Item | Value |
---|---|
geneid | 23654 |
ensemblid | ENSG00000196576.16 |
hgncid | 9104 |
symbol | PLXNB2 |
name | plexin B2 |
refseq_nuc | NM_012401.4 |
refseq_prot | NP_036533.2 |
ensembl_nuc | ENST00000359337.9 |
ensembl_prot | ENSP00000352288.4 |
mane_status | MANE Select |
chr | chr22 |
start | 50274979 |
end | 50307646 |
strand | - |
ver | v1.2 |
region | chr22:50274979-50307646 |
region5000 | chr22:50269979-50312646 |
regionname0 | PLXNB2_chr22_50274979_50307646 |
regionname5000 | PLXNB2_chr22_50269979_50312646 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 1838 | 86 | 10 | 22 | 28 | 5 | 21 | 18 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | MALQL others(1833): Show |
chr22 | 50269979 | 50312646 |
a0002 | 0/0 | 1838 | 77 | 41 | 3 | 29 | 1 | 3 | 17 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | MALQL others(1833): Show |
chr22 | 50269979 | 50312646 |
a0003 | 1/1 | 1838 | 51 | 9 | 15 | 21 | 1 | 3 | 9 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | MALQL others(1833): Show |
chr22 | 50269979 | 50312646 |
a0004 | 0/0 | 1838 | 37 | 9 | 2 | 21 | 1 | 4 | 15 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | MALQL others(1833): Show |
chr22 | 50269979 | 50312646 |
a0005 | 0/0 | 1838 | 6 | 0 | 0 | 4 | 1 | 1 | 3 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | MALQL others(1833): Show |
chr22 | 50269979 | 50312646 |
a0006 | 0/0 | 1838 | 6 | 0 | 5 | 0 | 0 | 1 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | MALQL others(1833): Show |
chr22 | 50269979 | 50312646 |
a0007 | 0/0 | 1838 | 4 | 0 | 1 | 3 | 0 | 0 | 2 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | MALQL others(1833): Show |
chr22 | 50269979 | 50312646 |
a0008 | 0/0 | 1838 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | MALQL others(1833): Show |
chr22 | 50269979 | 50312646 |
a0009 | 0/0 | 1838 | 3 | 0 | 1 | 0 | 0 | 2 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | MALQL others(1833): Show |
chr22 | 50269979 | 50312646 |
a0010 | 0/0 | 1838 | 3 | 0 | 2 | 0 | 0 | 1 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | MALQL others(1833): Show |
chr22 | 50269979 | 50312646 |
a0011 | 0/0 | 1838 | 3 | 0 | 1 | 2 | 0 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | MALQL others(1833): Show |
chr22 | 50269979 | 50312646 |
a0012 | 0/0 | 1838 | 3 | 0 | 2 | 1 | 0 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | MALQL others(1833): Show |
chr22 | 50269979 | 50312646 |
a0013 | 0/0 | 1838 | 2 | 0 | 0 | 1 | 1 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | MALQL others(1833): Show |
chr22 | 50269979 | 50312646 |
a0014 | 0/0 | 1838 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | MALQL others(1833): Show |
chr22 | 50269979 | 50312646 |
a0015 | 0/0 | 1838 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | MALQL others(1833): Show |
chr22 | 50269979 | 50312646 |
a0016 | 0/0 | 1838 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | MALQL others(1833): Show |
chr22 | 50269979 | 50312646 |
a0017 | 0/0 | 1838 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | MALQL others(1833): Show |
chr22 | 50269979 | 50312646 |
a0018 | 0/0 | 1838 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | MALQL others(1833): Show |
chr22 | 50269979 | 50312646 |
a0019 | 0/0 | 1838 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | MALPL others(1833): Show |
chr22 | 50269979 | 50312646 |
a0020 | 0/0 | 1838 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | MALQL others(1833): Show |
chr22 | 50269979 | 50312646 |
a0021 | 0/0 | 1838 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | MALQL others(1833): Show |
chr22 | 50269979 | 50312646 |
a0022 | 0/0 | 1838 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | MALQL others(1833): Show |
chr22 | 50269979 | 50312646 |
a0023 | 0/0 | 1838 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | MALQL others(1833): Show |
chr22 | 50269979 | 50312646 |
a0024 | 0/0 | 1838 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | MALQL others(1833): Show |
chr22 | 50269979 | 50312646 |
a0025 | 0/0 | 1838 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | MALQL others(1833): Show |
chr22 | 50269979 | 50312646 |
a0026 | 0/0 | 1838 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | MALQL others(1833): Show |
chr22 | 50269979 | 50312646 |
a0027 | 0/0 | 1838 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | MALQL others(1833): Show |
chr22 | 50269979 | 50312646 |
a0028 | 0/0 | 1838 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | MALQL others(1833): Show |
chr22 | 50269979 | 50312646 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002 | 0/0 | 5514 | 34 | 0 | 10 | 9 | 2 | 13 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0001c0003 | 0/0 | 5514 | 30 | 4 | 6 | 11 | 2 | 7 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0001c0006 | 0/0 | 5514 | 13 | 0 | 5 | 7 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0001c0038 | 0/0 | 5514 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0001c0046 | 0/0 | 5514 | 1 | 0 | 0 | 0 | 1 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0001c0047 | 0/0 | 5514 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0001c0049 | 0/0 | 5514 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0001c0050 | 0/0 | 5514 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0001c0051 | 0/0 | 5514 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0001c0052 | 0/0 | 5514 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0001c0078 | 0/0 | 5514 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0001c0080 | 0/0 | 5514 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0002c0005 | 0/0 | 5514 | 16 | 0 | 0 | 16 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0002c0007 | 0/0 | 5514 | 9 | 7 | 0 | 2 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0002c0009 | 0/0 | 5514 | 8 | 0 | 2 | 3 | 1 | 2 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0002c0010 | 0/0 | 5514 | 7 | 7 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0002c0011 | 0/0 | 5514 | 6 | 6 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0002c0013 | 0/0 | 5514 | 5 | 5 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0002c0014 | 0/0 | 5514 | 5 | 4 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0002c0017 | 0/0 | 5514 | 4 | 4 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0002c0019 | 0/0 | 5514 | 3 | 0 | 0 | 2 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0002c0028 | 0/0 | 5514 | 2 | 0 | 0 | 2 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0002c0032 | 0/0 | 5514 | 2 | 2 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0002c0034 | 0/0 | 5514 | 2 | 0 | 0 | 2 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0002c0060 | 0/0 | 5514 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0002c0063 | 0/0 | 5514 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0002c0064 | 0/0 | 5514 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0002c0065 | 0/0 | 5514 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0002c0071 | 0/0 | 5514 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0002c0072 | 0/0 | 5514 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0002c0073 | 0/0 | 5514 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0002c0077 | 0/0 | 5514 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0003c0001 | 1/0 | 5514 | 36 | 4 | 13 | 14 | 1 | 3 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0003c0015 | 0/1 | 5514 | 4 | 0 | 1 | 2 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0003c0018 | 0/0 | 5514 | 3 | 1 | 0 | 2 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0003c0022 | 0/0 | 5514 | 2 | 2 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0003c0039 | 0/0 | 5514 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0003c0041 | 0/0 | 5514 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0003c0042 | 0/0 | 5514 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0003c0043 | 0/0 | 5514 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0003c0044 | 0/0 | 5514 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0003c0045 | 0/0 | 5514 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0004c0004 | 0/0 | 5514 | 19 | 1 | 0 | 13 | 1 | 4 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0004c0008 | 0/0 | 5514 | 8 | 4 | 1 | 3 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0004c0021 | 0/0 | 5514 | 3 | 0 | 0 | 3 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0004c0025 | 0/0 | 5514 | 2 | 2 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0004c0026 | 0/0 | 5514 | 2 | 2 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0004c0033 | 0/0 | 5514 | 2 | 0 | 0 | 2 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0004c0070 | 0/0 | 5514 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0005c0016 | 0/0 | 5514 | 4 | 0 | 0 | 4 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0005c0067 | 0/0 | 5514 | 1 | 0 | 0 | 0 | 1 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0005c0068 | 0/0 | 5514 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0006c0012 | 0/0 | 5514 | 5 | 0 | 4 | 0 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0006c0058 | 0/0 | 5514 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0007c0029 | 0/0 | 5514 | 2 | 0 | 0 | 2 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0007c0066 | 0/0 | 5514 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0007c0076 | 0/0 | 5514 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0008c0035 | 0/0 | 5514 | 2 | 2 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0008c0036 | 0/0 | 5514 | 2 | 2 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0009c0020 | 0/0 | 5514 | 3 | 0 | 1 | 0 | 0 | 2 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0010c0031 | 0/0 | 5514 | 2 | 0 | 2 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0010c0069 | 0/0 | 5514 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0011c0023 | 0/0 | 5514 | 2 | 0 | 1 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0011c0057 | 0/0 | 5514 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0012c0024 | 0/0 | 5514 | 2 | 0 | 2 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0012c0062 | 0/0 | 5514 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0013c0030 | 0/0 | 5514 | 2 | 0 | 0 | 1 | 1 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0014c0027 | 0/0 | 5514 | 2 | 2 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0015c0037 | 0/0 | 5514 | 2 | 2 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0016c0048 | 0/0 | 5514 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0017c0055 | 0/0 | 5514 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0018c0054 | 0/0 | 5514 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0019c0082 | 0/0 | 5514 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0020c0079 | 0/0 | 5514 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0021c0040 | 0/0 | 5514 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0022c0074 | 0/0 | 5514 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0023c0059 | 0/0 | 5514 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0024c0081 | 0/0 | 5514 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0025c0061 | 0/0 | 5514 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0026c0075 | 0/0 | 5514 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0027c0053 | 0/0 | 5514 | 1 | 0 | 0 | 0 | 1 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 | ||
a0028c0056 | 0/0 | 5514 | 1 | 0 | 0 | 0 | 1 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ATGGC others(5509): Show |
chr22 | 50269979 | 50312646 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001 | 0/0 | 6409 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0001c0002t0002 | 0/0 | 6409 | 32 | 0 | 10 | 9 | 2 | 11 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0001c0002t0009 | 0/0 | 6409 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0001c0003t0001 | 0/0 | 6409 | 30 | 4 | 6 | 11 | 2 | 7 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0001c0006t0001 | 0/0 | 6409 | 12 | 0 | 5 | 6 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0001c0006t0002 | 0/0 | 6409 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0001c0038t0002 | 0/0 | 6409 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0001c0046t0006 | 0/0 | 6409 | 1 | 0 | 0 | 0 | 1 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0001c0047t0001 | 0/0 | 6409 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0001c0049t0001 | 0/0 | 6409 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0001c0050t0001 | 0/0 | 6409 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0001c0051t0003 | 0/0 | 6410 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6405): Show |
chr22 | 50269979 | 50312646 |
a0001c0052t0001 | 0/0 | 6409 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0001c0078t0002 | 0/0 | 6409 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0001c0080t0001 | 0/0 | 6409 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0002c0005t0002 | 0/0 | 6409 | 16 | 0 | 0 | 16 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0002c0007t0001 | 0/0 | 6409 | 9 | 7 | 0 | 2 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0002c0009t0002 | 0/0 | 6409 | 8 | 0 | 2 | 3 | 1 | 2 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0002c0010t0003 | 0/0 | 6410 | 7 | 7 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6405): Show |
chr22 | 50269979 | 50312646 |
a0002c0011t0002 | 0/0 | 6409 | 6 | 6 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0002c0013t0003 | 0/0 | 6410 | 5 | 5 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6405): Show |
chr22 | 50269979 | 50312646 |
a0002c0014t0003 | 0/0 | 6410 | 3 | 2 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6405): Show |
chr22 | 50269979 | 50312646 |
a0002c0014t0008 | 0/0 | 6409 | 2 | 2 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0002c0017t0004 | 0/0 | 6409 | 4 | 4 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0002c0019t0002 | 0/0 | 6409 | 3 | 0 | 0 | 2 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0002c0028t0001 | 0/0 | 6409 | 2 | 0 | 0 | 2 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0002c0032t0001 | 0/0 | 6409 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0002c0032t0012 | 0/0 | 6409 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0002c0034t0001 | 0/0 | 6409 | 2 | 0 | 0 | 2 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0002c0060t0002 | 0/0 | 6409 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0002c0063t0002 | 0/0 | 6409 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0002c0064t0003 | 0/0 | 6410 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6405): Show |
chr22 | 50269979 | 50312646 |
a0002c0065t0001 | 0/0 | 6409 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0002c0071t0003 | 0/0 | 6410 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6405): Show |
chr22 | 50269979 | 50312646 |
a0002c0072t0002 | 0/0 | 6409 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0002c0073t0001 | 0/0 | 6409 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0002c0077t0001 | 0/0 | 6409 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0003c0001t0001 | 0/0 | 6409 | 33 | 4 | 13 | 13 | 1 | 2 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0003c0001t0002 | 0/0 | 6409 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0003c0001t0006 | 1/0 | 6409 | 1 | 0 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0003c0001t0010 | 0/0 | 6392 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6387): Show |
chr22 | 50269979 | 50312646 |
a0003c0015t0001 | 0/0 | 6409 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0003c0015t0002 | 0/1 | 6409 | 3 | 0 | 0 | 2 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0003c0018t0002 | 0/0 | 6409 | 3 | 1 | 0 | 2 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0003c0022t0001 | 0/0 | 6409 | 2 | 2 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0003c0039t0001 | 0/0 | 6409 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0003c0041t0003 | 0/0 | 6410 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6405): Show |
chr22 | 50269979 | 50312646 |
a0003c0042t0001 | 0/0 | 6409 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0003c0043t0001 | 0/0 | 6409 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0003c0044t0001 | 0/0 | 6409 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0003c0045t0001 | 0/0 | 6409 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0004c0004t0002 | 0/0 | 6409 | 19 | 1 | 0 | 13 | 1 | 4 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0004c0008t0001 | 0/0 | 6409 | 6 | 4 | 1 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0004c0008t0005 | 0/0 | 6409 | 2 | 0 | 0 | 2 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0004c0021t0001 | 0/0 | 6409 | 3 | 0 | 0 | 3 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0004c0025t0002 | 0/0 | 6409 | 2 | 2 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0004c0026t0003 | 0/0 | 6410 | 2 | 2 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6405): Show |
chr22 | 50269979 | 50312646 |
a0004c0033t0001 | 0/0 | 6409 | 2 | 0 | 0 | 2 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0004c0070t0002 | 0/0 | 6409 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0005c0016t0002 | 0/0 | 6409 | 3 | 0 | 0 | 3 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0005c0016t0011 | 0/0 | 6409 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0005c0067t0001 | 0/0 | 6409 | 1 | 0 | 0 | 0 | 1 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0005c0068t0005 | 0/0 | 6409 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0006c0012t0001 | 0/0 | 6409 | 5 | 0 | 4 | 0 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0006c0058t0002 | 0/0 | 6409 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0007c0029t0001 | 0/0 | 6409 | 2 | 0 | 0 | 2 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0007c0066t0001 | 0/0 | 6409 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0007c0076t0001 | 0/0 | 6409 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0008c0035t0003 | 0/0 | 6410 | 2 | 2 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6405): Show |
chr22 | 50269979 | 50312646 |
a0008c0036t0003 | 0/0 | 6410 | 2 | 2 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6405): Show |
chr22 | 50269979 | 50312646 |
a0009c0020t0002 | 0/0 | 6409 | 3 | 0 | 1 | 0 | 0 | 2 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0010c0031t0002 | 0/0 | 6409 | 2 | 0 | 2 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0010c0069t0001 | 0/0 | 6409 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0011c0023t0001 | 0/0 | 6409 | 2 | 0 | 1 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0011c0057t0002 | 0/0 | 6409 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0012c0024t0001 | 0/0 | 6409 | 2 | 0 | 2 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0012c0062t0001 | 0/0 | 6409 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0013c0030t0001 | 0/0 | 6409 | 2 | 0 | 0 | 1 | 1 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0014c0027t0001 | 0/0 | 6409 | 2 | 2 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0015c0037t0007 | 0/0 | 6409 | 2 | 2 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0016c0048t0001 | 0/0 | 6409 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0017c0055t0001 | 0/0 | 6409 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0018c0054t0001 | 0/0 | 6409 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0019c0082t0002 | 0/0 | 6409 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0020c0079t0001 | 0/0 | 6409 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0021c0040t0001 | 0/0 | 6409 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0022c0074t0002 | 0/0 | 6409 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0023c0059t0001 | 0/0 | 6409 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0024c0081t0001 | 0/0 | 6409 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0025c0061t0002 | 0/0 | 6409 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0026c0075t0002 | 0/0 | 6409 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0027c0053t0002 | 0/0 | 6409 | 1 | 0 | 0 | 0 | 1 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
a0028c0056t0001 | 0/0 | 6409 | 1 | 0 | 0 | 0 | 1 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | ACACA others(6404): Show |
chr22 | 50269979 | 50312646 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0002t0002g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0002t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0002t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0002t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0002t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0002t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0002t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0002t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0002t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0002t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0002t0009g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0003t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0003t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0003t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0003t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0003t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0003t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0003t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0003t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0003t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0003t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0003t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0003t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0003t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0003t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0003t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0003t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0003t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0003t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0003t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0003t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0003t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0003t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0003t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0003t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0003t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0003t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0003t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0006t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0006t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0006t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0006t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0006t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0006t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0006t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0006t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0006t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0006t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0006t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0006t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0006t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0038t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0046t0006g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0047t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0049t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0050t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0051t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0052t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0078t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0001c0080t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0005t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0005t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0005t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0005t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0005t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0005t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0005t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0005t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0005t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0005t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0005t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0005t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0005t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0005t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0005t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0007t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0007t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0007t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0007t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0007t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0007t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0007t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0007t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0009t0002g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0009t0002g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0009t0002g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0009t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0009t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0009t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0009t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0009t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0010t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0010t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0010t0003g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0010t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0010t0003g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0010t0003g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0010t0003g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0011t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0011t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0011t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0011t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0011t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0011t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0013t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0013t0003g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0013t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0013t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0013t0003g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0014t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0014t0003g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0014t0003g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0014t0008g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0014t0008g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0017t0004g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0017t0004g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0017t0004g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0017t0004g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0019t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0019t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0019t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0028t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0028t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0032t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0032t0012g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0034t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0034t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0060t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0063t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0064t0003g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0065t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0071t0003g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0072t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0073t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0002c0077t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0003c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0003c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0003c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0003c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0003c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0003c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0003c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0003c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0003c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0003c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0003c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0003c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0003c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0003c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0003c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0003c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0003c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0003c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0003c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0003c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0003c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0003c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0003c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0003c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0003c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0003c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0003c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0003c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0003c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0003c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0003c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0003c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0003c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0003c0001t0006g0040 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0003c0001t0010g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0003c0015t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0003c0015t0002g0029 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0003c0015t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0003c0015t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0003c0018t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0003c0018t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0003c0018t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0003c0022t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0003c0022t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0003c0039t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0003c0041t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0003c0042t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0003c0043t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0003c0044t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0003c0045t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0004c0004t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0004c0004t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0004c0004t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0004c0004t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0004c0004t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0004c0004t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0004c0004t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0004c0004t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0004c0004t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0004c0004t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0004c0004t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0004c0004t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0004c0004t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0004c0004t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0004c0004t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0004c0004t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0004c0004t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0004c0004t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0004c0004t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0004c0008t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0004c0008t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0004c0008t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0004c0008t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0004c0008t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0004c0008t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0004c0008t0005g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0004c0021t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0004c0021t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0004c0021t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0004c0025t0002g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0004c0026t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0004c0026t0003g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0004c0033t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0004c0033t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0004c0070t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0005c0016t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0005c0016t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0005c0016t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0005c0016t0011g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0005c0067t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0005c0068t0005g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0006c0012t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0006c0012t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0006c0012t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0006c0012t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0006c0012t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0006c0058t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0007c0029t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0007c0029t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0007c0066t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0007c0076t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0008c0035t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0008c0035t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0008c0036t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0008c0036t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0009c0020t0002g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0009c0020t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0009c0020t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0010c0031t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0010c0031t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0010c0069t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0011c0023t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0011c0023t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0011c0057t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0012c0024t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0012c0062t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0013c0030t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0013c0030t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0014c0027t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0014c0027t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0015c0037t0007g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0016c0048t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0017c0055t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0018c0054t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0019c0082t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0020c0079t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0021c0040t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0022c0074t0002g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0023c0059t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0024c0081t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0025c0061t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0026c0075t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0027c0053t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
a0028c0056t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0002 | g0161 | EUR | GBR | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG00099 | hp2 | a0001 | c0046 | t0006 | g0199 | EUR | GBR | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG00280 | hp1 | a0004 | c0004 | t0002 | g0083 | EUR | FIN | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG00280 | hp2 | a0002 | c0009 | t0002 | g0021 | EUR | FIN | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG00408 | hp1 | a0003 | c0039 | t0001 | g0056 | EAS | CHS | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG00408 | hp2 | a0002 | c0028 | t0001 | g0226 | EAS | CHS | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG00423 | hp1 | a0005 | c0016 | t0011 | g0256 | EAS | CHS | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG00423 | hp2 | a0003 | c0001 | t0001 | g0066 | EAS | CHS | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG00438 | hp1 | a0001 | c0003 | t0001 | g0020 | EAS | CHS | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG00438 | hp2 | a0001 | c0006 | t0002 | g0155 | EAS | CHS | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG00544 | hp1 | a0002 | c0005 | t0002 | g0102 | EAS | CHS | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG00544 | hp2 | a0001 | c0003 | t0001 | g0151 | EAS | CHS | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG00558 | hp1 | a0002 | c0005 | t0002 | g0106 | EAS | CHS | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG00558 | hp2 | a0001 | c0002 | t0002 | g0033 | EAS | CHS | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG00597 | hp1 | a0002 | c0072 | t0002 | g0044 | EAS | CHS | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG00597 | hp2 | a0016 | c0048 | t0001 | g0143 | EAS | CHS | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG00609 | hp1 | a0003 | c0001 | t0001 | g0108 | EAS | CHS | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG00609 | hp2 | a0001 | c0006 | t0001 | g0144 | EAS | CHS | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG00621 | hp1 | a0003 | c0001 | t0001 | g0076 | EAS | CHS | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG00621 | hp2 | a0003 | c0018 | t0002 | g0171 | EAS | CHS | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG00639 | hp1 | a0003 | c0001 | t0001 | g0273 | AMR | PUR | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG00639 | hp2 | a0001 | c0006 | t0001 | g0186 | AMR | PUR | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG00673 | hp1 | a0007 | c0029 | t0001 | g0089 | EAS | CHS | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG00673 | hp2 | a0003 | c0043 | t0001 | g0175 | EAS | CHS | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG00733 | hp1 | a0002 | c0009 | t0002 | g0015 | AMR | PUR | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG00733 | hp2 | a0009 | c0020 | t0002 | g0047 | AMR | PUR | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG00735 | hp1 | a0006 | c0012 | t0001 | g0208 | AMR | PUR | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG00735 | hp2 | a0002 | c0009 | t0002 | g0016 | AMR | PUR | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG01071 | hp1 | a0001 | c0003 | t0001 | g0198 | AMR | PUR | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG01071 | hp2 | a0003 | c0001 | t0001 | g0017 | AMR | PUR | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG01081 | hp1 | a0003 | c0001 | t0001 | g0049 | AMR | PUR | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG01081 | hp2 | a0001 | c0006 | t0001 | g0215 | AMR | PUR | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG01099 | hp1 | a0001 | c0003 | t0001 | g0170 | AMR | PUR | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG01099 | hp2 | a0003 | c0001 | t0001 | g0050 | AMR | PUR | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG01106 | hp1 | a0017 | c0055 | t0001 | g0217 | AMR | PUR | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG01106 | hp2 | a0001 | c0002 | t0002 | g0154 | AMR | PUR | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG01109 | hp1 | a0002 | c0014 | t0003 | g0260 | AMR | PUR | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG01109 | hp2 | a0004 | c0070 | t0002 | g0239 | AMR | PUR | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG01168 | hp1 | a0001 | c0002 | t0002 | g0181 | AMR | PUR | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG01168 | hp2 | a0010 | c0031 | t0002 | g0082 | AMR | PUR | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG01169 | hp1 | a0010 | c0031 | t0002 | g0086 | AMR | PUR | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG01169 | hp2 | a0001 | c0002 | t0002 | g0133 | AMR | PUR | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG01175 | hp1 | a0006 | c0012 | t0001 | g0216 | AMR | PUR | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG01175 | hp2 | a0001 | c0003 | t0001 | g0184 | AMR | PUR | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG01192 | hp1 | a0001 | c0002 | t0002 | g0185 | AMR | PUR | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG01192 | hp2 | a0001 | c0002 | t0002 | g0231 | AMR | PUR | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG01258 | hp1 | a0001 | c0003 | t0001 | g0080 | AMR | CLM | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG01258 | hp2 | a0001 | c0002 | t0002 | g0201 | AMR | CLM | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG01261 | hp1 | a0001 | c0006 | t0001 | g0138 | AMR | CLM | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG01261 | hp2 | a0006 | c0012 | t0001 | g0237 | AMR | CLM | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG01346 | hp1 | a0011 | c0023 | t0001 | g0023 | AMR | CLM | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG01346 | hp2 | a0001 | c0003 | t0001 | g0028 | AMR | CLM | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG01361 | hp1 | a0004 | c0008 | t0001 | g0254 | AMR | CLM | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG01361 | hp2 | a0006 | c0058 | t0002 | g0197 | AMR | CLM | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG01496 | hp1 | a0001 | c0003 | t0001 | g0025 | AMR | CLM | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG01496 | hp2 | a0001 | c0002 | t0002 | g0013 | AMR | CLM | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG01515 | hp1 | a0001 | c0003 | t0001 | g0207 | EUR | IBS | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG01515 | hp2 | a0013 | c0030 | t0001 | g0220 | EUR | IBS | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG01517 | hp1 | a0001 | c0002 | t0002 | g0234 | EUR | IBS | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG01517 | hp2 | a0001 | c0003 | t0001 | g0210 | EUR | IBS | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG01884 | hp1 | a0002 | c0014 | t0008 | g0135 | AFR | ACB | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG01884 | hp2 | a0002 | c0007 | t0001 | g0001 | AFR | ACB | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG01891 | hp1 | a0002 | c0010 | t0003 | g0245 | AFR | ACB | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG01891 | hp2 | a0002 | c0011 | t0002 | g0285 | AFR | ACB | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG01934 | hp1 | a0001 | c0006 | t0001 | g0159 | AMR | PEL | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG01934 | hp2 | a0007 | c0066 | t0001 | g0061 | AMR | PEL | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG01943 | hp1 | a0003 | c0001 | t0001 | g0003 | AMR | PEL | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG01943 | hp2 | a0018 | c0054 | t0001 | g0041 | AMR | PEL | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG01952 | hp1 | a0003 | c0001 | t0001 | g0203 | AMR | PEL | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG01952 | hp2 | a0003 | c0001 | t0001 | g0052 | AMR | PEL | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG01975 | hp1 | a0003 | c0001 | t0001 | g0179 | AMR | PEL | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG01975 | hp2 | a0001 | c0002 | t0002 | g0200 | AMR | PEL | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG01978 | hp1 | a0003 | c0001 | t0001 | g0063 | AMR | PEL | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG01978 | hp2 | a0003 | c0015 | t0001 | g0048 | AMR | PEL | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG01993 | hp1 | a0003 | c0045 | t0001 | g0074 | AMR | PEL | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG01993 | hp2 | a0001 | c0002 | t0002 | g0187 | AMR | PEL | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02004 | hp1 | a0012 | c0024 | t0001 | g0002 | AMR | PEL | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02004 | hp2 | a0001 | c0050 | t0001 | g0060 | AMR | PEL | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02015 | hp1 | a0003 | c0001 | t0001 | g0030 | EAS | KHV | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02015 | hp2 | a0003 | c0001 | t0001 | g0026 | EAS | KHV | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02027 | hp1 | a0003 | c0042 | t0001 | g0018 | EAS | KHV | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02027 | hp2 | a0002 | c0005 | t0002 | g0113 | EAS | KHV | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02040 | hp1 | a0004 | c0008 | t0005 | g0008 | EAS | KHV | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02040 | hp2 | a0001 | c0002 | t0002 | g0188 | EAS | KHV | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02055 | hp1 | a0002 | c0013 | t0003 | g0228 | AFR | ACB | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02055 | hp2 | a0002 | c0017 | t0004 | g0124 | AFR | ACB | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02056 | hp1 | a0003 | c0001 | t0001 | g0073 | EAS | KHV | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02056 | hp2 | a0003 | c0001 | t0001 | g0070 | EAS | KHV | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02071 | hp1 | a0004 | c0033 | t0001 | g0290 | EAS | KHV | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02071 | hp2 | a0002 | c0019 | t0002 | g0104 | EAS | KHV | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02074 | hp1 | a0011 | c0023 | t0001 | g0035 | EAS | KHV | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02074 | hp2 | a0002 | c0007 | t0001 | g0227 | EAS | KHV | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02080 | hp1 | a0002 | c0005 | t0002 | g0164 | EAS | KHV | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02080 | hp2 | a0004 | c0004 | t0002 | g0176 | EAS | KHV | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02083 | hp1 | a0004 | c0004 | t0002 | g0174 | EAS | KHV | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02083 | hp2 | a0002 | c0005 | t0002 | g0211 | EAS | KHV | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02132 | hp1 | a0001 | c0006 | t0001 | g0169 | EAS | KHV | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02132 | hp2 | a0002 | c0005 | t0002 | g0103 | EAS | KHV | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02135 | hp1 | a0001 | c0003 | t0001 | g0069 | EAS | KHV | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02135 | hp2 | a0004 | c0004 | t0002 | g0101 | EAS | KHV | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02145 | hp1 | a0003 | c0022 | t0001 | g0294 | AFR | ACB | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02145 | hp2 | a0002 | c0010 | t0003 | g0278 | AFR | ACB | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02148 | hp1 | a0006 | c0012 | t0001 | g0209 | AMR | PEL | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02148 | hp2 | a0003 | c0001 | t0001 | g0055 | AMR | PEL | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02155 | hp1 | a0002 | c0028 | t0001 | g0225 | EAS | CDX | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02155 | hp2 | a0004 | c0008 | t0001 | g0195 | EAS | CDX | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02165 | hp1 | a0002 | c0005 | t0002 | g0212 | EAS | CDX | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02165 | hp2 | a0001 | c0078 | t0002 | g0214 | EAS | CDX | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02258 | hp1 | a0001 | c0003 | t0001 | g0267 | AFR | ACB | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02258 | hp2 | a0002 | c0017 | t0004 | g0128 | AFR | ACB | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02273 | hp1 | a0012 | c0024 | t0001 | g0002 | AMR | PEL | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02273 | hp2 | a0003 | c0001 | t0001 | g0003 | AMR | PEL | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02280 | hp1 | a0001 | c0003 | t0001 | g0027 | AFR | ACB | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02280 | hp2 | a0002 | c0064 | t0003 | g0282 | AFR | ACB | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02293 | hp1 | a0003 | c0001 | t0001 | g0071 | AMR | PEL | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02293 | hp2 | a0001 | c0006 | t0001 | g0190 | AMR | PEL | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02451 | hp1 | a0003 | c0018 | t0002 | g0114 | AFR | ACB | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02451 | hp2 | a0002 | c0010 | t0003 | g0279 | AFR | ACB | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02572 | hp1 | a0003 | c0001 | t0001 | g0115 | AFR | GWD | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02572 | hp2 | a0004 | c0026 | t0003 | g0261 | AFR | GWD | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02602 | hp1 | a0001 | c0003 | t0001 | g0205 | SAS | PJL | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02602 | hp2 | a0010 | c0069 | t0001 | g0236 | SAS | PJL | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02630 | hp1 | a0001 | c0047 | t0001 | g0078 | AFR | GWD | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02630 | hp2 | a0002 | c0014 | t0003 | g0259 | AFR | GWD | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02647 | hp1 | a0004 | c0008 | t0001 | g0250 | AFR | GWD | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02647 | hp2 | a0002 | c0011 | t0002 | g0042 | AFR | GWD | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02683 | hp1 | a0001 | c0002 | t0002 | g0142 | SAS | PJL | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02683 | hp2 | a0001 | c0003 | t0001 | g0121 | SAS | PJL | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02717 | hp1 | a0001 | c0080 | t0001 | g0079 | AFR | GWD | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02717 | hp2 | a0001 | c0051 | t0003 | g0120 | AFR | GWD | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02735 | hp1 | a0019 | c0082 | t0002 | g0130 | SAS | PJL | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02735 | hp2 | a0001 | c0006 | t0001 | g0192 | SAS | PJL | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02809 | hp1 | a0001 | c0038 | t0002 | g0136 | AFR | GWD | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02809 | hp2 | a0002 | c0014 | t0003 | g0036 | AFR | GWD | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02818 | hp1 | a0002 | c0007 | t0001 | g0131 | AFR | GWD | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02818 | hp2 | a0008 | c0035 | t0003 | g0095 | AFR | GWD | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02886 | hp1 | a0008 | c0036 | t0003 | g0054 | AFR | GWD | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02886 | hp2 | a0001 | c0003 | t0001 | g0043 | AFR | GWD | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02895 | hp1 | a0002 | c0013 | t0003 | g0248 | AFR | GWD | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02895 | hp2 | a0004 | c0025 | t0002 | g0006 | AFR | GWD | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02896 | hp1 | a0002 | c0013 | t0003 | g0165 | AFR | GWD | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02896 | hp2 | a0014 | c0027 | t0001 | g0014 | AFR | GWD | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02897 | hp1 | a0004 | c0025 | t0002 | g0006 | AFR | GWD | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02897 | hp2 | a0014 | c0027 | t0001 | g0011 | AFR | GWD | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02922 | hp1 | a0015 | c0037 | t0007 | g0007 | AFR | ESN | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02922 | hp2 | a0002 | c0077 | t0001 | g0292 | AFR | ESN | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02965 | hp1 | a0004 | c0008 | t0001 | g0249 | AFR | ESN | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02965 | hp2 | a0020 | c0079 | t0001 | g0126 | AFR | ESN | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02976 | hp1 | a0003 | c0001 | t0001 | g0280 | AFR | ESN | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02976 | hp2 | a0015 | c0037 | t0007 | g0007 | AFR | ESN | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG03017 | hp1 | a0001 | c0002 | t0002 | g0146 | SAS | PJL | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG03017 | hp2 | a0001 | c0002 | t0002 | g0232 | SAS | PJL | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG03130 | hp1 | a0002 | c0007 | t0001 | g0122 | AFR | ESN | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG03130 | hp2 | a0003 | c0044 | t0001 | g0276 | AFR | ESN | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG03139 | hp1 | a0004 | c0026 | t0003 | g0123 | AFR | ESN | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG03139 | hp2 | a0002 | c0011 | t0002 | g0281 | AFR | ESN | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG03209 | hp1 | a0001 | c0052 | t0001 | g0077 | AFR | MSL | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG03209 | hp2 | a0002 | c0011 | t0002 | g0284 | AFR | MSL | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG03225 | hp1 | a0002 | c0014 | t0008 | g0134 | AFR | MSL | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG03225 | hp2 | a0002 | c0073 | t0001 | g0263 | AFR | MSL | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG03239 | hp1 | a0001 | c0002 | t0001 | g0182 | SAS | PJL | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG03239 | hp2 | a0002 | c0009 | t0002 | g0037 | SAS | PJL | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG03453 | hp1 | a0002 | c0032 | t0001 | g0286 | AFR | MSL | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG03453 | hp2 | a0002 | c0011 | t0002 | g0283 | AFR | MSL | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG03486 | hp1 | a0002 | c0007 | t0001 | g0252 | AFR | MSL | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG03486 | hp2 | a0001 | c0003 | t0001 | g0266 | AFR | MSL | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG03492 | hp1 | a0021 | c0040 | t0001 | g0032 | SAS | PJL | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG03492 | hp2 | a0001 | c0003 | t0001 | g0202 | SAS | PJL | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG03540 | hp1 | a0002 | c0071 | t0003 | g0094 | AFR | GWD | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG03540 | hp2 | a0002 | c0010 | t0003 | g0243 | AFR | GWD | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG03579 | hp1 | a0002 | c0017 | t0004 | g0127 | AFR | MSL | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG03579 | hp2 | a0002 | c0011 | t0002 | g0275 | AFR | MSL | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG03654 | hp1 | a0001 | c0002 | t0002 | g0235 | SAS | PJL | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG03654 | hp2 | a0001 | c0002 | t0002 | g0229 | SAS | PJL | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG03669 | hp1 | a0001 | c0003 | t0001 | g0068 | SAS | PJL | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG03669 | hp2 | a0022 | c0074 | t0002 | g0019 | SAS | PJL | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG03688 | hp1 | a0001 | c0002 | t0002 | g0233 | SAS | STU | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG03688 | hp2 | a0002 | c0009 | t0002 | g0100 | SAS | STU | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG03704 | hp1 | a0009 | c0020 | t0002 | g0022 | SAS | PJL | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG03704 | hp2 | a0005 | c0068 | t0005 | g0257 | SAS | PJL | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG03831 | hp1 | a0009 | c0020 | t0002 | g0105 | SAS | BEB | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG03831 | hp2 | a0002 | c0019 | t0002 | g0272 | SAS | BEB | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG03834 | hp1 | a0003 | c0001 | t0002 | g0031 | SAS | BEB | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG03834 | hp2 | a0001 | c0003 | t0001 | g0262 | SAS | BEB | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG03927 | hp1 | a0004 | c0004 | t0002 | g0168 | SAS | BEB | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG03927 | hp2 | a0001 | c0002 | t0002 | g0167 | SAS | BEB | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG03942 | hp1 | a0004 | c0004 | t0002 | g0129 | SAS | BEB | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG03942 | hp2 | a0003 | c0001 | t0001 | g0118 | SAS | BEB | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG04115 | hp1 | a0001 | c0003 | t0001 | g0242 | SAS | STU | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG04115 | hp2 | a0004 | c0004 | t0002 | g0081 | SAS | STU | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG04184 | hp1 | a0001 | c0002 | t0009 | g0009 | SAS | BEB | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG04184 | hp2 | a0001 | c0002 | t0002 | g0221 | SAS | BEB | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG04199 | hp1 | a0001 | c0003 | t0001 | g0204 | SAS | STU | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG04199 | hp2 | a0006 | c0012 | t0001 | g0059 | SAS | STU | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG04204 | hp1 | a0001 | c0002 | t0002 | g0180 | SAS | STU | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG04204 | hp2 | a0023 | c0059 | t0001 | g0072 | SAS | STU | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG04228 | hp1 | a0003 | c0001 | t0001 | g0097 | SAS | STU | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG04228 | hp2 | a0004 | c0004 | t0002 | g0091 | SAS | STU | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA18522 | hp1 | a0002 | c0063 | t0002 | g0255 | AFR | YRI | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA18522 | hp2 | a0008 | c0035 | t0003 | g0093 | AFR | YRI | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA18747 | hp1 | a0001 | c0003 | t0001 | g0109 | EAS | CHB | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA18747 | hp2 | a0003 | c0001 | t0001 | g0064 | EAS | CHB | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA18906 | hp1 | a0002 | c0013 | t0003 | g0230 | AFR | YRI | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA18906 | hp2 | a0002 | c0017 | t0004 | g0125 | AFR | YRI | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA18944 | hp1 | a0002 | c0005 | t0002 | g0098 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA18944 | hp2 | a0004 | c0021 | t0001 | g0270 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA18945 | hp1 | a0002 | c0019 | t0002 | g0213 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA18945 | hp2 | a0004 | c0021 | t0001 | g0268 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA18947 | hp1 | a0002 | c0060 | t0002 | g0111 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA18947 | hp2 | a0001 | c0003 | t0001 | g0160 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA18950 | hp1 | a0004 | c0008 | t0005 | g0008 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA18950 | hp2 | a0004 | c0004 | t0002 | g0157 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA18952 | hp1 | a0001 | c0006 | t0001 | g0149 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA18952 | hp2 | a0002 | c0034 | t0001 | g0088 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA18954 | hp1 | a0001 | c0003 | t0001 | g0067 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA18954 | hp2 | a0004 | c0004 | t0002 | g0153 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA18956 | hp1 | a0024 | c0081 | t0001 | g0166 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA18956 | hp2 | a0001 | c0002 | t0002 | g0173 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA18957 | hp1 | a0002 | c0009 | t0002 | g0240 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA18957 | hp2 | a0002 | c0005 | t0002 | g0117 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA18966 | hp1 | a0003 | c0015 | t0002 | g0119 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA18966 | hp2 | a0003 | c0001 | t0001 | g0206 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA18967 | hp1 | a0004 | c0004 | t0002 | g0092 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA18967 | hp2 | a0025 | c0061 | t0002 | g0193 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA18969 | hp1 | a0004 | c0004 | t0002 | g0156 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA18969 | hp2 | a0005 | c0016 | t0002 | g0132 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA18970 | hp1 | a0001 | c0006 | t0001 | g0139 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA18970 | hp2 | a0012 | c0062 | t0001 | g0084 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA18971 | hp1 | a0001 | c0006 | t0001 | g0148 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA18971 | hp2 | a0004 | c0004 | t0002 | g0223 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA18973 | hp1 | a0002 | c0034 | t0001 | g0271 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA18973 | hp2 | a0004 | c0033 | t0001 | g0264 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA18975 | hp1 | a0004 | c0004 | t0002 | g0057 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA18975 | hp2 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA18980 | hp1 | a0002 | c0005 | t0002 | g0112 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA18980 | hp2 | a0003 | c0001 | t0001 | g0024 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA18983 | hp1 | a0003 | c0001 | t0001 | g0147 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA18983 | hp2 | a0004 | c0004 | t0002 | g0222 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA18990 | hp1 | a0004 | c0004 | t0002 | g0241 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA18990 | hp2 | a0007 | c0076 | t0001 | g0258 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA18993 | hp1 | a0004 | c0004 | t0002 | g0218 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA18993 | hp2 | a0004 | c0021 | t0001 | g0269 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA18995 | hp1 | a0026 | c0075 | t0002 | g0096 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA18995 | hp2 | a0003 | c0001 | t0010 | g0010 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA18997 | hp1 | a0001 | c0002 | t0002 | g0141 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA18997 | hp2 | a0002 | c0005 | t0002 | g0107 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA18999 | hp1 | a0001 | c0002 | t0002 | g0177 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA18999 | hp2 | a0005 | c0016 | t0002 | g0265 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA19000 | hp1 | a0003 | c0001 | t0001 | g0274 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA19000 | hp2 | a0002 | c0005 | t0002 | g0178 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA19005 | hp1 | a0001 | c0002 | t0002 | g0172 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA19005 | hp2 | a0002 | c0009 | t0002 | g0090 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA19007 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA19007 | hp2 | a0007 | c0029 | t0001 | g0085 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA19010 | hp1 | a0002 | c0005 | t0002 | g0005 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA19010 | hp2 | a0001 | c0003 | t0001 | g0293 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA19011 | hp1 | a0002 | c0005 | t0002 | g0238 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA19011 | hp2 | a0003 | c0001 | t0001 | g0110 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA19012 | hp1 | a0004 | c0004 | t0002 | g0219 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA19012 | hp2 | a0003 | c0015 | t0002 | g0034 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA19043 | hp1 | a0002 | c0013 | t0003 | g0291 | AFR | LWK | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA19043 | hp2 | a0002 | c0007 | t0001 | g0251 | AFR | LWK | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA19057 | hp1 | a0002 | c0009 | t0002 | g0152 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA19057 | hp2 | a0001 | c0003 | t0001 | g0062 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA19064 | hp1 | a0001 | c0002 | t0002 | g0163 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA19064 | hp2 | a0001 | c0006 | t0001 | g0046 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA19065 | hp1 | a0011 | c0057 | t0002 | g0065 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA19065 | hp2 | a0002 | c0005 | t0002 | g0099 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA19079 | hp1 | a0001 | c0002 | t0002 | g0140 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA19079 | hp2 | a0003 | c0018 | t0002 | g0137 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA19081 | hp1 | a0013 | c0030 | t0001 | g0087 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA19081 | hp2 | a0001 | c0003 | t0001 | g0145 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA19085 | hp1 | a0001 | c0002 | t0002 | g0150 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA19085 | hp2 | a0002 | c0007 | t0001 | g0058 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA19088 | hp1 | a0002 | c0005 | t0002 | g0005 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA19088 | hp2 | a0005 | c0016 | t0002 | g0224 | EAS | JPT | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA20129 | hp1 | a0003 | c0001 | t0001 | g0288 | AFR | ASW | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA20129 | hp2 | a0004 | c0008 | t0001 | g0253 | AFR | ASW | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA20752 | hp1 | a0027 | c0053 | t0002 | g0162 | EUR | TSI | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA20752 | hp2 | a0003 | c0001 | t0001 | g0194 | EUR | TSI | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA20805 | hp1 | a0005 | c0067 | t0001 | g0045 | EUR | TSI | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA20805 | hp2 | a0028 | c0056 | t0001 | g0189 | EUR | TSI | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA20905 | hp1 | a0001 | c0002 | t0002 | g0183 | SAS | GIH | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA20905 | hp2 | a0001 | c0002 | t0002 | g0191 | SAS | GIH | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG01123 | hp1 | a0001 | c0002 | t0002 | g0196 | AMR | CLM | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG01123 | hp2 | a0003 | c0001 | t0001 | g0051 | AMR | CLM | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02109 | hp1 | a0002 | c0007 | t0001 | g0012 | AFR | ACB | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02109 | hp2 | a0002 | c0032 | t0012 | g0287 | AFR | ACB | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02486 | hp1 | a0002 | c0010 | t0003 | g0246 | AFR | ACB | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02486 | hp2 | a0004 | c0008 | t0001 | g0116 | AFR | ACB | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02559 | hp1 | a0001 | c0049 | t0001 | g0158 | AFR | ACB | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG02559 | hp2 | a0008 | c0036 | t0003 | g0039 | AFR | ACB | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG03471 | hp1 | a0002 | c0065 | t0001 | g0289 | AFR | MSL | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG03471 | hp2 | a0003 | c0022 | t0001 | g0277 | AFR | MSL | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG06807 | hp1 | a0002 | c0007 | t0001 | g0001 | AFR | USA | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
HG06807 | hp2 | a0002 | c0010 | t0003 | g0244 | AFR | USA | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA20300 | hp1 | a0003 | c0001 | t0001 | g0053 | AFR | USA | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA20300 | hp2 | a0002 | c0010 | t0003 | g0247 | AFR | USA | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA21309 | hp1 | a0004 | c0004 | t0002 | g0038 | AFR | LWK | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
NA21309 | hp2 | a0003 | c0041 | t0003 | g0075 | AFR | LWK | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
homoSapiens | chm13v2 | a0003 | c0015 | t0002 | g0029 | REF | REF | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
homoSapiens | grch38p0 | a0003 | c0001 | t0006 | g0040 | REF | REF | PLXNB2_chr22_50269979_50312646 | PLXNB2 | chr22 | 50269979 | 50312646 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:50274980 | A | G | 21 | a0001 a0002 a0003 others(18): Show |
158 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(155): Show |
splice_region_variant | LOW | c.*724T>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 37/37 | chr22 | 50274980 | |||||||
chr22:50278631 | G | A | 1 | a0016 | 1 | HG00597.hp2 | missense_variant | MODERATE | c.4612C>T | p.Arg1538Trp | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 29/37 | 4779/6409 | 4612/5517 | 1538/1838 | chr22 | 50278631 | |||
chr22:50281979 | C | T | 1 | a0014 | 2 | HG02896.hp2 HG02897.hp2 |
missense_variant | MODERATE | c.3220G>A | p.Glu1074Lys | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 20/37 | 3387/6409 | 3220/5517 | 1074/1838 | chr22 | 50281979 | |||
chr22:50282796 | A | C | 1 | a0024 | 1 | NA18956.hp1 | missense_variant | MODERATE | c.2902T>G | p.Ser968Ala | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 18/37 | 3069/6409 | 2902/5517 | 968/1838 | chr22 | 50282796 | |||
chr22:50282823 | T | C | 1 | a0027 | 1 | NA20752.hp1 | missense_variant | MODERATE | c.2875A>G | p.Met959Val | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 18/37 | 3042/6409 | 2875/5517 | 959/1838 | chr22 | 50282823 | |||
chr22:50282867 | G | A | 1 | a0008 | 4 | HG02559.hp2 HG02818.hp2 HG02886.hp1 others(1): Show |
missense_variant | MODERATE | c.2831C>T | p.Ala944Val | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 18/37 | 2998/6409 | 2831/5517 | 944/1838 | chr22 | 50282867 | |||
chr22:50283063 | C | T | 4 | a0007 a0012 a0013 others(1): Show |
10 | HG00673.hp1 HG01106.hp1 HG01515.hp2 others(7): Show |
missense_variant | MODERATE | c.2803G>A | p.Val935Ile | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 17/37 | 2970/6409 | 2803/5517 | 935/1838 | chr22 | 50283063 | |||
chr22:50283705 | T | C | 13 | a0001 a0002 a0006 others(10): Show |
187 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(184): Show |
missense_variant | MODERATE | c.2467A>G | p.Ile823Val | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 15/37 | 2634/6409 | 2467/5517 | 823/1838 | chr22 | 50283705 | |||
chr22:50283738 | T | C | 5 | a0009 a0017 a0018 others(2): Show |
7 | HG00733.hp2 HG01106.hp1 HG01943.hp2 others(4): Show |
missense_variant | MODERATE | c.2434A>G | p.Thr812Ala | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 15/37 | 2601/6409 | 2434/5517 | 812/1838 | chr22 | 50283738 | |||
chr22:50283979 | T | C | 7 | a0005 a0006 a0007 others(4): Show |
25 | HG00423.hp1 HG00673.hp1 HG00735.hp1 others(22): Show |
missense_variant | MODERATE | c.2275A>G | p.Asn759Asp | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 14/37 | 2442/6409 | 2275/5517 | 759/1838 | chr22 | 50283979 | |||
chr22:50286075 | C | T | 1 | a0021 | 1 | HG03492.hp1 | missense_variant | MODERATE | c.1901G>A | p.Arg634His | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 10/37 | 2068/6409 | 1901/5517 | 634/1838 | chr22 | 50286075 | |||
chr22:50287122 | G | A | 1 | a0023 | 1 | HG04204.hp2 | missense_variant | MODERATE | c.1751C>T | p.Pro584Leu | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 8/37 | 1918/6409 | 1751/5517 | 584/1838 | chr22 | 50287122 | |||
chr22:50288024 | G | A | 1 | a0026 | 1 | NA18995.hp1 | missense_variant | MODERATE | c.1394C>T | p.Pro465Leu | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 6/37 | 1561/6409 | 1394/5517 | 465/1838 | chr22 | 50288024 | |||
chr22:50288030 | C | T | 1 | a0025 | 1 | NA18967.hp2 | missense_variant | MODERATE | c.1388G>A | p.Arg463Gln | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 6/37 | 1555/6409 | 1388/5517 | 463/1838 | chr22 | 50288030 | |||
chr22:50289633 | T | C | 17 | a0002 a0004 a0005 others(14): Show |
149 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(146): Show |
missense_variant | MODERATE | c.952A>G | p.Lys318Glu | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 3/37 | 1119/6409 | 952/5517 | 318/1838 | chr22 | 50289633 | |||
chr22:50289926 | G | A | 2 | a0015 a0020 |
3 | HG02922.hp1 HG02965.hp2 HG02976.hp2 |
missense_variant | MODERATE | c.659C>T | p.Ala220Val | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 3/37 | 826/6409 | 659/5517 | 220/1838 | chr22 | 50289926 | |||
chr22:50290574 | T | G | 1 | a0019 | 1 | HG02735.hp1 | missense_variant | MODERATE | c.11A>C | p.Gln4Pro | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 3/37 | 178/6409 | 11/5517 | 4/1838 | chr22 | 50290574 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:50275779 | G | A | 1 | a0001c0049 | 1 | HG02559.hp1 | synonymous_variant | LOW | c.5442C>T | p.Ala1814Ala | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 37/37 | 5609/6409 | 5442/5517 | 1814/1838 | chr22 | 50275779 | |||
chr22:50275782 | A | G | 2 | a0002c0071 a0008c0035 |
3 | HG02818.hp2 HG03540.hp1 NA18522.hp2 |
synonymous_variant | LOW | c.5439T>C | p.Pro1813Pro | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 37/37 | 5606/6409 | 5439/5517 | 1813/1838 | chr22 | 50275782 | |||
chr22:50277639 | C | T | 12 | a0001c0051 a0002c0010 a0002c0013 others(9): Show |
30 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(27): Show |
synonymous_variant | LOW | c.5148G>A | p.Ala1716Ala | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 33/37 | 5315/6409 | 5148/5517 | 1716/1838 | chr22 | 50277639 | |||
chr22:50277738 | G | A | 29 | a0001c0002 a0001c0006 a0001c0038 others(26): Show |
132 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(129): Show |
splice_region_variant&synonymous_variant | LOW | c.5049C>T | p.Ser1683Ser | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 33/37 | 5216/6409 | 5049/5517 | 1683/1838 | chr22 | 50277738 | |||
chr22:50277873 | G | A | 1 | a0007c0076 | 1 | NA18990.hp2 | synonymous_variant | LOW | c.5028C>T | p.Ile1676Ile | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 32/37 | 5195/6409 | 5028/5517 | 1676/1838 | chr22 | 50277873 | |||
chr22:50280512 | C | T | 4 | a0001c0051 a0002c0010 a0002c0013 others(1): Show |
14 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(11): Show |
synonymous_variant | LOW | c.4152G>A | p.Lys1384Lys | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 25/37 | 4319/6409 | 4152/5517 | 1384/1838 | chr22 | 50280512 | |||
chr22:50280611 | C | A | 1 | a0003c0044 | 1 | HG03130.hp2 | synonymous_variant | LOW | c.4053G>T | p.Ala1351Ala | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 25/37 | 4220/6409 | 4053/5517 | 1351/1838 | chr22 | 50280611 | |||
chr22:50280822 | A | G | 49 | a0001c0002 a0001c0006 a0001c0038 others(46): Show |
172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
synonymous_variant | LOW | c.3915T>C | p.Pro1305Pro | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 24/37 | 4082/6409 | 3915/5517 | 1305/1838 | chr22 | 50280822 | |||
chr22:50280888 | G | A | 1 | a0002c0072 | 1 | HG00597.hp1 | synonymous_variant | LOW | c.3849C>T | p.Arg1283Arg | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 24/37 | 4016/6409 | 3849/5517 | 1283/1838 | chr22 | 50280888 | |||
chr22:50280918 | G | A | 1 | a0001c0050 | 1 | HG02004.hp2 | synonymous_variant | LOW | c.3819C>T | p.Pro1273Pro | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 24/37 | 3986/6409 | 3819/5517 | 1273/1838 | chr22 | 50280918 | |||
chr22:50281120 | G | A | 1 | a0005c0068 | 1 | HG03704.hp2 | synonymous_variant | LOW | c.3732C>T | p.Ser1244Ser | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 23/37 | 3899/6409 | 3732/5517 | 1244/1838 | chr22 | 50281120 | |||
chr22:50281431 | C | T | 1 | a0002c0011 | 6 | HG01891.hp2 HG02647.hp2 HG03139.hp2 others(3): Show |
synonymous_variant | LOW | c.3591G>A | p.Pro1197Pro | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 22/37 | 3758/6409 | 3591/5517 | 1197/1838 | chr22 | 50281431 | |||
chr22:50281866 | G | A | 3 | a0001c0051 a0001c0052 a0002c0064 |
3 | HG02280.hp2 HG02717.hp2 HG03209.hp1 |
synonymous_variant | LOW | c.3333C>T | p.Leu1111Leu | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 20/37 | 3500/6409 | 3333/5517 | 1111/1838 | chr22 | 50281866 | |||
chr22:50281890 | G | A | 2 | a0002c0077 a0015c0037 |
3 | HG02922.hp1 HG02922.hp2 HG02976.hp2 |
synonymous_variant | LOW | c.3309C>T | p.Gly1103Gly | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 20/37 | 3476/6409 | 3309/5517 | 1103/1838 | chr22 | 50281890 | |||
chr22:50281989 | C | T | 1 | a0001c0046 | 1 | HG00099.hp2 | synonymous_variant | LOW | c.3210G>A | p.Thr1070Thr | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 20/37 | 3377/6409 | 3210/5517 | 1070/1838 | chr22 | 50281989 | |||
chr22:50282001 | G | C | 10 | a0001c0080 a0002c0010 a0002c0013 others(7): Show |
27 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(24): Show |
synonymous_variant | LOW | c.3198C>G | p.Ala1066Ala | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 20/37 | 3365/6409 | 3198/5517 | 1066/1838 | chr22 | 50282001 | |||
chr22:50282193 | C | T | 24 | a0001c0002 a0001c0038 a0001c0046 others(21): Show |
98 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(95): Show |
synonymous_variant | LOW | c.3108G>A | p.Gln1036Gln | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 19/37 | 3275/6409 | 3108/5517 | 1036/1838 | chr22 | 50282193 | |||
chr22:50282797 | C | A | 1 | a0003c0045 | 1 | HG01993.hp1 | synonymous_variant | LOW | c.2901G>T | p.Gly967Gly | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 18/37 | 3068/6409 | 2901/5517 | 967/1838 | chr22 | 50282797 | |||
chr22:50283848 | C | T | 2 | a0002c0013 a0002c0032 |
7 | HG02055.hp1 HG02109.hp2 HG02895.hp1 others(4): Show |
synonymous_variant | LOW | c.2406G>A | p.Pro802Pro | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 14/37 | 2573/6409 | 2406/5517 | 802/1838 | chr22 | 50283848 | |||
chr22:50286232 | C | T | 1 | a0003c0039 | 1 | HG00408.hp1 | synonymous_variant | LOW | c.1818G>A | p.Thr606Thr | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 9/37 | 1985/6409 | 1818/5517 | 606/1838 | chr22 | 50286232 | |||
chr22:50287124 | T | C | 20 | a0002c0005 a0002c0019 a0002c0032 others(17): Show |
47 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(44): Show |
synonymous_variant | LOW | c.1749A>G | p.Thr583Thr | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 8/37 | 1916/6409 | 1749/5517 | 583/1838 | chr22 | 50287124 | |||
chr22:50289014 | G | C | 1 | a0007c0076 | 1 | NA18990.hp2 | synonymous_variant | LOW | c.1197C>G | p.Ala399Ala | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 4/37 | 1364/6409 | 1197/5517 | 399/1838 | chr22 | 50289014 | |||
chr22:50289029 | G | T | 1 | a0002c0060 | 1 | NA18947.hp1 | synonymous_variant | LOW | c.1182C>A | p.Ala394Ala | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 4/37 | 1349/6409 | 1182/5517 | 394/1838 | chr22 | 50289029 | |||
chr22:50289083 | G | A | 1 | a0002c0017 | 4 | HG02055.hp2 HG02258.hp2 HG03579.hp1 others(1): Show |
synonymous_variant | LOW | c.1128C>T | p.Arg376Arg | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 4/37 | 1295/6409 | 1128/5517 | 376/1838 | chr22 | 50289083 | |||
chr22:50289739 | G | A | 1 | a0002c0077 | 1 | HG02922.hp2 | synonymous_variant | LOW | c.846C>T | p.Ala282Ala | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 3/37 | 1013/6409 | 846/5517 | 282/1838 | chr22 | 50289739 | |||
chr22:50289778 | G | A | 1 | a0001c0078 | 1 | HG02165.hp2 | synonymous_variant | LOW | c.807C>T | p.Pro269Pro | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 3/37 | 974/6409 | 807/5517 | 269/1838 | chr22 | 50289778 | |||
chr22:50290290 | G | A | 1 | a0001c0080 | 1 | HG02717.hp1 | synonymous_variant | LOW | c.295C>T | p.Leu99Leu | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 3/37 | 462/6409 | 295/5517 | 99/1838 | chr22 | 50290290 | |||
chr22:50290345 | C | T | 1 | a0001c0038 | 1 | HG02809.hp1 | synonymous_variant | LOW | c.240G>A | p.Pro80Pro | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 3/37 | 407/6409 | 240/5517 | 80/1838 | chr22 | 50290345 | |||
chr22:50290537 | T | C | 2 | a0004c0021 a0024c0081 |
4 | NA18944.hp2 NA18945.hp2 NA18956.hp1 others(1): Show |
synonymous_variant | LOW | c.48A>G | p.Ala16Ala | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 3/37 | 215/6409 | 48/5517 | 16/1838 | chr22 | 50290537 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:50274993 | C | CG | 10 | a0001c0051t0003 a0002c0010t0003 a0002c0013t0003 others(7): Show |
25 | HG01109.hp1 HG01891.hp1 HG02055.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*710dupC | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 37/37 | 710 | chr22 | 50274993 | ||||||
chr22:50275016 | C | A | 1 | a0002c0017t0004 | 4 | HG02055.hp2 HG02258.hp2 HG03579.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*688G>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 37/37 | 688 | chr22 | 50275016 | ||||||
chr22:50275067 | C | T | 11 | a0001c0051t0003 a0002c0010t0003 a0002c0013t0003 others(8): Show |
27 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*637G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 37/37 | 637 | chr22 | 50275067 | ||||||
chr22:50275379 | C | T | 1 | a0015c0037t0007 | 2 | HG02922.hp1 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*325G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 37/37 | 325 | chr22 | 50275379 | ||||||
chr22:50275437 | G | C | 91 | a0001c0002t0001 a0001c0002t0002 a0001c0002t0009 others(88): Show |
299 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(296): Show |
3_prime_UTR_variant | MODIFIER | c.*267C>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 37/37 | 267 | chr22 | 50275437 | ||||||
chr22:50275477 | G | A | 1 | a0002c0032t0012 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*227C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 37/37 | 227 | chr22 | 50275477 | ||||||
chr22:50294768 | A | G | 3 | a0004c0008t0005 a0005c0016t0011 a0005c0068t0005 |
4 | HG00423.hp1 HG02040.hp1 HG03704.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-63T>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 2/37 | 4184 | chr22 | 50294768 | ||||||
chr22:50307597 | GGCGCTGC others(10): Show |
G | 1 | a0003c0001t0010 | 1 | NA18995.hp2 | 5_prime_UTR_variant | MODIFIER | c.-135_-119delGGGCCA others(11): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/37 | 17014 | chr22 | 50307597 | ||||||
chr22:50307610 | G | T | 1 | a0009c0020t0002 | 1 | HG03704.hp1 | 5_prime_UTR_variant | MODIFIER | c.-131C>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/37 | 17026 | chr22 | 50307610 | ||||||
chr22:50307638 | C | T | 1 | a0001c0002t0009 | 1 | HG04184.hp1 | 5_prime_UTR_variant | MODIFIER | c.-159G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/37 | 17054 | chr22 | 50307638 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:50275821 | C | T | 14 | a0001c0051t0003g0120 a0002c0010t0003g0243 a0002c0010t0003g0244 others(11): Show |
14 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.5413-13G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 36/36 | chr22 | 50275821 | |||||||
chr22:50275860 | T | C | 224 | a0001c0002t0001g0182 a0001c0002t0002g0154 a0001c0003t0001g0004 others(221): Show |
231 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.5412+29A>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 36/36 | chr22 | 50275860 | |||||||
chr22:50275860 | T | G | 1 | a0002c0013t0003g0165 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.5412+29A>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 36/36 | chr22 | 50275860 | |||||||
chr22:50275861 | G | C | 1 | a0002c0013t0003g0165 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.5412+28C>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 36/36 | chr22 | 50275861 | |||||||
chr22:50275861 | G | GC | 5 | a0002c0013t0003g0228 a0002c0017t0004g0124 a0003c0001t0001g0274 others(2): Show |
5 | HG01993.hp1 HG02055.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.5412+27dupG | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 36/36 | chr22 | 50275861 | |||||||
chr22:50275997 | G | T | 1 | a0001c0003t0001g0020 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.5338-34C>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50275997 | |||||||
chr22:50276062 | A | C | 178 | a0001c0002t0001g0182 a0001c0003t0001g0004 a0001c0003t0001g0020 others(175): Show |
184 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.5338-99T>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276062 | |||||||
chr22:50276100 | C | A | 1 | a0001c0003t0001g0020 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.5338-137G>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276100 | |||||||
chr22:50276112 | A | G | 178 | a0001c0002t0001g0182 a0001c0003t0001g0004 a0001c0003t0001g0020 others(175): Show |
184 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.5338-149T>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276112 | |||||||
chr22:50276133 | C | T | 1 | a0001c0003t0001g0062 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.5338-170G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276133 | |||||||
chr22:50276187 | G | A | 164 | a0001c0003t0001g0004 a0001c0003t0001g0020 a0001c0003t0001g0025 others(161): Show |
168 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.5338-224C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276187 | |||||||
chr22:50276197 | G | A | 6 | a0001c0003t0001g0043 a0001c0003t0001g0266 a0001c0003t0001g0267 others(3): Show |
6 | HG02258.hp1 HG02572.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.5338-234C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276197 | |||||||
chr22:50276302 | A | G | 2 | a0002c0014t0008g0134 a0002c0014t0008g0135 |
2 | HG01884.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.5337+327T>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276302 | |||||||
chr22:50276309 | C | T | 163 | a0001c0003t0001g0004 a0001c0003t0001g0020 a0001c0003t0001g0025 others(160): Show |
167 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.5337+320G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276309 | |||||||
chr22:50276314 | A | G | 2 | a0002c0014t0008g0134 a0002c0014t0008g0135 |
2 | HG01884.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.5337+315T>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276314 | |||||||
chr22:50276317 | G | C | 2 | a0002c0014t0008g0134 a0002c0014t0008g0135 |
2 | HG01884.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.5337+312C>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276317 | |||||||
chr22:50276322 | G | GCAGGGAG others(747): Show |
1 | a0004c0070t0002g0239 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.5337+306_5337+307i others(756): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276322 | |||||||
chr22:50276345 | C | G | 1 | a0011c0023t0001g0035 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.5337+284G>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276345 | |||||||
chr22:50276351 | A | AGGGTGCA others(747): Show |
2 | a0001c0002t0002g0142 a0001c0002t0002g0232 |
2 | HG02683.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.5337+277_5337+278i others(756): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276351 | |||||||
chr22:50276351 | A | AGGGTGCA others(790): Show |
1 | a0001c0002t0002g0141 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.5337+277_5337+278i others(799): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276351 | |||||||
chr22:50276351 | A | AGGGTGCA others(787): Show |
1 | a0001c0002t0002g0163 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.5337+277_5337+278i others(796): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276351 | |||||||
chr22:50276351 | A | AGGGTGCA others(947): Show |
1 | a0003c0015t0002g0119 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.5337+277_5337+278i others(956): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276351 | |||||||
chr22:50276351 | A | AGGGTGCA others(1067): Show |
1 | a0011c0057t0002g0065 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.5337+277_5337+278i others(1076): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276351 | |||||||
chr22:50276351 | A | AGGGTGCA others(747): Show |
1 | a0004c0004t0002g0083 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.5337+277_5337+278i others(756): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276351 | |||||||
chr22:50276351 | A | AGGGTGCA others(790): Show |
1 | a0001c0002t0002g0231 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.5337+277_5337+278i others(799): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276351 | |||||||
chr22:50276351 | A | AGGGTGCA others(787): Show |
6 | a0002c0011t0002g0042 a0002c0011t0002g0275 a0002c0011t0002g0281 others(3): Show |
6 | HG01891.hp2 HG02647.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.5337+277_5337+278i others(796): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276351 | |||||||
chr22:50276351 | A | AGGGTGCA others(787): Show |
1 | a0001c0002t0002g0013 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.5337+277_5337+278i others(796): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276351 | |||||||
chr22:50276351 | A | AGGGTGCA others(787): Show |
1 | a0009c0020t0002g0047 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.5337+277_5337+278i others(796): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276351 | |||||||
chr22:50276351 | A | AGGGTGCA others(787): Show |
50 | a0001c0002t0002g0033 a0001c0002t0002g0133 a0001c0002t0002g0140 others(47): Show |
51 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.5337+277_5337+278i others(796): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276351 | |||||||
chr22:50276351 | A | AGGGTGCA others(788): Show |
1 | a0002c0019t0002g0272 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.5337+277_5337+278i others(797): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276351 | |||||||
chr22:50276351 | A | AGGGTGCA others(787): Show |
36 | a0001c0002t0002g0154 a0002c0009t0002g0015 a0002c0009t0002g0016 others(33): Show |
36 | HG00280.hp2 HG00423.hp1 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.5337+277_5337+278i others(796): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276351 | |||||||
chr22:50276351 | A | AGGGTGCA others(788): Show |
1 | a0004c0004t0002g0101 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.5337+277_5337+278i others(797): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276351 | |||||||
chr22:50276351 | A | AGGGTGCA others(787): Show |
1 | a0001c0002t0002g0221 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.5337+277_5337+278i others(796): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276351 | |||||||
chr22:50276351 | A | AGGGTGCA others(788): Show |
1 | a0001c0002t0009g0009 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.5337+277_5337+278i others(797): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276351 | |||||||
chr22:50276351 | A | AGGGTGCA others(787): Show |
2 | a0002c0063t0002g0255 a0004c0025t0002g0006 |
3 | HG02895.hp2 HG02897.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.5337+277_5337+278i others(796): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276351 | |||||||
chr22:50276351 | A | AGGGTGCA others(788): Show |
1 | a0009c0020t0002g0105 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.5337+277_5337+278i others(797): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276351 | |||||||
chr22:50276351 | A | AGGGTGCA others(789): Show |
1 | a0002c0072t0002g0044 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.5337+277_5337+278i others(798): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276351 | |||||||
chr22:50276351 | A | AGGGTGCA others(789): Show |
1 | a0004c0004t0002g0153 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.5337+277_5337+278i others(798): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276351 | |||||||
chr22:50276351 | A | AGGGTGCA others(789): Show |
1 | a0022c0074t0002g0019 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.5337+277_5337+278i others(798): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276351 | |||||||
chr22:50276351 | A | T | 3 | a0002c0014t0008g0134 a0002c0014t0008g0135 a0004c0070t0002g0239 |
3 | HG01109.hp2 HG01884.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.5337+278T>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276351 | |||||||
chr22:50276354 | G | A | 2 | a0002c0014t0008g0134 a0002c0014t0008g0135 |
2 | HG01884.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.5337+275C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276354 | |||||||
chr22:50276357 | C | G | 2 | a0002c0014t0008g0134 a0002c0014t0008g0135 |
2 | HG01884.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.5337+272G>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276357 | |||||||
chr22:50276361 | C | A | 2 | a0002c0014t0008g0134 a0002c0014t0008g0135 |
2 | HG01884.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.5337+268G>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276361 | |||||||
chr22:50276362 | G | A | 3 | a0002c0014t0008g0134 a0002c0014t0008g0135 a0003c0001t0001g0110 |
3 | HG01884.hp1 HG03225.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.5337+267C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276362 | |||||||
chr22:50276362 | G | GCAGGGAG others(830): Show |
1 | a0017c0055t0001g0217 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.5337+266_5337+267i others(839): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276362 | |||||||
chr22:50276362 | G | GCAGGGAG others(830): Show |
12 | a0001c0002t0001g0182 a0003c0042t0001g0018 a0004c0008t0005g0008 others(9): Show |
14 | HG00673.hp1 HG01934.hp2 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.5337+266_5337+267i others(839): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276362 | |||||||
chr22:50276362 | G | GCAGGGAG others(832): Show |
1 | a0013c0030t0001g0220 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.5337+266_5337+267i others(841): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276362 | |||||||
chr22:50276365 | G | GGGAGGGG others(789): Show |
1 | a0002c0005t0002g0178 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.5337+263_5337+264i others(798): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276365 | |||||||
chr22:50276391 | T | A | 1 | a0001c0047t0001g0078 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.5337+238A>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276391 | |||||||
chr22:50276402 | G | GCAGGGAG others(1348): Show |
1 | a0003c0001t0001g0147 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.5337+226_5337+227i others(1357): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276402 | |||||||
chr22:50276402 | G | GCAGGGAG others(1367): Show |
1 | a0001c0003t0001g0020 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.5337+226_5337+227i others(1376): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276402 | |||||||
chr22:50276402 | G | GCAGGGAG others(988): Show |
1 | a0004c0008t0001g0254 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.5337+226_5337+227i others(997): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276402 | |||||||
chr22:50276402 | G | GCAGGGAG others(790): Show |
1 | a0002c0013t0003g0248 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.5337+226_5337+227i others(799): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276402 | |||||||
chr22:50276402 | G | GCAGGGAG others(1268): Show |
2 | a0004c0021t0001g0268 a0024c0081t0001g0166 |
2 | NA18945.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.5337+226_5337+227i others(1277): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276402 | |||||||
chr22:50276402 | G | GCAGGGAG others(1268): Show |
1 | a0004c0021t0001g0269 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.5337+226_5337+227i others(1277): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276402 | |||||||
chr22:50276402 | G | GCAGGGAG others(1028): Show |
3 | a0004c0008t0001g0249 a0004c0008t0001g0250 a0004c0008t0001g0253 |
3 | HG02647.hp1 HG02965.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.5337+226_5337+227i others(1037): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276402 | |||||||
chr22:50276402 | G | GCAGGGAG others(1348): Show |
7 | a0001c0003t0001g0145 a0001c0003t0001g0160 a0001c0003t0001g0242 others(4): Show |
7 | HG02074.hp2 HG02155.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.5337+226_5337+227i others(1357): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276402 | |||||||
chr22:50276402 | G | GCAGGGAG others(1629): Show |
1 | a0001c0003t0001g0202 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.5337+226_5337+227i others(1638): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276402 | |||||||
chr22:50276402 | G | GCAGGGAG others(1350): Show |
1 | a0010c0069t0001g0236 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.5337+226_5337+227i others(1359): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276402 | |||||||
chr22:50276402 | G | GCAGGGAG others(1349): Show |
1 | a0001c0003t0001g0204 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.5337+226_5337+227i others(1358): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276402 | |||||||
chr22:50276402 | G | GCAGGGAG others(1350): Show |
1 | a0006c0012t0001g0059 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.5337+226_5337+227i others(1359): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276402 | |||||||
chr22:50276402 | G | GCAGGGAG others(1348): Show |
1 | a0006c0012t0001g0237 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.5337+226_5337+227i others(1357): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276402 | |||||||
chr22:50276402 | G | GCAGGGAG others(1349): Show |
1 | a0006c0012t0001g0216 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.5337+226_5337+227i others(1358): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276402 | |||||||
chr22:50276402 | G | GCAGGGAG others(1350): Show |
1 | a0006c0012t0001g0209 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.5337+226_5337+227i others(1359): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276402 | |||||||
chr22:50276402 | G | GCAGGGAG others(792): Show |
1 | a0002c0013t0003g0165 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.5337+226_5337+227i others(801): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276402 | |||||||
chr22:50276402 | G | GCAGGGAG others(1188): Show |
3 | a0001c0006t0001g0046 a0002c0028t0001g0225 a0016c0048t0001g0143 |
3 | HG00597.hp2 HG02155.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.5337+226_5337+227i others(1197): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276402 | |||||||
chr22:50276402 | G | GCAGGGAG others(1028): Show |
13 | a0001c0006t0001g0138 a0001c0006t0001g0139 a0001c0006t0001g0144 others(10): Show |
13 | HG00609.hp2 HG00639.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.5337+226_5337+227i others(1037): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276402 | |||||||
chr22:50276402 | G | GCAGGGAG others(1029): Show |
1 | a0001c0006t0001g0159 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.5337+226_5337+227i others(1038): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276402 | |||||||
chr22:50276402 | G | GCAGGGAG others(789): Show |
4 | a0002c0007t0001g0001 a0002c0007t0001g0012 a0014c0027t0001g0011 others(1): Show |
5 | HG01884.hp2 HG02109.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.5337+226_5337+227i others(798): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276402 | |||||||
chr22:50276402 | G | GCAGGGAG others(1028): Show |
3 | a0002c0032t0001g0286 a0002c0032t0012g0287 a0002c0073t0001g0263 |
3 | HG02109.hp2 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.5337+226_5337+227i others(1037): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276402 | |||||||
chr22:50276402 | G | GCAGGGAG others(1028): Show |
10 | a0001c0052t0001g0077 a0001c0080t0001g0079 a0002c0007t0001g0122 others(7): Show |
11 | HG02145.hp1 HG02717.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.5337+226_5337+227i others(1037): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276402 | |||||||
chr22:50276402 | G | GCAGGGAG others(789): Show |
13 | a0001c0051t0003g0120 a0002c0010t0003g0243 a0002c0010t0003g0244 others(10): Show |
13 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.5337+226_5337+227i others(798): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276402 | |||||||
chr22:50276402 | G | GCAGGGAG others(790): Show |
1 | a0002c0010t0003g0247 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.5337+226_5337+227i others(799): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276402 | |||||||
chr22:50276402 | G | GCAGGGAG others(1028): Show |
4 | a0002c0017t0004g0124 a0002c0017t0004g0125 a0002c0017t0004g0127 others(1): Show |
4 | HG02055.hp2 HG02258.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.5337+226_5337+227i others(1037): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276402 | |||||||
chr22:50276402 | G | GCAGGGAG others(1069): Show |
1 | a0003c0022t0001g0277 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.5337+226_5337+227i others(1078): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276402 | |||||||
chr22:50276402 | G | GCAGGGAG others(1268): Show |
1 | a0003c0001t0001g0206 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.5337+226_5337+227i others(1277): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276402 | |||||||
chr22:50276402 | G | GCAGGGAG others(1348): Show |
38 | a0001c0003t0001g0004 a0001c0003t0001g0027 a0001c0003t0001g0028 others(35): Show |
40 | HG00423.hp2 HG00639.hp1 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.5337+226_5337+227i others(1357): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276402 | |||||||
chr22:50276402 | G | GCAGGGAG others(1587): Show |
1 | a0003c0001t0001g0118 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.5337+226_5337+227i others(1596): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276402 | |||||||
chr22:50276402 | G | GCAGGGAG others(1349): Show |
1 | a0001c0003t0001g0062 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.5337+226_5337+227i others(1358): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276402 | |||||||
chr22:50276402 | G | GCAGGGAG others(1349): Show |
1 | a0003c0001t0001g0076 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.5337+226_5337+227i others(1358): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276402 | |||||||
chr22:50276402 | G | GCAGGGAG others(1349): Show |
1 | a0003c0001t0001g0052 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.5337+226_5337+227i others(1358): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276402 | |||||||
chr22:50276402 | G | GCAGGGAG others(1351): Show |
1 | a0001c0003t0001g0025 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.5337+226_5337+227i others(1360): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276402 | |||||||
chr22:50276402 | G | GCAGGGAG others(1351): Show |
1 | a0003c0001t0001g0097 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.5337+226_5337+227i others(1360): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276402 | |||||||
chr22:50276402 | G | GCAGGGAG others(1351): Show |
1 | a0003c0001t0001g0063 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.5337+226_5337+227i others(1360): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276402 | |||||||
chr22:50276402 | G | GCAGGGAG others(1350): Show |
1 | a0011c0023t0001g0035 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.5337+226_5337+227i others(1359): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276402 | |||||||
chr22:50276402 | G | GCAGGGAG others(1349): Show |
1 | a0003c0001t0001g0071 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.5337+226_5337+227i others(1358): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276402 | |||||||
chr22:50276402 | G | GCAGGGAG others(1349): Show |
1 | a0003c0001t0001g0050 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.5337+226_5337+227i others(1358): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276402 | |||||||
chr22:50276402 | G | GCAGGGAG others(1348): Show |
1 | a0001c0003t0001g0067 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.5337+226_5337+227i others(1357): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276402 | |||||||
chr22:50276402 | G | GCAGGGAG others(1388): Show |
1 | a0018c0054t0001g0041 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.5337+226_5337+227i others(1397): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276402 | |||||||
chr22:50276402 | G | GCAGGGAG others(1393): Show |
1 | a0001c0003t0001g0184 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.5337+226_5337+227i others(1402): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276402 | |||||||
chr22:50276402 | G | GCAGGGAG others(1348): Show |
4 | a0002c0007t0001g0058 a0002c0034t0001g0088 a0004c0021t0001g0270 others(1): Show |
4 | HG02071.hp1 NA18944.hp2 NA18952.hp2 others(1): Show |
intron_variant | MODIFIER | c.5337+226_5337+227i others(1357): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276402 | |||||||
chr22:50276402 | G | GCAGGGAG others(1348): Show |
2 | a0001c0003t0001g0207 a0001c0003t0001g0210 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.5337+226_5337+227i others(1357): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276402 | |||||||
chr22:50276402 | G | GCAGGGAG others(1350): Show |
1 | a0004c0033t0001g0264 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.5337+226_5337+227i others(1359): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276402 | |||||||
chr22:50276402 | G | GCAGGGAG others(1349): Show |
1 | a0002c0034t0001g0271 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.5337+226_5337+227i others(1358): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276402 | |||||||
chr22:50276402 | G | GCAGGGAG others(1350): Show |
1 | a0003c0001t0001g0108 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.5337+226_5337+227i others(1359): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276402 | |||||||
chr22:50276402 | G | GCAGGGAG others(947): Show |
1 | a0008c0036t0003g0039 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.5337+226_5337+227i others(956): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276402 | |||||||
chr22:50276402 | G | GCAGGGAG others(948): Show |
4 | a0002c0071t0003g0094 a0008c0035t0003g0093 a0008c0035t0003g0095 others(1): Show |
4 | HG02818.hp2 HG02886.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.5337+226_5337+227i others(957): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276402 | |||||||
chr22:50276402 | G | GCAGGGAG others(1352): Show |
1 | a0006c0012t0001g0208 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.5337+226_5337+227i others(1361): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276402 | |||||||
chr22:50276402 | G | GCAGGGAG others(1351): Show |
1 | a0001c0003t0001g0151 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.5337+226_5337+227i others(1360): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276402 | |||||||
chr22:50276402 | G | GCAGGGAG others(1189): Show |
1 | a0002c0028t0001g0226 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.5337+226_5337+227i others(1198): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276402 | |||||||
chr22:50276402 | G | GCAGGGAG others(1029): Show |
1 | a0003c0015t0001g0048 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.5337+226_5337+227i others(1038): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276402 | |||||||
chr22:50276402 | G | GCAGGGAG others(1349): Show |
1 | a0023c0059t0001g0072 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.5337+226_5337+227i others(1358): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276402 | |||||||
chr22:50276402 | G | GCAGGGAG others(1350): Show |
1 | a0001c0003t0001g0069 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.5337+226_5337+227i others(1359): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276402 | |||||||
chr22:50276402 | G | GCAGGGAG others(1352): Show |
1 | a0003c0045t0001g0074 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.5337+226_5337+227i others(1361): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276402 | |||||||
chr22:50276402 | G | GCAGGGAG others(949): Show |
1 | a0002c0014t0003g0259 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.5337+226_5337+227i others(958): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276402 | |||||||
chr22:50276402 | G | GCAGGGAG others(1388): Show |
2 | a0001c0047t0001g0078 a0003c0001t0001g0115 |
2 | HG02572.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.5337+226_5337+227i others(1397): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276402 | |||||||
chr22:50276402 | G | GCAGGGAG others(989): Show |
1 | a0002c0014t0003g0260 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.5337+226_5337+227i others(998): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276402 | |||||||
chr22:50276402 | G | GCAGGGAG others(989): Show |
2 | a0004c0026t0003g0123 a0004c0026t0003g0261 |
2 | HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.5337+226_5337+227i others(998): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276402 | |||||||
chr22:50276402 | G | GCAGGGAG others(1229): Show |
1 | a0003c0001t0001g0055 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.5337+226_5337+227i others(1238): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276402 | |||||||
chr22:50276402 | G | GCAGGGAG others(1353): Show |
1 | a0004c0008t0001g0116 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.5337+226_5337+227i others(1362): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276402 | |||||||
chr22:50276402 | G | GCAGGGAG others(1312): Show |
1 | a0001c0003t0001g0205 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.5337+226_5337+227i others(1321): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276402 | |||||||
chr22:50276402 | G | GCAGGGAG others(1189): Show |
1 | a0003c0039t0001g0056 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.5337+226_5337+227i others(1198): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276402 | |||||||
chr22:50276402 | G | GCAGGGAG others(1350): Show |
1 | a0001c0003t0001g0068 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.5337+226_5337+227i others(1359): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276402 | |||||||
chr22:50276402 | G | GCAGGGAT others(193): Show |
2 | a0002c0014t0008g0134 a0002c0014t0008g0135 |
2 | HG01884.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.5337+226_5337+227i others(202): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276402 | |||||||
chr22:50276465 | G | A | 1 | a0001c0002t0002g0150 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.5337+164C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276465 | |||||||
chr22:50276497 | A | T | 1 | a0003c0001t0001g0063 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.5337+132T>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276497 | |||||||
chr22:50276502 | G | A | 2 | a0004c0021t0001g0268 a0004c0021t0001g0269 |
2 | NA18945.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.5337+127C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276502 | |||||||
chr22:50276510 | G | A | 3 | a0002c0007t0001g0058 a0002c0034t0001g0088 a0002c0034t0001g0271 |
3 | NA18952.hp2 NA18973.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.5337+119C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276510 | |||||||
chr22:50276535 | C | G | 15 | a0001c0002t0001g0182 a0001c0003t0001g0062 a0003c0042t0001g0018 others(12): Show |
17 | HG00673.hp1 HG01106.hp1 HG01515.hp2 others(14): Show |
intron_variant | MODIFIER | c.5337+94G>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276535 | |||||||
chr22:50276600 | T | C | 289 | a0001c0002t0001g0182 a0001c0002t0002g0013 a0001c0002t0002g0033 others(286): Show |
297 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(294): Show |
intron_variant | MODIFIER | c.5337+29A>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 35/36 | chr22 | 50276600 | |||||||
chr22:50276736 | C | T | 1 | a0004c0026t0003g0261 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.5262-32G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 34/36 | chr22 | 50276736 | |||||||
chr22:50276808 | A | C | 1 | a0001c0003t0001g0151 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.5261+34T>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 34/36 | chr22 | 50276808 | |||||||
chr22:50277093 | G | A | 1 | a0005c0068t0005g0257 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.5197-187C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 33/36 | chr22 | 50277093 | |||||||
chr22:50277102 | T | G | 2 | a0002c0014t0008g0134 a0002c0014t0008g0135 |
2 | HG01884.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.5197-196A>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 33/36 | chr22 | 50277102 | |||||||
chr22:50277180 | A | G | 7 | a0002c0014t0003g0259 a0002c0014t0003g0260 a0002c0014t0008g0134 others(4): Show |
7 | HG01109.hp1 HG01884.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.5197-274T>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 33/36 | chr22 | 50277180 | |||||||
chr22:50277264 | G | A | 3 | a0002c0032t0001g0286 a0002c0032t0012g0287 a0002c0073t0001g0263 |
3 | HG02109.hp2 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.5196+327C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 33/36 | chr22 | 50277264 | |||||||
chr22:50277280 | G | A | 1 | a0001c0006t0002g0155 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.5196+311C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 33/36 | chr22 | 50277280 | |||||||
chr22:50277300 | C | CA | 144 | a0001c0002t0001g0182 a0001c0002t0002g0013 a0001c0002t0002g0033 others(141): Show |
146 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.5196+290dupT | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 33/36 | chr22 | 50277300 | |||||||
chr22:50277300 | C | CAA | 13 | a0002c0014t0003g0036 a0003c0042t0001g0018 a0004c0008t0005g0008 others(10): Show |
15 | HG00673.hp1 HG01106.hp1 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.5196+289_5196+290d others(4): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 33/36 | chr22 | 50277300 | |||||||
chr22:50277383 | C | G | 8 | a0002c0014t0003g0036 a0002c0014t0003g0259 a0002c0014t0003g0260 others(5): Show |
8 | HG01109.hp1 HG01884.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.5196+208G>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 33/36 | chr22 | 50277383 | |||||||
chr22:50277428 | C | T | 2 | a0002c0077t0001g0292 a0015c0037t0007g0007 |
3 | HG02922.hp1 HG02922.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.5196+163G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 33/36 | chr22 | 50277428 | |||||||
chr22:50277544 | G | T | 113 | a0001c0002t0001g0182 a0001c0002t0002g0013 a0001c0002t0002g0033 others(110): Show |
114 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.5196+47C>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 33/36 | chr22 | 50277544 | |||||||
chr22:50278051 | C | T | 2 | a0010c0031t0002g0082 a0010c0031t0002g0086 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.4888-38G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 31/36 | chr22 | 50278051 | |||||||
chr22:50278063 | G | A | 5 | a0002c0071t0003g0094 a0008c0035t0003g0093 a0008c0035t0003g0095 others(2): Show |
5 | HG02559.hp2 HG02818.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.4888-50C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 31/36 | chr22 | 50278063 | |||||||
chr22:50278078 | T | C | 1 | a0003c0022t0001g0277 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4887+39A>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 31/36 | chr22 | 50278078 | |||||||
chr22:50278530 | C | T | 1 | a0002c0011t0002g0281 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4648-11G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 29/36 | chr22 | 50278530 | |||||||
chr22:50278586 | A | G | 3 | a0002c0007t0001g0058 a0002c0034t0001g0088 a0002c0034t0001g0271 |
3 | NA18952.hp2 NA18973.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.4647+10T>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 29/36 | chr22 | 50278586 | |||||||
chr22:50278700 | T | G | 134 | a0001c0002t0001g0182 a0001c0002t0002g0013 a0001c0002t0002g0033 others(131): Show |
136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
splice_region_variant&intron_variant | LOW | c.4547-4A>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 28/36 | chr22 | 50278700 | |||||||
chr22:50279047 | C | A | 22 | a0001c0051t0003g0120 a0002c0010t0003g0243 a0002c0010t0003g0244 others(19): Show |
22 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.4390-36G>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 27/36 | chr22 | 50279047 | |||||||
chr22:50279118 | T | C | 132 | a0001c0002t0001g0182 a0001c0002t0002g0013 a0001c0002t0002g0033 others(129): Show |
133 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.4390-107A>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 27/36 | chr22 | 50279118 | |||||||
chr22:50279166 | A | G | 1 | a0003c0022t0001g0294 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.4390-155T>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 27/36 | chr22 | 50279166 | |||||||
chr22:50279201 | G | A | 1 | a0002c0019t0002g0104 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.4390-190C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 27/36 | chr22 | 50279201 | |||||||
chr22:50279330 | A | C | 1 | a0002c0013t0003g0248 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.4389+300T>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 27/36 | chr22 | 50279330 | |||||||
chr22:50279331 | C | A | 1 | a0002c0013t0003g0248 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.4389+299G>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 27/36 | chr22 | 50279331 | |||||||
chr22:50279358 | C | A | 1 | a0001c0003t0001g0121 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.4389+272G>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 27/36 | chr22 | 50279358 | |||||||
chr22:50279404 | C | T | 111 | a0001c0002t0001g0182 a0001c0002t0002g0013 a0001c0002t0002g0033 others(108): Show |
112 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.4389+226G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 27/36 | chr22 | 50279404 | |||||||
chr22:50279527 | T | C | 4 | a0002c0009t0002g0152 a0004c0004t0002g0153 a0004c0004t0002g0156 others(1): Show |
4 | NA18950.hp2 NA18954.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.4389+103A>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 27/36 | chr22 | 50279527 | |||||||
chr22:50279555 | C | A | 14 | a0001c0051t0003g0120 a0002c0010t0003g0243 a0002c0010t0003g0244 others(11): Show |
14 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.4389+75G>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 27/36 | chr22 | 50279555 | |||||||
chr22:50279818 | G | C | 1 | a0005c0068t0005g0257 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.4243-42C>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 26/36 | chr22 | 50279818 | |||||||
chr22:50279829 | G | A | 1 | a0002c0013t0003g0165 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.4243-53C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 26/36 | chr22 | 50279829 | |||||||
chr22:50279868 | G | A | 1 | a0001c0006t0001g0192 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.4243-92C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 26/36 | chr22 | 50279868 | |||||||
chr22:50279968 | A | G | 169 | a0001c0002t0001g0182 a0001c0002t0002g0013 a0001c0002t0002g0033 others(166): Show |
173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.4242+37T>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 26/36 | chr22 | 50279968 | |||||||
chr22:50280123 | C | G | 1 | a0002c0013t0003g0248 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.4176-52G>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 25/36 | chr22 | 50280123 | |||||||
chr22:50280154 | C | G | 1 | a0001c0080t0001g0079 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.4176-83G>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 25/36 | chr22 | 50280154 | |||||||
chr22:50280328 | T | C | 13 | a0003c0042t0001g0018 a0004c0008t0005g0008 a0005c0067t0001g0045 others(10): Show |
15 | HG00673.hp1 HG01106.hp1 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.4175+161A>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 25/36 | chr22 | 50280328 | |||||||
chr22:50280330 | G | C | 1 | a0001c0002t0002g0141 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.4175+159C>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 25/36 | chr22 | 50280330 | |||||||
chr22:50280332 | C | G | 1 | a0001c0002t0002g0141 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.4175+157G>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 25/36 | chr22 | 50280332 | |||||||
chr22:50280444 | G | A | 14 | a0001c0051t0003g0120 a0002c0010t0003g0243 a0002c0010t0003g0244 others(11): Show |
14 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.4175+45C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 25/36 | chr22 | 50280444 | |||||||
chr22:50280677 | G | T | 1 | a0002c0013t0003g0248 | 1 | HG02895.hp1 | splice_region_variant&intron_variant | LOW | c.3994-7C>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 24/36 | chr22 | 50280677 | |||||||
chr22:50280684 | C | T | 1 | a0001c0002t0002g0234 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.3994-14G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 24/36 | chr22 | 50280684 | |||||||
chr22:50280736 | T | C | 154 | a0001c0002t0001g0182 a0001c0002t0002g0013 a0001c0002t0002g0033 others(151): Show |
157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
splice_region_variant&intron_variant | LOW | c.3993+8A>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 24/36 | chr22 | 50280736 | |||||||
chr22:50281014 | G | A | 3 | a0002c0007t0001g0058 a0002c0034t0001g0088 a0002c0034t0001g0271 |
3 | NA18952.hp2 NA18973.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.3764-41C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 23/36 | chr22 | 50281014 | |||||||
chr22:50281214 | G | C | 1 | a0002c0034t0001g0271 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.3663-25C>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 22/36 | chr22 | 50281214 | |||||||
chr22:50281223 | G | A | 2 | a0001c0006t0001g0186 a0001c0006t0001g0215 |
2 | HG00639.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.3663-34C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 22/36 | chr22 | 50281223 | |||||||
chr22:50281239 | C | T | 1 | a0002c0013t0003g0248 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3663-50G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 22/36 | chr22 | 50281239 | |||||||
chr22:50281241 | G | C | 1 | a0004c0008t0001g0249 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3663-52C>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 22/36 | chr22 | 50281241 | |||||||
chr22:50281346 | G | C | 1 | a0002c0014t0003g0260 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3662+14C>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 22/36 | chr22 | 50281346 | |||||||
chr22:50281547 | C | T | 20 | a0001c0002t0002g0154 a0002c0009t0002g0015 a0002c0009t0002g0016 others(17): Show |
20 | HG00280.hp1 HG00280.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.3522+19G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 21/36 | chr22 | 50281547 | |||||||
chr22:50281556 | G | A | 1 | a0016c0048t0001g0143 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.3522+10C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 21/36 | chr22 | 50281556 | |||||||
chr22:50281752 | C | G | 99 | a0001c0002t0001g0182 a0001c0002t0002g0013 a0001c0002t0002g0033 others(96): Show |
100 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.3346-10G>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 20/36 | chr22 | 50281752 | |||||||
chr22:50281762 | C | T | 5 | a0002c0005t0002g0164 a0002c0005t0002g0211 a0003c0015t0002g0034 others(2): Show |
5 | HG02080.hp1 HG02083.hp2 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.3346-20G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 20/36 | chr22 | 50281762 | |||||||
chr22:50281786 | G | A | 1 | a0006c0058t0002g0197 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.3346-44C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 20/36 | chr22 | 50281786 | |||||||
chr22:50281835 | G | A | 1 | a0028c0056t0001g0189 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.3345+19C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 20/36 | chr22 | 50281835 | |||||||
chr22:50282151 | C | T | 1 | a0003c0001t0001g0052 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.3117+33G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 19/36 | chr22 | 50282151 | |||||||
chr22:50282373 | C | A | 11 | a0004c0008t0005g0008 a0005c0067t0001g0045 a0007c0029t0001g0085 others(8): Show |
13 | HG00673.hp1 HG01106.hp1 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.2988-60G>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 18/36 | chr22 | 50282373 | |||||||
chr22:50282391 | C | G | 1 | a0002c0063t0002g0255 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2988-78G>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 18/36 | chr22 | 50282391 | |||||||
chr22:50282391 | C | T | 1 | a0006c0058t0002g0197 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2988-78G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 18/36 | chr22 | 50282391 | |||||||
chr22:50282445 | A | C | 1 | a0003c0001t0001g0194 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2988-132T>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 18/36 | chr22 | 50282445 | |||||||
chr22:50282463 | C | T | 1 | a0001c0003t0001g0067 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.2988-150G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 18/36 | chr22 | 50282463 | |||||||
chr22:50282464 | G | A | 1 | a0003c0001t0001g0194 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2988-151C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 18/36 | chr22 | 50282464 | |||||||
chr22:50282474 | C | T | 2 | a0002c0077t0001g0292 a0015c0037t0007g0007 |
3 | HG02922.hp1 HG02922.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2988-161G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 18/36 | chr22 | 50282474 | |||||||
chr22:50282475 | G | C | 24 | a0002c0005t0002g0005 a0002c0005t0002g0098 a0002c0005t0002g0099 others(21): Show |
25 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(22): Show |
intron_variant | MODIFIER | c.2988-162C>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 18/36 | chr22 | 50282475 | |||||||
chr22:50282480 | T | A | 4 | a0002c0017t0004g0124 a0002c0017t0004g0125 a0002c0017t0004g0127 others(1): Show |
4 | HG02055.hp2 HG02258.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2988-167A>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 18/36 | chr22 | 50282480 | |||||||
chr22:50282485 | C | T | 3 | a0001c0006t0001g0046 a0002c0028t0001g0225 a0002c0028t0001g0226 |
3 | HG00408.hp2 HG02155.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.2988-172G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 18/36 | chr22 | 50282485 | |||||||
chr22:50282569 | G | A | 1 | a0007c0076t0001g0258 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.2987+142C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 18/36 | chr22 | 50282569 | |||||||
chr22:50282571 | A | G | 2 | a0002c0077t0001g0292 a0015c0037t0007g0007 |
3 | HG02922.hp1 HG02922.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2987+140T>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 18/36 | chr22 | 50282571 | |||||||
chr22:50282574 | G | A | 67 | a0001c0002t0001g0182 a0001c0002t0002g0013 a0001c0002t0002g0033 others(64): Show |
67 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.2987+137C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 18/36 | chr22 | 50282574 | |||||||
chr22:50282648 | A | AAGGGCAC others(40): Show |
35 | a0001c0006t0001g0138 a0001c0006t0001g0148 a0001c0006t0001g0149 others(32): Show |
38 | HG00673.hp1 HG01106.hp1 HG01261.hp1 others(35): Show |
intron_variant | MODIFIER | c.2987+62_2987+63ins others(47): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 18/36 | chr22 | 50282648 | |||||||
chr22:50282686 | G | A | 1 | a0004c0004t0002g0038 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2987+25C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 18/36 | chr22 | 50282686 | |||||||
chr22:50282689 | G | C | 16 | a0002c0010t0003g0243 a0002c0010t0003g0244 a0002c0010t0003g0245 others(13): Show |
16 | HG01109.hp1 HG01891.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.2987+22C>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 18/36 | chr22 | 50282689 | |||||||
chr22:50283037 | C | T | 1 | a0001c0002t0009g0009 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2816+13G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 17/36 | chr22 | 50283037 | |||||||
chr22:50283262 | C | T | 2 | a0004c0004t0002g0174 a0004c0004t0002g0222 |
2 | HG02083.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.2679+75G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 16/36 | chr22 | 50283262 | |||||||
chr22:50283295 | G | A | 1 | a0001c0003t0001g0121 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2679+42C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 16/36 | chr22 | 50283295 | |||||||
chr22:50283327 | G | A | 35 | a0001c0046t0006g0199 a0002c0007t0001g0001 a0002c0007t0001g0012 others(32): Show |
38 | HG00099.hp2 HG00673.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.2679+10C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 16/36 | chr22 | 50283327 | |||||||
chr22:50283450 | C | T | 2 | a0001c0006t0001g0139 a0006c0012t0001g0237 |
2 | HG01261.hp2 NA18970.hp1 |
splice_region_variant&intron_variant | LOW | c.2571-5G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 15/36 | chr22 | 50283450 | |||||||
chr22:50283798 | G | A | 2 | a0002c0014t0008g0134 a0002c0014t0008g0135 |
2 | HG01884.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2421+35C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 14/36 | chr22 | 50283798 | |||||||
chr22:50284039 | G | A | 5 | a0001c0051t0003g0120 a0002c0010t0003g0244 a0002c0010t0003g0245 others(2): Show |
5 | HG01891.hp1 HG02451.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.2264-49C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 13/36 | chr22 | 50284039 | |||||||
chr22:50284105 | G | A | 1 | a0002c0063t0002g0255 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2263+27C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 13/36 | chr22 | 50284105 | |||||||
chr22:50284262 | C | T | 1 | a0025c0061t0002g0193 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2182-49G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 12/36 | chr22 | 50284262 | |||||||
chr22:50284281 | G | C | 1 | a0020c0079t0001g0126 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2182-68C>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 12/36 | chr22 | 50284281 | |||||||
chr22:50284348 | G | A | 9 | a0002c0013t0003g0248 a0002c0013t0003g0291 a0002c0032t0001g0286 others(6): Show |
9 | HG02109.hp2 HG02559.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.2182-135C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 12/36 | chr22 | 50284348 | |||||||
chr22:50284442 | C | T | 2 | a0004c0004t0002g0153 a0004c0004t0002g0157 |
2 | NA18950.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.2181+131G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 12/36 | chr22 | 50284442 | |||||||
chr22:50284482 | T | A | 52 | a0002c0007t0001g0001 a0002c0007t0001g0012 a0002c0007t0001g0122 others(49): Show |
54 | HG01109.hp2 HG01361.hp1 HG01884.hp1 others(51): Show |
intron_variant | MODIFIER | c.2181+91A>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 12/36 | chr22 | 50284482 | |||||||
chr22:50284510 | A | AC | 55 | a0001c0002t0002g0140 a0001c0002t0002g0141 a0001c0002t0002g0150 others(52): Show |
57 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.2181+62dupG | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 12/36 | chr22 | 50284510 | |||||||
chr22:50284823 | G | A | 1 | a0002c0009t0002g0090 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2089-158C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50284823 | |||||||
chr22:50284853 | G | C | 8 | a0002c0032t0001g0286 a0002c0032t0012g0287 a0002c0071t0003g0094 others(5): Show |
8 | HG02109.hp2 HG02559.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.2089-188C>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50284853 | |||||||
chr22:50284944 | G | A | 1 | a0002c0019t0002g0272 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2089-279C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50284944 | |||||||
chr22:50284982 | C | G | 3 | a0001c0002t0002g0161 a0001c0006t0001g0186 a0001c0006t0001g0215 |
3 | HG00099.hp1 HG00639.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.2089-317G>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50284982 | |||||||
chr22:50284983 | C | T | 1 | a0001c0002t0002g0163 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.2089-318G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50284983 | |||||||
chr22:50284992 | T | G | 1 | a0002c0065t0001g0289 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2089-327A>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50284992 | |||||||
chr22:50285045 | G | A | 81 | a0001c0002t0001g0182 a0001c0002t0002g0013 a0001c0002t0002g0140 others(78): Show |
81 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.2089-380C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285045 | |||||||
chr22:50285049 | G | A | 1 | a0002c0017t0004g0125 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2089-384C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285049 | |||||||
chr22:50285072 | G | C | 45 | a0001c0002t0002g0133 a0002c0007t0001g0058 a0002c0007t0001g0227 others(42): Show |
45 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.2089-407C>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285072 | |||||||
chr22:50285114 | G | A | 1 | a0002c0010t0003g0243 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2089-449C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285114 | |||||||
chr22:50285139 | T | C | 44 | a0002c0007t0001g0058 a0002c0007t0001g0227 a0002c0009t0002g0015 others(41): Show |
44 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.2089-474A>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285139 | |||||||
chr22:50285159 | TGGCCGGC others(76): Show |
T | 1 | a0003c0001t0001g0055 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2088+558_2089-495d others(85): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285159 | |||||||
chr22:50285164 | G | A | 2 | a0010c0031t0002g0082 a0010c0031t0002g0086 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.2089-499C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285164 | |||||||
chr22:50285178 | C | T | 2 | a0002c0014t0008g0134 a0002c0014t0008g0135 |
2 | HG01884.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2089-513G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285178 | |||||||
chr22:50285179 | G | A | 43 | a0002c0007t0001g0058 a0002c0007t0001g0227 a0002c0009t0002g0015 others(40): Show |
43 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(40): Show |
intron_variant | MODIFIER | c.2089-514C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285179 | |||||||
chr22:50285180 | T | C | 2 | a0002c0014t0008g0134 a0002c0014t0008g0135 |
2 | HG01884.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2089-515A>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285180 | |||||||
chr22:50285201 | A | G | 2 | a0002c0014t0008g0134 a0002c0014t0008g0135 |
2 | HG01884.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2089-536T>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285201 | |||||||
chr22:50285202 | A | G | 10 | a0002c0014t0008g0134 a0002c0014t0008g0135 a0004c0008t0005g0008 others(7): Show |
12 | HG00423.hp1 HG01515.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.2089-537T>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285202 | |||||||
chr22:50285209 | C | CCCCCTCC others(117): Show |
1 | a0004c0026t0003g0123 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2089-545_2089-544i others(126): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285209 | |||||||
chr22:50285209 | C | CCCCCTCC others(158): Show |
1 | a0003c0001t0001g0070 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2088+426_2089-545d others(167): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285209 | |||||||
chr22:50285220 | C | T | 7 | a0002c0014t0008g0134 a0002c0014t0008g0135 a0002c0071t0003g0094 others(4): Show |
7 | HG01884.hp1 HG02559.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2089-555G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285220 | |||||||
chr22:50285227 | G | T | 2 | a0002c0014t0008g0134 a0002c0014t0008g0135 |
2 | HG01884.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2089-562C>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285227 | |||||||
chr22:50285240 | ACCGGCCG others(446): Show |
A | 2 | a0002c0014t0008g0134 a0002c0014t0008g0135 |
2 | HG01884.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2088+107_2088+559d others(2): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285240 | |||||||
chr22:50285243 | G | A | 3 | a0002c0014t0003g0259 a0002c0014t0003g0260 a0004c0026t0003g0261 |
3 | HG01109.hp1 HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2088+557C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285243 | |||||||
chr22:50285244 | G | A | 3 | a0002c0014t0003g0259 a0002c0014t0003g0260 a0004c0026t0003g0261 |
3 | HG01109.hp1 HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2088+556C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285244 | |||||||
chr22:50285250 | A | AC | 4 | a0002c0014t0003g0259 a0002c0014t0003g0260 a0004c0026t0003g0123 others(1): Show |
4 | HG01109.hp1 HG02572.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.2088+549dupG | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285250 | |||||||
chr22:50285250 | A | ACCCCTCC others(77): Show |
1 | a0005c0016t0002g0265 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2088+466_2088+549d others(86): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285250 | |||||||
chr22:50285250 | A | ACCCCTCC others(118): Show |
1 | a0024c0081t0001g0166 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.2088+549_2088+550i others(127): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285250 | |||||||
chr22:50285281 | ACCAACCG others(36): Show |
A | 5 | a0002c0007t0001g0251 a0004c0008t0001g0249 a0004c0008t0001g0250 others(2): Show |
5 | HG01361.hp1 HG02647.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2088+476_2088+518d others(45): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285281 | |||||||
chr22:50285284 | A | G | 18 | a0002c0014t0003g0259 a0002c0014t0003g0260 a0002c0034t0001g0088 others(15): Show |
20 | HG00423.hp1 HG01109.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.2088+516T>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285284 | |||||||
chr22:50285285 | A | G | 19 | a0002c0014t0003g0259 a0002c0014t0003g0260 a0002c0034t0001g0088 others(16): Show |
21 | HG00423.hp1 HG01109.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.2088+515T>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285285 | |||||||
chr22:50285287 | C | T | 1 | a0001c0006t0001g0186 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2088+513G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285287 | |||||||
chr22:50285291 | AC | A | 13 | a0002c0014t0003g0259 a0002c0014t0003g0260 a0004c0008t0005g0008 others(10): Show |
15 | HG00423.hp1 HG01109.hp1 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.2088+508delG | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285291 | |||||||
chr22:50285292 | C | CCCCTCCC others(281): Show |
6 | a0002c0034t0001g0088 a0002c0034t0001g0271 a0004c0021t0001g0268 others(3): Show |
6 | HG01109.hp2 HG02071.hp1 NA18945.hp2 others(3): Show |
intron_variant | MODIFIER | c.2088+507_2088+508i others(290): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285292 | |||||||
chr22:50285305 | C | T | 3 | a0004c0004t0002g0092 a0004c0026t0003g0123 a0024c0081t0001g0166 |
3 | HG03139.hp1 NA18956.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.2088+495G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285305 | |||||||
chr22:50285326 | G | A | 5 | a0002c0007t0001g0251 a0004c0008t0001g0249 a0004c0008t0001g0250 others(2): Show |
5 | HG01361.hp1 HG02647.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2088+474C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285326 | |||||||
chr22:50285333 | A | AC | 43 | a0002c0007t0001g0058 a0002c0007t0001g0227 a0002c0009t0002g0015 others(40): Show |
45 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(42): Show |
intron_variant | MODIFIER | c.2088+466dupG | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285333 | |||||||
chr22:50285333 | A | ACCCCCTC others(36): Show |
4 | a0002c0009t0002g0240 a0002c0028t0001g0226 a0004c0004t0002g0219 others(1): Show |
4 | HG00408.hp2 NA18957.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.2088+466_2088+467i others(45): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285333 | |||||||
chr22:50285338 | T | C | 1 | a0002c0005t0002g0102 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2088+462A>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285338 | |||||||
chr22:50285346 | C | CACCTGAG others(35): Show |
2 | a0004c0004t0002g0057 a0004c0004t0002g0176 |
2 | HG02080.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.2088+453_2088+454i others(44): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285346 | |||||||
chr22:50285346 | C | T | 5 | a0002c0009t0002g0240 a0002c0028t0001g0226 a0004c0004t0002g0219 others(2): Show |
5 | HG00408.hp2 HG02602.hp2 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.2088+454G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285346 | |||||||
chr22:50285364 | AC | A | 10 | a0002c0007t0001g0001 a0002c0007t0001g0012 a0002c0017t0004g0124 others(7): Show |
11 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.2088+435delG | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285364 | |||||||
chr22:50285367 | G | A | 55 | a0002c0007t0001g0001 a0002c0007t0001g0012 a0002c0007t0001g0058 others(52): Show |
58 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.2088+433C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285367 | |||||||
chr22:50285368 | G | A | 45 | a0002c0007t0001g0058 a0002c0007t0001g0227 a0002c0009t0002g0015 others(42): Show |
47 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(44): Show |
intron_variant | MODIFIER | c.2088+432C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285368 | |||||||
chr22:50285374 | A | AC | 49 | a0001c0002t0002g0173 a0002c0007t0001g0058 a0002c0007t0001g0227 others(46): Show |
51 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.2088+425dupG | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285374 | |||||||
chr22:50285374 | A | ACCCCCTC others(77): Show |
1 | a0026c0075t0002g0096 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2088+425_2088+426i others(86): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285374 | |||||||
chr22:50285387 | C | T | 49 | a0002c0007t0001g0058 a0002c0007t0001g0227 a0002c0009t0002g0015 others(46): Show |
51 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.2088+413G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285387 | |||||||
chr22:50285408 | G | A | 4 | a0002c0014t0003g0259 a0002c0014t0003g0260 a0004c0021t0001g0269 others(1): Show |
4 | HG01109.hp1 HG02630.hp2 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.2088+392C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285408 | |||||||
chr22:50285409 | G | A | 4 | a0002c0014t0003g0259 a0002c0014t0003g0260 a0004c0021t0001g0269 others(1): Show |
4 | HG01109.hp1 HG02630.hp2 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.2088+391C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285409 | |||||||
chr22:50285415 | A | AC | 7 | a0001c0002t0002g0141 a0001c0003t0001g0151 a0001c0003t0001g0205 others(4): Show |
7 | HG00544.hp1 HG00544.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.2088+384dupG | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285415 | |||||||
chr22:50285415 | AC | A | 83 | a0002c0007t0001g0001 a0002c0007t0001g0012 a0002c0007t0001g0058 others(80): Show |
86 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.2088+384delG | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285415 | |||||||
chr22:50285415 | ACCCCCTC others(36): Show |
A | 1 | a0004c0004t0002g0092 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2088+342_2088+384d others(45): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285415 | |||||||
chr22:50285416 | C | CCCCCCTC others(35): Show |
1 | a0001c0002t0002g0154 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2088+383_2088+384i others(44): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285416 | |||||||
chr22:50285429 | C | T | 8 | a0001c0003t0001g0170 a0001c0003t0001g0198 a0001c0049t0001g0158 others(5): Show |
8 | HG01071.hp1 HG01099.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.2088+371G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285429 | |||||||
chr22:50285444 | G | A | 1 | a0001c0049t0001g0158 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2088+356C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285444 | |||||||
chr22:50285447 | AC | A | 22 | a0002c0007t0001g0122 a0002c0007t0001g0131 a0002c0007t0001g0251 others(19): Show |
22 | HG01361.hp1 HG01891.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.2088+352delG | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285447 | |||||||
chr22:50285450 | A | G | 69 | a0001c0002t0002g0154 a0001c0003t0001g0170 a0001c0003t0001g0198 others(66): Show |
72 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.2088+350T>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285450 | |||||||
chr22:50285451 | A | G | 91 | a0001c0002t0002g0154 a0001c0003t0001g0170 a0001c0003t0001g0198 others(88): Show |
94 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.2088+349T>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285451 | |||||||
chr22:50285457 | AC | A | 81 | a0001c0002t0002g0154 a0001c0003t0001g0170 a0001c0003t0001g0198 others(78): Show |
82 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.2088+342delG | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285457 | |||||||
chr22:50285458 | C | CCCCCCTC others(331): Show |
1 | a0002c0005t0002g0102 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2088+341_2088+342i others(340): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285458 | |||||||
chr22:50285458 | C | CCCCCTCC others(321): Show |
1 | a0019c0082t0002g0130 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2088+341_2088+342i others(330): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285458 | |||||||
chr22:50285458 | C | CCCCTCCC others(33): Show |
2 | a0002c0028t0001g0225 a0004c0021t0001g0270 |
2 | HG02155.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.2088+341_2088+342i others(42): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285458 | |||||||
chr22:50285464 | C | T | 8 | a0004c0008t0005g0008 a0005c0016t0011g0256 a0005c0068t0005g0257 others(5): Show |
10 | HG00423.hp1 HG01515.hp2 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.2088+336G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285464 | |||||||
chr22:50285471 | T | C | 86 | a0001c0002t0002g0154 a0001c0003t0001g0170 a0001c0003t0001g0198 others(83): Show |
89 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.2088+329A>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285471 | |||||||
chr22:50285486 | G | A | 77 | a0001c0002t0001g0182 a0001c0002t0002g0013 a0001c0002t0002g0133 others(74): Show |
77 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.2088+314C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285486 | |||||||
chr22:50285489 | AC | A | 6 | a0001c0002t0002g0154 a0002c0007t0001g0001 a0002c0007t0001g0012 others(3): Show |
7 | HG01106.hp2 HG01884.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.2088+310delG | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285489 | |||||||
chr22:50285492 | G | A | 6 | a0001c0002t0002g0154 a0002c0007t0001g0001 a0002c0007t0001g0012 others(3): Show |
7 | HG01106.hp2 HG01884.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.2088+308C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285492 | |||||||
chr22:50285492 | G | GGCCGGCA others(33): Show |
2 | a0001c0003t0001g0198 a0001c0049t0001g0158 |
2 | HG01071.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.2088+307_2088+308i others(42): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285492 | |||||||
chr22:50285512 | C | CACCTGAG others(321): Show |
18 | a0002c0005t0002g0005 a0002c0005t0002g0098 a0002c0005t0002g0099 others(15): Show |
19 | HG00558.hp1 HG00597.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.2088+287_2088+288i others(330): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285512 | |||||||
chr22:50285512 | C | CACCTGAG others(198): Show |
1 | a0002c0019t0002g0272 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2088+287_2088+288i others(207): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285512 | |||||||
chr22:50285512 | C | T | 7 | a0002c0005t0002g0102 a0002c0034t0001g0088 a0002c0034t0001g0271 others(4): Show |
7 | HG00544.hp1 HG01109.hp2 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.2088+288G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285512 | |||||||
chr22:50285530 | A | ACCGGCCG others(322): Show |
1 | a0002c0005t0002g0117 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.2088+269_2088+270i others(331): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285530 | |||||||
chr22:50285533 | G | A | 2 | a0001c0003t0001g0170 a0004c0004t0002g0092 |
2 | HG01099.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.2088+267C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285533 | |||||||
chr22:50285533 | GGCCGGCA others(33): Show |
G | 6 | a0002c0011t0002g0275 a0002c0011t0002g0281 a0002c0011t0002g0283 others(3): Show |
6 | HG01891.hp2 HG02280.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.2088+227_2088+266d others(42): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285533 | |||||||
chr22:50285553 | C | T | 1 | a0024c0081t0001g0166 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.2088+247G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285553 | |||||||
chr22:50285558 | G | T | 5 | a0002c0034t0001g0088 a0002c0034t0001g0271 a0004c0021t0001g0268 others(2): Show |
5 | HG01109.hp2 HG02071.hp1 NA18945.hp2 others(2): Show |
intron_variant | MODIFIER | c.2088+242C>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285558 | |||||||
chr22:50285571 | A | AC | 38 | a0001c0002t0002g0200 a0001c0003t0001g0170 a0001c0006t0001g0149 others(35): Show |
39 | HG01099.hp1 HG01109.hp2 HG01361.hp1 others(36): Show |
intron_variant | MODIFIER | c.2088+228dupG | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285571 | |||||||
chr22:50285571 | A | ACCAACCG others(446): Show |
1 | a0002c0077t0001g0292 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2088+228_2088+229i others(455): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285571 | |||||||
chr22:50285571 | A | ACCGGCCG others(322): Show |
3 | a0002c0005t0002g0238 a0002c0019t0002g0104 a0002c0019t0002g0213 |
3 | HG02071.hp2 NA18945.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.2088+228_2088+229i others(331): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285571 | |||||||
chr22:50285573 | A | AGCCGGCA others(75): Show |
1 | a0001c0002t0002g0154 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2088+226_2088+227i others(84): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285573 | |||||||
chr22:50285573 | A | G | 35 | a0001c0002t0002g0200 a0001c0003t0001g0170 a0001c0006t0001g0149 others(32): Show |
36 | HG01099.hp1 HG01361.hp1 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.2088+227T>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285573 | |||||||
chr22:50285573 | AGCCGGCA others(34): Show |
A | 1 | a0003c0001t0001g0076 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2088+186_2088+226d others(43): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285573 | |||||||
chr22:50285574 | G | A | 7 | a0002c0034t0001g0088 a0002c0034t0001g0271 a0002c0077t0001g0292 others(4): Show |
7 | HG01109.hp2 HG02071.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.2088+226C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285574 | |||||||
chr22:50285593 | C | T | 23 | a0002c0007t0001g0122 a0002c0007t0001g0131 a0002c0007t0001g0251 others(20): Show |
23 | HG01361.hp1 HG01891.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.2088+207G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285593 | |||||||
chr22:50285593 | CACCTGAG others(115): Show |
C | 1 | a0003c0001t0001g0097 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2088+85_2088+206de others(1): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285593 | |||||||
chr22:50285598 | G | T | 1 | a0004c0026t0003g0123 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2088+202C>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285598 | |||||||
chr22:50285613 | C | T | 2 | a0001c0003t0001g0198 a0001c0049t0001g0158 |
2 | HG01071.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.2088+187G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285613 | |||||||
chr22:50285614 | GGCCGGCA others(33): Show |
G | 2 | a0004c0008t0001g0116 a0004c0025t0002g0006 |
3 | HG02486.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2088+146_2088+185d others(42): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285614 | |||||||
chr22:50285634 | C | T | 61 | a0001c0002t0002g0154 a0001c0003t0001g0198 a0001c0049t0001g0158 others(58): Show |
62 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.2088+166G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285634 | |||||||
chr22:50285639 | G | T | 2 | a0004c0026t0003g0123 a0007c0066t0001g0061 |
2 | HG01934.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2088+161C>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285639 | |||||||
chr22:50285652 | A | AC | 81 | a0001c0002t0002g0154 a0001c0003t0001g0198 a0001c0049t0001g0158 others(78): Show |
82 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.2088+147dupG | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285652 | |||||||
chr22:50285652 | A | ACCGGCCG others(571): Show |
1 | a0004c0026t0003g0261 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2088+147_2088+148i others(580): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285652 | |||||||
chr22:50285652 | A | ACCGGCCG others(735): Show |
2 | a0002c0014t0003g0259 a0002c0014t0003g0260 |
2 | HG01109.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.2088+147_2088+148i others(744): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285652 | |||||||
chr22:50285652 | A | ACCGGCCG others(280): Show |
1 | a0004c0021t0001g0269 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2088+147_2088+148i others(289): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285652 | |||||||
chr22:50285652 | A | ACCGGCCG others(158): Show |
1 | a0024c0081t0001g0166 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.2088+147_2088+148i others(167): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285652 | |||||||
chr22:50285654 | A | G | 86 | a0001c0002t0002g0154 a0001c0003t0001g0198 a0001c0049t0001g0158 others(83): Show |
87 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.2088+146T>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285654 | |||||||
chr22:50285674 | C | CACCTGAG others(402): Show |
2 | a0015c0037t0007g0007 a0020c0079t0001g0126 |
3 | HG02922.hp1 HG02965.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2088+125_2088+126i others(411): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285674 | |||||||
chr22:50285674 | C | CACCTGAG others(239): Show |
1 | a0004c0021t0001g0270 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2088+125_2088+126i others(248): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285674 | |||||||
chr22:50285674 | C | CACCTTAG others(198): Show |
8 | a0002c0032t0001g0286 a0002c0032t0012g0287 a0002c0071t0003g0094 others(5): Show |
8 | HG02109.hp2 HG02559.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.2088+125_2088+126i others(207): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285674 | |||||||
chr22:50285674 | C | CACCTTAG others(34): Show |
1 | a0005c0016t0011g0256 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2088+125_2088+126i others(43): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285674 | |||||||
chr22:50285674 | C | T | 28 | a0001c0002t0002g0154 a0002c0007t0001g0122 a0002c0007t0001g0131 others(25): Show |
28 | HG01106.hp2 HG01109.hp2 HG01361.hp1 others(25): Show |
intron_variant | MODIFIER | c.2088+126G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285674 | |||||||
chr22:50285679 | G | T | 6 | a0004c0008t0005g0008 a0005c0068t0005g0257 a0007c0076t0001g0258 others(3): Show |
8 | HG01515.hp2 HG02004.hp1 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.2088+121C>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285679 | |||||||
chr22:50285694 | C | T | 69 | a0001c0002t0001g0182 a0001c0002t0002g0133 a0001c0002t0002g0140 others(66): Show |
69 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.2088+106G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285694 | |||||||
chr22:50285695 | G | A | 2 | a0002c0014t0008g0134 a0002c0014t0008g0135 |
2 | HG01884.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2088+105C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285695 | |||||||
chr22:50285715 | T | C | 8 | a0001c0003t0001g0207 a0001c0003t0001g0210 a0002c0014t0003g0259 others(5): Show |
8 | HG01109.hp1 HG01515.hp1 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.2088+85A>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285715 | |||||||
chr22:50285720 | G | T | 3 | a0002c0014t0003g0259 a0002c0014t0003g0260 a0004c0026t0003g0261 |
3 | HG01109.hp1 HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2088+80C>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285720 | |||||||
chr22:50285724 | C | CTGCCTGT others(34): Show |
12 | a0002c0010t0003g0243 a0002c0010t0003g0244 a0002c0010t0003g0245 others(9): Show |
12 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.2088+75_2088+76ins others(41): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285724 | |||||||
chr22:50285736 | G | A | 3 | a0002c0014t0003g0259 a0002c0014t0003g0260 a0004c0026t0003g0261 |
3 | HG01109.hp1 HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2088+64C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285736 | |||||||
chr22:50285737 | G | A | 3 | a0002c0014t0003g0259 a0002c0014t0003g0260 a0004c0026t0003g0261 |
3 | HG01109.hp1 HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2088+63C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285737 | |||||||
chr22:50285737 | G | GCCGGCAC others(609): Show |
1 | a0004c0026t0003g0123 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2088+62_2088+63ins others(616): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285737 | |||||||
chr22:50285743 | A | AC | 40 | a0001c0002t0002g0154 a0002c0005t0002g0102 a0002c0007t0001g0122 others(37): Show |
40 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.2088+56dupG | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285743 | |||||||
chr22:50285743 | A | ACCCCTCC others(35): Show |
34 | a0002c0007t0001g0001 a0002c0007t0001g0012 a0002c0007t0001g0058 others(31): Show |
37 | HG00280.hp1 HG00673.hp1 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.2088+56_2088+57ins others(42): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285743 | |||||||
chr22:50285743 | A | ACCCCTCC others(36): Show |
1 | a0010c0069t0001g0236 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2088+56_2088+57ins others(43): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285743 | |||||||
chr22:50285743 | A | ACCCCTCC others(199): Show |
1 | a0001c0006t0001g0215 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2088+56_2088+57ins others(206): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285743 | |||||||
chr22:50285743 | A | ACCCCTCC others(76): Show |
2 | a0001c0003t0001g0198 a0001c0049t0001g0158 |
2 | HG01071.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.2088+56_2088+57ins others(83): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285743 | |||||||
chr22:50285755 | G | A | 1 | a0003c0001t0001g0052 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2088+45C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285755 | |||||||
chr22:50285756 | C | T | 10 | a0002c0009t0002g0015 a0002c0009t0002g0021 a0004c0004t0002g0156 others(7): Show |
10 | HG00280.hp2 HG00733.hp1 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.2088+44G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285756 | |||||||
chr22:50285761 | G | GAGCCTGC others(35): Show |
10 | a0002c0009t0002g0015 a0002c0009t0002g0021 a0004c0004t0002g0156 others(7): Show |
10 | HG00280.hp2 HG00733.hp1 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.2088+38_2088+39ins others(42): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285761 | |||||||
chr22:50285761 | G | GAGCCTGC others(117): Show |
4 | a0001c0003t0001g0160 a0002c0009t0002g0240 a0005c0016t0002g0265 others(1): Show |
4 | NA18947.hp2 NA18957.hp1 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.2088+38_2088+39ins others(124): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285761 | |||||||
chr22:50285761 | G | GAGCCTGC others(159): Show |
1 | a0006c0012t0001g0216 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2088+38_2088+39ins others(166): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285761 | |||||||
chr22:50285761 | G | GAGCCTGC others(158): Show |
73 | a0001c0002t0001g0182 a0001c0002t0002g0013 a0001c0002t0002g0133 others(70): Show |
73 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.2088+38_2088+39ins others(165): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285761 | |||||||
chr22:50285761 | G | T | 107 | a0001c0002t0002g0154 a0001c0003t0001g0198 a0001c0006t0001g0215 others(104): Show |
111 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.2088+39C>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285761 | |||||||
chr22:50285777 | A | G | 7 | a0001c0002t0002g0177 a0001c0003t0001g0151 a0002c0005t0002g0164 others(4): Show |
7 | HG00544.hp2 HG01109.hp1 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.2088+23T>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285777 | |||||||
chr22:50285778 | G | A | 66 | a0002c0007t0001g0001 a0002c0007t0001g0012 a0002c0007t0001g0122 others(63): Show |
70 | HG00423.hp1 HG01109.hp2 HG01361.hp1 others(67): Show |
intron_variant | MODIFIER | c.2088+22C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285778 | |||||||
chr22:50285781 | G | A | 1 | a0001c0002t0002g0191 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2088+19C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285781 | |||||||
chr22:50285784 | A | ACCCCTCC others(159): Show |
2 | a0001c0002t0002g0177 a0001c0003t0001g0151 |
2 | HG00544.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.2088+15_2088+16ins others(166): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 11/36 | chr22 | 50285784 | |||||||
chr22:50285972 | G | C | 2 | a0015c0037t0007g0007 a0020c0079t0001g0126 |
3 | HG02922.hp1 HG02965.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1986+18C>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 10/36 | chr22 | 50285972 | |||||||
chr22:50286164 | G | A | 5 | a0007c0066t0001g0061 a0007c0076t0001g0258 a0010c0069t0001g0236 others(2): Show |
6 | HG01515.hp2 HG01934.hp2 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.1877+9C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 9/36 | chr22 | 50286164 | |||||||
chr22:50286304 | G | T | 70 | a0002c0007t0001g0058 a0002c0007t0001g0227 a0002c0009t0002g0015 others(67): Show |
72 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.1763-17C>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 8/36 | chr22 | 50286304 | |||||||
chr22:50286333 | C | T | 1 | a0002c0065t0001g0289 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1763-46G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 8/36 | chr22 | 50286333 | |||||||
chr22:50286481 | G | A | 2 | a0002c0010t0003g0245 a0002c0010t0003g0247 |
2 | HG01891.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1763-194C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 8/36 | chr22 | 50286481 | |||||||
chr22:50286536 | C | T | 1 | a0002c0013t0003g0165 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1763-249G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 8/36 | chr22 | 50286536 | |||||||
chr22:50286574 | A | G | 1 | a0004c0004t0002g0168 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1763-287T>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 8/36 | chr22 | 50286574 | |||||||
chr22:50286601 | C | A | 2 | a0002c0014t0008g0134 a0002c0014t0008g0135 |
2 | HG01884.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1763-314G>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 8/36 | chr22 | 50286601 | |||||||
chr22:50286706 | G | A | 1 | a0004c0004t0002g0091 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1762+405C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 8/36 | chr22 | 50286706 | |||||||
chr22:50286808 | G | C | 8 | a0004c0008t0005g0008 a0005c0016t0011g0256 a0005c0068t0005g0257 others(5): Show |
10 | HG00423.hp1 HG01515.hp2 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.1762+303C>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 8/36 | chr22 | 50286808 | |||||||
chr22:50286810 | C | T | 1 | a0002c0011t0002g0284 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1762+301G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 8/36 | chr22 | 50286810 | |||||||
chr22:50286872 | G | A | 37 | a0002c0005t0002g0005 a0002c0005t0002g0098 a0002c0005t0002g0099 others(34): Show |
39 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.1762+239C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 8/36 | chr22 | 50286872 | |||||||
chr22:50287069 | C | A | 1 | a0001c0003t0001g0202 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1762+42G>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 8/36 | chr22 | 50287069 | |||||||
chr22:50287085 | C | T | 2 | a0015c0037t0007g0007 a0020c0079t0001g0126 |
3 | HG02922.hp1 HG02965.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1762+26G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 8/36 | chr22 | 50287085 | |||||||
chr22:50287087 | C | T | 12 | a0002c0005t0002g0005 a0002c0005t0002g0098 a0002c0005t0002g0099 others(9): Show |
13 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(10): Show |
intron_variant | MODIFIER | c.1762+24G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 8/36 | chr22 | 50287087 | |||||||
chr22:50287421 | C | A | 2 | a0002c0014t0008g0134 a0002c0014t0008g0135 |
2 | HG01884.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1609-157G>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 7/36 | chr22 | 50287421 | |||||||
chr22:50287490 | C | T | 3 | a0002c0005t0002g0178 a0002c0005t0002g0212 a0002c0005t0002g0238 |
3 | HG02165.hp1 NA19000.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.1608+177G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 7/36 | chr22 | 50287490 | |||||||
chr22:50287558 | G | A | 1 | a0003c0001t0001g0288 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1608+109C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 7/36 | chr22 | 50287558 | |||||||
chr22:50287625 | C | A | 1 | a0003c0045t0001g0074 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1608+42G>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 7/36 | chr22 | 50287625 | |||||||
chr22:50287625 | C | T | 1 | a0022c0074t0002g0019 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1608+42G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 7/36 | chr22 | 50287625 | |||||||
chr22:50287811 | G | A | 6 | a0002c0011t0002g0275 a0002c0011t0002g0281 a0002c0011t0002g0283 others(3): Show |
6 | HG01891.hp2 HG02280.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1482-18C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 6/36 | chr22 | 50287811 | |||||||
chr22:50287857 | C | T | 1 | a0003c0001t0001g0288 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1482-64G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 6/36 | chr22 | 50287857 | |||||||
chr22:50288047 | C | T | 1 | a0004c0004t0002g0083 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1381-10G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 5/36 | chr22 | 50288047 | |||||||
chr22:50288054 | G | A | 1 | a0003c0001t0001g0030 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1381-17C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 5/36 | chr22 | 50288054 | |||||||
chr22:50288081 | C | T | 5 | a0002c0017t0004g0124 a0002c0017t0004g0125 a0002c0017t0004g0127 others(2): Show |
5 | HG02055.hp2 HG02258.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1381-44G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 5/36 | chr22 | 50288081 | |||||||
chr22:50288095 | A | C | 12 | a0002c0007t0001g0122 a0002c0007t0001g0131 a0002c0007t0001g0252 others(9): Show |
12 | HG01891.hp2 HG02280.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.1381-58T>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 5/36 | chr22 | 50288095 | |||||||
chr22:50288127 | C | G | 2 | a0001c0003t0001g0020 a0003c0042t0001g0018 |
2 | HG00438.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.1381-90G>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 5/36 | chr22 | 50288127 | |||||||
chr22:50288182 | G | A | 12 | a0002c0007t0001g0122 a0002c0007t0001g0131 a0002c0007t0001g0252 others(9): Show |
12 | HG01891.hp2 HG02280.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.1381-145C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 5/36 | chr22 | 50288182 | |||||||
chr22:50288198 | G | A | 10 | a0002c0034t0001g0088 a0002c0034t0001g0271 a0002c0077t0001g0292 others(7): Show |
10 | HG01109.hp2 HG02071.hp1 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.1381-161C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 5/36 | chr22 | 50288198 | |||||||
chr22:50288244 | G | A | 1 | a0004c0004t0002g0083 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1381-207C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 5/36 | chr22 | 50288244 | |||||||
chr22:50288694 | A | G | 1 | a0001c0002t0002g0033 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1380+49T>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 5/36 | chr22 | 50288694 | |||||||
chr22:50288723 | C | T | 2 | a0002c0010t0003g0243 a0002c0010t0003g0246 |
2 | HG02486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1380+20G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 5/36 | chr22 | 50288723 | |||||||
chr22:50288879 | C | A | 1 | a0019c0082t0002g0130 | 1 | HG02735.hp1 | splice_region_variant&intron_variant | LOW | c.1252-8G>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 4/36 | chr22 | 50288879 | |||||||
chr22:50288898 | G | T | 3 | a0001c0006t0001g0139 a0003c0001t0001g0147 a0003c0018t0002g0137 |
3 | NA18970.hp1 NA18983.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1252-27C>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 4/36 | chr22 | 50288898 | |||||||
chr22:50288904 | G | A | 1 | a0002c0009t0002g0037 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1252-33C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 4/36 | chr22 | 50288904 | |||||||
chr22:50289266 | G | A | 2 | a0015c0037t0007g0007 a0020c0079t0001g0126 |
3 | HG02922.hp1 HG02965.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1069-124C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 3/36 | chr22 | 50289266 | |||||||
chr22:50289281 | A | G | 6 | a0001c0003t0001g0043 a0001c0003t0001g0266 a0001c0003t0001g0267 others(3): Show |
6 | HG02258.hp1 HG02572.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1069-139T>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 3/36 | chr22 | 50289281 | |||||||
chr22:50289293 | C | T | 1 | a0004c0004t0002g0057 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1069-151G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 3/36 | chr22 | 50289293 | |||||||
chr22:50289353 | G | A | 2 | a0001c0002t0002g0235 a0001c0046t0006g0199 |
2 | HG00099.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1068+164C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 3/36 | chr22 | 50289353 | |||||||
chr22:50289363 | T | C | 129 | a0002c0005t0002g0005 a0002c0005t0002g0098 a0002c0005t0002g0099 others(126): Show |
134 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.1068+154A>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 3/36 | chr22 | 50289363 | |||||||
chr22:50289390 | A | G | 1 | a0002c0009t0002g0037 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1068+127T>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 3/36 | chr22 | 50289390 | |||||||
chr22:50289474 | C | T | 1 | a0001c0002t0002g0167 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1068+43G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 3/36 | chr22 | 50289474 | |||||||
chr22:50289492 | T | C | 125 | a0002c0005t0002g0005 a0002c0005t0002g0098 a0002c0005t0002g0099 others(122): Show |
130 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.1068+25A>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 3/36 | chr22 | 50289492 | |||||||
chr22:50290865 | G | A | 1 | a0002c0005t0002g0099 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-13-268C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 2/36 | chr22 | 50290865 | |||||||
chr22:50290914 | G | A | 1 | a0007c0076t0001g0258 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-13-317C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 2/36 | chr22 | 50290914 | |||||||
chr22:50290926 | G | A | 6 | a0002c0071t0003g0094 a0004c0026t0003g0261 a0008c0035t0003g0093 others(3): Show |
6 | HG02559.hp2 HG02572.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.-13-329C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 2/36 | chr22 | 50290926 | |||||||
chr22:50291272 | C | G | 3 | a0002c0014t0003g0259 a0004c0026t0003g0123 a0004c0026t0003g0261 |
3 | HG02572.hp2 HG02630.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-13-675G>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 2/36 | chr22 | 50291272 | |||||||
chr22:50291678 | C | T | 1 | a0002c0064t0003g0282 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-13-1081G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 2/36 | chr22 | 50291678 | |||||||
chr22:50291760 | G | GCTCACAA others(9): Show |
1 | a0004c0004t0002g0057 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-13-1179_-13-1164d others(18): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 2/36 | chr22 | 50291760 | |||||||
chr22:50291791 | A | G | 103 | a0002c0007t0001g0001 a0002c0007t0001g0012 a0002c0007t0001g0058 others(100): Show |
106 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.-13-1194T>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 2/36 | chr22 | 50291791 | |||||||
chr22:50291821 | G | A | 1 | a0006c0012t0001g0216 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-13-1224C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 2/36 | chr22 | 50291821 | |||||||
chr22:50291875 | C | G | 25 | a0002c0007t0001g0122 a0002c0007t0001g0131 a0002c0007t0001g0252 others(22): Show |
25 | HG01109.hp2 HG01361.hp1 HG02071.hp1 others(22): Show |
intron_variant | MODIFIER | c.-13-1278G>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 2/36 | chr22 | 50291875 | |||||||
chr22:50291890 | T | C | 3 | a0003c0001t0002g0031 a0011c0023t0001g0023 a0021c0040t0001g0032 |
3 | HG01346.hp1 HG03492.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-13-1293A>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 2/36 | chr22 | 50291890 | |||||||
chr22:50291891 | T | C | 135 | a0001c0003t0001g0145 a0001c0003t0001g0151 a0001c0003t0001g0160 others(132): Show |
141 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.-13-1294A>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 2/36 | chr22 | 50291891 | |||||||
chr22:50292029 | G | T | 189 | a0001c0002t0002g0133 a0001c0002t0002g0140 a0001c0002t0002g0141 others(186): Show |
191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.-13-1432C>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 2/36 | chr22 | 50292029 | |||||||
chr22:50292075 | C | T | 6 | a0002c0011t0002g0275 a0002c0011t0002g0281 a0002c0011t0002g0283 others(3): Show |
6 | HG01891.hp2 HG02280.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.-13-1478G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 2/36 | chr22 | 50292075 | |||||||
chr22:50292293 | G | A | 1 | a0019c0082t0002g0130 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-13-1696C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 2/36 | chr22 | 50292293 | |||||||
chr22:50292317 | G | A | 1 | a0023c0059t0001g0072 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-13-1720C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 2/36 | chr22 | 50292317 | |||||||
chr22:50292337 | C | CA | 41 | a0001c0003t0001g0266 a0001c0051t0003g0120 a0002c0005t0002g0113 others(38): Show |
43 | HG00597.hp1 HG00735.hp2 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.-13-1741dupT | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 2/36 | chr22 | 50292337 | |||||||
chr22:50292337 | CA | C | 84 | a0001c0002t0001g0182 a0001c0002t0002g0133 a0001c0002t0002g0140 others(81): Show |
85 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.-13-1741delT | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 2/36 | chr22 | 50292337 | |||||||
chr22:50292543 | T | G | 10 | a0002c0034t0001g0271 a0004c0021t0001g0268 a0004c0021t0001g0269 others(7): Show |
10 | HG01109.hp2 HG02071.hp1 NA18944.hp2 others(7): Show |
intron_variant | MODIFIER | c.-13-1946A>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 2/36 | chr22 | 50292543 | |||||||
chr22:50292746 | G | T | 1 | a0002c0077t0001g0292 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-14+1973C>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 2/36 | chr22 | 50292746 | |||||||
chr22:50292796 | G | A | 18 | a0001c0003t0001g0043 a0001c0003t0001g0266 a0001c0003t0001g0267 others(15): Show |
18 | HG01891.hp2 HG02145.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.-14+1923C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 2/36 | chr22 | 50292796 | |||||||
chr22:50292881 | A | G | 51 | a0002c0007t0001g0058 a0002c0007t0001g0227 a0002c0009t0002g0015 others(48): Show |
52 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(49): Show |
intron_variant | MODIFIER | c.-14+1838T>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 2/36 | chr22 | 50292881 | |||||||
chr22:50292967 | GC | G | 109 | a0001c0002t0002g0013 a0001c0003t0001g0043 a0001c0003t0001g0266 others(106): Show |
112 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.-14+1751delG | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 2/36 | chr22 | 50292967 | |||||||
chr22:50293064 | G | A | 1 | a0001c0003t0001g0242 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-14+1655C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 2/36 | chr22 | 50293064 | |||||||
chr22:50293090 | G | A | 1 | a0003c0001t0001g0097 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-14+1629C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 2/36 | chr22 | 50293090 | |||||||
chr22:50293152 | C | G | 1 | a0004c0004t0002g0168 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-14+1567G>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 2/36 | chr22 | 50293152 | |||||||
chr22:50293179 | G | T | 2 | a0001c0006t0001g0169 a0016c0048t0001g0143 |
2 | HG00597.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.-14+1540C>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 2/36 | chr22 | 50293179 | |||||||
chr22:50293275 | C | T | 11 | a0002c0014t0008g0134 a0002c0014t0008g0135 a0002c0032t0001g0286 others(8): Show |
11 | HG01884.hp1 HG02109.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-14+1444G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 2/36 | chr22 | 50293275 | |||||||
chr22:50293379 | C | T | 43 | a0002c0007t0001g0058 a0002c0007t0001g0122 a0002c0007t0001g0227 others(40): Show |
44 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.-14+1340G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 2/36 | chr22 | 50293379 | |||||||
chr22:50293390 | C | T | 5 | a0001c0002t0002g0013 a0002c0007t0001g0001 a0002c0007t0001g0012 others(2): Show |
6 | HG01496.hp2 HG01884.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.-14+1329G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 2/36 | chr22 | 50293390 | |||||||
chr22:50293474 | T | C | 93 | a0001c0002t0002g0013 a0001c0003t0001g0043 a0001c0003t0001g0266 others(90): Show |
95 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.-14+1245A>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 2/36 | chr22 | 50293474 | |||||||
chr22:50293544 | C | T | 1 | a0002c0073t0001g0263 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-14+1175G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 2/36 | chr22 | 50293544 | |||||||
chr22:50293586 | G | A | 2 | a0002c0007t0001g0058 a0004c0004t0002g0101 |
2 | HG02135.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.-14+1133C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 2/36 | chr22 | 50293586 | |||||||
chr22:50293652 | G | A | 4 | a0002c0014t0003g0259 a0002c0014t0003g0260 a0004c0026t0003g0123 others(1): Show |
4 | HG01109.hp1 HG02572.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14+1067C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 2/36 | chr22 | 50293652 | |||||||
chr22:50293846 | C | A | 2 | a0002c0071t0003g0094 a0008c0035t0003g0095 |
2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-14+873G>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 2/36 | chr22 | 50293846 | |||||||
chr22:50293955 | C | T | 1 | a0002c0077t0001g0292 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-14+764G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 2/36 | chr22 | 50293955 | |||||||
chr22:50294080 | C | T | 5 | a0001c0006t0001g0138 a0001c0006t0001g0148 a0001c0006t0001g0149 others(2): Show |
5 | HG01261.hp1 HG01934.hp1 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.-14+639G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 2/36 | chr22 | 50294080 | |||||||
chr22:50294081 | G | A | 37 | a0002c0007t0001g0058 a0002c0007t0001g0227 a0002c0009t0002g0015 others(34): Show |
37 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(34): Show |
intron_variant | MODIFIER | c.-14+638C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 2/36 | chr22 | 50294081 | |||||||
chr22:50294143 | G | A | 1 | a0002c0063t0002g0255 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-14+576C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 2/36 | chr22 | 50294143 | |||||||
chr22:50294382 | A | AC | 9 | a0001c0002t0002g0221 a0002c0005t0002g0117 a0002c0011t0002g0042 others(6): Show |
9 | HG01109.hp1 HG01175.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-14+336dupG | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 2/36 | chr22 | 50294382 | |||||||
chr22:50294540 | C | T | 1 | a0004c0008t0005g0008 | 2 | HG02040.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.-14+179G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 2/36 | chr22 | 50294540 | |||||||
chr22:50294601 | C | T | 9 | a0002c0007t0001g0251 a0002c0007t0001g0252 a0002c0014t0008g0134 others(6): Show |
9 | HG01361.hp1 HG01884.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.-14+118G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 2/36 | chr22 | 50294601 | |||||||
chr22:50294798 | C | T | 37 | a0002c0007t0001g0058 a0002c0007t0001g0227 a0002c0009t0002g0015 others(34): Show |
37 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(34): Show |
intron_variant | MODIFIER | c.-73-20G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50294798 | |||||||
chr22:50295043 | G | A | 4 | a0002c0014t0003g0259 a0002c0014t0003g0260 a0004c0026t0003g0123 others(1): Show |
4 | HG01109.hp1 HG02572.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.-73-265C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50295043 | |||||||
chr22:50295058 | C | T | 1 | a0003c0001t0001g0071 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-73-280G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50295058 | |||||||
chr22:50295078 | T | C | 2 | a0002c0014t0008g0134 a0002c0014t0008g0135 |
2 | HG01884.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-73-300A>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50295078 | |||||||
chr22:50295105 | G | A | 1 | a0002c0007t0001g0122 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-73-327C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50295105 | |||||||
chr22:50295147 | C | T | 1 | a0003c0001t0001g0288 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-73-369G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50295147 | |||||||
chr22:50295194 | A | G | 95 | a0001c0002t0002g0013 a0001c0003t0001g0043 a0001c0003t0001g0266 others(92): Show |
97 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.-73-416T>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50295194 | |||||||
chr22:50295248 | C | T | 7 | a0002c0007t0001g0251 a0002c0007t0001g0252 a0002c0063t0002g0255 others(4): Show |
7 | HG01361.hp1 HG02647.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.-73-470G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50295248 | |||||||
chr22:50295249 | C | G | 60 | a0002c0007t0001g0058 a0002c0007t0001g0227 a0002c0007t0001g0251 others(57): Show |
61 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.-73-471G>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50295249 | |||||||
chr22:50295269 | G | A | 9 | a0002c0007t0001g0251 a0002c0007t0001g0252 a0002c0014t0008g0134 others(6): Show |
9 | HG01361.hp1 HG01884.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.-73-491C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50295269 | |||||||
chr22:50295306 | C | CA | 17 | a0001c0002t0002g0187 a0001c0002t0002g0196 a0001c0002t0002g0200 others(14): Show |
17 | HG01123.hp1 HG01258.hp2 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.-73-529dupT | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50295306 | |||||||
chr22:50295306 | CA | C | 52 | a0001c0003t0001g0025 a0001c0003t0001g0062 a0001c0003t0001g0262 others(49): Show |
53 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.-73-529delT | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50295306 | |||||||
chr22:50295306 | CAA | C | 6 | a0002c0009t0002g0021 a0002c0013t0003g0165 a0004c0004t0002g0168 others(3): Show |
6 | HG00280.hp2 HG01168.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.-73-530_-73-529del others(2): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50295306 | |||||||
chr22:50295324 | A | G | 1 | a0001c0052t0001g0077 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-73-546T>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50295324 | |||||||
chr22:50295389 | G | C | 60 | a0002c0007t0001g0058 a0002c0007t0001g0227 a0002c0007t0001g0251 others(57): Show |
61 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.-73-611C>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50295389 | |||||||
chr22:50295538 | T | C | 3 | a0001c0002t0002g0140 a0001c0002t0002g0172 a0001c0002t0002g0173 |
3 | NA18956.hp2 NA19005.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.-73-760A>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50295538 | |||||||
chr22:50295545 | G | C | 6 | a0002c0007t0001g0251 a0002c0007t0001g0252 a0004c0008t0001g0249 others(3): Show |
6 | HG01361.hp1 HG02647.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-73-767C>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50295545 | |||||||
chr22:50295629 | C | T | 2 | a0003c0001t0001g0024 a0003c0001t0010g0010 |
2 | NA18980.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.-73-851G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50295629 | |||||||
chr22:50295701 | G | C | 9 | a0002c0032t0001g0286 a0002c0032t0012g0287 a0002c0065t0001g0289 others(6): Show |
9 | HG02109.hp2 HG02559.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.-73-923C>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50295701 | |||||||
chr22:50295714 | G | A | 9 | a0002c0032t0001g0286 a0002c0032t0012g0287 a0002c0065t0001g0289 others(6): Show |
9 | HG02109.hp2 HG02559.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.-73-936C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50295714 | |||||||
chr22:50295815 | C | T | 14 | a0002c0032t0001g0286 a0002c0032t0012g0287 a0002c0065t0001g0289 others(11): Show |
15 | HG00423.hp1 HG01515.hp2 HG02040.hp1 others(12): Show |
intron_variant | MODIFIER | c.-73-1037G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50295815 | |||||||
chr22:50295872 | A | G | 9 | a0002c0007t0001g0251 a0002c0007t0001g0252 a0002c0014t0008g0134 others(6): Show |
9 | HG01361.hp1 HG01884.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.-73-1094T>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50295872 | |||||||
chr22:50295879 | G | A | 1 | a0001c0003t0001g0242 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-73-1101C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50295879 | |||||||
chr22:50295939 | T | A | 9 | a0002c0032t0001g0286 a0002c0032t0012g0287 a0002c0065t0001g0289 others(6): Show |
9 | HG02109.hp2 HG02559.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.-73-1161A>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50295939 | |||||||
chr22:50295963 | G | A | 19 | a0001c0002t0002g0154 a0001c0002t0002g0187 a0001c0002t0002g0196 others(16): Show |
19 | HG00099.hp2 HG01071.hp1 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.-73-1185C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50295963 | |||||||
chr22:50295974 | C | T | 2 | a0002c0014t0008g0134 a0002c0014t0008g0135 |
2 | HG01884.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-73-1196G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50295974 | |||||||
chr22:50295989 | C | T | 51 | a0002c0007t0001g0058 a0002c0007t0001g0227 a0002c0009t0002g0015 others(48): Show |
52 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(49): Show |
intron_variant | MODIFIER | c.-73-1211G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50295989 | |||||||
chr22:50296033 | T | C | 107 | a0001c0002t0002g0013 a0001c0002t0002g0173 a0001c0003t0001g0043 others(104): Show |
110 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.-73-1255A>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50296033 | |||||||
chr22:50296162 | G | A | 5 | a0002c0017t0004g0124 a0002c0017t0004g0125 a0002c0017t0004g0127 others(2): Show |
5 | HG02055.hp2 HG02258.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.-73-1384C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50296162 | |||||||
chr22:50296193 | T | TAC | 29 | a0001c0002t0002g0177 a0001c0003t0001g0062 a0001c0051t0003g0120 others(26): Show |
31 | HG01081.hp1 HG01884.hp1 HG01943.hp2 others(28): Show |
intron_variant | MODIFIER | c.-73-1417_-73-1416d others(4): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50296193 | |||||||
chr22:50296193 | T | TACAC | 89 | a0001c0002t0002g0033 a0001c0002t0002g0133 a0001c0002t0002g0140 others(86): Show |
92 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.-73-1419_-73-1416d others(6): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50296193 | |||||||
chr22:50296193 | T | TACACAC | 53 | a0001c0002t0002g0146 a0001c0002t0002g0161 a0001c0002t0002g0196 others(50): Show |
53 | HG00099.hp1 HG00438.hp2 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.-73-1421_-73-1416d others(8): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50296193 | |||||||
chr22:50296193 | T | TACACACA others(1): Show |
30 | a0001c0002t0002g0154 a0001c0002t0002g0180 a0001c0002t0002g0181 others(27): Show |
30 | HG00099.hp2 HG00597.hp2 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.-73-1423_-73-1416d others(10): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50296193 | |||||||
chr22:50296193 | T | TACACACA others(3): Show |
14 | a0001c0002t0001g0182 a0001c0002t0002g0183 a0001c0002t0002g0185 others(11): Show |
14 | HG01192.hp1 HG01517.hp1 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.-73-1425_-73-1416d others(12): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50296193 | |||||||
chr22:50296193 | T | TACACACA others(5): Show |
3 | a0001c0002t0002g0142 a0001c0002t0002g0167 a0002c0007t0001g0131 |
3 | HG02683.hp1 HG02818.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.-73-1427_-73-1416d others(14): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50296193 | |||||||
chr22:50296193 | T | TACACACA others(9): Show |
1 | a0003c0022t0001g0294 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-73-1431_-73-1416d others(18): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50296193 | |||||||
chr22:50296193 | TACAC | T | 3 | a0004c0008t0005g0008 a0005c0016t0011g0256 a0005c0068t0005g0257 |
4 | HG00423.hp1 HG02040.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.-73-1419_-73-1416d others(6): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50296193 | |||||||
chr22:50296193 | TACACACA others(5): Show |
T | 4 | a0001c0002t0002g0013 a0002c0007t0001g0001 a0002c0007t0001g0012 others(1): Show |
5 | HG01496.hp2 HG01884.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.-73-1427_-73-1416d others(14): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50296193 | |||||||
chr22:50296193 | TACACACA others(7): Show |
T | 1 | a0014c0027t0001g0011 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.-73-1429_-73-1416d others(16): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50296193 | |||||||
chr22:50296261 | C | A | 5 | a0001c0002t0002g0013 a0002c0007t0001g0001 a0002c0007t0001g0012 others(2): Show |
6 | HG01496.hp2 HG01884.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.-73-1483G>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50296261 | |||||||
chr22:50296300 | G | A | 1 | a0001c0003t0001g0202 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-73-1522C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50296300 | |||||||
chr22:50296305 | C | CTGAGGAG others(59): Show |
9 | a0002c0007t0001g0251 a0002c0007t0001g0252 a0002c0014t0008g0134 others(6): Show |
9 | HG01361.hp1 HG01884.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.-73-1528_-73-1527i others(68): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50296305 | |||||||
chr22:50296361 | A | G | 9 | a0002c0007t0001g0251 a0002c0007t0001g0252 a0002c0014t0008g0134 others(6): Show |
9 | HG01361.hp1 HG01884.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.-73-1583T>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50296361 | |||||||
chr22:50296461 | C | T | 46 | a0002c0007t0001g0058 a0002c0007t0001g0227 a0002c0009t0002g0015 others(43): Show |
46 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(43): Show |
intron_variant | MODIFIER | c.-73-1683G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50296461 | |||||||
chr22:50296468 | C | T | 1 | a0002c0010t0003g0243 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-73-1690G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50296468 | |||||||
chr22:50296477 | A | G | 1 | a0003c0043t0001g0175 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-73-1699T>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50296477 | |||||||
chr22:50296512 | G | A | 1 | a0010c0069t0001g0236 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-73-1734C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50296512 | |||||||
chr22:50296589 | T | A | 8 | a0001c0051t0003g0120 a0002c0017t0004g0124 a0002c0017t0004g0125 others(5): Show |
9 | HG02055.hp2 HG02258.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-73-1811A>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50296589 | |||||||
chr22:50296590 | C | CA | 43 | a0001c0002t0002g0033 a0001c0002t0002g0133 a0001c0002t0002g0185 others(40): Show |
45 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.-73-1813dupT | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50296590 | |||||||
chr22:50296590 | C | CAA | 7 | a0001c0002t0002g0173 a0001c0051t0003g0120 a0002c0010t0003g0245 others(4): Show |
7 | HG01109.hp1 HG01891.hp1 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.-73-1814_-73-1813d others(4): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50296590 | |||||||
chr22:50296590 | C | CAAAAAAA | 7 | a0002c0007t0001g0251 a0002c0007t0001g0252 a0002c0014t0008g0135 others(4): Show |
7 | HG01361.hp1 HG01884.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-73-1819_-73-1813d others(9): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50296590 | |||||||
chr22:50296590 | CA | C | 44 | a0001c0003t0001g0145 a0001c0006t0001g0186 a0002c0007t0001g0058 others(41): Show |
45 | HG00280.hp2 HG00408.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.-73-1813delT | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50296590 | |||||||
chr22:50296590 | CAA | C | 6 | a0002c0009t0002g0015 a0002c0009t0002g0240 a0004c0004t0002g0083 others(3): Show |
6 | HG00280.hp1 HG00733.hp1 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.-73-1814_-73-1813d others(4): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50296590 | |||||||
chr22:50296801 | A | G | 63 | a0002c0007t0001g0058 a0002c0007t0001g0227 a0002c0007t0001g0251 others(60): Show |
64 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.-73-2023T>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50296801 | |||||||
chr22:50296844 | C | T | 1 | a0004c0008t0001g0249 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-73-2066G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50296844 | |||||||
chr22:50296855 | G | A | 1 | a0002c0011t0002g0042 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-73-2077C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50296855 | |||||||
chr22:50296863 | T | G | 1 | a0002c0034t0001g0088 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-73-2085A>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50296863 | |||||||
chr22:50297003 | A | G | 13 | a0002c0007t0001g0251 a0002c0007t0001g0252 a0002c0014t0003g0259 others(10): Show |
13 | HG01109.hp1 HG01361.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.-73-2225T>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50297003 | |||||||
chr22:50297145 | C | T | 1 | a0010c0069t0001g0236 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-73-2367G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50297145 | |||||||
chr22:50297175 | G | A | 13 | a0002c0007t0001g0251 a0002c0007t0001g0252 a0002c0014t0003g0259 others(10): Show |
13 | HG01109.hp1 HG01361.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.-73-2397C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50297175 | |||||||
chr22:50297220 | T | C | 1 | a0002c0019t0002g0272 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-73-2442A>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50297220 | |||||||
chr22:50297443 | C | T | 24 | a0001c0002t0002g0173 a0001c0003t0001g0043 a0001c0003t0001g0266 others(21): Show |
24 | HG01891.hp2 HG02071.hp1 HG02258.hp1 others(21): Show |
intron_variant | MODIFIER | c.-73-2665G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50297443 | |||||||
chr22:50297633 | C | T | 2 | a0002c0071t0003g0094 a0005c0068t0005g0257 |
2 | HG03540.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.-73-2855G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50297633 | |||||||
chr22:50297673 | G | A | 1 | a0011c0023t0001g0035 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-73-2895C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50297673 | |||||||
chr22:50297879 | G | A | 27 | a0001c0002t0002g0173 a0001c0003t0001g0043 a0001c0003t0001g0266 others(24): Show |
27 | HG01891.hp2 HG02071.hp1 HG02145.hp2 others(24): Show |
intron_variant | MODIFIER | c.-73-3101C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50297879 | |||||||
chr22:50297905 | C | T | 2 | a0004c0004t0002g0081 a0004c0004t0002g0129 |
2 | HG03942.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.-73-3127G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50297905 | |||||||
chr22:50297941 | C | T | 5 | a0001c0006t0001g0138 a0001c0006t0001g0148 a0001c0006t0001g0149 others(2): Show |
5 | HG01261.hp1 HG01934.hp1 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.-73-3163G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50297941 | |||||||
chr22:50297980 | T | C | 28 | a0001c0002t0002g0173 a0001c0003t0001g0043 a0001c0003t0001g0266 others(25): Show |
28 | HG01891.hp2 HG02071.hp1 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.-73-3202A>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50297980 | |||||||
chr22:50298072 | G | C | 2 | a0002c0014t0008g0134 a0002c0014t0008g0135 |
2 | HG01884.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-73-3294C>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50298072 | |||||||
chr22:50298192 | C | T | 1 | a0011c0023t0001g0023 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-73-3414G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50298192 | |||||||
chr22:50298217 | G | C | 1 | a0003c0001t0001g0288 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-73-3439C>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50298217 | |||||||
chr22:50298253 | T | C | 16 | a0002c0007t0001g0122 a0002c0007t0001g0252 a0002c0010t0003g0244 others(13): Show |
16 | HG01109.hp1 HG01361.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.-73-3475A>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50298253 | |||||||
chr22:50298358 | A | G | 68 | a0001c0003t0001g0242 a0002c0007t0001g0058 a0002c0007t0001g0227 others(65): Show |
69 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.-73-3580T>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50298358 | |||||||
chr22:50298409 | G | A | 1 | a0003c0015t0002g0034 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-73-3631C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50298409 | |||||||
chr22:50298427 | G | A | 1 | a0001c0049t0001g0158 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-73-3649C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50298427 | |||||||
chr22:50298665 | G | A | 1 | a0003c0001t0001g0070 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-73-3887C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50298665 | |||||||
chr22:50298700 | T | C | 95 | a0001c0002t0002g0013 a0001c0002t0002g0173 a0001c0003t0001g0043 others(92): Show |
97 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.-73-3922A>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50298700 | |||||||
chr22:50298777 | C | G | 1 | a0001c0002t0002g0235 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-73-3999G>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50298777 | |||||||
chr22:50298835 | G | A | 6 | a0002c0014t0003g0259 a0002c0014t0003g0260 a0002c0014t0008g0134 others(3): Show |
6 | HG01109.hp1 HG01884.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.-73-4057C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50298835 | |||||||
chr22:50298843 | A | C | 1 | a0002c0063t0002g0255 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-73-4065T>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50298843 | |||||||
chr22:50299024 | G | A | 2 | a0003c0039t0001g0056 a0011c0023t0001g0035 |
2 | HG00408.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.-73-4246C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50299024 | |||||||
chr22:50299155 | G | T | 54 | a0002c0007t0001g0058 a0002c0007t0001g0227 a0002c0007t0001g0251 others(51): Show |
55 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.-73-4377C>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50299155 | |||||||
chr22:50299300 | T | TG | 70 | a0001c0002t0002g0013 a0001c0002t0002g0146 a0001c0002t0002g0161 others(67): Show |
71 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.-73-4523dupC | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50299300 | |||||||
chr22:50299300 | T | TGG | 26 | a0001c0002t0002g0177 a0002c0005t0002g0102 a0002c0005t0002g0103 others(23): Show |
26 | HG00408.hp2 HG00544.hp1 HG00558.hp1 others(23): Show |
intron_variant | MODIFIER | c.-73-4524_-73-4523d others(4): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50299300 | |||||||
chr22:50299326 | G | A | 1 | a0001c0003t0001g0121 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-73-4548C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50299326 | |||||||
chr22:50299340 | G | T | 2 | a0015c0037t0007g0007 a0020c0079t0001g0126 |
3 | HG02922.hp1 HG02965.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-73-4562C>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50299340 | |||||||
chr22:50299575 | G | C | 3 | a0002c0009t0002g0090 a0004c0004t0002g0091 a0004c0004t0002g0092 |
3 | HG04228.hp2 NA18967.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.-73-4797C>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50299575 | |||||||
chr22:50299697 | G | C | 1 | a0002c0013t0003g0228 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-73-4919C>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50299697 | |||||||
chr22:50299794 | G | A | 8 | a0001c0002t0002g0140 a0001c0002t0002g0141 a0001c0002t0002g0163 others(5): Show |
8 | HG00621.hp2 HG01109.hp2 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.-73-5016C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50299794 | |||||||
chr22:50300005 | A | G | 82 | a0001c0002t0002g0013 a0001c0002t0002g0173 a0001c0003t0001g0043 others(79): Show |
84 | HG00408.hp2 HG00423.hp1 HG01106.hp1 others(81): Show |
intron_variant | MODIFIER | c.-73-5227T>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50300005 | |||||||
chr22:50300151 | G | T | 1 | a0003c0001t0001g0118 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-73-5373C>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50300151 | |||||||
chr22:50300291 | A | ATCG | 5 | a0001c0002t0002g0013 a0002c0007t0001g0001 a0002c0007t0001g0012 others(2): Show |
6 | HG01496.hp2 HG01884.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.-73-5516_-73-5514d others(5): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50300291 | |||||||
chr22:50300315 | C | A | 1 | a0003c0022t0001g0277 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-73-5537G>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50300315 | |||||||
chr22:50300473 | G | A | 9 | a0002c0010t0003g0243 a0002c0010t0003g0245 a0002c0010t0003g0246 others(6): Show |
9 | HG01891.hp1 HG02055.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-73-5695C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50300473 | |||||||
chr22:50300501 | A | G | 43 | a0001c0002t0002g0188 a0001c0038t0002g0136 a0002c0007t0001g0227 others(40): Show |
44 | HG00408.hp2 HG00423.hp1 HG01109.hp1 others(41): Show |
intron_variant | MODIFIER | c.-73-5723T>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50300501 | |||||||
chr22:50300524 | C | G | 6 | a0001c0002t0002g0188 a0004c0008t0005g0008 a0005c0016t0011g0256 others(3): Show |
7 | HG00423.hp1 HG01515.hp2 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.-73-5746G>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50300524 | |||||||
chr22:50300531 | C | G | 1 | a0001c0002t0002g0187 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-73-5753G>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50300531 | |||||||
chr22:50300538 | G | C | 14 | a0002c0007t0001g0251 a0002c0007t0001g0252 a0002c0014t0003g0259 others(11): Show |
14 | HG01109.hp1 HG01361.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.-73-5760C>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50300538 | |||||||
chr22:50300543 | T | TGGGGC | 5 | a0001c0002t0002g0013 a0002c0007t0001g0001 a0002c0007t0001g0012 others(2): Show |
6 | HG01496.hp2 HG01884.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.-73-5770_-73-5766d others(7): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50300543 | |||||||
chr22:50300543 | T | TGGGGCGG others(3): Show |
2 | a0002c0071t0003g0094 a0008c0035t0003g0095 |
2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-73-5775_-73-5766d others(12): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50300543 | |||||||
chr22:50300620 | G | A | 23 | a0002c0007t0001g0227 a0002c0009t0002g0240 a0002c0010t0003g0243 others(20): Show |
23 | HG00408.hp2 HG01993.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.-73-5842C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50300620 | |||||||
chr22:50300709 | T | A | 8 | a0001c0051t0003g0120 a0002c0071t0003g0094 a0004c0008t0001g0116 others(5): Show |
9 | HG02486.hp2 HG02559.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.-73-5931A>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50300709 | |||||||
chr22:50301013 | T | C | 5 | a0004c0008t0005g0008 a0005c0016t0011g0256 a0005c0068t0005g0257 others(2): Show |
6 | HG00423.hp1 HG01515.hp2 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.-73-6235A>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50301013 | |||||||
chr22:50301314 | G | C | 1 | a0002c0063t0002g0255 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-74+6239C>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50301314 | |||||||
chr22:50301409 | G | GCACA | 229 | a0001c0002t0001g0182 a0001c0002t0002g0013 a0001c0002t0002g0133 others(226): Show |
234 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.-74+6140_-74+6143d others(6): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50301409 | |||||||
chr22:50301414 | C | CACAT | 9 | a0002c0010t0003g0243 a0002c0010t0003g0245 a0002c0010t0003g0246 others(6): Show |
9 | HG01891.hp1 HG02055.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-74+6138_-74+6139i others(6): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50301414 | |||||||
chr22:50301460 | C | T | 4 | a0002c0017t0004g0124 a0002c0017t0004g0125 a0002c0017t0004g0127 others(1): Show |
4 | HG02055.hp2 HG02258.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-74+6093G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50301460 | |||||||
chr22:50301560 | T | G | 69 | a0001c0002t0002g0177 a0001c0003t0001g0043 a0001c0003t0001g0121 others(66): Show |
70 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.-74+5993A>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50301560 | |||||||
chr22:50301612 | C | G | 7 | a0001c0002t0001g0182 a0001c0002t0002g0180 a0001c0002t0002g0181 others(4): Show |
7 | HG01168.hp1 HG01175.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.-74+5941G>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50301612 | |||||||
chr22:50301839 | G | A | 3 | a0004c0008t0005g0008 a0005c0016t0011g0256 a0007c0076t0001g0258 |
4 | HG00423.hp1 HG02040.hp1 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.-74+5714C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50301839 | |||||||
chr22:50301975 | C | A | 1 | a0009c0020t0002g0105 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-74+5578G>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50301975 | |||||||
chr22:50302098 | A | C | 1 | a0001c0002t0002g0146 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-74+5455T>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50302098 | |||||||
chr22:50302134 | G | A | 7 | a0002c0007t0001g0251 a0002c0007t0001g0252 a0002c0063t0002g0255 others(4): Show |
7 | HG01361.hp1 HG02647.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.-74+5419C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50302134 | |||||||
chr22:50302272 | T | TCAGGGCT others(43): Show |
1 | a0001c0002t0002g0221 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-74+5231_-74+5280d others(52): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50302272 | |||||||
chr22:50302315 | GA | G | 8 | a0002c0011t0002g0275 a0002c0011t0002g0281 a0002c0011t0002g0283 others(5): Show |
8 | HG01891.hp2 HG02280.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.-74+5237delT | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50302315 | |||||||
chr22:50302428 | G | A | 14 | a0002c0007t0001g0227 a0002c0009t0002g0240 a0002c0028t0001g0225 others(11): Show |
14 | HG00408.hp2 HG02074.hp2 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.-74+5125C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50302428 | |||||||
chr22:50302440 | T | C | 2 | a0002c0014t0008g0134 a0002c0014t0008g0135 |
2 | HG01884.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-74+5113A>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50302440 | |||||||
chr22:50302466 | C | G | 4 | a0002c0014t0003g0259 a0002c0014t0003g0260 a0004c0026t0003g0123 others(1): Show |
4 | HG01109.hp1 HG02572.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.-74+5087G>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50302466 | |||||||
chr22:50302564 | C | T | 7 | a0002c0007t0001g0251 a0002c0007t0001g0252 a0002c0063t0002g0255 others(4): Show |
7 | HG01361.hp1 HG02647.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.-74+4989G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50302564 | |||||||
chr22:50302621 | C | A | 1 | a0002c0005t0002g0106 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-74+4932G>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50302621 | |||||||
chr22:50302648 | G | A | 7 | a0002c0007t0001g0251 a0002c0007t0001g0252 a0002c0063t0002g0255 others(4): Show |
7 | HG01361.hp1 HG02647.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.-74+4905C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50302648 | |||||||
chr22:50302657 | G | C | 1 | a0008c0036t0003g0054 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-74+4896C>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50302657 | |||||||
chr22:50302674 | C | A | 5 | a0001c0002t0002g0013 a0002c0007t0001g0001 a0002c0007t0001g0012 others(2): Show |
6 | HG01496.hp2 HG01884.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.-74+4879G>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50302674 | |||||||
chr22:50302702 | G | C | 4 | a0002c0014t0003g0259 a0002c0014t0003g0260 a0004c0026t0003g0123 others(1): Show |
4 | HG01109.hp1 HG02572.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.-74+4851C>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50302702 | |||||||
chr22:50302865 | G | A | 1 | a0002c0011t0002g0042 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-74+4688C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50302865 | |||||||
chr22:50302898 | C | G | 3 | a0001c0003t0001g0043 a0003c0022t0001g0277 a0003c0044t0001g0276 |
3 | HG02886.hp2 HG03130.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-74+4655G>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50302898 | |||||||
chr22:50302909 | C | A | 2 | a0014c0027t0001g0011 a0014c0027t0001g0014 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-74+4644G>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50302909 | |||||||
chr22:50303075 | C | T | 133 | a0001c0002t0001g0182 a0001c0002t0002g0133 a0001c0002t0002g0140 others(130): Show |
134 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.-74+4478G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50303075 | |||||||
chr22:50303152 | C | T | 1 | a0002c0063t0002g0255 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-74+4401G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50303152 | |||||||
chr22:50303160 | C | T | 9 | a0001c0003t0001g0043 a0001c0003t0001g0266 a0001c0003t0001g0267 others(6): Show |
9 | HG02145.hp2 HG02258.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.-74+4393G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50303160 | |||||||
chr22:50303284 | C | T | 1 | a0001c0002t0002g0146 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-74+4269G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50303284 | |||||||
chr22:50303408 | C | A | 1 | a0002c0034t0001g0271 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-74+4145G>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50303408 | |||||||
chr22:50303453 | G | A | 4 | a0004c0008t0005g0008 a0005c0016t0011g0256 a0005c0068t0005g0257 others(1): Show |
5 | HG00423.hp1 HG02040.hp1 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.-74+4100C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50303453 | |||||||
chr22:50303490 | G | A | 1 | a0002c0007t0001g0227 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-74+4063C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50303490 | |||||||
chr22:50303696 | A | AGGGCCCC others(21): Show |
1 | a0009c0020t0002g0022 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-74+3829_-74+3856d others(30): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50303696 | |||||||
chr22:50303859 | G | A | 7 | a0002c0007t0001g0251 a0002c0007t0001g0252 a0002c0063t0002g0255 others(4): Show |
7 | HG01361.hp1 HG02647.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.-74+3694C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50303859 | |||||||
chr22:50303917 | G | C | 97 | a0001c0002t0001g0182 a0001c0002t0002g0133 a0001c0002t0002g0140 others(94): Show |
97 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.-74+3636C>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50303917 | |||||||
chr22:50303965 | G | A | 5 | a0001c0002t0002g0013 a0002c0007t0001g0001 a0002c0007t0001g0012 others(2): Show |
6 | HG01496.hp2 HG01884.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.-74+3588C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50303965 | |||||||
chr22:50304155 | C | A | 1 | a0002c0005t0002g0107 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-74+3398G>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50304155 | |||||||
chr22:50304178 | C | G | 1 | a0005c0067t0001g0045 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-74+3375G>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50304178 | |||||||
chr22:50304182 | C | A | 121 | a0001c0002t0001g0182 a0001c0002t0002g0133 a0001c0002t0002g0140 others(118): Show |
121 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.-74+3371G>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50304182 | |||||||
chr22:50304282 | T | C | 1 | a0001c0003t0001g0062 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-74+3271A>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50304282 | |||||||
chr22:50304292 | T | A | 3 | a0002c0009t0002g0015 a0002c0009t0002g0016 a0002c0009t0002g0021 |
3 | HG00280.hp2 HG00733.hp1 HG00735.hp2 |
intron_variant | MODIFIER | c.-74+3261A>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50304292 | |||||||
chr22:50304321 | G | C | 2 | a0002c0007t0001g0251 a0002c0007t0001g0252 |
2 | HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-74+3232C>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50304321 | |||||||
chr22:50304324 | C | CG | 10 | a0001c0002t0002g0173 a0001c0002t0002g0229 a0001c0003t0001g0145 others(7): Show |
10 | HG02055.hp1 HG02055.hp2 HG03540.hp2 others(7): Show |
intron_variant | MODIFIER | c.-74+3228dupC | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50304324 | |||||||
chr22:50304506 | A | G | 182 | a0001c0002t0002g0013 a0001c0002t0002g0033 a0001c0003t0001g0004 others(179): Show |
190 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.-74+3047T>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50304506 | |||||||
chr22:50304530 | TG | T | 14 | a0001c0002t0002g0177 a0002c0005t0002g0117 a0002c0007t0001g0227 others(11): Show |
14 | HG00408.hp2 HG02074.hp2 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.-74+3022delC | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50304530 | |||||||
chr22:50304545 | C | T | 1 | a0001c0006t0001g0144 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-74+3008G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50304545 | |||||||
chr22:50304632 | G | A | 1 | a0002c0063t0002g0255 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-74+2921C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50304632 | |||||||
chr22:50304651 | AC | A | 7 | a0001c0078t0002g0214 a0003c0001t0001g0053 a0003c0001t0001g0110 others(4): Show |
8 | HG00423.hp1 HG02040.hp1 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.-74+2901delG | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50304651 | |||||||
chr22:50304657 | C | A | 1 | a0004c0026t0003g0123 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-74+2896G>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50304657 | |||||||
chr22:50304705 | G | C | 1 | a0018c0054t0001g0041 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-74+2848C>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50304705 | |||||||
chr22:50304841 | G | T | 1 | a0002c0007t0001g0252 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-74+2712C>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50304841 | |||||||
chr22:50304974 | G | C | 1 | a0002c0011t0002g0042 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-74+2579C>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50304974 | |||||||
chr22:50305026 | G | A | 1 | a0002c0007t0001g0251 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-74+2527C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50305026 | |||||||
chr22:50305061 | A | G | 1 | a0003c0043t0001g0175 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-74+2492T>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50305061 | |||||||
chr22:50305081 | G | A | 139 | a0001c0002t0001g0182 a0001c0002t0002g0013 a0001c0002t0002g0133 others(136): Show |
141 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.-74+2472C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50305081 | |||||||
chr22:50305088 | C | T | 1 | a0004c0004t0002g0174 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-74+2465G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50305088 | |||||||
chr22:50305141 | C | T | 9 | a0002c0007t0001g0251 a0002c0007t0001g0252 a0002c0014t0008g0134 others(6): Show |
9 | HG01361.hp1 HG01884.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.-74+2412G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50305141 | |||||||
chr22:50305201 | C | A | 5 | a0001c0002t0002g0013 a0002c0007t0001g0001 a0002c0007t0001g0012 others(2): Show |
6 | HG01496.hp2 HG01884.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.-74+2352G>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50305201 | |||||||
chr22:50305204 | G | A | 5 | a0001c0002t0002g0013 a0002c0007t0001g0001 a0002c0007t0001g0012 others(2): Show |
6 | HG01496.hp2 HG01884.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.-74+2349C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50305204 | |||||||
chr22:50305209 | G | A | 7 | a0002c0007t0001g0251 a0002c0007t0001g0252 a0002c0063t0002g0255 others(4): Show |
7 | HG01361.hp1 HG02647.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.-74+2344C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50305209 | |||||||
chr22:50305255 | C | A | 1 | a0002c0007t0001g0058 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-74+2298G>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50305255 | |||||||
chr22:50305357 | CCCCGATG others(23): Show |
C | 1 | a0001c0038t0002g0136 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-74+2166_-74+2195d others(32): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50305357 | |||||||
chr22:50305388 | C | G | 1 | a0001c0002t0002g0173 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-74+2165G>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50305388 | |||||||
chr22:50305398 | G | A | 121 | a0001c0002t0001g0182 a0001c0002t0002g0133 a0001c0002t0002g0140 others(118): Show |
121 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.-74+2155C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50305398 | |||||||
chr22:50305543 | G | A | 1 | a0004c0008t0001g0116 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-74+2010C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50305543 | |||||||
chr22:50305619 | G | A | 7 | a0002c0007t0001g0251 a0002c0007t0001g0252 a0002c0063t0002g0255 others(4): Show |
7 | HG01361.hp1 HG02647.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.-74+1934C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50305619 | |||||||
chr22:50305795 | A | AG | 16 | a0001c0002t0002g0167 a0001c0002t0002g0172 a0001c0002t0002g0221 others(13): Show |
16 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(13): Show |
intron_variant | MODIFIER | c.-74+1757dupC | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50305795 | |||||||
chr22:50305816 | A | AG | 8 | a0001c0002t0002g0142 a0001c0003t0001g0170 a0001c0003t0001g0242 others(5): Show |
8 | HG00735.hp2 HG01099.hp1 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.-74+1736dupC | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50305816 | |||||||
chr22:50305875 | T | TG | 5 | a0002c0007t0001g0252 a0004c0008t0001g0249 a0004c0008t0001g0250 others(2): Show |
5 | HG01361.hp1 HG02647.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-74+1677dupC | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50305875 | |||||||
chr22:50305877 | G | A | 1 | a0001c0006t0001g0215 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-74+1676C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50305877 | |||||||
chr22:50305910 | C | G | 29 | a0001c0003t0001g0043 a0001c0003t0001g0266 a0001c0003t0001g0267 others(26): Show |
29 | HG01891.hp2 HG02071.hp1 HG02109.hp2 others(26): Show |
intron_variant | MODIFIER | c.-74+1643G>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50305910 | |||||||
chr22:50305947 | T | A | 4 | a0002c0005t0002g0005 a0002c0005t0002g0112 a0002c0005t0002g0113 others(1): Show |
5 | HG02027.hp2 NA18947.hp1 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.-74+1606A>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50305947 | |||||||
chr22:50306001 | A | C | 7 | a0003c0001t0001g0049 a0003c0001t0001g0050 a0003c0001t0001g0051 others(4): Show |
8 | HG01081.hp1 HG01099.hp2 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.-74+1552T>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50306001 | |||||||
chr22:50306094 | G | A | 2 | a0002c0009t0002g0240 a0004c0004t0002g0241 |
2 | NA18957.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.-74+1459C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50306094 | |||||||
chr22:50306119 | TCTTGGCA others(6): Show |
T | 1 | a0002c0013t0003g0165 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-74+1421_-74+1433d others(15): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50306119 | |||||||
chr22:50306137 | G | C | 1 | a0004c0021t0001g0268 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-74+1416C>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50306137 | |||||||
chr22:50306260 | CATAGGTA others(4): Show |
C | 1 | a0006c0012t0001g0216 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-74+1282_-74+1292d others(13): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50306260 | |||||||
chr22:50306331 | T | C | 1 | a0001c0003t0001g0020 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-74+1222A>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50306331 | |||||||
chr22:50306392 | A | G | 172 | a0001c0002t0001g0182 a0001c0002t0002g0013 a0001c0002t0002g0133 others(169): Show |
175 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.-74+1161T>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50306392 | |||||||
chr22:50306508 | G | A | 1 | a0003c0018t0002g0114 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-74+1045C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50306508 | |||||||
chr22:50306551 | A | C | 1 | a0002c0009t0002g0015 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-74+1002T>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50306551 | |||||||
chr22:50306610 | G | A | 28 | a0001c0003t0001g0043 a0001c0003t0001g0266 a0001c0003t0001g0267 others(25): Show |
28 | HG01891.hp2 HG02071.hp1 HG02109.hp2 others(25): Show |
intron_variant | MODIFIER | c.-74+943C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50306610 | |||||||
chr22:50306613 | C | CG | 14 | a0001c0002t0002g0013 a0001c0002t0002g0167 a0001c0006t0001g0169 others(11): Show |
14 | HG00597.hp1 HG00733.hp1 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.-74+939dupC | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50306613 | |||||||
chr22:50306679 | G | A | 2 | a0002c0009t0002g0240 a0004c0004t0002g0241 |
2 | NA18957.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.-74+874C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50306679 | |||||||
chr22:50306681 | C | CCACCCT | 30 | a0001c0002t0002g0133 a0001c0002t0002g0142 a0001c0002t0002g0146 others(27): Show |
30 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(27): Show |
intron_variant | MODIFIER | c.-74+866_-74+871dup others(6): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50306681 | |||||||
chr22:50306681 | C | CCACCCTC others(5): Show |
7 | a0001c0002t0002g0140 a0001c0006t0001g0138 a0001c0006t0001g0139 others(4): Show |
7 | HG01261.hp1 HG01884.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-74+860_-74+871dup others(12): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50306681 | |||||||
chr22:50306681 | C | CCCACCCT others(6): Show |
1 | a0001c0002t0002g0141 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-74+871_-74+872ins others(13): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50306681 | |||||||
chr22:50306681 | CCACCCT | C | 133 | a0001c0002t0002g0013 a0001c0002t0002g0221 a0001c0002t0002g0229 others(130): Show |
139 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.-74+866_-74+871del others(6): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50306681 | |||||||
chr22:50306681 | CCACCCTC others(5): Show |
C | 18 | a0001c0003t0001g0121 a0001c0003t0001g0242 a0001c0051t0003g0120 others(15): Show |
19 | HG01891.hp1 HG02486.hp1 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.-74+860_-74+871del others(12): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50306681 | |||||||
chr22:50306681 | CCACCCTC others(11): Show |
C | 9 | a0002c0017t0004g0124 a0002c0017t0004g0125 a0002c0017t0004g0127 others(6): Show |
10 | HG02055.hp2 HG02258.hp2 HG02735.hp1 others(7): Show |
intron_variant | MODIFIER | c.-74+854_-74+871del others(18): Show |
PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50306681 | |||||||
chr22:50306684 | C | G | 1 | a0002c0013t0003g0165 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-74+869G>C | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50306684 | |||||||
chr22:50306687 | T | C | 1 | a0002c0013t0003g0165 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-74+866A>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50306687 | |||||||
chr22:50306689 | A | C | 1 | a0002c0009t0002g0015 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-74+864T>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50306689 | |||||||
chr22:50306734 | C | A | 1 | a0002c0007t0001g0131 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-74+819G>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50306734 | |||||||
chr22:50306798 | G | A | 1 | a0005c0016t0002g0132 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-74+755C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50306798 | |||||||
chr22:50306803 | G | A | 10 | a0001c0002t0002g0013 a0002c0007t0001g0001 a0002c0007t0001g0012 others(7): Show |
12 | HG01109.hp1 HG01496.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.-74+750C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50306803 | |||||||
chr22:50306852 | T | C | 5 | a0001c0002t0002g0013 a0002c0007t0001g0001 a0002c0007t0001g0012 others(2): Show |
6 | HG01496.hp2 HG01884.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.-74+701A>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50306852 | |||||||
chr22:50307025 | T | C | 7 | a0002c0007t0001g0251 a0002c0007t0001g0252 a0002c0063t0002g0255 others(4): Show |
7 | HG01361.hp1 HG02647.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.-74+528A>G | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50307025 | |||||||
chr22:50307027 | C | CA | 4 | a0004c0008t0005g0008 a0005c0016t0011g0256 a0005c0068t0005g0257 others(1): Show |
5 | HG00423.hp1 HG02040.hp1 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.-74+525dupT | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50307027 | |||||||
chr22:50307155 | C | T | 1 | a0001c0002t0002g0133 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-74+398G>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50307155 | |||||||
chr22:50307389 | G | A | 3 | a0002c0014t0003g0259 a0002c0014t0003g0260 a0004c0026t0003g0261 |
3 | HG01109.hp1 HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-74+164C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50307389 | |||||||
chr22:50307403 | G | T | 5 | a0001c0002t0002g0013 a0002c0007t0001g0001 a0002c0007t0001g0012 others(2): Show |
6 | HG01496.hp2 HG01884.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.-74+150C>A | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50307403 | |||||||
chr22:50307408 | G | A | 1 | a0001c0003t0001g0262 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-74+145C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50307408 | |||||||
chr22:50307473 | G | A | 134 | a0001c0002t0001g0182 a0001c0002t0002g0133 a0001c0002t0002g0140 others(131): Show |
135 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.-74+80C>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50307473 | |||||||
chr22:50307497 | G | GC | 31 | a0001c0003t0001g0266 a0001c0003t0001g0267 a0001c0003t0001g0293 others(28): Show |
31 | HG00639.hp1 HG01891.hp2 HG02071.hp1 others(28): Show |
intron_variant | MODIFIER | c.-74+55dupG | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50307497 | |||||||
chr22:50307499 | C | A | 1 | a0003c0022t0001g0294 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-74+54G>T | PLXNB2 | ENSG00000196576.16 | transcript | ENST00000359337.9 | protein_coding | 1/36 | chr22 | 50307499 |