Item | Value |
---|---|
geneid | 267012 |
ensemblid | ENSG00000182346.22 |
hgncid | 21191 |
symbol | DAOA |
name | D-amino acid oxidase activator |
refseq_nuc | NM_172370.5 |
refseq_prot | NP_758958.3 |
ensembl_nuc | ENST00000375936.9 |
ensembl_prot | ENSP00000365103.3 |
mane_status | MANE Select |
chr | chr13 |
start | 105466045 |
end | 105491034 |
strand | + |
ver | v1.2 |
region | chr13:105466045-105491034 |
region5000 | chr13:105461045-105496034 |
regionname0 | DAOA_chr13_105466045_105491034 |
regionname5000 | DAOA_chr13_105461045_105496034 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 153 | 242 | 88 | 51 | 68 | 7 | 27 | 53 | DAOA_chr13_105461045_105496034 | DAOA | MLEKL others(148): Show |
chr13 | 105461045 | 105496034 |
a0002 | 0/1 | 153 | 162 | 8 | 27 | 102 | 7 | 17 | 81 | DAOA_chr13_105461045_105496034 | DAOA | MLEKL others(148): Show |
chr13 | 105461045 | 105496034 |
a0003 | 0/0 | 153 | 8 | 0 | 0 | 8 | 0 | 0 | 6 | DAOA_chr13_105461045_105496034 | DAOA | MLEKL others(148): Show |
chr13 | 105461045 | 105496034 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 459 | 242 | 88 | 51 | 68 | 7 | 27 | DAOA_chr13_105461045_105496034 | DAOA | ATGCT others(454): Show |
chr13 | 105461045 | 105496034 | ||
a0002c0002 | 0/1 | 459 | 162 | 8 | 27 | 102 | 7 | 17 | DAOA_chr13_105461045_105496034 | DAOA | ATGCT others(454): Show |
chr13 | 105461045 | 105496034 | ||
a0003c0003 | 0/0 | 459 | 8 | 0 | 0 | 8 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | ATGCT others(454): Show |
chr13 | 105461045 | 105496034 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 785 | 184 | 63 | 40 | 50 | 5 | 25 | DAOA_chr13_105461045_105496034 | DAOA | AGCAA others(780): Show |
chr13 | 105461045 | 105496034 |
a0001c0001t0002 | 0/0 | 785 | 35 | 24 | 9 | 0 | 1 | 1 | DAOA_chr13_105461045_105496034 | DAOA | AGCAA others(780): Show |
chr13 | 105461045 | 105496034 |
a0001c0001t0003 | 0/0 | 785 | 21 | 0 | 2 | 17 | 1 | 1 | DAOA_chr13_105461045_105496034 | DAOA | AGCAA others(780): Show |
chr13 | 105461045 | 105496034 |
a0001c0001t0005 | 0/0 | 785 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | AGCAA others(780): Show |
chr13 | 105461045 | 105496034 |
a0001c0001t0007 | 0/0 | 785 | 1 | 1 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | AGCAA others(780): Show |
chr13 | 105461045 | 105496034 |
a0002c0002t0001 | 0/1 | 785 | 157 | 7 | 26 | 102 | 6 | 15 | DAOA_chr13_105461045_105496034 | DAOA | AGCAA others(780): Show |
chr13 | 105461045 | 105496034 |
a0002c0002t0002 | 0/0 | 785 | 2 | 1 | 1 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | AGCAA others(780): Show |
chr13 | 105461045 | 105496034 |
a0002c0002t0004 | 0/0 | 785 | 2 | 0 | 0 | 0 | 0 | 2 | DAOA_chr13_105461045_105496034 | DAOA | AGCAA others(780): Show |
chr13 | 105461045 | 105496034 |
a0002c0002t0006 | 0/0 | 785 | 1 | 0 | 0 | 0 | 1 | 0 | DAOA_chr13_105461045_105496034 | DAOA | AGCAA others(780): Show |
chr13 | 105461045 | 105496034 |
a0003c0003t0001 | 0/0 | 785 | 8 | 0 | 0 | 8 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | AGCAA others(780): Show |
chr13 | 105461045 | 105496034 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0003 | 0/0 | 14 | 2 | 6 | 4 | 0 | 2 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0004 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0005 | 0/0 | 8 | 2 | 2 | 3 | 0 | 1 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0007 | 0/0 | 7 | 5 | 1 | 0 | 1 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0010 | 0/0 | 5 | 0 | 4 | 0 | 0 | 1 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0018 | 1/0 | 3 | 2 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0020 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0051 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0053 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0055 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0056 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0057 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0058 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0002g0009 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0002g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0002g0016 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0002g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0002g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0002g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0002g0059 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0003g0006 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0003g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0003g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0005g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0001c0001t0007g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0001 | 0/0 | 22 | 0 | 1 | 16 | 1 | 4 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0002 | 0/0 | 14 | 0 | 1 | 8 | 1 | 4 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0008 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0012 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0014 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0035 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0036 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0244 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0002g0040 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0004g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0002c0002t0006g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0003c0003t0001g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0003c0003t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0003c0003t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
a0003c0003t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0203 | EUR | GBR | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG00099 | hp2 | a0002 | c0002 | t0001 | g0035 | EUR | GBR | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG00140 | hp1 | a0002 | c0002 | t0001 | g0001 | EUR | GBR | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0016 | EUR | GBR | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0217 | EUR | FIN | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG00280 | hp2 | a0002 | c0002 | t0001 | g0177 | EUR | FIN | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG00323 | hp1 | a0002 | c0002 | t0001 | g0002 | EUR | FIN | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG00323 | hp2 | a0002 | c0002 | t0006 | g0119 | EUR | FIN | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG00408 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG00408 | hp2 | a0002 | c0002 | t0001 | g0200 | EAS | CHS | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | CHS | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG00544 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG00544 | hp2 | a0002 | c0002 | t0001 | g0013 | EAS | CHS | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG00558 | hp1 | a0002 | c0002 | t0001 | g0246 | EAS | CHS | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG00558 | hp2 | a0002 | c0002 | t0001 | g0147 | EAS | CHS | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG00609 | hp1 | a0002 | c0002 | t0001 | g0170 | EAS | CHS | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG00609 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | CHS | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG00621 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | CHS | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG00621 | hp2 | a0003 | c0003 | t0001 | g0011 | EAS | CHS | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG00639 | hp1 | a0002 | c0002 | t0001 | g0044 | AMR | PUR | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG00642 | hp1 | a0002 | c0002 | t0001 | g0164 | AMR | PUR | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG00673 | hp1 | a0002 | c0002 | t0001 | g0175 | EAS | CHS | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG00673 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0102 | AMR | PUR | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG01070 | hp1 | a0002 | c0002 | t0001 | g0039 | AMR | PUR | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG01070 | hp2 | a0002 | c0002 | t0001 | g0035 | AMR | PUR | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG01071 | hp1 | a0002 | c0002 | t0001 | g0039 | AMR | PUR | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG01071 | hp2 | a0002 | c0002 | t0001 | g0189 | AMR | PUR | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG01081 | hp1 | a0002 | c0002 | t0001 | g0145 | AMR | PUR | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG01099 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG01109 | hp1 | a0002 | c0002 | t0002 | g0040 | AMR | PUR | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0028 | AMR | PUR | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0028 | AMR | PUR | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG01175 | hp1 | a0002 | c0002 | t0001 | g0152 | AMR | PUR | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | CLM | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG01257 | hp1 | a0002 | c0002 | t0001 | g0154 | AMR | CLM | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | CLM | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG01258 | hp2 | a0002 | c0002 | t0001 | g0153 | AMR | CLM | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG01346 | hp1 | a0002 | c0002 | t0001 | g0012 | AMR | CLM | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG01346 | hp2 | a0002 | c0002 | t0001 | g0085 | AMR | CLM | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | CLM | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG01358 | hp2 | a0002 | c0002 | t0001 | g0036 | AMR | CLM | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG01361 | hp1 | a0002 | c0002 | t0001 | g0012 | AMR | CLM | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | CLM | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG01433 | hp1 | a0002 | c0002 | t0001 | g0084 | AMR | CLM | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | CLM | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG01496 | hp2 | a0001 | c0001 | t0003 | g0061 | AMR | CLM | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG01515 | hp1 | a0001 | c0001 | t0003 | g0065 | EUR | IBS | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0109 | EUR | IBS | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG01516 | hp2 | a0002 | c0002 | t0001 | g0188 | EUR | IBS | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | ACB | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG01928 | hp1 | a0002 | c0002 | t0001 | g0012 | AMR | PEL | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG01943 | hp1 | a0002 | c0002 | t0001 | g0115 | AMR | PEL | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG01952 | hp2 | a0002 | c0002 | t0001 | g0149 | AMR | PEL | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0059 | AMR | PEL | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG01978 | hp2 | a0002 | c0002 | t0001 | g0044 | AMR | PEL | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0089 | AMR | PEL | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG01981 | hp2 | a0002 | c0002 | t0001 | g0041 | AMR | PEL | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PEL | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02004 | hp1 | a0002 | c0002 | t0001 | g0012 | AMR | PEL | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02027 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02040 | hp2 | a0002 | c0002 | t0001 | g0174 | EAS | KHV | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | ACB | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0025 | AFR | ACB | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02071 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02074 | hp2 | a0002 | c0002 | t0001 | g0034 | EAS | KHV | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02080 | hp2 | a0001 | c0001 | t0003 | g0068 | EAS | KHV | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02083 | hp1 | a0002 | c0002 | t0001 | g0173 | EAS | KHV | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02083 | hp2 | a0003 | c0003 | t0001 | g0130 | EAS | KHV | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02132 | hp1 | a0002 | c0002 | t0001 | g0034 | EAS | KHV | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02132 | hp2 | a0002 | c0002 | t0001 | g0150 | EAS | KHV | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02135 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | KHV | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02135 | hp2 | a0002 | c0002 | t0001 | g0243 | EAS | KHV | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02145 | hp1 | a0002 | c0002 | t0001 | g0114 | AFR | ACB | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02165 | hp1 | a0002 | c0002 | t0001 | g0120 | EAS | CDX | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0122 | AFR | ACB | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | ACB | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | ACB | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02273 | hp1 | a0002 | c0002 | t0001 | g0041 | AMR | PEL | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PEL | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0113 | AFR | ACB | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02293 | hp1 | a0002 | c0002 | t0001 | g0193 | AMR | PEL | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02293 | hp2 | a0002 | c0002 | t0001 | g0143 | AMR | PEL | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02300 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02300 | hp2 | a0001 | c0001 | t0003 | g0063 | AMR | PEL | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0080 | AFR | GWD | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0101 | AFR | GWD | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02735 | hp1 | a0001 | c0001 | t0003 | g0064 | SAS | PJL | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02735 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02738 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02809 | hp1 | a0002 | c0002 | t0001 | g0162 | AFR | GWD | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02818 | hp2 | a0002 | c0002 | t0002 | g0040 | AFR | GWD | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0087 | AFR | GWD | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | GWD | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | ESN | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ESN | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ESN | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | ESN | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | ESN | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | MSL | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0117 | AFR | MSL | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0090 | AFR | ESN | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | ESN | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | ESN | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | ESN | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ESN | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | ESN | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | MSL | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | MSL | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG03225 | hp1 | a0002 | c0002 | t0001 | g0032 | AFR | MSL | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | MSL | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0123 | SAS | PJL | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | MSL | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | MSL | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG03490 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG03491 | hp1 | a0002 | c0002 | t0004 | g0033 | SAS | PJL | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG03492 | hp2 | a0002 | c0002 | t0004 | g0033 | SAS | PJL | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | ESN | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG03540 | hp1 | a0002 | c0002 | t0001 | g0032 | AFR | GWD | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0088 | AFR | MSL | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG03654 | hp1 | a0002 | c0002 | t0001 | g0184 | SAS | PJL | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG03688 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | STU | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | STU | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG03704 | hp1 | a0002 | c0002 | t0001 | g0178 | SAS | PJL | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG03704 | hp2 | a0002 | c0002 | t0001 | g0166 | SAS | PJL | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG03710 | hp1 | a0002 | c0002 | t0001 | g0179 | SAS | PJL | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG03831 | hp1 | a0002 | c0002 | t0001 | g0181 | SAS | BEB | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG03831 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | BEB | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | BEB | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG03834 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | BEB | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | BEB | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG03942 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | BEB | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG04115 | hp1 | a0002 | c0002 | t0001 | g0183 | SAS | STU | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0218 | SAS | STU | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG04184 | hp1 | a0002 | c0002 | t0001 | g0191 | SAS | BEB | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | STU | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0252 | SAS | STU | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | STU | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG04204 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | STU | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | STU | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | STU | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0247 | AFR | YRI | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | YRI | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18612 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CHB | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18612 | hp2 | a0001 | c0001 | t0003 | g0062 | EAS | CHB | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18747 | hp1 | a0002 | c0002 | t0001 | g0187 | EAS | CHB | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | YRI | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | YRI | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18939 | hp1 | a0003 | c0003 | t0001 | g0129 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18940 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18942 | hp1 | a0001 | c0001 | t0003 | g0069 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18942 | hp2 | a0002 | c0002 | t0001 | g0031 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18944 | hp1 | a0002 | c0002 | t0001 | g0042 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18944 | hp2 | a0002 | c0002 | t0001 | g0172 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18945 | hp1 | a0002 | c0002 | t0001 | g0043 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18945 | hp2 | a0003 | c0003 | t0001 | g0011 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18946 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18946 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18948 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18948 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18950 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18950 | hp2 | a0002 | c0002 | t0001 | g0186 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18952 | hp1 | a0002 | c0002 | t0001 | g0192 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18952 | hp2 | a0002 | c0002 | t0001 | g0045 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18953 | hp1 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18954 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18954 | hp2 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18956 | hp1 | a0002 | c0002 | t0001 | g0238 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18957 | hp2 | a0002 | c0002 | t0001 | g0096 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18960 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18960 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18961 | hp1 | a0002 | c0002 | t0001 | g0072 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18961 | hp2 | a0002 | c0002 | t0001 | g0190 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18962 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18964 | hp2 | a0002 | c0002 | t0001 | g0141 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18965 | hp1 | a0002 | c0002 | t0001 | g0086 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18965 | hp2 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18969 | hp2 | a0002 | c0002 | t0001 | g0201 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18970 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18971 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18971 | hp2 | a0002 | c0002 | t0001 | g0168 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18972 | hp2 | a0002 | c0002 | t0001 | g0027 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18977 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18977 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18979 | hp2 | a0002 | c0002 | t0001 | g0169 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18983 | hp1 | a0003 | c0003 | t0001 | g0011 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18983 | hp2 | a0002 | c0002 | t0001 | g0167 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18984 | hp1 | a0002 | c0002 | t0001 | g0182 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18984 | hp2 | a0002 | c0002 | t0001 | g0180 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18985 | hp2 | a0002 | c0002 | t0001 | g0142 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18986 | hp1 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18988 | hp1 | a0002 | c0002 | t0001 | g0194 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18992 | hp1 | a0002 | c0002 | t0001 | g0156 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18992 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18994 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18994 | hp2 | a0002 | c0002 | t0001 | g0043 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18998 | hp1 | a0002 | c0002 | t0001 | g0042 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18998 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18999 | hp2 | a0002 | c0002 | t0001 | g0161 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19000 | hp2 | a0002 | c0002 | t0001 | g0196 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19002 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19003 | hp2 | a0002 | c0002 | t0001 | g0151 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19005 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19005 | hp2 | a0002 | c0002 | t0001 | g0146 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19006 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19007 | hp1 | a0002 | c0002 | t0001 | g0031 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19007 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19009 | hp1 | a0002 | c0002 | t0001 | g0037 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19010 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19012 | hp1 | a0002 | c0002 | t0001 | g0038 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19012 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | LWK | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19030 | hp2 | a0002 | c0002 | t0001 | g0185 | AFR | LWK | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | LWK | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | LWK | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19054 | hp1 | a0002 | c0002 | t0001 | g0160 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19055 | hp1 | a0002 | c0002 | t0001 | g0097 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19056 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19057 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19058 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19058 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19060 | hp1 | a0002 | c0002 | t0001 | g0037 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19060 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19062 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19062 | hp2 | a0001 | c0001 | t0005 | g0054 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19064 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19064 | hp2 | a0002 | c0002 | t0001 | g0038 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19068 | hp1 | a0001 | c0001 | t0003 | g0060 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19068 | hp2 | a0003 | c0003 | t0001 | g0100 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19070 | hp1 | a0002 | c0002 | t0001 | g0148 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19070 | hp2 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19074 | hp2 | a0002 | c0002 | t0001 | g0027 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19075 | hp1 | a0002 | c0002 | t0001 | g0165 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19075 | hp2 | a0002 | c0002 | t0001 | g0158 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19076 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19078 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19079 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19079 | hp2 | a0003 | c0003 | t0001 | g0011 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19080 | hp1 | a0002 | c0002 | t0001 | g0045 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19081 | hp2 | a0002 | c0002 | t0001 | g0157 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19082 | hp1 | a0002 | c0002 | t0001 | g0195 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19082 | hp2 | a0002 | c0002 | t0001 | g0163 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19083 | hp1 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19083 | hp2 | a0002 | c0002 | t0001 | g0155 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19084 | hp1 | a0002 | c0002 | t0001 | g0176 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19084 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19085 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19086 | hp1 | a0003 | c0003 | t0001 | g0011 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19086 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19088 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19090 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | ASW | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ASW | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0227 | EUR | TSI | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA20752 | hp2 | a0002 | c0002 | t0001 | g0144 | EUR | TSI | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | GIH | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | GIH | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02109 | hp1 | a0001 | c0001 | t0007 | g0248 | AFR | ACB | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02109 | hp2 | a0002 | c0002 | t0001 | g0171 | AFR | ACB | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02486 | hp2 | a0002 | c0002 | t0001 | g0036 | AFR | ACB | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | ACB | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0059 | AFR | ACB | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | MSL | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | MSL | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | USA | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | USA | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18955 | hp1 | a0002 | c0002 | t0001 | g0159 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA18955 | hp2 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0103 | AFR | USA | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | USA | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | LWK | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0251 | AFR | LWK | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0244 | REF | REF | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0018 | REF | REF | DAOA_chr13_105461045_105496034 | DAOA | chr13 | 105461045 | 105496034 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:105467097 | G | A | 1 | a0002 | 161 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(158): Show |
missense_variant | MODERATE | c.89G>A | p.Arg30Lys | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/6 | 178/785 | 89/462 | 30/153 | chr13 | 105467097 | |||
chr13:105472588 | A | G | 1 | a0003 | 8 | HG00621.hp2 HG02083.hp2 NA18939.hp1 others(5): Show |
missense_variant | MODERATE | c.184A>G | p.Lys62Glu | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/6 | 273/785 | 184/462 | 62/153 | chr13 | 105472588 | |||
chr13:105490190 | G | A | 1 | a0002 | 1 | HG00323.hp2 | splice_region_variant | LOW | c.*109G>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 5/6 | chr13 | 105490190 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:105466263 | C | T | 1 | a0001c0001t0003 | 21 | HG00609.hp2 HG00621.hp1 HG01496.hp2 others(18): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-26C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 2/6 | chr13 | 105466263 | |||||||
chr13:105490087 | G | A | 1 | a0001c0001t0005 | 1 | NA19062.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6G>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 5/6 | 6 | chr13 | 105490087 | ||||||
chr13:105490915 | A | G | 1 | a0001c0001t0007 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*115A>G | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 6/6 | 834 | chr13 | 105490915 | ||||||
chr13:105490916 | T | A | 1 | a0001c0001t0007 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*116T>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 6/6 | 835 | chr13 | 105490916 | ||||||
chr13:105490917 | G | T | 1 | a0001c0001t0007 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*117G>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 6/6 | 836 | chr13 | 105490917 | ||||||
chr13:105490933 | C | T | 2 | a0001c0001t0002 a0002c0002t0002 |
37 | HG00140.hp2 HG00733.hp2 HG00741.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*133C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 6/6 | 852 | chr13 | 105490933 | ||||||
chr13:105491000 | C | T | 1 | a0002c0002t0004 | 2 | HG03491.hp1 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*200C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 6/6 | 919 | chr13 | 105491000 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:105466153 | C | T | 1 | a0001c0001t0001g0252 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-73-63C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 1/5 | chr13 | 105466153 | |||||||
chr13:105466811 | A | C | 4 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0002g0251 others(1): Show |
4 | HG02055.hp1 HG02109.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.45-242A>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 2/5 | chr13 | 105466811 | |||||||
chr13:105466855 | T | TA | 14 | a0001c0001t0003g0006 a0001c0001t0003g0021 a0001c0001t0003g0060 others(11): Show |
21 | HG00609.hp2 HG00621.hp1 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.45-188dupA | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 105466855 | ||||||
chr13:105466929 | A | C | 1 | a0001c0001t0002g0247 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.45-124A>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 2/5 | chr13 | 105466929 | |||||||
chr13:105466963 | T | A | 3 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0007g0248 |
3 | HG02055.hp1 HG02109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.45-90T>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 2/5 | chr13 | 105466963 | |||||||
chr13:105467142 | G | A | 1 | a0002c0002t0001g0072 | 1 | NA18961.hp1 | splice_donor_variant&intron_variant | HIGH | c.133+1G>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105467142 | |||||||
chr13:105467143 | T | A | 1 | a0001c0001t0001g0073 | 1 | HG02630.hp2 | splice_donor_variant&intron_variant | HIGH | c.133+2T>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105467143 | |||||||
chr13:105467207 | G | T | 1 | a0002c0002t0001g0246 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.133+66G>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105467207 | |||||||
chr13:105467250 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.133+109C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105467250 | |||||||
chr13:105467266 | T | C | 1 | a0001c0001t0002g0251 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.133+125T>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105467266 | |||||||
chr13:105467354 | C | A | 6 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(3): Show |
6 | HG01243.hp2 HG01943.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.133+213C>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105467354 | |||||||
chr13:105467392 | C | A | 1 | a0001c0001t0002g0080 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.133+251C>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105467392 | |||||||
chr13:105467392 | C | T | 4 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0002g0251 others(1): Show |
4 | HG02055.hp1 HG02109.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.133+251C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105467392 | |||||||
chr13:105467472 | T | C | 2 | a0001c0001t0001g0081 a0001c0001t0001g0082 |
2 | HG02965.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.133+331T>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105467472 | |||||||
chr13:105467513 | A | G | 1 | a0002c0002t0001g0243 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.133+372A>G | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105467513 | |||||||
chr13:105467514 | T | C | 1 | a0001c0001t0001g0083 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.133+373T>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105467514 | |||||||
chr13:105467524 | C | T | 4 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0242 others(1): Show |
5 | HG01975.hp1 HG02258.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.133+383C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105467524 | |||||||
chr13:105467568 | C | T | 1 | a0001c0001t0001g0239 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.133+427C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105467568 | |||||||
chr13:105467583 | C | CT | 71 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0020 others(68): Show |
112 | HG00099.hp1 HG00280.hp1 HG00609.hp2 others(109): Show |
intron_variant | MODIFIER | c.133+458dupT | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr13 | 105467583 | ||||||
chr13:105467583 | CT | C | 10 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(7): Show |
10 | HG01243.hp2 HG01346.hp2 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.133+458delT | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr13 | 105467583 | ||||||
chr13:105467601 | T | C | 1 | a0002c0002t0001g0086 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.133+460T>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105467601 | |||||||
chr13:105467646 | G | A | 8 | a0001c0001t0001g0023 a0001c0001t0001g0091 a0001c0001t0002g0009 others(5): Show |
15 | HG00733.hp2 HG01361.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.133+505G>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105467646 | |||||||
chr13:105467719 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.133+578G>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105467719 | |||||||
chr13:105467729 | C | CT | 126 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(123): Show |
218 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.133+606dupT | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr13 | 105467729 | ||||||
chr13:105467729 | C | CTT | 6 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 others(3): Show |
7 | HG00408.hp2 HG00738.hp1 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.133+605_133+606dup others(2): Show |
DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr13 | 105467729 | ||||||
chr13:105467729 | CT | C | 6 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0095 others(3): Show |
6 | HG00099.hp1 HG02622.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.133+606delT | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr13 | 105467729 | ||||||
chr13:105467729 | CTT | C | 14 | a0001c0001t0003g0006 a0001c0001t0003g0021 a0001c0001t0003g0060 others(11): Show |
21 | HG00609.hp2 HG00621.hp1 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.133+605_133+606del others(2): Show |
DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr13 | 105467729 | ||||||
chr13:105467742 | T | G | 14 | a0001c0001t0003g0006 a0001c0001t0003g0021 a0001c0001t0003g0060 others(11): Show |
21 | HG00609.hp2 HG00621.hp1 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.133+601T>G | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105467742 | |||||||
chr13:105467787 | C | A | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(247): Show |
405 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(402): Show |
intron_variant | MODIFIER | c.133+646C>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105467787 | |||||||
chr13:105467838 | A | AG | 5 | a0002c0002t0001g0027 a0002c0002t0001g0096 a0002c0002t0001g0097 others(2): Show |
6 | HG00323.hp2 HG02165.hp1 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.133+698dupG | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr13 | 105467838 | ||||||
chr13:105467857 | A | T | 1 | a0001c0001t0001g0116 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.133+716A>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105467857 | |||||||
chr13:105468022 | T | C | 1 | a0001c0001t0002g0251 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.133+881T>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105468022 | |||||||
chr13:105468053 | G | T | 1 | a0002c0002t0001g0044 | 2 | HG00639.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.133+912G>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105468053 | |||||||
chr13:105468070 | A | G | 104 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0020 others(101): Show |
176 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.133+929A>G | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105468070 | |||||||
chr13:105468074 | T | C | 16 | a0001c0001t0001g0073 a0001c0001t0001g0098 a0001c0001t0003g0006 others(13): Show |
23 | HG00609.hp2 HG00621.hp1 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.133+933T>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105468074 | |||||||
chr13:105468357 | A | C | 14 | a0001c0001t0003g0006 a0001c0001t0003g0021 a0001c0001t0003g0060 others(11): Show |
21 | HG00609.hp2 HG00621.hp1 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.133+1216A>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105468357 | |||||||
chr13:105468470 | G | T | 1 | a0002c0002t0001g0196 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.133+1329G>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105468470 | |||||||
chr13:105468595 | T | C | 1 | a0001c0001t0002g0087 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.133+1454T>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105468595 | |||||||
chr13:105468636 | G | T | 15 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0017 others(12): Show |
30 | HG00140.hp2 HG00639.hp2 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.133+1495G>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105468636 | |||||||
chr13:105468757 | T | C | 1 | a0001c0001t0001g0116 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.133+1616T>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105468757 | |||||||
chr13:105468765 | T | G | 1 | a0002c0002t0006g0119 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.133+1624T>G | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105468765 | |||||||
chr13:105468775 | C | T | 13 | a0001c0001t0003g0006 a0001c0001t0003g0021 a0001c0001t0003g0061 others(10): Show |
20 | HG00609.hp2 HG00621.hp1 HG01496.hp2 others(17): Show |
intron_variant | MODIFIER | c.133+1634C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105468775 | |||||||
chr13:105469064 | G | A | 13 | a0001c0001t0003g0006 a0001c0001t0003g0021 a0001c0001t0003g0061 others(10): Show |
20 | HG00609.hp2 HG00621.hp1 HG01496.hp2 others(17): Show |
intron_variant | MODIFIER | c.133+1923G>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105469064 | |||||||
chr13:105469113 | G | A | 1 | a0002c0002t0001g0141 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.133+1972G>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105469113 | |||||||
chr13:105469137 | T | C | 3 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0079 |
3 | HG01943.hp2 HG02145.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.133+1996T>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105469137 | |||||||
chr13:105469475 | C | T | 1 | a0002c0002t0001g0195 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.133+2334C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105469475 | |||||||
chr13:105469553 | G | A | 13 | a0001c0001t0003g0006 a0001c0001t0003g0021 a0001c0001t0003g0061 others(10): Show |
20 | HG00609.hp2 HG00621.hp1 HG01496.hp2 others(17): Show |
intron_variant | MODIFIER | c.133+2412G>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105469553 | |||||||
chr13:105469735 | A | C | 1 | a0002c0002t0001g0141 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.133+2594A>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105469735 | |||||||
chr13:105469801 | A | T | 1 | a0001c0001t0002g0087 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.133+2660A>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105469801 | |||||||
chr13:105469835 | C | G | 1 | a0001c0001t0002g0087 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.133+2694C>G | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105469835 | |||||||
chr13:105469847 | C | G | 1 | a0001c0001t0002g0087 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.134-2691C>G | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105469847 | |||||||
chr13:105469855 | A | G | 1 | a0001c0001t0002g0087 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.134-2683A>G | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105469855 | |||||||
chr13:105469856 | G | T | 1 | a0001c0001t0002g0087 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.134-2682G>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105469856 | |||||||
chr13:105469871 | C | A | 1 | a0001c0001t0002g0087 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.134-2667C>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105469871 | |||||||
chr13:105469882 | G | A | 1 | a0001c0001t0002g0087 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.134-2656G>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105469882 | |||||||
chr13:105469882 | G | T | 1 | a0002c0002t0001g0194 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.134-2656G>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105469882 | |||||||
chr13:105469886 | T | A | 1 | a0001c0001t0002g0087 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.134-2652T>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105469886 | |||||||
chr13:105469887 | C | T | 1 | a0001c0001t0002g0087 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.134-2651C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105469887 | |||||||
chr13:105469889 | C | T | 1 | a0001c0001t0002g0087 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.134-2649C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105469889 | |||||||
chr13:105469890 | A | G | 1 | a0001c0001t0002g0087 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.134-2648A>G | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105469890 | |||||||
chr13:105469922 | T | C | 1 | a0002c0002t0001g0142 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.134-2616T>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105469922 | |||||||
chr13:105469932 | T | A | 1 | a0001c0001t0002g0087 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.134-2606T>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105469932 | |||||||
chr13:105469933 | A | T | 1 | a0001c0001t0002g0087 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.134-2605A>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105469933 | |||||||
chr13:105469935 | T | C | 1 | a0001c0001t0002g0087 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.134-2603T>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105469935 | |||||||
chr13:105469947 | G | A | 13 | a0001c0001t0003g0006 a0001c0001t0003g0021 a0001c0001t0003g0061 others(10): Show |
20 | HG00609.hp2 HG00621.hp1 HG01496.hp2 others(17): Show |
intron_variant | MODIFIER | c.134-2591G>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105469947 | |||||||
chr13:105469956 | A | G | 13 | a0001c0001t0003g0006 a0001c0001t0003g0021 a0001c0001t0003g0061 others(10): Show |
20 | HG00609.hp2 HG00621.hp1 HG01496.hp2 others(17): Show |
intron_variant | MODIFIER | c.134-2582A>G | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105469956 | |||||||
chr13:105469972 | G | C | 1 | a0001c0001t0001g0121 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.134-2566G>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105469972 | |||||||
chr13:105470116 | A | AT | 80 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(77): Show |
130 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.134-2407dupT | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr13 | 105470116 | ||||||
chr13:105470116 | A | ATT | 8 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0091 others(5): Show |
10 | HG01109.hp2 HG01433.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.134-2408_134-2407d others(4): Show |
DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr13 | 105470116 | ||||||
chr13:105470116 | A | ATTTTTTT | 11 | a0001c0001t0003g0006 a0001c0001t0003g0021 a0001c0001t0003g0063 others(8): Show |
18 | HG00609.hp2 HG00621.hp1 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.134-2413_134-2407d others(9): Show |
DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr13 | 105470116 | ||||||
chr13:105470268 | T | A | 1 | a0001c0001t0001g0207 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.134-2270T>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105470268 | |||||||
chr13:105470431 | A | T | 2 | a0001c0001t0001g0139 a0001c0001t0001g0140 |
2 | NA18939.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.134-2107A>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105470431 | |||||||
chr13:105470514 | C | T | 13 | a0001c0001t0003g0006 a0001c0001t0003g0021 a0001c0001t0003g0061 others(10): Show |
20 | HG00609.hp2 HG00621.hp1 HG01496.hp2 others(17): Show |
intron_variant | MODIFIER | c.134-2024C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105470514 | |||||||
chr13:105470588 | A | T | 6 | a0001c0001t0001g0017 a0001c0001t0001g0023 a0001c0001t0001g0110 others(3): Show |
9 | HG02280.hp1 HG02647.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.134-1950A>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105470588 | |||||||
chr13:105470636 | G | A | 1 | a0002c0002t0001g0143 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.134-1902G>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105470636 | |||||||
chr13:105470646 | G | A | 14 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0205 others(11): Show |
18 | HG00639.hp1 HG00741.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.134-1892G>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105470646 | |||||||
chr13:105470688 | C | A | 1 | a0001c0001t0001g0116 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.134-1850C>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105470688 | |||||||
chr13:105470697 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.134-1841C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105470697 | |||||||
chr13:105470815 | GAGT | G | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(213): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.134-1722_134-1720d others(5): Show |
DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105470815 | |||||||
chr13:105470854 | G | A | 1 | a0002c0002t0001g0146 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.134-1684G>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105470854 | |||||||
chr13:105470936 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.134-1602G>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105470936 | |||||||
chr13:105470940 | A | G | 5 | a0001c0001t0001g0054 a0001c0001t0001g0230 a0001c0001t0001g0231 others(2): Show |
5 | NA18940.hp2 NA19062.hp2 NA19081.hp1 others(2): Show |
intron_variant | MODIFIER | c.134-1598A>G | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105470940 | |||||||
chr13:105470947 | A | C | 1 | a0001c0001t0003g0070 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.134-1591A>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105470947 | |||||||
chr13:105470965 | T | A | 14 | a0001c0001t0001g0046 a0001c0001t0001g0208 a0001c0001t0003g0006 others(11): Show |
22 | HG00609.hp2 HG00621.hp1 HG01496.hp2 others(19): Show |
intron_variant | MODIFIER | c.134-1573T>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105470965 | |||||||
chr13:105470988 | T | C | 1 | a0001c0001t0001g0048 | 2 | NA18956.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.134-1550T>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105470988 | |||||||
chr13:105471000 | T | G | 17 | a0001c0001t0001g0046 a0001c0001t0001g0208 a0001c0001t0003g0006 others(14): Show |
25 | HG00558.hp2 HG00609.hp2 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.134-1538T>G | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105471000 | |||||||
chr13:105471005 | G | A | 15 | a0001c0001t0001g0046 a0001c0001t0001g0208 a0001c0001t0003g0006 others(12): Show |
23 | HG00558.hp2 HG00609.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.134-1533G>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105471005 | |||||||
chr13:105471015 | C | T | 2 | a0002c0002t0001g0188 a0002c0002t0001g0189 |
2 | HG01071.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.134-1523C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105471015 | |||||||
chr13:105471032 | C | T | 2 | a0001c0001t0001g0073 a0001c0001t0001g0093 |
2 | HG02622.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.134-1506C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105471032 | |||||||
chr13:105471035 | G | T | 2 | a0001c0001t0001g0073 a0001c0001t0001g0093 |
2 | HG02622.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.134-1503G>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105471035 | |||||||
chr13:105471079 | T | C | 2 | a0001c0001t0001g0017 a0001c0001t0001g0110 |
4 | HG02717.hp2 HG02976.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.134-1459T>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105471079 | |||||||
chr13:105471090 | T | C | 1 | a0001c0001t0003g0063 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.134-1448T>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105471090 | |||||||
chr13:105471168 | G | A | 1 | a0001c0001t0001g0211 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.134-1370G>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105471168 | |||||||
chr13:105471210 | G | A | 12 | a0001c0001t0001g0020 a0001c0001t0001g0091 a0001c0001t0001g0237 others(9): Show |
19 | HG01256.hp2 HG01258.hp1 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.134-1328G>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105471210 | |||||||
chr13:105471256 | T | C | 1 | a0001c0001t0002g0059 | 2 | HG01975.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.134-1282T>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105471256 | |||||||
chr13:105471339 | A | ATG | 3 | a0001c0001t0002g0015 a0001c0001t0002g0101 a0001c0001t0002g0251 |
6 | HG02572.hp1 HG02615.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.134-1198_134-1197i others(4): Show |
DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr13 | 105471339 | ||||||
chr13:105471342 | T | A | 3 | a0001c0001t0002g0015 a0001c0001t0002g0101 a0001c0001t0002g0251 |
6 | HG02572.hp1 HG02615.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.134-1196T>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105471342 | |||||||
chr13:105471342 | T | TAA | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(243): Show |
398 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(395): Show |
intron_variant | MODIFIER | c.134-1196_134-1195i others(4): Show |
DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105471342 | |||||||
chr13:105471351 | T | C | 1 | a0002c0002t0001g0114 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.134-1187T>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105471351 | |||||||
chr13:105471515 | T | C | 14 | a0001c0001t0001g0046 a0001c0001t0001g0208 a0001c0001t0003g0006 others(11): Show |
22 | HG00609.hp2 HG00621.hp1 HG01496.hp2 others(19): Show |
intron_variant | MODIFIER | c.134-1023T>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105471515 | |||||||
chr13:105471545 | G | C | 16 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0017 others(13): Show |
29 | HG00639.hp2 HG01081.hp2 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.134-993G>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105471545 | |||||||
chr13:105471660 | A | G | 4 | a0001c0001t0001g0091 a0001c0001t0001g0249 a0001c0001t0001g0250 others(1): Show |
4 | HG02055.hp1 HG02109.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.134-878A>G | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105471660 | |||||||
chr13:105471661 | C | A | 1 | a0001c0001t0002g0089 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.134-877C>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105471661 | |||||||
chr13:105471707 | C | T | 1 | a0002c0002t0001g0187 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.134-831C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105471707 | |||||||
chr13:105471763 | C | CT | 249 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(246): Show |
404 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(401): Show |
intron_variant | MODIFIER | c.134-775_134-774ins others(1): Show |
DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105471763 | |||||||
chr13:105471770 | A | G | 1 | a0002c0002t0001g0152 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.134-768A>G | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105471770 | |||||||
chr13:105471830 | A | G | 14 | a0001c0001t0001g0046 a0001c0001t0001g0208 a0001c0001t0003g0006 others(11): Show |
22 | HG00609.hp2 HG00621.hp1 HG01496.hp2 others(19): Show |
intron_variant | MODIFIER | c.134-708A>G | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105471830 | |||||||
chr13:105472046 | A | T | 14 | a0001c0001t0001g0046 a0001c0001t0001g0208 a0001c0001t0003g0006 others(11): Show |
22 | HG00609.hp2 HG00621.hp1 HG01496.hp2 others(19): Show |
intron_variant | MODIFIER | c.134-492A>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105472046 | |||||||
chr13:105472108 | G | C | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(228): Show |
372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.134-430G>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105472108 | |||||||
chr13:105472142 | C | T | 1 | a0001c0001t0002g0028 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.134-396C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105472142 | |||||||
chr13:105472255 | T | G | 1 | a0001c0001t0001g0239 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.134-283T>G | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105472255 | |||||||
chr13:105472327 | G | A | 2 | a0002c0002t0001g0153 a0002c0002t0001g0154 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.134-211G>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105472327 | |||||||
chr13:105472507 | G | A | 1 | a0001c0001t0001g0029 | 2 | NA18966.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.134-31G>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 3/5 | chr13 | 105472507 | |||||||
chr13:105472739 | G | C | 14 | a0001c0001t0001g0046 a0001c0001t0001g0208 a0001c0001t0003g0006 others(11): Show |
22 | HG00609.hp2 HG00621.hp1 HG01496.hp2 others(19): Show |
intron_variant | MODIFIER | c.281+54G>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105472739 | |||||||
chr13:105472750 | C | T | 1 | a0002c0002t0001g0042 | 2 | NA18944.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.281+65C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105472750 | |||||||
chr13:105472767 | G | A | 1 | a0002c0002t0001g0032 | 2 | HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.281+82G>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105472767 | |||||||
chr13:105472884 | A | C | 14 | a0001c0001t0001g0046 a0001c0001t0001g0208 a0001c0001t0003g0006 others(11): Show |
22 | HG00609.hp2 HG00621.hp1 HG01496.hp2 others(19): Show |
intron_variant | MODIFIER | c.281+199A>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105472884 | |||||||
chr13:105472905 | T | C | 5 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0126 others(2): Show |
5 | HG00438.hp1 NA18957.hp1 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.281+220T>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105472905 | |||||||
chr13:105472980 | G | C | 1 | a0002c0002t0001g0147 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.281+295G>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105472980 | |||||||
chr13:105472996 | C | T | 1 | a0002c0002t0001g0186 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.281+311C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105472996 | |||||||
chr13:105473057 | T | C | 249 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(246): Show |
404 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(401): Show |
intron_variant | MODIFIER | c.281+372T>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105473057 | |||||||
chr13:105473060 | A | G | 4 | a0001c0001t0001g0091 a0001c0001t0001g0249 a0001c0001t0001g0250 others(1): Show |
4 | HG02055.hp1 HG02109.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.281+375A>G | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105473060 | |||||||
chr13:105473130 | T | A | 1 | a0001c0001t0002g0102 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.281+445T>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105473130 | |||||||
chr13:105473156 | A | AGT | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(142): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.281+492_281+493dup others(2): Show |
DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 105473156 | ||||||
chr13:105473156 | A | T | 1 | a0002c0002t0001g0041 | 2 | HG01981.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.281+471A>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105473156 | |||||||
chr13:105473156 | AGT | A | 10 | a0001c0001t0002g0009 a0001c0001t0002g0015 a0001c0001t0002g0022 others(7): Show |
20 | HG00733.hp2 HG01109.hp1 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.281+492_281+493del others(2): Show |
DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 105473156 | ||||||
chr13:105473237 | C | A | 229 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(226): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.281+552C>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105473237 | |||||||
chr13:105473247 | C | A | 1 | a0001c0001t0001g0212 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.281+562C>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105473247 | |||||||
chr13:105473404 | G | A | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0020 others(108): Show |
180 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.281+719G>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105473404 | |||||||
chr13:105473459 | A | G | 1 | a0002c0002t0001g0086 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.281+774A>G | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105473459 | |||||||
chr13:105473617 | G | T | 1 | a0001c0001t0002g0088 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.281+932G>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105473617 | |||||||
chr13:105473633 | G | T | 3 | a0001c0001t0002g0028 a0001c0001t0002g0122 a0001c0001t0002g0123 |
4 | HG01168.hp1 HG01169.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.281+948G>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105473633 | |||||||
chr13:105473656 | T | C | 4 | a0001c0001t0001g0091 a0001c0001t0001g0249 a0001c0001t0001g0250 others(1): Show |
4 | HG02055.hp1 HG02109.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.281+971T>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105473656 | |||||||
chr13:105473783 | C | T | 1 | a0002c0002t0001g0181 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.281+1098C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105473783 | |||||||
chr13:105473784 | G | A | 2 | a0001c0001t0001g0249 a0001c0001t0001g0250 |
2 | HG02055.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.281+1099G>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105473784 | |||||||
chr13:105473859 | C | A | 49 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0026 others(46): Show |
83 | HG00099.hp1 HG00280.hp1 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.281+1174C>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105473859 | |||||||
chr13:105473959 | C | T | 63 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0026 others(60): Show |
105 | HG00099.hp1 HG00280.hp1 HG00609.hp2 others(102): Show |
intron_variant | MODIFIER | c.281+1274C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105473959 | |||||||
chr13:105474168 | A | G | 1 | a0001c0001t0001g0227 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.281+1483A>G | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105474168 | |||||||
chr13:105474231 | C | T | 1 | a0002c0002t0001g0178 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.281+1546C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105474231 | |||||||
chr13:105474244 | C | A | 2 | a0001c0001t0001g0073 a0001c0001t0001g0093 |
2 | HG02622.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.281+1559C>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105474244 | |||||||
chr13:105474303 | C | T | 13 | a0001c0001t0001g0046 a0001c0001t0001g0208 a0001c0001t0003g0006 others(10): Show |
21 | HG00609.hp2 HG00621.hp1 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.281+1618C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105474303 | |||||||
chr13:105474380 | G | A | 49 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0026 others(46): Show |
83 | HG00099.hp1 HG00280.hp1 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.281+1695G>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105474380 | |||||||
chr13:105474478 | G | T | 249 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(246): Show |
404 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(401): Show |
intron_variant | MODIFIER | c.281+1793G>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105474478 | |||||||
chr13:105474537 | A | G | 16 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0017 others(13): Show |
29 | HG00639.hp2 HG01081.hp2 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.281+1852A>G | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105474537 | |||||||
chr13:105474549 | C | T | 1 | a0001c0001t0001g0053 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.281+1864C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105474549 | |||||||
chr13:105474567 | G | T | 3 | a0002c0002t0001g0044 a0002c0002t0001g0144 a0002c0002t0001g0145 |
4 | HG00639.hp1 HG01081.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.281+1882G>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105474567 | |||||||
chr13:105474620 | T | C | 249 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(246): Show |
404 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(401): Show |
intron_variant | MODIFIER | c.281+1935T>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105474620 | |||||||
chr13:105474809 | G | C | 1 | a0001c0001t0002g0102 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.281+2124G>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105474809 | |||||||
chr13:105474943 | G | T | 1 | a0001c0001t0001g0109 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.281+2258G>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105474943 | |||||||
chr13:105475046 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.281+2361G>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105475046 | |||||||
chr13:105475080 | T | A | 1 | a0001c0001t0001g0023 | 2 | HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.281+2395T>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105475080 | |||||||
chr13:105475095 | C | T | 1 | a0001c0001t0003g0069 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.281+2410C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105475095 | |||||||
chr13:105475153 | T | C | 1 | a0001c0001t0001g0092 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.281+2468T>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105475153 | |||||||
chr13:105475180 | C | T | 71 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0010 others(68): Show |
115 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.281+2495C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105475180 | |||||||
chr13:105475407 | G | T | 1 | a0001c0001t0001g0073 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.281+2722G>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105475407 | |||||||
chr13:105475485 | T | C | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(243): Show |
400 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(397): Show |
intron_variant | MODIFIER | c.281+2800T>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105475485 | |||||||
chr13:105475501 | AC | A | 10 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(7): Show |
10 | HG01243.hp2 HG01943.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.281+2817delC | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105475501 | |||||||
chr13:105475549 | A | G | 1 | a0001c0001t0001g0094 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.281+2864A>G | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105475549 | |||||||
chr13:105475561 | GTGTT | G | 14 | a0001c0001t0001g0046 a0001c0001t0001g0208 a0001c0001t0003g0006 others(11): Show |
22 | HG00609.hp2 HG00621.hp1 HG01496.hp2 others(19): Show |
intron_variant | MODIFIER | c.281+2879_281+2882d others(6): Show |
DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 105475561 | ||||||
chr13:105475739 | A | G | 14 | a0001c0001t0001g0046 a0001c0001t0001g0208 a0001c0001t0003g0006 others(11): Show |
22 | HG00609.hp2 HG00621.hp1 HG01496.hp2 others(19): Show |
intron_variant | MODIFIER | c.281+3054A>G | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105475739 | |||||||
chr13:105475787 | A | C | 106 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0020 others(103): Show |
172 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.281+3102A>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105475787 | |||||||
chr13:105475848 | T | C | 14 | a0001c0001t0001g0046 a0001c0001t0001g0208 a0001c0001t0003g0006 others(11): Show |
22 | HG00609.hp2 HG00621.hp1 HG01496.hp2 others(19): Show |
intron_variant | MODIFIER | c.281+3163T>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105475848 | |||||||
chr13:105475914 | T | C | 1 | a0001c0001t0001g0094 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.281+3229T>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105475914 | |||||||
chr13:105475956 | C | T | 1 | a0002c0002t0001g0114 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.281+3271C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105475956 | |||||||
chr13:105476157 | C | T | 1 | a0002c0002t0001g0039 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.281+3472C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105476157 | |||||||
chr13:105476340 | G | A | 1 | a0001c0001t0001g0026 | 2 | HG02451.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.281+3655G>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105476340 | |||||||
chr13:105476415 | C | T | 7 | a0001c0001t0002g0009 a0001c0001t0002g0022 a0001c0001t0002g0087 others(4): Show |
14 | HG00733.hp2 HG01109.hp1 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.281+3730C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105476415 | |||||||
chr13:105476462 | C | T | 89 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0020 others(86): Show |
148 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.281+3777C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105476462 | |||||||
chr13:105476477 | A | T | 49 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0026 others(46): Show |
83 | HG00099.hp1 HG00280.hp1 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.281+3792A>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105476477 | |||||||
chr13:105476502 | T | TA | 21 | a0001c0001t0001g0046 a0001c0001t0001g0073 a0001c0001t0001g0074 others(18): Show |
29 | HG00558.hp1 HG00609.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.281+3834dupA | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 105476502 | ||||||
chr13:105476502 | T | TAAA | 41 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0026 others(38): Show |
75 | HG00099.hp1 HG00280.hp1 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.281+3832_281+3834d others(5): Show |
DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 105476502 | ||||||
chr13:105476502 | T | TAAAA | 6 | a0001c0001t0001g0104 a0001c0001t0001g0212 a0001c0001t0001g0215 others(3): Show |
6 | HG01496.hp1 HG02258.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.281+3831_281+3834d others(6): Show |
DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 105476502 | ||||||
chr13:105476502 | TA | T | 57 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0024 others(54): Show |
91 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.281+3834delA | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 105476502 | ||||||
chr13:105476524 | A | G | 14 | a0001c0001t0001g0046 a0001c0001t0001g0208 a0001c0001t0003g0006 others(11): Show |
22 | HG00609.hp2 HG00621.hp1 HG01496.hp2 others(19): Show |
intron_variant | MODIFIER | c.281+3839A>G | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105476524 | |||||||
chr13:105476648 | A | T | 1 | a0001c0001t0001g0138 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.281+3963A>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105476648 | |||||||
chr13:105476657 | C | T | 1 | a0002c0002t0001g0177 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.281+3972C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105476657 | |||||||
chr13:105476771 | T | C | 1 | a0001c0001t0002g0059 | 2 | HG01975.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.281+4086T>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105476771 | |||||||
chr13:105476817 | GT | G | 14 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0017 others(11): Show |
27 | HG00639.hp2 HG01081.hp2 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.281+4135delT | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 105476817 | ||||||
chr13:105476896 | G | C | 235 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(232): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.281+4211G>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105476896 | |||||||
chr13:105476969 | T | C | 1 | a0002c0002t0001g0158 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.281+4284T>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105476969 | |||||||
chr13:105476996 | T | A | 1 | a0002c0002t0001g0187 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.281+4311T>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105476996 | |||||||
chr13:105477175 | G | C | 63 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0026 others(60): Show |
105 | HG00099.hp1 HG00280.hp1 HG00609.hp2 others(102): Show |
intron_variant | MODIFIER | c.281+4490G>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105477175 | |||||||
chr13:105477188 | C | A | 63 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0026 others(60): Show |
105 | HG00099.hp1 HG00280.hp1 HG00609.hp2 others(102): Show |
intron_variant | MODIFIER | c.281+4503C>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105477188 | |||||||
chr13:105477250 | G | T | 63 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0026 others(60): Show |
105 | HG00099.hp1 HG00280.hp1 HG00609.hp2 others(102): Show |
intron_variant | MODIFIER | c.281+4565G>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105477250 | |||||||
chr13:105477270 | T | C | 8 | a0001c0001t0002g0009 a0001c0001t0002g0022 a0001c0001t0002g0087 others(5): Show |
15 | HG00733.hp2 HG01109.hp1 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.281+4585T>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105477270 | |||||||
chr13:105477275 | G | T | 73 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0026 others(70): Show |
117 | HG00099.hp1 HG00280.hp1 HG00609.hp2 others(114): Show |
intron_variant | MODIFIER | c.281+4590G>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105477275 | |||||||
chr13:105477327 | C | T | 1 | a0002c0002t0001g0176 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.281+4642C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105477327 | |||||||
chr13:105477371 | A | T | 71 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0026 others(68): Show |
115 | HG00099.hp1 HG00280.hp1 HG00609.hp2 others(112): Show |
intron_variant | MODIFIER | c.281+4686A>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105477371 | |||||||
chr13:105477422 | A | G | 71 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0026 others(68): Show |
115 | HG00099.hp1 HG00280.hp1 HG00609.hp2 others(112): Show |
intron_variant | MODIFIER | c.281+4737A>G | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105477422 | |||||||
chr13:105477452 | G | C | 1 | a0001c0001t0001g0227 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.281+4767G>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105477452 | |||||||
chr13:105477502 | G | A | 71 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0026 others(68): Show |
115 | HG00099.hp1 HG00280.hp1 HG00609.hp2 others(112): Show |
intron_variant | MODIFIER | c.281+4817G>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105477502 | |||||||
chr13:105477504 | A | G | 71 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0026 others(68): Show |
115 | HG00099.hp1 HG00280.hp1 HG00609.hp2 others(112): Show |
intron_variant | MODIFIER | c.281+4819A>G | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105477504 | |||||||
chr13:105477549 | T | A | 71 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0026 others(68): Show |
115 | HG00099.hp1 HG00280.hp1 HG00609.hp2 others(112): Show |
intron_variant | MODIFIER | c.281+4864T>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105477549 | |||||||
chr13:105477569 | T | A | 71 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0026 others(68): Show |
115 | HG00099.hp1 HG00280.hp1 HG00609.hp2 others(112): Show |
intron_variant | MODIFIER | c.281+4884T>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105477569 | |||||||
chr13:105477598 | C | T | 49 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0026 others(46): Show |
83 | HG00099.hp1 HG00280.hp1 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.281+4913C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105477598 | |||||||
chr13:105477632 | G | A | 14 | a0001c0001t0001g0046 a0001c0001t0001g0208 a0001c0001t0003g0006 others(11): Show |
22 | HG00609.hp2 HG00621.hp1 HG01496.hp2 others(19): Show |
intron_variant | MODIFIER | c.281+4947G>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105477632 | |||||||
chr13:105477689 | A | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0020 others(104): Show |
173 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.281+5004A>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105477689 | |||||||
chr13:105477693 | C | G | 1 | a0002c0002t0001g0185 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.281+5008C>G | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105477693 | |||||||
chr13:105477788 | G | A | 71 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0026 others(68): Show |
115 | HG00099.hp1 HG00280.hp1 HG00609.hp2 others(112): Show |
intron_variant | MODIFIER | c.281+5103G>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105477788 | |||||||
chr13:105477893 | C | T | 2 | a0002c0002t0001g0174 a0002c0002t0001g0175 |
2 | HG00673.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.281+5208C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105477893 | |||||||
chr13:105477960 | T | A | 8 | a0001c0001t0001g0073 a0001c0001t0001g0093 a0001c0001t0001g0239 others(5): Show |
10 | HG01168.hp1 HG01169.hp2 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.281+5275T>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105477960 | |||||||
chr13:105477961 | C | T | 8 | a0001c0001t0001g0073 a0001c0001t0001g0093 a0001c0001t0001g0239 others(5): Show |
10 | HG01168.hp1 HG01169.hp2 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.281+5276C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105477961 | |||||||
chr13:105477992 | T | C | 63 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0026 others(60): Show |
105 | HG00099.hp1 HG00280.hp1 HG00609.hp2 others(102): Show |
intron_variant | MODIFIER | c.281+5307T>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105477992 | |||||||
chr13:105478030 | C | G | 66 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0026 others(63): Show |
111 | HG00099.hp1 HG00280.hp1 HG00609.hp2 others(108): Show |
intron_variant | MODIFIER | c.281+5345C>G | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105478030 | |||||||
chr13:105478049 | A | T | 3 | a0002c0002t0001g0014 a0002c0002t0001g0043 a0002c0002t0001g0180 |
8 | NA18945.hp1 NA18953.hp1 NA18977.hp2 others(5): Show |
intron_variant | MODIFIER | c.281+5364A>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105478049 | |||||||
chr13:105478405 | A | G | 1 | a0002c0002t0001g0173 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.281+5720A>G | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105478405 | |||||||
chr13:105478424 | C | G | 1 | a0001c0001t0001g0056 | 2 | NA18962.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.281+5739C>G | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105478424 | |||||||
chr13:105478470 | G | T | 3 | a0001c0001t0002g0028 a0001c0001t0002g0122 a0001c0001t0002g0123 |
4 | HG01168.hp1 HG01169.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.281+5785G>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105478470 | |||||||
chr13:105478597 | T | C | 13 | a0001c0001t0001g0046 a0001c0001t0001g0208 a0001c0001t0003g0006 others(10): Show |
21 | HG00609.hp2 HG00621.hp1 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.281+5912T>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105478597 | |||||||
chr13:105478603 | A | G | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(161): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.281+5918A>G | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105478603 | |||||||
chr13:105478631 | G | T | 49 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0026 others(46): Show |
83 | HG00099.hp1 HG00280.hp1 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.281+5946G>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105478631 | |||||||
chr13:105478723 | A | T | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0020 others(91): Show |
153 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.281+6038A>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105478723 | |||||||
chr13:105478733 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.281+6048C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105478733 | |||||||
chr13:105478752 | C | T | 4 | a0001c0001t0001g0091 a0001c0001t0001g0249 a0001c0001t0001g0250 others(1): Show |
4 | HG02055.hp1 HG02109.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.281+6067C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105478752 | |||||||
chr13:105478789 | C | T | 187 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(184): Show |
296 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(293): Show |
intron_variant | MODIFIER | c.281+6104C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105478789 | |||||||
chr13:105478851 | A | G | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0020 others(105): Show |
181 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.281+6166A>G | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105478851 | |||||||
chr13:105478880 | A | C | 1 | a0001c0001t0001g0230 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.281+6195A>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105478880 | |||||||
chr13:105478934 | G | T | 3 | a0001c0001t0001g0239 a0001c0001t0002g0059 a0001c0001t0002g0117 |
4 | HG01975.hp1 HG02559.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.281+6249G>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105478934 | |||||||
chr13:105479021 | A | G | 1 | a0001c0001t0001g0226 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.281+6336A>G | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105479021 | |||||||
chr13:105479101 | C | T | 1 | a0001c0001t0002g0059 | 2 | HG01975.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.281+6416C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105479101 | |||||||
chr13:105479141 | T | C | 13 | a0001c0001t0001g0046 a0001c0001t0001g0208 a0001c0001t0003g0006 others(10): Show |
21 | HG00609.hp2 HG00621.hp1 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.281+6456T>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105479141 | |||||||
chr13:105479189 | T | C | 13 | a0001c0001t0001g0046 a0001c0001t0001g0208 a0001c0001t0003g0006 others(10): Show |
21 | HG00609.hp2 HG00621.hp1 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.281+6504T>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105479189 | |||||||
chr13:105479194 | G | A | 1 | a0002c0002t0001g0159 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.281+6509G>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105479194 | |||||||
chr13:105479245 | A | T | 90 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0020 others(87): Show |
149 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.281+6560A>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105479245 | |||||||
chr13:105479247 | T | C | 1 | a0002c0002t0001g0115 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.281+6562T>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105479247 | |||||||
chr13:105479268 | C | A | 49 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0048 others(46): Show |
82 | HG00099.hp1 HG00280.hp1 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.281+6583C>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105479268 | |||||||
chr13:105479303 | C | G | 1 | a0002c0002t0001g0150 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.281+6618C>G | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105479303 | |||||||
chr13:105479309 | T | G | 13 | a0001c0001t0001g0046 a0001c0001t0001g0208 a0001c0001t0003g0006 others(10): Show |
21 | HG00609.hp2 HG00621.hp1 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.281+6624T>G | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105479309 | |||||||
chr13:105479418 | A | C | 13 | a0001c0001t0001g0046 a0001c0001t0001g0208 a0001c0001t0003g0006 others(10): Show |
21 | HG00609.hp2 HG00621.hp1 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.281+6733A>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105479418 | |||||||
chr13:105479496 | A | G | 8 | a0001c0001t0001g0026 a0001c0001t0001g0093 a0001c0001t0001g0239 others(5): Show |
13 | HG01975.hp1 HG02451.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.281+6811A>G | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105479496 | |||||||
chr13:105479523 | C | T | 21 | a0001c0001t0001g0026 a0001c0001t0001g0046 a0001c0001t0001g0093 others(18): Show |
34 | HG00609.hp2 HG00621.hp1 HG01496.hp2 others(31): Show |
intron_variant | MODIFIER | c.281+6838C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105479523 | |||||||
chr13:105479533 | A | G | 21 | a0001c0001t0001g0026 a0001c0001t0001g0046 a0001c0001t0001g0093 others(18): Show |
34 | HG00609.hp2 HG00621.hp1 HG01496.hp2 others(31): Show |
intron_variant | MODIFIER | c.281+6848A>G | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105479533 | |||||||
chr13:105479583 | A | G | 1 | a0001c0001t0001g0104 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.281+6898A>G | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105479583 | |||||||
chr13:105479596 | T | C | 4 | a0001c0001t0002g0016 a0001c0001t0002g0028 a0001c0001t0002g0122 others(1): Show |
7 | HG00140.hp2 HG01167.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.281+6911T>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105479596 | |||||||
chr13:105479646 | C | A | 2 | a0001c0001t0003g0064 a0001c0001t0003g0065 |
2 | HG01515.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.281+6961C>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105479646 | |||||||
chr13:105479675 | C | T | 2 | a0001c0001t0001g0017 a0001c0001t0001g0110 |
4 | HG02717.hp2 HG02976.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.281+6990C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105479675 | |||||||
chr13:105479870 | A | C | 90 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0020 others(87): Show |
149 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.281+7185A>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105479870 | |||||||
chr13:105479890 | T | C | 21 | a0001c0001t0001g0026 a0001c0001t0001g0046 a0001c0001t0001g0093 others(18): Show |
34 | HG00609.hp2 HG00621.hp1 HG01496.hp2 others(31): Show |
intron_variant | MODIFIER | c.281+7205T>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105479890 | |||||||
chr13:105479918 | C | T | 10 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(7): Show |
10 | HG01243.hp2 HG01943.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.281+7233C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105479918 | |||||||
chr13:105479987 | G | A | 15 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0017 others(12): Show |
28 | HG00639.hp2 HG01081.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.281+7302G>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105479987 | |||||||
chr13:105480036 | T | C | 2 | a0001c0001t0001g0049 a0001c0001t0001g0050 |
4 | HG02280.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.281+7351T>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105480036 | |||||||
chr13:105480189 | C | A | 13 | a0001c0001t0001g0046 a0001c0001t0001g0208 a0001c0001t0003g0006 others(10): Show |
21 | HG00609.hp2 HG00621.hp1 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.281+7504C>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105480189 | |||||||
chr13:105480237 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.281+7552G>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105480237 | |||||||
chr13:105480285 | G | A | 2 | a0002c0002t0001g0044 a0002c0002t0001g0144 |
3 | HG00639.hp1 HG01978.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.281+7600G>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105480285 | |||||||
chr13:105480370 | C | A | 90 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0020 others(87): Show |
149 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.281+7685C>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105480370 | |||||||
chr13:105480462 | CAGAT | C | 13 | a0001c0001t0001g0046 a0001c0001t0001g0208 a0001c0001t0003g0006 others(10): Show |
21 | HG00609.hp2 HG00621.hp1 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.281+7781_281+7784d others(6): Show |
DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 105480462 | ||||||
chr13:105480495 | G | A | 18 | a0001c0001t0001g0026 a0001c0001t0001g0046 a0001c0001t0001g0093 others(15): Show |
28 | HG00609.hp2 HG00621.hp1 HG01496.hp2 others(25): Show |
intron_variant | MODIFIER | c.281+7810G>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105480495 | |||||||
chr13:105480527 | C | CATAG | 60 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0019 others(57): Show |
98 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.281+7883_281+7886d others(6): Show |
DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 105480527 | ||||||
chr13:105480527 | C | CATAGATA others(1): Show |
14 | a0001c0001t0001g0051 a0001c0001t0001g0094 a0001c0001t0001g0118 others(11): Show |
18 | HG00738.hp2 HG01106.hp2 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.281+7879_281+7886d others(10): Show |
DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 105480527 | ||||||
chr13:105480527 | C | CATAGATA others(5): Show |
2 | a0002c0002t0001g0148 a0002c0002t0001g0160 |
2 | NA19054.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.281+7875_281+7886d others(14): Show |
DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 105480527 | ||||||
chr13:105480527 | CATAG | C | 29 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0049 others(26): Show |
44 | HG00639.hp2 HG00741.hp2 HG01106.hp1 others(41): Show |
intron_variant | MODIFIER | c.281+7883_281+7886d others(6): Show |
DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 105480527 | ||||||
chr13:105480527 | CATAGATA others(1): Show |
C | 6 | a0001c0001t0001g0026 a0001c0001t0001g0078 a0001c0001t0001g0136 others(3): Show |
8 | HG01099.hp1 HG01358.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.281+7879_281+7886d others(10): Show |
DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 105480527 | ||||||
chr13:105480527 | CATAGATA others(5): Show |
C | 5 | a0001c0001t0001g0093 a0001c0001t0001g0239 a0001c0001t0002g0059 others(2): Show |
6 | HG01515.hp1 HG01975.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.281+7875_281+7886d others(14): Show |
DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 105480527 | ||||||
chr13:105480527 | CATAGATA others(9): Show |
C | 12 | a0001c0001t0001g0046 a0001c0001t0001g0208 a0001c0001t0002g0117 others(9): Show |
20 | HG00609.hp2 HG00621.hp1 HG01496.hp2 others(17): Show |
intron_variant | MODIFIER | c.281+7871_281+7886d others(18): Show |
DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 105480527 | ||||||
chr13:105480550 | A | AGATAGAT | 5 | a0001c0001t0002g0009 a0001c0001t0002g0022 a0001c0001t0002g0087 others(2): Show |
11 | HG00733.hp2 HG01361.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.281+7866_281+7872d others(9): Show |
DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 105480550 | ||||||
chr13:105480550 | A | AGATAGAT others(4): Show |
3 | a0001c0001t0002g0088 a0001c0001t0002g0090 a0002c0002t0002g0040 |
4 | HG01109.hp1 HG02818.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.281+7866_281+7876d others(13): Show |
DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 105480550 | ||||||
chr13:105480571 | G | A | 2 | a0001c0001t0003g0071 a0002c0002t0001g0147 |
2 | HG00558.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.281+7886G>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105480571 | |||||||
chr13:105480594 | G | A | 2 | a0001c0001t0001g0240 a0001c0001t0001g0242 |
2 | HG02258.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.281+7909G>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105480594 | |||||||
chr13:105480634 | C | T | 49 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0048 others(46): Show |
82 | HG00099.hp1 HG00280.hp1 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.281+7949C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105480634 | |||||||
chr13:105480809 | G | T | 18 | a0001c0001t0001g0026 a0001c0001t0001g0046 a0001c0001t0001g0093 others(15): Show |
28 | HG00609.hp2 HG00621.hp1 HG01496.hp2 others(25): Show |
intron_variant | MODIFIER | c.281+8124G>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105480809 | |||||||
chr13:105480917 | G | T | 1 | a0001c0001t0001g0094 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.281+8232G>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105480917 | |||||||
chr13:105480918 | T | TCCACTGA | 7 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(4): Show |
7 | HG01243.hp2 HG02896.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.281+8235_281+8241d others(9): Show |
DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 105480918 | ||||||
chr13:105480926 | C | T | 18 | a0001c0001t0001g0026 a0001c0001t0001g0046 a0001c0001t0001g0093 others(15): Show |
28 | HG00609.hp2 HG00621.hp1 HG01496.hp2 others(25): Show |
intron_variant | MODIFIER | c.281+8241C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105480926 | |||||||
chr13:105480990 | C | T | 18 | a0001c0001t0001g0026 a0001c0001t0001g0046 a0001c0001t0001g0093 others(15): Show |
28 | HG00609.hp2 HG00621.hp1 HG01496.hp2 others(25): Show |
intron_variant | MODIFIER | c.281+8305C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105480990 | |||||||
chr13:105481016 | A | C | 18 | a0001c0001t0001g0026 a0001c0001t0001g0046 a0001c0001t0001g0093 others(15): Show |
28 | HG00609.hp2 HG00621.hp1 HG01496.hp2 others(25): Show |
intron_variant | MODIFIER | c.281+8331A>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105481016 | |||||||
chr13:105481084 | T | C | 18 | a0001c0001t0001g0026 a0001c0001t0001g0046 a0001c0001t0001g0093 others(15): Show |
28 | HG00609.hp2 HG00621.hp1 HG01496.hp2 others(25): Show |
intron_variant | MODIFIER | c.281+8399T>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105481084 | |||||||
chr13:105481090 | A | G | 1 | a0001c0001t0001g0203 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.281+8405A>G | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105481090 | |||||||
chr13:105481110 | A | G | 18 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(15): Show |
25 | HG00733.hp2 HG01109.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.281+8425A>G | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105481110 | |||||||
chr13:105481199 | C | T | 13 | a0001c0001t0001g0046 a0001c0001t0001g0208 a0001c0001t0003g0006 others(10): Show |
21 | HG00609.hp2 HG00621.hp1 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.281+8514C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105481199 | |||||||
chr13:105481258 | T | C | 1 | a0002c0002t0001g0173 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.281+8573T>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105481258 | |||||||
chr13:105481283 | T | C | 18 | a0001c0001t0001g0026 a0001c0001t0001g0046 a0001c0001t0001g0093 others(15): Show |
28 | HG00609.hp2 HG00621.hp1 HG01496.hp2 others(25): Show |
intron_variant | MODIFIER | c.281+8598T>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105481283 | |||||||
chr13:105481410 | C | T | 14 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0017 others(11): Show |
27 | HG00639.hp2 HG01081.hp2 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.282-8491C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105481410 | |||||||
chr13:105481445 | C | G | 1 | a0001c0001t0001g0222 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.282-8456C>G | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105481445 | |||||||
chr13:105481560 | A | T | 1 | a0001c0001t0001g0202 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.282-8341A>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105481560 | |||||||
chr13:105481605 | G | A | 3 | a0001c0001t0002g0015 a0001c0001t0002g0101 a0001c0001t0002g0251 |
6 | HG02572.hp1 HG02615.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.282-8296G>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105481605 | |||||||
chr13:105481700 | G | A | 2 | a0001c0001t0002g0059 a0001c0001t0002g0117 |
3 | HG01975.hp1 HG02559.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.282-8201G>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105481700 | |||||||
chr13:105481733 | C | A | 7 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(4): Show |
7 | HG01243.hp2 HG02896.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.282-8168C>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105481733 | |||||||
chr13:105481796 | A | C | 13 | a0001c0001t0001g0046 a0001c0001t0001g0208 a0001c0001t0003g0006 others(10): Show |
21 | HG00609.hp2 HG00621.hp1 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.282-8105A>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105481796 | |||||||
chr13:105481820 | C | T | 6 | a0001c0001t0002g0015 a0001c0001t0002g0028 a0001c0001t0002g0101 others(3): Show |
10 | HG01168.hp1 HG01169.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.282-8081C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105481820 | |||||||
chr13:105481849 | G | A | 8 | a0001c0001t0002g0009 a0001c0001t0002g0022 a0001c0001t0002g0087 others(5): Show |
15 | HG00733.hp2 HG01109.hp1 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.282-8052G>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105481849 | |||||||
chr13:105482005 | C | A | 8 | a0001c0001t0002g0009 a0001c0001t0002g0022 a0001c0001t0002g0087 others(5): Show |
15 | HG00733.hp2 HG01109.hp1 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.282-7896C>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105482005 | |||||||
chr13:105482010 | G | A | 13 | a0001c0001t0001g0046 a0001c0001t0001g0208 a0001c0001t0003g0006 others(10): Show |
21 | HG00609.hp2 HG00621.hp1 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.282-7891G>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105482010 | |||||||
chr13:105482061 | T | C | 90 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0020 others(87): Show |
149 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.282-7840T>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105482061 | |||||||
chr13:105482108 | C | T | 1 | a0001c0001t0003g0067 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.282-7793C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105482108 | |||||||
chr13:105482110 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.282-7791G>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105482110 | |||||||
chr13:105482149 | A | ACT | 13 | a0001c0001t0001g0046 a0001c0001t0001g0208 a0001c0001t0003g0006 others(10): Show |
21 | HG00609.hp2 HG00621.hp1 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.282-7752_282-7751i others(4): Show |
DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105482149 | |||||||
chr13:105482167 | C | G | 1 | a0001c0001t0001g0116 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.282-7734C>G | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105482167 | |||||||
chr13:105482168 | G | T | 13 | a0001c0001t0001g0046 a0001c0001t0001g0208 a0001c0001t0003g0006 others(10): Show |
21 | HG00609.hp2 HG00621.hp1 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.282-7733G>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105482168 | |||||||
chr13:105482201 | T | C | 6 | a0001c0001t0001g0046 a0001c0001t0001g0208 a0001c0001t0003g0061 others(3): Show |
7 | HG01496.hp2 HG01515.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.282-7700T>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105482201 | |||||||
chr13:105482243 | A | G | 4 | a0001c0001t0001g0091 a0001c0001t0001g0249 a0001c0001t0001g0250 others(1): Show |
4 | HG02055.hp1 HG02109.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.282-7658A>G | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105482243 | |||||||
chr13:105482357 | AT | A | 6 | a0001c0001t0002g0015 a0001c0001t0002g0028 a0001c0001t0002g0101 others(3): Show |
10 | HG01168.hp1 HG01169.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.282-7533delT | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 105482357 | ||||||
chr13:105482357 | ATT | A | 16 | a0001c0001t0001g0026 a0001c0001t0001g0046 a0001c0001t0001g0093 others(13): Show |
25 | HG00609.hp2 HG00621.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.282-7534_282-7533d others(4): Show |
DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 105482357 | ||||||
chr13:105482393 | A | G | 1 | a0001c0001t0001g0202 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.282-7508A>G | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105482393 | |||||||
chr13:105482419 | C | T | 13 | a0001c0001t0001g0046 a0001c0001t0001g0208 a0001c0001t0003g0006 others(10): Show |
21 | HG00609.hp2 HG00621.hp1 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.282-7482C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105482419 | |||||||
chr13:105482420 | G | A | 3 | a0001c0001t0001g0026 a0001c0001t0001g0093 a0001c0001t0001g0239 |
4 | HG02451.hp2 HG02622.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.282-7481G>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105482420 | |||||||
chr13:105482457 | C | A | 3 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0007g0248 |
3 | HG02055.hp1 HG02109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.282-7444C>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105482457 | |||||||
chr13:105482505 | A | C | 49 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0048 others(46): Show |
82 | HG00099.hp1 HG00280.hp1 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.282-7396A>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105482505 | |||||||
chr13:105482506 | GT | G | 24 | a0001c0001t0001g0026 a0001c0001t0001g0074 a0001c0001t0001g0075 others(21): Show |
33 | HG00733.hp1 HG00733.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.282-7378delT | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 105482506 | ||||||
chr13:105482595 | C | T | 46 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0024 others(43): Show |
71 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.282-7306C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105482595 | |||||||
chr13:105482640 | T | A | 90 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0020 others(87): Show |
149 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.282-7261T>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105482640 | |||||||
chr13:105482708 | A | G | 16 | a0001c0001t0001g0047 a0001c0001t0001g0205 a0001c0001t0001g0207 others(13): Show |
25 | HG00544.hp2 HG00741.hp2 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.282-7193A>G | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105482708 | |||||||
chr13:105482742 | G | A | 10 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(7): Show |
10 | HG01243.hp2 HG01943.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.282-7159G>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105482742 | |||||||
chr13:105482798 | T | G | 6 | a0001c0001t0001g0026 a0001c0001t0001g0093 a0001c0001t0001g0239 others(3): Show |
10 | HG02451.hp2 HG02572.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.282-7103T>G | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105482798 | |||||||
chr13:105482955 | A | C | 15 | a0001c0001t0002g0009 a0001c0001t0002g0015 a0001c0001t0002g0016 others(12): Show |
28 | HG00140.hp2 HG00733.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.282-6946A>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105482955 | |||||||
chr13:105482967 | A | G | 3 | a0001c0001t0001g0026 a0001c0001t0001g0093 a0001c0001t0001g0239 |
4 | HG02451.hp2 HG02622.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.282-6934A>G | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105482967 | |||||||
chr13:105482978 | A | C | 3 | a0001c0001t0001g0026 a0001c0001t0001g0093 a0001c0001t0001g0239 |
4 | HG02451.hp2 HG02622.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.282-6923A>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105482978 | |||||||
chr13:105483047 | C | A | 1 | a0001c0001t0001g0133 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.282-6854C>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105483047 | |||||||
chr13:105483139 | A | T | 1 | a0002c0002t0001g0171 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.282-6762A>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105483139 | |||||||
chr13:105483193 | T | C | 3 | a0001c0001t0002g0015 a0001c0001t0002g0101 a0001c0001t0002g0251 |
6 | HG02572.hp1 HG02615.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.282-6708T>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105483193 | |||||||
chr13:105483203 | G | C | 1 | a0001c0001t0001g0078 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.282-6698G>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105483203 | |||||||
chr13:105483258 | T | C | 104 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0020 others(101): Show |
172 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.282-6643T>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105483258 | |||||||
chr13:105483356 | G | T | 7 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(4): Show |
7 | HG01243.hp2 HG02896.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.282-6545G>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105483356 | |||||||
chr13:105483392 | G | T | 1 | a0001c0001t0003g0066 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.282-6509G>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105483392 | |||||||
chr13:105483486 | G | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0110 |
4 | HG02717.hp2 HG02976.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.282-6415G>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105483486 | |||||||
chr13:105483568 | A | G | 3 | a0001c0001t0001g0026 a0001c0001t0001g0093 a0001c0001t0001g0239 |
4 | HG02451.hp2 HG02622.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.282-6333A>G | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105483568 | |||||||
chr13:105483623 | T | C | 106 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0020 others(103): Show |
175 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.282-6278T>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105483623 | |||||||
chr13:105483685 | A | AT | 4 | a0001c0001t0001g0026 a0001c0001t0001g0050 a0001c0001t0001g0093 others(1): Show |
6 | HG02451.hp2 HG02622.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.282-6208dupT | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 105483685 | ||||||
chr13:105483708 | T | G | 1 | a0001c0001t0001g0232 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.282-6193T>G | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105483708 | |||||||
chr13:105483709 | G | A | 1 | a0001c0001t0002g0022 | 2 | HG00733.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.282-6192G>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105483709 | |||||||
chr13:105483748 | G | A | 1 | a0001c0001t0001g0030 | 2 | HG01074.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.282-6153G>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105483748 | |||||||
chr13:105483958 | C | T | 28 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0024 others(25): Show |
42 | HG00438.hp2 HG00609.hp1 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.282-5943C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105483958 | |||||||
chr13:105483999 | G | A | 1 | a0002c0002t0001g0177 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.282-5902G>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105483999 | |||||||
chr13:105484032 | T | C | 1 | a0002c0002t0001g0163 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.282-5869T>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105484032 | |||||||
chr13:105484107 | G | A | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.282-5794G>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105484107 | |||||||
chr13:105484163 | G | A | 4 | a0001c0001t0001g0026 a0001c0001t0001g0050 a0001c0001t0001g0093 others(1): Show |
6 | HG02451.hp2 HG02622.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.282-5738G>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105484163 | |||||||
chr13:105484325 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.282-5576G>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105484325 | |||||||
chr13:105484383 | T | A | 106 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0020 others(103): Show |
175 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.282-5518T>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105484383 | |||||||
chr13:105484484 | T | A | 2 | a0001c0001t0001g0124 a0001c0001t0001g0126 |
2 | HG00438.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.282-5417T>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105484484 | |||||||
chr13:105484493 | C | T | 3 | a0001c0001t0002g0015 a0001c0001t0002g0101 a0001c0001t0002g0251 |
6 | HG02572.hp1 HG02615.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.282-5408C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105484493 | |||||||
chr13:105484643 | G | A | 4 | a0001c0001t0001g0091 a0001c0001t0001g0249 a0001c0001t0001g0250 others(1): Show |
4 | HG02055.hp1 HG02109.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.282-5258G>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105484643 | |||||||
chr13:105484737 | G | A | 10 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(7): Show |
10 | HG01243.hp2 HG01943.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.282-5164G>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105484737 | |||||||
chr13:105484805 | C | T | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(121): Show |
210 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.282-5096C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105484805 | |||||||
chr13:105484821 | T | G | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(248): Show |
406 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(403): Show |
intron_variant | MODIFIER | c.282-5080T>G | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105484821 | |||||||
chr13:105484855 | A | G | 1 | a0001c0001t0001g0216 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.282-5046A>G | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105484855 | |||||||
chr13:105485001 | C | T | 1 | a0002c0002t0001g0027 | 2 | NA18972.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.282-4900C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105485001 | |||||||
chr13:105485112 | A | C | 105 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0020 others(102): Show |
174 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.282-4789A>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105485112 | |||||||
chr13:105485215 | C | A | 1 | a0001c0001t0001g0078 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.282-4686C>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105485215 | |||||||
chr13:105485324 | C | T | 2 | a0001c0001t0002g0059 a0001c0001t0002g0117 |
3 | HG01975.hp1 HG02559.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.282-4577C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105485324 | |||||||
chr13:105485395 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.282-4506G>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105485395 | |||||||
chr13:105485404 | G | A | 10 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(7): Show |
10 | HG01243.hp2 HG01943.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.282-4497G>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105485404 | |||||||
chr13:105485736 | G | A | 16 | a0001c0001t0001g0020 a0001c0001t0001g0237 a0001c0001t0003g0068 others(13): Show |
24 | HG01256.hp2 HG01258.hp1 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.282-4165G>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105485736 | |||||||
chr13:105485767 | T | A | 1 | a0001c0001t0001g0077 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.282-4134T>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105485767 | |||||||
chr13:105485911 | G | C | 104 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0020 others(101): Show |
173 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.282-3990G>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105485911 | |||||||
chr13:105485980 | C | T | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(248): Show |
406 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(403): Show |
intron_variant | MODIFIER | c.282-3921C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105485980 | |||||||
chr13:105486017 | C | T | 89 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0020 others(86): Show |
148 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.282-3884C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105486017 | |||||||
chr13:105486110 | T | C | 1 | a0001c0001t0001g0217 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.282-3791T>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105486110 | |||||||
chr13:105486111 | G | A | 4 | a0001c0001t0001g0052 a0001c0001t0001g0073 a0001c0001t0001g0220 others(1): Show |
5 | HG01884.hp2 HG02630.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.282-3790G>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105486111 | |||||||
chr13:105486147 | C | G | 1 | a0001c0001t0001g0215 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.282-3754C>G | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105486147 | |||||||
chr13:105486575 | C | T | 10 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(7): Show |
10 | HG01243.hp2 HG01943.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.282-3326C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105486575 | |||||||
chr13:105486617 | C | CT | 16 | a0001c0001t0001g0046 a0001c0001t0001g0131 a0001c0001t0001g0208 others(13): Show |
29 | HG00099.hp2 HG00544.hp2 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.282-3281dupT | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 105486617 | ||||||
chr13:105486619 | TTC | T | 46 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0048 others(43): Show |
77 | HG00099.hp1 HG00280.hp1 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.282-3280_282-3279d others(4): Show |
DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 105486619 | ||||||
chr13:105486621 | C | T | 204 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(201): Show |
328 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.282-3280C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105486621 | |||||||
chr13:105486743 | C | T | 1 | a0001c0001t0001g0218 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.282-3158C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105486743 | |||||||
chr13:105486901 | T | C | 3 | a0002c0002t0001g0161 a0002c0002t0001g0168 a0002c0002t0001g0190 |
3 | NA18961.hp2 NA18971.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.282-3000T>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105486901 | |||||||
chr13:105486923 | G | A | 1 | a0001c0001t0007g0248 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.282-2978G>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105486923 | |||||||
chr13:105486986 | A | C | 3 | a0002c0002t0001g0014 a0002c0002t0001g0043 a0002c0002t0001g0180 |
8 | NA18945.hp1 NA18953.hp1 NA18977.hp2 others(5): Show |
intron_variant | MODIFIER | c.282-2915A>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105486986 | |||||||
chr13:105487086 | G | A | 3 | a0001c0001t0001g0046 a0001c0001t0001g0208 a0001c0001t0003g0061 |
4 | HG01496.hp2 HG02602.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.282-2815G>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105487086 | |||||||
chr13:105487170 | C | T | 1 | a0001c0001t0002g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.282-2731C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105487170 | |||||||
chr13:105487171 | G | A | 2 | a0002c0002t0001g0037 a0002c0002t0001g0182 |
3 | NA18984.hp1 NA19009.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.282-2730G>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105487171 | |||||||
chr13:105487313 | T | G | 127 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(124): Show |
196 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.282-2588T>G | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105487313 | |||||||
chr13:105487328 | A | T | 21 | a0001c0001t0002g0009 a0001c0001t0002g0015 a0001c0001t0002g0022 others(18): Show |
34 | HG00733.hp2 HG00741.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.282-2573A>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105487328 | |||||||
chr13:105487338 | T | C | 1 | a0001c0001t0001g0093 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.282-2563T>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105487338 | |||||||
chr13:105487397 | T | C | 10 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(7): Show |
10 | HG01243.hp2 HG01943.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.282-2504T>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105487397 | |||||||
chr13:105487421 | G | C | 3 | a0001c0001t0002g0015 a0001c0001t0002g0101 a0001c0001t0002g0251 |
6 | HG02572.hp1 HG02615.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.282-2480G>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105487421 | |||||||
chr13:105487455 | T | G | 2 | a0001c0001t0002g0059 a0001c0001t0002g0117 |
3 | HG01975.hp1 HG02559.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.282-2446T>G | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105487455 | |||||||
chr13:105487470 | T | C | 1 | a0001c0001t0001g0093 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.282-2431T>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105487470 | |||||||
chr13:105487497 | C | A | 2 | a0001c0001t0002g0059 a0001c0001t0002g0117 |
3 | HG01975.hp1 HG02559.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.282-2404C>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105487497 | |||||||
chr13:105487539 | C | G | 1 | a0002c0002t0001g0167 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.282-2362C>G | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105487539 | |||||||
chr13:105487591 | GA | G | 52 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0048 others(49): Show |
83 | HG00099.hp1 HG00280.hp1 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.282-2298delA | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 105487591 | ||||||
chr13:105487591 | GAA | G | 67 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0024 others(64): Show |
105 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(102): Show |
intron_variant | MODIFIER | c.282-2299_282-2298d others(4): Show |
DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 105487591 | ||||||
chr13:105487591 | GAAA | G | 10 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(7): Show |
10 | HG01243.hp2 HG01943.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.282-2300_282-2298d others(5): Show |
DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 105487591 | ||||||
chr13:105487628 | G | C | 1 | a0001c0001t0001g0077 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.282-2273G>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105487628 | |||||||
chr13:105487754 | G | T | 12 | a0001c0001t0001g0046 a0001c0001t0001g0131 a0001c0001t0001g0208 others(9): Show |
19 | HG00609.hp2 HG00621.hp1 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.282-2147G>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105487754 | |||||||
chr13:105487759 | C | A | 1 | a0001c0001t0001g0108 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.282-2142C>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105487759 | |||||||
chr13:105487811 | C | T | 2 | a0001c0001t0002g0025 a0001c0001t0002g0080 |
3 | HG02055.hp2 HG02559.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.282-2090C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105487811 | |||||||
chr13:105487843 | C | A | 10 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(7): Show |
10 | HG01243.hp2 HG01943.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.282-2058C>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105487843 | |||||||
chr13:105487859 | A | G | 4 | a0001c0001t0002g0016 a0001c0001t0002g0028 a0001c0001t0002g0122 others(1): Show |
7 | HG00140.hp2 HG01167.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.282-2042A>G | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105487859 | |||||||
chr13:105487873 | T | A | 3 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0206 |
3 | HG02965.hp1 HG03195.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.282-2028T>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105487873 | |||||||
chr13:105487983 | A | G | 1 | a0002c0002t0001g0114 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.282-1918A>G | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105487983 | |||||||
chr13:105488053 | C | G | 1 | a0001c0001t0001g0239 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.282-1848C>G | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105488053 | |||||||
chr13:105488066 | A | G | 1 | a0001c0001t0001g0207 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.282-1835A>G | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105488066 | |||||||
chr13:105488337 | G | T | 2 | a0001c0001t0002g0059 a0001c0001t0002g0117 |
3 | HG01975.hp1 HG02559.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.282-1564G>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105488337 | |||||||
chr13:105488387 | C | T | 3 | a0001c0001t0003g0063 a0001c0001t0003g0064 a0001c0001t0003g0065 |
3 | HG01515.hp1 HG02300.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.282-1514C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105488387 | |||||||
chr13:105488431 | G | A | 77 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0024 others(74): Show |
115 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.282-1470G>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105488431 | |||||||
chr13:105488438 | G | T | 1 | a0001c0001t0002g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.282-1463G>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105488438 | |||||||
chr13:105488459 | G | A | 1 | a0001c0001t0001g0052 | 2 | HG01884.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.282-1442G>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105488459 | |||||||
chr13:105488694 | A | G | 1 | a0001c0001t0001g0213 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.282-1207A>G | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105488694 | |||||||
chr13:105488727 | G | A | 12 | a0001c0001t0001g0046 a0001c0001t0001g0131 a0001c0001t0001g0208 others(9): Show |
19 | HG00609.hp2 HG00621.hp1 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.282-1174G>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105488727 | |||||||
chr13:105488873 | C | T | 2 | a0001c0001t0002g0028 a0001c0001t0002g0123 |
3 | HG01168.hp1 HG01169.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.282-1028C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105488873 | |||||||
chr13:105489014 | A | G | 1 | a0002c0002t0001g0178 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.282-887A>G | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105489014 | |||||||
chr13:105489036 | A | C | 9 | a0001c0001t0001g0017 a0001c0001t0001g0023 a0001c0001t0001g0110 others(6): Show |
16 | HG00621.hp2 HG02083.hp2 HG02647.hp1 others(13): Show |
intron_variant | MODIFIER | c.282-865A>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105489036 | |||||||
chr13:105489066 | C | T | 3 | a0001c0001t0001g0125 a0001c0001t0001g0127 a0001c0001t0001g0128 |
3 | NA18999.hp1 NA19057.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.282-835C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105489066 | |||||||
chr13:105489096 | T | C | 1 | a0002c0002t0001g0114 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.282-805T>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105489096 | |||||||
chr13:105489140 | T | G | 3 | a0002c0002t0001g0164 a0002c0002t0001g0191 a0002c0002t0004g0033 |
4 | HG00642.hp1 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.282-761T>G | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105489140 | |||||||
chr13:105489160 | G | A | 1 | a0001c0001t0002g0059 | 2 | HG01975.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.282-741G>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105489160 | |||||||
chr13:105489210 | A | T | 1 | a0002c0002t0001g0158 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.282-691A>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105489210 | |||||||
chr13:105489313 | CAA | C | 2 | a0002c0002t0001g0034 a0002c0002t0001g0163 |
3 | HG02074.hp2 HG02132.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.282-585_282-584del others(2): Show |
DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 105489313 | ||||||
chr13:105489483 | G | A | 1 | a0002c0002t0001g0172 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.282-418G>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105489483 | |||||||
chr13:105489603 | T | G | 105 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0020 others(102): Show |
174 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.282-298T>G | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105489603 | |||||||
chr13:105489646 | T | C | 127 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(124): Show |
196 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.282-255T>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105489646 | |||||||
chr13:105489826 | G | T | 7 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(4): Show |
7 | HG01243.hp2 HG02896.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.282-75G>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105489826 | |||||||
chr13:105489836 | C | T | 2 | a0002c0002t0001g0200 a0002c0002t0001g0201 |
2 | HG00408.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.282-65C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105489836 | |||||||
chr13:105489844 | C | A | 8 | a0001c0001t0002g0009 a0001c0001t0002g0022 a0001c0001t0002g0087 others(5): Show |
14 | HG00733.hp2 HG01361.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.282-57C>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105489844 | |||||||
chr13:105489886 | C | T | 46 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0048 others(43): Show |
77 | HG00099.hp1 HG00280.hp1 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.282-15C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105489886 | |||||||
chr13:105489887 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.282-14G>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 4/5 | chr13 | 105489887 | |||||||
chr13:105490409 | C | T | 2 | a0001c0001t0002g0059 a0001c0001t0002g0117 |
3 | HG01975.hp1 HG02559.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.*111+217C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 5/5 | chr13 | 105490409 | |||||||
chr13:105490425 | C | A | 1 | a0002c0002t0001g0196 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.*111+233C>A | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 5/5 | chr13 | 105490425 | |||||||
chr13:105490700 | C | T | 1 | a0001c0001t0002g0088 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.*112-212C>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 5/5 | chr13 | 105490700 | |||||||
chr13:105490780 | T | TAAGGTAA others(20): Show |
1 | a0001c0001t0007g0248 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.*112-131_*112-105d others(29): Show |
DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr13 | 105490780 | ||||||
chr13:105490825 | A | C | 105 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0020 others(102): Show |
174 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.*112-87A>C | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 5/5 | chr13 | 105490825 | |||||||
chr13:105490867 | A | T | 1 | a0001c0001t0001g0128 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.*112-45A>T | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 5/5 | chr13 | 105490867 | |||||||
chr13:105490876 | AG | A | 3 | a0001c0001t0001g0026 a0001c0001t0001g0050 a0001c0001t0001g0093 |
5 | HG02451.hp2 HG02622.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.*112-35delG | DAOA | ENSG00000182346.22 | transcript | ENST00000375936.9 | protein_coding | 5/5 | chr13 | 105490876 |