Item | Value |
---|---|
geneid | 7984 |
ensemblid | ENSG00000050327.15 |
hgncid | 13209 |
symbol | ARHGEF5 |
name | Rho guanine nucleotide exchange factor 5 |
refseq_nuc | NM_005435.4 |
refseq_prot | NP_005426.2 |
ensembl_nuc | ENST00000056217.10 |
ensembl_prot | ENSP00000056217.5 |
mane_status | MANE Select |
chr | chr7 |
start | 144355402 |
end | 144380632 |
strand | + |
ver | v1.2 |
region | chr7:144355402-144380632 |
region5000 | chr7:144350402-144385632 |
regionname0 | ARHGEF5_chr7_144355402_144380632 |
regionname5000 | ARHGEF5_chr7_144350402_144385632 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 1597 | 49 | 9 | 11 | 18 | 2 | 8 | 16 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | MEAEE others(1592): Show |
chr7 | 144350402 | 144385632 |
a0002 | 0/0 | 1597 | 47 | 1 | 15 | 24 | 1 | 6 | 13 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | MEAEE others(1592): Show |
chr7 | 144350402 | 144385632 |
a0003 | 0/1 | 1597 | 35 | 9 | 10 | 4 | 4 | 7 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | MEAEE others(1592): Show |
chr7 | 144350402 | 144385632 |
a0004 | 0/0 | 1597 | 25 | 1 | 11 | 2 | 4 | 7 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | MEAEE others(1592): Show |
chr7 | 144350402 | 144385632 |
a0005 | 0/0 | 1597 | 17 | 2 | 1 | 11 | 2 | 1 | 9 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | MEAEE others(1592): Show |
chr7 | 144350402 | 144385632 |
a0006 | 0/0 | 1597 | 17 | 4 | 0 | 5 | 2 | 6 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | MEAEE others(1592): Show |
chr7 | 144350402 | 144385632 |
a0007 | 0/0 | 1597 | 17 | 16 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | MEAEE others(1592): Show |
chr7 | 144350402 | 144385632 |
a0008 | 0/0 | 1597 | 11 | 9 | 1 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | MEAEE others(1592): Show |
chr7 | 144350402 | 144385632 |
a0009 | 0/0 | 10 | 9 | 1 | 1 | 7 | 0 | 0 | 7 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | MEAEE others(5): Show |
chr7 | 144350402 | 144385632 |
a0010 | 0/0 | 1597 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | MEAEE others(1592): Show |
chr7 | 144350402 | 144385632 |
a0011 | 0/0 | 1597 | 5 | 3 | 0 | 2 | 0 | 0 | 2 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | MEAEE others(1592): Show |
chr7 | 144350402 | 144385632 |
a0012 | 0/0 | 1597 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | MEAEE others(1592): Show |
chr7 | 144350402 | 144385632 |
a0013 | 0/0 | 1597 | 3 | 0 | 0 | 3 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | MEAEE others(1592): Show |
chr7 | 144350402 | 144385632 |
a0014 | 0/0 | 1597 | 3 | 0 | 1 | 0 | 2 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | MEAEE others(1592): Show |
chr7 | 144350402 | 144385632 |
a0015 | 0/0 | 817 | 2 | 0 | 1 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | MEAEE others(812): Show |
chr7 | 144350402 | 144385632 |
a0016 | 0/0 | 1597 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | MEAEE others(1592): Show |
chr7 | 144350402 | 144385632 |
a0017 | 0/0 | 1597 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | MEAEE others(1592): Show |
chr7 | 144350402 | 144385632 |
a0018 | 0/0 | 817 | 2 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | MEAEE others(812): Show |
chr7 | 144350402 | 144385632 |
a0019 | 0/0 | 1597 | 2 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | MEAEE others(1592): Show |
chr7 | 144350402 | 144385632 |
a0020 | 0/0 | 817 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | MEAEE others(812): Show |
chr7 | 144350402 | 144385632 |
a0021 | 0/0 | 817 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | MEAEE others(812): Show |
chr7 | 144350402 | 144385632 |
a0022 | 0/0 | 1597 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | MEAEE others(1592): Show |
chr7 | 144350402 | 144385632 |
a0023 | 0/0 | 817 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | MEAEE others(812): Show |
chr7 | 144350402 | 144385632 |
a0024 | 0/0 | 1597 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | MEAEE others(1592): Show |
chr7 | 144350402 | 144385632 |
a0025 | 0/0 | 817 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | MEAEE others(812): Show |
chr7 | 144350402 | 144385632 |
a0026 | 0/0 | 1597 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | MEAEE others(1592): Show |
chr7 | 144350402 | 144385632 |
a0027 | 0/0 | 1597 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | MEAEE others(1592): Show |
chr7 | 144350402 | 144385632 |
a0028 | 0/0 | 1597 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | MEAEE others(1592): Show |
chr7 | 144350402 | 144385632 |
a0029 | 0/0 | 817 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | MEAEE others(812): Show |
chr7 | 144350402 | 144385632 |
a0030 | 0/0 | 1597 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | MEAEE others(1592): Show |
chr7 | 144350402 | 144385632 |
a0031 | 0/0 | 1597 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | MEAEE others(1592): Show |
chr7 | 144350402 | 144385632 |
a0032 | 0/0 | 1597 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | MEAEE others(1592): Show |
chr7 | 144350402 | 144385632 |
a0033 | 0/0 | 1597 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | MEAEE others(1592): Show |
chr7 | 144350402 | 144385632 |
a0034 | 0/0 | 817 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | MEAEE others(812): Show |
chr7 | 144350402 | 144385632 |
a0035 | 0/0 | 1597 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | MEAEE others(1592): Show |
chr7 | 144350402 | 144385632 |
a0036 | 0/0 | 1597 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | MEAEE others(1592): Show |
chr7 | 144350402 | 144385632 |
a0037 | 0/0 | 817 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | MEAEE others(812): Show |
chr7 | 144350402 | 144385632 |
a0038 | 0/0 | 1597 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | MEAEE others(1592): Show |
chr7 | 144350402 | 144385632 |
a0039 | 0/0 | 1597 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | MEAEE others(1592): Show |
chr7 | 144350402 | 144385632 |
a0040 | 0/0 | 817 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | MEAEE others(812): Show |
chr7 | 144350402 | 144385632 |
a0041 | 0/0 | 1597 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | MEAEE others(1592): Show |
chr7 | 144350402 | 144385632 |
a0042 | 0/0 | 1597 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | MEAEE others(1592): Show |
chr7 | 144350402 | 144385632 |
a0043 | 0/0 | 1597 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | MEAEE others(1592): Show |
chr7 | 144350402 | 144385632 |
a0044 | 0/0 | 817 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | MEAEE others(812): Show |
chr7 | 144350402 | 144385632 |
a0045 | 0/0 | 1597 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | MEAEE others(1592): Show |
chr7 | 144350402 | 144385632 |
a0046 | 0/0 | 817 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | MEAEE others(812): Show |
chr7 | 144350402 | 144385632 |
a0047 | 0/0 | 817 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | MEAEE others(812): Show |
chr7 | 144350402 | 144385632 |
a0048 | 0/0 | 1597 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | MEAEE others(1592): Show |
chr7 | 144350402 | 144385632 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002 | 1/0 | 4791 | 37 | 3 | 10 | 16 | 2 | 5 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4786): Show |
chr7 | 144350402 | 144385632 | ||
a0001c0010 | 0/0 | 4791 | 6 | 6 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4786): Show |
chr7 | 144350402 | 144385632 | ||
a0001c0020 | 0/0 | 4791 | 2 | 0 | 1 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4786): Show |
chr7 | 144350402 | 144385632 | ||
a0001c0021 | 0/0 | 4791 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4786): Show |
chr7 | 144350402 | 144385632 | ||
a0001c0036 | 0/0 | 4791 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4786): Show |
chr7 | 144350402 | 144385632 | ||
a0001c0039 | 0/0 | 4791 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4786): Show |
chr7 | 144350402 | 144385632 | ||
a0002c0001 | 0/0 | 4791 | 41 | 1 | 13 | 21 | 1 | 5 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4786): Show |
chr7 | 144350402 | 144385632 | ||
a0002c0016 | 0/0 | 4791 | 3 | 0 | 1 | 1 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4786): Show |
chr7 | 144350402 | 144385632 | ||
a0002c0061 | 0/0 | 4791 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4786): Show |
chr7 | 144350402 | 144385632 | ||
a0002c0063 | 0/0 | 4791 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4786): Show |
chr7 | 144350402 | 144385632 | ||
a0002c0064 | 0/0 | 4791 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4786): Show |
chr7 | 144350402 | 144385632 | ||
a0003c0004 | 0/1 | 4791 | 25 | 1 | 8 | 4 | 4 | 7 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4786): Show |
chr7 | 144350402 | 144385632 | ||
a0003c0012 | 0/0 | 4791 | 5 | 5 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4786): Show |
chr7 | 144350402 | 144385632 | ||
a0003c0014 | 0/0 | 4791 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4786): Show |
chr7 | 144350402 | 144385632 | ||
a0003c0032 | 0/0 | 4791 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4786): Show |
chr7 | 144350402 | 144385632 | ||
a0003c0047 | 0/0 | 4791 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4786): Show |
chr7 | 144350402 | 144385632 | ||
a0004c0003 | 0/0 | 4791 | 25 | 1 | 11 | 2 | 4 | 7 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4786): Show |
chr7 | 144350402 | 144385632 | ||
a0005c0005 | 0/0 | 4791 | 17 | 2 | 1 | 11 | 2 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4786): Show |
chr7 | 144350402 | 144385632 | ||
a0006c0006 | 0/0 | 4791 | 17 | 4 | 0 | 5 | 2 | 6 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4786): Show |
chr7 | 144350402 | 144385632 | ||
a0007c0007 | 0/0 | 4791 | 10 | 10 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4786): Show |
chr7 | 144350402 | 144385632 | ||
a0007c0011 | 0/0 | 4791 | 5 | 5 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4786): Show |
chr7 | 144350402 | 144385632 | ||
a0007c0041 | 0/0 | 4791 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4786): Show |
chr7 | 144350402 | 144385632 | ||
a0007c0042 | 0/0 | 4791 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4786): Show |
chr7 | 144350402 | 144385632 | ||
a0008c0008 | 0/0 | 4791 | 10 | 8 | 1 | 0 | 1 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4786): Show |
chr7 | 144350402 | 144385632 | ||
a0008c0055 | 0/0 | 4791 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4786): Show |
chr7 | 144350402 | 144385632 | ||
a0009c0026 | 0/0 | 4813 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4808): Show |
chr7 | 144350402 | 144385632 | ||
a0009c0070 | 0/0 | 4813 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4808): Show |
chr7 | 144350402 | 144385632 | ||
a0009c0071 | 0/0 | 4813 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4808): Show |
chr7 | 144350402 | 144385632 | ||
a0009c0072 | 0/0 | 4813 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4808): Show |
chr7 | 144350402 | 144385632 | ||
a0009c0073 | 0/0 | 4814 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4809): Show |
chr7 | 144350402 | 144385632 | ||
a0009c0074 | 0/0 | 4813 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4808): Show |
chr7 | 144350402 | 144385632 | ||
a0009c0075 | 0/0 | 4813 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4808): Show |
chr7 | 144350402 | 144385632 | ||
a0009c0076 | 0/0 | 4813 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4808): Show |
chr7 | 144350402 | 144385632 | ||
a0010c0009 | 0/0 | 4791 | 6 | 6 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4786): Show |
chr7 | 144350402 | 144385632 | ||
a0011c0023 | 0/0 | 4791 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4786): Show |
chr7 | 144350402 | 144385632 | ||
a0011c0043 | 0/0 | 4791 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4786): Show |
chr7 | 144350402 | 144385632 | ||
a0011c0044 | 0/0 | 4791 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4786): Show |
chr7 | 144350402 | 144385632 | ||
a0011c0045 | 0/0 | 4791 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4786): Show |
chr7 | 144350402 | 144385632 | ||
a0012c0013 | 0/0 | 4791 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4786): Show |
chr7 | 144350402 | 144385632 | ||
a0013c0017 | 0/0 | 4791 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4786): Show |
chr7 | 144350402 | 144385632 | ||
a0014c0015 | 0/0 | 4791 | 3 | 0 | 1 | 0 | 2 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4786): Show |
chr7 | 144350402 | 144385632 | ||
a0015c0019 | 0/0 | 4792 | 2 | 0 | 1 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4787): Show |
chr7 | 144350402 | 144385632 | ||
a0016c0022 | 0/0 | 4791 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4786): Show |
chr7 | 144350402 | 144385632 | ||
a0017c0025 | 0/0 | 4791 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4786): Show |
chr7 | 144350402 | 144385632 | ||
a0018c0054 | 0/0 | 4792 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4787): Show |
chr7 | 144350402 | 144385632 | ||
a0018c0065 | 0/0 | 4792 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4787): Show |
chr7 | 144350402 | 144385632 | ||
a0019c0018 | 0/0 | 4791 | 2 | 1 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4786): Show |
chr7 | 144350402 | 144385632 | ||
a0020c0024 | 0/0 | 4792 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4787): Show |
chr7 | 144350402 | 144385632 | ||
a0021c0057 | 0/0 | 4792 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4787): Show |
chr7 | 144350402 | 144385632 | ||
a0022c0038 | 0/0 | 4791 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4786): Show |
chr7 | 144350402 | 144385632 | ||
a0023c0050 | 0/0 | 4792 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4787): Show |
chr7 | 144350402 | 144385632 | ||
a0024c0066 | 0/0 | 4791 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4786): Show |
chr7 | 144350402 | 144385632 | ||
a0025c0046 | 0/0 | 4792 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4787): Show |
chr7 | 144350402 | 144385632 | ||
a0026c0034 | 0/0 | 4791 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4786): Show |
chr7 | 144350402 | 144385632 | ||
a0027c0069 | 0/0 | 4791 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4786): Show |
chr7 | 144350402 | 144385632 | ||
a0028c0037 | 0/0 | 4791 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4786): Show |
chr7 | 144350402 | 144385632 | ||
a0029c0040 | 0/0 | 4792 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4787): Show |
chr7 | 144350402 | 144385632 | ||
a0030c0035 | 0/0 | 4791 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4786): Show |
chr7 | 144350402 | 144385632 | ||
a0031c0059 | 0/0 | 4791 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4786): Show |
chr7 | 144350402 | 144385632 | ||
a0032c0067 | 0/0 | 4791 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4786): Show |
chr7 | 144350402 | 144385632 | ||
a0033c0033 | 0/0 | 4791 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4786): Show |
chr7 | 144350402 | 144385632 | ||
a0034c0029 | 0/0 | 4792 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4787): Show |
chr7 | 144350402 | 144385632 | ||
a0035c0053 | 0/0 | 4791 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4786): Show |
chr7 | 144350402 | 144385632 | ||
a0036c0058 | 0/0 | 4791 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4786): Show |
chr7 | 144350402 | 144385632 | ||
a0037c0028 | 0/0 | 4792 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4787): Show |
chr7 | 144350402 | 144385632 | ||
a0038c0030 | 0/0 | 4791 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4786): Show |
chr7 | 144350402 | 144385632 | ||
a0039c0027 | 0/0 | 4791 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4786): Show |
chr7 | 144350402 | 144385632 | ||
a0040c0056 | 0/0 | 4792 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4787): Show |
chr7 | 144350402 | 144385632 | ||
a0041c0062 | 0/0 | 4791 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4786): Show |
chr7 | 144350402 | 144385632 | ||
a0042c0048 | 0/0 | 4791 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4786): Show |
chr7 | 144350402 | 144385632 | ||
a0043c0051 | 0/0 | 4791 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4786): Show |
chr7 | 144350402 | 144385632 | ||
a0044c0068 | 0/0 | 4792 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4787): Show |
chr7 | 144350402 | 144385632 | ||
a0045c0052 | 0/0 | 4791 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4786): Show |
chr7 | 144350402 | 144385632 | ||
a0046c0060 | 0/0 | 4792 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4787): Show |
chr7 | 144350402 | 144385632 | ||
a0047c0031 | 0/0 | 4792 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4787): Show |
chr7 | 144350402 | 144385632 | ||
a0048c0049 | 0/0 | 4791 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | ATGGA others(4786): Show |
chr7 | 144350402 | 144385632 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0002 | 1/0 | 5482 | 35 | 3 | 8 | 16 | 2 | 5 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5477): Show |
chr7 | 144350402 | 144385632 |
a0001c0002t0004 | 0/0 | 5482 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5477): Show |
chr7 | 144350402 | 144385632 |
a0001c0010t0002 | 0/0 | 5482 | 6 | 6 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5477): Show |
chr7 | 144350402 | 144385632 |
a0001c0020t0002 | 0/0 | 5482 | 2 | 0 | 1 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5477): Show |
chr7 | 144350402 | 144385632 |
a0001c0021t0002 | 0/0 | 5482 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5477): Show |
chr7 | 144350402 | 144385632 |
a0001c0036t0002 | 0/0 | 5482 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5477): Show |
chr7 | 144350402 | 144385632 |
a0001c0039t0002 | 0/0 | 5482 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5477): Show |
chr7 | 144350402 | 144385632 |
a0002c0001t0001 | 0/0 | 5482 | 41 | 1 | 13 | 21 | 1 | 5 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5477): Show |
chr7 | 144350402 | 144385632 |
a0002c0016t0001 | 0/0 | 5482 | 3 | 0 | 1 | 1 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5477): Show |
chr7 | 144350402 | 144385632 |
a0002c0061t0001 | 0/0 | 5482 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5477): Show |
chr7 | 144350402 | 144385632 |
a0002c0063t0001 | 0/0 | 5482 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5477): Show |
chr7 | 144350402 | 144385632 |
a0002c0064t0001 | 0/0 | 5482 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5477): Show |
chr7 | 144350402 | 144385632 |
a0003c0004t0002 | 0/1 | 5482 | 24 | 1 | 8 | 4 | 3 | 7 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5477): Show |
chr7 | 144350402 | 144385632 |
a0003c0004t0005 | 0/0 | 5482 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5477): Show |
chr7 | 144350402 | 144385632 |
a0003c0012t0002 | 0/0 | 5482 | 5 | 5 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5477): Show |
chr7 | 144350402 | 144385632 |
a0003c0014t0002 | 0/0 | 5482 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5477): Show |
chr7 | 144350402 | 144385632 |
a0003c0032t0002 | 0/0 | 5482 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5477): Show |
chr7 | 144350402 | 144385632 |
a0003c0047t0002 | 0/0 | 5482 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5477): Show |
chr7 | 144350402 | 144385632 |
a0004c0003t0001 | 0/0 | 5482 | 25 | 1 | 11 | 2 | 4 | 7 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5477): Show |
chr7 | 144350402 | 144385632 |
a0005c0005t0001 | 0/0 | 5482 | 17 | 2 | 1 | 11 | 2 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5477): Show |
chr7 | 144350402 | 144385632 |
a0006c0006t0001 | 0/0 | 5482 | 17 | 4 | 0 | 5 | 2 | 6 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5477): Show |
chr7 | 144350402 | 144385632 |
a0007c0007t0003 | 0/0 | 5482 | 10 | 10 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5477): Show |
chr7 | 144350402 | 144385632 |
a0007c0011t0002 | 0/0 | 5482 | 5 | 5 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5477): Show |
chr7 | 144350402 | 144385632 |
a0007c0041t0001 | 0/0 | 5482 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5477): Show |
chr7 | 144350402 | 144385632 |
a0007c0042t0001 | 0/0 | 5482 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5477): Show |
chr7 | 144350402 | 144385632 |
a0008c0008t0001 | 0/0 | 5482 | 10 | 8 | 1 | 0 | 1 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5477): Show |
chr7 | 144350402 | 144385632 |
a0008c0055t0001 | 0/0 | 5482 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5477): Show |
chr7 | 144350402 | 144385632 |
a0009c0026t0001 | 0/0 | 5504 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5499): Show |
chr7 | 144350402 | 144385632 |
a0009c0070t0001 | 0/0 | 5504 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5499): Show |
chr7 | 144350402 | 144385632 |
a0009c0071t0001 | 0/0 | 5504 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5499): Show |
chr7 | 144350402 | 144385632 |
a0009c0072t0001 | 0/0 | 5504 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5499): Show |
chr7 | 144350402 | 144385632 |
a0009c0073t0001 | 0/0 | 5505 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5500): Show |
chr7 | 144350402 | 144385632 |
a0009c0074t0001 | 0/0 | 5504 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5499): Show |
chr7 | 144350402 | 144385632 |
a0009c0075t0002 | 0/0 | 5504 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5499): Show |
chr7 | 144350402 | 144385632 |
a0009c0076t0001 | 0/0 | 5504 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5499): Show |
chr7 | 144350402 | 144385632 |
a0010c0009t0001 | 0/0 | 5482 | 6 | 6 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5477): Show |
chr7 | 144350402 | 144385632 |
a0011c0023t0002 | 0/0 | 5482 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5477): Show |
chr7 | 144350402 | 144385632 |
a0011c0043t0002 | 0/0 | 5482 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5477): Show |
chr7 | 144350402 | 144385632 |
a0011c0044t0001 | 0/0 | 5482 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5477): Show |
chr7 | 144350402 | 144385632 |
a0011c0045t0001 | 0/0 | 5482 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5477): Show |
chr7 | 144350402 | 144385632 |
a0012c0013t0002 | 0/0 | 5482 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5477): Show |
chr7 | 144350402 | 144385632 |
a0013c0017t0001 | 0/0 | 5482 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5477): Show |
chr7 | 144350402 | 144385632 |
a0014c0015t0002 | 0/0 | 5482 | 3 | 0 | 1 | 0 | 2 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5477): Show |
chr7 | 144350402 | 144385632 |
a0015c0019t0002 | 0/0 | 5483 | 2 | 0 | 1 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5478): Show |
chr7 | 144350402 | 144385632 |
a0016c0022t0002 | 0/0 | 5482 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5477): Show |
chr7 | 144350402 | 144385632 |
a0017c0025t0001 | 0/0 | 5482 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5477): Show |
chr7 | 144350402 | 144385632 |
a0018c0054t0001 | 0/0 | 5483 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5478): Show |
chr7 | 144350402 | 144385632 |
a0018c0065t0001 | 0/0 | 5483 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5478): Show |
chr7 | 144350402 | 144385632 |
a0019c0018t0001 | 0/0 | 5482 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5477): Show |
chr7 | 144350402 | 144385632 |
a0019c0018t0002 | 0/0 | 5482 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5477): Show |
chr7 | 144350402 | 144385632 |
a0020c0024t0001 | 0/0 | 5483 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5478): Show |
chr7 | 144350402 | 144385632 |
a0021c0057t0001 | 0/0 | 5483 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5478): Show |
chr7 | 144350402 | 144385632 |
a0022c0038t0002 | 0/0 | 5482 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5477): Show |
chr7 | 144350402 | 144385632 |
a0023c0050t0001 | 0/0 | 5483 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5478): Show |
chr7 | 144350402 | 144385632 |
a0024c0066t0001 | 0/0 | 5482 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5477): Show |
chr7 | 144350402 | 144385632 |
a0025c0046t0002 | 0/0 | 5483 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5478): Show |
chr7 | 144350402 | 144385632 |
a0026c0034t0002 | 0/0 | 5482 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5477): Show |
chr7 | 144350402 | 144385632 |
a0027c0069t0002 | 0/0 | 5482 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5477): Show |
chr7 | 144350402 | 144385632 |
a0028c0037t0002 | 0/0 | 5482 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5477): Show |
chr7 | 144350402 | 144385632 |
a0029c0040t0002 | 0/0 | 5483 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5478): Show |
chr7 | 144350402 | 144385632 |
a0030c0035t0002 | 0/0 | 5482 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5477): Show |
chr7 | 144350402 | 144385632 |
a0031c0059t0001 | 0/0 | 5482 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5477): Show |
chr7 | 144350402 | 144385632 |
a0032c0067t0001 | 0/0 | 5482 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5477): Show |
chr7 | 144350402 | 144385632 |
a0033c0033t0002 | 0/0 | 5482 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5477): Show |
chr7 | 144350402 | 144385632 |
a0034c0029t0001 | 0/0 | 5483 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5478): Show |
chr7 | 144350402 | 144385632 |
a0035c0053t0001 | 0/0 | 5482 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5477): Show |
chr7 | 144350402 | 144385632 |
a0036c0058t0001 | 0/0 | 5482 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5477): Show |
chr7 | 144350402 | 144385632 |
a0037c0028t0001 | 0/0 | 5483 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5478): Show |
chr7 | 144350402 | 144385632 |
a0038c0030t0001 | 0/0 | 5482 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5477): Show |
chr7 | 144350402 | 144385632 |
a0039c0027t0002 | 0/0 | 5482 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5477): Show |
chr7 | 144350402 | 144385632 |
a0040c0056t0001 | 0/0 | 5483 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5478): Show |
chr7 | 144350402 | 144385632 |
a0041c0062t0001 | 0/0 | 5482 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5477): Show |
chr7 | 144350402 | 144385632 |
a0042c0048t0001 | 0/0 | 5482 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5477): Show |
chr7 | 144350402 | 144385632 |
a0043c0051t0001 | 0/0 | 5482 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5477): Show |
chr7 | 144350402 | 144385632 |
a0044c0068t0001 | 0/0 | 5483 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5478): Show |
chr7 | 144350402 | 144385632 |
a0045c0052t0001 | 0/0 | 5482 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5477): Show |
chr7 | 144350402 | 144385632 |
a0046c0060t0001 | 0/0 | 5483 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5478): Show |
chr7 | 144350402 | 144385632 |
a0047c0031t0003 | 0/0 | 5483 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5478): Show |
chr7 | 144350402 | 144385632 |
a0048c0049t0002 | 0/0 | 5482 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | GGGGC others(5477): Show |
chr7 | 144350402 | 144385632 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0002g0002 | 0/0 | 9 | 0 | 5 | 4 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0001c0002t0002g0005 | 1/0 | 5 | 0 | 1 | 3 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0001c0002t0002g0016 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0001c0002t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0001c0002t0002g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0001c0002t0002g0041 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0001c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0001c0002t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0001c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0001c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0001c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0001c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0001c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0001c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0001c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0001c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0001c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0001c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0001c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0001c0002t0004g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0001c0010t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0001c0010t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0001c0010t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0001c0010t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0001c0010t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0001c0010t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0001c0020t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0001c0020t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0001c0021t0002g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0001c0036t0002g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0001c0039t0002g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0001t0001g0001 | 0/0 | 11 | 0 | 7 | 2 | 0 | 2 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0001t0001g0012 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0016t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0016t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0016t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0061t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0063t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0002c0064t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0003c0004t0002g0004 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0003c0004t0002g0011 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0003c0004t0002g0015 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0003c0004t0002g0019 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0003c0004t0002g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0003c0004t0002g0022 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0003c0004t0002g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0003c0004t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0003c0004t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0003c0004t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0003c0004t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0003c0004t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0003c0004t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0003c0004t0002g0125 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0003c0004t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0003c0004t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0003c0004t0005g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0003c0012t0002g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0003c0012t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0003c0014t0002g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0003c0014t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0003c0032t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0003c0047t0002g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0004c0003t0001g0003 | 0/0 | 12 | 1 | 4 | 1 | 3 | 3 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0004c0003t0001g0043 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0004c0003t0001g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0004c0003t0001g0046 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0004c0003t0001g0048 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0004c0003t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0004c0003t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0004c0003t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0004c0003t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0004c0003t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0005c0005t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0005c0005t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0005c0005t0001g0009 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0005c0005t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0005c0005t0001g0027 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0005c0005t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0005c0005t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0005c0005t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0005c0005t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0005c0005t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0005c0005t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0005c0005t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0006c0006t0001g0007 | 0/0 | 4 | 0 | 0 | 0 | 1 | 3 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0006c0006t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0006c0006t0001g0028 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0006c0006t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0006c0006t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0006c0006t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0006c0006t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0006c0006t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0006c0006t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0006c0006t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0006c0006t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0006c0006t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0006c0006t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0007c0007t0003g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0007c0007t0003g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0007c0007t0003g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0007c0007t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0007c0007t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0007c0007t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0007c0011t0002g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0007c0011t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0007c0041t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0007c0042t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0008c0008t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0008c0008t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0008c0008t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0008c0008t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0008c0008t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0008c0008t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0008c0008t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0008c0008t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0008c0055t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0009c0026t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0009c0026t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0009c0070t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0009c0071t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0009c0072t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0009c0073t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0009c0074t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0009c0075t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0009c0076t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0010c0009t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0010c0009t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0010c0009t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0010c0009t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0010c0009t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0011c0023t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0011c0023t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0011c0043t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0011c0044t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0011c0045t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0012c0013t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0012c0013t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0012c0013t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0012c0013t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0013c0017t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0013c0017t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0013c0017t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0014c0015t0002g0004 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0014c0015t0002g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0015c0019t0002g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0015c0019t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0016c0022t0002g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0017c0025t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0018c0054t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0018c0065t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0019c0018t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0019c0018t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0020c0024t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0020c0024t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0021c0057t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0022c0038t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0023c0050t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0024c0066t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0025c0046t0002g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0026c0034t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0027c0069t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0028c0037t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0029c0040t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0030c0035t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0031c0059t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0032c0067t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0033c0033t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0034c0029t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0035c0053t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0036c0058t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0037c0028t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0038c0030t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0039c0027t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0040c0056t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0041c0062t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0042c0048t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0043c0051t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0044c0068t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0045c0052t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0046c0060t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0047c0031t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
a0048c0049t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0002 | g0162 | EUR | GBR | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG00099 | hp2 | a0005 | c0005 | t0001 | g0009 | EUR | GBR | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG00140 | hp1 | a0003 | c0004 | t0002 | g0156 | EUR | GBR | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG00140 | hp2 | a0004 | c0003 | t0001 | g0003 | EUR | GBR | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG00280 | hp1 | a0001 | c0002 | t0002 | g0163 | EUR | FIN | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG00280 | hp2 | a0004 | c0003 | t0001 | g0003 | EUR | FIN | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG00323 | hp1 | a0005 | c0005 | t0001 | g0152 | EUR | FIN | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG00323 | hp2 | a0004 | c0003 | t0001 | g0171 | EUR | FIN | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG00423 | hp1 | a0005 | c0005 | t0001 | g0008 | EAS | CHS | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG00423 | hp2 | a0015 | c0019 | t0002 | g0005 | EAS | CHS | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG00438 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | CHS | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG00438 | hp2 | a0002 | c0001 | t0001 | g0090 | EAS | CHS | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG00544 | hp1 | a0006 | c0006 | t0001 | g0031 | EAS | CHS | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG00544 | hp2 | a0002 | c0001 | t0001 | g0093 | EAS | CHS | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG00558 | hp1 | a0002 | c0001 | t0001 | g0092 | EAS | CHS | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG00558 | hp2 | a0002 | c0001 | t0001 | g0078 | EAS | CHS | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG00597 | hp1 | a0013 | c0017 | t0001 | g0154 | EAS | CHS | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG00597 | hp2 | a0021 | c0057 | t0001 | g0031 | EAS | CHS | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG00621 | hp1 | a0002 | c0001 | t0001 | g0108 | EAS | CHS | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG00621 | hp2 | a0006 | c0006 | t0001 | g0099 | EAS | CHS | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG00639 | hp1 | a0004 | c0003 | t0001 | g0003 | AMR | PUR | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG00639 | hp2 | a0016 | c0022 | t0002 | g0034 | AMR | PUR | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG00642 | hp1 | a0004 | c0003 | t0001 | g0045 | AMR | PUR | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG00642 | hp2 | a0022 | c0038 | t0002 | g0036 | AMR | PUR | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG00673 | hp1 | a0023 | c0050 | t0001 | g0030 | EAS | CHS | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG00673 | hp2 | a0024 | c0066 | t0001 | g0001 | EAS | CHS | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG00735 | hp1 | a0008 | c0008 | t0001 | g0033 | AMR | PUR | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG00735 | hp2 | a0001 | c0020 | t0002 | g0137 | AMR | PUR | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG00741 | hp1 | a0002 | c0061 | t0001 | g0094 | AMR | PUR | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG00741 | hp2 | a0025 | c0046 | t0002 | g0015 | AMR | PUR | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01069 | hp1 | a0017 | c0025 | t0001 | g0009 | AMR | PUR | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01069 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01071 | hp1 | a0005 | c0005 | t0001 | g0027 | AMR | PUR | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01071 | hp2 | a0017 | c0025 | t0001 | g0009 | AMR | PUR | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01074 | hp1 | a0003 | c0004 | t0002 | g0004 | AMR | PUR | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01074 | hp2 | a0026 | c0034 | t0002 | g0164 | AMR | PUR | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01099 | hp1 | a0014 | c0015 | t0002 | g0004 | AMR | PUR | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01099 | hp2 | a0016 | c0022 | t0002 | g0034 | AMR | PUR | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01167 | hp1 | a0001 | c0002 | t0004 | g0002 | AMR | PUR | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01167 | hp2 | a0004 | c0003 | t0001 | g0048 | AMR | PUR | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01168 | hp1 | a0003 | c0004 | t0002 | g0015 | AMR | PUR | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01168 | hp2 | a0002 | c0001 | t0001 | g0032 | AMR | PUR | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01169 | hp1 | a0002 | c0001 | t0001 | g0032 | AMR | PUR | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01169 | hp2 | a0001 | c0002 | t0004 | g0002 | AMR | PUR | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01192 | hp1 | a0002 | c0001 | t0001 | g0103 | AMR | PUR | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01192 | hp2 | a0003 | c0004 | t0002 | g0011 | AMR | PUR | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01243 | hp1 | a0015 | c0019 | t0002 | g0002 | AMR | PUR | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01243 | hp2 | a0004 | c0003 | t0001 | g0046 | AMR | PUR | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01255 | hp1 | a0002 | c0001 | t0001 | g0012 | AMR | CLM | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01255 | hp2 | a0003 | c0032 | t0002 | g0063 | AMR | CLM | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01256 | hp1 | a0003 | c0004 | t0002 | g0004 | AMR | CLM | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01256 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | CLM | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01258 | hp1 | a0003 | c0004 | t0002 | g0004 | AMR | CLM | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01258 | hp2 | a0002 | c0001 | t0001 | g0001 | AMR | CLM | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01261 | hp1 | a0003 | c0004 | t0002 | g0061 | AMR | CLM | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01261 | hp2 | a0003 | c0047 | t0002 | g0004 | AMR | CLM | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01346 | hp1 | a0001 | c0002 | t0002 | g0016 | AMR | CLM | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01346 | hp2 | a0004 | c0003 | t0001 | g0003 | AMR | CLM | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01361 | hp1 | a0004 | c0003 | t0001 | g0003 | AMR | CLM | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01361 | hp2 | a0027 | c0069 | t0002 | g0157 | AMR | CLM | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01433 | hp1 | a0003 | c0004 | t0002 | g0022 | AMR | CLM | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01433 | hp2 | a0004 | c0003 | t0001 | g0003 | AMR | CLM | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01496 | hp1 | a0009 | c0071 | t0001 | g0173 | AMR | CLM | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01496 | hp2 | a0004 | c0003 | t0001 | g0043 | AMR | CLM | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01515 | hp1 | a0014 | c0015 | t0002 | g0004 | EUR | IBS | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01515 | hp2 | a0002 | c0001 | t0001 | g0089 | EUR | IBS | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01516 | hp1 | a0003 | c0004 | t0002 | g0019 | EUR | IBS | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01516 | hp2 | a0006 | c0006 | t0001 | g0086 | EUR | IBS | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01517 | hp1 | a0014 | c0015 | t0002 | g0020 | EUR | IBS | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01517 | hp2 | a0006 | c0006 | t0001 | g0007 | EUR | IBS | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01884 | hp1 | a0012 | c0013 | t0002 | g0120 | AFR | ACB | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01884 | hp2 | a0009 | c0076 | t0001 | g0053 | AFR | ACB | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01891 | hp1 | a0007 | c0007 | t0003 | g0038 | AFR | ACB | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01891 | hp2 | a0008 | c0008 | t0001 | g0114 | AFR | ACB | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01928 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01928 | hp2 | a0002 | c0001 | t0001 | g0001 | AMR | PEL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01934 | hp1 | a0003 | c0004 | t0002 | g0069 | AMR | PEL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01934 | hp2 | a0002 | c0016 | t0001 | g0102 | AMR | PEL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01975 | hp1 | a0002 | c0001 | t0001 | g0001 | AMR | PEL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01975 | hp2 | a0028 | c0037 | t0002 | g0140 | AMR | PEL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01993 | hp1 | a0004 | c0003 | t0001 | g0172 | AMR | PEL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01993 | hp2 | a0002 | c0001 | t0001 | g0095 | AMR | PEL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02004 | hp1 | a0002 | c0001 | t0001 | g0001 | AMR | PEL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02004 | hp2 | a0001 | c0002 | t0002 | g0041 | AMR | PEL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02015 | hp1 | a0004 | c0003 | t0001 | g0003 | EAS | KHV | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02015 | hp2 | a0005 | c0005 | t0001 | g0087 | EAS | KHV | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02027 | hp1 | a0029 | c0040 | t0002 | g0002 | EAS | KHV | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02027 | hp2 | a0002 | c0001 | t0001 | g0047 | EAS | KHV | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02040 | hp1 | a0030 | c0035 | t0002 | g0141 | EAS | KHV | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02040 | hp2 | a0002 | c0064 | t0001 | g0074 | EAS | KHV | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02074 | hp1 | a0013 | c0017 | t0001 | g0110 | EAS | KHV | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02074 | hp2 | a0001 | c0002 | t0002 | g0142 | EAS | KHV | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02083 | hp1 | a0003 | c0004 | t0002 | g0158 | EAS | KHV | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02083 | hp2 | a0002 | c0001 | t0001 | g0026 | EAS | KHV | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02132 | hp1 | a0031 | c0059 | t0001 | g0083 | EAS | KHV | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02132 | hp2 | a0002 | c0001 | t0001 | g0047 | EAS | KHV | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02135 | hp1 | a0006 | c0006 | t0001 | g0073 | EAS | KHV | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02135 | hp2 | a0019 | c0018 | t0001 | g0147 | EAS | KHV | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02145 | hp1 | a0003 | c0004 | t0002 | g0065 | AFR | ACB | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02145 | hp2 | a0001 | c0010 | t0002 | g0126 | AFR | ACB | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02148 | hp1 | a0002 | c0001 | t0001 | g0001 | AMR | PEL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02148 | hp2 | a0007 | c0042 | t0001 | g0170 | AMR | PEL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02165 | hp1 | a0003 | c0004 | t0002 | g0066 | EAS | CDX | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02165 | hp2 | a0013 | c0017 | t0001 | g0111 | EAS | CDX | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02258 | hp1 | a0007 | c0011 | t0002 | g0010 | AFR | ACB | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02258 | hp2 | a0001 | c0010 | t0002 | g0119 | AFR | ACB | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02273 | hp1 | a0002 | c0001 | t0001 | g0177 | AMR | PEL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02273 | hp2 | a0001 | c0002 | t0002 | g0005 | AMR | PEL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02293 | hp1 | a0004 | c0003 | t0001 | g0045 | AMR | PEL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02293 | hp2 | a0002 | c0001 | t0001 | g0001 | AMR | PEL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02300 | hp1 | a0002 | c0001 | t0001 | g0001 | AMR | PEL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02300 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02451 | hp1 | a0003 | c0012 | t0002 | g0006 | AFR | ACB | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02451 | hp2 | a0032 | c0067 | t0001 | g0169 | AFR | ACB | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02622 | hp1 | a0006 | c0006 | t0001 | g0096 | AFR | GWD | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02622 | hp2 | a0007 | c0007 | t0003 | g0014 | AFR | GWD | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02630 | hp1 | a0006 | c0006 | t0001 | g0008 | AFR | GWD | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02630 | hp2 | a0007 | c0007 | t0003 | g0117 | AFR | GWD | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02647 | hp1 | a0007 | c0007 | t0003 | g0014 | AFR | GWD | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02647 | hp2 | a0019 | c0018 | t0002 | g0062 | AFR | GWD | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02683 | hp1 | a0005 | c0005 | t0001 | g0150 | SAS | PJL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02683 | hp2 | a0001 | c0002 | t0002 | g0016 | SAS | PJL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02698 | hp1 | a0004 | c0003 | t0001 | g0003 | SAS | PJL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02698 | hp2 | a0002 | c0001 | t0001 | g0001 | SAS | PJL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02723 | hp1 | a0007 | c0007 | t0003 | g0037 | AFR | GWD | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02723 | hp2 | a0033 | c0033 | t0002 | g0131 | AFR | GWD | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02735 | hp1 | a0004 | c0003 | t0001 | g0161 | SAS | PJL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02735 | hp2 | a0001 | c0020 | t0002 | g0135 | SAS | PJL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02738 | hp1 | a0034 | c0029 | t0001 | g0001 | SAS | PJL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02738 | hp2 | a0003 | c0004 | t0002 | g0022 | SAS | PJL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02809 | hp1 | a0003 | c0014 | t0002 | g0023 | AFR | GWD | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02809 | hp2 | a0011 | c0043 | t0002 | g0064 | AFR | GWD | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02818 | hp1 | a0007 | c0011 | t0002 | g0010 | AFR | GWD | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02818 | hp2 | a0007 | c0007 | t0003 | g0014 | AFR | GWD | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02886 | hp1 | a0005 | c0005 | t0001 | g0009 | AFR | GWD | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02886 | hp2 | a0003 | c0014 | t0002 | g0021 | AFR | GWD | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02895 | hp1 | a0006 | c0006 | t0001 | g0107 | AFR | GWD | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02895 | hp2 | a0008 | c0008 | t0001 | g0029 | AFR | GWD | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02897 | hp1 | a0008 | c0008 | t0001 | g0029 | AFR | GWD | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02897 | hp2 | a0010 | c0009 | t0001 | g0018 | AFR | GWD | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02922 | hp1 | a0001 | c0002 | t0002 | g0040 | AFR | ESN | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02922 | hp2 | a0011 | c0023 | t0002 | g0070 | AFR | ESN | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02965 | hp1 | a0010 | c0009 | t0001 | g0058 | AFR | ESN | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02965 | hp2 | a0003 | c0012 | t0002 | g0006 | AFR | ESN | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02970 | hp1 | a0007 | c0011 | t0002 | g0155 | AFR | ESN | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02970 | hp2 | a0012 | c0013 | t0002 | g0121 | AFR | ESN | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02976 | hp1 | a0007 | c0007 | t0003 | g0035 | AFR | ESN | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02976 | hp2 | a0035 | c0053 | t0001 | g0116 | AFR | ESN | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03017 | hp1 | a0006 | c0006 | t0001 | g0084 | SAS | PJL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03017 | hp2 | a0002 | c0001 | t0001 | g0001 | SAS | PJL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03041 | hp1 | a0005 | c0005 | t0001 | g0072 | AFR | GWD | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03041 | hp2 | a0001 | c0010 | t0002 | g0128 | AFR | GWD | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03130 | hp1 | a0001 | c0002 | t0002 | g0040 | AFR | ESN | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03130 | hp2 | a0007 | c0007 | t0003 | g0035 | AFR | ESN | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03139 | hp1 | a0008 | c0008 | t0001 | g0044 | AFR | ESN | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03139 | hp2 | a0006 | c0006 | t0001 | g0097 | AFR | ESN | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03195 | hp1 | a0008 | c0008 | t0001 | g0044 | AFR | ESN | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03195 | hp2 | a0007 | c0011 | t0002 | g0010 | AFR | ESN | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03209 | hp1 | a0036 | c0058 | t0001 | g0098 | AFR | MSL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03209 | hp2 | a0003 | c0012 | t0002 | g0006 | AFR | MSL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03239 | hp1 | a0003 | c0004 | t0002 | g0020 | SAS | PJL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03239 | hp2 | a0006 | c0006 | t0001 | g0007 | SAS | PJL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03453 | hp1 | a0010 | c0009 | t0001 | g0018 | AFR | MSL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03453 | hp2 | a0003 | c0012 | t0002 | g0068 | AFR | MSL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03486 | hp1 | a0012 | c0013 | t0002 | g0123 | AFR | MSL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03486 | hp2 | a0007 | c0007 | t0003 | g0037 | AFR | MSL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03490 | hp1 | a0006 | c0006 | t0001 | g0007 | SAS | PJL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03490 | hp2 | a0004 | c0003 | t0001 | g0046 | SAS | PJL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03491 | hp1 | a0006 | c0006 | t0001 | g0028 | SAS | PJL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03491 | hp2 | a0003 | c0004 | t0002 | g0024 | SAS | PJL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03492 | hp1 | a0006 | c0006 | t0001 | g0007 | SAS | PJL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03492 | hp2 | a0003 | c0004 | t0002 | g0024 | SAS | PJL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03516 | hp1 | a0037 | c0028 | t0001 | g0017 | AFR | ESN | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03516 | hp2 | a0004 | c0003 | t0001 | g0003 | AFR | ESN | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03540 | hp1 | a0008 | c0008 | t0001 | g0151 | AFR | GWD | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03540 | hp2 | a0007 | c0011 | t0002 | g0010 | AFR | GWD | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03579 | hp1 | a0001 | c0002 | t0002 | g0124 | AFR | MSL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03579 | hp2 | a0001 | c0010 | t0002 | g0118 | AFR | MSL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03669 | hp1 | a0001 | c0036 | t0002 | g0002 | SAS | PJL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03669 | hp2 | a0038 | c0030 | t0001 | g0001 | SAS | PJL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03704 | hp1 | a0001 | c0002 | t0002 | g0134 | SAS | PJL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03704 | hp2 | a0004 | c0003 | t0001 | g0043 | SAS | PJL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03710 | hp1 | a0003 | c0004 | t0002 | g0019 | SAS | PJL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03710 | hp2 | a0004 | c0003 | t0001 | g0160 | SAS | PJL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03831 | hp1 | a0002 | c0001 | t0001 | g0081 | SAS | BEB | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03831 | hp2 | a0004 | c0003 | t0001 | g0003 | SAS | BEB | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03834 | hp1 | a0003 | c0004 | t0002 | g0049 | SAS | BEB | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03834 | hp2 | a0001 | c0002 | t0002 | g0130 | SAS | BEB | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03927 | hp1 | a0006 | c0006 | t0001 | g0106 | SAS | BEB | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03927 | hp2 | a0018 | c0065 | t0001 | g0148 | SAS | BEB | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG04184 | hp1 | a0001 | c0002 | t0002 | g0136 | SAS | BEB | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG04184 | hp2 | a0001 | c0039 | t0002 | g0016 | SAS | BEB | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG04204 | hp1 | a0003 | c0004 | t0002 | g0004 | SAS | STU | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG04204 | hp2 | a0002 | c0016 | t0001 | g0077 | SAS | STU | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG04228 | hp1 | a0002 | c0001 | t0001 | g0100 | SAS | STU | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG04228 | hp2 | a0001 | c0002 | t0002 | g0112 | SAS | STU | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18522 | hp1 | a0007 | c0007 | t0003 | g0129 | AFR | YRI | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18522 | hp2 | a0010 | c0009 | t0001 | g0017 | AFR | YRI | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18612 | hp1 | a0003 | c0004 | t0002 | g0067 | EAS | CHB | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18612 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | CHB | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18747 | hp1 | a0006 | c0006 | t0001 | g0028 | EAS | CHB | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18747 | hp2 | a0002 | c0001 | t0001 | g0025 | EAS | CHB | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18906 | hp1 | a0007 | c0041 | t0001 | g0003 | AFR | YRI | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18906 | hp2 | a0039 | c0027 | t0002 | g0059 | AFR | YRI | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18939 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18939 | hp2 | a0002 | c0001 | t0001 | g0109 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18941 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18941 | hp2 | a0005 | c0005 | t0001 | g0101 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18944 | hp1 | a0002 | c0001 | t0001 | g0105 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18944 | hp2 | a0040 | c0056 | t0001 | g0082 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18945 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18945 | hp2 | a0001 | c0002 | t0002 | g0165 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18951 | hp1 | a0009 | c0075 | t0002 | g0174 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18951 | hp2 | a0011 | c0045 | t0001 | g0143 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18962 | hp1 | a0041 | c0062 | t0001 | g0026 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18962 | hp2 | a0001 | c0002 | t0002 | g0139 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18964 | hp1 | a0042 | c0048 | t0001 | g0146 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18964 | hp2 | a0001 | c0002 | t0002 | g0039 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18970 | hp1 | a0043 | c0051 | t0001 | g0176 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18970 | hp2 | a0001 | c0021 | t0002 | g0042 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18971 | hp1 | a0002 | c0001 | t0001 | g0012 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18971 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18977 | hp1 | a0009 | c0026 | t0001 | g0052 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18977 | hp2 | a0020 | c0024 | t0001 | g0025 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18982 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18982 | hp2 | a0002 | c0063 | t0001 | g0079 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18985 | hp1 | a0009 | c0073 | t0001 | g0055 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18985 | hp2 | a0001 | c0002 | t0002 | g0039 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18986 | hp1 | a0002 | c0001 | t0001 | g0076 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18986 | hp2 | a0009 | c0070 | t0001 | g0175 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18990 | hp1 | a0002 | c0016 | t0001 | g0167 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18990 | hp2 | a0002 | c0001 | t0001 | g0104 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18999 | hp1 | a0005 | c0005 | t0001 | g0001 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18999 | hp2 | a0002 | c0001 | t0001 | g0012 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA19000 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA19000 | hp2 | a0002 | c0001 | t0001 | g0080 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA19001 | hp1 | a0003 | c0004 | t0002 | g0011 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA19001 | hp2 | a0005 | c0005 | t0001 | g0088 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA19002 | hp1 | a0004 | c0003 | t0001 | g0048 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA19002 | hp2 | a0005 | c0005 | t0001 | g0001 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA19010 | hp1 | a0002 | c0001 | t0001 | g0085 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA19010 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA19011 | hp1 | a0005 | c0005 | t0001 | g0113 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA19011 | hp2 | a0001 | c0002 | t0002 | g0133 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA19012 | hp1 | a0044 | c0068 | t0001 | g0145 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA19012 | hp2 | a0009 | c0074 | t0001 | g0054 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA19030 | hp1 | a0045 | c0052 | t0001 | g0008 | AFR | LWK | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA19030 | hp2 | a0008 | c0008 | t0001 | g0153 | AFR | LWK | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA19055 | hp1 | a0009 | c0026 | t0001 | g0051 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA19055 | hp2 | a0001 | c0002 | t0002 | g0132 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA19057 | hp1 | a0005 | c0005 | t0001 | g0013 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA19057 | hp2 | a0001 | c0002 | t0002 | g0138 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA19065 | hp1 | a0005 | c0005 | t0001 | g0013 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA19065 | hp2 | a0001 | c0021 | t0002 | g0042 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA19083 | hp1 | a0020 | c0024 | t0001 | g0091 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA19083 | hp2 | a0046 | c0060 | t0001 | g0168 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA19084 | hp1 | a0009 | c0072 | t0001 | g0056 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA19084 | hp2 | a0011 | c0044 | t0001 | g0144 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA19088 | hp1 | a0006 | c0006 | t0001 | g0030 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA19088 | hp2 | a0005 | c0005 | t0001 | g0013 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA19091 | hp1 | a0005 | c0005 | t0001 | g0027 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA19091 | hp2 | a0001 | c0002 | t0002 | g0041 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA19240 | hp1 | a0012 | c0013 | t0002 | g0122 | AFR | YRI | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA19240 | hp2 | a0047 | c0031 | t0003 | g0038 | AFR | YRI | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA20129 | hp1 | a0010 | c0009 | t0001 | g0060 | AFR | ASW | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA20129 | hp2 | a0003 | c0014 | t0002 | g0021 | AFR | ASW | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA20752 | hp1 | a0008 | c0008 | t0001 | g0149 | EUR | TSI | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA20752 | hp2 | a0003 | c0004 | t0005 | g0011 | EUR | TSI | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA20805 | hp1 | a0003 | c0004 | t0002 | g0015 | EUR | TSI | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA20805 | hp2 | a0004 | c0003 | t0001 | g0003 | EUR | TSI | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA20905 | hp1 | a0002 | c0001 | t0001 | g0050 | SAS | GIH | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA20905 | hp2 | a0004 | c0003 | t0001 | g0003 | SAS | GIH | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01123 | hp1 | a0004 | c0003 | t0001 | g0159 | AMR | CLM | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG01123 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | CLM | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02109 | hp1 | a0001 | c0010 | t0002 | g0036 | AFR | ACB | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02109 | hp2 | a0018 | c0054 | t0001 | g0033 | AFR | ACB | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02486 | hp1 | a0003 | c0012 | t0002 | g0006 | AFR | ACB | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG02486 | hp2 | a0002 | c0001 | t0001 | g0008 | AFR | ACB | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03471 | hp1 | a0008 | c0008 | t0001 | g0115 | AFR | MSL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG03471 | hp2 | a0011 | c0023 | t0002 | g0071 | AFR | MSL | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG06807 | hp1 | a0010 | c0009 | t0001 | g0057 | AFR | USA | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
HG06807 | hp2 | a0008 | c0055 | t0001 | g0001 | AFR | USA | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18955 | hp1 | a0002 | c0001 | t0001 | g0075 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA18955 | hp2 | a0002 | c0001 | t0001 | g0166 | EAS | JPT | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA21309 | hp1 | a0048 | c0049 | t0002 | g0023 | AFR | LWK | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
NA21309 | hp2 | a0001 | c0010 | t0002 | g0127 | AFR | LWK | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
homoSapiens | chm13v2 | a0003 | c0004 | t0002 | g0125 | REF | REF | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
homoSapiens | grch38p0 | a0001 | c0002 | t0002 | g0005 | REF | REF | ARHGEF5_chr7_144350402_144385632 | ARHGEF5 | chr7 | 144350402 | 144385632 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:144362670 | A | ATGGAGGC others(15): Show |
1 | a0009 | 9 | HG01496.hp1 HG01884.hp2 NA18951.hp1 others(6): Show |
frameshift_variant&stop_gained | HIGH | c.7_28dupGCTGAGGAGGC others(11): Show |
p.Ala10fs | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 141/5482 | 29/4794 | 10/1597 | INFO_REALIGN_3_PRIME | chr7 | 144362670 | ||
chr7:144362742 | G | A | 1 | a0019 | 2 | HG02135.hp2 HG02647.hp2 |
missense_variant | MODERATE | c.73G>A | p.Glu25Lys | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 185/5482 | 73/4794 | 25/1597 | chr7 | 144362742 | |||
chr7:144362991 | C | T | 1 | a0027 | 1 | HG01361.hp2 | missense_variant | MODERATE | c.322C>T | p.Pro108Ser | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 434/5482 | 322/4794 | 108/1597 | chr7 | 144362991 | |||
chr7:144363042 | T | C | 1 | a0012 | 4 | HG01884.hp1 HG02970.hp2 HG03486.hp1 others(1): Show |
missense_variant | MODERATE | c.373T>C | p.Trp125Arg | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 485/5482 | 373/4794 | 125/1597 | chr7 | 144363042 | |||
chr7:144363102 | A | G | 22 | a0002 a0005 a0006 others(19): Show |
116 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(113): Show |
missense_variant | MODERATE | c.433A>G | p.Ser145Gly | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 545/5482 | 433/4794 | 145/1597 | chr7 | 144363102 | |||
chr7:144363193 | A | G | 3 | a0042 a0044 a0048 |
3 | NA18964.hp1 NA19012.hp1 NA21309.hp1 |
missense_variant | MODERATE | c.524A>G | p.Asp175Gly | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 636/5482 | 524/4794 | 175/1597 | chr7 | 144363193 | |||
chr7:144363264 | T | G | 25 | a0002 a0005 a0006 others(22): Show |
124 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(121): Show |
missense_variant | MODERATE | c.595T>G | p.Ser199Ala | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 707/5482 | 595/4794 | 199/1597 | chr7 | 144363264 | |||
chr7:144363303 | C | T | 25 | a0002 a0005 a0006 others(22): Show |
124 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(121): Show |
missense_variant | MODERATE | c.634C>T | p.Pro212Ser | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 746/5482 | 634/4794 | 212/1597 | chr7 | 144363303 | |||
chr7:144363352 | A | C | 1 | a0013 | 3 | HG00597.hp1 HG02074.hp1 HG02165.hp2 |
missense_variant | MODERATE | c.683A>C | p.Gln228Pro | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 795/5482 | 683/4794 | 228/1597 | chr7 | 144363352 | |||
chr7:144363488 | G | C | 1 | a0024 | 1 | HG00673.hp2 | missense_variant | MODERATE | c.819G>C | p.Lys273Asn | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 931/5482 | 819/4794 | 273/1597 | chr7 | 144363488 | |||
chr7:144363594 | G | A | 2 | a0023 a0043 |
2 | HG00673.hp1 NA18970.hp1 |
missense_variant | MODERATE | c.925G>A | p.Asp309Asn | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 1037/5482 | 925/4794 | 309/1597 | chr7 | 144363594 | |||
chr7:144363606 | A | C | 1 | a0017 | 2 | HG01069.hp1 HG01071.hp2 |
missense_variant | MODERATE | c.937A>C | p.Lys313Gln | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 1049/5482 | 937/4794 | 313/1597 | chr7 | 144363606 | |||
chr7:144363647 | G | C | 1 | a0045 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.978G>C | p.Arg326Ser | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 1090/5482 | 978/4794 | 326/1597 | chr7 | 144363647 | |||
chr7:144363709 | C | T | 1 | a0009 | 7 | HG01496.hp1 HG01884.hp2 NA18951.hp1 others(4): Show |
missense_variant | MODERATE | c.1040C>T | p.Thr347Ile | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 1152/5482 | 1040/4794 | 347/1597 | chr7 | 144363709 | |||
chr7:144363729 | G | A | 1 | a0033 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1060G>A | p.Glu354Lys | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 1172/5482 | 1060/4794 | 354/1597 | chr7 | 144363729 | |||
chr7:144363954 | A | G | 32 | a0002 a0003 a0005 others(29): Show |
171 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(168): Show |
missense_variant | MODERATE | c.1285A>G | p.Met429Val | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 1397/5482 | 1285/4794 | 429/1597 | chr7 | 144363954 | |||
chr7:144364024 | C | T | 1 | a0019 | 2 | HG02135.hp2 HG02647.hp2 |
missense_variant | MODERATE | c.1355C>T | p.Ser452Leu | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 1467/5482 | 1355/4794 | 452/1597 | chr7 | 144364024 | |||
chr7:144364111 | A | G | 5 | a0003 a0014 a0025 others(2): Show |
40 | HG00140.hp1 HG00741.hp2 HG01074.hp1 others(37): Show |
missense_variant | MODERATE | c.1442A>G | p.Gln481Arg | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 1554/5482 | 1442/4794 | 481/1597 | chr7 | 144364111 | |||
chr7:144364129 | A | G | 36 | a0002 a0003 a0004 others(33): Show |
221 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(218): Show |
missense_variant | MODERATE | c.1460A>G | p.Glu487Gly | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 1572/5482 | 1460/4794 | 487/1597 | chr7 | 144364129 | |||
chr7:144364321 | G | A | 1 | a0009 | 2 | NA18985.hp1 NA19012.hp2 |
missense_variant | MODERATE | c.1652G>A | p.Arg551His | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 1764/5482 | 1652/4794 | 551/1597 | chr7 | 144364321 | |||
chr7:144364393 | C | A | 1 | a0004 | 25 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(22): Show |
missense_variant | MODERATE | c.1724C>A | p.Pro575Gln | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 1836/5482 | 1724/4794 | 575/1597 | chr7 | 144364393 | |||
chr7:144364407 | G | T | 16 | a0002 a0006 a0013 others(13): Show |
81 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(78): Show |
missense_variant | MODERATE | c.1738G>T | p.Gly580Cys | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 1850/5482 | 1738/4794 | 580/1597 | chr7 | 144364407 | |||
chr7:144364479 | A | C | 1 | a0029 | 1 | HG02027.hp1 | missense_variant | MODERATE | c.1810A>C | p.Ser604Arg | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 1922/5482 | 1810/4794 | 604/1597 | chr7 | 144364479 | |||
chr7:144364514 | G | C | 13 | a0006 a0008 a0010 others(10): Show |
47 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(44): Show |
missense_variant | MODERATE | c.1845G>C | p.Gln615His | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 1957/5482 | 1845/4794 | 615/1597 | chr7 | 144364514 | |||
chr7:144364839 | C | T | 1 | a0032 | 1 | HG02451.hp2 | missense_variant | MODERATE | c.2170C>T | p.Pro724Ser | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 2282/5482 | 2170/4794 | 724/1597 | chr7 | 144364839 | |||
chr7:144365046 | T | A | 1 | a0046 | 1 | NA19083.hp2 | missense_variant | MODERATE | c.2377T>A | p.Ser793Thr | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 2489/5482 | 2377/4794 | 793/1597 | chr7 | 144365046 | |||
chr7:144365108 | A | AC | 14 | a0009 a0015 a0018 others(11): Show |
17 | HG00423.hp2 HG00597.hp2 HG00673.hp1 others(14): Show |
frameshift_variant | HIGH | c.2444dupC | p.Thr816fs | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 2557/5482 | 2445/4794 | 815/1597 | INFO_REALIGN_3_PRIME | chr7 | 144365108 | ||
chr7:144365112 | C | G | 2 | a0016 a0022 |
3 | HG00639.hp2 HG00642.hp2 HG01099.hp2 |
missense_variant | MODERATE | c.2443C>G | p.Pro815Ala | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 2555/5482 | 2443/4794 | 815/1597 | chr7 | 144365112 | |||
chr7:144365322 | T | C | 1 | a0026 | 1 | HG01074.hp2 | missense_variant | MODERATE | c.2653T>C | p.Trp885Arg | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 2765/5482 | 2653/4794 | 885/1597 | chr7 | 144365322 | |||
chr7:144365350 | G | T | 1 | a0031 | 1 | HG02132.hp1 | missense_variant | MODERATE | c.2681G>T | p.Gly894Val | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 2793/5482 | 2681/4794 | 894/1597 | chr7 | 144365350 | |||
chr7:144365352 | C | T | 1 | a0028 | 1 | HG01975.hp2 | missense_variant | MODERATE | c.2683C>T | p.Arg895Cys | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 2795/5482 | 2683/4794 | 895/1597 | chr7 | 144365352 | |||
chr7:144365490 | T | G | 1 | a0046 | 1 | NA19083.hp2 | missense_variant | MODERATE | c.2821T>G | p.Trp941Gly | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 2933/5482 | 2821/4794 | 941/1597 | chr7 | 144365490 | |||
chr7:144365539 | C | G | 1 | a0009 | 1 | HG01884.hp2 | stop_gained | HIGH | c.2870C>G | p.Ser957* | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 2982/5482 | 2870/4794 | 957/1597 | chr7 | 144365539 | |||
chr7:144365640 | C | G | 1 | a0014 | 3 | HG01099.hp1 HG01515.hp1 HG01517.hp1 |
missense_variant | MODERATE | c.2971C>G | p.Pro991Ala | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 3083/5482 | 2971/4794 | 991/1597 | chr7 | 144365640 | |||
chr7:144365641 | C | A | 1 | a0014 | 3 | HG01099.hp1 HG01515.hp1 HG01517.hp1 |
missense_variant | MODERATE | c.2972C>A | p.Pro991Gln | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 3084/5482 | 2972/4794 | 991/1597 | chr7 | 144365641 | |||
chr7:144365751 | G | T | 1 | a0022 | 1 | HG00642.hp2 | missense_variant | MODERATE | c.3082G>T | p.Gly1028Trp | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 3194/5482 | 3082/4794 | 1028/1597 | chr7 | 144365751 | |||
chr7:144367261 | T | C | 1 | a0033 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.3437T>C | p.Met1146Thr | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/15 | 3549/5482 | 3437/4794 | 1146/1597 | chr7 | 144367261 | |||
chr7:144367296 | G | A | 1 | a0036 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.3472G>A | p.Val1158Met | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/15 | 3584/5482 | 3472/4794 | 1158/1597 | chr7 | 144367296 | |||
chr7:144371236 | T | A | 1 | a0030 | 1 | HG02040.hp1 | missense_variant | MODERATE | c.3607T>A | p.Ser1203Thr | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 6/15 | 3719/5482 | 3607/4794 | 1203/1597 | chr7 | 144371236 | |||
chr7:144379913 | G | A | 1 | a0041 | 1 | NA18962.hp1 | missense_variant | MODERATE | c.4651G>A | p.Val1551Met | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 15/15 | 4763/5482 | 4651/4794 | 1551/1597 | chr7 | 144379913 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:144363275 | G | A | 2 | a0007c0007 a0047c0031 |
11 | HG01891.hp1 HG02622.hp2 HG02630.hp2 others(8): Show |
synonymous_variant | LOW | c.606G>A | p.Gly202Gly | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 718/5482 | 606/4794 | 202/1597 | chr7 | 144363275 | |||
chr7:144363476 | G | A | 29 | a0002c0001 a0002c0016 a0002c0061 others(26): Show |
122 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(119): Show |
synonymous_variant | LOW | c.807G>A | p.Lys269Lys | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 919/5482 | 807/4794 | 269/1597 | chr7 | 144363476 | |||
chr7:144363575 | C | T | 1 | a0002c0064 | 1 | HG02040.hp2 | synonymous_variant | LOW | c.906C>T | p.Asp302Asp | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 1018/5482 | 906/4794 | 302/1597 | chr7 | 144363575 | |||
chr7:144363677 | T | C | 36 | a0001c0010 a0002c0001 a0002c0016 others(33): Show |
134 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(131): Show |
synonymous_variant | LOW | c.1008T>C | p.Asn336Asn | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 1120/5482 | 1008/4794 | 336/1597 | chr7 | 144363677 | |||
chr7:144363953 | C | T | 5 | a0003c0004 a0003c0032 a0003c0047 others(2): Show |
30 | HG00140.hp1 HG00741.hp2 HG01074.hp1 others(27): Show |
synonymous_variant | LOW | c.1284C>T | p.Leu428Leu | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 1396/5482 | 1284/4794 | 428/1597 | chr7 | 144363953 | |||
chr7:144364026 | C | T | 2 | a0004c0003 a0007c0042 |
26 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(23): Show |
synonymous_variant | LOW | c.1357C>T | p.Leu453Leu | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 1469/5482 | 1357/4794 | 453/1597 | chr7 | 144364026 | |||
chr7:144364436 | G | A | 2 | a0004c0003 a0007c0041 |
26 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(23): Show |
synonymous_variant | LOW | c.1767G>A | p.Pro589Pro | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 1879/5482 | 1767/4794 | 589/1597 | chr7 | 144364436 | |||
chr7:144364691 | A | G | 1 | a0001c0039 | 1 | HG04184.hp2 | synonymous_variant | LOW | c.2022A>G | p.Gln674Gln | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 2134/5482 | 2022/4794 | 674/1597 | chr7 | 144364691 | |||
chr7:144365369 | G | A | 1 | a0002c0061 | 1 | HG00741.hp1 | synonymous_variant | LOW | c.2700G>A | p.Pro900Pro | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 2812/5482 | 2700/4794 | 900/1597 | chr7 | 144365369 | |||
chr7:144365498 | G | A | 1 | a0032c0067 | 1 | HG02451.hp2 | synonymous_variant | LOW | c.2829G>A | p.Pro943Pro | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 2941/5482 | 2829/4794 | 943/1597 | chr7 | 144365498 | |||
chr7:144365546 | C | T | 2 | a0003c0047 a0014c0015 |
4 | HG01099.hp1 HG01261.hp2 HG01515.hp1 others(1): Show |
synonymous_variant | LOW | c.2877C>T | p.His959His | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 2989/5482 | 2877/4794 | 959/1597 | chr7 | 144365546 | |||
chr7:144365600 | C | G | 3 | a0001c0021 a0011c0044 a0011c0045 |
4 | NA18951.hp2 NA18970.hp2 NA19065.hp2 others(1): Show |
synonymous_variant | LOW | c.2931C>G | p.Ala977Ala | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/15 | 3043/5482 | 2931/4794 | 977/1597 | chr7 | 144365600 | |||
chr7:144373245 | A | G | 48 | a0001c0020 a0002c0001 a0002c0061 others(45): Show |
180 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(177): Show |
synonymous_variant | LOW | c.4101A>G | p.Glu1367Glu | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 10/15 | 4213/5482 | 4101/4794 | 1367/1597 | chr7 | 144373245 | |||
chr7:144374740 | G | A | 1 | a0001c0036 | 1 | HG03669.hp1 | synonymous_variant | LOW | c.4149G>A | p.Pro1383Pro | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 11/15 | 4261/5482 | 4149/4794 | 1383/1597 | chr7 | 144374740 | |||
chr7:144375547 | C | T | 1 | a0008c0055 | 1 | HG06807.hp2 | synonymous_variant | LOW | c.4332C>T | p.Pro1444Pro | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 12/15 | 4444/5482 | 4332/4794 | 1444/1597 | chr7 | 144375547 | |||
chr7:144379966 | C | T | 1 | a0007c0011 | 5 | HG02258.hp1 HG02818.hp1 HG02970.hp1 others(2): Show |
synonymous_variant | LOW | c.4704C>T | p.Phe1568Phe | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 15/15 | 4816/5482 | 4704/4794 | 1568/1597 | chr7 | 144379966 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:144380074 | T | A | 1 | a0001c0002t0004 | 2 | HG01167.hp1 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*18T>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 15/15 | 18 | chr7 | 144380074 | ||||||
chr7:144380078 | G | A | 2 | a0007c0007t0003 a0047c0031t0003 |
11 | HG01891.hp1 HG02622.hp2 HG02630.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*22G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 15/15 | 22 | chr7 | 144380078 | ||||||
chr7:144380496 | C | T | 1 | a0003c0004t0005 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*440C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 15/15 | 440 | chr7 | 144380496 | ||||||
chr7:144380523 | T | C | 47 | a0002c0001t0001 a0002c0016t0001 a0002c0061t0001 others(44): Show |
173 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(170): Show |
3_prime_UTR_variant | MODIFIER | c.*467T>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 15/15 | 467 | chr7 | 144380523 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:144355651 | G | T | 5 | a0002c0001t0001g0177 a0009c0070t0001g0175 a0009c0071t0001g0173 others(2): Show |
5 | HG01496.hp1 HG02273.hp1 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13+150G>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144355651 | |||||||
chr7:144355660 | C | G | 4 | a0004c0003t0001g0048 a0004c0003t0001g0171 a0004c0003t0001g0172 others(1): Show |
5 | HG00323.hp2 HG01167.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13+159C>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144355660 | |||||||
chr7:144355971 | T | G | 1 | a0003c0004t0002g0049 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-13+470T>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144355971 | |||||||
chr7:144355998 | T | G | 1 | a0007c0042t0001g0170 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-13+497T>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144355998 | |||||||
chr7:144356069 | T | C | 17 | a0002c0001t0001g0050 a0009c0026t0001g0051 a0009c0026t0001g0052 others(14): Show |
18 | HG01496.hp1 HG01884.hp2 HG02897.hp2 others(15): Show |
intron_variant | MODIFIER | c.-13+568T>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144356069 | |||||||
chr7:144356228 | TC | T | 2 | a0010c0009t0001g0018 a0010c0009t0001g0060 |
3 | HG02897.hp2 HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-13+729delC | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 144356228 | ||||||
chr7:144356238 | C | A | 24 | a0003c0004t0002g0004 a0003c0004t0002g0011 a0003c0004t0002g0019 others(21): Show |
36 | HG01074.hp1 HG01099.hp1 HG01192.hp2 others(33): Show |
intron_variant | MODIFIER | c.-13+737C>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144356238 | |||||||
chr7:144356248 | A | G | 1 | a0032c0067t0001g0169 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-13+747A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144356248 | |||||||
chr7:144356251 | G | C | 2 | a0011c0023t0002g0070 a0011c0023t0002g0071 |
2 | HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-13+750G>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144356251 | |||||||
chr7:144356267 | C | T | 4 | a0002c0001t0001g0047 a0002c0001t0001g0166 a0002c0016t0001g0167 others(1): Show |
5 | HG02027.hp2 HG02132.hp2 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.-13+766C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144356267 | |||||||
chr7:144356346 | A | G | 1 | a0001c0002t0002g0165 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-13+845A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144356346 | |||||||
chr7:144356422 | C | A | 1 | a0005c0005t0001g0072 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-13+921C>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144356422 | |||||||
chr7:144356605 | G | A | 74 | a0002c0001t0001g0001 a0002c0001t0001g0008 a0002c0001t0001g0012 others(71): Show |
98 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.-13+1104G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144356605 | |||||||
chr7:144356648 | A | G | 39 | a0001c0002t0002g0016 a0001c0002t0002g0162 a0001c0002t0002g0163 others(36): Show |
62 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(59): Show |
intron_variant | MODIFIER | c.-13+1147A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144356648 | |||||||
chr7:144356659 | A | C | 1 | a0003c0004t0002g0024 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-13+1158A>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144356659 | |||||||
chr7:144356724 | G | A | 2 | a0010c0009t0001g0018 a0010c0009t0001g0060 |
3 | HG02897.hp2 HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-13+1223G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144356724 | |||||||
chr7:144356770 | G | A | 2 | a0011c0044t0001g0144 a0011c0045t0001g0143 |
2 | NA18951.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.-13+1269G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144356770 | |||||||
chr7:144356794 | A | G | 1 | a0039c0027t0002g0059 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-13+1293A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144356794 | |||||||
chr7:144356864 | G | A | 9 | a0009c0026t0001g0051 a0009c0026t0001g0052 a0009c0070t0001g0175 others(6): Show |
9 | HG01496.hp1 HG01884.hp2 NA18951.hp1 others(6): Show |
intron_variant | MODIFIER | c.-13+1363G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144356864 | |||||||
chr7:144356902 | G | A | 10 | a0009c0026t0001g0051 a0009c0026t0001g0052 a0009c0070t0001g0175 others(7): Show |
10 | HG01496.hp1 HG01884.hp2 NA18906.hp2 others(7): Show |
intron_variant | MODIFIER | c.-13+1401G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144356902 | |||||||
chr7:144357116 | G | A | 1 | a0003c0004t0002g0061 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-13+1615G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144357116 | |||||||
chr7:144357123 | C | T | 10 | a0009c0026t0001g0051 a0009c0026t0001g0052 a0009c0070t0001g0175 others(7): Show |
10 | HG01496.hp1 HG01884.hp2 NA18906.hp2 others(7): Show |
intron_variant | MODIFIER | c.-13+1622C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144357123 | |||||||
chr7:144357124 | C | T | 10 | a0009c0026t0001g0051 a0009c0026t0001g0052 a0009c0070t0001g0175 others(7): Show |
10 | HG01496.hp1 HG01884.hp2 NA18906.hp2 others(7): Show |
intron_variant | MODIFIER | c.-13+1623C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144357124 | |||||||
chr7:144357178 | G | A | 16 | a0004c0003t0001g0043 a0006c0006t0001g0073 a0009c0026t0001g0051 others(13): Show |
17 | HG01496.hp1 HG01496.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-13+1677G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144357178 | |||||||
chr7:144357191 | A | C | 1 | a0039c0027t0002g0059 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-13+1690A>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144357191 | |||||||
chr7:144357210 | T | C | 1 | a0001c0002t0002g0112 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-13+1709T>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144357210 | |||||||
chr7:144357221 | T | C | 1 | a0032c0067t0001g0169 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-13+1720T>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144357221 | |||||||
chr7:144357223 | T | G | 160 | a0001c0002t0002g0124 a0001c0010t0002g0036 a0001c0010t0002g0118 others(157): Show |
208 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.-13+1722T>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144357223 | |||||||
chr7:144357378 | G | A | 91 | a0002c0001t0001g0001 a0002c0001t0001g0008 a0002c0001t0001g0012 others(88): Show |
118 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.-13+1877G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144357378 | |||||||
chr7:144357390 | T | C | 102 | a0002c0001t0001g0001 a0002c0001t0001g0008 a0002c0001t0001g0012 others(99): Show |
129 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.-13+1889T>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144357390 | |||||||
chr7:144357410 | C | T | 105 | a0002c0001t0001g0001 a0002c0001t0001g0008 a0002c0001t0001g0012 others(102): Show |
133 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.-13+1909C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144357410 | |||||||
chr7:144357425 | G | A | 3 | a0013c0017t0001g0110 a0013c0017t0001g0111 a0013c0017t0001g0154 |
3 | HG00597.hp1 HG02074.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.-13+1924G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144357425 | |||||||
chr7:144357588 | A | G | 9 | a0009c0026t0001g0051 a0009c0026t0001g0052 a0009c0070t0001g0175 others(6): Show |
9 | HG01496.hp1 HG01884.hp2 NA18951.hp1 others(6): Show |
intron_variant | MODIFIER | c.-13+2087A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144357588 | |||||||
chr7:144357662 | G | A | 10 | a0009c0026t0001g0051 a0009c0026t0001g0052 a0009c0070t0001g0175 others(7): Show |
10 | HG01496.hp1 HG01884.hp2 NA18906.hp2 others(7): Show |
intron_variant | MODIFIER | c.-13+2161G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144357662 | |||||||
chr7:144357680 | A | G | 1 | a0032c0067t0001g0169 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-13+2179A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144357680 | |||||||
chr7:144357767 | A | G | 10 | a0009c0026t0001g0051 a0009c0026t0001g0052 a0009c0070t0001g0175 others(7): Show |
10 | HG01496.hp1 HG01884.hp2 NA18906.hp2 others(7): Show |
intron_variant | MODIFIER | c.-13+2266A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144357767 | |||||||
chr7:144357835 | G | A | 30 | a0004c0003t0001g0003 a0004c0003t0001g0043 a0004c0003t0001g0045 others(27): Show |
48 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.-13+2334G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144357835 | |||||||
chr7:144357861 | G | A | 1 | a0004c0003t0001g0171 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-13+2360G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144357861 | |||||||
chr7:144357959 | C | T | 12 | a0009c0026t0001g0051 a0009c0026t0001g0052 a0009c0070t0001g0175 others(9): Show |
12 | HG01496.hp1 HG01884.hp2 NA18906.hp2 others(9): Show |
intron_variant | MODIFIER | c.-13+2458C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144357959 | |||||||
chr7:144358071 | C | T | 2 | a0009c0070t0001g0175 a0009c0072t0001g0056 |
2 | NA18986.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.-13+2570C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144358071 | |||||||
chr7:144358227 | C | T | 1 | a0002c0001t0001g0109 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-13+2726C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144358227 | |||||||
chr7:144358434 | G | A | 1 | a0039c0027t0002g0059 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-13+2933G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144358434 | |||||||
chr7:144358444 | A | G | 11 | a0002c0001t0001g0108 a0009c0026t0001g0051 a0009c0026t0001g0052 others(8): Show |
11 | HG00621.hp1 HG01496.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.-13+2943A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144358444 | |||||||
chr7:144358460 | C | T | 1 | a0032c0067t0001g0169 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-13+2959C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144358460 | |||||||
chr7:144358464 | G | C | 1 | a0005c0005t0001g0113 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-13+2963G>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144358464 | |||||||
chr7:144358467 | T | G | 1 | a0005c0005t0001g0113 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-13+2966T>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144358467 | |||||||
chr7:144358515 | G | C | 2 | a0011c0023t0002g0070 a0011c0023t0002g0071 |
2 | HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-13+3014G>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144358515 | |||||||
chr7:144358536 | G | A | 2 | a0042c0048t0001g0146 a0044c0068t0001g0145 |
2 | NA18964.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.-13+3035G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144358536 | |||||||
chr7:144358633 | C | A | 1 | a0032c0067t0001g0169 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-13+3132C>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144358633 | |||||||
chr7:144358661 | A | G | 1 | a0005c0005t0001g0013 | 3 | NA19057.hp1 NA19065.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.-13+3160A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144358661 | |||||||
chr7:144358745 | G | A | 2 | a0011c0023t0002g0070 a0011c0023t0002g0071 |
2 | HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-13+3244G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144358745 | |||||||
chr7:144358758 | A | AGT | 24 | a0001c0002t0002g0002 a0001c0002t0002g0039 a0001c0002t0002g0112 others(21): Show |
35 | HG00323.hp1 HG00642.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.-13+3300_-13+3301d others(4): Show |
ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 144358758 | ||||||
chr7:144358758 | A | AGTGT | 17 | a0001c0002t0002g0040 a0001c0002t0002g0041 a0001c0002t0002g0142 others(14): Show |
25 | HG00741.hp2 HG01168.hp1 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.-13+3298_-13+3301d others(6): Show |
ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 144358758 | ||||||
chr7:144358758 | A | AGTGTGT | 6 | a0001c0010t0002g0128 a0003c0004t0002g0004 a0003c0004t0002g0066 others(3): Show |
10 | HG01074.hp1 HG01099.hp1 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.-13+3296_-13+3301d others(8): Show |
ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 144358758 | ||||||
chr7:144358758 | A | AGTGTGTG others(1): Show |
5 | a0003c0004t0002g0020 a0003c0004t0002g0067 a0003c0012t0002g0068 others(2): Show |
6 | HG01517.hp1 HG02886.hp2 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13+3294_-13+3301d others(10): Show |
ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 144358758 | ||||||
chr7:144358758 | A | AGTGTGTG others(3): Show |
3 | a0003c0004t0002g0022 a0003c0014t0002g0023 a0048c0049t0002g0023 |
4 | HG01433.hp1 HG02738.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+3292_-13+3301d others(12): Show |
ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 144358758 | ||||||
chr7:144358758 | A | AGTGTGTG others(5): Show |
1 | a0003c0004t0002g0069 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-13+3290_-13+3301d others(14): Show |
ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 144358758 | ||||||
chr7:144358758 | AGT | A | 65 | a0001c0002t0002g0016 a0001c0002t0002g0130 a0001c0002t0002g0162 others(62): Show |
91 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.-13+3300_-13+3301d others(4): Show |
ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 144358758 | ||||||
chr7:144358758 | AGTGT | A | 13 | a0001c0010t0002g0118 a0001c0010t0002g0119 a0002c0001t0001g0085 others(10): Show |
14 | HG00597.hp1 HG01891.hp1 HG02074.hp1 others(11): Show |
intron_variant | MODIFIER | c.-13+3298_-13+3301d others(6): Show |
ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 144358758 | ||||||
chr7:144358758 | AGTGTGT | A | 6 | a0002c0001t0001g0080 a0002c0001t0001g0081 a0002c0063t0001g0079 others(3): Show |
8 | HG02622.hp2 HG02630.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.-13+3296_-13+3301d others(8): Show |
ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 144358758 | ||||||
chr7:144358758 | AGTGTGTG others(1): Show |
A | 5 | a0002c0001t0001g0075 a0002c0001t0001g0076 a0002c0001t0001g0078 others(2): Show |
5 | HG00558.hp2 HG02040.hp2 HG04204.hp2 others(2): Show |
intron_variant | MODIFIER | c.-13+3294_-13+3301d others(10): Show |
ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 144358758 | ||||||
chr7:144358758 | AGTGTGTG others(3): Show |
A | 1 | a0007c0007t0003g0129 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-13+3292_-13+3301d others(12): Show |
ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 144358758 | ||||||
chr7:144358784 | TGTGTGTG others(15): Show |
T | 11 | a0004c0003t0001g0003 a0004c0003t0001g0043 a0004c0003t0001g0045 others(8): Show |
26 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(23): Show |
intron_variant | MODIFIER | c.-13+3284_-13+3305d others(24): Show |
ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144358784 | |||||||
chr7:144358786 | TGTGTGTG others(13): Show |
T | 1 | a0004c0003t0001g0161 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-13+3286_-13+3305d others(22): Show |
ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144358786 | |||||||
chr7:144358792 | TGTGTGTG others(7): Show |
T | 5 | a0009c0026t0001g0052 a0009c0071t0001g0173 a0009c0073t0001g0055 others(2): Show |
5 | HG01496.hp1 HG01884.hp2 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13+3292_-13+3305d others(16): Show |
ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144358792 | |||||||
chr7:144358794 | TGTGTGTG others(5): Show |
T | 4 | a0009c0026t0001g0051 a0009c0070t0001g0175 a0009c0072t0001g0056 others(1): Show |
4 | NA18951.hp1 NA18986.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+3294_-13+3305d others(14): Show |
ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144358794 | |||||||
chr7:144358796 | TGTGTGTA others(3): Show |
T | 1 | a0039c0027t0002g0059 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-13+3296_-13+3305d others(12): Show |
ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144358796 | |||||||
chr7:144358800 | TGTACAC | T | 4 | a0007c0007t0003g0035 a0011c0044t0001g0144 a0011c0045t0001g0143 others(1): Show |
4 | HG02451.hp2 HG03130.hp2 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+3300_-13+3305d others(8): Show |
ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144358800 | |||||||
chr7:144358803 | A | G | 5 | a0007c0011t0002g0010 a0007c0011t0002g0155 a0010c0009t0001g0017 others(2): Show |
8 | HG02258.hp1 HG02647.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-13+3302A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144358803 | |||||||
chr7:144358804 | C | T | 5 | a0007c0011t0002g0010 a0007c0011t0002g0155 a0010c0009t0001g0017 others(2): Show |
8 | HG02258.hp1 HG02647.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-13+3303C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144358804 | |||||||
chr7:144358805 | A | G | 3 | a0007c0011t0002g0010 a0007c0011t0002g0155 a0010c0009t0001g0017 |
6 | HG02258.hp1 HG02818.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13+3304A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144358805 | |||||||
chr7:144358806 | C | T | 3 | a0007c0011t0002g0010 a0007c0011t0002g0155 a0010c0009t0001g0017 |
6 | HG02258.hp1 HG02818.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13+3305C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144358806 | |||||||
chr7:144358812 | G | A | 10 | a0009c0026t0001g0051 a0009c0026t0001g0052 a0009c0070t0001g0175 others(7): Show |
10 | HG01496.hp1 HG01884.hp2 NA18906.hp2 others(7): Show |
intron_variant | MODIFIER | c.-13+3311G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144358812 | |||||||
chr7:144358884 | G | A | 1 | a0039c0027t0002g0059 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-13+3383G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144358884 | |||||||
chr7:144358929 | G | T | 12 | a0004c0003t0001g0003 a0004c0003t0001g0043 a0004c0003t0001g0045 others(9): Show |
27 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.-13+3428G>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144358929 | |||||||
chr7:144358970 | T | C | 2 | a0011c0044t0001g0144 a0011c0045t0001g0143 |
2 | NA18951.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.-13+3469T>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144358970 | |||||||
chr7:144358988 | G | A | 3 | a0019c0018t0001g0147 a0042c0048t0001g0146 a0044c0068t0001g0145 |
3 | HG02135.hp2 NA18964.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.-13+3487G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144358988 | |||||||
chr7:144358991 | A | C | 1 | a0002c0001t0001g0078 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-13+3490A>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144358991 | |||||||
chr7:144359134 | G | A | 12 | a0005c0005t0001g0101 a0005c0005t0001g0113 a0009c0026t0001g0051 others(9): Show |
12 | HG01496.hp1 HG01884.hp2 NA18906.hp2 others(9): Show |
intron_variant | MODIFIER | c.-12-3524G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144359134 | |||||||
chr7:144359386 | C | T | 95 | a0002c0001t0001g0001 a0002c0001t0001g0008 a0002c0001t0001g0012 others(92): Show |
122 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.-12-3272C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144359386 | |||||||
chr7:144359423 | T | C | 6 | a0001c0002t0002g0134 a0007c0011t0002g0155 a0011c0044t0001g0144 others(3): Show |
6 | HG02970.hp1 HG03704.hp1 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.-12-3235T>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144359423 | |||||||
chr7:144359426 | G | A | 106 | a0002c0001t0001g0001 a0002c0001t0001g0008 a0002c0001t0001g0012 others(103): Show |
133 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.-12-3232G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144359426 | |||||||
chr7:144359658 | T | A | 1 | a0006c0006t0001g0086 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-12-3000T>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144359658 | |||||||
chr7:144359681 | A | G | 2 | a0011c0044t0001g0144 a0011c0045t0001g0143 |
2 | NA18951.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.-12-2977A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144359681 | |||||||
chr7:144359682 | GA | G | 2 | a0005c0005t0001g0013 a0042c0048t0001g0146 |
4 | NA18964.hp1 NA19057.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-2975delA | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144359682 | |||||||
chr7:144359683 | A | G | 5 | a0011c0044t0001g0144 a0011c0045t0001g0143 a0019c0018t0001g0147 others(2): Show |
5 | HG02135.hp2 NA18906.hp2 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.-12-2975A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144359683 | |||||||
chr7:144359683 | AG | A | 57 | a0003c0004t0002g0004 a0003c0004t0002g0011 a0003c0004t0002g0015 others(54): Show |
90 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.-12-2967delG | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 144359683 | ||||||
chr7:144359691 | G | A | 1 | a0046c0060t0001g0168 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-12-2967G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144359691 | |||||||
chr7:144359692 | A | T | 1 | a0046c0060t0001g0168 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-12-2966A>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144359692 | |||||||
chr7:144359693 | T | G | 1 | a0046c0060t0001g0168 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-12-2965T>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144359693 | |||||||
chr7:144359752 | G | A | 2 | a0042c0048t0001g0146 a0044c0068t0001g0145 |
2 | NA18964.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.-12-2906G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144359752 | |||||||
chr7:144359755 | G | T | 1 | a0006c0006t0001g0086 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-12-2903G>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144359755 | |||||||
chr7:144359814 | T | A | 1 | a0006c0006t0001g0086 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-12-2844T>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144359814 | |||||||
chr7:144359887 | G | A | 98 | a0002c0001t0001g0001 a0002c0001t0001g0008 a0002c0001t0001g0012 others(95): Show |
125 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.-12-2771G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144359887 | |||||||
chr7:144359899 | T | C | 1 | a0005c0005t0001g0087 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-12-2759T>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144359899 | |||||||
chr7:144359903 | G | C | 1 | a0019c0018t0001g0147 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-12-2755G>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144359903 | |||||||
chr7:144360105 | T | A | 126 | a0002c0001t0001g0001 a0002c0001t0001g0008 a0002c0001t0001g0012 others(123): Show |
171 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.-12-2553T>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144360105 | |||||||
chr7:144360107 | T | C | 2 | a0008c0008t0001g0033 a0018c0054t0001g0033 |
2 | HG00735.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.-12-2551T>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144360107 | |||||||
chr7:144360148 | G | A | 1 | a0019c0018t0001g0147 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-12-2510G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144360148 | |||||||
chr7:144360149 | A | T | 109 | a0002c0001t0001g0001 a0002c0001t0001g0008 a0002c0001t0001g0012 others(106): Show |
136 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.-12-2509A>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144360149 | |||||||
chr7:144360202 | T | A | 16 | a0004c0003t0001g0003 a0004c0003t0001g0043 a0004c0003t0001g0045 others(13): Show |
34 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.-12-2456T>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144360202 | |||||||
chr7:144360209 | AGGATCCC others(7): Show |
A | 109 | a0002c0001t0001g0001 a0002c0001t0001g0008 a0002c0001t0001g0012 others(106): Show |
136 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.-12-2448_-12-2435d others(16): Show |
ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144360209 | |||||||
chr7:144360224 | C | T | 109 | a0002c0001t0001g0001 a0002c0001t0001g0008 a0002c0001t0001g0012 others(106): Show |
136 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.-12-2434C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144360224 | |||||||
chr7:144360231 | CT | C | 108 | a0002c0001t0001g0001 a0002c0001t0001g0008 a0002c0001t0001g0012 others(105): Show |
135 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.-12-2426delT | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144360231 | |||||||
chr7:144360236 | G | A | 109 | a0002c0001t0001g0001 a0002c0001t0001g0008 a0002c0001t0001g0012 others(106): Show |
136 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.-12-2422G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144360236 | |||||||
chr7:144360298 | A | C | 1 | a0046c0060t0001g0168 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-12-2360A>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144360298 | |||||||
chr7:144360350 | A | G | 13 | a0009c0026t0001g0051 a0009c0026t0001g0052 a0009c0070t0001g0175 others(10): Show |
13 | HG01496.hp1 HG01884.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.-12-2308A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144360350 | |||||||
chr7:144360359 | C | T | 1 | a0002c0001t0001g0100 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-12-2299C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144360359 | |||||||
chr7:144360390 | C | T | 157 | a0002c0001t0001g0001 a0002c0001t0001g0008 a0002c0001t0001g0012 others(154): Show |
218 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.-12-2268C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144360390 | |||||||
chr7:144360476 | T | C | 1 | a0011c0043t0002g0064 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-12-2182T>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144360476 | |||||||
chr7:144360584 | G | C | 13 | a0007c0011t0002g0010 a0007c0011t0002g0155 a0009c0026t0001g0051 others(10): Show |
16 | HG01496.hp1 HG01884.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-12-2074G>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144360584 | |||||||
chr7:144360609 | G | A | 2 | a0042c0048t0001g0146 a0044c0068t0001g0145 |
2 | NA18964.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.-12-2049G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144360609 | |||||||
chr7:144360631 | A | G | 95 | a0002c0001t0001g0001 a0002c0001t0001g0008 a0002c0001t0001g0012 others(92): Show |
122 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.-12-2027A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144360631 | |||||||
chr7:144360638 | G | T | 1 | a0001c0002t0002g0124 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-12-2020G>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144360638 | |||||||
chr7:144360689 | T | C | 2 | a0042c0048t0001g0146 a0044c0068t0001g0145 |
2 | NA18964.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.-12-1969T>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144360689 | |||||||
chr7:144360709 | A | G | 1 | a0001c0002t0002g0142 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-12-1949A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144360709 | |||||||
chr7:144360739 | A | G | 94 | a0002c0001t0001g0001 a0002c0001t0001g0008 a0002c0001t0001g0012 others(91): Show |
121 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.-12-1919A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144360739 | |||||||
chr7:144360868 | C | A | 9 | a0009c0026t0001g0051 a0009c0026t0001g0052 a0009c0070t0001g0175 others(6): Show |
9 | HG01496.hp1 HG01884.hp2 NA18951.hp1 others(6): Show |
intron_variant | MODIFIER | c.-12-1790C>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144360868 | |||||||
chr7:144360884 | A | T | 96 | a0002c0001t0001g0001 a0002c0001t0001g0008 a0002c0001t0001g0012 others(93): Show |
123 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.-12-1774A>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144360884 | |||||||
chr7:144360912 | A | C | 2 | a0042c0048t0001g0146 a0044c0068t0001g0145 |
2 | NA18964.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.-12-1746A>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144360912 | |||||||
chr7:144360957 | T | C | 98 | a0002c0001t0001g0001 a0002c0001t0001g0008 a0002c0001t0001g0012 others(95): Show |
125 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.-12-1701T>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144360957 | |||||||
chr7:144360958 | G | A | 98 | a0002c0001t0001g0001 a0002c0001t0001g0008 a0002c0001t0001g0012 others(95): Show |
125 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.-12-1700G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144360958 | |||||||
chr7:144361001 | G | T | 1 | a0032c0067t0001g0169 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-12-1657G>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144361001 | |||||||
chr7:144361014 | G | A | 2 | a0042c0048t0001g0146 a0044c0068t0001g0145 |
2 | NA18964.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.-12-1644G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144361014 | |||||||
chr7:144361042 | G | A | 98 | a0002c0001t0001g0001 a0002c0001t0001g0008 a0002c0001t0001g0012 others(95): Show |
125 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.-12-1616G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144361042 | |||||||
chr7:144361042 | G | T | 1 | a0004c0003t0001g0161 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-12-1616G>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144361042 | |||||||
chr7:144361107 | A | G | 1 | a0010c0009t0001g0018 | 2 | HG02897.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-12-1551A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144361107 | |||||||
chr7:144361142 | G | C | 107 | a0002c0001t0001g0001 a0002c0001t0001g0008 a0002c0001t0001g0012 others(104): Show |
134 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.-12-1516G>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144361142 | |||||||
chr7:144361143 | G | T | 94 | a0002c0001t0001g0001 a0002c0001t0001g0008 a0002c0001t0001g0012 others(91): Show |
121 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.-12-1515G>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144361143 | |||||||
chr7:144361157 | A | G | 99 | a0002c0001t0001g0001 a0002c0001t0001g0008 a0002c0001t0001g0012 others(96): Show |
126 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.-12-1501A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144361157 | |||||||
chr7:144361167 | C | T | 1 | a0002c0001t0001g0085 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-12-1491C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144361167 | |||||||
chr7:144361188 | C | T | 8 | a0009c0026t0001g0051 a0009c0026t0001g0052 a0009c0070t0001g0175 others(5): Show |
8 | HG01884.hp2 NA18951.hp1 NA18977.hp1 others(5): Show |
intron_variant | MODIFIER | c.-12-1470C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144361188 | |||||||
chr7:144361190 | G | A | 4 | a0012c0013t0002g0120 a0012c0013t0002g0121 a0012c0013t0002g0122 others(1): Show |
4 | HG01884.hp1 HG02970.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-1468G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144361190 | |||||||
chr7:144361226 | C | CA | 14 | a0001c0020t0002g0135 a0002c0001t0001g0080 a0002c0001t0001g0085 others(11): Show |
19 | HG01192.hp1 HG01515.hp2 HG01517.hp2 others(16): Show |
intron_variant | MODIFIER | c.-12-1417dupA | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 144361226 | ||||||
chr7:144361232 | AAAAAAAA others(3): Show |
A | 59 | a0003c0004t0002g0004 a0003c0004t0002g0011 a0003c0004t0002g0015 others(56): Show |
93 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.-12-1421_-12-1412d others(12): Show |
ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 144361232 | ||||||
chr7:144361232 | AAAAAAAA others(8): Show |
A | 1 | a0005c0005t0001g0087 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-12-1416_-12-1402d others(17): Show |
ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 144361232 | ||||||
chr7:144361241 | AG | A | 3 | a0002c0001t0001g0001 a0005c0005t0001g0072 a0019c0018t0001g0147 |
3 | HG01975.hp1 HG02135.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-12-1416delG | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144361241 | |||||||
chr7:144361242 | G | A | 96 | a0001c0002t0002g0139 a0002c0001t0001g0001 a0002c0001t0001g0008 others(93): Show |
121 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.-12-1416G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144361242 | |||||||
chr7:144361247 | G | A | 1 | a0006c0006t0001g0086 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-12-1411G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144361247 | |||||||
chr7:144361247 | GA | G | 4 | a0005c0005t0001g0009 a0005c0005t0001g0150 a0005c0005t0001g0152 others(1): Show |
6 | HG00099.hp2 HG00323.hp1 HG01069.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-1398delA | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 144361247 | ||||||
chr7:144361251 | A | G | 64 | a0001c0002t0002g0139 a0002c0001t0001g0100 a0003c0004t0002g0004 others(61): Show |
98 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.-12-1407A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144361251 | |||||||
chr7:144361448 | A | G | 24 | a0004c0003t0001g0003 a0004c0003t0001g0043 a0004c0003t0001g0045 others(21): Show |
42 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.-12-1210A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144361448 | |||||||
chr7:144361509 | C | T | 2 | a0007c0007t0003g0038 a0047c0031t0003g0038 |
2 | HG01891.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-12-1149C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144361509 | |||||||
chr7:144361592 | T | C | 34 | a0001c0002t0002g0124 a0001c0010t0002g0036 a0001c0010t0002g0118 others(31): Show |
53 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.-12-1066T>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144361592 | |||||||
chr7:144361610 | C | T | 1 | a0003c0032t0002g0063 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-12-1048C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144361610 | |||||||
chr7:144361702 | G | A | 89 | a0001c0002t0002g0130 a0002c0001t0001g0001 a0002c0001t0001g0008 others(86): Show |
114 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.-12-956G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144361702 | |||||||
chr7:144361799 | G | A | 1 | a0033c0033t0002g0131 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-12-859G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144361799 | |||||||
chr7:144362044 | C | T | 36 | a0001c0002t0002g0124 a0001c0010t0002g0036 a0001c0010t0002g0118 others(33): Show |
55 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.-12-614C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144362044 | |||||||
chr7:144362416 | C | T | 9 | a0009c0026t0001g0051 a0009c0026t0001g0052 a0009c0070t0001g0175 others(6): Show |
9 | HG01496.hp1 HG01884.hp2 NA18951.hp1 others(6): Show |
intron_variant | MODIFIER | c.-12-242C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144362416 | |||||||
chr7:144362419 | T | C | 15 | a0004c0003t0001g0003 a0004c0003t0001g0043 a0004c0003t0001g0045 others(12): Show |
33 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.-12-239T>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144362419 | |||||||
chr7:144362513 | T | C | 11 | a0002c0001t0001g0012 a0002c0001t0001g0025 a0002c0001t0001g0026 others(8): Show |
13 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(10): Show |
intron_variant | MODIFIER | c.-12-145T>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 1/14 | chr7 | 144362513 | |||||||
chr7:144365934 | C | T | 2 | a0007c0011t0002g0010 a0007c0011t0002g0155 |
5 | HG02258.hp1 HG02818.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.3154+111C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/14 | chr7 | 144365934 | |||||||
chr7:144366128 | G | T | 1 | a0036c0058t0001g0098 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3155-227G>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/14 | chr7 | 144366128 | |||||||
chr7:144366277 | G | A | 1 | a0009c0070t0001g0175 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.3155-78G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 2/14 | chr7 | 144366277 | |||||||
chr7:144366492 | T | C | 1 | a0009c0070t0001g0175 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.3212+80T>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 3/14 | chr7 | 144366492 | |||||||
chr7:144366938 | A | C | 162 | a0001c0021t0002g0042 a0002c0001t0001g0001 a0002c0001t0001g0008 others(159): Show |
225 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.3277+28A>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 4/14 | chr7 | 144366938 | |||||||
chr7:144367761 | G | A | 1 | a0002c0064t0001g0074 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.3531+406G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144367761 | |||||||
chr7:144367898 | T | G | 2 | a0001c0010t0002g0126 a0027c0069t0002g0157 |
2 | HG01361.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.3531+543T>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144367898 | |||||||
chr7:144368058 | G | GAT | 1 | a0007c0007t0003g0014 | 3 | HG02622.hp2 HG02647.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.3531+706_3531+707d others(4): Show |
ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr7 | 144368058 | ||||||
chr7:144368080 | A | T | 184 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0016 others(181): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.3531+725A>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144368080 | |||||||
chr7:144368178 | C | T | 1 | a0003c0012t0002g0006 | 4 | HG02451.hp1 HG02486.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.3531+823C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144368178 | |||||||
chr7:144368179 | G | C | 3 | a0009c0070t0001g0175 a0042c0048t0001g0146 a0046c0060t0001g0168 |
3 | NA18964.hp1 NA18986.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.3531+824G>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144368179 | |||||||
chr7:144368288 | C | T | 1 | a0003c0012t0002g0006 | 4 | HG02451.hp1 HG02486.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.3531+933C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144368288 | |||||||
chr7:144368294 | T | C | 1 | a0002c0061t0001g0094 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.3531+939T>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144368294 | |||||||
chr7:144368386 | C | T | 1 | a0009c0073t0001g0055 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.3531+1031C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144368386 | |||||||
chr7:144368497 | A | G | 4 | a0009c0070t0001g0175 a0020c0024t0001g0025 a0044c0068t0001g0145 others(1): Show |
4 | NA18977.hp2 NA18986.hp2 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.3531+1142A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144368497 | |||||||
chr7:144368499 | A | C | 2 | a0003c0004t0002g0065 a0003c0032t0002g0063 |
2 | HG01255.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.3531+1144A>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144368499 | |||||||
chr7:144368750 | A | T | 13 | a0004c0003t0001g0003 a0004c0003t0001g0043 a0004c0003t0001g0045 others(10): Show |
28 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.3531+1395A>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144368750 | |||||||
chr7:144368996 | A | C | 98 | a0001c0021t0002g0042 a0002c0001t0001g0001 a0002c0001t0001g0008 others(95): Show |
128 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.3531+1641A>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144368996 | |||||||
chr7:144369131 | A | G | 27 | a0003c0004t0002g0004 a0003c0004t0002g0011 a0003c0004t0002g0015 others(24): Show |
40 | HG00140.hp1 HG00741.hp2 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.3531+1776A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144369131 | |||||||
chr7:144369227 | TC | T | 21 | a0003c0004t0002g0004 a0003c0004t0002g0011 a0003c0004t0002g0015 others(18): Show |
30 | HG00140.hp1 HG00741.hp2 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.3531+1873delC | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144369227 | |||||||
chr7:144369465 | C | T | 93 | a0002c0001t0001g0001 a0002c0001t0001g0008 a0002c0001t0001g0012 others(90): Show |
117 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.3532-1696C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144369465 | |||||||
chr7:144369577 | G | T | 161 | a0002c0001t0001g0001 a0002c0001t0001g0008 a0002c0001t0001g0012 others(158): Show |
223 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.3532-1584G>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144369577 | |||||||
chr7:144369673 | A | G | 1 | a0012c0013t0002g0123 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3532-1488A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144369673 | |||||||
chr7:144370024 | G | T | 2 | a0006c0006t0001g0031 a0021c0057t0001g0031 |
2 | HG00544.hp1 HG00597.hp2 |
intron_variant | MODIFIER | c.3532-1137G>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144370024 | |||||||
chr7:144370058 | C | G | 1 | a0044c0068t0001g0145 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.3532-1103C>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144370058 | |||||||
chr7:144370059 | T | A | 1 | a0005c0005t0001g0088 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.3532-1102T>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144370059 | |||||||
chr7:144370121 | C | T | 1 | a0001c0002t0002g0162 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.3532-1040C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144370121 | |||||||
chr7:144370205 | C | T | 1 | a0001c0002t0002g0162 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.3532-956C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144370205 | |||||||
chr7:144370356 | A | G | 1 | a0032c0067t0001g0169 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3532-805A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144370356 | |||||||
chr7:144370468 | A | T | 13 | a0004c0003t0001g0003 a0004c0003t0001g0043 a0004c0003t0001g0045 others(10): Show |
28 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.3532-693A>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144370468 | |||||||
chr7:144370483 | T | C | 1 | a0003c0012t0002g0068 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3532-678T>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144370483 | |||||||
chr7:144370664 | C | G | 113 | a0001c0002t0002g0134 a0001c0002t0002g0139 a0001c0002t0002g0142 others(110): Show |
141 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.3532-497C>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144370664 | |||||||
chr7:144370667 | C | T | 2 | a0002c0001t0001g0026 a0041c0062t0001g0026 |
2 | HG02083.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.3532-494C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144370667 | |||||||
chr7:144370668 | G | A | 2 | a0007c0007t0003g0014 a0007c0007t0003g0117 |
4 | HG02622.hp2 HG02630.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.3532-493G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144370668 | |||||||
chr7:144370744 | G | C | 1 | a0009c0073t0001g0055 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.3532-417G>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144370744 | |||||||
chr7:144370955 | C | T | 1 | a0006c0006t0001g0084 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3532-206C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144370955 | |||||||
chr7:144371015 | C | T | 16 | a0006c0006t0001g0007 a0006c0006t0001g0028 a0006c0006t0001g0030 others(13): Show |
20 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(17): Show |
intron_variant | MODIFIER | c.3532-146C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144371015 | |||||||
chr7:144371070 | T | C | 64 | a0001c0002t0002g0134 a0002c0001t0001g0008 a0002c0016t0001g0167 others(61): Show |
95 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.3532-91T>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144371070 | |||||||
chr7:144371071 | G | A | 2 | a0007c0011t0002g0010 a0007c0011t0002g0155 |
5 | HG02258.hp1 HG02818.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.3532-90G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144371071 | |||||||
chr7:144371114 | G | C | 1 | a0009c0026t0001g0051 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.3532-47G>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144371114 | |||||||
chr7:144371121 | T | C | 26 | a0003c0004t0002g0004 a0003c0004t0002g0011 a0003c0004t0002g0015 others(23): Show |
39 | HG00140.hp1 HG00741.hp2 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.3532-40T>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 5/14 | chr7 | 144371121 | |||||||
chr7:144371383 | T | C | 2 | a0007c0007t0003g0014 a0007c0007t0003g0117 |
4 | HG02622.hp2 HG02630.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.3692+62T>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 6/14 | chr7 | 144371383 | |||||||
chr7:144371387 | G | A | 118 | a0001c0010t0002g0118 a0002c0001t0001g0001 a0002c0001t0001g0008 others(115): Show |
148 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.3692+66G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 6/14 | chr7 | 144371387 | |||||||
chr7:144371480 | G | A | 99 | a0002c0001t0001g0001 a0002c0001t0001g0012 a0002c0001t0001g0025 others(96): Show |
129 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.3692+159G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 6/14 | chr7 | 144371480 | |||||||
chr7:144371561 | G | C | 2 | a0011c0043t0002g0064 a0019c0018t0002g0062 |
2 | HG02647.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.3692+240G>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 6/14 | chr7 | 144371561 | |||||||
chr7:144371721 | G | A | 1 | a0008c0008t0001g0029 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.3693-156G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 6/14 | chr7 | 144371721 | |||||||
chr7:144372168 | G | A | 1 | a0004c0003t0001g0045 | 2 | HG00642.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.3846-131G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 7/14 | chr7 | 144372168 | |||||||
chr7:144372517 | C | T | 2 | a0001c0002t0002g0133 a0001c0002t0002g0138 |
2 | NA19011.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.3975+89C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 8/14 | chr7 | 144372517 | |||||||
chr7:144372815 | C | T | 2 | a0006c0006t0001g0096 a0006c0006t0001g0097 |
2 | HG02622.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.4050+58C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 9/14 | chr7 | 144372815 | |||||||
chr7:144372891 | G | T | 3 | a0001c0020t0002g0137 a0003c0012t0002g0006 a0033c0033t0002g0131 |
6 | HG00735.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.4050+134G>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 9/14 | chr7 | 144372891 | |||||||
chr7:144372934 | G | A | 1 | a0003c0012t0002g0006 | 4 | HG02451.hp1 HG02486.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.4050+177G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 9/14 | chr7 | 144372934 | |||||||
chr7:144372979 | C | A | 5 | a0001c0010t0002g0118 a0001c0010t0002g0119 a0007c0011t0002g0010 others(2): Show |
8 | HG02258.hp1 HG02258.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.4051-216C>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 9/14 | chr7 | 144372979 | |||||||
chr7:144372984 | C | A | 117 | a0001c0010t0002g0118 a0001c0010t0002g0119 a0001c0020t0002g0137 others(114): Show |
167 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.4051-211C>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 9/14 | chr7 | 144372984 | |||||||
chr7:144373022 | G | C | 8 | a0001c0002t0002g0040 a0001c0020t0002g0137 a0003c0012t0002g0006 others(5): Show |
15 | HG00735.hp2 HG02258.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.4051-173G>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 9/14 | chr7 | 144373022 | |||||||
chr7:144373291 | C | T | 1 | a0002c0001t0001g0100 | 1 | HG04228.hp1 | splice_region_variant&intron_variant | LOW | c.4140+7C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 10/14 | chr7 | 144373291 | |||||||
chr7:144373299 | T | G | 1 | a0002c0001t0001g0090 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.4140+15T>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 10/14 | chr7 | 144373299 | |||||||
chr7:144373472 | T | A | 131 | a0001c0020t0002g0137 a0002c0001t0001g0001 a0002c0001t0001g0008 others(128): Show |
180 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.4140+188T>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 10/14 | chr7 | 144373472 | |||||||
chr7:144373538 | T | G | 11 | a0005c0005t0001g0009 a0005c0005t0001g0150 a0005c0005t0001g0152 others(8): Show |
14 | HG00099.hp2 HG00323.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.4140+254T>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 10/14 | chr7 | 144373538 | |||||||
chr7:144373547 | G | A | 1 | a0032c0067t0001g0169 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4140+263G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 10/14 | chr7 | 144373547 | |||||||
chr7:144373692 | G | C | 12 | a0004c0003t0001g0003 a0004c0003t0001g0043 a0004c0003t0001g0045 others(9): Show |
27 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.4140+408G>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 10/14 | chr7 | 144373692 | |||||||
chr7:144373757 | G | T | 4 | a0007c0011t0002g0010 a0007c0011t0002g0155 a0009c0070t0001g0175 others(1): Show |
7 | HG02258.hp1 HG02723.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.4140+473G>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 10/14 | chr7 | 144373757 | |||||||
chr7:144373846 | C | CT | 7 | a0002c0016t0001g0077 a0002c0016t0001g0102 a0002c0016t0001g0167 others(4): Show |
10 | HG01934.hp2 HG02083.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.4140+576dupT | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr7 | 144373846 | ||||||
chr7:144373880 | G | A | 159 | a0002c0001t0001g0001 a0002c0001t0001g0008 a0002c0001t0001g0012 others(156): Show |
218 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.4140+596G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 10/14 | chr7 | 144373880 | |||||||
chr7:144373912 | G | C | 1 | a0006c0006t0001g0096 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4140+628G>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 10/14 | chr7 | 144373912 | |||||||
chr7:144374003 | G | A | 1 | a0019c0018t0001g0147 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.4140+719G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 10/14 | chr7 | 144374003 | |||||||
chr7:144374054 | C | T | 1 | a0032c0067t0001g0169 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4141-678C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 10/14 | chr7 | 144374054 | |||||||
chr7:144374067 | C | T | 1 | a0033c0033t0002g0131 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.4141-665C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 10/14 | chr7 | 144374067 | |||||||
chr7:144374111 | G | T | 116 | a0001c0002t0002g0162 a0002c0001t0001g0001 a0002c0001t0001g0008 others(113): Show |
149 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.4141-621G>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 10/14 | chr7 | 144374111 | |||||||
chr7:144374118 | AG | A | 4 | a0012c0013t0002g0120 a0012c0013t0002g0121 a0012c0013t0002g0122 others(1): Show |
4 | HG01884.hp1 HG02970.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.4141-612delG | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr7 | 144374118 | ||||||
chr7:144374122 | G | A | 5 | a0007c0007t0003g0035 a0007c0007t0003g0037 a0007c0007t0003g0038 others(2): Show |
7 | HG01891.hp1 HG02723.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.4141-610G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 10/14 | chr7 | 144374122 | |||||||
chr7:144374136 | T | C | 166 | a0001c0002t0002g0132 a0002c0001t0001g0001 a0002c0001t0001g0008 others(163): Show |
228 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.4141-596T>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 10/14 | chr7 | 144374136 | |||||||
chr7:144374197 | A | T | 2 | a0011c0043t0002g0064 a0019c0018t0002g0062 |
2 | HG02647.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.4141-535A>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 10/14 | chr7 | 144374197 | |||||||
chr7:144374218 | C | T | 1 | a0001c0002t0002g0165 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.4141-514C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 10/14 | chr7 | 144374218 | |||||||
chr7:144374238 | A | T | 1 | a0006c0006t0001g0096 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4141-494A>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 10/14 | chr7 | 144374238 | |||||||
chr7:144374269 | C | A | 2 | a0004c0003t0001g0159 a0009c0070t0001g0175 |
2 | HG01123.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.4141-463C>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 10/14 | chr7 | 144374269 | |||||||
chr7:144374445 | C | T | 1 | a0004c0003t0001g0046 | 2 | HG01243.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.4141-287C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 10/14 | chr7 | 144374445 | |||||||
chr7:144374512 | A | G | 110 | a0001c0002t0002g0136 a0002c0001t0001g0001 a0002c0001t0001g0008 others(107): Show |
140 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.4141-220A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 10/14 | chr7 | 144374512 | |||||||
chr7:144374626 | G | A | 1 | a0003c0012t0002g0068 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.4141-106G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 10/14 | chr7 | 144374626 | |||||||
chr7:144374670 | G | A | 1 | a0001c0002t0002g0130 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.4141-62G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 10/14 | chr7 | 144374670 | |||||||
chr7:144375183 | T | A | 2 | a0002c0001t0001g0104 a0002c0016t0001g0167 |
2 | NA18990.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.4298+294T>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 11/14 | chr7 | 144375183 | |||||||
chr7:144375232 | G | T | 132 | a0002c0001t0001g0001 a0002c0001t0001g0008 a0002c0001t0001g0012 others(129): Show |
181 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.4299-282G>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 11/14 | chr7 | 144375232 | |||||||
chr7:144375350 | C | T | 3 | a0003c0004t0002g0066 a0003c0004t0002g0067 a0003c0004t0002g0069 |
3 | HG01934.hp1 HG02165.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.4299-164C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 11/14 | chr7 | 144375350 | |||||||
chr7:144375714 | A | G | 2 | a0011c0043t0002g0064 a0019c0018t0002g0062 |
2 | HG02647.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.4460+39A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 12/14 | chr7 | 144375714 | |||||||
chr7:144375721 | C | T | 2 | a0001c0002t0002g0039 a0001c0002t0002g0136 |
3 | HG04184.hp1 NA18964.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.4460+46C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 12/14 | chr7 | 144375721 | |||||||
chr7:144375923 | G | A | 1 | a0001c0020t0002g0135 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.4460+248G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 12/14 | chr7 | 144375923 | |||||||
chr7:144376457 | C | T | 1 | a0032c0067t0001g0169 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4461-663C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 12/14 | chr7 | 144376457 | |||||||
chr7:144376702 | T | G | 1 | a0020c0024t0001g0091 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.4461-418T>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 12/14 | chr7 | 144376702 | |||||||
chr7:144376737 | G | A | 12 | a0004c0003t0001g0003 a0004c0003t0001g0043 a0004c0003t0001g0045 others(9): Show |
27 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.4461-383G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 12/14 | chr7 | 144376737 | |||||||
chr7:144376808 | G | A | 1 | a0002c0001t0001g0092 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.4461-312G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 12/14 | chr7 | 144376808 | |||||||
chr7:144376860 | A | T | 128 | a0002c0001t0001g0001 a0002c0001t0001g0008 a0002c0001t0001g0012 others(125): Show |
177 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.4461-260A>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 12/14 | chr7 | 144376860 | |||||||
chr7:144376902 | T | G | 107 | a0002c0001t0001g0001 a0002c0001t0001g0008 a0002c0001t0001g0012 others(104): Show |
135 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.4461-218T>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 12/14 | chr7 | 144376902 | |||||||
chr7:144377062 | C | T | 1 | a0002c0001t0001g0095 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.4461-58C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 12/14 | chr7 | 144377062 | |||||||
chr7:144377466 | A | T | 7 | a0007c0007t0003g0014 a0007c0007t0003g0035 a0007c0007t0003g0037 others(4): Show |
11 | HG01891.hp1 HG02622.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.4531+276A>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 13/14 | chr7 | 144377466 | |||||||
chr7:144377536 | A | G | 127 | a0002c0001t0001g0001 a0002c0001t0001g0008 a0002c0001t0001g0012 others(124): Show |
173 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.4531+346A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 13/14 | chr7 | 144377536 | |||||||
chr7:144377630 | G | A | 1 | a0035c0053t0001g0116 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4531+440G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 13/14 | chr7 | 144377630 | |||||||
chr7:144377677 | A | C | 1 | a0002c0001t0001g0075 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.4531+487A>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 13/14 | chr7 | 144377677 | |||||||
chr7:144377680 | C | G | 2 | a0007c0007t0003g0037 a0007c0007t0003g0129 |
3 | HG02723.hp1 HG03486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.4531+490C>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 13/14 | chr7 | 144377680 | |||||||
chr7:144377836 | G | A | 26 | a0003c0004t0002g0004 a0003c0004t0002g0011 a0003c0004t0002g0015 others(23): Show |
39 | HG00140.hp1 HG00741.hp2 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.4531+646G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 13/14 | chr7 | 144377836 | |||||||
chr7:144377920 | C | T | 13 | a0004c0003t0001g0003 a0004c0003t0001g0043 a0004c0003t0001g0045 others(10): Show |
28 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.4531+730C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 13/14 | chr7 | 144377920 | |||||||
chr7:144378024 | A | G | 1 | a0008c0008t0001g0115 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.4532-738A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 13/14 | chr7 | 144378024 | |||||||
chr7:144378544 | C | G | 1 | a0001c0010t0002g0118 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.4532-218C>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 13/14 | chr7 | 144378544 | |||||||
chr7:144378578 | A | G | 1 | a0001c0010t0002g0118 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.4532-184A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 13/14 | chr7 | 144378578 | |||||||
chr7:144378656 | A | G | 127 | a0002c0001t0001g0001 a0002c0001t0001g0008 a0002c0001t0001g0012 others(124): Show |
173 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.4532-106A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 13/14 | chr7 | 144378656 | |||||||
chr7:144378895 | C | T | 1 | a0002c0001t0001g0050 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.4636+29C>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 14/14 | chr7 | 144378895 | |||||||
chr7:144378899 | G | T | 2 | a0003c0004t0002g0024 a0003c0004t0002g0061 |
3 | HG01261.hp1 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.4636+33G>T | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 14/14 | chr7 | 144378899 | |||||||
chr7:144379338 | G | A | 4 | a0012c0013t0002g0120 a0012c0013t0002g0121 a0012c0013t0002g0122 others(1): Show |
4 | HG01884.hp1 HG02970.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.4636+472G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 14/14 | chr7 | 144379338 | |||||||
chr7:144379399 | G | A | 1 | a0003c0004t0002g0065 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.4637-500G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 14/14 | chr7 | 144379399 | |||||||
chr7:144379457 | A | G | 131 | a0002c0001t0001g0001 a0002c0001t0001g0008 a0002c0001t0001g0012 others(128): Show |
180 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.4637-442A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 14/14 | chr7 | 144379457 | |||||||
chr7:144379606 | G | A | 1 | a0006c0006t0001g0097 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4637-293G>A | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 14/14 | chr7 | 144379606 | |||||||
chr7:144379671 | A | G | 129 | a0002c0001t0001g0001 a0002c0001t0001g0008 a0002c0001t0001g0012 others(126): Show |
178 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.4637-228A>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 14/14 | chr7 | 144379671 | |||||||
chr7:144379822 | C | G | 127 | a0002c0001t0001g0001 a0002c0001t0001g0008 a0002c0001t0001g0012 others(124): Show |
173 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.4637-77C>G | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 14/14 | chr7 | 144379822 | |||||||
chr7:144379860 | T | C | 1 | a0002c0001t0001g0085 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.4637-39T>C | ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 14/14 | chr7 | 144379860 |