Item | Value |
---|---|
geneid | 167227 |
ensemblid | ENSG00000172795.17 |
hgncid | 24452 |
symbol | DCP2 |
name | decapping mRNA 2 |
refseq_nuc | NM_152624.6 |
refseq_prot | NP_689837.2 |
ensembl_nuc | ENST00000389063.3 |
ensembl_prot | ENSP00000373715.2 |
mane_status | MANE Select |
chr | chr5 |
start | 112976798 |
end | 113022195 |
strand | + |
ver | v1.2 |
region | chr5:112976798-113022195 |
region5000 | chr5:112971798-113027195 |
regionname0 | DCP2_chr5_112976798_113022195 |
regionname5000 | DCP2_chr5_112971798_113027195 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1260 | 252 | 67 | 38 | 107 | 11 | 28 | DCP2_chr5_112971798_113027195 | DCP2 | ATGGA others(1255): Show |
chr5 | 112971798 | 113027195 | ||
a0001c0002 | 1/0 | 1260 | 86 | 13 | 20 | 44 | 3 | 5 | DCP2_chr5_112971798_113027195 | DCP2 | ATGGA others(1255): Show |
chr5 | 112971798 | 113027195 | ||
a0001c0003 | 0/0 | 1260 | 9 | 9 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | ATGGA others(1255): Show |
chr5 | 112971798 | 113027195 | ||
a0001c0004 | 0/0 | 1260 | 6 | 4 | 1 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | ATGGA others(1255): Show |
chr5 | 112971798 | 113027195 | ||
a0001c0005 | 0/0 | 1260 | 3 | 0 | 0 | 3 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | ATGGA others(1255): Show |
chr5 | 112971798 | 113027195 | ||
a0001c0006 | 0/0 | 1260 | 3 | 0 | 0 | 3 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | ATGGA others(1255): Show |
chr5 | 112971798 | 113027195 | ||
a0001c0007 | 0/0 | 1260 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | ATGGA others(1255): Show |
chr5 | 112971798 | 113027195 | ||
a0001c0008 | 0/0 | 1260 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | ATGGA others(1255): Show |
chr5 | 112971798 | 113027195 | ||
a0001c0009 | 0/0 | 1260 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | ATGGA others(1255): Show |
chr5 | 112971798 | 113027195 | ||
a0001c0010 | 0/0 | 1260 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | ATGGA others(1255): Show |
chr5 | 112971798 | 113027195 | ||
a0001c0011 | 0/0 | 1260 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | ATGGA others(1255): Show |
chr5 | 112971798 | 113027195 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 10108 | 76 | 3 | 18 | 40 | 3 | 11 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10103): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0003 | 0/0 | 10109 | 24 | 5 | 1 | 11 | 2 | 5 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10104): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0004 | 0/0 | 10109 | 10 | 0 | 3 | 7 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10104): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0005 | 0/0 | 10108 | 3 | 3 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10103): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0006 | 0/0 | 10109 | 11 | 1 | 0 | 9 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10104): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0007 | 0/0 | 10108 | 10 | 1 | 0 | 9 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10103): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0010 | 0/0 | 10108 | 5 | 0 | 0 | 5 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10103): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0011 | 0/0 | 10110 | 5 | 5 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10105): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0012 | 0/0 | 10113 | 5 | 4 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10108): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0013 | 0/0 | 10109 | 5 | 4 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10104): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0015 | 0/0 | 10109 | 4 | 4 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10104): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0016 | 0/0 | 10109 | 4 | 0 | 0 | 2 | 2 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10104): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0017 | 0/0 | 10109 | 4 | 4 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10104): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0018 | 0/0 | 10113 | 4 | 4 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10108): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0020 | 0/0 | 10112 | 3 | 0 | 0 | 3 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10107): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0021 | 0/0 | 10108 | 2 | 0 | 2 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10103): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0022 | 0/0 | 10107 | 3 | 3 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10102): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0023 | 0/0 | 10108 | 3 | 3 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10103): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0024 | 0/0 | 10110 | 3 | 3 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10105): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0029 | 0/0 | 10108 | 2 | 2 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10103): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0030 | 0/0 | 10109 | 2 | 2 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10104): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0031 | 0/0 | 10110 | 2 | 0 | 0 | 2 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10105): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0032 | 0/0 | 10109 | 2 | 0 | 0 | 0 | 0 | 2 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10104): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0033 | 0/0 | 10109 | 2 | 0 | 0 | 2 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10104): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0034 | 0/0 | 10110 | 2 | 0 | 0 | 0 | 0 | 2 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10105): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0036 | 0/0 | 10108 | 2 | 0 | 2 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10103): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0037 | 0/0 | 10108 | 2 | 0 | 0 | 0 | 2 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10103): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0038 | 0/0 | 10109 | 2 | 2 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10104): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0040 | 0/0 | 10108 | 2 | 0 | 2 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10103): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0042 | 0/0 | 10108 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10103): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0043 | 0/0 | 10110 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10105): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0044 | 0/0 | 10111 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10106): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0045 | 0/0 | 10108 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10103): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0047 | 0/0 | 10111 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10106): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0065 | 0/0 | 10108 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10103): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0066 | 0/0 | 10107 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10102): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0067 | 0/0 | 10110 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10105): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0068 | 0/0 | 10109 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10104): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0069 | 0/0 | 10111 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10106): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0071 | 0/0 | 10109 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10104): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0072 | 0/0 | 10109 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10104): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0073 | 0/0 | 10109 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10104): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0074 | 0/0 | 10109 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10104): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0075 | 0/0 | 10109 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10104): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0076 | 0/0 | 10111 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10106): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0077 | 0/0 | 10111 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10106): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0078 | 0/0 | 10110 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10105): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0080 | 0/0 | 10108 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10103): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0081 | 0/0 | 10107 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10102): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0082 | 0/0 | 10108 | 1 | 0 | 0 | 0 | 1 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10103): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0083 | 0/0 | 10108 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10103): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0084 | 0/0 | 10108 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10103): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0085 | 0/0 | 10108 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10103): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0086 | 0/0 | 10108 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10103): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0087 | 0/0 | 10109 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10104): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0088 | 0/0 | 10108 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10103): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0089 | 0/0 | 10108 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10103): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0090 | 0/0 | 10108 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10103): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0091 | 0/0 | 10108 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10103): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0092 | 0/0 | 10108 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10103): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0093 | 0/0 | 10109 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10104): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0094 | 0/0 | 10108 | 1 | 0 | 0 | 0 | 1 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10103): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0095 | 0/0 | 10109 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10104): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0096 | 0/0 | 10108 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10103): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0097 | 0/0 | 10109 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10104): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0098 | 0/0 | 10108 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10103): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0099 | 0/0 | 10109 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10104): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0100 | 0/0 | 10108 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10103): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0101 | 0/0 | 10108 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10103): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0104 | 0/0 | 10110 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10105): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0105 | 0/0 | 10109 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10104): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0107 | 0/0 | 10111 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10106): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0109 | 0/0 | 10112 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10107): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0110 | 0/0 | 10109 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10104): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0111 | 0/0 | 10109 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10104): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0112 | 0/0 | 10110 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10105): Show |
chr5 | 112971798 | 113027195 |
a0001c0001t0113 | 0/0 | 10110 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10105): Show |
chr5 | 112971798 | 113027195 |
a0001c0002t0002 | 0/0 | 10110 | 39 | 6 | 15 | 13 | 2 | 3 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10105): Show |
chr5 | 112971798 | 113027195 |
a0001c0002t0008 | 0/0 | 10112 | 9 | 0 | 2 | 7 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10107): Show |
chr5 | 112971798 | 113027195 |
a0001c0002t0009 | 0/0 | 10111 | 5 | 0 | 0 | 5 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10106): Show |
chr5 | 112971798 | 113027195 |
a0001c0002t0014 | 0/0 | 10110 | 4 | 0 | 0 | 4 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10105): Show |
chr5 | 112971798 | 113027195 |
a0001c0002t0025 | 0/0 | 10110 | 2 | 1 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10105): Show |
chr5 | 112971798 | 113027195 |
a0001c0002t0026 | 0/0 | 10110 | 2 | 0 | 0 | 2 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10105): Show |
chr5 | 112971798 | 113027195 |
a0001c0002t0027 | 0/0 | 10111 | 2 | 0 | 0 | 2 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10106): Show |
chr5 | 112971798 | 113027195 |
a0001c0002t0028 | 0/0 | 10111 | 2 | 0 | 0 | 2 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10106): Show |
chr5 | 112971798 | 113027195 |
a0001c0002t0039 | 1/0 | 10110 | 2 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10105): Show |
chr5 | 112971798 | 113027195 |
a0001c0002t0041 | 0/0 | 10110 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10105): Show |
chr5 | 112971798 | 113027195 |
a0001c0002t0048 | 0/0 | 10110 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10105): Show |
chr5 | 112971798 | 113027195 |
a0001c0002t0049 | 0/0 | 10110 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10105): Show |
chr5 | 112971798 | 113027195 |
a0001c0002t0050 | 0/0 | 10110 | 1 | 0 | 0 | 0 | 1 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10105): Show |
chr5 | 112971798 | 113027195 |
a0001c0002t0051 | 0/0 | 10111 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10106): Show |
chr5 | 112971798 | 113027195 |
a0001c0002t0052 | 0/0 | 10109 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10104): Show |
chr5 | 112971798 | 113027195 |
a0001c0002t0053 | 0/0 | 10111 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10106): Show |
chr5 | 112971798 | 113027195 |
a0001c0002t0054 | 0/0 | 10109 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10104): Show |
chr5 | 112971798 | 113027195 |
a0001c0002t0056 | 0/0 | 10111 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10106): Show |
chr5 | 112971798 | 113027195 |
a0001c0002t0057 | 0/0 | 10111 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10106): Show |
chr5 | 112971798 | 113027195 |
a0001c0002t0058 | 0/0 | 10112 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10107): Show |
chr5 | 112971798 | 113027195 |
a0001c0002t0059 | 0/0 | 10112 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10107): Show |
chr5 | 112971798 | 113027195 |
a0001c0002t0061 | 0/0 | 10113 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10108): Show |
chr5 | 112971798 | 113027195 |
a0001c0002t0063 | 0/0 | 10110 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10105): Show |
chr5 | 112971798 | 113027195 |
a0001c0002t0064 | 0/0 | 10110 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10105): Show |
chr5 | 112971798 | 113027195 |
a0001c0002t0102 | 0/0 | 10110 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10105): Show |
chr5 | 112971798 | 113027195 |
a0001c0002t0103 | 0/0 | 10110 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10105): Show |
chr5 | 112971798 | 113027195 |
a0001c0002t0106 | 0/0 | 10110 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10105): Show |
chr5 | 112971798 | 113027195 |
a0001c0002t0114 | 0/0 | 10110 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10105): Show |
chr5 | 112971798 | 113027195 |
a0001c0003t0005 | 0/0 | 10108 | 9 | 9 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10103): Show |
chr5 | 112971798 | 113027195 |
a0001c0004t0019 | 0/0 | 10108 | 3 | 2 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10103): Show |
chr5 | 112971798 | 113027195 |
a0001c0004t0046 | 0/0 | 10110 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10105): Show |
chr5 | 112971798 | 113027195 |
a0001c0004t0060 | 0/0 | 10109 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10104): Show |
chr5 | 112971798 | 113027195 |
a0001c0004t0062 | 0/0 | 10109 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10104): Show |
chr5 | 112971798 | 113027195 |
a0001c0005t0004 | 0/0 | 10109 | 3 | 0 | 0 | 3 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10104): Show |
chr5 | 112971798 | 113027195 |
a0001c0006t0035 | 0/0 | 10108 | 2 | 0 | 0 | 2 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10103): Show |
chr5 | 112971798 | 113027195 |
a0001c0006t0079 | 0/0 | 10109 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10104): Show |
chr5 | 112971798 | 113027195 |
a0001c0007t0055 | 0/0 | 10109 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10104): Show |
chr5 | 112971798 | 113027195 |
a0001c0008t0108 | 0/0 | 10113 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10108): Show |
chr5 | 112971798 | 113027195 |
a0001c0009t0021 | 0/0 | 10108 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10103): Show |
chr5 | 112971798 | 113027195 |
a0001c0010t0070 | 0/0 | 10110 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10105): Show |
chr5 | 112971798 | 113027195 |
a0001c0011t0001 | 0/0 | 10108 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | CTCGT others(10103): Show |
chr5 | 112971798 | 113027195 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0310 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0004g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0004g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0004g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0004g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0004g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0004g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0004g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0004g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0005g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0005g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0005g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0006g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0006g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0006g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0006g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0006g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0006g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0006g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0006g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0006g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0006g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0006g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0007g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0007g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0007g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0007g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0007g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0007g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0007g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0007g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0007g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0007g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0010g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0010g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0010g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0010g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0011g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0011g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0011g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0011g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0012g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0012g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0012g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0012g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0013g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0013g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0013g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0013g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0013g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0015g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0015g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0015g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0015g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0016g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0016g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0016g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0016g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0017g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0017g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0018g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0018g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0018g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0018g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0020g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0020g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0020g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0021g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0021g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0022g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0022g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0022g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0023g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0023g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0023g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0024g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0024g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0024g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0029g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0029g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0030g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0030g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0031g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0031g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0032g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0033g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0033g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0034g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0034g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0036g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0036g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0037g0005 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0038g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0038g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0040g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0040g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0042g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0043g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0044g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0045g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0047g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0065g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0066g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0067g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0068g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0069g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0071g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0072g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0073g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0074g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0075g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0076g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0077g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0078g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0080g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0081g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0082g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0083g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0084g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0085g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0086g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0087g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0088g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0089g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0090g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0091g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0092g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0093g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0094g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0095g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0096g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0097g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0098g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0099g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0100g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0101g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0104g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0105g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0107g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0109g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0110g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0111g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0112g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0001t0113g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0001 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0008g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0008g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0008g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0008g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0008g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0008g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0008g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0008g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0009g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0009g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0009g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0009g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0009g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0014g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0014g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0014g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0025g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0025g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0026g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0026g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0027g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0027g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0028g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0028g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0039g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0039g0230 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0041g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0048g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0049g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0050g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0051g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0052g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0053g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0054g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0056g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0057g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0058g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0059g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0061g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0063g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0064g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0102g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0103g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0106g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0002t0114g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0003t0005g0003 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0003t0005g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0003t0005g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0003t0005g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0003t0005g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0004t0019g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0004t0019g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0004t0019g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0004t0046g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0004t0060g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0004t0062g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0005t0004g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0005t0004g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0005t0004g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0006t0035g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0006t0035g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0006t0079g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0007t0055g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0008t0108g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0009t0021g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0010t0070g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
a0001c0011t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0094 | g0208 | EUR | GBR | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0256 | EUR | GBR | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG00280 | hp1 | a0001 | c0001 | t0082 | g0300 | EUR | FIN | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG00280 | hp2 | a0001 | c0002 | t0002 | g0091 | EUR | FIN | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG00408 | hp1 | a0001 | c0002 | t0014 | g0001 | EAS | CHS | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | CHS | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG00423 | hp1 | a0001 | c0001 | t0010 | g0002 | EAS | CHS | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG00423 | hp2 | a0001 | c0002 | t0008 | g0086 | EAS | CHS | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG00609 | hp1 | a0001 | c0001 | t0007 | g0042 | EAS | CHS | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG00609 | hp2 | a0001 | c0002 | t0002 | g0075 | EAS | CHS | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG00621 | hp1 | a0001 | c0002 | t0058 | g0011 | EAS | CHS | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG00621 | hp2 | a0001 | c0001 | t0093 | g0224 | EAS | CHS | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG00639 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG00639 | hp2 | a0001 | c0002 | t0025 | g0093 | AMR | PUR | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | CHS | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | CHS | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG00733 | hp2 | a0001 | c0002 | t0002 | g0108 | AMR | PUR | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG00735 | hp1 | a0001 | c0002 | t0041 | g0001 | AMR | PUR | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG00735 | hp2 | a0001 | c0001 | t0004 | g0257 | AMR | PUR | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0320 | AMR | PUR | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG00738 | hp2 | a0001 | c0002 | t0002 | g0109 | AMR | PUR | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG00741 | hp1 | a0001 | c0004 | t0019 | g0124 | AMR | PUR | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01070 | hp1 | a0001 | c0001 | t0040 | g0314 | AMR | PUR | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01070 | hp2 | a0001 | c0001 | t0091 | g0210 | AMR | PUR | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01071 | hp1 | a0001 | c0001 | t0036 | g0239 | AMR | PUR | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01071 | hp2 | a0001 | c0001 | t0040 | g0313 | AMR | PUR | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01074 | hp2 | a0001 | c0001 | t0012 | g0014 | AMR | PUR | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01081 | hp2 | a0001 | c0002 | t0002 | g0205 | AMR | PUR | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01099 | hp1 | a0001 | c0001 | t0090 | g0271 | AMR | PUR | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01099 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01106 | hp1 | a0001 | c0001 | t0003 | g0173 | AMR | PUR | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01167 | hp1 | a0001 | c0002 | t0002 | g0067 | AMR | PUR | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01167 | hp2 | a0001 | c0001 | t0004 | g0267 | AMR | PUR | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01192 | hp2 | a0001 | c0001 | t0096 | g0262 | AMR | PUR | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01243 | hp1 | a0001 | c0002 | t0102 | g0142 | AMR | PUR | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01243 | hp2 | a0001 | c0002 | t0002 | g0026 | AMR | PUR | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01256 | hp1 | a0001 | c0001 | t0021 | g0263 | AMR | CLM | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01256 | hp2 | a0001 | c0001 | t0047 | g0110 | AMR | CLM | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01258 | hp1 | a0001 | c0001 | t0021 | g0264 | AMR | CLM | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | CLM | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01261 | hp2 | a0001 | c0011 | t0001 | g0309 | AMR | CLM | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01346 | hp1 | a0001 | c0002 | t0002 | g0051 | AMR | CLM | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01346 | hp2 | a0001 | c0002 | t0002 | g0096 | AMR | CLM | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01358 | hp1 | a0001 | c0001 | t0045 | g0082 | AMR | CLM | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01358 | hp2 | a0001 | c0002 | t0002 | g0092 | AMR | CLM | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01433 | hp1 | a0001 | c0002 | t0002 | g0076 | AMR | CLM | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01433 | hp2 | a0001 | c0001 | t0004 | g0292 | AMR | CLM | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01496 | hp1 | a0001 | c0001 | t0072 | g0323 | AMR | CLM | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01496 | hp2 | a0001 | c0001 | t0013 | g0145 | AMR | CLM | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01515 | hp1 | a0001 | c0001 | t0003 | g0165 | EUR | IBS | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01515 | hp2 | a0001 | c0001 | t0016 | g0222 | EUR | IBS | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01516 | hp1 | a0001 | c0002 | t0002 | g0199 | EUR | IBS | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01516 | hp2 | a0001 | c0001 | t0037 | g0005 | EUR | IBS | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01517 | hp1 | a0001 | c0001 | t0016 | g0223 | EUR | IBS | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01517 | hp2 | a0001 | c0001 | t0037 | g0005 | EUR | IBS | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01884 | hp1 | a0001 | c0003 | t0005 | g0012 | AFR | ACB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01884 | hp2 | a0001 | c0001 | t0109 | g0217 | AFR | ACB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01891 | hp1 | a0001 | c0004 | t0019 | g0125 | AFR | ACB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01891 | hp2 | a0001 | c0001 | t0012 | g0156 | AFR | ACB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01928 | hp1 | a0001 | c0002 | t0008 | g0060 | AMR | PEL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0291 | AMR | PEL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01934 | hp2 | a0001 | c0001 | t0036 | g0250 | AMR | PEL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01943 | hp1 | a0001 | c0002 | t0008 | g0066 | AMR | PEL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PEL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01975 | hp1 | a0001 | c0002 | t0002 | g0074 | AMR | PEL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0296 | AMR | PEL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01978 | hp2 | a0001 | c0001 | t0110 | g0315 | AMR | PEL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0294 | AMR | PEL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG01981 | hp2 | a0001 | c0002 | t0002 | g0102 | AMR | PEL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02015 | hp1 | a0001 | c0001 | t0075 | g0168 | EAS | KHV | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02027 | hp1 | a0001 | c0001 | t0010 | g0021 | EAS | KHV | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | KHV | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02040 | hp1 | a0001 | c0002 | t0002 | g0068 | EAS | KHV | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02040 | hp2 | a0001 | c0002 | t0002 | g0127 | EAS | KHV | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02055 | hp1 | a0001 | c0004 | t0060 | g0122 | AFR | ACB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02055 | hp2 | a0001 | c0001 | t0113 | g0147 | AFR | ACB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | KHV | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02074 | hp2 | a0001 | c0002 | t0051 | g0070 | EAS | KHV | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02129 | hp1 | a0001 | c0001 | t0007 | g0041 | EAS | KHV | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02129 | hp2 | a0001 | c0004 | t0046 | g0069 | EAS | KHV | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02135 | hp2 | a0001 | c0002 | t0009 | g0011 | EAS | KHV | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02145 | hp1 | a0001 | c0003 | t0005 | g0112 | AFR | ACB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02145 | hp2 | a0001 | c0001 | t0003 | g0169 | AFR | ACB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02155 | hp1 | a0001 | c0002 | t0014 | g0100 | EAS | CDX | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02155 | hp2 | a0001 | c0001 | t0006 | g0129 | EAS | CDX | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02257 | hp1 | a0001 | c0002 | t0002 | g0098 | AFR | ACB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02257 | hp2 | a0001 | c0001 | t0015 | g0028 | AFR | ACB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02258 | hp1 | a0001 | c0001 | t0011 | g0150 | AFR | ACB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02258 | hp2 | a0001 | c0001 | t0023 | g0004 | AFR | ACB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02280 | hp1 | a0001 | c0001 | t0100 | g0004 | AFR | ACB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02280 | hp2 | a0001 | c0001 | t0105 | g0141 | AFR | ACB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02293 | hp1 | a0001 | c0002 | t0002 | g0095 | AMR | PEL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02293 | hp2 | a0001 | c0002 | t0002 | g0072 | AMR | PEL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02300 | hp1 | a0001 | c0001 | t0073 | g0170 | AMR | PEL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02451 | hp1 | a0001 | c0001 | t0012 | g0014 | AFR | ACB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02451 | hp2 | a0001 | c0010 | t0070 | g0048 | AFR | ACB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02523 | hp1 | a0001 | c0002 | t0027 | g0055 | EAS | KHV | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02523 | hp2 | a0001 | c0001 | t0007 | g0023 | EAS | KHV | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02572 | hp1 | a0001 | c0003 | t0005 | g0003 | AFR | GWD | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02572 | hp2 | a0001 | c0001 | t0018 | g0311 | AFR | GWD | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0174 | SAS | PJL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02602 | hp2 | a0001 | c0002 | t0002 | g0105 | SAS | PJL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02615 | hp1 | a0001 | c0003 | t0005 | g0012 | AFR | GWD | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02615 | hp2 | a0001 | c0002 | t0057 | g0061 | AFR | GWD | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02622 | hp1 | a0001 | c0001 | t0011 | g0013 | AFR | GWD | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02622 | hp2 | a0001 | c0001 | t0018 | g0215 | AFR | GWD | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02630 | hp1 | a0001 | c0001 | t0018 | g0312 | AFR | GWD | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02630 | hp2 | a0001 | c0001 | t0038 | g0151 | AFR | GWD | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02647 | hp1 | a0001 | c0002 | t0048 | g0057 | AFR | GWD | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02647 | hp2 | a0001 | c0001 | t0029 | g0034 | AFR | GWD | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02683 | hp1 | a0001 | c0002 | t0002 | g0104 | SAS | PJL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02683 | hp2 | a0001 | c0001 | t0086 | g0209 | SAS | PJL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | GWD | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02717 | hp2 | a0001 | c0003 | t0005 | g0003 | AFR | GWD | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02723 | hp1 | a0001 | c0003 | t0005 | g0111 | AFR | GWD | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02723 | hp2 | a0001 | c0001 | t0084 | g0133 | AFR | GWD | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02735 | hp1 | a0001 | c0001 | t0081 | g0254 | SAS | PJL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0302 | SAS | PJL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0270 | SAS | PJL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02738 | hp2 | a0001 | c0001 | t0077 | g0167 | SAS | PJL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02809 | hp1 | a0001 | c0001 | t0023 | g0200 | AFR | GWD | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02809 | hp2 | a0001 | c0001 | t0013 | g0143 | AFR | GWD | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02818 | hp1 | a0001 | c0001 | t0071 | g0033 | AFR | GWD | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02818 | hp2 | a0001 | c0001 | t0023 | g0201 | AFR | GWD | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02886 | hp1 | a0001 | c0001 | t0022 | g0203 | AFR | GWD | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02886 | hp2 | a0001 | c0001 | t0013 | g0146 | AFR | GWD | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02895 | hp1 | a0001 | c0001 | t0022 | g0204 | AFR | GWD | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02895 | hp2 | a0001 | c0002 | t0054 | g0053 | AFR | GWD | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02896 | hp1 | a0001 | c0001 | t0024 | g0191 | AFR | GWD | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02896 | hp2 | a0001 | c0001 | t0011 | g0013 | AFR | GWD | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02897 | hp1 | a0001 | c0001 | t0022 | g0202 | AFR | GWD | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02897 | hp2 | a0001 | c0001 | t0024 | g0190 | AFR | GWD | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02922 | hp1 | a0001 | c0007 | t0055 | g0052 | AFR | ESN | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02922 | hp2 | a0001 | c0001 | t0005 | g0154 | AFR | ESN | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02970 | hp1 | a0001 | c0002 | t0002 | g0062 | AFR | ESN | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02970 | hp2 | a0001 | c0001 | t0030 | g0114 | AFR | ESN | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02976 | hp1 | a0001 | c0001 | t0017 | g0004 | AFR | ESN | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02976 | hp2 | a0001 | c0002 | t0052 | g0054 | AFR | ESN | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0290 | SAS | PJL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03041 | hp1 | a0001 | c0001 | t0015 | g0030 | AFR | GWD | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0303 | AFR | GWD | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03098 | hp1 | a0001 | c0002 | t0002 | g0059 | AFR | MSL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03098 | hp2 | a0001 | c0001 | t0012 | g0139 | AFR | MSL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03130 | hp1 | a0001 | c0001 | t0029 | g0035 | AFR | ESN | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03130 | hp2 | a0001 | c0008 | t0108 | g0301 | AFR | ESN | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03195 | hp1 | a0001 | c0001 | t0015 | g0031 | AFR | ESN | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03195 | hp2 | a0001 | c0004 | t0062 | g0123 | AFR | ESN | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03209 | hp1 | a0001 | c0001 | t0013 | g0144 | AFR | MSL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03209 | hp2 | a0001 | c0001 | t0067 | g0045 | AFR | MSL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03225 | hp1 | a0001 | c0001 | t0112 | g0119 | AFR | MSL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03225 | hp2 | a0001 | c0001 | t0011 | g0152 | AFR | MSL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03453 | hp1 | a0001 | c0003 | t0005 | g0113 | AFR | MSL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03453 | hp2 | a0001 | c0001 | t0069 | g0046 | AFR | MSL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03486 | hp1 | a0001 | c0002 | t0103 | g0140 | AFR | MSL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03486 | hp2 | a0001 | c0004 | t0019 | g0025 | AFR | MSL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03490 | hp2 | a0001 | c0001 | t0003 | g0159 | SAS | PJL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0304 | SAS | PJL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03491 | hp2 | a0001 | c0001 | t0032 | g0015 | SAS | PJL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03492 | hp1 | a0001 | c0001 | t0032 | g0015 | SAS | PJL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0160 | SAS | PJL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03516 | hp1 | a0001 | c0001 | t0024 | g0155 | AFR | ESN | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03516 | hp2 | a0001 | c0001 | t0011 | g0153 | AFR | ESN | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03540 | hp1 | a0001 | c0001 | t0005 | g0206 | AFR | GWD | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03540 | hp2 | a0001 | c0003 | t0005 | g0003 | AFR | GWD | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03579 | hp1 | a0001 | c0001 | t0038 | g0029 | AFR | MSL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0317 | AFR | MSL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03669 | hp1 | a0001 | c0001 | t0034 | g0171 | SAS | PJL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0316 | SAS | PJL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03710 | hp2 | a0001 | c0002 | t0002 | g0056 | SAS | PJL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03831 | hp1 | a0001 | c0001 | t0078 | g0178 | SAS | BEB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0293 | SAS | BEB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03834 | hp1 | a0001 | c0009 | t0021 | g0221 | SAS | BEB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03834 | hp2 | a0001 | c0001 | t0074 | g0166 | SAS | BEB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03927 | hp1 | a0001 | c0002 | t0114 | g0212 | SAS | BEB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0306 | SAS | BEB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03942 | hp1 | a0001 | c0001 | t0083 | g0299 | SAS | BEB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0318 | SAS | BEB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG04115 | hp1 | a0001 | c0001 | t0080 | g0024 | SAS | STU | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG04115 | hp2 | a0001 | c0001 | t0003 | g0175 | SAS | STU | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG04199 | hp1 | a0001 | c0001 | t0034 | g0172 | SAS | STU | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG04199 | hp2 | a0001 | c0002 | t0049 | g0103 | SAS | STU | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18522 | hp1 | a0001 | c0001 | t0015 | g0032 | AFR | YRI | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18522 | hp2 | a0001 | c0001 | t0006 | g0027 | AFR | YRI | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18612 | hp1 | a0001 | c0002 | t0056 | g0106 | EAS | CHB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | CHB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18747 | hp1 | a0001 | c0001 | t0006 | g0186 | EAS | CHB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18747 | hp2 | a0001 | c0002 | t0009 | g0078 | EAS | CHB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18906 | hp1 | a0001 | c0002 | t0002 | g0064 | AFR | YRI | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18906 | hp2 | a0001 | c0001 | t0018 | g0216 | AFR | YRI | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18940 | hp1 | a0001 | c0002 | t0064 | g0065 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18942 | hp1 | a0001 | c0001 | t0020 | g0008 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18942 | hp2 | a0001 | c0002 | t0008 | g0010 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18943 | hp1 | a0001 | c0001 | t0088 | g0018 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18943 | hp2 | a0001 | c0001 | t0043 | g0184 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18945 | hp1 | a0001 | c0001 | t0003 | g0180 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18945 | hp2 | a0001 | c0002 | t0002 | g0101 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18947 | hp1 | a0001 | c0001 | t0065 | g0049 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18947 | hp2 | a0001 | c0002 | t0026 | g0009 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18948 | hp1 | a0001 | c0001 | t0042 | g0130 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18950 | hp1 | a0001 | c0001 | t0007 | g0043 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18952 | hp1 | a0001 | c0001 | t0006 | g0131 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18952 | hp2 | a0001 | c0001 | t0033 | g0183 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18954 | hp1 | a0001 | c0002 | t0002 | g0081 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18957 | hp1 | a0001 | c0001 | t0003 | g0193 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18957 | hp2 | a0001 | c0001 | t0007 | g0038 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18960 | hp1 | a0001 | c0001 | t0004 | g0020 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18960 | hp2 | a0001 | c0001 | t0006 | g0187 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18963 | hp1 | a0001 | c0001 | t0031 | g0195 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18965 | hp1 | a0001 | c0002 | t0026 | g0001 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18966 | hp2 | a0001 | c0001 | t0099 | g0234 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18968 | hp1 | a0001 | c0002 | t0059 | g0089 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18968 | hp2 | a0001 | c0001 | t0006 | g0132 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18969 | hp1 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18969 | hp2 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18970 | hp1 | a0001 | c0001 | t0006 | g0128 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18970 | hp2 | a0001 | c0002 | t0002 | g0073 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18972 | hp1 | a0001 | c0002 | t0053 | g0090 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18973 | hp1 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18973 | hp2 | a0001 | c0002 | t0008 | g0088 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18974 | hp1 | a0001 | c0001 | t0010 | g0286 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18974 | hp2 | a0001 | c0001 | t0003 | g0162 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18975 | hp1 | a0001 | c0001 | t0003 | g0196 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18975 | hp2 | a0001 | c0001 | t0020 | g0233 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18977 | hp1 | a0001 | c0002 | t0002 | g0087 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18977 | hp2 | a0001 | c0001 | t0089 | g0272 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18981 | hp2 | a0001 | c0002 | t0027 | g0085 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18983 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18984 | hp1 | a0001 | c0001 | t0016 | g0020 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18984 | hp2 | a0001 | c0001 | t0016 | g0279 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18985 | hp1 | a0001 | c0001 | t0004 | g0274 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18985 | hp2 | a0001 | c0001 | t0003 | g0176 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18986 | hp1 | a0001 | c0002 | t0106 | g0241 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18987 | hp1 | a0001 | c0002 | t0008 | g0058 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18987 | hp2 | a0001 | c0001 | t0087 | g0018 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18989 | hp1 | a0001 | c0002 | t0009 | g0077 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18989 | hp2 | a0001 | c0001 | t0010 | g0002 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18990 | hp2 | a0001 | c0002 | t0063 | g0009 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18992 | hp1 | a0001 | c0001 | t0068 | g0040 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18992 | hp2 | a0001 | c0005 | t0004 | g0319 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18995 | hp1 | a0001 | c0001 | t0004 | g0232 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18995 | hp2 | a0001 | c0001 | t0004 | g0288 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18998 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18999 | hp1 | a0001 | c0002 | t0008 | g0079 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19000 | hp1 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19000 | hp2 | a0001 | c0001 | t0010 | g0276 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19001 | hp1 | a0001 | c0001 | t0066 | g0044 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19002 | hp1 | a0001 | c0001 | t0003 | g0179 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19002 | hp2 | a0001 | c0001 | t0007 | g0036 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19004 | hp1 | a0001 | c0001 | t0097 | g0265 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19004 | hp2 | a0001 | c0002 | t0008 | g0010 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19006 | hp1 | a0001 | c0002 | t0061 | g0083 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19007 | hp1 | a0001 | c0006 | t0035 | g0237 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19007 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19009 | hp2 | a0001 | c0001 | t0006 | g0185 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19010 | hp1 | a0001 | c0001 | t0076 | g0177 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19011 | hp1 | a0001 | c0002 | t0008 | g0120 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19030 | hp1 | a0001 | c0001 | t0107 | g0117 | AFR | LWK | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19030 | hp2 | a0001 | c0001 | t0017 | g0016 | AFR | LWK | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19043 | hp1 | a0001 | c0001 | t0003 | g0136 | AFR | LWK | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19043 | hp2 | a0001 | c0002 | t0002 | g0094 | AFR | LWK | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19054 | hp1 | a0001 | c0001 | t0033 | g0198 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19055 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19057 | hp1 | a0001 | c0001 | t0007 | g0050 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19058 | hp1 | a0001 | c0005 | t0004 | g0258 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19058 | hp2 | a0001 | c0001 | t0031 | g0194 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19060 | hp1 | a0001 | c0002 | t0014 | g0099 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19063 | hp2 | a0001 | c0006 | t0079 | g0297 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19064 | hp1 | a0001 | c0002 | t0002 | g0080 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19065 | hp1 | a0001 | c0002 | t0014 | g0001 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19065 | hp2 | a0001 | c0001 | t0007 | g0037 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19066 | hp2 | a0001 | c0001 | t0006 | g0188 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19070 | hp1 | a0001 | c0001 | t0003 | g0197 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19074 | hp1 | a0001 | c0002 | t0028 | g0116 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19074 | hp2 | a0001 | c0001 | t0006 | g0189 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19077 | hp1 | a0001 | c0002 | t0028 | g0126 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19078 | hp1 | a0001 | c0006 | t0035 | g0321 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19078 | hp2 | a0001 | c0002 | t0009 | g0084 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19079 | hp2 | a0001 | c0001 | t0092 | g0207 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19080 | hp1 | a0001 | c0001 | t0098 | g0252 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19080 | hp2 | a0001 | c0001 | t0004 | g0287 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19082 | hp1 | a0001 | c0001 | t0003 | g0181 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19082 | hp2 | a0001 | c0001 | t0085 | g0305 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19083 | hp2 | a0001 | c0002 | t0009 | g0071 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19084 | hp2 | a0001 | c0001 | t0003 | g0182 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19085 | hp1 | a0001 | c0001 | t0007 | g0039 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19087 | hp1 | a0001 | c0001 | t0044 | g0134 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19087 | hp2 | a0001 | c0005 | t0004 | g0281 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19240 | hp1 | a0001 | c0003 | t0005 | g0003 | AFR | YRI | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA19240 | hp2 | a0001 | c0001 | t0013 | g0138 | AFR | YRI | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA20129 | hp1 | a0001 | c0001 | t0104 | g0149 | AFR | ASW | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA20129 | hp2 | a0001 | c0001 | t0101 | g0322 | AFR | ASW | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA20752 | hp1 | a0001 | c0002 | t0050 | g0097 | EUR | TSI | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0280 | EUR | TSI | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA20805 | hp1 | a0001 | c0001 | t0003 | g0164 | EUR | TSI | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0284 | EUR | TSI | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA20905 | hp1 | a0001 | c0001 | t0003 | g0158 | SAS | GIH | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA20905 | hp2 | a0001 | c0001 | t0006 | g0107 | SAS | GIH | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02109 | hp1 | a0001 | c0002 | t0039 | g0211 | AFR | ACB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02109 | hp2 | a0001 | c0001 | t0095 | g0261 | AFR | ACB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02486 | hp1 | a0001 | c0001 | t0017 | g0016 | AFR | ACB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02486 | hp2 | a0001 | c0001 | t0012 | g0157 | AFR | ACB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02559 | hp1 | a0001 | c0002 | t0002 | g0063 | AFR | ACB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG02559 | hp2 | a0001 | c0001 | t0017 | g0004 | AFR | ACB | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03471 | hp1 | a0001 | c0001 | t0003 | g0137 | AFR | MSL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG03471 | hp2 | a0001 | c0001 | t0111 | g0148 | AFR | MSL | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG06807 | hp1 | a0001 | c0002 | t0025 | g0121 | AFR | USA | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
HG06807 | hp2 | a0001 | c0001 | t0003 | g0135 | AFR | USA | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18955 | hp1 | a0001 | c0001 | t0020 | g0285 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA18955 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA20300 | hp1 | a0001 | c0001 | t0030 | g0115 | AFR | USA | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA20300 | hp2 | a0001 | c0001 | t0003 | g0161 | AFR | USA | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA21309 | hp1 | a0001 | c0001 | t0007 | g0047 | AFR | LWK | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
NA21309 | hp2 | a0001 | c0001 | t0005 | g0118 | AFR | LWK | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0310 | REF | REF | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
homoSapiens | grch38p0 | a0001 | c0002 | t0039 | g0230 | REF | REF | DCP2_chr5_112971798_113027195 | DCP2 | chr5 | 112971798 | 113027195 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:113022192 | AC | A | 1 | a0001 | 3 | HG02895.hp2 HG02922.hp1 HG02976.hp2 |
splice_region_variant | LOW | c.*8709delC | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | chr5 | 113022192 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:112992137 | G | T | 1 | a0001c0011 | 1 | HG01261.hp2 | synonymous_variant | LOW | c.222G>T | p.Pro74Pro | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 3/11 | 358/10110 | 222/1263 | 74/420 | chr5 | 112992137 | |||
chr5:112992215 | T | C | 1 | a0001c0003 | 9 | HG01884.hp1 HG02145.hp1 HG02572.hp1 others(6): Show |
synonymous_variant | LOW | c.300T>C | p.Tyr100Tyr | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 3/11 | 436/10110 | 300/1263 | 100/420 | chr5 | 112992215 | |||
chr5:112992680 | A | G | 8 | a0001c0001 a0001c0003 a0001c0005 others(5): Show |
270 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
synonymous_variant | LOW | c.342A>G | p.Leu114Leu | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/11 | 478/10110 | 342/1263 | 114/420 | chr5 | 112992680 | |||
chr5:113001101 | T | C | 1 | a0001c0008 | 1 | HG03130.hp2 | synonymous_variant | LOW | c.450T>C | p.Gly150Gly | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 5/11 | 586/10110 | 450/1263 | 150/420 | chr5 | 113001101 | |||
chr5:113001206 | A | G | 1 | a0001c0007 | 1 | HG02922.hp1 | synonymous_variant | LOW | c.555A>G | p.Lys185Lys | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 5/11 | 691/10110 | 555/1263 | 185/420 | chr5 | 113001206 | |||
chr5:113001233 | T | A | 1 | a0001c0005 | 3 | NA18992.hp2 NA19058.hp1 NA19087.hp2 |
synonymous_variant | LOW | c.582T>A | p.Ile194Ile | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 5/11 | 718/10110 | 582/1263 | 194/420 | chr5 | 113001233 | |||
chr5:113001624 | A | G | 1 | a0001c0010 | 1 | HG02451.hp2 | synonymous_variant | LOW | c.756A>G | p.Gly252Gly | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 7/11 | 892/10110 | 756/1263 | 252/420 | chr5 | 113001624 | |||
chr5:113013373 | T | C | 9 | a0001c0001 a0001c0003 a0001c0004 others(6): Show |
276 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(273): Show |
synonymous_variant | LOW | c.1152T>C | p.Ala384Ala | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 1288/10110 | 1152/1263 | 384/420 | chr5 | 113013373 | |||
chr5:113013397 | T | C | 1 | a0001c0006 | 3 | NA19007.hp1 NA19063.hp2 NA19078.hp1 |
synonymous_variant | LOW | c.1176T>C | p.Asn392Asn | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 1312/10110 | 1176/1263 | 392/420 | chr5 | 113013397 | |||
chr5:113013412 | C | T | 1 | a0001c0009 | 1 | HG03834.hp1 | synonymous_variant | LOW | c.1191C>T | p.Phe397Phe | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 1327/10110 | 1191/1263 | 397/420 | chr5 | 113013412 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:112976805 | C | A | 1 | a0001c0002t0041 | 1 | HG00735.hp1 | 5_prime_UTR_variant | MODIFIER | c.-129C>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/11 | 129 | chr5 | 112976805 | ||||||
chr5:112976831 | T | C | 34 | a0001c0001t0006 a0001c0001t0042 a0001c0001t0043 others(31): Show |
103 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(100): Show |
5_prime_UTR_variant | MODIFIER | c.-103T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/11 | 103 | chr5 | 112976831 | ||||||
chr5:112976883 | T | C | 8 | a0001c0001t0007 a0001c0001t0029 a0001c0001t0065 others(5): Show |
18 | HG00609.hp1 HG02129.hp1 HG02451.hp2 others(15): Show |
5_prime_UTR_variant | MODIFIER | c.-51T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/11 | 51 | chr5 | 112976883 | ||||||
chr5:113013597 | G | A | 4 | a0001c0001t0015 a0001c0001t0030 a0001c0001t0071 others(1): Show |
8 | HG01496.hp1 HG02257.hp2 HG02818.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*113G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 113 | chr5 | 113013597 | ||||||
chr5:113013600 | T | C | 15 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0031 others(12): Show |
52 | HG01106.hp1 HG01515.hp1 HG02015.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*116T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 116 | chr5 | 113013600 | ||||||
chr5:113013682 | T | C | 35 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0010 others(32): Show |
133 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*198T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 198 | chr5 | 113013682 | ||||||
chr5:113013682 | T | G | 1 | a0001c0001t0099 | 1 | NA18966.hp2 | 3_prime_UTR_variant | MODIFIER | c.*198T>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 198 | chr5 | 113013682 | ||||||
chr5:113013710 | T | C | 5 | a0001c0001t0015 a0001c0001t0030 a0001c0001t0038 others(2): Show |
10 | HG01496.hp1 HG02257.hp2 HG02630.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*226T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 226 | chr5 | 113013710 | ||||||
chr5:113013953 | A | G | 1 | a0001c0002t0064 | 1 | NA18940.hp1 | 3_prime_UTR_variant | MODIFIER | c.*469A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 469 | chr5 | 113013953 | ||||||
chr5:113013980 | T | A | 1 | a0001c0002t0025 | 2 | HG00639.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*496T>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 496 | chr5 | 113013980 | ||||||
chr5:113013993 | T | G | 1 | a0001c0001t0022 | 3 | HG02886.hp1 HG02895.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*509T>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 509 | chr5 | 113013993 | ||||||
chr5:113014000 | C | G | 1 | a0001c0002t0114 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*516C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 516 | chr5 | 113014000 | ||||||
chr5:113014084 | G | A | 1 | a0001c0001t0100 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*600G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 600 | chr5 | 113014084 | ||||||
chr5:113014157 | G | A | 2 | a0001c0006t0035 a0001c0006t0079 |
3 | NA19007.hp1 NA19063.hp2 NA19078.hp1 |
3_prime_UTR_variant | MODIFIER | c.*673G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 673 | chr5 | 113014157 | ||||||
chr5:113014158 | G | T | 1 | a0001c0010t0070 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*674G>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 674 | chr5 | 113014158 | ||||||
chr5:113014333 | G | A | 1 | a0001c0001t0101 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*849G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 849 | chr5 | 113014333 | ||||||
chr5:113014370 | C | T | 1 | a0001c0001t0030 | 2 | HG02970.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*886C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 886 | chr5 | 113014370 | ||||||
chr5:113014401 | C | T | 19 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0013 others(16): Show |
60 | HG01106.hp1 HG01496.hp2 HG01515.hp1 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*917C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 917 | chr5 | 113014401 | ||||||
chr5:113014474 | A | C | 1 | a0001c0002t0063 | 1 | NA18990.hp2 | 3_prime_UTR_variant | MODIFIER | c.*990A>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 990 | chr5 | 113014474 | ||||||
chr5:113014609 | T | A | 1 | a0001c0001t0073 | 1 | HG02300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1125T>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 1125 | chr5 | 113014609 | ||||||
chr5:113014632 | G | C | 1 | a0001c0001t0111 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1148G>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 1148 | chr5 | 113014632 | ||||||
chr5:113014677 | G | C | 2 | a0001c0002t0048 a0001c0002t0102 |
2 | HG01243.hp1 HG02647.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1193G>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 1193 | chr5 | 113014677 | ||||||
chr5:113014758 | A | ATG | 1 | a0001c0001t0012 | 5 | HG01074.hp2 HG01891.hp2 HG02451.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1286_*1287dupGT | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 1288 | INFO_REALIGN_3_PRIME | chr5 | 113014758 | |||||
chr5:113014838 | A | C | 1 | a0001c0010t0070 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1354A>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 1354 | chr5 | 113014838 | ||||||
chr5:113014883 | T | C | 1 | a0001c0001t0029 | 2 | HG02647.hp2 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1399T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 1399 | chr5 | 113014883 | ||||||
chr5:113015010 | G | A | 33 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0010 others(30): Show |
131 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(128): Show |
3_prime_UTR_variant | MODIFIER | c.*1526G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 1526 | chr5 | 113015010 | ||||||
chr5:113015177 | G | A | 1 | a0001c0001t0065 | 1 | NA18947.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1693G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 1693 | chr5 | 113015177 | ||||||
chr5:113015361 | G | GT | 4 | a0001c0001t0024 a0001c0001t0044 a0001c0004t0062 others(1): Show |
6 | HG02896.hp1 HG02897.hp2 HG03195.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1888dupT | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 1889 | INFO_REALIGN_3_PRIME | chr5 | 113015361 | |||||
chr5:113015600 | A | G | 2 | a0001c0001t0095 a0001c0001t0096 |
2 | HG01192.hp2 HG02109.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2116A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 2116 | chr5 | 113015600 | ||||||
chr5:113015920 | A | C | 2 | a0001c0001t0021 a0001c0009t0021 |
3 | HG01256.hp1 HG01258.hp1 HG03834.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2436A>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 2436 | chr5 | 113015920 | ||||||
chr5:113015957 | G | T | 1 | a0001c0001t0012 | 5 | HG01074.hp2 HG01891.hp2 HG02451.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2473G>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 2473 | chr5 | 113015957 | ||||||
chr5:113016187 | G | C | 1 | a0001c0002t0049 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2703G>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 2703 | chr5 | 113016187 | ||||||
chr5:113016188 | G | T | 1 | a0001c0001t0094 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2704G>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 2704 | chr5 | 113016188 | ||||||
chr5:113016310 | C | G | 1 | a0001c0001t0010 | 5 | HG00423.hp1 HG02027.hp1 NA18974.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2826C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 2826 | chr5 | 113016310 | ||||||
chr5:113016350 | A | G | 1 | a0001c0010t0070 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2866A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 2866 | chr5 | 113016350 | ||||||
chr5:113016464 | T | C | 1 | a0001c0010t0070 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2980T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 2980 | chr5 | 113016464 | ||||||
chr5:113016531 | G | A | 1 | a0001c0001t0022 | 3 | HG02886.hp1 HG02895.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3047G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 3047 | chr5 | 113016531 | ||||||
chr5:113016572 | G | A | 1 | a0001c0001t0022 | 3 | HG02886.hp1 HG02895.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3088G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 3088 | chr5 | 113016572 | ||||||
chr5:113016594 | C | A | 1 | a0001c0002t0049 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3110C>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 3110 | chr5 | 113016594 | ||||||
chr5:113016840 | C | CT | 72 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(69): Show |
254 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
3_prime_UTR_variant | MODIFIER | c.*3374dupT | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 3375 | INFO_REALIGN_3_PRIME | chr5 | 113016840 | |||||
chr5:113016840 | C | CTT | 9 | a0001c0001t0012 a0001c0001t0016 a0001c0001t0034 others(6): Show |
17 | HG00621.hp2 HG01074.hp2 HG01515.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*3373_*3374dupTT | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 3375 | INFO_REALIGN_3_PRIME | chr5 | 113016840 | |||||
chr5:113016919 | G | T | 1 | a0001c0007t0055 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3435G>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 3435 | chr5 | 113016919 | ||||||
chr5:113016947 | T | C | 1 | a0001c0001t0111 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3463T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 3463 | chr5 | 113016947 | ||||||
chr5:113016966 | C | G | 1 | a0001c0001t0037 | 2 | HG01516.hp2 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3482C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 3482 | chr5 | 113016966 | ||||||
chr5:113016968 | A | G | 1 | a0001c0001t0112 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3484A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 3484 | chr5 | 113016968 | ||||||
chr5:113017047 | G | C | 1 | a0001c0001t0065 | 1 | NA18947.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3563G>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 3563 | chr5 | 113017047 | ||||||
chr5:113017096 | C | G | 1 | a0001c0001t0112 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3612C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 3612 | chr5 | 113017096 | ||||||
chr5:113017133 | T | C | 1 | a0001c0002t0056 | 1 | NA18612.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3649T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 3649 | chr5 | 113017133 | ||||||
chr5:113017169 | G | T | 1 | a0001c0001t0112 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3685G>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 3685 | chr5 | 113017169 | ||||||
chr5:113017304 | CTG | C | 11 | a0001c0001t0007 a0001c0001t0029 a0001c0001t0040 others(8): Show |
24 | HG00609.hp1 HG00741.hp1 HG01070.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*3822_*3823delGT | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 3822 | INFO_REALIGN_3_PRIME | chr5 | 113017304 | |||||
chr5:113017346 | G | A | 1 | a0001c0001t0082 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3862G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 3862 | chr5 | 113017346 | ||||||
chr5:113017408 | T | G | 4 | a0001c0001t0017 a0001c0001t0023 a0001c0001t0100 others(1): Show |
9 | HG02258.hp2 HG02280.hp1 HG02486.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3924T>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 3924 | chr5 | 113017408 | ||||||
chr5:113017411 | G | T | 1 | a0001c0001t0097 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3927G>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 3927 | chr5 | 113017411 | ||||||
chr5:113017627 | G | T | 5 | a0001c0001t0015 a0001c0001t0030 a0001c0001t0038 others(2): Show |
10 | HG01496.hp1 HG02257.hp2 HG02630.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4143G>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 4143 | chr5 | 113017627 | ||||||
chr5:113017752 | G | A | 2 | a0001c0002t0009 a0001c0002t0058 |
6 | HG00621.hp1 HG02135.hp2 NA18747.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4268G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 4268 | chr5 | 113017752 | ||||||
chr5:113017814 | A | G | 1 | a0001c0001t0011 | 5 | HG02258.hp1 HG02622.hp1 HG02896.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4330A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 4330 | chr5 | 113017814 | ||||||
chr5:113017840 | C | G | 3 | a0001c0002t0014 a0001c0002t0063 a0001c0002t0106 |
6 | HG00408.hp1 HG02155.hp1 NA18986.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4356C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 4356 | chr5 | 113017840 | ||||||
chr5:113017937 | A | G | 1 | a0001c0002t0054 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4453A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 4453 | chr5 | 113017937 | ||||||
chr5:113018190 | A | C | 1 | a0001c0001t0092 | 1 | NA19079.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4706A>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 4706 | chr5 | 113018190 | ||||||
chr5:113018372 | A | T | 1 | a0001c0010t0070 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4888A>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 4888 | chr5 | 113018372 | ||||||
chr5:113018401 | G | A | 1 | a0001c0001t0074 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4917G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 4917 | chr5 | 113018401 | ||||||
chr5:113018669 | G | A | 1 | a0001c0002t0050 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5185G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 5185 | chr5 | 113018669 | ||||||
chr5:113018715 | C | G | 1 | a0001c0002t0028 | 2 | NA19074.hp1 NA19077.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5231C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 5231 | chr5 | 113018715 | ||||||
chr5:113018720 | T | A | 10 | a0001c0001t0007 a0001c0001t0029 a0001c0001t0040 others(7): Show |
21 | HG00609.hp1 HG01070.hp1 HG01071.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*5236T>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 5236 | chr5 | 113018720 | ||||||
chr5:113018856 | G | C | 1 | a0001c0001t0040 | 2 | HG01070.hp1 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5372G>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 5372 | chr5 | 113018856 | ||||||
chr5:113018857 | C | G | 1 | a0001c0002t0026 | 2 | NA18947.hp2 NA18965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5373C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 5373 | chr5 | 113018857 | ||||||
chr5:113018889 | G | A | 1 | a0001c0001t0093 | 1 | HG00621.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5405G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 5405 | chr5 | 113018889 | ||||||
chr5:113019126 | C | T | 1 | a0001c0001t0072 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5642C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 5642 | chr5 | 113019126 | ||||||
chr5:113019201 | C | G | 43 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(40): Show |
159 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(156): Show |
3_prime_UTR_variant | MODIFIER | c.*5717C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 5717 | chr5 | 113019201 | ||||||
chr5:113019313 | G | A | 1 | a0001c0001t0083 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5829G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 5829 | chr5 | 113019313 | ||||||
chr5:113019320 | C | G | 1 | a0001c0001t0107 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5836C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 5836 | chr5 | 113019320 | ||||||
chr5:113019534 | G | C | 2 | a0001c0002t0009 a0001c0002t0058 |
6 | HG00621.hp1 HG02135.hp2 NA18747.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*6050G>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 6050 | chr5 | 113019534 | ||||||
chr5:113019571 | A | G | 1 | a0001c0010t0070 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6087A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 6087 | chr5 | 113019571 | ||||||
chr5:113019578 | G | C | 1 | a0001c0001t0022 | 3 | HG02886.hp1 HG02895.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6094G>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 6094 | chr5 | 113019578 | ||||||
chr5:113019971 | C | G | 31 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0010 others(28): Show |
129 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*6487C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 6487 | chr5 | 113019971 | ||||||
chr5:113020002 | G | T | 2 | a0001c0002t0053 a0001c0002t0059 |
2 | NA18968.hp1 NA18972.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6518G>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 6518 | chr5 | 113020002 | ||||||
chr5:113020157 | A | G | 2 | a0001c0001t0104 a0001c0001t0105 |
2 | HG02280.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6673A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 6673 | chr5 | 113020157 | ||||||
chr5:113020162 | A | G | 1 | a0001c0010t0070 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6678A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 6678 | chr5 | 113020162 | ||||||
chr5:113020211 | A | G | 43 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(40): Show |
161 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(158): Show |
3_prime_UTR_variant | MODIFIER | c.*6727A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 6727 | chr5 | 113020211 | ||||||
chr5:113020369 | CTA | C | 41 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(38): Show |
157 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
3_prime_UTR_variant | MODIFIER | c.*6888_*6889delTA | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 6888 | INFO_REALIGN_3_PRIME | chr5 | 113020369 | |||||
chr5:113020609 | C | T | 1 | a0001c0001t0036 | 2 | HG01071.hp1 HG01934.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7125C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 7125 | chr5 | 113020609 | ||||||
chr5:113020652 | A | G | 1 | a0001c0001t0091 | 1 | HG01070.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7168A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 7168 | chr5 | 113020652 | ||||||
chr5:113020744 | A | G | 1 | a0001c0001t0090 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7260A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 7260 | chr5 | 113020744 | ||||||
chr5:113020763 | G | T | 1 | a0001c0001t0033 | 2 | NA18952.hp2 NA19054.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7279G>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 7279 | chr5 | 113020763 | ||||||
chr5:113020766 | T | G | 10 | a0001c0001t0007 a0001c0001t0029 a0001c0001t0040 others(7): Show |
21 | HG00609.hp1 HG01070.hp1 HG01071.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*7282T>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 7282 | chr5 | 113020766 | ||||||
chr5:113020789 | T | G | 1 | a0001c0001t0085 | 1 | NA19082.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7305T>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 7305 | chr5 | 113020789 | ||||||
chr5:113020847 | A | G | 2 | a0001c0001t0018 a0001c0001t0109 |
5 | HG01884.hp2 HG02572.hp2 HG02622.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*7363A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 7363 | chr5 | 113020847 | ||||||
chr5:113020952 | G | A | 41 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(38): Show |
157 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
3_prime_UTR_variant | MODIFIER | c.*7468G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 7468 | chr5 | 113020952 | ||||||
chr5:113021001 | C | T | 1 | a0001c0001t0078 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7517C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 7517 | chr5 | 113021001 | ||||||
chr5:113021042 | A | G | 3 | a0001c0001t0013 a0001c0001t0111 a0001c0001t0113 |
7 | HG01496.hp2 HG02055.hp2 HG02809.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*7558A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 7558 | chr5 | 113021042 | ||||||
chr5:113021087 | A | T | 1 | a0001c0001t0071 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7603A>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 7603 | chr5 | 113021087 | ||||||
chr5:113021175 | C | G | 1 | a0001c0001t0089 | 1 | NA18977.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7691C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 7691 | chr5 | 113021175 | ||||||
chr5:113021219 | T | C | 1 | a0001c0001t0075 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7735T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 7735 | chr5 | 113021219 | ||||||
chr5:113021358 | ACT | A | 1 | a0001c0001t0022 | 3 | HG02886.hp1 HG02895.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7877_*7878delCT | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 7877 | INFO_REALIGN_3_PRIME | chr5 | 113021358 | |||||
chr5:113021381 | A | C | 1 | a0001c0001t0078 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7897A>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 7897 | chr5 | 113021381 | ||||||
chr5:113021386 | C | CA | 15 | a0001c0001t0004 a0001c0001t0017 a0001c0001t0018 others(12): Show |
40 | HG00423.hp2 HG00621.hp1 HG00735.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*7920dupA | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 7921 | INFO_REALIGN_3_PRIME | chr5 | 113021386 | |||||
chr5:113021386 | CA | C | 22 | a0001c0001t0007 a0001c0001t0011 a0001c0001t0012 others(19): Show |
51 | HG00609.hp1 HG01070.hp1 HG01071.hp2 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*7920delA | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 7920 | INFO_REALIGN_3_PRIME | chr5 | 113021386 | |||||
chr5:113021386 | CAA | C | 14 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0013 others(11): Show |
54 | HG01106.hp1 HG01496.hp2 HG01515.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*7919_*7920delAA | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 7919 | INFO_REALIGN_3_PRIME | chr5 | 113021386 | |||||
chr5:113021404 | A | C | 1 | a0001c0001t0112 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7920A>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 7920 | chr5 | 113021404 | ||||||
chr5:113021405 | C | A | 1 | a0001c0001t0086 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7921C>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 7921 | chr5 | 113021405 | ||||||
chr5:113021461 | TTAAG | T | 3 | a0001c0004t0019 a0001c0004t0060 a0001c0004t0062 |
5 | HG00741.hp1 HG01891.hp1 HG02055.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*7979_*7982delAAGT | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 7979 | INFO_REALIGN_3_PRIME | chr5 | 113021461 | |||||
chr5:113021541 | T | TTAAG | 1 | a0001c0001t0020 | 3 | NA18942.hp1 NA18955.hp1 NA18975.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8059_*8062dupAAGT | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 8063 | INFO_REALIGN_3_PRIME | chr5 | 113021541 | |||||
chr5:113021599 | G | A | 1 | a0001c0001t0032 | 2 | HG03491.hp2 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8115G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 8115 | chr5 | 113021599 | ||||||
chr5:113021646 | G | GTAAC | 3 | a0001c0001t0018 a0001c0001t0109 a0001c0008t0108 |
6 | HG01884.hp2 HG02572.hp2 HG02622.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*8164_*8167dupAACT | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 8168 | INFO_REALIGN_3_PRIME | chr5 | 113021646 | |||||
chr5:113021705 | AG | A | 42 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(39): Show |
158 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*8222delG | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 8222 | chr5 | 113021705 | ||||||
chr5:113021782 | A | G | 2 | a0001c0001t0087 a0001c0001t0088 |
2 | NA18943.hp1 NA18987.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8298A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 8298 | chr5 | 113021782 | ||||||
chr5:113022033 | T | C | 1 | a0001c0002t0103 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8549T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 8549 | chr5 | 113022033 | ||||||
chr5:113022070 | G | A | 8 | a0001c0001t0007 a0001c0001t0029 a0001c0001t0065 others(5): Show |
18 | HG00609.hp1 HG02129.hp1 HG02523.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*8586G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 11/11 | 8586 | chr5 | 113022070 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:112977016 | C | T | 1 | a0001c0001t0001g0324 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.53+30C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112977016 | |||||||
chr5:112977018 | G | C | 1 | a0001c0001t0007g0023 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.53+32G>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112977018 | |||||||
chr5:112977028 | C | A | 1 | a0001c0001t0080g0024 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.53+42C>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112977028 | |||||||
chr5:112977039 | G | C | 202 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0137 others(199): Show |
218 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(215): Show |
intron_variant | MODIFIER | c.53+53G>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112977039 | |||||||
chr5:112977045 | C | T | 1 | a0001c0001t0005g0206 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.53+59C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112977045 | |||||||
chr5:112977157 | C | T | 1 | a0001c0001t0072g0323 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.53+171C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112977157 | |||||||
chr5:112977185 | C | T | 1 | a0001c0002t0002g0205 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.53+199C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112977185 | |||||||
chr5:112977257 | A | T | 9 | a0001c0001t0017g0004 a0001c0001t0017g0016 a0001c0001t0022g0202 others(6): Show |
11 | HG02258.hp2 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.53+271A>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112977257 | |||||||
chr5:112977292 | G | A | 1 | a0001c0004t0019g0025 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.53+306G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112977292 | |||||||
chr5:112977545 | C | T | 1 | a0001c0002t0002g0199 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.53+559C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112977545 | |||||||
chr5:112977636 | C | G | 1 | a0001c0001t0033g0198 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.53+650C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112977636 | |||||||
chr5:112977660 | G | C | 1 | a0001c0001t0005g0206 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.53+674G>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112977660 | |||||||
chr5:112977761 | C | G | 6 | a0001c0001t0003g0192 a0001c0001t0003g0193 a0001c0001t0003g0196 others(3): Show |
6 | NA18957.hp1 NA18963.hp1 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.53+775C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112977761 | |||||||
chr5:112977778 | G | A | 2 | a0001c0001t0006g0027 a0001c0002t0002g0026 |
2 | HG01243.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.53+792G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112977778 | |||||||
chr5:112977948 | G | GT | 83 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0137 others(80): Show |
88 | HG01074.hp2 HG01106.hp1 HG01243.hp1 others(85): Show |
intron_variant | MODIFIER | c.53+968dupT | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112977948 | ||||||
chr5:112977954 | T | TG | 6 | a0001c0001t0015g0028 a0001c0001t0015g0030 a0001c0001t0015g0031 others(3): Show |
6 | HG02257.hp2 HG02818.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.53+972dupG | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112977954 | ||||||
chr5:112977978 | T | G | 5 | a0001c0001t0006g0128 a0001c0001t0006g0129 a0001c0001t0006g0131 others(2): Show |
5 | HG02155.hp2 NA18948.hp1 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.53+992T>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112977978 | |||||||
chr5:112978040 | C | A | 6 | a0001c0001t0015g0028 a0001c0001t0015g0030 a0001c0001t0015g0031 others(3): Show |
6 | HG02257.hp2 HG02818.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.53+1054C>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112978040 | |||||||
chr5:112978135 | C | G | 1 | a0001c0002t0002g0127 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.53+1149C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112978135 | |||||||
chr5:112978274 | C | T | 79 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0137 others(76): Show |
82 | HG01074.hp2 HG01106.hp1 HG01243.hp1 others(79): Show |
intron_variant | MODIFIER | c.53+1288C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112978274 | |||||||
chr5:112978341 | G | A | 1 | a0001c0001t0044g0134 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.53+1355G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112978341 | |||||||
chr5:112978414 | T | C | 2 | a0001c0001t0029g0034 a0001c0001t0029g0035 |
2 | HG02647.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.53+1428T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112978414 | |||||||
chr5:112978445 | A | G | 2 | a0001c0001t0024g0190 a0001c0001t0024g0191 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.53+1459A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112978445 | |||||||
chr5:112978498 | A | G | 1 | a0001c0001t0101g0322 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.53+1512A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112978498 | |||||||
chr5:112978568 | T | G | 3 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0137 |
3 | HG03471.hp1 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.53+1582T>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112978568 | |||||||
chr5:112978581 | A | G | 49 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0137 others(46): Show |
50 | HG01106.hp1 HG01515.hp1 HG02015.hp1 others(47): Show |
intron_variant | MODIFIER | c.53+1595A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112978581 | |||||||
chr5:112978584 | A | G | 79 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0137 others(76): Show |
82 | HG01074.hp2 HG01106.hp1 HG01243.hp1 others(79): Show |
intron_variant | MODIFIER | c.53+1598A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112978584 | |||||||
chr5:112978611 | T | C | 18 | a0001c0001t0007g0023 a0001c0001t0007g0036 a0001c0001t0007g0037 others(15): Show |
18 | HG00609.hp1 HG02129.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.53+1625T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112978611 | |||||||
chr5:112978683 | T | TA | 89 | a0001c0001t0006g0027 a0001c0001t0006g0107 a0001c0001t0030g0114 others(86): Show |
100 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.53+1710dupA | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112978683 | ||||||
chr5:112978744 | C | T | 1 | a0001c0006t0035g0321 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.53+1758C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112978744 | |||||||
chr5:112978751 | C | T | 6 | a0001c0001t0015g0028 a0001c0001t0015g0030 a0001c0001t0015g0031 others(3): Show |
6 | HG02257.hp2 HG02818.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.53+1765C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112978751 | |||||||
chr5:112978755 | C | T | 2 | a0001c0002t0028g0116 a0001c0002t0028g0126 |
2 | NA19074.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.53+1769C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112978755 | |||||||
chr5:112978756 | A | G | 96 | a0001c0001t0006g0027 a0001c0001t0006g0107 a0001c0001t0030g0114 others(93): Show |
107 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.53+1770A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112978756 | |||||||
chr5:112978757 | A | G | 3 | a0001c0001t0012g0014 a0001c0001t0012g0156 a0001c0001t0012g0157 |
4 | HG01074.hp2 HG01891.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.53+1771A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112978757 | |||||||
chr5:112978910 | T | G | 1 | a0001c0001t0003g0158 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.53+1924T>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112978910 | |||||||
chr5:112978995 | A | G | 1 | a0001c0001t0001g0320 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.53+2009A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112978995 | |||||||
chr5:112979015 | CTGTTAAC others(7): Show |
C | 9 | a0001c0001t0017g0004 a0001c0001t0017g0016 a0001c0001t0022g0202 others(6): Show |
11 | HG02258.hp2 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.53+2033_53+2046del others(14): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112979015 | ||||||
chr5:112979039 | C | A | 1 | a0001c0002t0002g0051 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.53+2053C>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112979039 | |||||||
chr5:112979073 | A | G | 9 | a0001c0001t0005g0154 a0001c0001t0011g0013 a0001c0001t0011g0150 others(6): Show |
10 | HG02258.hp1 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.53+2087A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112979073 | |||||||
chr5:112979126 | GT | G | 88 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0137 others(85): Show |
93 | HG01074.hp2 HG01106.hp1 HG01243.hp1 others(90): Show |
intron_variant | MODIFIER | c.53+2141delT | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112979126 | |||||||
chr5:112979334 | C | G | 7 | a0001c0001t0030g0114 a0001c0001t0030g0115 a0001c0003t0005g0003 others(4): Show |
11 | HG01884.hp1 HG02145.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.53+2348C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112979334 | |||||||
chr5:112979469 | C | A | 1 | a0001c0001t0013g0138 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.53+2483C>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112979469 | |||||||
chr5:112979516 | G | T | 1 | a0001c0001t0112g0119 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.53+2530G>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112979516 | |||||||
chr5:112979718 | G | A | 1 | a0001c0007t0055g0052 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.53+2732G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112979718 | |||||||
chr5:112979786 | A | G | 11 | a0001c0001t0006g0129 a0001c0001t0006g0131 a0001c0001t0006g0132 others(8): Show |
11 | HG02155.hp2 NA18747.hp1 NA18943.hp2 others(8): Show |
intron_variant | MODIFIER | c.53+2800A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112979786 | |||||||
chr5:112979852 | T | A | 3 | a0001c0002t0052g0054 a0001c0002t0054g0053 a0001c0007t0055g0052 |
3 | HG02895.hp2 HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.53+2866T>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112979852 | |||||||
chr5:112979935 | C | T | 1 | a0001c0001t0006g0027 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.53+2949C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112979935 | |||||||
chr5:112980005 | G | A | 2 | a0001c0001t0029g0034 a0001c0001t0029g0035 |
2 | HG02647.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.53+3019G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112980005 | |||||||
chr5:112980062 | T | A | 2 | a0001c0001t0007g0036 a0001c0001t0007g0037 |
2 | NA19002.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.53+3076T>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112980062 | |||||||
chr5:112980156 | G | A | 170 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0137 others(167): Show |
182 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.53+3170G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112980156 | |||||||
chr5:112980165 | A | G | 3 | a0001c0001t0024g0155 a0001c0001t0024g0190 a0001c0001t0024g0191 |
3 | HG02896.hp1 HG02897.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.53+3179A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112980165 | |||||||
chr5:112980231 | A | G | 1 | a0001c0005t0004g0319 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.53+3245A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112980231 | |||||||
chr5:112980317 | C | G | 1 | a0001c0001t0013g0138 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.53+3331C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112980317 | |||||||
chr5:112980553 | A | G | 1 | a0001c0001t0071g0033 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.53+3567A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112980553 | |||||||
chr5:112980585 | A | AC | 170 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0137 others(167): Show |
182 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.53+3600dupC | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112980585 | ||||||
chr5:112980620 | C | A | 1 | a0001c0002t0027g0055 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.53+3634C>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112980620 | |||||||
chr5:112980645 | A | G | 2 | a0001c0001t0007g0050 a0001c0001t0065g0049 |
2 | NA18947.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.53+3659A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112980645 | |||||||
chr5:112980779 | A | C | 2 | a0001c0002t0002g0108 a0001c0002t0002g0109 |
2 | HG00733.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.53+3793A>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112980779 | |||||||
chr5:112980879 | A | G | 1 | a0001c0001t0001g0318 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.53+3893A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112980879 | |||||||
chr5:112981029 | A | AT | 89 | a0001c0001t0006g0027 a0001c0001t0006g0107 a0001c0001t0045g0082 others(86): Show |
96 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.53+4053dupT | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112981029 | ||||||
chr5:112981212 | C | T | 1 | a0001c0001t0006g0107 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.53+4226C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112981212 | |||||||
chr5:112981223 | C | G | 7 | a0001c0001t0030g0114 a0001c0001t0030g0115 a0001c0003t0005g0003 others(4): Show |
11 | HG01884.hp1 HG02145.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.53+4237C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112981223 | |||||||
chr5:112981230 | G | A | 12 | a0001c0001t0007g0023 a0001c0001t0007g0036 a0001c0001t0007g0037 others(9): Show |
12 | HG00609.hp1 HG02129.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.53+4244G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112981230 | |||||||
chr5:112981232 | A | G | 1 | a0001c0001t0044g0134 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.53+4246A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112981232 | |||||||
chr5:112981350 | G | A | 9 | a0001c0001t0017g0004 a0001c0001t0017g0016 a0001c0001t0022g0202 others(6): Show |
11 | HG02258.hp2 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.53+4364G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112981350 | |||||||
chr5:112981668 | G | C | 1 | a0001c0001t0001g0213 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.54-4167G>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112981668 | |||||||
chr5:112981720 | T | C | 112 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0137 others(109): Show |
121 | HG00609.hp1 HG01074.hp2 HG01106.hp1 others(118): Show |
intron_variant | MODIFIER | c.54-4115T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112981720 | |||||||
chr5:112981733 | T | C | 2 | a0001c0001t0001g0007 a0001c0001t0001g0214 |
4 | NA18940.hp2 NA19070.hp2 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.54-4102T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112981733 | |||||||
chr5:112982033 | G | A | 1 | a0001c0002t0028g0126 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.54-3802G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112982033 | |||||||
chr5:112982069 | C | T | 3 | a0001c0002t0052g0054 a0001c0002t0054g0053 a0001c0007t0055g0052 |
3 | HG02895.hp2 HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.54-3766C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112982069 | |||||||
chr5:112982087 | A | G | 1 | a0001c0002t0056g0106 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.54-3748A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112982087 | |||||||
chr5:112982137 | T | G | 1 | a0001c0001t0112g0119 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.54-3698T>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112982137 | |||||||
chr5:112982175 | A | G | 14 | a0001c0001t0007g0023 a0001c0001t0007g0036 a0001c0001t0007g0037 others(11): Show |
14 | HG00609.hp1 HG02129.hp1 HG02523.hp2 others(11): Show |
intron_variant | MODIFIER | c.54-3660A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112982175 | |||||||
chr5:112982191 | T | TTA | 112 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0137 others(109): Show |
121 | HG00609.hp1 HG01074.hp2 HG01106.hp1 others(118): Show |
intron_variant | MODIFIER | c.54-3644_54-3643ins others(2): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112982191 | |||||||
chr5:112982233 | C | T | 2 | a0001c0001t0001g0317 a0001c0002t0002g0105 |
2 | HG02602.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.54-3602C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112982233 | |||||||
chr5:112982287 | A | T | 80 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0137 others(77): Show |
85 | HG00609.hp1 HG01106.hp1 HG01496.hp2 others(82): Show |
intron_variant | MODIFIER | c.54-3548A>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112982287 | |||||||
chr5:112982315 | C | T | 3 | a0001c0002t0002g0102 a0001c0002t0002g0104 a0001c0002t0049g0103 |
3 | HG01981.hp2 HG02683.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.54-3520C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112982315 | |||||||
chr5:112982467 | T | A | 5 | a0001c0001t0012g0014 a0001c0001t0012g0139 a0001c0001t0012g0156 others(2): Show |
6 | HG01074.hp2 HG01891.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.54-3368T>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112982467 | |||||||
chr5:112982561 | C | A | 3 | a0001c0001t0024g0155 a0001c0001t0024g0190 a0001c0001t0024g0191 |
3 | HG02896.hp1 HG02897.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.54-3274C>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112982561 | |||||||
chr5:112982598 | G | A | 1 | a0001c0001t0012g0139 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.54-3237G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112982598 | |||||||
chr5:112982624 | C | G | 2 | a0001c0001t0033g0183 a0001c0001t0033g0198 |
2 | NA18952.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.54-3211C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112982624 | |||||||
chr5:112982651 | GT | G | 6 | a0001c0001t0005g0154 a0001c0001t0011g0013 a0001c0001t0011g0150 others(3): Show |
7 | HG02258.hp1 HG02622.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.54-3176delT | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112982651 | ||||||
chr5:112982672 | TCTTA | T | 9 | a0001c0001t0005g0154 a0001c0001t0011g0013 a0001c0001t0011g0150 others(6): Show |
10 | HG02258.hp1 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.54-3158_54-3155del others(4): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112982672 | ||||||
chr5:112982690 | C | A | 6 | a0001c0001t0015g0028 a0001c0001t0015g0030 a0001c0001t0015g0031 others(3): Show |
6 | HG02257.hp2 HG02818.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.54-3145C>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112982690 | |||||||
chr5:112982716 | G | A | 9 | a0001c0001t0017g0004 a0001c0001t0017g0016 a0001c0001t0022g0202 others(6): Show |
11 | HG02258.hp2 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.54-3119G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112982716 | |||||||
chr5:112982848 | A | G | 1 | a0001c0001t0001g0316 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.54-2987A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112982848 | |||||||
chr5:112983231 | C | T | 166 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0137 others(163): Show |
178 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.54-2604C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112983231 | |||||||
chr5:112983344 | C | T | 80 | a0001c0001t0006g0027 a0001c0001t0006g0107 a0001c0001t0045g0082 others(77): Show |
87 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.54-2491C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112983344 | |||||||
chr5:112983399 | A | G | 10 | a0001c0001t0005g0118 a0001c0001t0005g0206 a0001c0001t0030g0114 others(7): Show |
14 | HG01884.hp1 HG02145.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.54-2436A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112983399 | |||||||
chr5:112983415 | T | A | 165 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0137 others(162): Show |
177 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.54-2420T>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112983415 | |||||||
chr5:112983429 | C | T | 1 | a0001c0010t0070g0048 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.54-2406C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112983429 | |||||||
chr5:112983571 | A | G | 2 | a0001c0001t0007g0036 a0001c0001t0007g0037 |
2 | NA19002.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.54-2264A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112983571 | |||||||
chr5:112983660 | G | T | 1 | a0001c0002t0002g0101 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.54-2175G>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112983660 | |||||||
chr5:112983670 | G | A | 1 | a0001c0002t0008g0058 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.54-2165G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112983670 | |||||||
chr5:112983699 | A | G | 4 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0182 others(1): Show |
4 | NA18945.hp1 NA19030.hp1 NA19082.hp1 others(1): Show |
intron_variant | MODIFIER | c.54-2136A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112983699 | |||||||
chr5:112983794 | G | A | 9 | a0001c0001t0017g0004 a0001c0001t0017g0016 a0001c0001t0022g0202 others(6): Show |
11 | HG02258.hp2 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.54-2041G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112983794 | |||||||
chr5:112984103 | G | A | 3 | a0001c0001t0022g0202 a0001c0001t0022g0203 a0001c0001t0022g0204 |
3 | HG02886.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.54-1732G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984103 | |||||||
chr5:112984208 | A | G | 1 | a0001c0001t0006g0107 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.54-1627A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984208 | |||||||
chr5:112984273 | G | C | 6 | a0001c0001t0005g0154 a0001c0001t0011g0013 a0001c0001t0011g0150 others(3): Show |
7 | HG02258.hp1 HG02622.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.54-1562G>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984273 | |||||||
chr5:112984420 | C | G | 4 | a0001c0001t0040g0313 a0001c0001t0040g0314 a0001c0001t0107g0117 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.54-1415C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984420 | |||||||
chr5:112984561 | C | T | 8 | a0001c0001t0015g0028 a0001c0001t0015g0030 a0001c0001t0015g0031 others(5): Show |
8 | HG02257.hp2 HG02818.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.54-1274C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984561 | |||||||
chr5:112984641 | G | A | 1 | a0001c0002t0002g0059 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.54-1194G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984641 | |||||||
chr5:112984643 | C | G | 1 | a0001c0002t0002g0026 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.54-1192C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984643 | |||||||
chr5:112984652 | C | T | 9 | a0001c0001t0017g0004 a0001c0001t0017g0016 a0001c0001t0022g0202 others(6): Show |
11 | HG02258.hp2 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.54-1183C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984652 | |||||||
chr5:112984663 | C | G | 2 | a0001c0001t0018g0311 a0001c0001t0018g0312 |
2 | HG02572.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.54-1172C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984663 | |||||||
chr5:112984684 | A | AT | 12 | a0001c0001t0003g0158 a0001c0001t0003g0169 a0001c0001t0003g0173 others(9): Show |
12 | HG01106.hp1 HG02015.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.54-1149dupT | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984684 | ||||||
chr5:112984686 | T | TTA | 4 | a0001c0001t0003g0137 a0001c0001t0003g0164 a0001c0001t0003g0165 others(1): Show |
4 | HG01515.hp1 HG03471.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.54-1149_54-1148ins others(2): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984686 | |||||||
chr5:112984686 | T | TTAA | 13 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0159 others(10): Show |
14 | HG03490.hp2 HG03491.hp2 HG03492.hp1 others(11): Show |
intron_variant | MODIFIER | c.54-1149_54-1148ins others(3): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984686 | |||||||
chr5:112984686 | TA | T | 11 | a0001c0001t0001g0007 a0001c0001t0001g0214 a0001c0001t0001g0302 others(8): Show |
13 | HG01261.hp2 HG02735.hp2 HG03041.hp2 others(10): Show |
intron_variant | MODIFIER | c.54-1131delA | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984686 | ||||||
chr5:112984687 | A | T | 151 | a0001c0001t0003g0175 a0001c0001t0003g0176 a0001c0001t0003g0179 others(148): Show |
160 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.54-1148A>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984687 | |||||||
chr5:112984693 | A | ATATATAT others(4): Show |
2 | a0001c0001t0024g0190 a0001c0001t0024g0191 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.54-1142_54-1141ins others(11): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984693 | |||||||
chr5:112984693 | A | ATATATAT others(24): Show |
1 | a0001c0002t0014g0100 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.54-1142_54-1141ins others(31): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984693 | |||||||
chr5:112984693 | A | T | 5 | a0001c0004t0019g0025 a0001c0004t0019g0124 a0001c0004t0019g0125 others(2): Show |
5 | HG00741.hp1 HG01891.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.54-1142A>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984693 | |||||||
chr5:112984694 | AAAAAAAA others(6): Show |
A | 1 | a0001c0002t0014g0099 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.54-1139_54-1127del others(13): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984694 | ||||||
chr5:112984695 | A | AATATATA others(7): Show |
1 | a0001c0002t0064g0065 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.54-1139_54-1138ins others(14): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984695 | ||||||
chr5:112984695 | A | ATATATAT others(16): Show |
1 | a0001c0002t0002g0091 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.54-1140_54-1139ins others(23): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984695 | |||||||
chr5:112984695 | A | T | 8 | a0001c0001t0024g0190 a0001c0001t0024g0191 a0001c0002t0014g0100 others(5): Show |
8 | HG00741.hp1 HG01891.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.54-1140A>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984695 | |||||||
chr5:112984697 | A | AAT | 5 | a0001c0002t0048g0057 a0001c0003t0005g0003 a0001c0003t0005g0012 others(2): Show |
7 | HG01884.hp1 HG02572.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.54-1137_54-1136ins others(2): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984697 | ||||||
chr5:112984697 | A | AATATATA others(3): Show |
1 | a0001c0002t0027g0055 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.54-1137_54-1136ins others(10): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984697 | ||||||
chr5:112984697 | A | AATATATA others(11): Show |
1 | a0001c0001t0015g0032 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.54-1137_54-1136ins others(18): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984697 | ||||||
chr5:112984697 | A | AATATATA others(13): Show |
2 | a0001c0001t0015g0031 a0001c0001t0044g0134 |
2 | HG03195.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.54-1137_54-1136ins others(20): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984697 | ||||||
chr5:112984697 | A | AATATATA others(17): Show |
2 | a0001c0001t0015g0030 a0001c0002t0002g0062 |
2 | HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.54-1137_54-1136ins others(24): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984697 | ||||||
chr5:112984697 | A | AATATATA others(21): Show |
3 | a0001c0001t0015g0028 a0001c0002t0002g0063 a0001c0002t0002g0067 |
3 | HG01167.hp1 HG02257.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.54-1137_54-1136ins others(28): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984697 | ||||||
chr5:112984697 | A | AATATATA others(23): Show |
2 | a0001c0002t0028g0116 a0001c0002t0028g0126 |
2 | NA19074.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.54-1137_54-1136ins others(30): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984697 | ||||||
chr5:112984697 | A | AATATATA others(27): Show |
1 | a0001c0002t0002g0051 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.54-1137_54-1136ins others(34): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984697 | ||||||
chr5:112984697 | A | ATATATAT others(6): Show |
1 | a0001c0004t0046g0069 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.54-1138_54-1137ins others(13): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984697 | |||||||
chr5:112984697 | A | ATATATAT others(8): Show |
1 | a0001c0002t0008g0058 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.54-1138_54-1137ins others(15): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984697 | |||||||
chr5:112984697 | A | ATATATAT others(26): Show |
2 | a0001c0001t0030g0115 a0001c0002t0063g0009 |
2 | NA18990.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.54-1138_54-1137ins others(33): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984697 | |||||||
chr5:112984697 | A | T | 11 | a0001c0001t0024g0190 a0001c0001t0024g0191 a0001c0002t0002g0091 others(8): Show |
11 | HG00280.hp2 HG00741.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.54-1138A>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984697 | |||||||
chr5:112984699 | A | AATATATA others(9): Show |
2 | a0001c0001t0011g0150 a0001c0002t0059g0089 |
2 | HG02258.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.54-1135_54-1134ins others(16): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984699 | ||||||
chr5:112984699 | A | AATATATA others(13): Show |
3 | a0001c0002t0002g0001 a0001c0002t0002g0087 a0001c0002t0053g0090 |
3 | NA18972.hp1 NA18977.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.54-1135_54-1134ins others(20): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984699 | ||||||
chr5:112984699 | A | AATATATA others(15): Show |
1 | a0001c0002t0009g0071 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.54-1135_54-1134ins others(22): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984699 | ||||||
chr5:112984699 | A | AATATATA others(17): Show |
1 | a0001c0001t0038g0029 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.54-1135_54-1134ins others(24): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984699 | ||||||
chr5:112984699 | A | AATATATA others(19): Show |
1 | a0001c0002t0009g0084 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.54-1135_54-1134ins others(26): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984699 | ||||||
chr5:112984699 | A | AATATATA others(21): Show |
2 | a0001c0001t0071g0033 a0001c0002t0009g0011 |
2 | HG02135.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.54-1135_54-1134ins others(28): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984699 | ||||||
chr5:112984699 | A | AATATATA others(31): Show |
1 | a0001c0002t0002g0073 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.54-1135_54-1134ins others(38): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984699 | ||||||
chr5:112984699 | A | AATATATA others(35): Show |
1 | a0001c0002t0002g0072 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.54-1135_54-1134ins others(42): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984699 | ||||||
chr5:112984699 | A | AT | 5 | a0001c0001t0001g0227 a0001c0001t0001g0266 a0001c0001t0001g0291 others(2): Show |
5 | HG00140.hp1 HG01192.hp1 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.54-1136_54-1135ins others(1): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984699 | |||||||
chr5:112984699 | A | ATAT | 1 | a0001c0002t0002g0006 | 3 | NA18955.hp2 NA18983.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.54-1136_54-1135ins others(3): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984699 | |||||||
chr5:112984699 | A | ATATATAT others(4): Show |
2 | a0001c0001t0104g0149 a0001c0001t0105g0141 |
2 | HG02280.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.54-1136_54-1135ins others(11): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984699 | |||||||
chr5:112984699 | A | ATATATAT others(6): Show |
2 | a0001c0002t0008g0010 a0001c0002t0061g0083 |
2 | NA18942.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.54-1136_54-1135ins others(13): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984699 | |||||||
chr5:112984699 | A | ATATATAT others(8): Show |
1 | a0001c0002t0008g0010 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.54-1136_54-1135ins others(15): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984699 | |||||||
chr5:112984699 | A | ATATATAT others(10): Show |
1 | a0001c0002t0002g0080 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.54-1136_54-1135ins others(17): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984699 | |||||||
chr5:112984699 | A | ATATATAT others(14): Show |
2 | a0001c0001t0024g0155 a0001c0002t0008g0120 |
2 | HG03516.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.54-1136_54-1135ins others(21): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984699 | |||||||
chr5:112984699 | A | ATATATAT others(16): Show |
2 | a0001c0001t0011g0013 a0001c0002t0002g0056 |
2 | HG02622.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.54-1136_54-1135ins others(23): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984699 | |||||||
chr5:112984699 | A | ATATATAT others(20): Show |
2 | a0001c0002t0051g0070 a0001c0002t0057g0061 |
2 | HG02074.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.54-1136_54-1135ins others(27): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984699 | |||||||
chr5:112984699 | A | ATATATAT others(24): Show |
1 | a0001c0001t0030g0114 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.54-1136_54-1135ins others(31): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984699 | |||||||
chr5:112984699 | A | T | 37 | a0001c0001t0001g0249 a0001c0001t0005g0118 a0001c0001t0015g0028 others(34): Show |
40 | HG00280.hp2 HG00735.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.54-1136A>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984699 | |||||||
chr5:112984701 | A | AATATATA others(3): Show |
1 | a0001c0001t0107g0117 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.54-1133_54-1132ins others(10): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984701 | ||||||
chr5:112984701 | A | AATATATA others(17): Show |
1 | a0001c0002t0027g0085 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.54-1133_54-1132ins others(24): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984701 | ||||||
chr5:112984701 | A | AATATATA others(19): Show |
1 | a0001c0002t0002g0101 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.54-1133_54-1132ins others(26): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984701 | ||||||
chr5:112984701 | A | AATATATA others(21): Show |
1 | a0001c0002t0002g0076 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.54-1133_54-1132ins others(28): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984701 | ||||||
chr5:112984701 | A | AATATATA others(23): Show |
1 | a0001c0001t0005g0154 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.54-1133_54-1132ins others(30): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984701 | ||||||
chr5:112984701 | A | AATATATA others(25): Show |
1 | a0001c0002t0002g0001 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.54-1133_54-1132ins others(32): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984701 | ||||||
chr5:112984701 | A | AATATATA others(27): Show |
2 | a0001c0002t0009g0077 a0001c0002t0014g0001 |
3 | HG00408.hp1 NA18989.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.54-1133_54-1132ins others(34): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984701 | ||||||
chr5:112984701 | A | AATATATA others(51): Show |
1 | a0001c0001t0006g0027 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.54-1133_54-1132ins others(58): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984701 | ||||||
chr5:112984701 | A | AT | 14 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0219 others(11): Show |
15 | HG00423.hp1 HG01256.hp1 HG01258.hp1 others(12): Show |
intron_variant | MODIFIER | c.54-1134_54-1133ins others(1): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984701 | |||||||
chr5:112984701 | A | ATATATAT others(10): Show |
3 | a0001c0002t0008g0066 a0001c0002t0008g0086 a0001c0002t0008g0088 |
3 | HG00423.hp2 HG01943.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.54-1134_54-1133ins others(17): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984701 | |||||||
chr5:112984701 | A | ATATATAT others(14): Show |
1 | a0001c0001t0006g0187 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.54-1134_54-1133ins others(21): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984701 | |||||||
chr5:112984701 | A | ATATATAT others(16): Show |
2 | a0001c0001t0011g0013 a0001c0002t0056g0106 |
2 | HG02896.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.54-1134_54-1133ins others(23): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984701 | |||||||
chr5:112984701 | A | ATATATAT others(18): Show |
2 | a0001c0002t0008g0060 a0001c0002t0058g0011 |
2 | HG00621.hp1 HG01928.hp1 |
intron_variant | MODIFIER | c.54-1134_54-1133ins others(25): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984701 | |||||||
chr5:112984701 | A | ATATATAT others(24): Show |
1 | a0001c0002t0002g0075 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.54-1134_54-1133ins others(31): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984701 | |||||||
chr5:112984701 | A | ATATATAT others(26): Show |
1 | a0001c0002t0009g0078 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.54-1134_54-1133ins others(33): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984701 | |||||||
chr5:112984701 | A | ATATATAT others(28): Show |
2 | a0001c0002t0002g0064 a0001c0002t0002g0074 |
2 | HG01975.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.54-1134_54-1133ins others(35): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984701 | |||||||
chr5:112984701 | A | T | 92 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0227 others(89): Show |
103 | HG00140.hp1 HG00280.hp2 HG00673.hp1 others(100): Show |
intron_variant | MODIFIER | c.54-1134A>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984701 | |||||||
chr5:112984703 | A | AAAAAAAA others(11): Show |
1 | a0001c0001t0065g0049 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.54-1131_54-1130ins others(18): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | ||||||
chr5:112984703 | A | AAAAAAAA others(13): Show |
1 | a0001c0001t0007g0036 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.54-1131_54-1130ins others(20): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | ||||||
chr5:112984703 | A | AAAAAAAT others(6): Show |
1 | a0001c0001t0111g0148 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.54-1131_54-1130ins others(13): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | ||||||
chr5:112984703 | A | AAAAAAAT others(8): Show |
1 | a0001c0001t0007g0038 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.54-1131_54-1130ins others(15): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | ||||||
chr5:112984703 | A | AAAAAAAT others(16): Show |
1 | a0001c0001t0069g0046 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.54-1131_54-1130ins others(23): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | ||||||
chr5:112984703 | A | AAAAAATA others(9): Show |
2 | a0001c0001t0007g0043 a0001c0001t0013g0144 |
2 | HG03209.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.54-1131_54-1130ins others(16): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | ||||||
chr5:112984703 | A | AAAAAATA others(11): Show |
3 | a0001c0001t0007g0039 a0001c0001t0007g0050 a0001c0001t0013g0146 |
3 | HG02886.hp2 NA19057.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.54-1131_54-1130ins others(18): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | ||||||
chr5:112984703 | A | AAAAAATA others(13): Show |
2 | a0001c0001t0007g0037 a0001c0001t0007g0047 |
2 | NA19065.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.54-1131_54-1130ins others(20): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | ||||||
chr5:112984703 | A | AAAAAATA others(19): Show |
1 | a0001c0001t0013g0145 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.54-1131_54-1130ins others(26): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | ||||||
chr5:112984703 | A | AAAAATAT others(6): Show |
2 | a0001c0001t0013g0138 a0001c0001t0113g0147 |
2 | HG02055.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.54-1131_54-1130ins others(13): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | ||||||
chr5:112984703 | A | AAAAATAT others(14): Show |
1 | a0001c0001t0067g0045 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.54-1131_54-1130ins others(21): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | ||||||
chr5:112984703 | A | AAAAATAT others(22): Show |
2 | a0001c0002t0002g0059 a0001c0002t0002g0205 |
2 | HG01081.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.54-1131_54-1130ins others(29): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | ||||||
chr5:112984703 | A | AAAAATAT others(32): Show |
1 | a0001c0002t0025g0093 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.54-1131_54-1130ins others(39): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | ||||||
chr5:112984703 | A | AAAAATAT others(34): Show |
1 | a0001c0010t0070g0048 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.54-1131_54-1130ins others(41): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | ||||||
chr5:112984703 | A | AAAATATA others(3): Show |
1 | a0001c0002t0049g0103 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.54-1131_54-1130ins others(10): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | ||||||
chr5:112984703 | A | AAAATATA others(9): Show |
1 | a0001c0001t0007g0042 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.54-1131_54-1130ins others(16): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | ||||||
chr5:112984703 | A | AAAATATA others(11): Show |
2 | a0001c0001t0007g0041 a0001c0001t0068g0040 |
2 | HG02129.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.54-1131_54-1130ins others(18): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | ||||||
chr5:112984703 | A | AAAATATA others(13): Show |
1 | a0001c0002t0002g0098 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.54-1131_54-1130ins others(20): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | ||||||
chr5:112984703 | A | AAAATATA others(15): Show |
2 | a0001c0001t0066g0044 a0001c0002t0002g0127 |
2 | HG02040.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.54-1131_54-1130ins others(22): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | ||||||
chr5:112984703 | A | AAAATATA others(17): Show |
3 | a0001c0001t0006g0129 a0001c0001t0042g0130 a0001c0002t0002g0102 |
3 | HG01981.hp2 HG02155.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.54-1131_54-1130ins others(24): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | ||||||
chr5:112984703 | A | AAAATATA others(19): Show |
2 | a0001c0001t0006g0188 a0001c0002t0002g0104 |
2 | HG02683.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.54-1131_54-1130ins others(26): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | ||||||
chr5:112984703 | A | AAAATATA others(29): Show |
1 | a0001c0002t0002g0108 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.54-1131_54-1130ins others(36): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | ||||||
chr5:112984703 | A | AAATAT | 6 | a0001c0001t0003g0175 a0001c0001t0003g0176 a0001c0001t0003g0179 others(3): Show |
6 | HG04115.hp2 NA18945.hp1 NA18985.hp2 others(3): Show |
intron_variant | MODIFIER | c.54-1131_54-1130ins others(5): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | ||||||
chr5:112984703 | A | AAATATAT others(8): Show |
1 | a0001c0001t0029g0035 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.54-1131_54-1130ins others(15): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | ||||||
chr5:112984703 | A | AAATATAT others(10): Show |
1 | a0001c0001t0007g0023 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.54-1131_54-1130ins others(17): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | ||||||
chr5:112984703 | A | AAATATAT others(12): Show |
1 | a0001c0002t0002g0092 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.54-1131_54-1130ins others(19): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | ||||||
chr5:112984703 | A | AAATATAT others(16): Show |
1 | a0001c0001t0006g0131 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.54-1131_54-1130ins others(23): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | ||||||
chr5:112984703 | A | AAATATAT others(22): Show |
1 | a0001c0002t0054g0053 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.54-1131_54-1130ins others(29): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | ||||||
chr5:112984703 | A | AAATATAT others(24): Show |
1 | a0001c0002t0025g0121 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.54-1131_54-1130ins others(31): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | ||||||
chr5:112984703 | A | AAATATAT others(26): Show |
2 | a0001c0002t0002g0068 a0001c0002t0002g0096 |
2 | HG01346.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.54-1131_54-1130ins others(33): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | ||||||
chr5:112984703 | A | AAATATAT others(36): Show |
1 | a0001c0002t0052g0054 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.54-1131_54-1130ins others(43): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | ||||||
chr5:112984703 | A | AAATATAT others(38): Show |
1 | a0001c0002t0002g0199 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.54-1131_54-1130ins others(45): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | ||||||
chr5:112984703 | A | AATATATA others(7): Show |
1 | a0001c0001t0029g0034 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.54-1123_54-1110dup others(14): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | ||||||
chr5:112984703 | A | AATATATA others(17): Show |
4 | a0001c0001t0006g0186 a0001c0001t0006g0189 a0001c0001t0043g0184 others(1): Show |
4 | HG01243.hp1 NA18747.hp1 NA18943.hp2 others(1): Show |
intron_variant | MODIFIER | c.54-1110_54-1109ins others(24): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | ||||||
chr5:112984703 | A | AATATATA others(19): Show |
1 | a0001c0001t0011g0152 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.54-1110_54-1109ins others(26): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | ||||||
chr5:112984703 | A | AATATATA others(23): Show |
2 | a0001c0002t0050g0097 a0001c0007t0055g0052 |
2 | HG02922.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.54-1110_54-1109ins others(30): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | ||||||
chr5:112984703 | A | AATATATA others(25): Show |
1 | a0001c0002t0002g0001 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.54-1110_54-1109ins others(32): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | ||||||
chr5:112984703 | A | AATATATA others(27): Show |
1 | a0001c0002t0002g0109 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.54-1110_54-1109ins others(34): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | ||||||
chr5:112984703 | A | AATATATA others(29): Show |
1 | a0001c0002t0002g0081 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.54-1110_54-1109ins others(36): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | ||||||
chr5:112984703 | A | AATATATA others(35): Show |
1 | a0001c0002t0002g0095 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.54-1110_54-1109ins others(42): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984703 | ||||||
chr5:112984703 | A | ATATATAT others(4): Show |
1 | a0001c0002t0002g0105 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.54-1132_54-1131ins others(11): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984703 | |||||||
chr5:112984703 | A | ATATATAT others(8): Show |
1 | a0001c0001t0013g0143 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.54-1132_54-1131ins others(15): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984703 | |||||||
chr5:112984703 | A | ATATATAT others(10): Show |
2 | a0001c0001t0006g0132 a0001c0002t0008g0079 |
2 | NA18968.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.54-1132_54-1131ins others(17): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984703 | |||||||
chr5:112984703 | A | ATATATAT others(16): Show |
2 | a0001c0001t0006g0107 a0001c0001t0038g0151 |
2 | HG02630.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.54-1132_54-1131ins others(23): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984703 | |||||||
chr5:112984703 | A | ATATATAT others(18): Show |
1 | a0001c0001t0045g0082 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.54-1132_54-1131ins others(25): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984703 | |||||||
chr5:112984703 | A | ATATATAT others(20): Show |
2 | a0001c0001t0006g0185 a0001c0001t0011g0153 |
2 | HG03516.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.54-1132_54-1131ins others(27): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984703 | |||||||
chr5:112984703 | A | ATATATAT others(22): Show |
1 | a0001c0001t0006g0128 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.54-1132_54-1131ins others(29): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984703 | |||||||
chr5:112984703 | A | ATATATAT others(24): Show |
2 | a0001c0002t0002g0026 a0001c0002t0002g0094 |
2 | HG01243.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.54-1132_54-1131ins others(31): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984703 | |||||||
chr5:112984703 | A | ATATATAT others(32): Show |
1 | a0001c0002t0002g0001 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.54-1132_54-1131ins others(39): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984703 | |||||||
chr5:112984703 | A | T | 228 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(225): Show |
253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.54-1132A>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984703 | |||||||
chr5:112984720 | A | ATG | 9 | a0001c0001t0017g0004 a0001c0001t0017g0016 a0001c0001t0022g0202 others(6): Show |
11 | HG02258.hp2 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.54-1114_54-1113ins others(2): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984720 | ||||||
chr5:112984722 | A | ATATATAT others(31): Show |
1 | a0001c0001t0012g0139 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.54-1110_54-1109ins others(38): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984722 | ||||||
chr5:112984722 | A | ATATATAT others(25): Show |
1 | a0001c0002t0103g0140 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.54-1110_54-1109ins others(32): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984722 | ||||||
chr5:112984740 | C | T | 2 | a0001c0001t0001g0318 a0001c0002t0103g0140 |
2 | HG03486.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.54-1095C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984740 | |||||||
chr5:112984829 | C | T | 1 | a0001c0001t0082g0300 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.54-1006C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984829 | |||||||
chr5:112984838 | AG | A | 179 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0137 others(176): Show |
189 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(186): Show |
intron_variant | MODIFIER | c.54-995delG | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 112984838 | ||||||
chr5:112984860 | A | G | 9 | a0001c0001t0017g0004 a0001c0001t0017g0016 a0001c0001t0022g0202 others(6): Show |
11 | HG02258.hp2 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.54-975A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984860 | |||||||
chr5:112984981 | G | A | 204 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0137 others(201): Show |
220 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(217): Show |
intron_variant | MODIFIER | c.54-854G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112984981 | |||||||
chr5:112985057 | C | G | 18 | a0001c0001t0007g0023 a0001c0001t0007g0036 a0001c0001t0007g0037 others(15): Show |
18 | HG00609.hp1 HG02129.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.54-778C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112985057 | |||||||
chr5:112985062 | G | A | 4 | a0001c0002t0002g0062 a0001c0002t0002g0063 a0001c0002t0002g0064 others(1): Show |
4 | HG02559.hp1 HG02615.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.54-773G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112985062 | |||||||
chr5:112985225 | G | A | 9 | a0001c0001t0017g0004 a0001c0001t0017g0016 a0001c0001t0022g0202 others(6): Show |
11 | HG02258.hp2 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.54-610G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112985225 | |||||||
chr5:112985228 | A | G | 1 | a0001c0001t0111g0148 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.54-607A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112985228 | |||||||
chr5:112985252 | G | A | 50 | a0001c0001t0006g0027 a0001c0001t0006g0107 a0001c0001t0045g0082 others(47): Show |
57 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.54-583G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112985252 | |||||||
chr5:112985256 | A | T | 1 | a0001c0001t0003g0174 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.54-579A>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112985256 | |||||||
chr5:112985270 | G | T | 92 | a0001c0001t0006g0027 a0001c0001t0006g0107 a0001c0001t0006g0128 others(89): Show |
99 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.54-565G>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112985270 | |||||||
chr5:112985334 | G | A | 188 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0137 others(185): Show |
200 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(197): Show |
intron_variant | MODIFIER | c.54-501G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112985334 | |||||||
chr5:112985373 | T | C | 188 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0137 others(185): Show |
200 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(197): Show |
intron_variant | MODIFIER | c.54-462T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112985373 | |||||||
chr5:112985426 | A | G | 6 | a0001c0001t0005g0154 a0001c0001t0011g0013 a0001c0001t0011g0150 others(3): Show |
7 | HG02258.hp1 HG02622.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.54-409A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112985426 | |||||||
chr5:112985478 | A | G | 1 | a0001c0003t0005g0113 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.54-357A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112985478 | |||||||
chr5:112985522 | A | G | 1 | a0001c0002t0002g0091 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.54-313A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112985522 | |||||||
chr5:112985603 | A | G | 3 | a0001c0001t0024g0155 a0001c0001t0024g0190 a0001c0001t0024g0191 |
3 | HG02896.hp1 HG02897.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.54-232A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112985603 | |||||||
chr5:112985681 | T | C | 1 | a0001c0001t0084g0133 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.54-154T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112985681 | |||||||
chr5:112985751 | G | T | 6 | a0001c0001t0017g0004 a0001c0001t0017g0016 a0001c0001t0023g0004 others(3): Show |
8 | HG02258.hp2 HG02280.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.54-84G>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112985751 | |||||||
chr5:112985769 | A | T | 2 | a0001c0001t0029g0034 a0001c0001t0029g0035 |
2 | HG02647.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.54-66A>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112985769 | |||||||
chr5:112985774 | G | T | 9 | a0001c0001t0017g0004 a0001c0001t0017g0016 a0001c0001t0022g0202 others(6): Show |
11 | HG02258.hp2 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.54-61G>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112985774 | |||||||
chr5:112985791 | A | G | 93 | a0001c0001t0006g0027 a0001c0001t0006g0107 a0001c0001t0006g0128 others(90): Show |
100 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.54-44A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112985791 | |||||||
chr5:112985827 | T | C | 1 | a0001c0001t0001g0218 | 1 | NA18612.hp2 | splice_region_variant&intron_variant | LOW | c.54-8T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 1/10 | chr5 | 112985827 | |||||||
chr5:112986046 | T | A | 2 | a0001c0001t0001g0219 a0001c0001t0001g0220 |
2 | NA18999.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.205+60T>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112986046 | |||||||
chr5:112986060 | C | T | 9 | a0001c0001t0017g0004 a0001c0001t0017g0016 a0001c0001t0022g0202 others(6): Show |
11 | HG02258.hp2 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.205+74C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112986060 | |||||||
chr5:112986069 | A | G | 5 | a0001c0003t0005g0003 a0001c0003t0005g0012 a0001c0003t0005g0111 others(2): Show |
9 | HG01884.hp1 HG02145.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.205+83A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112986069 | |||||||
chr5:112986246 | T | C | 1 | a0001c0001t0112g0119 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.205+260T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112986246 | |||||||
chr5:112986341 | CT | C | 87 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0137 others(84): Show |
90 | HG00609.hp1 HG01074.hp2 HG01106.hp1 others(87): Show |
intron_variant | MODIFIER | c.205+367delT | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 112986341 | ||||||
chr5:112986342 | T | C | 14 | a0001c0001t0006g0128 a0001c0001t0006g0129 a0001c0001t0006g0131 others(11): Show |
14 | HG02155.hp2 HG02602.hp2 NA18747.hp1 others(11): Show |
intron_variant | MODIFIER | c.205+356T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112986342 | |||||||
chr5:112986398 | T | C | 1 | a0001c0001t0001g0316 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.205+412T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112986398 | |||||||
chr5:112986499 | A | G | 9 | a0001c0001t0017g0004 a0001c0001t0017g0016 a0001c0001t0022g0202 others(6): Show |
11 | HG02258.hp2 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.205+513A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112986499 | |||||||
chr5:112986585 | A | G | 9 | a0001c0001t0017g0004 a0001c0001t0017g0016 a0001c0001t0022g0202 others(6): Show |
11 | HG02258.hp2 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.205+599A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112986585 | |||||||
chr5:112986623 | C | A | 1 | a0001c0009t0021g0221 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.205+637C>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112986623 | |||||||
chr5:112986624 | C | T | 1 | a0001c0001t0047g0110 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.205+638C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112986624 | |||||||
chr5:112986628 | G | A | 1 | a0001c0002t0002g0205 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.205+642G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112986628 | |||||||
chr5:112986753 | C | A | 1 | a0001c0001t0112g0119 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.205+767C>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112986753 | |||||||
chr5:112986842 | G | C | 1 | a0001c0002t0002g0006 | 3 | NA18955.hp2 NA18983.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.205+856G>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112986842 | |||||||
chr5:112986880 | A | G | 104 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0137 others(101): Show |
111 | HG00609.hp1 HG01074.hp2 HG01106.hp1 others(108): Show |
intron_variant | MODIFIER | c.205+894A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112986880 | |||||||
chr5:112986935 | G | A | 2 | a0001c0001t0016g0222 a0001c0001t0016g0223 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.205+949G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112986935 | |||||||
chr5:112987158 | C | T | 1 | a0001c0001t0006g0132 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.205+1172C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112987158 | |||||||
chr5:112987379 | G | T | 1 | a0001c0001t0003g0136 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.205+1393G>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112987379 | |||||||
chr5:112987440 | T | G | 3 | a0001c0001t0022g0202 a0001c0001t0022g0203 a0001c0001t0022g0204 |
3 | HG02886.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.205+1454T>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112987440 | |||||||
chr5:112987608 | A | G | 102 | a0001c0001t0001g0022 a0001c0001t0001g0294 a0001c0001t0001g0295 others(99): Show |
110 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.205+1622A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112987608 | |||||||
chr5:112987620 | C | CT | 79 | a0001c0001t0001g0021 a0001c0001t0001g0214 a0001c0001t0001g0220 others(76): Show |
82 | HG00673.hp1 HG01074.hp2 HG01099.hp1 others(79): Show |
intron_variant | MODIFIER | c.205+1659dupT | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 112987620 | ||||||
chr5:112987620 | C | CTT | 27 | a0001c0001t0001g0293 a0001c0001t0003g0158 a0001c0001t0003g0162 others(24): Show |
30 | HG01106.hp1 HG01433.hp2 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.205+1658_205+1659d others(4): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 112987620 | ||||||
chr5:112987620 | C | CTTT | 19 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0137 others(16): Show |
19 | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.205+1657_205+1659d others(5): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 112987620 | ||||||
chr5:112987620 | C | CTTTTT | 25 | a0001c0001t0006g0128 a0001c0001t0006g0129 a0001c0001t0006g0132 others(22): Show |
26 | HG00733.hp2 HG00738.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.205+1655_205+1659d others(7): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 112987620 | ||||||
chr5:112987620 | C | CTTTTTT | 45 | a0001c0001t0005g0154 a0001c0001t0006g0027 a0001c0001t0006g0131 others(42): Show |
52 | HG00408.hp1 HG00609.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.205+1654_205+1659d others(8): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 112987620 | ||||||
chr5:112987620 | C | CTTTTTTT | 22 | a0001c0001t0006g0189 a0001c0001t0045g0082 a0001c0001t0112g0119 others(19): Show |
22 | HG00280.hp2 HG00423.hp2 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.205+1653_205+1659d others(9): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 112987620 | ||||||
chr5:112987620 | C | CTTTTTTT others(3): Show |
1 | a0001c0002t0025g0121 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.205+1650_205+1659d others(12): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 112987620 | ||||||
chr5:112987620 | CTTT | C | 9 | a0001c0001t0017g0004 a0001c0001t0017g0016 a0001c0001t0022g0202 others(6): Show |
11 | HG02258.hp2 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.205+1657_205+1659d others(5): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 112987620 | ||||||
chr5:112987624 | T | C | 9 | a0001c0001t0017g0004 a0001c0001t0017g0016 a0001c0001t0022g0202 others(6): Show |
11 | HG02258.hp2 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.205+1638T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112987624 | |||||||
chr5:112987628 | T | G | 1 | a0001c0001t0094g0208 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.205+1642T>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112987628 | |||||||
chr5:112987661 | A | G | 1 | a0001c0001t0006g0132 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.205+1675A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112987661 | |||||||
chr5:112987705 | G | C | 205 | a0001c0001t0001g0022 a0001c0001t0001g0268 a0001c0001t0001g0294 others(202): Show |
222 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(219): Show |
intron_variant | MODIFIER | c.205+1719G>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112987705 | |||||||
chr5:112987744 | G | A | 1 | a0001c0002t0002g0104 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.205+1758G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112987744 | |||||||
chr5:112987745 | A | T | 6 | a0001c0002t0002g0092 a0001c0002t0002g0098 a0001c0002t0002g0127 others(3): Show |
6 | HG00639.hp2 HG01358.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.205+1759A>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112987745 | |||||||
chr5:112987747 | T | A | 1 | a0001c0001t0093g0224 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.205+1761T>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112987747 | |||||||
chr5:112987793 | C | CT | 9 | a0001c0001t0017g0004 a0001c0001t0017g0016 a0001c0001t0022g0202 others(6): Show |
11 | HG02258.hp2 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.205+1817dupT | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 112987793 | ||||||
chr5:112987830 | C | T | 2 | a0001c0001t0006g0131 a0001c0001t0042g0130 |
2 | NA18948.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.205+1844C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112987830 | |||||||
chr5:112987877 | C | T | 24 | a0001c0001t0003g0159 a0001c0001t0003g0160 a0001c0001t0003g0161 others(21): Show |
25 | HG02602.hp1 HG03490.hp2 HG03491.hp2 others(22): Show |
intron_variant | MODIFIER | c.205+1891C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112987877 | |||||||
chr5:112987878 | G | A | 1 | a0001c0001t0001g0269 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.205+1892G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112987878 | |||||||
chr5:112987909 | G | A | 1 | a0001c0001t0044g0134 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.205+1923G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112987909 | |||||||
chr5:112987914 | C | T | 113 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(110): Show |
124 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.205+1928C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112987914 | |||||||
chr5:112987915 | G | C | 1 | a0001c0002t0049g0103 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.205+1929G>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112987915 | |||||||
chr5:112988041 | A | G | 205 | a0001c0001t0001g0266 a0001c0001t0001g0290 a0001c0001t0001g0291 others(202): Show |
221 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(218): Show |
intron_variant | MODIFIER | c.205+2055A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112988041 | |||||||
chr5:112988089 | T | C | 1 | a0001c0010t0070g0048 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.205+2103T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112988089 | |||||||
chr5:112988159 | C | T | 4 | a0001c0001t0003g0158 a0001c0001t0003g0173 a0001c0001t0075g0168 others(1): Show |
4 | HG00280.hp2 HG01106.hp1 HG02015.hp1 others(1): Show |
intron_variant | MODIFIER | c.205+2173C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112988159 | |||||||
chr5:112988195 | A | G | 1 | a0001c0002t0050g0097 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.205+2209A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112988195 | |||||||
chr5:112988220 | T | C | 61 | a0001c0001t0001g0231 a0001c0001t0001g0269 a0001c0001t0001g0303 others(58): Show |
66 | HG01243.hp1 HG01496.hp1 HG01496.hp2 others(63): Show |
intron_variant | MODIFIER | c.205+2234T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112988220 | |||||||
chr5:112988232 | C | G | 1 | a0001c0001t0001g0308 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.205+2246C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112988232 | |||||||
chr5:112988318 | T | TA | 158 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(155): Show |
174 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.205+2347dupA | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 112988318 | ||||||
chr5:112988318 | T | TAA | 8 | a0001c0001t0001g0225 a0001c0001t0003g0135 a0001c0001t0003g0169 others(5): Show |
8 | HG01074.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.205+2346_205+2347d others(4): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 112988318 | ||||||
chr5:112988319 | A | G | 1 | a0001c0001t0013g0145 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.205+2333A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112988319 | |||||||
chr5:112988348 | T | C | 1 | a0001c0002t0002g0059 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.205+2362T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112988348 | |||||||
chr5:112988363 | G | A | 47 | a0001c0001t0001g0228 a0001c0001t0003g0136 a0001c0001t0003g0137 others(44): Show |
47 | HG00741.hp1 HG01891.hp1 HG02015.hp1 others(44): Show |
intron_variant | MODIFIER | c.205+2377G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112988363 | |||||||
chr5:112988441 | G | A | 1 | a0001c0002t0002g0205 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.205+2455G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112988441 | |||||||
chr5:112988449 | G | C | 2 | a0001c0001t0040g0313 a0001c0001t0040g0314 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.205+2463G>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112988449 | |||||||
chr5:112988494 | T | TA | 40 | a0001c0001t0001g0225 a0001c0001t0001g0227 a0001c0001t0001g0253 others(37): Show |
41 | HG00140.hp2 HG00609.hp1 HG01074.hp1 others(38): Show |
intron_variant | MODIFIER | c.205+2532dupA | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 112988494 | ||||||
chr5:112988494 | T | TAA | 141 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(138): Show |
152 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.205+2531_205+2532d others(4): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 112988494 | ||||||
chr5:112988494 | T | TAAA | 37 | a0001c0001t0001g0017 a0001c0001t0001g0235 a0001c0001t0001g0236 others(34): Show |
39 | HG00621.hp2 HG00735.hp2 HG01070.hp1 others(36): Show |
intron_variant | MODIFIER | c.205+2530_205+2532d others(5): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 112988494 | ||||||
chr5:112988494 | T | TAAAAA | 6 | a0001c0001t0001g0269 a0001c0001t0017g0004 a0001c0001t0023g0004 others(3): Show |
7 | HG02258.hp2 HG02280.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.205+2528_205+2532d others(7): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 112988494 | ||||||
chr5:112988494 | TA | T | 27 | a0001c0001t0006g0128 a0001c0001t0006g0129 a0001c0001t0006g0131 others(24): Show |
28 | HG00423.hp2 HG01243.hp1 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.205+2532delA | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 112988494 | ||||||
chr5:112988520 | G | A | 1 | a0001c0001t0004g0292 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.205+2534G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112988520 | |||||||
chr5:112988546 | G | A | 1 | a0001c0002t0002g0073 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.205+2560G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112988546 | |||||||
chr5:112988650 | C | A | 1 | a0001c0001t0036g0239 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.205+2664C>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112988650 | |||||||
chr5:112988655 | T | C | 1 | a0001c0001t0001g0278 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.205+2669T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112988655 | |||||||
chr5:112988703 | T | C | 5 | a0001c0004t0019g0025 a0001c0004t0019g0124 a0001c0004t0019g0125 others(2): Show |
5 | HG00741.hp1 HG01891.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.205+2717T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112988703 | |||||||
chr5:112988799 | G | A | 332 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(329): Show |
359 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(356): Show |
intron_variant | MODIFIER | c.205+2813G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112988799 | |||||||
chr5:112989047 | T | C | 15 | a0001c0001t0015g0028 a0001c0001t0015g0030 a0001c0001t0015g0031 others(12): Show |
19 | HG01496.hp1 HG01884.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.205+3061T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112989047 | |||||||
chr5:112989073 | A | G | 1 | a0001c0001t0001g0256 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.206-3048A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112989073 | |||||||
chr5:112989081 | G | C | 1 | a0001c0001t0001g0278 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.206-3040G>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112989081 | |||||||
chr5:112989090 | C | T | 1 | a0001c0001t0112g0119 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.206-3031C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112989090 | |||||||
chr5:112989092 | G | A | 77 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0137 others(74): Show |
84 | HG01074.hp2 HG01106.hp1 HG01496.hp1 others(81): Show |
intron_variant | MODIFIER | c.206-3029G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112989092 | |||||||
chr5:112989120 | G | C | 1 | a0001c0001t0074g0166 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.206-3001G>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112989120 | |||||||
chr5:112989205 | C | A | 1 | a0001c0001t0001g0240 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.206-2916C>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112989205 | |||||||
chr5:112989428 | C | CA | 7 | a0001c0001t0003g0180 a0001c0001t0006g0027 a0001c0001t0010g0286 others(4): Show |
7 | HG02280.hp2 HG03098.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.206-2680dupA | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 112989428 | ||||||
chr5:112989476 | A | T | 6 | a0001c0001t0017g0004 a0001c0001t0017g0016 a0001c0001t0023g0004 others(3): Show |
8 | HG02258.hp2 HG02280.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.206-2645A>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112989476 | |||||||
chr5:112989541 | A | G | 2 | a0001c0001t0021g0263 a0001c0001t0021g0264 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.206-2580A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112989541 | |||||||
chr5:112989597 | A | G | 1 | a0001c0001t0112g0119 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.206-2524A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112989597 | |||||||
chr5:112989650 | T | G | 1 | a0001c0001t0030g0115 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.206-2471T>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112989650 | |||||||
chr5:112989653 | G | T | 1 | a0001c0001t0112g0119 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.206-2468G>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112989653 | |||||||
chr5:112989854 | A | G | 1 | a0001c0002t0008g0060 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.206-2267A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112989854 | |||||||
chr5:112989899 | T | C | 1 | a0001c0001t0112g0119 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.206-2222T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112989899 | |||||||
chr5:112989919 | A | T | 1 | a0001c0001t0005g0154 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.206-2202A>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112989919 | |||||||
chr5:112989926 | GTGA | G | 90 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0137 others(87): Show |
97 | HG01074.hp2 HG01106.hp1 HG01496.hp1 others(94): Show |
intron_variant | MODIFIER | c.206-2190_206-2188d others(5): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 112989926 | ||||||
chr5:112990172 | C | T | 135 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(132): Show |
148 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.206-1949C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112990172 | |||||||
chr5:112990333 | T | C | 1 | a0001c0001t0004g0292 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.206-1788T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112990333 | |||||||
chr5:112990552 | T | C | 1 | a0001c0001t0066g0044 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.206-1569T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112990552 | |||||||
chr5:112990571 | C | T | 5 | a0001c0001t0001g0229 a0001c0001t0001g0238 a0001c0001t0004g0020 others(2): Show |
5 | NA18960.hp1 NA18963.hp2 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.206-1550C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112990571 | |||||||
chr5:112990713 | G | A | 139 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(136): Show |
152 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.206-1408G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112990713 | |||||||
chr5:112990729 | A | T | 1 | a0001c0001t0007g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.206-1392A>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112990729 | |||||||
chr5:112990802 | GTAC | G | 90 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0137 others(87): Show |
97 | HG01074.hp2 HG01106.hp1 HG01496.hp1 others(94): Show |
intron_variant | MODIFIER | c.206-1315_206-1313d others(5): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 112990802 | ||||||
chr5:112990883 | AT | A | 138 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(135): Show |
151 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.206-1227delT | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 112990883 | ||||||
chr5:112990953 | T | G | 15 | a0001c0001t0015g0028 a0001c0001t0015g0030 a0001c0001t0015g0031 others(12): Show |
19 | HG01496.hp1 HG01884.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.206-1168T>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112990953 | |||||||
chr5:112991050 | A | G | 3 | a0001c0001t0012g0014 a0001c0001t0012g0156 a0001c0001t0012g0157 |
4 | HG01074.hp2 HG01891.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.206-1071A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112991050 | |||||||
chr5:112991254 | C | G | 57 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0137 others(54): Show |
58 | HG01106.hp1 HG01496.hp2 HG01515.hp1 others(55): Show |
intron_variant | MODIFIER | c.206-867C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112991254 | |||||||
chr5:112991258 | A | G | 2 | a0001c0001t0005g0118 a0001c0001t0005g0206 |
2 | HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.206-863A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112991258 | |||||||
chr5:112991433 | C | T | 2 | a0001c0001t0001g0268 a0001c0001t0004g0267 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.206-688C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112991433 | |||||||
chr5:112991561 | A | G | 1 | a0001c0001t0107g0117 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.206-560A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112991561 | |||||||
chr5:112991633 | T | C | 1 | a0001c0002t0002g0074 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.206-488T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112991633 | |||||||
chr5:112991654 | T | G | 1 | a0001c0001t0112g0119 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.206-467T>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112991654 | |||||||
chr5:112991762 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.206-359C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112991762 | |||||||
chr5:112991936 | G | A | 1 | a0001c0001t0001g0308 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.206-185G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112991936 | |||||||
chr5:112992056 | C | T | 3 | a0001c0001t0012g0014 a0001c0001t0012g0156 a0001c0001t0012g0157 |
4 | HG01074.hp2 HG01891.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.206-65C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 2/10 | chr5 | 112992056 | |||||||
chr5:112992289 | C | T | 1 | a0001c0001t0107g0117 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.333+41C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 3/10 | chr5 | 112992289 | |||||||
chr5:112992394 | T | C | 2 | a0001c0001t0104g0149 a0001c0001t0105g0141 |
2 | HG02280.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.333+146T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 3/10 | chr5 | 112992394 | |||||||
chr5:112992396 | C | T | 1 | a0001c0001t0091g0210 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.333+148C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 3/10 | chr5 | 112992396 | |||||||
chr5:112992550 | A | G | 1 | a0001c0002t0008g0088 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.334-122A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 3/10 | chr5 | 112992550 | |||||||
chr5:112992570 | C | T | 107 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0137 others(104): Show |
114 | HG00609.hp1 HG01074.hp2 HG01106.hp1 others(111): Show |
intron_variant | MODIFIER | c.334-102C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 3/10 | chr5 | 112992570 | |||||||
chr5:112992900 | AC | A | 141 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(138): Show |
154 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.432+131delC | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112992900 | |||||||
chr5:112992901 | C | T | 1 | a0001c0001t0010g0286 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.432+131C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112992901 | |||||||
chr5:112992933 | T | G | 1 | a0001c0001t0015g0030 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.432+163T>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112992933 | |||||||
chr5:112993156 | T | A | 3 | a0001c0001t0022g0202 a0001c0001t0022g0203 a0001c0001t0022g0204 |
3 | HG02886.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.432+386T>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112993156 | |||||||
chr5:112993339 | A | G | 1 | a0001c0002t0050g0097 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.432+569A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112993339 | |||||||
chr5:112993366 | G | A | 137 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(134): Show |
150 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.432+596G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112993366 | |||||||
chr5:112993440 | C | A | 6 | a0001c0001t0001g0304 a0001c0004t0019g0025 a0001c0004t0019g0124 others(3): Show |
6 | HG00741.hp1 HG01891.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.432+670C>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112993440 | |||||||
chr5:112993595 | G | C | 1 | a0001c0001t0007g0039 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.432+825G>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112993595 | |||||||
chr5:112993616 | C | G | 1 | a0001c0002t0103g0140 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.432+846C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112993616 | |||||||
chr5:112993624 | C | CA | 14 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0137 others(11): Show |
14 | HG01891.hp2 HG01943.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.432+869dupA | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 112993624 | ||||||
chr5:112993639 | A | C | 3 | a0001c0001t0024g0155 a0001c0001t0024g0190 a0001c0001t0024g0191 |
3 | HG02896.hp1 HG02897.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.432+869A>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112993639 | |||||||
chr5:112993640 | C | A | 8 | a0001c0001t0001g0238 a0001c0001t0001g0243 a0001c0001t0001g0294 others(5): Show |
8 | HG01261.hp2 HG01981.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.432+870C>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112993640 | |||||||
chr5:112993642 | A | C | 7 | a0001c0001t0001g0238 a0001c0001t0001g0243 a0001c0001t0001g0294 others(4): Show |
7 | HG01261.hp2 HG01981.hp1 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.432+872A>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112993642 | |||||||
chr5:112993653 | AC | A | 130 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(127): Show |
143 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.432+885delC | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 112993653 | ||||||
chr5:112993654 | C | A | 7 | a0001c0001t0001g0238 a0001c0001t0001g0243 a0001c0001t0001g0294 others(4): Show |
7 | HG01261.hp2 HG01981.hp1 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.432+884C>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112993654 | |||||||
chr5:112993881 | A | C | 249 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(246): Show |
269 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.432+1111A>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112993881 | |||||||
chr5:112993943 | A | G | 19 | a0001c0001t0007g0023 a0001c0001t0007g0036 a0001c0001t0007g0037 others(16): Show |
19 | HG00609.hp1 HG01099.hp1 HG02129.hp1 others(16): Show |
intron_variant | MODIFIER | c.432+1173A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112993943 | |||||||
chr5:112993970 | A | T | 1 | a0001c0002t0064g0065 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.432+1200A>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112993970 | |||||||
chr5:112994086 | C | T | 1 | a0001c0001t0001g0295 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.432+1316C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112994086 | |||||||
chr5:112994163 | C | CT | 41 | a0001c0001t0001g0021 a0001c0001t0001g0238 a0001c0001t0001g0243 others(38): Show |
41 | HG00621.hp2 HG00741.hp1 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.432+1418dupT | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 112994163 | ||||||
chr5:112994163 | CT | C | 21 | a0001c0001t0001g0235 a0001c0001t0001g0244 a0001c0001t0001g0280 others(18): Show |
22 | HG01071.hp2 HG01256.hp1 HG02155.hp1 others(19): Show |
intron_variant | MODIFIER | c.432+1418delT | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 112994163 | ||||||
chr5:112994221 | G | GA | 6 | a0001c0001t0017g0004 a0001c0001t0017g0016 a0001c0001t0023g0004 others(3): Show |
8 | HG02258.hp2 HG02280.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.432+1452dupA | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 112994221 | ||||||
chr5:112994260 | C | T | 15 | a0001c0001t0015g0028 a0001c0001t0015g0030 a0001c0001t0015g0031 others(12): Show |
19 | HG01496.hp1 HG01884.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.432+1490C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112994260 | |||||||
chr5:112994276 | A | G | 2 | a0001c0001t0001g0235 a0001c0006t0035g0237 |
2 | NA19006.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.432+1506A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112994276 | |||||||
chr5:112994380 | C | T | 1 | a0001c0002t0002g0074 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.432+1610C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112994380 | |||||||
chr5:112994398 | CTAGGCTT others(7): Show |
C | 1 | a0001c0002t0061g0083 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.432+1629_432+1642d others(16): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112994398 | |||||||
chr5:112994451 | C | T | 2 | a0001c0002t0002g0075 a0001c0002t0051g0070 |
2 | HG00609.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.432+1681C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112994451 | |||||||
chr5:112994452 | G | C | 1 | a0001c0010t0070g0048 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.432+1682G>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112994452 | |||||||
chr5:112994660 | T | C | 2 | a0001c0001t0001g0268 a0001c0001t0004g0267 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.432+1890T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112994660 | |||||||
chr5:112994900 | T | G | 7 | a0001c0001t0013g0138 a0001c0001t0013g0143 a0001c0001t0013g0144 others(4): Show |
7 | HG01496.hp2 HG02055.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.432+2130T>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112994900 | |||||||
chr5:112995041 | A | C | 136 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(133): Show |
149 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.432+2271A>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112995041 | |||||||
chr5:112995058 | G | A | 1 | a0001c0001t0003g0164 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.432+2288G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112995058 | |||||||
chr5:112995058 | G | C | 1 | a0001c0001t0004g0232 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.432+2288G>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112995058 | |||||||
chr5:112995111 | C | CAAAAAAT others(6): Show |
1 | a0001c0002t0061g0083 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.432+2345_432+2357d others(15): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 112995111 | ||||||
chr5:112995190 | A | G | 1 | a0001c0001t0024g0155 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.432+2420A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112995190 | |||||||
chr5:112995232 | T | G | 3 | a0001c0001t0024g0155 a0001c0001t0024g0190 a0001c0001t0024g0191 |
3 | HG02896.hp1 HG02897.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.432+2462T>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112995232 | |||||||
chr5:112995282 | C | T | 15 | a0001c0001t0015g0028 a0001c0001t0015g0030 a0001c0001t0015g0031 others(12): Show |
19 | HG01496.hp1 HG01884.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.432+2512C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112995282 | |||||||
chr5:112995344 | C | T | 1 | a0001c0001t0111g0148 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.432+2574C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112995344 | |||||||
chr5:112995394 | G | C | 248 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(245): Show |
268 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.432+2624G>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112995394 | |||||||
chr5:112995465 | A | T | 1 | a0001c0001t0112g0119 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.432+2695A>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112995465 | |||||||
chr5:112995582 | G | A | 1 | a0001c0001t0024g0155 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.432+2812G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112995582 | |||||||
chr5:112995680 | C | T | 5 | a0001c0001t0001g0005 a0001c0001t0001g0256 a0001c0001t0004g0257 others(2): Show |
7 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(4): Show |
intron_variant | MODIFIER | c.432+2910C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112995680 | |||||||
chr5:112995685 | T | C | 5 | a0001c0001t0001g0005 a0001c0001t0001g0256 a0001c0001t0004g0257 others(2): Show |
7 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(4): Show |
intron_variant | MODIFIER | c.432+2915T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112995685 | |||||||
chr5:112995782 | A | G | 1 | a0001c0010t0070g0048 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.432+3012A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112995782 | |||||||
chr5:112995973 | T | C | 1 | a0001c0008t0108g0301 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.432+3203T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112995973 | |||||||
chr5:112996057 | C | G | 5 | a0001c0004t0019g0025 a0001c0004t0019g0124 a0001c0004t0019g0125 others(2): Show |
5 | HG00741.hp1 HG01891.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.432+3287C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112996057 | |||||||
chr5:112996105 | C | A | 1 | a0001c0003t0005g0111 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.432+3335C>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112996105 | |||||||
chr5:112996109 | T | C | 6 | a0001c0001t0004g0274 a0001c0001t0004g0288 a0001c0001t0099g0234 others(3): Show |
6 | NA18966.hp2 NA18985.hp1 NA18992.hp2 others(3): Show |
intron_variant | MODIFIER | c.432+3339T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112996109 | |||||||
chr5:112996161 | G | C | 10 | a0001c0001t0015g0028 a0001c0001t0015g0030 a0001c0001t0015g0031 others(7): Show |
10 | HG01496.hp1 HG02257.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.432+3391G>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112996161 | |||||||
chr5:112996256 | A | G | 1 | a0001c0001t0004g0232 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.432+3486A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112996256 | |||||||
chr5:112996328 | C | T | 1 | a0001c0001t0045g0082 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.432+3558C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112996328 | |||||||
chr5:112996410 | T | A | 4 | a0001c0001t0001g0240 a0001c0001t0001g0273 a0001c0001t0087g0018 others(1): Show |
4 | NA18943.hp1 NA18966.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.432+3640T>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112996410 | |||||||
chr5:112996519 | T | C | 1 | a0001c0001t0001g0282 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.432+3749T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112996519 | |||||||
chr5:112996626 | A | G | 4 | a0001c0001t0012g0014 a0001c0001t0012g0139 a0001c0001t0012g0156 others(1): Show |
5 | HG01074.hp2 HG01891.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.432+3856A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112996626 | |||||||
chr5:112996750 | C | A | 1 | a0001c0001t0001g0307 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.432+3980C>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112996750 | |||||||
chr5:112996960 | G | C | 1 | a0001c0001t0001g0275 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.433-4124G>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112996960 | |||||||
chr5:112997009 | C | T | 3 | a0001c0001t0024g0155 a0001c0001t0024g0190 a0001c0001t0024g0191 |
3 | HG02896.hp1 HG02897.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.433-4075C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112997009 | |||||||
chr5:112997029 | T | C | 1 | a0001c0001t0023g0201 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.433-4055T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112997029 | |||||||
chr5:112997030 | C | T | 1 | a0001c0001t0023g0201 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.433-4054C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112997030 | |||||||
chr5:112997098 | A | G | 1 | a0001c0010t0070g0048 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.433-3986A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112997098 | |||||||
chr5:112997191 | G | A | 1 | a0001c0001t0001g0228 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.433-3893G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112997191 | |||||||
chr5:112997202 | T | C | 3 | a0001c0001t0007g0047 a0001c0001t0067g0045 a0001c0001t0069g0046 |
3 | HG03209.hp2 HG03453.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.433-3882T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112997202 | |||||||
chr5:112997317 | G | T | 5 | a0001c0001t0005g0154 a0001c0001t0011g0013 a0001c0001t0011g0150 others(2): Show |
6 | HG02258.hp1 HG02622.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.433-3767G>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112997317 | |||||||
chr5:112997359 | G | A | 1 | a0001c0001t0034g0172 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.433-3725G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112997359 | |||||||
chr5:112997486 | T | C | 10 | a0001c0001t0003g0158 a0001c0001t0003g0164 a0001c0001t0003g0165 others(7): Show |
10 | HG01106.hp1 HG01515.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.433-3598T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112997486 | |||||||
chr5:112997623 | T | C | 1 | a0001c0001t0012g0139 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.433-3461T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112997623 | |||||||
chr5:112997637 | T | A | 1 | a0001c0001t0001g0277 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.433-3447T>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112997637 | |||||||
chr5:112997826 | G | A | 1 | a0001c0008t0108g0301 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.433-3258G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112997826 | |||||||
chr5:112997846 | C | T | 1 | a0001c0001t0111g0148 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.433-3238C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112997846 | |||||||
chr5:112997849 | G | A | 6 | a0001c0001t0004g0274 a0001c0001t0004g0288 a0001c0001t0099g0234 others(3): Show |
6 | NA18966.hp2 NA18985.hp1 NA18992.hp2 others(3): Show |
intron_variant | MODIFIER | c.433-3235G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112997849 | |||||||
chr5:112997928 | TA | T | 4 | a0001c0001t0004g0008 a0001c0001t0020g0008 a0001c0001t0020g0285 others(1): Show |
5 | NA18942.hp1 NA18948.hp1 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.433-3148delA | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 112997928 | ||||||
chr5:112997975 | T | G | 1 | a0001c0001t0003g0136 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.433-3109T>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112997975 | |||||||
chr5:112998274 | ATTCCTGG others(20): Show |
A | 1 | a0001c0001t0003g0164 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.433-2807_433-2781d others(29): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 112998274 | ||||||
chr5:112998315 | G | A | 1 | a0001c0001t0012g0139 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.433-2769G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112998315 | |||||||
chr5:112998445 | T | C | 251 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(248): Show |
271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.433-2639T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112998445 | |||||||
chr5:112998490 | G | T | 144 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(141): Show |
161 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.433-2594G>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112998490 | |||||||
chr5:112998525 | G | A | 1 | a0001c0001t0043g0184 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.433-2559G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112998525 | |||||||
chr5:112998822 | T | G | 1 | a0001c0001t0101g0322 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.433-2262T>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112998822 | |||||||
chr5:112998841 | C | T | 1 | a0001c0002t0052g0054 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.433-2243C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112998841 | |||||||
chr5:112998912 | T | A | 2 | a0001c0002t0039g0211 a0001c0002t0114g0212 |
2 | HG02109.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.433-2172T>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112998912 | |||||||
chr5:112999031 | T | G | 1 | a0001c0001t0001g0324 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.433-2053T>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112999031 | |||||||
chr5:112999160 | C | T | 252 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(249): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.433-1924C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112999160 | |||||||
chr5:112999171 | A | C | 1 | a0001c0001t0001g0303 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.433-1913A>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112999171 | |||||||
chr5:112999279 | T | C | 147 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(144): Show |
164 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.433-1805T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112999279 | |||||||
chr5:112999454 | G | A | 3 | a0001c0004t0019g0025 a0001c0004t0019g0125 a0001c0004t0060g0122 |
3 | HG01891.hp1 HG02055.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.433-1630G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112999454 | |||||||
chr5:112999476 | G | A | 7 | a0001c0001t0013g0138 a0001c0001t0013g0143 a0001c0001t0013g0144 others(4): Show |
7 | HG01496.hp2 HG02055.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.433-1608G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112999476 | |||||||
chr5:112999478 | G | A | 147 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(144): Show |
164 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.433-1606G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112999478 | |||||||
chr5:112999565 | A | G | 1 | a0001c0001t0020g0285 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.433-1519A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112999565 | |||||||
chr5:112999625 | C | A | 1 | a0001c0001t0112g0119 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.433-1459C>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112999625 | |||||||
chr5:112999626 | C | CT | 9 | a0001c0001t0003g0196 a0001c0001t0005g0118 a0001c0001t0005g0206 others(6): Show |
9 | HG01243.hp2 HG01256.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.433-1441dupT | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 112999626 | ||||||
chr5:112999626 | CT | C | 18 | a0001c0001t0004g0287 a0001c0001t0013g0138 a0001c0001t0013g0143 others(15): Show |
18 | HG01256.hp2 HG01496.hp1 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.433-1441delT | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 112999626 | ||||||
chr5:112999651 | G | A | 147 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(144): Show |
164 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.433-1433G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112999651 | |||||||
chr5:112999953 | C | T | 141 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(138): Show |
158 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.433-1131C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 112999953 | |||||||
chr5:113000061 | C | CA | 65 | a0001c0001t0001g0324 a0001c0001t0003g0135 a0001c0001t0003g0136 others(62): Show |
67 | HG00609.hp1 HG01106.hp1 HG01515.hp1 others(64): Show |
intron_variant | MODIFIER | c.433-1002dupA | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 113000061 | ||||||
chr5:113000061 | C | CAA | 12 | a0001c0001t0003g0159 a0001c0001t0006g0128 a0001c0001t0006g0129 others(9): Show |
12 | HG02155.hp2 HG03490.hp2 HG03831.hp1 others(9): Show |
intron_variant | MODIFIER | c.433-1003_433-1002d others(4): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 113000061 | ||||||
chr5:113000061 | CA | C | 136 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(133): Show |
153 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.433-1002delA | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 113000061 | ||||||
chr5:113000061 | CAA | C | 7 | a0001c0001t0001g0255 a0001c0001t0001g0278 a0001c0001t0085g0305 others(4): Show |
7 | HG01070.hp2 HG03225.hp1 NA18986.hp2 others(4): Show |
intron_variant | MODIFIER | c.433-1003_433-1002d others(4): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 113000061 | ||||||
chr5:113000155 | C | T | 4 | a0001c0001t0040g0313 a0001c0001t0040g0314 a0001c0001t0110g0315 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.433-929C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 113000155 | |||||||
chr5:113000167 | A | C | 1 | a0001c0001t0001g0226 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.433-917A>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 113000167 | |||||||
chr5:113000318 | G | T | 148 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(145): Show |
165 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.433-766G>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 113000318 | |||||||
chr5:113000372 | T | G | 4 | a0001c0001t0040g0313 a0001c0001t0040g0314 a0001c0001t0110g0315 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.433-712T>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 113000372 | |||||||
chr5:113000399 | T | TACAC | 13 | a0001c0002t0008g0010 a0001c0002t0008g0058 a0001c0002t0008g0060 others(10): Show |
14 | HG00423.hp2 HG01928.hp1 HG01943.hp1 others(11): Show |
intron_variant | MODIFIER | c.433-662_433-659dup others(4): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 113000399 | ||||||
chr5:113000399 | T | TACACAC | 11 | a0001c0001t0012g0014 a0001c0001t0012g0156 a0001c0001t0012g0157 others(8): Show |
12 | HG00621.hp1 HG01074.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.433-664_433-659dup others(6): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 113000399 | ||||||
chr5:113000399 | TAC | T | 4 | a0001c0002t0002g0096 a0001c0002t0002g0108 a0001c0002t0002g0205 others(1): Show |
4 | HG00733.hp2 HG01081.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.433-660_433-659del others(2): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 113000399 | ||||||
chr5:113000406 | A | ACACACAC others(3): Show |
2 | a0001c0001t0006g0185 a0001c0001t0006g0187 |
2 | NA18960.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.433-669_433-668ins others(10): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 113000406 | ||||||
chr5:113000408 | A | ACACCCAC others(9): Show |
5 | a0001c0001t0005g0154 a0001c0001t0011g0013 a0001c0001t0011g0150 others(2): Show |
6 | HG02258.hp1 HG02622.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.433-673_433-672ins others(16): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 113000408 | ||||||
chr5:113000420 | A | ACACACAC others(6): Show |
1 | a0001c0001t0003g0160 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.433-659_433-658ins others(13): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 113000420 | ||||||
chr5:113000420 | A | ACACACAC others(8): Show |
1 | a0001c0001t0015g0031 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.433-659_433-658ins others(15): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 113000420 | ||||||
chr5:113000420 | A | ACACACAC others(15): Show |
1 | a0001c0001t0112g0119 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.433-659_433-658ins others(22): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 113000420 | ||||||
chr5:113000420 | A | ACACACAC others(9): Show |
1 | a0001c0001t0072g0323 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.433-659_433-658ins others(16): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 113000420 | ||||||
chr5:113000420 | A | ACACACAC others(11): Show |
3 | a0001c0001t0040g0313 a0001c0001t0040g0314 a0001c0001t0110g0315 |
3 | HG01070.hp1 HG01071.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.433-659_433-658ins others(18): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 113000420 | ||||||
chr5:113000420 | A | ACACACAC others(7): Show |
10 | a0001c0001t0003g0161 a0001c0001t0013g0146 a0001c0001t0015g0028 others(7): Show |
11 | HG02257.hp2 HG02630.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.433-659_433-658ins others(14): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 113000420 | ||||||
chr5:113000420 | A | ACACACAC others(5): Show |
10 | a0001c0001t0013g0138 a0001c0001t0013g0143 a0001c0001t0013g0145 others(7): Show |
10 | HG01496.hp2 HG02055.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.433-659_433-658ins others(12): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 113000420 | ||||||
chr5:113000420 | A | ACACACAC others(7): Show |
1 | a0001c0010t0070g0048 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.433-659_433-658ins others(14): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 113000420 | ||||||
chr5:113000420 | A | ACACACAC others(3): Show |
40 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0137 others(37): Show |
40 | HG01106.hp1 HG01515.hp1 HG02155.hp2 others(37): Show |
intron_variant | MODIFIER | c.433-659_433-658ins others(10): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 113000420 | ||||||
chr5:113000420 | A | ACACACAC others(1): Show |
5 | a0001c0001t0022g0202 a0001c0001t0022g0203 a0001c0001t0022g0204 others(2): Show |
5 | HG02886.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.433-659_433-658ins others(8): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 113000420 | ||||||
chr5:113000420 | A | ACACACAC others(3): Show |
1 | a0001c0001t0003g0158 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.433-659_433-658ins others(10): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 113000420 | ||||||
chr5:113000420 | A | ACACACC | 8 | a0001c0001t0001g0293 a0001c0001t0003g0164 a0001c0001t0003g0169 others(5): Show |
8 | HG00621.hp2 HG02015.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.433-658_433-653dup others(6): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 113000420 | ||||||
chr5:113000420 | A | ACACACCC others(1): Show |
18 | a0001c0001t0007g0023 a0001c0001t0007g0036 a0001c0001t0007g0037 others(15): Show |
18 | HG00609.hp1 HG02129.hp1 HG02523.hp2 others(15): Show |
intron_variant | MODIFIER | c.433-657_433-656ins others(8): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 113000420 | ||||||
chr5:113000420 | A | ACACC | 119 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(116): Show |
130 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.433-661_433-660ins others(4): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 113000420 | ||||||
chr5:113000420 | A | ACC | 20 | a0001c0001t0017g0004 a0001c0001t0017g0016 a0001c0001t0018g0215 others(17): Show |
26 | HG01884.hp1 HG01884.hp2 HG02145.hp1 others(23): Show |
intron_variant | MODIFIER | c.433-663_433-662ins others(2): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 113000420 | ||||||
chr5:113000420 | A | C | 39 | a0001c0001t0005g0118 a0001c0001t0005g0154 a0001c0001t0005g0206 others(36): Show |
40 | HG00639.hp2 HG00733.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.433-664A>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 113000420 | |||||||
chr5:113000550 | G | A | 1 | a0001c0001t0016g0279 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.433-534G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 113000550 | |||||||
chr5:113000580 | A | T | 5 | a0001c0001t0001g0005 a0001c0001t0001g0256 a0001c0001t0004g0257 others(2): Show |
7 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(4): Show |
intron_variant | MODIFIER | c.433-504A>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 113000580 | |||||||
chr5:113000606 | G | C | 1 | a0001c0002t0048g0057 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.433-478G>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 113000606 | |||||||
chr5:113000680 | C | G | 10 | a0001c0001t0015g0028 a0001c0001t0015g0030 a0001c0001t0015g0031 others(7): Show |
10 | HG01496.hp1 HG02257.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.433-404C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 113000680 | |||||||
chr5:113000759 | G | T | 1 | a0001c0001t0012g0139 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.433-325G>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 113000759 | |||||||
chr5:113000821 | T | G | 1 | a0001c0001t0112g0119 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.433-263T>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 113000821 | |||||||
chr5:113000844 | A | G | 5 | a0001c0001t0005g0154 a0001c0001t0011g0013 a0001c0001t0011g0150 others(2): Show |
6 | HG02258.hp1 HG02622.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.433-240A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 113000844 | |||||||
chr5:113000891 | C | T | 147 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(144): Show |
164 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.433-193C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 113000891 | |||||||
chr5:113000910 | G | A | 1 | a0001c0001t0001g0283 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.433-174G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 113000910 | |||||||
chr5:113000937 | T | C | 147 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(144): Show |
164 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.433-147T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 113000937 | |||||||
chr5:113000993 | T | C | 3 | a0001c0001t0007g0047 a0001c0001t0067g0045 a0001c0001t0069g0046 |
3 | HG03209.hp2 HG03453.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.433-91T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 4/10 | chr5 | 113000993 | |||||||
chr5:113001308 | G | A | 1 | a0001c0001t0001g0220 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.586-49G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 5/10 | chr5 | 113001308 | |||||||
chr5:113001796 | T | G | 1 | a0001c0001t0003g0176 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.806+122T>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 7/10 | chr5 | 113001796 | |||||||
chr5:113001958 | G | A | 1 | a0001c0002t0002g0026 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.806+284G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 7/10 | chr5 | 113001958 | |||||||
chr5:113002058 | T | A | 1 | a0001c0001t0003g0161 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.806+384T>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 7/10 | chr5 | 113002058 | |||||||
chr5:113002162 | C | G | 2 | a0001c0002t0039g0211 a0001c0002t0114g0212 |
2 | HG02109.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.806+488C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 7/10 | chr5 | 113002162 | |||||||
chr5:113002162 | C | T | 1 | a0001c0001t0006g0107 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.806+488C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 7/10 | chr5 | 113002162 | |||||||
chr5:113002262 | G | A | 146 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(143): Show |
163 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.806+588G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 7/10 | chr5 | 113002262 | |||||||
chr5:113002422 | C | CA | 21 | a0001c0001t0001g0017 a0001c0001t0001g0240 a0001c0001t0001g0242 others(18): Show |
22 | HG00621.hp2 HG00673.hp2 HG01358.hp1 others(19): Show |
intron_variant | MODIFIER | c.806+765dupA | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr5 | 113002422 | ||||||
chr5:113002422 | CA | C | 7 | a0001c0001t0001g0268 a0001c0001t0003g0135 a0001c0001t0068g0040 others(4): Show |
7 | HG00609.hp2 HG01169.hp1 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.806+765delA | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr5 | 113002422 | ||||||
chr5:113002423 | A | G | 1 | a0001c0001t0077g0167 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.806+749A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 7/10 | chr5 | 113002423 | |||||||
chr5:113002714 | GC | G | 2 | a0001c0001t0003g0161 a0001c0001t0032g0015 |
3 | HG03491.hp2 HG03492.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.806+1041delC | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 7/10 | chr5 | 113002714 | |||||||
chr5:113002729 | C | T | 1 | a0001c0001t0081g0254 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.806+1055C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 7/10 | chr5 | 113002729 | |||||||
chr5:113002773 | T | C | 3 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0137 |
3 | HG03471.hp1 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.806+1099T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 7/10 | chr5 | 113002773 | |||||||
chr5:113003111 | C | T | 1 | a0001c0010t0070g0048 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.807-831C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 7/10 | chr5 | 113003111 | |||||||
chr5:113003164 | G | GGTC | 251 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(248): Show |
271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.807-778_807-777ins others(3): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 7/10 | chr5 | 113003164 | |||||||
chr5:113003165 | A | T | 251 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(248): Show |
271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.807-777A>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 7/10 | chr5 | 113003165 | |||||||
chr5:113003167 | T | G | 251 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(248): Show |
271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.807-775T>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 7/10 | chr5 | 113003167 | |||||||
chr5:113003220 | T | G | 2 | a0001c0002t0002g0051 a0001c0002t0002g0056 |
2 | HG01346.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.807-722T>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 7/10 | chr5 | 113003220 | |||||||
chr5:113003242 | C | T | 6 | a0001c0001t0018g0215 a0001c0001t0018g0216 a0001c0001t0018g0311 others(3): Show |
6 | HG01884.hp2 HG02572.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.807-700C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 7/10 | chr5 | 113003242 | |||||||
chr5:113003250 | A | G | 1 | a0001c0001t0112g0119 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.807-692A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 7/10 | chr5 | 113003250 | |||||||
chr5:113003351 | T | C | 11 | a0001c0001t0017g0004 a0001c0001t0017g0016 a0001c0001t0023g0004 others(8): Show |
17 | HG01884.hp1 HG02145.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.807-591T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 7/10 | chr5 | 113003351 | |||||||
chr5:113003701 | GA | G | 50 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0137 others(47): Show |
51 | HG01106.hp1 HG01515.hp1 HG02015.hp1 others(48): Show |
intron_variant | MODIFIER | c.807-233delA | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr5 | 113003701 | ||||||
chr5:113003712 | G | A | 1 | a0001c0001t0112g0119 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.807-230G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 7/10 | chr5 | 113003712 | |||||||
chr5:113003881 | G | T | 2 | a0001c0001t0003g0158 a0001c0001t0003g0173 |
2 | HG01106.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.807-61G>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 7/10 | chr5 | 113003881 | |||||||
chr5:113004214 | T | C | 1 | a0001c0001t0080g0024 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.942+137T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113004214 | |||||||
chr5:113004462 | C | G | 1 | a0001c0001t0013g0146 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.942+385C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113004462 | |||||||
chr5:113004503 | C | T | 3 | a0001c0001t0022g0202 a0001c0001t0022g0203 a0001c0001t0022g0204 |
3 | HG02886.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.942+426C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113004503 | |||||||
chr5:113004674 | C | G | 3 | a0001c0001t0024g0155 a0001c0001t0024g0190 a0001c0001t0024g0191 |
3 | HG02896.hp1 HG02897.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.942+597C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113004674 | |||||||
chr5:113004794 | A | G | 1 | a0001c0001t0001g0302 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.942+717A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113004794 | |||||||
chr5:113004819 | T | A | 144 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(141): Show |
161 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.942+742T>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113004819 | |||||||
chr5:113004850 | A | G | 4 | a0001c0001t0040g0313 a0001c0001t0040g0314 a0001c0001t0110g0315 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.942+773A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113004850 | |||||||
chr5:113004952 | C | T | 1 | a0001c0002t0002g0098 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.942+875C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113004952 | |||||||
chr5:113004994 | G | A | 12 | a0001c0001t0017g0004 a0001c0001t0017g0016 a0001c0001t0023g0004 others(9): Show |
18 | HG01884.hp1 HG02145.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.942+917G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113004994 | |||||||
chr5:113005145 | C | CGTGTGTG others(1): Show |
5 | a0001c0001t0011g0013 a0001c0001t0011g0150 a0001c0001t0011g0152 others(2): Show |
6 | HG01192.hp2 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.942+1073_942+1074i others(10): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 113005145 | ||||||
chr5:113005145 | C | CGTGTGTG others(5): Show |
2 | a0001c0001t0033g0183 a0001c0001t0033g0198 |
2 | NA18952.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.942+1073_942+1074i others(14): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 113005145 | ||||||
chr5:113005145 | C | T | 1 | a0001c0002t0014g0100 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.942+1068C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113005145 | |||||||
chr5:113005151 | G | GGTGTGGG others(9): Show |
1 | a0001c0001t0003g0162 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.942+1079_942+1080i others(18): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 113005151 | ||||||
chr5:113005151 | G | GGTGTGT | 73 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0026 others(70): Show |
80 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.942+1087_942+1092d others(8): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 113005151 | ||||||
chr5:113005151 | G | GGTGTGTG others(5): Show |
140 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(137): Show |
157 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.942+1081_942+1082i others(14): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 113005151 | ||||||
chr5:113005151 | G | GGTGTGTG others(7): Show |
6 | a0001c0001t0001g0284 a0001c0001t0005g0118 a0001c0001t0005g0206 others(3): Show |
6 | HG03130.hp2 HG03540.hp1 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.942+1081_942+1082i others(16): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 113005151 | ||||||
chr5:113005151 | G | GGTGTGTG others(3): Show |
6 | a0001c0001t0024g0155 a0001c0001t0024g0190 a0001c0001t0024g0191 others(3): Show |
6 | HG01358.hp2 HG01516.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.942+1083_942+1092d others(12): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 113005151 | ||||||
chr5:113005151 | G | GGTGTGTG others(5): Show |
25 | a0001c0001t0007g0023 a0001c0001t0007g0036 a0001c0001t0007g0037 others(22): Show |
26 | HG00609.hp1 HG01496.hp2 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.942+1081_942+1092d others(14): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 113005151 | ||||||
chr5:113005151 | G | GGTGTGTG others(7): Show |
49 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0137 others(46): Show |
49 | HG01496.hp1 HG02155.hp2 HG02257.hp2 others(46): Show |
intron_variant | MODIFIER | c.942+1079_942+1092d others(16): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 113005151 | ||||||
chr5:113005151 | G | GGTGTGTG others(9): Show |
11 | a0001c0001t0003g0158 a0001c0001t0003g0164 a0001c0001t0003g0165 others(8): Show |
11 | HG01106.hp1 HG01515.hp1 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.942+1077_942+1092d others(18): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 113005151 | ||||||
chr5:113005151 | G | GGTGTGTG others(11): Show |
2 | a0001c0001t0003g0169 a0001c0001t0012g0157 |
2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.942+1075_942+1092d others(20): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 113005151 | ||||||
chr5:113005151 | G | GGTGTGTG others(13): Show |
9 | a0001c0001t0012g0014 a0001c0001t0012g0139 a0001c0001t0012g0156 others(6): Show |
10 | HG01070.hp1 HG01071.hp2 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.942+1092_942+1093i others(22): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 113005151 | ||||||
chr5:113005151 | G | T | 9 | a0001c0001t0005g0154 a0001c0001t0011g0013 a0001c0001t0011g0150 others(6): Show |
10 | HG01192.hp2 HG02040.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.942+1074G>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113005151 | |||||||
chr5:113005157 | T | TGTGTGTG others(7): Show |
1 | a0001c0010t0070g0048 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.942+1092_942+1093i others(16): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 113005157 | ||||||
chr5:113005383 | T | C | 5 | a0001c0001t0001g0005 a0001c0001t0001g0256 a0001c0001t0004g0257 others(2): Show |
7 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(4): Show |
intron_variant | MODIFIER | c.942+1306T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113005383 | |||||||
chr5:113005389 | TG | T | 11 | a0001c0001t0015g0028 a0001c0001t0015g0030 a0001c0001t0015g0031 others(8): Show |
11 | HG01496.hp1 HG02257.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.942+1314delG | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 113005389 | ||||||
chr5:113005390 | G | T | 1 | a0001c0001t0001g0318 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.942+1313G>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113005390 | |||||||
chr5:113005551 | T | C | 149 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(146): Show |
166 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.942+1474T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113005551 | |||||||
chr5:113005701 | A | G | 5 | a0001c0001t0018g0215 a0001c0001t0018g0216 a0001c0001t0018g0311 others(2): Show |
5 | HG01884.hp2 HG02572.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.942+1624A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113005701 | |||||||
chr5:113005705 | A | G | 3 | a0001c0002t0002g0056 a0001c0004t0019g0124 a0001c0004t0062g0123 |
3 | HG00741.hp1 HG03195.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.942+1628A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113005705 | |||||||
chr5:113005809 | A | G | 1 | a0001c0001t0045g0082 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.942+1732A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113005809 | |||||||
chr5:113005894 | A | G | 1 | a0001c0001t0013g0145 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.942+1817A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113005894 | |||||||
chr5:113005931 | G | A | 1 | a0001c0001t0003g0179 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.942+1854G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113005931 | |||||||
chr5:113005941 | T | G | 3 | a0001c0001t0022g0202 a0001c0001t0022g0203 a0001c0001t0022g0204 |
3 | HG02886.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.942+1864T>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113005941 | |||||||
chr5:113005989 | G | C | 51 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0137 others(48): Show |
52 | HG01106.hp1 HG01515.hp1 HG02015.hp1 others(49): Show |
intron_variant | MODIFIER | c.942+1912G>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113005989 | |||||||
chr5:113006117 | C | CA | 55 | a0001c0001t0001g0022 a0001c0001t0001g0269 a0001c0001t0001g0270 others(52): Show |
58 | HG00280.hp2 HG00609.hp1 HG01074.hp2 others(55): Show |
intron_variant | MODIFIER | c.943-1799dupA | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 113006117 | ||||||
chr5:113006117 | C | CAA | 8 | a0001c0001t0001g0246 a0001c0001t0001g0255 a0001c0001t0011g0152 others(5): Show |
8 | HG00408.hp2 HG02896.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.943-1800_943-1799d others(4): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 113006117 | ||||||
chr5:113006182 | T | C | 1 | a0001c0002t0002g0091 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.943-1756T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113006182 | |||||||
chr5:113006431 | A | G | 24 | a0001c0001t0007g0023 a0001c0001t0007g0036 a0001c0001t0007g0037 others(21): Show |
25 | HG00609.hp1 HG01070.hp1 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.943-1507A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113006431 | |||||||
chr5:113006585 | C | G | 59 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0137 others(56): Show |
60 | HG01106.hp1 HG01496.hp2 HG01515.hp1 others(57): Show |
intron_variant | MODIFIER | c.943-1353C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113006585 | |||||||
chr5:113006648 | CTATT | C | 5 | a0001c0001t0005g0154 a0001c0001t0011g0013 a0001c0001t0011g0150 others(2): Show |
6 | HG02258.hp1 HG02622.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.943-1285_943-1282d others(6): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 113006648 | ||||||
chr5:113006662 | T | G | 1 | a0001c0001t0074g0166 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.943-1276T>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113006662 | |||||||
chr5:113006692 | A | G | 2 | a0001c0001t0038g0029 a0001c0001t0038g0151 |
2 | HG02630.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.943-1246A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113006692 | |||||||
chr5:113006727 | G | A | 3 | a0001c0001t0024g0155 a0001c0001t0024g0190 a0001c0001t0024g0191 |
3 | HG02896.hp1 HG02897.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.943-1211G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113006727 | |||||||
chr5:113007140 | T | A | 1 | a0001c0001t0022g0203 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.943-798T>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113007140 | |||||||
chr5:113007143 | T | C | 3 | a0001c0001t0040g0313 a0001c0001t0040g0314 a0001c0001t0110g0315 |
3 | HG01070.hp1 HG01071.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.943-795T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113007143 | |||||||
chr5:113007243 | A | G | 1 | a0001c0001t0006g0107 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.943-695A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113007243 | |||||||
chr5:113007297 | C | G | 1 | a0001c0001t0001g0298 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.943-641C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113007297 | |||||||
chr5:113007376 | ATTTC | A | 224 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(221): Show |
243 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.943-538_943-535del others(4): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 113007376 | ||||||
chr5:113007396 | CTTTCT | C | 24 | a0001c0001t0001g0308 a0001c0001t0007g0023 a0001c0001t0007g0036 others(21): Show |
25 | HG00609.hp1 HG01070.hp1 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.943-538_943-534del others(5): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 113007396 | ||||||
chr5:113007591 | G | A | 3 | a0001c0001t0024g0155 a0001c0001t0024g0190 a0001c0001t0024g0191 |
3 | HG02896.hp1 HG02897.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.943-347G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113007591 | |||||||
chr5:113007676 | C | T | 19 | a0001c0001t0005g0154 a0001c0001t0011g0013 a0001c0001t0011g0150 others(16): Show |
20 | HG01496.hp1 HG02257.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.943-262C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113007676 | |||||||
chr5:113007690 | C | T | 1 | a0001c0001t0001g0249 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.943-248C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113007690 | |||||||
chr5:113007712 | T | A | 10 | a0001c0001t0003g0158 a0001c0001t0003g0164 a0001c0001t0003g0165 others(7): Show |
10 | HG01106.hp1 HG01515.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.943-226T>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113007712 | |||||||
chr5:113007847 | G | A | 252 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(249): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.943-91G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113007847 | |||||||
chr5:113007876 | A | G | 1 | a0001c0001t0001g0295 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.943-62A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 8/10 | chr5 | 113007876 | |||||||
chr5:113008097 | C | A | 1 | a0001c0001t0003g0169 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1047+55C>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113008097 | |||||||
chr5:113008098 | A | G | 4 | a0001c0001t0001g0213 a0001c0001t0021g0263 a0001c0001t0021g0264 others(1): Show |
4 | HG01256.hp1 HG01258.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.1047+56A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113008098 | |||||||
chr5:113008162 | G | T | 2 | a0001c0001t0005g0118 a0001c0001t0005g0206 |
2 | HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1047+120G>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113008162 | |||||||
chr5:113008181 | T | C | 2 | a0001c0001t0001g0247 a0001c0001t0001g0320 |
2 | HG00738.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.1047+139T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113008181 | |||||||
chr5:113008190 | A | G | 2 | a0001c0001t0003g0161 a0001c0001t0032g0015 |
3 | HG03491.hp2 HG03492.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1047+148A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113008190 | |||||||
chr5:113008385 | G | A | 208 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(205): Show |
226 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.1047+343G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113008385 | |||||||
chr5:113008389 | A | G | 1 | a0001c0002t0048g0057 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1047+347A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113008389 | |||||||
chr5:113008476 | C | CTGAAT | 251 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(248): Show |
271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.1047+434_1047+435i others(7): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113008476 | |||||||
chr5:113008572 | A | C | 1 | a0001c0001t0030g0114 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1047+530A>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113008572 | |||||||
chr5:113008572 | A | G | 3 | a0001c0001t0022g0202 a0001c0001t0022g0203 a0001c0001t0022g0204 |
3 | HG02886.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1047+530A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113008572 | |||||||
chr5:113008846 | T | C | 4 | a0001c0001t0012g0014 a0001c0001t0012g0139 a0001c0001t0012g0156 others(1): Show |
5 | HG01074.hp2 HG01891.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1047+804T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113008846 | |||||||
chr5:113008849 | C | CT | 78 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0137 others(75): Show |
79 | HG00639.hp2 HG01106.hp1 HG01243.hp1 others(76): Show |
intron_variant | MODIFIER | c.1047+820dupT | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr5 | 113008849 | ||||||
chr5:113008958 | C | G | 1 | a0001c0001t0020g0285 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1047+916C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113008958 | |||||||
chr5:113008958 | C | T | 120 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(117): Show |
131 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.1047+916C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113008958 | |||||||
chr5:113009094 | C | T | 2 | a0001c0002t0039g0211 a0001c0002t0114g0212 |
2 | HG02109.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1047+1052C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113009094 | |||||||
chr5:113009134 | C | T | 5 | a0001c0001t0005g0154 a0001c0001t0011g0013 a0001c0001t0011g0150 others(2): Show |
6 | HG02258.hp1 HG02622.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1047+1092C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113009134 | |||||||
chr5:113009255 | C | G | 5 | a0001c0001t0006g0128 a0001c0001t0006g0129 a0001c0001t0006g0131 others(2): Show |
5 | HG02155.hp2 NA18948.hp1 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.1047+1213C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113009255 | |||||||
chr5:113009268 | C | A | 249 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(246): Show |
269 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.1047+1226C>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113009268 | |||||||
chr5:113009274 | T | A | 1 | a0001c0001t0001g0304 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1047+1232T>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113009274 | |||||||
chr5:113009315 | C | T | 1 | a0001c0001t0001g0019 | 2 | HG01081.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.1047+1273C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113009315 | |||||||
chr5:113009654 | A | AGAT | 59 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0137 others(56): Show |
60 | HG01106.hp1 HG01496.hp2 HG01515.hp1 others(57): Show |
intron_variant | MODIFIER | c.1048-1101_1048-109 others(7): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr5 | 113009654 | ||||||
chr5:113009698 | C | G | 59 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0137 others(56): Show |
60 | HG01106.hp1 HG01496.hp2 HG01515.hp1 others(57): Show |
intron_variant | MODIFIER | c.1048-1058C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113009698 | |||||||
chr5:113009748 | CATTAT | C | 11 | a0001c0002t0008g0010 a0001c0002t0008g0058 a0001c0002t0008g0060 others(8): Show |
12 | HG00423.hp2 HG01928.hp1 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.1048-1004_1048-100 others(9): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr5 | 113009748 | ||||||
chr5:113009750 | T | A | 59 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0137 others(56): Show |
60 | HG01106.hp1 HG01496.hp2 HG01515.hp1 others(57): Show |
intron_variant | MODIFIER | c.1048-1006T>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113009750 | |||||||
chr5:113009759 | A | G | 60 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0137 others(57): Show |
61 | HG01106.hp1 HG01496.hp2 HG01515.hp1 others(58): Show |
intron_variant | MODIFIER | c.1048-997A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113009759 | |||||||
chr5:113009856 | C | T | 6 | a0001c0001t0004g0274 a0001c0001t0004g0288 a0001c0001t0099g0234 others(3): Show |
6 | NA18966.hp2 NA18985.hp1 NA18992.hp2 others(3): Show |
intron_variant | MODIFIER | c.1048-900C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113009856 | |||||||
chr5:113009921 | C | CTTT | 57 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0158 others(54): Show |
58 | HG01106.hp1 HG01496.hp2 HG01515.hp1 others(55): Show |
intron_variant | MODIFIER | c.1048-823_1048-821d others(5): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr5 | 113009921 | ||||||
chr5:113009969 | A | G | 1 | a0001c0002t0002g0059 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1048-787A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113009969 | |||||||
chr5:113009977 | T | C | 1 | a0001c0001t0004g0274 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1048-779T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113009977 | |||||||
chr5:113010034 | C | CT | 54 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0137 others(51): Show |
55 | HG01106.hp1 HG01515.hp1 HG02015.hp1 others(52): Show |
intron_variant | MODIFIER | c.1048-706dupT | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr5 | 113010034 | ||||||
chr5:113010034 | C | CTT | 8 | a0001c0001t0003g0161 a0001c0001t0013g0138 a0001c0001t0013g0143 others(5): Show |
8 | HG01496.hp2 HG02055.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1048-707_1048-706d others(4): Show |
DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr5 | 113010034 | ||||||
chr5:113010034 | CT | C | 6 | a0001c0001t0001g0227 a0001c0001t0001g0308 a0001c0001t0024g0190 others(3): Show |
6 | HG00280.hp1 HG01167.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1048-706delT | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr5 | 113010034 | ||||||
chr5:113010207 | A | AT | 38 | a0001c0001t0001g0236 a0001c0001t0001g0307 a0001c0001t0001g0308 others(35): Show |
40 | HG00609.hp1 HG00621.hp2 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.1048-530dupT | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr5 | 113010207 | ||||||
chr5:113010207 | AT | A | 56 | a0001c0001t0001g0290 a0001c0001t0003g0135 a0001c0001t0003g0136 others(53): Show |
57 | HG01106.hp1 HG01496.hp2 HG01515.hp1 others(54): Show |
intron_variant | MODIFIER | c.1048-530delT | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr5 | 113010207 | ||||||
chr5:113010246 | A | G | 143 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(140): Show |
160 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.1048-510A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113010246 | |||||||
chr5:113010253 | C | A | 3 | a0001c0001t0024g0155 a0001c0001t0024g0190 a0001c0001t0024g0191 |
3 | HG02896.hp1 HG02897.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1048-503C>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113010253 | |||||||
chr5:113010339 | T | C | 59 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0137 others(56): Show |
60 | HG01106.hp1 HG01496.hp2 HG01515.hp1 others(57): Show |
intron_variant | MODIFIER | c.1048-417T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113010339 | |||||||
chr5:113010365 | G | C | 1 | a0001c0001t0003g0181 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1048-391G>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113010365 | |||||||
chr5:113010389 | T | G | 59 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0137 others(56): Show |
60 | HG01106.hp1 HG01496.hp2 HG01515.hp1 others(57): Show |
intron_variant | MODIFIER | c.1048-367T>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113010389 | |||||||
chr5:113010486 | A | G | 59 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0137 others(56): Show |
60 | HG01106.hp1 HG01496.hp2 HG01515.hp1 others(57): Show |
intron_variant | MODIFIER | c.1048-270A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113010486 | |||||||
chr5:113010719 | A | G | 2 | a0001c0001t0001g0306 a0001c0001t0045g0082 |
2 | HG01358.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1048-37A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113010719 | |||||||
chr5:113010734 | TG | T | 157 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(154): Show |
175 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.1048-21delG | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113010734 | |||||||
chr5:113010735 | G | T | 9 | a0001c0001t0005g0118 a0001c0001t0005g0154 a0001c0001t0005g0206 others(6): Show |
10 | HG02258.hp1 HG02622.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.1048-21G>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113010735 | |||||||
chr5:113010735 | GTT | G | 59 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0137 others(56): Show |
60 | HG01106.hp1 HG01496.hp2 HG01515.hp1 others(57): Show |
splice_region_variant&intron_variant | LOW | c.1048-8_1048-7delTT | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr5 | 113010735 | ||||||
chr5:113010737 | T | G | 2 | a0001c0001t0007g0036 a0001c0002t0102g0142 |
2 | HG01243.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.1048-19T>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 9/10 | chr5 | 113010737 | |||||||
chr5:113010940 | G | A | 1 | a0001c0001t0001g0266 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1099+133G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 10/10 | chr5 | 113010940 | |||||||
chr5:113010941 | T | G | 1 | a0001c0001t0001g0266 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1099+134T>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 10/10 | chr5 | 113010941 | |||||||
chr5:113011023 | C | A | 1 | a0001c0001t0001g0295 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1099+216C>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 10/10 | chr5 | 113011023 | |||||||
chr5:113011211 | T | A | 1 | a0001c0007t0055g0052 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1099+404T>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 10/10 | chr5 | 113011211 | |||||||
chr5:113011337 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1099+530C>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 10/10 | chr5 | 113011337 | |||||||
chr5:113011614 | A | T | 1 | a0001c0002t0002g0205 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1099+807A>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 10/10 | chr5 | 113011614 | |||||||
chr5:113011785 | A | C | 1 | a0001c0001t0001g0282 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1099+978A>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 10/10 | chr5 | 113011785 | |||||||
chr5:113011841 | G | A | 21 | a0001c0001t0007g0023 a0001c0001t0007g0036 a0001c0001t0007g0037 others(18): Show |
21 | HG00609.hp1 HG01070.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.1099+1034G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 10/10 | chr5 | 113011841 | |||||||
chr5:113011966 | T | A | 1 | a0001c0001t0001g0304 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1099+1159T>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 10/10 | chr5 | 113011966 | |||||||
chr5:113011969 | C | A | 1 | a0001c0001t0001g0304 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1099+1162C>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 10/10 | chr5 | 113011969 | |||||||
chr5:113012010 | G | A | 1 | a0001c0001t0081g0254 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1099+1203G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 10/10 | chr5 | 113012010 | |||||||
chr5:113012013 | T | C | 202 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(199): Show |
220 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.1099+1206T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 10/10 | chr5 | 113012013 | |||||||
chr5:113012099 | T | C | 7 | a0001c0001t0013g0138 a0001c0001t0013g0143 a0001c0001t0013g0144 others(4): Show |
7 | HG01496.hp2 HG02055.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1100-1222T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 10/10 | chr5 | 113012099 | |||||||
chr5:113012131 | A | G | 146 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(143): Show |
163 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.1100-1190A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 10/10 | chr5 | 113012131 | |||||||
chr5:113012275 | A | T | 1 | a0001c0001t0001g0251 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1100-1046A>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 10/10 | chr5 | 113012275 | |||||||
chr5:113012281 | G | A | 3 | a0001c0001t0007g0047 a0001c0001t0067g0045 a0001c0001t0069g0046 |
3 | HG03209.hp2 HG03453.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1100-1040G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 10/10 | chr5 | 113012281 | |||||||
chr5:113012442 | A | C | 1 | a0001c0001t0083g0299 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1100-879A>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 10/10 | chr5 | 113012442 | |||||||
chr5:113012569 | GA | G | 3 | a0001c0001t0024g0155 a0001c0001t0024g0190 a0001c0001t0024g0191 |
3 | HG02896.hp1 HG02897.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1100-746delA | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 113012569 | ||||||
chr5:113012587 | T | C | 10 | a0001c0001t0005g0154 a0001c0001t0011g0013 a0001c0001t0011g0150 others(7): Show |
11 | HG02258.hp1 HG02280.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1100-734T>C | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 10/10 | chr5 | 113012587 | |||||||
chr5:113012600 | G | T | 57 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0137 others(54): Show |
58 | HG01106.hp1 HG01496.hp2 HG01515.hp1 others(55): Show |
intron_variant | MODIFIER | c.1100-721G>T | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 10/10 | chr5 | 113012600 | |||||||
chr5:113012730 | G | A | 3 | a0001c0001t0022g0202 a0001c0001t0022g0203 a0001c0001t0022g0204 |
3 | HG02886.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1100-591G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 10/10 | chr5 | 113012730 | |||||||
chr5:113012747 | C | G | 1 | a0001c0001t0007g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1100-574C>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 10/10 | chr5 | 113012747 | |||||||
chr5:113012750 | T | A | 1 | a0001c0001t0005g0206 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1100-571T>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 10/10 | chr5 | 113012750 | |||||||
chr5:113012932 | A | G | 1 | a0001c0001t0004g0274 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1100-389A>G | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 10/10 | chr5 | 113012932 | |||||||
chr5:113013054 | G | A | 2 | a0001c0001t0021g0263 a0001c0001t0021g0264 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1100-267G>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 10/10 | chr5 | 113013054 | |||||||
chr5:113013094 | C | A | 1 | a0001c0002t0103g0140 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1100-227C>A | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 10/10 | chr5 | 113013094 | |||||||
chr5:113013233 | T | TA | 3 | a0001c0001t0022g0202 a0001c0001t0022g0203 a0001c0001t0022g0204 |
3 | HG02886.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1100-86dupA | DCP2 | ENSG00000172795.17 | transcript | ENST00000389063.3 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 113013233 |