Item | Value |
---|---|
geneid | 23129 |
ensemblid | ENSG00000004399.13 |
hgncid | 9107 |
symbol | PLXND1 |
name | plexin D1 |
refseq_nuc | NM_015103.3 |
refseq_prot | NP_055918.3 |
ensembl_nuc | ENST00000324093.9 |
ensembl_prot | ENSP00000317128.4 |
mane_status | MANE Select |
chr | chr3 |
start | 129555214 |
end | 129606676 |
strand | - |
ver | v1.2 |
region | chr3:129555214-129606676 |
region5000 | chr3:129550214-129611676 |
regionname0 | PLXND1_chr3_129555214_129606676 |
regionname5000 | PLXND1_chr3_129550214_129611676 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 1925 | 181 | 18 | 32 | 100 | 6 | 25 | 80 | PLXND1_chr3_129550214_129611676 | PLXND1 | MAPRA others(1920): Show |
chr3 | 129550214 | 129611676 |
a0002 | 0/0 | 1925 | 109 | 34 | 17 | 48 | 2 | 8 | 32 | PLXND1_chr3_129550214_129611676 | PLXND1 | MAPRA others(1920): Show |
chr3 | 129550214 | 129611676 |
a0003 | 0/0 | 1925 | 41 | 13 | 16 | 0 | 6 | 6 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | MAPRA others(1920): Show |
chr3 | 129550214 | 129611676 |
a0004 | 0/0 | 1925 | 27 | 6 | 3 | 13 | 1 | 4 | 11 | PLXND1_chr3_129550214_129611676 | PLXND1 | MAPRA others(1920): Show |
chr3 | 129550214 | 129611676 |
a0005 | 0/0 | 1925 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | MAPRA others(1920): Show |
chr3 | 129550214 | 129611676 |
a0006 | 0/0 | 1925 | 4 | 3 | 0 | 0 | 0 | 1 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | MAPRA others(1920): Show |
chr3 | 129550214 | 129611676 |
a0007 | 0/0 | 1925 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | MAPRA others(1920): Show |
chr3 | 129550214 | 129611676 |
a0008 | 0/0 | 1925 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | MAPRA others(1920): Show |
chr3 | 129550214 | 129611676 |
a0009 | 0/0 | 1925 | 2 | 0 | 0 | 0 | 1 | 1 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | MAPRA others(1920): Show |
chr3 | 129550214 | 129611676 |
a0010 | 0/0 | 1925 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | MAPRA others(1920): Show |
chr3 | 129550214 | 129611676 |
a0011 | 0/0 | 1925 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | MAPRA others(1920): Show |
chr3 | 129550214 | 129611676 |
a0012 | 0/0 | 1925 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | MAPRA others(1920): Show |
chr3 | 129550214 | 129611676 |
a0013 | 0/0 | 1925 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | PLXND1_chr3_129550214_129611676 | PLXND1 | MAPRA others(1920): Show |
chr3 | 129550214 | 129611676 |
a0014 | 0/0 | 1925 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | PLXND1_chr3_129550214_129611676 | PLXND1 | MAPRA others(1920): Show |
chr3 | 129550214 | 129611676 |
a0015 | 0/0 | 1925 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | PLXND1_chr3_129550214_129611676 | PLXND1 | MAPRA others(1920): Show |
chr3 | 129550214 | 129611676 |
a0017 | 0/0 | 1925 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | MAPRA others(1920): Show |
chr3 | 129550214 | 129611676 |
a0018 | 0/0 | 1925 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | MAPRA others(1920): Show |
chr3 | 129550214 | 129611676 |
a0019 | 0/0 | 1925 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | MAPRA others(1920): Show |
chr3 | 129550214 | 129611676 |
a0020 | 0/0 | 1925 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | MAPRA others(1920): Show |
chr3 | 129550214 | 129611676 |
a0021 | 0/0 | 1925 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | MAPRA others(1920): Show |
chr3 | 129550214 | 129611676 |
a0022 | 0/0 | 1925 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | MAPRA others(1920): Show |
chr3 | 129550214 | 129611676 |
a0023 | 0/0 | 1925 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | MAPRA others(1920): Show |
chr3 | 129550214 | 129611676 |
a0024 | 0/0 | 1925 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | MAPRA others(1920): Show |
chr3 | 129550214 | 129611676 |
a0025 | 0/0 | 1925 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | MAPRA others(1920): Show |
chr3 | 129550214 | 129611676 |
a0026 | 0/0 | 1925 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | MAPRA others(1920): Show |
chr3 | 129550214 | 129611676 |
a0027 | 0/0 | 589 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | MAPRA others(584): Show |
chr3 | 129550214 | 129611676 |
a0028 | 0/0 | 1925 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | MAPRA others(1920): Show |
chr3 | 129550214 | 129611676 |
a0029 | 0/0 | 1542 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | MAPRA others(1537): Show |
chr3 | 129550214 | 129611676 |
a0030 | 0/0 | 961 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | MAPRA others(956): Show |
chr3 | 129550214 | 129611676 |
a0031 | 0/0 | 800 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | MAPRA others(795): Show |
chr3 | 129550214 | 129611676 |
a0032 | 0/0 | 1607 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | MAPRA others(1602): Show |
chr3 | 129550214 | 129611676 |
a0033 | 0/0 | 1925 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | MAPRA others(1920): Show |
chr3 | 129550214 | 129611676 |
a0034 | 0/0 | 87 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | MAPRA others(82): Show |
chr3 | 129550214 | 129611676 |
a0035 | 0/0 | 86 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | MAPRA others(81): Show |
chr3 | 129550214 | 129611676 |
a0036 | 0/0 | 1925 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | MAPRA others(1920): Show |
chr3 | 129550214 | 129611676 |
a0037 | 0/0 | 1300 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | MAPRA others(1295): Show |
chr3 | 129550214 | 129611676 |
a0038 | 0/0 | 498 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | MAPRA others(493): Show |
chr3 | 129550214 | 129611676 |
a0039 | 0/0 | 1300 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | MAPRA others(1295): Show |
chr3 | 129550214 | 129611676 |
a0040 | 0/0 | 1925 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | MAPRA others(1920): Show |
chr3 | 129550214 | 129611676 |
a0041 | 0/0 | 1925 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | MAPRA others(1920): Show |
chr3 | 129550214 | 129611676 |
a0042 | 0/0 | 460 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | MAPRA others(455): Show |
chr3 | 129550214 | 129611676 |
a0043 | 0/0 | 525 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | MAPRA others(520): Show |
chr3 | 129550214 | 129611676 |
a0044 | 0/0 | 1327 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | MAPRA others(1322): Show |
chr3 | 129550214 | 129611676 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 5775 | 105 | 8 | 27 | 49 | 6 | 15 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0001c0002 | 0/0 | 5775 | 52 | 2 | 5 | 38 | 0 | 7 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0001c0011 | 0/0 | 5775 | 6 | 4 | 0 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0001c0013 | 0/0 | 5775 | 5 | 0 | 0 | 5 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0001c0020 | 0/0 | 5775 | 3 | 0 | 0 | 0 | 0 | 3 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0001c0028 | 0/0 | 5775 | 2 | 0 | 0 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0001c0045 | 0/0 | 5775 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0001c0050 | 0/0 | 5775 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0001c0054 | 0/0 | 5775 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0001c0056 | 0/0 | 5775 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0001c0064 | 0/0 | 5775 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0001c0070 | 0/0 | 5775 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0001c0073 | 0/0 | 5775 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0001c0078 | 0/0 | 5775 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0002c0003 | 0/0 | 5775 | 43 | 0 | 0 | 39 | 0 | 4 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0002c0004 | 0/0 | 5775 | 23 | 9 | 8 | 1 | 1 | 4 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0002c0006 | 0/0 | 5775 | 13 | 11 | 2 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0002c0009 | 0/0 | 5775 | 9 | 0 | 4 | 5 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0002c0012 | 0/0 | 5775 | 6 | 5 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0002c0015 | 0/0 | 5775 | 5 | 5 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0002c0017 | 0/0 | 5775 | 4 | 2 | 1 | 0 | 1 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0002c0048 | 0/0 | 5775 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0002c0057 | 0/0 | 5775 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0002c0058 | 0/0 | 5775 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0002c0060 | 0/0 | 5775 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0002c0075 | 0/0 | 5775 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0002c0079 | 0/0 | 5775 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0003c0007 | 0/0 | 5775 | 13 | 2 | 5 | 0 | 5 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0003c0008 | 0/0 | 5775 | 11 | 1 | 8 | 0 | 1 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0003c0010 | 0/0 | 5775 | 7 | 0 | 3 | 0 | 0 | 4 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0003c0014 | 0/0 | 5775 | 5 | 5 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0003c0018 | 0/0 | 5775 | 4 | 4 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0003c0059 | 0/0 | 5775 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0004c0005 | 0/0 | 5775 | 22 | 3 | 1 | 13 | 1 | 4 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0004c0019 | 0/0 | 5775 | 3 | 2 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0004c0040 | 0/0 | 5775 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0004c0076 | 0/0 | 5775 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0005c0016 | 0/0 | 5775 | 5 | 5 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0006c0023 | 0/0 | 5775 | 2 | 2 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0006c0046 | 0/0 | 5775 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0006c0047 | 0/0 | 5775 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0007c0021 | 0/0 | 5775 | 3 | 2 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0008c0024 | 0/0 | 5775 | 2 | 0 | 0 | 0 | 2 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0009c0022 | 0/0 | 5775 | 2 | 0 | 0 | 0 | 1 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0010c0035 | 0/0 | 5775 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0010c0036 | 0/0 | 5775 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0011c0026 | 0/0 | 5775 | 2 | 2 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0012c0029 | 0/0 | 5775 | 2 | 2 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0013c0025 | 0/0 | 5775 | 2 | 0 | 0 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0014c0061 | 0/0 | 5775 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0014c0062 | 0/0 | 5775 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0015c0027 | 0/0 | 5775 | 2 | 0 | 0 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0017c0071 | 0/0 | 5775 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0018c0067 | 0/0 | 5775 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0019c0066 | 0/0 | 5775 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0020c0072 | 0/0 | 5775 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0021c0043 | 0/0 | 5775 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0022c0065 | 0/0 | 5775 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0023c0049 | 0/0 | 5775 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0024c0038 | 0/0 | 5775 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0025c0051 | 0/0 | 5775 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0026c0063 | 0/0 | 5775 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0027c0042 | 0/0 | 5774 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5769): Show |
chr3 | 129550214 | 129611676 | ||
a0028c0044 | 0/0 | 5775 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0029c0052 | 0/0 | 5776 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5771): Show |
chr3 | 129550214 | 129611676 | ||
a0030c0039 | 0/0 | 5775 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0031c0037 | 0/0 | 5775 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0032c0053 | 0/0 | 5773 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5768): Show |
chr3 | 129550214 | 129611676 | ||
a0033c0041 | 0/0 | 5775 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0034c0032 | 0/0 | 5776 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5771): Show |
chr3 | 129550214 | 129611676 | ||
a0035c0081 | 0/0 | 5776 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5771): Show |
chr3 | 129550214 | 129611676 | ||
a0036c0068 | 0/0 | 5775 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0037c0069 | 0/0 | 5777 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5772): Show |
chr3 | 129550214 | 129611676 | ||
a0038c0034 | 0/0 | 5775 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0039c0055 | 0/0 | 5776 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5771): Show |
chr3 | 129550214 | 129611676 | ||
a0040c0080 | 0/0 | 5775 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0041c0074 | 0/0 | 5775 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 | ||
a0042c0030 | 0/0 | 5777 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5772): Show |
chr3 | 129550214 | 129611676 | ||
a0043c0031 | 0/0 | 5776 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5771): Show |
chr3 | 129550214 | 129611676 | ||
a0044c0033 | 0/0 | 5775 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGGC others(5770): Show |
chr3 | 129550214 | 129611676 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6913 | 101 | 7 | 25 | 49 | 6 | 14 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0001c0001t0008 | 0/0 | 6913 | 3 | 1 | 1 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0001c0001t0013 | 0/0 | 6913 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0001c0002t0002 | 0/0 | 6913 | 51 | 2 | 5 | 37 | 0 | 7 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0001c0002t0012 | 0/0 | 6913 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0001c0011t0001 | 0/0 | 6913 | 6 | 4 | 0 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0001c0013t0003 | 0/0 | 6913 | 5 | 0 | 0 | 5 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0001c0020t0001 | 0/0 | 6913 | 3 | 0 | 0 | 0 | 0 | 3 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0001c0028t0001 | 0/0 | 6913 | 2 | 0 | 0 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0001c0045t0002 | 0/0 | 6913 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0001c0050t0001 | 0/0 | 6913 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0001c0054t0002 | 0/0 | 6913 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0001c0056t0002 | 0/0 | 6913 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0001c0064t0001 | 0/0 | 6913 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0001c0070t0001 | 0/0 | 6913 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0001c0073t0001 | 0/0 | 6913 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0001c0078t0011 | 0/0 | 6913 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0002c0003t0001 | 0/0 | 6913 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0002c0003t0003 | 0/0 | 6913 | 42 | 0 | 0 | 38 | 0 | 4 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0002c0004t0001 | 0/0 | 6913 | 23 | 9 | 8 | 1 | 1 | 4 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0002c0006t0001 | 0/0 | 6913 | 13 | 11 | 2 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0002c0009t0001 | 0/0 | 6913 | 3 | 0 | 1 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0002c0009t0003 | 0/0 | 6913 | 6 | 0 | 3 | 3 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0002c0012t0001 | 0/0 | 6913 | 6 | 5 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0002c0015t0006 | 0/0 | 6913 | 5 | 5 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0002c0017t0004 | 0/0 | 6913 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0002c0017t0007 | 0/0 | 6913 | 3 | 1 | 1 | 0 | 1 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0002c0048t0003 | 0/0 | 6913 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0002c0057t0001 | 0/0 | 6913 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0002c0058t0009 | 0/0 | 6913 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0002c0060t0003 | 0/0 | 6913 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0002c0075t0002 | 0/0 | 6913 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0002c0079t0011 | 0/0 | 6913 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0003c0007t0001 | 0/0 | 6913 | 13 | 2 | 5 | 0 | 5 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0003c0008t0004 | 0/0 | 6913 | 11 | 1 | 8 | 0 | 1 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0003c0010t0001 | 0/0 | 6913 | 7 | 0 | 3 | 0 | 0 | 4 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0003c0014t0004 | 0/0 | 6913 | 5 | 5 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0003c0018t0005 | 0/0 | 6913 | 4 | 4 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0003c0059t0004 | 0/0 | 6913 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0004c0005t0001 | 0/0 | 6913 | 22 | 3 | 1 | 13 | 1 | 4 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0004c0019t0004 | 0/0 | 6913 | 3 | 2 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0004c0040t0004 | 0/0 | 6913 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0004c0076t0004 | 0/0 | 6913 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0005c0016t0001 | 0/0 | 6913 | 5 | 5 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0006c0023t0001 | 0/0 | 6913 | 2 | 2 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0006c0046t0004 | 0/0 | 6913 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0006c0047t0001 | 0/0 | 6913 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0007c0021t0002 | 0/0 | 6913 | 2 | 1 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0007c0021t0004 | 0/0 | 6913 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0008c0024t0004 | 0/0 | 6913 | 2 | 0 | 0 | 0 | 2 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0009c0022t0001 | 0/0 | 6913 | 2 | 0 | 0 | 0 | 1 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0010c0035t0005 | 0/0 | 6913 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0010c0036t0005 | 0/0 | 6913 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0011c0026t0004 | 0/0 | 6913 | 2 | 2 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0012c0029t0010 | 0/0 | 6913 | 2 | 2 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0013c0025t0001 | 0/0 | 6913 | 2 | 0 | 0 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0014c0061t0003 | 0/0 | 6913 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0014c0062t0003 | 0/0 | 6913 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0015c0027t0001 | 0/0 | 6913 | 2 | 0 | 0 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0017c0071t0002 | 0/0 | 6913 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0018c0067t0002 | 0/0 | 6913 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0019c0066t0014 | 0/0 | 6913 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0020c0072t0002 | 0/0 | 6913 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0021c0043t0001 | 0/0 | 6913 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0022c0065t0009 | 0/0 | 6913 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0023c0049t0001 | 0/0 | 6913 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0024c0038t0001 | 0/0 | 6913 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0025c0051t0001 | 0/0 | 6913 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0026c0063t0001 | 0/0 | 6913 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0027c0042t0001 | 0/0 | 6912 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6907): Show |
chr3 | 129550214 | 129611676 |
a0028c0044t0003 | 0/0 | 6913 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0029c0052t0001 | 0/0 | 6914 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6909): Show |
chr3 | 129550214 | 129611676 |
a0030c0039t0001 | 0/0 | 6913 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0031c0037t0001 | 0/0 | 6913 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0032c0053t0001 | 0/0 | 6911 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6906): Show |
chr3 | 129550214 | 129611676 |
a0033c0041t0001 | 0/0 | 6913 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0034c0032t0001 | 0/0 | 6914 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6909): Show |
chr3 | 129550214 | 129611676 |
a0035c0081t0001 | 0/0 | 6914 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6909): Show |
chr3 | 129550214 | 129611676 |
a0036c0068t0002 | 0/0 | 6913 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0037c0069t0002 | 0/0 | 6915 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6910): Show |
chr3 | 129550214 | 129611676 |
a0038c0034t0003 | 0/0 | 6913 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0039c0055t0001 | 0/0 | 6914 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6909): Show |
chr3 | 129550214 | 129611676 |
a0040c0080t0003 | 0/0 | 6913 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0041c0074t0002 | 0/0 | 6913 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
a0042c0030t0003 | 0/0 | 6915 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6910): Show |
chr3 | 129550214 | 129611676 |
a0043c0031t0003 | 0/0 | 6914 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6909): Show |
chr3 | 129550214 | 129611676 |
a0044c0033t0002 | 0/0 | 6913 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | ATGCA others(6908): Show |
chr3 | 129550214 | 129611676 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 6 | 0 | 4 | 0 | 1 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0003 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0011 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0012 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0008g0036 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0008g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0001t0013g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0002t0002g0005 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0002t0002g0008 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0002t0002g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0002t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0002t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0002t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0002t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0002t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0002t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0002t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0002t0012g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0011t0001g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0011t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0011t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0013t0003g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0013t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0020t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0020t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0020t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0028t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0045t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0050t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0054t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0056t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0064t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0070t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0073t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0001c0078t0011g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0003t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0003t0003g0001 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0003t0003g0013 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0003t0003g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0003t0003g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0003t0003g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0003t0003g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0003t0003g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0003t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0003t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0003t0003g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0003t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0003t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0003t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0003t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0003t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0003t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0003t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0003t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0003t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0003t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0003t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0003t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0003t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0003t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0003t0003g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0003t0003g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0003t0003g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0004t0001g0004 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0004t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0004t0001g0052 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0004t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0004t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0004t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0004t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0004t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0004t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0004t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0004t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0004t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0004t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0004t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0004t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0004t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0006t0001g0007 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0006t0001g0010 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0006t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0006t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0006t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0006t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0009t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0009t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0009t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0009t0003g0018 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0009t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0009t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0009t0003g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0012t0001g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0012t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0012t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0012t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0012t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0015t0006g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0015t0006g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0015t0006g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0015t0006g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0015t0006g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0017t0004g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0017t0007g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0017t0007g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0048t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0057t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0058t0009g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0060t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0075t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0002c0079t0011g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0003c0007t0001g0009 | 0/0 | 4 | 1 | 2 | 0 | 1 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0003c0007t0001g0026 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0003c0007t0001g0027 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0003c0007t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0003c0007t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0003c0007t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0003c0007t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0003c0007t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0003c0008t0004g0017 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0003c0008t0004g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0003c0008t0004g0039 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0003c0008t0004g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0003c0008t0004g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0003c0008t0004g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0003c0008t0004g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0003c0010t0001g0020 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0003c0010t0001g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0003c0010t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0003c0010t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0003c0014t0004g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0003c0014t0004g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0003c0014t0004g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0003c0014t0004g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0003c0018t0005g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0003c0018t0005g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0003c0018t0005g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0003c0059t0004g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0004c0005t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0004c0005t0001g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0004c0005t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0004c0005t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0004c0005t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0004c0005t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0004c0005t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0004c0005t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0004c0005t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0004c0005t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0004c0005t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0004c0005t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0004c0005t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0004c0005t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0004c0005t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0004c0005t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0004c0005t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0004c0005t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0004c0005t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0004c0019t0004g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0004c0019t0004g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0004c0019t0004g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0004c0040t0004g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0004c0076t0004g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0005c0016t0001g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0005c0016t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0005c0016t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0006c0023t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0006c0023t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0006c0046t0004g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0006c0047t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0007c0021t0002g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0007c0021t0004g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0008c0024t0004g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0008c0024t0004g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0009c0022t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0009c0022t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0010c0035t0005g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0010c0036t0005g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0011c0026t0004g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0012c0029t0010g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0013c0025t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0013c0025t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0014c0061t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0014c0062t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0015c0027t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0015c0027t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0017c0071t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0018c0067t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0019c0066t0014g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0020c0072t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0021c0043t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0022c0065t0009g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0023c0049t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0024c0038t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0025c0051t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0026c0063t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0027c0042t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0028c0044t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0029c0052t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0030c0039t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0031c0037t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0032c0053t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0033c0041t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0034c0032t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0035c0081t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0036c0068t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0037c0069t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0038c0034t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0039c0055t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0040c0080t0003g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0041c0074t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0042c0030t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0043c0031t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
a0044c0033t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0144 | EUR | GBR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0032 | EUR | GBR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG00140 | hp1 | a0002 | c0017 | t0007 | g0142 | EUR | GBR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG00140 | hp2 | a0003 | c0007 | t0001 | g0102 | EUR | GBR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG00280 | hp1 | a0003 | c0007 | t0001 | g0026 | EUR | FIN | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG00323 | hp1 | a0003 | c0008 | t0004 | g0176 | EUR | FIN | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0021 | EUR | FIN | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | CHS | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG00408 | hp2 | a0004 | c0005 | t0001 | g0254 | EAS | CHS | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG00423 | hp1 | a0001 | c0002 | t0002 | g0078 | EAS | CHS | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG00438 | hp1 | a0001 | c0070 | t0001 | g0076 | EAS | CHS | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG00438 | hp2 | a0001 | c0011 | t0001 | g0211 | EAS | CHS | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG00558 | hp1 | a0002 | c0003 | t0003 | g0001 | EAS | CHS | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | CHS | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | CHS | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG00597 | hp2 | a0002 | c0075 | t0002 | g0091 | EAS | CHS | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG00609 | hp1 | a0001 | c0028 | t0001 | g0025 | EAS | CHS | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG00621 | hp1 | a0002 | c0003 | t0003 | g0045 | EAS | CHS | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG00621 | hp2 | a0002 | c0003 | t0001 | g0230 | EAS | CHS | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG00639 | hp1 | a0001 | c0001 | t0008 | g0172 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG00639 | hp2 | a0004 | c0019 | t0004 | g0251 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG00642 | hp1 | a0003 | c0007 | t0001 | g0079 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG00642 | hp2 | a0003 | c0008 | t0004 | g0039 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG00673 | hp1 | a0002 | c0003 | t0003 | g0044 | EAS | CHS | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG00733 | hp1 | a0001 | c0001 | t0013 | g0146 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG00733 | hp2 | a0003 | c0007 | t0001 | g0009 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG00735 | hp1 | a0002 | c0058 | t0009 | g0119 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG00735 | hp2 | a0003 | c0007 | t0001 | g0098 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG00738 | hp1 | a0002 | c0017 | t0007 | g0033 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG00738 | hp2 | a0002 | c0004 | t0001 | g0052 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG01069 | hp1 | a0002 | c0004 | t0001 | g0028 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG01069 | hp2 | a0003 | c0007 | t0001 | g0027 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG01070 | hp2 | a0003 | c0008 | t0004 | g0038 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG01071 | hp1 | a0003 | c0008 | t0004 | g0038 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG01071 | hp2 | a0002 | c0004 | t0001 | g0028 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG01081 | hp1 | a0001 | c0002 | t0002 | g0099 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG01099 | hp1 | a0003 | c0010 | t0001 | g0265 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG01099 | hp2 | a0002 | c0004 | t0001 | g0149 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG01109 | hp1 | a0003 | c0007 | t0001 | g0009 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG01109 | hp2 | a0002 | c0006 | t0001 | g0010 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG01167 | hp1 | a0002 | c0004 | t0001 | g0293 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0297 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG01168 | hp1 | a0003 | c0008 | t0004 | g0296 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG01169 | hp1 | a0002 | c0004 | t0001 | g0052 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG01175 | hp2 | a0003 | c0008 | t0004 | g0017 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG01192 | hp1 | a0003 | c0008 | t0004 | g0178 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG01243 | hp1 | a0007 | c0021 | t0002 | g0023 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG01255 | hp1 | a0002 | c0006 | t0001 | g0007 | AMR | CLM | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG01255 | hp2 | a0002 | c0009 | t0003 | g0232 | AMR | CLM | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG01257 | hp1 | a0003 | c0010 | t0001 | g0047 | AMR | CLM | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG01258 | hp2 | a0003 | c0010 | t0001 | g0047 | AMR | CLM | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG01346 | hp1 | a0002 | c0004 | t0001 | g0004 | AMR | CLM | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG01346 | hp2 | a0017 | c0071 | t0002 | g0095 | AMR | CLM | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | CLM | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG01433 | hp1 | a0001 | c0002 | t0002 | g0005 | AMR | CLM | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG01433 | hp2 | a0003 | c0008 | t0004 | g0295 | AMR | CLM | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG01496 | hp1 | a0002 | c0012 | t0001 | g0283 | AMR | CLM | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG01515 | hp1 | a0002 | c0004 | t0001 | g0134 | EUR | IBS | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG01515 | hp2 | a0003 | c0007 | t0001 | g0009 | EUR | IBS | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG01516 | hp1 | a0008 | c0024 | t0004 | g0139 | EUR | IBS | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG01516 | hp2 | a0009 | c0022 | t0001 | g0060 | EUR | IBS | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG01517 | hp1 | a0008 | c0024 | t0004 | g0177 | EUR | IBS | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG01517 | hp2 | a0003 | c0007 | t0001 | g0027 | EUR | IBS | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG01884 | hp1 | a0002 | c0004 | t0001 | g0289 | AFR | ACB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG01884 | hp2 | a0001 | c0002 | t0002 | g0070 | AFR | ACB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG01891 | hp1 | a0005 | c0016 | t0001 | g0309 | AFR | ACB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG01891 | hp2 | a0002 | c0012 | t0001 | g0280 | AFR | ACB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG01975 | hp2 | a0002 | c0009 | t0003 | g0018 | AMR | PEL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG01978 | hp1 | a0002 | c0009 | t0003 | g0018 | AMR | PEL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG01978 | hp2 | a0002 | c0004 | t0001 | g0147 | AMR | PEL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG01981 | hp2 | a0004 | c0040 | t0004 | g0252 | AMR | PEL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG01993 | hp1 | a0001 | c0002 | t0002 | g0100 | AMR | PEL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG01993 | hp2 | a0001 | c0002 | t0002 | g0086 | AMR | PEL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02015 | hp1 | a0004 | c0005 | t0001 | g0019 | EAS | KHV | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02015 | hp2 | a0002 | c0003 | t0003 | g0001 | EAS | KHV | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02027 | hp2 | a0002 | c0003 | t0003 | g0001 | EAS | KHV | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02055 | hp1 | a0002 | c0015 | t0006 | g0120 | AFR | ACB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02055 | hp2 | a0002 | c0006 | t0001 | g0291 | AFR | ACB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02056 | hp1 | a0002 | c0003 | t0003 | g0233 | EAS | KHV | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02074 | hp2 | a0002 | c0003 | t0003 | g0218 | EAS | KHV | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02080 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | KHV | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02083 | hp2 | a0001 | c0002 | t0002 | g0096 | EAS | KHV | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02129 | hp1 | a0002 | c0003 | t0003 | g0209 | EAS | KHV | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02129 | hp2 | a0001 | c0002 | t0002 | g0081 | EAS | KHV | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02132 | hp1 | a0002 | c0003 | t0003 | g0045 | EAS | KHV | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02132 | hp2 | a0002 | c0003 | t0003 | g0225 | EAS | KHV | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02145 | hp1 | a0002 | c0017 | t0007 | g0033 | AFR | ACB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02145 | hp2 | a0002 | c0015 | t0006 | g0145 | AFR | ACB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02148 | hp2 | a0004 | c0005 | t0001 | g0245 | AMR | PEL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02155 | hp1 | a0001 | c0002 | t0002 | g0084 | EAS | CDX | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02155 | hp2 | a0002 | c0003 | t0003 | g0234 | EAS | CDX | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02165 | hp1 | a0018 | c0067 | t0002 | g0085 | EAS | CDX | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02165 | hp2 | a0002 | c0003 | t0003 | g0001 | EAS | CDX | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02257 | hp1 | a0019 | c0066 | t0014 | g0272 | AFR | ACB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02257 | hp2 | a0006 | c0023 | t0001 | g0143 | AFR | ACB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02258 | hp1 | a0003 | c0018 | t0005 | g0048 | AFR | ACB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02258 | hp2 | a0003 | c0008 | t0004 | g0017 | AFR | ACB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02273 | hp1 | a0001 | c0002 | t0002 | g0093 | AMR | PEL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02280 | hp2 | a0005 | c0016 | t0001 | g0022 | AFR | ACB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02293 | hp2 | a0002 | c0009 | t0001 | g0229 | AMR | PEL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02451 | hp1 | a0002 | c0012 | t0001 | g0049 | AFR | ACB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | ACB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02523 | hp1 | a0002 | c0003 | t0003 | g0224 | EAS | KHV | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02523 | hp2 | a0020 | c0072 | t0002 | g0073 | EAS | KHV | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02602 | hp2 | a0003 | c0010 | t0001 | g0020 | SAS | PJL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02615 | hp1 | a0002 | c0017 | t0004 | g0277 | AFR | GWD | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02615 | hp2 | a0002 | c0006 | t0001 | g0007 | AFR | GWD | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02622 | hp1 | a0003 | c0007 | t0001 | g0009 | AFR | GWD | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02622 | hp2 | a0021 | c0043 | t0001 | g0259 | AFR | GWD | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02630 | hp1 | a0004 | c0076 | t0004 | g0305 | AFR | GWD | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02630 | hp2 | a0002 | c0004 | t0001 | g0274 | AFR | GWD | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02647 | hp2 | a0003 | c0014 | t0004 | g0050 | AFR | GWD | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02698 | hp1 | a0006 | c0047 | t0001 | g0263 | SAS | PJL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02698 | hp2 | a0003 | c0007 | t0001 | g0026 | SAS | PJL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02717 | hp1 | a0002 | c0004 | t0001 | g0004 | AFR | GWD | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02717 | hp2 | a0011 | c0026 | t0004 | g0051 | AFR | GWD | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02723 | hp1 | a0010 | c0036 | t0005 | g0269 | AFR | GWD | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02723 | hp2 | a0003 | c0014 | t0004 | g0294 | AFR | GWD | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02735 | hp1 | a0001 | c0001 | t0008 | g0036 | SAS | PJL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02735 | hp2 | a0002 | c0004 | t0001 | g0126 | SAS | PJL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02809 | hp1 | a0002 | c0012 | t0001 | g0284 | AFR | GWD | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02809 | hp2 | a0001 | c0054 | t0002 | g0285 | AFR | GWD | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02818 | hp1 | a0002 | c0015 | t0006 | g0117 | AFR | GWD | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02818 | hp2 | a0002 | c0057 | t0001 | g0282 | AFR | GWD | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02886 | hp1 | a0002 | c0079 | t0011 | g0307 | AFR | GWD | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02886 | hp2 | a0004 | c0005 | t0001 | g0246 | AFR | GWD | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02896 | hp1 | a0001 | c0011 | t0001 | g0015 | AFR | GWD | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02896 | hp2 | a0002 | c0006 | t0001 | g0007 | AFR | GWD | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02897 | hp1 | a0002 | c0004 | t0001 | g0278 | AFR | GWD | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02897 | hp2 | a0002 | c0006 | t0001 | g0007 | AFR | GWD | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02922 | hp1 | a0006 | c0023 | t0001 | g0137 | AFR | ESN | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02922 | hp2 | a0001 | c0011 | t0001 | g0015 | AFR | ESN | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02965 | hp1 | a0002 | c0015 | t0006 | g0118 | AFR | ESN | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02965 | hp2 | a0001 | c0011 | t0001 | g0015 | AFR | ESN | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02970 | hp1 | a0003 | c0014 | t0004 | g0286 | AFR | ESN | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02970 | hp2 | a0004 | c0005 | t0001 | g0244 | AFR | ESN | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02976 | hp1 | a0003 | c0014 | t0004 | g0290 | AFR | ESN | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02976 | hp2 | a0003 | c0014 | t0004 | g0050 | AFR | ESN | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG03017 | hp2 | a0003 | c0010 | t0001 | g0020 | SAS | PJL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG03041 | hp1 | a0006 | c0046 | t0004 | g0264 | AFR | GWD | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG03041 | hp2 | a0002 | c0012 | t0001 | g0049 | AFR | GWD | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG03139 | hp1 | a0004 | c0019 | t0004 | g0247 | AFR | ESN | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG03139 | hp2 | a0003 | c0018 | t0005 | g0048 | AFR | ESN | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG03195 | hp1 | a0002 | c0015 | t0006 | g0116 | AFR | ESN | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG03195 | hp2 | a0002 | c0004 | t0001 | g0004 | AFR | ESN | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG03209 | hp1 | a0002 | c0006 | t0001 | g0010 | AFR | MSL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG03209 | hp2 | a0005 | c0016 | t0001 | g0310 | AFR | MSL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG03225 | hp1 | a0002 | c0006 | t0001 | g0010 | AFR | MSL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG03225 | hp2 | a0004 | c0005 | t0001 | g0301 | AFR | MSL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG03239 | hp1 | a0003 | c0008 | t0004 | g0039 | SAS | PJL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG03239 | hp2 | a0009 | c0022 | t0001 | g0059 | SAS | PJL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG03453 | hp1 | a0002 | c0004 | t0001 | g0004 | AFR | MSL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG03453 | hp2 | a0012 | c0029 | t0010 | g0054 | AFR | MSL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG03486 | hp1 | a0001 | c0011 | t0001 | g0015 | AFR | MSL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG03486 | hp2 | a0003 | c0059 | t0004 | g0281 | AFR | MSL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG03490 | hp1 | a0002 | c0003 | t0003 | g0013 | SAS | PJL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG03491 | hp1 | a0001 | c0002 | t0002 | g0107 | SAS | PJL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG03492 | hp1 | a0002 | c0003 | t0003 | g0013 | SAS | PJL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG03516 | hp1 | a0004 | c0019 | t0004 | g0240 | AFR | ESN | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG03516 | hp2 | a0002 | c0004 | t0001 | g0004 | AFR | ESN | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG03540 | hp1 | a0005 | c0016 | t0001 | g0022 | AFR | GWD | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG03540 | hp2 | a0001 | c0078 | t0011 | g0308 | AFR | GWD | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG03579 | hp1 | a0003 | c0018 | t0005 | g0262 | AFR | MSL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG03579 | hp2 | a0007 | c0021 | t0004 | g0068 | AFR | MSL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG03654 | hp1 | a0002 | c0003 | t0003 | g0208 | SAS | PJL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG03654 | hp2 | a0023 | c0049 | t0001 | g0130 | SAS | PJL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG03669 | hp1 | a0001 | c0002 | t0002 | g0111 | SAS | PJL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG03688 | hp1 | a0004 | c0005 | t0001 | g0239 | SAS | STU | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG03688 | hp2 | a0001 | c0002 | t0002 | g0106 | SAS | STU | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG03704 | hp1 | a0003 | c0010 | t0001 | g0020 | SAS | PJL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG03710 | hp2 | a0002 | c0003 | t0003 | g0303 | SAS | PJL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | BEB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | BEB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG03834 | hp1 | a0001 | c0002 | t0002 | g0008 | SAS | BEB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG03834 | hp2 | a0002 | c0004 | t0001 | g0154 | SAS | BEB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | BEB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG03927 | hp2 | a0004 | c0005 | t0001 | g0256 | SAS | BEB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG03942 | hp1 | a0002 | c0004 | t0001 | g0125 | SAS | BEB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG03942 | hp2 | a0001 | c0002 | t0002 | g0108 | SAS | BEB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG04115 | hp1 | a0001 | c0002 | t0002 | g0088 | SAS | STU | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG04115 | hp2 | a0024 | c0038 | t0001 | g0242 | SAS | STU | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG04184 | hp1 | a0001 | c0020 | t0001 | g0165 | SAS | BEB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG04184 | hp2 | a0025 | c0051 | t0001 | g0181 | SAS | BEB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG04199 | hp1 | a0001 | c0020 | t0001 | g0131 | SAS | STU | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG04199 | hp2 | a0003 | c0010 | t0001 | g0267 | SAS | STU | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | STU | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG04204 | hp2 | a0004 | c0005 | t0001 | g0241 | SAS | STU | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG04228 | hp1 | a0002 | c0004 | t0001 | g0138 | SAS | STU | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG04228 | hp2 | a0004 | c0005 | t0001 | g0248 | SAS | STU | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18522 | hp1 | a0026 | c0063 | t0001 | g0121 | AFR | YRI | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18522 | hp2 | a0002 | c0006 | t0001 | g0271 | AFR | YRI | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18747 | hp1 | a0002 | c0003 | t0003 | g0213 | EAS | CHB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | CHB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18906 | hp1 | a0001 | c0050 | t0001 | g0148 | AFR | YRI | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | YRI | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18939 | hp1 | a0002 | c0003 | t0003 | g0226 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18939 | hp2 | a0001 | c0002 | t0002 | g0067 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18940 | hp2 | a0001 | c0002 | t0012 | g0094 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18941 | hp1 | a0002 | c0003 | t0003 | g0042 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18942 | hp1 | a0027 | c0042 | t0001 | g0156 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18942 | hp2 | a0001 | c0013 | t0003 | g0014 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18943 | hp1 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18943 | hp2 | a0004 | c0005 | t0001 | g0053 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18944 | hp1 | a0002 | c0003 | t0003 | g0236 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18944 | hp2 | a0001 | c0002 | t0002 | g0109 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18946 | hp1 | a0004 | c0005 | t0001 | g0053 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18946 | hp2 | a0002 | c0003 | t0003 | g0001 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18947 | hp2 | a0002 | c0009 | t0003 | g0219 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18950 | hp1 | a0004 | c0005 | t0001 | g0019 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18951 | hp1 | a0001 | c0002 | t0002 | g0202 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18951 | hp2 | a0013 | c0025 | t0001 | g0257 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18952 | hp1 | a0001 | c0002 | t0002 | g0112 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18952 | hp2 | a0004 | c0005 | t0001 | g0193 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18954 | hp2 | a0002 | c0003 | t0003 | g0237 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18957 | hp1 | a0001 | c0002 | t0002 | g0024 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18959 | hp1 | a0028 | c0044 | t0003 | g0212 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18959 | hp2 | a0013 | c0025 | t0001 | g0153 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18960 | hp2 | a0002 | c0003 | t0003 | g0046 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18963 | hp2 | a0001 | c0002 | t0002 | g0205 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18965 | hp1 | a0014 | c0061 | t0003 | g0221 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18965 | hp2 | a0014 | c0062 | t0003 | g0220 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18966 | hp1 | a0001 | c0002 | t0002 | g0024 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18966 | hp2 | a0002 | c0060 | t0003 | g0167 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18967 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18968 | hp2 | a0002 | c0003 | t0003 | g0044 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18969 | hp2 | a0002 | c0009 | t0001 | g0228 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18970 | hp1 | a0001 | c0002 | t0002 | g0204 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18970 | hp2 | a0001 | c0002 | t0002 | g0082 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18971 | hp2 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18972 | hp1 | a0001 | c0002 | t0002 | g0061 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18972 | hp2 | a0029 | c0052 | t0001 | g0136 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18973 | hp1 | a0004 | c0005 | t0001 | g0194 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18973 | hp2 | a0002 | c0003 | t0003 | g0046 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18974 | hp1 | a0030 | c0039 | t0001 | g0255 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18974 | hp2 | a0015 | c0027 | t0001 | g0201 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18975 | hp1 | a0001 | c0002 | t0002 | g0105 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18975 | hp2 | a0002 | c0003 | t0003 | g0001 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18977 | hp1 | a0001 | c0011 | t0001 | g0214 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18977 | hp2 | a0031 | c0037 | t0001 | g0249 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18979 | hp1 | a0001 | c0028 | t0001 | g0025 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18980 | hp1 | a0002 | c0004 | t0001 | g0188 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18980 | hp2 | a0002 | c0009 | t0001 | g0217 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18981 | hp1 | a0032 | c0053 | t0001 | g0140 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18981 | hp2 | a0002 | c0003 | t0003 | g0013 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18983 | hp1 | a0002 | c0003 | t0003 | g0013 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18983 | hp2 | a0001 | c0002 | t0002 | g0097 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18984 | hp2 | a0001 | c0013 | t0003 | g0014 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18986 | hp1 | a0002 | c0003 | t0003 | g0227 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18988 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18988 | hp2 | a0033 | c0041 | t0001 | g0238 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18990 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18992 | hp2 | a0015 | c0027 | t0001 | g0195 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18993 | hp1 | a0034 | c0032 | t0001 | g0057 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18993 | hp2 | a0002 | c0003 | t0003 | g0043 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18994 | hp1 | a0001 | c0013 | t0003 | g0014 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18994 | hp2 | a0035 | c0081 | t0001 | g0312 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18995 | hp1 | a0002 | c0003 | t0003 | g0304 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18997 | hp2 | a0001 | c0002 | t0002 | g0066 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18999 | hp1 | a0004 | c0005 | t0001 | g0253 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18999 | hp2 | a0002 | c0003 | t0003 | g0222 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA19000 | hp1 | a0002 | c0003 | t0003 | g0206 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA19000 | hp2 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA19002 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA19003 | hp2 | a0002 | c0009 | t0003 | g0215 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA19004 | hp1 | a0002 | c0003 | t0003 | g0216 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA19004 | hp2 | a0001 | c0002 | t0002 | g0071 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA19005 | hp1 | a0002 | c0003 | t0003 | g0001 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA19005 | hp2 | a0001 | c0002 | t0002 | g0065 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA19007 | hp1 | a0004 | c0005 | t0001 | g0250 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA19007 | hp2 | a0001 | c0002 | t0002 | g0083 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA19009 | hp2 | a0002 | c0003 | t0003 | g0235 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA19011 | hp1 | a0001 | c0002 | t0002 | g0110 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA19011 | hp2 | a0002 | c0003 | t0003 | g0043 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA19012 | hp1 | a0004 | c0005 | t0001 | g0300 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA19012 | hp2 | a0001 | c0002 | t0002 | g0104 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA19030 | hp1 | a0002 | c0006 | t0001 | g0122 | AFR | LWK | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | LWK | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA19043 | hp1 | a0036 | c0068 | t0002 | g0069 | AFR | LWK | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA19043 | hp2 | a0001 | c0064 | t0001 | g0261 | AFR | LWK | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA19055 | hp2 | a0037 | c0069 | t0002 | g0075 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA19056 | hp1 | a0038 | c0034 | t0003 | g0210 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA19056 | hp2 | a0001 | c0002 | t0002 | g0090 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA19057 | hp1 | a0039 | c0055 | t0001 | g0174 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA19057 | hp2 | a0002 | c0003 | t0003 | g0302 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA19058 | hp1 | a0040 | c0080 | t0003 | g0311 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA19058 | hp2 | a0001 | c0002 | t0002 | g0077 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA19060 | hp1 | a0001 | c0073 | t0001 | g0092 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA19060 | hp2 | a0002 | c0003 | t0003 | g0207 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA19062 | hp1 | a0001 | c0056 | t0002 | g0133 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA19062 | hp2 | a0001 | c0013 | t0003 | g0124 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA19063 | hp1 | a0001 | c0002 | t0002 | g0087 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA19063 | hp2 | a0002 | c0048 | t0003 | g0223 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA19065 | hp2 | a0041 | c0074 | t0002 | g0089 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA19066 | hp2 | a0004 | c0005 | t0001 | g0019 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA19068 | hp1 | a0042 | c0030 | t0003 | g0055 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA19070 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA19074 | hp1 | a0001 | c0045 | t0002 | g0231 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA19077 | hp1 | a0002 | c0009 | t0003 | g0018 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA19079 | hp1 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA19079 | hp2 | a0002 | c0003 | t0003 | g0001 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA19083 | hp2 | a0001 | c0002 | t0002 | g0072 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA19084 | hp1 | a0001 | c0002 | t0002 | g0074 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA19084 | hp2 | a0043 | c0031 | t0003 | g0056 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA19085 | hp2 | a0002 | c0003 | t0003 | g0042 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA19087 | hp1 | a0001 | c0013 | t0003 | g0014 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA19087 | hp2 | a0044 | c0033 | t0002 | g0058 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA19090 | hp1 | a0004 | c0005 | t0001 | g0243 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA19090 | hp2 | a0004 | c0005 | t0001 | g0299 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA19240 | hp1 | a0002 | c0012 | t0001 | g0292 | AFR | YRI | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA19240 | hp2 | a0007 | c0021 | t0002 | g0023 | AFR | YRI | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA20129 | hp1 | a0003 | c0018 | t0005 | g0260 | AFR | ASW | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | ASW | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0161 | EUR | TSI | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0021 | EUR | TSI | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA20805 | hp1 | a0003 | c0007 | t0001 | g0101 | EUR | TSI | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA20805 | hp2 | a0004 | c0005 | t0001 | g0197 | EUR | TSI | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA20905 | hp1 | a0001 | c0020 | t0001 | g0166 | SAS | GIH | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA20905 | hp2 | a0001 | c0002 | t0002 | g0103 | SAS | GIH | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG01123 | hp2 | a0003 | c0008 | t0004 | g0017 | AMR | CLM | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02109 | hp1 | a0005 | c0016 | t0001 | g0022 | AFR | ACB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02109 | hp2 | a0002 | c0004 | t0001 | g0279 | AFR | ACB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02486 | hp1 | a0002 | c0004 | t0001 | g0004 | AFR | ACB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02486 | hp2 | a0010 | c0035 | t0005 | g0270 | AFR | ACB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02559 | hp1 | a0011 | c0026 | t0004 | g0051 | AFR | ACB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG02559 | hp2 | a0012 | c0029 | t0010 | g0054 | AFR | ACB | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG03471 | hp1 | a0002 | c0006 | t0001 | g0010 | AFR | MSL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG03471 | hp2 | a0022 | c0065 | t0009 | g0288 | AFR | MSL | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG06807 | hp1 | a0002 | c0006 | t0001 | g0007 | AFR | USA | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
HG06807 | hp2 | a0002 | c0006 | t0001 | g0287 | AFR | USA | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA20300 | hp1 | a0001 | c0001 | t0008 | g0036 | AFR | USA | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA20300 | hp2 | a0003 | c0007 | t0001 | g0268 | AFR | USA | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | LWK | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
NA21309 | hp2 | a0001 | c0002 | t0002 | g0080 | AFR | LWK | PLXND1_chr3_129550214_129611676 | PLXND1 | chr3 | 129550214 | 129611676 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:129556419 | C | T | 1 | a0020 | 1 | HG02523.hp2 | missense_variant | MODERATE | c.5671G>A | p.Ala1891Thr | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 36/36 | 5708/6913 | 5671/5778 | 1891/1925 | chr3 | 129556419 | |||
chr3:129557159 | C | T | 1 | a0017 | 1 | HG01346.hp2 | missense_variant | MODERATE | c.5510G>A | p.Arg1837His | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 34/36 | 5547/6913 | 5510/5778 | 1837/1925 | chr3 | 129557159 | |||
chr3:129559775 | C | CA | 1 | a0037 | 1 | NA19055.hp2 | frameshift_variant | HIGH | c.5141dupT | p.Leu1714fs | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 32/36 | 5178/6913 | 5141/5778 | 1714/1925 | chr3 | 129559775 | |||
chr3:129562889 | T | TG | 1 | a0035 | 1 | NA18994.hp2 | frameshift_variant | HIGH | c.4722dupC | p.Met1575fs | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 27/36 | 4759/6913 | 4722/5778 | 1574/1925 | chr3 | 129562889 | |||
chr3:129562928 | A | AG | 1 | a0035 | 1 | NA18994.hp2 | frameshift_variant | HIGH | c.4683dupC | p.Phe1562fs | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 27/36 | 4720/6913 | 4683/5778 | 1561/1925 | chr3 | 129562928 | |||
chr3:129563095 | CG | C | 1 | a0032 | 1 | NA18981.hp1 | frameshift_variant&splice_region_variant | HIGH | c.4666delC | p.Arg1556fs | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 26/36 | 4703/6913 | 4666/5778 | 1556/1925 | chr3 | 129563095 | |||
chr3:129563116 | T | TC | 1 | a0031 | 1 | NA18977.hp2 | frameshift_variant | HIGH | c.4645dupG | p.Glu1549fs | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 26/36 | 4682/6913 | 4645/5778 | 1549/1925 | chr3 | 129563116 | |||
chr3:129563137 | C | T | 43 | a0001 a0002 a0003 others(40): Show |
415 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(412): Show |
missense_variant | MODERATE | c.4625G>A | p.Ser1542Asn | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 26/36 | 4662/6913 | 4625/5778 | 1542/1925 | chr3 | 129563137 | |||
chr3:129563227 | TC | T | 1 | a0032 | 1 | NA18981.hp1 | frameshift_variant | HIGH | c.4534delG | p.Glu1512fs | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 26/36 | 4571/6913 | 4534/5778 | 1512/1925 | chr3 | 129563227 | |||
chr3:129565397 | A | AG | 1 | a0029 | 1 | NA18972.hp2 | frameshift_variant | HIGH | c.4463dupC | p.Val1489fs | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 25/36 | 4500/6913 | 4463/5778 | 1488/1925 | chr3 | 129565397 | |||
chr3:129565975 | A | C | 7 | a0003 a0006 a0007 others(4): Show |
56 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(53): Show |
missense_variant | MODERATE | c.4234T>G | p.Leu1412Val | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 24/36 | 4271/6913 | 4234/5778 | 1412/1925 | chr3 | 129565975 | |||
chr3:129565993 | T | G | 1 | a0033 | 1 | NA18988.hp2 | missense_variant | MODERATE | c.4216A>C | p.Met1406Leu | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 24/36 | 4253/6913 | 4216/5778 | 1406/1925 | chr3 | 129565993 | |||
chr3:129566552 | GT | G | 1 | a0044 | 1 | NA19087.hp2 | frameshift_variant | HIGH | c.4165delA | p.Thr1389fs | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 23/36 | 4202/6913 | 4165/5778 | 1389/1925 | chr3 | 129566552 | |||
chr3:129566580 | A | AG | 1 | a0044 | 1 | NA19087.hp2 | frameshift_variant | HIGH | c.4137dupC | p.Ser1380fs | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 23/36 | 4174/6913 | 4137/5778 | 1379/1925 | chr3 | 129566580 | |||
chr3:129566585 | AG | A | 1 | a0044 | 1 | NA19087.hp2 | frameshift_variant | HIGH | c.4132delC | p.Leu1378fs | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 23/36 | 4169/6913 | 4132/5778 | 1378/1925 | chr3 | 129566585 | |||
chr3:129567745 | A | C | 1 | a0044 | 1 | NA19087.hp2 | missense_variant | MODERATE | c.3926T>G | p.Leu1309Arg | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 21/36 | 3963/6913 | 3926/5778 | 1309/1925 | chr3 | 129567745 | |||
chr3:129567758 | G | GC | 1 | a0044 | 1 | NA19087.hp2 | frameshift_variant | HIGH | c.3912dupG | p.Gln1305fs | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 21/36 | 3949/6913 | 3912/5778 | 1304/1925 | chr3 | 129567758 | |||
chr3:129569907 | G | GC | 1 | a0039 | 1 | NA19057.hp1 | frameshift_variant | HIGH | c.3800dupG | p.Ser1268fs | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 20/36 | 3837/6913 | 3800/5778 | 1267/1925 | chr3 | 129569907 | |||
chr3:129569927 | C | T | 1 | a0025 | 1 | HG04184.hp2 | missense_variant | MODERATE | c.3781G>A | p.Ala1261Thr | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 20/36 | 3818/6913 | 3781/5778 | 1261/1925 | chr3 | 129569927 | |||
chr3:129570817 | A | AG | 1 | a0037 | 1 | NA19055.hp2 | frameshift_variant | HIGH | c.3718dupC | p.Leu1240fs | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 19/36 | 3755/6913 | 3718/5778 | 1240/1925 | chr3 | 129570817 | |||
chr3:129571135 | G | A | 1 | a0008 | 2 | HG01516.hp1 HG01517.hp1 |
missense_variant | MODERATE | c.3505C>T | p.Arg1169Cys | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 18/36 | 3542/6913 | 3505/5778 | 1169/1925 | chr3 | 129571135 | |||
chr3:129571240 | A | AT | 1 | a0030 | 1 | NA18974.hp1 | frameshift_variant | HIGH | c.3399dupA | p.Ser1134fs | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 18/36 | 3436/6913 | 3399/5778 | 1133/1925 | chr3 | 129571240 | |||
chr3:129571254 | G | GC | 1 | a0030 | 1 | NA18974.hp1 | frameshift_variant | HIGH | c.3385dupG | p.Ala1129fs | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 18/36 | 3422/6913 | 3385/5778 | 1129/1925 | chr3 | 129571254 | |||
chr3:129571725 | A | G | 1 | a0036 | 1 | NA19043.hp1 | missense_variant | MODERATE | c.3197T>C | p.Met1066Thr | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 16/36 | 3234/6913 | 3197/5778 | 1066/1925 | chr3 | 129571725 | |||
chr3:129571757 | G | GC | 1 | a0030 | 1 | NA18974.hp1 | frameshift_variant | HIGH | c.3164dupG | p.Cys1056fs | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 16/36 | 3201/6913 | 3164/5778 | 1055/1925 | chr3 | 129571757 | |||
chr3:129571843 | G | A | 1 | a0041 | 1 | NA19065.hp2 | missense_variant&splice_region_variant | MODERATE | c.3079C>T | p.Arg1027Cys | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 16/36 | 3116/6913 | 3079/5778 | 1027/1925 | chr3 | 129571843 | |||
chr3:129572713 | GC | G | 1 | a0030 | 1 | NA18974.hp1 | frameshift_variant | HIGH | c.2972delG | p.Gly991fs | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 15/36 | 3009/6913 | 2972/5778 | 991/1925 | chr3 | 129572713 | |||
chr3:129572858 | TC | T | 1 | a0030 | 1 | NA18974.hp1 | frameshift_variant | HIGH | c.2920delG | p.Asp974fs | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 14/36 | 2957/6913 | 2920/5778 | 974/1925 | chr3 | 129572858 | |||
chr3:129572861 | C | T | 1 | a0023 | 1 | HG03654.hp2 | missense_variant | MODERATE | c.2918G>A | p.Arg973Gln | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 14/36 | 2955/6913 | 2918/5778 | 973/1925 | chr3 | 129572861 | |||
chr3:129573643 | CA | C | 1 | a0030 | 1 | NA18974.hp1 | frameshift_variant | HIGH | c.2787delT | p.Ile929fs | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 13/36 | 2824/6913 | 2787/5778 | 929/1925 | chr3 | 129573643 | |||
chr3:129574340 | T | C | 42 | a0001 a0002 a0003 others(39): Show |
413 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(410): Show |
missense_variant | MODERATE | c.2681A>G | p.His894Arg | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 12/36 | 2718/6913 | 2681/5778 | 894/1925 | chr3 | 129574340 | |||
chr3:129574369 | C | T | 1 | a0018 | 1 | HG02165.hp1 | missense_variant | MODERATE | c.2652G>A | p.Met884Ile | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 12/36 | 2689/6913 | 2652/5778 | 884/1925 | chr3 | 129574369 | |||
chr3:129574413 | T | C | 22 | a0002 a0003 a0004 others(19): Show |
208 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(205): Show |
missense_variant | MODERATE | c.2608A>G | p.Met870Val | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 12/36 | 2645/6913 | 2608/5778 | 870/1925 | chr3 | 129574413 | |||
chr3:129575498 | C | T | 1 | a0028 | 1 | NA18959.hp1 | missense_variant | MODERATE | c.2501G>A | p.Arg834Gln | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 11/36 | 2538/6913 | 2501/5778 | 834/1925 | chr3 | 129575498 | |||
chr3:129575549 | C | T | 1 | a0021 | 1 | HG02622.hp2 | missense_variant | MODERATE | c.2450G>A | p.Arg817Gln | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 11/36 | 2487/6913 | 2450/5778 | 817/1925 | chr3 | 129575549 | |||
chr3:129578412 | TC | T | 1 | a0031 | 1 | NA18977.hp2 | frameshift_variant | HIGH | c.2262delG | p.Thr755fs | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 9/36 | 2299/6913 | 2262/5778 | 754/1925 | chr3 | 129578412 | |||
chr3:129584393 | G | C | 1 | a0014 | 2 | NA18965.hp1 NA18965.hp2 |
missense_variant | MODERATE | c.2021C>G | p.Pro674Arg | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 6/36 | 2058/6913 | 2021/5778 | 674/1925 | chr3 | 129584393 | |||
chr3:129584543 | G | A | 1 | a0026 | 1 | NA18522.hp1 | missense_variant | MODERATE | c.1871C>T | p.Ser624Leu | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 6/36 | 1908/6913 | 1871/5778 | 624/1925 | chr3 | 129584543 | |||
chr3:129585954 | G | A | 7 | a0004 a0015 a0024 others(4): Show |
34 | HG00408.hp2 HG00639.hp2 HG01981.hp2 others(31): Show |
missense_variant&splice_region_variant | MODERATE | c.1849C>T | p.Pro617Ser | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 5/36 | 1886/6913 | 1849/5778 | 617/1925 | chr3 | 129585954 | |||
chr3:129586032 | TC | T | 1 | a0027 | 1 | NA18942.hp1 | frameshift_variant | HIGH | c.1770delG | p.Trp590fs | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 5/36 | 1807/6913 | 1770/5778 | 590/1925 | chr3 | 129586032 | |||
chr3:129586616 | C | A | 1 | a0013 | 2 | NA18951.hp2 NA18959.hp2 |
missense_variant | MODERATE | c.1592G>T | p.Gly531Val | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 3/36 | 1629/6913 | 1592/5778 | 531/1925 | chr3 | 129586616 | |||
chr3:129586617 | C | T | 8 | a0004 a0005 a0015 others(5): Show |
39 | HG00408.hp2 HG00639.hp2 HG01891.hp1 others(36): Show |
missense_variant | MODERATE | c.1591G>A | p.Gly531Ser | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 3/36 | 1628/6913 | 1591/5778 | 531/1925 | chr3 | 129586617 | |||
chr3:129586664 | T | C | 2 | a0011 a0022 |
3 | HG02559.hp1 HG02717.hp2 HG03471.hp2 |
missense_variant | MODERATE | c.1544A>G | p.Tyr515Cys | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 3/36 | 1581/6913 | 1544/5778 | 515/1925 | chr3 | 129586664 | |||
chr3:129586679 | A | AC | 1 | a0038 | 1 | NA19056.hp1 | frameshift_variant | HIGH | c.1528dupG | p.Val510fs | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 3/36 | 1565/6913 | 1528/5778 | 510/1925 | chr3 | 129586679 | |||
chr3:129586695 | C | G | 2 | a0010 a0019 |
3 | HG02257.hp1 HG02486.hp2 HG02723.hp1 |
missense_variant | MODERATE | c.1513G>C | p.Val505Leu | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 3/36 | 1550/6913 | 1513/5778 | 505/1925 | chr3 | 129586695 | |||
chr3:129586697 | T | C | 1 | a0015 | 2 | NA18974.hp2 NA18992.hp2 |
missense_variant | MODERATE | c.1511A>G | p.Gln504Arg | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 3/36 | 1548/6913 | 1511/5778 | 504/1925 | chr3 | 129586697 | |||
chr3:129586707 | C | T | 1 | a0007 | 3 | HG01243.hp1 HG03579.hp2 NA19240.hp2 |
missense_variant | MODERATE | c.1501G>A | p.Glu501Lys | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 3/36 | 1538/6913 | 1501/5778 | 501/1925 | chr3 | 129586707 | |||
chr3:129589362 | TC | T | 1 | a0038 | 1 | NA19056.hp1 | frameshift_variant | HIGH | c.1476delG | p.Arg493fs | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/36 | 1513/6913 | 1476/5778 | 492/1925 | chr3 | 129589362 | |||
chr3:129605495 | C | CG | 1 | a0042 | 1 | NA19068.hp1 | frameshift_variant | HIGH | c.1144dupC | p.Arg382fs | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/36 | 1181/6913 | 1144/5778 | 382/1925 | chr3 | 129605495 | |||
chr3:129605502 | C | CG | 1 | a0042 | 1 | NA19068.hp1 | frameshift_variant | HIGH | c.1137dupC | p.Ala380fs | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/36 | 1174/6913 | 1137/5778 | 379/1925 | chr3 | 129605502 | |||
chr3:129605765 | C | G | 1 | a0009 | 2 | HG01516.hp2 HG03239.hp2 |
missense_variant | MODERATE | c.875G>C | p.Gly292Ala | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/36 | 912/6913 | 875/5778 | 292/1925 | chr3 | 129605765 | |||
chr3:129605787 | G | A | 1 | a0040 | 1 | NA19058.hp1 | missense_variant | MODERATE | c.853C>T | p.His285Tyr | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/36 | 890/6913 | 853/5778 | 285/1925 | chr3 | 129605787 | |||
chr3:129605912 | AG | A | 1 | a0042 | 1 | NA19068.hp1 | frameshift_variant | HIGH | c.727delC | p.Leu243fs | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/36 | 764/6913 | 727/5778 | 243/1925 | chr3 | 129605912 | |||
chr3:129606289 | CG | C | 1 | a0034 | 1 | NA18993.hp1 | frameshift_variant | HIGH | c.350delC | p.Pro117fs | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/36 | 387/6913 | 350/5778 | 117/1925 | chr3 | 129606289 | |||
chr3:129606476 | G | GGA | 1 | a0034 | 1 | NA18993.hp1 | frameshift_variant | HIGH | c.163_164insTC | p.Ser55fs | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/36 | 200/6913 | 163/5778 | 55/1925 | chr3 | 129606476 | |||
chr3:129606477 | A | G | 1 | a0034 | 1 | NA18993.hp1 | missense_variant | MODERATE | c.163T>C | p.Ser55Pro | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/36 | 200/6913 | 163/5778 | 55/1925 | chr3 | 129606477 | |||
chr3:129606577 | C | CG | 1 | a0043 | 1 | NA19084.hp2 | frameshift_variant | HIGH | c.62dupC | p.Pro22fs | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/36 | 99/6913 | 62/5778 | 21/1925 | chr3 | 129606577 | |||
chr3:129606577 | CG | C | 1 | a0035 | 1 | NA18994.hp2 | frameshift_variant | HIGH | c.62delC | p.Pro21fs | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/36 | 99/6913 | 62/5778 | 21/1925 | chr3 | 129606577 | |||
chr3:129606599 | C | CG | 1 | a0042 | 1 | NA19068.hp1 | frameshift_variant | HIGH | c.40dupC | p.Arg14fs | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/36 | 77/6913 | 40/5778 | 14/1925 | chr3 | 129606599 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:129556363 | C | T | 26 | a0001c0002 a0001c0045 a0001c0054 others(23): Show |
105 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(102): Show |
synonymous_variant | LOW | c.5727G>A | p.Gln1909Gln | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 36/36 | 5764/6913 | 5727/5778 | 1909/1925 | chr3 | 129556363 | |||
chr3:129556632 | C | T | 1 | a0003c0059 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.5646G>A | p.Lys1882Lys | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 35/36 | 5683/6913 | 5646/5778 | 1882/1925 | chr3 | 129556632 | |||
chr3:129559661 | T | G | 1 | a0042c0030 | 1 | NA19068.hp1 | synonymous_variant | LOW | c.5256A>C | p.Gly1752Gly | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 32/36 | 5293/6913 | 5256/5778 | 1752/1925 | chr3 | 129559661 | |||
chr3:129562875 | C | T | 13 | a0001c0002 a0001c0045 a0001c0054 others(10): Show |
64 | HG00423.hp1 HG00597.hp2 HG01081.hp1 others(61): Show |
synonymous_variant | LOW | c.4737G>A | p.Thr1579Thr | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 27/36 | 4774/6913 | 4737/5778 | 1579/1925 | chr3 | 129562875 | |||
chr3:129567516 | G | A | 1 | a0002c0048 | 1 | NA19063.hp2 | synonymous_variant | LOW | c.4062C>T | p.Phe1354Phe | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 22/36 | 4099/6913 | 4062/5778 | 1354/1925 | chr3 | 129567516 | |||
chr3:129567570 | G | C | 55 | a0001c0002 a0001c0013 a0001c0028 others(52): Show |
252 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(249): Show |
synonymous_variant | LOW | c.4008C>G | p.Leu1336Leu | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 22/36 | 4045/6913 | 4008/5778 | 1336/1925 | chr3 | 129567570 | |||
chr3:129567792 | G | A | 25 | a0001c0013 a0001c0078 a0002c0003 others(22): Show |
113 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(110): Show |
synonymous_variant | LOW | c.3879C>T | p.Phe1293Phe | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 21/36 | 3916/6913 | 3879/5778 | 1293/1925 | chr3 | 129567792 | |||
chr3:129570909 | C | T | 14 | a0002c0006 a0002c0012 a0002c0015 others(11): Show |
63 | HG00408.hp2 HG00639.hp2 HG01109.hp2 others(60): Show |
synonymous_variant | LOW | c.3627G>A | p.Gln1209Gln | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 19/36 | 3664/6913 | 3627/5778 | 1209/1925 | chr3 | 129570909 | |||
chr3:129571244 | G | A | 13 | a0001c0002 a0001c0028 a0001c0045 others(10): Show |
65 | HG00423.hp1 HG00438.hp1 HG00597.hp2 others(62): Show |
synonymous_variant | LOW | c.3396C>T | p.Asn1132Asn | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 18/36 | 3433/6913 | 3396/5778 | 1132/1925 | chr3 | 129571244 | |||
chr3:129571259 | G | A | 1 | a0010c0036 | 1 | HG02723.hp1 | synonymous_variant | LOW | c.3381C>T | p.Pro1127Pro | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 18/36 | 3418/6913 | 3381/5778 | 1127/1925 | chr3 | 129571259 | |||
chr3:129571706 | C | T | 1 | a0001c0050 | 1 | NA18906.hp1 | synonymous_variant | LOW | c.3216G>A | p.Thr1072Thr | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 16/36 | 3253/6913 | 3216/5778 | 1072/1925 | chr3 | 129571706 | |||
chr3:129572656 | G | A | 14 | a0001c0078 a0002c0006 a0002c0012 others(11): Show |
59 | HG00408.hp2 HG00639.hp2 HG01109.hp2 others(56): Show |
synonymous_variant | LOW | c.3030C>T | p.Ser1010Ser | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 15/36 | 3067/6913 | 3030/5778 | 1010/1925 | chr3 | 129572656 | |||
chr3:129572908 | T | C | 43 | a0001c0013 a0001c0056 a0001c0078 others(40): Show |
187 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(184): Show |
synonymous_variant | LOW | c.2871A>G | p.Pro957Pro | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 14/36 | 2908/6913 | 2871/5778 | 957/1925 | chr3 | 129572908 | |||
chr3:129573602 | C | T | 3 | a0010c0035 a0010c0036 a0019c0066 |
3 | HG02257.hp1 HG02486.hp2 HG02723.hp1 |
synonymous_variant | LOW | c.2829G>A | p.Val943Val | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 13/36 | 2866/6913 | 2829/5778 | 943/1925 | chr3 | 129573602 | |||
chr3:129573719 | G | A | 1 | a0002c0012 | 6 | HG01496.hp1 HG01891.hp2 HG02451.hp1 others(3): Show |
synonymous_variant | LOW | c.2712C>T | p.Asp904Asp | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 13/36 | 2749/6913 | 2712/5778 | 904/1925 | chr3 | 129573719 | |||
chr3:129574348 | G | A | 1 | a0001c0020 | 3 | HG04184.hp1 HG04199.hp1 NA20905.hp1 |
synonymous_variant | LOW | c.2673C>T | p.Pro891Pro | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 12/36 | 2710/6913 | 2673/5778 | 891/1925 | chr3 | 129574348 | |||
chr3:129578380 | C | G | 25 | a0001c0011 a0001c0013 a0001c0045 others(22): Show |
109 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(106): Show |
synonymous_variant | LOW | c.2295G>C | p.Thr765Thr | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 9/36 | 2332/6913 | 2295/5778 | 765/1925 | chr3 | 129578380 | |||
chr3:129583612 | G | A | 10 | a0004c0005 a0004c0019 a0004c0040 others(7): Show |
34 | HG00408.hp2 HG00639.hp2 HG01981.hp2 others(31): Show |
synonymous_variant | LOW | c.2196C>T | p.Ser732Ser | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/36 | 2233/6913 | 2196/5778 | 732/1925 | chr3 | 129583612 | |||
chr3:129584229 | G | A | 10 | a0004c0005 a0004c0019 a0004c0040 others(7): Show |
34 | HG00408.hp2 HG00639.hp2 HG01981.hp2 others(31): Show |
synonymous_variant | LOW | c.2034C>T | p.His678His | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 7/36 | 2071/6913 | 2034/5778 | 678/1925 | chr3 | 129584229 | |||
chr3:129584434 | G | A | 1 | a0003c0018 | 4 | HG02258.hp1 HG03139.hp2 HG03579.hp1 others(1): Show |
synonymous_variant | LOW | c.1980C>T | p.Tyr660Tyr | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 6/36 | 2017/6913 | 1980/5778 | 660/1925 | chr3 | 129584434 | |||
chr3:129586195 | G | A | 1 | a0001c0064 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.1698C>T | p.Cys566Cys | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 4/36 | 1735/6913 | 1698/5778 | 566/1925 | chr3 | 129586195 | |||
chr3:129589366 | G | A | 15 | a0001c0002 a0001c0028 a0001c0070 others(12): Show |
81 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(78): Show |
synonymous_variant | LOW | c.1473C>T | p.Asn491Asn | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/36 | 1510/6913 | 1473/5778 | 491/1925 | chr3 | 129589366 | |||
chr3:129605350 | A | G | 75 | a0001c0001 a0001c0002 a0001c0011 others(72): Show |
405 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(402): Show |
synonymous_variant | LOW | c.1290T>C | p.Cys430Cys | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/36 | 1327/6913 | 1290/5778 | 430/1925 | chr3 | 129605350 | |||
chr3:129605893 | C | T | 1 | a0044c0033 | 1 | NA19087.hp2 | synonymous_variant | LOW | c.747G>A | p.Leu249Leu | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/36 | 784/6913 | 747/5778 | 249/1925 | chr3 | 129605893 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:129555225 | G | A | 4 | a0003c0018t0005 a0010c0035t0005 a0010c0036t0005 others(1): Show |
7 | HG02257.hp1 HG02258.hp1 HG02486.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1087C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 36/36 | 1087 | chr3 | 129555225 | ||||||
chr3:129555268 | C | A | 1 | a0001c0002t0012 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1044G>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 36/36 | 1044 | chr3 | 129555268 | ||||||
chr3:129555357 | C | T | 1 | a0002c0015t0006 | 5 | HG02055.hp1 HG02145.hp2 HG02818.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*955G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 36/36 | 955 | chr3 | 129555357 | ||||||
chr3:129555372 | C | T | 3 | a0002c0015t0006 a0002c0058t0009 a0022c0065t0009 |
7 | HG00735.hp1 HG02055.hp1 HG02145.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*940G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 36/36 | 940 | chr3 | 129555372 | ||||||
chr3:129555520 | G | A | 28 | a0001c0002t0002 a0001c0002t0012 a0001c0045t0002 others(25): Show |
100 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*792C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 36/36 | 792 | chr3 | 129555520 | ||||||
chr3:129555613 | C | T | 12 | a0002c0017t0004 a0002c0017t0007 a0003c0008t0004 others(9): Show |
33 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*699G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 36/36 | 699 | chr3 | 129555613 | ||||||
chr3:129555640 | C | T | 1 | a0001c0001t0013 | 1 | HG00733.hp1 | 3_prime_UTR_variant | MODIFIER | c.*672G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 36/36 | 672 | chr3 | 129555640 | ||||||
chr3:129555731 | G | A | 1 | a0002c0017t0007 | 3 | HG00140.hp1 HG00738.hp1 HG02145.hp1 |
3_prime_UTR_variant | MODIFIER | c.*581C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 36/36 | 581 | chr3 | 129555731 | ||||||
chr3:129555812 | C | T | 29 | a0001c0002t0002 a0001c0002t0012 a0001c0045t0002 others(26): Show |
102 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*500G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 36/36 | 500 | chr3 | 129555812 | ||||||
chr3:129555971 | G | A | 27 | a0001c0013t0003 a0002c0003t0003 a0002c0009t0003 others(24): Show |
102 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*341C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 36/36 | 341 | chr3 | 129555971 | ||||||
chr3:129556035 | C | T | 1 | a0001c0001t0008 | 3 | HG00639.hp1 HG02735.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*277G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 36/36 | 277 | chr3 | 129556035 | ||||||
chr3:129556046 | G | A | 1 | a0019c0066t0014 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*266C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 36/36 | 266 | chr3 | 129556046 | ||||||
chr3:129556093 | A | G | 15 | a0002c0015t0006 a0002c0017t0004 a0002c0017t0007 others(12): Show |
40 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*219T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 36/36 | 219 | chr3 | 129556093 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:129556455 | G | C | 1 | a0002c0012t0001g0280 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.5662-27C>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 35/35 | chr3 | 129556455 | |||||||
chr3:129556509 | C | T | 3 | a0003c0014t0004g0290 a0003c0014t0004g0294 a0007c0021t0004g0068 |
3 | HG02723.hp2 HG02976.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.5662-81G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 35/35 | chr3 | 129556509 | |||||||
chr3:129556560 | C | A | 33 | a0002c0015t0006g0116 a0002c0015t0006g0117 a0002c0015t0006g0118 others(30): Show |
40 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.5661+57G>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 35/35 | chr3 | 129556560 | |||||||
chr3:129556712 | G | A | 1 | a0002c0003t0003g0213 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.5587-21C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 34/35 | chr3 | 129556712 | |||||||
chr3:129556776 | T | C | 88 | a0001c0001t0001g0160 a0001c0002t0002g0005 a0001c0002t0002g0008 others(85): Show |
106 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.5587-85A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 34/35 | chr3 | 129556776 | |||||||
chr3:129556837 | A | G | 8 | a0002c0003t0001g0230 a0004c0005t0001g0053 a0004c0005t0001g0241 others(5): Show |
9 | HG00408.hp2 HG00621.hp2 HG03927.hp2 others(6): Show |
intron_variant | MODIFIER | c.5587-146T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 34/35 | chr3 | 129556837 | |||||||
chr3:129556903 | C | T | 53 | a0001c0002t0002g0005 a0001c0002t0002g0008 a0001c0002t0002g0016 others(50): Show |
63 | HG00423.hp1 HG00597.hp2 HG01081.hp1 others(60): Show |
intron_variant | MODIFIER | c.5586+180G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 34/35 | chr3 | 129556903 | |||||||
chr3:129557065 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.5586+18C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 34/35 | chr3 | 129557065 | |||||||
chr3:129557070 | C | T | 1 | a0002c0003t0003g0045 | 2 | HG00621.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.5586+13G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 34/35 | chr3 | 129557070 | |||||||
chr3:129557270 | C | G | 5 | a0002c0015t0006g0116 a0002c0015t0006g0117 a0002c0015t0006g0118 others(2): Show |
5 | HG02055.hp1 HG02145.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.5446-47G>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 33/35 | chr3 | 129557270 | |||||||
chr3:129557270 | C | T | 1 | a0002c0004t0001g0289 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.5446-47G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 33/35 | chr3 | 129557270 | |||||||
chr3:129557400 | G | T | 1 | a0001c0002t0002g0111 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.5446-177C>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 33/35 | chr3 | 129557400 | |||||||
chr3:129557425 | C | T | 3 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0162 |
3 | HG01106.hp2 HG02148.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.5446-202G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 33/35 | chr3 | 129557425 | |||||||
chr3:129557487 | A | AG | 195 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 others(192): Show |
257 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(254): Show |
intron_variant | MODIFIER | c.5446-265dupC | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 33/35 | chr3 | 129557487 | |||||||
chr3:129557502 | G | C | 2 | a0001c0078t0011g0308 a0002c0079t0011g0307 |
2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.5446-279C>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 33/35 | chr3 | 129557502 | |||||||
chr3:129557533 | A | G | 3 | a0004c0005t0001g0019 a0004c0005t0001g0248 a0004c0005t0001g0253 |
5 | HG02015.hp1 HG04228.hp2 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.5446-310T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 33/35 | chr3 | 129557533 | |||||||
chr3:129557569 | T | C | 27 | a0002c0017t0004g0277 a0002c0017t0007g0033 a0002c0017t0007g0142 others(24): Show |
35 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.5446-346A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 33/35 | chr3 | 129557569 | |||||||
chr3:129557643 | C | T | 43 | a0001c0013t0003g0014 a0001c0013t0003g0124 a0002c0003t0003g0001 others(40): Show |
63 | HG00558.hp1 HG00621.hp1 HG00673.hp1 others(60): Show |
intron_variant | MODIFIER | c.5446-420G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 33/35 | chr3 | 129557643 | |||||||
chr3:129557751 | C | T | 1 | a0009c0022t0001g0059 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.5446-528G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 33/35 | chr3 | 129557751 | |||||||
chr3:129557758 | C | T | 2 | a0001c0001t0001g0258 a0039c0055t0001g0174 |
2 | NA18957.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.5446-535G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 33/35 | chr3 | 129557758 | |||||||
chr3:129558098 | T | C | 2 | a0001c0078t0011g0308 a0002c0079t0011g0307 |
2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.5445+330A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 33/35 | chr3 | 129558098 | |||||||
chr3:129558149 | C | T | 2 | a0001c0002t0002g0078 a0001c0002t0002g0083 |
2 | HG00423.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.5445+279G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 33/35 | chr3 | 129558149 | |||||||
chr3:129558303 | A | C | 92 | a0001c0001t0001g0160 a0001c0002t0002g0005 a0001c0002t0002g0008 others(89): Show |
112 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.5445+125T>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 33/35 | chr3 | 129558303 | |||||||
chr3:129558638 | T | C | 29 | a0002c0017t0004g0277 a0002c0017t0007g0033 a0002c0017t0007g0142 others(26): Show |
37 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.5298-63A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 32/35 | chr3 | 129558638 | |||||||
chr3:129558875 | G | A | 1 | a0001c0001t0001g0164 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.5298-300C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 32/35 | chr3 | 129558875 | |||||||
chr3:129559098 | G | A | 1 | a0005c0016t0001g0309 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.5297+522C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 32/35 | chr3 | 129559098 | |||||||
chr3:129559149 | C | T | 26 | a0002c0017t0004g0277 a0002c0017t0007g0033 a0002c0017t0007g0142 others(23): Show |
33 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.5297+471G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 32/35 | chr3 | 129559149 | |||||||
chr3:129559339 | A | G | 92 | a0001c0001t0001g0160 a0001c0002t0002g0005 a0001c0002t0002g0008 others(89): Show |
112 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.5297+281T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 32/35 | chr3 | 129559339 | |||||||
chr3:129559358 | G | C | 3 | a0004c0005t0001g0193 a0004c0005t0001g0194 a0015c0027t0001g0195 |
3 | NA18952.hp2 NA18973.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.5297+262C>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 32/35 | chr3 | 129559358 | |||||||
chr3:129559462 | A | G | 1 | a0025c0051t0001g0181 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.5297+158T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 32/35 | chr3 | 129559462 | |||||||
chr3:129559603 | GC | G | 52 | a0001c0001t0001g0266 a0001c0002t0002g0005 a0001c0002t0002g0067 others(49): Show |
63 | HG00140.hp1 HG00323.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.5297+16delG | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 32/35 | chr3 | 129559603 | |||||||
chr3:129559823 | C | T | 2 | a0002c0058t0009g0119 a0022c0065t0009g0288 |
2 | HG00735.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.5134-40G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 31/35 | chr3 | 129559823 | |||||||
chr3:129559917 | C | T | 3 | a0001c0001t0001g0297 a0001c0002t0002g0106 a0001c0013t0003g0124 |
3 | HG01167.hp2 HG03688.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.5134-134G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 31/35 | chr3 | 129559917 | |||||||
chr3:129559950 | G | A | 5 | a0002c0015t0006g0116 a0002c0015t0006g0117 a0002c0015t0006g0118 others(2): Show |
5 | HG02055.hp1 HG02145.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.5134-167C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 31/35 | chr3 | 129559950 | |||||||
chr3:129560057 | C | T | 2 | a0002c0058t0009g0119 a0022c0065t0009g0288 |
2 | HG00735.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.5133+273G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 31/35 | chr3 | 129560057 | |||||||
chr3:129560121 | A | G | 1 | a0004c0005t0001g0241 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.5133+209T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 31/35 | chr3 | 129560121 | |||||||
chr3:129560188 | T | G | 1 | a0003c0008t0004g0298 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.5133+142A>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 31/35 | chr3 | 129560188 | |||||||
chr3:129560190 | C | T | 1 | a0002c0004t0001g0289 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.5133+140G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 31/35 | chr3 | 129560190 | |||||||
chr3:129560235 | C | T | 2 | a0001c0078t0011g0308 a0002c0079t0011g0307 |
2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.5133+95G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 31/35 | chr3 | 129560235 | |||||||
chr3:129560238 | G | A | 2 | a0001c0078t0011g0308 a0002c0079t0011g0307 |
2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.5133+92C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 31/35 | chr3 | 129560238 | |||||||
chr3:129560727 | T | C | 88 | a0001c0001t0001g0160 a0001c0002t0002g0005 a0001c0002t0002g0008 others(85): Show |
106 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(103): Show |
splice_region_variant&intron_variant | LOW | c.4994-4A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 29/35 | chr3 | 129560727 | |||||||
chr3:129560754 | C | T | 311 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(308): Show |
415 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(412): Show |
intron_variant | MODIFIER | c.4994-31G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 29/35 | chr3 | 129560754 | |||||||
chr3:129560828 | G | A | 3 | a0001c0011t0001g0015 a0001c0064t0001g0261 a0021c0043t0001g0259 |
6 | HG02622.hp2 HG02896.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.4994-105C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 29/35 | chr3 | 129560828 | |||||||
chr3:129560877 | G | A | 6 | a0003c0008t0004g0038 a0003c0008t0004g0039 a0003c0008t0004g0176 others(3): Show |
8 | HG00323.hp1 HG00642.hp2 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.4994-154C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 29/35 | chr3 | 129560877 | |||||||
chr3:129560930 | C | T | 1 | a0001c0001t0001g0171 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.4994-207G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 29/35 | chr3 | 129560930 | |||||||
chr3:129560992 | A | G | 60 | a0001c0001t0001g0160 a0001c0002t0002g0005 a0001c0002t0002g0008 others(57): Show |
73 | HG00423.hp1 HG00597.hp2 HG01081.hp1 others(70): Show |
intron_variant | MODIFIER | c.4994-269T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 29/35 | chr3 | 129560992 | |||||||
chr3:129561021 | G | A | 1 | a0006c0023t0001g0143 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.4994-298C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 29/35 | chr3 | 129561021 | |||||||
chr3:129561127 | C | T | 5 | a0002c0015t0006g0116 a0002c0015t0006g0117 a0002c0015t0006g0118 others(2): Show |
5 | HG02055.hp1 HG02145.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.4994-404G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 29/35 | chr3 | 129561127 | |||||||
chr3:129561313 | G | A | 1 | a0003c0059t0004g0281 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.4993+333C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 29/35 | chr3 | 129561313 | |||||||
chr3:129561418 | C | T | 27 | a0002c0017t0004g0277 a0002c0017t0007g0033 a0002c0017t0007g0142 others(24): Show |
34 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.4993+228G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 29/35 | chr3 | 129561418 | |||||||
chr3:129561639 | G | A | 1 | a0001c0001t0001g0179 | 1 | NA19077.hp2 | splice_region_variant&intron_variant | LOW | c.4993+7C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 29/35 | chr3 | 129561639 | |||||||
chr3:129561730 | G | A | 1 | a0003c0008t0004g0298 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.4930-21C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 28/35 | chr3 | 129561730 | |||||||
chr3:129561782 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.4929+18G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 28/35 | chr3 | 129561782 | |||||||
chr3:129561967 | G | C | 1 | a0002c0004t0001g0279 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4826-64C>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 27/35 | chr3 | 129561967 | |||||||
chr3:129562101 | C | T | 32 | a0002c0017t0004g0277 a0002c0017t0007g0033 a0002c0017t0007g0142 others(29): Show |
40 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.4826-198G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 27/35 | chr3 | 129562101 | |||||||
chr3:129562163 | A | G | 5 | a0002c0015t0006g0116 a0002c0015t0006g0117 a0002c0015t0006g0118 others(2): Show |
5 | HG02055.hp1 HG02145.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.4826-260T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 27/35 | chr3 | 129562163 | |||||||
chr3:129562194 | C | T | 1 | a0002c0009t0001g0217 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.4826-291G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 27/35 | chr3 | 129562194 | |||||||
chr3:129562236 | C | T | 1 | a0004c0005t0001g0253 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.4826-333G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 27/35 | chr3 | 129562236 | |||||||
chr3:129562245 | GCTCACAC others(4): Show |
G | 53 | a0001c0002t0002g0005 a0001c0002t0002g0008 a0001c0002t0002g0016 others(50): Show |
63 | HG00423.hp1 HG00597.hp2 HG01081.hp1 others(60): Show |
intron_variant | MODIFIER | c.4826-353_4826-343d others(13): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 27/35 | chr3 | 129562245 | |||||||
chr3:129562370 | TGTG | T | 53 | a0001c0002t0002g0005 a0001c0002t0002g0008 a0001c0002t0002g0016 others(50): Show |
63 | HG00423.hp1 HG00597.hp2 HG01081.hp1 others(60): Show |
intron_variant | MODIFIER | c.4825+414_4825+416d others(5): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 27/35 | chr3 | 129562370 | |||||||
chr3:129562378 | T | C | 1 | a0001c0064t0001g0261 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4825+409A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 27/35 | chr3 | 129562378 | |||||||
chr3:129562595 | C | T | 30 | a0002c0017t0004g0277 a0002c0058t0009g0119 a0003c0008t0004g0017 others(27): Show |
37 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.4825+192G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 27/35 | chr3 | 129562595 | |||||||
chr3:129562615 | G | A | 30 | a0001c0001t0001g0031 a0001c0001t0001g0062 a0001c0001t0001g0141 others(27): Show |
40 | HG00140.hp2 HG00280.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.4825+172C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 27/35 | chr3 | 129562615 | |||||||
chr3:129563023 | G | C | 44 | a0001c0078t0011g0308 a0002c0004t0001g0289 a0002c0017t0004g0277 others(41): Show |
60 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.4668+71C>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 26/35 | chr3 | 129563023 | |||||||
chr3:129563270 | G | C | 1 | a0002c0012t0001g0292 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.4522-30C>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 25/35 | chr3 | 129563270 | |||||||
chr3:129563294 | T | C | 213 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 others(210): Show |
279 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(276): Show |
intron_variant | MODIFIER | c.4522-54A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 25/35 | chr3 | 129563294 | |||||||
chr3:129563295 | G | A | 30 | a0002c0004t0001g0154 a0003c0007t0001g0009 a0003c0007t0001g0026 others(27): Show |
43 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(40): Show |
intron_variant | MODIFIER | c.4522-55C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 25/35 | chr3 | 129563295 | |||||||
chr3:129563510 | C | T | 55 | a0001c0001t0001g0160 a0001c0002t0002g0005 a0001c0002t0002g0008 others(52): Show |
66 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.4522-270G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 25/35 | chr3 | 129563510 | |||||||
chr3:129563579 | C | T | 2 | a0009c0022t0001g0059 a0009c0022t0001g0060 |
2 | HG01516.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.4522-339G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 25/35 | chr3 | 129563579 | |||||||
chr3:129563697 | A | G | 55 | a0001c0001t0008g0172 a0001c0078t0011g0308 a0002c0006t0001g0007 others(52): Show |
68 | HG00408.hp2 HG00639.hp1 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.4522-457T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 25/35 | chr3 | 129563697 | |||||||
chr3:129563784 | A | G | 1 | a0001c0001t0001g0161 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.4522-544T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 25/35 | chr3 | 129563784 | |||||||
chr3:129564024 | T | C | 1 | a0002c0006t0001g0271 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4522-784A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 25/35 | chr3 | 129564024 | |||||||
chr3:129564027 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.4522-787C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 25/35 | chr3 | 129564027 | |||||||
chr3:129564125 | C | T | 1 | a0001c0001t0001g0275 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.4522-885G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 25/35 | chr3 | 129564125 | |||||||
chr3:129564134 | C | T | 82 | a0001c0078t0011g0308 a0002c0006t0001g0007 a0002c0006t0001g0271 others(79): Show |
108 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.4522-894G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 25/35 | chr3 | 129564134 | |||||||
chr3:129564269 | G | A | 2 | a0007c0021t0002g0023 a0007c0021t0004g0068 |
3 | HG01243.hp1 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.4522-1029C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 25/35 | chr3 | 129564269 | |||||||
chr3:129564416 | C | T | 4 | a0002c0003t0003g0045 a0002c0003t0003g0233 a0014c0062t0003g0220 others(1): Show |
5 | HG00621.hp1 HG02056.hp1 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.4521+924G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 25/35 | chr3 | 129564416 | |||||||
chr3:129564510 | T | G | 46 | a0002c0006t0001g0007 a0002c0006t0001g0010 a0002c0006t0001g0122 others(43): Show |
57 | HG00408.hp2 HG00639.hp2 HG01109.hp2 others(54): Show |
intron_variant | MODIFIER | c.4521+830A>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 25/35 | chr3 | 129564510 | |||||||
chr3:129564606 | C | T | 3 | a0001c0002t0002g0008 a0001c0002t0002g0096 a0020c0072t0002g0073 |
6 | HG02080.hp2 HG02083.hp2 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.4521+734G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 25/35 | chr3 | 129564606 | |||||||
chr3:129564698 | G | A | 8 | a0002c0006t0001g0010 a0002c0006t0001g0122 a0002c0006t0001g0287 others(5): Show |
11 | HG01109.hp2 HG02055.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.4521+642C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 25/35 | chr3 | 129564698 | |||||||
chr3:129564710 | T | C | 1 | a0001c0002t0002g0088 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.4521+630A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 25/35 | chr3 | 129564710 | |||||||
chr3:129564766 | C | T | 4 | a0002c0003t0003g0045 a0002c0003t0003g0233 a0014c0062t0003g0220 others(1): Show |
5 | HG00621.hp1 HG02056.hp1 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.4521+574G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 25/35 | chr3 | 129564766 | |||||||
chr3:129564769 | A | T | 1 | a0002c0079t0011g0307 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.4521+571T>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 25/35 | chr3 | 129564769 | |||||||
chr3:129564783 | C | T | 55 | a0001c0001t0001g0160 a0001c0002t0002g0005 a0001c0002t0002g0008 others(52): Show |
66 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.4521+557G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 25/35 | chr3 | 129564783 | |||||||
chr3:129564832 | A | G | 4 | a0002c0057t0001g0282 a0005c0016t0001g0022 a0005c0016t0001g0309 others(1): Show |
6 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.4521+508T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 25/35 | chr3 | 129564832 | |||||||
chr3:129564839 | G | T | 21 | a0004c0005t0001g0019 a0004c0005t0001g0053 a0004c0005t0001g0239 others(18): Show |
24 | HG00408.hp2 HG02015.hp1 HG02148.hp2 others(21): Show |
intron_variant | MODIFIER | c.4521+501C>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 25/35 | chr3 | 129564839 | |||||||
chr3:129564922 | G | A | 90 | a0001c0078t0011g0308 a0002c0006t0001g0007 a0002c0006t0001g0010 others(87): Show |
119 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.4521+418C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 25/35 | chr3 | 129564922 | |||||||
chr3:129565060 | G | A | 1 | a0002c0004t0001g0278 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.4521+280C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 25/35 | chr3 | 129565060 | |||||||
chr3:129565217 | C | T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0063 |
6 | NA18945.hp1 NA18947.hp1 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.4521+123G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 25/35 | chr3 | 129565217 | |||||||
chr3:129565270 | G | A | 1 | a0001c0020t0001g0165 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.4521+70C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 25/35 | chr3 | 129565270 | |||||||
chr3:129565284 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.4521+56C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 25/35 | chr3 | 129565284 | |||||||
chr3:129565307 | G | A | 38 | a0002c0006t0001g0007 a0002c0006t0001g0271 a0002c0006t0001g0291 others(35): Show |
46 | HG00408.hp2 HG00639.hp2 HG01255.hp1 others(43): Show |
intron_variant | MODIFIER | c.4521+33C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 25/35 | chr3 | 129565307 | |||||||
chr3:129565546 | C | T | 1 | a0015c0027t0001g0201 | 1 | NA18974.hp2 | splice_region_variant&intron_variant | LOW | c.4323-8G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 24/35 | chr3 | 129565546 | |||||||
chr3:129565572 | G | T | 40 | a0001c0078t0011g0308 a0002c0079t0011g0307 a0003c0007t0001g0009 others(37): Show |
56 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.4323-34C>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 24/35 | chr3 | 129565572 | |||||||
chr3:129565619 | C | G | 4 | a0002c0057t0001g0282 a0005c0016t0001g0022 a0005c0016t0001g0309 others(1): Show |
6 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.4323-81G>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 24/35 | chr3 | 129565619 | |||||||
chr3:129565711 | C | G | 55 | a0001c0001t0001g0160 a0001c0002t0002g0005 a0001c0002t0002g0008 others(52): Show |
66 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.4323-173G>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 24/35 | chr3 | 129565711 | |||||||
chr3:129565794 | A | G | 92 | a0001c0078t0011g0308 a0002c0006t0001g0007 a0002c0006t0001g0010 others(89): Show |
121 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.4322+93T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 24/35 | chr3 | 129565794 | |||||||
chr3:129566138 | C | T | 1 | a0001c0020t0001g0131 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.4192-121G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 23/35 | chr3 | 129566138 | |||||||
chr3:129566156 | C | T | 1 | a0001c0020t0001g0166 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.4192-139G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 23/35 | chr3 | 129566156 | |||||||
chr3:129566332 | G | A | 46 | a0002c0006t0001g0007 a0002c0006t0001g0010 a0002c0006t0001g0122 others(43): Show |
57 | HG00408.hp2 HG00639.hp2 HG01109.hp2 others(54): Show |
intron_variant | MODIFIER | c.4191+195C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 23/35 | chr3 | 129566332 | |||||||
chr3:129566425 | G | A | 3 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0162 |
3 | HG01106.hp2 HG02148.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.4191+102C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 23/35 | chr3 | 129566425 | |||||||
chr3:129566433 | G | A | 1 | a0001c0002t0002g0097 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.4191+94C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 23/35 | chr3 | 129566433 | |||||||
chr3:129566480 | G | A | 1 | a0004c0005t0001g0256 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.4191+47C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 23/35 | chr3 | 129566480 | |||||||
chr3:129566734 | A | C | 46 | a0002c0006t0001g0007 a0002c0006t0001g0010 a0002c0006t0001g0122 others(43): Show |
57 | HG00408.hp2 HG00639.hp2 HG01109.hp2 others(54): Show |
intron_variant | MODIFIER | c.4087-103T>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 22/35 | chr3 | 129566734 | |||||||
chr3:129566744 | G | A | 46 | a0002c0006t0001g0007 a0002c0006t0001g0010 a0002c0006t0001g0122 others(43): Show |
57 | HG00408.hp2 HG00639.hp2 HG01109.hp2 others(54): Show |
intron_variant | MODIFIER | c.4087-113C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 22/35 | chr3 | 129566744 | |||||||
chr3:129566757 | C | T | 1 | a0001c0002t0002g0100 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.4087-126G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 22/35 | chr3 | 129566757 | |||||||
chr3:129567060 | G | GGGCA | 46 | a0002c0006t0001g0007 a0002c0006t0001g0010 a0002c0006t0001g0122 others(43): Show |
57 | HG00408.hp2 HG00639.hp2 HG01109.hp2 others(54): Show |
intron_variant | MODIFIER | c.4086+428_4087-430d others(6): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 22/35 | chr3 | 129567060 | |||||||
chr3:129567118 | G | T | 1 | a0044c0033t0002g0058 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.4086+374C>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 22/35 | chr3 | 129567118 | |||||||
chr3:129567205 | GC | G | 46 | a0002c0006t0001g0007 a0002c0006t0001g0010 a0002c0006t0001g0122 others(43): Show |
57 | HG00408.hp2 HG00639.hp2 HG01109.hp2 others(54): Show |
intron_variant | MODIFIER | c.4086+286delG | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 22/35 | chr3 | 129567205 | |||||||
chr3:129567366 | C | T | 3 | a0002c0006t0001g0010 a0002c0006t0001g0122 a0002c0006t0001g0287 |
6 | HG01109.hp2 HG03209.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.4086+126G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 22/35 | chr3 | 129567366 | |||||||
chr3:129567484 | G | A | 1 | a0001c0001t0001g0200 | 1 | NA21309.hp1 | splice_region_variant&intron_variant | LOW | c.4086+8C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 22/35 | chr3 | 129567484 | |||||||
chr3:129567688 | C | A | 127 | a0001c0013t0003g0014 a0001c0013t0003g0124 a0001c0078t0011g0308 others(124): Show |
172 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.3973+10G>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 21/35 | chr3 | 129567688 | |||||||
chr3:129567810 | G | A | 1 | a0001c0001t0001g0128 | 1 | NA18968.hp1 | splice_region_variant&intron_variant | LOW | c.3866-5C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 20/35 | chr3 | 129567810 | |||||||
chr3:129567983 | C | T | 1 | a0001c0002t0002g0104 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.3866-178G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 20/35 | chr3 | 129567983 | |||||||
chr3:129568032 | C | T | 1 | a0003c0059t0004g0281 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3866-227G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 20/35 | chr3 | 129568032 | |||||||
chr3:129568033 | G | A | 8 | a0002c0006t0001g0010 a0002c0006t0001g0122 a0002c0006t0001g0287 others(5): Show |
11 | HG01109.hp2 HG02055.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.3866-228C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 20/35 | chr3 | 129568033 | |||||||
chr3:129568088 | C | G | 1 | a0044c0033t0002g0058 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.3866-283G>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 20/35 | chr3 | 129568088 | |||||||
chr3:129568089 | G | T | 1 | a0044c0033t0002g0058 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.3866-284C>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 20/35 | chr3 | 129568089 | |||||||
chr3:129568091 | T | A | 1 | a0044c0033t0002g0058 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.3866-286A>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 20/35 | chr3 | 129568091 | |||||||
chr3:129568161 | A | G | 52 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0021 others(49): Show |
69 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.3866-356T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 20/35 | chr3 | 129568161 | |||||||
chr3:129568333 | A | G | 1 | a0001c0002t0002g0087 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.3866-528T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 20/35 | chr3 | 129568333 | |||||||
chr3:129568506 | C | T | 1 | a0015c0027t0001g0195 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3866-701G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 20/35 | chr3 | 129568506 | |||||||
chr3:129568630 | C | T | 89 | a0001c0013t0003g0014 a0001c0013t0003g0124 a0001c0078t0011g0308 others(86): Show |
125 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.3866-825G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 20/35 | chr3 | 129568630 | |||||||
chr3:129568714 | A | G | 4 | a0002c0057t0001g0282 a0005c0016t0001g0022 a0005c0016t0001g0309 others(1): Show |
6 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.3866-909T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 20/35 | chr3 | 129568714 | |||||||
chr3:129568733 | G | C | 1 | a0003c0008t0004g0298 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.3866-928C>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 20/35 | chr3 | 129568733 | |||||||
chr3:129569173 | A | T | 1 | a0003c0010t0001g0020 | 3 | HG02602.hp2 HG03017.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.3865+670T>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 20/35 | chr3 | 129569173 | |||||||
chr3:129569194 | T | A | 1 | a0039c0055t0001g0174 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.3865+649A>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 20/35 | chr3 | 129569194 | |||||||
chr3:129569195 | A | T | 1 | a0039c0055t0001g0174 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.3865+648T>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 20/35 | chr3 | 129569195 | |||||||
chr3:129569197 | T | G | 1 | a0039c0055t0001g0174 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.3865+646A>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 20/35 | chr3 | 129569197 | |||||||
chr3:129569256 | A | AAC | 137 | a0001c0013t0003g0014 a0001c0013t0003g0124 a0001c0056t0002g0133 others(134): Show |
186 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.3865+585_3865+586d others(4): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 20/35 | chr3 | 129569256 | |||||||
chr3:129569258 | C | CAT | 158 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(155): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.3865+584_3865+585i others(4): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 20/35 | chr3 | 129569258 | |||||||
chr3:129569285 | G | A | 9 | a0003c0008t0004g0038 a0003c0008t0004g0039 a0003c0008t0004g0176 others(6): Show |
11 | HG00323.hp1 HG00642.hp2 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.3865+558C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 20/35 | chr3 | 129569285 | |||||||
chr3:129569463 | T | C | 2 | a0001c0078t0011g0308 a0002c0079t0011g0307 |
2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.3865+380A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 20/35 | chr3 | 129569463 | |||||||
chr3:129569562 | A | G | 1 | a0001c0002t0002g0070 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3865+281T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 20/35 | chr3 | 129569562 | |||||||
chr3:129569632 | C | T | 3 | a0001c0001t0001g0041 a0001c0001t0001g0064 a0001c0001t0001g0199 |
4 | HG00673.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.3865+211G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 20/35 | chr3 | 129569632 | |||||||
chr3:129569707 | C | A | 1 | a0001c0020t0001g0166 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3865+136G>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 20/35 | chr3 | 129569707 | |||||||
chr3:129569726 | CT | C | 4 | a0002c0003t0003g0045 a0002c0003t0003g0233 a0014c0062t0003g0220 others(1): Show |
5 | HG00621.hp1 HG02056.hp1 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.3865+116delA | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 20/35 | chr3 | 129569726 | |||||||
chr3:129569805 | C | T | 1 | a0001c0001t0001g0115 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3865+38G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 20/35 | chr3 | 129569805 | |||||||
chr3:129570008 | A | G | 2 | a0001c0078t0011g0308 a0002c0079t0011g0307 |
2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.3751-51T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 19/35 | chr3 | 129570008 | |||||||
chr3:129570215 | G | C | 9 | a0001c0001t0001g0040 a0001c0001t0001g0157 a0001c0001t0001g0163 others(6): Show |
10 | HG00558.hp2 HG01934.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.3751-258C>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 19/35 | chr3 | 129570215 | |||||||
chr3:129570236 | G | A | 1 | a0002c0009t0001g0217 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.3751-279C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 19/35 | chr3 | 129570236 | |||||||
chr3:129570247 | C | T | 50 | a0002c0006t0001g0007 a0002c0006t0001g0010 a0002c0006t0001g0122 others(47): Show |
63 | HG00408.hp2 HG00639.hp2 HG01109.hp2 others(60): Show |
intron_variant | MODIFIER | c.3751-290G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 19/35 | chr3 | 129570247 | |||||||
chr3:129570415 | T | C | 87 | a0001c0013t0003g0014 a0001c0013t0003g0124 a0001c0056t0002g0133 others(84): Show |
123 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.3750+371A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 19/35 | chr3 | 129570415 | |||||||
chr3:129570419 | C | CA | 47 | a0001c0013t0003g0014 a0001c0013t0003g0124 a0001c0056t0002g0133 others(44): Show |
67 | HG00558.hp1 HG00621.hp1 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.3750+366dupT | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 19/35 | chr3 | 129570419 | |||||||
chr3:129570458 | T | A | 1 | a0002c0003t0003g0218 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.3750+328A>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 19/35 | chr3 | 129570458 | |||||||
chr3:129570504 | C | T | 1 | a0001c0001t0001g0175 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.3750+282G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 19/35 | chr3 | 129570504 | |||||||
chr3:129570752 | A | G | 2 | a0001c0078t0011g0308 a0002c0079t0011g0307 |
2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.3750+34T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 19/35 | chr3 | 129570752 | |||||||
chr3:129570774 | C | T | 1 | a0001c0045t0002g0231 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.3750+12G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 19/35 | chr3 | 129570774 | |||||||
chr3:129570988 | A | G | 194 | a0001c0002t0002g0005 a0001c0002t0002g0008 a0001c0002t0002g0016 others(191): Show |
254 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.3600+52T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 18/35 | chr3 | 129570988 | |||||||
chr3:129571002 | C | T | 1 | a0004c0019t0004g0240 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3600+38G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 18/35 | chr3 | 129571002 | |||||||
chr3:129571018 | C | T | 1 | a0003c0018t0005g0260 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3600+22G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 18/35 | chr3 | 129571018 | |||||||
chr3:129571344 | T | C | 89 | a0001c0013t0003g0014 a0001c0013t0003g0124 a0001c0056t0002g0133 others(86): Show |
125 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.3337-41A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 17/35 | chr3 | 129571344 | |||||||
chr3:129571425 | G | A | 1 | a0003c0008t0004g0017 | 3 | HG01123.hp2 HG01175.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.3336+84C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 17/35 | chr3 | 129571425 | |||||||
chr3:129571484 | C | T | 1 | a0004c0005t0001g0197 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.3336+25G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 17/35 | chr3 | 129571484 | |||||||
chr3:129571876 | T | C | 1 | a0005c0016t0001g0309 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3078-32A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 15/35 | chr3 | 129571876 | |||||||
chr3:129571898 | G | A | 1 | a0006c0046t0004g0264 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3078-54C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 15/35 | chr3 | 129571898 | |||||||
chr3:129571934 | A | G | 1 | a0005c0016t0001g0309 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3078-90T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 15/35 | chr3 | 129571934 | |||||||
chr3:129571941 | C | T | 1 | a0002c0003t0003g0206 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.3078-97G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 15/35 | chr3 | 129571941 | |||||||
chr3:129571981 | C | T | 1 | a0001c0002t0002g0096 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.3078-137G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 15/35 | chr3 | 129571981 | |||||||
chr3:129572013 | C | T | 1 | a0003c0010t0001g0265 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.3078-169G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 15/35 | chr3 | 129572013 | |||||||
chr3:129572025 | G | T | 1 | a0030c0039t0001g0255 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.3078-181C>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 15/35 | chr3 | 129572025 | |||||||
chr3:129572089 | GTC | G | 54 | a0001c0002t0002g0005 a0001c0002t0002g0008 a0001c0002t0002g0016 others(51): Show |
65 | HG00423.hp1 HG00438.hp1 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.3078-247_3078-246d others(4): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 15/35 | chr3 | 129572089 | |||||||
chr3:129572302 | G | A | 1 | a0002c0012t0001g0283 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.3077+307C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 15/35 | chr3 | 129572302 | |||||||
chr3:129572587 | T | C | 1 | a0001c0002t0002g0090 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.3077+22A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 15/35 | chr3 | 129572587 | |||||||
chr3:129572800 | C | T | 2 | a0001c0078t0011g0308 a0002c0079t0011g0307 |
2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2937+42G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 14/35 | chr3 | 129572800 | |||||||
chr3:129573025 | C | T | 53 | a0001c0002t0002g0005 a0001c0002t0002g0008 a0001c0002t0002g0016 others(50): Show |
64 | HG00423.hp1 HG00438.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.2838-84G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 13/35 | chr3 | 129573025 | |||||||
chr3:129573093 | A | G | 2 | a0002c0058t0009g0119 a0022c0065t0009g0288 |
2 | HG00735.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2838-152T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 13/35 | chr3 | 129573093 | |||||||
chr3:129573222 | C | T | 83 | a0001c0013t0003g0014 a0001c0013t0003g0124 a0002c0003t0001g0230 others(80): Show |
119 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.2838-281G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 13/35 | chr3 | 129573222 | |||||||
chr3:129573424 | C | T | 2 | a0003c0014t0004g0050 a0003c0014t0004g0286 |
3 | HG02647.hp2 HG02970.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2837+170G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 13/35 | chr3 | 129573424 | |||||||
chr3:129573520 | A | G | 1 | a0030c0039t0001g0255 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2837+74T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 13/35 | chr3 | 129573520 | |||||||
chr3:129573521 | G | A | 1 | a0030c0039t0001g0255 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2837+73C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 13/35 | chr3 | 129573521 | |||||||
chr3:129573578 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2837+16G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 13/35 | chr3 | 129573578 | |||||||
chr3:129573843 | C | G | 1 | a0001c0002t0002g0086 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2686-98G>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 12/35 | chr3 | 129573843 | |||||||
chr3:129574034 | T | C | 1 | a0002c0003t0003g0234 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2686-289A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 12/35 | chr3 | 129574034 | |||||||
chr3:129574105 | C | T | 17 | a0003c0007t0001g0009 a0003c0007t0001g0026 a0003c0007t0001g0027 others(14): Show |
25 | HG00140.hp2 HG00280.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.2685+231G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 12/35 | chr3 | 129574105 | |||||||
chr3:129574181 | G | A | 2 | a0001c0001t0001g0006 a0001c0001t0001g0063 |
6 | NA18945.hp1 NA18947.hp1 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.2685+155C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 12/35 | chr3 | 129574181 | |||||||
chr3:129574263 | G | C | 166 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(163): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.2685+73C>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 12/35 | chr3 | 129574263 | |||||||
chr3:129574303 | C | T | 1 | a0003c0007t0001g0026 | 2 | HG00280.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.2685+33G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 12/35 | chr3 | 129574303 | |||||||
chr3:129574522 | C | T | 1 | a0014c0062t0003g0220 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2531-32G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 11/35 | chr3 | 129574522 | |||||||
chr3:129574587 | G | A | 1 | a0001c0050t0001g0148 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2531-97C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 11/35 | chr3 | 129574587 | |||||||
chr3:129574764 | A | G | 36 | a0002c0006t0001g0007 a0002c0006t0001g0271 a0002c0006t0001g0291 others(33): Show |
44 | HG00408.hp2 HG00639.hp2 HG01255.hp1 others(41): Show |
intron_variant | MODIFIER | c.2531-274T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 11/35 | chr3 | 129574764 | |||||||
chr3:129574804 | C | T | 2 | a0001c0002t0002g0111 a0004c0019t0004g0251 |
2 | HG00639.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.2531-314G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 11/35 | chr3 | 129574804 | |||||||
chr3:129574821 | C | G | 2 | a0001c0002t0002g0070 a0001c0002t0002g0080 |
2 | HG01884.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2531-331G>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 11/35 | chr3 | 129574821 | |||||||
chr3:129574847 | C | T | 38 | a0001c0078t0011g0308 a0002c0006t0001g0010 a0002c0006t0001g0122 others(35): Show |
44 | HG00408.hp2 HG00639.hp2 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.2531-357G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 11/35 | chr3 | 129574847 | |||||||
chr3:129574853 | C | A | 1 | a0001c0002t0002g0110 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2531-363G>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 11/35 | chr3 | 129574853 | |||||||
chr3:129574946 | C | T | 3 | a0005c0016t0001g0022 a0005c0016t0001g0309 a0005c0016t0001g0310 |
5 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2531-456G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 11/35 | chr3 | 129574946 | |||||||
chr3:129574996 | G | A | 25 | a0004c0005t0001g0019 a0004c0005t0001g0053 a0004c0005t0001g0193 others(22): Show |
28 | HG00639.hp2 HG01981.hp2 HG02015.hp1 others(25): Show |
intron_variant | MODIFIER | c.2530+473C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 11/35 | chr3 | 129574996 | |||||||
chr3:129575106 | A | C | 14 | a0001c0001t0001g0034 a0001c0001t0001g0037 a0001c0001t0001g0158 others(11): Show |
20 | HG00597.hp1 HG00609.hp2 HG03490.hp1 others(17): Show |
intron_variant | MODIFIER | c.2530+363T>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 11/35 | chr3 | 129575106 | |||||||
chr3:129575130 | T | C | 60 | a0001c0078t0011g0308 a0002c0006t0001g0007 a0002c0006t0001g0010 others(57): Show |
76 | HG00408.hp2 HG00639.hp2 HG01109.hp2 others(73): Show |
intron_variant | MODIFIER | c.2530+339A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 11/35 | chr3 | 129575130 | |||||||
chr3:129575240 | T | A | 1 | a0001c0050t0001g0148 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2530+229A>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 11/35 | chr3 | 129575240 | |||||||
chr3:129575273 | CTA | C | 93 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(90): Show |
127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.2530+194_2530+195d others(4): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 11/35 | chr3 | 129575273 | |||||||
chr3:129575401 | G | A | 3 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 |
3 | HG02280.hp1 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2530+68C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 11/35 | chr3 | 129575401 | |||||||
chr3:129575451 | G | C | 40 | a0001c0078t0011g0308 a0002c0006t0001g0010 a0002c0006t0001g0122 others(37): Show |
46 | HG00408.hp2 HG00639.hp2 HG01109.hp2 others(43): Show |
intron_variant | MODIFIER | c.2530+18C>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 11/35 | chr3 | 129575451 | |||||||
chr3:129575613 | C | T | 74 | a0001c0011t0001g0015 a0001c0011t0001g0211 a0001c0011t0001g0214 others(71): Show |
106 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.2437-51G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 10/35 | chr3 | 129575613 | |||||||
chr3:129575615 | G | A | 1 | a0003c0007t0001g0098 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2437-53C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 10/35 | chr3 | 129575615 | |||||||
chr3:129575719 | C | T | 1 | a0004c0005t0001g0197 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2436+47G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 10/35 | chr3 | 129575719 | |||||||
chr3:129575725 | G | A | 62 | a0001c0002t0002g0005 a0001c0002t0002g0008 a0001c0002t0002g0016 others(59): Show |
78 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.2436+41C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 10/35 | chr3 | 129575725 | |||||||
chr3:129575880 | C | T | 1 | a0001c0001t0001g0021 | 3 | HG00323.hp2 HG03704.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.2347-25G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 9/35 | chr3 | 129575880 | |||||||
chr3:129575998 | G | A | 2 | a0001c0002t0002g0078 a0001c0002t0002g0083 |
2 | HG00423.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.2347-143C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 9/35 | chr3 | 129575998 | |||||||
chr3:129576170 | C | A | 1 | a0001c0001t0001g0150 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2347-315G>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 9/35 | chr3 | 129576170 | |||||||
chr3:129576244 | G | A | 3 | a0002c0006t0001g0010 a0002c0006t0001g0122 a0002c0006t0001g0287 |
6 | HG01109.hp2 HG03209.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.2347-389C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 9/35 | chr3 | 129576244 | |||||||
chr3:129576272 | G | A | 1 | a0022c0065t0009g0288 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2347-417C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 9/35 | chr3 | 129576272 | |||||||
chr3:129576289 | T | C | 1 | a0003c0014t0004g0290 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2347-434A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 9/35 | chr3 | 129576289 | |||||||
chr3:129576356 | A | G | 1 | a0002c0003t0003g0303 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2347-501T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 9/35 | chr3 | 129576356 | |||||||
chr3:129576592 | A | T | 1 | a0001c0002t0002g0097 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2347-737T>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 9/35 | chr3 | 129576592 | |||||||
chr3:129576622 | T | G | 1 | a0001c0001t0001g0168 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2347-767A>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 9/35 | chr3 | 129576622 | |||||||
chr3:129576687 | G | A | 1 | a0001c0002t0002g0099 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2347-832C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 9/35 | chr3 | 129576687 | |||||||
chr3:129576776 | C | T | 1 | a0001c0001t0001g0032 | 2 | HG00099.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.2347-921G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 9/35 | chr3 | 129576776 | |||||||
chr3:129576811 | A | G | 2 | a0007c0021t0002g0023 a0007c0021t0004g0068 |
3 | HG01243.hp1 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2347-956T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 9/35 | chr3 | 129576811 | |||||||
chr3:129576863 | C | T | 1 | a0036c0068t0002g0069 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2347-1008G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 9/35 | chr3 | 129576863 | |||||||
chr3:129577137 | CCT | C | 3 | a0005c0016t0001g0022 a0005c0016t0001g0309 a0005c0016t0001g0310 |
5 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2346+1190_2346+119 others(6): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 9/35 | chr3 | 129577137 | |||||||
chr3:129577177 | C | T | 117 | a0001c0011t0001g0015 a0001c0011t0001g0211 a0001c0011t0001g0214 others(114): Show |
157 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(154): Show |
intron_variant | MODIFIER | c.2346+1152G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 9/35 | chr3 | 129577177 | |||||||
chr3:129577224 | G | A | 1 | a0004c0005t0001g0194 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.2346+1105C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 9/35 | chr3 | 129577224 | |||||||
chr3:129577233 | G | A | 1 | a0004c0005t0001g0194 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.2346+1096C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 9/35 | chr3 | 129577233 | |||||||
chr3:129577635 | A | G | 1 | a0001c0002t0002g0072 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.2346+694T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 9/35 | chr3 | 129577635 | |||||||
chr3:129577913 | G | T | 43 | a0001c0078t0011g0308 a0002c0006t0001g0010 a0002c0006t0001g0122 others(40): Show |
51 | HG00408.hp2 HG00639.hp2 HG01109.hp2 others(48): Show |
intron_variant | MODIFIER | c.2346+416C>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 9/35 | chr3 | 129577913 | |||||||
chr3:129577939 | G | A | 60 | a0001c0002t0002g0005 a0001c0002t0002g0008 a0001c0002t0002g0016 others(57): Show |
76 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.2346+390C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 9/35 | chr3 | 129577939 | |||||||
chr3:129578004 | A | G | 77 | a0001c0011t0001g0015 a0001c0011t0001g0211 a0001c0011t0001g0214 others(74): Show |
109 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(106): Show |
intron_variant | MODIFIER | c.2346+325T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 9/35 | chr3 | 129578004 | |||||||
chr3:129578035 | C | T | 1 | a0002c0004t0001g0138 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2346+294G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 9/35 | chr3 | 129578035 | |||||||
chr3:129578152 | G | A | 2 | a0007c0021t0002g0023 a0007c0021t0004g0068 |
3 | HG01243.hp1 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2346+177C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 9/35 | chr3 | 129578152 | |||||||
chr3:129578169 | G | C | 310 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(307): Show |
413 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(410): Show |
intron_variant | MODIFIER | c.2346+160C>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 9/35 | chr3 | 129578169 | |||||||
chr3:129578554 | T | C | 1 | a0005c0016t0001g0022 | 3 | HG02109.hp1 HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2242-121A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129578554 | |||||||
chr3:129578635 | C | T | 60 | a0001c0002t0002g0005 a0001c0002t0002g0008 a0001c0002t0002g0016 others(57): Show |
76 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.2242-202G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129578635 | |||||||
chr3:129578750 | A | G | 30 | a0004c0005t0001g0019 a0004c0005t0001g0053 a0004c0005t0001g0193 others(27): Show |
33 | HG00408.hp2 HG00639.hp2 HG01981.hp2 others(30): Show |
intron_variant | MODIFIER | c.2242-317T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129578750 | |||||||
chr3:129578834 | G | A | 1 | a0001c0001t0001g0183 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.2242-401C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129578834 | |||||||
chr3:129579049 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2242-616G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129579049 | |||||||
chr3:129579232 | A | C | 1 | a0001c0001t0001g0135 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2242-799T>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129579232 | |||||||
chr3:129579255 | C | T | 1 | a0001c0002t0002g0084 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2242-822G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129579255 | |||||||
chr3:129579263 | A | T | 2 | a0001c0001t0001g0151 a0001c0001t0001g0152 |
2 | HG01106.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.2242-830T>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129579263 | |||||||
chr3:129579286 | G | A | 36 | a0002c0006t0001g0010 a0002c0006t0001g0122 a0002c0015t0006g0116 others(33): Show |
42 | HG00408.hp2 HG00639.hp2 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.2242-853C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129579286 | |||||||
chr3:129579320 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2242-887G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129579320 | |||||||
chr3:129579466 | G | A | 1 | a0002c0058t0009g0119 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2242-1033C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129579466 | |||||||
chr3:129579510 | A | C | 1 | a0010c0035t0005g0270 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2242-1077T>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129579510 | |||||||
chr3:129579577 | C | T | 2 | a0005c0016t0001g0022 a0005c0016t0001g0310 |
4 | HG02109.hp1 HG02280.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2242-1144G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129579577 | |||||||
chr3:129579702 | T | A | 1 | a0004c0005t0001g0245 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2242-1269A>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129579702 | |||||||
chr3:129579843 | C | T | 74 | a0001c0011t0001g0015 a0001c0011t0001g0211 a0001c0011t0001g0214 others(71): Show |
105 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.2242-1410G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129579843 | |||||||
chr3:129579950 | A | G | 1 | a0004c0005t0001g0254 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2242-1517T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129579950 | |||||||
chr3:129580151 | G | T | 234 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(231): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.2242-1718C>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129580151 | |||||||
chr3:129580182 | C | G | 4 | a0001c0002t0002g0078 a0001c0002t0002g0083 a0001c0002t0002g0205 others(1): Show |
4 | HG00423.hp1 NA18963.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.2242-1749G>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129580182 | |||||||
chr3:129580235 | G | A | 2 | a0001c0002t0002g0008 a0001c0002t0002g0096 |
5 | HG02080.hp2 HG02083.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.2242-1802C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129580235 | |||||||
chr3:129580236 | G | GC | 76 | a0001c0001t0001g0062 a0001c0001t0001g0266 a0001c0011t0001g0015 others(73): Show |
107 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.2242-1804dupG | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129580236 | |||||||
chr3:129580422 | G | A | 12 | a0001c0001t0001g0062 a0001c0001t0001g0266 a0003c0010t0001g0020 others(9): Show |
15 | HG01099.hp1 HG01257.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.2242-1989C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129580422 | |||||||
chr3:129580438 | T | C | 110 | a0001c0001t0001g0062 a0001c0001t0001g0266 a0001c0011t0001g0015 others(107): Show |
146 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.2242-2005A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129580438 | |||||||
chr3:129580560 | G | C | 1 | a0004c0005t0001g0301 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2242-2127C>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129580560 | |||||||
chr3:129580715 | T | C | 283 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(280): Show |
373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.2242-2282A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129580715 | |||||||
chr3:129580745 | G | A | 6 | a0004c0005t0001g0243 a0004c0005t0001g0250 a0015c0027t0001g0201 others(3): Show |
6 | NA18974.hp2 NA18977.hp2 NA18988.hp2 others(3): Show |
intron_variant | MODIFIER | c.2242-2312C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129580745 | |||||||
chr3:129581039 | T | C | 235 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(232): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.2241+2528A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129581039 | |||||||
chr3:129581039 | T | G | 76 | a0001c0001t0001g0062 a0001c0001t0001g0266 a0001c0011t0001g0015 others(73): Show |
107 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.2241+2528A>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129581039 | |||||||
chr3:129581055 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2241+2512C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129581055 | |||||||
chr3:129581316 | C | A | 76 | a0001c0001t0001g0062 a0001c0001t0001g0266 a0001c0011t0001g0015 others(73): Show |
107 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.2241+2251G>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129581316 | |||||||
chr3:129581333 | C | T | 3 | a0005c0016t0001g0022 a0005c0016t0001g0309 a0005c0016t0001g0310 |
5 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2241+2234G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129581333 | |||||||
chr3:129581446 | C | T | 2 | a0002c0003t0003g0235 a0002c0004t0001g0289 |
2 | HG01884.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.2241+2121G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129581446 | |||||||
chr3:129581448 | A | C | 97 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(94): Show |
131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.2241+2119T>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129581448 | |||||||
chr3:129581464 | AGAAATCC others(7): Show |
A | 1 | a0001c0001t0001g0129 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2241+2089_2241+210 others(18): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129581464 | |||||||
chr3:129581733 | T | C | 3 | a0005c0016t0001g0022 a0005c0016t0001g0309 a0005c0016t0001g0310 |
5 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2241+1834A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129581733 | |||||||
chr3:129581760 | G | A | 1 | a0026c0063t0001g0121 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2241+1807C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129581760 | |||||||
chr3:129581820 | C | T | 1 | a0026c0063t0001g0121 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2241+1747G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129581820 | |||||||
chr3:129581864 | C | A | 110 | a0001c0001t0001g0062 a0001c0001t0001g0266 a0001c0011t0001g0015 others(107): Show |
146 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.2241+1703G>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129581864 | |||||||
chr3:129581909 | A | G | 76 | a0001c0001t0001g0062 a0001c0001t0001g0266 a0001c0011t0001g0015 others(73): Show |
107 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.2241+1658T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129581909 | |||||||
chr3:129581990 | G | GGAGCAGG others(19): Show |
1 | a0038c0034t0003g0210 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2241+1551_2241+157 others(30): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129581990 | |||||||
chr3:129581997 | G | A | 31 | a0004c0005t0001g0019 a0004c0005t0001g0053 a0004c0005t0001g0193 others(28): Show |
34 | HG00408.hp2 HG00639.hp2 HG01981.hp2 others(31): Show |
intron_variant | MODIFIER | c.2241+1570C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129581997 | |||||||
chr3:129582024 | A | G | 76 | a0001c0001t0001g0062 a0001c0001t0001g0266 a0001c0011t0001g0015 others(73): Show |
107 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.2241+1543T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129582024 | |||||||
chr3:129582056 | G | A | 1 | a0004c0005t0001g0245 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2241+1511C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129582056 | |||||||
chr3:129582090 | C | T | 76 | a0001c0001t0001g0062 a0001c0001t0001g0266 a0001c0011t0001g0015 others(73): Show |
107 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.2241+1477G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129582090 | |||||||
chr3:129582315 | A | G | 1 | a0001c0054t0002g0285 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2241+1252T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129582315 | |||||||
chr3:129582428 | T | C | 3 | a0005c0016t0001g0022 a0005c0016t0001g0309 a0005c0016t0001g0310 |
5 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2241+1139A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129582428 | |||||||
chr3:129582522 | C | T | 2 | a0001c0001t0001g0258 a0039c0055t0001g0174 |
2 | NA18957.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.2241+1045G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129582522 | |||||||
chr3:129582543 | G | C | 2 | a0007c0021t0002g0023 a0007c0021t0004g0068 |
3 | HG01243.hp1 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2241+1024C>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129582543 | |||||||
chr3:129582575 | CCCTGGCA others(7): Show |
C | 1 | a0001c0054t0002g0285 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2241+978_2241+991d others(16): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129582575 | |||||||
chr3:129582608 | C | T | 1 | a0003c0008t0004g0176 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2241+959G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129582608 | |||||||
chr3:129582705 | G | A | 1 | a0001c0073t0001g0092 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2241+862C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129582705 | |||||||
chr3:129582726 | A | G | 3 | a0005c0016t0001g0022 a0005c0016t0001g0309 a0005c0016t0001g0310 |
5 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2241+841T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129582726 | |||||||
chr3:129583031 | G | A | 77 | a0001c0001t0001g0062 a0001c0001t0001g0187 a0001c0001t0001g0266 others(74): Show |
108 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.2241+536C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129583031 | |||||||
chr3:129583102 | T | G | 31 | a0004c0005t0001g0019 a0004c0005t0001g0053 a0004c0005t0001g0193 others(28): Show |
34 | HG00408.hp2 HG00639.hp2 HG01981.hp2 others(31): Show |
intron_variant | MODIFIER | c.2241+465A>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129583102 | |||||||
chr3:129583277 | T | C | 3 | a0005c0016t0001g0022 a0005c0016t0001g0309 a0005c0016t0001g0310 |
5 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2241+290A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129583277 | |||||||
chr3:129583316 | G | A | 31 | a0004c0005t0001g0019 a0004c0005t0001g0053 a0004c0005t0001g0193 others(28): Show |
34 | HG00408.hp2 HG00639.hp2 HG01981.hp2 others(31): Show |
intron_variant | MODIFIER | c.2241+251C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129583316 | |||||||
chr3:129583418 | C | T | 3 | a0005c0016t0001g0022 a0005c0016t0001g0309 a0005c0016t0001g0310 |
5 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2241+149G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129583418 | |||||||
chr3:129583424 | G | A | 1 | a0010c0036t0005g0269 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2241+143C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 8/35 | chr3 | 129583424 | |||||||
chr3:129583786 | G | A | 63 | a0001c0002t0002g0005 a0001c0002t0002g0008 a0001c0002t0002g0016 others(60): Show |
80 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.2139-117C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 7/35 | chr3 | 129583786 | |||||||
chr3:129584029 | T | C | 1 | a0001c0001t0001g0169 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2138+96A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 7/35 | chr3 | 129584029 | |||||||
chr3:129584049 | C | G | 2 | a0006c0023t0001g0137 a0006c0023t0001g0143 |
2 | HG02257.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2138+76G>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 7/35 | chr3 | 129584049 | |||||||
chr3:129584055 | A | G | 1 | a0002c0004t0001g0289 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2138+70T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 7/35 | chr3 | 129584055 | |||||||
chr3:129584354 | T | C | 309 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(306): Show |
412 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(409): Show |
intron_variant | MODIFIER | c.2029+31A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 6/35 | chr3 | 129584354 | |||||||
chr3:129584355 | G | A | 1 | a0002c0004t0001g0289 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2029+30C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 6/35 | chr3 | 129584355 | |||||||
chr3:129584593 | T | G | 133 | a0001c0001t0001g0062 a0001c0001t0001g0266 a0001c0002t0002g0005 others(130): Show |
179 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.1852-31A>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 5/35 | chr3 | 129584593 | |||||||
chr3:129584645 | C | G | 63 | a0001c0002t0002g0005 a0001c0002t0002g0008 a0001c0002t0002g0016 others(60): Show |
80 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.1852-83G>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 5/35 | chr3 | 129584645 | |||||||
chr3:129584660 | T | A | 2 | a0010c0035t0005g0270 a0010c0036t0005g0269 |
2 | HG02486.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1852-98A>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 5/35 | chr3 | 129584660 | |||||||
chr3:129584729 | T | A | 31 | a0004c0005t0001g0019 a0004c0005t0001g0053 a0004c0005t0001g0193 others(28): Show |
34 | HG00408.hp2 HG00639.hp2 HG01981.hp2 others(31): Show |
intron_variant | MODIFIER | c.1852-167A>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 5/35 | chr3 | 129584729 | |||||||
chr3:129584742 | T | G | 1 | a0002c0015t0006g0120 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1852-180A>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 5/35 | chr3 | 129584742 | |||||||
chr3:129584901 | G | A | 167 | a0001c0001t0001g0062 a0001c0001t0001g0266 a0001c0002t0002g0005 others(164): Show |
218 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.1852-339C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 5/35 | chr3 | 129584901 | |||||||
chr3:129584989 | C | T | 3 | a0005c0016t0001g0022 a0005c0016t0001g0309 a0005c0016t0001g0310 |
5 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1852-427G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 5/35 | chr3 | 129584989 | |||||||
chr3:129585081 | G | A | 1 | a0001c0002t0002g0109 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1852-519C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 5/35 | chr3 | 129585081 | |||||||
chr3:129585139 | G | A | 1 | a0002c0012t0001g0283 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1852-577C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 5/35 | chr3 | 129585139 | |||||||
chr3:129585207 | A | G | 7 | a0002c0006t0001g0010 a0002c0006t0001g0122 a0002c0015t0006g0116 others(4): Show |
10 | HG01109.hp2 HG02055.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1852-645T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 5/35 | chr3 | 129585207 | |||||||
chr3:129585380 | G | A | 2 | a0001c0001t0001g0152 a0001c0050t0001g0148 |
2 | HG01106.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1851+572C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 5/35 | chr3 | 129585380 | |||||||
chr3:129585407 | G | A | 31 | a0004c0005t0001g0019 a0004c0005t0001g0053 a0004c0005t0001g0193 others(28): Show |
34 | HG00408.hp2 HG00639.hp2 HG01981.hp2 others(31): Show |
intron_variant | MODIFIER | c.1851+545C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 5/35 | chr3 | 129585407 | |||||||
chr3:129585463 | G | A | 63 | a0001c0002t0002g0005 a0001c0002t0002g0008 a0001c0002t0002g0016 others(60): Show |
80 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.1851+489C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 5/35 | chr3 | 129585463 | |||||||
chr3:129585472 | T | C | 48 | a0001c0011t0001g0211 a0001c0011t0001g0214 a0001c0013t0003g0014 others(45): Show |
68 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.1851+480A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 5/35 | chr3 | 129585472 | |||||||
chr3:129585502 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1851+450G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 5/35 | chr3 | 129585502 | |||||||
chr3:129585607 | C | G | 31 | a0004c0005t0001g0019 a0004c0005t0001g0053 a0004c0005t0001g0193 others(28): Show |
34 | HG00408.hp2 HG00639.hp2 HG01981.hp2 others(31): Show |
intron_variant | MODIFIER | c.1851+345G>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 5/35 | chr3 | 129585607 | |||||||
chr3:129586391 | A | G | 2 | a0001c0078t0011g0308 a0002c0079t0011g0307 |
2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1621-119T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 3/35 | chr3 | 129586391 | |||||||
chr3:129586450 | A | G | 2 | a0005c0016t0001g0022 a0005c0016t0001g0310 |
4 | HG02109.hp1 HG02280.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1620+138T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 3/35 | chr3 | 129586450 | |||||||
chr3:129586476 | G | C | 1 | a0003c0008t0004g0017 | 3 | HG01123.hp2 HG01175.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1620+112C>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 3/35 | chr3 | 129586476 | |||||||
chr3:129586527 | C | T | 1 | a0001c0001t0001g0155 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1620+61G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 3/35 | chr3 | 129586527 | |||||||
chr3:129586558 | G | A | 2 | a0001c0001t0001g0184 a0001c0050t0001g0148 |
2 | HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1620+30C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 3/35 | chr3 | 129586558 | |||||||
chr3:129586727 | G | C | 1 | a0001c0001t0001g0185 | 1 | NA18945.hp2 | splice_region_variant&intron_variant | LOW | c.1489-8C>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129586727 | |||||||
chr3:129586756 | T | C | 3 | a0002c0003t0003g0222 a0002c0003t0003g0235 a0002c0048t0003g0223 |
3 | NA18999.hp2 NA19009.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1489-37A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129586756 | |||||||
chr3:129586779 | G | A | 1 | a0002c0004t0001g0138 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1489-60C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129586779 | |||||||
chr3:129586863 | A | C | 1 | a0003c0010t0001g0047 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1489-144T>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129586863 | |||||||
chr3:129586989 | C | T | 3 | a0005c0016t0001g0022 a0005c0016t0001g0309 a0005c0016t0001g0310 |
5 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1489-270G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129586989 | |||||||
chr3:129586995 | C | G | 1 | a0001c0001t0013g0146 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1489-276G>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129586995 | |||||||
chr3:129587076 | T | C | 63 | a0001c0002t0002g0005 a0001c0002t0002g0008 a0001c0002t0002g0016 others(60): Show |
80 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.1489-357A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129587076 | |||||||
chr3:129587189 | G | T | 1 | a0001c0001t0001g0297 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1489-470C>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129587189 | |||||||
chr3:129587222 | C | A | 2 | a0003c0010t0001g0020 a0003c0010t0001g0267 |
4 | HG02602.hp2 HG03017.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.1489-503G>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129587222 | |||||||
chr3:129587222 | C | G | 70 | a0001c0001t0001g0062 a0001c0001t0001g0266 a0001c0002t0002g0093 others(67): Show |
97 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(94): Show |
intron_variant | MODIFIER | c.1489-503G>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129587222 | |||||||
chr3:129587224 | G | C | 167 | a0001c0001t0001g0062 a0001c0001t0001g0113 a0001c0001t0001g0114 others(164): Show |
217 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(214): Show |
intron_variant | MODIFIER | c.1489-505C>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129587224 | |||||||
chr3:129587361 | G | A | 63 | a0001c0002t0002g0005 a0001c0002t0002g0008 a0001c0002t0002g0016 others(60): Show |
80 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.1489-642C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129587361 | |||||||
chr3:129587366 | T | C | 1 | a0002c0004t0001g0149 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1489-647A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129587366 | |||||||
chr3:129587437 | C | A | 70 | a0001c0001t0001g0062 a0001c0001t0001g0266 a0001c0011t0001g0015 others(67): Show |
99 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.1489-718G>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129587437 | |||||||
chr3:129587470 | G | A | 2 | a0002c0004t0001g0125 a0002c0004t0001g0126 |
2 | HG02735.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1489-751C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129587470 | |||||||
chr3:129587498 | T | C | 3 | a0005c0016t0001g0022 a0005c0016t0001g0309 a0005c0016t0001g0310 |
5 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1489-779A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129587498 | |||||||
chr3:129587648 | T | C | 2 | a0006c0023t0001g0137 a0006c0023t0001g0143 |
2 | HG02257.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1489-929A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129587648 | |||||||
chr3:129587686 | C | T | 1 | a0004c0005t0001g0244 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1489-967G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129587686 | |||||||
chr3:129587968 | C | T | 1 | a0002c0003t0003g0206 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1489-1249G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129587968 | |||||||
chr3:129587971 | A | AC | 146 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(143): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.1489-1253dupG | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129587971 | |||||||
chr3:129588050 | C | T | 70 | a0001c0001t0001g0062 a0001c0001t0001g0266 a0001c0011t0001g0015 others(67): Show |
99 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.1488+1301G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129588050 | |||||||
chr3:129588172 | A | G | 307 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(304): Show |
408 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(405): Show |
intron_variant | MODIFIER | c.1488+1179T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129588172 | |||||||
chr3:129588277 | G | A | 1 | a0024c0038t0001g0242 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1488+1074C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129588277 | |||||||
chr3:129588348 | C | T | 63 | a0001c0002t0002g0005 a0001c0002t0002g0008 a0001c0002t0002g0016 others(60): Show |
80 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.1488+1003G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129588348 | |||||||
chr3:129588412 | A | T | 1 | a0001c0002t0002g0103 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1488+939T>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129588412 | |||||||
chr3:129588428 | GC | G | 63 | a0001c0002t0002g0005 a0001c0002t0002g0008 a0001c0002t0002g0016 others(60): Show |
80 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.1488+922delG | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129588428 | |||||||
chr3:129588471 | TGTGA | T | 161 | a0001c0001t0001g0062 a0001c0001t0001g0266 a0001c0002t0002g0005 others(158): Show |
209 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(206): Show |
intron_variant | MODIFIER | c.1488+876_1488+879d others(6): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129588471 | |||||||
chr3:129588560 | A | G | 2 | a0006c0023t0001g0137 a0006c0023t0001g0143 |
2 | HG02257.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1488+791T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129588560 | |||||||
chr3:129588609 | G | C | 5 | a0002c0004t0001g0289 a0002c0006t0001g0007 a0002c0006t0001g0271 others(2): Show |
9 | HG01255.hp1 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1488+742C>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129588609 | |||||||
chr3:129588645 | G | C | 1 | a0001c0001t0001g0152 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1488+706C>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129588645 | |||||||
chr3:129588658 | G | A | 1 | a0002c0003t0003g0208 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1488+693C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129588658 | |||||||
chr3:129588803 | C | T | 69 | a0001c0001t0001g0062 a0001c0001t0001g0266 a0001c0011t0001g0015 others(66): Show |
98 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.1488+548G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129588803 | |||||||
chr3:129588814 | C | T | 3 | a0010c0035t0005g0270 a0010c0036t0005g0269 a0019c0066t0014g0272 |
3 | HG02257.hp1 HG02486.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1488+537G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129588814 | |||||||
chr3:129588884 | G | C | 1 | a0003c0010t0001g0047 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1488+467C>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129588884 | |||||||
chr3:129588969 | G | A | 8 | a0002c0006t0001g0010 a0002c0006t0001g0122 a0002c0015t0006g0116 others(5): Show |
11 | HG01109.hp2 HG02055.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1488+382C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129588969 | |||||||
chr3:129589114 | T | G | 63 | a0001c0002t0002g0005 a0001c0002t0002g0008 a0001c0002t0002g0016 others(60): Show |
80 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.1488+237A>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129589114 | |||||||
chr3:129589149 | T | C | 306 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(303): Show |
407 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(404): Show |
intron_variant | MODIFIER | c.1488+202A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129589149 | |||||||
chr3:129589253 | G | A | 143 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(140): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.1488+98C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 2/35 | chr3 | 129589253 | |||||||
chr3:129589545 | C | T | 1 | a0002c0004t0001g0274 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1312-18G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129589545 | |||||||
chr3:129589582 | G | A | 31 | a0001c0078t0011g0308 a0002c0079t0011g0307 a0003c0010t0001g0047 others(28): Show |
34 | HG00408.hp2 HG00639.hp2 HG01257.hp1 others(31): Show |
intron_variant | MODIFIER | c.1312-55C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129589582 | |||||||
chr3:129589594 | G | A | 1 | a0001c0001t0001g0035 | 2 | HG01070.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1312-67C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129589594 | |||||||
chr3:129589654 | A | C | 31 | a0001c0078t0011g0308 a0002c0079t0011g0307 a0003c0010t0001g0047 others(28): Show |
34 | HG00408.hp2 HG00639.hp2 HG01257.hp1 others(31): Show |
intron_variant | MODIFIER | c.1312-127T>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129589654 | |||||||
chr3:129589874 | T | C | 307 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(304): Show |
408 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(405): Show |
intron_variant | MODIFIER | c.1312-347A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129589874 | |||||||
chr3:129589900 | G | A | 2 | a0001c0001t0001g0170 a0001c0001t0001g0190 |
2 | NA18990.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1312-373C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129589900 | |||||||
chr3:129590041 | C | A | 1 | a0002c0003t0003g0224 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1312-514G>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129590041 | |||||||
chr3:129590062 | G | T | 1 | a0001c0054t0002g0285 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1312-535C>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129590062 | |||||||
chr3:129590083 | A | C | 1 | a0002c0003t0003g0227 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1312-556T>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129590083 | |||||||
chr3:129590304 | G | A | 69 | a0001c0001t0001g0062 a0001c0001t0001g0266 a0001c0011t0001g0015 others(66): Show |
97 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(94): Show |
intron_variant | MODIFIER | c.1312-777C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129590304 | |||||||
chr3:129590304 | G | C | 143 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(140): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.1312-777C>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129590304 | |||||||
chr3:129590307 | CT | C | 144 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(141): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.1312-781delA | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129590307 | |||||||
chr3:129590349 | G | A | 1 | a0001c0001t0001g0171 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1312-822C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129590349 | |||||||
chr3:129590420 | T | C | 144 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(141): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.1312-893A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129590420 | |||||||
chr3:129590442 | C | T | 1 | a0004c0005t0001g0239 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1312-915G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129590442 | |||||||
chr3:129590558 | C | T | 2 | a0002c0004t0001g0052 a0002c0004t0001g0293 |
3 | HG00738.hp2 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1312-1031G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129590558 | |||||||
chr3:129590607 | T | C | 1 | a0001c0002t0002g0204 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1312-1080A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129590607 | |||||||
chr3:129590612 | G | A | 62 | a0001c0001t0001g0062 a0001c0001t0001g0266 a0001c0011t0001g0211 others(59): Show |
84 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.1312-1085C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129590612 | |||||||
chr3:129590735 | C | A | 1 | a0005c0016t0001g0309 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1312-1208G>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129590735 | |||||||
chr3:129590746 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1312-1219C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129590746 | |||||||
chr3:129591018 | C | CAA | 307 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(304): Show |
408 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(405): Show |
intron_variant | MODIFIER | c.1312-1492_1312-149 others(6): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129591018 | |||||||
chr3:129591044 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1312-1517C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129591044 | |||||||
chr3:129591059 | T | C | 1 | a0005c0016t0001g0309 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1312-1532A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129591059 | |||||||
chr3:129591102 | G | A | 6 | a0001c0011t0001g0015 a0001c0064t0001g0261 a0003c0018t0005g0048 others(3): Show |
10 | HG02258.hp1 HG02622.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.1312-1575C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129591102 | |||||||
chr3:129591222 | C | T | 1 | a0002c0006t0001g0271 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1312-1695G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129591222 | |||||||
chr3:129591241 | G | A | 2 | a0001c0002t0002g0093 a0001c0002t0002g0100 |
2 | HG01993.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.1312-1714C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129591241 | |||||||
chr3:129591348 | C | T | 63 | a0001c0002t0002g0005 a0001c0002t0002g0008 a0001c0002t0002g0016 others(60): Show |
80 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.1312-1821G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129591348 | |||||||
chr3:129591350 | C | T | 3 | a0002c0003t0003g0045 a0002c0003t0003g0233 a0038c0034t0003g0210 |
4 | HG00621.hp1 HG02056.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.1312-1823G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129591350 | |||||||
chr3:129591353 | G | A | 2 | a0001c0001t0001g0151 a0001c0001t0001g0152 |
2 | HG01106.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.1312-1826C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129591353 | |||||||
chr3:129591431 | G | C | 2 | a0001c0001t0008g0036 a0001c0001t0008g0172 |
3 | HG00639.hp1 HG02735.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1312-1904C>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129591431 | |||||||
chr3:129591437 | A | G | 3 | a0004c0005t0001g0053 a0004c0005t0001g0299 a0004c0005t0001g0300 |
4 | NA18943.hp2 NA18946.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.1312-1910T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129591437 | |||||||
chr3:129591524 | G | A | 4 | a0004c0005t0001g0241 a0004c0005t0001g0254 a0004c0005t0001g0256 others(1): Show |
4 | HG00408.hp2 HG03927.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.1312-1997C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129591524 | |||||||
chr3:129591562 | A | G | 29 | a0003c0010t0001g0047 a0004c0005t0001g0019 a0004c0005t0001g0193 others(26): Show |
32 | HG00408.hp2 HG00639.hp2 HG01257.hp1 others(29): Show |
intron_variant | MODIFIER | c.1312-2035T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129591562 | |||||||
chr3:129591799 | C | T | 1 | a0006c0047t0001g0263 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1312-2272G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129591799 | |||||||
chr3:129591856 | C | G | 1 | a0003c0008t0004g0296 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1312-2329G>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129591856 | |||||||
chr3:129592057 | C | A | 1 | a0030c0039t0001g0255 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1312-2530G>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129592057 | |||||||
chr3:129592068 | C | T | 2 | a0003c0008t0004g0295 a0003c0008t0004g0296 |
2 | HG01168.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.1312-2541G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129592068 | |||||||
chr3:129592109 | C | G | 3 | a0002c0003t0003g0045 a0002c0006t0001g0271 a0033c0041t0001g0238 |
4 | HG00621.hp1 HG02132.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1312-2582G>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129592109 | |||||||
chr3:129592375 | A | T | 1 | a0002c0004t0001g0154 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1312-2848T>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129592375 | |||||||
chr3:129592380 | T | G | 29 | a0003c0010t0001g0047 a0004c0005t0001g0019 a0004c0005t0001g0193 others(26): Show |
32 | HG00408.hp2 HG00639.hp2 HG01257.hp1 others(29): Show |
intron_variant | MODIFIER | c.1312-2853A>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129592380 | |||||||
chr3:129592569 | G | A | 2 | a0013c0025t0001g0153 a0013c0025t0001g0257 |
2 | NA18951.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.1312-3042C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129592569 | |||||||
chr3:129592651 | T | C | 1 | a0001c0002t0012g0094 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1312-3124A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129592651 | |||||||
chr3:129592686 | T | C | 63 | a0001c0001t0001g0266 a0001c0011t0001g0015 a0001c0011t0001g0211 others(60): Show |
89 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.1312-3159A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129592686 | |||||||
chr3:129592721 | A | G | 2 | a0002c0015t0006g0116 a0002c0015t0006g0145 |
2 | HG02145.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1312-3194T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129592721 | |||||||
chr3:129592725 | T | A | 149 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(146): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.1312-3198A>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129592725 | |||||||
chr3:129592773 | G | A | 60 | a0001c0002t0002g0005 a0001c0002t0002g0008 a0001c0002t0002g0016 others(57): Show |
76 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.1312-3246C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129592773 | |||||||
chr3:129592839 | C | T | 1 | a0001c0002t0002g0096 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1312-3312G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129592839 | |||||||
chr3:129592959 | G | A | 3 | a0001c0001t0001g0037 a0001c0001t0001g0173 a0002c0004t0001g0188 |
4 | NA18980.hp1 NA18986.hp2 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1312-3432C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129592959 | |||||||
chr3:129592977 | C | T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0144 |
5 | HG00099.hp1 HG01123.hp1 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.1312-3450G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129592977 | |||||||
chr3:129593034 | G | C | 2 | a0002c0006t0001g0007 a0002c0006t0001g0291 |
6 | HG01255.hp1 HG02055.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1312-3507C>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129593034 | |||||||
chr3:129593135 | C | T | 63 | a0001c0002t0002g0005 a0001c0002t0002g0008 a0001c0002t0002g0016 others(60): Show |
80 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.1312-3608G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129593135 | |||||||
chr3:129593161 | C | T | 6 | a0001c0011t0001g0015 a0001c0064t0001g0261 a0003c0018t0005g0048 others(3): Show |
10 | HG02258.hp1 HG02622.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.1312-3634G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129593161 | |||||||
chr3:129593169 | T | C | 307 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(304): Show |
408 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(405): Show |
intron_variant | MODIFIER | c.1312-3642A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129593169 | |||||||
chr3:129593264 | C | T | 1 | a0003c0014t0004g0290 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1312-3737G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129593264 | |||||||
chr3:129593433 | G | A | 1 | a0017c0071t0002g0095 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1312-3906C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129593433 | |||||||
chr3:129593495 | G | A | 1 | a0003c0007t0001g0101 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1312-3968C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129593495 | |||||||
chr3:129593588 | C | G | 149 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(146): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.1312-4061G>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129593588 | |||||||
chr3:129593845 | C | T | 1 | a0024c0038t0001g0242 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1312-4318G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129593845 | |||||||
chr3:129593858 | G | A | 2 | a0001c0001t0001g0258 a0039c0055t0001g0174 |
2 | NA18957.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.1312-4331C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129593858 | |||||||
chr3:129594059 | C | T | 1 | a0004c0005t0001g0245 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1312-4532G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129594059 | |||||||
chr3:129594138 | G | A | 63 | a0001c0002t0002g0005 a0001c0002t0002g0008 a0001c0002t0002g0016 others(60): Show |
80 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.1312-4611C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129594138 | |||||||
chr3:129594146 | A | G | 156 | a0001c0001t0001g0266 a0001c0002t0002g0005 a0001c0002t0002g0008 others(153): Show |
202 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(199): Show |
intron_variant | MODIFIER | c.1312-4619T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129594146 | |||||||
chr3:129594384 | G | A | 1 | a0002c0058t0009g0119 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1312-4857C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129594384 | |||||||
chr3:129594387 | C | T | 1 | a0001c0001t0001g0273 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1312-4860G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129594387 | |||||||
chr3:129594478 | T | A | 1 | a0002c0003t0003g0225 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1312-4951A>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129594478 | |||||||
chr3:129594530 | T | C | 1 | a0001c0002t0002g0072 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1312-5003A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129594530 | |||||||
chr3:129594564 | C | T | 1 | a0001c0002t0002g0070 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1312-5037G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129594564 | |||||||
chr3:129594566 | T | C | 1 | a0001c0002t0002g0070 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1312-5039A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129594566 | |||||||
chr3:129594567 | C | T | 1 | a0001c0002t0002g0070 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1312-5040G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129594567 | |||||||
chr3:129594586 | C | A | 1 | a0015c0027t0001g0195 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1312-5059G>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129594586 | |||||||
chr3:129594595 | C | A | 1 | a0002c0003t0003g0207 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1312-5068G>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129594595 | |||||||
chr3:129594646 | A | G | 307 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(304): Show |
408 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(405): Show |
intron_variant | MODIFIER | c.1312-5119T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129594646 | |||||||
chr3:129594661 | A | G | 1 | a0008c0024t0004g0139 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1312-5134T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129594661 | |||||||
chr3:129594662 | G | A | 1 | a0008c0024t0004g0139 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1312-5135C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129594662 | |||||||
chr3:129594678 | G | A | 1 | a0004c0019t0004g0251 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1312-5151C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129594678 | |||||||
chr3:129594707 | A | G | 1 | a0003c0008t0004g0038 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1312-5180T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129594707 | |||||||
chr3:129594754 | C | T | 1 | a0001c0002t0002g0071 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1312-5227G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129594754 | |||||||
chr3:129594788 | C | T | 2 | a0002c0006t0001g0010 a0002c0006t0001g0122 |
5 | HG01109.hp2 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1312-5261G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129594788 | |||||||
chr3:129594806 | C | G | 1 | a0003c0014t0004g0294 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1312-5279G>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129594806 | |||||||
chr3:129594869 | T | TA | 8 | a0001c0001t0001g0175 a0001c0001t0001g0191 a0001c0002t0002g0070 others(5): Show |
8 | HG01192.hp1 HG01884.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.1312-5343dupT | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129594869 | |||||||
chr3:129594869 | T | TAA | 146 | a0001c0001t0001g0266 a0001c0002t0002g0005 a0001c0002t0002g0008 others(143): Show |
192 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.1312-5344_1312-534 others(6): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129594869 | |||||||
chr3:129594869 | T | TAAA | 6 | a0001c0002t0002g0072 a0002c0003t0003g0207 a0002c0003t0003g0237 others(3): Show |
6 | HG03239.hp2 NA18954.hp2 NA19055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1312-5345_1312-534 others(7): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129594869 | |||||||
chr3:129594991 | A | G | 3 | a0001c0001t0001g0031 a0001c0001t0001g0141 a0002c0017t0007g0142 |
4 | HG00140.hp1 HG01258.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.1312-5464T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129594991 | |||||||
chr3:129595102 | G | GATGGGCT others(1): Show |
17 | a0001c0001t0001g0273 a0001c0001t0001g0275 a0001c0001t0001g0276 others(14): Show |
24 | HG00738.hp2 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.1312-5576_1312-557 others(12): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595102 | |||||||
chr3:129595104 | C | A | 17 | a0001c0001t0001g0273 a0001c0001t0001g0275 a0001c0001t0001g0276 others(14): Show |
24 | HG00738.hp2 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.1312-5577G>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595104 | |||||||
chr3:129595107 | T | TGG | 17 | a0001c0001t0001g0273 a0001c0001t0001g0275 a0001c0001t0001g0276 others(14): Show |
24 | HG00738.hp2 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.1312-5581_1312-558 others(6): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595107 | |||||||
chr3:129595189 | T | G | 3 | a0007c0021t0002g0023 a0007c0021t0004g0068 a0036c0068t0002g0069 |
4 | HG01243.hp1 HG03579.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1312-5662A>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595189 | |||||||
chr3:129595242 | T | C | 307 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(304): Show |
408 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(405): Show |
intron_variant | MODIFIER | c.1312-5715A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595242 | |||||||
chr3:129595345 | C | T | 1 | a0002c0004t0001g0125 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1312-5818G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595345 | |||||||
chr3:129595416 | T | A | 1 | a0002c0003t0003g0207 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1312-5889A>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595416 | |||||||
chr3:129595416 | T | G | 153 | a0001c0001t0001g0266 a0001c0002t0002g0005 a0001c0002t0002g0008 others(150): Show |
199 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(196): Show |
intron_variant | MODIFIER | c.1312-5889A>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595416 | |||||||
chr3:129595427 | G | A | 6 | a0003c0008t0004g0038 a0003c0008t0004g0039 a0003c0008t0004g0176 others(3): Show |
8 | HG00323.hp1 HG00642.hp2 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.1312-5900C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595427 | |||||||
chr3:129595546 | G | C | 1 | a0002c0012t0001g0283 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1312-6019C>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595546 | |||||||
chr3:129595596 | G | A | 62 | a0001c0001t0001g0266 a0001c0011t0001g0015 a0001c0011t0001g0211 others(59): Show |
88 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.1312-6069C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595596 | |||||||
chr3:129595654 | A | G | 1 | a0003c0007t0001g0102 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1312-6127T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595654 | |||||||
chr3:129595916 | C | T | 2 | a0001c0078t0011g0308 a0002c0079t0011g0307 |
2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1312-6389G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595916 | |||||||
chr3:129595919 | A | ACG | 2 | a0007c0021t0002g0023 a0007c0021t0004g0068 |
3 | HG01243.hp1 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1312-6394_1312-639 others(6): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595919 | |||||||
chr3:129595921 | G | GCA | 19 | a0002c0003t0003g0209 a0003c0010t0001g0047 a0004c0005t0001g0193 others(16): Show |
20 | HG00639.hp2 HG01257.hp1 HG01258.hp2 others(17): Show |
intron_variant | MODIFIER | c.1312-6396_1312-639 others(6): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595921 | |||||||
chr3:129595921 | G | GCACA | 22 | a0001c0001t0001g0141 a0001c0001t0001g0266 a0001c0011t0001g0015 others(19): Show |
31 | HG00408.hp2 HG00673.hp1 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.1312-6398_1312-639 others(8): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595921 | |||||||
chr3:129595921 | G | GCACACA | 34 | a0001c0011t0001g0211 a0001c0011t0001g0214 a0001c0013t0003g0014 others(31): Show |
49 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.1312-6400_1312-639 others(10): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595921 | |||||||
chr3:129595921 | G | GCACACAC others(1): Show |
63 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0029 others(60): Show |
92 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(89): Show |
intron_variant | MODIFIER | c.1312-6402_1312-639 others(12): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595921 | |||||||
chr3:129595921 | G | GCACACAC others(3): Show |
73 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0011 others(70): Show |
101 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.1312-6404_1312-639 others(14): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595921 | |||||||
chr3:129595921 | G | GCACACAC others(5): Show |
19 | a0001c0001t0001g0040 a0001c0001t0001g0064 a0001c0001t0001g0135 others(16): Show |
20 | HG00597.hp1 HG01255.hp2 HG02056.hp2 others(17): Show |
intron_variant | MODIFIER | c.1312-6406_1312-639 others(16): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595921 | |||||||
chr3:129595921 | G | GCACACAC others(7): Show |
1 | a0001c0001t0001g0192 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1312-6408_1312-639 others(18): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595921 | |||||||
chr3:129595921 | G | GCACACAC others(9): Show |
1 | a0001c0054t0002g0285 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1312-6410_1312-639 others(20): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595921 | |||||||
chr3:129595921 | G | GCACACAC others(11): Show |
2 | a0001c0020t0001g0131 a0002c0058t0009g0119 |
2 | HG00735.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1312-6412_1312-639 others(22): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595921 | |||||||
chr3:129595921 | G | GCACGCAC others(5): Show |
1 | a0002c0079t0011g0307 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1312-6395_1312-639 others(16): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595921 | |||||||
chr3:129595921 | G | GCACGCAC others(7): Show |
1 | a0001c0078t0011g0308 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1312-6395_1312-639 others(18): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595921 | |||||||
chr3:129595921 | G | GCCACACA others(4): Show |
1 | a0001c0001t0001g0179 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1312-6395_1312-639 others(15): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595921 | |||||||
chr3:129595921 | G | GCGCACA | 3 | a0001c0002t0002g0074 a0020c0072t0002g0073 a0037c0069t0002g0075 |
3 | HG02523.hp2 NA19055.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1312-6395_1312-639 others(10): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595921 | |||||||
chr3:129595921 | G | GCGCACAC others(1): Show |
2 | a0001c0002t0002g0008 a0001c0002t0002g0111 |
5 | HG02080.hp2 HG03669.hp1 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.1312-6395_1312-639 others(12): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595921 | |||||||
chr3:129595921 | G | GCGCACAC others(3): Show |
5 | a0001c0002t0002g0061 a0001c0002t0002g0077 a0001c0002t0002g0109 others(2): Show |
5 | HG00438.hp1 NA18944.hp2 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.1312-6395_1312-639 others(14): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595921 | |||||||
chr3:129595921 | G | GCGCACAC others(5): Show |
4 | a0001c0002t0002g0078 a0001c0002t0002g0080 a0001c0002t0002g0081 others(1): Show |
4 | HG00423.hp1 HG00642.hp1 HG02129.hp2 others(1): Show |
intron_variant | MODIFIER | c.1312-6395_1312-639 others(16): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595921 | |||||||
chr3:129595921 | G | GCGCACAC others(7): Show |
18 | a0001c0002t0002g0005 a0001c0002t0002g0024 a0001c0002t0002g0067 others(15): Show |
24 | HG00597.hp2 HG00609.hp1 HG01346.hp2 others(21): Show |
intron_variant | MODIFIER | c.1312-6395_1312-639 others(18): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595921 | |||||||
chr3:129595921 | G | GCGCACAC others(9): Show |
11 | a0001c0002t0002g0016 a0001c0002t0002g0072 a0001c0002t0002g0096 others(8): Show |
17 | HG00280.hp1 HG00733.hp2 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.1312-6395_1312-639 others(20): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595921 | |||||||
chr3:129595921 | G | GCGCACAC others(11): Show |
10 | a0001c0002t0002g0065 a0001c0002t0002g0066 a0001c0002t0002g0103 others(7): Show |
11 | HG00140.hp2 HG01069.hp2 HG01517.hp2 others(8): Show |
intron_variant | MODIFIER | c.1312-6395_1312-639 others(22): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595921 | |||||||
chr3:129595921 | G | GCGCACAC others(13): Show |
1 | a0001c0002t0002g0205 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1312-6395_1312-639 others(24): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595921 | |||||||
chr3:129595921 | G | GCGCACAC others(15): Show |
2 | a0001c0002t0002g0110 a0001c0002t0002g0112 |
2 | NA18952.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1312-6395_1312-639 others(26): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595921 | |||||||
chr3:129595921 | G | GCGCGCAC others(7): Show |
1 | a0001c0002t0002g0071 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1312-6395_1312-639 others(18): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595921 | |||||||
chr3:129595921 | G | GCGCGCAC others(9): Show |
1 | a0001c0002t0002g0082 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1312-6395_1312-639 others(20): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595921 | |||||||
chr3:129595921 | G | GCGCGCAC others(17): Show |
1 | a0001c0002t0002g0107 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1312-6395_1312-639 others(28): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595921 | |||||||
chr3:129595921 | G | GCGCGCAC others(19): Show |
1 | a0001c0002t0002g0108 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1312-6395_1312-639 others(30): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595921 | |||||||
chr3:129595923 | A | G | 1 | a0001c0002t0002g0070 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1312-6396T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595923 | |||||||
chr3:129595946 | C | CACACACA others(7): Show |
1 | a0001c0002t0002g0070 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1312-6420_1312-641 others(18): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595946 | |||||||
chr3:129595949 | T | A | 152 | a0001c0001t0001g0266 a0001c0002t0002g0005 a0001c0002t0002g0008 others(149): Show |
198 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.1312-6422A>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129595949 | |||||||
chr3:129596024 | A | G | 307 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(304): Show |
408 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(405): Show |
intron_variant | MODIFIER | c.1312-6497T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129596024 | |||||||
chr3:129596052 | G | A | 12 | a0002c0004t0001g0289 a0002c0006t0001g0007 a0002c0006t0001g0271 others(9): Show |
18 | HG01255.hp1 HG01884.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1312-6525C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129596052 | |||||||
chr3:129596189 | G | C | 3 | a0007c0021t0002g0023 a0007c0021t0004g0068 a0036c0068t0002g0069 |
4 | HG01243.hp1 HG03579.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1312-6662C>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129596189 | |||||||
chr3:129596236 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1312-6709C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129596236 | |||||||
chr3:129596262 | C | G | 1 | a0004c0005t0001g0243 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1312-6735G>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129596262 | |||||||
chr3:129596294 | C | T | 1 | a0001c0002t0002g0072 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1312-6767G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129596294 | |||||||
chr3:129596301 | G | A | 1 | a0001c0001t0001g0187 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1312-6774C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129596301 | |||||||
chr3:129596408 | C | G | 1 | a0002c0015t0006g0120 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1312-6881G>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129596408 | |||||||
chr3:129596445 | C | A | 1 | a0002c0004t0001g0188 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1312-6918G>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129596445 | |||||||
chr3:129596453 | C | T | 17 | a0001c0001t0001g0273 a0001c0001t0001g0275 a0001c0001t0001g0276 others(14): Show |
24 | HG00738.hp2 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.1312-6926G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129596453 | |||||||
chr3:129596526 | T | A | 1 | a0001c0002t0002g0070 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1312-6999A>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129596526 | |||||||
chr3:129596624 | C | G | 2 | a0001c0078t0011g0308 a0002c0079t0011g0307 |
2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1312-7097G>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129596624 | |||||||
chr3:129596644 | G | A | 64 | a0001c0001t0001g0189 a0001c0002t0002g0005 a0001c0002t0002g0008 others(61): Show |
81 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.1312-7117C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129596644 | |||||||
chr3:129596735 | C | T | 2 | a0001c0001t0001g0030 a0032c0053t0001g0140 |
3 | NA18981.hp1 NA19066.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1312-7208G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129596735 | |||||||
chr3:129596736 | A | G | 307 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(304): Show |
408 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(405): Show |
intron_variant | MODIFIER | c.1312-7209T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129596736 | |||||||
chr3:129596738 | C | G | 1 | a0008c0024t0004g0139 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1312-7211G>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129596738 | |||||||
chr3:129596843 | A | T | 1 | a0002c0003t0003g0208 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1312-7316T>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129596843 | |||||||
chr3:129596886 | C | T | 1 | a0001c0002t0002g0071 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1312-7359G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129596886 | |||||||
chr3:129596887 | G | A | 1 | a0026c0063t0001g0121 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1312-7360C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129596887 | |||||||
chr3:129596926 | G | A | 151 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(148): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.1312-7399C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129596926 | |||||||
chr3:129596988 | C | A | 125 | a0001c0001t0001g0266 a0001c0002t0002g0005 a0001c0002t0002g0008 others(122): Show |
168 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.1312-7461G>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129596988 | |||||||
chr3:129597176 | G | C | 157 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(154): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.1312-7649C>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129597176 | |||||||
chr3:129597212 | T | C | 2 | a0001c0078t0011g0308 a0002c0079t0011g0307 |
2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1312-7685A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129597212 | |||||||
chr3:129597417 | G | T | 1 | a0001c0002t0002g0070 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1312-7890C>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129597417 | |||||||
chr3:129597424 | G | C | 11 | a0002c0004t0001g0289 a0002c0006t0001g0007 a0002c0006t0001g0287 others(8): Show |
17 | HG01255.hp1 HG01884.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1312-7897C>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129597424 | |||||||
chr3:129597483 | G | GC | 17 | a0001c0001t0001g0132 a0001c0001t0001g0135 a0001c0001t0001g0190 others(14): Show |
17 | HG00423.hp2 HG01515.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1311+7845dupG | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129597483 | |||||||
chr3:129597492 | C | CCCA | 24 | a0003c0010t0001g0047 a0004c0005t0001g0019 a0004c0005t0001g0193 others(21): Show |
27 | HG00408.hp2 HG00639.hp2 HG01257.hp1 others(24): Show |
intron_variant | MODIFIER | c.1311+7836_1311+783 others(7): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129597492 | |||||||
chr3:129597559 | G | A | 1 | a0001c0078t0011g0308 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1311+7770C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129597559 | |||||||
chr3:129597585 | C | G | 2 | a0001c0001t0001g0203 a0002c0004t0001g0138 |
2 | HG02738.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1311+7744G>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129597585 | |||||||
chr3:129597636 | G | A | 2 | a0001c0078t0011g0308 a0002c0079t0011g0307 |
2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1311+7693C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129597636 | |||||||
chr3:129597701 | G | T | 1 | a0001c0002t0002g0070 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1311+7628C>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129597701 | |||||||
chr3:129597751 | G | A | 305 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(302): Show |
406 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(403): Show |
intron_variant | MODIFIER | c.1311+7578C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129597751 | |||||||
chr3:129597801 | G | C | 1 | a0002c0003t0003g0206 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1311+7528C>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129597801 | |||||||
chr3:129597824 | C | T | 2 | a0001c0078t0011g0308 a0002c0079t0011g0307 |
2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1311+7505G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129597824 | |||||||
chr3:129597930 | T | G | 1 | a0001c0001t0001g0196 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1311+7399A>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129597930 | |||||||
chr3:129598134 | G | A | 1 | a0002c0003t0003g0237 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1311+7195C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129598134 | |||||||
chr3:129598284 | C | T | 2 | a0002c0006t0001g0010 a0002c0006t0001g0122 |
5 | HG01109.hp2 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1311+7045G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129598284 | |||||||
chr3:129598402 | T | C | 60 | a0001c0002t0002g0005 a0001c0002t0002g0008 a0001c0002t0002g0016 others(57): Show |
76 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.1311+6927A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129598402 | |||||||
chr3:129598461 | G | C | 156 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(153): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.1311+6868C>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129598461 | |||||||
chr3:129598472 | C | A | 1 | a0019c0066t0014g0272 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1311+6857G>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129598472 | |||||||
chr3:129598504 | T | C | 2 | a0001c0078t0011g0308 a0002c0079t0011g0307 |
2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1311+6825A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129598504 | |||||||
chr3:129598509 | G | A | 62 | a0001c0001t0001g0266 a0001c0011t0001g0015 a0001c0011t0001g0211 others(59): Show |
88 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.1311+6820C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129598509 | |||||||
chr3:129598644 | G | T | 1 | a0002c0003t0003g0207 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1311+6685C>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129598644 | |||||||
chr3:129598658 | C | T | 1 | a0006c0023t0001g0137 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1311+6671G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129598658 | |||||||
chr3:129598659 | G | A | 1 | a0002c0006t0001g0271 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1311+6670C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129598659 | |||||||
chr3:129598742 | C | T | 62 | a0001c0001t0001g0266 a0001c0011t0001g0015 a0001c0011t0001g0211 others(59): Show |
88 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.1311+6587G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129598742 | |||||||
chr3:129598838 | A | G | 1 | a0001c0002t0002g0067 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1311+6491T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129598838 | |||||||
chr3:129598902 | G | T | 307 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(304): Show |
408 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(405): Show |
intron_variant | MODIFIER | c.1311+6427C>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129598902 | |||||||
chr3:129598931 | T | C | 1 | a0001c0002t0002g0111 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1311+6398A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129598931 | |||||||
chr3:129598936 | A | G | 1 | a0029c0052t0001g0136 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1311+6393T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129598936 | |||||||
chr3:129599213 | C | T | 1 | a0002c0003t0003g0042 | 2 | NA18941.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1311+6116G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129599213 | |||||||
chr3:129599260 | C | T | 1 | a0001c0002t0002g0066 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1311+6069G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129599260 | |||||||
chr3:129599435 | C | A | 281 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(278): Show |
379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.1311+5894G>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129599435 | |||||||
chr3:129599451 | C | T | 4 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 others(1): Show |
4 | HG02280.hp1 NA18522.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1311+5878G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129599451 | |||||||
chr3:129599751 | A | G | 13 | a0001c0001t0001g0011 a0001c0001t0001g0029 a0001c0001t0001g0123 others(10): Show |
17 | HG01106.hp1 HG01496.hp2 HG01515.hp1 others(14): Show |
intron_variant | MODIFIER | c.1311+5578T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129599751 | |||||||
chr3:129599880 | C | T | 2 | a0001c0078t0011g0308 a0002c0079t0011g0307 |
2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1311+5449G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129599880 | |||||||
chr3:129600020 | A | T | 2 | a0001c0078t0011g0308 a0002c0079t0011g0307 |
2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1311+5309T>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129600020 | |||||||
chr3:129600026 | G | A | 1 | a0004c0005t0001g0197 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1311+5303C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129600026 | |||||||
chr3:129600039 | C | T | 1 | a0001c0002t0002g0065 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1311+5290G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129600039 | |||||||
chr3:129600206 | G | A | 63 | a0001c0002t0002g0005 a0001c0002t0002g0008 a0001c0002t0002g0016 others(60): Show |
80 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.1311+5123C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129600206 | |||||||
chr3:129600439 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1311+4890C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129600439 | |||||||
chr3:129600655 | G | A | 1 | a0009c0022t0001g0059 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1311+4674C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129600655 | |||||||
chr3:129600719 | C | G | 156 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(153): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.1311+4610G>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129600719 | |||||||
chr3:129600741 | C | G | 1 | a0019c0066t0014g0272 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1311+4588G>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129600741 | |||||||
chr3:129601293 | G | C | 242 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(239): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.1311+4036C>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129601293 | |||||||
chr3:129601325 | T | C | 1 | a0026c0063t0001g0121 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1311+4004A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129601325 | |||||||
chr3:129601330 | G | A | 3 | a0001c0001t0001g0041 a0001c0001t0001g0064 a0001c0001t0001g0199 |
4 | HG00673.hp2 HG02027.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.1311+3999C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129601330 | |||||||
chr3:129601443 | G | A | 1 | a0001c0001t0001g0200 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1311+3886C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129601443 | |||||||
chr3:129601458 | G | A | 218 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(215): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.1311+3871C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129601458 | |||||||
chr3:129601465 | C | T | 3 | a0002c0004t0001g0028 a0002c0004t0001g0125 a0002c0004t0001g0126 |
4 | HG01069.hp1 HG01071.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.1311+3864G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129601465 | |||||||
chr3:129601655 | A | G | 1 | a0003c0008t0004g0295 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1311+3674T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129601655 | |||||||
chr3:129601685 | A | G | 242 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(239): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.1311+3644T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129601685 | |||||||
chr3:129601687 | A | G | 56 | a0001c0001t0001g0266 a0001c0011t0001g0211 a0001c0011t0001g0214 others(53): Show |
78 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.1311+3642T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129601687 | |||||||
chr3:129601914 | C | T | 241 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(238): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.1311+3415G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129601914 | |||||||
chr3:129601957 | C | T | 1 | a0002c0003t0003g0206 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1311+3372G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129601957 | |||||||
chr3:129602225 | C | T | 2 | a0001c0078t0011g0308 a0002c0079t0011g0307 |
2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1311+3104G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129602225 | |||||||
chr3:129602272 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1311+3057G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129602272 | |||||||
chr3:129602477 | C | T | 2 | a0002c0006t0001g0010 a0002c0006t0001g0122 |
5 | HG01109.hp2 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1311+2852G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129602477 | |||||||
chr3:129602478 | G | A | 9 | a0001c0001t0001g0266 a0003c0007t0001g0268 a0003c0010t0001g0020 others(6): Show |
11 | HG01099.hp1 HG01358.hp1 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.1311+2851C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129602478 | |||||||
chr3:129602649 | T | C | 1 | a0002c0012t0001g0292 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1311+2680A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129602649 | |||||||
chr3:129602767 | A | G | 304 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(301): Show |
405 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(402): Show |
intron_variant | MODIFIER | c.1311+2562T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129602767 | |||||||
chr3:129602922 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1311+2407C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129602922 | |||||||
chr3:129602997 | A | T | 3 | a0004c0005t0001g0053 a0004c0005t0001g0299 a0004c0005t0001g0300 |
4 | NA18943.hp2 NA18946.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.1311+2332T>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129602997 | |||||||
chr3:129603010 | A | G | 304 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(301): Show |
405 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(402): Show |
intron_variant | MODIFIER | c.1311+2319T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129603010 | |||||||
chr3:129603555 | G | A | 2 | a0002c0004t0001g0052 a0002c0004t0001g0293 |
3 | HG00738.hp2 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1311+1774C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129603555 | |||||||
chr3:129603679 | G | A | 1 | a0003c0014t0004g0294 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1311+1650C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129603679 | |||||||
chr3:129603768 | C | T | 1 | a0009c0022t0001g0059 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1311+1561G>A | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129603768 | |||||||
chr3:129603973 | A | G | 62 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0002t0002g0005 others(59): Show |
79 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.1311+1356T>C | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129603973 | |||||||
chr3:129603981 | G | A | 178 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0258 others(175): Show |
237 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(234): Show |
intron_variant | MODIFIER | c.1311+1348C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129603981 | |||||||
chr3:129604176 | T | C | 310 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(307): Show |
414 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(411): Show |
intron_variant | MODIFIER | c.1311+1153A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129604176 | |||||||
chr3:129604298 | C | A | 3 | a0010c0035t0005g0270 a0010c0036t0005g0269 a0019c0066t0014g0272 |
3 | HG02257.hp1 HG02486.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1311+1031G>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129604298 | |||||||
chr3:129604465 | T | C | 1 | a0002c0006t0001g0271 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1311+864A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129604465 | |||||||
chr3:129604479 | T | C | 1 | a0001c0001t0001g0021 | 3 | HG00323.hp2 HG03704.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1311+850A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129604479 | |||||||
chr3:129605133 | G | A | 1 | a0019c0066t0014g0272 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1311+196C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129605133 | |||||||
chr3:129605162 | G | A | 28 | a0001c0001t0001g0273 a0001c0001t0001g0275 a0001c0001t0001g0276 others(25): Show |
41 | HG00738.hp2 HG01167.hp1 HG01169.hp1 others(38): Show |
intron_variant | MODIFIER | c.1311+167C>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129605162 | |||||||
chr3:129605173 | T | C | 4 | a0001c0001t0001g0297 a0003c0008t0004g0295 a0003c0008t0004g0296 others(1): Show |
4 | HG01167.hp2 HG01168.hp1 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.1311+156A>G | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129605173 | |||||||
chr3:129605265 | G | GCCCGCC | 3 | a0004c0005t0001g0053 a0004c0005t0001g0299 a0004c0005t0001g0300 |
4 | NA18943.hp2 NA18946.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.1311+58_1311+63dup others(6): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129605265 | |||||||
chr3:129605265 | GCCCGCC | G | 9 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 others(6): Show |
9 | HG00735.hp1 HG02055.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1311+58_1311+63del others(6): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129605265 | |||||||
chr3:129605284 | C | CCCG | 61 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0064 others(58): Show |
78 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.1311+42_1311+44dup others(3): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129605284 | |||||||
chr3:129605284 | C | CCCGCCGC others(8): Show |
1 | a0001c0002t0002g0061 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1311+30_1311+44dup others(15): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129605284 | |||||||
chr3:129605284 | CCCGCCGC others(5): Show |
C | 3 | a0002c0003t0003g0302 a0002c0003t0003g0303 a0002c0003t0003g0304 |
3 | HG03710.hp2 NA18995.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1311+33_1311+44del others(12): Show |
PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129605284 | |||||||
chr3:129605285 | C | A | 1 | a0004c0005t0001g0301 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1311+44G>T | PLXND1 | ENSG00000004399.13 | transcript | ENST00000324093.9 | protein_coding | 1/35 | chr3 | 129605285 |