01074.hp1 HG01361.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.70-3000G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115863670 | |||||||
chr5:115863722 | A | G | 1 | a0001c0001t0001g0324 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.70-2948A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115863722 | |||||||
chr5:115863743 | A | G | 3 | a0001c0001t0001g0325 a0001c0001t0001g0326 a0001c0001t0001g0327 |
3 | HG00735.hp1 HG01358.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.70-2927A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115863743 | |||||||
chr5:115863924 | G | A | 2 | a0001c0001t0001g0027 a0001c0001t0001g0028 |
2 | HG03704.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.70-2746G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115863924 | |||||||
chr5:115863964 | T | C | 1 | a0001c0001t0001g0324 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.70-2706T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115863964 | |||||||
chr5:115864123 | A | G | 8 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0336 others(5): Show |
8 | HG02559.hp1 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.70-2547A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115864123 | |||||||
chr5:115864161 | C | T | 1 | a0001c0001t0001g0351 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.70-2509C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115864161 | |||||||
chr5:115864211 | A | G | 1 | a0001c0001t0001g0339 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.70-2459A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115864211 | |||||||
chr5:115864253 | A | G | 1 | a0001c0001t0001g0304 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.70-2417A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115864253 | |||||||
chr5:115864353 | C | G | 13 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0336 others(10): Show |
13 | HG02257.hp1 HG02559.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.70-2317C>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115864353 | |||||||
chr5:115864388 | C | A | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(134): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.70-2282C>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115864388 | |||||||
chr5:115864494 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.70-2176G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115864494 | |||||||
chr5:115864581 | G | A | 1 | a0001c0001t0001g0159 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.70-2089G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115864581 | |||||||
chr5:115864622 | G | T | 77 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(74): Show |
88 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.70-2048G>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115864622 | |||||||
chr5:115864663 | A | G | 1 | a0001c0001t0001g0087 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.70-2007A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115864663 | |||||||
chr5:115864665 | C | G | 4 | a0001c0001t0001g0020 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG02717.hp1 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.70-2005C>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115864665 | |||||||
chr5:115864679 | C | T | 1 | a0001c0001t0004g0350 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.70-1991C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115864679 | |||||||
chr5:115864762 | A | G | 1 | a0001c0001t0001g0258 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.70-1908A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115864762 | |||||||
chr5:115864992 | A | G | 13 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0336 others(10): Show |
13 | HG02257.hp1 HG02559.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.70-1678A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115864992 | |||||||
chr5:115865166 | G | A | 16 | a0001c0001t0001g0170 a0001c0001t0001g0192 a0001c0001t0001g0333 others(13): Show |
16 | HG02257.hp1 HG02559.hp1 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.70-1504G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115865166 | |||||||
chr5:115865410 | T | C | 1 | a0001c0001t0001g0324 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.70-1260T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115865410 | |||||||
chr5:115865448 | A | G | 1 | a0001c0001t0001g0041 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.70-1222A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115865448 | |||||||
chr5:115865473 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.70-1197G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115865473 | |||||||
chr5:115865632 | C | A | 4 | a0001c0001t0001g0233 a0001c0001t0002g0232 a0002c0002t0001g0228 others(1): Show |
4 | HG02258.hp2 HG02922.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.70-1038C>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115865632 | |||||||
chr5:115865649 | G | A | 4 | a0001c0001t0001g0001 a0001c0001t0001g0240 a0001c0001t0001g0241 others(1): Show |
8 | NA18939.hp2 NA18962.hp2 NA18974.hp1 others(5): Show |
intron_variant | MODIFIER | c.70-1021G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115865649 | |||||||
chr5:115865859 | C | T | 1 | a0001c0001t0001g0137 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.70-811C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115865859 | |||||||
chr5:115865965 | T | C | 2 | a0001c0001t0001g0044 a0001c0001t0001g0202 |
2 | HG02683.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.70-705T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115865965 | |||||||
chr5:115865987 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.70-683G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115865987 | |||||||
chr5:115866091 | C | T | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(88): Show |
103 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(100): Show |
intron_variant | MODIFIER | c.70-579C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115866091 | |||||||
chr5:115866171 | T | C | 1 | a0001c0001t0001g0351 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.70-499T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115866171 | |||||||
chr5:115866182 | A | T | 1 | a0001c0001t0001g0019 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.70-488A>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115866182 | |||||||
chr5:115866187 | A | G | 1 | a0001c0001t0001g0324 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.70-483A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115866187 | |||||||
chr5:115866192 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.70-478G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115866192 | |||||||
chr5:115866254 | C | A | 1 | a0001c0001t0001g0207 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.70-416C>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115866254 | |||||||
chr5:115866313 | T | A | 1 | a0001c0001t0001g0351 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.70-357T>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115866313 | |||||||
chr5:115866591 | A | G | 1 | a0001c0001t0002g0345 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.70-79A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115866591 | |||||||
chr5:115866641 | C | G | 1 | a0001c0001t0001g0303 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.70-29C>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 1/5 | chr5 | 115866641 | |||||||
chr5:115867094 | T | C | 2 | a0001c0001t0001g0103 a0001c0001t0001g0163 |
2 | HG02976.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.161+333T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 2/5 | chr5 | 115867094 | |||||||
chr5:115867095 | A | T | 1 | a0001c0001t0001g0324 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.161+334A>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 2/5 | chr5 | 115867095 | |||||||
chr5:115867165 | A | T | 2 | a0001c0001t0001g0302 a0001c0001t0001g0312 |
2 | NA19005.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.161+404A>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 2/5 | chr5 | 115867165 | |||||||
chr5:115867176 | C | T | 1 | a0001c0001t0001g0179 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.161+415C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 2/5 | chr5 | 115867176 | |||||||
chr5:115867216 | T | C | 1 | a0001c0001t0001g0324 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.161+455T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 2/5 | chr5 | 115867216 | |||||||
chr5:115867232 | G | T | 1 | a0001c0001t0001g0324 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.161+471G>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 2/5 | chr5 | 115867232 | |||||||
chr5:115867450 | A | G | 1 | a0001c0001t0001g0308 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.161+689A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 2/5 | chr5 | 115867450 | |||||||
chr5:115867457 | T | C | 1 | a0001c0001t0001g0324 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.161+696T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 2/5 | chr5 | 115867457 | |||||||
chr5:115867467 | T | G | 4 | a0001c0001t0001g0233 a0001c0001t0002g0232 a0002c0002t0001g0228 others(1): Show |
4 | HG02258.hp2 HG02922.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.161+706T>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 2/5 | chr5 | 115867467 | |||||||
chr5:115867500 | T | G | 1 | a0001c0001t0001g0117 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.161+739T>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 2/5 | chr5 | 115867500 | |||||||
chr5:115867529 | G | T | 1 | a0001c0001t0001g0076 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.161+768G>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 2/5 | chr5 | 115867529 | |||||||
chr5:115867554 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.161+793C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 2/5 | chr5 | 115867554 | |||||||
chr5:115867566 | G | T | 1 | a0001c0001t0001g0324 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.161+805G>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 2/5 | chr5 | 115867566 | |||||||
chr5:115867653 | T | C | 1 | a0001c0001t0001g0305 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.161+892T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 2/5 | chr5 | 115867653 | |||||||
chr5:115867867 | A | G | 4 | a0001c0001t0001g0020 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG02717.hp1 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.161+1106A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 2/5 | chr5 | 115867867 | |||||||
chr5:115868181 | T | C | 1 | a0001c0001t0001g0335 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.161+1420T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 2/5 | chr5 | 115868181 | |||||||
chr5:115868244 | A | G | 2 | a0001c0001t0001g0283 a0001c0001t0001g0284 |
2 | NA18965.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.161+1483A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 2/5 | chr5 | 115868244 | |||||||
chr5:115868393 | C | G | 2 | a0001c0001t0001g0114 a0001c0001t0001g0169 |
2 | NA18955.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.162-1624C>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 2/5 | chr5 | 115868393 | |||||||
chr5:115868450 | G | T | 2 | a0001c0001t0001g0039 a0001c0001t0001g0052 |
2 | NA18965.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.162-1567G>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 2/5 | chr5 | 115868450 | |||||||
chr5:115868458 | C | T | 77 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(74): Show |
88 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.162-1559C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 2/5 | chr5 | 115868458 | |||||||
chr5:115868511 | A | G | 1 | a0001c0001t0001g0268 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.162-1506A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 2/5 | chr5 | 115868511 | |||||||
chr5:115868524 | A | T | 1 | a0001c0001t0001g0301 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.162-1493A>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 2/5 | chr5 | 115868524 | |||||||
chr5:115868571 | T | G | 1 | a0001c0001t0001g0139 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.162-1446T>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 2/5 | chr5 | 115868571 | |||||||
chr5:115868668 | G | A | 1 | a0001c0001t0001g0129 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.162-1349G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 2/5 | chr5 | 115868668 | |||||||
chr5:115868806 | C | A | 3 | a0001c0001t0001g0013 a0001c0001t0001g0198 a0001c0001t0004g0196 |
4 | HG02486.hp2 HG02615.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.162-1211C>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 2/5 | chr5 | 115868806 | |||||||
chr5:115868816 | A | G | 1 | a0001c0001t0001g0330 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.162-1201A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 2/5 | chr5 | 115868816 | |||||||
chr5:115868843 | T | C | 139 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(136): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.162-1174T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 2/5 | chr5 | 115868843 | |||||||
chr5:115868893 | G | GAGAGAGA others(5): Show |
137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(134): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.162-1118_162-1107d others(14): Show |
AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 115868893 | ||||||
chr5:115868911 | A | G | 1 | a0001c0001t0001g0339 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.162-1106A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 2/5 | chr5 | 115868911 | |||||||
chr5:115868918 | G | A | 1 | a0001c0001t0001g0339 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.162-1099G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 2/5 | chr5 | 115868918 | |||||||
chr5:115868920 | T | A | 1 | a0001c0001t0001g0339 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.162-1097T>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 2/5 | chr5 | 115868920 | |||||||
chr5:115868923 | A | G | 1 | a0001c0001t0001g0339 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.162-1094A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 2/5 | chr5 | 115868923 | |||||||
chr5:115868924 | G | A | 1 | a0001c0001t0001g0339 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.162-1093G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 2/5 | chr5 | 115868924 | |||||||
chr5:115868928 | G | T | 1 | a0001c0001t0001g0339 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.162-1089G>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 2/5 | chr5 | 115868928 | |||||||
chr5:115868930 | G | A | 1 | a0001c0001t0001g0339 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.162-1087G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 2/5 | chr5 | 115868930 | |||||||
chr5:115868936 | GGGAA | G | 7 | a0001c0001t0001g0020 a0001c0001t0001g0030 a0001c0001t0001g0031 others(4): Show |
7 | HG01243.hp2 HG02717.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.162-1066_162-1063d others(6): Show |
AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 115868936 | ||||||
chr5:115868940 | A | G | 1 | a0001c0001t0001g0339 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.162-1077A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 2/5 | chr5 | 115868940 | |||||||
chr5:115868943 | A | AAGGG | 4 | a0001c0001t0002g0343 a0001c0001t0002g0344 a0001c0001t0002g0345 others(1): Show |
4 | HG02615.hp2 HG02630.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.162-1071_162-1070i others(6): Show |
AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 115868943 | ||||||
chr5:115868943 | A | AAGGGAGG others(5): Show |
1 | a0001c0001t0001g0351 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.162-1071_162-1070i others(14): Show |
AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 115868943 | ||||||
chr5:115868944 | A | G | 1 | a0001c0001t0001g0339 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.162-1073A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 2/5 | chr5 | 115868944 | |||||||
chr5:115868947 | A | AAGGG | 74 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(71): Show |
85 | HG00280.hp1 HG00735.hp2 HG00738.hp2 others(82): Show |
intron_variant | MODIFIER | c.162-1067_162-1066i others(6): Show |
AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 115868947 | ||||||
chr5:115868947 | A | AAGGGAGG others(1): Show |
6 | a0001c0001t0001g0017 a0001c0001t0001g0218 a0001c0001t0001g0280 others(3): Show |
7 | HG00099.hp2 HG01978.hp1 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.162-1067_162-1066i others(10): Show |
AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 115868947 | ||||||
chr5:115868947 | A | G | 28 | a0001c0001t0001g0009 a0001c0001t0001g0088 a0001c0001t0001g0089 others(25): Show |
29 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.162-1070A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 2/5 | chr5 | 115868947 | |||||||
chr5:115868951 | A | AAGGG | 3 | a0001c0001t0001g0348 a0001c0001t0001g0349 a0001c0001t0004g0350 |
3 | HG02809.hp1 HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.162-1035_162-1032d others(6): Show |
AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 115868951 | ||||||
chr5:115868951 | A | AAGGGAGG others(13): Show |
1 | a0001c0001t0001g0324 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.162-1051_162-1032d others(22): Show |
AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 115868951 | ||||||
chr5:115868951 | A | G | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(116): Show |
132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.162-1066A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 2/5 | chr5 | 115868951 | |||||||
chr5:115868951 | AAGGG | A | 142 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0012 others(139): Show |
147 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.162-1035_162-1032d others(6): Show |
AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 115868951 | ||||||
chr5:115868980 | AGG | A | 3 | a0001c0001t0001g0214 a0001c0001t0001g0315 a0001c0001t0005g0215 |
3 | HG02965.hp2 HG03041.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.162-1035_162-1034d others(4): Show |
AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 115868980 | ||||||
chr5:115868982 | G | GGAGGGAG others(3): Show |
10 | a0001c0001t0001g0009 a0001c0001t0001g0088 a0001c0001t0001g0089 others(7): Show |
11 | HG00140.hp1 HG00639.hp1 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.162-1032_162-1031i others(12): Show |
AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 115868982 | ||||||
chr5:115868982 | G | GGAGGGAG others(7): Show |
8 | a0001c0001t0001g0013 a0001c0001t0001g0127 a0001c0001t0001g0128 others(5): Show |
9 | HG00099.hp1 HG01256.hp1 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.162-1032_162-1031i others(16): Show |
AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 115868982 | ||||||
chr5:115868982 | G | GGAGGGAG others(11): Show |
5 | a0001c0001t0001g0210 a0001c0001t0001g0212 a0001c0001t0003g0022 others(2): Show |
5 | HG02145.hp1 HG03225.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.162-1032_162-1031i others(20): Show |
AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 115868982 | ||||||
chr5:115868982 | G | GGAGGGAG others(19): Show |
3 | a0001c0001t0001g0209 a0001c0001t0001g0211 a0001c0001t0001g0213 |
3 | HG02486.hp1 HG02559.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.162-1032_162-1031i others(28): Show |
AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 115868982 | ||||||
chr5:115869226 | G | A | 3 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0317 |
3 | HG03688.hp2 HG03834.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.162-791G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 2/5 | chr5 | 115869226 | |||||||
chr5:115869342 | G | A | 1 | a0001c0001t0001g0324 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.162-675G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 2/5 | chr5 | 115869342 | |||||||
chr5:115869408 | C | G | 1 | a0001c0001t0001g0208 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.162-609C>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 2/5 | chr5 | 115869408 | |||||||
chr5:115869527 | T | G | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(138): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.162-490T>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 2/5 | chr5 | 115869527 | |||||||
chr5:115869596 | A | G | 1 | a0001c0001t0001g0339 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.162-421A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 2/5 | chr5 | 115869596 | |||||||
chr5:115869705 | C | CTGA | 13 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0336 others(10): Show |
13 | HG02257.hp1 HG02559.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.162-306_162-304dup others(3): Show |
AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 115869705 | ||||||
chr5:115869742 | C | T | 1 | a0001c0001t0001g0239 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.162-275C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 2/5 | chr5 | 115869742 | |||||||
chr5:115869763 | A | G | 1 | a0001c0001t0001g0324 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.162-254A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 2/5 | chr5 | 115869763 | |||||||
chr5:115869892 | A | G | 1 | a0001c0001t0001g0324 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.162-125A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 2/5 | chr5 | 115869892 | |||||||
chr5:115870309 | A | G | 13 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0336 others(10): Show |
13 | HG02257.hp1 HG02559.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.273+181A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115870309 | |||||||
chr5:115870354 | T | C | 2 | a0001c0001t0001g0205 a0001c0001t0001g0206 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.273+226T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115870354 | |||||||
chr5:115870381 | G | A | 2 | a0001c0001t0002g0328 a0001c0001t0002g0329 |
2 | HG02809.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.273+253G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115870381 | |||||||
chr5:115870565 | T | C | 1 | a0001c0001t0001g0208 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.273+437T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115870565 | |||||||
chr5:115870651 | A | G | 66 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(63): Show |
77 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.273+523A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115870651 | |||||||
chr5:115870683 | A | T | 1 | a0001c0001t0001g0332 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.273+555A>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115870683 | |||||||
chr5:115870814 | T | C | 1 | a0001c0001t0001g0332 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.273+686T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115870814 | |||||||
chr5:115870840 | C | A | 3 | a0001c0001t0001g0013 a0001c0001t0001g0198 a0001c0001t0004g0196 |
4 | HG02486.hp2 HG02615.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.273+712C>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115870840 | |||||||
chr5:115870846 | T | G | 1 | a0001c0001t0001g0332 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.273+718T>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115870846 | |||||||
chr5:115870948 | C | T | 2 | a0001c0001t0001g0283 a0001c0001t0001g0284 |
2 | NA18965.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.273+820C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115870948 | |||||||
chr5:115871003 | C | A | 2 | a0001c0001t0001g0253 a0001c0001t0001g0317 |
2 | HG03688.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.273+875C>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115871003 | |||||||
chr5:115871011 | A | G | 2 | a0001c0001t0001g0205 a0001c0001t0001g0206 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.273+883A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115871011 | |||||||
chr5:115871168 | G | C | 14 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0336 others(11): Show |
14 | HG02257.hp1 HG02559.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.273+1040G>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115871168 | |||||||
chr5:115871170 | C | T | 14 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0336 others(11): Show |
14 | HG02257.hp1 HG02559.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.273+1042C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115871170 | |||||||
chr5:115871182 | C | T | 57 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0024 others(54): Show |
59 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.273+1054C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115871182 | |||||||
chr5:115871236 | A | G | 1 | a0001c0001t0001g0197 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.273+1108A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115871236 | |||||||
chr5:115871240 | C | T | 139 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(136): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.273+1112C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115871240 | |||||||
chr5:115871261 | T | C | 1 | a0001c0001t0001g0052 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.273+1133T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115871261 | |||||||
chr5:115871275 | C | G | 4 | a0001c0001t0001g0020 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG02717.hp1 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+1147C>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115871275 | |||||||
chr5:115871324 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.273+1196G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115871324 | |||||||
chr5:115871347 | A | G | 28 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0061 others(25): Show |
30 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.273+1219A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115871347 | |||||||
chr5:115871637 | G | A | 1 | a0001c0001t0001g0349 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.273+1509G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115871637 | |||||||
chr5:115871782 | C | T | 1 | a0001c0001t0001g0211 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.273+1654C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115871782 | |||||||
chr5:115871786 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.273+1658G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115871786 | |||||||
chr5:115871909 | A | C | 2 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
2 | HG02735.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.273+1781A>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115871909 | |||||||
chr5:115871914 | G | A | 9 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0231 others(6): Show |
11 | HG01074.hp1 HG01361.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.273+1786G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115871914 | |||||||
chr5:115871940 | G | A | 7 | a0001c0001t0001g0245 a0001c0001t0001g0277 a0001c0001t0001g0288 others(4): Show |
7 | HG01943.hp2 HG02004.hp2 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.273+1812G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115871940 | |||||||
chr5:115872174 | C | G | 5 | a0001c0001t0001g0020 a0001c0001t0001g0225 a0001c0001t0001g0226 others(2): Show |
5 | HG02717.hp1 HG02809.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.273+2046C>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115872174 | |||||||
chr5:115872281 | C | CA | 5 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0035 others(2): Show |
5 | HG01243.hp2 HG03139.hp2 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.273+2161dupA | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr5 | 115872281 | ||||||
chr5:115872305 | T | A | 1 | a0001c0001t0001g0324 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.273+2177T>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115872305 | |||||||
chr5:115872450 | T | C | 2 | a0001c0001t0002g0328 a0001c0001t0002g0329 |
2 | HG02809.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.273+2322T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115872450 | |||||||
chr5:115872565 | G | T | 2 | a0001c0001t0001g0133 a0001c0001t0001g0186 |
2 | NA18975.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.273+2437G>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115872565 | |||||||
chr5:115872672 | T | C | 1 | a0001c0001t0001g0162 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.273+2544T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115872672 | |||||||
chr5:115872739 | A | AGG | 45 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0088 others(42): Show |
47 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.273+2613_273+2614d others(4): Show |
AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr5 | 115872739 | ||||||
chr5:115872888 | C | A | 2 | a0001c0001t0001g0348 a0001c0001t0001g0349 |
2 | HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.273+2760C>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115872888 | |||||||
chr5:115872897 | C | G | 1 | a0001c0001t0001g0324 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.273+2769C>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115872897 | |||||||
chr5:115873140 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.273+3012A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115873140 | |||||||
chr5:115873146 | A | G | 92 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(89): Show |
104 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(101): Show |
intron_variant | MODIFIER | c.273+3018A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115873146 | |||||||
chr5:115873216 | A | T | 1 | a0001c0001t0001g0324 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.273+3088A>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115873216 | |||||||
chr5:115873341 | C | T | 4 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0131 others(1): Show |
4 | HG02572.hp2 HG02818.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.273+3213C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115873341 | |||||||
chr5:115873342 | G | A | 3 | a0001c0001t0001g0324 a0001c0001t0003g0021 a0001c0001t0003g0023 |
3 | HG01256.hp1 HG01258.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.273+3214G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115873342 | |||||||
chr5:115873345 | G | A | 7 | a0001c0001t0001g0245 a0001c0001t0001g0277 a0001c0001t0001g0288 others(4): Show |
7 | HG01943.hp2 HG02004.hp2 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.273+3217G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115873345 | |||||||
chr5:115873374 | C | G | 14 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0336 others(11): Show |
14 | HG02257.hp1 HG02559.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.273+3246C>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115873374 | |||||||
chr5:115873411 | G | A | 3 | a0001c0001t0001g0013 a0001c0001t0001g0198 a0001c0001t0004g0196 |
4 | HG02486.hp2 HG02615.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.273+3283G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115873411 | |||||||
chr5:115873697 | G | T | 4 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0212 others(1): Show |
4 | HG02486.hp1 HG02559.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.273+3569G>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115873697 | |||||||
chr5:115873725 | C | G | 14 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0336 others(11): Show |
14 | HG02257.hp1 HG02559.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.273+3597C>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115873725 | |||||||
chr5:115873726 | T | G | 2 | a0001c0001t0001g0266 a0001c0001t0001g0272 |
2 | HG00639.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.273+3598T>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115873726 | |||||||
chr5:115874014 | T | A | 1 | a0001c0001t0001g0089 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.273+3886T>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115874014 | |||||||
chr5:115874104 | G | A | 4 | a0001c0001t0001g0233 a0001c0001t0002g0232 a0002c0002t0001g0228 others(1): Show |
4 | HG02258.hp2 HG02922.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.273+3976G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115874104 | |||||||
chr5:115874221 | A | G | 2 | a0001c0001t0001g0348 a0001c0001t0001g0349 |
2 | HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.273+4093A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115874221 | |||||||
chr5:115874443 | G | T | 1 | a0001c0001t0001g0324 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.273+4315G>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115874443 | |||||||
chr5:115874549 | A | G | 4 | a0001c0001t0002g0343 a0001c0001t0002g0344 a0001c0001t0002g0345 others(1): Show |
4 | HG02615.hp2 HG02630.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+4421A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115874549 | |||||||
chr5:115874561 | A | G | 1 | a0001c0001t0001g0324 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.273+4433A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115874561 | |||||||
chr5:115874600 | C | A | 1 | a0001c0001t0001g0141 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.273+4472C>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115874600 | |||||||
chr5:115874818 | A | AG | 3 | a0001c0001t0001g0044 a0001c0001t0001g0063 a0001c0001t0001g0202 |
3 | HG01516.hp2 HG02683.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.273+4692dupG | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr5 | 115874818 | ||||||
chr5:115874997 | G | A | 2 | a0001c0001t0001g0039 a0001c0001t0001g0052 |
2 | NA18965.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.273+4869G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115874997 | |||||||
chr5:115875023 | C | T | 1 | a0001c0001t0001g0324 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.273+4895C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115875023 | |||||||
chr5:115875118 | A | C | 2 | a0001c0001t0003g0091 a0001c0001t0003g0156 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.273+4990A>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115875118 | |||||||
chr5:115875242 | A | T | 2 | a0001c0001t0001g0214 a0001c0001t0001g0315 |
2 | HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.273+5114A>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115875242 | |||||||
chr5:115875284 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.273+5156G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115875284 | |||||||
chr5:115875366 | G | A | 1 | a0001c0001t0001g0280 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.273+5238G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115875366 | |||||||
chr5:115875369 | T | C | 1 | a0001c0001t0001g0351 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.273+5241T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115875369 | |||||||
chr5:115875388 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.273+5260C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115875388 | |||||||
chr5:115875527 | A | G | 139 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(136): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.273+5399A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115875527 | |||||||
chr5:115875663 | C | G | 13 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0336 others(10): Show |
13 | HG02257.hp1 HG02559.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.273+5535C>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115875663 | |||||||
chr5:115875902 | G | A | 1 | a0001c0001t0001g0324 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.273+5774G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115875902 | |||||||
chr5:115875912 | A | G | 14 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0336 others(11): Show |
14 | HG02257.hp1 HG02559.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.273+5784A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115875912 | |||||||
chr5:115876191 | C | G | 1 | a0001c0001t0001g0351 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.273+6063C>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115876191 | |||||||
chr5:115876546 | T | C | 14 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0336 others(11): Show |
14 | HG02257.hp1 HG02559.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.273+6418T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115876546 | |||||||
chr5:115876803 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.273+6675G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115876803 | |||||||
chr5:115876915 | G | A | 1 | a0001c0001t0001g0351 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.273+6787G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115876915 | |||||||
chr5:115877013 | T | C | 2 | a0001c0001t0001g0216 a0001c0001t0001g0217 |
2 | HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.273+6885T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115877013 | |||||||
chr5:115877054 | T | C | 31 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0088 others(28): Show |
33 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.273+6926T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115877054 | |||||||
chr5:115877121 | G | T | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(75): Show |
89 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.273+6993G>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115877121 | |||||||
chr5:115877230 | A | G | 1 | a0001c0001t0001g0313 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.273+7102A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115877230 | |||||||
chr5:115877250 | A | G | 14 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0336 others(11): Show |
14 | HG02257.hp1 HG02559.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.273+7122A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115877250 | |||||||
chr5:115877366 | G | T | 1 | a0001c0001t0001g0330 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.273+7238G>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115877366 | |||||||
chr5:115877583 | C | A | 1 | a0001c0001t0001g0330 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.273+7455C>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115877583 | |||||||
chr5:115877830 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.273+7702G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115877830 | |||||||
chr5:115877859 | T | C | 3 | a0001c0001t0001g0013 a0001c0001t0001g0198 a0001c0001t0004g0196 |
4 | HG02486.hp2 HG02615.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.273+7731T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115877859 | |||||||
chr5:115877961 | G | A | 4 | a0001c0001t0002g0343 a0001c0001t0002g0344 a0001c0001t0002g0345 others(1): Show |
4 | HG02615.hp2 HG02630.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+7833G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115877961 | |||||||
chr5:115878079 | C | G | 6 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(3): Show |
6 | HG02055.hp2 HG02572.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.273+7951C>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115878079 | |||||||
chr5:115878214 | A | G | 4 | a0001c0001t0001g0020 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG02717.hp1 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+8086A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115878214 | |||||||
chr5:115878222 | A | G | 1 | a0001c0001t0001g0351 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.273+8094A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115878222 | |||||||
chr5:115878256 | T | C | 31 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0088 others(28): Show |
33 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.273+8128T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115878256 | |||||||
chr5:115878361 | T | G | 1 | a0001c0001t0001g0303 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.273+8233T>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115878361 | |||||||
chr5:115878423 | A | G | 1 | a0001c0001t0001g0136 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.273+8295A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115878423 | |||||||
chr5:115878441 | C | CATT | 143 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(140): Show |
157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.273+8313_273+8314i others(5): Show |
AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115878441 | |||||||
chr5:115878446 | A | T | 14 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0336 others(11): Show |
14 | HG02257.hp1 HG02559.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.273+8318A>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115878446 | |||||||
chr5:115878450 | A | G | 1 | a0001c0001t0001g0019 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.273+8322A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115878450 | |||||||
chr5:115878482 | G | A | 4 | a0001c0001t0001g0020 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG02717.hp1 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+8354G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115878482 | |||||||
chr5:115878487 | A | T | 1 | a0001c0001t0001g0255 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.273+8359A>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115878487 | |||||||
chr5:115878584 | G | A | 45 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0088 others(42): Show |
47 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.273+8456G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115878584 | |||||||
chr5:115878660 | G | T | 1 | a0001c0001t0001g0086 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.273+8532G>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115878660 | |||||||
chr5:115878776 | A | G | 2 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
2 | HG00099.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.273+8648A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115878776 | |||||||
chr5:115878780 | C | T | 1 | a0001c0001t0001g0300 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.273+8652C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115878780 | |||||||
chr5:115878831 | A | T | 1 | a0001c0001t0001g0269 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.273+8703A>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115878831 | |||||||
chr5:115878921 | T | TAAGTTGT others(341): Show |
2 | a0001c0001t0001g0039 a0001c0001t0001g0052 |
2 | NA18965.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.273+8809_273+8810i others(350): Show |
AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr5 | 115878921 | ||||||
chr5:115879053 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.273+8925C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115879053 | |||||||
chr5:115879201 | C | T | 4 | a0001c0001t0001g0233 a0001c0001t0002g0232 a0002c0002t0001g0228 others(1): Show |
4 | HG02258.hp2 HG02922.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.273+9073C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115879201 | |||||||
chr5:115879366 | T | C | 1 | a0001c0001t0001g0254 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.273+9238T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115879366 | |||||||
chr5:115879403 | G | A | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(134): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.273+9275G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115879403 | |||||||
chr5:115879512 | G | A | 1 | a0001c0001t0001g0289 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.273+9384G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115879512 | |||||||
chr5:115879537 | A | G | 1 | a0001c0001t0001g0049 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.273+9409A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115879537 | |||||||
chr5:115879539 | G | A | 1 | a0001c0001t0001g0324 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.273+9411G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115879539 | |||||||
chr5:115879560 | G | GT | 3 | a0001c0001t0001g0017 a0001c0001t0001g0257 a0001c0001t0001g0318 |
4 | HG01884.hp2 HG02451.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.273+9434dupT | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr5 | 115879560 | ||||||
chr5:115879594 | G | A | 2 | a0001c0001t0001g0227 a0001c0001t0001g0304 |
2 | HG02129.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.273+9466G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115879594 | |||||||
chr5:115879640 | G | T | 1 | a0001c0001t0001g0178 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.273+9512G>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115879640 | |||||||
chr5:115879679 | C | G | 1 | a0001c0001t0001g0316 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.273+9551C>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115879679 | |||||||
chr5:115879813 | G | A | 54 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0024 others(51): Show |
56 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.273+9685G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115879813 | |||||||
chr5:115879846 | G | C | 13 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0336 others(10): Show |
13 | HG02257.hp1 HG02559.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.273+9718G>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115879846 | |||||||
chr5:115880146 | A | G | 32 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0088 others(29): Show |
34 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.273+10018A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115880146 | |||||||
chr5:115880162 | G | A | 2 | a0001c0001t0001g0348 a0001c0001t0001g0349 |
2 | HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.273+10034G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115880162 | |||||||
chr5:115880275 | T | C | 2 | a0001c0001t0002g0328 a0001c0001t0002g0329 |
2 | HG02809.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.273+10147T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115880275 | |||||||
chr5:115880315 | C | T | 4 | a0001c0001t0001g0233 a0001c0001t0002g0232 a0002c0002t0001g0228 others(1): Show |
4 | HG02258.hp2 HG02922.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.273+10187C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115880315 | |||||||
chr5:115880408 | C | G | 10 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0068 others(7): Show |
10 | HG01243.hp2 HG02055.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.273+10280C>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115880408 | |||||||
chr5:115880730 | G | A | 2 | a0001c0001t0001g0348 a0001c0001t0001g0349 |
2 | HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.273+10602G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115880730 | |||||||
chr5:115880752 | C | G | 4 | a0001c0001t0001g0233 a0001c0001t0002g0232 a0002c0002t0001g0228 others(1): Show |
4 | HG02258.hp2 HG02922.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.273+10624C>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115880752 | |||||||
chr5:115880800 | T | C | 4 | a0001c0001t0001g0109 a0001c0001t0001g0162 a0001c0001t0001g0164 others(1): Show |
4 | HG02602.hp1 HG02698.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.273+10672T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115880800 | |||||||
chr5:115880871 | C | T | 4 | a0001c0001t0001g0233 a0001c0001t0002g0232 a0002c0002t0001g0228 others(1): Show |
4 | HG02258.hp2 HG02922.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.273+10743C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115880871 | |||||||
chr5:115880972 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.273+10844G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115880972 | |||||||
chr5:115881100 | C | T | 1 | a0001c0001t0001g0270 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.273+10972C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115881100 | |||||||
chr5:115881129 | T | C | 20 | a0001c0001t0001g0009 a0001c0001t0001g0088 a0001c0001t0001g0089 others(17): Show |
21 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.273+11001T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115881129 | |||||||
chr5:115881274 | G | A | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(138): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.273+11146G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115881274 | |||||||
chr5:115881277 | C | T | 19 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(16): Show |
28 | HG01255.hp2 HG01934.hp2 HG01981.hp2 others(25): Show |
intron_variant | MODIFIER | c.273+11149C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115881277 | |||||||
chr5:115881315 | A | G | 1 | a0001c0001t0001g0324 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.273+11187A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115881315 | |||||||
chr5:115881338 | G | A | 8 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0336 others(5): Show |
8 | HG02559.hp1 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.273+11210G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115881338 | |||||||
chr5:115881372 | G | T | 4 | a0001c0001t0001g0233 a0001c0001t0002g0232 a0002c0002t0001g0228 others(1): Show |
4 | HG02258.hp2 HG02922.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.273+11244G>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115881372 | |||||||
chr5:115881413 | G | A | 1 | a0001c0001t0001g0020 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.273+11285G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115881413 | |||||||
chr5:115881685 | G | A | 1 | a0001c0001t0001g0351 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.273+11557G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115881685 | |||||||
chr5:115881702 | G | A | 1 | a0001c0001t0001g0339 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.273+11574G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115881702 | |||||||
chr5:115881728 | G | A | 6 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(3): Show |
6 | HG02055.hp2 HG02572.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.273+11600G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115881728 | |||||||
chr5:115881770 | C | G | 1 | a0001c0001t0001g0050 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.273+11642C>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115881770 | |||||||
chr5:115881810 | A | T | 13 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0336 others(10): Show |
13 | HG02257.hp1 HG02559.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.273+11682A>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115881810 | |||||||
chr5:115881821 | C | T | 13 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0336 others(10): Show |
13 | HG02257.hp1 HG02559.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.273+11693C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115881821 | |||||||
chr5:115881867 | G | C | 2 | a0001c0001t0001g0103 a0001c0001t0001g0163 |
2 | HG02976.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.273+11739G>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115881867 | |||||||
chr5:115881996 | A | G | 1 | a0001c0001t0005g0059 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.273+11868A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115881996 | |||||||
chr5:115882000 | A | G | 1 | a0001c0001t0001g0208 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.273+11872A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115882000 | |||||||
chr5:115882271 | A | G | 1 | a0001c0001t0001g0208 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.273+12143A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115882271 | |||||||
chr5:115882394 | A | G | 2 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
2 | HG02735.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.273+12266A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115882394 | |||||||
chr5:115882548 | T | C | 85 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(82): Show |
97 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(94): Show |
intron_variant | MODIFIER | c.273+12420T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115882548 | |||||||
chr5:115882576 | C | G | 2 | a0001c0001t0002g0343 a0001c0001t0002g0344 |
2 | HG02615.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.273+12448C>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115882576 | |||||||
chr5:115882598 | G | T | 30 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0088 others(27): Show |
32 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.273+12470G>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115882598 | |||||||
chr5:115882612 | C | T | 1 | a0001c0001t0001g0287 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.274-12475C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115882612 | |||||||
chr5:115882671 | CG | C | 3 | a0001c0001t0001g0017 a0001c0001t0001g0257 a0001c0001t0001g0318 |
4 | HG01884.hp2 HG02451.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.274-12411delG | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr5 | 115882671 | ||||||
chr5:115882725 | A | G | 2 | a0001c0001t0001g0325 a0001c0001t0001g0326 |
2 | HG00735.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.274-12362A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115882725 | |||||||
chr5:115882736 | A | G | 1 | a0001c0001t0001g0019 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.274-12351A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115882736 | |||||||
chr5:115882750 | A | T | 2 | a0001c0001t0001g0256 a0001c0001t0001g0298 |
2 | HG00738.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.274-12337A>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115882750 | |||||||
chr5:115882946 | A | G | 2 | a0001c0001t0003g0021 a0001c0001t0003g0023 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.274-12141A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115882946 | |||||||
chr5:115882984 | G | A | 1 | a0001c0001t0001g0274 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.274-12103G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115882984 | |||||||
chr5:115883040 | C | T | 1 | a0001c0001t0001g0230 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.274-12047C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115883040 | |||||||
chr5:115883051 | C | T | 62 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0024 others(59): Show |
64 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.274-12036C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115883051 | |||||||
chr5:115883054 | C | G | 1 | a0001c0001t0001g0351 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.274-12033C>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115883054 | |||||||
chr5:115883483 | T | C | 1 | a0001c0001t0001g0324 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.274-11604T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115883483 | |||||||
chr5:115883558 | G | A | 1 | a0001c0001t0002g0094 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.274-11529G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115883558 | |||||||
chr5:115883588 | G | A | 2 | a0001c0001t0002g0328 a0001c0001t0002g0329 |
2 | HG02809.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.274-11499G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115883588 | |||||||
chr5:115883621 | G | A | 2 | a0001c0001t0001g0161 a0001c0001t0001g0173 |
2 | NA18959.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.274-11466G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115883621 | |||||||
chr5:115883759 | G | C | 289 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(286): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.274-11328G>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115883759 | |||||||
chr5:115883813 | A | C | 1 | a0001c0001t0001g0154 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.274-11274A>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115883813 | |||||||
chr5:115884097 | A | G | 1 | a0001c0001t0001g0324 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.274-10990A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115884097 | |||||||
chr5:115884145 | C | G | 1 | a0001c0001t0001g0324 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.274-10942C>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115884145 | |||||||
chr5:115884301 | A | G | 1 | a0001c0001t0001g0216 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.274-10786A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115884301 | |||||||
chr5:115884361 | T | G | 1 | a0001c0001t0001g0330 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.274-10726T>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115884361 | |||||||
chr5:115884437 | C | T | 8 | a0001c0001t0001g0120 a0001c0001t0001g0153 a0001c0001t0001g0208 others(5): Show |
8 | HG01891.hp1 HG03139.hp1 HG03579.hp1 others(5): Show |
intron_variant | MODIFIER | c.274-10650C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115884437 | |||||||
chr5:115884520 | A | G | 1 | a0001c0001t0001g0324 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.274-10567A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115884520 | |||||||
chr5:115884522 | T | C | 142 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(139): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.274-10565T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115884522 | |||||||
chr5:115884761 | A | G | 13 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0336 others(10): Show |
13 | HG02257.hp1 HG02559.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.274-10326A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115884761 | |||||||
chr5:115884807 | G | T | 2 | a0001c0001t0002g0328 a0001c0001t0002g0329 |
2 | HG02809.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.274-10280G>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115884807 | |||||||
chr5:115884849 | A | C | 2 | a0001c0001t0001g0090 a0001c0001t0001g0155 |
2 | HG00140.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.274-10238A>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115884849 | |||||||
chr5:115885326 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.274-9761G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115885326 | |||||||
chr5:115885371 | A | T | 2 | a0001c0001t0001g0348 a0001c0001t0001g0349 |
2 | HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.274-9716A>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115885371 | |||||||
chr5:115885548 | T | C | 21 | a0001c0001t0001g0061 a0001c0001t0001g0093 a0001c0001t0001g0157 others(18): Show |
21 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.274-9539T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115885548 | |||||||
chr5:115885646 | A | G | 31 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0088 others(28): Show |
33 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.274-9441A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115885646 | |||||||
chr5:115885746 | C | A | 1 | a0001c0001t0001g0324 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.274-9341C>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115885746 | |||||||
chr5:115885761 | T | C | 3 | a0001c0001t0001g0017 a0001c0001t0001g0257 a0001c0001t0001g0318 |
4 | HG01884.hp2 HG02451.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.274-9326T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115885761 | |||||||
chr5:115885922 | A | T | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(138): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.274-9165A>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115885922 | |||||||
chr5:115886022 | T | G | 4 | a0001c0001t0001g0233 a0001c0001t0002g0232 a0002c0002t0001g0228 others(1): Show |
4 | HG02258.hp2 HG02922.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.274-9065T>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115886022 | |||||||
chr5:115886166 | A | G | 2 | a0001c0001t0003g0091 a0001c0001t0003g0156 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.274-8921A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115886166 | |||||||
chr5:115886208 | C | T | 31 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0088 others(28): Show |
33 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.274-8879C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115886208 | |||||||
chr5:115886309 | A | G | 23 | a0001c0001t0001g0017 a0001c0001t0001g0068 a0001c0001t0001g0069 others(20): Show |
24 | HG01884.hp2 HG02055.hp1 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.274-8778A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115886309 | |||||||
chr5:115886432 | G | A | 1 | a0001c0001t0005g0215 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.274-8655G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115886432 | |||||||
chr5:115886499 | T | C | 1 | a0001c0001t0001g0335 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.274-8588T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115886499 | |||||||
chr5:115886579 | A | G | 1 | a0001c0001t0001g0318 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.274-8508A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115886579 | |||||||
chr5:115886585 | C | T | 1 | a0001c0001t0001g0230 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.274-8502C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115886585 | |||||||
chr5:115886602 | G | A | 1 | a0001c0001t0004g0350 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.274-8485G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115886602 | |||||||
chr5:115886810 | T | TA | 4 | a0001c0001t0001g0060 a0001c0001t0001g0078 a0001c0001t0001g0079 others(1): Show |
4 | HG00733.hp2 HG01070.hp1 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-8276dupA | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr5 | 115886810 | ||||||
chr5:115887008 | A | G | 1 | a0001c0001t0001g0297 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.274-8079A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115887008 | |||||||
chr5:115887143 | T | A | 1 | a0001c0001t0001g0324 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.274-7944T>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115887143 | |||||||
chr5:115887338 | G | C | 142 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(139): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.274-7749G>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115887338 | |||||||
chr5:115887364 | CT | C | 344 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(341): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.274-7712delT | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr5 | 115887364 | ||||||
chr5:115887453 | A | T | 4 | a0001c0001t0001g0020 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG02717.hp1 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-7634A>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115887453 | |||||||
chr5:115887625 | G | T | 1 | a0001c0001t0001g0324 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.274-7462G>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115887625 | |||||||
chr5:115887807 | C | T | 32 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0088 others(29): Show |
34 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.274-7280C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115887807 | |||||||
chr5:115888098 | A | G | 2 | a0001c0001t0002g0328 a0001c0001t0002g0329 |
2 | HG02809.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.274-6989A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115888098 | |||||||
chr5:115888177 | G | C | 1 | a0001c0001t0001g0230 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.274-6910G>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115888177 | |||||||
chr5:115888221 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.274-6866C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115888221 | |||||||
chr5:115888223 | G | A | 1 | a0001c0001t0001g0324 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.274-6864G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115888223 | |||||||
chr5:115888418 | G | A | 47 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0088 others(44): Show |
49 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.274-6669G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115888418 | |||||||
chr5:115888702 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.274-6385G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115888702 | |||||||
chr5:115888718 | G | A | 2 | a0001c0001t0001g0077 a0001c0001t0001g0174 |
2 | HG00733.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.274-6369G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115888718 | |||||||
chr5:115888721 | A | G | 4 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0257 others(1): Show |
5 | HG01884.hp2 HG02280.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.274-6366A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115888721 | |||||||
chr5:115888927 | T | A | 2 | a0001c0001t0001g0348 a0001c0001t0001g0349 |
2 | HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.274-6160T>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115888927 | |||||||
chr5:115889221 | A | C | 1 | a0001c0001t0001g0330 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.274-5866A>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115889221 | |||||||
chr5:115889509 | T | A | 2 | a0001c0001t0001g0348 a0001c0001t0001g0349 |
2 | HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.274-5578T>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115889509 | |||||||
chr5:115889580 | G | C | 1 | a0001c0001t0001g0324 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.274-5507G>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115889580 | |||||||
chr5:115889664 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.274-5423G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115889664 | |||||||
chr5:115889713 | C | T | 1 | a0001c0001t0001g0339 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.274-5374C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115889713 | |||||||
chr5:115889714 | C | G | 47 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0088 others(44): Show |
49 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.274-5373C>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115889714 | |||||||
chr5:115889810 | TA | T | 33 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0088 others(30): Show |
35 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.274-5268delA | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr5 | 115889810 | ||||||
chr5:115889820 | T | A | 2 | a0001c0001t0001g0348 a0001c0001t0001g0349 |
2 | HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.274-5267T>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115889820 | |||||||
chr5:115889828 | A | G | 1 | a0001c0001t0001g0330 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.274-5259A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115889828 | |||||||
chr5:115890109 | A | T | 2 | a0001c0001t0001g0037 a0001c0001t0001g0166 |
2 | HG01256.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.274-4978A>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115890109 | |||||||
chr5:115890418 | A | G | 49 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0088 others(46): Show |
51 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.274-4669A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115890418 | |||||||
chr5:115890562 | G | C | 2 | a0001c0001t0002g0328 a0001c0001t0002g0329 |
2 | HG02809.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.274-4525G>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115890562 | |||||||
chr5:115890797 | G | GT | 34 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0088 others(31): Show |
36 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.274-4287dupT | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr5 | 115890797 | ||||||
chr5:115890884 | C | T | 2 | a0001c0001t0002g0328 a0001c0001t0002g0329 |
2 | HG02809.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.274-4203C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115890884 | |||||||
chr5:115891225 | G | A | 48 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0088 others(45): Show |
50 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.274-3862G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115891225 | |||||||
chr5:115891376 | T | C | 2 | a0001c0001t0001g0227 a0001c0001t0001g0304 |
2 | HG02129.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.274-3711T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115891376 | |||||||
chr5:115891519 | C | G | 1 | a0001c0001t0001g0351 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.274-3568C>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115891519 | |||||||
chr5:115891526 | C | T | 1 | a0001c0001t0001g0330 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.274-3561C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115891526 | |||||||
chr5:115891556 | C | T | 1 | a0001c0001t0001g0208 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.274-3531C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115891556 | |||||||
chr5:115891655 | C | T | 2 | a0001c0001t0001g0039 a0001c0001t0001g0052 |
2 | NA18965.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.274-3432C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115891655 | |||||||
chr5:115891671 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.274-3416G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115891671 | |||||||
chr5:115891713 | G | C | 47 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0088 others(44): Show |
49 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.274-3374G>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115891713 | |||||||
chr5:115891756 | C | T | 1 | a0001c0001t0001g0330 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.274-3331C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115891756 | |||||||
chr5:115892128 | A | G | 14 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0336 others(11): Show |
14 | HG02257.hp1 HG02559.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.274-2959A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115892128 | |||||||
chr5:115892142 | ATTTGCAA others(2): Show |
A | 4 | a0001c0001t0001g0007 a0001c0001t0001g0076 a0001c0001t0001g0134 others(1): Show |
5 | NA18991.hp1 NA18995.hp1 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.274-2943_274-2935d others(11): Show |
AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr5 | 115892142 | ||||||
chr5:115892218 | T | C | 2 | a0001c0001t0002g0328 a0001c0001t0002g0329 |
2 | HG02809.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.274-2869T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115892218 | |||||||
chr5:115892469 | C | T | 7 | a0001c0001t0001g0008 a0001c0001t0001g0045 a0001c0001t0001g0096 others(4): Show |
8 | HG01168.hp1 HG02280.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.274-2618C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115892469 | |||||||
chr5:115892517 | A | G | 3 | a0001c0001t0002g0343 a0001c0001t0002g0344 a0001c0001t0002g0345 |
3 | HG02615.hp2 HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.274-2570A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115892517 | |||||||
chr5:115892567 | A | G | 1 | a0001c0001t0001g0048 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.274-2520A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115892567 | |||||||
chr5:115892577 | C | T | 1 | a0001c0001t0001g0108 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.274-2510C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115892577 | |||||||
chr5:115892590 | G | A | 4 | a0001c0001t0001g0020 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG02717.hp1 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-2497G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115892590 | |||||||
chr5:115892645 | G | A | 139 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(136): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.274-2442G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115892645 | |||||||
chr5:115892681 | A | G | 92 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(89): Show |
104 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(101): Show |
intron_variant | MODIFIER | c.274-2406A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115892681 | |||||||
chr5:115892843 | A | C | 1 | a0001c0001t0001g0019 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.274-2244A>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115892843 | |||||||
chr5:115892889 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.274-2198T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115892889 | |||||||
chr5:115893206 | G | A | 1 | a0001c0001t0001g0192 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.274-1881G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115893206 | |||||||
chr5:115893380 | T | G | 3 | a0001c0001t0002g0343 a0001c0001t0002g0344 a0001c0001t0002g0345 |
3 | HG02615.hp2 HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.274-1707T>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115893380 | |||||||
chr5:115893686 | C | G | 1 | a0001c0001t0001g0207 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.274-1401C>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115893686 | |||||||
chr5:115893959 | A | C | 81 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(78): Show |
93 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.274-1128A>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115893959 | |||||||
chr5:115894028 | G | A | 47 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0088 others(44): Show |
49 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.274-1059G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115894028 | |||||||
chr5:115894228 | C | T | 4 | a0001c0001t0001g0020 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG02717.hp1 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-859C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115894228 | |||||||
chr5:115894336 | C | T | 2 | a0001c0001t0001g0039 a0001c0001t0001g0052 |
2 | NA18965.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.274-751C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115894336 | |||||||
chr5:115894522 | A | G | 1 | a0001c0001t0001g0113 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.274-565A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115894522 | |||||||
chr5:115894541 | C | T | 1 | a0001c0001t0001g0333 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.274-546C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115894541 | |||||||
chr5:115894550 | G | C | 1 | a0001c0001t0005g0215 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.274-537G>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115894550 | |||||||
chr5:115894584 | T | C | 89 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(86): Show |
101 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.274-503T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115894584 | |||||||
chr5:115894716 | T | G | 1 | a0001c0001t0001g0087 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.274-371T>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115894716 | |||||||
chr5:115894743 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.274-344G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115894743 | |||||||
chr5:115894791 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.274-296T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115894791 | |||||||
chr5:115894868 | T | G | 3 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0084 |
3 | HG02129.hp1 NA18980.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.274-219T>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115894868 | |||||||
chr5:115894991 | C | T | 2 | a0001c0001t0001g0093 a0001c0001t0001g0157 |
2 | HG01106.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.274-96C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115894991 | |||||||
chr5:115895012 | A | G | 1 | a0001c0001t0001g0222 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.274-75A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115895012 | |||||||
chr5:115895052 | A | G | 1 | a0001c0001t0001g0019 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.274-35A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115895052 | |||||||
chr5:115895055 | C | T | 1 | a0001c0001t0001g0309 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.274-32C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115895055 | |||||||
chr5:115895080 | T | C | 1 | a0001c0001t0001g0158 | 1 | NA18970.hp1 | splice_region_variant&intron_variant | LOW | c.274-7T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 3/5 | chr5 | 115895080 | |||||||
chr5:115895346 | A | T | 1 | a0001c0001t0001g0251 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.345+188A>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115895346 | |||||||
chr5:115895355 | G | A | 4 | a0001c0001t0001g0020 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG02717.hp1 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.345+197G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115895355 | |||||||
chr5:115895503 | A | G | 2 | a0001c0001t0001g0039 a0001c0001t0001g0052 |
2 | NA18965.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.345+345A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115895503 | |||||||
chr5:115895504 | T | C | 8 | a0001c0001t0001g0036 a0001c0001t0001g0049 a0001c0001t0001g0050 others(5): Show |
8 | HG00738.hp1 HG01081.hp1 HG02015.hp1 others(5): Show |
intron_variant | MODIFIER | c.345+346T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115895504 | |||||||
chr5:115895603 | A | G | 2 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.345+445A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115895603 | |||||||
chr5:115895693 | A | G | 36 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0080 others(33): Show |
38 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.345+535A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115895693 | |||||||
chr5:115895927 | G | T | 1 | a0001c0001t0001g0077 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.345+769G>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115895927 | |||||||
chr5:115895960 | C | T | 12 | a0001c0001t0001g0020 a0001c0001t0001g0036 a0001c0001t0001g0049 others(9): Show |
12 | HG00738.hp1 HG01081.hp1 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.345+802C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115895960 | |||||||
chr5:115895961 | G | C | 1 | a0001c0001t0001g0077 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.345+803G>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115895961 | |||||||
chr5:115896097 | G | T | 1 | a0001c0001t0001g0125 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.345+939G>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115896097 | |||||||
chr5:115896235 | A | G | 1 | a0001c0001t0001g0324 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.345+1077A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115896235 | |||||||
chr5:115896340 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.345+1182A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115896340 | |||||||
chr5:115896390 | G | A | 3 | a0001c0001t0001g0238 a0001c0001t0001g0263 a0001c0001t0001g0265 |
3 | HG00140.hp2 HG01175.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.345+1232G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115896390 | |||||||
chr5:115896463 | A | G | 1 | a0001c0001t0001g0216 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.345+1305A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115896463 | |||||||
chr5:115896868 | T | G | 1 | a0001c0001t0001g0324 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.345+1710T>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115896868 | |||||||
chr5:115896912 | C | T | 1 | a0001c0001t0001g0257 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.345+1754C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115896912 | |||||||
chr5:115896946 | T | A | 1 | a0001c0001t0001g0019 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.345+1788T>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115896946 | |||||||
chr5:115896946 | T | C | 1 | a0001c0001t0001g0175 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.345+1788T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115896946 | |||||||
chr5:115896946 | TA | T | 15 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0336 others(12): Show |
15 | HG02257.hp1 HG02559.hp1 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.345+1789delA | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115896946 | |||||||
chr5:115896972 | A | G | 33 | a0001c0001t0001g0009 a0001c0001t0001g0080 a0001c0001t0001g0088 others(30): Show |
34 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.345+1814A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115896972 | |||||||
chr5:115897009 | A | T | 1 | a0001c0001t0001g0097 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.345+1851A>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115897009 | |||||||
chr5:115897153 | T | A | 1 | a0001c0001t0001g0336 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.345+1995T>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115897153 | |||||||
chr5:115897269 | C | T | 1 | a0001c0001t0001g0320 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.345+2111C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115897269 | |||||||
chr5:115897274 | C | A | 31 | a0001c0001t0001g0009 a0001c0001t0001g0080 a0001c0001t0001g0088 others(28): Show |
32 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.345+2116C>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115897274 | |||||||
chr5:115897419 | G | A | 96 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(93): Show |
102 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.345+2261G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115897419 | |||||||
chr5:115897600 | C | T | 2 | a0001c0001t0001g0177 a0001c0001t0001g0179 |
2 | NA18993.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.345+2442C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115897600 | |||||||
chr5:115897684 | C | T | 1 | a0001c0001t0001g0230 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.345+2526C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115897684 | |||||||
chr5:115897694 | G | A | 1 | a0001c0001t0002g0094 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.345+2536G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115897694 | |||||||
chr5:115897708 | C | T | 1 | a0001c0001t0001g0280 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.345+2550C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115897708 | |||||||
chr5:115897783 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.345+2625C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115897783 | |||||||
chr5:115897853 | C | T | 2 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
2 | HG02735.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.345+2695C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115897853 | |||||||
chr5:115898092 | G | A | 14 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0336 others(11): Show |
14 | HG02257.hp1 HG02559.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.345+2934G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115898092 | |||||||
chr5:115898106 | A | T | 1 | a0001c0001t0001g0150 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.345+2948A>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115898106 | |||||||
chr5:115898146 | G | A | 1 | a0001c0001t0001g0324 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.345+2988G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115898146 | |||||||
chr5:115898168 | A | G | 8 | a0001c0001t0001g0036 a0001c0001t0001g0049 a0001c0001t0001g0050 others(5): Show |
8 | HG00738.hp1 HG01081.hp1 HG02015.hp1 others(5): Show |
intron_variant | MODIFIER | c.345+3010A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115898168 | |||||||
chr5:115898382 | A | T | 1 | a0001c0001t0001g0150 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.345+3224A>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115898382 | |||||||
chr5:115898397 | T | G | 3 | a0001c0001t0001g0013 a0001c0001t0001g0198 a0001c0001t0004g0196 |
4 | HG02486.hp2 HG02615.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.345+3239T>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115898397 | |||||||
chr5:115898445 | C | G | 1 | a0001c0001t0001g0283 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.345+3287C>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115898445 | |||||||
chr5:115898594 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.345+3436G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115898594 | |||||||
chr5:115898628 | G | T | 4 | a0001c0001t0001g0020 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG02717.hp1 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.345+3470G>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115898628 | |||||||
chr5:115898841 | G | C | 1 | a0001c0001t0001g0299 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.345+3683G>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115898841 | |||||||
chr5:115898882 | G | A | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(148): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.345+3724G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115898882 | |||||||
chr5:115898915 | A | T | 1 | a0001c0001t0001g0150 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.345+3757A>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115898915 | |||||||
chr5:115898946 | T | A | 1 | a0001c0001t0001g0351 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.345+3788T>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115898946 | |||||||
chr5:115899064 | A | G | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(148): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.346-3821A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115899064 | |||||||
chr5:115899105 | T | A | 79 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(76): Show |
90 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.346-3780T>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115899105 | |||||||
chr5:115899140 | A | T | 2 | a0001c0001t0001g0056 a0001c0001t0005g0059 |
2 | HG02055.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.346-3745A>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115899140 | |||||||
chr5:115899387 | A | G | 2 | a0001c0001t0002g0328 a0001c0001t0002g0329 |
2 | HG02809.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.346-3498A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115899387 | |||||||
chr5:115899393 | C | T | 32 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0024 others(29): Show |
34 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(31): Show |
intron_variant | MODIFIER | c.346-3492C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115899393 | |||||||
chr5:115899434 | T | C | 3 | a0001c0001t0001g0330 a0001c0001t0001g0348 a0001c0001t0001g0349 |
3 | HG03098.hp1 HG03471.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.346-3451T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115899434 | |||||||
chr5:115899469 | G | A | 1 | a0001c0001t0001g0019 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.346-3416G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115899469 | |||||||
chr5:115899656 | T | C | 7 | a0001c0001t0001g0080 a0001c0001t0001g0209 a0001c0001t0001g0210 others(4): Show |
7 | HG02486.hp1 HG02559.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.346-3229T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115899656 | |||||||
chr5:115899820 | A | G | 1 | a0001c0001t0001g0324 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.346-3065A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115899820 | |||||||
chr5:115899824 | C | T | 4 | a0001c0001t0001g0020 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG02717.hp1 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.346-3061C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115899824 | |||||||
chr5:115899999 | T | C | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(150): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.346-2886T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115899999 | |||||||
chr5:115900062 | AAG | A | 6 | a0001c0001t0001g0030 a0001c0001t0001g0068 a0001c0001t0001g0069 others(3): Show |
6 | HG02055.hp1 HG02572.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.346-2819_346-2818d others(4): Show |
AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 115900062 | ||||||
chr5:115900130 | A | G | 1 | a0001c0001t0001g0016 | 2 | HG02145.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.346-2755A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115900130 | |||||||
chr5:115900219 | A | G | 12 | a0001c0001t0001g0080 a0001c0001t0001g0103 a0001c0001t0001g0163 others(9): Show |
12 | HG01891.hp1 HG02486.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.346-2666A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115900219 | |||||||
chr5:115900841 | A | G | 6 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(3): Show |
6 | HG02055.hp2 HG02572.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.346-2044A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115900841 | |||||||
chr5:115900915 | T | C | 1 | a0001c0001t0001g0150 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.346-1970T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115900915 | |||||||
chr5:115900993 | A | C | 33 | a0001c0001t0001g0009 a0001c0001t0001g0080 a0001c0001t0001g0088 others(30): Show |
34 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.346-1892A>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115900993 | |||||||
chr5:115901069 | G | C | 15 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0336 others(12): Show |
15 | HG02257.hp1 HG02559.hp1 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.346-1816G>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115901069 | |||||||
chr5:115901100 | A | T | 1 | a0001c0001t0001g0324 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.346-1785A>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115901100 | |||||||
chr5:115901231 | G | T | 90 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(87): Show |
102 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.346-1654G>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115901231 | |||||||
chr5:115901277 | T | C | 3 | a0001c0001t0001g0069 a0001c0001t0001g0131 a0001c0001t0001g0132 |
3 | HG02572.hp2 HG02818.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.346-1608T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115901277 | |||||||
chr5:115901357 | G | A | 1 | a0001c0001t0001g0326 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.346-1528G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115901357 | |||||||
chr5:115901387 | A | G | 2 | a0001c0001t0001g0112 a0001c0001t0001g0176 |
2 | HG03239.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.346-1498A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115901387 | |||||||
chr5:115901392 | CT | C | 147 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(144): Show |
160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.346-1472delT | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 115901392 | ||||||
chr5:115901392 | CTT | C | 19 | a0001c0001t0001g0024 a0001c0001t0001g0080 a0001c0001t0001g0143 others(16): Show |
19 | HG01516.hp1 HG01891.hp1 HG01943.hp1 others(16): Show |
intron_variant | MODIFIER | c.346-1473_346-1472d others(4): Show |
AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 115901392 | ||||||
chr5:115901599 | T | C | 4 | a0001c0001t0001g0103 a0001c0001t0001g0163 a0001c0001t0001g0216 others(1): Show |
4 | HG01891.hp1 HG02976.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.346-1286T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115901599 | |||||||
chr5:115901672 | A | G | 4 | a0001c0001t0001g0033 a0001c0001t0001g0065 a0001c0001t0001g0348 others(1): Show |
4 | HG00438.hp2 HG03098.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.346-1213A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115901672 | |||||||
chr5:115901680 | G | C | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(77): Show |
91 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.346-1205G>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115901680 | |||||||
chr5:115901722 | T | C | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(77): Show |
91 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.346-1163T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115901722 | |||||||
chr5:115901780 | T | C | 287 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(284): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.346-1105T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115901780 | |||||||
chr5:115901864 | G | A | 63 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0020 others(60): Show |
64 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.346-1021G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115901864 | |||||||
chr5:115901927 | G | GA | 8 | a0001c0001t0001g0035 a0001c0001t0001g0083 a0001c0001t0001g0087 others(5): Show |
8 | NA18945.hp1 NA18949.hp1 NA18952.hp1 others(5): Show |
intron_variant | MODIFIER | c.346-949dupA | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 115901927 | ||||||
chr5:115901942 | G | A | 2 | a0001c0001t0001g0135 a0001c0001t0001g0183 |
2 | HG00597.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.346-943G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115901942 | |||||||
chr5:115901978 | T | G | 1 | a0001c0001t0001g0246 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.346-907T>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115901978 | |||||||
chr5:115902123 | C | G | 2 | a0001c0001t0002g0328 a0001c0001t0002g0329 |
2 | HG02809.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.346-762C>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115902123 | |||||||
chr5:115902126 | A | G | 2 | a0001c0001t0001g0103 a0001c0001t0001g0163 |
2 | HG02976.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.346-759A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115902126 | |||||||
chr5:115902169 | T | A | 1 | a0001c0001t0001g0339 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.346-716T>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115902169 | |||||||
chr5:115902182 | G | A | 14 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0336 others(11): Show |
14 | HG02257.hp1 HG02559.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.346-703G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115902182 | |||||||
chr5:115902370 | A | G | 49 | a0001c0001t0001g0009 a0001c0001t0001g0080 a0001c0001t0001g0088 others(46): Show |
50 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.346-515A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115902370 | |||||||
chr5:115902417 | C | G | 2 | a0001c0001t0001g0260 a0001c0001t0001g0261 |
2 | HG01255.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.346-468C>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115902417 | |||||||
chr5:115902518 | T | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(151): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.346-367T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115902518 | |||||||
chr5:115902553 | A | C | 3 | a0001c0001t0001g0180 a0001c0001t0001g0193 a0001c0001t0001g0203 |
3 | HG01496.hp2 HG01891.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.346-332A>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115902553 | |||||||
chr5:115902635 | T | C | 2 | a0001c0001t0001g0291 a0001c0001t0001g0301 |
2 | HG02074.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.346-250T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115902635 | |||||||
chr5:115902699 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.346-186G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115902699 | |||||||
chr5:115902712 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.346-173C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 4/5 | chr5 | 115902712 | |||||||
chr5:115903019 | G | A | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(77): Show |
91 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.453+27G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115903019 | |||||||
chr5:115903101 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.453+109C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115903101 | |||||||
chr5:115903163 | C | G | 1 | a0001c0001t0001g0051 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.453+171C>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115903163 | |||||||
chr5:115903163 | C | T | 2 | a0001c0001t0002g0328 a0001c0001t0002g0329 |
2 | HG02809.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.453+171C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115903163 | |||||||
chr5:115903212 | A | G | 90 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(87): Show |
102 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.453+220A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115903212 | |||||||
chr5:115903307 | G | A | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(146): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.453+315G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115903307 | |||||||
chr5:115903480 | T | C | 7 | a0001c0001t0001g0060 a0001c0001t0001g0066 a0001c0001t0001g0078 others(4): Show |
7 | HG00733.hp2 HG01070.hp1 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.453+488T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115903480 | |||||||
chr5:115903492 | T | C | 2 | a0001c0001t0001g0144 a0001c0001t0001g0160 |
2 | NA18946.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.453+500T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115903492 | |||||||
chr5:115903496 | A | G | 3 | a0001c0001t0001g0330 a0001c0001t0001g0348 a0001c0001t0001g0349 |
3 | HG03098.hp1 HG03471.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.453+504A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115903496 | |||||||
chr5:115903559 | A | G | 47 | a0001c0001t0001g0009 a0001c0001t0001g0080 a0001c0001t0001g0088 others(44): Show |
48 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.453+567A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115903559 | |||||||
chr5:115903616 | G | A | 18 | a0001c0001t0001g0009 a0001c0001t0001g0088 a0001c0001t0001g0089 others(15): Show |
19 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.453+624G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115903616 | |||||||
chr5:115903669 | A | C | 1 | a0001c0001t0001g0049 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.453+677A>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115903669 | |||||||
chr5:115903783 | T | C | 49 | a0001c0001t0001g0009 a0001c0001t0001g0080 a0001c0001t0001g0088 others(46): Show |
50 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.453+791T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115903783 | |||||||
chr5:115903963 | T | C | 1 | a0001c0001t0001g0337 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.453+971T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115903963 | |||||||
chr5:115904013 | T | G | 13 | a0001c0001t0001g0007 a0001c0001t0001g0026 a0001c0001t0001g0048 others(10): Show |
14 | HG00597.hp2 HG02080.hp2 HG02083.hp2 others(11): Show |
intron_variant | MODIFIER | c.453+1021T>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115904013 | |||||||
chr5:115904030 | C | A | 10 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0240 others(7): Show |
16 | HG01934.hp2 HG02293.hp2 NA18939.hp2 others(13): Show |
intron_variant | MODIFIER | c.453+1038C>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115904030 | |||||||
chr5:115904090 | A | G | 1 | a0001c0001t0001g0049 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.453+1098A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115904090 | |||||||
chr5:115904324 | G | T | 1 | a0001c0001t0001g0324 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.453+1332G>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115904324 | |||||||
chr5:115904354 | A | G | 3 | a0001c0001t0001g0180 a0001c0001t0001g0193 a0001c0001t0001g0203 |
3 | HG01496.hp2 HG01891.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.453+1362A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115904354 | |||||||
chr5:115904443 | T | G | 7 | a0001c0001t0001g0245 a0001c0001t0001g0277 a0001c0001t0001g0288 others(4): Show |
7 | HG01943.hp2 HG02004.hp2 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.453+1451T>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115904443 | |||||||
chr5:115904458 | T | G | 33 | a0001c0001t0001g0009 a0001c0001t0001g0080 a0001c0001t0001g0088 others(30): Show |
34 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.453+1466T>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115904458 | |||||||
chr5:115904821 | G | A | 1 | a0001c0001t0001g0262 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.453+1829G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115904821 | |||||||
chr5:115904822 | GT | G | 14 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0336 others(11): Show |
14 | HG02257.hp1 HG02559.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.453+1832delT | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 115904822 | ||||||
chr5:115905015 | A | G | 1 | a0001c0001t0001g0168 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.453+2023A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115905015 | |||||||
chr5:115905286 | T | C | 4 | a0001c0001t0001g0032 a0001c0001t0001g0180 a0001c0001t0001g0193 others(1): Show |
4 | HG01496.hp2 HG01891.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.453+2294T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115905286 | |||||||
chr5:115905437 | A | G | 14 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0336 others(11): Show |
14 | HG02257.hp1 HG02559.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.453+2445A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115905437 | |||||||
chr5:115905729 | T | A | 1 | a0001c0001t0001g0348 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.453+2737T>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115905729 | |||||||
chr5:115905808 | T | C | 4 | a0001c0001t0001g0020 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG02717.hp1 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.453+2816T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115905808 | |||||||
chr5:115905816 | T | A | 1 | a0001c0001t0001g0129 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.453+2824T>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115905816 | |||||||
chr5:115905857 | A | G | 12 | a0001c0001t0001g0020 a0001c0001t0001g0036 a0001c0001t0001g0049 others(9): Show |
12 | HG00738.hp1 HG01081.hp1 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.453+2865A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115905857 | |||||||
chr5:115905933 | C | T | 1 | a0001c0001t0001g0318 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.453+2941C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115905933 | |||||||
chr5:115905942 | G | A | 4 | a0001c0001t0001g0267 a0001c0001t0001g0270 a0001c0001t0001g0274 others(1): Show |
4 | HG02683.hp2 HG03654.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.453+2950G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115905942 | |||||||
chr5:115906008 | A | T | 1 | a0001c0001t0001g0193 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.453+3016A>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115906008 | |||||||
chr5:115906061 | C | A | 79 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(76): Show |
90 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.453+3069C>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115906061 | |||||||
chr5:115906061 | C | G | 49 | a0001c0001t0001g0009 a0001c0001t0001g0080 a0001c0001t0001g0088 others(46): Show |
50 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.453+3069C>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115906061 | |||||||
chr5:115906135 | G | A | 2 | a0001c0001t0002g0328 a0001c0001t0002g0329 |
2 | HG02809.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.453+3143G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115906135 | |||||||
chr5:115906335 | T | C | 1 | a0001c0001t0001g0146 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.453+3343T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115906335 | |||||||
chr5:115906445 | G | A | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(148): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.453+3453G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115906445 | |||||||
chr5:115906532 | G | A | 4 | a0001c0001t0001g0233 a0001c0001t0002g0232 a0002c0002t0001g0228 others(1): Show |
4 | HG02258.hp2 HG02922.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.453+3540G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115906532 | |||||||
chr5:115906578 | G | C | 3 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0185 |
3 | NA18972.hp2 NA18998.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.453+3586G>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115906578 | |||||||
chr5:115907156 | T | C | 1 | a0001c0001t0001g0270 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.453+4164T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115907156 | |||||||
chr5:115907213 | A | G | 1 | a0001c0001t0001g0235 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.453+4221A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115907213 | |||||||
chr5:115907222 | C | T | 3 | a0001c0001t0001g0096 a0001c0001t0001g0098 a0001c0001t0005g0095 |
3 | HG02622.hp2 HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.453+4230C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115907222 | |||||||
chr5:115907425 | A | C | 5 | a0001c0001t0003g0021 a0001c0001t0003g0022 a0001c0001t0003g0023 others(2): Show |
5 | HG01256.hp1 HG01258.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.453+4433A>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115907425 | |||||||
chr5:115907522 | T | C | 2 | a0001c0001t0001g0279 a0001c0001t0001g0292 |
2 | NA18963.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.453+4530T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115907522 | |||||||
chr5:115907567 | A | T | 1 | a0001c0001t0001g0311 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.453+4575A>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115907567 | |||||||
chr5:115907951 | A | G | 2 | a0001c0001t0001g0037 a0001c0001t0001g0166 |
2 | HG01256.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.453+4959A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115907951 | |||||||
chr5:115907964 | C | T | 1 | a0001c0001t0001g0136 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.453+4972C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115907964 | |||||||
chr5:115908074 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.453+5082G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115908074 | |||||||
chr5:115908239 | G | A | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(149): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.454-5123G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115908239 | |||||||
chr5:115908507 | A | C | 1 | a0001c0001t0001g0332 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.454-4855A>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115908507 | |||||||
chr5:115908538 | A | G | 3 | a0001c0001t0001g0330 a0001c0001t0001g0348 a0001c0001t0001g0349 |
3 | HG03098.hp1 HG03471.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.454-4824A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115908538 | |||||||
chr5:115908575 | C | G | 1 | a0001c0001t0001g0324 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.454-4787C>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115908575 | |||||||
chr5:115908633 | C | T | 2 | a0001c0001t0001g0170 a0001c0001t0001g0192 |
2 | NA18945.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.454-4729C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115908633 | |||||||
chr5:115908677 | G | A | 63 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0020 others(60): Show |
64 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.454-4685G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115908677 | |||||||
chr5:115909049 | T | A | 47 | a0001c0001t0001g0009 a0001c0001t0001g0077 a0001c0001t0001g0080 others(44): Show |
48 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.454-4313T>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115909049 | |||||||
chr5:115909089 | GA | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(152): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.454-4262delA | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 115909089 | ||||||
chr5:115909234 | C | T | 5 | a0001c0001t0001g0018 a0001c0001t0001g0252 a0001c0001t0001g0253 others(2): Show |
6 | HG02258.hp1 HG03041.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.454-4128C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115909234 | |||||||
chr5:115909402 | A | T | 1 | a0001c0001t0001g0160 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.454-3960A>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115909402 | |||||||
chr5:115909422 | G | T | 1 | a0001c0001t0001g0163 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.454-3940G>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115909422 | |||||||
chr5:115909750 | C | T | 2 | a0001c0001t0001g0109 a0001c0001t0001g0172 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.454-3612C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115909750 | |||||||
chr5:115909764 | T | C | 2 | a0001c0001t0001g0080 a0001c0001t0001g0211 |
2 | HG02818.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.454-3598T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115909764 | |||||||
chr5:115909807 | C | T | 1 | a0001c0001t0001g0330 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.454-3555C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115909807 | |||||||
chr5:115909827 | CTG | C | 3 | a0001c0001t0002g0232 a0002c0002t0001g0228 a0002c0002t0001g0229 |
3 | HG02922.hp2 HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.454-3531_454-3530d others(4): Show |
AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 115909827 | ||||||
chr5:115909934 | A | C | 1 | a0001c0001t0001g0324 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.454-3428A>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115909934 | |||||||
chr5:115909981 | A | G | 2 | a0001c0001t0001g0133 a0001c0001t0001g0186 |
2 | NA18975.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.454-3381A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115909981 | |||||||
chr5:115909982 | G | A | 8 | a0001c0001t0001g0339 a0001c0001t0001g0351 a0001c0001t0002g0328 others(5): Show |
8 | HG02257.hp1 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.454-3380G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115909982 | |||||||
chr5:115909997 | C | T | 10 | a0001c0001t0001g0007 a0001c0001t0001g0026 a0001c0001t0001g0048 others(7): Show |
11 | HG02080.hp2 NA18953.hp2 NA18960.hp1 others(8): Show |
intron_variant | MODIFIER | c.454-3365C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115909997 | |||||||
chr5:115910001 | C | T | 1 | a0001c0001t0001g0019 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.454-3361C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115910001 | |||||||
chr5:115910128 | G | T | 1 | a0001c0001t0001g0044 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.454-3234G>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115910128 | |||||||
chr5:115910180 | A | G | 4 | a0001c0001t0001g0233 a0001c0001t0002g0232 a0002c0002t0001g0228 others(1): Show |
4 | HG02258.hp2 HG02922.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.454-3182A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115910180 | |||||||
chr5:115910265 | T | TA | 14 | a0001c0001t0001g0039 a0001c0001t0001g0052 a0001c0001t0001g0112 others(11): Show |
14 | HG01168.hp2 HG02258.hp2 HG02717.hp2 others(11): Show |
intron_variant | MODIFIER | c.454-3075dupA | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 115910265 | ||||||
chr5:115910265 | TA | T | 47 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0037 others(44): Show |
51 | HG01069.hp1 HG01255.hp2 HG01256.hp2 others(48): Show |
intron_variant | MODIFIER | c.454-3075delA | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 115910265 | ||||||
chr5:115910265 | TAA | T | 30 | a0001c0001t0001g0009 a0001c0001t0001g0088 a0001c0001t0001g0089 others(27): Show |
31 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(28): Show |
intron_variant | MODIFIER | c.454-3076_454-3075d others(4): Show |
AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 115910265 | ||||||
chr5:115910452 | C | T | 6 | a0001c0001t0001g0163 a0001c0001t0001g0186 a0001c0001t0001g0210 others(3): Show |
6 | HG02976.hp1 HG03139.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.454-2910C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115910452 | |||||||
chr5:115910453 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.454-2909G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115910453 | |||||||
chr5:115910500 | A | G | 2 | a0001c0001t0001g0348 a0001c0001t0001g0349 |
2 | HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.454-2862A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115910500 | |||||||
chr5:115910503 | T | C | 10 | a0001c0001t0001g0245 a0001c0001t0001g0249 a0001c0001t0001g0258 others(7): Show |
10 | HG01943.hp2 HG02004.hp2 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.454-2859T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115910503 | |||||||
chr5:115910509 | GA | G | 9 | a0001c0001t0001g0020 a0001c0001t0001g0225 a0001c0001t0001g0278 others(6): Show |
9 | HG00609.hp2 HG02717.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.454-2841delA | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | 115910509 | ||||||
chr5:115910727 | A | G | 1 | a0001c0001t0001g0230 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.454-2635A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115910727 | |||||||
chr5:115910805 | A | G | 3 | a0001c0001t0001g0072 a0001c0001t0001g0188 a0001c0001t0001g0189 |
3 | HG01070.hp2 HG01071.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.454-2557A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115910805 | |||||||
chr5:115910849 | C | T | 2 | a0001c0001t0001g0168 a0001c0001t0001g0204 |
2 | NA18948.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.454-2513C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115910849 | |||||||
chr5:115910855 | C | G | 3 | a0001c0001t0001g0233 a0002c0002t0001g0228 a0002c0002t0001g0229 |
3 | HG02258.hp2 HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.454-2507C>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115910855 | |||||||
chr5:115910906 | T | C | 9 | a0001c0001t0001g0020 a0001c0001t0001g0080 a0001c0001t0001g0211 others(6): Show |
9 | HG02257.hp1 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.454-2456T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115910906 | |||||||
chr5:115910931 | A | T | 1 | a0001c0001t0001g0161 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.454-2431A>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115910931 | |||||||
chr5:115911142 | A | G | 1 | a0001c0001t0001g0162 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.454-2220A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115911142 | |||||||
chr5:115911194 | T | A | 2 | a0001c0001t0002g0328 a0001c0001t0002g0329 |
2 | HG02809.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.454-2168T>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115911194 | |||||||
chr5:115911197 | T | C | 1 | a0001c0001t0001g0341 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.454-2165T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115911197 | |||||||
chr5:115911282 | A | G | 2 | a0001c0001t0001g0027 a0001c0001t0001g0028 |
2 | HG03704.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.454-2080A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115911282 | |||||||
chr5:115911473 | C | T | 1 | a0001c0001t0001g0324 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.454-1889C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115911473 | |||||||
chr5:115911487 | G | A | 2 | a0001c0001t0001g0216 a0001c0001t0001g0217 |
2 | HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.454-1875G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115911487 | |||||||
chr5:115911626 | A | G | 1 | a0001c0001t0001g0336 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.454-1736A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115911626 | |||||||
chr5:115911738 | A | C | 2 | a0001c0001t0001g0348 a0001c0001t0001g0349 |
2 | HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.454-1624A>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115911738 | |||||||
chr5:115911772 | A | G | 1 | a0001c0001t0001g0320 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.454-1590A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115911772 | |||||||
chr5:115911807 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.454-1555C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115911807 | |||||||
chr5:115911934 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.454-1428A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115911934 | |||||||
chr5:115912365 | A | G | 1 | a0001c0001t0001g0149 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.454-997A>G | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115912365 | |||||||
chr5:115912426 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.454-936C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115912426 | |||||||
chr5:115912447 | G | A | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(152): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.454-915G>A | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115912447 | |||||||
chr5:115912540 | C | T | 5 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0212 others(2): Show |
5 | HG02486.hp1 HG02965.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.454-822C>T | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115912540 | |||||||
chr5:115912688 | T | C | 1 | a0001c0001t0001g0116 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.454-674T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115912688 | |||||||
chr5:115913090 | T | C | 1 | a0001c0001t0001g0110 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.454-272T>C | AP3S1 | ENSG00000177879.17 | transcript | ENST00000316788.12 | protein_coding | 5/5 | chr5 | 115913090 |