Item | Value |
---|---|
geneid | 27237 |
ensemblid | ENSG00000130762.15 |
hgncid | 15515 |
symbol | ARHGEF16 |
name | Rho guanine nucleotide exchange factor 16 |
refseq_nuc | NM_014448.4 |
refseq_prot | NP_055263.2 |
ensembl_nuc | ENST00000378378.9 |
ensembl_prot | ENSP00000367629.4 |
mane_status | MANE Select |
chr | chr1 |
start | 3454665 |
end | 3481113 |
strand | + |
ver | v1.2 |
region | chr1:3454665-3481113 |
region5000 | chr1:3449665-3486113 |
regionname0 | ARHGEF16_chr1_3454665_3481113 |
regionname5000 | ARHGEF16_chr1_3449665_3486113 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 709 | 202 | 25 | 48 | 81 | 15 | 32 | 61 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | MAQRH others(704): Show |
chr1 | 3449665 | 3486113 |
a0002 | 1/0 | 709 | 81 | 38 | 16 | 22 | 0 | 4 | 7 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | MAQRH others(704): Show |
chr1 | 3449665 | 3486113 |
a0003 | 0/0 | 709 | 29 | 10 | 3 | 16 | 0 | 0 | 14 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | MAQRH others(704): Show |
chr1 | 3449665 | 3486113 |
a0004 | 0/0 | 709 | 5 | 2 | 2 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | MAQRH others(704): Show |
chr1 | 3449665 | 3486113 |
a0005 | 0/0 | 709 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | MAQRH others(704): Show |
chr1 | 3449665 | 3486113 |
a0006 | 0/0 | 709 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | MAQRH others(704): Show |
chr1 | 3449665 | 3486113 |
a0007 | 0/0 | 709 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | MAQRH others(704): Show |
chr1 | 3449665 | 3486113 |
a0008 | 0/0 | 709 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | MAQRH others(704): Show |
chr1 | 3449665 | 3486113 |
a0009 | 0/0 | 709 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | MAQRH others(704): Show |
chr1 | 3449665 | 3486113 |
a0010 | 0/0 | 709 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | MAQRH others(704): Show |
chr1 | 3449665 | 3486113 |
a0011 | 0/0 | 709 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | MAQRH others(704): Show |
chr1 | 3449665 | 3486113 |
a0012 | 0/0 | 709 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | MAQRH others(704): Show |
chr1 | 3449665 | 3486113 |
a0013 | 0/0 | 709 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | MAQRH others(704): Show |
chr1 | 3449665 | 3486113 |
a0014 | 0/0 | 709 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | MAQRH others(704): Show |
chr1 | 3449665 | 3486113 |
a0015 | 0/0 | 709 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | MAQRH others(704): Show |
chr1 | 3449665 | 3486113 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 2127 | 189 | 25 | 47 | 69 | 15 | 32 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | ATGGC others(2122): Show |
chr1 | 3449665 | 3486113 | ||
a0001c0005 | 0/0 | 2127 | 9 | 0 | 1 | 8 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | ATGGC others(2122): Show |
chr1 | 3449665 | 3486113 | ||
a0001c0009 | 0/0 | 2127 | 4 | 0 | 0 | 4 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | ATGGC others(2122): Show |
chr1 | 3449665 | 3486113 | ||
a0002c0002 | 0/0 | 2127 | 27 | 0 | 10 | 16 | 0 | 1 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | ATGGC others(2122): Show |
chr1 | 3449665 | 3486113 | ||
a0002c0003 | 0/0 | 2127 | 18 | 16 | 2 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | ATGGC others(2122): Show |
chr1 | 3449665 | 3486113 | ||
a0002c0007 | 0/0 | 2127 | 8 | 0 | 1 | 6 | 0 | 1 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | ATGGC others(2122): Show |
chr1 | 3449665 | 3486113 | ||
a0002c0008 | 1/0 | 2127 | 5 | 4 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | ATGGC others(2122): Show |
chr1 | 3449665 | 3486113 | ||
a0002c0011 | 0/0 | 2127 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | ATGGC others(2122): Show |
chr1 | 3449665 | 3486113 | ||
a0002c0012 | 0/0 | 2127 | 4 | 3 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | ATGGC others(2122): Show |
chr1 | 3449665 | 3486113 | ||
a0002c0014 | 0/0 | 2127 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | ATGGC others(2122): Show |
chr1 | 3449665 | 3486113 | ||
a0002c0017 | 0/0 | 2127 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | ATGGC others(2122): Show |
chr1 | 3449665 | 3486113 | ||
a0002c0020 | 0/0 | 2127 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | ATGGC others(2122): Show |
chr1 | 3449665 | 3486113 | ||
a0002c0021 | 0/0 | 2127 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | ATGGC others(2122): Show |
chr1 | 3449665 | 3486113 | ||
a0002c0022 | 0/0 | 2127 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | ATGGC others(2122): Show |
chr1 | 3449665 | 3486113 | ||
a0002c0024 | 0/0 | 2127 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | ATGGC others(2122): Show |
chr1 | 3449665 | 3486113 | ||
a0002c0028 | 0/0 | 2127 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | ATGGC others(2122): Show |
chr1 | 3449665 | 3486113 | ||
a0002c0030 | 0/0 | 2127 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | ATGGC others(2122): Show |
chr1 | 3449665 | 3486113 | ||
a0002c0035 | 0/0 | 2127 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | ATGGC others(2122): Show |
chr1 | 3449665 | 3486113 | ||
a0003c0004 | 0/0 | 2127 | 16 | 0 | 2 | 14 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | ATGGC others(2122): Show |
chr1 | 3449665 | 3486113 | ||
a0003c0006 | 0/0 | 2127 | 8 | 8 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | ATGGC others(2122): Show |
chr1 | 3449665 | 3486113 | ||
a0003c0015 | 0/0 | 2127 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | ATGGC others(2122): Show |
chr1 | 3449665 | 3486113 | ||
a0003c0016 | 0/0 | 2127 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | ATGGC others(2122): Show |
chr1 | 3449665 | 3486113 | ||
a0003c0026 | 0/0 | 2127 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | ATGGC others(2122): Show |
chr1 | 3449665 | 3486113 | ||
a0004c0010 | 0/0 | 2127 | 4 | 1 | 2 | 0 | 1 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | ATGGC others(2122): Show |
chr1 | 3449665 | 3486113 | ||
a0004c0029 | 0/0 | 2127 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | ATGGC others(2122): Show |
chr1 | 3449665 | 3486113 | ||
a0005c0013 | 0/0 | 2127 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | ATGGC others(2122): Show |
chr1 | 3449665 | 3486113 | ||
a0006c0023 | 0/0 | 2127 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | ATGGC others(2122): Show |
chr1 | 3449665 | 3486113 | ||
a0007c0018 | 0/0 | 2127 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | ATGGC others(2122): Show |
chr1 | 3449665 | 3486113 | ||
a0008c0019 | 0/0 | 2127 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | ATGGC others(2122): Show |
chr1 | 3449665 | 3486113 | ||
a0009c0036 | 0/0 | 2127 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | ATGGC others(2122): Show |
chr1 | 3449665 | 3486113 | ||
a0010c0032 | 0/0 | 2127 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | ATGGC others(2122): Show |
chr1 | 3449665 | 3486113 | ||
a0011c0034 | 0/0 | 2127 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | ATGGC others(2122): Show |
chr1 | 3449665 | 3486113 | ||
a0012c0025 | 0/0 | 2127 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | ATGGC others(2122): Show |
chr1 | 3449665 | 3486113 | ||
a0013c0031 | 0/0 | 2127 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | ATGGC others(2122): Show |
chr1 | 3449665 | 3486113 | ||
a0014c0033 | 0/0 | 2127 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | ATGGC others(2122): Show |
chr1 | 3449665 | 3486113 | ||
a0015c0027 | 0/0 | 2127 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | ATGGC others(2122): Show |
chr1 | 3449665 | 3486113 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 2824 | 179 | 25 | 46 | 61 | 15 | 31 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | AGCCA others(2819): Show |
chr1 | 3449665 | 3486113 |
a0001c0001t0004 | 0/0 | 2824 | 5 | 0 | 0 | 5 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | AGCCA others(2819): Show |
chr1 | 3449665 | 3486113 |
a0001c0001t0011 | 0/0 | 2824 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | AGCCA others(2819): Show |
chr1 | 3449665 | 3486113 |
a0001c0001t0013 | 0/0 | 2824 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | AGCCA others(2819): Show |
chr1 | 3449665 | 3486113 |
a0001c0001t0016 | 0/0 | 2824 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | AGCCA others(2819): Show |
chr1 | 3449665 | 3486113 |
a0001c0001t0017 | 0/0 | 2824 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | AGCCA others(2819): Show |
chr1 | 3449665 | 3486113 |
a0001c0001t0018 | 0/0 | 2824 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | AGCCA others(2819): Show |
chr1 | 3449665 | 3486113 |
a0001c0005t0001 | 0/0 | 2824 | 8 | 0 | 1 | 7 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | AGCCA others(2819): Show |
chr1 | 3449665 | 3486113 |
a0001c0005t0019 | 0/0 | 2824 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | AGCCA others(2819): Show |
chr1 | 3449665 | 3486113 |
a0001c0009t0001 | 0/0 | 2824 | 4 | 0 | 0 | 4 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | AGCCA others(2819): Show |
chr1 | 3449665 | 3486113 |
a0002c0002t0001 | 0/0 | 2824 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | AGCCA others(2819): Show |
chr1 | 3449665 | 3486113 |
a0002c0002t0002 | 0/0 | 2824 | 16 | 0 | 10 | 5 | 0 | 1 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | AGCCA others(2819): Show |
chr1 | 3449665 | 3486113 |
a0002c0002t0003 | 0/0 | 2824 | 10 | 0 | 0 | 10 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | AGCCA others(2819): Show |
chr1 | 3449665 | 3486113 |
a0002c0003t0002 | 0/0 | 2824 | 18 | 16 | 2 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | AGCCA others(2819): Show |
chr1 | 3449665 | 3486113 |
a0002c0007t0002 | 0/0 | 2824 | 8 | 0 | 1 | 6 | 0 | 1 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | AGCCA others(2819): Show |
chr1 | 3449665 | 3486113 |
a0002c0008t0007 | 0/0 | 2822 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | AGCCA others(2817): Show |
chr1 | 3449665 | 3486113 |
a0002c0008t0008 | 1/0 | 2822 | 3 | 2 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | AGCCA others(2817): Show |
chr1 | 3449665 | 3486113 |
a0002c0008t0014 | 0/0 | 2822 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | AGCCA others(2817): Show |
chr1 | 3449665 | 3486113 |
a0002c0011t0002 | 0/0 | 2824 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | AGCCA others(2819): Show |
chr1 | 3449665 | 3486113 |
a0002c0011t0009 | 0/0 | 2824 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | AGCCA others(2819): Show |
chr1 | 3449665 | 3486113 |
a0002c0012t0001 | 0/0 | 2824 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | AGCCA others(2819): Show |
chr1 | 3449665 | 3486113 |
a0002c0012t0002 | 0/0 | 2824 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | AGCCA others(2819): Show |
chr1 | 3449665 | 3486113 |
a0002c0012t0010 | 0/0 | 2824 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | AGCCA others(2819): Show |
chr1 | 3449665 | 3486113 |
a0002c0014t0006 | 0/0 | 2824 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | AGCCA others(2819): Show |
chr1 | 3449665 | 3486113 |
a0002c0017t0001 | 0/0 | 2824 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | AGCCA others(2819): Show |
chr1 | 3449665 | 3486113 |
a0002c0020t0001 | 0/0 | 2824 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | AGCCA others(2819): Show |
chr1 | 3449665 | 3486113 |
a0002c0021t0002 | 0/0 | 2824 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | AGCCA others(2819): Show |
chr1 | 3449665 | 3486113 |
a0002c0022t0002 | 0/0 | 2824 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | AGCCA others(2819): Show |
chr1 | 3449665 | 3486113 |
a0002c0024t0002 | 0/0 | 2824 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | AGCCA others(2819): Show |
chr1 | 3449665 | 3486113 |
a0002c0028t0002 | 0/0 | 2824 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | AGCCA others(2819): Show |
chr1 | 3449665 | 3486113 |
a0002c0030t0007 | 0/0 | 2822 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | AGCCA others(2817): Show |
chr1 | 3449665 | 3486113 |
a0002c0035t0002 | 0/0 | 2824 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | AGCCA others(2819): Show |
chr1 | 3449665 | 3486113 |
a0003c0004t0002 | 0/0 | 2824 | 16 | 0 | 2 | 14 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | AGCCA others(2819): Show |
chr1 | 3449665 | 3486113 |
a0003c0006t0002 | 0/0 | 2824 | 7 | 7 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | AGCCA others(2819): Show |
chr1 | 3449665 | 3486113 |
a0003c0006t0015 | 0/0 | 2824 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | AGCCA others(2819): Show |
chr1 | 3449665 | 3486113 |
a0003c0015t0002 | 0/0 | 2824 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | AGCCA others(2819): Show |
chr1 | 3449665 | 3486113 |
a0003c0016t0002 | 0/0 | 2824 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | AGCCA others(2819): Show |
chr1 | 3449665 | 3486113 |
a0003c0016t0007 | 0/0 | 2822 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | AGCCA others(2817): Show |
chr1 | 3449665 | 3486113 |
a0003c0026t0001 | 0/0 | 2824 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | AGCCA others(2819): Show |
chr1 | 3449665 | 3486113 |
a0004c0010t0002 | 0/0 | 2824 | 4 | 1 | 2 | 0 | 1 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | AGCCA others(2819): Show |
chr1 | 3449665 | 3486113 |
a0004c0029t0002 | 0/0 | 2824 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | AGCCA others(2819): Show |
chr1 | 3449665 | 3486113 |
a0005c0013t0005 | 0/0 | 2824 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | AGCCA others(2819): Show |
chr1 | 3449665 | 3486113 |
a0005c0013t0009 | 0/0 | 2824 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | AGCCA others(2819): Show |
chr1 | 3449665 | 3486113 |
a0006c0023t0001 | 0/0 | 2824 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | AGCCA others(2819): Show |
chr1 | 3449665 | 3486113 |
a0007c0018t0001 | 0/0 | 2824 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | AGCCA others(2819): Show |
chr1 | 3449665 | 3486113 |
a0008c0019t0001 | 0/0 | 2824 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | AGCCA others(2819): Show |
chr1 | 3449665 | 3486113 |
a0009c0036t0001 | 0/0 | 2824 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | AGCCA others(2819): Show |
chr1 | 3449665 | 3486113 |
a0010c0032t0002 | 0/0 | 2824 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | AGCCA others(2819): Show |
chr1 | 3449665 | 3486113 |
a0011c0034t0005 | 0/0 | 2824 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | AGCCA others(2819): Show |
chr1 | 3449665 | 3486113 |
a0012c0025t0012 | 0/0 | 2824 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | AGCCA others(2819): Show |
chr1 | 3449665 | 3486113 |
a0013c0031t0002 | 0/0 | 2824 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | AGCCA others(2819): Show |
chr1 | 3449665 | 3486113 |
a0014c0033t0001 | 0/0 | 2824 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | AGCCA others(2819): Show |
chr1 | 3449665 | 3486113 |
a0015c0027t0001 | 0/0 | 2824 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | AGCCA others(2819): Show |
chr1 | 3449665 | 3486113 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0147 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0004g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0004g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0004g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0004g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0011g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0013g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0016g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0017g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0001t0018g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0005t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0005t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0005t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0005t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0005t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0005t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0005t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0005t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0005t0019g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0009t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0009t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0001c0009t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0002t0002g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0002t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0002t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0002t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0002t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0002t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0002t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0002t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0002t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0002t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0002t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0002t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0002t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0002t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0002t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0002t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0002t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0002t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0002t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0003t0002g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0003t0002g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0003t0002g0005 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0003t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0003t0002g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0003t0002g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0003t0002g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0003t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0003t0002g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0003t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0007t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0007t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0007t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0007t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0007t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0007t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0007t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0007t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0008t0007g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0008t0008g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0008t0008g0095 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0008t0014g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0011t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0011t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0011t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0011t0009g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0012t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0012t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0012t0002g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0012t0010g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0014t0006g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0014t0006g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0017t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0017t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0020t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0020t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0021t0002g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0022t0002g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0024t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0028t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0030t0007g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0002c0035t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0003c0004t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0003c0004t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0003c0004t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0003c0004t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0003c0004t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0003c0004t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0003c0004t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0003c0004t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0003c0004t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0003c0004t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0003c0004t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0003c0004t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0003c0004t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0003c0004t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0003c0004t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0003c0006t0002g0001 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0003c0006t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0003c0006t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0003c0006t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0003c0006t0015g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0003c0015t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0003c0015t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0003c0016t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0003c0016t0007g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0003c0026t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0004c0010t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0004c0010t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0004c0010t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0004c0010t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0004c0029t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0005c0013t0005g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0005c0013t0005g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0005c0013t0005g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0005c0013t0009g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0006c0023t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0006c0023t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0007c0018t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0007c0018t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0008c0019t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0008c0019t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0009c0036t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0010c0032t0002g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0011c0034t0005g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0012c0025t0012g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0013c0031t0002g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0014c0033t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
a0015c0027t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0092 | EUR | GBR | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0083 | EUR | GBR | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0091 | EUR | GBR | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0213 | EUR | GBR | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0169 | EUR | FIN | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0207 | EUR | FIN | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0176 | EUR | FIN | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0236 | EUR | FIN | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG00423 | hp1 | a0002 | c0002 | t0002 | g0043 | EAS | CHS | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG00423 | hp2 | a0002 | c0002 | t0003 | g0034 | EAS | CHS | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG00438 | hp1 | a0009 | c0036 | t0001 | g0143 | EAS | CHS | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG00438 | hp2 | a0002 | c0007 | t0002 | g0158 | EAS | CHS | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG00544 | hp2 | a0002 | c0002 | t0003 | g0031 | EAS | CHS | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG00558 | hp1 | a0006 | c0023 | t0001 | g0135 | EAS | CHS | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG00597 | hp1 | a0001 | c0001 | t0011 | g0217 | EAS | CHS | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG00597 | hp2 | a0002 | c0002 | t0002 | g0042 | EAS | CHS | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG00609 | hp1 | a0002 | c0002 | t0003 | g0033 | EAS | CHS | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG00609 | hp2 | a0002 | c0002 | t0003 | g0036 | EAS | CHS | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG00621 | hp2 | a0002 | c0002 | t0002 | g0035 | EAS | CHS | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG00642 | hp2 | a0004 | c0010 | t0002 | g0058 | AMR | PUR | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | CHS | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | CHS | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG01070 | hp1 | a0003 | c0004 | t0002 | g0073 | AMR | PUR | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG01081 | hp1 | a0003 | c0026 | t0001 | g0070 | AMR | PUR | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG01081 | hp2 | a0002 | c0002 | t0002 | g0046 | AMR | PUR | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG01109 | hp2 | a0002 | c0012 | t0002 | g0291 | AMR | PUR | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG01243 | hp1 | a0010 | c0032 | t0002 | g0017 | AMR | PUR | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG01243 | hp2 | a0002 | c0017 | t0001 | g0283 | AMR | PUR | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG01255 | hp1 | a0002 | c0020 | t0001 | g0189 | AMR | CLM | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG01257 | hp1 | a0002 | c0002 | t0002 | g0006 | AMR | CLM | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG01258 | hp1 | a0002 | c0002 | t0002 | g0006 | AMR | CLM | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG01261 | hp1 | a0002 | c0003 | t0002 | g0005 | AMR | CLM | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | CLM | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG01358 | hp1 | a0001 | c0005 | t0001 | g0053 | AMR | CLM | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG01361 | hp1 | a0003 | c0004 | t0002 | g0075 | AMR | CLM | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | CLM | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | CLM | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG01515 | hp1 | a0004 | c0010 | t0002 | g0059 | EUR | IBS | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0212 | EUR | IBS | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0160 | EUR | IBS | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0156 | EUR | IBS | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG01884 | hp1 | a0002 | c0008 | t0007 | g0096 | AFR | ACB | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG01884 | hp2 | a0002 | c0003 | t0002 | g0004 | AFR | ACB | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG01928 | hp1 | a0002 | c0007 | t0002 | g0119 | AMR | PEL | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG01928 | hp2 | a0002 | c0002 | t0002 | g0051 | AMR | PEL | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG01934 | hp1 | a0002 | c0002 | t0002 | g0054 | AMR | PEL | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG01978 | hp1 | a0002 | c0002 | t0002 | g0050 | AMR | PEL | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG01981 | hp1 | a0002 | c0002 | t0002 | g0048 | AMR | PEL | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG01981 | hp2 | a0002 | c0002 | t0002 | g0052 | AMR | PEL | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PEL | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0274 | AMR | PEL | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02004 | hp2 | a0004 | c0010 | t0002 | g0060 | AMR | PEL | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02027 | hp2 | a0003 | c0004 | t0002 | g0007 | EAS | KHV | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02055 | hp2 | a0011 | c0034 | t0005 | g0282 | AFR | ACB | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | KHV | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | KHV | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02074 | hp1 | a0002 | c0002 | t0003 | g0037 | EAS | KHV | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | KHV | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02083 | hp2 | a0002 | c0002 | t0001 | g0021 | EAS | KHV | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02129 | hp1 | a0002 | c0002 | t0002 | g0039 | EAS | KHV | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02132 | hp1 | a0002 | c0007 | t0002 | g0159 | EAS | KHV | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02132 | hp2 | a0002 | c0002 | t0002 | g0041 | EAS | KHV | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02135 | hp2 | a0003 | c0004 | t0002 | g0076 | EAS | KHV | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02155 | hp1 | a0002 | c0002 | t0003 | g0044 | EAS | CDX | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | CDX | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | CDX | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | CDX | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02258 | hp1 | a0004 | c0010 | t0002 | g0057 | AFR | ACB | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02258 | hp2 | a0002 | c0003 | t0002 | g0018 | AFR | ACB | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02273 | hp2 | a0001 | c0001 | t0016 | g0164 | AMR | PEL | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02280 | hp2 | a0002 | c0028 | t0002 | g0094 | AFR | ACB | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02293 | hp1 | a0002 | c0002 | t0002 | g0047 | AMR | PEL | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PEL | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02451 | hp1 | a0002 | c0022 | t0002 | g0008 | AFR | ACB | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02451 | hp2 | a0003 | c0016 | t0002 | g0293 | AFR | ACB | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02572 | hp2 | a0005 | c0013 | t0005 | g0280 | AFR | GWD | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | PJL | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | GWD | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | GWD | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02630 | hp2 | a0002 | c0011 | t0009 | g0285 | AFR | GWD | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02647 | hp1 | a0002 | c0003 | t0002 | g0002 | AFR | GWD | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02647 | hp2 | a0003 | c0006 | t0002 | g0065 | AFR | GWD | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0251 | SAS | PJL | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02717 | hp1 | a0002 | c0011 | t0002 | g0287 | AFR | GWD | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02717 | hp2 | a0002 | c0012 | t0001 | g0090 | AFR | GWD | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02723 | hp2 | a0002 | c0011 | t0002 | g0286 | AFR | GWD | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0278 | SAS | PJL | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02809 | hp1 | a0003 | c0006 | t0002 | g0001 | AFR | GWD | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02809 | hp2 | a0002 | c0014 | t0006 | g0009 | AFR | GWD | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02818 | hp1 | a0002 | c0030 | t0007 | g0261 | AFR | GWD | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02818 | hp2 | a0002 | c0003 | t0002 | g0295 | AFR | GWD | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02895 | hp1 | a0005 | c0013 | t0005 | g0279 | AFR | GWD | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02896 | hp1 | a0002 | c0003 | t0002 | g0005 | AFR | GWD | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02896 | hp2 | a0003 | c0006 | t0002 | g0063 | AFR | GWD | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02897 | hp2 | a0002 | c0003 | t0002 | g0005 | AFR | GWD | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ESN | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02965 | hp1 | a0005 | c0013 | t0009 | g0289 | AFR | ESN | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02965 | hp2 | a0002 | c0014 | t0006 | g0009 | AFR | ESN | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ESN | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02970 | hp2 | a0003 | c0006 | t0002 | g0001 | AFR | ESN | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ESN | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02976 | hp2 | a0002 | c0003 | t0002 | g0002 | AFR | ESN | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | MSL | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG03098 | hp2 | a0002 | c0014 | t0006 | g0088 | AFR | MSL | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG03130 | hp1 | a0002 | c0003 | t0002 | g0002 | AFR | ESN | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG03130 | hp2 | a0002 | c0024 | t0002 | g0290 | AFR | ESN | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG03139 | hp1 | a0004 | c0029 | t0002 | g0252 | AFR | ESN | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG03139 | hp2 | a0003 | c0006 | t0015 | g0064 | AFR | ESN | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0308 | AFR | ESN | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG03195 | hp2 | a0002 | c0003 | t0002 | g0004 | AFR | ESN | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG03209 | hp1 | a0002 | c0012 | t0010 | g0277 | AFR | MSL | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG03209 | hp2 | a0002 | c0003 | t0002 | g0300 | AFR | MSL | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG03225 | hp1 | a0002 | c0011 | t0002 | g0288 | AFR | MSL | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG03225 | hp2 | a0002 | c0003 | t0002 | g0297 | AFR | MSL | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG03453 | hp1 | a0002 | c0003 | t0002 | g0296 | AFR | MSL | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | MSL | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | MSL | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | MSL | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG03490 | hp2 | a0002 | c0021 | t0002 | g0013 | SAS | PJL | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG03492 | hp2 | a0002 | c0021 | t0002 | g0013 | SAS | PJL | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG03516 | hp1 | a0012 | c0025 | t0012 | g0292 | AFR | ESN | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG03516 | hp2 | a0002 | c0003 | t0002 | g0004 | AFR | ESN | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG03579 | hp1 | a0003 | c0006 | t0002 | g0062 | AFR | MSL | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG03579 | hp2 | a0002 | c0035 | t0002 | g0301 | AFR | MSL | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | STU | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0243 | SAS | STU | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | BEB | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | BEB | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | BEB | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | BEB | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG03927 | hp1 | a0002 | c0002 | t0002 | g0055 | SAS | BEB | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG03927 | hp2 | a0007 | c0018 | t0001 | g0118 | SAS | BEB | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0268 | SAS | BEB | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | BEB | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG04115 | hp1 | a0001 | c0001 | t0018 | g0245 | SAS | STU | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0256 | SAS | STU | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0270 | SAS | STU | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG04199 | hp2 | a0002 | c0007 | t0002 | g0152 | SAS | STU | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | STU | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | STU | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA18522 | hp1 | a0002 | c0020 | t0001 | g0056 | AFR | YRI | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | CHB | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA18612 | hp2 | a0001 | c0001 | t0013 | g0163 | EAS | CHB | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA18747 | hp1 | a0006 | c0023 | t0001 | g0136 | EAS | CHB | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA18747 | hp2 | a0002 | c0007 | t0002 | g0045 | EAS | CHB | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA18906 | hp1 | a0003 | c0006 | t0002 | g0001 | AFR | YRI | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA18906 | hp2 | a0013 | c0031 | t0002 | g0298 | AFR | YRI | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA18941 | hp2 | a0002 | c0007 | t0002 | g0195 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA18945 | hp1 | a0001 | c0001 | t0004 | g0130 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA18946 | hp1 | a0003 | c0015 | t0002 | g0079 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA18946 | hp2 | a0001 | c0001 | t0017 | g0148 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA18950 | hp2 | a0002 | c0002 | t0003 | g0040 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA18954 | hp1 | a0003 | c0004 | t0002 | g0066 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA18960 | hp1 | a0002 | c0002 | t0003 | g0038 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA18961 | hp1 | a0001 | c0001 | t0004 | g0129 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA18961 | hp2 | a0003 | c0004 | t0002 | g0077 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA18966 | hp1 | a0001 | c0009 | t0001 | g0199 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA18967 | hp2 | a0001 | c0009 | t0001 | g0015 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA18970 | hp1 | a0001 | c0005 | t0001 | g0022 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA18970 | hp2 | a0003 | c0004 | t0002 | g0071 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA18971 | hp1 | a0001 | c0005 | t0001 | g0026 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA18977 | hp2 | a0001 | c0001 | t0004 | g0140 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA18980 | hp2 | a0003 | c0004 | t0002 | g0007 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA18986 | hp2 | a0003 | c0004 | t0002 | g0067 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA18989 | hp1 | a0003 | c0015 | t0002 | g0069 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA18990 | hp2 | a0001 | c0005 | t0001 | g0029 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA18991 | hp1 | a0003 | c0004 | t0002 | g0081 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA18991 | hp2 | a0014 | c0033 | t0001 | g0255 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA18992 | hp2 | a0001 | c0005 | t0019 | g0030 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA18994 | hp2 | a0003 | c0004 | t0002 | g0078 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA18995 | hp1 | a0003 | c0004 | t0002 | g0082 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA18999 | hp2 | a0002 | c0007 | t0002 | g0157 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA19003 | hp1 | a0003 | c0004 | t0002 | g0074 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA19003 | hp2 | a0015 | c0027 | t0001 | g0306 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA19005 | hp1 | a0008 | c0019 | t0001 | g0210 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA19007 | hp2 | a0001 | c0009 | t0001 | g0015 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA19011 | hp1 | a0001 | c0001 | t0004 | g0126 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA19043 | hp1 | a0005 | c0013 | t0005 | g0281 | AFR | LWK | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA19043 | hp2 | a0002 | c0008 | t0008 | g0010 | AFR | LWK | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA19057 | hp1 | a0002 | c0002 | t0003 | g0020 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA19057 | hp2 | a0008 | c0019 | t0001 | g0244 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA19064 | hp1 | a0002 | c0002 | t0003 | g0032 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA19065 | hp2 | a0001 | c0009 | t0001 | g0223 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA19068 | hp1 | a0001 | c0005 | t0001 | g0027 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA19070 | hp1 | a0002 | c0007 | t0002 | g0266 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA19079 | hp1 | a0001 | c0005 | t0001 | g0024 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA19079 | hp2 | a0003 | c0004 | t0002 | g0068 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA19080 | hp1 | a0003 | c0004 | t0002 | g0072 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA19081 | hp1 | a0001 | c0005 | t0001 | g0025 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA19090 | hp1 | a0003 | c0004 | t0002 | g0080 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA19090 | hp2 | a0001 | c0005 | t0001 | g0028 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA19091 | hp1 | a0001 | c0001 | t0004 | g0139 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA19240 | hp1 | a0002 | c0003 | t0002 | g0299 | AFR | YRI | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA19240 | hp2 | a0002 | c0012 | t0002 | g0249 | AFR | YRI | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0262 | EUR | TSI | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0131 | EUR | TSI | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0155 | EUR | TSI | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0269 | EUR | TSI | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | GIH | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA20905 | hp2 | a0007 | c0018 | t0001 | g0250 | SAS | GIH | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG01123 | hp1 | a0002 | c0002 | t0002 | g0049 | AMR | CLM | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG01123 | hp2 | a0002 | c0003 | t0002 | g0018 | AMR | CLM | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02109 | hp1 | a0002 | c0008 | t0008 | g0010 | AFR | ACB | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02559 | hp1 | a0003 | c0016 | t0007 | g0294 | AFR | ACB | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG03471 | hp1 | a0002 | c0003 | t0002 | g0017 | AFR | MSL | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG03471 | hp2 | a0002 | c0008 | t0014 | g0097 | AFR | MSL | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG06807 | hp1 | a0002 | c0003 | t0002 | g0002 | AFR | USA | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
HG06807 | hp2 | a0002 | c0017 | t0001 | g0284 | AFR | USA | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA20300 | hp1 | a0003 | c0006 | t0002 | g0001 | AFR | USA | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
NA20300 | hp2 | a0002 | c0022 | t0002 | g0008 | AFR | USA | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0147 | REF | REF | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
homoSapiens | grch38p0 | a0002 | c0008 | t0008 | g0095 | REF | REF | ARHGEF16_chr1_3449665_3486113 | ARHGEF16 | chr1 | 3449665 | 3486113 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:3463193 | A | G | 1 | a0006 | 2 | HG00558.hp1 NA18747.hp1 |
missense_variant | MODERATE | c.109A>G | p.Met37Val | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 2/15 | 275/2822 | 109/2130 | 37/709 | chr1 | 3463193 | |||
chr1:3463209 | C | T | 1 | a0009 | 1 | HG00438.hp1 | missense_variant | MODERATE | c.125C>T | p.Pro42Leu | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 2/15 | 291/2822 | 125/2130 | 42/709 | chr1 | 3463209 | |||
chr1:3463266 | G | A | 1 | a0012 | 1 | HG03516.hp1 | missense_variant | MODERATE | c.182G>A | p.Arg61Gln | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 2/15 | 348/2822 | 182/2130 | 61/709 | chr1 | 3463266 | |||
chr1:3463493 | G | A | 2 | a0003 a0015 |
30 | HG01070.hp1 HG01081.hp1 HG01361.hp1 others(27): Show |
missense_variant | MODERATE | c.409G>A | p.Val137Met | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 2/15 | 575/2822 | 409/2130 | 137/709 | chr1 | 3463493 | |||
chr1:3469503 | T | G | 1 | a0007 | 2 | HG03927.hp2 NA20905.hp2 |
missense_variant | MODERATE | c.932T>G | p.Leu311Arg | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/15 | 1098/2822 | 932/2130 | 311/709 | chr1 | 3469503 | |||
chr1:3469508 | T | C | 1 | a0008 | 2 | NA19005.hp1 NA19057.hp2 |
missense_variant | MODERATE | c.937T>C | p.Ser313Pro | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/15 | 1103/2822 | 937/2130 | 313/709 | chr1 | 3469508 | |||
chr1:3473163 | C | T | 9 | a0001 a0005 a0006 others(6): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
missense_variant | MODERATE | c.1108C>T | p.His370Tyr | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 7/15 | 1274/2822 | 1108/2130 | 370/709 | chr1 | 3473163 | |||
chr1:3476001 | G | A | 1 | a0014 | 1 | NA18991.hp2 | missense_variant | MODERATE | c.1412G>A | p.Arg471Lys | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/15 | 1578/2822 | 1412/2130 | 471/709 | chr1 | 3476001 | |||
chr1:3478438 | T | C | 2 | a0005 a0011 |
5 | HG02055.hp2 HG02572.hp2 HG02895.hp1 others(2): Show |
missense_variant | MODERATE | c.1640T>C | p.Met547Thr | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 12/15 | 1806/2822 | 1640/2130 | 547/709 | chr1 | 3478438 | |||
chr1:3478612 | C | T | 1 | a0010 | 1 | HG01243.hp1 | missense_variant&splice_region_variant | MODERATE | c.1814C>T | p.Ala605Val | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 12/15 | 1980/2822 | 1814/2130 | 605/709 | chr1 | 3478612 | |||
chr1:3480498 | G | A | 1 | a0004 | 5 | HG00642.hp2 HG01515.hp1 HG02004.hp2 others(2): Show |
missense_variant | MODERATE | c.2041G>A | p.Glu681Lys | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 15/15 | 2207/2822 | 2041/2130 | 681/709 | chr1 | 3480498 | |||
chr1:3480534 | G | A | 2 | a0011 a0013 |
2 | HG02055.hp2 NA18906.hp2 |
missense_variant | MODERATE | c.2077G>A | p.Val693Met | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 15/15 | 2243/2822 | 2077/2130 | 693/709 | chr1 | 3480534 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:3463114 | G | A | 1 | a0002c0024 | 1 | HG03130.hp2 | synonymous_variant | LOW | c.30G>A | p.Leu10Leu | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 2/15 | 196/2822 | 30/2130 | 10/709 | chr1 | 3463114 | |||
chr1:3463432 | G | A | 1 | a0001c0009 | 4 | NA18966.hp1 NA18967.hp2 NA19007.hp2 others(1): Show |
synonymous_variant | LOW | c.348G>A | p.Glu116Glu | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 2/15 | 514/2822 | 348/2130 | 116/709 | chr1 | 3463432 | |||
chr1:3463435 | C | T | 1 | a0002c0035 | 1 | HG03579.hp2 | synonymous_variant | LOW | c.351C>T | p.Ala117Ala | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 2/15 | 517/2822 | 351/2130 | 117/709 | chr1 | 3463435 | |||
chr1:3463660 | G | A | 1 | a0003c0015 | 2 | NA18946.hp1 NA18989.hp1 |
synonymous_variant | LOW | c.576G>A | p.Pro192Pro | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 2/15 | 742/2822 | 576/2130 | 192/709 | chr1 | 3463660 | |||
chr1:3467334 | A | G | 28 | a0001c0001 a0001c0009 a0002c0003 others(25): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
synonymous_variant | LOW | c.801A>G | p.Pro267Pro | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 4/15 | 967/2822 | 801/2130 | 267/709 | chr1 | 3467334 | |||
chr1:3469525 | G | A | 1 | a0003c0006 | 8 | HG02647.hp2 HG02809.hp1 HG02896.hp2 others(5): Show |
synonymous_variant | LOW | c.954G>A | p.Ala318Ala | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/15 | 1120/2822 | 954/2130 | 318/709 | chr1 | 3469525 | |||
chr1:3473444 | G | A | 1 | a0002c0014 | 3 | HG02809.hp2 HG02965.hp2 HG03098.hp2 |
synonymous_variant | LOW | c.1227G>A | p.Pro409Pro | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 8/15 | 1393/2822 | 1227/2130 | 409/709 | chr1 | 3473444 | |||
chr1:3477877 | C | T | 8 | a0002c0003 a0002c0014 a0002c0022 others(5): Show |
28 | HG01123.hp2 HG01243.hp1 HG01261.hp1 others(25): Show |
splice_region_variant&synonymous_variant | LOW | c.1476C>T | p.Ser492Ser | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 11/15 | 1642/2822 | 1476/2130 | 492/709 | chr1 | 3477877 | |||
chr1:3477892 | T | C | 33 | a0001c0001 a0001c0005 a0001c0009 others(30): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
synonymous_variant | LOW | c.1491T>C | p.Ser497Ser | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 11/15 | 1657/2822 | 1491/2130 | 497/709 | chr1 | 3477892 | |||
chr1:3478424 | C | T | 1 | a0002c0021 | 2 | HG03490.hp2 HG03492.hp2 |
splice_region_variant&synonymous_variant | LOW | c.1626C>T | p.Ser542Ser | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 12/15 | 1792/2822 | 1626/2130 | 542/709 | chr1 | 3478424 | |||
chr1:3478475 | G | A | 14 | a0001c0001 a0001c0005 a0001c0009 others(11): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
synonymous_variant | LOW | c.1677G>A | p.Val559Val | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 12/15 | 1843/2822 | 1677/2130 | 559/709 | chr1 | 3478475 | |||
chr1:3478610 | C | A | 2 | a0002c0002 a0002c0007 |
35 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(32): Show |
splice_region_variant&synonymous_variant | LOW | c.1812C>A | p.Ser604Ser | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 12/15 | 1978/2822 | 1812/2130 | 604/709 | chr1 | 3478610 | |||
chr1:3479532 | G | A | 1 | a0002c0014 | 3 | HG02809.hp2 HG02965.hp2 HG03098.hp2 |
synonymous_variant | LOW | c.1830G>A | p.Arg610Arg | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 13/15 | 1996/2822 | 1830/2130 | 610/709 | chr1 | 3479532 | |||
chr1:3480485 | G | A | 1 | a0002c0014 | 3 | HG02809.hp2 HG02965.hp2 HG03098.hp2 |
synonymous_variant | LOW | c.2028G>A | p.Thr676Thr | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 15/15 | 2194/2822 | 2028/2130 | 676/709 | chr1 | 3480485 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:3454705 | G | C | 4 | a0002c0012t0010 a0002c0014t0006 a0005c0013t0005 others(1): Show |
8 | HG02055.hp2 HG02572.hp2 HG02809.hp2 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-126G>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/15 | 8380 | chr1 | 3454705 | ||||||
chr1:3454783 | C | T | 1 | a0001c0005t0019 | 1 | NA18992.hp2 | 5_prime_UTR_variant | MODIFIER | c.-48C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/15 | 8302 | chr1 | 3454783 | ||||||
chr1:3463078 | G | A | 1 | a0002c0012t0010 | 1 | HG03209.hp1 | 5_prime_UTR_variant | MODIFIER | c.-7G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 2/15 | 7 | chr1 | 3463078 | ||||||
chr1:3480605 | G | A | 1 | a0001c0001t0011 | 1 | HG00597.hp1 | 3_prime_UTR_variant | MODIFIER | c.*18G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 15/15 | 18 | chr1 | 3480605 | ||||||
chr1:3480624 | T | C | 52 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0011 others(49): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
3_prime_UTR_variant | MODIFIER | c.*37T>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 15/15 | 37 | chr1 | 3480624 | ||||||
chr1:3480747 | C | A | 1 | a0012c0025t0012 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*160C>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 15/15 | 160 | chr1 | 3480747 | ||||||
chr1:3480785 | G | A | 1 | a0001c0001t0013 | 1 | NA18612.hp2 | 3_prime_UTR_variant | MODIFIER | c.*198G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 15/15 | 198 | chr1 | 3480785 | ||||||
chr1:3480851 | C | CCT | 48 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0011 others(45): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
3_prime_UTR_variant | MODIFIER | c.*266_*267dupTC | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 15/15 | 268 | INFO_REALIGN_3_PRIME | chr1 | 3480851 | |||||
chr1:3480883 | C | T | 1 | a0001c0001t0018 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*296C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 15/15 | 296 | chr1 | 3480883 | ||||||
chr1:3480891 | G | A | 22 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0011 others(19): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
3_prime_UTR_variant | MODIFIER | c.*304G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 15/15 | 304 | chr1 | 3480891 | ||||||
chr1:3480950 | C | T | 1 | a0001c0001t0004 | 5 | NA18945.hp1 NA18961.hp1 NA18977.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*363C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 15/15 | 363 | chr1 | 3480950 | ||||||
chr1:3480976 | C | T | 1 | a0002c0014t0006 | 3 | HG02809.hp2 HG02965.hp2 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*389C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 15/15 | 389 | chr1 | 3480976 | ||||||
chr1:3481000 | C | T | 21 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0011 others(18): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
3_prime_UTR_variant | MODIFIER | c.*413C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 15/15 | 413 | chr1 | 3481000 | ||||||
chr1:3481038 | C | T | 1 | a0001c0001t0016 | 1 | HG02273.hp2 | 3_prime_UTR_variant | MODIFIER | c.*451C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 15/15 | 451 | chr1 | 3481038 | ||||||
chr1:3481053 | G | A | 4 | a0002c0011t0009 a0005c0013t0005 a0005c0013t0009 others(1): Show |
6 | HG02055.hp2 HG02572.hp2 HG02630.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*466G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 15/15 | 466 | chr1 | 3481053 | ||||||
chr1:3481106 | C | G | 1 | a0002c0002t0003 | 10 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*519C>G | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 15/15 | 519 | chr1 | 3481106 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:3454830 | T | C | 1 | a0001c0001t0001g0019 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-20+19T>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3454830 | |||||||
chr1:3454845 | G | A | 37 | a0001c0001t0001g0023 a0001c0005t0001g0022 a0001c0005t0001g0024 others(34): Show |
38 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.-20+34G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3454845 | |||||||
chr1:3454906 | G | C | 29 | a0001c0001t0001g0061 a0002c0020t0001g0056 a0003c0004t0002g0007 others(26): Show |
33 | HG00639.hp2 HG00642.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.-20+95G>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3454906 | |||||||
chr1:3454956 | C | T | 1 | a0001c0001t0001g0309 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-20+145C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3454956 | |||||||
chr1:3455007 | G | T | 1 | a0001c0001t0001g0308 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-20+196G>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3455007 | |||||||
chr1:3455047 | C | A | 1 | a0002c0022t0002g0008 | 2 | HG02451.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-20+236C>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3455047 | |||||||
chr1:3455048 | C | T | 23 | a0003c0004t0002g0007 a0003c0004t0002g0066 a0003c0004t0002g0067 others(20): Show |
27 | HG01070.hp1 HG01081.hp1 HG01361.hp1 others(24): Show |
intron_variant | MODIFIER | c.-20+237C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3455048 | |||||||
chr1:3455177 | G | T | 6 | a0001c0001t0001g0302 a0001c0001t0001g0303 a0001c0001t0001g0304 others(3): Show |
6 | NA18983.hp2 NA18994.hp1 NA18999.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20+366G>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3455177 | |||||||
chr1:3455223 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-20+412G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3455223 | |||||||
chr1:3455224 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-20+413G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3455224 | |||||||
chr1:3455298 | T | A | 37 | a0001c0001t0001g0023 a0001c0005t0001g0022 a0001c0005t0001g0024 others(34): Show |
38 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.-20+487T>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3455298 | |||||||
chr1:3455299 | C | A | 37 | a0001c0001t0001g0023 a0001c0005t0001g0022 a0001c0005t0001g0024 others(34): Show |
38 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.-20+488C>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3455299 | |||||||
chr1:3455391 | G | A | 4 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(1): Show |
4 | HG02723.hp1 HG02976.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+580G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3455391 | |||||||
chr1:3455417 | G | C | 7 | a0002c0014t0006g0009 a0002c0014t0006g0088 a0002c0020t0001g0056 others(4): Show |
8 | HG00642.hp2 HG01515.hp1 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.-20+606G>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3455417 | |||||||
chr1:3455436 | G | A | 1 | a0002c0002t0003g0020 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-20+625G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3455436 | |||||||
chr1:3455528 | T | C | 1 | a0002c0002t0001g0021 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-20+717T>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3455528 | |||||||
chr1:3455548 | G | C | 1 | a0001c0001t0001g0089 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-20+737G>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3455548 | |||||||
chr1:3455594 | T | C | 1 | a0002c0012t0001g0090 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-20+783T>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3455594 | |||||||
chr1:3455642 | A | T | 1 | a0002c0035t0002g0301 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-20+831A>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3455642 | |||||||
chr1:3455660 | C | T | 1 | a0003c0004t0002g0082 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-20+849C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3455660 | |||||||
chr1:3455668 | C | T | 37 | a0001c0001t0001g0023 a0001c0005t0001g0022 a0001c0005t0001g0024 others(34): Show |
38 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.-20+857C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3455668 | |||||||
chr1:3455907 | A | C | 98 | a0001c0001t0001g0023 a0001c0005t0001g0022 a0001c0005t0001g0024 others(95): Show |
113 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.-20+1096A>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3455907 | |||||||
chr1:3456101 | T | G | 4 | a0005c0013t0005g0279 a0005c0013t0005g0280 a0005c0013t0005g0281 others(1): Show |
4 | HG02055.hp2 HG02572.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+1290T>G | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3456101 | |||||||
chr1:3456105 | T | C | 7 | a0002c0014t0006g0009 a0002c0014t0006g0088 a0002c0020t0001g0056 others(4): Show |
8 | HG00642.hp2 HG01515.hp1 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.-20+1294T>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3456105 | |||||||
chr1:3456191 | C | A | 3 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 |
3 | HG00099.hp1 HG00140.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.-20+1380C>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3456191 | |||||||
chr1:3456293 | A | G | 5 | a0002c0020t0001g0056 a0004c0010t0002g0057 a0004c0010t0002g0058 others(2): Show |
5 | HG00642.hp2 HG01515.hp1 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20+1482A>G | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3456293 | |||||||
chr1:3456361 | G | A | 1 | a0002c0012t0001g0090 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-20+1550G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3456361 | |||||||
chr1:3456539 | G | A | 1 | a0002c0012t0001g0090 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-20+1728G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3456539 | |||||||
chr1:3456753 | G | T | 1 | a0002c0002t0002g0055 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-20+1942G>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3456753 | |||||||
chr1:3456911 | C | T | 23 | a0003c0004t0002g0007 a0003c0004t0002g0066 a0003c0004t0002g0067 others(20): Show |
27 | HG01070.hp1 HG01081.hp1 HG01361.hp1 others(24): Show |
intron_variant | MODIFIER | c.-20+2100C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3456911 | |||||||
chr1:3457047 | C | G | 5 | a0002c0020t0001g0056 a0004c0010t0002g0057 a0004c0010t0002g0058 others(2): Show |
5 | HG00642.hp2 HG01515.hp1 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20+2236C>G | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3457047 | |||||||
chr1:3457303 | C | T | 1 | a0004c0010t0002g0060 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-20+2492C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3457303 | |||||||
chr1:3457330 | C | T | 1 | a0001c0001t0001g0278 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-20+2519C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3457330 | |||||||
chr1:3457403 | A | G | 99 | a0001c0001t0001g0023 a0001c0005t0001g0022 a0001c0005t0001g0024 others(96): Show |
114 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.-20+2592A>G | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3457403 | |||||||
chr1:3457413 | C | T | 2 | a0002c0003t0002g0018 a0002c0003t0002g0300 |
3 | HG01123.hp2 HG02258.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-20+2602C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3457413 | |||||||
chr1:3457453 | C | T | 25 | a0002c0003t0002g0002 a0002c0003t0002g0004 a0002c0003t0002g0005 others(22): Show |
34 | HG01109.hp2 HG01123.hp2 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.-20+2642C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3457453 | |||||||
chr1:3457454 | G | A | 23 | a0003c0004t0002g0007 a0003c0004t0002g0066 a0003c0004t0002g0067 others(20): Show |
27 | HG01070.hp1 HG01081.hp1 HG01361.hp1 others(24): Show |
intron_variant | MODIFIER | c.-20+2643G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3457454 | |||||||
chr1:3457589 | GC | G | 4 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(1): Show |
4 | HG02723.hp1 HG02976.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+2779delC | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3457589 | |||||||
chr1:3457594 | G | A | 23 | a0003c0004t0002g0007 a0003c0004t0002g0066 a0003c0004t0002g0067 others(20): Show |
27 | HG01070.hp1 HG01081.hp1 HG01361.hp1 others(24): Show |
intron_variant | MODIFIER | c.-20+2783G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3457594 | |||||||
chr1:3457698 | T | C | 6 | a0002c0011t0002g0286 a0002c0011t0002g0287 a0002c0011t0002g0288 others(3): Show |
6 | HG01243.hp2 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20+2887T>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3457698 | |||||||
chr1:3457796 | C | T | 205 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(202): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.-20+2985C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3457796 | |||||||
chr1:3457820 | T | A | 205 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(202): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.-20+3009T>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3457820 | |||||||
chr1:3458379 | A | G | 7 | a0002c0014t0006g0009 a0002c0014t0006g0088 a0002c0020t0001g0056 others(4): Show |
8 | HG00642.hp2 HG01515.hp1 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.-20+3568A>G | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3458379 | |||||||
chr1:3458388 | G | A | 1 | a0002c0020t0001g0056 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-20+3577G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3458388 | |||||||
chr1:3458511 | G | A | 1 | a0001c0001t0001g0098 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-20+3700G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3458511 | |||||||
chr1:3458593 | C | A | 2 | a0001c0001t0001g0099 a0001c0001t0001g0100 |
2 | HG02622.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-20+3782C>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3458593 | |||||||
chr1:3458617 | C | T | 37 | a0001c0001t0001g0023 a0001c0005t0001g0022 a0001c0005t0001g0024 others(34): Show |
38 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.-20+3806C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3458617 | |||||||
chr1:3458654 | A | G | 1 | a0002c0012t0001g0090 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-20+3843A>G | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3458654 | |||||||
chr1:3458787 | C | T | 1 | a0002c0020t0001g0056 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-20+3976C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3458787 | |||||||
chr1:3458804 | A | G | 4 | a0004c0010t0002g0057 a0004c0010t0002g0058 a0004c0010t0002g0059 others(1): Show |
4 | HG00642.hp2 HG01515.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20+3993A>G | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3458804 | |||||||
chr1:3458931 | A | G | 1 | a0002c0012t0001g0090 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-20+4120A>G | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3458931 | |||||||
chr1:3459159 | C | G | 5 | a0002c0020t0001g0056 a0004c0010t0002g0057 a0004c0010t0002g0058 others(2): Show |
5 | HG00642.hp2 HG01515.hp1 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.-19-3907C>G | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3459159 | |||||||
chr1:3459160 | G | A | 1 | a0002c0012t0010g0277 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-19-3906G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3459160 | |||||||
chr1:3459208 | C | T | 2 | a0002c0014t0006g0009 a0002c0014t0006g0088 |
3 | HG02809.hp2 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-19-3858C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3459208 | |||||||
chr1:3459255 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-19-3811C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3459255 | |||||||
chr1:3459369 | C | T | 18 | a0003c0004t0002g0007 a0003c0004t0002g0066 a0003c0004t0002g0067 others(15): Show |
19 | HG01070.hp1 HG01081.hp1 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.-19-3697C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3459369 | |||||||
chr1:3459420 | CAG | C | 13 | a0002c0003t0002g0002 a0002c0003t0002g0004 a0002c0003t0002g0005 others(10): Show |
22 | HG01123.hp2 HG01243.hp1 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.-19-3645_-19-3644d others(4): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3459420 | |||||||
chr1:3459574 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-19-3492G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3459574 | |||||||
chr1:3459619 | C | T | 1 | a0001c0001t0001g0276 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-19-3447C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3459619 | |||||||
chr1:3459629 | C | T | 7 | a0002c0014t0006g0009 a0002c0014t0006g0088 a0002c0020t0001g0056 others(4): Show |
8 | HG00642.hp2 HG01515.hp1 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.-19-3437C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3459629 | |||||||
chr1:3459768 | G | C | 2 | a0002c0017t0001g0283 a0002c0017t0001g0284 |
2 | HG01243.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-19-3298G>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3459768 | |||||||
chr1:3459778 | C | T | 1 | a0001c0001t0001g0275 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-19-3288C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3459778 | |||||||
chr1:3459808 | G | T | 1 | a0003c0004t0002g0081 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-19-3258G>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3459808 | |||||||
chr1:3459841 | G | A | 5 | a0005c0013t0005g0279 a0005c0013t0005g0280 a0005c0013t0005g0281 others(2): Show |
5 | HG02055.hp2 HG02572.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19-3225G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3459841 | |||||||
chr1:3459850 | G | A | 1 | a0002c0014t0006g0088 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-19-3216G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3459850 | |||||||
chr1:3459934 | G | A | 1 | a0002c0028t0002g0094 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-19-3132G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3459934 | |||||||
chr1:3459969 | T | C | 7 | a0002c0014t0006g0009 a0002c0014t0006g0088 a0002c0020t0001g0056 others(4): Show |
8 | HG00642.hp2 HG01515.hp1 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.-19-3097T>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3459969 | |||||||
chr1:3459995 | A | ATGCTAAG others(14): Show |
1 | a0004c0010t0002g0059 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-19-3068_-19-3048d others(23): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 3459995 | ||||||
chr1:3460099 | C | T | 1 | a0002c0020t0001g0056 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-19-2967C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3460099 | |||||||
chr1:3460112 | C | A | 2 | a0001c0001t0001g0102 a0001c0001t0001g0103 |
2 | HG03017.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.-19-2954C>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3460112 | |||||||
chr1:3460174 | C | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0274 |
3 | HG01069.hp1 HG01070.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.-19-2892C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3460174 | |||||||
chr1:3460175 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-19-2891G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3460175 | |||||||
chr1:3460265 | G | T | 3 | a0003c0016t0002g0293 a0003c0016t0007g0294 a0012c0025t0012g0292 |
3 | HG02451.hp2 HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-19-2801G>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3460265 | |||||||
chr1:3460334 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-19-2732G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3460334 | |||||||
chr1:3460559 | C | T | 7 | a0002c0014t0006g0009 a0002c0014t0006g0088 a0002c0020t0001g0056 others(4): Show |
8 | HG00642.hp2 HG01515.hp1 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.-19-2507C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3460559 | |||||||
chr1:3460560 | G | A | 5 | a0005c0013t0005g0279 a0005c0013t0005g0280 a0005c0013t0005g0281 others(2): Show |
5 | HG02055.hp2 HG02572.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19-2506G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3460560 | |||||||
chr1:3460567 | C | T | 1 | a0001c0001t0001g0273 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-19-2499C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3460567 | |||||||
chr1:3460614 | G | A | 1 | a0001c0005t0001g0022 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-19-2452G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3460614 | |||||||
chr1:3460724 | G | A | 23 | a0003c0004t0002g0007 a0003c0004t0002g0066 a0003c0004t0002g0067 others(20): Show |
27 | HG01070.hp1 HG01081.hp1 HG01361.hp1 others(24): Show |
intron_variant | MODIFIER | c.-19-2342G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3460724 | |||||||
chr1:3460747 | C | T | 1 | a0001c0001t0001g0272 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-19-2319C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3460747 | |||||||
chr1:3460752 | G | C | 1 | a0001c0001t0001g0098 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-19-2314G>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3460752 | |||||||
chr1:3460779 | T | C | 99 | a0001c0001t0001g0023 a0001c0005t0001g0022 a0001c0005t0001g0024 others(96): Show |
114 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.-19-2287T>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3460779 | |||||||
chr1:3460878 | T | C | 37 | a0001c0001t0001g0023 a0001c0005t0001g0022 a0001c0005t0001g0024 others(34): Show |
38 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.-19-2188T>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3460878 | |||||||
chr1:3460934 | TGAGCAGG others(4): Show |
T | 26 | a0002c0003t0002g0002 a0002c0003t0002g0004 a0002c0003t0002g0005 others(23): Show |
35 | HG01109.hp2 HG01123.hp2 HG01243.hp1 others(32): Show |
intron_variant | MODIFIER | c.-19-2128_-19-2118d others(13): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 3460934 | ||||||
chr1:3461051 | G | A | 6 | a0001c0001t0001g0011 a0001c0001t0001g0089 a0001c0001t0001g0099 others(3): Show |
7 | HG01167.hp2 HG02622.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-19-2015G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3461051 | |||||||
chr1:3461125 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-19-1941C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3461125 | |||||||
chr1:3461207 | A | C | 3 | a0002c0003t0002g0299 a0002c0022t0002g0008 a0013c0031t0002g0298 |
4 | HG02451.hp1 NA18906.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19-1859A>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3461207 | |||||||
chr1:3461630 | A | G | 2 | a0002c0014t0006g0009 a0002c0014t0006g0088 |
3 | HG02809.hp2 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-19-1436A>G | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3461630 | |||||||
chr1:3461653 | C | T | 3 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 |
3 | HG03942.hp1 HG04199.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.-19-1413C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3461653 | |||||||
chr1:3461747 | G | A | 2 | a0001c0001t0001g0101 a0001c0001t0001g0108 |
2 | HG02280.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.-19-1319G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3461747 | |||||||
chr1:3461768 | C | T | 1 | a0001c0001t0001g0267 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-19-1298C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3461768 | |||||||
chr1:3461847 | G | A | 2 | a0002c0014t0006g0009 a0002c0014t0006g0088 |
3 | HG02809.hp2 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-19-1219G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3461847 | |||||||
chr1:3461960 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-19-1106G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3461960 | |||||||
chr1:3461979 | T | G | 1 | a0005c0013t0005g0279 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-19-1087T>G | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3461979 | |||||||
chr1:3462023 | G | A | 1 | a0001c0001t0001g0098 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-19-1043G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3462023 | |||||||
chr1:3462066 | C | G | 9 | a0002c0011t0002g0286 a0002c0011t0002g0287 a0002c0011t0002g0288 others(6): Show |
9 | HG01109.hp2 HG02451.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.-19-1000C>G | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3462066 | |||||||
chr1:3462090 | G | A | 1 | a0002c0017t0001g0283 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-19-976G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3462090 | |||||||
chr1:3462099 | G | A | 2 | a0002c0014t0006g0009 a0002c0014t0006g0088 |
3 | HG02809.hp2 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-19-967G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3462099 | |||||||
chr1:3462418 | GGGCTCGG others(3): Show |
G | 1 | a0004c0010t0002g0059 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-19-645_-19-636del others(10): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 3462418 | ||||||
chr1:3462760 | A | G | 2 | a0002c0014t0006g0009 a0002c0014t0006g0088 |
3 | HG02809.hp2 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-19-306A>G | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3462760 | |||||||
chr1:3462821 | A | C | 38 | a0001c0001t0001g0023 a0001c0005t0001g0022 a0001c0005t0001g0024 others(35): Show |
39 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.-19-245A>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3462821 | |||||||
chr1:3462967 | G | A | 2 | a0002c0014t0006g0009 a0002c0014t0006g0088 |
3 | HG02809.hp2 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-19-99G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 1/14 | chr1 | 3462967 | |||||||
chr1:3463746 | G | A | 5 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(2): Show |
5 | HG00621.hp1 HG02027.hp1 NA18944.hp2 others(2): Show |
intron_variant | MODIFIER | c.588+74G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 2/14 | chr1 | 3463746 | |||||||
chr1:3463756 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.588+84G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 2/14 | chr1 | 3463756 | |||||||
chr1:3463773 | G | A | 23 | a0003c0004t0002g0007 a0003c0004t0002g0066 a0003c0004t0002g0067 others(20): Show |
27 | HG01070.hp1 HG01081.hp1 HG01361.hp1 others(24): Show |
intron_variant | MODIFIER | c.588+101G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 2/14 | chr1 | 3463773 | |||||||
chr1:3463804 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.588+132G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 2/14 | chr1 | 3463804 | |||||||
chr1:3463898 | G | A | 22 | a0002c0003t0002g0002 a0002c0003t0002g0004 a0002c0003t0002g0005 others(19): Show |
31 | HG01109.hp2 HG01123.hp2 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.588+226G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 2/14 | chr1 | 3463898 | |||||||
chr1:3463941 | G | A | 23 | a0003c0004t0002g0007 a0003c0004t0002g0066 a0003c0004t0002g0067 others(20): Show |
27 | HG01070.hp1 HG01081.hp1 HG01361.hp1 others(24): Show |
intron_variant | MODIFIER | c.588+269G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 2/14 | chr1 | 3463941 | |||||||
chr1:3463960 | C | G | 2 | a0002c0014t0006g0009 a0002c0014t0006g0088 |
3 | HG02809.hp2 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.588+288C>G | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 2/14 | chr1 | 3463960 | |||||||
chr1:3463976 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.588+304G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 2/14 | chr1 | 3463976 | |||||||
chr1:3463981 | C | T | 1 | a0001c0001t0001g0278 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.588+309C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 2/14 | chr1 | 3463981 | |||||||
chr1:3463991 | G | T | 1 | a0001c0001t0001g0265 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.588+319G>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 2/14 | chr1 | 3463991 | |||||||
chr1:3463993 | C | T | 10 | a0001c0005t0001g0053 a0002c0002t0002g0006 a0002c0002t0002g0046 others(7): Show |
11 | HG01081.hp2 HG01123.hp1 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.588+321C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 2/14 | chr1 | 3463993 | |||||||
chr1:3464031 | G | A | 3 | a0002c0011t0009g0285 a0002c0017t0001g0283 a0002c0017t0001g0284 |
3 | HG01243.hp2 HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.588+359G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 2/14 | chr1 | 3464031 | |||||||
chr1:3464151 | CTG | C | 194 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(191): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.588+481_588+482del others(2): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 3464151 | ||||||
chr1:3464155 | A | T | 1 | a0002c0002t0003g0020 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.588+483A>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 2/14 | chr1 | 3464155 | |||||||
chr1:3464245 | ACTGCATG others(10): Show |
A | 1 | a0002c0002t0001g0021 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.588+574_588+590del others(17): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 2/14 | chr1 | 3464245 | |||||||
chr1:3464282 | C | T | 6 | a0002c0035t0002g0301 a0005c0013t0005g0279 a0005c0013t0005g0280 others(3): Show |
6 | HG02055.hp2 HG02572.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.588+610C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 2/14 | chr1 | 3464282 | |||||||
chr1:3464418 | A | G | 2 | a0002c0014t0006g0009 a0002c0014t0006g0088 |
3 | HG02809.hp2 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.588+746A>G | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 2/14 | chr1 | 3464418 | |||||||
chr1:3464419 | C | G | 3 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 |
3 | HG03942.hp1 HG04199.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.588+747C>G | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 2/14 | chr1 | 3464419 | |||||||
chr1:3464475 | G | A | 1 | a0001c0001t0001g0110 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.588+803G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 2/14 | chr1 | 3464475 | |||||||
chr1:3464548 | G | A | 2 | a0003c0004t0002g0066 a0003c0004t0002g0067 |
2 | NA18954.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.588+876G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 2/14 | chr1 | 3464548 | |||||||
chr1:3464553 | C | T | 1 | a0014c0033t0001g0255 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.588+881C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 2/14 | chr1 | 3464553 | |||||||
chr1:3464592 | C | T | 4 | a0001c0001t0001g0253 a0001c0001t0001g0254 a0002c0014t0006g0009 others(1): Show |
5 | HG02809.hp2 HG02965.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.588+920C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 2/14 | chr1 | 3464592 | |||||||
chr1:3464695 | C | T | 1 | a0001c0001t0001g0272 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.588+1023C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 2/14 | chr1 | 3464695 | |||||||
chr1:3464808 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.588+1136G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 2/14 | chr1 | 3464808 | |||||||
chr1:3464925 | C | T | 13 | a0002c0003t0002g0002 a0002c0003t0002g0004 a0002c0003t0002g0005 others(10): Show |
22 | HG01123.hp2 HG01243.hp1 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.589-1223C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 2/14 | chr1 | 3464925 | |||||||
chr1:3464926 | G | A | 37 | a0001c0001t0001g0023 a0001c0005t0001g0022 a0001c0005t0001g0024 others(34): Show |
38 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.589-1222G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 2/14 | chr1 | 3464926 | |||||||
chr1:3465023 | C | T | 27 | a0001c0001t0001g0023 a0001c0005t0001g0022 a0001c0005t0001g0024 others(24): Show |
27 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(24): Show |
intron_variant | MODIFIER | c.589-1125C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 2/14 | chr1 | 3465023 | |||||||
chr1:3465134 | G | A | 31 | a0002c0012t0010g0277 a0003c0004t0002g0007 a0003c0004t0002g0066 others(28): Show |
35 | HG01070.hp1 HG01081.hp1 HG01361.hp1 others(32): Show |
intron_variant | MODIFIER | c.589-1014G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 2/14 | chr1 | 3465134 | |||||||
chr1:3465224 | C | T | 1 | a0004c0029t0002g0252 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.589-924C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 2/14 | chr1 | 3465224 | |||||||
chr1:3465571 | C | T | 36 | a0001c0005t0001g0022 a0001c0005t0001g0024 a0001c0005t0001g0025 others(33): Show |
37 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.589-577C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 2/14 | chr1 | 3465571 | |||||||
chr1:3465594 | CG | C | 210 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(207): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.589-551delG | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 3465594 | ||||||
chr1:3465616 | G | T | 209 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(206): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.589-532G>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 2/14 | chr1 | 3465616 | |||||||
chr1:3465641 | G | A | 1 | a0002c0003t0002g0295 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.589-507G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 2/14 | chr1 | 3465641 | |||||||
chr1:3465704 | G | A | 33 | a0001c0005t0001g0022 a0001c0005t0001g0024 a0001c0005t0001g0025 others(30): Show |
34 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.589-444G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 2/14 | chr1 | 3465704 | |||||||
chr1:3465704 | G | C | 43 | a0001c0001t0001g0019 a0001c0001t0001g0061 a0001c0001t0001g0091 others(40): Show |
43 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.589-444G>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 2/14 | chr1 | 3465704 | |||||||
chr1:3465756 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.589-392G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 2/14 | chr1 | 3465756 | |||||||
chr1:3465766 | G | C | 33 | a0002c0012t0001g0090 a0002c0014t0006g0009 a0002c0014t0006g0088 others(30): Show |
38 | HG01070.hp1 HG01081.hp1 HG01361.hp1 others(35): Show |
intron_variant | MODIFIER | c.589-382G>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 2/14 | chr1 | 3465766 | |||||||
chr1:3465781 | G | C | 1 | a0002c0011t0009g0285 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.589-367G>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 2/14 | chr1 | 3465781 | |||||||
chr1:3465794 | G | T | 1 | a0002c0003t0002g0300 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.589-354G>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 2/14 | chr1 | 3465794 | |||||||
chr1:3466219 | C | T | 2 | a0002c0008t0007g0096 a0002c0008t0014g0097 |
2 | HG01884.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.634+26C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 3/14 | chr1 | 3466219 | |||||||
chr1:3466350 | C | T | 1 | a0002c0012t0002g0291 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.634+157C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 3/14 | chr1 | 3466350 | |||||||
chr1:3466370 | AGTCTAGA others(3): Show |
A | 1 | a0002c0020t0001g0056 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.634+188_634+197del others(10): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 3466370 | ||||||
chr1:3466397 | T | C | 1 | a0001c0001t0001g0149 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.634+204T>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 3/14 | chr1 | 3466397 | |||||||
chr1:3466474 | G | A | 47 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0083 others(44): Show |
49 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.634+281G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 3/14 | chr1 | 3466474 | |||||||
chr1:3466531 | G | A | 1 | a0001c0001t0001g0185 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.634+338G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 3/14 | chr1 | 3466531 | |||||||
chr1:3466543 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.634+350C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 3/14 | chr1 | 3466543 | |||||||
chr1:3466613 | G | A | 36 | a0001c0005t0001g0022 a0001c0005t0001g0024 a0001c0005t0001g0025 others(33): Show |
37 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.634+420G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 3/14 | chr1 | 3466613 | |||||||
chr1:3466632 | G | A | 2 | a0002c0014t0006g0009 a0002c0014t0006g0088 |
3 | HG02809.hp2 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.634+439G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 3/14 | chr1 | 3466632 | |||||||
chr1:3466633 | G | A | 8 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0188 others(5): Show |
8 | HG00735.hp1 HG01069.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.634+440G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 3/14 | chr1 | 3466633 | |||||||
chr1:3466705 | G | C | 8 | a0001c0005t0001g0022 a0001c0005t0001g0024 a0001c0005t0001g0025 others(5): Show |
8 | NA18970.hp1 NA18971.hp1 NA18990.hp2 others(5): Show |
intron_variant | MODIFIER | c.635-463G>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 3/14 | chr1 | 3466705 | |||||||
chr1:3466722 | G | A | 35 | a0001c0005t0001g0022 a0001c0005t0001g0024 a0001c0005t0001g0025 others(32): Show |
36 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.635-446G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 3/14 | chr1 | 3466722 | |||||||
chr1:3466734 | G | A | 2 | a0002c0014t0006g0009 a0002c0014t0006g0088 |
3 | HG02809.hp2 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.635-434G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 3/14 | chr1 | 3466734 | |||||||
chr1:3466737 | G | C | 1 | a0001c0001t0001g0150 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.635-431G>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 3/14 | chr1 | 3466737 | |||||||
chr1:3466791 | G | A | 3 | a0002c0011t0002g0286 a0002c0011t0002g0287 a0002c0011t0002g0288 |
3 | HG02717.hp1 HG02723.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.635-377G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 3/14 | chr1 | 3466791 | |||||||
chr1:3466827 | T | C | 1 | a0001c0001t0001g0193 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.635-341T>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 3/14 | chr1 | 3466827 | |||||||
chr1:3466839 | GGGGTACC others(31): Show |
G | 1 | a0001c0001t0017g0148 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.635-327_635-290del others(38): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 3466839 | ||||||
chr1:3466912 | A | G | 1 | a0001c0001t0001g0264 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.635-256A>G | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 3/14 | chr1 | 3466912 | |||||||
chr1:3467029 | G | T | 208 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(205): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.635-139G>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 3/14 | chr1 | 3467029 | |||||||
chr1:3467101 | G | A | 206 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(203): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.635-67G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 3/14 | chr1 | 3467101 | |||||||
chr1:3467372 | A | G | 1 | a0012c0025t0012g0292 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.804+35A>G | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 4/14 | chr1 | 3467372 | |||||||
chr1:3467429 | C | G | 2 | a0003c0016t0002g0293 a0003c0016t0007g0294 |
2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.804+92C>G | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 4/14 | chr1 | 3467429 | |||||||
chr1:3467486 | G | A | 1 | a0003c0004t0002g0068 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.804+149G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 4/14 | chr1 | 3467486 | |||||||
chr1:3467488 | C | T | 5 | a0004c0010t0002g0057 a0004c0010t0002g0058 a0004c0010t0002g0059 others(2): Show |
5 | HG00642.hp2 HG01515.hp1 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.804+151C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 4/14 | chr1 | 3467488 | |||||||
chr1:3467571 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.804+234G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 4/14 | chr1 | 3467571 | |||||||
chr1:3467626 | C | A | 1 | a0001c0001t0001g0194 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.804+289C>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 4/14 | chr1 | 3467626 | |||||||
chr1:3467665 | G | A | 1 | a0002c0008t0007g0096 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.804+328G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 4/14 | chr1 | 3467665 | |||||||
chr1:3467667 | A | G | 211 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(208): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.804+330A>G | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 4/14 | chr1 | 3467667 | |||||||
chr1:3467795 | C | CCCGGCAT others(18): Show |
1 | a0001c0001t0001g0186 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.804+459_804+483dup others(25): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 3467795 | ||||||
chr1:3467811 | A | G | 13 | a0002c0003t0002g0002 a0002c0003t0002g0004 a0002c0003t0002g0005 others(10): Show |
22 | HG01123.hp2 HG01243.hp1 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.804+474A>G | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 4/14 | chr1 | 3467811 | |||||||
chr1:3467853 | A | C | 2 | a0001c0001t0001g0262 a0001c0001t0001g0263 |
2 | HG00642.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.804+516A>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 4/14 | chr1 | 3467853 | |||||||
chr1:3467864 | A | C | 1 | a0001c0001t0001g0248 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.804+527A>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 4/14 | chr1 | 3467864 | |||||||
chr1:3467866 | C | T | 1 | a0001c0001t0001g0275 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.804+529C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 4/14 | chr1 | 3467866 | |||||||
chr1:3467885 | G | A | 1 | a0002c0002t0003g0031 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.804+548G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 4/14 | chr1 | 3467885 | |||||||
chr1:3468013 | T | A | 1 | a0002c0007t0002g0152 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.804+676T>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 4/14 | chr1 | 3468013 | |||||||
chr1:3468042 | A | G | 209 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(206): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.804+705A>G | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 4/14 | chr1 | 3468042 | |||||||
chr1:3468111 | CTCCTGCT others(3): Show |
C | 1 | a0001c0001t0001g0302 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.805-768_805-759del others(10): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 4/14 | chr1 | 3468111 | |||||||
chr1:3468149 | C | T | 1 | a0002c0012t0010g0277 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.805-731C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 4/14 | chr1 | 3468149 | |||||||
chr1:3468194 | C | T | 4 | a0002c0003t0002g0017 a0002c0003t0002g0295 a0002c0003t0002g0297 others(1): Show |
4 | HG01243.hp1 HG02818.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.805-686C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 4/14 | chr1 | 3468194 | |||||||
chr1:3468339 | C | T | 2 | a0003c0004t0002g0066 a0003c0004t0002g0067 |
2 | NA18954.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.805-541C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 4/14 | chr1 | 3468339 | |||||||
chr1:3468379 | C | A | 1 | a0002c0035t0002g0301 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.805-501C>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 4/14 | chr1 | 3468379 | |||||||
chr1:3468406 | G | A | 2 | a0003c0016t0002g0293 a0003c0016t0007g0294 |
2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.805-474G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 4/14 | chr1 | 3468406 | |||||||
chr1:3468451 | G | A | 3 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0155 |
3 | HG01074.hp2 HG03831.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.805-429G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 4/14 | chr1 | 3468451 | |||||||
chr1:3468565 | G | A | 278 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(275): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.805-315G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 4/14 | chr1 | 3468565 | |||||||
chr1:3468575 | G | T | 263 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(260): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.805-305G>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 4/14 | chr1 | 3468575 | |||||||
chr1:3468655 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.805-225C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 4/14 | chr1 | 3468655 | |||||||
chr1:3468661 | G | C | 22 | a0001c0001t0001g0309 a0002c0002t0002g0046 a0002c0007t0002g0045 others(19): Show |
24 | HG01070.hp1 HG01081.hp1 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.805-219G>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 4/14 | chr1 | 3468661 | |||||||
chr1:3468662 | G | C | 2 | a0004c0010t0002g0057 a0004c0029t0002g0252 |
2 | HG02258.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.805-218G>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 4/14 | chr1 | 3468662 | |||||||
chr1:3468662 | G | T | 5 | a0005c0013t0005g0279 a0005c0013t0005g0280 a0005c0013t0005g0281 others(2): Show |
5 | HG02055.hp2 HG02572.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.805-218G>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 4/14 | chr1 | 3468662 | |||||||
chr1:3468663 | G | A | 17 | a0002c0002t0001g0021 a0002c0002t0002g0006 a0002c0002t0002g0035 others(14): Show |
18 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(15): Show |
intron_variant | MODIFIER | c.805-217G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 4/14 | chr1 | 3468663 | |||||||
chr1:3468669 | G | A | 5 | a0005c0013t0005g0279 a0005c0013t0005g0280 a0005c0013t0005g0281 others(2): Show |
5 | HG02055.hp2 HG02572.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.805-211G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 4/14 | chr1 | 3468669 | |||||||
chr1:3468686 | C | A | 178 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0014 others(175): Show |
184 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.805-194C>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 4/14 | chr1 | 3468686 | |||||||
chr1:3468692 | A | G | 140 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0019 others(137): Show |
158 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.805-188A>G | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 4/14 | chr1 | 3468692 | |||||||
chr1:3468724 | C | T | 1 | a0002c0017t0001g0283 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.805-156C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 4/14 | chr1 | 3468724 | |||||||
chr1:3468766 | T | C | 300 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(297): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.805-114T>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 4/14 | chr1 | 3468766 | |||||||
chr1:3468782 | A | G | 1 | a0001c0001t0001g0240 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.805-98A>G | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 4/14 | chr1 | 3468782 | |||||||
chr1:3469150 | T | G | 1 | a0002c0011t0009g0285 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.861+214T>G | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 5/14 | chr1 | 3469150 | |||||||
chr1:3469219 | C | T | 3 | a0002c0011t0002g0286 a0002c0011t0002g0287 a0002c0011t0002g0288 |
3 | HG02717.hp1 HG02723.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.862-214C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 5/14 | chr1 | 3469219 | |||||||
chr1:3469351 | G | A | 13 | a0002c0002t0002g0035 a0002c0002t0002g0055 a0002c0002t0003g0020 others(10): Show |
13 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(10): Show |
intron_variant | MODIFIER | c.862-82G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 5/14 | chr1 | 3469351 | |||||||
chr1:3469356 | C | T | 1 | a0002c0003t0002g0299 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.862-77C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 5/14 | chr1 | 3469356 | |||||||
chr1:3469738 | G | A | 3 | a0002c0002t0003g0020 a0002c0002t0003g0031 a0002c0002t0003g0032 |
3 | HG00544.hp2 NA19057.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.1022+145G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/14 | chr1 | 3469738 | |||||||
chr1:3469808 | G | A | 1 | a0002c0002t0003g0033 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1022+215G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/14 | chr1 | 3469808 | |||||||
chr1:3469821 | G | C | 1 | a0002c0011t0009g0285 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1022+228G>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/14 | chr1 | 3469821 | |||||||
chr1:3469894 | C | T | 2 | a0001c0001t0001g0239 a0001c0001t0001g0271 |
2 | HG02056.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.1022+301C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/14 | chr1 | 3469894 | |||||||
chr1:3469967 | G | A | 9 | a0002c0012t0001g0090 a0002c0012t0002g0249 a0002c0012t0002g0291 others(6): Show |
9 | HG01109.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1022+374G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/14 | chr1 | 3469967 | |||||||
chr1:3470094 | G | C | 5 | a0003c0006t0002g0001 a0003c0006t0002g0062 a0003c0006t0002g0063 others(2): Show |
8 | HG02647.hp2 HG02809.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1022+501G>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/14 | chr1 | 3470094 | |||||||
chr1:3470101 | T | G | 1 | a0003c0015t0002g0069 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1022+508T>G | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/14 | chr1 | 3470101 | |||||||
chr1:3470104 | G | T | 1 | a0003c0015t0002g0069 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1022+511G>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/14 | chr1 | 3470104 | |||||||
chr1:3470115 | G | A | 30 | a0002c0002t0001g0021 a0002c0002t0002g0006 a0002c0002t0002g0035 others(27): Show |
31 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.1022+522G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/14 | chr1 | 3470115 | |||||||
chr1:3470233 | T | A | 1 | a0002c0020t0001g0056 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1022+640T>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/14 | chr1 | 3470233 | |||||||
chr1:3470253 | G | GGGGCAGG others(13): Show |
1 | a0012c0025t0012g0292 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1022+666_1022+685d others(22): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr1 | 3470253 | ||||||
chr1:3470301 | GGTGTCTG others(7): Show |
G | 13 | a0002c0003t0002g0002 a0002c0003t0002g0004 a0002c0003t0002g0005 others(10): Show |
22 | HG01123.hp2 HG01243.hp1 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.1022+727_1022+740d others(16): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr1 | 3470301 | ||||||
chr1:3470354 | G | A | 10 | a0001c0001t0001g0120 a0002c0012t0001g0090 a0002c0012t0002g0249 others(7): Show |
10 | HG01109.hp2 HG02055.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1022+761G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/14 | chr1 | 3470354 | |||||||
chr1:3470449 | T | G | 9 | a0002c0012t0001g0090 a0002c0012t0002g0249 a0002c0012t0002g0291 others(6): Show |
9 | HG01109.hp2 HG02055.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1022+856T>G | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/14 | chr1 | 3470449 | |||||||
chr1:3470459 | G | A | 1 | a0001c0001t0001g0262 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1022+866G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/14 | chr1 | 3470459 | |||||||
chr1:3470550 | G | T | 1 | a0001c0001t0001g0238 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1022+957G>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/14 | chr1 | 3470550 | |||||||
chr1:3470594 | C | T | 4 | a0001c0001t0001g0256 a0002c0017t0001g0283 a0002c0017t0001g0284 others(1): Show |
4 | HG01243.hp2 HG04115.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1022+1001C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/14 | chr1 | 3470594 | |||||||
chr1:3470718 | C | T | 1 | a0004c0010t0002g0057 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1022+1125C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/14 | chr1 | 3470718 | |||||||
chr1:3470863 | CGTGGGCA others(45): Show |
C | 5 | a0004c0010t0002g0057 a0004c0010t0002g0058 a0004c0010t0002g0059 others(2): Show |
5 | HG00642.hp2 HG01515.hp1 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.1022+1285_1022+133 others(56): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr1 | 3470863 | ||||||
chr1:3470884 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1022+1291G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/14 | chr1 | 3470884 | |||||||
chr1:3471083 | GGGGTGTG others(7): Show |
G | 2 | a0002c0014t0006g0009 a0002c0014t0006g0088 |
3 | HG02809.hp2 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1022+1503_1022+151 others(18): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr1 | 3471083 | ||||||
chr1:3471096 | G | A | 4 | a0004c0010t0002g0057 a0004c0010t0002g0058 a0004c0010t0002g0059 others(1): Show |
4 | HG00642.hp2 HG01515.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.1022+1503G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/14 | chr1 | 3471096 | |||||||
chr1:3471109 | CCTGGGCA others(7): Show |
C | 1 | a0002c0002t0003g0037 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1022+1517_1022+153 others(18): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/14 | chr1 | 3471109 | |||||||
chr1:3471114 | G | GC | 4 | a0002c0012t0001g0090 a0002c0012t0002g0249 a0002c0012t0002g0291 others(1): Show |
4 | HG01109.hp2 HG02717.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1022+1522dupC | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr1 | 3471114 | ||||||
chr1:3471130 | G | C | 1 | a0012c0025t0012g0292 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1022+1537G>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/14 | chr1 | 3471130 | |||||||
chr1:3471163 | G | A | 2 | a0002c0014t0006g0009 a0002c0014t0006g0088 |
3 | HG02809.hp2 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1022+1570G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/14 | chr1 | 3471163 | |||||||
chr1:3471269 | G | A | 1 | a0004c0010t0002g0057 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1022+1676G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/14 | chr1 | 3471269 | |||||||
chr1:3471350 | G | A | 2 | a0001c0001t0001g0014 a0001c0001t0001g0196 |
3 | HG01256.hp2 HG01258.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.1023-1728G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/14 | chr1 | 3471350 | |||||||
chr1:3471390 | TCTGCTGC others(17): Show |
T | 1 | a0004c0010t0002g0060 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1023-1687_1023-166 others(28): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/14 | chr1 | 3471390 | |||||||
chr1:3471411 | T | C | 1 | a0001c0001t0001g0182 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1023-1667T>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/14 | chr1 | 3471411 | |||||||
chr1:3471414 | C | T | 33 | a0002c0002t0001g0021 a0002c0002t0002g0006 a0002c0002t0002g0035 others(30): Show |
34 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.1023-1664C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/14 | chr1 | 3471414 | |||||||
chr1:3471427 | C | A | 2 | a0001c0001t0001g0012 a0001c0001t0001g0160 |
3 | HG00735.hp2 HG01109.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.1023-1651C>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/14 | chr1 | 3471427 | |||||||
chr1:3471455 | T | A | 2 | a0001c0001t0001g0197 a0001c0001t0001g0241 |
2 | HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1023-1623T>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/14 | chr1 | 3471455 | |||||||
chr1:3471466 | A | G | 2 | a0002c0024t0002g0290 a0002c0028t0002g0094 |
2 | HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1023-1612A>G | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/14 | chr1 | 3471466 | |||||||
chr1:3471619 | G | A | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG01496.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.1023-1459G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/14 | chr1 | 3471619 | |||||||
chr1:3471632 | C | A | 2 | a0002c0014t0006g0009 a0002c0014t0006g0088 |
3 | HG02809.hp2 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1023-1446C>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/14 | chr1 | 3471632 | |||||||
chr1:3471660 | G | A | 1 | a0002c0007t0002g0045 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1023-1418G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/14 | chr1 | 3471660 | |||||||
chr1:3471705 | G | A | 4 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0155 others(1): Show |
4 | HG01074.hp2 HG01516.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.1023-1373G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/14 | chr1 | 3471705 | |||||||
chr1:3471727 | C | G | 2 | a0002c0024t0002g0290 a0002c0028t0002g0094 |
2 | HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1023-1351C>G | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/14 | chr1 | 3471727 | |||||||
chr1:3471787 | T | C | 2 | a0002c0024t0002g0290 a0002c0028t0002g0094 |
2 | HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1023-1291T>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/14 | chr1 | 3471787 | |||||||
chr1:3471842 | A | G | 36 | a0001c0001t0001g0188 a0002c0002t0001g0021 a0002c0002t0002g0006 others(33): Show |
38 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.1023-1236A>G | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/14 | chr1 | 3471842 | |||||||
chr1:3471977 | T | G | 1 | a0002c0012t0002g0249 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1023-1101T>G | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/14 | chr1 | 3471977 | |||||||
chr1:3471992 | A | G | 50 | a0001c0001t0001g0188 a0002c0002t0001g0021 a0002c0002t0002g0006 others(47): Show |
52 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.1023-1086A>G | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/14 | chr1 | 3471992 | |||||||
chr1:3472051 | C | T | 8 | a0001c0005t0001g0022 a0001c0005t0001g0024 a0001c0005t0001g0025 others(5): Show |
8 | NA18970.hp1 NA18971.hp1 NA18990.hp2 others(5): Show |
intron_variant | MODIFIER | c.1023-1027C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/14 | chr1 | 3472051 | |||||||
chr1:3472058 | C | T | 2 | a0002c0014t0006g0009 a0002c0014t0006g0088 |
3 | HG02809.hp2 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1023-1020C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/14 | chr1 | 3472058 | |||||||
chr1:3472087 | A | G | 1 | a0002c0030t0007g0261 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1023-991A>G | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/14 | chr1 | 3472087 | |||||||
chr1:3472440 | GC | G | 53 | a0001c0001t0001g0146 a0002c0002t0001g0021 a0002c0002t0002g0006 others(50): Show |
64 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.1023-629delC | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr1 | 3472440 | ||||||
chr1:3472472 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1023-606C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/14 | chr1 | 3472472 | |||||||
chr1:3472583 | C | T | 1 | a0002c0003t0002g0296 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1023-495C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/14 | chr1 | 3472583 | |||||||
chr1:3472588 | C | G | 1 | a0002c0008t0007g0096 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1023-490C>G | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/14 | chr1 | 3472588 | |||||||
chr1:3472607 | T | G | 5 | a0003c0006t0002g0001 a0003c0006t0002g0062 a0003c0006t0002g0063 others(2): Show |
8 | HG02647.hp2 HG02809.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1023-471T>G | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/14 | chr1 | 3472607 | |||||||
chr1:3472675 | G | A | 4 | a0005c0013t0005g0279 a0005c0013t0005g0280 a0005c0013t0005g0281 others(1): Show |
4 | HG02055.hp2 HG02572.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1023-403G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/14 | chr1 | 3472675 | |||||||
chr1:3472709 | T | C | 207 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(204): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.1023-369T>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/14 | chr1 | 3472709 | |||||||
chr1:3472757 | C | T | 268 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(265): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.1023-321C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/14 | chr1 | 3472757 | |||||||
chr1:3472769 | C | T | 1 | a0001c0001t0001g0247 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1023-309C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/14 | chr1 | 3472769 | |||||||
chr1:3472921 | C | T | 1 | a0001c0001t0001g0278 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1023-157C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/14 | chr1 | 3472921 | |||||||
chr1:3472945 | C | T | 5 | a0003c0006t0002g0001 a0003c0006t0002g0062 a0003c0006t0002g0063 others(2): Show |
8 | HG02647.hp2 HG02809.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1023-133C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/14 | chr1 | 3472945 | |||||||
chr1:3472979 | T | C | 34 | a0001c0001t0001g0188 a0002c0002t0001g0021 a0002c0002t0002g0006 others(31): Show |
35 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.1023-99T>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/14 | chr1 | 3472979 | |||||||
chr1:3473023 | C | T | 4 | a0002c0011t0009g0285 a0002c0012t0002g0249 a0002c0012t0002g0291 others(1): Show |
4 | HG01109.hp2 HG02630.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1023-55C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/14 | chr1 | 3473023 | |||||||
chr1:3473321 | C | T | 11 | a0002c0002t0002g0006 a0002c0002t0002g0046 a0002c0002t0002g0047 others(8): Show |
12 | HG01081.hp2 HG01123.hp1 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1176-72C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 7/14 | chr1 | 3473321 | |||||||
chr1:3473655 | C | G | 9 | a0001c0001t0001g0019 a0001c0001t0001g0142 a0001c0001t0001g0144 others(6): Show |
9 | HG00438.hp1 HG01358.hp1 HG02074.hp2 others(6): Show |
intron_variant | MODIFIER | c.1305+133C>G | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 8/14 | chr1 | 3473655 | |||||||
chr1:3473655 | C | T | 21 | a0002c0007t0002g0045 a0002c0021t0002g0013 a0002c0024t0002g0290 others(18): Show |
23 | HG01070.hp1 HG01361.hp1 HG02027.hp2 others(20): Show |
intron_variant | MODIFIER | c.1305+133C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 8/14 | chr1 | 3473655 | |||||||
chr1:3473674 | T | A | 302 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(299): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.1305+152T>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 8/14 | chr1 | 3473674 | |||||||
chr1:3473697 | G | A | 14 | a0002c0003t0002g0002 a0002c0003t0002g0004 a0002c0003t0002g0005 others(11): Show |
23 | HG01123.hp2 HG01243.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.1305+175G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 8/14 | chr1 | 3473697 | |||||||
chr1:3473769 | G | T | 5 | a0003c0006t0002g0001 a0003c0006t0002g0062 a0003c0006t0002g0063 others(2): Show |
8 | HG02647.hp2 HG02809.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1305+247G>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 8/14 | chr1 | 3473769 | |||||||
chr1:3473799 | T | C | 1 | a0001c0001t0001g0263 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1305+277T>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 8/14 | chr1 | 3473799 | |||||||
chr1:3473803 | A | ACTGGCAT others(17): Show |
1 | a0001c0001t0001g0192 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1305+282_1305+305d others(26): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr1 | 3473803 | ||||||
chr1:3473973 | G | C | 1 | a0002c0008t0014g0097 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1305+451G>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 8/14 | chr1 | 3473973 | |||||||
chr1:3473989 | G | A | 2 | a0002c0014t0006g0009 a0002c0014t0006g0088 |
3 | HG02809.hp2 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1305+467G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 8/14 | chr1 | 3473989 | |||||||
chr1:3474164 | C | T | 4 | a0001c0001t0001g0084 a0002c0011t0002g0286 a0002c0011t0002g0287 others(1): Show |
4 | HG02717.hp1 HG02723.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1306-544C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 8/14 | chr1 | 3474164 | |||||||
chr1:3474202 | GCACCCGG others(12): Show |
G | 1 | a0001c0001t0001g0262 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1306-502_1306-484d others(21): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr1 | 3474202 | ||||||
chr1:3474217 | A | G | 19 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(16): Show |
19 | HG00544.hp1 HG00558.hp1 HG00621.hp1 others(16): Show |
intron_variant | MODIFIER | c.1306-491A>G | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 8/14 | chr1 | 3474217 | |||||||
chr1:3474275 | T | A | 8 | a0002c0012t0002g0249 a0002c0012t0002g0291 a0002c0012t0010g0277 others(5): Show |
8 | HG01109.hp2 HG02055.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1306-433T>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 8/14 | chr1 | 3474275 | |||||||
chr1:3474315 | T | C | 1 | a0001c0001t0001g0185 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1306-393T>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 8/14 | chr1 | 3474315 | |||||||
chr1:3474336 | A | ACACATGG others(38): Show |
1 | a0002c0002t0003g0034 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1306-371_1306-327d others(47): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr1 | 3474336 | ||||||
chr1:3474337 | C | T | 4 | a0001c0001t0001g0012 a0001c0001t0001g0160 a0001c0001t0001g0161 others(1): Show |
5 | HG00735.hp2 HG01109.hp1 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.1306-371C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 8/14 | chr1 | 3474337 | |||||||
chr1:3474340 | A | G | 1 | a0001c0001t0001g0239 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1306-368A>G | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 8/14 | chr1 | 3474340 | |||||||
chr1:3474373 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1306-335A>G | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 8/14 | chr1 | 3474373 | |||||||
chr1:3474453 | TGGCCGAG others(15): Show |
T | 1 | a0001c0001t0001g0181 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1306-253_1306-232d others(24): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr1 | 3474453 | ||||||
chr1:3474458 | G | A | 268 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(265): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.1306-250G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 8/14 | chr1 | 3474458 | |||||||
chr1:3474573 | G | A | 1 | a0001c0001t0001g0121 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1306-135G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 8/14 | chr1 | 3474573 | |||||||
chr1:3474586 | G | A | 1 | a0002c0012t0001g0090 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1306-122G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 8/14 | chr1 | 3474586 | |||||||
chr1:3474614 | C | T | 1 | a0002c0002t0002g0055 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1306-94C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 8/14 | chr1 | 3474614 | |||||||
chr1:3474657 | C | T | 2 | a0002c0007t0002g0159 a0002c0007t0002g0266 |
2 | HG02132.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.1306-51C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 8/14 | chr1 | 3474657 | |||||||
chr1:3474685 | T | C | 13 | a0002c0003t0002g0002 a0002c0003t0002g0004 a0002c0003t0002g0005 others(10): Show |
22 | HG01123.hp2 HG01243.hp1 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.1306-23T>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 8/14 | chr1 | 3474685 | |||||||
chr1:3474687 | C | A | 13 | a0002c0003t0002g0002 a0002c0003t0002g0004 a0002c0003t0002g0005 others(10): Show |
22 | HG01123.hp2 HG01243.hp1 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.1306-21C>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 8/14 | chr1 | 3474687 | |||||||
chr1:3474827 | G | A | 2 | a0001c0001t0001g0186 a0001c0001t0001g0192 |
2 | HG03704.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1380+45G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 9/14 | chr1 | 3474827 | |||||||
chr1:3474840 | C | T | 1 | a0001c0001t0001g0197 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1380+58C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 9/14 | chr1 | 3474840 | |||||||
chr1:3474873 | G | C | 1 | a0003c0004t0002g0071 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1380+91G>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 9/14 | chr1 | 3474873 | |||||||
chr1:3474897 | G | A | 1 | a0001c0001t0001g0276 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1380+115G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 9/14 | chr1 | 3474897 | |||||||
chr1:3474905 | T | TCAGATTA others(53): Show |
1 | a0002c0011t0009g0285 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1380+165_1380+166i others(62): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr1 | 3474905 | ||||||
chr1:3474905 | T | TCAGATTA others(53): Show |
8 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0198 others(5): Show |
8 | HG02083.hp1 HG02165.hp1 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.1380+260_1380+319d others(62): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr1 | 3474905 | ||||||
chr1:3474932 | AGCGCTGA others(233): Show |
A | 1 | a0002c0002t0002g0043 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1380+200_1380+439d others(2): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr1 | 3474932 | ||||||
chr1:3474935 | G | A | 1 | a0001c0001t0001g0137 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1380+153G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 9/14 | chr1 | 3474935 | |||||||
chr1:3475042 | A | AGCCTTTC others(113): Show |
1 | a0002c0002t0002g0051 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1380+319_1380+320i others(122): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr1 | 3475042 | ||||||
chr1:3475042 | A | AGCCTTTC others(173): Show |
2 | a0002c0002t0003g0033 a0002c0007t0002g0045 |
2 | HG00609.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.1380+319_1380+320i others(182): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr1 | 3475042 | ||||||
chr1:3475042 | A | AGCCTTTC others(173): Show |
7 | a0002c0002t0002g0006 a0002c0002t0002g0046 a0002c0002t0002g0048 others(4): Show |
8 | HG01081.hp2 HG01123.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1380+319_1380+320i others(182): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr1 | 3475042 | ||||||
chr1:3475042 | A | AGCCTTTC others(113): Show |
1 | a0002c0002t0002g0039 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1380+319_1380+320i others(122): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr1 | 3475042 | ||||||
chr1:3475042 | A | AGCCTTTC others(173): Show |
19 | a0002c0002t0001g0021 a0002c0002t0002g0035 a0002c0002t0002g0041 others(16): Show |
19 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(16): Show |
intron_variant | MODIFIER | c.1380+319_1380+320i others(182): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr1 | 3475042 | ||||||
chr1:3475042 | A | AGCCTTTC others(233): Show |
1 | a0002c0011t0009g0285 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1380+329_1380+330i others(242): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr1 | 3475042 | ||||||
chr1:3475042 | A | AGCCTTTC others(113): Show |
1 | a0002c0002t0002g0047 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1380+271_1380+272i others(122): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr1 | 3475042 | ||||||
chr1:3475042 | A | AGCCTTTC others(53): Show |
1 | a0012c0025t0012g0292 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1380+271_1380+272i others(62): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr1 | 3475042 | ||||||
chr1:3475052 | AGCGCTGA others(53): Show |
A | 13 | a0002c0003t0002g0002 a0002c0003t0002g0004 a0002c0003t0002g0005 others(10): Show |
22 | HG01123.hp2 HG01243.hp1 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.1380+570_1381-559d others(62): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr1 | 3475052 | ||||||
chr1:3475052 | AGCGCTGA others(113): Show |
A | 7 | a0002c0002t0002g0054 a0002c0035t0002g0301 a0003c0006t0002g0001 others(4): Show |
10 | HG01934.hp1 HG02647.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.1380+510_1381-559d others(2): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr1 | 3475052 | ||||||
chr1:3475052 | AGCGCTGA others(173): Show |
A | 1 | a0001c0001t0001g0236 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1380+450_1381-559d others(2): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr1 | 3475052 | ||||||
chr1:3475052 | AGCGCTGA others(233): Show |
A | 1 | a0001c0001t0001g0246 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1380+390_1381-559d others(2): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr1 | 3475052 | ||||||
chr1:3475054 | C | CGCTGACA others(53): Show |
2 | a0002c0007t0002g0119 a0002c0012t0010g0277 |
2 | HG01928.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1380+319_1380+320i others(62): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr1 | 3475054 | ||||||
chr1:3475102 | G | A | 225 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(222): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.1380+320G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 9/14 | chr1 | 3475102 | |||||||
chr1:3475112 | G | A | 278 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(275): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.1380+330G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 9/14 | chr1 | 3475112 | |||||||
chr1:3475112 | G | C | 1 | a0001c0001t0017g0148 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1380+330G>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 9/14 | chr1 | 3475112 | |||||||
chr1:3475114 | C | T | 1 | a0002c0012t0002g0291 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1380+332C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 9/14 | chr1 | 3475114 | |||||||
chr1:3475127 | A | T | 13 | a0002c0003t0002g0002 a0002c0003t0002g0004 a0002c0003t0002g0005 others(10): Show |
22 | HG01123.hp2 HG01243.hp1 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.1380+345A>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 9/14 | chr1 | 3475127 | |||||||
chr1:3475162 | G | A | 16 | a0001c0001t0001g0101 a0002c0003t0002g0002 a0002c0003t0002g0004 others(13): Show |
26 | HG01123.hp2 HG01243.hp1 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.1380+380G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 9/14 | chr1 | 3475162 | |||||||
chr1:3475172 | G | A | 292 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(289): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.1380+390G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 9/14 | chr1 | 3475172 | |||||||
chr1:3475174 | C | CGCTGACA others(53): Show |
2 | a0002c0014t0006g0009 a0002c0014t0006g0088 |
3 | HG02809.hp2 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1380+439_1380+440i others(62): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr1 | 3475174 | ||||||
chr1:3475174 | C | T | 13 | a0002c0003t0002g0002 a0002c0003t0002g0004 a0002c0003t0002g0005 others(10): Show |
22 | HG01123.hp2 HG01243.hp1 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.1380+392C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 9/14 | chr1 | 3475174 | |||||||
chr1:3475222 | G | A | 6 | a0002c0002t0002g0054 a0003c0006t0002g0001 a0003c0006t0002g0062 others(3): Show |
9 | HG01934.hp1 HG02647.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1380+440G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 9/14 | chr1 | 3475222 | |||||||
chr1:3475232 | G | A | 289 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(286): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.1380+450G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 9/14 | chr1 | 3475232 | |||||||
chr1:3475232 | G | GGCGCTGA others(53): Show |
2 | a0003c0016t0002g0293 a0003c0016t0007g0294 |
2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1380+509_1380+510i others(62): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr1 | 3475232 | ||||||
chr1:3475234 | C | T | 1 | a0002c0002t0002g0054 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1380+452C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 9/14 | chr1 | 3475234 | |||||||
chr1:3475282 | G | A | 2 | a0001c0001t0001g0236 a0002c0002t0002g0054 |
2 | HG00323.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.1380+500G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 9/14 | chr1 | 3475282 | |||||||
chr1:3475292 | G | A | 274 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(271): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.1380+510G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 9/14 | chr1 | 3475292 | |||||||
chr1:3475292 | G | GGCGCTGA others(53): Show |
1 | a0002c0008t0014g0097 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1380+569_1380+570i others(62): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr1 | 3475292 | ||||||
chr1:3475295 | G | GCTGACAG others(53): Show |
1 | a0002c0030t0007g0261 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1380+569_1380+570i others(62): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr1 | 3475295 | ||||||
chr1:3475342 | G | A | 1 | a0001c0001t0001g0246 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1380+560G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 9/14 | chr1 | 3475342 | |||||||
chr1:3475352 | G | A | 276 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(273): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.1380+570G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 9/14 | chr1 | 3475352 | |||||||
chr1:3475352 | G | GGCGCTGA others(53): Show |
1 | a0002c0008t0008g0010 | 2 | HG02109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1381-268_1381-209d others(62): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr1 | 3475352 | ||||||
chr1:3475352 | GGCGCTGA others(53): Show |
G | 7 | a0003c0004t0002g0072 a0003c0004t0002g0080 a0003c0015t0002g0069 others(4): Show |
7 | HG00642.hp2 HG01515.hp1 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.1381-268_1381-209d others(62): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr1 | 3475352 | ||||||
chr1:3475352 | GGCGCTGA others(113): Show |
G | 2 | a0003c0004t0002g0007 a0003c0004t0002g0082 |
3 | HG02027.hp2 NA18980.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.1381-328_1381-209d others(2): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr1 | 3475352 | ||||||
chr1:3475402 | G | A | 1 | a0001c0001t0001g0268 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1381-568G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 9/14 | chr1 | 3475402 | |||||||
chr1:3475402 | G | GGCCTTTC others(53): Show |
5 | a0005c0013t0005g0279 a0005c0013t0005g0280 a0005c0013t0005g0281 others(2): Show |
5 | HG02055.hp2 HG02572.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1381-509_1381-508i others(62): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr1 | 3475402 | ||||||
chr1:3475411 | C | T | 4 | a0003c0004t0002g0068 a0003c0004t0002g0071 a0003c0004t0002g0077 others(1): Show |
4 | NA18961.hp2 NA18970.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.1381-559C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 9/14 | chr1 | 3475411 | |||||||
chr1:3475412 | A | G | 21 | a0002c0011t0002g0286 a0002c0011t0002g0287 a0002c0011t0002g0288 others(18): Show |
22 | HG01070.hp1 HG01361.hp1 HG02135.hp2 others(19): Show |
intron_variant | MODIFIER | c.1381-558A>G | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 9/14 | chr1 | 3475412 | |||||||
chr1:3475413 | G | GCGCTGAC others(9): Show |
1 | a0002c0007t0002g0159 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1381-556_1381-541d others(18): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr1 | 3475413 | ||||||
chr1:3475472 | A | G | 10 | a0002c0011t0002g0286 a0002c0011t0002g0287 a0002c0011t0002g0288 others(7): Show |
10 | HG00642.hp2 HG01515.hp1 HG02004.hp2 others(7): Show |
intron_variant | MODIFIER | c.1381-498A>G | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 9/14 | chr1 | 3475472 | |||||||
chr1:3475474 | C | CGCTGACA others(113): Show |
1 | a0002c0012t0010g0277 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1381-377_1381-376i others(122): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr1 | 3475474 | ||||||
chr1:3475474 | C | CGCTGACA others(173): Show |
1 | a0002c0012t0002g0291 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1381-437_1381-436i others(182): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr1 | 3475474 | ||||||
chr1:3475474 | C | T | 5 | a0005c0013t0005g0279 a0005c0013t0005g0280 a0005c0013t0005g0281 others(2): Show |
5 | HG02055.hp2 HG02572.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1381-496C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 9/14 | chr1 | 3475474 | |||||||
chr1:3475489 | T | A | 1 | a0001c0001t0001g0240 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1381-481T>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 9/14 | chr1 | 3475489 | |||||||
chr1:3475532 | A | G | 8 | a0002c0011t0002g0286 a0002c0011t0002g0287 a0002c0011t0002g0288 others(5): Show |
8 | HG00642.hp2 HG01515.hp1 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.1381-438A>G | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 9/14 | chr1 | 3475532 | |||||||
chr1:3475592 | A | G | 3 | a0004c0010t0002g0058 a0004c0010t0002g0059 a0004c0010t0002g0060 |
3 | HG00642.hp2 HG01515.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1381-378A>G | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 9/14 | chr1 | 3475592 | |||||||
chr1:3475594 | C | T | 1 | a0001c0001t0001g0308 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1381-376C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 9/14 | chr1 | 3475594 | |||||||
chr1:3475616 | C | CAGAGGTT others(53): Show |
1 | a0001c0001t0001g0101 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1381-295_1381-294i others(62): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr1 | 3475616 | ||||||
chr1:3475616 | C | T | 7 | a0001c0001t0001g0108 a0001c0001t0001g0257 a0001c0001t0001g0258 others(4): Show |
7 | HG00642.hp1 HG01099.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1381-354C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 9/14 | chr1 | 3475616 | |||||||
chr1:3475642 | G | A | 18 | a0002c0021t0002g0013 a0003c0004t0002g0007 a0003c0004t0002g0066 others(15): Show |
20 | HG01070.hp1 HG01361.hp1 HG02027.hp2 others(17): Show |
intron_variant | MODIFIER | c.1381-328G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 9/14 | chr1 | 3475642 | |||||||
chr1:3475652 | A | G | 1 | a0004c0010t0002g0058 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1381-318A>G | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 9/14 | chr1 | 3475652 | |||||||
chr1:3475702 | GGCCTTTC others(53): Show |
G | 10 | a0001c0001t0001g0003 a0001c0001t0001g0086 a0001c0001t0001g0109 others(7): Show |
12 | HG01255.hp2 HG02109.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.1381-256_1381-197d others(62): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr1 | 3475702 | ||||||
chr1:3475762 | A | G | 237 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0014 others(234): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.1381-208A>G | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 9/14 | chr1 | 3475762 | |||||||
chr1:3475853 | A | AGGCACTG others(70): Show |
1 | a0001c0009t0001g0199 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1381-116_1381-40du others(78): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr1 | 3475853 | ||||||
chr1:3476070 | G | C | 1 | a0014c0033t0001g0255 | 1 | NA18991.hp2 | splice_region_variant&intron_variant | LOW | c.1473+8G>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | chr1 | 3476070 | |||||||
chr1:3476071 | C | G | 1 | a0014c0033t0001g0255 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1473+9C>G | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | chr1 | 3476071 | |||||||
chr1:3476079 | A | G | 16 | a0002c0003t0002g0002 a0002c0003t0002g0004 a0002c0003t0002g0005 others(13): Show |
26 | HG01123.hp2 HG01243.hp1 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.1473+17A>G | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | chr1 | 3476079 | |||||||
chr1:3476167 | G | A | 2 | a0002c0014t0006g0009 a0002c0014t0006g0088 |
3 | HG02809.hp2 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1473+105G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | chr1 | 3476167 | |||||||
chr1:3476303 | C | T | 18 | a0002c0003t0002g0002 a0002c0003t0002g0004 a0002c0003t0002g0005 others(15): Show |
28 | HG01123.hp2 HG01243.hp1 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.1473+241C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | chr1 | 3476303 | |||||||
chr1:3476378 | G | C | 3 | a0002c0011t0002g0286 a0002c0011t0002g0287 a0002c0011t0002g0288 |
3 | HG02717.hp1 HG02723.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1473+316G>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | chr1 | 3476378 | |||||||
chr1:3476386 | CCTGTCAG others(41): Show |
C | 1 | a0001c0001t0001g0251 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1473+325_1473+372d others(50): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | chr1 | 3476386 | |||||||
chr1:3476422 | C | T | 1 | a0002c0011t0009g0285 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1473+360C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | chr1 | 3476422 | |||||||
chr1:3476473 | G | T | 208 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(205): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.1473+411G>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | chr1 | 3476473 | |||||||
chr1:3476510 | T | C | 1 | a0001c0001t0001g0200 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1473+448T>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | chr1 | 3476510 | |||||||
chr1:3476566 | A | G | 1 | a0012c0025t0012g0292 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1473+504A>G | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | chr1 | 3476566 | |||||||
chr1:3476674 | CTCCCCTA others(37): Show |
C | 1 | a0001c0001t0001g0201 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1473+616_1473+659d others(46): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3476674 | ||||||
chr1:3476678 | C | G | 20 | a0002c0021t0002g0013 a0002c0024t0002g0290 a0002c0028t0002g0094 others(17): Show |
22 | HG01070.hp1 HG01361.hp1 HG02027.hp2 others(19): Show |
intron_variant | MODIFIER | c.1473+616C>G | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | chr1 | 3476678 | |||||||
chr1:3476835 | C | CCCGGGGT others(16): Show |
1 | a0001c0001t0001g0186 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1473+776_1473+798d others(25): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3476835 | ||||||
chr1:3476889 | C | T | 1 | a0012c0025t0012g0292 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1473+827C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | chr1 | 3476889 | |||||||
chr1:3477097 | G | A | 2 | a0002c0014t0006g0009 a0002c0014t0006g0088 |
3 | HG02809.hp2 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1474-778G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | chr1 | 3477097 | |||||||
chr1:3477100 | G | A | 1 | a0002c0011t0009g0285 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1474-775G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | chr1 | 3477100 | |||||||
chr1:3477141 | G | A | 1 | a0002c0002t0003g0044 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1474-734G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | chr1 | 3477141 | |||||||
chr1:3477171 | G | A | 3 | a0002c0014t0006g0009 a0002c0014t0006g0088 a0002c0035t0002g0301 |
4 | HG02809.hp2 HG02965.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1474-704G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | chr1 | 3477171 | |||||||
chr1:3477212 | G | C | 1 | a0001c0001t0001g0101 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1474-663G>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | chr1 | 3477212 | |||||||
chr1:3477213 | A | T | 1 | a0001c0001t0001g0101 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1474-662A>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | chr1 | 3477213 | |||||||
chr1:3477214 | G | T | 1 | a0001c0001t0001g0101 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1474-661G>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | chr1 | 3477214 | |||||||
chr1:3477216 | A | C | 1 | a0001c0001t0001g0101 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1474-659A>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | chr1 | 3477216 | |||||||
chr1:3477217 | G | C | 1 | a0001c0001t0001g0101 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1474-658G>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | chr1 | 3477217 | |||||||
chr1:3477219 | G | T | 1 | a0001c0001t0001g0101 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1474-656G>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | chr1 | 3477219 | |||||||
chr1:3477220 | G | C | 1 | a0001c0001t0001g0101 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1474-655G>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | chr1 | 3477220 | |||||||
chr1:3477223 | G | C | 1 | a0001c0001t0001g0101 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1474-652G>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | chr1 | 3477223 | |||||||
chr1:3477226 | G | T | 1 | a0001c0001t0001g0101 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1474-649G>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | chr1 | 3477226 | |||||||
chr1:3477227 | G | C | 1 | a0001c0001t0001g0101 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1474-648G>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | chr1 | 3477227 | |||||||
chr1:3477229 | G | C | 1 | a0001c0001t0001g0101 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1474-646G>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | chr1 | 3477229 | |||||||
chr1:3477230 | G | C | 1 | a0001c0001t0001g0101 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1474-645G>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | chr1 | 3477230 | |||||||
chr1:3477231 | G | T | 1 | a0001c0001t0001g0101 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1474-644G>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | chr1 | 3477231 | |||||||
chr1:3477234 | G | C | 1 | a0001c0001t0001g0101 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1474-641G>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | chr1 | 3477234 | |||||||
chr1:3477235 | G | C | 1 | a0001c0001t0001g0101 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1474-640G>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | chr1 | 3477235 | |||||||
chr1:3477237 | T | A | 1 | a0001c0001t0001g0101 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1474-638T>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | chr1 | 3477237 | |||||||
chr1:3477240 | T | C | 1 | a0001c0001t0001g0101 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1474-635T>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | chr1 | 3477240 | |||||||
chr1:3477250 | T | C | 1 | a0001c0001t0001g0101 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1474-625T>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | chr1 | 3477250 | |||||||
chr1:3477252 | T | A | 1 | a0001c0001t0001g0101 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1474-623T>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | chr1 | 3477252 | |||||||
chr1:3477290 | G | C | 1 | a0001c0001t0001g0101 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1474-585G>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | chr1 | 3477290 | |||||||
chr1:3477291 | A | C | 1 | a0001c0001t0001g0101 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1474-584A>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | chr1 | 3477291 | |||||||
chr1:3477298 | T | TCACCCCC others(1993): Show |
1 | a0001c0001t0001g0101 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1474-576_1474-575i others(2002): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477298 | ||||||
chr1:3477298 | T | TCCCTGTC others(825): Show |
1 | a0012c0025t0012g0292 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1474-574_1474-573i others(834): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477298 | ||||||
chr1:3477303 | G | A | 3 | a0001c0001t0001g0101 a0002c0002t0002g0047 a0012c0025t0012g0292 |
3 | HG02280.hp1 HG02293.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1474-572G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | chr1 | 3477303 | |||||||
chr1:3477303 | G | GTCACCCC others(829): Show |
1 | a0003c0015t0002g0079 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(838): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(447): Show |
1 | a0003c0004t0002g0073 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(456): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2815): Show |
1 | a0002c0008t0014g0097 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2824): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2363): Show |
1 | a0001c0001t0001g0161 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2372): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(1939): Show |
1 | a0002c0020t0001g0056 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(1948): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2063): Show |
1 | a0002c0030t0007g0261 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2072): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2532): Show |
1 | a0002c0017t0001g0284 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2541): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2741): Show |
1 | a0002c0017t0001g0283 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2750): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(3827): Show |
1 | a0001c0001t0016g0164 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(3836): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2890): Show |
1 | a0001c0001t0001g0165 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2899): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(3876): Show |
1 | a0001c0001t0001g0166 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(3885): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(3948): Show |
1 | a0001c0001t0001g0167 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(3957): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(3833): Show |
1 | a0001c0001t0001g0168 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(3842): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(1265): Show |
1 | a0001c0001t0001g0124 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(1274): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(3023): Show |
1 | a0001c0001t0001g0241 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(3032): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2929): Show |
1 | a0001c0001t0001g0197 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2938): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(977): Show |
1 | a0001c0001t0001g0271 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(986): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2110): Show |
1 | a0002c0012t0002g0249 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2119): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2007): Show |
1 | a0001c0001t0013g0163 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2016): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(3032): Show |
1 | a0001c0001t0001g0202 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(3041): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2033): Show |
1 | a0002c0020t0001g0189 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2042): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2385): Show |
1 | a0002c0008t0007g0096 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2394): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2135): Show |
1 | a0001c0001t0001g0151 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2144): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2035): Show |
1 | a0001c0001t0001g0183 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2044): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(1285): Show |
1 | a0001c0001t0001g0198 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(1294): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2240): Show |
1 | a0001c0001t0001g0256 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2249): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(1877): Show |
1 | a0001c0001t0001g0203 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(1886): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2458): Show |
1 | a0001c0001t0001g0193 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2467): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2084): Show |
1 | a0001c0001t0001g0023 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2093): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2045): Show |
1 | a0001c0001t0001g0125 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2054): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(1814): Show |
1 | a0001c0001t0001g0169 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(1823): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(1839): Show |
1 | a0001c0001t0001g0275 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(1848): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2548): Show |
1 | a0001c0001t0001g0274 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2557): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(3566): Show |
1 | a0001c0001t0001g0149 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(3575): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2625): Show |
1 | a0001c0001t0001g0204 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2634): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(1860): Show |
1 | a0001c0001t0001g0257 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(1869): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2000): Show |
1 | a0001c0001t0001g0258 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2009): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2049): Show |
1 | a0001c0001t0001g0108 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2058): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2351): Show |
1 | a0001c0001t0001g0205 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2360): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(3139): Show |
1 | a0001c0001t0001g0206 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(3148): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2462): Show |
1 | a0001c0001t0001g0242 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2471): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2510): Show |
1 | a0001c0001t0001g0207 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2519): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2173): Show |
1 | a0001c0001t0001g0243 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2182): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2835): Show |
1 | a0001c0001t0001g0278 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2844): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2573): Show |
1 | a0001c0001t0001g0247 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2582): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2550): Show |
1 | a0001c0001t0001g0170 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2559): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2077): Show |
1 | a0001c0001t0001g0182 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2086): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2369): Show |
1 | a0001c0001t0001g0084 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2378): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(1999): Show |
1 | a0001c0001t0001g0208 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2008): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2023): Show |
1 | a0001c0001t0001g0209 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2032): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2047): Show |
1 | a0001c0001t0001g0185 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2056): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(1951): Show |
1 | a0001c0001t0001g0308 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(1960): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(1613): Show |
1 | a0008c0019t0001g0210 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(1622): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(1614): Show |
1 | a0001c0001t0001g0194 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(1623): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(1614): Show |
1 | a0008c0019t0001g0244 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(1623): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(1243): Show |
1 | a0001c0001t0001g0083 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(1252): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2358): Show |
1 | a0001c0001t0001g0171 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2367): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2704): Show |
1 | a0001c0001t0001g0098 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2713): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(1663): Show |
1 | a0001c0001t0001g0253 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(1672): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2176): Show |
1 | a0001c0001t0001g0264 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2185): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2650): Show |
1 | a0001c0001t0001g0117 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2659): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2509): Show |
1 | a0001c0001t0001g0211 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2518): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2816): Show |
1 | a0001c0001t0001g0212 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2825): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2703): Show |
1 | a0001c0001t0001g0014 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1474-550_1474-549i others(2712): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2318): Show |
1 | a0003c0026t0001g0070 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2327): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2660): Show |
1 | a0001c0001t0001g0115 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2669): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2304): Show |
1 | a0001c0001t0001g0213 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2313): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2090): Show |
1 | a0001c0001t0001g0214 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2099): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(3448): Show |
1 | a0001c0001t0001g0106 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(3457): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2494): Show |
1 | a0001c0001t0001g0089 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2503): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(3495): Show |
1 | a0001c0001t0001g0099 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(3504): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2065): Show |
1 | a0001c0001t0001g0104 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2074): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(3494): Show |
1 | a0001c0001t0001g0011 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1474-550_1474-549i others(3503): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(1980): Show |
1 | a0001c0001t0018g0245 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(1989): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2360): Show |
1 | a0001c0001t0001g0186 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2369): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2103): Show |
1 | a0001c0001t0001g0192 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2112): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(3542): Show |
1 | a0001c0001t0001g0100 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(3551): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2933): Show |
1 | a0001c0001t0001g0153 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2942): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2799): Show |
1 | a0001c0001t0001g0154 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2808): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2777): Show |
1 | a0001c0001t0001g0155 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2786): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(4068): Show |
1 | a0001c0001t0001g0184 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(4077): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2802): Show |
1 | a0001c0001t0001g0156 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2811): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(1814): Show |
1 | a0001c0001t0001g0172 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(1823): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2508): Show |
1 | a0001c0001t0001g0173 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2517): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2134): Show |
1 | a0001c0001t0001g0012 | 2 | HG00735.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.1474-550_1474-549i others(2143): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(1602): Show |
1 | a0001c0001t0001g0160 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(1611): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(1982): Show |
1 | a0001c0001t0001g0016 | 2 | HG01069.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.1474-550_1474-549i others(1991): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2242): Show |
1 | a0001c0001t0001g0162 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2251): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2353): Show |
1 | a0001c0001t0001g0251 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2362): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2482): Show |
1 | a0001c0001t0001g0174 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2491): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(1980): Show |
1 | a0001c0001t0001g0175 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(1989): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2617): Show |
1 | a0001c0001t0001g0176 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2626): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2217): Show |
1 | a0001c0001t0001g0177 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2226): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(1855): Show |
1 | a0001c0001t0001g0087 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(1864): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(3328): Show |
1 | a0001c0001t0001g0215 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(3337): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(3428): Show |
1 | a0001c0001t0001g0107 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(3437): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2360): Show |
1 | a0001c0001t0001g0178 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2369): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(1925): Show |
1 | a0001c0001t0001g0259 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(1934): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2144): Show |
1 | a0001c0001t0001g0102 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2153): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2598): Show |
1 | a0001c0001t0001g0265 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2607): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(1765): Show |
1 | a0001c0001t0001g0086 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(1774): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(1673): Show |
1 | a0001c0001t0001g0150 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(1682): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2601): Show |
2 | a0001c0001t0004g0126 a0001c0001t0004g0139 |
2 | NA19011.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1474-550_1474-549i others(2610): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2602): Show |
1 | a0001c0001t0004g0140 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2611): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2464): Show |
1 | a0001c0001t0001g0127 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2473): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(3084): Show |
1 | a0001c0001t0001g0121 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(3093): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2578): Show |
1 | a0001c0001t0001g0216 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2587): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(3656): Show |
1 | a0001c0001t0001g0128 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(3665): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(3097): Show |
1 | a0001c0001t0004g0129 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(3106): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(1496): Show |
1 | a0001c0001t0004g0130 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(1505): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2570): Show |
1 | a0001c0001t0001g0269 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2579): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2498): Show |
1 | a0001c0001t0001g0270 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2507): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2980): Show |
1 | a0001c0001t0001g0268 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2989): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2552): Show |
1 | a0001c0005t0001g0024 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2561): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2509): Show |
1 | a0001c0005t0001g0025 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2518): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(3981): Show |
1 | a0001c0001t0001g0120 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(3990): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(1102): Show |
1 | a0001c0001t0011g0217 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(1111): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2536): Show |
1 | a0001c0001t0001g0218 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2545): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2882): Show |
1 | a0001c0001t0001g0219 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2891): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(3899): Show |
1 | a0001c0001t0001g0272 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(3908): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2415): Show |
1 | a0001c0001t0001g0220 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2424): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(1950): Show |
1 | a0001c0001t0001g0142 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(1959): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2371): Show |
1 | a0001c0001t0001g0262 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2380): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2043): Show |
1 | a0001c0001t0001g0122 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2052): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2065): Show |
1 | a0001c0005t0001g0053 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2074): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(1951): Show |
3 | a0001c0001t0001g0019 a0001c0001t0001g0146 a0001c0001t0001g0237 |
3 | HG02074.hp2 NA18992.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1474-550_1474-549i others(1960): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(1904): Show |
1 | a0001c0001t0001g0103 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(1913): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2301): Show |
1 | a0001c0001t0001g0091 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2310): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(1859): Show |
1 | a0001c0001t0001g0092 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(1868): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(1836): Show |
1 | a0001c0001t0001g0131 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(1845): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2138): Show |
1 | a0001c0001t0001g0221 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2147): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2823): Show |
1 | a0001c0001t0001g0222 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2832): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2044): Show |
1 | a0001c0001t0001g0132 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2053): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2049): Show |
1 | a0001c0001t0001g0141 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2058): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(1307): Show |
1 | a0001c0001t0001g0109 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(1316): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(1903): Show |
1 | a0001c0001t0001g0133 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(1912): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(1978): Show |
1 | a0009c0036t0001g0143 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(1987): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(1859): Show |
1 | a0001c0001t0001g0093 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(1868): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(3301): Show |
1 | a0001c0001t0001g0116 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(3310): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2276): Show |
1 | a0001c0001t0001g0105 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2285): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2750): Show |
1 | a0001c0009t0001g0223 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2759): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2614): Show |
1 | a0001c0009t0001g0015 | 2 | NA18967.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1474-550_1474-549i others(2623): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2615): Show |
1 | a0001c0001t0001g0224 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2624): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2071): Show |
1 | a0001c0001t0001g0225 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2080): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2593): Show |
1 | a0001c0009t0001g0199 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2602): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2622): Show |
1 | a0001c0001t0001g0226 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2631): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2575): Show |
1 | a0001c0001t0001g0227 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2584): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2742): Show |
1 | a0001c0001t0001g0228 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2751): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2369): Show |
1 | a0001c0001t0001g0309 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2378): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(3360): Show |
1 | a0001c0001t0001g0229 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(3369): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2813): Show |
1 | a0001c0001t0001g0273 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2822): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2326): Show |
1 | a0007c0018t0001g0250 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2335): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(1978): Show |
1 | a0015c0027t0001g0306 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(1987): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2000): Show |
1 | a0001c0001t0001g0267 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2009): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(1952): Show |
1 | a0001c0001t0001g0303 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(1961): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(1632): Show |
1 | a0001c0001t0001g0307 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(1641): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(1999): Show |
1 | a0001c0001t0001g0304 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2008): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2484): Show |
1 | a0001c0001t0001g0239 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2493): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(1519): Show |
1 | a0001c0001t0001g0230 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(1528): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(3706): Show |
1 | a0001c0001t0001g0231 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(3715): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(1976): Show |
1 | a0001c0001t0001g0302 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(1985): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2396): Show |
1 | a0001c0001t0001g0248 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2405): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(1030): Show |
1 | a0001c0001t0001g0123 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(1039): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2628): Show |
1 | a0001c0005t0001g0026 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2637): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2332): Show |
1 | a0007c0018t0001g0118 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2341): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2657): Show |
1 | a0001c0001t0001g0190 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2666): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2787): Show |
1 | a0001c0001t0001g0188 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2796): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2738): Show |
1 | a0001c0001t0001g0187 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2747): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2770): Show |
1 | a0001c0005t0001g0027 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2779): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2918): Show |
1 | a0001c0005t0001g0028 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2927): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2031): Show |
1 | a0001c0005t0001g0029 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2040): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2571): Show |
1 | a0001c0001t0001g0232 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2580): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2116): Show |
1 | a0001c0001t0001g0134 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2125): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2332): Show |
1 | a0001c0001t0001g0233 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2341): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(1485): Show |
1 | a0001c0001t0001g0196 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(1494): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(1808): Show |
1 | a0001c0001t0001g0240 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(1817): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(915): Show |
1 | a0001c0001t0001g0061 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(924): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(539): Show |
1 | a0002c0011t0009g0285 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(548): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2890): Show |
1 | a0002c0008t0008g0010 | 2 | HG02109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1474-550_1474-549i others(2899): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(1627): Show |
1 | a0001c0001t0001g0200 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(1636): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2731): Show |
1 | a0001c0001t0001g0246 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2740): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(3278): Show |
1 | a0005c0013t0005g0279 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(3287): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(3293): Show |
1 | a0005c0013t0005g0280 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(3302): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2925): Show |
1 | a0005c0013t0005g0281 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2934): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(1378): Show |
1 | a0001c0005t0019g0030 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(1387): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(1551): Show |
1 | a0003c0006t0002g0062 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(1560): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(1251): Show |
1 | a0003c0006t0002g0063 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(1260): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(1320): Show |
1 | a0003c0006t0002g0001 | 4 | HG02809.hp1 HG02970.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1474-550_1474-549i others(1329): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(1410): Show |
1 | a0003c0006t0015g0064 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(1419): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(1861): Show |
1 | a0003c0006t0002g0065 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(1870): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(3287): Show |
1 | a0011c0034t0005g0282 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(3296): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2717): Show |
1 | a0006c0023t0001g0135 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2726): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2767): Show |
1 | a0006c0023t0001g0136 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2776): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(1471): Show |
1 | a0001c0001t0001g0137 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(1480): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(3238): Show |
1 | a0001c0001t0001g0179 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(3247): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(751): Show |
1 | a0001c0001t0001g0144 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(760): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(3643): Show |
1 | a0001c0001t0001g0110 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(3652): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2719): Show |
1 | a0001c0001t0001g0111 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2728): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2717): Show |
1 | a0001c0001t0001g0112 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2726): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2718): Show |
1 | a0001c0001t0001g0113 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2727): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(3023): Show |
1 | a0001c0001t0001g0114 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(3032): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(1689): Show |
1 | a0001c0001t0001g0138 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(1698): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(1213): Show |
1 | a0001c0001t0001g0260 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(1222): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(1006): Show |
1 | a0001c0001t0001g0234 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(1015): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(1907): Show |
1 | a0001c0001t0017g0148 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(1916): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2256): Show |
1 | a0001c0001t0001g0238 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2265): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(1937): Show |
1 | a0002c0012t0001g0090 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(1946): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(1951): Show |
1 | a0004c0010t0002g0057 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(1960): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2402): Show |
1 | a0004c0029t0002g0252 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2411): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2074): Show |
1 | a0002c0012t0002g0291 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2083): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(3272): Show |
1 | a0002c0012t0010g0277 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(3281): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2154): Show |
1 | a0003c0016t0002g0293 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2163): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2295): Show |
1 | a0003c0016t0007g0294 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2304): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(3030): Show |
1 | a0001c0005t0001g0022 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(3039): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(1498): Show |
1 | a0004c0010t0002g0059 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(1507): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2082): Show |
1 | a0004c0010t0002g0058 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2091): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2107): Show |
1 | a0004c0010t0002g0060 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2116): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(1663): Show |
1 | a0001c0001t0001g0254 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(1672): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2008): Show |
1 | a0001c0001t0001g0305 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2017): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(865): Show |
1 | a0001c0001t0001g0145 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(874): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(1647): Show |
1 | a0001c0001t0001g0263 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(1656): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(705): Show |
1 | a0002c0003t0002g0296 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(714): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(705): Show |
1 | a0002c0003t0002g0300 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(714): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(683): Show |
1 | a0002c0003t0002g0002 | 4 | HG02647.hp1 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1474-550_1474-549i others(692): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(706): Show |
1 | a0002c0003t0002g0005 | 3 | HG01261.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1474-550_1474-549i others(715): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(729): Show |
5 | a0002c0003t0002g0018 a0002c0003t0002g0297 a0002c0003t0002g0299 others(2): Show |
7 | HG01123.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1474-550_1474-549i others(738): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(729): Show |
1 | a0002c0003t0002g0004 | 3 | HG01884.hp2 HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1474-550_1474-549i others(738): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(729): Show |
3 | a0002c0003t0002g0017 a0002c0003t0002g0295 a0010c0032t0002g0017 |
3 | HG01243.hp1 HG02818.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1474-550_1474-549i others(738): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(1647): Show |
1 | a0002c0035t0002g0301 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(1656): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(470): Show |
1 | a0003c0004t0002g0074 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(479): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(3009): Show |
1 | a0002c0011t0002g0286 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(3018): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2554): Show |
1 | a0002c0011t0002g0287 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2563): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2893): Show |
1 | a0002c0011t0002g0288 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2902): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(588): Show |
1 | a0002c0021t0002g0013 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1474-550_1474-549i others(597): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(518): Show |
3 | a0003c0004t0002g0007 a0003c0004t0002g0072 a0003c0004t0002g0082 |
4 | HG02027.hp2 NA18980.hp2 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.1474-550_1474-549i others(527): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(541): Show |
6 | a0003c0004t0002g0066 a0003c0004t0002g0068 a0003c0004t0002g0071 others(3): Show |
6 | HG01361.hp1 NA18954.hp1 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.1474-550_1474-549i others(550): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(542): Show |
1 | a0003c0004t0002g0080 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(551): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(518): Show |
1 | a0003c0004t0002g0076 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(527): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(3566): Show |
1 | a0005c0013t0009g0289 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(3575): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(1435): Show |
1 | a0001c0001t0001g0276 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(1444): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2135): Show |
1 | a0001c0001t0001g0085 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2144): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(474): Show |
1 | a0003c0004t0002g0078 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(483): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2143): Show |
1 | a0014c0033t0001g0255 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1474-564_1474-563i others(2152): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477303 | G | GTCACCCC others(2029): Show |
1 | a0001c0001t0001g0235 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1474-564_1474-563i others(2038): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477303 | ||||||
chr1:3477306 | A | ACCCCCAC others(2605): Show |
1 | a0001c0001t0001g0236 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2614): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477306 | ||||||
chr1:3477306 | A | ACCCCCAC others(831): Show |
1 | a0003c0015t0002g0069 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(840): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477306 | ||||||
chr1:3477316 | T | TACCCACC others(4262): Show |
1 | a0001c0001t0001g0201 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(4271): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477316 | ||||||
chr1:3477317 | A | ACCCACCC others(1810): Show |
1 | a0001c0001t0001g0003 | 3 | HG02559.hp2 HG02922.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1474-550_1474-549i others(1819): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477317 | ||||||
chr1:3477317 | A | ACCCACCC others(2452): Show |
1 | a0002c0007t0002g0152 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2461): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477317 | ||||||
chr1:3477317 | A | ACCCACCC others(4883): Show |
1 | a0002c0002t0002g0046 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(4892): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477317 | ||||||
chr1:3477317 | A | ACCCACCC others(3929): Show |
1 | a0002c0002t0002g0054 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(3938): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477317 | ||||||
chr1:3477317 | A | ACCCACCC others(2936): Show |
1 | a0002c0002t0002g0047 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2945): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477317 | ||||||
chr1:3477317 | A | ACCCACCC others(2169): Show |
1 | a0002c0002t0002g0048 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2178): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477317 | ||||||
chr1:3477317 | A | ACCCACCC others(2330): Show |
1 | a0002c0002t0002g0006 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1474-550_1474-549i others(2339): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477317 | ||||||
chr1:3477317 | A | ACCCACCC others(2491): Show |
1 | a0002c0002t0002g0049 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2500): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477317 | ||||||
chr1:3477317 | A | ACCCACCC others(2043): Show |
1 | a0002c0002t0002g0050 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2052): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477317 | ||||||
chr1:3477317 | A | ACCCACCC others(747): Show |
1 | a0002c0007t0002g0045 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(756): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477317 | ||||||
chr1:3477317 | A | ACCCACCC others(1927): Show |
1 | a0002c0002t0002g0035 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(1936): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477317 | ||||||
chr1:3477317 | A | ACCCACCC others(2473): Show |
1 | a0002c0002t0003g0020 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2482): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477317 | ||||||
chr1:3477317 | A | ACCCACCC others(2618): Show |
1 | a0002c0002t0003g0034 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2627): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477317 | ||||||
chr1:3477317 | A | ACCCACCC others(2430): Show |
3 | a0002c0002t0003g0031 a0002c0002t0003g0033 a0002c0002t0003g0037 |
3 | HG00544.hp2 HG00609.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.1474-550_1474-549i others(2439): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477317 | ||||||
chr1:3477317 | A | ACCCACCC others(2431): Show |
1 | a0002c0002t0003g0040 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2440): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477317 | ||||||
chr1:3477317 | A | ACCCACCC others(2478): Show |
1 | a0002c0002t0003g0036 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2487): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477317 | ||||||
chr1:3477317 | A | ACCCACCC others(2660): Show |
1 | a0002c0002t0003g0032 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2669): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477317 | ||||||
chr1:3477317 | A | ACCCACCC others(2431): Show |
1 | a0002c0002t0003g0038 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2440): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477317 | ||||||
chr1:3477317 | A | ACCCACCC others(2250): Show |
1 | a0002c0007t0002g0157 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2259): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477317 | ||||||
chr1:3477317 | A | ACCCACCC others(2021): Show |
1 | a0002c0002t0002g0039 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2030): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477317 | ||||||
chr1:3477317 | A | ACCCACCC others(1818): Show |
1 | a0002c0002t0002g0042 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(1827): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477317 | ||||||
chr1:3477317 | A | ACCCACCC others(2324): Show |
1 | a0002c0002t0001g0021 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2333): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477317 | ||||||
chr1:3477317 | A | ACCCACCC others(2226): Show |
1 | a0002c0007t0002g0195 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2235): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477317 | ||||||
chr1:3477317 | A | ACCCACCC others(2228): Show |
1 | a0002c0007t0002g0266 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2237): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477317 | ||||||
chr1:3477317 | A | ACCCACCC others(2236): Show |
1 | a0002c0007t0002g0159 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2245): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477317 | ||||||
chr1:3477317 | A | ACCCACCC others(2252): Show |
1 | a0002c0007t0002g0158 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2261): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477317 | ||||||
chr1:3477317 | A | ACCCACCC others(2660): Show |
1 | a0002c0002t0002g0043 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2669): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477317 | ||||||
chr1:3477317 | A | ACCCACCC others(2102): Show |
1 | a0002c0002t0002g0041 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2111): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477317 | ||||||
chr1:3477317 | A | ACCCACCC others(2685): Show |
1 | a0002c0002t0002g0055 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2694): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477317 | ||||||
chr1:3477317 | A | ACCCACCC others(1818): Show |
1 | a0002c0002t0003g0044 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(1827): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477317 | ||||||
chr1:3477317 | A | ACCCACCC others(2447): Show |
1 | a0002c0002t0002g0051 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2456): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477317 | ||||||
chr1:3477317 | A | ACCCACCC others(2604): Show |
1 | a0002c0007t0002g0119 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2613): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477317 | ||||||
chr1:3477317 | A | ACCCACCC others(541): Show |
1 | a0003c0004t0002g0067 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(550): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477317 | ||||||
chr1:3477317 | A | ACCCACCC others(1983): Show |
1 | a0002c0002t0002g0052 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(1992): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477317 | ||||||
chr1:3477321 | A | ACCCCCAT others(2658): Show |
1 | a0001c0001t0001g0191 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2667): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477321 | ||||||
chr1:3477321 | A | ACCCCCAT others(2383): Show |
1 | a0001c0001t0001g0181 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2392): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477321 | ||||||
chr1:3477321 | A | ACCCCCAT others(2171): Show |
2 | a0002c0024t0002g0290 a0002c0028t0002g0094 |
2 | HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1474-550_1474-549i others(2180): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477321 | ||||||
chr1:3477321 | A | ACCCCCAT others(764): Show |
2 | a0002c0014t0006g0009 a0002c0014t0006g0088 |
3 | HG02809.hp2 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1474-550_1474-549i others(773): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477321 | ||||||
chr1:3477321 | A | ACCCCCCA others(2573): Show |
1 | a0001c0001t0001g0180 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1474-550_1474-549i others(2582): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477321 | ||||||
chr1:3477335 | A | C | 1 | a0002c0012t0002g0249 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1474-540A>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | chr1 | 3477335 | |||||||
chr1:3477337 | A | G | 1 | a0003c0004t0002g0067 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1474-538A>G | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | chr1 | 3477337 | |||||||
chr1:3477339 | T | C | 1 | a0003c0004t0002g0067 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1474-536T>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | chr1 | 3477339 | |||||||
chr1:3477343 | C | T | 3 | a0002c0011t0002g0286 a0002c0011t0002g0287 a0002c0011t0002g0288 |
3 | HG02717.hp1 HG02723.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1474-532C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | chr1 | 3477343 | |||||||
chr1:3477370 | C | T | 1 | a0002c0011t0009g0285 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1474-505C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | chr1 | 3477370 | |||||||
chr1:3477412 | G | A | 8 | a0002c0011t0009g0285 a0002c0012t0002g0291 a0002c0012t0010g0277 others(5): Show |
8 | HG01109.hp2 HG02055.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1474-463G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | chr1 | 3477412 | |||||||
chr1:3477453 | G | A | 8 | a0002c0011t0009g0285 a0002c0012t0002g0291 a0002c0012t0010g0277 others(5): Show |
8 | HG01109.hp2 HG02055.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1474-422G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | chr1 | 3477453 | |||||||
chr1:3477534 | G | A | 8 | a0002c0011t0009g0285 a0002c0012t0002g0291 a0002c0012t0010g0277 others(5): Show |
8 | HG01109.hp2 HG02055.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1474-341G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | chr1 | 3477534 | |||||||
chr1:3477539 | C | T | 7 | a0002c0012t0002g0291 a0002c0012t0010g0277 a0005c0013t0005g0279 others(4): Show |
7 | HG01109.hp2 HG02055.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1474-336C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | chr1 | 3477539 | |||||||
chr1:3477557 | G | T | 24 | a0002c0012t0001g0090 a0002c0012t0002g0249 a0002c0021t0002g0013 others(21): Show |
26 | HG00642.hp2 HG01515.hp1 HG02004.hp2 others(23): Show |
intron_variant | MODIFIER | c.1474-318G>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | chr1 | 3477557 | |||||||
chr1:3477660 | C | CG | 276 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(273): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.1474-213dupG | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 3477660 | ||||||
chr1:3477686 | C | T | 211 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(208): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.1474-189C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | chr1 | 3477686 | |||||||
chr1:3477715 | C | T | 34 | a0002c0002t0001g0021 a0002c0002t0002g0006 a0002c0002t0002g0035 others(31): Show |
35 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.1474-160C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | chr1 | 3477715 | |||||||
chr1:3478042 | G | A | 1 | a0002c0011t0009g0285 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1625+16G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 11/14 | chr1 | 3478042 | |||||||
chr1:3478076 | A | G | 276 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(273): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.1625+50A>G | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 11/14 | chr1 | 3478076 | |||||||
chr1:3478110 | T | C | 302 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(299): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.1625+84T>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 11/14 | chr1 | 3478110 | |||||||
chr1:3478235 | G | A | 1 | a0005c0013t0005g0280 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1626-189G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 11/14 | chr1 | 3478235 | |||||||
chr1:3478253 | G | T | 1 | a0002c0012t0010g0277 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1626-171G>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 11/14 | chr1 | 3478253 | |||||||
chr1:3478288 | C | T | 7 | a0002c0024t0002g0290 a0002c0028t0002g0094 a0003c0006t0002g0001 others(4): Show |
10 | HG02280.hp2 HG02647.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.1626-136C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 11/14 | chr1 | 3478288 | |||||||
chr1:3478290 | C | T | 3 | a0002c0011t0002g0286 a0002c0011t0002g0287 a0002c0011t0002g0288 |
3 | HG02717.hp1 HG02723.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1626-134C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 11/14 | chr1 | 3478290 | |||||||
chr1:3478307 | C | T | 7 | a0002c0012t0002g0291 a0002c0012t0010g0277 a0005c0013t0005g0279 others(4): Show |
7 | HG01109.hp2 HG02055.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1626-117C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 11/14 | chr1 | 3478307 | |||||||
chr1:3478357 | C | A | 1 | a0002c0008t0007g0096 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1626-67C>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 11/14 | chr1 | 3478357 | |||||||
chr1:3478368 | C | T | 1 | a0002c0002t0003g0031 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1626-56C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 11/14 | chr1 | 3478368 | |||||||
chr1:3478396 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1626-28G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 11/14 | chr1 | 3478396 | |||||||
chr1:3478651 | G | A | 1 | a0004c0010t0002g0060 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1814+39G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 12/14 | chr1 | 3478651 | |||||||
chr1:3478663 | C | T | 1 | a0002c0012t0001g0090 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1814+51C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 12/14 | chr1 | 3478663 | |||||||
chr1:3478665 | T | C | 300 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(297): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.1814+53T>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 12/14 | chr1 | 3478665 | |||||||
chr1:3478695 | G | A | 1 | a0012c0025t0012g0292 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1814+83G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 12/14 | chr1 | 3478695 | |||||||
chr1:3478718 | C | T | 5 | a0002c0014t0006g0009 a0002c0014t0006g0088 a0002c0024t0002g0290 others(2): Show |
6 | HG02280.hp2 HG02809.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1814+106C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 12/14 | chr1 | 3478718 | |||||||
chr1:3478765 | A | T | 2 | a0002c0017t0001g0283 a0002c0017t0001g0284 |
2 | HG01243.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1814+153A>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 12/14 | chr1 | 3478765 | |||||||
chr1:3478824 | C | G | 24 | a0002c0012t0002g0249 a0002c0021t0002g0013 a0003c0004t0002g0007 others(21): Show |
26 | HG00642.hp2 HG01070.hp1 HG01361.hp1 others(23): Show |
intron_variant | MODIFIER | c.1814+212C>G | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 12/14 | chr1 | 3478824 | |||||||
chr1:3478880 | G | A | 1 | a0001c0001t0001g0137 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1814+268G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 12/14 | chr1 | 3478880 | |||||||
chr1:3478967 | GGAGAGCC others(2): Show |
G | 14 | a0002c0003t0002g0002 a0002c0003t0002g0004 a0002c0003t0002g0005 others(11): Show |
23 | HG01123.hp2 HG01243.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.1814+359_1814+367d others(11): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 3478967 | ||||||
chr1:3479040 | G | A | 2 | a0002c0003t0002g0017 a0010c0032t0002g0017 |
2 | HG01243.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1814+428G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 12/14 | chr1 | 3479040 | |||||||
chr1:3479151 | C | G | 1 | a0001c0001t0001g0177 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1815-366C>G | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 12/14 | chr1 | 3479151 | |||||||
chr1:3479170 | G | A | 20 | a0001c0001t0001g0219 a0001c0001t0001g0226 a0001c0001t0001g0227 others(17): Show |
29 | HG00673.hp1 HG01123.hp2 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.1815-347G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 12/14 | chr1 | 3479170 | |||||||
chr1:3479191 | G | A | 30 | a0002c0002t0001g0021 a0002c0002t0002g0006 a0002c0002t0002g0035 others(27): Show |
31 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.1815-326G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 12/14 | chr1 | 3479191 | |||||||
chr1:3479196 | G | A | 1 | a0004c0010t0002g0057 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1815-321G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 12/14 | chr1 | 3479196 | |||||||
chr1:3479238 | C | T | 3 | a0002c0002t0002g0046 a0002c0002t0002g0050 a0002c0002t0002g0054 |
3 | HG01081.hp2 HG01934.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.1815-279C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 12/14 | chr1 | 3479238 | |||||||
chr1:3479239 | G | A | 1 | a0003c0006t0002g0065 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1815-278G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 12/14 | chr1 | 3479239 | |||||||
chr1:3479247 | C | A | 1 | a0002c0011t0009g0285 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1815-270C>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 12/14 | chr1 | 3479247 | |||||||
chr1:3479385 | C | T | 1 | a0003c0004t0002g0072 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1815-132C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 12/14 | chr1 | 3479385 | |||||||
chr1:3479409 | ACC | A | 237 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(234): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.1815-104_1815-103d others(4): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 3479409 | ||||||
chr1:3479428 | G | A | 1 | a0003c0006t0002g0065 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1815-89G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 12/14 | chr1 | 3479428 | |||||||
chr1:3479436 | T | C | 1 | a0001c0001t0001g0121 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1815-81T>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 12/14 | chr1 | 3479436 | |||||||
chr1:3479468 | C | T | 1 | a0002c0011t0009g0285 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1815-49C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 12/14 | chr1 | 3479468 | |||||||
chr1:3479599 | G | A | 5 | a0005c0013t0005g0279 a0005c0013t0005g0280 a0005c0013t0005g0281 others(2): Show |
5 | HG02055.hp2 HG02572.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1888+9G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 13/14 | chr1 | 3479599 | |||||||
chr1:3479622 | C | A | 1 | a0001c0001t0001g0258 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1888+32C>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 13/14 | chr1 | 3479622 | |||||||
chr1:3479714 | T | TGCCCCG | 7 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 others(4): Show |
7 | HG00280.hp2 HG00741.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.1889-90_1889-85dup others(6): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr1 | 3479714 | ||||||
chr1:3479928 | G | A | 2 | a0001c0001t0001g0178 a0001c0001t0001g0183 |
2 | HG02683.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1990+15G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 14/14 | chr1 | 3479928 | |||||||
chr1:3479963 | G | A | 2 | a0002c0024t0002g0290 a0002c0028t0002g0094 |
2 | HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1990+50G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 14/14 | chr1 | 3479963 | |||||||
chr1:3480045 | C | T | 209 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(206): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.1990+132C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 14/14 | chr1 | 3480045 | |||||||
chr1:3480134 | C | G | 1 | a0001c0001t0001g0194 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1990+221C>G | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 14/14 | chr1 | 3480134 | |||||||
chr1:3480142 | C | T | 1 | a0002c0007t0002g0157 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1990+229C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 14/14 | chr1 | 3480142 | |||||||
chr1:3480173 | C | T | 20 | a0002c0003t0002g0002 a0002c0003t0002g0004 a0002c0003t0002g0005 others(17): Show |
32 | HG01123.hp2 HG01243.hp1 HG01261.hp1 others(29): Show |
intron_variant | MODIFIER | c.1990+260C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 14/14 | chr1 | 3480173 | |||||||
chr1:3480200 | C | T | 1 | a0003c0006t0002g0065 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1991-248C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 14/14 | chr1 | 3480200 | |||||||
chr1:3480264 | C | T | 1 | a0002c0008t0007g0096 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1991-184C>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 14/14 | chr1 | 3480264 | |||||||
chr1:3480396 | G | T | 7 | a0002c0012t0002g0291 a0002c0012t0010g0277 a0005c0013t0005g0279 others(4): Show |
7 | HG01109.hp2 HG02055.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1991-52G>T | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 14/14 | chr1 | 3480396 | |||||||
chr1:3480407 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1991-41G>A | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 14/14 | chr1 | 3480407 | |||||||
chr1:3480435 | T | C | 1 | a0012c0025t0012g0292 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1991-13T>C | ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 14/14 | chr1 | 3480435 |