Item | Value |
---|---|
geneid | 4883 |
ensemblid | ENSG00000113389.16 |
hgncid | 7945 |
symbol | NPR3 |
name | natriuretic peptide receptor 3 |
refseq_nuc | NM_001204375.2 |
refseq_prot | NP_001191304.1 |
ensembl_nuc | ENST00000265074.13 |
ensembl_prot | ENSP00000265074.8 |
mane_status | MANE Select |
chr | chr5 |
start | 32711321 |
end | 32791720 |
strand | + |
ver | v1.2 |
region | chr5:32711321-32791720 |
region5000 | chr5:32706321-32796720 |
regionname0 | NPR3_chr5_32711321_32791720 |
regionname5000 | NPR3_chr5_32706321_32796720 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 541 | 252 | 80 | 47 | 91 | 8 | 24 | 64 | NPR3_chr5_32706321_32796720 | NPR3 | MPSLL others(536): Show |
chr5 | 32706321 | 32796720 |
a0002 | 0/0 | 541 | 68 | 8 | 11 | 33 | 4 | 12 | 28 | NPR3_chr5_32706321_32796720 | NPR3 | MPSLL others(536): Show |
chr5 | 32706321 | 32796720 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1623 | 235 | 64 | 46 | 91 | 8 | 24 | NPR3_chr5_32706321_32796720 | NPR3 | ATGCC others(1618): Show |
chr5 | 32706321 | 32796720 | ||
a0001c0003 | 0/0 | 1623 | 14 | 13 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | ATGCC others(1618): Show |
chr5 | 32706321 | 32796720 | ||
a0001c0004 | 0/0 | 1623 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | ATGCC others(1618): Show |
chr5 | 32706321 | 32796720 | ||
a0001c0005 | 0/0 | 1623 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | ATGCC others(1618): Show |
chr5 | 32706321 | 32796720 | ||
a0001c0006 | 0/0 | 1623 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | ATGCC others(1618): Show |
chr5 | 32706321 | 32796720 | ||
a0002c0002 | 0/0 | 1623 | 68 | 8 | 11 | 33 | 4 | 12 | NPR3_chr5_32706321_32796720 | NPR3 | ATGCC others(1618): Show |
chr5 | 32706321 | 32796720 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 7463 | 90 | 14 | 16 | 41 | 4 | 15 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7458): Show |
chr5 | 32706321 | 32796720 |
a0001c0001t0002 | 0/0 | 7463 | 2 | 2 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7458): Show |
chr5 | 32706321 | 32796720 |
a0001c0001t0003 | 0/0 | 7461 | 47 | 1 | 3 | 39 | 0 | 4 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7456): Show |
chr5 | 32706321 | 32796720 |
a0001c0001t0004 | 0/0 | 7463 | 17 | 7 | 5 | 0 | 1 | 4 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7458): Show |
chr5 | 32706321 | 32796720 |
a0001c0001t0005 | 0/0 | 7477 | 3 | 3 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7472): Show |
chr5 | 32706321 | 32796720 |
a0001c0001t0006 | 0/0 | 7463 | 6 | 5 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7458): Show |
chr5 | 32706321 | 32796720 |
a0001c0001t0007 | 0/0 | 7463 | 6 | 4 | 2 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7458): Show |
chr5 | 32706321 | 32796720 |
a0001c0001t0008 | 0/0 | 7478 | 4 | 4 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7473): Show |
chr5 | 32706321 | 32796720 |
a0001c0001t0009 | 1/0 | 7457 | 5 | 0 | 1 | 3 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7452): Show |
chr5 | 32706321 | 32796720 |
a0001c0001t0010 | 0/1 | 7461 | 4 | 0 | 3 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7456): Show |
chr5 | 32706321 | 32796720 |
a0001c0001t0013 | 0/0 | 7469 | 3 | 0 | 3 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7464): Show |
chr5 | 32706321 | 32796720 |
a0001c0001t0014 | 0/0 | 7463 | 2 | 0 | 2 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7458): Show |
chr5 | 32706321 | 32796720 |
a0001c0001t0015 | 0/0 | 7463 | 2 | 0 | 1 | 0 | 1 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7458): Show |
chr5 | 32706321 | 32796720 |
a0001c0001t0017 | 0/0 | 7463 | 2 | 2 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7458): Show |
chr5 | 32706321 | 32796720 |
a0001c0001t0019 | 0/0 | 7463 | 2 | 2 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7458): Show |
chr5 | 32706321 | 32796720 |
a0001c0001t0021 | 0/0 | 7463 | 2 | 2 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7458): Show |
chr5 | 32706321 | 32796720 |
a0001c0001t0022 | 0/0 | 7461 | 2 | 0 | 0 | 0 | 1 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7456): Show |
chr5 | 32706321 | 32796720 |
a0001c0001t0024 | 0/0 | 7477 | 2 | 2 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7472): Show |
chr5 | 32706321 | 32796720 |
a0001c0001t0025 | 0/0 | 7464 | 2 | 2 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7459): Show |
chr5 | 32706321 | 32796720 |
a0001c0001t0026 | 0/0 | 7478 | 2 | 2 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7473): Show |
chr5 | 32706321 | 32796720 |
a0001c0001t0028 | 0/0 | 7461 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7456): Show |
chr5 | 32706321 | 32796720 |
a0001c0001t0030 | 0/0 | 7466 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7461): Show |
chr5 | 32706321 | 32796720 |
a0001c0001t0031 | 0/0 | 7467 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7462): Show |
chr5 | 32706321 | 32796720 |
a0001c0001t0032 | 0/0 | 7461 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7456): Show |
chr5 | 32706321 | 32796720 |
a0001c0001t0034 | 0/0 | 7463 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7458): Show |
chr5 | 32706321 | 32796720 |
a0001c0001t0036 | 0/0 | 7463 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7458): Show |
chr5 | 32706321 | 32796720 |
a0001c0001t0037 | 0/0 | 7463 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7458): Show |
chr5 | 32706321 | 32796720 |
a0001c0001t0038 | 0/0 | 7463 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7458): Show |
chr5 | 32706321 | 32796720 |
a0001c0001t0039 | 0/0 | 7463 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7458): Show |
chr5 | 32706321 | 32796720 |
a0001c0001t0040 | 0/0 | 7463 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7458): Show |
chr5 | 32706321 | 32796720 |
a0001c0001t0041 | 0/0 | 7463 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7458): Show |
chr5 | 32706321 | 32796720 |
a0001c0001t0042 | 0/0 | 7463 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7458): Show |
chr5 | 32706321 | 32796720 |
a0001c0001t0043 | 0/0 | 7463 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7458): Show |
chr5 | 32706321 | 32796720 |
a0001c0001t0045 | 0/0 | 7463 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7458): Show |
chr5 | 32706321 | 32796720 |
a0001c0001t0046 | 0/0 | 7463 | 1 | 0 | 0 | 0 | 1 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7458): Show |
chr5 | 32706321 | 32796720 |
a0001c0001t0047 | 0/0 | 7463 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7458): Show |
chr5 | 32706321 | 32796720 |
a0001c0001t0048 | 0/0 | 7463 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7458): Show |
chr5 | 32706321 | 32796720 |
a0001c0001t0049 | 0/0 | 7463 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7458): Show |
chr5 | 32706321 | 32796720 |
a0001c0001t0050 | 0/0 | 7463 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7458): Show |
chr5 | 32706321 | 32796720 |
a0001c0001t0051 | 0/0 | 7463 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7458): Show |
chr5 | 32706321 | 32796720 |
a0001c0001t0053 | 0/0 | 7461 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7456): Show |
chr5 | 32706321 | 32796720 |
a0001c0001t0055 | 0/0 | 7463 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7458): Show |
chr5 | 32706321 | 32796720 |
a0001c0001t0057 | 0/0 | 7463 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7458): Show |
chr5 | 32706321 | 32796720 |
a0001c0001t0059 | 0/0 | 7465 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7460): Show |
chr5 | 32706321 | 32796720 |
a0001c0001t0060 | 0/0 | 7477 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7472): Show |
chr5 | 32706321 | 32796720 |
a0001c0001t0064 | 0/0 | 7464 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7459): Show |
chr5 | 32706321 | 32796720 |
a0001c0001t0065 | 0/0 | 7464 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7459): Show |
chr5 | 32706321 | 32796720 |
a0001c0001t0066 | 0/0 | 7462 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7457): Show |
chr5 | 32706321 | 32796720 |
a0001c0001t0067 | 0/0 | 7455 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7450): Show |
chr5 | 32706321 | 32796720 |
a0001c0001t0068 | 0/0 | 7455 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7450): Show |
chr5 | 32706321 | 32796720 |
a0001c0003t0001 | 0/0 | 7463 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7458): Show |
chr5 | 32706321 | 32796720 |
a0001c0003t0004 | 0/0 | 7463 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7458): Show |
chr5 | 32706321 | 32796720 |
a0001c0003t0005 | 0/0 | 7477 | 6 | 6 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7472): Show |
chr5 | 32706321 | 32796720 |
a0001c0003t0008 | 0/0 | 7478 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7473): Show |
chr5 | 32706321 | 32796720 |
a0001c0003t0023 | 0/0 | 7477 | 2 | 2 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7472): Show |
chr5 | 32706321 | 32796720 |
a0001c0003t0044 | 0/0 | 7463 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7458): Show |
chr5 | 32706321 | 32796720 |
a0001c0003t0058 | 0/0 | 7463 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7458): Show |
chr5 | 32706321 | 32796720 |
a0001c0003t0063 | 0/0 | 7477 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7472): Show |
chr5 | 32706321 | 32796720 |
a0001c0004t0062 | 0/0 | 7477 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7472): Show |
chr5 | 32706321 | 32796720 |
a0001c0005t0056 | 0/0 | 7463 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7458): Show |
chr5 | 32706321 | 32796720 |
a0001c0006t0061 | 0/0 | 7478 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7473): Show |
chr5 | 32706321 | 32796720 |
a0002c0002t0002 | 0/0 | 7463 | 47 | 5 | 4 | 28 | 3 | 7 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7458): Show |
chr5 | 32706321 | 32796720 |
a0002c0002t0011 | 0/0 | 7463 | 4 | 0 | 1 | 1 | 1 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7458): Show |
chr5 | 32706321 | 32796720 |
a0002c0002t0012 | 0/0 | 7463 | 4 | 0 | 4 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7458): Show |
chr5 | 32706321 | 32796720 |
a0002c0002t0016 | 0/0 | 7469 | 2 | 0 | 2 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7464): Show |
chr5 | 32706321 | 32796720 |
a0002c0002t0018 | 0/0 | 7463 | 2 | 2 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7458): Show |
chr5 | 32706321 | 32796720 |
a0002c0002t0020 | 0/0 | 7463 | 2 | 0 | 0 | 2 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7458): Show |
chr5 | 32706321 | 32796720 |
a0002c0002t0027 | 0/0 | 7457 | 2 | 1 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7452): Show |
chr5 | 32706321 | 32796720 |
a0002c0002t0029 | 0/0 | 7463 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7458): Show |
chr5 | 32706321 | 32796720 |
a0002c0002t0033 | 0/0 | 7463 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7458): Show |
chr5 | 32706321 | 32796720 |
a0002c0002t0035 | 0/0 | 7463 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7458): Show |
chr5 | 32706321 | 32796720 |
a0002c0002t0052 | 0/0 | 7463 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7458): Show |
chr5 | 32706321 | 32796720 |
a0002c0002t0054 | 0/0 | 7463 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | GGCGC others(7458): Show |
chr5 | 32706321 | 32796720 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0003g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0003g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0003g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0003g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0003g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0003g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0003g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0004g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0004g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0004g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0004g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0004g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0004g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0004g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0004g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0004g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0004g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0004g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0004g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0004g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0004g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0004g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0004g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0004g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0005g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0005g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0005g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0006g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0006g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0006g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0006g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0006g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0006g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0007g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0007g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0007g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0007g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0007g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0007g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0008g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0008g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0008g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0008g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0009g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0009g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0009g0190 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0009g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0009g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0010g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0010g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0010g0131 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0013g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0013g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0013g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0014g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0014g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0015g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0015g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0017g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0017g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0019g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0019g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0021g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0021g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0022g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0022g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0024g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0024g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0025g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0025g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0026g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0026g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0028g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0030g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0031g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0032g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0034g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0036g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0037g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0038g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0039g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0040g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0041g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0042g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0043g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0045g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0046g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0047g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0048g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0049g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0050g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0051g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0053g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0055g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0057g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0059g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0060g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0064g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0065g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0066g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0067g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0001t0068g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0003t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0003t0004g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0003t0005g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0003t0005g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0003t0005g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0003t0005g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0003t0005g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0003t0008g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0003t0023g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0003t0023g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0003t0044g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0003t0058g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0003t0063g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0004t0062g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0005t0056g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0001c0006t0061g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0002g0005 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0002g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0002g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0011g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0011g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0011g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0011g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0012g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0012g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0012g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0012g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0016g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0016g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0018g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0018g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0020g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0020g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0027g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0027g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0029g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0033g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0035g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0052g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
a0002c0002t0054g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0093 | EUR | GBR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG00099 | hp2 | a0002 | c0002 | t0002 | g0226 | EUR | GBR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG00280 | hp1 | a0001 | c0001 | t0015 | g0103 | EUR | FIN | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG00280 | hp2 | a0001 | c0001 | t0022 | g0221 | EUR | FIN | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0223 | EUR | FIN | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG00323 | hp2 | a0001 | c0001 | t0046 | g0285 | EUR | FIN | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG00423 | hp1 | a0001 | c0001 | t0003 | g0246 | EAS | CHS | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG00423 | hp2 | a0001 | c0001 | t0003 | g0087 | EAS | CHS | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | CHS | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG00544 | hp2 | a0001 | c0001 | t0003 | g0245 | EAS | CHS | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG00609 | hp1 | a0002 | c0002 | t0002 | g0217 | EAS | CHS | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG00609 | hp2 | a0001 | c0001 | t0003 | g0164 | EAS | CHS | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG00621 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | CHS | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | CHS | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG00639 | hp1 | a0002 | c0002 | t0002 | g0158 | AMR | PUR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG00642 | hp2 | a0002 | c0002 | t0012 | g0108 | AMR | PUR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG00735 | hp2 | a0001 | c0001 | t0045 | g0099 | AMR | PUR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG00738 | hp1 | a0002 | c0002 | t0002 | g0081 | AMR | PUR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG00738 | hp2 | a0001 | c0001 | t0038 | g0022 | AMR | PUR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG00741 | hp1 | a0001 | c0001 | t0004 | g0148 | AMR | PUR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG01069 | hp1 | a0001 | c0001 | t0003 | g0115 | AMR | PUR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG01070 | hp1 | a0001 | c0001 | t0010 | g0120 | AMR | PUR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG01070 | hp2 | a0001 | c0001 | t0004 | g0102 | AMR | PUR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG01074 | hp1 | a0001 | c0001 | t0047 | g0104 | AMR | PUR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG01074 | hp2 | a0001 | c0001 | t0003 | g0075 | AMR | PUR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG01099 | hp2 | a0002 | c0002 | t0012 | g0293 | AMR | PUR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG01106 | hp1 | a0002 | c0002 | t0012 | g0107 | AMR | PUR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG01106 | hp2 | a0001 | c0001 | t0007 | g0150 | AMR | PUR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG01109 | hp1 | a0001 | c0001 | t0003 | g0118 | AMR | PUR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG01109 | hp2 | a0001 | c0003 | t0001 | g0034 | AMR | PUR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG01168 | hp1 | a0001 | c0001 | t0010 | g0003 | AMR | PUR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG01168 | hp2 | a0001 | c0001 | t0049 | g0015 | AMR | PUR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG01169 | hp1 | a0001 | c0001 | t0010 | g0003 | AMR | PUR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG01175 | hp2 | a0001 | c0001 | t0036 | g0013 | AMR | PUR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG01192 | hp1 | a0001 | c0001 | t0055 | g0147 | AMR | PUR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG01243 | hp1 | a0001 | c0001 | t0006 | g0109 | AMR | PUR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG01256 | hp1 | a0001 | c0001 | t0028 | g0094 | AMR | CLM | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG01257 | hp1 | a0002 | c0002 | t0002 | g0009 | AMR | CLM | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG01257 | hp2 | a0001 | c0001 | t0014 | g0105 | AMR | CLM | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG01258 | hp2 | a0001 | c0001 | t0014 | g0106 | AMR | CLM | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG01261 | hp1 | a0001 | c0001 | t0040 | g0162 | AMR | CLM | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG01261 | hp2 | a0001 | c0001 | t0004 | g0154 | AMR | CLM | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG01346 | hp1 | a0002 | c0002 | t0002 | g0005 | AMR | CLM | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | CLM | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG01433 | hp1 | a0002 | c0002 | t0012 | g0018 | AMR | CLM | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG01433 | hp2 | a0001 | c0001 | t0004 | g0016 | AMR | CLM | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG01496 | hp1 | a0001 | c0001 | t0004 | g0027 | AMR | CLM | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | CLM | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG01516 | hp1 | a0002 | c0002 | t0011 | g0130 | EUR | IBS | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG01516 | hp2 | a0001 | c0001 | t0004 | g0149 | EUR | IBS | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG01884 | hp1 | a0001 | c0001 | t0021 | g0080 | AFR | ACB | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG01891 | hp1 | a0001 | c0001 | t0004 | g0139 | AFR | ACB | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG01891 | hp2 | a0001 | c0001 | t0006 | g0063 | AFR | ACB | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG01934 | hp1 | a0001 | c0001 | t0013 | g0282 | AMR | PEL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG01934 | hp2 | a0001 | c0001 | t0007 | g0138 | AMR | PEL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG01952 | hp1 | a0001 | c0001 | t0015 | g0123 | AMR | PEL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG01952 | hp2 | a0001 | c0001 | t0013 | g0283 | AMR | PEL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG01978 | hp1 | a0002 | c0002 | t0011 | g0261 | AMR | PEL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG01978 | hp2 | a0001 | c0001 | t0009 | g0160 | AMR | PEL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG01981 | hp2 | a0002 | c0002 | t0016 | g0276 | AMR | PEL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG01993 | hp2 | a0001 | c0001 | t0030 | g0284 | AMR | PEL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02015 | hp1 | a0001 | c0001 | t0003 | g0234 | EAS | KHV | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02015 | hp2 | a0001 | c0001 | t0003 | g0083 | EAS | KHV | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02027 | hp1 | a0001 | c0001 | t0003 | g0240 | EAS | KHV | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02040 | hp1 | a0002 | c0002 | t0020 | g0086 | EAS | KHV | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02055 | hp1 | a0002 | c0002 | t0027 | g0127 | AFR | ACB | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02055 | hp2 | a0001 | c0006 | t0061 | g0046 | AFR | ACB | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02071 | hp1 | a0001 | c0001 | t0003 | g0122 | EAS | KHV | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02074 | hp1 | a0001 | c0001 | t0053 | g0311 | EAS | KHV | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02074 | hp2 | a0001 | c0001 | t0003 | g0171 | EAS | KHV | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02080 | hp1 | a0001 | c0001 | t0032 | g0216 | EAS | KHV | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02080 | hp2 | a0002 | c0002 | t0002 | g0204 | EAS | KHV | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02083 | hp1 | a0001 | c0001 | t0003 | g0296 | EAS | KHV | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | KHV | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02129 | hp2 | a0001 | c0001 | t0003 | g0256 | EAS | KHV | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02135 | hp2 | a0002 | c0002 | t0002 | g0166 | EAS | KHV | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02145 | hp1 | a0001 | c0001 | t0005 | g0153 | AFR | ACB | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02155 | hp1 | a0001 | c0001 | t0003 | g0222 | EAS | CDX | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | CDX | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02257 | hp1 | a0001 | c0001 | t0008 | g0301 | AFR | ACB | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02257 | hp2 | a0001 | c0001 | t0004 | g0155 | AFR | ACB | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02258 | hp1 | a0001 | c0001 | t0006 | g0010 | AFR | ACB | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02258 | hp2 | a0001 | c0003 | t0005 | g0030 | AFR | ACB | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02280 | hp1 | a0001 | c0001 | t0005 | g0079 | AFR | ACB | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | ACB | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02293 | hp1 | a0001 | c0001 | t0013 | g0278 | AMR | PEL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02293 | hp2 | a0002 | c0002 | t0016 | g0290 | AMR | PEL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02451 | hp1 | a0002 | c0002 | t0002 | g0041 | AFR | ACB | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02451 | hp2 | a0001 | c0001 | t0007 | g0200 | AFR | ACB | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02523 | hp1 | a0001 | c0001 | t0003 | g0111 | EAS | KHV | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02523 | hp2 | a0002 | c0002 | t0002 | g0211 | EAS | KHV | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02602 | hp1 | a0001 | c0001 | t0004 | g0017 | SAS | PJL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02615 | hp1 | a0001 | c0001 | t0007 | g0058 | AFR | GWD | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02615 | hp2 | a0001 | c0001 | t0050 | g0047 | AFR | GWD | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02622 | hp1 | a0001 | c0003 | t0023 | g0038 | AFR | GWD | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02622 | hp2 | a0001 | c0001 | t0026 | g0049 | AFR | GWD | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02630 | hp1 | a0001 | c0001 | t0006 | g0066 | AFR | GWD | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02630 | hp2 | a0001 | c0001 | t0006 | g0110 | AFR | GWD | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02647 | hp1 | a0001 | c0001 | t0003 | g0101 | AFR | GWD | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02683 | hp1 | a0002 | c0002 | t0002 | g0012 | SAS | PJL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02698 | hp1 | a0002 | c0002 | t0054 | g0168 | SAS | PJL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02717 | hp1 | a0001 | c0001 | t0066 | g0053 | AFR | GWD | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02717 | hp2 | a0001 | c0003 | t0008 | g0032 | AFR | GWD | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02723 | hp1 | a0001 | c0001 | t0043 | g0067 | AFR | GWD | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | GWD | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02735 | hp1 | a0001 | c0001 | t0004 | g0294 | SAS | PJL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02735 | hp2 | a0001 | c0001 | t0022 | g0021 | SAS | PJL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02809 | hp1 | a0001 | c0001 | t0006 | g0065 | AFR | GWD | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02809 | hp2 | a0002 | c0002 | t0002 | g0055 | AFR | GWD | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02818 | hp1 | a0002 | c0002 | t0002 | g0270 | AFR | GWD | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02818 | hp2 | a0001 | c0001 | t0025 | g0048 | AFR | GWD | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02886 | hp1 | a0001 | c0003 | t0058 | g0035 | AFR | GWD | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02886 | hp2 | a0001 | c0001 | t0019 | g0007 | AFR | GWD | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02895 | hp1 | a0002 | c0002 | t0018 | g0077 | AFR | GWD | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02895 | hp2 | a0001 | c0001 | t0039 | g0265 | AFR | GWD | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02896 | hp1 | a0001 | c0003 | t0023 | g0039 | AFR | GWD | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02897 | hp1 | a0002 | c0002 | t0018 | g0076 | AFR | GWD | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02922 | hp1 | a0001 | c0001 | t0004 | g0300 | AFR | ESN | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02922 | hp2 | a0001 | c0001 | t0026 | g0052 | AFR | ESN | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02965 | hp1 | a0001 | c0001 | t0017 | g0064 | AFR | ESN | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02965 | hp2 | a0001 | c0003 | t0005 | g0029 | AFR | ESN | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02970 | hp1 | a0001 | c0003 | t0005 | g0031 | AFR | ESN | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02970 | hp2 | a0001 | c0001 | t0041 | g0146 | AFR | ESN | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02976 | hp1 | a0001 | c0001 | t0008 | g0128 | AFR | ESN | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02976 | hp2 | a0001 | c0001 | t0021 | g0141 | AFR | ESN | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG03041 | hp1 | a0001 | c0003 | t0005 | g0033 | AFR | GWD | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | MSL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG03098 | hp2 | a0001 | c0001 | t0004 | g0299 | AFR | MSL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG03130 | hp1 | a0001 | c0001 | t0060 | g0289 | AFR | ESN | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG03130 | hp2 | a0001 | c0001 | t0004 | g0302 | AFR | ESN | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG03139 | hp1 | a0001 | c0001 | t0059 | g0156 | AFR | ESN | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG03139 | hp2 | a0001 | c0001 | t0025 | g0050 | AFR | ESN | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG03195 | hp2 | a0002 | c0002 | t0002 | g0072 | AFR | ESN | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG03225 | hp1 | a0001 | c0001 | t0051 | g0269 | AFR | MSL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG03225 | hp2 | a0001 | c0003 | t0005 | g0002 | AFR | MSL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG03239 | hp1 | a0001 | c0001 | t0004 | g0028 | SAS | PJL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG03453 | hp1 | a0001 | c0001 | t0019 | g0006 | AFR | MSL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG03453 | hp2 | a0001 | c0001 | t0007 | g0074 | AFR | MSL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG03492 | hp2 | a0002 | c0002 | t0002 | g0232 | SAS | PJL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG03516 | hp1 | a0001 | c0001 | t0005 | g0143 | AFR | ESN | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG03516 | hp2 | a0001 | c0001 | t0042 | g0042 | AFR | ESN | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG03540 | hp1 | a0001 | c0001 | t0004 | g0044 | AFR | GWD | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG03540 | hp2 | a0001 | c0003 | t0044 | g0036 | AFR | GWD | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG03579 | hp1 | a0001 | c0001 | t0017 | g0057 | AFR | MSL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG03579 | hp2 | a0001 | c0003 | t0063 | g0040 | AFR | MSL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | PJL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG03654 | hp2 | a0001 | c0001 | t0004 | g0073 | SAS | PJL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG03688 | hp1 | a0001 | c0001 | t0003 | g0176 | SAS | STU | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG03688 | hp2 | a0002 | c0002 | t0002 | g0125 | SAS | STU | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG03831 | hp1 | a0002 | c0002 | t0002 | g0112 | SAS | BEB | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG03831 | hp2 | a0002 | c0002 | t0029 | g0100 | SAS | BEB | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG03834 | hp1 | a0002 | c0002 | t0052 | g0163 | SAS | BEB | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | BEB | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG03927 | hp1 | a0002 | c0002 | t0035 | g0124 | SAS | BEB | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | BEB | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG04115 | hp1 | a0002 | c0002 | t0002 | g0178 | SAS | STU | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG04115 | hp2 | a0001 | c0001 | t0003 | g0249 | SAS | STU | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG04184 | hp1 | a0002 | c0002 | t0002 | g0237 | SAS | BEB | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG04184 | hp2 | a0001 | c0001 | t0003 | g0116 | SAS | BEB | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG04199 | hp1 | a0002 | c0002 | t0002 | g0271 | SAS | STU | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG04199 | hp2 | a0001 | c0001 | t0003 | g0185 | SAS | STU | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | STU | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | STU | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | STU | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG04228 | hp2 | a0002 | c0002 | t0011 | g0262 | SAS | STU | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18522 | hp1 | a0001 | c0001 | t0064 | g0054 | AFR | YRI | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18522 | hp2 | a0001 | c0003 | t0005 | g0002 | AFR | YRI | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18612 | hp1 | a0001 | c0001 | t0048 | g0303 | EAS | CHB | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18612 | hp2 | a0001 | c0001 | t0003 | g0224 | EAS | CHB | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | YRI | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18906 | hp2 | a0002 | c0002 | t0002 | g0145 | AFR | YRI | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18940 | hp1 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18940 | hp2 | a0002 | c0002 | t0002 | g0082 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18941 | hp1 | a0001 | c0001 | t0003 | g0235 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18941 | hp2 | a0001 | c0001 | t0009 | g0304 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18942 | hp2 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18943 | hp2 | a0002 | c0002 | t0002 | g0275 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18945 | hp2 | a0001 | c0001 | t0003 | g0228 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18946 | hp2 | a0002 | c0002 | t0002 | g0308 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18949 | hp1 | a0002 | c0002 | t0002 | g0136 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18950 | hp1 | a0001 | c0001 | t0003 | g0298 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18952 | hp2 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18953 | hp1 | a0001 | c0001 | t0003 | g0157 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18954 | hp1 | a0001 | c0001 | t0003 | g0253 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18956 | hp1 | a0002 | c0002 | t0002 | g0220 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18960 | hp1 | a0001 | c0001 | t0003 | g0244 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18960 | hp2 | a0002 | c0002 | t0002 | g0295 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18961 | hp1 | a0001 | c0001 | t0003 | g0205 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18961 | hp2 | a0002 | c0002 | t0002 | g0165 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18962 | hp2 | a0002 | c0002 | t0002 | g0207 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18963 | hp1 | a0002 | c0002 | t0033 | g0219 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18967 | hp1 | a0001 | c0001 | t0009 | g0161 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18967 | hp2 | a0001 | c0001 | t0068 | g0231 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18973 | hp1 | a0001 | c0001 | t0003 | g0248 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18974 | hp1 | a0002 | c0002 | t0002 | g0212 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18975 | hp2 | a0002 | c0002 | t0002 | g0071 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18977 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18982 | hp2 | a0001 | c0001 | t0003 | g0095 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18983 | hp2 | a0002 | c0002 | t0002 | g0121 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18984 | hp2 | a0001 | c0001 | t0003 | g0091 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18986 | hp1 | a0001 | c0001 | t0003 | g0233 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18986 | hp2 | a0002 | c0002 | t0002 | g0070 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18988 | hp2 | a0002 | c0002 | t0011 | g0260 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18992 | hp1 | a0002 | c0002 | t0002 | g0259 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18992 | hp2 | a0001 | c0001 | t0003 | g0238 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18995 | hp1 | a0002 | c0002 | t0002 | g0119 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18995 | hp2 | a0001 | c0001 | t0003 | g0241 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18998 | hp2 | a0002 | c0002 | t0002 | g0213 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18999 | hp1 | a0002 | c0002 | t0002 | g0177 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA19000 | hp1 | a0002 | c0002 | t0002 | g0137 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA19002 | hp1 | a0002 | c0002 | t0002 | g0084 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA19004 | hp2 | a0001 | c0001 | t0003 | g0297 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA19011 | hp2 | a0001 | c0001 | t0009 | g0194 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA19030 | hp1 | a0001 | c0005 | t0056 | g0266 | AFR | LWK | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA19030 | hp2 | a0001 | c0001 | t0008 | g0045 | AFR | LWK | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA19043 | hp1 | a0001 | c0001 | t0024 | g0277 | AFR | LWK | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA19043 | hp2 | a0001 | c0001 | t0065 | g0051 | AFR | LWK | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA19058 | hp1 | a0001 | c0001 | t0003 | g0313 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA19058 | hp2 | a0002 | c0002 | t0027 | g0227 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA19060 | hp2 | a0002 | c0002 | t0020 | g0225 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA19062 | hp1 | a0001 | c0001 | t0003 | g0288 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA19062 | hp2 | a0002 | c0002 | t0002 | g0089 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA19070 | hp1 | a0001 | c0001 | t0031 | g0291 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA19077 | hp1 | a0002 | c0002 | t0002 | g0255 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA19078 | hp1 | a0002 | c0002 | t0002 | g0274 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA19078 | hp2 | a0001 | c0001 | t0003 | g0239 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA19081 | hp1 | a0001 | c0001 | t0057 | g0281 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA19081 | hp2 | a0002 | c0002 | t0002 | g0218 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA19083 | hp2 | a0001 | c0001 | t0003 | g0252 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA19087 | hp1 | a0001 | c0001 | t0034 | g0159 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA19088 | hp2 | a0001 | c0001 | t0067 | g0264 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA19090 | hp1 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA19090 | hp2 | a0002 | c0002 | t0002 | g0310 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | YRI | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA19240 | hp2 | a0001 | c0003 | t0004 | g0037 | AFR | YRI | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0129 | AFR | ASW | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | ASW | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0292 | EUR | TSI | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA20752 | hp2 | a0002 | c0002 | t0002 | g0272 | EUR | TSI | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0273 | EUR | TSI | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA20805 | hp2 | a0002 | c0002 | t0002 | g0005 | EUR | TSI | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02109 | hp1 | a0001 | c0001 | t0037 | g0059 | AFR | ACB | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02109 | hp2 | a0001 | c0004 | t0062 | g0135 | AFR | ACB | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02486 | hp1 | a0001 | c0001 | t0007 | g0152 | AFR | ACB | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG02486 | hp2 | a0001 | c0001 | t0008 | g0134 | AFR | ACB | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG03471 | hp1 | a0001 | c0001 | t0024 | g0263 | AFR | MSL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | MSL | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18955 | hp1 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA18955 | hp2 | a0002 | c0002 | t0002 | g0214 | EAS | JPT | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA21309 | hp1 | a0001 | c0001 | t0004 | g0140 | AFR | LWK | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | LWK | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
homoSapiens | chm13v2 | a0001 | c0001 | t0010 | g0131 | REF | REF | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
homoSapiens | grch38p0 | a0001 | c0001 | t0009 | g0190 | REF | REF | NPR3_chr5_32706321_32796720 | NPR3 | chr5 | 32706321 | 32796720 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:32786283 | A | G | 1 | a0002 | 68 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(65): Show |
missense_variant | MODERATE | c.1564A>G | p.Asn522Asp | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 2020/7457 | 1564/1626 | 522/541 | chr5 | 32786283 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:32712013 | T | C | 1 | a0001c0003 | 14 | HG01109.hp2 HG02258.hp2 HG02622.hp1 others(11): Show |
synonymous_variant | LOW | c.237T>C | p.Ala79Ala | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/8 | 693/7457 | 237/1626 | 79/541 | chr5 | 32712013 | |||
chr5:32774734 | C | T | 1 | a0001c0006 | 1 | HG02055.hp2 | synonymous_variant | LOW | c.1086C>T | p.His362His | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/8 | 1542/7457 | 1086/1626 | 362/541 | chr5 | 32774734 | |||
chr5:32780759 | C | T | 1 | a0001c0005 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.1233C>T | p.Asp411Asp | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 5/8 | 1689/7457 | 1233/1626 | 411/541 | chr5 | 32780759 | |||
chr5:32784833 | C | T | 2 | a0001c0004 a0001c0006 |
2 | HG02055.hp2 HG02109.hp2 |
synonymous_variant | LOW | c.1464C>T | p.Val488Val | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 7/8 | 1920/7457 | 1464/1626 | 488/541 | chr5 | 32784833 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:32711527 | C | A | 6 | a0001c0001t0010 a0001c0001t0014 a0001c0001t0015 others(3): Show |
13 | HG00280.hp1 HG01070.hp1 HG01168.hp1 others(10): Show |
5_prime_UTR_variant | MODIFIER | c.-250C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/8 | 250 | chr5 | 32711527 | ||||||
chr5:32711547 | A | ACTTTTT | 60 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(57): Show |
296 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(293): Show |
5_prime_UTR_variant | MODIFIER | c.-211_-206dupCTTTTT | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/8 | 205 | INFO_REALIGN_3_PRIME | chr5 | 32711547 | |||||
chr5:32711547 | A | ACTTTTTC others(5): Show |
3 | a0001c0001t0013 a0001c0001t0031 a0002c0002t0016 |
6 | HG01934.hp1 HG01952.hp2 HG01981.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-217_-206dupCTTTTT others(6): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/8 | 205 | INFO_REALIGN_3_PRIME | chr5 | 32711547 | |||||
chr5:32711566 | C | CTTTTTCT | 5 | a0001c0001t0025 a0001c0001t0026 a0001c0001t0064 others(2): Show |
7 | HG02622.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-206_-205insCTTTTT others(1): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/8 | 205 | INFO_REALIGN_3_PRIME | chr5 | 32711566 | |||||
chr5:32711567 | T | TTTTTCTT others(4): Show |
1 | a0001c0001t0030 | 1 | HG01993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-206_-205insCTTTTT others(5): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/8 | 205 | INFO_REALIGN_3_PRIME | chr5 | 32711567 | |||||
chr5:32711576 | T | A | 2 | a0001c0001t0006 a0001c0001t0017 |
8 | HG01243.hp1 HG01891.hp2 HG02258.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-201T>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/8 | 201 | chr5 | 32711576 | ||||||
chr5:32711771 | G | C | 5 | a0001c0001t0025 a0001c0001t0026 a0001c0001t0064 others(2): Show |
7 | HG02622.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-6G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/8 | 6 | chr5 | 32711771 | ||||||
chr5:32786531 | T | C | 1 | a0002c0002t0018 | 2 | HG02895.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*186T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 186 | chr5 | 32786531 | ||||||
chr5:32786545 | A | G | 7 | a0001c0001t0005 a0001c0001t0024 a0001c0001t0026 others(4): Show |
16 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*200A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 200 | chr5 | 32786545 | ||||||
chr5:32786573 | T | C | 1 | a0001c0001t0019 | 2 | HG02886.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*228T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 228 | chr5 | 32786573 | ||||||
chr5:32786600 | C | G | 12 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0024 others(9): Show |
25 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*255C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 255 | chr5 | 32786600 | ||||||
chr5:32786607 | G | A | 1 | a0001c0001t0032 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*262G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 262 | chr5 | 32786607 | ||||||
chr5:32786680 | T | C | 1 | a0002c0002t0020 | 2 | HG02040.hp1 NA19060.hp2 |
3_prime_UTR_variant | MODIFIER | c.*335T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 335 | chr5 | 32786680 | ||||||
chr5:32786738 | G | A | 1 | a0001c0001t0014 | 2 | HG01257.hp2 HG01258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*393G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 393 | chr5 | 32786738 | ||||||
chr5:32786894 | A | G | 7 | a0001c0001t0005 a0001c0001t0024 a0001c0001t0026 others(4): Show |
16 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*549A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 549 | chr5 | 32786894 | ||||||
chr5:32786942 | C | T | 12 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0024 others(9): Show |
25 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*597C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 597 | chr5 | 32786942 | ||||||
chr5:32787025 | T | TA | 8 | a0001c0001t0005 a0001c0001t0024 a0001c0001t0026 others(5): Show |
18 | HG02109.hp2 HG02145.hp1 HG02258.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*691dupA | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 692 | INFO_REALIGN_3_PRIME | chr5 | 32787025 | |||||
chr5:32787025 | T | TAA | 4 | a0001c0001t0008 a0001c0001t0059 a0001c0003t0008 others(1): Show |
7 | HG02055.hp2 HG02257.hp1 HG02486.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*690_*691dupAA | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 692 | INFO_REALIGN_3_PRIME | chr5 | 32787025 | |||||
chr5:32787047 | G | A | 1 | a0001c0003t0023 | 2 | HG02622.hp1 HG02896.hp1 |
3_prime_UTR_variant | MODIFIER | c.*702G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 702 | chr5 | 32787047 | ||||||
chr5:32787095 | A | G | 8 | a0001c0001t0005 a0001c0001t0024 a0001c0001t0026 others(5): Show |
17 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*750A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 750 | chr5 | 32787095 | ||||||
chr5:32787182 | G | C | 1 | a0002c0002t0033 | 1 | NA18963.hp1 | 3_prime_UTR_variant | MODIFIER | c.*837G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 837 | chr5 | 32787182 | ||||||
chr5:32787192 | A | C | 8 | a0001c0001t0005 a0001c0001t0024 a0001c0001t0026 others(5): Show |
17 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*847A>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 847 | chr5 | 32787192 | ||||||
chr5:32787311 | C | A | 5 | a0001c0001t0008 a0001c0001t0059 a0001c0001t0060 others(2): Show |
9 | HG02257.hp1 HG02486.hp2 HG02622.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*966C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 966 | chr5 | 32787311 | ||||||
chr5:32787328 | G | A | 1 | a0001c0001t0034 | 1 | NA19087.hp1 | 3_prime_UTR_variant | MODIFIER | c.*983G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 983 | chr5 | 32787328 | ||||||
chr5:32787387 | C | T | 1 | a0001c0001t0068 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1042C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 1042 | chr5 | 32787387 | ||||||
chr5:32787411 | T | C | 4 | a0001c0001t0008 a0001c0001t0059 a0001c0001t0060 others(1): Show |
7 | HG02257.hp1 HG02486.hp2 HG02717.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1066T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 1066 | chr5 | 32787411 | ||||||
chr5:32787526 | T | G | 1 | a0002c0002t0035 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1181T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 1181 | chr5 | 32787526 | ||||||
chr5:32787564 | T | A | 1 | a0001c0001t0036 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1219T>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 1219 | chr5 | 32787564 | ||||||
chr5:32787779 | T | C | 1 | a0001c0001t0037 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1434T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 1434 | chr5 | 32787779 | ||||||
chr5:32787871 | A | G | 1 | a0001c0001t0057 | 1 | NA19081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1526A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 1526 | chr5 | 32787871 | ||||||
chr5:32787877 | T | A | 1 | a0001c0001t0038 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1532T>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 1532 | chr5 | 32787877 | ||||||
chr5:32787939 | T | G | 13 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0024 others(10): Show |
26 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1594T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 1594 | chr5 | 32787939 | ||||||
chr5:32787995 | A | G | 5 | a0001c0001t0008 a0001c0001t0059 a0001c0001t0060 others(2): Show |
9 | HG02257.hp1 HG02486.hp2 HG02622.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1650A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 1650 | chr5 | 32787995 | ||||||
chr5:32788078 | C | T | 40 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(37): Show |
160 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(157): Show |
3_prime_UTR_variant | MODIFIER | c.*1733C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 1733 | chr5 | 32788078 | ||||||
chr5:32788263 | G | A | 25 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0010 others(22): Show |
132 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(129): Show |
3_prime_UTR_variant | MODIFIER | c.*1918G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 1918 | chr5 | 32788263 | ||||||
chr5:32788300 | C | A | 3 | a0001c0001t0007 a0001c0001t0039 a0001c0001t0064 |
8 | HG01106.hp2 HG01934.hp2 HG02451.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1955C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 1955 | chr5 | 32788300 | ||||||
chr5:32788362 | G | A | 1 | a0001c0001t0040 | 1 | HG01261.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2017G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 2017 | chr5 | 32788362 | ||||||
chr5:32788368 | C | T | 1 | a0001c0003t0063 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2023C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 2023 | chr5 | 32788368 | ||||||
chr5:32788420 | C | G | 8 | a0001c0001t0005 a0001c0001t0024 a0001c0001t0026 others(5): Show |
17 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2075C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 2075 | chr5 | 32788420 | ||||||
chr5:32788420 | C | T | 1 | a0001c0001t0034 | 1 | NA19087.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2075C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 2075 | chr5 | 32788420 | ||||||
chr5:32788441 | G | T | 1 | a0001c0001t0051 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2096G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 2096 | chr5 | 32788441 | ||||||
chr5:32788582 | C | T | 1 | a0001c0001t0055 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2237C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 2237 | chr5 | 32788582 | ||||||
chr5:32788590 | G | A | 2 | a0001c0001t0022 a0001c0001t0028 |
3 | HG00280.hp2 HG01256.hp1 HG02735.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2245G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 2245 | chr5 | 32788590 | ||||||
chr5:32788730 | G | A | 5 | a0001c0001t0008 a0001c0001t0059 a0001c0001t0060 others(2): Show |
9 | HG02257.hp1 HG02486.hp2 HG02622.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2385G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 2385 | chr5 | 32788730 | ||||||
chr5:32788832 | T | G | 1 | a0002c0002t0052 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2487T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 2487 | chr5 | 32788832 | ||||||
chr5:32788975 | G | A | 13 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0024 others(10): Show |
26 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*2630G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 2630 | chr5 | 32788975 | ||||||
chr5:32788999 | T | C | 13 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0024 others(10): Show |
26 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*2654T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 2654 | chr5 | 32788999 | ||||||
chr5:32789089 | CT | C | 11 | a0001c0001t0003 a0001c0001t0010 a0001c0001t0022 others(8): Show |
60 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*2747delT | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 2747 | INFO_REALIGN_3_PRIME | chr5 | 32789089 | |||||
chr5:32789286 | G | A | 25 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0010 others(22): Show |
132 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(129): Show |
3_prime_UTR_variant | MODIFIER | c.*2941G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 2941 | chr5 | 32789286 | ||||||
chr5:32789287 | TA | T | 11 | a0001c0001t0003 a0001c0001t0010 a0001c0001t0022 others(8): Show |
60 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*2943delA | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 2943 | chr5 | 32789287 | ||||||
chr5:32789366 | G | T | 1 | a0001c0001t0050 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3021G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 3021 | chr5 | 32789366 | ||||||
chr5:32789415 | T | C | 1 | a0001c0001t0065 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3070T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 3070 | chr5 | 32789415 | ||||||
chr5:32789507 | T | C | 1 | a0001c0001t0041 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3162T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 3162 | chr5 | 32789507 | ||||||
chr5:32789641 | A | T | 1 | a0001c0001t0049 | 1 | HG01168.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3296A>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 3296 | chr5 | 32789641 | ||||||
chr5:32789702 | A | T | 1 | a0001c0004t0062 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3357A>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 3357 | chr5 | 32789702 | ||||||
chr5:32789746 | T | C | 57 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(54): Show |
201 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(198): Show |
3_prime_UTR_variant | MODIFIER | c.*3401T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 3401 | chr5 | 32789746 | ||||||
chr5:32789813 | G | A | 1 | a0002c0002t0054 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3468G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 3468 | chr5 | 32789813 | ||||||
chr5:32789852 | G | A | 7 | a0001c0001t0005 a0001c0001t0024 a0001c0001t0026 others(4): Show |
16 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*3507G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 3507 | chr5 | 32789852 | ||||||
chr5:32790019 | A | G | 3 | a0001c0001t0037 a0001c0001t0065 a0001c0003t0058 |
3 | HG02109.hp1 HG02886.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3674A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 3674 | chr5 | 32790019 | ||||||
chr5:32790133 | T | C | 1 | a0001c0001t0064 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3788T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 3788 | chr5 | 32790133 | ||||||
chr5:32790168 | G | A | 1 | a0001c0001t0019 | 2 | HG02886.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3823G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 3823 | chr5 | 32790168 | ||||||
chr5:32790262 | C | CAGCAAGA others(16): Show |
11 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0024 others(8): Show |
24 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*3926_*3927insCATG others(19): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 3927 | INFO_REALIGN_3_PRIME | chr5 | 32790262 | |||||
chr5:32790325 | C | G | 1 | a0001c0001t0045 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3980C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 3980 | chr5 | 32790325 | ||||||
chr5:32790352 | CTCCACCC others(3): Show |
C | 11 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0024 others(8): Show |
24 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*4013_*4022delCCAC others(6): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 4013 | INFO_REALIGN_3_PRIME | chr5 | 32790352 | |||||
chr5:32790384 | A | G | 1 | a0001c0001t0019 | 2 | HG02886.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4039A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 4039 | chr5 | 32790384 | ||||||
chr5:32790429 | G | A | 5 | a0001c0001t0008 a0001c0001t0059 a0001c0001t0060 others(2): Show |
9 | HG02257.hp1 HG02486.hp2 HG02622.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4084G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 4084 | chr5 | 32790429 | ||||||
chr5:32790510 | T | C | 27 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0010 others(24): Show |
134 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(131): Show |
3_prime_UTR_variant | MODIFIER | c.*4165T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 4165 | chr5 | 32790510 | ||||||
chr5:32790535 | G | A | 1 | a0001c0001t0039 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4190G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 4190 | chr5 | 32790535 | ||||||
chr5:32790672 | G | T | 1 | a0001c0003t0044 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4327G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 4327 | chr5 | 32790672 | ||||||
chr5:32790673 | G | C | 1 | a0001c0003t0044 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4328G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 4328 | chr5 | 32790673 | ||||||
chr5:32790722 | C | T | 1 | a0001c0001t0019 | 2 | HG02886.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4377C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 4377 | chr5 | 32790722 | ||||||
chr5:32790729 | A | G | 11 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0024 others(8): Show |
24 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*4384A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 4384 | chr5 | 32790729 | ||||||
chr5:32790739 | A | T | 2 | a0001c0001t0024 a0001c0003t0063 |
3 | HG03471.hp1 HG03579.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4394A>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 4394 | chr5 | 32790739 | ||||||
chr5:32790812 | G | C | 13 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0014 others(10): Show |
37 | HG00735.hp2 HG00741.hp1 HG01070.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*4467G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 4467 | chr5 | 32790812 | ||||||
chr5:32790814 | T | C | 2 | a0001c0001t0037 a0001c0003t0058 |
2 | HG02109.hp1 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4469T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 4469 | chr5 | 32790814 | ||||||
chr5:32790865 | G | A | 1 | a0001c0001t0053 | 1 | HG02074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4520G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 4520 | chr5 | 32790865 | ||||||
chr5:32790933 | T | C | 12 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0024 others(9): Show |
25 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*4588T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 4588 | chr5 | 32790933 | ||||||
chr5:32791051 | G | A | 1 | a0001c0001t0041 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4706G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 4706 | chr5 | 32791051 | ||||||
chr5:32791058 | G | A | 7 | a0001c0001t0005 a0001c0001t0024 a0001c0001t0026 others(4): Show |
16 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*4713G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 4713 | chr5 | 32791058 | ||||||
chr5:32791147 | T | G | 3 | a0001c0001t0017 a0001c0001t0021 a0001c0003t0044 |
5 | HG01884.hp1 HG02965.hp1 HG02976.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4802T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 4802 | chr5 | 32791147 | ||||||
chr5:32791187 | A | T | 1 | a0001c0001t0048 | 1 | NA18612.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4842A>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 4842 | chr5 | 32791187 | ||||||
chr5:32791205 | G | C | 1 | a0001c0001t0046 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4860G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 4860 | chr5 | 32791205 | ||||||
chr5:32791215 | G | A | 12 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0024 others(9): Show |
25 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*4870G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 4870 | chr5 | 32791215 | ||||||
chr5:32791345 | C | T | 1 | a0002c0002t0012 | 4 | HG00642.hp2 HG01099.hp2 HG01106.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5000C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 5000 | chr5 | 32791345 | ||||||
chr5:32791371 | G | A | 1 | a0001c0001t0042 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5026G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 5026 | chr5 | 32791371 | ||||||
chr5:32791378 | C | T | 1 | a0001c0001t0057 | 1 | NA19081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5033C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 5033 | chr5 | 32791378 | ||||||
chr5:32791420 | G | A | 1 | a0001c0001t0065 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5075G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 5075 | chr5 | 32791420 | ||||||
chr5:32791571 | C | A | 1 | a0001c0001t0047 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5226C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 5226 | chr5 | 32791571 | ||||||
chr5:32791625 | T | C | 1 | a0001c0006t0061 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5280T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 8/8 | 5280 | chr5 | 32791625 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:32712568 | C | T | 13 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0001g0307 others(10): Show |
13 | HG00544.hp1 HG02074.hp1 NA18612.hp1 others(10): Show |
intron_variant | MODIFIER | c.769+23C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32712568 | |||||||
chr5:32712689 | C | T | 4 | a0001c0001t0004g0299 a0001c0001t0004g0300 a0001c0001t0004g0302 others(1): Show |
4 | HG02257.hp1 HG02922.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.769+144C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32712689 | |||||||
chr5:32712693 | T | A | 4 | a0001c0001t0002g0008 a0001c0001t0019g0006 a0001c0001t0019g0007 others(1): Show |
4 | HG01257.hp1 HG02886.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.769+148T>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32712693 | |||||||
chr5:32712725 | C | T | 34 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0273 others(31): Show |
35 | HG00323.hp2 HG01099.hp2 HG01346.hp1 others(32): Show |
intron_variant | MODIFIER | c.769+180C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32712725 | |||||||
chr5:32712795 | A | C | 1 | a0001c0001t0039g0265 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.769+250A>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32712795 | |||||||
chr5:32712843 | T | A | 1 | a0001c0001t0006g0010 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.769+298T>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32712843 | |||||||
chr5:32713002 | G | C | 103 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(100): Show |
106 | HG00323.hp2 HG00735.hp1 HG00738.hp2 others(103): Show |
intron_variant | MODIFIER | c.769+457G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32713002 | |||||||
chr5:32713026 | G | A | 34 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0273 others(31): Show |
35 | HG00323.hp2 HG01099.hp2 HG01346.hp1 others(32): Show |
intron_variant | MODIFIER | c.769+481G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32713026 | |||||||
chr5:32713151 | C | T | 1 | a0001c0001t0043g0067 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.769+606C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32713151 | |||||||
chr5:32713166 | T | C | 3 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0002c0002t0002g0070 |
3 | NA18954.hp2 NA18986.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.769+621T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32713166 | |||||||
chr5:32713221 | T | C | 79 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(76): Show |
82 | HG00323.hp2 HG00735.hp1 HG00738.hp2 others(79): Show |
intron_variant | MODIFIER | c.769+676T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32713221 | |||||||
chr5:32713259 | T | G | 19 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(16): Show |
20 | HG00735.hp1 HG00738.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.769+714T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32713259 | |||||||
chr5:32713392 | C | A | 1 | a0001c0001t0001g0011 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.769+847C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32713392 | |||||||
chr5:32713562 | C | A | 1 | a0001c0001t0043g0067 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.769+1017C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32713562 | |||||||
chr5:32713563 | G | T | 1 | a0001c0001t0067g0264 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.769+1018G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32713563 | |||||||
chr5:32713730 | A | G | 79 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(76): Show |
82 | HG00323.hp2 HG00735.hp1 HG00738.hp2 others(79): Show |
intron_variant | MODIFIER | c.769+1185A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32713730 | |||||||
chr5:32713781 | G | A | 1 | a0002c0002t0002g0071 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.769+1236G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32713781 | |||||||
chr5:32713900 | G | C | 1 | a0002c0002t0002g0072 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.769+1355G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32713900 | |||||||
chr5:32713932 | C | T | 1 | a0001c0001t0050g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.769+1387C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32713932 | |||||||
chr5:32714013 | A | G | 2 | a0001c0001t0004g0027 a0001c0001t0004g0028 |
2 | HG01496.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.769+1468A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32714013 | |||||||
chr5:32714017 | A | C | 1 | a0001c0001t0050g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.769+1472A>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32714017 | |||||||
chr5:32714079 | C | G | 4 | a0001c0001t0003g0296 a0001c0001t0003g0297 a0001c0001t0003g0298 others(1): Show |
4 | HG02083.hp1 NA18950.hp1 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.769+1534C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32714079 | |||||||
chr5:32714164 | C | G | 79 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(76): Show |
82 | HG00323.hp2 HG00735.hp1 HG00738.hp2 others(79): Show |
intron_variant | MODIFIER | c.769+1619C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32714164 | |||||||
chr5:32714165 | G | T | 1 | a0001c0001t0004g0302 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.769+1620G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32714165 | |||||||
chr5:32714170 | G | C | 1 | a0001c0001t0004g0073 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.769+1625G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32714170 | |||||||
chr5:32714188 | C | G | 1 | a0001c0001t0004g0294 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.769+1643C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32714188 | |||||||
chr5:32714258 | G | T | 6 | a0001c0001t0001g0043 a0001c0001t0004g0044 a0001c0001t0008g0045 others(3): Show |
6 | HG02055.hp2 HG02451.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.769+1713G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32714258 | |||||||
chr5:32714327 | C | T | 12 | a0001c0001t0001g0056 a0001c0001t0001g0060 a0001c0001t0001g0061 others(9): Show |
12 | HG01192.hp2 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.769+1782C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32714327 | |||||||
chr5:32714360 | C | G | 1 | a0001c0001t0001g0026 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.769+1815C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32714360 | |||||||
chr5:32714370 | G | C | 1 | a0001c0001t0007g0074 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.769+1825G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32714370 | |||||||
chr5:32714491 | C | A | 1 | a0001c0001t0001g0068 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.769+1946C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32714491 | |||||||
chr5:32714505 | CT | C | 80 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(77): Show |
82 | HG00323.hp2 HG00735.hp1 HG00738.hp2 others(79): Show |
intron_variant | MODIFIER | c.769+1975delT | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 32714505 | ||||||
chr5:32714505 | CTT | C | 7 | a0001c0003t0001g0034 a0001c0003t0005g0002 a0001c0003t0005g0029 others(4): Show |
8 | HG01109.hp2 HG02258.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.769+1974_769+1975d others(4): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 32714505 | ||||||
chr5:32714514 | T | C | 4 | a0001c0001t0002g0008 a0001c0001t0019g0006 a0001c0001t0019g0007 others(1): Show |
4 | HG01257.hp1 HG02886.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.769+1969T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32714514 | |||||||
chr5:32714555 | C | T | 40 | a0001c0001t0001g0043 a0001c0001t0001g0267 a0001c0001t0001g0268 others(37): Show |
41 | HG00323.hp2 HG01099.hp2 HG01346.hp1 others(38): Show |
intron_variant | MODIFIER | c.769+2010C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32714555 | |||||||
chr5:32714781 | A | G | 17 | a0001c0001t0001g0056 a0001c0001t0001g0060 a0001c0001t0001g0061 others(14): Show |
17 | HG01192.hp2 HG01884.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.769+2236A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32714781 | |||||||
chr5:32715029 | C | T | 41 | a0001c0001t0001g0043 a0001c0001t0001g0267 a0001c0001t0001g0268 others(38): Show |
42 | HG00323.hp2 HG01099.hp2 HG01346.hp1 others(39): Show |
intron_variant | MODIFIER | c.769+2484C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32715029 | |||||||
chr5:32715157 | C | A | 2 | a0002c0002t0018g0076 a0002c0002t0018g0077 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.769+2612C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32715157 | |||||||
chr5:32715414 | C | T | 1 | a0001c0001t0024g0263 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.769+2869C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32715414 | |||||||
chr5:32715804 | T | C | 4 | a0001c0001t0002g0008 a0001c0001t0019g0006 a0001c0001t0019g0007 others(1): Show |
4 | HG01257.hp1 HG02886.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.769+3259T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32715804 | |||||||
chr5:32716002 | C | T | 2 | a0001c0001t0043g0067 a0001c0001t0050g0047 |
2 | HG02615.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.769+3457C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32716002 | |||||||
chr5:32716060 | C | T | 3 | a0002c0002t0011g0260 a0002c0002t0011g0261 a0002c0002t0011g0262 |
3 | HG01978.hp1 HG04228.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.769+3515C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32716060 | |||||||
chr5:32716115 | A | C | 4 | a0001c0001t0002g0008 a0001c0001t0019g0006 a0001c0001t0019g0007 others(1): Show |
4 | HG01257.hp1 HG02886.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.769+3570A>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32716115 | |||||||
chr5:32716202 | A | G | 13 | a0001c0003t0001g0034 a0001c0003t0004g0037 a0001c0003t0005g0002 others(10): Show |
14 | HG01109.hp2 HG02258.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.769+3657A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32716202 | |||||||
chr5:32716281 | C | T | 1 | a0002c0002t0002g0259 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.769+3736C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32716281 | |||||||
chr5:32716368 | C | CT | 87 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(84): Show |
90 | HG00323.hp2 HG00735.hp1 HG00738.hp2 others(87): Show |
intron_variant | MODIFIER | c.769+3835dupT | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 32716368 | ||||||
chr5:32716368 | C | CTT | 16 | a0001c0001t0001g0056 a0001c0001t0001g0060 a0001c0001t0001g0061 others(13): Show |
16 | HG01192.hp2 HG01884.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.769+3834_769+3835d others(4): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 32716368 | ||||||
chr5:32716429 | C | T | 40 | a0001c0001t0001g0043 a0001c0001t0001g0267 a0001c0001t0001g0268 others(37): Show |
41 | HG00323.hp2 HG01099.hp2 HG01346.hp1 others(38): Show |
intron_variant | MODIFIER | c.769+3884C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32716429 | |||||||
chr5:32716446 | C | T | 16 | a0001c0001t0001g0056 a0001c0001t0001g0060 a0001c0001t0001g0061 others(13): Show |
16 | HG01192.hp2 HG01884.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.769+3901C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32716446 | |||||||
chr5:32716483 | T | C | 36 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(33): Show |
38 | HG00735.hp1 HG00738.hp2 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.769+3938T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32716483 | |||||||
chr5:32716658 | T | C | 2 | a0001c0001t0001g0078 a0001c0001t0005g0079 |
2 | HG02280.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.769+4113T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32716658 | |||||||
chr5:32716894 | G | A | 1 | a0001c0001t0067g0264 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.769+4349G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32716894 | |||||||
chr5:32716996 | AC | A | 79 | a0001c0001t0001g0085 a0001c0001t0001g0088 a0001c0001t0001g0090 others(76): Show |
80 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.769+4458delC | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 32716996 | ||||||
chr5:32716998 | C | A | 79 | a0001c0001t0001g0085 a0001c0001t0001g0088 a0001c0001t0001g0090 others(76): Show |
80 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.769+4453C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32716998 | |||||||
chr5:32717122 | C | T | 79 | a0001c0001t0001g0085 a0001c0001t0001g0088 a0001c0001t0001g0090 others(76): Show |
80 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.769+4577C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32717122 | |||||||
chr5:32717151 | G | A | 16 | a0001c0001t0001g0056 a0001c0001t0001g0060 a0001c0001t0001g0061 others(13): Show |
16 | HG01192.hp2 HG01884.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.769+4606G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32717151 | |||||||
chr5:32717175 | A | G | 4 | a0001c0001t0002g0008 a0001c0001t0019g0006 a0001c0001t0019g0007 others(1): Show |
4 | HG01257.hp1 HG02886.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.769+4630A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32717175 | |||||||
chr5:32717212 | A | G | 6 | a0001c0001t0001g0043 a0001c0001t0004g0044 a0001c0001t0008g0045 others(3): Show |
6 | HG02055.hp2 HG02451.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.769+4667A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32717212 | |||||||
chr5:32717283 | T | G | 4 | a0001c0001t0004g0299 a0001c0001t0004g0300 a0001c0001t0004g0302 others(1): Show |
4 | HG02257.hp1 HG02922.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.769+4738T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32717283 | |||||||
chr5:32717443 | G | A | 1 | a0001c0001t0024g0263 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.769+4898G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32717443 | |||||||
chr5:32717853 | AGT | A | 36 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(33): Show |
38 | HG00735.hp1 HG00738.hp2 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.769+5309_769+5310d others(4): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32717853 | |||||||
chr5:32717938 | C | T | 175 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(172): Show |
179 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.769+5393C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32717938 | |||||||
chr5:32718175 | C | T | 62 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0206 others(59): Show |
63 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.769+5630C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32718175 | |||||||
chr5:32718275 | A | G | 4 | a0001c0001t0006g0063 a0001c0001t0006g0065 a0001c0001t0006g0066 others(1): Show |
4 | HG01891.hp2 HG02630.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.769+5730A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32718275 | |||||||
chr5:32718391 | C | T | 1 | a0001c0001t0031g0291 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.769+5846C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32718391 | |||||||
chr5:32718501 | C | T | 79 | a0001c0001t0001g0085 a0001c0001t0001g0088 a0001c0001t0001g0090 others(76): Show |
80 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.769+5956C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32718501 | |||||||
chr5:32718752 | A | C | 32 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(29): Show |
34 | HG00735.hp1 HG00738.hp2 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.770-5946A>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32718752 | |||||||
chr5:32719324 | C | T | 1 | a0001c0001t0050g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.770-5374C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32719324 | |||||||
chr5:32719484 | T | C | 1 | a0001c0001t0001g0267 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.770-5214T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32719484 | |||||||
chr5:32719509 | G | A | 1 | a0001c0001t0003g0203 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.770-5189G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32719509 | |||||||
chr5:32719587 | C | T | 175 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(172): Show |
179 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.770-5111C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32719587 | |||||||
chr5:32719651 | A | C | 1 | a0001c0001t0043g0067 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.770-5047A>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32719651 | |||||||
chr5:32719705 | G | A | 79 | a0001c0001t0001g0085 a0001c0001t0001g0088 a0001c0001t0001g0090 others(76): Show |
80 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.770-4993G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32719705 | |||||||
chr5:32719723 | ATGCTAGA others(120): Show |
A | 1 | a0001c0001t0025g0048 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.770-4972_770-4846d others(2): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 32719723 | ||||||
chr5:32719785 | G | GT | 9 | a0001c0001t0001g0043 a0001c0001t0004g0044 a0001c0001t0004g0299 others(6): Show |
9 | HG02257.hp1 HG02451.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.770-4911dupT | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 32719785 | ||||||
chr5:32719787 | TG | T | 113 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(110): Show |
115 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.770-4910delG | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32719787 | |||||||
chr5:32719788 | G | T | 66 | a0001c0001t0001g0043 a0001c0001t0001g0056 a0001c0001t0001g0060 others(63): Show |
67 | HG00323.hp2 HG01099.hp2 HG01109.hp1 others(64): Show |
intron_variant | MODIFIER | c.770-4910G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32719788 | |||||||
chr5:32719790 | T | G | 3 | a0001c0001t0045g0099 a0002c0002t0012g0107 a0002c0002t0012g0108 |
3 | HG00642.hp2 HG00735.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.770-4908T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32719790 | |||||||
chr5:32719924 | A | G | 4 | a0001c0001t0002g0008 a0001c0001t0019g0006 a0001c0001t0019g0007 others(1): Show |
4 | HG01257.hp1 HG02886.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.770-4774A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32719924 | |||||||
chr5:32720000 | C | T | 1 | a0002c0002t0011g0130 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.770-4698C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32720000 | |||||||
chr5:32720039 | C | T | 4 | a0001c0001t0002g0008 a0001c0001t0019g0006 a0001c0001t0019g0007 others(1): Show |
4 | HG01257.hp1 HG02886.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.770-4659C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32720039 | |||||||
chr5:32720053 | G | T | 1 | a0001c0001t0001g0202 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.770-4645G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32720053 | |||||||
chr5:32720208 | A | T | 1 | a0002c0002t0016g0290 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.770-4490A>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32720208 | |||||||
chr5:32720393 | A | G | 4 | a0001c0001t0002g0008 a0001c0001t0019g0006 a0001c0001t0019g0007 others(1): Show |
4 | HG01257.hp1 HG02886.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.770-4305A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32720393 | |||||||
chr5:32720401 | A | C | 3 | a0001c0001t0002g0129 a0001c0001t0008g0128 a0002c0002t0027g0127 |
3 | HG02055.hp1 HG02976.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.770-4297A>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32720401 | |||||||
chr5:32720789 | T | C | 4 | a0001c0001t0004g0299 a0001c0001t0004g0300 a0001c0001t0004g0302 others(1): Show |
4 | HG02257.hp1 HG02922.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.770-3909T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32720789 | |||||||
chr5:32720798 | G | T | 1 | a0001c0001t0039g0265 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.770-3900G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32720798 | |||||||
chr5:32720823 | T | C | 1 | a0001c0001t0001g0268 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.770-3875T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32720823 | |||||||
chr5:32720877 | G | T | 1 | a0001c0001t0001g0257 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.770-3821G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32720877 | |||||||
chr5:32721010 | G | T | 12 | a0001c0001t0001g0056 a0001c0001t0001g0060 a0001c0001t0001g0061 others(9): Show |
12 | HG01192.hp2 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.770-3688G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32721010 | |||||||
chr5:32721283 | A | T | 1 | a0001c0001t0001g0201 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.770-3415A>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32721283 | |||||||
chr5:32721387 | C | T | 2 | a0001c0001t0001g0056 a0001c0001t0001g0062 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.770-3311C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32721387 | |||||||
chr5:32721439 | G | A | 25 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(22): Show |
26 | HG00735.hp1 HG00738.hp2 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.770-3259G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32721439 | |||||||
chr5:32721454 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.770-3244C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32721454 | |||||||
chr5:32721488 | C | G | 34 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0273 others(31): Show |
35 | HG00323.hp2 HG01099.hp2 HG01346.hp1 others(32): Show |
intron_variant | MODIFIER | c.770-3210C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32721488 | |||||||
chr5:32721500 | G | A | 2 | a0002c0002t0018g0076 a0002c0002t0018g0077 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.770-3198G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32721500 | |||||||
chr5:32721690 | A | C | 1 | a0001c0001t0067g0264 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.770-3008A>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32721690 | |||||||
chr5:32721691 | AG | A | 4 | a0001c0001t0002g0008 a0001c0001t0019g0006 a0001c0001t0019g0007 others(1): Show |
4 | HG01257.hp1 HG02886.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.770-3006delG | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32721691 | |||||||
chr5:32722213 | G | A | 32 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(29): Show |
34 | HG00735.hp1 HG00738.hp2 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.770-2485G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32722213 | |||||||
chr5:32722214 | G | A | 15 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0206 others(12): Show |
15 | HG01069.hp2 HG02080.hp2 HG02083.hp2 others(12): Show |
intron_variant | MODIFIER | c.770-2484G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32722214 | |||||||
chr5:32722224 | C | G | 17 | a0001c0001t0001g0056 a0001c0001t0001g0060 a0001c0001t0001g0061 others(14): Show |
17 | HG01192.hp2 HG01884.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.770-2474C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32722224 | |||||||
chr5:32722228 | G | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(178): Show |
185 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.770-2470G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32722228 | |||||||
chr5:32722321 | C | A | 4 | a0001c0001t0002g0008 a0001c0001t0019g0006 a0001c0001t0019g0007 others(1): Show |
4 | HG01257.hp1 HG02886.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.770-2377C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32722321 | |||||||
chr5:32722327 | T | A | 6 | a0001c0001t0001g0043 a0001c0001t0004g0044 a0001c0001t0008g0045 others(3): Show |
6 | HG02055.hp2 HG02451.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.770-2371T>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32722327 | |||||||
chr5:32722382 | A | G | 4 | a0001c0001t0004g0299 a0001c0001t0004g0300 a0001c0001t0004g0302 others(1): Show |
4 | HG02257.hp1 HG02922.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.770-2316A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32722382 | |||||||
chr5:32722393 | T | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(178): Show |
185 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.770-2305T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32722393 | |||||||
chr5:32722529 | T | C | 1 | a0001c0001t0048g0303 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.770-2169T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32722529 | |||||||
chr5:32722544 | A | G | 1 | a0001c0001t0007g0200 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.770-2154A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32722544 | |||||||
chr5:32722576 | C | G | 6 | a0001c0001t0001g0056 a0001c0001t0001g0060 a0001c0001t0001g0061 others(3): Show |
6 | HG01192.hp2 HG01884.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.770-2122C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32722576 | |||||||
chr5:32722615 | C | G | 1 | a0001c0001t0001g0199 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.770-2083C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32722615 | |||||||
chr5:32722642 | C | T | 3 | a0001c0001t0001g0025 a0001c0001t0004g0027 a0001c0001t0004g0028 |
3 | HG01496.hp1 HG03239.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.770-2056C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32722642 | |||||||
chr5:32722665 | T | C | 7 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0008g0134 others(4): Show |
7 | HG02145.hp2 HG02486.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.770-2033T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32722665 | |||||||
chr5:32722795 | A | T | 1 | a0001c0001t0039g0265 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.770-1903A>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32722795 | |||||||
chr5:32722930 | C | T | 1 | a0001c0001t0039g0265 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.770-1768C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32722930 | |||||||
chr5:32723029 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.770-1669G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32723029 | |||||||
chr5:32723057 | A | C | 2 | a0001c0001t0001g0197 a0001c0001t0001g0198 |
2 | HG04204.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.770-1641A>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32723057 | |||||||
chr5:32723171 | G | T | 1 | a0001c0001t0003g0256 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.770-1527G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32723171 | |||||||
chr5:32723285 | T | C | 1 | a0001c0001t0043g0067 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.770-1413T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32723285 | |||||||
chr5:32723372 | G | A | 76 | a0001c0001t0001g0085 a0001c0001t0001g0088 a0001c0001t0001g0090 others(73): Show |
77 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.770-1326G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32723372 | |||||||
chr5:32723463 | G | A | 1 | a0001c0001t0050g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.770-1235G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32723463 | |||||||
chr5:32723524 | C | T | 2 | a0001c0001t0001g0195 a0001c0001t0001g0196 |
2 | HG01993.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.770-1174C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32723524 | |||||||
chr5:32723649 | T | C | 1 | a0002c0002t0002g0204 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.770-1049T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32723649 | |||||||
chr5:32723652 | G | A | 1 | a0001c0001t0003g0075 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.770-1046G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32723652 | |||||||
chr5:32723692 | G | T | 1 | a0001c0001t0003g0122 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.770-1006G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32723692 | |||||||
chr5:32723835 | C | T | 1 | a0002c0002t0002g0255 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.770-863C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32723835 | |||||||
chr5:32723875 | C | T | 6 | a0001c0001t0001g0056 a0001c0001t0001g0060 a0001c0001t0001g0061 others(3): Show |
6 | HG01192.hp2 HG01884.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.770-823C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32723875 | |||||||
chr5:32723943 | A | G | 1 | a0002c0002t0002g0070 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.770-755A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32723943 | |||||||
chr5:32723972 | C | G | 131 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(128): Show |
134 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.770-726C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32723972 | |||||||
chr5:32724134 | A | T | 4 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0003g0075 others(1): Show |
4 | HG01074.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.770-564A>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32724134 | |||||||
chr5:32724257 | C | T | 1 | a0001c0001t0001g0024 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.770-441C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32724257 | |||||||
chr5:32724353 | C | T | 2 | a0001c0001t0060g0289 a0001c0005t0056g0266 |
2 | HG03130.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.770-345C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32724353 | |||||||
chr5:32724368 | T | C | 2 | a0002c0002t0002g0136 a0002c0002t0002g0137 |
2 | NA18949.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.770-330T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32724368 | |||||||
chr5:32724529 | G | A | 2 | a0001c0001t0051g0269 a0002c0002t0002g0270 |
2 | HG02818.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.770-169G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 1/7 | chr5 | 32724529 | |||||||
chr5:32724836 | C | A | 1 | a0001c0001t0007g0138 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.892+16C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32724836 | |||||||
chr5:32724846 | C | G | 1 | a0002c0002t0035g0124 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.892+26C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32724846 | |||||||
chr5:32724924 | C | G | 1 | a0001c0001t0002g0129 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.892+104C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32724924 | |||||||
chr5:32724965 | C | T | 1 | a0001c0005t0056g0266 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.892+145C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32724965 | |||||||
chr5:32724966 | T | C | 196 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(193): Show |
200 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.892+146T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32724966 | |||||||
chr5:32724991 | G | T | 2 | a0001c0001t0004g0155 a0001c0001t0059g0156 |
2 | HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.892+171G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32724991 | |||||||
chr5:32725053 | A | G | 4 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(1): Show |
4 | NA18963.hp2 NA18975.hp1 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.892+233A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32725053 | |||||||
chr5:32725082 | C | T | 1 | a0001c0001t0001g0254 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.892+262C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32725082 | |||||||
chr5:32725112 | G | A | 1 | a0001c0001t0003g0157 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.892+292G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32725112 | |||||||
chr5:32725132 | G | A | 1 | a0001c0001t0003g0224 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.892+312G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32725132 | |||||||
chr5:32725153 | T | C | 7 | a0001c0001t0002g0008 a0001c0001t0007g0200 a0001c0001t0019g0006 others(4): Show |
7 | HG02451.hp2 HG02622.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.892+333T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32725153 | |||||||
chr5:32725246 | G | C | 94 | a0001c0001t0001g0043 a0001c0001t0001g0056 a0001c0001t0001g0062 others(91): Show |
95 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.892+426G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32725246 | |||||||
chr5:32725425 | G | A | 70 | a0001c0001t0001g0085 a0001c0001t0001g0088 a0001c0001t0001g0090 others(67): Show |
70 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.892+605G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32725425 | |||||||
chr5:32725439 | T | C | 23 | a0001c0001t0001g0014 a0001c0001t0001g0078 a0001c0001t0001g0267 others(20): Show |
23 | HG01074.hp2 HG01175.hp1 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.892+619T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32725439 | |||||||
chr5:32725662 | G | A | 20 | a0001c0001t0001g0043 a0001c0001t0004g0016 a0001c0001t0004g0017 others(17): Show |
20 | HG00741.hp1 HG01070.hp2 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.892+842G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32725662 | |||||||
chr5:32725678 | A | G | 6 | a0001c0001t0002g0008 a0001c0001t0008g0134 a0001c0001t0019g0006 others(3): Show |
6 | HG02055.hp2 HG02486.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.892+858A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32725678 | |||||||
chr5:32725749 | T | C | 1 | a0001c0001t0004g0140 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.892+929T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32725749 | |||||||
chr5:32725813 | A | G | 1 | a0001c0001t0021g0080 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.892+993A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32725813 | |||||||
chr5:32725832 | G | C | 2 | a0001c0001t0050g0047 a0001c0003t0044g0036 |
2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.892+1012G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32725832 | |||||||
chr5:32726083 | C | T | 1 | a0001c0001t0065g0051 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.892+1263C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32726083 | |||||||
chr5:32726137 | A | G | 1 | a0001c0005t0056g0266 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.892+1317A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32726137 | |||||||
chr5:32726232 | G | A | 2 | a0001c0001t0068g0231 a0002c0002t0002g0272 |
2 | NA18967.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.892+1412G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32726232 | |||||||
chr5:32726529 | A | T | 1 | a0001c0003t0044g0036 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.892+1709A>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32726529 | |||||||
chr5:32726531 | G | A | 143 | a0001c0001t0001g0043 a0001c0001t0001g0085 a0001c0001t0001g0088 others(140): Show |
143 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(140): Show |
intron_variant | MODIFIER | c.892+1711G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32726531 | |||||||
chr5:32726601 | G | A | 1 | a0001c0001t0053g0311 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.892+1781G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32726601 | |||||||
chr5:32726628 | A | G | 2 | a0001c0001t0005g0143 a0001c0001t0043g0067 |
2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.892+1808A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32726628 | |||||||
chr5:32726910 | A | G | 1 | a0001c0001t0065g0051 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.892+2090A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32726910 | |||||||
chr5:32727395 | A | G | 1 | a0001c0001t0005g0079 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.892+2575A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32727395 | |||||||
chr5:32727560 | G | C | 3 | a0001c0001t0004g0027 a0001c0001t0004g0028 a0001c0001t0004g0102 |
3 | HG01070.hp2 HG01496.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.892+2740G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32727560 | |||||||
chr5:32727578 | G | T | 13 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0020 others(10): Show |
13 | HG00099.hp2 HG00323.hp2 HG00642.hp1 others(10): Show |
intron_variant | MODIFIER | c.892+2758G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32727578 | |||||||
chr5:32727924 | A | G | 1 | a0001c0001t0065g0051 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.892+3104A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32727924 | |||||||
chr5:32727990 | G | A | 1 | a0001c0001t0009g0160 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.892+3170G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32727990 | |||||||
chr5:32728070 | G | A | 1 | a0001c0005t0056g0266 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.892+3250G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32728070 | |||||||
chr5:32728217 | C | G | 60 | a0001c0001t0001g0085 a0001c0001t0001g0088 a0001c0001t0001g0117 others(57): Show |
60 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.892+3397C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32728217 | |||||||
chr5:32728288 | C | T | 11 | a0001c0001t0004g0140 a0001c0001t0005g0079 a0001c0001t0007g0152 others(8): Show |
11 | HG02055.hp1 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.892+3468C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32728288 | |||||||
chr5:32728465 | G | GA | 292 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(289): Show |
297 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.892+3660dupA | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728465 | ||||||
chr5:32728465 | G | GAA | 10 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0004g0027 others(7): Show |
10 | HG01496.hp1 HG02055.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.892+3659_892+3660d others(4): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728465 | ||||||
chr5:32728465 | G | GAAA | 6 | a0001c0001t0006g0063 a0001c0001t0006g0065 a0001c0001t0017g0057 others(3): Show |
6 | HG01891.hp2 HG02809.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.892+3658_892+3660d others(5): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728465 | ||||||
chr5:32728502 | A | G | 1 | a0002c0002t0002g0145 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.892+3682A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32728502 | |||||||
chr5:32728618 | G | A | 1 | a0001c0003t0058g0035 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.892+3798G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32728618 | |||||||
chr5:32728700 | A | G | 11 | a0001c0001t0004g0140 a0001c0001t0005g0079 a0001c0001t0007g0152 others(8): Show |
11 | HG02055.hp1 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.892+3880A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32728700 | |||||||
chr5:32728779 | T | C | 1 | a0001c0001t0002g0008 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.892+3959T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32728779 | |||||||
chr5:32728792 | C | A | 2 | a0001c0001t0002g0008 a0001c0004t0062g0135 |
2 | HG02109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.892+3972C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32728792 | |||||||
chr5:32728815 | TTG | T | 45 | a0001c0001t0001g0085 a0001c0001t0001g0117 a0001c0001t0001g0126 others(42): Show |
46 | HG00423.hp2 HG00621.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.892+4017_892+4018d others(4): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728815 | ||||||
chr5:32728815 | TTGTG | T | 26 | a0001c0001t0001g0043 a0001c0001t0001g0151 a0001c0001t0002g0008 others(23): Show |
26 | HG00280.hp1 HG00609.hp1 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.892+4015_892+4018d others(6): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728815 | ||||||
chr5:32728815 | TTGTGTG | T | 11 | a0001c0001t0001g0142 a0001c0001t0001g0314 a0001c0001t0001g0315 others(8): Show |
11 | HG00738.hp1 HG01106.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.892+4013_892+4018d others(8): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728815 | ||||||
chr5:32728815 | TTGTGTGT others(1): Show |
T | 3 | a0001c0001t0003g0228 a0001c0003t0044g0036 a0002c0002t0027g0227 |
3 | HG03540.hp2 NA18945.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.892+4011_892+4018d others(10): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728815 | ||||||
chr5:32728827 | GTGTGTGT others(7): Show |
G | 1 | a0002c0002t0002g0270 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.892+4009_892+4022d others(16): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728827 | ||||||
chr5:32728827 | GTGTGTGT others(17): Show |
G | 1 | a0001c0005t0056g0266 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.892+4009_892+4032d others(26): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728827 | ||||||
chr5:32728829 | G | GTA | 6 | a0001c0001t0001g0088 a0001c0001t0001g0229 a0001c0001t0001g0306 others(3): Show |
6 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.892+4010_892+4011i others(4): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728829 | ||||||
chr5:32728829 | G | GTATATAT others(3): Show |
1 | a0002c0002t0002g0119 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.892+4010_892+4011i others(12): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728829 | ||||||
chr5:32728829 | GTGTGTGT others(9): Show |
G | 1 | a0001c0001t0003g0075 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.892+4011_892+4026d others(18): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728829 | ||||||
chr5:32728829 | GTGTGTGT others(25): Show |
G | 2 | a0001c0001t0024g0263 a0002c0002t0002g0259 |
2 | HG03471.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.892+4011_892+4042d others(34): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728829 | ||||||
chr5:32728829 | GTGTGTGT others(31): Show |
G | 1 | a0002c0002t0002g0125 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.892+4011_892+4048d others(40): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728829 | ||||||
chr5:32728831 | G | A | 17 | a0001c0001t0001g0088 a0001c0001t0001g0133 a0001c0001t0001g0229 others(14): Show |
17 | HG00621.hp2 HG00642.hp2 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.892+4011G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32728831 | |||||||
chr5:32728831 | G | GTA | 10 | a0001c0001t0004g0016 a0001c0001t0004g0028 a0001c0001t0004g0148 others(7): Show |
10 | HG00741.hp1 HG01261.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.892+4012_892+4013i others(4): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728831 | ||||||
chr5:32728831 | G | GTATA | 7 | a0001c0001t0004g0017 a0001c0001t0004g0299 a0001c0001t0006g0063 others(4): Show |
7 | HG01192.hp1 HG01257.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.892+4012_892+4013i others(6): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728831 | ||||||
chr5:32728831 | GTGTGTGT others(3): Show |
G | 1 | a0001c0001t0051g0269 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.892+4013_892+4022d others(12): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728831 | ||||||
chr5:32728831 | GTGTGTGT others(15): Show |
G | 1 | a0001c0001t0007g0200 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.892+4013_892+4034d others(24): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728831 | ||||||
chr5:32728831 | GTGTGTGT others(19): Show |
G | 3 | a0001c0001t0007g0138 a0001c0001t0041g0146 a0001c0001t0050g0047 |
3 | HG01934.hp2 HG02615.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.892+4013_892+4038d others(28): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728831 | ||||||
chr5:32728831 | GTGTGTGT others(21): Show |
G | 1 | a0001c0001t0007g0058 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.892+4013_892+4040d others(30): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728831 | ||||||
chr5:32728831 | GTGTGTGT others(23): Show |
G | 1 | a0001c0001t0004g0073 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.892+4013_892+4042d others(32): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728831 | ||||||
chr5:32728833 | G | A | 69 | a0001c0001t0001g0085 a0001c0001t0001g0088 a0001c0001t0001g0117 others(66): Show |
69 | HG00280.hp1 HG00423.hp2 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.892+4013G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32728833 | |||||||
chr5:32728833 | G | GTATATA | 4 | a0001c0001t0001g0188 a0001c0001t0004g0027 a0001c0001t0019g0006 others(1): Show |
4 | HG01496.hp1 HG02886.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.892+4014_892+4015i others(8): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728833 | ||||||
chr5:32728833 | GTGTGTAT others(17): Show |
G | 1 | a0001c0001t0005g0079 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.892+4015_892+4038d others(26): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728833 | ||||||
chr5:32728833 | GTGTGTAT others(21): Show |
G | 2 | a0001c0006t0061g0046 a0002c0002t0002g0072 |
2 | HG02055.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.892+4015_892+4042d others(30): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728833 | ||||||
chr5:32728835 | G | A | 98 | a0001c0001t0001g0085 a0001c0001t0001g0088 a0001c0001t0001g0117 others(95): Show |
98 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.892+4015G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32728835 | |||||||
chr5:32728835 | G | GTA | 21 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0023 others(18): Show |
22 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.892+4016_892+4017i others(4): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728835 | ||||||
chr5:32728835 | G | GTATA | 30 | a0001c0001t0001g0001 a0001c0001t0001g0068 a0001c0001t0001g0090 others(27): Show |
30 | HG01109.hp2 HG01934.hp1 HG02027.hp2 others(27): Show |
intron_variant | MODIFIER | c.892+4016_892+4017i others(6): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728835 | ||||||
chr5:32728835 | G | GTATATA | 40 | a0001c0001t0001g0056 a0001c0001t0001g0061 a0001c0001t0001g0062 others(37): Show |
40 | HG00642.hp1 HG00738.hp2 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.892+4016_892+4017i others(8): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728835 | ||||||
chr5:32728835 | G | GTATATAT others(1): Show |
4 | a0001c0001t0001g0014 a0001c0001t0001g0192 a0001c0001t0001g0312 others(1): Show |
4 | HG00544.hp1 HG01069.hp1 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.892+4016_892+4017i others(10): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728835 | ||||||
chr5:32728835 | G | GTATATAT others(3): Show |
3 | a0001c0001t0001g0060 a0001c0001t0001g0069 a0002c0002t0002g0211 |
3 | HG01192.hp2 HG02523.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.892+4016_892+4017i others(12): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728835 | ||||||
chr5:32728835 | G | GTATATAT others(9): Show |
2 | a0001c0001t0001g0024 a0002c0002t0002g0112 |
2 | HG02698.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.892+4016_892+4017i others(18): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728835 | ||||||
chr5:32728835 | GTGTA | G | 4 | a0001c0001t0001g0173 a0001c0001t0025g0048 a0001c0001t0030g0284 others(1): Show |
4 | HG01993.hp2 HG02818.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.892+4017_892+4020d others(6): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728835 | ||||||
chr5:32728835 | GTGTATA | G | 3 | a0001c0001t0001g0195 a0002c0002t0018g0076 a0002c0002t0018g0077 |
3 | HG01993.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.892+4017_892+4022d others(8): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728835 | ||||||
chr5:32728835 | GTGTATAT others(11): Show |
G | 1 | a0001c0001t0001g0273 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.892+4017_892+4034d others(20): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728835 | ||||||
chr5:32728835 | GTGTATAT others(13): Show |
G | 1 | a0002c0002t0002g0145 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.892+4017_892+4036d others(22): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728835 | ||||||
chr5:32728835 | GTGTATAT others(15): Show |
G | 9 | a0001c0001t0004g0140 a0001c0001t0007g0152 a0001c0001t0008g0045 others(6): Show |
9 | HG02055.hp1 HG02257.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.892+4017_892+4038d others(24): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728835 | ||||||
chr5:32728837 | G | A | 225 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(222): Show |
228 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.892+4017G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32728837 | |||||||
chr5:32728837 | G | GTA | 4 | a0001c0001t0001g0093 a0001c0001t0001g0189 a0001c0001t0003g0174 others(1): Show |
4 | HG00099.hp1 HG02071.hp2 NA18952.hp2 others(1): Show |
intron_variant | MODIFIER | c.892+4055_892+4056d others(4): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728837 | ||||||
chr5:32728837 | G | GTATA | 6 | a0001c0001t0001g0019 a0001c0001t0003g0122 a0001c0001t0003g0183 others(3): Show |
6 | HG00423.hp1 HG01256.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.892+4053_892+4056d others(6): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728837 | ||||||
chr5:32728837 | G | GTATATA | 10 | a0001c0001t0001g0144 a0001c0001t0003g0111 a0001c0001t0003g0157 others(7): Show |
10 | HG02027.hp1 HG02523.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.892+4051_892+4056d others(8): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728837 | ||||||
chr5:32728837 | G | GTATATAT others(3): Show |
2 | a0001c0001t0003g0238 a0001c0001t0003g0239 |
2 | NA18992.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.892+4047_892+4056d others(12): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728837 | ||||||
chr5:32728837 | G | GTATATAT others(7): Show |
1 | a0001c0001t0003g0256 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.892+4043_892+4056d others(16): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728837 | ||||||
chr5:32728837 | G | GTATATAT others(11): Show |
1 | a0001c0001t0003g0245 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.892+4039_892+4056d others(20): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728837 | ||||||
chr5:32728837 | G | GTATATAT others(13): Show |
1 | a0001c0001t0001g0202 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.892+4037_892+4056d others(22): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728837 | ||||||
chr5:32728837 | GTA | G | 5 | a0001c0001t0003g0224 a0001c0001t0003g0249 a0001c0001t0010g0120 others(2): Show |
5 | HG01070.hp1 HG02074.hp1 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.892+4055_892+4056d others(4): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32728837 | ||||||
chr5:32728841 | A | G | 1 | a0001c0001t0003g0224 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.892+4021A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32728841 | |||||||
chr5:32728857 | A | G | 1 | a0001c0003t0044g0036 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.892+4037A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32728857 | |||||||
chr5:32728930 | A | C | 1 | a0001c0003t0001g0034 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.892+4110A>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32728930 | |||||||
chr5:32728976 | A | T | 143 | a0001c0001t0001g0043 a0001c0001t0001g0085 a0001c0001t0001g0088 others(140): Show |
143 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(140): Show |
intron_variant | MODIFIER | c.892+4156A>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32728976 | |||||||
chr5:32729014 | G | GT | 8 | a0001c0001t0001g0014 a0001c0001t0001g0068 a0001c0001t0001g0202 others(5): Show |
8 | HG01168.hp2 HG01175.hp1 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.892+4209dupT | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32729014 | ||||||
chr5:32729014 | G | T | 9 | a0001c0001t0001g0314 a0001c0001t0001g0315 a0001c0001t0003g0230 others(6): Show |
9 | HG00280.hp1 HG01175.hp2 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.892+4194G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32729014 | |||||||
chr5:32729014 | GTT | G | 9 | a0001c0001t0001g0229 a0001c0001t0003g0087 a0001c0001t0006g0066 others(6): Show |
9 | HG00423.hp2 HG00621.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.892+4208_892+4209d others(4): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32729014 | ||||||
chr5:32729016 | T | G | 1 | a0001c0001t0007g0058 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.892+4196T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32729016 | |||||||
chr5:32729025 | T | G | 3 | a0001c0001t0001g0170 a0001c0001t0001g0208 a0001c0001t0013g0278 |
3 | HG01169.hp2 HG02293.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.892+4205T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32729025 | |||||||
chr5:32729028 | TTG | T | 8 | a0001c0001t0006g0065 a0001c0001t0017g0064 a0001c0001t0019g0006 others(5): Show |
8 | HG02055.hp2 HG02809.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.892+4210_892+4211d others(4): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32729028 | ||||||
chr5:32729029 | TG | T | 51 | a0001c0001t0001g0085 a0001c0001t0001g0088 a0001c0001t0001g0117 others(48): Show |
51 | HG00609.hp1 HG00609.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.892+4210delG | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32729029 | |||||||
chr5:32729030 | G | T | 19 | a0001c0001t0001g0314 a0001c0001t0001g0315 a0001c0001t0002g0008 others(16): Show |
19 | HG00280.hp1 HG00642.hp2 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.892+4210G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32729030 | |||||||
chr5:32729032 | T | G | 51 | a0001c0001t0001g0085 a0001c0001t0001g0088 a0001c0001t0001g0117 others(48): Show |
51 | HG00609.hp1 HG00609.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.892+4212T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32729032 | |||||||
chr5:32729033 | T | G | 9 | a0001c0001t0001g0229 a0001c0001t0003g0087 a0001c0001t0006g0066 others(6): Show |
9 | HG00423.hp2 HG00621.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.892+4213T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32729033 | |||||||
chr5:32729033 | TTG | T | 11 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0003g0075 others(8): Show |
11 | HG00735.hp2 HG01074.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.892+4215_892+4216d others(4): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32729033 | ||||||
chr5:32729035 | G | T | 14 | a0001c0001t0001g0229 a0001c0001t0003g0087 a0001c0001t0005g0143 others(11): Show |
14 | HG00280.hp1 HG00423.hp2 HG00621.hp2 others(11): Show |
intron_variant | MODIFIER | c.892+4215G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32729035 | |||||||
chr5:32729035 | GT | G | 222 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(219): Show |
225 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(222): Show |
intron_variant | MODIFIER | c.892+4227delT | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32729035 | ||||||
chr5:32729036 | T | G | 23 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0229 others(20): Show |
23 | HG00280.hp1 HG00423.hp2 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.892+4216T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32729036 | |||||||
chr5:32729041 | T | G | 1 | a0001c0001t0036g0013 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.892+4221T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32729041 | |||||||
chr5:32729091 | G | A | 33 | a0001c0001t0001g0043 a0001c0001t0001g0142 a0001c0001t0001g0151 others(30): Show |
33 | HG00741.hp1 HG01070.hp2 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.892+4271G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32729091 | |||||||
chr5:32729103 | C | T | 2 | a0001c0001t0005g0143 a0001c0001t0043g0067 |
2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.892+4283C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32729103 | |||||||
chr5:32729112 | C | G | 8 | a0001c0001t0001g0314 a0001c0001t0001g0315 a0001c0001t0003g0230 others(5): Show |
8 | HG00280.hp1 HG01175.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.892+4292C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32729112 | |||||||
chr5:32729130 | C | T | 63 | a0001c0001t0001g0085 a0001c0001t0001g0088 a0001c0001t0001g0117 others(60): Show |
63 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.892+4310C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32729130 | |||||||
chr5:32729140 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.892+4320C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32729140 | |||||||
chr5:32729153 | C | A | 1 | a0002c0002t0002g0072 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.892+4333C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32729153 | |||||||
chr5:32729276 | A | G | 143 | a0001c0001t0001g0043 a0001c0001t0001g0085 a0001c0001t0001g0088 others(140): Show |
143 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(140): Show |
intron_variant | MODIFIER | c.892+4456A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32729276 | |||||||
chr5:32729313 | G | A | 1 | a0001c0001t0005g0079 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.892+4493G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32729313 | |||||||
chr5:32729421 | T | G | 1 | a0001c0001t0040g0162 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.892+4601T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32729421 | |||||||
chr5:32729655 | C | A | 1 | a0002c0002t0012g0293 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.892+4835C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32729655 | |||||||
chr5:32729908 | T | G | 1 | a0002c0002t0002g0232 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.892+5088T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32729908 | |||||||
chr5:32729963 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.892+5143C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32729963 | |||||||
chr5:32730115 | G | A | 1 | a0001c0001t0065g0051 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.892+5295G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32730115 | |||||||
chr5:32730122 | C | T | 4 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0006g0010 others(1): Show |
4 | HG02145.hp2 HG02258.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.892+5302C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32730122 | |||||||
chr5:32730198 | TA | T | 14 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0188 others(11): Show |
14 | HG00280.hp1 HG01175.hp2 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.892+5388delA | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32730198 | ||||||
chr5:32730222 | T | C | 1 | a0002c0002t0052g0163 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.892+5402T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32730222 | |||||||
chr5:32730314 | AG | A | 4 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0006g0010 others(1): Show |
4 | HG02145.hp2 HG02258.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.892+5498delG | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32730314 | ||||||
chr5:32730358 | G | T | 63 | a0001c0001t0001g0085 a0001c0001t0001g0088 a0001c0001t0001g0117 others(60): Show |
63 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.892+5538G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32730358 | |||||||
chr5:32730360 | A | G | 1 | a0001c0001t0007g0152 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.892+5540A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32730360 | |||||||
chr5:32730540 | T | C | 1 | a0001c0001t0008g0045 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.892+5720T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32730540 | |||||||
chr5:32730660 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.892+5840G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32730660 | |||||||
chr5:32730665 | T | A | 1 | a0002c0002t0002g0237 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.892+5845T>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32730665 | |||||||
chr5:32730859 | T | C | 10 | a0001c0001t0002g0129 a0001c0001t0004g0139 a0001c0001t0015g0123 others(7): Show |
10 | HG00735.hp2 HG01074.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.892+6039T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32730859 | |||||||
chr5:32731204 | C | T | 1 | a0002c0002t0002g0232 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.892+6384C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32731204 | |||||||
chr5:32731268 | A | G | 1 | a0001c0001t0015g0123 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.892+6448A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32731268 | |||||||
chr5:32731309 | C | T | 1 | a0001c0001t0050g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.892+6489C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32731309 | |||||||
chr5:32731313 | A | G | 1 | a0001c0001t0065g0051 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.892+6493A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32731313 | |||||||
chr5:32731368 | A | G | 2 | a0001c0001t0045g0099 a0002c0002t0029g0100 |
2 | HG00735.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.892+6548A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32731368 | |||||||
chr5:32731442 | A | G | 33 | a0001c0001t0001g0043 a0001c0001t0001g0142 a0001c0001t0001g0151 others(30): Show |
33 | HG00741.hp1 HG01070.hp2 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.892+6622A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32731442 | |||||||
chr5:32731534 | G | A | 6 | a0001c0001t0004g0139 a0001c0001t0015g0123 a0001c0001t0026g0049 others(3): Show |
6 | HG00735.hp2 HG01891.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.892+6714G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32731534 | |||||||
chr5:32731726 | T | C | 1 | a0001c0001t0050g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.892+6906T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32731726 | |||||||
chr5:32731820 | T | G | 8 | a0001c0001t0001g0314 a0001c0001t0001g0315 a0001c0001t0003g0230 others(5): Show |
8 | HG00280.hp1 HG01175.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.892+7000T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32731820 | |||||||
chr5:32731960 | G | A | 1 | a0001c0004t0062g0135 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.893-6904G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32731960 | |||||||
chr5:32732008 | A | G | 72 | a0001c0001t0001g0085 a0001c0001t0001g0088 a0001c0001t0001g0117 others(69): Show |
72 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.893-6856A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32732008 | |||||||
chr5:32732068 | C | T | 1 | a0001c0001t0003g0087 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.893-6796C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32732068 | |||||||
chr5:32732084 | A | G | 1 | a0001c0001t0003g0075 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.893-6780A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32732084 | |||||||
chr5:32732097 | C | T | 1 | a0001c0001t0007g0152 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.893-6767C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32732097 | |||||||
chr5:32732104 | G | A | 11 | a0001c0001t0001g0056 a0001c0001t0001g0060 a0001c0001t0001g0061 others(8): Show |
11 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.893-6760G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32732104 | |||||||
chr5:32732131 | C | T | 1 | a0001c0001t0003g0075 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.893-6733C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32732131 | |||||||
chr5:32732134 | G | C | 1 | a0001c0001t0001g0060 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.893-6730G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32732134 | |||||||
chr5:32732135 | G | A | 1 | a0001c0001t0003g0075 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.893-6729G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32732135 | |||||||
chr5:32732247 | C | CA | 74 | a0001c0001t0001g0014 a0001c0001t0001g0068 a0001c0001t0001g0096 others(71): Show |
76 | HG00423.hp1 HG00544.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.893-6586dupA | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32732247 | ||||||
chr5:32732247 | C | CAA | 23 | a0001c0001t0001g0043 a0001c0001t0001g0069 a0001c0001t0001g0314 others(20): Show |
23 | HG00280.hp1 HG01175.hp2 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.893-6587_893-6586d others(4): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32732247 | ||||||
chr5:32732247 | CA | C | 14 | a0001c0001t0001g0142 a0001c0001t0001g0198 a0001c0001t0003g0083 others(11): Show |
14 | HG00741.hp1 HG01516.hp2 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.893-6586delA | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32732247 | ||||||
chr5:32732247 | CAA | C | 33 | a0001c0001t0001g0085 a0001c0001t0001g0088 a0001c0001t0001g0306 others(30): Show |
33 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.893-6587_893-6586d others(4): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32732247 | ||||||
chr5:32732247 | CAAA | C | 43 | a0001c0001t0001g0117 a0001c0001t0001g0126 a0001c0001t0001g0229 others(40): Show |
43 | HG00621.hp2 HG00639.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.893-6588_893-6586d others(5): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32732247 | ||||||
chr5:32732247 | CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0005g0143 a0001c0001t0043g0067 |
2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.893-6596_893-6586d others(13): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32732247 | ||||||
chr5:32732369 | G | A | 14 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0113 others(11): Show |
14 | HG02040.hp2 HG02071.hp1 HG02083.hp2 others(11): Show |
intron_variant | MODIFIER | c.893-6495G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32732369 | |||||||
chr5:32732666 | T | C | 5 | a0001c0001t0008g0134 a0001c0001t0019g0006 a0001c0001t0019g0007 others(2): Show |
5 | HG02055.hp2 HG02486.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.893-6198T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32732666 | |||||||
chr5:32732754 | A | G | 8 | a0001c0001t0001g0314 a0001c0001t0001g0315 a0001c0001t0003g0230 others(5): Show |
8 | HG00280.hp1 HG01175.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.893-6110A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32732754 | |||||||
chr5:32732853 | C | T | 64 | a0001c0001t0001g0085 a0001c0001t0001g0088 a0001c0001t0001g0117 others(61): Show |
64 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.893-6011C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32732853 | |||||||
chr5:32733096 | C | T | 1 | a0001c0001t0004g0155 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.893-5768C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32733096 | |||||||
chr5:32733124 | C | T | 1 | a0002c0002t0002g0214 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.893-5740C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32733124 | |||||||
chr5:32733140 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.893-5724C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32733140 | |||||||
chr5:32733159 | T | C | 1 | a0002c0002t0002g0082 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.893-5705T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32733159 | |||||||
chr5:32733312 | C | T | 95 | a0001c0001t0001g0085 a0001c0001t0001g0088 a0001c0001t0001g0117 others(92): Show |
95 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.893-5552C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32733312 | |||||||
chr5:32733741 | A | G | 10 | a0001c0001t0002g0129 a0001c0001t0004g0139 a0001c0001t0015g0123 others(7): Show |
10 | HG00735.hp2 HG01074.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.893-5123A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32733741 | |||||||
chr5:32733747 | C | A | 1 | a0001c0001t0003g0238 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.893-5117C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32733747 | |||||||
chr5:32733806 | A | G | 1 | a0001c0004t0062g0135 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.893-5058A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32733806 | |||||||
chr5:32733807 | T | G | 2 | a0001c0001t0005g0143 a0001c0001t0043g0067 |
2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.893-5057T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32733807 | |||||||
chr5:32733834 | C | T | 11 | a0001c0001t0004g0140 a0001c0001t0005g0079 a0001c0001t0007g0152 others(8): Show |
11 | HG02055.hp1 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.893-5030C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32733834 | |||||||
chr5:32733862 | C | T | 8 | a0001c0001t0001g0314 a0001c0001t0001g0315 a0001c0001t0003g0230 others(5): Show |
8 | HG00280.hp1 HG01175.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.893-5002C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32733862 | |||||||
chr5:32733907 | T | C | 1 | a0002c0002t0002g0158 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.893-4957T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32733907 | |||||||
chr5:32734034 | A | G | 64 | a0001c0001t0001g0085 a0001c0001t0001g0088 a0001c0001t0001g0117 others(61): Show |
64 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.893-4830A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32734034 | |||||||
chr5:32734140 | G | A | 2 | a0001c0003t0023g0038 a0001c0003t0023g0039 |
2 | HG02622.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.893-4724G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32734140 | |||||||
chr5:32734187 | T | C | 1 | a0001c0001t0065g0051 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.893-4677T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32734187 | |||||||
chr5:32734221 | A | G | 60 | a0001c0001t0001g0085 a0001c0001t0001g0088 a0001c0001t0001g0117 others(57): Show |
60 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.893-4643A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32734221 | |||||||
chr5:32734302 | T | G | 44 | a0001c0001t0001g0043 a0001c0001t0001g0142 a0001c0001t0001g0151 others(41): Show |
44 | HG00741.hp1 HG01070.hp2 HG01106.hp2 others(41): Show |
intron_variant | MODIFIER | c.893-4562T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32734302 | |||||||
chr5:32734364 | C | T | 2 | a0001c0001t0003g0224 a0001c0001t0003g0288 |
2 | NA18612.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.893-4500C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32734364 | |||||||
chr5:32734377 | C | T | 1 | a0001c0001t0007g0152 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.893-4487C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32734377 | |||||||
chr5:32734405 | G | A | 64 | a0001c0001t0001g0085 a0001c0001t0001g0088 a0001c0001t0001g0117 others(61): Show |
64 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.893-4459G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32734405 | |||||||
chr5:32734427 | T | C | 1 | a0001c0003t0058g0035 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.893-4437T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32734427 | |||||||
chr5:32734463 | G | A | 4 | a0001c0001t0015g0123 a0001c0001t0045g0099 a0001c0001t0047g0104 others(1): Show |
4 | HG00735.hp2 HG01074.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.893-4401G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32734463 | |||||||
chr5:32734472 | A | G | 3 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0009g0194 |
3 | NA18963.hp2 NA18977.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.893-4392A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32734472 | |||||||
chr5:32734584 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.893-4280C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32734584 | |||||||
chr5:32734711 | G | A | 63 | a0001c0001t0001g0085 a0001c0001t0001g0088 a0001c0001t0001g0117 others(60): Show |
63 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.893-4153G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32734711 | |||||||
chr5:32734762 | A | G | 96 | a0001c0001t0001g0085 a0001c0001t0001g0088 a0001c0001t0001g0117 others(93): Show |
96 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.893-4102A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32734762 | |||||||
chr5:32734850 | C | T | 1 | a0001c0001t0003g0256 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.893-4014C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32734850 | |||||||
chr5:32735013 | T | A | 70 | a0001c0001t0001g0085 a0001c0001t0001g0088 a0001c0001t0001g0117 others(67): Show |
70 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.893-3851T>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32735013 | |||||||
chr5:32735039 | T | A | 4 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0006g0010 others(1): Show |
4 | HG02145.hp2 HG02258.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.893-3825T>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32735039 | |||||||
chr5:32735137 | T | C | 1 | a0002c0002t0002g0178 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.893-3727T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32735137 | |||||||
chr5:32735139 | C | T | 1 | a0001c0001t0004g0139 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.893-3725C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32735139 | |||||||
chr5:32735191 | G | A | 3 | a0001c0001t0001g0179 a0001c0001t0001g0242 a0001c0001t0003g0171 |
3 | HG02074.hp2 NA18949.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.893-3673G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32735191 | |||||||
chr5:32735213 | A | G | 1 | a0001c0001t0001g0199 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.893-3651A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32735213 | |||||||
chr5:32735289 | G | C | 1 | a0002c0002t0002g0295 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.893-3575G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32735289 | |||||||
chr5:32735302 | C | T | 31 | a0001c0001t0001g0314 a0001c0001t0001g0315 a0001c0001t0002g0129 others(28): Show |
31 | HG00280.hp1 HG00735.hp2 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.893-3562C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32735302 | |||||||
chr5:32735303 | T | A | 1 | a0001c0001t0005g0079 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.893-3561T>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32735303 | |||||||
chr5:32735412 | CTA | C | 6 | a0001c0001t0001g0056 a0001c0001t0001g0060 a0001c0001t0001g0061 others(3): Show |
6 | HG01109.hp2 HG01192.hp2 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.893-3450_893-3449d others(4): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32735412 | ||||||
chr5:32735426 | T | A | 8 | a0001c0001t0001g0314 a0001c0001t0001g0315 a0001c0001t0003g0230 others(5): Show |
8 | HG00280.hp1 HG01175.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.893-3438T>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32735426 | |||||||
chr5:32735479 | C | CA | 23 | a0001c0001t0001g0020 a0001c0001t0001g0090 a0001c0001t0001g0096 others(20): Show |
23 | HG00639.hp2 HG01099.hp1 HG01952.hp1 others(20): Show |
intron_variant | MODIFIER | c.893-3370dupA | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32735479 | ||||||
chr5:32735479 | C | CAAA | 58 | a0001c0001t0001g0085 a0001c0001t0001g0088 a0001c0001t0001g0117 others(55): Show |
58 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.893-3372_893-3370d others(5): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32735479 | ||||||
chr5:32735479 | CA | C | 36 | a0001c0001t0001g0142 a0001c0001t0001g0151 a0001c0001t0001g0198 others(33): Show |
36 | HG01074.hp2 HG01106.hp2 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.893-3370delA | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32735479 | ||||||
chr5:32735479 | CAA | C | 9 | a0001c0001t0001g0314 a0001c0001t0001g0315 a0001c0001t0003g0230 others(6): Show |
9 | HG00280.hp1 HG01175.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.893-3371_893-3370d others(4): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32735479 | ||||||
chr5:32735543 | G | A | 111 | a0001c0001t0001g0085 a0001c0001t0001g0088 a0001c0001t0001g0117 others(108): Show |
111 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.893-3321G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32735543 | |||||||
chr5:32735556 | G | A | 1 | a0001c0004t0062g0135 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.893-3308G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32735556 | |||||||
chr5:32735624 | C | T | 1 | a0001c0001t0006g0066 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.893-3240C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32735624 | |||||||
chr5:32735627 | C | G | 6 | a0001c0001t0004g0140 a0001c0001t0008g0045 a0001c0001t0008g0128 others(3): Show |
6 | HG02055.hp1 HG02257.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.893-3237C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32735627 | |||||||
chr5:32735679 | T | C | 5 | a0001c0001t0006g0063 a0001c0001t0006g0065 a0001c0001t0017g0057 others(2): Show |
5 | HG01891.hp2 HG02809.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.893-3185T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32735679 | |||||||
chr5:32735693 | A | T | 7 | a0001c0001t0004g0139 a0001c0001t0015g0123 a0001c0001t0026g0049 others(4): Show |
7 | HG00735.hp2 HG01074.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.893-3171A>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32735693 | |||||||
chr5:32735788 | C | G | 8 | a0001c0001t0001g0314 a0001c0001t0001g0315 a0001c0001t0003g0230 others(5): Show |
8 | HG00280.hp1 HG01175.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.893-3076C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32735788 | |||||||
chr5:32735844 | G | C | 23 | a0001c0001t0003g0075 a0001c0001t0004g0140 a0001c0001t0005g0079 others(20): Show |
23 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.893-3020G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32735844 | |||||||
chr5:32735853 | G | A | 6 | a0001c0001t0006g0063 a0001c0001t0006g0065 a0001c0001t0017g0057 others(3): Show |
6 | HG01891.hp2 HG02809.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.893-3011G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32735853 | |||||||
chr5:32735969 | G | A | 1 | a0002c0002t0002g0308 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.893-2895G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32735969 | |||||||
chr5:32736059 | T | C | 63 | a0001c0001t0001g0085 a0001c0001t0001g0088 a0001c0001t0001g0117 others(60): Show |
63 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.893-2805T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32736059 | |||||||
chr5:32736088 | G | A | 1 | a0001c0003t0058g0035 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.893-2776G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32736088 | |||||||
chr5:32736165 | AG | A | 4 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0009g0304 others(1): Show |
4 | NA18941.hp2 NA18984.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.893-2697delG | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32736165 | ||||||
chr5:32736213 | A | T | 10 | a0001c0001t0002g0129 a0001c0001t0004g0139 a0001c0001t0015g0123 others(7): Show |
10 | HG00735.hp2 HG01074.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.893-2651A>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32736213 | |||||||
chr5:32736230 | C | CA | 7 | a0001c0001t0001g0181 a0001c0001t0010g0120 a0001c0001t0065g0051 others(4): Show |
7 | HG01070.hp1 HG02109.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.893-2616dupA | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32736230 | ||||||
chr5:32736230 | CA | C | 43 | a0001c0001t0001g0043 a0001c0001t0001g0142 a0001c0001t0001g0151 others(40): Show |
43 | HG00741.hp1 HG01070.hp2 HG01106.hp1 others(40): Show |
intron_variant | MODIFIER | c.893-2616delA | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32736230 | ||||||
chr5:32736239 | A | G | 4 | a0001c0001t0003g0095 a0001c0001t0003g0296 a0001c0001t0003g0297 others(1): Show |
4 | HG02083.hp1 NA18950.hp1 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.893-2625A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32736239 | |||||||
chr5:32736248 | A | AAAG | 15 | a0001c0001t0002g0129 a0001c0001t0004g0139 a0001c0001t0008g0134 others(12): Show |
15 | HG00735.hp2 HG01074.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.893-2616_893-2615i others(5): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32736248 | |||||||
chr5:32736249 | G | A | 32 | a0001c0001t0001g0208 a0001c0001t0001g0314 a0001c0001t0001g0315 others(29): Show |
32 | HG00280.hp1 HG00735.hp2 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.893-2615G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32736249 | |||||||
chr5:32736250 | A | AAAG | 5 | a0001c0001t0015g0103 a0001c0001t0036g0013 a0001c0003t0044g0036 others(2): Show |
5 | HG00280.hp1 HG01175.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.893-2612_893-2611i others(5): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 32736250 | ||||||
chr5:32736363 | G | A | 86 | a0001c0001t0001g0085 a0001c0001t0001g0088 a0001c0001t0001g0117 others(83): Show |
86 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(83): Show |
intron_variant | MODIFIER | c.893-2501G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32736363 | |||||||
chr5:32736368 | G | A | 8 | a0001c0001t0001g0314 a0001c0001t0001g0315 a0001c0001t0003g0230 others(5): Show |
8 | HG00280.hp1 HG01175.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.893-2496G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32736368 | |||||||
chr5:32736394 | A | T | 3 | a0001c0001t0004g0139 a0001c0001t0026g0049 a0001c0001t0026g0052 |
3 | HG01891.hp1 HG02622.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.893-2470A>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32736394 | |||||||
chr5:32736614 | G | A | 1 | a0001c0001t0055g0147 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.893-2250G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32736614 | |||||||
chr5:32736629 | G | A | 23 | a0001c0001t0002g0129 a0001c0001t0003g0075 a0001c0001t0004g0139 others(20): Show |
23 | HG00735.hp2 HG01074.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.893-2235G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32736629 | |||||||
chr5:32736729 | C | T | 13 | a0001c0001t0003g0075 a0001c0001t0005g0079 a0001c0001t0006g0063 others(10): Show |
13 | HG01074.hp2 HG01891.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.893-2135C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32736729 | |||||||
chr5:32736821 | C | T | 1 | a0001c0001t0005g0079 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.893-2043C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32736821 | |||||||
chr5:32736895 | C | T | 23 | a0001c0001t0002g0129 a0001c0001t0003g0075 a0001c0001t0004g0139 others(20): Show |
23 | HG00735.hp2 HG01074.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.893-1969C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32736895 | |||||||
chr5:32737037 | T | C | 11 | a0001c0001t0004g0140 a0001c0001t0007g0152 a0001c0001t0008g0045 others(8): Show |
11 | HG01261.hp1 HG02055.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.893-1827T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32737037 | |||||||
chr5:32737128 | A | T | 11 | a0001c0001t0004g0140 a0001c0001t0007g0152 a0001c0001t0008g0045 others(8): Show |
11 | HG01261.hp1 HG02055.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.893-1736A>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32737128 | |||||||
chr5:32737204 | G | A | 23 | a0001c0001t0002g0129 a0001c0001t0003g0075 a0001c0001t0004g0139 others(20): Show |
23 | HG00735.hp2 HG01074.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.893-1660G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32737204 | |||||||
chr5:32737213 | T | C | 2 | a0001c0001t0005g0143 a0001c0001t0043g0067 |
2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.893-1651T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32737213 | |||||||
chr5:32737237 | T | C | 1 | a0001c0001t0010g0120 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.893-1627T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32737237 | |||||||
chr5:32737243 | C | T | 1 | a0001c0001t0008g0134 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.893-1621C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32737243 | |||||||
chr5:32737259 | T | C | 1 | a0001c0001t0003g0075 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.893-1605T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32737259 | |||||||
chr5:32737371 | G | A | 1 | a0002c0002t0002g0089 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.893-1493G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32737371 | |||||||
chr5:32737477 | C | T | 12 | a0001c0001t0003g0203 a0001c0001t0004g0140 a0001c0001t0007g0152 others(9): Show |
12 | HG01261.hp1 HG02055.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.893-1387C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32737477 | |||||||
chr5:32737478 | G | A | 1 | a0001c0001t0050g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.893-1386G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32737478 | |||||||
chr5:32737508 | C | A | 1 | a0001c0001t0001g0172 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.893-1356C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32737508 | |||||||
chr5:32737509 | T | C | 1 | a0001c0001t0001g0172 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.893-1355T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32737509 | |||||||
chr5:32737510 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.893-1354G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32737510 | |||||||
chr5:32737515 | G | T | 2 | a0002c0002t0002g0041 a0002c0002t0002g0055 |
2 | HG02451.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.893-1349G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32737515 | |||||||
chr5:32737516 | T | C | 1 | a0001c0001t0001g0172 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.893-1348T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32737516 | |||||||
chr5:32737653 | G | A | 1 | a0002c0002t0002g0308 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.893-1211G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32737653 | |||||||
chr5:32737826 | T | C | 7 | a0001c0001t0001g0314 a0001c0001t0001g0315 a0001c0001t0003g0230 others(4): Show |
7 | HG00280.hp1 HG01175.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.893-1038T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32737826 | |||||||
chr5:32737861 | C | T | 7 | a0001c0001t0001g0314 a0001c0001t0001g0315 a0001c0001t0003g0230 others(4): Show |
7 | HG00280.hp1 HG01175.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.893-1003C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32737861 | |||||||
chr5:32737942 | A | G | 2 | a0001c0001t0045g0099 a0002c0002t0029g0100 |
2 | HG00735.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.893-922A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32737942 | |||||||
chr5:32738122 | T | G | 1 | a0001c0001t0004g0139 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.893-742T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32738122 | |||||||
chr5:32738341 | T | C | 4 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0006g0010 others(1): Show |
4 | HG02145.hp2 HG02258.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.893-523T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32738341 | |||||||
chr5:32738401 | C | T | 4 | a0001c0001t0003g0222 a0001c0001t0003g0313 a0001c0001t0067g0264 others(1): Show |
4 | HG02155.hp1 NA18967.hp2 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.893-463C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32738401 | |||||||
chr5:32738433 | C | T | 2 | a0001c0003t0023g0038 a0001c0003t0023g0039 |
2 | HG02622.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.893-431C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32738433 | |||||||
chr5:32738547 | A | C | 8 | a0001c0001t0001g0314 a0001c0001t0001g0315 a0001c0001t0003g0230 others(5): Show |
8 | HG00280.hp1 HG01175.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.893-317A>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32738547 | |||||||
chr5:32738548 | G | A | 144 | a0001c0001t0001g0043 a0001c0001t0001g0085 a0001c0001t0001g0088 others(141): Show |
144 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(141): Show |
intron_variant | MODIFIER | c.893-316G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32738548 | |||||||
chr5:32738652 | G | A | 11 | a0001c0001t0002g0129 a0001c0001t0004g0139 a0001c0001t0015g0123 others(8): Show |
11 | HG00735.hp2 HG01891.hp1 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.893-212G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32738652 | |||||||
chr5:32738702 | G | A | 1 | a0002c0002t0002g0145 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.893-162G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32738702 | |||||||
chr5:32738758 | C | T | 1 | a0001c0001t0003g0176 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.893-106C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32738758 | |||||||
chr5:32738780 | G | A | 8 | a0001c0001t0001g0314 a0001c0001t0001g0315 a0001c0001t0003g0230 others(5): Show |
8 | HG00280.hp1 HG01175.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.893-84G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32738780 | |||||||
chr5:32738785 | C | T | 63 | a0001c0001t0001g0085 a0001c0001t0001g0088 a0001c0001t0001g0117 others(60): Show |
63 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.893-79C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 2/7 | chr5 | 32738785 | |||||||
chr5:32739165 | C | CTG | 5 | a0001c0001t0001g0092 a0001c0001t0001g0312 a0001c0001t0003g0238 others(2): Show |
5 | HG00544.hp1 HG00544.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.1059+153_1059+154d others(4): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32739165 | ||||||
chr5:32739165 | CTG | C | 16 | a0001c0001t0001g0001 a0001c0001t0001g0026 a0001c0001t0001g0170 others(13): Show |
17 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.1059+153_1059+154d others(4): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32739165 | ||||||
chr5:32739181 | G | T | 1 | a0001c0001t0002g0008 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1059+151G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32739181 | |||||||
chr5:32739183 | G | GT | 14 | a0001c0001t0004g0016 a0001c0001t0004g0017 a0001c0001t0004g0027 others(11): Show |
14 | HG00741.hp1 HG01070.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.1059+165dupT | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32739183 | ||||||
chr5:32739183 | G | T | 106 | a0001c0001t0001g0043 a0001c0001t0001g0085 a0001c0001t0001g0088 others(103): Show |
106 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(103): Show |
intron_variant | MODIFIER | c.1059+153G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32739183 | |||||||
chr5:32739185 | T | G | 30 | a0001c0001t0001g0169 a0001c0001t0001g0189 a0001c0001t0001g0243 others(27): Show |
32 | HG00621.hp1 HG01168.hp1 HG01169.hp1 others(29): Show |
intron_variant | MODIFIER | c.1059+155T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32739185 | |||||||
chr5:32739191 | T | TA | 16 | a0001c0001t0002g0129 a0001c0001t0003g0075 a0001c0001t0004g0139 others(13): Show |
16 | HG00735.hp2 HG01074.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.1059+161_1059+162i others(3): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32739191 | |||||||
chr5:32739191 | T | TTTA | 6 | a0001c0001t0006g0063 a0001c0001t0006g0065 a0001c0001t0017g0057 others(3): Show |
6 | HG01891.hp2 HG02809.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1059+163_1059+164i others(5): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32739191 | ||||||
chr5:32739555 | A | G | 71 | a0001c0001t0001g0085 a0001c0001t0001g0088 a0001c0001t0001g0117 others(68): Show |
71 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.1059+525A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32739555 | |||||||
chr5:32739556 | C | A | 1 | a0001c0001t0003g0234 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1059+526C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32739556 | |||||||
chr5:32739625 | G | T | 1 | a0001c0001t0065g0051 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1059+595G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32739625 | |||||||
chr5:32739642 | G | A | 1 | a0001c0001t0003g0256 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1059+612G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32739642 | |||||||
chr5:32739679 | C | T | 1 | a0002c0002t0002g0145 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1059+649C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32739679 | |||||||
chr5:32739854 | T | A | 1 | a0001c0001t0007g0138 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1059+824T>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32739854 | |||||||
chr5:32739869 | G | A | 3 | a0001c0001t0002g0008 a0001c0001t0065g0051 a0001c0004t0062g0135 |
3 | HG02109.hp2 HG03098.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1059+839G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32739869 | |||||||
chr5:32739953 | T | C | 63 | a0001c0001t0001g0085 a0001c0001t0001g0088 a0001c0001t0001g0117 others(60): Show |
63 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.1059+923T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32739953 | |||||||
chr5:32740078 | G | A | 1 | a0001c0001t0050g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1059+1048G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32740078 | |||||||
chr5:32740120 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1059+1090A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32740120 | |||||||
chr5:32740240 | G | T | 75 | a0001c0001t0001g0085 a0001c0001t0001g0088 a0001c0001t0001g0117 others(72): Show |
75 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.1059+1210G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32740240 | |||||||
chr5:32740255 | T | C | 75 | a0001c0001t0001g0085 a0001c0001t0001g0088 a0001c0001t0001g0117 others(72): Show |
75 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.1059+1225T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32740255 | |||||||
chr5:32740302 | T | C | 75 | a0001c0001t0001g0085 a0001c0001t0001g0088 a0001c0001t0001g0117 others(72): Show |
75 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.1059+1272T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32740302 | |||||||
chr5:32740326 | A | G | 143 | a0001c0001t0001g0043 a0001c0001t0001g0085 a0001c0001t0001g0088 others(140): Show |
143 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(140): Show |
intron_variant | MODIFIER | c.1059+1296A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32740326 | |||||||
chr5:32740437 | T | A | 139 | a0001c0001t0001g0043 a0001c0001t0001g0085 a0001c0001t0001g0088 others(136): Show |
139 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(136): Show |
intron_variant | MODIFIER | c.1059+1407T>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32740437 | |||||||
chr5:32740471 | A | G | 1 | a0001c0003t0058g0035 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1059+1441A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32740471 | |||||||
chr5:32740493 | T | C | 9 | a0001c0001t0001g0314 a0001c0001t0001g0315 a0001c0001t0003g0230 others(6): Show |
9 | HG00280.hp1 HG01175.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1059+1463T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32740493 | |||||||
chr5:32740608 | G | GA | 49 | a0001c0001t0001g0043 a0001c0001t0001g0142 a0001c0001t0001g0151 others(46): Show |
49 | HG00741.hp1 HG01070.hp2 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.1059+1588dupA | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32740608 | ||||||
chr5:32740630 | G | A | 143 | a0001c0001t0001g0043 a0001c0001t0001g0085 a0001c0001t0001g0088 others(140): Show |
143 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(140): Show |
intron_variant | MODIFIER | c.1059+1600G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32740630 | |||||||
chr5:32740660 | C | T | 1 | a0001c0001t0001g0236 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1059+1630C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32740660 | |||||||
chr5:32740674 | T | C | 8 | a0001c0001t0001g0314 a0001c0001t0001g0315 a0001c0001t0003g0230 others(5): Show |
8 | HG00280.hp1 HG01175.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1059+1644T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32740674 | |||||||
chr5:32740737 | G | A | 63 | a0001c0001t0001g0085 a0001c0001t0001g0088 a0001c0001t0001g0117 others(60): Show |
63 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.1059+1707G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32740737 | |||||||
chr5:32740767 | G | A | 1 | a0001c0001t0040g0162 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1059+1737G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32740767 | |||||||
chr5:32740878 | G | A | 65 | a0001c0001t0001g0085 a0001c0001t0001g0088 a0001c0001t0001g0117 others(62): Show |
65 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.1059+1848G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32740878 | |||||||
chr5:32740930 | A | C | 2 | a0001c0001t0005g0143 a0001c0001t0043g0067 |
2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1059+1900A>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32740930 | |||||||
chr5:32740953 | C | T | 1 | a0001c0001t0008g0134 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1059+1923C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32740953 | |||||||
chr5:32740977 | T | C | 85 | a0001c0001t0001g0085 a0001c0001t0001g0088 a0001c0001t0001g0117 others(82): Show |
85 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.1059+1947T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32740977 | |||||||
chr5:32741018 | TA | T | 11 | a0001c0001t0002g0129 a0001c0001t0004g0139 a0001c0001t0015g0123 others(8): Show |
11 | HG00735.hp2 HG01074.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1059+1989delA | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32741018 | |||||||
chr5:32741027 | C | T | 9 | a0001c0001t0004g0139 a0001c0001t0015g0123 a0001c0001t0026g0049 others(6): Show |
9 | HG00735.hp2 HG01074.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1059+1997C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32741027 | |||||||
chr5:32741050 | T | TAGGTTCA others(309): Show |
1 | a0002c0002t0054g0168 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1059+2037_1059+203 others(320): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32741050 | ||||||
chr5:32741050 | T | TAGGTTCA others(317): Show |
1 | a0002c0002t0011g0261 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1059+2037_1059+203 others(328): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32741050 | ||||||
chr5:32741050 | T | TAGGTTCA others(322): Show |
1 | a0001c0001t0003g0087 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1059+2037_1059+203 others(333): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32741050 | ||||||
chr5:32741050 | T | TAGGTTCA others(326): Show |
7 | a0001c0001t0001g0126 a0002c0002t0002g0070 a0002c0002t0002g0081 others(4): Show |
7 | HG00639.hp1 HG00738.hp1 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.1059+2037_1059+203 others(337): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32741050 | ||||||
chr5:32741050 | T | TAGGTTCA others(327): Show |
14 | a0001c0001t0001g0085 a0001c0001t0001g0305 a0001c0001t0032g0216 others(11): Show |
14 | HG01516.hp1 HG02080.hp1 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.1059+2037_1059+203 others(338): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32741050 | ||||||
chr5:32741050 | T | TAGGTTCA others(328): Show |
5 | a0001c0001t0001g0229 a0001c0001t0003g0167 a0001c0001t0009g0161 others(2): Show |
5 | HG00621.hp2 HG01981.hp2 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.1059+2037_1059+203 others(339): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32741050 | ||||||
chr5:32741050 | T | TAGGTTCA others(329): Show |
2 | a0001c0001t0009g0304 a0002c0002t0002g0274 |
2 | NA18941.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.1059+2037_1059+203 others(340): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32741050 | ||||||
chr5:32741050 | T | TAGGTTCA others(330): Show |
4 | a0001c0001t0003g0083 a0002c0002t0012g0108 a0002c0002t0012g0293 others(1): Show |
4 | HG00642.hp2 HG01099.hp2 HG02015.hp2 others(1): Show |
intron_variant | MODIFIER | c.1059+2037_1059+203 others(341): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32741050 | ||||||
chr5:32741050 | T | TAGGTTCA others(331): Show |
7 | a0001c0001t0001g0117 a0001c0001t0003g0164 a0002c0002t0002g0255 others(4): Show |
7 | HG00609.hp2 HG01106.hp1 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.1059+2037_1059+203 others(342): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32741050 | ||||||
chr5:32741050 | T | TAGGTTCA others(332): Show |
6 | a0001c0001t0001g0088 a0001c0001t0003g0228 a0001c0001t0021g0080 others(3): Show |
6 | HG00609.hp1 HG00741.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.1059+2037_1059+203 others(343): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32741050 | ||||||
chr5:32741050 | T | TAGGTTCA others(333): Show |
4 | a0002c0002t0002g0009 a0002c0002t0002g0218 a0002c0002t0020g0086 others(1): Show |
4 | HG01257.hp1 HG02040.hp1 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.1059+2037_1059+203 others(344): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32741050 | ||||||
chr5:32741050 | T | TAGGTTCA others(334): Show |
2 | a0002c0002t0002g0041 a0002c0002t0033g0219 |
2 | HG02451.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.1059+2037_1059+203 others(345): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32741050 | ||||||
chr5:32741050 | T | TAGGTTCA others(335): Show |
3 | a0001c0001t0001g0306 a0001c0001t0006g0066 a0002c0002t0002g0055 |
3 | HG02630.hp1 HG02809.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.1059+2037_1059+203 others(346): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32741050 | ||||||
chr5:32741050 | T | TAGGTTCA others(336): Show |
1 | a0002c0002t0011g0260 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1059+2037_1059+203 others(347): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32741050 | ||||||
chr5:32741050 | T | TAGGTTCA others(337): Show |
2 | a0002c0002t0002g0082 a0002c0002t0011g0262 |
2 | HG04228.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.1059+2037_1059+203 others(348): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32741050 | ||||||
chr5:32741097 | G | GTTGT | 8 | a0001c0001t0001g0314 a0001c0001t0001g0315 a0001c0001t0003g0230 others(5): Show |
8 | HG00280.hp1 HG01175.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1059+2068_1059+207 others(8): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32741097 | ||||||
chr5:32741116 | C | T | 111 | a0001c0001t0001g0085 a0001c0001t0001g0088 a0001c0001t0001g0117 others(108): Show |
111 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.1059+2086C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32741116 | |||||||
chr5:32741156 | C | T | 12 | a0001c0001t0002g0129 a0001c0001t0004g0139 a0001c0001t0015g0123 others(9): Show |
12 | HG00735.hp2 HG01074.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.1059+2126C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32741156 | |||||||
chr5:32741279 | A | G | 1 | a0002c0002t0002g0070 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1059+2249A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32741279 | |||||||
chr5:32741409 | A | T | 1 | a0001c0001t0060g0289 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1059+2379A>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32741409 | |||||||
chr5:32741482 | T | C | 9 | a0001c0001t0004g0139 a0001c0001t0015g0123 a0001c0001t0026g0049 others(6): Show |
9 | HG00735.hp2 HG01074.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1059+2452T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32741482 | |||||||
chr5:32741499 | T | G | 2 | a0001c0001t0005g0143 a0001c0001t0043g0067 |
2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1059+2469T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32741499 | |||||||
chr5:32741507 | A | G | 2 | a0001c0001t0005g0143 a0001c0001t0043g0067 |
2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1059+2477A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32741507 | |||||||
chr5:32741749 | G | T | 1 | a0001c0003t0008g0032 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1059+2719G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32741749 | |||||||
chr5:32741771 | C | CT | 64 | a0001c0001t0001g0085 a0001c0001t0001g0088 a0001c0001t0001g0117 others(61): Show |
64 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.1059+2752dupT | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32741771 | ||||||
chr5:32741771 | C | CTT | 13 | a0001c0001t0002g0129 a0001c0001t0004g0139 a0001c0001t0015g0123 others(10): Show |
13 | HG00735.hp2 HG01074.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.1059+2751_1059+275 others(6): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32741771 | ||||||
chr5:32741792 | C | G | 83 | a0001c0001t0001g0085 a0001c0001t0001g0088 a0001c0001t0001g0117 others(80): Show |
83 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.1059+2762C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32741792 | |||||||
chr5:32742046 | C | T | 1 | a0001c0003t0008g0032 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1059+3016C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32742046 | |||||||
chr5:32742047 | G | A | 5 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0006g0109 others(2): Show |
5 | HG01243.hp1 HG02280.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1059+3017G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32742047 | |||||||
chr5:32742186 | C | T | 1 | a0001c0003t0058g0035 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1059+3156C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32742186 | |||||||
chr5:32742240 | T | C | 77 | a0001c0001t0001g0085 a0001c0001t0001g0088 a0001c0001t0001g0117 others(74): Show |
77 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.1059+3210T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32742240 | |||||||
chr5:32742264 | C | G | 8 | a0001c0001t0001g0314 a0001c0001t0001g0315 a0001c0001t0003g0230 others(5): Show |
8 | HG00280.hp1 HG01175.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1059+3234C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32742264 | |||||||
chr5:32742353 | G | C | 1 | a0001c0001t0003g0075 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1059+3323G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32742353 | |||||||
chr5:32742359 | C | T | 84 | a0001c0001t0001g0085 a0001c0001t0001g0088 a0001c0001t0001g0117 others(81): Show |
84 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.1059+3329C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32742359 | |||||||
chr5:32742439 | T | A | 1 | a0001c0001t0017g0057 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1059+3409T>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32742439 | |||||||
chr5:32742857 | G | A | 1 | a0001c0001t0003g0185 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1059+3827G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32742857 | |||||||
chr5:32742982 | A | G | 1 | a0001c0001t0025g0048 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1059+3952A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32742982 | |||||||
chr5:32743134 | A | C | 3 | a0001c0001t0002g0008 a0001c0001t0065g0051 a0001c0004t0062g0135 |
3 | HG02109.hp2 HG03098.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1059+4104A>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32743134 | |||||||
chr5:32743392 | A | ATG | 8 | a0001c0001t0003g0122 a0001c0001t0005g0143 a0001c0001t0007g0058 others(5): Show |
8 | HG01257.hp1 HG01978.hp1 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1059+4378_1059+437 others(6): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32743392 | ||||||
chr5:32743392 | A | ATGTG | 7 | a0001c0001t0001g0314 a0001c0001t0001g0315 a0001c0001t0003g0230 others(4): Show |
7 | HG00280.hp1 HG01175.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1059+4376_1059+437 others(8): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32743392 | ||||||
chr5:32743648 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1059+4618C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32743648 | |||||||
chr5:32743696 | G | A | 1 | a0001c0001t0008g0301 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1059+4666G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32743696 | |||||||
chr5:32743717 | G | A | 1 | a0001c0001t0003g0075 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1059+4687G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32743717 | |||||||
chr5:32743832 | G | A | 1 | a0002c0002t0002g0112 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1059+4802G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32743832 | |||||||
chr5:32743919 | A | G | 6 | a0001c0001t0004g0140 a0001c0001t0008g0045 a0001c0001t0008g0128 others(3): Show |
6 | HG02055.hp1 HG02257.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1059+4889A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32743919 | |||||||
chr5:32743987 | A | AT | 31 | a0001c0001t0001g0023 a0001c0001t0001g0060 a0001c0001t0001g0090 others(28): Show |
31 | HG01192.hp2 HG01243.hp1 HG01261.hp2 others(28): Show |
intron_variant | MODIFIER | c.1059+4981dupT | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32743987 | ||||||
chr5:32743987 | A | ATCT | 11 | a0001c0001t0001g0043 a0001c0001t0004g0140 a0001c0001t0008g0045 others(8): Show |
11 | HG01257.hp2 HG01261.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1059+4958_1059+495 others(7): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32743987 | ||||||
chr5:32743987 | A | ATCTT | 32 | a0001c0001t0001g0142 a0001c0001t0001g0151 a0001c0001t0001g0314 others(29): Show |
32 | HG00280.hp1 HG00741.hp1 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.1059+4958_1059+495 others(8): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32743987 | ||||||
chr5:32743987 | A | ATCTTT | 14 | a0001c0001t0004g0017 a0001c0001t0004g0073 a0001c0001t0004g0299 others(11): Show |
14 | HG01106.hp2 HG01192.hp1 HG01934.hp2 others(11): Show |
intron_variant | MODIFIER | c.1059+4958_1059+495 others(9): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32743987 | ||||||
chr5:32743987 | AT | A | 13 | a0001c0001t0001g0093 a0001c0001t0001g0172 a0001c0001t0001g0173 others(10): Show |
13 | HG00099.hp1 HG00099.hp2 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.1059+4981delT | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32743987 | ||||||
chr5:32743987 | ATTTTTT | A | 74 | a0001c0001t0001g0085 a0001c0001t0001g0088 a0001c0001t0001g0117 others(71): Show |
74 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.1059+4976_1059+498 others(10): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32743987 | ||||||
chr5:32743989 | T | C | 2 | a0001c0003t0023g0038 a0001c0003t0023g0039 |
2 | HG02622.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1059+4959T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32743989 | |||||||
chr5:32743990 | T | C | 2 | a0001c0001t0005g0143 a0001c0001t0043g0067 |
2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1059+4960T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32743990 | |||||||
chr5:32743994 | T | C | 1 | a0001c0001t0004g0139 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1059+4964T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32743994 | |||||||
chr5:32743995 | T | C | 74 | a0001c0001t0001g0085 a0001c0001t0001g0088 a0001c0001t0001g0117 others(71): Show |
74 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.1059+4965T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32743995 | |||||||
chr5:32744123 | G | A | 1 | a0001c0001t0065g0051 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1059+5093G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32744123 | |||||||
chr5:32744125 | T | C | 1 | a0002c0002t0002g0125 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1059+5095T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32744125 | |||||||
chr5:32744135 | G | A | 2 | a0001c0001t0003g0246 a0001c0001t0003g0253 |
2 | HG00423.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.1059+5105G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32744135 | |||||||
chr5:32744273 | G | A | 8 | a0001c0001t0001g0314 a0001c0001t0001g0315 a0001c0001t0003g0230 others(5): Show |
8 | HG00280.hp1 HG01175.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1059+5243G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32744273 | |||||||
chr5:32744597 | G | A | 5 | a0002c0002t0002g0005 a0002c0002t0002g0012 a0002c0002t0002g0112 others(2): Show |
6 | HG01346.hp1 HG02683.hp1 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.1059+5567G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32744597 | |||||||
chr5:32744635 | C | T | 2 | a0001c0001t0002g0008 a0001c0004t0062g0135 |
2 | HG02109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1059+5605C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32744635 | |||||||
chr5:32744687 | C | T | 2 | a0001c0001t0014g0105 a0001c0001t0014g0106 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1059+5657C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32744687 | |||||||
chr5:32744731 | T | C | 83 | a0001c0001t0001g0085 a0001c0001t0001g0088 a0001c0001t0001g0117 others(80): Show |
83 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.1059+5701T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32744731 | |||||||
chr5:32744790 | C | T | 112 | a0001c0001t0001g0085 a0001c0001t0001g0088 a0001c0001t0001g0117 others(109): Show |
112 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.1059+5760C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32744790 | |||||||
chr5:32744803 | C | T | 61 | a0001c0001t0001g0085 a0001c0001t0001g0088 a0001c0001t0001g0117 others(58): Show |
61 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.1059+5773C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32744803 | |||||||
chr5:32744804 | A | G | 4 | a0001c0001t0001g0056 a0001c0001t0001g0060 a0001c0001t0001g0061 others(1): Show |
4 | HG01192.hp2 HG01884.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1059+5774A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32744804 | |||||||
chr5:32744810 | T | G | 4 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0006g0010 others(1): Show |
4 | HG02145.hp2 HG02258.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1059+5780T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32744810 | |||||||
chr5:32744901 | T | A | 6 | a0001c0001t0015g0123 a0001c0001t0045g0099 a0001c0001t0047g0104 others(3): Show |
6 | HG00735.hp2 HG01074.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.1059+5871T>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32744901 | |||||||
chr5:32744923 | C | T | 86 | a0001c0001t0001g0085 a0001c0001t0001g0088 a0001c0001t0001g0117 others(83): Show |
86 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.1059+5893C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32744923 | |||||||
chr5:32745105 | A | G | 1 | a0002c0002t0002g0204 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1059+6075A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32745105 | |||||||
chr5:32745153 | C | T | 7 | a0002c0002t0002g0070 a0002c0002t0002g0136 a0002c0002t0002g0274 others(4): Show |
7 | HG01981.hp2 HG02293.hp2 NA18943.hp2 others(4): Show |
intron_variant | MODIFIER | c.1059+6123C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32745153 | |||||||
chr5:32745177 | A | C | 124 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0026 others(121): Show |
125 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.1059+6147A>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32745177 | |||||||
chr5:32745242 | C | T | 2 | a0001c0001t0005g0143 a0001c0001t0043g0067 |
2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1059+6212C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32745242 | |||||||
chr5:32745251 | C | A | 14 | a0001c0001t0002g0008 a0001c0001t0003g0075 a0001c0001t0004g0140 others(11): Show |
14 | HG01074.hp2 HG02055.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1059+6221C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32745251 | |||||||
chr5:32745328 | A | C | 1 | a0001c0001t0003g0248 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1059+6298A>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32745328 | |||||||
chr5:32745490 | T | G | 1 | a0001c0001t0003g0075 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1059+6460T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32745490 | |||||||
chr5:32745527 | A | G | 8 | a0001c0001t0006g0063 a0001c0001t0006g0065 a0001c0001t0008g0134 others(5): Show |
8 | HG01891.hp2 HG02486.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1059+6497A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32745527 | |||||||
chr5:32745562 | A | G | 1 | a0001c0001t0004g0044 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1059+6532A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32745562 | |||||||
chr5:32745592 | A | G | 2 | a0001c0006t0061g0046 a0002c0002t0002g0072 |
2 | HG02055.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1059+6562A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32745592 | |||||||
chr5:32745646 | C | A | 145 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0026 others(142): Show |
146 | HG00323.hp1 HG00423.hp2 HG00609.hp1 others(143): Show |
intron_variant | MODIFIER | c.1059+6616C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32745646 | |||||||
chr5:32745720 | G | C | 1 | a0002c0002t0011g0260 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1059+6690G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32745720 | |||||||
chr5:32745949 | T | C | 1 | a0001c0001t0050g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1059+6919T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32745949 | |||||||
chr5:32746071 | G | A | 1 | a0002c0002t0027g0127 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1059+7041G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32746071 | |||||||
chr5:32746173 | T | C | 2 | a0001c0004t0062g0135 a0001c0005t0056g0266 |
2 | HG02109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1059+7143T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32746173 | |||||||
chr5:32746320 | T | C | 1 | a0001c0003t0008g0032 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1059+7290T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32746320 | |||||||
chr5:32746399 | C | T | 1 | a0001c0001t0001g0206 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1059+7369C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32746399 | |||||||
chr5:32746441 | A | G | 123 | a0001c0001t0001g0025 a0001c0001t0001g0085 a0001c0001t0001g0088 others(120): Show |
123 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(120): Show |
intron_variant | MODIFIER | c.1059+7411A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32746441 | |||||||
chr5:32746459 | G | A | 1 | a0001c0001t0015g0123 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1059+7429G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32746459 | |||||||
chr5:32746475 | A | C | 3 | a0001c0001t0001g0142 a0001c0001t0001g0151 a0001c0001t0066g0053 |
3 | HG01243.hp2 HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1059+7445A>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32746475 | |||||||
chr5:32747073 | T | C | 13 | a0001c0001t0005g0079 a0001c0001t0005g0153 a0001c0001t0024g0263 others(10): Show |
14 | HG02145.hp1 HG02258.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1059+8043T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32747073 | |||||||
chr5:32747082 | A | G | 63 | a0001c0001t0001g0085 a0001c0001t0001g0088 a0001c0001t0001g0117 others(60): Show |
63 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.1059+8052A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32747082 | |||||||
chr5:32747198 | C | A | 1 | a0001c0001t0004g0016 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1059+8168C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32747198 | |||||||
chr5:32747605 | C | T | 1 | a0001c0001t0002g0008 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1059+8575C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32747605 | |||||||
chr5:32747728 | C | T | 15 | a0001c0001t0004g0016 a0001c0001t0004g0017 a0001c0001t0004g0027 others(12): Show |
15 | HG00735.hp2 HG00741.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.1059+8698C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32747728 | |||||||
chr5:32747748 | G | A | 16 | a0001c0001t0005g0079 a0001c0001t0005g0143 a0001c0001t0005g0153 others(13): Show |
17 | HG02145.hp1 HG02258.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.1059+8718G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32747748 | |||||||
chr5:32747757 | AT | A | 113 | a0001c0001t0001g0085 a0001c0001t0001g0088 a0001c0001t0001g0117 others(110): Show |
113 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(110): Show |
intron_variant | MODIFIER | c.1059+8743delT | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32747757 | ||||||
chr5:32748049 | C | T | 1 | a0001c0001t0022g0221 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1059+9019C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32748049 | |||||||
chr5:32748156 | C | A | 1 | a0001c0006t0061g0046 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1059+9126C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32748156 | |||||||
chr5:32748206 | C | T | 4 | a0001c0001t0015g0123 a0001c0006t0061g0046 a0002c0002t0002g0072 others(1): Show |
4 | HG01952.hp1 HG02055.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1059+9176C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32748206 | |||||||
chr5:32748247 | A | G | 1 | a0001c0001t0057g0281 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1059+9217A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32748247 | |||||||
chr5:32748433 | A | AGCAT | 118 | a0001c0001t0001g0025 a0001c0001t0001g0085 a0001c0001t0001g0088 others(115): Show |
118 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(115): Show |
intron_variant | MODIFIER | c.1059+9404_1059+940 others(8): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32748433 | ||||||
chr5:32748531 | G | A | 118 | a0001c0001t0001g0025 a0001c0001t0001g0085 a0001c0001t0001g0088 others(115): Show |
118 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(115): Show |
intron_variant | MODIFIER | c.1059+9501G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32748531 | |||||||
chr5:32748552 | G | A | 118 | a0001c0001t0001g0025 a0001c0001t0001g0085 a0001c0001t0001g0088 others(115): Show |
118 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(115): Show |
intron_variant | MODIFIER | c.1059+9522G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32748552 | |||||||
chr5:32748582 | G | A | 1 | a0001c0001t0008g0134 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1059+9552G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32748582 | |||||||
chr5:32748635 | A | G | 5 | a0001c0001t0004g0140 a0001c0001t0008g0045 a0001c0001t0008g0128 others(2): Show |
5 | HG02257.hp1 HG02976.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1059+9605A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32748635 | |||||||
chr5:32748956 | A | G | 1 | a0001c0001t0003g0164 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1059+9926A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32748956 | |||||||
chr5:32748966 | T | C | 1 | a0001c0001t0040g0162 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1059+9936T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32748966 | |||||||
chr5:32749042 | G | A | 1 | a0001c0001t0034g0159 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1059+10012G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32749042 | |||||||
chr5:32749049 | C | T | 2 | a0001c0001t0004g0148 a0001c0001t0004g0149 |
2 | HG00741.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.1059+10019C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32749049 | |||||||
chr5:32749196 | AT | A | 152 | a0001c0001t0001g0025 a0001c0001t0001g0043 a0001c0001t0001g0085 others(149): Show |
153 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(150): Show |
intron_variant | MODIFIER | c.1059+10173delT | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32749196 | ||||||
chr5:32749228 | A | C | 1 | a0001c0001t0003g0245 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1059+10198A>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32749228 | |||||||
chr5:32749234 | C | T | 36 | a0001c0001t0001g0142 a0001c0001t0001g0151 a0001c0001t0004g0016 others(33): Show |
36 | HG00735.hp2 HG00741.hp1 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.1059+10204C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32749234 | |||||||
chr5:32749317 | T | A | 1 | a0001c0001t0065g0051 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1059+10287T>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32749317 | |||||||
chr5:32749318 | A | T | 128 | a0001c0001t0001g0024 a0001c0001t0001g0085 a0001c0001t0001g0088 others(125): Show |
128 | HG00423.hp1 HG00423.hp2 HG00609.hp1 others(125): Show |
intron_variant | MODIFIER | c.1059+10288A>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32749318 | |||||||
chr5:32749355 | C | T | 1 | a0001c0001t0003g0241 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1059+10325C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32749355 | |||||||
chr5:32749432 | T | C | 1 | a0001c0001t0004g0148 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1059+10402T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32749432 | |||||||
chr5:32749486 | G | A | 117 | a0001c0001t0001g0085 a0001c0001t0001g0088 a0001c0001t0001g0117 others(114): Show |
117 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(114): Show |
intron_variant | MODIFIER | c.1059+10456G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32749486 | |||||||
chr5:32749523 | A | G | 1 | a0001c0001t0003g0183 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1059+10493A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32749523 | |||||||
chr5:32749643 | T | C | 1 | a0002c0002t0002g0275 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1059+10613T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32749643 | |||||||
chr5:32749745 | C | T | 2 | a0001c0004t0062g0135 a0001c0005t0056g0266 |
2 | HG02109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1059+10715C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32749745 | |||||||
chr5:32749774 | C | A | 1 | a0002c0002t0002g0145 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1059+10744C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32749774 | |||||||
chr5:32749845 | C | T | 1 | a0002c0002t0002g0136 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1059+10815C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32749845 | |||||||
chr5:32749883 | C | T | 1 | a0001c0001t0025g0048 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1059+10853C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32749883 | |||||||
chr5:32749896 | A | G | 11 | a0001c0001t0003g0111 a0001c0001t0003g0116 a0001c0001t0003g0157 others(8): Show |
11 | HG00544.hp2 HG02027.hp1 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.1059+10866A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32749896 | |||||||
chr5:32749969 | A | G | 1 | a0001c0001t0040g0162 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1059+10939A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32749969 | |||||||
chr5:32750276 | C | T | 1 | a0001c0003t0005g0031 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1059+11246C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32750276 | |||||||
chr5:32750292 | C | T | 36 | a0001c0001t0001g0142 a0001c0001t0001g0151 a0001c0001t0004g0016 others(33): Show |
36 | HG00735.hp2 HG00741.hp1 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.1059+11262C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32750292 | |||||||
chr5:32750309 | G | T | 115 | a0001c0001t0001g0025 a0001c0001t0001g0085 a0001c0001t0001g0088 others(112): Show |
115 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.1059+11279G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32750309 | |||||||
chr5:32750641 | G | A | 1 | a0001c0001t0003g0083 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1059+11611G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32750641 | |||||||
chr5:32750675 | A | C | 1 | a0001c0001t0065g0051 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1059+11645A>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32750675 | |||||||
chr5:32750783 | T | C | 1 | a0001c0001t0064g0054 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1059+11753T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32750783 | |||||||
chr5:32750784 | C | T | 1 | a0002c0002t0002g0125 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1059+11754C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32750784 | |||||||
chr5:32750801 | C | T | 2 | a0001c0001t0019g0006 a0001c0001t0019g0007 |
2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1059+11771C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32750801 | |||||||
chr5:32750877 | T | C | 140 | a0001c0001t0001g0025 a0001c0001t0001g0043 a0001c0001t0001g0088 others(137): Show |
141 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(138): Show |
intron_variant | MODIFIER | c.1059+11847T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32750877 | |||||||
chr5:32751044 | G | A | 1 | a0001c0001t0040g0162 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1059+12014G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32751044 | |||||||
chr5:32751155 | TA | T | 63 | a0001c0001t0001g0088 a0001c0001t0001g0126 a0001c0001t0001g0229 others(60): Show |
63 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.1059+12131delA | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32751155 | ||||||
chr5:32751155 | TAA | T | 5 | a0001c0001t0001g0182 a0001c0001t0003g0176 a0001c0001t0013g0278 others(2): Show |
5 | HG01496.hp2 HG01934.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.1059+12130_1059+12 others(8): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32751155 | ||||||
chr5:32751436 | G | A | 5 | a0001c0001t0015g0123 a0001c0001t0047g0104 a0001c0006t0061g0046 others(2): Show |
5 | HG01074.hp1 HG01952.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1059+12406G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32751436 | |||||||
chr5:32751560 | G | A | 5 | a0001c0001t0015g0123 a0001c0001t0047g0104 a0001c0006t0061g0046 others(2): Show |
5 | HG01074.hp1 HG01952.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1059+12530G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32751560 | |||||||
chr5:32751683 | G | A | 2 | a0001c0001t0019g0006 a0001c0001t0019g0007 |
2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1059+12653G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32751683 | |||||||
chr5:32751880 | G | A | 5 | a0001c0001t0004g0140 a0001c0001t0008g0045 a0001c0001t0008g0128 others(2): Show |
5 | HG02257.hp1 HG02976.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1059+12850G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32751880 | |||||||
chr5:32751921 | G | A | 43 | a0001c0001t0001g0142 a0001c0001t0001g0151 a0001c0001t0004g0016 others(40): Show |
43 | HG00735.hp2 HG00741.hp1 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.1059+12891G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32751921 | |||||||
chr5:32751989 | G | A | 1 | a0001c0001t0007g0152 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1059+12959G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32751989 | |||||||
chr5:32751992 | G | A | 72 | a0001c0001t0001g0025 a0001c0001t0001g0088 a0001c0001t0001g0126 others(69): Show |
72 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.1059+12962G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32751992 | |||||||
chr5:32752022 | T | G | 67 | a0001c0001t0001g0025 a0001c0001t0001g0088 a0001c0001t0001g0126 others(64): Show |
67 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.1059+12992T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32752022 | |||||||
chr5:32752029 | C | T | 2 | a0001c0001t0004g0044 a0001c0001t0042g0042 |
2 | HG03516.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1059+12999C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32752029 | |||||||
chr5:32752030 | C | T | 1 | a0001c0001t0024g0263 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1059+13000C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32752030 | |||||||
chr5:32752045 | T | C | 72 | a0001c0001t0001g0025 a0001c0001t0001g0088 a0001c0001t0001g0126 others(69): Show |
72 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.1059+13015T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32752045 | |||||||
chr5:32752051 | A | C | 1 | a0001c0001t0004g0073 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1059+13021A>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32752051 | |||||||
chr5:32752068 | G | T | 5 | a0001c0001t0015g0123 a0001c0001t0047g0104 a0001c0006t0061g0046 others(2): Show |
5 | HG01074.hp1 HG01952.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1059+13038G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32752068 | |||||||
chr5:32752160 | T | C | 4 | a0001c0001t0004g0299 a0001c0001t0004g0300 a0001c0001t0004g0302 others(1): Show |
4 | HG02922.hp1 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1059+13130T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32752160 | |||||||
chr5:32752201 | C | T | 4 | a0001c0001t0003g0095 a0001c0001t0003g0296 a0001c0001t0003g0297 others(1): Show |
4 | HG02083.hp1 NA18950.hp1 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.1059+13171C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32752201 | |||||||
chr5:32752207 | CCAAAAA | C | 52 | a0001c0001t0001g0043 a0001c0001t0001g0142 a0001c0001t0001g0151 others(49): Show |
52 | HG00735.hp2 HG00741.hp1 HG01070.hp2 others(49): Show |
intron_variant | MODIFIER | c.1059+13216_1059+13 others(12): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32752207 | ||||||
chr5:32752207 | CCAAAAAC others(5): Show |
C | 73 | a0001c0001t0001g0025 a0001c0001t0001g0088 a0001c0001t0001g0126 others(70): Show |
73 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.1059+13210_1059+13 others(18): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32752207 | ||||||
chr5:32752207 | CCAAAAAC others(11): Show |
C | 15 | a0001c0001t0005g0079 a0001c0001t0005g0153 a0001c0001t0007g0152 others(12): Show |
16 | HG02145.hp1 HG02258.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1059+13204_1059+13 others(24): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32752207 | ||||||
chr5:32752258 | C | T | 1 | a0001c0001t0003g0101 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1059+13228C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32752258 | |||||||
chr5:32752333 | C | T | 5 | a0001c0001t0003g0111 a0001c0001t0003g0157 a0001c0001t0003g0174 others(2): Show |
5 | HG02027.hp1 HG02523.hp1 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.1059+13303C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32752333 | |||||||
chr5:32752469 | C | T | 1 | a0002c0002t0002g0220 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1059+13439C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32752469 | |||||||
chr5:32752493 | G | T | 41 | a0001c0001t0001g0142 a0001c0001t0001g0151 a0001c0001t0004g0016 others(38): Show |
41 | HG00735.hp2 HG00741.hp1 HG01070.hp2 others(38): Show |
intron_variant | MODIFIER | c.1059+13463G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32752493 | |||||||
chr5:32752533 | G | T | 4 | a0001c0001t0004g0299 a0001c0001t0004g0300 a0001c0001t0004g0302 others(1): Show |
4 | HG02922.hp1 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1059+13503G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32752533 | |||||||
chr5:32752545 | C | T | 1 | a0001c0001t0006g0066 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1059+13515C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32752545 | |||||||
chr5:32752582 | A | G | 2 | a0001c0001t0001g0195 a0001c0001t0001g0312 |
2 | HG00544.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.1059+13552A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32752582 | |||||||
chr5:32753080 | G | A | 1 | a0001c0001t0050g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1059+14050G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32753080 | |||||||
chr5:32753120 | A | G | 1 | a0001c0001t0003g0176 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1059+14090A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32753120 | |||||||
chr5:32753190 | A | G | 1 | a0001c0001t0021g0080 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1059+14160A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32753190 | |||||||
chr5:32753323 | C | CT | 6 | a0001c0001t0006g0063 a0001c0001t0006g0065 a0001c0001t0017g0057 others(3): Show |
6 | HG01891.hp2 HG02809.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1059+14306dupT | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32753323 | ||||||
chr5:32753323 | C | T | 6 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0026 others(3): Show |
7 | HG00323.hp1 HG00639.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.1059+14293C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32753323 | |||||||
chr5:32753323 | CTT | C | 69 | a0001c0001t0001g0025 a0001c0001t0001g0088 a0001c0001t0001g0126 others(66): Show |
69 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.1059+14305_1059+14 others(8): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32753323 | ||||||
chr5:32753331 | T | C | 5 | a0001c0001t0015g0123 a0001c0001t0047g0104 a0001c0006t0061g0046 others(2): Show |
5 | HG01074.hp1 HG01952.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1059+14301T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32753331 | |||||||
chr5:32753387 | A | G | 1 | a0001c0001t0003g0298 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1059+14357A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32753387 | |||||||
chr5:32753439 | G | A | 2 | a0001c0001t0026g0049 a0001c0001t0026g0052 |
2 | HG02622.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1059+14409G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32753439 | |||||||
chr5:32753501 | C | G | 2 | a0001c0001t0004g0139 a0001c0001t0055g0147 |
2 | HG01192.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.1059+14471C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32753501 | |||||||
chr5:32753501 | C | T | 5 | a0001c0001t0015g0123 a0001c0001t0047g0104 a0001c0006t0061g0046 others(2): Show |
5 | HG01074.hp1 HG01952.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1059+14471C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32753501 | |||||||
chr5:32753566 | T | C | 64 | a0001c0001t0001g0025 a0001c0001t0001g0088 a0001c0001t0001g0126 others(61): Show |
64 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.1059+14536T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32753566 | |||||||
chr5:32753585 | C | T | 1 | a0001c0001t0001g0247 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1059+14555C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32753585 | |||||||
chr5:32753624 | C | CT | 27 | a0001c0001t0001g0060 a0001c0001t0001g0172 a0001c0001t0001g0188 others(24): Show |
28 | HG01069.hp1 HG01069.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.1059+14620dupT | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32753624 | ||||||
chr5:32753624 | CT | C | 22 | a0001c0001t0001g0019 a0001c0001t0001g0043 a0001c0001t0001g0062 others(19): Show |
22 | HG01074.hp2 HG01192.hp1 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.1059+14620delT | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32753624 | ||||||
chr5:32753624 | CTT | C | 59 | a0001c0001t0001g0069 a0001c0001t0001g0088 a0001c0001t0001g0229 others(56): Show |
59 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.1059+14619_1059+14 others(8): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32753624 | ||||||
chr5:32753624 | CTTT | C | 8 | a0001c0001t0001g0126 a0001c0001t0005g0143 a0001c0001t0015g0103 others(5): Show |
8 | HG00280.hp1 HG01261.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1059+14618_1059+14 others(9): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32753624 | ||||||
chr5:32753624 | CTTTT | C | 16 | a0001c0001t0001g0025 a0001c0001t0005g0079 a0001c0001t0005g0153 others(13): Show |
17 | HG02145.hp1 HG02258.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.1059+14617_1059+14 others(10): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32753624 | ||||||
chr5:32753624 | CTTTTT | C | 34 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0142 others(31): Show |
34 | HG00735.hp2 HG00741.hp1 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.1059+14616_1059+14 others(11): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32753624 | ||||||
chr5:32753624 | CTTTTTT | C | 12 | a0001c0001t0006g0063 a0001c0001t0006g0065 a0001c0001t0008g0134 others(9): Show |
12 | HG01891.hp2 HG02486.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.1059+14615_1059+14 others(12): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32753624 | ||||||
chr5:32753674 | A | G | 1 | a0001c0001t0008g0134 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1059+14644A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32753674 | |||||||
chr5:32753744 | A | G | 5 | a0001c0001t0015g0123 a0001c0001t0047g0104 a0001c0006t0061g0046 others(2): Show |
5 | HG01074.hp1 HG01952.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1059+14714A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32753744 | |||||||
chr5:32754004 | C | T | 2 | a0001c0004t0062g0135 a0001c0005t0056g0266 |
2 | HG02109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1059+14974C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32754004 | |||||||
chr5:32754053 | C | T | 1 | a0001c0001t0003g0164 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1059+15023C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32754053 | |||||||
chr5:32754129 | A | G | 2 | a0001c0001t0001g0267 a0001c0001t0009g0194 |
2 | NA19011.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.1059+15099A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32754129 | |||||||
chr5:32754326 | T | C | 3 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0006g0010 |
3 | HG02145.hp2 HG02258.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1059+15296T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32754326 | |||||||
chr5:32754347 | G | GT | 55 | a0001c0001t0001g0025 a0001c0001t0001g0090 a0001c0001t0001g0132 others(52): Show |
55 | HG00280.hp1 HG00735.hp2 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.1059+15327dupT | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32754347 | ||||||
chr5:32754384 | T | C | 1 | a0001c0003t0044g0036 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1059+15354T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32754384 | |||||||
chr5:32754696 | G | T | 5 | a0001c0001t0015g0123 a0001c0001t0047g0104 a0001c0006t0061g0046 others(2): Show |
5 | HG01074.hp1 HG01952.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1059+15666G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32754696 | |||||||
chr5:32754979 | G | C | 6 | a0001c0001t0001g0025 a0001c0001t0001g0132 a0001c0001t0001g0133 others(3): Show |
6 | HG00280.hp1 HG02145.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1059+15949G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32754979 | |||||||
chr5:32754996 | G | A | 5 | a0001c0001t0015g0123 a0001c0001t0047g0104 a0001c0006t0061g0046 others(2): Show |
5 | HG01074.hp1 HG01952.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1059+15966G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32754996 | |||||||
chr5:32755093 | C | T | 1 | a0002c0002t0002g0145 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1059+16063C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32755093 | |||||||
chr5:32755155 | C | T | 1 | a0001c0001t0003g0101 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1059+16125C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32755155 | |||||||
chr5:32755248 | T | C | 1 | a0001c0001t0007g0152 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1059+16218T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32755248 | |||||||
chr5:32755275 | G | C | 1 | a0001c0001t0001g0179 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1059+16245G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32755275 | |||||||
chr5:32755416 | T | C | 43 | a0001c0001t0001g0142 a0001c0001t0001g0151 a0001c0001t0004g0016 others(40): Show |
43 | HG00735.hp2 HG00741.hp1 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.1059+16386T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32755416 | |||||||
chr5:32755418 | G | T | 3 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0006g0010 |
3 | HG02145.hp2 HG02258.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1059+16388G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32755418 | |||||||
chr5:32755483 | T | C | 70 | a0001c0001t0001g0025 a0001c0001t0001g0088 a0001c0001t0001g0126 others(67): Show |
70 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.1059+16453T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32755483 | |||||||
chr5:32755858 | G | T | 6 | a0001c0001t0001g0025 a0001c0001t0001g0132 a0001c0001t0001g0133 others(3): Show |
6 | HG00280.hp1 HG02145.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1059+16828G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32755858 | |||||||
chr5:32756101 | C | T | 3 | a0001c0001t0001g0026 a0001c0001t0001g0197 a0001c0001t0001g0198 |
3 | HG02683.hp2 HG04204.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1059+17071C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32756101 | |||||||
chr5:32756162 | T | C | 1 | a0001c0001t0007g0152 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1059+17132T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32756162 | |||||||
chr5:32756237 | A | T | 2 | a0002c0002t0002g0041 a0002c0002t0002g0055 |
2 | HG02451.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1059+17207A>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32756237 | |||||||
chr5:32756238 | G | A | 2 | a0002c0002t0002g0041 a0002c0002t0002g0055 |
2 | HG02451.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1059+17208G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32756238 | |||||||
chr5:32756288 | C | T | 1 | a0002c0002t0027g0127 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1059+17258C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32756288 | |||||||
chr5:32756289 | A | G | 1 | a0002c0002t0027g0127 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1059+17259A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32756289 | |||||||
chr5:32756321 | T | A | 36 | a0001c0001t0001g0142 a0001c0001t0001g0151 a0001c0001t0004g0016 others(33): Show |
36 | HG00735.hp2 HG00741.hp1 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.1059+17291T>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32756321 | |||||||
chr5:32756373 | A | T | 1 | a0001c0001t0007g0152 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1059+17343A>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32756373 | |||||||
chr5:32756433 | T | C | 70 | a0001c0001t0001g0025 a0001c0001t0001g0088 a0001c0001t0001g0126 others(67): Show |
70 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.1059+17403T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32756433 | |||||||
chr5:32756486 | G | A | 5 | a0001c0001t0004g0140 a0001c0001t0008g0045 a0001c0001t0008g0128 others(2): Show |
5 | HG02257.hp1 HG02976.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1059+17456G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32756486 | |||||||
chr5:32756494 | C | T | 1 | a0001c0001t0065g0051 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1059+17464C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32756494 | |||||||
chr5:32756544 | T | A | 2 | a0001c0003t0023g0038 a0001c0003t0023g0039 |
2 | HG02622.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1059+17514T>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32756544 | |||||||
chr5:32756669 | C | G | 6 | a0001c0001t0003g0095 a0001c0001t0003g0296 a0001c0001t0003g0297 others(3): Show |
6 | HG02083.hp1 HG02723.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.1059+17639C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32756669 | |||||||
chr5:32756683 | C | T | 1 | a0001c0001t0021g0080 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1059+17653C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32756683 | |||||||
chr5:32756854 | A | C | 1 | a0002c0002t0002g0145 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1059+17824A>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32756854 | |||||||
chr5:32756857 | G | C | 2 | a0001c0001t0001g0088 a0001c0001t0001g0126 |
2 | HG00741.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1059+17827G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32756857 | |||||||
chr5:32756875 | T | G | 1 | a0001c0001t0001g0169 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1060-17833T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32756875 | |||||||
chr5:32756911 | T | A | 1 | a0001c0001t0003g0095 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1060-17797T>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32756911 | |||||||
chr5:32756938 | G | C | 3 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0006g0010 |
3 | HG02145.hp2 HG02258.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1060-17770G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32756938 | |||||||
chr5:32757035 | C | T | 1 | a0001c0001t0007g0152 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1060-17673C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32757035 | |||||||
chr5:32757036 | A | G | 1 | a0001c0001t0007g0152 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1060-17672A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32757036 | |||||||
chr5:32757062 | G | A | 1 | a0001c0001t0010g0003 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1060-17646G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32757062 | |||||||
chr5:32757102 | C | T | 1 | a0001c0001t0007g0152 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1060-17606C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32757102 | |||||||
chr5:32757143 | A | C | 8 | a0001c0001t0001g0243 a0001c0001t0003g0004 a0001c0001t0003g0167 others(5): Show |
9 | HG00621.hp1 HG02015.hp1 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.1060-17565A>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32757143 | |||||||
chr5:32757166 | A | T | 70 | a0001c0001t0001g0025 a0001c0001t0001g0088 a0001c0001t0001g0126 others(67): Show |
70 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.1060-17542A>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32757166 | |||||||
chr5:32757175 | A | G | 28 | a0001c0001t0001g0243 a0001c0001t0003g0004 a0001c0001t0003g0091 others(25): Show |
30 | HG00621.hp1 HG01109.hp1 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.1060-17533A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32757175 | |||||||
chr5:32757185 | G | T | 2 | a0002c0002t0020g0086 a0002c0002t0020g0225 |
2 | HG02040.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.1060-17523G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32757185 | |||||||
chr5:32757202 | C | A | 4 | a0001c0001t0015g0123 a0001c0001t0047g0104 a0001c0006t0061g0046 others(1): Show |
4 | HG01074.hp1 HG01952.hp1 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.1060-17506C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32757202 | |||||||
chr5:32757211 | C | T | 2 | a0001c0001t0006g0109 a0001c0001t0006g0110 |
2 | HG01243.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1060-17497C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32757211 | |||||||
chr5:32757226 | C | G | 1 | a0001c0001t0015g0123 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1060-17482C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32757226 | |||||||
chr5:32757299 | T | C | 1 | a0001c0001t0003g0122 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1060-17409T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32757299 | |||||||
chr5:32757335 | G | T | 1 | a0001c0001t0040g0162 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1060-17373G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32757335 | |||||||
chr5:32757349 | T | G | 1 | a0001c0001t0040g0162 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1060-17359T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32757349 | |||||||
chr5:32757538 | A | C | 4 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0023 others(1): Show |
4 | HG00735.hp1 HG00738.hp2 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.1060-17170A>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32757538 | |||||||
chr5:32757546 | A | C | 1 | a0001c0001t0001g0114 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1060-17162A>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32757546 | |||||||
chr5:32757585 | C | G | 1 | a0002c0002t0002g0145 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1060-17123C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32757585 | |||||||
chr5:32757679 | A | G | 1 | a0002c0002t0002g0310 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1060-17029A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32757679 | |||||||
chr5:32757756 | T | C | 2 | a0001c0001t0001g0314 a0001c0001t0001g0315 |
2 | NA19060.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1060-16952T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32757756 | |||||||
chr5:32757759 | T | A | 6 | a0001c0001t0001g0025 a0001c0001t0001g0132 a0001c0001t0001g0133 others(3): Show |
6 | HG00280.hp1 HG02145.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1060-16949T>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32757759 | |||||||
chr5:32757797 | G | A | 1 | a0002c0002t0002g0204 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1060-16911G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32757797 | |||||||
chr5:32757817 | T | C | 1 | a0001c0001t0001g0020 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1060-16891T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32757817 | |||||||
chr5:32757832 | G | A | 2 | a0001c0003t0023g0038 a0001c0003t0023g0039 |
2 | HG02622.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1060-16876G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32757832 | |||||||
chr5:32758043 | G | T | 2 | a0001c0001t0003g0091 a0001c0001t0003g0203 |
2 | NA18940.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.1060-16665G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32758043 | |||||||
chr5:32758051 | T | C | 1 | a0001c0001t0040g0162 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1060-16657T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32758051 | |||||||
chr5:32758060 | CT | C | 3 | a0001c0001t0001g0025 a0001c0001t0015g0103 a0002c0002t0002g0270 |
3 | HG00280.hp1 HG02818.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1060-16647delT | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32758060 | |||||||
chr5:32758062 | CT | C | 133 | a0001c0001t0001g0043 a0001c0001t0001g0088 a0001c0001t0001g0126 others(130): Show |
134 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(131): Show |
intron_variant | MODIFIER | c.1060-16638delT | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32758062 | ||||||
chr5:32758063 | T | C | 3 | a0001c0001t0001g0025 a0001c0001t0015g0103 a0002c0002t0002g0270 |
3 | HG00280.hp1 HG02818.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1060-16645T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32758063 | |||||||
chr5:32758114 | C | G | 1 | a0001c0001t0040g0162 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1060-16594C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32758114 | |||||||
chr5:32758256 | A | C | 1 | a0001c0001t0001g0133 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1060-16452A>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32758256 | |||||||
chr5:32758348 | G | A | 43 | a0001c0001t0001g0142 a0001c0001t0001g0151 a0001c0001t0004g0016 others(40): Show |
43 | HG00735.hp2 HG00741.hp1 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.1060-16360G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32758348 | |||||||
chr5:32758404 | T | C | 60 | a0001c0001t0001g0088 a0001c0001t0001g0126 a0001c0001t0001g0229 others(57): Show |
60 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.1060-16304T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32758404 | |||||||
chr5:32758472 | G | A | 2 | a0002c0002t0011g0262 a0002c0002t0054g0168 |
2 | HG02698.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1060-16236G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32758472 | |||||||
chr5:32758551 | T | C | 70 | a0001c0001t0001g0025 a0001c0001t0001g0088 a0001c0001t0001g0126 others(67): Show |
70 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.1060-16157T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32758551 | |||||||
chr5:32758582 | G | GT | 69 | a0001c0001t0001g0025 a0001c0001t0001g0088 a0001c0001t0001g0126 others(66): Show |
69 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.1060-16120dupT | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32758582 | ||||||
chr5:32758758 | T | G | 1 | a0001c0001t0051g0269 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1060-15950T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32758758 | |||||||
chr5:32758815 | A | G | 1 | a0001c0001t0008g0134 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1060-15893A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32758815 | |||||||
chr5:32758923 | T | A | 16 | a0001c0001t0005g0079 a0001c0001t0005g0143 a0001c0001t0005g0153 others(13): Show |
17 | HG02145.hp1 HG02258.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.1060-15785T>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32758923 | |||||||
chr5:32758939 | T | G | 5 | a0001c0001t0015g0123 a0001c0001t0047g0104 a0001c0006t0061g0046 others(2): Show |
5 | HG01074.hp1 HG01952.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1060-15769T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32758939 | |||||||
chr5:32758980 | A | C | 5 | a0001c0001t0004g0140 a0001c0001t0008g0045 a0001c0001t0008g0128 others(2): Show |
5 | HG02257.hp1 HG02976.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1060-15728A>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32758980 | |||||||
chr5:32759035 | A | G | 1 | a0001c0005t0056g0266 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1060-15673A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32759035 | |||||||
chr5:32759233 | G | A | 1 | a0002c0002t0002g0136 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1060-15475G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32759233 | |||||||
chr5:32759285 | T | C | 70 | a0001c0001t0001g0025 a0001c0001t0001g0088 a0001c0001t0001g0126 others(67): Show |
70 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.1060-15423T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32759285 | |||||||
chr5:32759422 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1060-15286G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32759422 | |||||||
chr5:32759436 | T | G | 70 | a0001c0001t0001g0025 a0001c0001t0001g0088 a0001c0001t0001g0126 others(67): Show |
70 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.1060-15272T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32759436 | |||||||
chr5:32759446 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1060-15262T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32759446 | |||||||
chr5:32759451 | T | G | 1 | a0001c0001t0001g0113 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1060-15257T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32759451 | |||||||
chr5:32759457 | C | G | 1 | a0001c0001t0001g0113 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1060-15251C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32759457 | |||||||
chr5:32759458 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1060-15250C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32759458 | |||||||
chr5:32759475 | C | T | 14 | a0001c0001t0001g0113 a0001c0001t0005g0079 a0001c0001t0005g0153 others(11): Show |
15 | HG02040.hp2 HG02145.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1060-15233C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32759475 | |||||||
chr5:32759487 | C | T | 6 | a0001c0001t0001g0025 a0001c0001t0001g0132 a0001c0001t0001g0133 others(3): Show |
6 | HG00280.hp1 HG02145.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1060-15221C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32759487 | |||||||
chr5:32759488 | G | A | 1 | a0001c0001t0065g0051 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1060-15220G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32759488 | |||||||
chr5:32759488 | G | C | 1 | a0001c0001t0001g0113 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1060-15220G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32759488 | |||||||
chr5:32759507 | T | G | 43 | a0001c0001t0001g0142 a0001c0001t0001g0151 a0001c0001t0004g0016 others(40): Show |
43 | HG00735.hp2 HG00741.hp1 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.1060-15201T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32759507 | |||||||
chr5:32759515 | G | T | 1 | a0001c0001t0053g0311 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1060-15193G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32759515 | |||||||
chr5:32759538 | T | C | 1 | a0002c0002t0052g0163 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1060-15170T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32759538 | |||||||
chr5:32759652 | G | T | 1 | a0001c0001t0001g0273 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1060-15056G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32759652 | |||||||
chr5:32759671 | C | T | 6 | a0001c0001t0001g0025 a0001c0001t0001g0132 a0001c0001t0001g0133 others(3): Show |
6 | HG00280.hp1 HG02145.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1060-15037C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32759671 | |||||||
chr5:32759681 | TG | T | 6 | a0001c0001t0001g0025 a0001c0001t0001g0132 a0001c0001t0001g0133 others(3): Show |
6 | HG00280.hp1 HG02145.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1060-15025delG | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32759681 | ||||||
chr5:32759713 | C | T | 3 | a0001c0001t0008g0128 a0001c0001t0008g0301 a0001c0001t0059g0156 |
3 | HG02257.hp1 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1060-14995C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32759713 | |||||||
chr5:32759716 | T | G | 6 | a0001c0001t0001g0025 a0001c0001t0001g0132 a0001c0001t0001g0133 others(3): Show |
6 | HG00280.hp1 HG02145.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1060-14992T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32759716 | |||||||
chr5:32759740 | G | C | 1 | a0001c0001t0040g0162 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1060-14968G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32759740 | |||||||
chr5:32759830 | G | T | 1 | a0001c0004t0062g0135 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1060-14878G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32759830 | |||||||
chr5:32760089 | G | A | 1 | a0001c0001t0001g0236 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1060-14619G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32760089 | |||||||
chr5:32760125 | GT | G | 53 | a0001c0001t0001g0088 a0001c0001t0001g0126 a0001c0001t0001g0229 others(50): Show |
53 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.1060-14572delT | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32760125 | ||||||
chr5:32760159 | G | A | 1 | a0001c0001t0007g0058 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1060-14549G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32760159 | |||||||
chr5:32760269 | T | C | 70 | a0001c0001t0001g0025 a0001c0001t0001g0088 a0001c0001t0001g0126 others(67): Show |
70 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.1060-14439T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32760269 | |||||||
chr5:32760277 | T | C | 53 | a0001c0001t0001g0088 a0001c0001t0001g0126 a0001c0001t0001g0229 others(50): Show |
53 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.1060-14431T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32760277 | |||||||
chr5:32760547 | T | C | 2 | a0001c0001t0003g0246 a0001c0001t0003g0253 |
2 | HG00423.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.1060-14161T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32760547 | |||||||
chr5:32760574 | T | C | 2 | a0001c0001t0005g0143 a0001c0001t0043g0067 |
2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1060-14134T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32760574 | |||||||
chr5:32760649 | G | A | 6 | a0001c0001t0015g0123 a0001c0001t0040g0162 a0001c0001t0047g0104 others(3): Show |
6 | HG01074.hp1 HG01261.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.1060-14059G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32760649 | |||||||
chr5:32760655 | T | G | 2 | a0001c0001t0005g0143 a0001c0001t0043g0067 |
2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1060-14053T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32760655 | |||||||
chr5:32760667 | G | T | 58 | a0001c0001t0001g0088 a0001c0001t0001g0126 a0001c0001t0001g0229 others(55): Show |
58 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.1060-14041G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32760667 | |||||||
chr5:32760667 | GT | G | 9 | a0001c0001t0015g0123 a0001c0001t0019g0006 a0001c0001t0047g0104 others(6): Show |
9 | HG01074.hp1 HG01952.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1060-14028delT | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32760667 | ||||||
chr5:32760681 | A | T | 5 | a0001c0001t0001g0043 a0001c0001t0002g0008 a0001c0001t0002g0129 others(2): Show |
5 | HG02109.hp1 HG03098.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.1060-14027A>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32760681 | |||||||
chr5:32760742 | T | C | 2 | a0001c0001t0004g0027 a0001c0001t0004g0028 |
2 | HG01496.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.1060-13966T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32760742 | |||||||
chr5:32760988 | G | T | 6 | a0001c0001t0001g0025 a0001c0001t0001g0132 a0001c0001t0001g0133 others(3): Show |
6 | HG00280.hp1 HG02145.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1060-13720G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32760988 | |||||||
chr5:32761211 | TA | T | 13 | a0001c0001t0001g0025 a0001c0001t0001g0043 a0001c0001t0001g0132 others(10): Show |
13 | HG00280.hp1 HG02109.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1060-13486delA | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32761211 | ||||||
chr5:32761231 | T | C | 1 | a0001c0001t0003g0118 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1060-13477T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32761231 | |||||||
chr5:32761258 | C | T | 5 | a0001c0001t0015g0123 a0001c0001t0047g0104 a0001c0006t0061g0046 others(2): Show |
5 | HG01074.hp1 HG01952.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1060-13450C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32761258 | |||||||
chr5:32761323 | C | T | 59 | a0001c0001t0001g0088 a0001c0001t0001g0126 a0001c0001t0001g0229 others(56): Show |
59 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.1060-13385C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32761323 | |||||||
chr5:32761349 | A | G | 1 | a0001c0001t0001g0117 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1060-13359A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32761349 | |||||||
chr5:32761404 | A | T | 2 | a0001c0001t0001g0173 a0001c0001t0003g0183 |
2 | HG03704.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.1060-13304A>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32761404 | |||||||
chr5:32761472 | T | C | 5 | a0002c0002t0002g0005 a0002c0002t0002g0012 a0002c0002t0002g0112 others(2): Show |
6 | HG01346.hp1 HG02683.hp1 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.1060-13236T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32761472 | |||||||
chr5:32761512 | T | C | 5 | a0001c0001t0015g0123 a0001c0001t0047g0104 a0001c0006t0061g0046 others(2): Show |
5 | HG01074.hp1 HG01952.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1060-13196T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32761512 | |||||||
chr5:32761591 | C | T | 13 | a0001c0001t0005g0079 a0001c0001t0005g0153 a0001c0001t0024g0263 others(10): Show |
14 | HG02145.hp1 HG02258.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1060-13117C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32761591 | |||||||
chr5:32761646 | T | G | 1 | a0001c0001t0065g0051 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1060-13062T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32761646 | |||||||
chr5:32761658 | AT | A | 5 | a0001c0001t0015g0123 a0001c0001t0047g0104 a0001c0006t0061g0046 others(2): Show |
5 | HG01074.hp1 HG01952.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1060-13041delT | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32761658 | ||||||
chr5:32761737 | T | TTTTTA | 70 | a0001c0001t0001g0025 a0001c0001t0001g0088 a0001c0001t0001g0126 others(67): Show |
70 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.1060-12961_1060-12 others(11): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32761737 | ||||||
chr5:32761794 | A | T | 1 | a0001c0005t0056g0266 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1060-12914A>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32761794 | |||||||
chr5:32761962 | G | T | 4 | a0001c0001t0004g0299 a0001c0001t0004g0300 a0001c0001t0004g0302 others(1): Show |
4 | HG02922.hp1 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1060-12746G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32761962 | |||||||
chr5:32762012 | A | T | 4 | a0001c0001t0001g0056 a0001c0001t0001g0060 a0001c0001t0001g0061 others(1): Show |
4 | HG01192.hp2 HG01884.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1060-12696A>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32762012 | |||||||
chr5:32762148 | A | G | 1 | a0001c0001t0001g0113 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1060-12560A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32762148 | |||||||
chr5:32762196 | A | G | 2 | a0001c0001t0005g0143 a0001c0001t0043g0067 |
2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1060-12512A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32762196 | |||||||
chr5:32762332 | T | C | 2 | a0001c0003t0005g0031 a0001c0003t0005g0033 |
2 | HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1060-12376T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32762332 | |||||||
chr5:32762333 | G | A | 43 | a0001c0001t0001g0142 a0001c0001t0001g0151 a0001c0001t0004g0016 others(40): Show |
43 | HG00735.hp2 HG00741.hp1 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.1060-12375G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32762333 | |||||||
chr5:32762427 | C | T | 2 | a0001c0001t0004g0139 a0001c0001t0055g0147 |
2 | HG01192.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.1060-12281C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32762427 | |||||||
chr5:32762456 | T | TTGTTTCC others(326): Show |
2 | a0002c0002t0002g0212 a0002c0002t0002g0213 |
2 | NA18974.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.1060-12236_1060-12 others(339): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32762456 | ||||||
chr5:32762456 | T | TTGTTTCC others(327): Show |
32 | a0001c0001t0003g0091 a0001c0001t0003g0111 a0001c0001t0003g0115 others(29): Show |
33 | HG00280.hp2 HG01069.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.1060-12236_1060-12 others(340): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32762456 | ||||||
chr5:32762456 | T | TTGTTTCC others(327): Show |
1 | a0001c0001t0003g0118 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1060-12236_1060-12 others(340): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32762456 | ||||||
chr5:32762456 | T | TTGTTTCC others(328): Show |
23 | a0001c0001t0001g0243 a0001c0001t0003g0095 a0001c0001t0003g0101 others(20): Show |
23 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.1060-12236_1060-12 others(341): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32762456 | ||||||
chr5:32762456 | T | TTGTTTCC others(328): Show |
1 | a0001c0001t0003g0116 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1060-12236_1060-12 others(341): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32762456 | ||||||
chr5:32762456 | T | TTGTTTCC others(329): Show |
3 | a0001c0001t0003g0004 a0001c0001t0003g0256 a0001c0001t0010g0003 |
5 | HG00621.hp1 HG01168.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.1060-12236_1060-12 others(342): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32762456 | ||||||
chr5:32762583 | A | G | 1 | a0002c0002t0002g0178 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1060-12125A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32762583 | |||||||
chr5:32762913 | A | G | 1 | a0001c0003t0008g0032 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1060-11795A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32762913 | |||||||
chr5:32763012 | G | A | 65 | a0001c0001t0001g0025 a0001c0001t0001g0088 a0001c0001t0001g0126 others(62): Show |
65 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.1060-11696G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32763012 | |||||||
chr5:32763022 | A | C | 1 | a0001c0003t0058g0035 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1060-11686A>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32763022 | |||||||
chr5:32763154 | T | C | 1 | a0002c0002t0054g0168 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1060-11554T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32763154 | |||||||
chr5:32763181 | A | C | 70 | a0001c0001t0001g0025 a0001c0001t0001g0088 a0001c0001t0001g0126 others(67): Show |
70 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.1060-11527A>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32763181 | |||||||
chr5:32763363 | A | C | 70 | a0001c0001t0001g0025 a0001c0001t0001g0088 a0001c0001t0001g0126 others(67): Show |
70 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.1060-11345A>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32763363 | |||||||
chr5:32763461 | C | T | 1 | a0001c0001t0003g0288 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1060-11247C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32763461 | |||||||
chr5:32763466 | C | T | 1 | a0001c0001t0008g0134 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1060-11242C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32763466 | |||||||
chr5:32763476 | A | AT | 28 | a0001c0001t0001g0043 a0001c0001t0001g0172 a0001c0001t0001g0258 others(25): Show |
30 | HG00639.hp1 HG01069.hp1 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.1060-11213dupT | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32763476 | ||||||
chr5:32763476 | A | ATT | 61 | a0001c0001t0001g0025 a0001c0001t0001g0088 a0001c0001t0001g0126 others(58): Show |
61 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.1060-11214_1060-11 others(8): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32763476 | ||||||
chr5:32763476 | AT | A | 9 | a0001c0001t0001g0062 a0001c0001t0001g0096 a0001c0001t0001g0179 others(6): Show |
9 | HG00099.hp2 HG02280.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1060-11213delT | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32763476 | ||||||
chr5:32763657 | A | G | 1 | a0001c0001t0064g0054 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1060-11051A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32763657 | |||||||
chr5:32763740 | G | A | 139 | a0001c0001t0001g0025 a0001c0001t0001g0043 a0001c0001t0001g0088 others(136): Show |
140 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(137): Show |
intron_variant | MODIFIER | c.1060-10968G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32763740 | |||||||
chr5:32764025 | T | C | 43 | a0001c0001t0001g0142 a0001c0001t0001g0151 a0001c0001t0004g0016 others(40): Show |
43 | HG00735.hp2 HG00741.hp1 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.1060-10683T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32764025 | |||||||
chr5:32764091 | G | A | 6 | a0001c0001t0015g0123 a0001c0001t0040g0162 a0001c0001t0047g0104 others(3): Show |
6 | HG01074.hp1 HG01261.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.1060-10617G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32764091 | |||||||
chr5:32764120 | C | T | 1 | a0001c0001t0008g0134 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1060-10588C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32764120 | |||||||
chr5:32764219 | C | G | 4 | a0001c0001t0001g0043 a0001c0001t0002g0008 a0001c0001t0002g0129 others(1): Show |
4 | HG02109.hp1 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1060-10489C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32764219 | |||||||
chr5:32764466 | A | G | 59 | a0001c0001t0001g0088 a0001c0001t0001g0126 a0001c0001t0001g0229 others(56): Show |
59 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.1060-10242A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32764466 | |||||||
chr5:32764516 | G | A | 43 | a0001c0001t0001g0142 a0001c0001t0001g0151 a0001c0001t0004g0016 others(40): Show |
43 | HG00735.hp2 HG00741.hp1 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.1060-10192G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32764516 | |||||||
chr5:32764655 | G | T | 1 | a0001c0001t0051g0269 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1060-10053G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32764655 | |||||||
chr5:32764657 | G | A | 1 | a0002c0002t0002g0145 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1060-10051G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32764657 | |||||||
chr5:32764785 | T | A | 2 | a0001c0001t0001g0314 a0001c0001t0001g0315 |
2 | NA19060.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1060-9923T>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32764785 | |||||||
chr5:32764788 | C | CA | 20 | a0001c0001t0001g0085 a0001c0001t0001g0114 a0001c0001t0001g0175 others(17): Show |
20 | HG01952.hp1 HG01952.hp2 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1060-9892dupA | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32764788 | ||||||
chr5:32764788 | C | CAAAAAAA others(1): Show |
9 | a0001c0001t0001g0132 a0001c0001t0004g0027 a0001c0001t0004g0028 others(6): Show |
9 | HG00735.hp2 HG01070.hp2 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1060-9899_1060-989 others(12): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32764788 | ||||||
chr5:32764788 | C | CAAAAAAA others(2): Show |
7 | a0001c0001t0004g0016 a0001c0001t0004g0017 a0001c0001t0004g0073 others(4): Show |
7 | HG00741.hp1 HG01168.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1060-9900_1060-989 others(13): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32764788 | ||||||
chr5:32764788 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0001g0142 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1060-9901_1060-989 others(14): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32764788 | ||||||
chr5:32764788 | C | CAAAAAAA others(4): Show |
3 | a0001c0001t0004g0155 a0001c0001t0007g0200 a0001c0001t0066g0053 |
3 | HG02257.hp2 HG02451.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1060-9902_1060-989 others(15): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32764788 | ||||||
chr5:32764788 | C | CAAAAAAA others(5): Show |
5 | a0001c0001t0001g0151 a0001c0001t0021g0080 a0001c0001t0039g0265 others(2): Show |
5 | HG01243.hp2 HG01884.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1060-9903_1060-989 others(16): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32764788 | ||||||
chr5:32764788 | C | CAAAAAAA others(6): Show |
3 | a0001c0001t0007g0058 a0001c0001t0007g0074 a0001c0001t0007g0150 |
3 | HG01106.hp2 HG02615.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1060-9904_1060-989 others(17): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32764788 | ||||||
chr5:32764788 | C | CAAAAAAA others(7): Show |
3 | a0001c0001t0007g0138 a0001c0001t0008g0134 a0001c0001t0040g0162 |
3 | HG01261.hp1 HG01934.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1060-9905_1060-989 others(18): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32764788 | ||||||
chr5:32764788 | C | CAAAAAAA others(8): Show |
3 | a0001c0001t0004g0044 a0001c0001t0019g0006 a0001c0001t0042g0042 |
3 | HG03453.hp1 HG03516.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1060-9906_1060-989 others(19): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32764788 | ||||||
chr5:32764788 | C | CAAAAAAA others(10): Show |
1 | a0001c0001t0019g0007 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1060-9908_1060-989 others(21): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32764788 | ||||||
chr5:32764788 | CA | C | 35 | a0001c0001t0001g0043 a0001c0001t0001g0113 a0001c0001t0001g0189 others(32): Show |
36 | HG00609.hp2 HG00621.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.1060-9892delA | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32764788 | ||||||
chr5:32764788 | CAA | C | 60 | a0001c0001t0001g0088 a0001c0001t0001g0126 a0001c0001t0001g0229 others(57): Show |
60 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.1060-9893_1060-989 others(6): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32764788 | ||||||
chr5:32764788 | CAAAAAAA others(8): Show |
C | 3 | a0001c0001t0001g0025 a0001c0001t0015g0103 a0002c0002t0002g0270 |
3 | HG00280.hp1 HG02818.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1060-9906_1060-989 others(19): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32764788 | ||||||
chr5:32765010 | C | T | 1 | a0001c0004t0062g0135 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1060-9698C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32765010 | |||||||
chr5:32765036 | T | C | 1 | a0001c0001t0007g0152 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1060-9672T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32765036 | |||||||
chr5:32765105 | G | C | 6 | a0001c0001t0001g0025 a0001c0001t0001g0132 a0001c0001t0001g0133 others(3): Show |
6 | HG00280.hp1 HG02145.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1060-9603G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32765105 | |||||||
chr5:32765351 | C | A | 6 | a0001c0001t0001g0025 a0001c0001t0001g0132 a0001c0001t0001g0133 others(3): Show |
6 | HG00280.hp1 HG02145.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1060-9357C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32765351 | |||||||
chr5:32765383 | C | A | 115 | a0001c0001t0001g0025 a0001c0001t0001g0088 a0001c0001t0001g0126 others(112): Show |
115 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.1060-9325C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32765383 | |||||||
chr5:32765398 | C | G | 1 | a0001c0005t0056g0266 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1060-9310C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32765398 | |||||||
chr5:32765468 | C | T | 10 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0006g0063 others(7): Show |
10 | HG01243.hp1 HG01891.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1060-9240C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32765468 | |||||||
chr5:32765477 | T | A | 1 | a0001c0001t0006g0063 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1060-9231T>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32765477 | |||||||
chr5:32765560 | C | A | 16 | a0001c0001t0005g0079 a0001c0001t0005g0143 a0001c0001t0005g0153 others(13): Show |
17 | HG02145.hp1 HG02258.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.1060-9148C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32765560 | |||||||
chr5:32765685 | G | A | 2 | a0001c0006t0061g0046 a0002c0002t0002g0072 |
2 | HG02055.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1060-9023G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32765685 | |||||||
chr5:32765830 | A | G | 1 | a0001c0005t0056g0266 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1060-8878A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32765830 | |||||||
chr5:32765983 | A | G | 219 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0025 others(216): Show |
224 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.1060-8725A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32765983 | |||||||
chr5:32765991 | C | G | 134 | a0001c0001t0001g0025 a0001c0001t0001g0088 a0001c0001t0001g0126 others(131): Show |
135 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(132): Show |
intron_variant | MODIFIER | c.1060-8717C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32765991 | |||||||
chr5:32765991 | C | T | 1 | a0002c0002t0002g0226 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1060-8717C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32765991 | |||||||
chr5:32766039 | T | A | 61 | a0001c0001t0001g0088 a0001c0001t0001g0126 a0001c0001t0001g0229 others(58): Show |
61 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.1060-8669T>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32766039 | |||||||
chr5:32766102 | G | A | 1 | a0002c0002t0002g0204 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1060-8606G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32766102 | |||||||
chr5:32766106 | G | T | 43 | a0001c0001t0001g0142 a0001c0001t0001g0151 a0001c0001t0004g0016 others(40): Show |
43 | HG00735.hp2 HG00741.hp1 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.1060-8602G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32766106 | |||||||
chr5:32766149 | G | A | 1 | a0001c0001t0001g0196 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1060-8559G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32766149 | |||||||
chr5:32766159 | G | A | 1 | a0001c0001t0001g0250 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1060-8549G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32766159 | |||||||
chr5:32766174 | G | A | 61 | a0001c0001t0001g0088 a0001c0001t0001g0126 a0001c0001t0001g0229 others(58): Show |
61 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.1060-8534G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32766174 | |||||||
chr5:32766311 | T | C | 138 | a0001c0001t0001g0025 a0001c0001t0001g0043 a0001c0001t0001g0088 others(135): Show |
139 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(136): Show |
intron_variant | MODIFIER | c.1060-8397T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32766311 | |||||||
chr5:32766327 | A | G | 1 | a0002c0002t0002g0145 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1060-8381A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32766327 | |||||||
chr5:32766360 | A | G | 112 | a0001c0001t0001g0025 a0001c0001t0001g0088 a0001c0001t0001g0126 others(109): Show |
112 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.1060-8348A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32766360 | |||||||
chr5:32766400 | C | G | 2 | a0001c0001t0007g0138 a0001c0001t0041g0146 |
2 | HG01934.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1060-8308C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32766400 | |||||||
chr5:32766487 | C | G | 1 | a0001c0001t0007g0074 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1060-8221C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32766487 | |||||||
chr5:32766577 | A | G | 61 | a0001c0001t0001g0088 a0001c0001t0001g0126 a0001c0001t0001g0229 others(58): Show |
61 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.1060-8131A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32766577 | |||||||
chr5:32766623 | T | C | 3 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0006g0010 |
3 | HG02145.hp2 HG02258.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1060-8085T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32766623 | |||||||
chr5:32766716 | T | C | 112 | a0001c0001t0001g0025 a0001c0001t0001g0088 a0001c0001t0001g0126 others(109): Show |
112 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.1060-7992T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32766716 | |||||||
chr5:32766920 | C | A | 1 | a0001c0001t0024g0277 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1060-7788C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32766920 | |||||||
chr5:32767341 | T | C | 1 | a0001c0001t0007g0152 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1060-7367T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32767341 | |||||||
chr5:32767351 | C | G | 1 | a0001c0001t0004g0140 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1060-7357C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32767351 | |||||||
chr5:32767580 | A | T | 1 | a0001c0001t0003g0083 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1060-7128A>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32767580 | |||||||
chr5:32767621 | A | G | 112 | a0001c0001t0001g0025 a0001c0001t0001g0088 a0001c0001t0001g0126 others(109): Show |
112 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.1060-7087A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32767621 | |||||||
chr5:32767663 | C | T | 1 | a0001c0001t0043g0067 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1060-7045C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32767663 | |||||||
chr5:32767676 | T | C | 112 | a0001c0001t0001g0025 a0001c0001t0001g0088 a0001c0001t0001g0126 others(109): Show |
112 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.1060-7032T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32767676 | |||||||
chr5:32767775 | C | A | 1 | a0001c0001t0040g0162 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1060-6933C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32767775 | |||||||
chr5:32767822 | T | G | 110 | a0001c0001t0001g0025 a0001c0001t0001g0088 a0001c0001t0001g0126 others(107): Show |
110 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.1060-6886T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32767822 | |||||||
chr5:32768009 | T | G | 1 | a0001c0001t0047g0104 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1060-6699T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32768009 | |||||||
chr5:32768064 | C | T | 1 | a0001c0001t0004g0139 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1060-6644C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32768064 | |||||||
chr5:32768151 | G | A | 6 | a0001c0001t0001g0025 a0001c0001t0001g0132 a0001c0001t0001g0133 others(3): Show |
6 | HG00280.hp1 HG02145.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1060-6557G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32768151 | |||||||
chr5:32768347 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1060-6361G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32768347 | |||||||
chr5:32768367 | G | A | 2 | a0001c0004t0062g0135 a0001c0005t0056g0266 |
2 | HG02109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1060-6341G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32768367 | |||||||
chr5:32768416 | T | C | 2 | a0001c0001t0019g0006 a0001c0001t0019g0007 |
2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1060-6292T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32768416 | |||||||
chr5:32768428 | G | A | 2 | a0001c0001t0001g0184 a0001c0001t0001g0201 |
2 | NA18956.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.1060-6280G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32768428 | |||||||
chr5:32768520 | C | A | 2 | a0001c0001t0004g0139 a0001c0001t0055g0147 |
2 | HG01192.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.1060-6188C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32768520 | |||||||
chr5:32768528 | A | G | 112 | a0001c0001t0001g0025 a0001c0001t0001g0088 a0001c0001t0001g0126 others(109): Show |
112 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.1060-6180A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32768528 | |||||||
chr5:32768594 | T | C | 2 | a0001c0001t0001g0088 a0001c0001t0001g0126 |
2 | HG00741.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1060-6114T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32768594 | |||||||
chr5:32768614 | G | C | 1 | a0002c0002t0033g0219 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1060-6094G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32768614 | |||||||
chr5:32768789 | C | T | 2 | a0001c0006t0061g0046 a0002c0002t0002g0072 |
2 | HG02055.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1060-5919C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32768789 | |||||||
chr5:32768829 | C | A | 2 | a0001c0006t0061g0046 a0002c0002t0002g0072 |
2 | HG02055.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1060-5879C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32768829 | |||||||
chr5:32768864 | G | A | 1 | a0001c0003t0001g0034 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1060-5844G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32768864 | |||||||
chr5:32768963 | C | T | 3 | a0001c0001t0001g0142 a0001c0001t0001g0151 a0001c0001t0066g0053 |
3 | HG01243.hp2 HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1060-5745C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32768963 | |||||||
chr5:32769072 | A | G | 1 | a0001c0001t0001g0024 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1060-5636A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32769072 | |||||||
chr5:32769075 | C | T | 61 | a0001c0001t0001g0088 a0001c0001t0001g0126 a0001c0001t0001g0229 others(58): Show |
61 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.1060-5633C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32769075 | |||||||
chr5:32769081 | A | G | 1 | a0001c0005t0056g0266 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1060-5627A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32769081 | |||||||
chr5:32769197 | A | G | 1 | a0001c0001t0001g0020 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1060-5511A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32769197 | |||||||
chr5:32769251 | A | T | 2 | a0001c0001t0005g0143 a0001c0001t0043g0067 |
2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1060-5457A>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32769251 | |||||||
chr5:32769354 | A | G | 14 | a0001c0001t0004g0016 a0001c0001t0004g0017 a0001c0001t0004g0027 others(11): Show |
14 | HG00735.hp2 HG00741.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.1060-5354A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32769354 | |||||||
chr5:32769421 | C | G | 1 | a0001c0001t0001g0251 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1060-5287C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32769421 | |||||||
chr5:32769602 | A | G | 7 | a0001c0001t0004g0140 a0001c0001t0008g0045 a0001c0001t0008g0128 others(4): Show |
7 | HG02257.hp1 HG02976.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1060-5106A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32769602 | |||||||
chr5:32769663 | C | T | 1 | a0001c0001t0019g0006 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1060-5045C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32769663 | |||||||
chr5:32769857 | T | C | 3 | a0001c0001t0036g0013 a0001c0004t0062g0135 a0001c0005t0056g0266 |
3 | HG01175.hp2 HG02109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1060-4851T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32769857 | |||||||
chr5:32769987 | A | G | 5 | a0001c0001t0006g0063 a0001c0001t0006g0065 a0001c0001t0017g0057 others(2): Show |
5 | HG01891.hp2 HG02809.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1060-4721A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32769987 | |||||||
chr5:32769993 | G | T | 115 | a0001c0001t0001g0025 a0001c0001t0001g0088 a0001c0001t0001g0126 others(112): Show |
115 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.1060-4715G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32769993 | |||||||
chr5:32770116 | T | G | 1 | a0001c0001t0003g0224 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1060-4592T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32770116 | |||||||
chr5:32770220 | T | G | 2 | a0001c0004t0062g0135 a0001c0005t0056g0266 |
2 | HG02109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1060-4488T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32770220 | |||||||
chr5:32770266 | C | CA | 7 | a0001c0001t0004g0140 a0001c0001t0008g0045 a0001c0001t0008g0128 others(4): Show |
7 | HG02257.hp1 HG02976.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1060-4436dupA | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32770266 | ||||||
chr5:32770362 | C | A | 2 | a0001c0001t0026g0049 a0001c0001t0026g0052 |
2 | HG02622.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1060-4346C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32770362 | |||||||
chr5:32770429 | C | CA | 16 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0026 others(13): Show |
17 | HG00323.hp1 HG00639.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.1060-4268dupA | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32770429 | ||||||
chr5:32770431 | A | G | 1 | a0002c0002t0002g0137 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1060-4277A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32770431 | |||||||
chr5:32770483 | C | T | 2 | a0001c0006t0061g0046 a0002c0002t0002g0072 |
2 | HG02055.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1060-4225C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32770483 | |||||||
chr5:32770644 | G | A | 52 | a0001c0001t0001g0088 a0001c0001t0001g0126 a0001c0001t0001g0229 others(49): Show |
52 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.1060-4064G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32770644 | |||||||
chr5:32770707 | A | G | 1 | a0001c0001t0017g0064 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1060-4001A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32770707 | |||||||
chr5:32770913 | A | G | 6 | a0001c0001t0001g0043 a0001c0001t0002g0008 a0001c0001t0002g0129 others(3): Show |
6 | HG02109.hp1 HG02615.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1060-3795A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32770913 | |||||||
chr5:32771089 | C | T | 5 | a0001c0001t0004g0140 a0001c0001t0008g0045 a0001c0001t0008g0128 others(2): Show |
5 | HG02257.hp1 HG02976.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1060-3619C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32771089 | |||||||
chr5:32771273 | A | G | 139 | a0001c0001t0001g0025 a0001c0001t0001g0043 a0001c0001t0001g0088 others(136): Show |
140 | HG00280.hp1 HG00423.hp2 HG00609.hp1 others(137): Show |
intron_variant | MODIFIER | c.1060-3435A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32771273 | |||||||
chr5:32771286 | C | T | 1 | a0001c0001t0001g0114 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1060-3422C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32771286 | |||||||
chr5:32771336 | G | C | 4 | a0001c0001t0001g0090 a0001c0001t0001g0096 a0001c0001t0001g0097 others(1): Show |
4 | NA18962.hp1 NA18974.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.1060-3372G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32771336 | |||||||
chr5:32771443 | G | A | 2 | a0001c0001t0006g0109 a0001c0001t0006g0110 |
2 | HG01243.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1060-3265G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32771443 | |||||||
chr5:32771445 | C | T | 1 | a0002c0002t0002g0213 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1060-3263C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32771445 | |||||||
chr5:32771476 | A | G | 1 | a0001c0001t0040g0162 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1060-3232A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32771476 | |||||||
chr5:32771706 | C | T | 61 | a0001c0001t0001g0088 a0001c0001t0001g0126 a0001c0001t0001g0229 others(58): Show |
61 | HG00609.hp1 HG00621.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.1060-3002C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32771706 | |||||||
chr5:32771719 | A | G | 117 | a0001c0001t0001g0025 a0001c0001t0001g0088 a0001c0001t0001g0126 others(114): Show |
117 | HG00280.hp1 HG00609.hp1 HG00621.hp2 others(114): Show |
intron_variant | MODIFIER | c.1060-2989A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32771719 | |||||||
chr5:32771730 | G | C | 2 | a0001c0001t0026g0049 a0001c0001t0026g0052 |
2 | HG02622.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1060-2978G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32771730 | |||||||
chr5:32771832 | A | G | 137 | a0001c0001t0001g0025 a0001c0001t0001g0043 a0001c0001t0001g0088 others(134): Show |
138 | HG00280.hp1 HG00609.hp1 HG00621.hp2 others(135): Show |
intron_variant | MODIFIER | c.1060-2876A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32771832 | |||||||
chr5:32771937 | A | G | 115 | a0001c0001t0001g0025 a0001c0001t0001g0088 a0001c0001t0001g0126 others(112): Show |
115 | HG00280.hp1 HG00609.hp1 HG00621.hp2 others(112): Show |
intron_variant | MODIFIER | c.1060-2771A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32771937 | |||||||
chr5:32771967 | A | T | 1 | a0001c0006t0061g0046 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1060-2741A>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32771967 | |||||||
chr5:32771974 | A | G | 1 | a0001c0001t0040g0162 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1060-2734A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32771974 | |||||||
chr5:32772221 | C | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0023 |
2 | HG00735.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.1060-2487C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32772221 | |||||||
chr5:32772230 | T | C | 25 | a0001c0001t0001g0043 a0001c0001t0002g0008 a0001c0001t0002g0129 others(22): Show |
26 | HG01074.hp2 HG01192.hp1 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.1060-2478T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32772230 | |||||||
chr5:32772237 | C | T | 1 | a0001c0001t0040g0162 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1060-2471C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32772237 | |||||||
chr5:32772520 | G | A | 3 | a0001c0001t0001g0142 a0001c0001t0001g0151 a0001c0001t0066g0053 |
3 | HG01243.hp2 HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1060-2188G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32772520 | |||||||
chr5:32772585 | T | C | 113 | a0001c0001t0001g0088 a0001c0001t0001g0126 a0001c0001t0001g0142 others(110): Show |
114 | HG00099.hp2 HG00609.hp1 HG00621.hp2 others(111): Show |
intron_variant | MODIFIER | c.1060-2123T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32772585 | |||||||
chr5:32772656 | A | G | 1 | a0002c0002t0035g0124 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1060-2052A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32772656 | |||||||
chr5:32772658 | T | C | 1 | a0001c0001t0001g0257 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1060-2050T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32772658 | |||||||
chr5:32772781 | A | AT | 25 | a0001c0001t0001g0043 a0001c0001t0002g0008 a0001c0001t0002g0129 others(22): Show |
26 | HG01074.hp2 HG01192.hp1 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.1060-1921dupT | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 32772781 | ||||||
chr5:32772796 | C | T | 25 | a0001c0001t0001g0043 a0001c0001t0002g0008 a0001c0001t0002g0129 others(22): Show |
26 | HG01074.hp2 HG01192.hp1 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.1060-1912C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32772796 | |||||||
chr5:32772807 | C | T | 1 | a0001c0001t0004g0294 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1060-1901C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32772807 | |||||||
chr5:32772808 | G | A | 3 | a0001c0001t0005g0143 a0001c0001t0043g0067 a0001c0001t0065g0051 |
3 | HG02723.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1060-1900G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32772808 | |||||||
chr5:32772886 | G | C | 61 | a0001c0001t0001g0088 a0001c0001t0001g0126 a0001c0001t0001g0229 others(58): Show |
62 | HG00099.hp2 HG00609.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.1060-1822G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32772886 | |||||||
chr5:32772910 | T | A | 21 | a0001c0001t0001g0043 a0001c0001t0002g0008 a0001c0001t0002g0129 others(18): Show |
22 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.1060-1798T>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32772910 | |||||||
chr5:32772927 | G | A | 24 | a0001c0001t0001g0043 a0001c0001t0002g0008 a0001c0001t0002g0129 others(21): Show |
25 | HG01074.hp2 HG01192.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.1060-1781G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32772927 | |||||||
chr5:32772948 | C | T | 1 | a0001c0001t0007g0200 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1060-1760C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32772948 | |||||||
chr5:32772964 | G | A | 25 | a0001c0001t0001g0043 a0001c0001t0002g0008 a0001c0001t0002g0129 others(22): Show |
26 | HG01074.hp2 HG01192.hp1 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.1060-1744G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32772964 | |||||||
chr5:32773035 | A | G | 1 | a0001c0001t0001g0023 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1060-1673A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32773035 | |||||||
chr5:32773049 | TG | T | 59 | a0001c0001t0001g0088 a0001c0001t0001g0126 a0001c0001t0001g0229 others(56): Show |
60 | HG00099.hp2 HG00609.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.1060-1658delG | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32773049 | |||||||
chr5:32773169 | A | G | 5 | a0001c0001t0001g0025 a0001c0001t0015g0103 a0001c0001t0019g0006 others(2): Show |
5 | HG00280.hp1 HG02818.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1060-1539A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32773169 | |||||||
chr5:32773208 | C | T | 109 | a0001c0001t0001g0025 a0001c0001t0001g0088 a0001c0001t0001g0126 others(106): Show |
110 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.1060-1500C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32773208 | |||||||
chr5:32773250 | C | T | 63 | a0001c0001t0001g0088 a0001c0001t0001g0126 a0001c0001t0001g0229 others(60): Show |
64 | HG00099.hp2 HG00609.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.1060-1458C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32773250 | |||||||
chr5:32773363 | G | A | 2 | a0001c0001t0005g0143 a0001c0001t0043g0067 |
2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1060-1345G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32773363 | |||||||
chr5:32773542 | A | C | 9 | a0001c0001t0004g0139 a0001c0001t0041g0146 a0001c0001t0043g0067 others(6): Show |
9 | HG01192.hp1 HG01891.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1060-1166A>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32773542 | |||||||
chr5:32773545 | C | T | 64 | a0001c0001t0001g0088 a0001c0001t0001g0126 a0001c0001t0001g0229 others(61): Show |
65 | HG00099.hp2 HG00609.hp1 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.1060-1163C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32773545 | |||||||
chr5:32773580 | T | G | 1 | a0001c0001t0049g0015 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1060-1128T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32773580 | |||||||
chr5:32773667 | C | G | 2 | a0001c0001t0019g0007 a0001c0001t0037g0059 |
2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1060-1041C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32773667 | |||||||
chr5:32773683 | A | G | 2 | a0001c0001t0001g0286 a0001c0001t0001g0287 |
2 | HG03471.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1060-1025A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32773683 | |||||||
chr5:32774153 | G | A | 1 | a0001c0006t0061g0046 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1060-555G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32774153 | |||||||
chr5:32774225 | A | G | 1 | a0001c0001t0003g0115 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1060-483A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32774225 | |||||||
chr5:32774228 | A | G | 1 | a0001c0001t0050g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1060-480A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32774228 | |||||||
chr5:32774240 | A | G | 2 | a0001c0001t0043g0067 a0001c0001t0065g0051 |
2 | HG02723.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1060-468A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32774240 | |||||||
chr5:32774327 | T | C | 1 | a0001c0006t0061g0046 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1060-381T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 3/7 | chr5 | 32774327 | |||||||
chr5:32774889 | G | A | 2 | a0001c0003t0023g0038 a0001c0003t0023g0039 |
2 | HG02622.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1195+46G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32774889 | |||||||
chr5:32774908 | A | T | 1 | a0001c0006t0061g0046 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1195+65A>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32774908 | |||||||
chr5:32774941 | G | T | 196 | a0001c0001t0001g0085 a0001c0001t0001g0088 a0001c0001t0001g0126 others(193): Show |
200 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(197): Show |
intron_variant | MODIFIER | c.1195+98G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32774941 | |||||||
chr5:32775144 | T | C | 72 | a0001c0001t0001g0088 a0001c0001t0001g0126 a0001c0001t0004g0140 others(69): Show |
73 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.1195+301T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32775144 | |||||||
chr5:32775155 | G | A | 16 | a0001c0001t0005g0079 a0001c0001t0005g0143 a0001c0001t0005g0153 others(13): Show |
17 | HG02145.hp1 HG02258.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.1195+312G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32775155 | |||||||
chr5:32775294 | AT | A | 53 | a0001c0001t0004g0016 a0001c0001t0004g0017 a0001c0001t0004g0027 others(50): Show |
54 | HG00735.hp2 HG00741.hp1 HG01070.hp2 others(51): Show |
intron_variant | MODIFIER | c.1195+467delT | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 32775294 | ||||||
chr5:32775294 | ATT | A | 68 | a0001c0001t0001g0088 a0001c0001t0001g0126 a0001c0001t0002g0008 others(65): Show |
70 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.1195+466_1195+467d others(4): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 32775294 | ||||||
chr5:32775294 | ATTT | A | 71 | a0001c0001t0004g0140 a0001c0001t0008g0045 a0001c0001t0008g0128 others(68): Show |
72 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.1195+465_1195+467d others(5): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 32775294 | ||||||
chr5:32775358 | G | A | 1 | a0001c0001t0017g0064 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1195+515G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32775358 | |||||||
chr5:32775577 | T | A | 1 | a0002c0002t0016g0276 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1195+734T>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32775577 | |||||||
chr5:32775738 | C | T | 1 | a0001c0001t0003g0164 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1195+895C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32775738 | |||||||
chr5:32775907 | A | C | 2 | a0001c0001t0001g0188 a0001c0001t0001g0206 |
2 | NA18942.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1195+1064A>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32775907 | |||||||
chr5:32775909 | T | A | 139 | a0001c0001t0001g0088 a0001c0001t0001g0126 a0001c0001t0002g0008 others(136): Show |
142 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.1195+1066T>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32775909 | |||||||
chr5:32776291 | T | C | 77 | a0001c0001t0001g0088 a0001c0001t0001g0126 a0001c0001t0004g0140 others(74): Show |
78 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.1195+1448T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32776291 | |||||||
chr5:32776335 | A | T | 1 | a0001c0006t0061g0046 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1195+1492A>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32776335 | |||||||
chr5:32776356 | A | G | 1 | a0001c0001t0015g0123 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1195+1513A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32776356 | |||||||
chr5:32776426 | C | T | 1 | a0001c0006t0061g0046 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1195+1583C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32776426 | |||||||
chr5:32776567 | C | T | 73 | a0001c0001t0001g0088 a0001c0001t0001g0126 a0001c0001t0004g0140 others(70): Show |
74 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.1195+1724C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32776567 | |||||||
chr5:32776617 | C | T | 1 | a0001c0001t0001g0025 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1195+1774C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32776617 | |||||||
chr5:32776938 | A | C | 1 | a0001c0006t0061g0046 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1195+2095A>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32776938 | |||||||
chr5:32776949 | C | A | 1 | a0001c0001t0001g0184 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1195+2106C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32776949 | |||||||
chr5:32776994 | G | A | 1 | a0001c0003t0008g0032 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1195+2151G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32776994 | |||||||
chr5:32777035 | C | T | 3 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0006g0010 |
3 | HG02145.hp2 HG02258.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1195+2192C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32777035 | |||||||
chr5:32777239 | G | C | 62 | a0001c0001t0002g0008 a0001c0001t0002g0129 a0001c0001t0003g0004 others(59): Show |
64 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.1195+2396G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32777239 | |||||||
chr5:32777289 | A | G | 1 | a0001c0001t0049g0015 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1195+2446A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32777289 | |||||||
chr5:32777548 | G | A | 1 | a0001c0006t0061g0046 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1195+2705G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32777548 | |||||||
chr5:32777549 | T | C | 2 | a0001c0001t0002g0008 a0001c0001t0002g0129 |
2 | HG03098.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1195+2706T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32777549 | |||||||
chr5:32777564 | C | T | 13 | a0001c0001t0005g0079 a0001c0001t0005g0143 a0001c0001t0005g0153 others(10): Show |
14 | HG02145.hp1 HG02258.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1195+2721C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32777564 | |||||||
chr5:32777580 | G | A | 5 | a0001c0001t0004g0139 a0001c0001t0004g0299 a0001c0001t0004g0300 others(2): Show |
5 | HG01891.hp1 HG02922.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1195+2737G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32777580 | |||||||
chr5:32777713 | G | A | 1 | a0001c0005t0056g0266 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1195+2870G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32777713 | |||||||
chr5:32777830 | A | G | 1 | a0001c0001t0003g0252 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1196-2892A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32777830 | |||||||
chr5:32777853 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1196-2869A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32777853 | |||||||
chr5:32778062 | G | A | 3 | a0001c0001t0019g0006 a0001c0001t0019g0007 a0001c0001t0055g0147 |
3 | HG01192.hp1 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1196-2660G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32778062 | |||||||
chr5:32778127 | A | C | 78 | a0001c0001t0001g0088 a0001c0001t0001g0126 a0001c0001t0004g0140 others(75): Show |
79 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.1196-2595A>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32778127 | |||||||
chr5:32778295 | C | T | 1 | a0001c0001t0001g0043 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1196-2427C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32778295 | |||||||
chr5:32778588 | T | C | 3 | a0001c0001t0019g0006 a0001c0001t0019g0007 a0001c0001t0055g0147 |
3 | HG01192.hp1 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1196-2134T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32778588 | |||||||
chr5:32778813 | C | G | 3 | a0001c0001t0008g0128 a0001c0001t0008g0301 a0001c0001t0059g0156 |
3 | HG02257.hp1 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1196-1909C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32778813 | |||||||
chr5:32778932 | G | T | 1 | a0001c0006t0061g0046 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1196-1790G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32778932 | |||||||
chr5:32779205 | T | C | 2 | a0001c0001t0043g0067 a0001c0001t0065g0051 |
2 | HG02723.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1196-1517T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32779205 | |||||||
chr5:32779228 | GAGAGAAC others(6): Show |
G | 9 | a0001c0001t0004g0016 a0001c0001t0004g0017 a0001c0001t0004g0027 others(6): Show |
9 | HG00735.hp2 HG01070.hp2 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.1196-1479_1196-146 others(17): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 32779228 | ||||||
chr5:32779341 | G | A | 1 | a0001c0001t0001g0306 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1196-1381G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32779341 | |||||||
chr5:32779396 | G | A | 1 | a0001c0006t0061g0046 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1196-1326G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32779396 | |||||||
chr5:32779490 | C | T | 1 | a0001c0001t0001g0184 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1196-1232C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32779490 | |||||||
chr5:32779491 | G | A | 13 | a0001c0001t0005g0079 a0001c0001t0005g0143 a0001c0001t0005g0153 others(10): Show |
14 | HG02145.hp1 HG02258.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1196-1231G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32779491 | |||||||
chr5:32779504 | G | A | 1 | a0001c0006t0061g0046 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1196-1218G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32779504 | |||||||
chr5:32779541 | C | T | 1 | a0001c0001t0003g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1196-1181C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32779541 | |||||||
chr5:32779643 | G | T | 1 | a0001c0004t0062g0135 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1196-1079G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32779643 | |||||||
chr5:32779715 | A | G | 2 | a0002c0002t0002g0041 a0002c0002t0002g0055 |
2 | HG02451.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1196-1007A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32779715 | |||||||
chr5:32779819 | C | T | 1 | a0001c0001t0047g0104 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1196-903C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32779819 | |||||||
chr5:32779847 | C | T | 1 | a0001c0001t0039g0265 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1196-875C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32779847 | |||||||
chr5:32779908 | G | T | 2 | a0001c0001t0004g0044 a0001c0001t0042g0042 |
2 | HG03516.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1196-814G>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32779908 | |||||||
chr5:32779926 | T | C | 1 | a0001c0001t0003g0087 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1196-796T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32779926 | |||||||
chr5:32780021 | G | A | 1 | a0001c0006t0061g0046 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1196-701G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32780021 | |||||||
chr5:32780167 | T | C | 1 | a0001c0006t0061g0046 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1196-555T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32780167 | |||||||
chr5:32780185 | A | G | 78 | a0001c0001t0001g0088 a0001c0001t0001g0126 a0001c0001t0008g0045 others(75): Show |
79 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.1196-537A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32780185 | |||||||
chr5:32780210 | G | C | 37 | a0001c0001t0004g0016 a0001c0001t0004g0017 a0001c0001t0004g0027 others(34): Show |
37 | HG00735.hp2 HG00741.hp1 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.1196-512G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32780210 | |||||||
chr5:32780341 | G | A | 1 | a0001c0006t0061g0046 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1196-381G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32780341 | |||||||
chr5:32780452 | AATCTTTT others(9): Show |
A | 1 | a0001c0001t0037g0059 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1196-266_1196-251d others(18): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 32780452 | ||||||
chr5:32780575 | A | G | 1 | a0001c0001t0001g0254 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1196-147A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32780575 | |||||||
chr5:32780695 | T | C | 2 | a0001c0001t0001g0314 a0001c0001t0001g0315 |
2 | NA19060.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1196-27T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 4/7 | chr5 | 32780695 | |||||||
chr5:32780828 | AG | A | 3 | a0001c0001t0001g0151 a0001c0001t0006g0066 a0001c0001t0006g0110 |
3 | HG01243.hp2 HG02630.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1290+13delG | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 5/7 | chr5 | 32780828 | |||||||
chr5:32780857 | C | T | 1 | a0001c0001t0038g0022 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1290+41C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 5/7 | chr5 | 32780857 | |||||||
chr5:32781090 | T | G | 75 | a0001c0001t0001g0088 a0001c0001t0001g0126 a0001c0001t0008g0045 others(72): Show |
76 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.1290+274T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 5/7 | chr5 | 32781090 | |||||||
chr5:32781298 | C | T | 74 | a0001c0001t0001g0088 a0001c0001t0001g0126 a0001c0001t0008g0045 others(71): Show |
75 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.1290+482C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 5/7 | chr5 | 32781298 | |||||||
chr5:32781415 | T | C | 65 | a0001c0001t0001g0088 a0001c0001t0001g0126 a0002c0002t0002g0005 others(62): Show |
66 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.1290+599T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 5/7 | chr5 | 32781415 | |||||||
chr5:32781422 | T | C | 1 | a0001c0006t0061g0046 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1290+606T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 5/7 | chr5 | 32781422 | |||||||
chr5:32781475 | G | GT | 198 | a0001c0001t0001g0088 a0001c0001t0001g0126 a0001c0001t0002g0008 others(195): Show |
202 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.1290+659_1290+660i others(3): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 5/7 | chr5 | 32781475 | |||||||
chr5:32781495 | A | G | 37 | a0001c0001t0004g0016 a0001c0001t0004g0017 a0001c0001t0004g0027 others(34): Show |
37 | HG00735.hp2 HG00741.hp1 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.1290+679A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 5/7 | chr5 | 32781495 | |||||||
chr5:32781747 | C | A | 1 | a0001c0006t0061g0046 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1290+931C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 5/7 | chr5 | 32781747 | |||||||
chr5:32781808 | G | A | 1 | a0001c0001t0003g0075 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1290+992G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 5/7 | chr5 | 32781808 | |||||||
chr5:32782046 | C | A | 198 | a0001c0001t0001g0088 a0001c0001t0001g0126 a0001c0001t0002g0008 others(195): Show |
202 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.1291-847C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 5/7 | chr5 | 32782046 | |||||||
chr5:32782188 | A | G | 2 | a0002c0002t0020g0086 a0002c0002t0020g0225 |
2 | HG02040.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.1291-705A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 5/7 | chr5 | 32782188 | |||||||
chr5:32782270 | T | C | 1 | a0001c0005t0056g0266 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1291-623T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 5/7 | chr5 | 32782270 | |||||||
chr5:32782325 | C | T | 1 | a0001c0001t0003g0256 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1291-568C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 5/7 | chr5 | 32782325 | |||||||
chr5:32782339 | ACCCTGGC others(14): Show |
A | 37 | a0001c0001t0004g0016 a0001c0001t0004g0017 a0001c0001t0004g0027 others(34): Show |
37 | HG00735.hp2 HG00741.hp1 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.1291-548_1291-528d others(23): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 32782339 | ||||||
chr5:32782487 | C | A | 1 | a0001c0005t0056g0266 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1291-406C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 5/7 | chr5 | 32782487 | |||||||
chr5:32782573 | C | T | 1 | a0001c0006t0061g0046 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1291-320C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 5/7 | chr5 | 32782573 | |||||||
chr5:32782576 | C | T | 2 | a0001c0001t0043g0067 a0001c0001t0065g0051 |
2 | HG02723.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1291-317C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 5/7 | chr5 | 32782576 | |||||||
chr5:32782687 | T | A | 3 | a0001c0001t0003g0004 a0001c0001t0003g0234 a0001c0001t0003g0256 |
4 | HG00621.hp1 HG02015.hp1 HG02129.hp2 others(1): Show |
intron_variant | MODIFIER | c.1291-206T>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 5/7 | chr5 | 32782687 | |||||||
chr5:32782698 | G | A | 1 | a0001c0001t0003g0234 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1291-195G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 5/7 | chr5 | 32782698 | |||||||
chr5:32782720 | C | T | 1 | a0002c0002t0002g0125 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1291-173C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 5/7 | chr5 | 32782720 | |||||||
chr5:32782783 | C | T | 2 | a0001c0001t0050g0047 a0001c0003t0058g0035 |
2 | HG02615.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1291-110C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 5/7 | chr5 | 32782783 | |||||||
chr5:32782834 | C | T | 1 | a0001c0001t0036g0013 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1291-59C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 5/7 | chr5 | 32782834 | |||||||
chr5:32783490 | A | G | 2 | a0001c0001t0043g0067 a0001c0001t0065g0051 |
2 | HG02723.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1426+462A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 6/7 | chr5 | 32783490 | |||||||
chr5:32783560 | T | A | 1 | a0001c0001t0037g0059 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1426+532T>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 6/7 | chr5 | 32783560 | |||||||
chr5:32783602 | C | T | 27 | a0001c0001t0003g0004 a0001c0001t0003g0087 a0001c0001t0003g0091 others(24): Show |
29 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.1426+574C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 6/7 | chr5 | 32783602 | |||||||
chr5:32783603 | C | T | 74 | a0001c0001t0001g0088 a0001c0001t0001g0126 a0001c0001t0008g0045 others(71): Show |
75 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.1426+575C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 6/7 | chr5 | 32783603 | |||||||
chr5:32783631 | C | G | 1 | a0001c0006t0061g0046 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1426+603C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 6/7 | chr5 | 32783631 | |||||||
chr5:32783690 | A | T | 1 | a0001c0001t0003g0122 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1426+662A>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 6/7 | chr5 | 32783690 | |||||||
chr5:32783990 | T | G | 1 | a0001c0001t0008g0134 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1427-806T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 6/7 | chr5 | 32783990 | |||||||
chr5:32784020 | T | C | 2 | a0001c0004t0062g0135 a0001c0006t0061g0046 |
2 | HG02055.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.1427-776T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 6/7 | chr5 | 32784020 | |||||||
chr5:32784023 | A | G | 1 | a0001c0001t0060g0289 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1427-773A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 6/7 | chr5 | 32784023 | |||||||
chr5:32784087 | A | G | 2 | a0001c0004t0062g0135 a0001c0006t0061g0046 |
2 | HG02055.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.1427-709A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 6/7 | chr5 | 32784087 | |||||||
chr5:32784097 | C | A | 1 | a0001c0001t0040g0162 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1427-699C>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 6/7 | chr5 | 32784097 | |||||||
chr5:32784177 | G | C | 5 | a0001c0001t0008g0045 a0001c0001t0008g0128 a0001c0001t0008g0134 others(2): Show |
5 | HG02257.hp1 HG02486.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1427-619G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 6/7 | chr5 | 32784177 | |||||||
chr5:32784251 | T | C | 76 | a0001c0001t0001g0088 a0001c0001t0001g0126 a0001c0001t0008g0045 others(73): Show |
77 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.1427-545T>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 6/7 | chr5 | 32784251 | |||||||
chr5:32784262 | C | T | 1 | a0001c0001t0017g0064 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1427-534C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 6/7 | chr5 | 32784262 | |||||||
chr5:32784670 | A | G | 73 | a0001c0001t0001g0088 a0001c0001t0001g0126 a0001c0001t0008g0045 others(70): Show |
74 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.1427-126A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 6/7 | chr5 | 32784670 | |||||||
chr5:32784891 | C | T | 1 | a0001c0001t0001g0096 | 1 | NA18962.hp1 | splice_region_variant&intron_variant | LOW | c.1514+8C>T | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 7/7 | chr5 | 32784891 | |||||||
chr5:32784991 | G | A | 1 | a0001c0001t0004g0016 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1514+108G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 7/7 | chr5 | 32784991 | |||||||
chr5:32785101 | A | G | 2 | a0001c0001t0009g0161 a0001c0001t0048g0303 |
2 | NA18612.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.1514+218A>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 7/7 | chr5 | 32785101 | |||||||
chr5:32785138 | A | AT | 60 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0019 others(57): Show |
61 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.1514+283dupT | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 32785138 | ||||||
chr5:32785138 | A | ATT | 7 | a0001c0001t0001g0132 a0001c0001t0006g0010 a0001c0001t0006g0063 others(4): Show |
7 | HG01891.hp2 HG01978.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1514+282_1514+283d others(4): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 32785138 | ||||||
chr5:32785138 | AT | A | 6 | a0001c0001t0004g0149 a0001c0001t0007g0200 a0001c0001t0037g0059 others(3): Show |
6 | HG01516.hp2 HG02109.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1514+283delT | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 32785138 | ||||||
chr5:32785138 | ATT | A | 8 | a0001c0001t0008g0045 a0001c0001t0008g0128 a0001c0001t0008g0134 others(5): Show |
8 | HG02257.hp1 HG02486.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1514+282_1514+283d others(4): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 32785138 | ||||||
chr5:32785138 | ATTTT | A | 12 | a0001c0001t0001g0088 a0001c0001t0019g0007 a0001c0006t0061g0046 others(9): Show |
12 | HG00741.hp2 HG01433.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1514+280_1514+283d others(6): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 32785138 | ||||||
chr5:32785138 | ATTTTT | A | 65 | a0001c0001t0001g0126 a0001c0001t0003g0101 a0001c0001t0003g0167 others(62): Show |
66 | HG00099.hp2 HG00544.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.1514+279_1514+283d others(7): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 32785138 | ||||||
chr5:32785138 | ATTTTTT | A | 52 | a0001c0001t0002g0008 a0001c0001t0002g0129 a0001c0001t0003g0004 others(49): Show |
54 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.1514+278_1514+283d others(8): Show |
NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 32785138 | ||||||
chr5:32785177 | C | G | 1 | a0001c0001t0002g0008 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1514+294C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 7/7 | chr5 | 32785177 | |||||||
chr5:32785181 | G | C | 10 | a0001c0001t0008g0045 a0001c0001t0008g0128 a0001c0001t0008g0134 others(7): Show |
10 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1514+298G>C | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 7/7 | chr5 | 32785181 | |||||||
chr5:32785314 | T | G | 10 | a0001c0001t0008g0045 a0001c0001t0008g0128 a0001c0001t0008g0134 others(7): Show |
10 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1514+431T>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 7/7 | chr5 | 32785314 | |||||||
chr5:32785720 | G | A | 4 | a0001c0003t0005g0002 a0001c0003t0005g0030 a0001c0003t0005g0031 others(1): Show |
5 | HG02258.hp2 HG02970.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1515-514G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 7/7 | chr5 | 32785720 | |||||||
chr5:32785749 | G | A | 4 | a0001c0001t0017g0057 a0001c0001t0017g0064 a0001c0001t0021g0080 others(1): Show |
4 | HG01884.hp1 HG02965.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1515-485G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 7/7 | chr5 | 32785749 | |||||||
chr5:32785807 | G | A | 1 | a0001c0004t0062g0135 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1515-427G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 7/7 | chr5 | 32785807 | |||||||
chr5:32785973 | C | G | 1 | a0001c0005t0056g0266 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1515-261C>G | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 7/7 | chr5 | 32785973 | |||||||
chr5:32786009 | G | A | 9 | a0001c0001t0008g0045 a0001c0001t0008g0128 a0001c0001t0008g0134 others(6): Show |
9 | HG02257.hp1 HG02486.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1515-225G>A | NPR3 | ENSG00000113389.16 | transcript | ENST00000265074.13 | protein_coding | 7/7 | chr5 | 32786009 |