Item | Value |
---|---|
geneid | 50650 |
ensemblid | ENSG00000163947.12 |
hgncid | 683 |
symbol | ARHGEF3 |
name | Rho guanine nucleotide exchange factor 3 |
refseq_nuc | NM_019555.3 |
refseq_prot | NP_062455.1 |
ensembl_nuc | ENST00000296315.8 |
ensembl_prot | ENSP00000296315.3 |
mane_status | MANE Select |
chr | chr3 |
start | 56727420 |
end | 56801949 |
strand | - |
ver | v1.2 |
region | chr3:56727420-56801949 |
region5000 | chr3:56722420-56806949 |
regionname0 | ARHGEF3_chr3_56727420_56801949 |
regionname5000 | ARHGEF3_chr3_56722420_56806949 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 526 | 209 | 37 | 33 | 99 | 10 | 29 | 80 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | MVAKD others(521): Show |
chr3 | 56722420 | 56806949 |
a0002 | 0/1 | 526 | 145 | 44 | 21 | 60 | 6 | 13 | 48 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | MVAKD others(521): Show |
chr3 | 56722420 | 56806949 |
a0003 | 0/0 | 526 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | MVAKD others(521): Show |
chr3 | 56722420 | 56806949 |
a0004 | 0/0 | 526 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | MVAKD others(521): Show |
chr3 | 56722420 | 56806949 |
a0005 | 0/0 | 526 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | MVAKD others(521): Show |
chr3 | 56722420 | 56806949 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002 | 0/0 | 1578 | 81 | 19 | 4 | 46 | 0 | 12 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | ATGGT others(1573): Show |
chr3 | 56722420 | 56806949 | ||
a0001c0003 | 1/0 | 1578 | 55 | 7 | 14 | 26 | 4 | 3 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | ATGGT others(1573): Show |
chr3 | 56722420 | 56806949 | ||
a0001c0005 | 0/0 | 1578 | 25 | 1 | 6 | 10 | 5 | 3 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | ATGGT others(1573): Show |
chr3 | 56722420 | 56806949 | ||
a0001c0006 | 0/0 | 1578 | 23 | 1 | 3 | 9 | 1 | 9 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | ATGGT others(1573): Show |
chr3 | 56722420 | 56806949 | ||
a0001c0007 | 0/0 | 1578 | 19 | 7 | 5 | 5 | 0 | 2 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | ATGGT others(1573): Show |
chr3 | 56722420 | 56806949 | ||
a0001c0008 | 0/0 | 1578 | 3 | 0 | 1 | 2 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | ATGGT others(1573): Show |
chr3 | 56722420 | 56806949 | ||
a0001c0009 | 0/0 | 1578 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | ATGGT others(1573): Show |
chr3 | 56722420 | 56806949 | ||
a0001c0012 | 0/0 | 1578 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | ATGGT others(1573): Show |
chr3 | 56722420 | 56806949 | ||
a0001c0013 | 0/0 | 1578 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | ATGGT others(1573): Show |
chr3 | 56722420 | 56806949 | ||
a0002c0001 | 0/0 | 1578 | 108 | 43 | 10 | 47 | 1 | 7 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | ATGGT others(1573): Show |
chr3 | 56722420 | 56806949 | ||
a0002c0004 | 0/1 | 1578 | 37 | 1 | 11 | 13 | 5 | 6 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | ATGGT others(1573): Show |
chr3 | 56722420 | 56806949 | ||
a0003c0010 | 0/0 | 1578 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | ATGGT others(1573): Show |
chr3 | 56722420 | 56806949 | ||
a0003c0014 | 0/0 | 1578 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | ATGGT others(1573): Show |
chr3 | 56722420 | 56806949 | ||
a0004c0011 | 0/0 | 1578 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | ATGGT others(1573): Show |
chr3 | 56722420 | 56806949 | ||
a0005c0015 | 0/0 | 1578 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | ATGGT others(1573): Show |
chr3 | 56722420 | 56806949 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0002 | 0/0 | 3582 | 73 | 11 | 4 | 46 | 0 | 12 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | AGTCG others(3577): Show |
chr3 | 56722420 | 56806949 |
a0001c0002t0005 | 0/0 | 3578 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | AGTCG others(3573): Show |
chr3 | 56722420 | 56806949 |
a0001c0002t0006 | 0/0 | 3582 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | AGTCG others(3577): Show |
chr3 | 56722420 | 56806949 |
a0001c0002t0008 | 0/0 | 3578 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | AGTCG others(3573): Show |
chr3 | 56722420 | 56806949 |
a0001c0002t0010 | 0/0 | 3582 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | AGTCG others(3577): Show |
chr3 | 56722420 | 56806949 |
a0001c0002t0017 | 0/0 | 3578 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | AGTCG others(3573): Show |
chr3 | 56722420 | 56806949 |
a0001c0003t0001 | 1/0 | 3582 | 53 | 7 | 14 | 24 | 4 | 3 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | AGTCG others(3577): Show |
chr3 | 56722420 | 56806949 |
a0001c0003t0011 | 0/0 | 3582 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | AGTCG others(3577): Show |
chr3 | 56722420 | 56806949 |
a0001c0003t0015 | 0/0 | 3582 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | AGTCG others(3577): Show |
chr3 | 56722420 | 56806949 |
a0001c0005t0001 | 0/0 | 3582 | 25 | 1 | 6 | 10 | 5 | 3 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | AGTCG others(3577): Show |
chr3 | 56722420 | 56806949 |
a0001c0006t0002 | 0/0 | 3582 | 22 | 1 | 3 | 8 | 1 | 9 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | AGTCG others(3577): Show |
chr3 | 56722420 | 56806949 |
a0001c0006t0018 | 0/0 | 3582 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | AGTCG others(3577): Show |
chr3 | 56722420 | 56806949 |
a0001c0007t0001 | 0/0 | 3582 | 8 | 7 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | AGTCG others(3577): Show |
chr3 | 56722420 | 56806949 |
a0001c0007t0004 | 0/0 | 3582 | 11 | 0 | 4 | 5 | 0 | 2 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | AGTCG others(3577): Show |
chr3 | 56722420 | 56806949 |
a0001c0008t0004 | 0/0 | 3582 | 3 | 0 | 1 | 2 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | AGTCG others(3577): Show |
chr3 | 56722420 | 56806949 |
a0001c0009t0002 | 0/0 | 3582 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | AGTCG others(3577): Show |
chr3 | 56722420 | 56806949 |
a0001c0012t0001 | 0/0 | 3582 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | AGTCG others(3577): Show |
chr3 | 56722420 | 56806949 |
a0001c0013t0001 | 0/0 | 3582 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | AGTCG others(3577): Show |
chr3 | 56722420 | 56806949 |
a0002c0001t0001 | 0/0 | 3582 | 69 | 33 | 8 | 25 | 1 | 2 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | AGTCG others(3577): Show |
chr3 | 56722420 | 56806949 |
a0002c0001t0003 | 0/0 | 3582 | 34 | 6 | 2 | 22 | 0 | 4 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | AGTCG others(3577): Show |
chr3 | 56722420 | 56806949 |
a0002c0001t0007 | 0/0 | 3582 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | AGTCG others(3577): Show |
chr3 | 56722420 | 56806949 |
a0002c0001t0009 | 0/0 | 3582 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | AGTCG others(3577): Show |
chr3 | 56722420 | 56806949 |
a0002c0001t0013 | 0/0 | 3582 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | AGTCG others(3577): Show |
chr3 | 56722420 | 56806949 |
a0002c0001t0016 | 0/0 | 3582 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | AGTCG others(3577): Show |
chr3 | 56722420 | 56806949 |
a0002c0004t0001 | 0/0 | 3582 | 12 | 1 | 5 | 2 | 2 | 2 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | AGTCG others(3577): Show |
chr3 | 56722420 | 56806949 |
a0002c0004t0003 | 0/1 | 3582 | 23 | 0 | 5 | 10 | 3 | 4 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | AGTCG others(3577): Show |
chr3 | 56722420 | 56806949 |
a0002c0004t0012 | 0/0 | 3582 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | AGTCG others(3577): Show |
chr3 | 56722420 | 56806949 |
a0002c0004t0014 | 0/0 | 3582 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | AGTCG others(3577): Show |
chr3 | 56722420 | 56806949 |
a0003c0010t0003 | 0/0 | 3582 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | AGTCG others(3577): Show |
chr3 | 56722420 | 56806949 |
a0003c0014t0003 | 0/0 | 3582 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | AGTCG others(3577): Show |
chr3 | 56722420 | 56806949 |
a0004c0011t0008 | 0/0 | 3578 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | AGTCG others(3573): Show |
chr3 | 56722420 | 56806949 |
a0005c0015t0002 | 0/0 | 3582 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | AGTCG others(3577): Show |
chr3 | 56722420 | 56806949 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0005g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0005g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0005g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0006g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0006g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0008g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0010g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0002t0017g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0150 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0011g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0003t0015g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0005t0001g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0005t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0005t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0005t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0005t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0005t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0005t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0005t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0005t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0005t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0005t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0005t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0005t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0005t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0005t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0005t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0005t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0005t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0005t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0005t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0005t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0005t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0005t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0005t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0006t0002g0009 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0006t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0006t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0006t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0006t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0006t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0006t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0006t0002g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0006t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0006t0002g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0006t0002g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0006t0002g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0006t0002g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0006t0002g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0006t0002g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0006t0002g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0006t0002g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0006t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0006t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0006t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0006t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0006t0018g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0007t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0007t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0007t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0007t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0007t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0007t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0007t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0007t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0007t0004g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0007t0004g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0007t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0007t0004g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0007t0004g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0007t0004g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0007t0004g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0007t0004g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0007t0004g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0007t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0007t0004g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0008t0004g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0008t0004g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0008t0004g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0009t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0012t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0001c0013t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0007g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0009g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0013g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0001t0016g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0001g0346 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0003g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0003g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0003g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0003g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0003g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0003g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0003g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0003g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0003g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0003g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0003g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0003g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0003g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0003g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0003g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0003g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0003g0345 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0012g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0002c0004t0014g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0003c0010t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0003c0014t0003g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0004c0011t0008g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
a0005c0015t0002g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0003 | t0001 | g0173 | EUR | GBR | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG00099 | hp2 | a0001 | c0003 | t0001 | g0166 | EUR | GBR | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG00140 | hp1 | a0002 | c0004 | t0003 | g0301 | EUR | GBR | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG00140 | hp2 | a0001 | c0005 | t0001 | g0322 | EUR | GBR | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG00280 | hp1 | a0001 | c0003 | t0001 | g0167 | EUR | FIN | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG00280 | hp2 | a0001 | c0006 | t0002 | g0009 | EUR | FIN | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG00323 | hp1 | a0001 | c0005 | t0001 | g0296 | EUR | FIN | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG00323 | hp2 | a0002 | c0004 | t0001 | g0346 | EUR | FIN | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG00544 | hp1 | a0002 | c0001 | t0003 | g0044 | EAS | CHS | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG00544 | hp2 | a0001 | c0002 | t0002 | g0058 | EAS | CHS | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG00558 | hp1 | a0001 | c0003 | t0001 | g0051 | EAS | CHS | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG00558 | hp2 | a0003 | c0014 | t0003 | g0311 | EAS | CHS | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG00597 | hp1 | a0001 | c0002 | t0002 | g0212 | EAS | CHS | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG00597 | hp2 | a0002 | c0001 | t0003 | g0113 | EAS | CHS | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG00621 | hp1 | a0001 | c0002 | t0002 | g0190 | EAS | CHS | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG00621 | hp2 | a0002 | c0004 | t0003 | g0339 | EAS | CHS | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG00639 | hp1 | a0001 | c0003 | t0001 | g0128 | AMR | PUR | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG00639 | hp2 | a0001 | c0002 | t0002 | g0168 | AMR | PUR | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG00642 | hp1 | a0001 | c0003 | t0001 | g0204 | AMR | PUR | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG00642 | hp2 | a0001 | c0005 | t0001 | g0299 | AMR | PUR | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG00673 | hp1 | a0001 | c0002 | t0002 | g0195 | EAS | CHS | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG00673 | hp2 | a0002 | c0001 | t0003 | g0263 | EAS | CHS | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG00733 | hp1 | a0002 | c0004 | t0012 | g0266 | AMR | PUR | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG00733 | hp2 | a0002 | c0004 | t0001 | g0008 | AMR | PUR | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG00738 | hp1 | a0001 | c0006 | t0002 | g0009 | AMR | PUR | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG00738 | hp2 | a0001 | c0005 | t0001 | g0010 | AMR | PUR | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG00741 | hp1 | a0001 | c0005 | t0001 | g0265 | AMR | PUR | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG00741 | hp2 | a0001 | c0003 | t0001 | g0104 | AMR | PUR | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01070 | hp1 | a0001 | c0007 | t0001 | g0162 | AMR | PUR | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01070 | hp2 | a0002 | c0004 | t0001 | g0282 | AMR | PUR | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01071 | hp1 | a0001 | c0003 | t0001 | g0174 | AMR | PUR | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01071 | hp2 | a0002 | c0004 | t0001 | g0008 | AMR | PUR | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01099 | hp1 | a0001 | c0002 | t0002 | g0086 | AMR | PUR | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01099 | hp2 | a0001 | c0003 | t0001 | g0182 | AMR | PUR | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01106 | hp1 | a0001 | c0005 | t0001 | g0271 | AMR | PUR | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01106 | hp2 | a0001 | c0005 | t0001 | g0321 | AMR | PUR | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01109 | hp1 | a0002 | c0001 | t0001 | g0226 | AMR | PUR | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01109 | hp2 | a0001 | c0003 | t0001 | g0017 | AMR | PUR | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01167 | hp1 | a0001 | c0003 | t0001 | g0006 | AMR | PUR | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01167 | hp2 | a0002 | c0001 | t0001 | g0003 | AMR | PUR | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01169 | hp1 | a0002 | c0001 | t0001 | g0003 | AMR | PUR | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01169 | hp2 | a0001 | c0003 | t0001 | g0180 | AMR | PUR | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01175 | hp1 | a0002 | c0004 | t0003 | g0303 | AMR | PUR | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01175 | hp2 | a0001 | c0003 | t0001 | g0184 | AMR | PUR | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01256 | hp1 | a0001 | c0006 | t0002 | g0268 | AMR | CLM | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01256 | hp2 | a0001 | c0003 | t0001 | g0148 | AMR | CLM | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01258 | hp1 | a0001 | c0006 | t0002 | g0269 | AMR | CLM | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01258 | hp2 | a0001 | c0003 | t0001 | g0006 | AMR | CLM | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01261 | hp1 | a0002 | c0001 | t0003 | g0154 | AMR | CLM | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01261 | hp2 | a0001 | c0003 | t0001 | g0176 | AMR | CLM | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01361 | hp1 | a0002 | c0004 | t0001 | g0309 | AMR | CLM | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01361 | hp2 | a0001 | c0007 | t0004 | g0117 | AMR | CLM | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01496 | hp1 | a0001 | c0003 | t0001 | g0091 | AMR | CLM | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01496 | hp2 | a0002 | c0004 | t0001 | g0279 | AMR | CLM | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01515 | hp1 | a0001 | c0003 | t0001 | g0171 | EUR | IBS | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01515 | hp2 | a0002 | c0004 | t0003 | g0306 | EUR | IBS | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01516 | hp1 | a0001 | c0005 | t0001 | g0323 | EUR | IBS | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01516 | hp2 | a0001 | c0005 | t0001 | g0293 | EUR | IBS | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01517 | hp1 | a0001 | c0005 | t0001 | g0292 | EUR | IBS | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01517 | hp2 | a0002 | c0004 | t0003 | g0305 | EUR | IBS | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01884 | hp1 | a0002 | c0001 | t0001 | g0094 | AFR | ACB | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01884 | hp2 | a0001 | c0003 | t0001 | g0100 | AFR | ACB | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01891 | hp1 | a0001 | c0003 | t0001 | g0255 | AFR | ACB | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01891 | hp2 | a0001 | c0002 | t0002 | g0153 | AFR | ACB | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01928 | hp1 | a0001 | c0007 | t0004 | g0114 | AMR | PEL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01928 | hp2 | a0002 | c0004 | t0003 | g0330 | AMR | PEL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01934 | hp1 | a0002 | c0004 | t0003 | g0302 | AMR | PEL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01934 | hp2 | a0002 | c0001 | t0001 | g0097 | AMR | PEL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01952 | hp1 | a0001 | c0008 | t0004 | g0315 | AMR | PEL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01952 | hp2 | a0002 | c0001 | t0001 | g0118 | AMR | PEL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01975 | hp1 | a0002 | c0001 | t0001 | g0262 | AMR | PEL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01975 | hp2 | a0002 | c0001 | t0003 | g0116 | AMR | PEL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01981 | hp1 | a0001 | c0005 | t0001 | g0310 | AMR | PEL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01981 | hp2 | a0001 | c0002 | t0002 | g0025 | AMR | PEL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02027 | hp1 | a0001 | c0002 | t0002 | g0023 | EAS | KHV | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02027 | hp2 | a0002 | c0004 | t0003 | g0277 | EAS | KHV | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02040 | hp1 | a0001 | c0003 | t0001 | g0259 | EAS | KHV | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02040 | hp2 | a0002 | c0001 | t0001 | g0247 | EAS | KHV | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02055 | hp1 | a0001 | c0002 | t0005 | g0250 | AFR | ACB | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02055 | hp2 | a0001 | c0003 | t0001 | g0170 | AFR | ACB | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02071 | hp1 | a0001 | c0006 | t0002 | g0338 | EAS | KHV | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02071 | hp2 | a0002 | c0001 | t0003 | g0224 | EAS | KHV | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02074 | hp1 | a0002 | c0001 | t0003 | g0163 | EAS | KHV | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02074 | hp2 | a0001 | c0002 | t0002 | g0124 | EAS | KHV | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02080 | hp1 | a0001 | c0002 | t0002 | g0131 | EAS | KHV | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02080 | hp2 | a0001 | c0002 | t0002 | g0056 | EAS | KHV | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02083 | hp1 | a0002 | c0004 | t0003 | g0276 | EAS | KHV | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02083 | hp2 | a0001 | c0002 | t0002 | g0125 | EAS | KHV | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02135 | hp1 | a0001 | c0002 | t0002 | g0130 | EAS | KHV | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02135 | hp2 | a0002 | c0004 | t0003 | g0267 | EAS | KHV | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02145 | hp1 | a0001 | c0006 | t0002 | g0289 | AFR | ACB | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02145 | hp2 | a0001 | c0003 | t0001 | g0016 | AFR | ACB | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02155 | hp1 | a0002 | c0004 | t0003 | g0278 | EAS | CDX | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02155 | hp2 | a0001 | c0002 | t0002 | g0066 | EAS | CDX | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02165 | hp1 | a0001 | c0002 | t0002 | g0028 | EAS | CDX | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02165 | hp2 | a0001 | c0003 | t0001 | g0172 | EAS | CDX | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02257 | hp1 | a0001 | c0005 | t0001 | g0010 | AFR | ACB | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02257 | hp2 | a0002 | c0001 | t0003 | g0202 | AFR | ACB | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02258 | hp1 | a0002 | c0001 | t0003 | g0089 | AFR | ACB | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02258 | hp2 | a0001 | c0002 | t0010 | g0014 | AFR | ACB | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02273 | hp1 | a0001 | c0007 | t0004 | g0039 | AMR | PEL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02273 | hp2 | a0002 | c0001 | t0001 | g0260 | AMR | PEL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02280 | hp1 | a0001 | c0007 | t0001 | g0093 | AFR | ACB | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02280 | hp2 | a0001 | c0002 | t0002 | g0083 | AFR | ACB | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02293 | hp1 | a0001 | c0007 | t0004 | g0115 | AMR | PEL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02293 | hp2 | a0002 | c0004 | t0003 | g0316 | AMR | PEL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02300 | hp1 | a0002 | c0004 | t0003 | g0300 | AMR | PEL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02300 | hp2 | a0001 | c0003 | t0001 | g0149 | AMR | PEL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02451 | hp1 | a0002 | c0001 | t0007 | g0004 | AFR | ACB | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02451 | hp2 | a0002 | c0001 | t0001 | g0001 | AFR | ACB | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02523 | hp1 | a0001 | c0007 | t0004 | g0059 | EAS | KHV | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02523 | hp2 | a0001 | c0005 | t0001 | g0290 | EAS | KHV | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02572 | hp1 | a0002 | c0001 | t0016 | g0146 | AFR | GWD | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02572 | hp2 | a0002 | c0001 | t0001 | g0155 | AFR | GWD | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02602 | hp1 | a0001 | c0006 | t0002 | g0328 | SAS | PJL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02602 | hp2 | a0001 | c0007 | t0004 | g0112 | SAS | PJL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02615 | hp1 | a0002 | c0001 | t0001 | g0225 | AFR | GWD | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02615 | hp2 | a0002 | c0001 | t0001 | g0160 | AFR | GWD | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02622 | hp1 | a0002 | c0001 | t0001 | g0103 | AFR | GWD | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02622 | hp2 | a0002 | c0001 | t0001 | g0084 | AFR | GWD | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02630 | hp1 | a0001 | c0003 | t0001 | g0244 | AFR | GWD | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02630 | hp2 | a0002 | c0001 | t0001 | g0245 | AFR | GWD | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02647 | hp1 | a0004 | c0011 | t0008 | g0073 | AFR | GWD | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02647 | hp2 | a0002 | c0001 | t0003 | g0151 | AFR | GWD | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02683 | hp1 | a0001 | c0003 | t0001 | g0177 | SAS | PJL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02683 | hp2 | a0001 | c0006 | t0002 | g0326 | SAS | PJL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02698 | hp1 | a0002 | c0001 | t0001 | g0264 | SAS | PJL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02698 | hp2 | a0001 | c0005 | t0001 | g0273 | SAS | PJL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02723 | hp1 | a0001 | c0002 | t0006 | g0013 | AFR | GWD | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02723 | hp2 | a0002 | c0001 | t0001 | g0019 | AFR | GWD | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02735 | hp1 | a0001 | c0002 | t0002 | g0029 | SAS | PJL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02735 | hp2 | a0001 | c0002 | t0002 | g0194 | SAS | PJL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02818 | hp1 | a0002 | c0001 | t0001 | g0156 | AFR | GWD | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02818 | hp2 | a0002 | c0001 | t0001 | g0159 | AFR | GWD | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02886 | hp1 | a0001 | c0002 | t0002 | g0077 | AFR | GWD | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02886 | hp2 | a0002 | c0001 | t0001 | g0099 | AFR | GWD | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02896 | hp1 | a0001 | c0002 | t0002 | g0257 | AFR | GWD | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02896 | hp2 | a0002 | c0001 | t0001 | g0152 | AFR | GWD | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02897 | hp1 | a0001 | c0002 | t0002 | g0256 | AFR | GWD | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02897 | hp2 | a0002 | c0001 | t0003 | g0208 | AFR | GWD | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02922 | hp1 | a0002 | c0001 | t0001 | g0081 | AFR | ESN | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02922 | hp2 | a0002 | c0001 | t0001 | g0015 | AFR | ESN | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02965 | hp1 | a0002 | c0001 | t0001 | g0175 | AFR | ESN | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02965 | hp2 | a0001 | c0007 | t0001 | g0074 | AFR | ESN | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02976 | hp1 | a0001 | c0002 | t0005 | g0142 | AFR | ESN | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02976 | hp2 | a0002 | c0001 | t0007 | g0004 | AFR | ESN | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03017 | hp1 | a0001 | c0002 | t0002 | g0069 | SAS | PJL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03017 | hp2 | a0001 | c0006 | t0002 | g0320 | SAS | PJL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03098 | hp1 | a0001 | c0002 | t0017 | g0161 | AFR | MSL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03098 | hp2 | a0002 | c0001 | t0001 | g0200 | AFR | MSL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03139 | hp1 | a0001 | c0007 | t0001 | g0098 | AFR | ESN | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03139 | hp2 | a0001 | c0003 | t0001 | g0018 | AFR | ESN | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03195 | hp1 | a0002 | c0001 | t0001 | g0075 | AFR | ESN | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03195 | hp2 | a0002 | c0001 | t0003 | g0080 | AFR | ESN | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03225 | hp1 | a0002 | c0001 | t0001 | g0227 | AFR | MSL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03225 | hp2 | a0002 | c0001 | t0001 | g0096 | AFR | MSL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03239 | hp1 | a0002 | c0001 | t0003 | g0027 | SAS | PJL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03239 | hp2 | a0001 | c0006 | t0002 | g0325 | SAS | PJL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03486 | hp1 | a0001 | c0002 | t0002 | g0138 | AFR | MSL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03486 | hp2 | a0002 | c0001 | t0001 | g0088 | AFR | MSL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03490 | hp1 | a0002 | c0001 | t0001 | g0090 | SAS | PJL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03490 | hp2 | a0001 | c0002 | t0002 | g0063 | SAS | PJL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03491 | hp1 | a0001 | c0002 | t0002 | g0064 | SAS | PJL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03491 | hp2 | a0001 | c0006 | t0002 | g0319 | SAS | PJL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03516 | hp1 | a0002 | c0001 | t0001 | g0258 | AFR | ESN | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03516 | hp2 | a0001 | c0013 | t0001 | g0140 | AFR | ESN | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03540 | hp1 | a0001 | c0012 | t0001 | g0105 | AFR | GWD | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03540 | hp2 | a0002 | c0001 | t0001 | g0141 | AFR | GWD | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03579 | hp1 | a0001 | c0003 | t0001 | g0216 | AFR | MSL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03579 | hp2 | a0002 | c0001 | t0001 | g0085 | AFR | MSL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03654 | hp1 | a0002 | c0004 | t0003 | g0331 | SAS | PJL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03654 | hp2 | a0002 | c0001 | t0013 | g0201 | SAS | PJL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03669 | hp1 | a0001 | c0002 | t0002 | g0207 | SAS | PJL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03669 | hp2 | a0002 | c0001 | t0003 | g0203 | SAS | PJL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03688 | hp1 | a0002 | c0004 | t0003 | g0298 | SAS | STU | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03688 | hp2 | a0001 | c0005 | t0001 | g0308 | SAS | STU | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03704 | hp1 | a0001 | c0002 | t0002 | g0110 | SAS | PJL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03704 | hp2 | a0001 | c0005 | t0001 | g0297 | SAS | PJL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03710 | hp1 | a0002 | c0004 | t0001 | g0283 | SAS | PJL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03710 | hp2 | a0002 | c0004 | t0003 | g0329 | SAS | PJL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03834 | hp1 | a0001 | c0002 | t0002 | g0022 | SAS | BEB | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03834 | hp2 | a0001 | c0003 | t0001 | g0109 | SAS | BEB | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03927 | hp1 | a0002 | c0001 | t0003 | g0219 | SAS | BEB | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03927 | hp2 | a0001 | c0003 | t0001 | g0092 | SAS | BEB | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03942 | hp1 | a0002 | c0004 | t0003 | g0335 | SAS | BEB | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03942 | hp2 | a0001 | c0006 | t0002 | g0327 | SAS | BEB | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG04115 | hp1 | a0001 | c0006 | t0002 | g0291 | SAS | STU | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG04115 | hp2 | a0002 | c0004 | t0001 | g0332 | SAS | STU | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG04184 | hp1 | a0001 | c0002 | t0002 | g0192 | SAS | BEB | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG04184 | hp2 | a0001 | c0006 | t0002 | g0324 | SAS | BEB | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG04199 | hp1 | a0001 | c0002 | t0002 | g0065 | SAS | STU | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG04199 | hp2 | a0001 | c0002 | t0002 | g0068 | SAS | STU | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG04204 | hp1 | a0001 | c0006 | t0002 | g0333 | SAS | STU | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG04204 | hp2 | a0001 | c0007 | t0004 | g0111 | SAS | STU | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG04228 | hp1 | a0001 | c0002 | t0002 | g0157 | SAS | STU | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG04228 | hp2 | a0002 | c0001 | t0003 | g0243 | SAS | STU | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18522 | hp1 | a0001 | c0007 | t0001 | g0102 | AFR | YRI | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18522 | hp2 | a0001 | c0002 | t0002 | g0078 | AFR | YRI | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18612 | hp1 | a0002 | c0001 | t0001 | g0232 | EAS | CHB | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18612 | hp2 | a0001 | c0006 | t0002 | g0341 | EAS | CHB | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18906 | hp1 | a0001 | c0002 | t0005 | g0249 | AFR | YRI | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18906 | hp2 | a0002 | c0001 | t0001 | g0147 | AFR | YRI | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18940 | hp1 | a0001 | c0002 | t0002 | g0214 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18940 | hp2 | a0002 | c0001 | t0001 | g0062 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18941 | hp1 | a0001 | c0003 | t0001 | g0070 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18941 | hp2 | a0001 | c0002 | t0002 | g0042 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18942 | hp1 | a0002 | c0001 | t0001 | g0239 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18942 | hp2 | a0002 | c0001 | t0003 | g0106 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18944 | hp1 | a0001 | c0003 | t0001 | g0241 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18944 | hp2 | a0002 | c0001 | t0003 | g0221 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18945 | hp1 | a0001 | c0005 | t0001 | g0285 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18945 | hp2 | a0002 | c0001 | t0001 | g0231 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18946 | hp1 | a0001 | c0008 | t0004 | g0313 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18946 | hp2 | a0001 | c0002 | t0002 | g0187 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18947 | hp1 | a0001 | c0002 | t0002 | g0188 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18947 | hp2 | a0001 | c0003 | t0001 | g0050 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18950 | hp1 | a0001 | c0002 | t0002 | g0021 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18950 | hp2 | a0001 | c0006 | t0002 | g0275 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18952 | hp1 | a0001 | c0002 | t0002 | g0040 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18952 | hp2 | a0001 | c0005 | t0001 | g0343 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18953 | hp1 | a0001 | c0003 | t0001 | g0209 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18953 | hp2 | a0001 | c0002 | t0002 | g0191 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18954 | hp1 | a0002 | c0004 | t0003 | g0274 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18954 | hp2 | a0001 | c0003 | t0001 | g0246 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18956 | hp1 | a0001 | c0005 | t0001 | g0317 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18956 | hp2 | a0002 | c0001 | t0001 | g0211 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18960 | hp1 | a0001 | c0006 | t0002 | g0337 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18960 | hp2 | a0002 | c0001 | t0003 | g0035 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18961 | hp1 | a0001 | c0003 | t0001 | g0061 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18961 | hp2 | a0002 | c0001 | t0001 | g0237 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18962 | hp1 | a0001 | c0003 | t0001 | g0048 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18962 | hp2 | a0002 | c0004 | t0014 | g0284 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18963 | hp1 | a0001 | c0003 | t0001 | g0033 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18963 | hp2 | a0001 | c0005 | t0001 | g0270 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18964 | hp1 | a0002 | c0004 | t0001 | g0340 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18964 | hp2 | a0002 | c0001 | t0001 | g0055 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18965 | hp1 | a0001 | c0003 | t0001 | g0183 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18965 | hp2 | a0001 | c0007 | t0004 | g0031 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18966 | hp1 | a0001 | c0006 | t0002 | g0281 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18966 | hp2 | a0002 | c0001 | t0001 | g0107 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18967 | hp1 | a0001 | c0002 | t0002 | g0253 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18967 | hp2 | a0002 | c0001 | t0003 | g0045 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18968 | hp1 | a0001 | c0002 | t0002 | g0026 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18968 | hp2 | a0002 | c0001 | t0003 | g0067 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18969 | hp1 | a0001 | c0002 | t0002 | g0054 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18969 | hp2 | a0001 | c0003 | t0001 | g0046 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18970 | hp1 | a0001 | c0005 | t0001 | g0344 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18970 | hp2 | a0001 | c0002 | t0002 | g0052 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18972 | hp1 | a0001 | c0006 | t0018 | g0348 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18972 | hp2 | a0002 | c0001 | t0003 | g0036 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18973 | hp1 | a0001 | c0003 | t0001 | g0179 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18973 | hp2 | a0002 | c0001 | t0003 | g0223 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18977 | hp1 | a0002 | c0001 | t0001 | g0206 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18977 | hp2 | a0001 | c0005 | t0001 | g0272 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18979 | hp1 | a0002 | c0001 | t0001 | g0248 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18979 | hp2 | a0001 | c0002 | t0002 | g0178 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18980 | hp1 | a0001 | c0003 | t0001 | g0134 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18980 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18982 | hp1 | a0001 | c0003 | t0001 | g0049 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18982 | hp2 | a0001 | c0002 | t0002 | g0252 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18984 | hp1 | a0001 | c0003 | t0015 | g0108 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18984 | hp2 | a0001 | c0002 | t0002 | g0037 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18986 | hp1 | a0001 | c0002 | t0002 | g0043 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18986 | hp2 | a0002 | c0004 | t0003 | g0318 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18990 | hp1 | a0002 | c0001 | t0003 | g0002 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18990 | hp2 | a0001 | c0002 | t0002 | g0215 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18994 | hp1 | a0001 | c0003 | t0001 | g0251 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18994 | hp2 | a0002 | c0001 | t0001 | g0233 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18995 | hp1 | a0002 | c0001 | t0003 | g0199 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18995 | hp2 | a0001 | c0002 | t0002 | g0038 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18999 | hp1 | a0001 | c0007 | t0004 | g0123 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18999 | hp2 | a0002 | c0001 | t0001 | g0240 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19000 | hp1 | a0002 | c0001 | t0001 | g0205 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19000 | hp2 | a0001 | c0006 | t0002 | g0336 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19001 | hp1 | a0002 | c0001 | t0001 | g0229 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19001 | hp2 | a0001 | c0002 | t0002 | g0165 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19004 | hp1 | a0002 | c0001 | t0001 | g0230 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19004 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19005 | hp1 | a0001 | c0002 | t0002 | g0034 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19005 | hp2 | a0001 | c0002 | t0002 | g0218 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19006 | hp1 | a0001 | c0002 | t0002 | g0129 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19006 | hp2 | a0001 | c0005 | t0001 | g0286 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19007 | hp1 | a0001 | c0002 | t0002 | g0032 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19007 | hp2 | a0002 | c0001 | t0001 | g0210 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19012 | hp1 | a0002 | c0001 | t0001 | g0236 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19012 | hp2 | a0001 | c0008 | t0004 | g0314 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19030 | hp1 | a0001 | c0002 | t0002 | g0139 | AFR | LWK | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19030 | hp2 | a0002 | c0001 | t0001 | g0144 | AFR | LWK | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19043 | hp1 | a0001 | c0007 | t0001 | g0101 | AFR | LWK | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19043 | hp2 | a0001 | c0002 | t0002 | g0079 | AFR | LWK | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19054 | hp1 | a0001 | c0005 | t0001 | g0287 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19054 | hp2 | a0001 | c0002 | t0002 | g0193 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19055 | hp1 | a0002 | c0001 | t0003 | g0060 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19055 | hp2 | a0001 | c0003 | t0011 | g0120 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19056 | hp1 | a0002 | c0001 | t0001 | g0228 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19056 | hp2 | a0005 | c0015 | t0002 | g0347 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19057 | hp1 | a0001 | c0002 | t0002 | g0197 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19057 | hp2 | a0002 | c0001 | t0003 | g0186 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19060 | hp1 | a0001 | c0002 | t0002 | g0196 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19060 | hp2 | a0002 | c0004 | t0003 | g0294 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19063 | hp1 | a0001 | c0007 | t0004 | g0126 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19063 | hp2 | a0001 | c0003 | t0001 | g0181 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19064 | hp1 | a0001 | c0005 | t0001 | g0295 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19064 | hp2 | a0001 | c0007 | t0004 | g0122 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19065 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19065 | hp2 | a0001 | c0003 | t0001 | g0041 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19066 | hp1 | a0001 | c0002 | t0002 | g0242 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19066 | hp2 | a0002 | c0001 | t0001 | g0235 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19067 | hp1 | a0002 | c0001 | t0001 | g0132 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19067 | hp2 | a0001 | c0006 | t0002 | g0312 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19068 | hp1 | a0001 | c0003 | t0001 | g0071 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19068 | hp2 | a0002 | c0004 | t0003 | g0307 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19070 | hp1 | a0002 | c0001 | t0003 | g0198 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19070 | hp2 | a0002 | c0001 | t0001 | g0185 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19078 | hp1 | a0002 | c0001 | t0001 | g0238 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19078 | hp2 | a0001 | c0003 | t0001 | g0047 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19079 | hp1 | a0002 | c0001 | t0003 | g0222 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19079 | hp2 | a0002 | c0001 | t0001 | g0254 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19081 | hp1 | a0002 | c0004 | t0001 | g0342 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19081 | hp2 | a0001 | c0003 | t0001 | g0121 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19084 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19084 | hp2 | a0002 | c0001 | t0003 | g0220 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19085 | hp1 | a0001 | c0002 | t0002 | g0057 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19085 | hp2 | a0002 | c0001 | t0003 | g0002 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19086 | hp1 | a0001 | c0006 | t0002 | g0280 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19086 | hp2 | a0002 | c0004 | t0003 | g0304 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19087 | hp1 | a0001 | c0002 | t0002 | g0217 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19087 | hp2 | a0001 | c0002 | t0002 | g0189 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19088 | hp1 | a0002 | c0001 | t0001 | g0234 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19088 | hp2 | a0002 | c0001 | t0003 | g0024 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19090 | hp1 | a0003 | c0010 | t0003 | g0119 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19090 | hp2 | a0001 | c0002 | t0002 | g0213 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19091 | hp1 | a0001 | c0009 | t0002 | g0020 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA19091 | hp2 | a0001 | c0003 | t0001 | g0053 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA20129 | hp1 | a0002 | c0001 | t0001 | g0143 | AFR | ASW | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA20129 | hp2 | a0002 | c0001 | t0001 | g0145 | AFR | ASW | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA20752 | hp1 | a0002 | c0004 | t0001 | g0288 | EUR | TSI | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA20752 | hp2 | a0002 | c0001 | t0001 | g0137 | EUR | TSI | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01123 | hp1 | a0002 | c0001 | t0001 | g0261 | AMR | CLM | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG01123 | hp2 | a0001 | c0002 | t0002 | g0169 | AMR | CLM | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02109 | hp1 | a0002 | c0001 | t0009 | g0012 | AFR | ACB | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02109 | hp2 | a0002 | c0001 | t0001 | g0136 | AFR | ACB | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02486 | hp1 | a0002 | c0001 | t0003 | g0082 | AFR | ACB | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02486 | hp2 | a0001 | c0002 | t0002 | g0127 | AFR | ACB | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02559 | hp1 | a0001 | c0002 | t0008 | g0135 | AFR | ACB | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG02559 | hp2 | a0002 | c0001 | t0001 | g0133 | AFR | ACB | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03471 | hp1 | a0002 | c0001 | t0001 | g0158 | AFR | MSL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG03471 | hp2 | a0002 | c0001 | t0001 | g0095 | AFR | MSL | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG06807 | hp1 | a0002 | c0001 | t0001 | g0001 | AFR | USA | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
HG06807 | hp2 | a0001 | c0007 | t0001 | g0164 | AFR | USA | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18955 | hp1 | a0002 | c0001 | t0003 | g0030 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA18955 | hp2 | a0001 | c0003 | t0001 | g0072 | EAS | JPT | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA20300 | hp1 | a0001 | c0007 | t0001 | g0076 | AFR | USA | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA20300 | hp2 | a0001 | c0002 | t0006 | g0011 | AFR | USA | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA21309 | hp1 | a0001 | c0002 | t0002 | g0087 | AFR | LWK | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
NA21309 | hp2 | a0002 | c0004 | t0001 | g0334 | AFR | LWK | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
homoSapiens | chm13v2 | a0002 | c0004 | t0003 | g0345 | REF | REF | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
homoSapiens | grch38p0 | a0001 | c0003 | t0001 | g0150 | REF | REF | ARHGEF3_chr3_56722420_56806949 | ARHGEF3 | chr3 | 56722420 | 56806949 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:56729329 | G | A | 1 | a0003 | 2 | HG00558.hp2 NA19090.hp1 |
missense_variant | MODERATE | c.1522C>T | p.Arg508Cys | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 10/10 | 1673/3582 | 1522/1581 | 508/526 | chr3 | 56729329 | |||
chr3:56732325 | C | T | 1 | a0004 | 1 | HG02647.hp1 | missense_variant | MODERATE | c.1141G>A | p.Val381Met | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/10 | 1292/3582 | 1141/1581 | 381/526 | chr3 | 56732325 | |||
chr3:56737223 | A | C | 2 | a0002 a0003 |
146 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(143): Show |
missense_variant | MODERATE | c.1003T>G | p.Leu335Val | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/10 | 1154/3582 | 1003/1581 | 335/526 | chr3 | 56737223 | |||
chr3:56801761 | T | C | 1 | a0005 | 1 | NA19056.hp2 | missense_variant | MODERATE | c.38A>G | p.Lys13Arg | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/10 | 189/3582 | 38/1581 | 13/526 | chr3 | 56801761 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:56729288 | G | A | 12 | a0001c0002 a0001c0006 a0001c0007 others(9): Show |
276 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(273): Show |
synonymous_variant | LOW | c.1563C>T | p.His521His | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 10/10 | 1714/3582 | 1563/1581 | 521/526 | chr3 | 56729288 | |||
chr3:56729300 | T | C | 11 | a0001c0002 a0001c0006 a0001c0007 others(8): Show |
275 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(272): Show |
synonymous_variant | LOW | c.1551A>G | p.Gly517Gly | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 10/10 | 1702/3582 | 1551/1581 | 517/526 | chr3 | 56729300 | |||
chr3:56729497 | A | G | 5 | a0001c0002 a0001c0006 a0001c0009 others(2): Show |
107 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(104): Show |
synonymous_variant | LOW | c.1354T>C | p.Leu452Leu | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 10/10 | 1505/3582 | 1354/1581 | 452/526 | chr3 | 56729497 | |||
chr3:56729507 | T | C | 1 | a0001c0013 | 1 | HG03516.hp2 | synonymous_variant | LOW | c.1344A>G | p.Lys448Lys | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 10/10 | 1495/3582 | 1344/1581 | 448/526 | chr3 | 56729507 | |||
chr3:56729591 | A | G | 5 | a0001c0002 a0001c0006 a0001c0009 others(2): Show |
107 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(104): Show |
synonymous_variant | LOW | c.1260T>C | p.Asn420Asn | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 10/10 | 1411/3582 | 1260/1581 | 420/526 | chr3 | 56729591 | |||
chr3:56732407 | C | G | 5 | a0001c0002 a0001c0006 a0001c0009 others(2): Show |
107 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(104): Show |
synonymous_variant | LOW | c.1059G>C | p.Leu353Leu | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/10 | 1210/3582 | 1059/1581 | 353/526 | chr3 | 56732407 | |||
chr3:56773772 | C | T | 1 | a0001c0009 | 1 | NA19091.hp1 | synonymous_variant | LOW | c.141G>A | p.Ser47Ser | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/10 | 292/3582 | 141/1581 | 47/526 | chr3 | 56773772 | |||
chr3:56801733 | G | A | 5 | a0001c0005 a0001c0006 a0001c0008 others(2): Show |
88 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(85): Show |
synonymous_variant | LOW | c.66C>T | p.Pro22Pro | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/10 | 217/3582 | 66/1581 | 22/526 | chr3 | 56801733 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:56727622 | A | G | 7 | a0002c0001t0003 a0002c0001t0013 a0002c0004t0003 others(4): Show |
61 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*1648T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 10/10 | 1648 | chr3 | 56727622 | ||||||
chr3:56727665 | G | C | 1 | a0002c0001t0013 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1605C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 10/10 | 1605 | chr3 | 56727665 | ||||||
chr3:56727687 | G | A | 7 | a0001c0002t0002 a0001c0002t0006 a0001c0002t0010 others(4): Show |
101 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*1583C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 10/10 | 1583 | chr3 | 56727687 | ||||||
chr3:56727893 | C | T | 1 | a0002c0004t0012 | 1 | HG00733.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1377G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 10/10 | 1377 | chr3 | 56727893 | ||||||
chr3:56728013 | A | G | 2 | a0001c0002t0005 a0001c0002t0017 |
4 | HG02055.hp1 HG02976.hp1 HG03098.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1257T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 10/10 | 1257 | chr3 | 56728013 | ||||||
chr3:56728217 | T | C | 11 | a0001c0002t0002 a0001c0002t0005 a0001c0002t0006 others(8): Show |
107 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*1053A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 10/10 | 1053 | chr3 | 56728217 | ||||||
chr3:56728221 | C | T | 2 | a0001c0007t0004 a0001c0008t0004 |
14 | HG01361.hp2 HG01928.hp1 HG01952.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1049G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 10/10 | 1049 | chr3 | 56728221 | ||||||
chr3:56728307 | G | A | 1 | a0002c0004t0014 | 1 | NA18962.hp2 | 3_prime_UTR_variant | MODIFIER | c.*963C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 10/10 | 963 | chr3 | 56728307 | ||||||
chr3:56728449 | C | T | 2 | a0001c0002t0008 a0004c0011t0008 |
2 | HG02559.hp1 HG02647.hp1 |
3_prime_UTR_variant | MODIFIER | c.*821G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 10/10 | 821 | chr3 | 56728449 | ||||||
chr3:56728679 | C | T | 1 | a0001c0003t0011 | 1 | NA19055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*591G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 10/10 | 591 | chr3 | 56728679 | ||||||
chr3:56728712 | T | G | 1 | a0001c0003t0015 | 1 | NA18984.hp1 | 3_prime_UTR_variant | MODIFIER | c.*558A>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 10/10 | 558 | chr3 | 56728712 | ||||||
chr3:56728736 | T | C | 4 | a0001c0002t0005 a0001c0002t0008 a0001c0002t0017 others(1): Show |
6 | HG02055.hp1 HG02559.hp1 HG02647.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*534A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 10/10 | 534 | chr3 | 56728736 | ||||||
chr3:56728737 | G | A | 1 | a0001c0002t0017 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*533C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 10/10 | 533 | chr3 | 56728737 | ||||||
chr3:56728746 | C | G | 4 | a0001c0002t0005 a0001c0002t0008 a0001c0002t0017 others(1): Show |
6 | HG02055.hp1 HG02559.hp1 HG02647.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*524G>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 10/10 | 524 | chr3 | 56728746 | ||||||
chr3:56728905 | A | G | 1 | a0002c0001t0007 | 2 | HG02451.hp1 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*365T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 10/10 | 365 | chr3 | 56728905 | ||||||
chr3:56728920 | C | A | 1 | a0002c0001t0016 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*350G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 10/10 | 350 | chr3 | 56728920 | ||||||
chr3:56728939 | A | G | 11 | a0001c0002t0002 a0001c0002t0005 a0001c0002t0006 others(8): Show |
107 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*331T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 10/10 | 331 | chr3 | 56728939 | ||||||
chr3:56728940 | A | G | 11 | a0001c0002t0002 a0001c0002t0005 a0001c0002t0006 others(8): Show |
107 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*330T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 10/10 | 330 | chr3 | 56728940 | ||||||
chr3:56728968 | ATTCT | A | 4 | a0001c0002t0005 a0001c0002t0008 a0001c0002t0017 others(1): Show |
6 | HG02055.hp1 HG02559.hp1 HG02647.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*298_*301delAGAA | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 10/10 | 298 | chr3 | 56728968 | ||||||
chr3:56729200 | T | C | 7 | a0001c0002t0002 a0001c0002t0006 a0001c0002t0010 others(4): Show |
101 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*70A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 10/10 | 70 | chr3 | 56729200 | ||||||
chr3:56801868 | A | G | 1 | a0001c0006t0018 | 1 | NA18972.hp1 | 5_prime_UTR_variant | MODIFIER | c.-70T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/10 | 70 | chr3 | 56801868 | ||||||
chr3:56801873 | G | C | 1 | a0001c0006t0018 | 1 | NA18972.hp1 | 5_prime_UTR_variant | MODIFIER | c.-75C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/10 | 75 | chr3 | 56801873 | ||||||
chr3:56801919 | C | T | 1 | a0001c0002t0010 | 1 | HG02258.hp2 | 5_prime_UTR_variant | MODIFIER | c.-121G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/10 | 121 | chr3 | 56801919 | ||||||
chr3:56801933 | C | T | 2 | a0001c0002t0006 a0002c0001t0009 |
3 | HG02109.hp1 HG02723.hp1 NA20300.hp2 |
5_prime_UTR_variant | MODIFIER | c.-135G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/10 | 135 | chr3 | 56801933 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:56729746 | T | A | 2 | a0001c0007t0001g0098 a0001c0007t0001g0164 |
2 | HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1229-124A>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56729746 | |||||||
chr3:56729853 | C | CTCTCAGA | 104 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(101): Show |
107 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.1229-232_1229-231i others(9): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56729853 | |||||||
chr3:56729855 | G | A | 104 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(101): Show |
107 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.1229-233C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56729855 | |||||||
chr3:56729856 | G | C | 104 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(101): Show |
107 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.1229-234C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56729856 | |||||||
chr3:56729857 | T | C | 104 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(101): Show |
107 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.1229-235A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56729857 | |||||||
chr3:56729946 | G | A | 2 | a0001c0002t0002g0157 a0001c0003t0001g0184 |
2 | HG01175.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1229-324C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56729946 | |||||||
chr3:56729947 | G | T | 1 | a0001c0003t0001g0184 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1229-325C>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56729947 | |||||||
chr3:56729974 | C | T | 104 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(101): Show |
107 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.1229-352G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56729974 | |||||||
chr3:56730102 | G | A | 98 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(95): Show |
101 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.1229-480C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56730102 | |||||||
chr3:56730130 | C | G | 2 | a0002c0001t0001g0155 a0002c0001t0001g0156 |
2 | HG02572.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1229-508G>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56730130 | |||||||
chr3:56730169 | G | A | 1 | a0002c0001t0003g0036 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1229-547C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56730169 | |||||||
chr3:56730301 | C | T | 104 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(101): Show |
107 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.1229-679G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56730301 | |||||||
chr3:56730352 | A | T | 1 | a0001c0002t0002g0194 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1229-730T>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56730352 | |||||||
chr3:56730365 | A | G | 7 | a0001c0007t0001g0076 a0001c0007t0001g0093 a0001c0007t0001g0098 others(4): Show |
7 | HG01070.hp1 HG02280.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.1229-743T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56730365 | |||||||
chr3:56730388 | C | CT | 9 | a0001c0003t0001g0072 a0001c0003t0001g0183 a0001c0003t0001g0251 others(6): Show |
9 | HG00597.hp2 HG02074.hp1 HG04115.hp2 others(6): Show |
intron_variant | MODIFIER | c.1229-767dupA | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56730388 | |||||||
chr3:56730388 | CT | C | 17 | a0001c0002t0005g0142 a0001c0002t0005g0249 a0001c0002t0005g0250 others(14): Show |
19 | HG00642.hp2 HG01167.hp2 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.1229-767delA | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56730388 | |||||||
chr3:56730388 | CTTTTTTT others(4): Show |
C | 98 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(95): Show |
101 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.1229-777_1229-767d others(13): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56730388 | |||||||
chr3:56730413 | A | G | 104 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(101): Show |
107 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.1229-791T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56730413 | |||||||
chr3:56730447 | C | T | 14 | a0001c0007t0004g0031 a0001c0007t0004g0039 a0001c0007t0004g0059 others(11): Show |
14 | HG01361.hp2 HG01928.hp1 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.1229-825G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56730447 | |||||||
chr3:56730625 | C | T | 1 | a0001c0007t0001g0162 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1229-1003G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56730625 | |||||||
chr3:56730792 | G | T | 3 | a0001c0007t0004g0031 a0001c0007t0004g0059 a0001c0008t0004g0314 |
3 | HG02523.hp1 NA18965.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1229-1170C>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56730792 | |||||||
chr3:56730816 | A | G | 12 | a0001c0007t0004g0031 a0001c0007t0004g0039 a0001c0007t0004g0059 others(9): Show |
12 | HG01361.hp2 HG01928.hp1 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.1229-1194T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56730816 | |||||||
chr3:56730825 | G | A | 2 | a0001c0005t0001g0265 a0001c0005t0001g0273 |
2 | HG00741.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1229-1203C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56730825 | |||||||
chr3:56730903 | C | T | 164 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(161): Show |
169 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(166): Show |
intron_variant | MODIFIER | c.1229-1281G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56730903 | |||||||
chr3:56730966 | A | C | 1 | a0001c0002t0002g0212 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1228+1272T>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56730966 | |||||||
chr3:56730984 | T | C | 6 | a0001c0002t0005g0142 a0001c0002t0005g0249 a0001c0002t0005g0250 others(3): Show |
6 | HG02055.hp1 HG02559.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1228+1254A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56730984 | |||||||
chr3:56731008 | T | C | 98 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(95): Show |
101 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.1228+1230A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56731008 | |||||||
chr3:56731156 | G | A | 155 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(152): Show |
158 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(155): Show |
intron_variant | MODIFIER | c.1228+1082C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56731156 | |||||||
chr3:56731219 | A | T | 98 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(95): Show |
101 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.1228+1019T>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56731219 | |||||||
chr3:56731411 | C | T | 104 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(101): Show |
107 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.1228+827G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56731411 | |||||||
chr3:56731449 | T | C | 2 | a0002c0001t0003g0027 a0002c0004t0003g0335 |
2 | HG03239.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1228+789A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56731449 | |||||||
chr3:56731517 | G | T | 155 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(152): Show |
158 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(155): Show |
intron_variant | MODIFIER | c.1228+721C>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56731517 | |||||||
chr3:56731592 | C | CCGGGTTT others(598): Show |
1 | a0001c0002t0008g0135 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1228+645_1228+646i others(607): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56731592 | |||||||
chr3:56731592 | C | CCGGGTTT others(609): Show |
1 | a0004c0011t0008g0073 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1228+645_1228+646i others(618): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56731592 | |||||||
chr3:56731592 | C | CCGGGTTT others(598): Show |
6 | a0001c0002t0002g0077 a0001c0002t0002g0078 a0001c0002t0002g0079 others(3): Show |
6 | HG01099.hp1 HG02280.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1228+645_1228+646i others(607): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56731592 | |||||||
chr3:56731592 | C | CCGGGTTT others(612): Show |
1 | a0001c0002t0005g0142 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1228+645_1228+646i others(621): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56731592 | |||||||
chr3:56731592 | C | CCGGGTTT others(613): Show |
2 | a0001c0002t0005g0249 a0001c0002t0017g0161 |
2 | HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1228+645_1228+646i others(622): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56731592 | |||||||
chr3:56731592 | C | CCGGGTTT others(614): Show |
1 | a0001c0002t0005g0250 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1228+645_1228+646i others(623): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56731592 | |||||||
chr3:56731592 | C | CCGGGTTT others(596): Show |
3 | a0001c0002t0002g0026 a0001c0002t0002g0043 a0001c0006t0002g0281 |
3 | NA18966.hp1 NA18968.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.1228+645_1228+646i others(605): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56731592 | |||||||
chr3:56731592 | C | CCGGGTTT others(597): Show |
62 | a0001c0002t0002g0007 a0001c0002t0002g0021 a0001c0002t0002g0022 others(59): Show |
64 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.1228+645_1228+646i others(606): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56731592 | |||||||
chr3:56731592 | C | CCGGGTTT others(598): Show |
24 | a0001c0002t0002g0005 a0001c0002t0002g0023 a0001c0002t0002g0032 others(21): Show |
25 | HG00621.hp1 HG00673.hp1 HG02027.hp1 others(22): Show |
intron_variant | MODIFIER | c.1228+645_1228+646i others(607): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56731592 | |||||||
chr3:56731592 | C | CCGGGTTT others(599): Show |
1 | a0001c0002t0002g0187 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1228+645_1228+646i others(608): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56731592 | |||||||
chr3:56731592 | C | CCGGGTTT others(599): Show |
2 | a0001c0002t0002g0191 a0001c0002t0002g0253 |
2 | NA18953.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.1228+645_1228+646i others(608): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56731592 | |||||||
chr3:56731594 | G | A | 29 | a0001c0003t0001g0016 a0001c0003t0001g0017 a0001c0003t0001g0018 others(26): Show |
29 | HG00558.hp1 HG01106.hp2 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.1228+644C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56731594 | |||||||
chr3:56731621 | G | A | 104 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(101): Show |
107 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.1228+617C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56731621 | |||||||
chr3:56731775 | A | C | 1 | a0001c0003t0001g0167 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1228+463T>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56731775 | |||||||
chr3:56731778 | T | G | 1 | a0002c0001t0001g0145 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1228+460A>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56731778 | |||||||
chr3:56731786 | C | G | 1 | a0004c0011t0008g0073 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1228+452G>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56731786 | |||||||
chr3:56731977 | T | C | 4 | a0001c0002t0005g0142 a0001c0002t0005g0249 a0001c0002t0005g0250 others(1): Show |
4 | HG02055.hp1 HG02976.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1228+261A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56731977 | |||||||
chr3:56731978 | G | A | 1 | a0001c0002t0017g0161 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1228+260C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56731978 | |||||||
chr3:56731986 | T | G | 105 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(102): Show |
108 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.1228+252A>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56731986 | |||||||
chr3:56732110 | G | A | 29 | a0001c0003t0001g0016 a0001c0003t0001g0017 a0001c0003t0001g0018 others(26): Show |
29 | HG00558.hp1 HG01106.hp2 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.1228+128C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 9/9 | chr3 | 56732110 | |||||||
chr3:56732655 | C | T | 1 | a0002c0001t0001g0055 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1042-231G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56732655 | |||||||
chr3:56732656 | C | T | 1 | a0001c0003t0001g0134 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1042-232G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56732656 | |||||||
chr3:56732922 | C | T | 1 | a0001c0012t0001g0105 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1042-498G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56732922 | |||||||
chr3:56732951 | T | C | 104 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(101): Show |
107 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.1042-527A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56732951 | |||||||
chr3:56732997 | A | G | 1 | a0001c0003t0001g0051 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1042-573T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56732997 | |||||||
chr3:56733066 | C | T | 1 | a0001c0003t0001g0180 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1042-642G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733066 | |||||||
chr3:56733082 | G | C | 2 | a0001c0003t0001g0017 a0001c0003t0001g0216 |
2 | HG01109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1042-658C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733082 | |||||||
chr3:56733140 | G | A | 23 | a0001c0002t0002g0043 a0001c0002t0002g0064 a0001c0002t0002g0065 others(20): Show |
24 | HG00280.hp2 HG00639.hp2 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.1042-716C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733140 | |||||||
chr3:56733152 | G | A | 18 | a0001c0002t0002g0043 a0001c0002t0002g0064 a0001c0002t0002g0065 others(15): Show |
19 | HG00280.hp2 HG00639.hp2 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.1042-728C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733152 | |||||||
chr3:56733258 | G | C | 1 | a0001c0003t0001g0134 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1042-834C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733258 | |||||||
chr3:56733281 | TA | T | 53 | a0001c0002t0002g0253 a0001c0003t0001g0016 a0001c0003t0001g0017 others(50): Show |
53 | HG00558.hp1 HG01070.hp1 HG01106.hp2 others(50): Show |
intron_variant | MODIFIER | c.1042-858delT | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733281 | |||||||
chr3:56733281 | TAA | T | 103 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(100): Show |
106 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.1042-859_1042-858d others(4): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733281 | |||||||
chr3:56733317 | C | T | 3 | a0001c0002t0005g0142 a0001c0002t0005g0249 a0001c0002t0005g0250 |
3 | HG02055.hp1 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1042-893G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733317 | |||||||
chr3:56733319 | A | G | 3 | a0001c0002t0005g0142 a0001c0002t0005g0249 a0001c0002t0005g0250 |
3 | HG02055.hp1 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1042-895T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733319 | |||||||
chr3:56733321 | G | C | 3 | a0001c0002t0005g0142 a0001c0002t0005g0249 a0001c0002t0005g0250 |
3 | HG02055.hp1 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1042-897C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733321 | |||||||
chr3:56733322 | T | G | 3 | a0001c0002t0005g0142 a0001c0002t0005g0249 a0001c0002t0005g0250 |
3 | HG02055.hp1 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1042-898A>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733322 | |||||||
chr3:56733331 | C | CG | 31 | a0001c0003t0001g0047 a0001c0003t0001g0100 a0001c0003t0001g0134 others(28): Show |
31 | HG00099.hp1 HG00140.hp2 HG01256.hp2 others(28): Show |
intron_variant | MODIFIER | c.1042-908dupC | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733331 | |||||||
chr3:56733331 | C | G | 2 | a0001c0002t0005g0249 a0001c0002t0005g0250 |
2 | HG02055.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1042-907G>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733331 | |||||||
chr3:56733331 | CG | C | 96 | a0001c0002t0002g0007 a0001c0002t0002g0022 a0001c0002t0002g0026 others(93): Show |
98 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.1042-908delC | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733331 | |||||||
chr3:56733331 | CGG | C | 49 | a0001c0002t0002g0005 a0001c0002t0002g0021 a0001c0002t0002g0023 others(46): Show |
51 | HG00140.hp1 HG00621.hp1 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.1042-909_1042-908d others(4): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733331 | |||||||
chr3:56733331 | CGGG | C | 30 | a0001c0002t0002g0037 a0001c0002t0002g0077 a0001c0002t0002g0083 others(27): Show |
30 | HG00323.hp2 HG01099.hp1 HG01928.hp1 others(27): Show |
intron_variant | MODIFIER | c.1042-910_1042-908d others(5): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733331 | |||||||
chr3:56733335 | G | GC | 4 | a0002c0004t0003g0267 a0002c0004t0003g0294 a0002c0004t0003g0304 others(1): Show |
4 | HG02135.hp2 NA19060.hp2 NA19086.hp2 others(1): Show |
intron_variant | MODIFIER | c.1042-912_1042-911i others(3): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733335 | |||||||
chr3:56733336 | G | C | 2 | a0002c0004t0003g0307 a0003c0014t0003g0311 |
2 | HG00558.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1042-912C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733336 | |||||||
chr3:56733337 | G | T | 1 | a0001c0002t0002g0022 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1042-913C>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733337 | |||||||
chr3:56733341 | G | C | 2 | a0001c0006t0002g0336 a0001c0006t0002g0337 |
2 | NA18960.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.1042-917C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733341 | |||||||
chr3:56733345 | G | T | 2 | a0001c0007t0001g0076 a0001c0007t0001g0093 |
2 | HG02280.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1042-921C>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733345 | |||||||
chr3:56733346 | G | A | 59 | a0001c0002t0002g0007 a0001c0002t0002g0021 a0001c0002t0002g0022 others(56): Show |
61 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.1042-922C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733346 | |||||||
chr3:56733346 | G | C | 4 | a0001c0002t0005g0142 a0001c0002t0005g0249 a0001c0002t0017g0161 others(1): Show |
4 | HG02647.hp1 HG02976.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1042-922C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733346 | |||||||
chr3:56733346 | G | GA | 5 | a0001c0002t0002g0043 a0001c0002t0002g0110 a0001c0002t0002g0256 others(2): Show |
5 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1042-923_1042-922i others(3): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733346 | |||||||
chr3:56733348 | C | T | 1 | a0002c0001t0003g0154 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1042-924G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733348 | |||||||
chr3:56733349 | G | A | 1 | a0001c0002t0002g0139 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1042-925C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733349 | |||||||
chr3:56733425 | C | A | 337 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(334): Show |
346 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(343): Show |
intron_variant | MODIFIER | c.1042-1001G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733425 | |||||||
chr3:56733443 | T | A | 1 | a0001c0002t0002g0139 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1042-1019A>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733443 | |||||||
chr3:56733521 | A | G | 7 | a0001c0007t0001g0076 a0001c0007t0001g0093 a0001c0007t0001g0098 others(4): Show |
7 | HG01070.hp1 HG02280.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.1042-1097T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733521 | |||||||
chr3:56733534 | C | T | 1 | a0001c0012t0001g0105 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1042-1110G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733534 | |||||||
chr3:56733606 | G | A | 3 | a0002c0001t0001g0143 a0002c0001t0001g0144 a0002c0004t0001g0334 |
3 | NA19030.hp2 NA20129.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1042-1182C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733606 | |||||||
chr3:56733645 | G | C | 104 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(101): Show |
107 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.1042-1221C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733645 | |||||||
chr3:56733661 | G | A | 3 | a0001c0003t0001g0100 a0001c0003t0001g0255 a0001c0005t0001g0321 |
3 | HG01106.hp2 HG01884.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.1042-1237C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733661 | |||||||
chr3:56733667 | G | C | 1 | a0001c0006t0002g0328 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1042-1243C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733667 | |||||||
chr3:56733752 | G | A | 1 | a0001c0002t0002g0054 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1042-1328C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733752 | |||||||
chr3:56733810 | C | T | 3 | a0002c0001t0001g0132 a0002c0001t0001g0235 a0002c0001t0001g0236 |
3 | NA19012.hp1 NA19066.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.1042-1386G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733810 | |||||||
chr3:56733845 | G | A | 3 | a0001c0002t0005g0142 a0001c0002t0005g0249 a0001c0002t0005g0250 |
3 | HG02055.hp1 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1042-1421C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733845 | |||||||
chr3:56733846 | C | T | 2 | a0001c0007t0001g0098 a0001c0007t0001g0164 |
2 | HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1042-1422G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733846 | |||||||
chr3:56733870 | G | A | 1 | a0001c0007t0001g0074 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1042-1446C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733870 | |||||||
chr3:56733902 | T | A | 1 | a0001c0002t0008g0135 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1042-1478A>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733902 | |||||||
chr3:56733963 | G | A | 1 | a0004c0011t0008g0073 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1042-1539C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733963 | |||||||
chr3:56733984 | C | CA | 21 | a0001c0002t0002g0189 a0001c0002t0010g0014 a0001c0002t0017g0161 others(18): Show |
21 | HG00140.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.1042-1561dupT | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733984 | |||||||
chr3:56733984 | C | CAA | 70 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(67): Show |
72 | HG00544.hp2 HG00597.hp1 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.1042-1562_1042-156 others(6): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733984 | |||||||
chr3:56733984 | C | CAAA | 11 | a0001c0002t0002g0025 a0001c0002t0002g0125 a0001c0002t0002g0129 others(8): Show |
11 | HG01981.hp2 HG02083.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.1042-1563_1042-156 others(7): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733984 | |||||||
chr3:56733984 | CA | C | 29 | a0001c0007t0001g0074 a0001c0007t0001g0076 a0001c0007t0001g0098 others(26): Show |
29 | HG01070.hp1 HG01361.hp2 HG01515.hp2 others(26): Show |
intron_variant | MODIFIER | c.1042-1561delT | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733984 | |||||||
chr3:56733984 | CAA | C | 25 | a0001c0003t0001g0016 a0001c0003t0001g0017 a0001c0003t0001g0018 others(22): Show |
25 | HG00558.hp1 HG01106.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.1042-1562_1042-156 others(6): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733984 | |||||||
chr3:56733984 | CAAAA | C | 18 | a0001c0002t0002g0043 a0001c0002t0002g0064 a0001c0002t0002g0065 others(15): Show |
19 | HG00280.hp2 HG00639.hp2 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.1042-1564_1042-156 others(8): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56733984 | |||||||
chr3:56734010 | G | C | 1 | a0001c0012t0001g0105 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1042-1586C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56734010 | |||||||
chr3:56734044 | C | G | 28 | a0001c0003t0001g0016 a0001c0003t0001g0017 a0001c0003t0001g0018 others(25): Show |
28 | HG00558.hp1 HG01106.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.1042-1620G>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56734044 | |||||||
chr3:56734214 | C | T | 100 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(97): Show |
103 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.1042-1790G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56734214 | |||||||
chr3:56734231 | C | G | 100 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(97): Show |
103 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.1042-1807G>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56734231 | |||||||
chr3:56734232 | G | A | 1 | a0001c0005t0001g0299 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1042-1808C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56734232 | |||||||
chr3:56734346 | G | T | 119 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(116): Show |
122 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(119): Show |
intron_variant | MODIFIER | c.1042-1922C>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56734346 | |||||||
chr3:56734376 | T | C | 2 | a0001c0002t0002g0213 a0001c0002t0002g0214 |
2 | NA18940.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1042-1952A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56734376 | |||||||
chr3:56734443 | G | A | 20 | a0001c0003t0001g0033 a0001c0003t0001g0041 a0001c0003t0001g0048 others(17): Show |
20 | HG00558.hp1 HG01496.hp1 HG02630.hp1 others(17): Show |
intron_variant | MODIFIER | c.1042-2019C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56734443 | |||||||
chr3:56734511 | T | C | 1 | a0001c0012t0001g0105 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1042-2087A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56734511 | |||||||
chr3:56734833 | G | C | 1 | a0001c0002t0002g0193 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1041+2352C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56734833 | |||||||
chr3:56734896 | T | G | 7 | a0002c0001t0001g0132 a0002c0001t0001g0228 a0002c0001t0001g0230 others(4): Show |
7 | NA18945.hp2 NA19004.hp1 NA19012.hp1 others(4): Show |
intron_variant | MODIFIER | c.1041+2289A>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56734896 | |||||||
chr3:56734972 | T | C | 148 | a0001c0007t0001g0076 a0001c0007t0001g0093 a0001c0007t0001g0098 others(145): Show |
153 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(150): Show |
intron_variant | MODIFIER | c.1041+2213A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56734972 | |||||||
chr3:56735058 | C | T | 1 | a0001c0003t0001g0244 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1041+2127G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56735058 | |||||||
chr3:56735235 | G | C | 2 | a0001c0002t0006g0011 a0001c0002t0006g0013 |
2 | HG02723.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1041+1950C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56735235 | |||||||
chr3:56735309 | A | G | 4 | a0001c0002t0005g0142 a0001c0002t0005g0249 a0001c0002t0005g0250 others(1): Show |
4 | HG02055.hp1 HG02976.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1041+1876T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56735309 | |||||||
chr3:56735392 | C | G | 1 | a0001c0012t0001g0105 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1041+1793G>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56735392 | |||||||
chr3:56735418 | C | T | 100 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(97): Show |
103 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.1041+1767G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56735418 | |||||||
chr3:56735433 | C | T | 4 | a0001c0002t0005g0142 a0001c0002t0005g0249 a0001c0002t0005g0250 others(1): Show |
4 | HG02055.hp1 HG02976.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1041+1752G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56735433 | |||||||
chr3:56735483 | A | C | 14 | a0001c0007t0004g0031 a0001c0007t0004g0039 a0001c0007t0004g0059 others(11): Show |
14 | HG01361.hp2 HG01928.hp1 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.1041+1702T>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56735483 | |||||||
chr3:56735519 | T | A | 1 | a0001c0002t0008g0135 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1041+1666A>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56735519 | |||||||
chr3:56735534 | C | T | 2 | a0001c0002t0002g0127 a0001c0002t0010g0014 |
2 | HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1041+1651G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56735534 | |||||||
chr3:56735575 | G | A | 1 | a0001c0003t0001g0104 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1041+1610C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56735575 | |||||||
chr3:56735603 | G | C | 1 | a0004c0011t0008g0073 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1041+1582C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56735603 | |||||||
chr3:56735646 | G | A | 1 | a0001c0002t0008g0135 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1041+1539C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56735646 | |||||||
chr3:56735688 | T | C | 100 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(97): Show |
103 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.1041+1497A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56735688 | |||||||
chr3:56735820 | C | T | 3 | a0001c0003t0001g0128 a0001c0003t0001g0170 a0001c0003t0001g0182 |
3 | HG00639.hp1 HG01099.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.1041+1365G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56735820 | |||||||
chr3:56735850 | T | C | 100 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(97): Show |
103 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.1041+1335A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56735850 | |||||||
chr3:56735945 | A | G | 1 | a0002c0004t0003g0274 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1041+1240T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56735945 | |||||||
chr3:56736035 | A | C | 2 | a0001c0007t0001g0101 a0001c0007t0001g0102 |
2 | NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1041+1150T>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56736035 | |||||||
chr3:56736038 | A | C | 1 | a0001c0003t0001g0180 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1041+1147T>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56736038 | |||||||
chr3:56736041 | G | A | 1 | a0002c0004t0003g0331 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1041+1144C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56736041 | |||||||
chr3:56736049 | A | AAC | 3 | a0001c0003t0001g0006 a0001c0003t0001g0092 a0001c0005t0001g0295 |
3 | HG01167.hp1 HG03927.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.1041+1134_1041+113 others(6): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56736049 | |||||||
chr3:56736049 | A | AACAC | 4 | a0001c0002t0005g0142 a0001c0002t0005g0249 a0001c0002t0005g0250 others(1): Show |
4 | HG02055.hp1 HG02647.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1041+1132_1041+113 others(8): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56736049 | |||||||
chr3:56736049 | A | AACACAC | 5 | a0001c0002t0017g0161 a0001c0003t0001g0016 a0001c0003t0001g0017 others(2): Show |
5 | HG01109.hp2 HG02145.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1041+1130_1041+113 others(10): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56736049 | |||||||
chr3:56736049 | AAC | A | 7 | a0001c0003t0001g0244 a0001c0005t0001g0010 a0001c0013t0001g0140 others(4): Show |
7 | HG01975.hp1 HG02257.hp1 HG02273.hp2 others(4): Show |
intron_variant | MODIFIER | c.1041+1134_1041+113 others(6): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56736049 | |||||||
chr3:56736049 | AACAC | A | 82 | a0001c0003t0001g0041 a0001c0003t0001g0048 a0001c0003t0001g0049 others(79): Show |
84 | HG00323.hp2 HG00558.hp1 HG00733.hp2 others(81): Show |
intron_variant | MODIFIER | c.1041+1132_1041+113 others(8): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56736049 | |||||||
chr3:56736049 | AACACAC | A | 78 | a0001c0007t0001g0076 a0001c0007t0001g0093 a0001c0007t0001g0098 others(75): Show |
81 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.1041+1130_1041+113 others(10): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56736049 | |||||||
chr3:56736049 | AACACACA others(7): Show |
A | 100 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(97): Show |
103 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.1041+1122_1041+113 others(18): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56736049 | |||||||
chr3:56736063 | C | CACAA | 14 | a0001c0007t0004g0031 a0001c0007t0004g0039 a0001c0007t0004g0059 others(11): Show |
14 | HG01361.hp2 HG01928.hp1 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.1041+1121_1041+112 others(8): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56736063 | |||||||
chr3:56736341 | A | G | 102 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(99): Show |
105 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.1041+844T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56736341 | |||||||
chr3:56736454 | A | T | 3 | a0001c0002t0002g0127 a0001c0002t0002g0139 a0001c0002t0010g0014 |
3 | HG02258.hp2 HG02486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1041+731T>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56736454 | |||||||
chr3:56736575 | C | T | 1 | a0001c0007t0001g0074 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1041+610G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56736575 | |||||||
chr3:56736645 | A | G | 1 | a0001c0003t0001g0134 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1041+540T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56736645 | |||||||
chr3:56736774 | T | C | 7 | a0002c0001t0001g0003 a0002c0001t0001g0015 a0002c0001t0001g0145 others(4): Show |
9 | HG01167.hp2 HG01169.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1041+411A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56736774 | |||||||
chr3:56736808 | G | A | 1 | a0002c0004t0003g0274 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1041+377C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56736808 | |||||||
chr3:56736818 | C | T | 1 | a0001c0002t0002g0023 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1041+367G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56736818 | |||||||
chr3:56736986 | T | C | 1 | a0001c0007t0004g0111 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1041+199A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 8/9 | chr3 | 56736986 | |||||||
chr3:56737414 | G | T | 2 | a0001c0002t0002g0077 a0001c0002t0002g0086 |
2 | HG01099.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.871-59C>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56737414 | |||||||
chr3:56737427 | A | T | 1 | a0001c0002t0002g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.871-72T>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56737427 | |||||||
chr3:56737484 | T | C | 8 | a0002c0001t0001g0001 a0002c0001t0001g0094 a0002c0001t0001g0136 others(5): Show |
9 | HG01884.hp1 HG02109.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.871-129A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56737484 | |||||||
chr3:56737495 | G | GA | 267 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(264): Show |
275 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(272): Show |
intron_variant | MODIFIER | c.871-141dupT | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56737495 | |||||||
chr3:56737527 | C | G | 1 | a0001c0002t0017g0161 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.871-172G>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56737527 | |||||||
chr3:56737677 | C | T | 1 | a0001c0002t0008g0135 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.871-322G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56737677 | |||||||
chr3:56737706 | A | G | 1 | a0001c0002t0002g0157 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.871-351T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56737706 | |||||||
chr3:56737803 | C | G | 2 | a0001c0002t0006g0011 a0001c0002t0006g0013 |
2 | HG02723.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.871-448G>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56737803 | |||||||
chr3:56737938 | A | G | 108 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(105): Show |
111 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.871-583T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56737938 | |||||||
chr3:56737971 | C | T | 96 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(93): Show |
99 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.871-616G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56737971 | |||||||
chr3:56738052 | T | C | 1 | a0001c0002t0002g0127 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.871-697A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56738052 | |||||||
chr3:56738087 | A | G | 1 | a0001c0003t0001g0174 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.871-732T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56738087 | |||||||
chr3:56738097 | G | A | 21 | a0002c0001t0003g0116 a0002c0001t0003g0154 a0002c0001t0003g0163 others(18): Show |
21 | HG00140.hp1 HG00558.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.871-742C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56738097 | |||||||
chr3:56738146 | T | G | 1 | a0002c0001t0001g0090 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.871-791A>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56738146 | |||||||
chr3:56738287 | C | A | 4 | a0001c0002t0005g0142 a0001c0002t0005g0249 a0001c0002t0005g0250 others(1): Show |
4 | HG02055.hp1 HG02976.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.871-932G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56738287 | |||||||
chr3:56738311 | T | C | 2 | a0001c0002t0002g0023 a0001c0002t0002g0188 |
2 | HG02027.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.871-956A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56738311 | |||||||
chr3:56738395 | C | T | 1 | a0001c0002t0017g0161 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.871-1040G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56738395 | |||||||
chr3:56738685 | G | A | 7 | a0001c0007t0001g0076 a0001c0007t0001g0093 a0001c0007t0001g0098 others(4): Show |
7 | HG01070.hp1 HG02280.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.871-1330C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56738685 | |||||||
chr3:56738806 | C | T | 4 | a0001c0002t0002g0168 a0001c0006t0002g0268 a0001c0006t0002g0269 others(1): Show |
4 | HG00639.hp2 HG01256.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.871-1451G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56738806 | |||||||
chr3:56738882 | G | C | 7 | a0001c0007t0001g0076 a0001c0007t0001g0093 a0001c0007t0001g0098 others(4): Show |
7 | HG01070.hp1 HG02280.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.871-1527C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56738882 | |||||||
chr3:56738981 | G | C | 1 | a0001c0005t0001g0290 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.871-1626C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56738981 | |||||||
chr3:56738985 | C | T | 1 | a0002c0001t0001g0085 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.871-1630G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56738985 | |||||||
chr3:56739146 | T | C | 1 | a0001c0006t0002g0328 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.871-1791A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56739146 | |||||||
chr3:56739205 | T | C | 1 | a0001c0007t0001g0162 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.871-1850A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56739205 | |||||||
chr3:56739232 | G | A | 1 | a0001c0003t0001g0173 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.871-1877C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56739232 | |||||||
chr3:56739309 | G | C | 1 | a0001c0005t0001g0287 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.871-1954C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56739309 | |||||||
chr3:56739377 | T | C | 2 | a0001c0007t0001g0076 a0001c0007t0001g0093 |
2 | HG02280.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.871-2022A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56739377 | |||||||
chr3:56739395 | C | T | 263 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(260): Show |
271 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(268): Show |
intron_variant | MODIFIER | c.871-2040G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56739395 | |||||||
chr3:56739396 | CT | C | 284 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(281): Show |
292 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(289): Show |
intron_variant | MODIFIER | c.871-2042delA | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56739396 | |||||||
chr3:56739659 | C | T | 2 | a0001c0002t0002g0127 a0001c0002t0010g0014 |
2 | HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.871-2304G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56739659 | |||||||
chr3:56739675 | C | T | 7 | a0002c0001t0001g0003 a0002c0001t0001g0015 a0002c0001t0001g0145 others(4): Show |
9 | HG01167.hp2 HG01169.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.871-2320G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56739675 | |||||||
chr3:56739679 | T | C | 2 | a0001c0002t0002g0127 a0001c0002t0010g0014 |
2 | HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.871-2324A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56739679 | |||||||
chr3:56739848 | T | C | 2 | a0001c0002t0002g0127 a0001c0002t0010g0014 |
2 | HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.871-2493A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56739848 | |||||||
chr3:56739851 | T | C | 2 | a0001c0002t0002g0127 a0001c0002t0010g0014 |
2 | HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.871-2496A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56739851 | |||||||
chr3:56739872 | T | C | 2 | a0001c0002t0002g0127 a0001c0002t0010g0014 |
2 | HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.871-2517A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56739872 | |||||||
chr3:56739891 | A | G | 2 | a0001c0007t0001g0098 a0001c0007t0001g0164 |
2 | HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.871-2536T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56739891 | |||||||
chr3:56739901 | A | AT | 77 | a0001c0002t0002g0007 a0001c0002t0002g0021 a0001c0002t0002g0022 others(74): Show |
79 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.871-2547dupA | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56739901 | |||||||
chr3:56739911 | T | C | 2 | a0001c0002t0002g0127 a0001c0002t0010g0014 |
2 | HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.871-2556A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56739911 | |||||||
chr3:56739994 | G | A | 1 | a0004c0011t0008g0073 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.871-2639C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56739994 | |||||||
chr3:56740000 | A | C | 14 | a0001c0007t0004g0031 a0001c0007t0004g0039 a0001c0007t0004g0059 others(11): Show |
14 | HG01361.hp2 HG01928.hp1 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.871-2645T>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56740000 | |||||||
chr3:56740041 | G | A | 108 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(105): Show |
111 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.871-2686C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56740041 | |||||||
chr3:56740125 | C | A | 1 | a0001c0002t0017g0161 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.871-2770G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56740125 | |||||||
chr3:56740132 | G | A | 8 | a0002c0001t0001g0001 a0002c0001t0001g0094 a0002c0001t0001g0136 others(5): Show |
9 | HG01884.hp1 HG02109.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.871-2777C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56740132 | |||||||
chr3:56740183 | C | T | 1 | a0001c0007t0004g0112 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.871-2828G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56740183 | |||||||
chr3:56740187 | C | CA | 144 | a0001c0002t0002g0026 a0001c0002t0002g0040 a0001c0005t0001g0290 others(141): Show |
149 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(146): Show |
intron_variant | MODIFIER | c.871-2833dupT | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56740187 | |||||||
chr3:56740270 | T | TA | 259 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(256): Show |
267 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(264): Show |
intron_variant | MODIFIER | c.871-2916dupT | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56740270 | |||||||
chr3:56740270 | T | TAA | 7 | a0001c0007t0001g0076 a0001c0007t0001g0093 a0001c0007t0001g0098 others(4): Show |
7 | HG01070.hp1 HG02280.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.871-2917_871-2916d others(4): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56740270 | |||||||
chr3:56740281 | A | AC | 4 | a0002c0004t0003g0267 a0002c0004t0003g0294 a0002c0004t0003g0304 others(1): Show |
4 | HG02135.hp2 NA19060.hp2 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.871-2927dupG | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56740281 | |||||||
chr3:56740569 | G | A | 1 | a0001c0002t0002g0139 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.871-3214C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56740569 | |||||||
chr3:56740620 | C | T | 1 | a0004c0011t0008g0073 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.871-3265G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56740620 | |||||||
chr3:56740621 | T | C | 1 | a0002c0001t0001g0094 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.871-3266A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56740621 | |||||||
chr3:56740833 | G | A | 1 | a0002c0001t0001g0107 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.871-3478C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56740833 | |||||||
chr3:56740957 | T | C | 14 | a0001c0007t0004g0031 a0001c0007t0004g0039 a0001c0007t0004g0059 others(11): Show |
14 | HG01361.hp2 HG01928.hp1 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.871-3602A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56740957 | |||||||
chr3:56741184 | C | CCTT | 3 | a0002c0001t0001g0001 a0002c0001t0001g0094 a0002c0001t0001g0200 |
4 | HG01884.hp1 HG02451.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.871-3830_871-3829i others(5): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56741184 | |||||||
chr3:56741184 | C | CCTTT | 5 | a0002c0001t0001g0136 a0002c0001t0001g0137 a0002c0001t0001g0158 others(2): Show |
5 | HG02109.hp2 HG02965.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.871-3830_871-3829i others(6): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56741184 | |||||||
chr3:56741184 | C | CT | 10 | a0001c0002t0002g0037 a0001c0002t0008g0135 a0001c0002t0017g0161 others(7): Show |
10 | HG01070.hp1 HG01175.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.871-3830dupA | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56741184 | |||||||
chr3:56741184 | C | CTT | 134 | a0001c0002t0002g0026 a0001c0002t0002g0040 a0001c0005t0001g0290 others(131): Show |
138 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(135): Show |
intron_variant | MODIFIER | c.871-3831_871-3830d others(4): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56741184 | |||||||
chr3:56741215 | C | T | 10 | a0001c0003t0001g0006 a0001c0003t0001g0092 a0001c0003t0001g0148 others(7): Show |
11 | HG00140.hp2 HG00280.hp1 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.871-3860G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56741215 | |||||||
chr3:56741427 | G | A | 1 | a0004c0011t0008g0073 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.870+3778C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56741427 | |||||||
chr3:56741482 | C | T | 1 | a0002c0001t0001g0260 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.870+3723G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56741482 | |||||||
chr3:56741496 | C | CT | 190 | a0001c0002t0002g0007 a0001c0002t0002g0021 a0001c0002t0002g0022 others(187): Show |
194 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.870+3708dupA | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56741496 | |||||||
chr3:56741496 | C | CTT | 33 | a0001c0002t0002g0054 a0001c0002t0002g0130 a0001c0002t0002g0168 others(30): Show |
33 | HG00597.hp2 HG00639.hp2 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.870+3707_870+3708d others(4): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56741496 | |||||||
chr3:56741496 | CTTTTTTT others(4): Show |
C | 2 | a0001c0002t0002g0192 a0001c0012t0001g0105 |
2 | HG03540.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.870+3698_870+3708d others(13): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56741496 | |||||||
chr3:56741496 | CTTTTTTT others(5): Show |
C | 1 | a0002c0001t0001g0245 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.870+3697_870+3708d others(14): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56741496 | |||||||
chr3:56741532 | G | A | 1 | a0004c0011t0008g0073 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.870+3673C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56741532 | |||||||
chr3:56741659 | A | G | 3 | a0002c0001t0001g0225 a0002c0001t0001g0226 a0002c0001t0001g0227 |
3 | HG01109.hp1 HG02615.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.870+3546T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56741659 | |||||||
chr3:56741689 | G | C | 1 | a0001c0005t0001g0290 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.870+3516C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56741689 | |||||||
chr3:56741694 | G | A | 1 | a0002c0001t0001g0062 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.870+3511C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56741694 | |||||||
chr3:56741707 | G | C | 3 | a0001c0002t0002g0038 a0001c0002t0002g0197 a0001c0006t0002g0275 |
3 | NA18950.hp2 NA18995.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.870+3498C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56741707 | |||||||
chr3:56742214 | G | A | 1 | a0001c0005t0001g0295 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.870+2991C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56742214 | |||||||
chr3:56742215 | G | A | 2 | a0001c0005t0001g0296 a0001c0005t0001g0297 |
2 | HG00323.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.870+2990C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56742215 | |||||||
chr3:56742391 | T | C | 4 | a0001c0002t0005g0142 a0001c0002t0005g0249 a0001c0002t0005g0250 others(1): Show |
4 | HG02055.hp1 HG02976.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.870+2814A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56742391 | |||||||
chr3:56742818 | C | T | 2 | a0001c0002t0002g0127 a0001c0002t0010g0014 |
2 | HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.870+2387G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56742818 | |||||||
chr3:56742823 | T | C | 2 | a0001c0002t0002g0127 a0001c0002t0010g0014 |
2 | HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.870+2382A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56742823 | |||||||
chr3:56742880 | T | C | 142 | a0001c0002t0002g0083 a0001c0002t0002g0138 a0002c0001t0001g0001 others(139): Show |
147 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.870+2325A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56742880 | |||||||
chr3:56743025 | G | T | 1 | a0001c0007t0001g0074 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.870+2180C>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56743025 | |||||||
chr3:56743086 | A | G | 2 | a0001c0002t0002g0127 a0001c0002t0010g0014 |
2 | HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.870+2119T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56743086 | |||||||
chr3:56743189 | G | T | 3 | a0001c0002t0002g0127 a0001c0002t0010g0014 a0001c0007t0001g0093 |
3 | HG02258.hp2 HG02280.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.870+2016C>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56743189 | |||||||
chr3:56743232 | C | T | 2 | a0001c0002t0002g0127 a0001c0002t0010g0014 |
2 | HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.870+1973G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56743232 | |||||||
chr3:56743265 | T | C | 2 | a0001c0002t0002g0127 a0001c0002t0010g0014 |
2 | HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.870+1940A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56743265 | |||||||
chr3:56743369 | C | A | 1 | a0001c0002t0008g0135 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.870+1836G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56743369 | |||||||
chr3:56743390 | T | C | 2 | a0001c0002t0005g0142 a0001c0002t0005g0249 |
2 | HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.870+1815A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56743390 | |||||||
chr3:56743468 | T | A | 16 | a0002c0001t0001g0055 a0002c0001t0001g0062 a0002c0001t0001g0185 others(13): Show |
16 | NA18612.hp1 NA18940.hp2 NA18942.hp1 others(13): Show |
intron_variant | MODIFIER | c.870+1737A>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56743468 | |||||||
chr3:56743474 | T | C | 1 | a0001c0006t0018g0348 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.870+1731A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56743474 | |||||||
chr3:56743493 | T | C | 1 | a0001c0003t0001g0051 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.870+1712A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56743493 | |||||||
chr3:56743557 | G | C | 3 | a0001c0003t0001g0070 a0001c0003t0001g0071 a0001c0003t0001g0072 |
3 | NA18941.hp1 NA18955.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.870+1648C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56743557 | |||||||
chr3:56743581 | T | C | 7 | a0002c0001t0001g0003 a0002c0001t0001g0015 a0002c0001t0001g0145 others(4): Show |
9 | HG01167.hp2 HG01169.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.870+1624A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56743581 | |||||||
chr3:56743583 | T | G | 7 | a0002c0001t0001g0003 a0002c0001t0001g0015 a0002c0001t0001g0145 others(4): Show |
9 | HG01167.hp2 HG01169.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.870+1622A>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56743583 | |||||||
chr3:56743753 | A | AT | 3 | a0001c0002t0002g0127 a0001c0002t0010g0014 a0004c0011t0008g0073 |
3 | HG02258.hp2 HG02486.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.870+1451dupA | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56743753 | |||||||
chr3:56743758 | TGTCCCAG | T | 3 | a0001c0002t0002g0127 a0001c0002t0010g0014 a0004c0011t0008g0073 |
3 | HG02258.hp2 HG02486.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.870+1440_870+1446d others(9): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56743758 | |||||||
chr3:56743785 | C | T | 2 | a0001c0002t0002g0038 a0001c0006t0002g0275 |
2 | NA18950.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.870+1420G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56743785 | |||||||
chr3:56743854 | A | C | 107 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(104): Show |
110 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(107): Show |
intron_variant | MODIFIER | c.870+1351T>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56743854 | |||||||
chr3:56743965 | A | G | 5 | a0001c0003t0001g0016 a0001c0003t0001g0017 a0001c0003t0001g0018 others(2): Show |
5 | HG01109.hp2 HG02145.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.870+1240T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56743965 | |||||||
chr3:56744067 | C | T | 2 | a0001c0007t0001g0101 a0002c0001t0001g0097 |
2 | HG01934.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.870+1138G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56744067 | |||||||
chr3:56744082 | T | C | 14 | a0001c0007t0004g0031 a0001c0007t0004g0039 a0001c0007t0004g0059 others(11): Show |
14 | HG01361.hp2 HG01928.hp1 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.870+1123A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56744082 | |||||||
chr3:56744222 | G | C | 1 | a0002c0001t0001g0175 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.870+983C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56744222 | |||||||
chr3:56744299 | C | T | 1 | a0001c0002t0002g0064 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.870+906G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56744299 | |||||||
chr3:56744320 | C | T | 2 | a0001c0002t0002g0127 a0004c0011t0008g0073 |
2 | HG02486.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.870+885G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56744320 | |||||||
chr3:56744397 | CT | C | 261 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(258): Show |
269 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(266): Show |
intron_variant | MODIFIER | c.870+807delA | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56744397 | |||||||
chr3:56744397 | CTT | C | 15 | a0001c0007t0004g0031 a0001c0007t0004g0039 a0001c0007t0004g0059 others(12): Show |
15 | HG01261.hp1 HG01361.hp2 HG01928.hp1 others(12): Show |
intron_variant | MODIFIER | c.870+806_870+807del others(2): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56744397 | |||||||
chr3:56744475 | T | G | 8 | a0002c0001t0001g0003 a0002c0001t0001g0075 a0002c0001t0001g0145 others(5): Show |
10 | HG01167.hp2 HG01169.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.870+730A>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56744475 | |||||||
chr3:56744519 | T | C | 2 | a0001c0002t0002g0127 a0004c0011t0008g0073 |
2 | HG02486.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.870+686A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56744519 | |||||||
chr3:56744555 | C | T | 4 | a0001c0007t0001g0076 a0001c0007t0001g0093 a0001c0007t0001g0101 others(1): Show |
4 | HG01934.hp2 HG02280.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.870+650G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56744555 | |||||||
chr3:56744736 | T | G | 1 | a0001c0006t0002g0338 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.870+469A>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56744736 | |||||||
chr3:56744760 | A | G | 1 | a0001c0002t0002g0083 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.870+445T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56744760 | |||||||
chr3:56744861 | AT | A | 37 | a0001c0002t0002g0007 a0001c0002t0002g0021 a0001c0002t0002g0022 others(34): Show |
38 | HG00544.hp2 HG00597.hp1 HG01123.hp2 others(35): Show |
intron_variant | MODIFIER | c.870+343delA | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56744861 | |||||||
chr3:56744889 | T | C | 4 | a0001c0002t0002g0139 a0001c0002t0008g0135 a0001c0002t0010g0014 others(1): Show |
4 | HG02109.hp2 HG02258.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.870+316A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56744889 | |||||||
chr3:56744945 | T | C | 2 | a0001c0002t0002g0077 a0001c0002t0002g0086 |
2 | HG01099.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.870+260A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56744945 | |||||||
chr3:56744983 | G | A | 135 | a0001c0002t0002g0083 a0001c0007t0001g0102 a0002c0001t0001g0001 others(132): Show |
140 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.870+222C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56744983 | |||||||
chr3:56745142 | C | A | 1 | a0001c0005t0001g0321 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.870+63G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 7/9 | chr3 | 56745142 | |||||||
chr3:56745467 | G | A | 1 | a0001c0005t0001g0272 | 1 | NA18977.hp2 | splice_region_variant&intron_variant | LOW | c.613-5C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56745467 | |||||||
chr3:56745792 | C | A | 2 | a0002c0001t0001g0228 a0002c0001t0001g0254 |
2 | NA19056.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.613-330G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56745792 | |||||||
chr3:56745975 | C | T | 124 | a0001c0002t0002g0083 a0001c0007t0001g0102 a0002c0001t0001g0019 others(121): Show |
126 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.613-513G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56745975 | |||||||
chr3:56746115 | C | T | 1 | a0002c0001t0001g0136 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.613-653G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56746115 | |||||||
chr3:56746467 | C | A | 2 | a0001c0007t0001g0076 a0001c0007t0001g0093 |
2 | HG02280.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.613-1005G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56746467 | |||||||
chr3:56746512 | A | C | 1 | a0001c0002t0002g0087 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.613-1050T>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56746512 | |||||||
chr3:56746547 | T | C | 4 | a0001c0002t0005g0142 a0001c0002t0005g0249 a0001c0002t0005g0250 others(1): Show |
4 | HG02055.hp1 HG02976.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.613-1085A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56746547 | |||||||
chr3:56746663 | G | A | 1 | a0001c0002t0002g0086 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.613-1201C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56746663 | |||||||
chr3:56746996 | T | C | 1 | a0001c0002t0002g0034 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.613-1534A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56746996 | |||||||
chr3:56747055 | A | G | 1 | a0001c0002t0002g0127 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.613-1593T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56747055 | |||||||
chr3:56747064 | C | CAG | 9 | a0001c0003t0001g0128 a0001c0003t0001g0170 a0001c0005t0001g0321 others(6): Show |
9 | HG00140.hp1 HG00639.hp1 HG00733.hp1 others(6): Show |
intron_variant | MODIFIER | c.613-1604_613-1603d others(4): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56747064 | |||||||
chr3:56747064 | C | CAGAG | 3 | a0001c0002t0005g0249 a0001c0002t0005g0250 a0001c0002t0017g0161 |
3 | HG02055.hp1 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.613-1606_613-1603d others(6): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56747064 | |||||||
chr3:56747064 | C | CAGAGAGA others(15): Show |
1 | a0001c0007t0001g0074 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.613-1624_613-1603d others(24): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56747064 | |||||||
chr3:56747064 | C | G | 16 | a0001c0007t0004g0031 a0001c0007t0004g0039 a0001c0007t0004g0059 others(13): Show |
16 | HG01361.hp2 HG01928.hp1 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.613-1602G>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56747064 | |||||||
chr3:56747064 | CAG | C | 107 | a0001c0002t0002g0083 a0001c0007t0001g0102 a0002c0001t0001g0019 others(104): Show |
109 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(106): Show |
intron_variant | MODIFIER | c.613-1604_613-1603d others(4): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56747064 | |||||||
chr3:56747064 | CAGAG | C | 11 | a0001c0002t0002g0077 a0001c0002t0002g0078 a0001c0002t0002g0079 others(8): Show |
12 | HG01070.hp1 HG01099.hp1 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.613-1606_613-1603d others(6): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56747064 | |||||||
chr3:56747064 | CAGAGAG | C | 34 | a0001c0002t0002g0005 a0001c0002t0002g0023 a0001c0002t0002g0032 others(31): Show |
35 | HG00323.hp2 HG00621.hp1 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.613-1608_613-1603d others(8): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56747064 | |||||||
chr3:56747064 | CAGAGAGA others(9): Show |
C | 64 | a0001c0002t0002g0007 a0001c0002t0002g0021 a0001c0002t0002g0022 others(61): Show |
66 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.613-1618_613-1603d others(18): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56747064 | |||||||
chr3:56747066 | G | C | 4 | a0001c0003t0001g0070 a0001c0003t0001g0071 a0001c0003t0001g0072 others(1): Show |
4 | HG03710.hp2 NA18941.hp1 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.613-1604C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56747066 | |||||||
chr3:56747068 | G | C | 1 | a0002c0001t0013g0201 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.613-1606C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56747068 | |||||||
chr3:56747112 | C | CG | 64 | a0001c0002t0002g0007 a0001c0002t0002g0021 a0001c0002t0002g0022 others(61): Show |
66 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.613-1651_613-1650i others(3): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56747112 | |||||||
chr3:56747216 | A | G | 4 | a0001c0002t0005g0142 a0001c0002t0005g0249 a0001c0002t0005g0250 others(1): Show |
4 | HG02055.hp1 HG02976.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.613-1754T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56747216 | |||||||
chr3:56747440 | G | C | 3 | a0002c0001t0003g0116 a0002c0004t0003g0316 a0002c0004t0003g0330 |
3 | HG01928.hp2 HG01975.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.613-1978C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56747440 | |||||||
chr3:56747497 | C | T | 2 | a0002c0001t0001g0260 a0002c0001t0001g0262 |
2 | HG01975.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.613-2035G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56747497 | |||||||
chr3:56747568 | T | C | 4 | a0001c0002t0005g0142 a0001c0002t0005g0249 a0001c0002t0005g0250 others(1): Show |
4 | HG02055.hp1 HG02976.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.613-2106A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56747568 | |||||||
chr3:56747631 | T | C | 1 | a0001c0005t0001g0322 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.613-2169A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56747631 | |||||||
chr3:56748060 | G | C | 4 | a0001c0007t0001g0076 a0001c0007t0001g0093 a0001c0007t0001g0101 others(1): Show |
4 | HG01934.hp2 HG02280.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.613-2598C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56748060 | |||||||
chr3:56748201 | T | C | 1 | a0001c0002t0002g0054 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.613-2739A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56748201 | |||||||
chr3:56748549 | A | AT | 11 | a0001c0003t0001g0016 a0001c0003t0001g0017 a0001c0003t0001g0018 others(8): Show |
11 | HG00323.hp1 HG01109.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.612+2506dupA | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56748549 | |||||||
chr3:56748549 | AT | A | 8 | a0001c0002t0005g0142 a0001c0002t0005g0249 a0001c0002t0005g0250 others(5): Show |
8 | HG02055.hp1 HG02965.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.612+2506delA | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56748549 | |||||||
chr3:56748549 | ATT | A | 218 | a0001c0002t0002g0007 a0001c0002t0002g0021 a0001c0002t0002g0022 others(215): Show |
225 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(222): Show |
intron_variant | MODIFIER | c.612+2505_612+2506d others(4): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56748549 | |||||||
chr3:56748549 | ATTT | A | 34 | a0001c0002t0002g0005 a0001c0002t0002g0023 a0001c0002t0002g0032 others(31): Show |
35 | HG00621.hp1 HG00673.hp1 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.612+2504_612+2506d others(5): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56748549 | |||||||
chr3:56748551 | T | A | 1 | a0002c0001t0001g0075 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.612+2505A>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56748551 | |||||||
chr3:56748784 | C | T | 2 | a0001c0007t0001g0098 a0002c0001t0001g0075 |
2 | HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.612+2272G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56748784 | |||||||
chr3:56748785 | G | A | 134 | a0001c0002t0002g0083 a0001c0002t0010g0014 a0001c0007t0001g0102 others(131): Show |
139 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(136): Show |
intron_variant | MODIFIER | c.612+2271C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56748785 | |||||||
chr3:56748921 | C | T | 3 | a0002c0001t0001g0133 a0002c0001t0001g0159 a0002c0001t0001g0160 |
3 | HG02559.hp2 HG02615.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.612+2135G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56748921 | |||||||
chr3:56749020 | G | A | 3 | a0001c0002t0005g0142 a0001c0002t0005g0249 a0001c0002t0005g0250 |
3 | HG02055.hp1 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.612+2036C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56749020 | |||||||
chr3:56749213 | C | T | 1 | a0002c0001t0003g0208 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.612+1843G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56749213 | |||||||
chr3:56749329 | G | A | 1 | a0001c0002t0002g0021 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.612+1727C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56749329 | |||||||
chr3:56749490 | T | A | 1 | a0001c0002t0002g0139 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.612+1566A>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56749490 | |||||||
chr3:56749563 | C | T | 2 | a0001c0007t0001g0076 a0001c0007t0001g0093 |
2 | HG02280.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.612+1493G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56749563 | |||||||
chr3:56749604 | C | T | 1 | a0001c0002t0002g0127 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.612+1452G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56749604 | |||||||
chr3:56749777 | C | A | 33 | a0001c0002t0002g0005 a0001c0002t0002g0023 a0001c0002t0002g0032 others(30): Show |
34 | HG00621.hp1 HG00673.hp1 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.612+1279G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56749777 | |||||||
chr3:56749778 | T | C | 261 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(258): Show |
269 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(266): Show |
intron_variant | MODIFIER | c.612+1278A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56749778 | |||||||
chr3:56749855 | T | C | 2 | a0001c0005t0001g0270 a0001c0005t0001g0272 |
2 | NA18963.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.612+1201A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56749855 | |||||||
chr3:56749873 | T | C | 1 | a0001c0007t0001g0162 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.612+1183A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56749873 | |||||||
chr3:56749902 | T | TAAAACTT others(32): Show |
1 | a0001c0002t0010g0014 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.612+1153_612+1154i others(41): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56749902 | |||||||
chr3:56749902 | T | TAAAACTT others(56): Show |
1 | a0002c0001t0001g0094 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.612+1153_612+1154i others(65): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56749902 | |||||||
chr3:56749902 | T | TAAAACTT others(65): Show |
1 | a0002c0001t0001g0001 | 2 | HG02451.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.612+1153_612+1154i others(74): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56749902 | |||||||
chr3:56749902 | T | TAAAACTT others(66): Show |
1 | a0002c0001t0001g0200 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.612+1153_612+1154i others(75): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56749902 | |||||||
chr3:56749908 | T | C | 1 | a0002c0001t0001g0003 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.612+1148A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56749908 | |||||||
chr3:56750670 | GT | G | 6 | a0001c0005t0001g0297 a0001c0007t0001g0076 a0001c0007t0001g0093 others(3): Show |
6 | HG01261.hp1 HG01934.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.612+385delA | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56750670 | |||||||
chr3:56750820 | C | G | 205 | a0001c0002t0002g0005 a0001c0002t0002g0023 a0001c0002t0002g0026 others(202): Show |
211 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(208): Show |
intron_variant | MODIFIER | c.612+236G>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56750820 | |||||||
chr3:56751023 | T | G | 1 | a0001c0002t0010g0014 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.612+33A>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 6/9 | chr3 | 56751023 | |||||||
chr3:56751148 | C | T | 1 | a0001c0003t0001g0179 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.536-16G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 5/9 | chr3 | 56751148 | |||||||
chr3:56751213 | T | C | 1 | a0001c0007t0001g0162 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.536-81A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 5/9 | chr3 | 56751213 | |||||||
chr3:56751528 | C | T | 209 | a0001c0002t0002g0005 a0001c0002t0002g0023 a0001c0002t0002g0026 others(206): Show |
216 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(213): Show |
intron_variant | MODIFIER | c.439-132G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 4/9 | chr3 | 56751528 | |||||||
chr3:56751849 | A | G | 2 | a0001c0007t0004g0059 a0002c0001t0003g0223 |
2 | HG02523.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.439-453T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 4/9 | chr3 | 56751849 | |||||||
chr3:56752082 | CT | C | 208 | a0001c0002t0002g0005 a0001c0002t0002g0023 a0001c0002t0002g0026 others(205): Show |
215 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(212): Show |
intron_variant | MODIFIER | c.439-687delA | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 4/9 | chr3 | 56752082 | |||||||
chr3:56752117 | T | C | 8 | a0002c0001t0001g0003 a0002c0001t0001g0075 a0002c0001t0001g0145 others(5): Show |
10 | HG01167.hp2 HG01169.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.439-721A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 4/9 | chr3 | 56752117 | |||||||
chr3:56752167 | C | T | 1 | a0001c0007t0001g0093 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.439-771G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 4/9 | chr3 | 56752167 | |||||||
chr3:56752170 | C | T | 1 | a0001c0002t0002g0127 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.439-774G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 4/9 | chr3 | 56752170 | |||||||
chr3:56752172 | C | T | 1 | a0002c0001t0001g0205 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.439-776G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 4/9 | chr3 | 56752172 | |||||||
chr3:56752192 | A | G | 24 | a0001c0002t0002g0207 a0001c0003t0001g0167 a0001c0003t0001g0259 others(21): Show |
24 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.439-796T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 4/9 | chr3 | 56752192 | |||||||
chr3:56752214 | C | T | 7 | a0001c0002t0005g0142 a0001c0002t0005g0249 a0001c0002t0005g0250 others(4): Show |
7 | HG01934.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.439-818G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 4/9 | chr3 | 56752214 | |||||||
chr3:56752227 | T | C | 158 | a0001c0002t0002g0005 a0001c0002t0002g0023 a0001c0002t0002g0026 others(155): Show |
165 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(162): Show |
intron_variant | MODIFIER | c.439-831A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 4/9 | chr3 | 56752227 | |||||||
chr3:56752325 | C | T | 208 | a0001c0002t0002g0005 a0001c0002t0002g0023 a0001c0002t0002g0026 others(205): Show |
215 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(212): Show |
intron_variant | MODIFIER | c.439-929G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 4/9 | chr3 | 56752325 | |||||||
chr3:56752346 | C | T | 1 | a0001c0002t0002g0077 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.439-950G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 4/9 | chr3 | 56752346 | |||||||
chr3:56752348 | G | A | 2 | a0001c0002t0002g0256 a0001c0002t0002g0257 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.439-952C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 4/9 | chr3 | 56752348 | |||||||
chr3:56752354 | G | A | 1 | a0002c0001t0001g0136 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.439-958C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 4/9 | chr3 | 56752354 | |||||||
chr3:56752602 | G | A | 5 | a0001c0002t0005g0142 a0001c0002t0005g0249 a0001c0002t0005g0250 others(2): Show |
5 | HG01934.hp2 HG02055.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.438+902C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 4/9 | chr3 | 56752602 | |||||||
chr3:56752702 | T | C | 2 | a0001c0006t0002g0291 a0001c0006t0002g0319 |
2 | HG03491.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.438+802A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 4/9 | chr3 | 56752702 | |||||||
chr3:56752808 | G | C | 1 | a0002c0001t0001g0205 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.438+696C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 4/9 | chr3 | 56752808 | |||||||
chr3:56752944 | T | C | 1 | a0001c0005t0001g0290 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.438+560A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 4/9 | chr3 | 56752944 | |||||||
chr3:56752954 | G | C | 1 | a0001c0002t0002g0022 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.438+550C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 4/9 | chr3 | 56752954 | |||||||
chr3:56752982 | G | T | 1 | a0001c0007t0001g0098 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.438+522C>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 4/9 | chr3 | 56752982 | |||||||
chr3:56753005 | G | C | 7 | a0001c0002t0005g0142 a0001c0002t0005g0249 a0001c0002t0005g0250 others(4): Show |
7 | HG01934.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.438+499C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 4/9 | chr3 | 56753005 | |||||||
chr3:56753423 | C | T | 287 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(284): Show |
295 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.438+81G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 4/9 | chr3 | 56753423 | |||||||
chr3:56753441 | T | C | 1 | a0001c0007t0001g0074 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.438+63A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 4/9 | chr3 | 56753441 | |||||||
chr3:56753664 | A | G | 123 | a0001c0002t0002g0054 a0001c0002t0002g0083 a0001c0002t0002g0139 others(120): Show |
129 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(126): Show |
intron_variant | MODIFIER | c.376-98T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 3/9 | chr3 | 56753664 | |||||||
chr3:56753686 | G | A | 1 | a0002c0004t0003g0267 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.376-120C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 3/9 | chr3 | 56753686 | |||||||
chr3:56753949 | T | C | 1 | a0001c0002t0002g0138 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.376-383A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 3/9 | chr3 | 56753949 | |||||||
chr3:56754008 | C | T | 1 | a0002c0001t0001g0055 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.376-442G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 3/9 | chr3 | 56754008 | |||||||
chr3:56754037 | T | C | 2 | a0002c0001t0001g0062 a0002c0001t0001g0237 |
2 | NA18940.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.376-471A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 3/9 | chr3 | 56754037 | |||||||
chr3:56754047 | C | T | 1 | a0002c0001t0013g0201 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.376-481G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 3/9 | chr3 | 56754047 | |||||||
chr3:56754149 | C | T | 1 | a0001c0002t0002g0215 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.376-583G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 3/9 | chr3 | 56754149 | |||||||
chr3:56754368 | T | C | 287 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(284): Show |
295 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.375+613A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 3/9 | chr3 | 56754368 | |||||||
chr3:56754417 | G | A | 7 | a0001c0002t0005g0142 a0001c0002t0005g0249 a0001c0002t0005g0250 others(4): Show |
7 | HG01934.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.375+564C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 3/9 | chr3 | 56754417 | |||||||
chr3:56755311 | C | T | 1 | a0001c0007t0001g0102 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.205-160G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56755311 | |||||||
chr3:56755427 | G | A | 1 | a0001c0005t0001g0308 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.205-276C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56755427 | |||||||
chr3:56755434 | G | A | 2 | a0002c0001t0001g0155 a0002c0001t0001g0156 |
2 | HG02572.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.205-283C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56755434 | |||||||
chr3:56755619 | T | C | 1 | a0002c0001t0001g0096 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.205-468A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56755619 | |||||||
chr3:56755706 | T | TA | 14 | a0001c0002t0002g0032 a0001c0007t0004g0031 a0001c0007t0004g0039 others(11): Show |
14 | HG01361.hp2 HG01928.hp1 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.205-556dupT | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56755706 | |||||||
chr3:56755708 | C | T | 26 | a0001c0002t0002g0052 a0001c0002t0002g0064 a0001c0003t0001g0016 others(23): Show |
26 | HG00558.hp1 HG01109.hp2 HG01496.hp1 others(23): Show |
intron_variant | MODIFIER | c.205-557G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56755708 | |||||||
chr3:56755715 | A | C | 28 | a0001c0002t0002g0052 a0001c0002t0002g0064 a0001c0002t0017g0161 others(25): Show |
28 | HG00558.hp1 HG01109.hp2 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.205-564T>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56755715 | |||||||
chr3:56755715 | A | G | 138 | a0001c0002t0002g0032 a0001c0002t0002g0054 a0001c0002t0002g0083 others(135): Show |
144 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.205-564T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56755715 | |||||||
chr3:56755778 | G | A | 1 | a0001c0002t0002g0169 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.205-627C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56755778 | |||||||
chr3:56755848 | G | A | 3 | a0001c0002t0005g0142 a0001c0002t0005g0249 a0001c0002t0005g0250 |
3 | HG02055.hp1 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.205-697C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56755848 | |||||||
chr3:56755876 | G | A | 1 | a0002c0004t0003g0298 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.205-725C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56755876 | |||||||
chr3:56755965 | T | C | 1 | a0001c0002t0002g0187 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.205-814A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56755965 | |||||||
chr3:56756034 | C | G | 1 | a0001c0005t0001g0322 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.205-883G>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56756034 | |||||||
chr3:56756545 | C | CT | 41 | a0001c0002t0002g0007 a0001c0002t0002g0021 a0001c0002t0002g0022 others(38): Show |
42 | HG00544.hp2 HG00597.hp1 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.205-1395dupA | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56756545 | |||||||
chr3:56756545 | C | CTT | 6 | a0001c0002t0002g0038 a0001c0002t0002g0214 a0001c0002t0002g0215 others(3): Show |
6 | HG03491.hp2 HG03942.hp2 NA18940.hp1 others(3): Show |
intron_variant | MODIFIER | c.205-1396_205-1395d others(4): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56756545 | |||||||
chr3:56756545 | CT | C | 64 | a0001c0002t0002g0032 a0001c0002t0002g0043 a0001c0002t0002g0078 others(61): Show |
66 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.205-1395delA | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56756545 | |||||||
chr3:56756545 | CTT | C | 44 | a0001c0002t0002g0005 a0001c0002t0002g0023 a0001c0002t0002g0037 others(41): Show |
45 | HG00621.hp1 HG00673.hp1 HG01070.hp1 others(42): Show |
intron_variant | MODIFIER | c.205-1396_205-1395d others(4): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56756545 | |||||||
chr3:56756545 | CTTT | C | 22 | a0001c0002t0002g0026 a0001c0002t0002g0052 a0001c0002t0002g0064 others(19): Show |
22 | HG00558.hp1 HG01109.hp2 HG01496.hp1 others(19): Show |
intron_variant | MODIFIER | c.205-1397_205-1395d others(5): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56756545 | |||||||
chr3:56756546 | T | TTTTTTTT others(2621): Show |
3 | a0002c0004t0001g0008 a0002c0004t0001g0279 a0002c0004t0001g0282 |
4 | HG00733.hp2 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.205-1396_205-1395i others(2630): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56756546 | |||||||
chr3:56756651 | G | A | 1 | a0002c0001t0003g0243 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.205-1500C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56756651 | |||||||
chr3:56756680 | G | T | 1 | a0002c0001t0003g0036 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.205-1529C>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56756680 | |||||||
chr3:56756875 | C | T | 1 | a0001c0002t0002g0069 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.205-1724G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56756875 | |||||||
chr3:56756966 | T | G | 2 | a0001c0002t0017g0161 a0002c0001t0001g0141 |
2 | HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.205-1815A>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56756966 | |||||||
chr3:56757014 | C | T | 1 | a0001c0002t0002g0187 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.205-1863G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56757014 | |||||||
chr3:56757097 | T | C | 2 | a0001c0007t0001g0076 a0001c0007t0001g0093 |
2 | HG02280.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.205-1946A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56757097 | |||||||
chr3:56757128 | A | G | 2 | a0002c0001t0001g0095 a0002c0001t0001g0096 |
2 | HG03225.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.205-1977T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56757128 | |||||||
chr3:56757185 | G | C | 5 | a0001c0002t0002g0078 a0001c0002t0002g0079 a0001c0002t0006g0011 others(2): Show |
5 | HG02723.hp1 HG03540.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.205-2034C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56757185 | |||||||
chr3:56757213 | C | T | 109 | a0001c0002t0002g0054 a0001c0002t0002g0083 a0001c0002t0002g0157 others(106): Show |
112 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.205-2062G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56757213 | |||||||
chr3:56757335 | G | A | 1 | a0002c0001t0003g0202 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.205-2184C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56757335 | |||||||
chr3:56757452 | C | T | 1 | a0001c0006t0002g0328 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.205-2301G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56757452 | |||||||
chr3:56757470 | G | A | 1 | a0001c0007t0001g0098 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.205-2319C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56757470 | |||||||
chr3:56757476 | G | C | 7 | a0001c0002t0005g0142 a0001c0002t0005g0249 a0001c0002t0005g0250 others(4): Show |
7 | HG01934.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.205-2325C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56757476 | |||||||
chr3:56757715 | T | A | 1 | a0002c0001t0003g0024 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.205-2564A>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56757715 | |||||||
chr3:56757761 | C | T | 1 | a0002c0001t0001g0136 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.205-2610G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56757761 | |||||||
chr3:56757816 | G | A | 7 | a0001c0002t0005g0142 a0001c0002t0005g0249 a0001c0002t0005g0250 others(4): Show |
7 | HG01934.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.205-2665C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56757816 | |||||||
chr3:56757849 | A | G | 1 | a0001c0006t0002g0324 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.205-2698T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56757849 | |||||||
chr3:56758016 | G | A | 1 | a0002c0001t0001g0175 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.205-2865C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56758016 | |||||||
chr3:56758017 | C | T | 1 | a0001c0006t0002g0341 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.205-2866G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56758017 | |||||||
chr3:56758048 | C | T | 2 | a0001c0007t0001g0076 a0001c0007t0001g0093 |
2 | HG02280.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.205-2897G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56758048 | |||||||
chr3:56758123 | C | CA | 29 | a0001c0002t0002g0052 a0001c0002t0002g0064 a0001c0002t0017g0161 others(26): Show |
29 | HG00558.hp1 HG01109.hp2 HG01496.hp1 others(26): Show |
intron_variant | MODIFIER | c.205-2973dupT | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56758123 | |||||||
chr3:56758158 | G | T | 5 | a0001c0002t0005g0142 a0001c0002t0005g0249 a0001c0002t0005g0250 others(2): Show |
5 | HG01934.hp2 HG02055.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.205-3007C>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56758158 | |||||||
chr3:56758243 | T | C | 1 | a0002c0001t0001g0094 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.205-3092A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56758243 | |||||||
chr3:56758619 | T | C | 1 | a0001c0008t0004g0315 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.205-3468A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56758619 | |||||||
chr3:56758727 | C | G | 122 | a0001c0002t0002g0054 a0001c0002t0002g0083 a0001c0002t0002g0139 others(119): Show |
128 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.205-3576G>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56758727 | |||||||
chr3:56758757 | G | A | 22 | a0001c0002t0002g0052 a0001c0002t0002g0064 a0001c0003t0001g0033 others(19): Show |
22 | HG00558.hp1 HG01496.hp1 HG02523.hp2 others(19): Show |
intron_variant | MODIFIER | c.205-3606C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56758757 | |||||||
chr3:56758955 | C | G | 2 | a0001c0007t0001g0098 a0001c0007t0001g0164 |
2 | HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.205-3804G>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56758955 | |||||||
chr3:56759174 | A | AT | 65 | a0001c0002t0002g0043 a0001c0002t0002g0052 a0001c0002t0002g0054 others(62): Show |
65 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.205-4024dupA | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56759174 | |||||||
chr3:56759174 | A | ATT | 7 | a0001c0003t0001g0048 a0001c0003t0011g0120 a0001c0006t0002g0268 others(4): Show |
7 | HG01175.hp1 HG01256.hp1 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.205-4025_205-4024d others(4): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56759174 | |||||||
chr3:56759174 | AT | A | 21 | a0001c0002t0002g0032 a0001c0002t0002g0087 a0001c0002t0008g0135 others(18): Show |
22 | HG01361.hp2 HG01884.hp1 HG01928.hp1 others(19): Show |
intron_variant | MODIFIER | c.205-4024delA | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56759174 | |||||||
chr3:56759326 | C | T | 8 | a0002c0001t0001g0003 a0002c0001t0001g0075 a0002c0001t0001g0145 others(5): Show |
10 | HG01167.hp2 HG01169.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.205-4175G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56759326 | |||||||
chr3:56759331 | C | G | 1 | a0001c0006t0002g0281 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.205-4180G>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56759331 | |||||||
chr3:56759428 | C | T | 5 | a0001c0002t0002g0078 a0001c0002t0002g0079 a0001c0002t0006g0011 others(2): Show |
5 | HG02723.hp1 HG03540.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.205-4277G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56759428 | |||||||
chr3:56759594 | C | T | 29 | a0001c0002t0002g0052 a0001c0002t0002g0064 a0001c0002t0017g0161 others(26): Show |
29 | HG00558.hp1 HG01109.hp2 HG01496.hp1 others(26): Show |
intron_variant | MODIFIER | c.205-4443G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56759594 | |||||||
chr3:56759694 | A | G | 209 | a0001c0002t0002g0005 a0001c0002t0002g0023 a0001c0002t0002g0026 others(206): Show |
216 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(213): Show |
intron_variant | MODIFIER | c.205-4543T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56759694 | |||||||
chr3:56759773 | T | C | 14 | a0001c0002t0002g0032 a0001c0007t0004g0031 a0001c0007t0004g0039 others(11): Show |
14 | HG01361.hp2 HG01928.hp1 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.205-4622A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56759773 | |||||||
chr3:56759968 | A | G | 1 | a0002c0001t0001g0062 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.205-4817T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56759968 | |||||||
chr3:56759969 | A | G | 136 | a0001c0002t0002g0032 a0001c0002t0002g0054 a0001c0002t0002g0083 others(133): Show |
142 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.205-4818T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56759969 | |||||||
chr3:56760047 | A | T | 7 | a0001c0002t0005g0142 a0001c0002t0005g0249 a0001c0002t0005g0250 others(4): Show |
7 | HG01934.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.205-4896T>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56760047 | |||||||
chr3:56760301 | AGG | A | 2 | a0002c0001t0001g0001 a0002c0001t0001g0200 |
3 | HG02451.hp2 HG03098.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.205-5152_205-5151d others(4): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56760301 | |||||||
chr3:56760305 | T | TATAATAA others(17): Show |
2 | a0002c0001t0001g0001 a0002c0001t0001g0200 |
3 | HG02451.hp2 HG03098.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.205-5155_205-5154i others(26): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56760305 | |||||||
chr3:56760414 | G | A | 2 | a0001c0002t0002g0217 a0001c0002t0002g0218 |
2 | NA19005.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.205-5263C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56760414 | |||||||
chr3:56760626 | A | G | 1 | a0002c0001t0001g0094 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.205-5475T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56760626 | |||||||
chr3:56760684 | C | T | 3 | a0001c0002t0002g0252 a0001c0002t0002g0253 a0001c0006t0002g0312 |
3 | NA18967.hp1 NA18982.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.205-5533G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56760684 | |||||||
chr3:56760991 | T | C | 7 | a0002c0001t0001g0081 a0002c0001t0001g0088 a0002c0001t0001g0225 others(4): Show |
7 | HG01109.hp1 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.205-5840A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56760991 | |||||||
chr3:56761051 | T | A | 1 | a0001c0006t0002g0325 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.205-5900A>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56761051 | |||||||
chr3:56761099 | C | T | 1 | a0004c0011t0008g0073 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.205-5948G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56761099 | |||||||
chr3:56761159 | G | A | 134 | a0001c0002t0002g0032 a0001c0002t0002g0054 a0001c0002t0002g0083 others(131): Show |
139 | HG00323.hp2 HG00544.hp1 HG00597.hp2 others(136): Show |
intron_variant | MODIFIER | c.205-6008C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56761159 | |||||||
chr3:56761192 | A | C | 287 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(284): Show |
295 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.205-6041T>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56761192 | |||||||
chr3:56761328 | G | C | 1 | a0001c0003t0001g0091 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.205-6177C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56761328 | |||||||
chr3:56761790 | C | T | 1 | a0002c0001t0003g0113 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.205-6639G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56761790 | |||||||
chr3:56761912 | G | A | 1 | a0001c0002t0002g0038 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.205-6761C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56761912 | |||||||
chr3:56761996 | G | A | 1 | a0002c0001t0003g0243 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.205-6845C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56761996 | |||||||
chr3:56761998 | C | T | 177 | a0001c0002t0002g0005 a0001c0002t0002g0023 a0001c0002t0002g0026 others(174): Show |
183 | HG00323.hp2 HG00544.hp1 HG00597.hp2 others(180): Show |
intron_variant | MODIFIER | c.205-6847G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56761998 | |||||||
chr3:56762152 | C | T | 102 | a0001c0002t0002g0054 a0001c0002t0002g0083 a0001c0002t0002g0157 others(99): Show |
104 | HG00323.hp2 HG00544.hp1 HG00597.hp2 others(101): Show |
intron_variant | MODIFIER | c.205-7001G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56762152 | |||||||
chr3:56762271 | G | A | 1 | a0002c0001t0003g0202 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.205-7120C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56762271 | |||||||
chr3:56762378 | G | C | 2 | a0002c0004t0001g0309 a0002c0004t0001g0346 |
2 | HG00323.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.205-7227C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56762378 | |||||||
chr3:56762507 | G | T | 2 | a0001c0003t0001g0104 a0001c0005t0001g0273 |
2 | HG00741.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.205-7356C>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56762507 | |||||||
chr3:56762510 | C | T | 1 | a0001c0003t0001g0046 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.205-7359G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56762510 | |||||||
chr3:56762511 | G | A | 1 | a0001c0006t0002g0326 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.205-7360C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56762511 | |||||||
chr3:56762593 | C | T | 1 | a0002c0001t0003g0263 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.205-7442G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56762593 | |||||||
chr3:56762594 | G | A | 1 | a0001c0002t0002g0190 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.205-7443C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56762594 | |||||||
chr3:56762710 | T | C | 39 | a0001c0002t0002g0007 a0001c0002t0002g0021 a0001c0002t0002g0022 others(36): Show |
41 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.205-7559A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56762710 | |||||||
chr3:56762718 | C | A | 1 | a0002c0001t0001g0081 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.205-7567G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56762718 | |||||||
chr3:56762973 | G | A | 4 | a0001c0002t0002g0077 a0001c0002t0002g0086 a0001c0002t0002g0087 others(1): Show |
4 | HG01099.hp1 HG02886.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.205-7822C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56762973 | |||||||
chr3:56763039 | C | T | 1 | a0002c0004t0003g0303 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.205-7888G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56763039 | |||||||
chr3:56763049 | A | T | 5 | a0001c0003t0001g0016 a0001c0003t0001g0017 a0001c0003t0001g0018 others(2): Show |
5 | HG01109.hp2 HG02145.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.205-7898T>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56763049 | |||||||
chr3:56763078 | A | G | 16 | a0001c0002t0002g0032 a0001c0002t0002g0110 a0001c0007t0004g0031 others(13): Show |
16 | HG01361.hp2 HG01928.hp1 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.205-7927T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56763078 | |||||||
chr3:56763092 | A | G | 9 | a0001c0007t0001g0101 a0002c0001t0001g0003 a0002c0001t0001g0075 others(6): Show |
11 | HG01167.hp2 HG01169.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.205-7941T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56763092 | |||||||
chr3:56763102 | T | C | 1 | a0001c0002t0002g0127 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.205-7951A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56763102 | |||||||
chr3:56763159 | C | G | 34 | a0001c0002t0002g0007 a0001c0002t0002g0021 a0001c0002t0002g0022 others(31): Show |
35 | HG00544.hp2 HG00597.hp1 HG01981.hp2 others(32): Show |
intron_variant | MODIFIER | c.205-8008G>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56763159 | |||||||
chr3:56763661 | T | G | 9 | a0001c0007t0001g0101 a0002c0001t0001g0003 a0002c0001t0001g0075 others(6): Show |
11 | HG01167.hp2 HG01169.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.205-8510A>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56763661 | |||||||
chr3:56763686 | C | T | 16 | a0001c0002t0002g0032 a0001c0002t0002g0110 a0001c0007t0004g0031 others(13): Show |
16 | HG01361.hp2 HG01928.hp1 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.205-8535G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56763686 | |||||||
chr3:56763740 | T | G | 215 | a0001c0002t0002g0005 a0001c0002t0002g0023 a0001c0002t0002g0026 others(212): Show |
221 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.205-8589A>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56763740 | |||||||
chr3:56763760 | G | A | 285 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(282): Show |
294 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(291): Show |
intron_variant | MODIFIER | c.205-8609C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56763760 | |||||||
chr3:56763802 | T | C | 72 | a0001c0002t0002g0054 a0001c0002t0002g0083 a0001c0003t0001g0244 others(69): Show |
74 | HG00280.hp2 HG00323.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.205-8651A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56763802 | |||||||
chr3:56763957 | G | A | 34 | a0001c0002t0002g0007 a0001c0002t0002g0021 a0001c0002t0002g0022 others(31): Show |
35 | HG00544.hp2 HG00597.hp1 HG01981.hp2 others(32): Show |
intron_variant | MODIFIER | c.205-8806C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56763957 | |||||||
chr3:56763991 | G | A | 1 | a0002c0001t0003g0202 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.205-8840C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56763991 | |||||||
chr3:56764067 | T | TAA | 111 | a0001c0002t0002g0052 a0001c0002t0002g0064 a0001c0002t0002g0129 others(108): Show |
113 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.205-8918_205-8917d others(4): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56764067 | |||||||
chr3:56764101 | T | C | 111 | a0001c0002t0002g0052 a0001c0002t0002g0064 a0001c0002t0002g0129 others(108): Show |
113 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.205-8950A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56764101 | |||||||
chr3:56764278 | C | T | 110 | a0001c0002t0002g0052 a0001c0002t0002g0064 a0001c0002t0002g0129 others(107): Show |
112 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.205-9127G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56764278 | |||||||
chr3:56764467 | C | T | 7 | a0001c0003t0001g0167 a0002c0001t0003g0163 a0002c0004t0003g0300 others(4): Show |
7 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(4): Show |
intron_variant | MODIFIER | c.204+9242G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56764467 | |||||||
chr3:56764525 | G | A | 2 | a0002c0001t0001g0233 a0002c0001t0001g0234 |
2 | NA18994.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.204+9184C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56764525 | |||||||
chr3:56764637 | C | CGATATGA others(9): Show |
1 | a0002c0001t0001g0211 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+9056_204+9071d others(18): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56764637 | |||||||
chr3:56764676 | C | G | 72 | a0001c0002t0002g0054 a0001c0002t0002g0083 a0001c0003t0001g0244 others(69): Show |
74 | HG00280.hp2 HG00323.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.204+9033G>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56764676 | |||||||
chr3:56764721 | A | G | 111 | a0001c0002t0002g0005 a0001c0002t0002g0023 a0001c0002t0002g0026 others(108): Show |
115 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(112): Show |
intron_variant | MODIFIER | c.204+8988T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56764721 | |||||||
chr3:56764746 | T | C | 111 | a0001c0002t0002g0052 a0001c0002t0002g0064 a0001c0002t0002g0129 others(108): Show |
113 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.204+8963A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56764746 | |||||||
chr3:56764756 | A | AT | 104 | a0001c0002t0002g0052 a0001c0002t0002g0064 a0001c0002t0002g0129 others(101): Show |
106 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.204+8952dupA | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56764756 | |||||||
chr3:56764756 | AT | A | 94 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(91): Show |
97 | HG00544.hp2 HG00597.hp1 HG00621.hp1 others(94): Show |
intron_variant | MODIFIER | c.204+8952delA | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56764756 | |||||||
chr3:56764756 | ATT | A | 9 | a0001c0002t0002g0069 a0002c0001t0001g0003 a0002c0001t0001g0075 others(6): Show |
11 | HG01167.hp2 HG01169.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.204+8951_204+8952d others(4): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56764756 | |||||||
chr3:56764919 | G | A | 16 | a0001c0002t0002g0032 a0001c0002t0002g0110 a0001c0007t0004g0031 others(13): Show |
16 | HG01361.hp2 HG01928.hp1 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.204+8790C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56764919 | |||||||
chr3:56765091 | A | G | 111 | a0001c0002t0002g0052 a0001c0002t0002g0064 a0001c0002t0002g0129 others(108): Show |
113 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.204+8618T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56765091 | |||||||
chr3:56765296 | C | T | 1 | a0001c0002t0002g0029 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.204+8413G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56765296 | |||||||
chr3:56765297 | G | A | 4 | a0002c0001t0003g0080 a0002c0001t0003g0082 a0002c0001t0003g0089 others(1): Show |
4 | HG02258.hp1 HG02486.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.204+8412C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56765297 | |||||||
chr3:56765389 | C | T | 1 | a0001c0003t0001g0166 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.204+8320G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56765389 | |||||||
chr3:56765764 | G | C | 4 | a0001c0002t0002g0212 a0001c0002t0002g0213 a0001c0002t0002g0214 others(1): Show |
4 | HG00597.hp1 NA18940.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.204+7945C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56765764 | |||||||
chr3:56765860 | T | A | 1 | a0001c0002t0002g0025 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.204+7849A>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56765860 | |||||||
chr3:56766193 | A | G | 1 | a0002c0004t0003g0276 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.204+7516T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56766193 | |||||||
chr3:56766536 | A | G | 2 | a0001c0002t0006g0011 a0001c0002t0006g0013 |
2 | HG02723.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.204+7173T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56766536 | |||||||
chr3:56766574 | A | T | 1 | a0001c0002t0010g0014 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.204+7135T>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56766574 | |||||||
chr3:56766593 | T | C | 1 | a0002c0001t0001g0075 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.204+7116A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56766593 | |||||||
chr3:56766626 | G | A | 2 | a0001c0007t0001g0076 a0001c0007t0001g0093 |
2 | HG02280.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.204+7083C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56766626 | |||||||
chr3:56766739 | T | C | 3 | a0001c0003t0001g0166 a0001c0005t0001g0292 a0001c0005t0001g0293 |
3 | HG00099.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.204+6970A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56766739 | |||||||
chr3:56767020 | A | C | 1 | a0002c0001t0001g0211 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6689T>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767020 | |||||||
chr3:56767021 | G | A | 1 | a0002c0001t0001g0211 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6688C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767021 | |||||||
chr3:56767027 | T | A | 1 | a0002c0001t0001g0211 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6682A>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767027 | |||||||
chr3:56767028 | G | A | 1 | a0002c0001t0001g0211 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6681C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767028 | |||||||
chr3:56767029 | G | T | 1 | a0002c0001t0001g0211 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6680C>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767029 | |||||||
chr3:56767031 | G | C | 1 | a0002c0001t0001g0211 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6678C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767031 | |||||||
chr3:56767036 | G | T | 1 | a0002c0001t0001g0211 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6673C>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767036 | |||||||
chr3:56767037 | T | A | 1 | a0002c0001t0001g0211 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6672A>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767037 | |||||||
chr3:56767039 | G | A | 1 | a0002c0001t0001g0211 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6670C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767039 | |||||||
chr3:56767040 | T | C | 1 | a0002c0001t0001g0211 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6669A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767040 | |||||||
chr3:56767045 | C | G | 1 | a0002c0001t0001g0211 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6664G>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767045 | |||||||
chr3:56767048 | G | A | 1 | a0002c0001t0001g0211 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6661C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767048 | |||||||
chr3:56767049 | C | G | 1 | a0002c0001t0001g0211 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6660G>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767049 | |||||||
chr3:56767066 | T | A | 1 | a0002c0001t0001g0211 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6643A>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767066 | |||||||
chr3:56767067 | TGGGAGGC others(5): Show |
T | 1 | a0002c0001t0001g0211 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6630_204+6641d others(14): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767067 | |||||||
chr3:56767081 | G | T | 1 | a0002c0001t0001g0211 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6628C>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767081 | |||||||
chr3:56767082 | G | T | 1 | a0002c0001t0001g0211 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6627C>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767082 | |||||||
chr3:56767088 | C | A | 1 | a0002c0001t0001g0211 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6621G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767088 | |||||||
chr3:56767090 | G | A | 1 | a0002c0001t0001g0211 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6619C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767090 | |||||||
chr3:56767091 | C | T | 1 | a0002c0001t0001g0211 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6618G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767091 | |||||||
chr3:56767093 | T | A | 1 | a0002c0001t0001g0211 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6616A>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767093 | |||||||
chr3:56767094 | G | A | 1 | a0002c0001t0001g0211 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6615C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767094 | |||||||
chr3:56767096 | G | A | 1 | a0002c0001t0001g0211 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6613C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767096 | |||||||
chr3:56767097 | G | A | 1 | a0002c0001t0001g0211 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6612C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767097 | |||||||
chr3:56767098 | C | A | 1 | a0002c0001t0001g0211 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6611G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767098 | |||||||
chr3:56767102 | G | A | 1 | a0002c0001t0001g0211 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6607C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767102 | |||||||
chr3:56767104 | G | A | 1 | a0002c0001t0001g0211 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6605C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767104 | |||||||
chr3:56767105 | T | A | 1 | a0002c0001t0001g0211 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6604A>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767105 | |||||||
chr3:56767107 | T | A | 1 | a0002c0001t0001g0211 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6602A>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767107 | |||||||
chr3:56767108 | G | A | 1 | a0002c0001t0001g0211 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6601C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767108 | |||||||
chr3:56767110 | G | A | 1 | a0002c0001t0001g0211 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6599C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767110 | |||||||
chr3:56767111 | A | T | 1 | a0002c0001t0001g0211 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6598T>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767111 | |||||||
chr3:56767113 | C | A | 1 | a0002c0001t0001g0211 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6596G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767113 | |||||||
chr3:56767119 | G | T | 1 | a0002c0001t0001g0211 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6590C>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767119 | |||||||
chr3:56767120 | G | T | 1 | a0002c0001t0001g0211 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6589C>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767120 | |||||||
chr3:56767122 | C | A | 1 | a0002c0001t0001g0211 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6587G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767122 | |||||||
chr3:56767125 | C | A | 1 | a0002c0001t0001g0211 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6584G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767125 | |||||||
chr3:56767126 | A | C | 1 | a0002c0001t0001g0211 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6583T>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767126 | |||||||
chr3:56767141 | T | A | 1 | a0002c0001t0001g0211 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6568A>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767141 | |||||||
chr3:56767144 | C | A | 1 | a0002c0001t0001g0211 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6565G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767144 | |||||||
chr3:56767145 | T | C | 1 | a0002c0001t0001g0211 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6564A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767145 | |||||||
chr3:56767188 | G | C | 1 | a0002c0001t0001g0211 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6521C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767188 | |||||||
chr3:56767189 | A | G | 1 | a0002c0001t0001g0211 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6520T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767189 | |||||||
chr3:56767190 | C | A | 1 | a0002c0001t0001g0211 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.204+6519G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767190 | |||||||
chr3:56767280 | T | C | 2 | a0001c0007t0001g0098 a0001c0007t0001g0164 |
2 | HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.204+6429A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767280 | |||||||
chr3:56767300 | C | T | 1 | a0004c0011t0008g0073 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.204+6409G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767300 | |||||||
chr3:56767310 | C | T | 17 | a0001c0002t0002g0032 a0001c0002t0002g0110 a0001c0007t0004g0031 others(14): Show |
17 | HG01361.hp2 HG01928.hp1 HG01952.hp1 others(14): Show |
intron_variant | MODIFIER | c.204+6399G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767310 | |||||||
chr3:56767441 | G | A | 33 | a0001c0002t0002g0007 a0001c0002t0002g0021 a0001c0002t0002g0022 others(30): Show |
35 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.204+6268C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767441 | |||||||
chr3:56767583 | C | CA | 108 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(105): Show |
112 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(109): Show |
intron_variant | MODIFIER | c.204+6125dupT | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767583 | |||||||
chr3:56767583 | C | CAA | 51 | a0001c0002t0002g0023 a0001c0002t0002g0032 a0001c0002t0002g0034 others(48): Show |
52 | HG00544.hp2 HG00621.hp1 HG01884.hp1 others(49): Show |
intron_variant | MODIFIER | c.204+6124_204+6125d others(4): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767583 | |||||||
chr3:56767583 | C | CAAA | 9 | a0001c0002t0002g0124 a0001c0002t0002g0127 a0001c0007t0004g0114 others(6): Show |
9 | HG01361.hp2 HG01928.hp1 HG02074.hp2 others(6): Show |
intron_variant | MODIFIER | c.204+6123_204+6125d others(5): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767583 | |||||||
chr3:56767583 | CAAAAAAA | C | 108 | a0001c0002t0002g0052 a0001c0002t0002g0064 a0001c0002t0002g0129 others(105): Show |
110 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.204+6119_204+6125d others(9): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767583 | |||||||
chr3:56767999 | C | T | 35 | a0001c0002t0002g0129 a0001c0002t0002g0130 a0001c0002t0002g0131 others(32): Show |
36 | HG00544.hp1 HG00597.hp2 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.204+5710G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56767999 | |||||||
chr3:56768117 | C | G | 2 | a0001c0002t0017g0161 a0002c0001t0001g0141 |
2 | HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.204+5592G>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56768117 | |||||||
chr3:56768257 | C | A | 1 | a0001c0003t0001g0180 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.204+5452G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56768257 | |||||||
chr3:56768581 | C | A | 2 | a0001c0002t0002g0127 a0004c0011t0008g0073 |
2 | HG02486.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.204+5128G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56768581 | |||||||
chr3:56768667 | C | CA | 15 | a0001c0002t0002g0034 a0001c0002t0002g0058 a0001c0002t0002g0069 others(12): Show |
15 | HG00544.hp2 HG01099.hp1 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.204+5041dupT | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56768667 | |||||||
chr3:56768667 | CA | C | 31 | a0001c0002t0002g0032 a0001c0002t0002g0110 a0001c0003t0001g0016 others(28): Show |
33 | HG01109.hp2 HG01167.hp2 HG01169.hp1 others(30): Show |
intron_variant | MODIFIER | c.204+5041delT | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56768667 | |||||||
chr3:56768683 | AG | A | 98 | a0001c0002t0002g0005 a0001c0002t0002g0023 a0001c0002t0002g0026 others(95): Show |
101 | HG00323.hp2 HG00621.hp1 HG00673.hp1 others(98): Show |
intron_variant | MODIFIER | c.204+5025delC | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56768683 | |||||||
chr3:56768684 | G | A | 157 | a0001c0002t0002g0007 a0001c0002t0002g0021 a0001c0002t0002g0022 others(154): Show |
161 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.204+5025C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56768684 | |||||||
chr3:56768753 | A | G | 1 | a0001c0002t0002g0187 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.204+4956T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56768753 | |||||||
chr3:56768941 | A | G | 8 | a0002c0001t0001g0003 a0002c0001t0001g0075 a0002c0001t0001g0145 others(5): Show |
10 | HG01167.hp2 HG01169.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.204+4768T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56768941 | |||||||
chr3:56769038 | G | A | 2 | a0001c0002t0002g0127 a0004c0011t0008g0073 |
2 | HG02486.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.204+4671C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56769038 | |||||||
chr3:56769147 | A | G | 74 | a0001c0002t0002g0054 a0001c0002t0002g0083 a0001c0002t0008g0135 others(71): Show |
76 | HG00323.hp2 HG00733.hp2 HG01070.hp2 others(73): Show |
intron_variant | MODIFIER | c.204+4562T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56769147 | |||||||
chr3:56769271 | G | A | 3 | a0001c0005t0001g0321 a0001c0007t0001g0162 a0002c0001t0001g0103 |
3 | HG01070.hp1 HG01106.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.204+4438C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56769271 | |||||||
chr3:56769454 | A | G | 1 | a0001c0002t0002g0056 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.204+4255T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56769454 | |||||||
chr3:56769488 | G | A | 1 | a0002c0001t0001g0055 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.204+4221C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56769488 | |||||||
chr3:56769832 | G | A | 17 | a0001c0002t0002g0032 a0001c0002t0002g0110 a0001c0007t0004g0031 others(14): Show |
17 | HG01361.hp2 HG01928.hp1 HG01952.hp1 others(14): Show |
intron_variant | MODIFIER | c.204+3877C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56769832 | |||||||
chr3:56769929 | A | G | 2 | a0001c0002t0002g0212 a0002c0001t0003g0030 |
2 | HG00597.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.204+3780T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56769929 | |||||||
chr3:56770025 | T | G | 9 | a0001c0007t0001g0101 a0002c0001t0001g0003 a0002c0001t0001g0075 others(6): Show |
11 | HG01167.hp2 HG01169.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.204+3684A>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56770025 | |||||||
chr3:56770069 | C | T | 2 | a0001c0002t0002g0127 a0004c0011t0008g0073 |
2 | HG02486.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.204+3640G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56770069 | |||||||
chr3:56770096 | C | G | 14 | a0001c0003t0001g0016 a0001c0003t0001g0017 a0001c0003t0001g0018 others(11): Show |
16 | HG01109.hp2 HG01167.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.204+3613G>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56770096 | |||||||
chr3:56770229 | T | A | 111 | a0001c0002t0002g0052 a0001c0002t0002g0064 a0001c0002t0002g0129 others(108): Show |
113 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.204+3480A>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56770229 | |||||||
chr3:56770239 | G | A | 5 | a0001c0003t0001g0016 a0001c0003t0001g0017 a0001c0003t0001g0018 others(2): Show |
5 | HG01109.hp2 HG02145.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.204+3470C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56770239 | |||||||
chr3:56770361 | G | C | 5 | a0001c0007t0004g0039 a0001c0007t0004g0114 a0001c0007t0004g0115 others(2): Show |
5 | HG01361.hp2 HG01928.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.204+3348C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56770361 | |||||||
chr3:56770404 | T | C | 4 | a0001c0002t0002g0212 a0001c0002t0002g0213 a0001c0002t0002g0214 others(1): Show |
4 | HG00597.hp1 NA18940.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.204+3305A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56770404 | |||||||
chr3:56770411 | A | AAAATT | 103 | a0001c0002t0002g0052 a0001c0002t0002g0054 a0001c0002t0002g0064 others(100): Show |
108 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.204+3293_204+3297d others(7): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56770411 | |||||||
chr3:56770411 | A | AAAATTAA others(3): Show |
4 | a0001c0002t0002g0127 a0001c0002t0010g0014 a0001c0007t0001g0101 others(1): Show |
4 | HG02258.hp2 HG02486.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.204+3288_204+3297d others(12): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56770411 | |||||||
chr3:56770411 | A | AAAATTAA others(8): Show |
1 | a0002c0001t0003g0208 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.204+3283_204+3297d others(17): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56770411 | |||||||
chr3:56770411 | AAAATT | A | 8 | a0001c0003t0001g0016 a0001c0003t0001g0017 a0001c0003t0001g0018 others(5): Show |
8 | HG01109.hp2 HG01884.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.204+3293_204+3297d others(7): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56770411 | |||||||
chr3:56770411 | AAAATTAA others(3): Show |
A | 20 | a0001c0002t0002g0032 a0001c0002t0002g0110 a0001c0002t0002g0153 others(17): Show |
20 | HG01361.hp2 HG01891.hp2 HG01928.hp1 others(17): Show |
intron_variant | MODIFIER | c.204+3288_204+3297d others(12): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56770411 | |||||||
chr3:56770518 | T | C | 2 | a0002c0001t0001g0001 a0002c0001t0001g0200 |
3 | HG02451.hp2 HG03098.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.204+3191A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56770518 | |||||||
chr3:56770645 | G | C | 1 | a0002c0004t0001g0334 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.204+3064C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56770645 | |||||||
chr3:56770772 | G | A | 2 | a0001c0002t0002g0139 a0002c0001t0001g0136 |
2 | HG02109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.204+2937C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56770772 | |||||||
chr3:56770933 | G | A | 2 | a0002c0001t0003g0060 a0002c0004t0003g0277 |
2 | HG02027.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.204+2776C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56770933 | |||||||
chr3:56770937 | C | G | 3 | a0002c0001t0001g0019 a0002c0001t0001g0095 a0002c0001t0001g0096 |
3 | HG02723.hp2 HG03225.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.204+2772G>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56770937 | |||||||
chr3:56770982 | G | A | 200 | a0001c0002t0002g0052 a0001c0002t0002g0054 a0001c0002t0002g0064 others(197): Show |
207 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.204+2727C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56770982 | |||||||
chr3:56771110 | T | C | 2 | a0001c0003t0001g0244 a0001c0013t0001g0140 |
2 | HG02630.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.204+2599A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56771110 | |||||||
chr3:56771113 | C | CAA | 6 | a0001c0003t0001g0016 a0001c0003t0001g0017 a0001c0003t0001g0018 others(3): Show |
6 | HG01109.hp2 HG02145.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.204+2594_204+2595d others(4): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56771113 | |||||||
chr3:56771184 | C | A | 2 | a0001c0002t0002g0139 a0002c0001t0001g0136 |
2 | HG02109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.204+2525G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56771184 | |||||||
chr3:56771204 | C | T | 5 | a0001c0003t0001g0109 a0001c0003t0001g0166 a0001c0003t0001g0180 others(2): Show |
5 | HG00099.hp2 HG01169.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.204+2505G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56771204 | |||||||
chr3:56771288 | T | C | 2 | a0001c0002t0002g0056 a0001c0002t0002g0187 |
2 | HG02080.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.204+2421A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56771288 | |||||||
chr3:56771328 | G | A | 1 | a0002c0004t0001g0340 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.204+2381C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56771328 | |||||||
chr3:56771348 | A | G | 121 | a0001c0002t0002g0007 a0001c0002t0002g0021 a0001c0002t0002g0022 others(118): Show |
127 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.204+2361T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56771348 | |||||||
chr3:56771392 | G | A | 1 | a0001c0002t0002g0029 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.204+2317C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56771392 | |||||||
chr3:56771610 | G | C | 2 | a0001c0006t0002g0275 a0002c0004t0014g0284 |
2 | NA18950.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.204+2099C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56771610 | |||||||
chr3:56771613 | C | T | 8 | a0002c0001t0001g0003 a0002c0001t0001g0075 a0002c0001t0001g0145 others(5): Show |
10 | HG01167.hp2 HG01169.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.204+2096G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56771613 | |||||||
chr3:56771615 | C | T | 4 | a0001c0002t0002g0077 a0001c0002t0002g0086 a0001c0002t0002g0087 others(1): Show |
4 | HG01099.hp1 HG02886.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.204+2094G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56771615 | |||||||
chr3:56771672 | T | C | 1 | a0002c0001t0001g0175 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.204+2037A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56771672 | |||||||
chr3:56771678 | C | T | 9 | a0001c0007t0001g0101 a0002c0001t0001g0003 a0002c0001t0001g0075 others(6): Show |
11 | HG01167.hp2 HG01169.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.204+2031G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56771678 | |||||||
chr3:56771792 | A | C | 1 | a0001c0005t0001g0286 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.204+1917T>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56771792 | |||||||
chr3:56771817 | A | T | 2 | a0001c0002t0002g0127 a0004c0011t0008g0073 |
2 | HG02486.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.204+1892T>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56771817 | |||||||
chr3:56771989 | G | A | 1 | a0002c0001t0001g0136 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.204+1720C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56771989 | |||||||
chr3:56771989 | G | T | 1 | a0001c0002t0002g0138 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.204+1720C>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56771989 | |||||||
chr3:56772117 | A | G | 154 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(151): Show |
161 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(158): Show |
intron_variant | MODIFIER | c.204+1592T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56772117 | |||||||
chr3:56772144 | G | C | 27 | a0001c0002t0002g0005 a0001c0002t0002g0023 a0001c0002t0002g0026 others(24): Show |
28 | HG00621.hp1 HG00673.hp1 HG02027.hp1 others(25): Show |
intron_variant | MODIFIER | c.204+1565C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56772144 | |||||||
chr3:56772159 | G | A | 4 | a0001c0003t0001g0006 a0001c0003t0001g0092 a0001c0003t0001g0176 others(1): Show |
5 | HG01167.hp1 HG01258.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.204+1550C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56772159 | |||||||
chr3:56772175 | T | C | 90 | a0001c0002t0002g0054 a0001c0002t0002g0083 a0001c0002t0002g0127 others(87): Show |
95 | HG00280.hp2 HG00323.hp2 HG00733.hp2 others(92): Show |
intron_variant | MODIFIER | c.204+1534A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56772175 | |||||||
chr3:56772409 | C | T | 1 | a0001c0012t0001g0105 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.204+1300G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56772409 | |||||||
chr3:56772648 | C | T | 1 | a0001c0002t0002g0195 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.204+1061G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56772648 | |||||||
chr3:56772739 | A | G | 1 | a0002c0001t0001g0137 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.204+970T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56772739 | |||||||
chr3:56772747 | G | T | 1 | a0002c0001t0001g0137 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.204+962C>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56772747 | |||||||
chr3:56772752 | C | T | 1 | a0002c0001t0001g0185 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.204+957G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56772752 | |||||||
chr3:56772914 | A | T | 1 | a0002c0004t0003g0278 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.204+795T>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56772914 | |||||||
chr3:56773198 | T | A | 3 | a0002c0001t0003g0203 a0002c0004t0003g0331 a0002c0004t0003g0335 |
3 | HG03654.hp1 HG03669.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.204+511A>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56773198 | |||||||
chr3:56773302 | A | G | 4 | a0002c0001t0003g0080 a0002c0001t0003g0082 a0002c0001t0003g0089 others(1): Show |
4 | HG02258.hp1 HG02486.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.204+407T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56773302 | |||||||
chr3:56773500 | C | T | 1 | a0001c0002t0002g0207 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.204+209G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56773500 | |||||||
chr3:56773662 | G | A | 2 | a0001c0007t0001g0076 a0001c0007t0001g0093 |
2 | HG02280.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.204+47C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 2/9 | chr3 | 56773662 | |||||||
chr3:56773826 | T | A | 1 | a0002c0004t0003g0278 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.97-10A>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56773826 | |||||||
chr3:56773961 | T | C | 1 | a0002c0004t0001g0340 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.97-145A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56773961 | |||||||
chr3:56774127 | C | A | 6 | a0001c0003t0001g0148 a0001c0003t0001g0149 a0001c0005t0001g0322 others(3): Show |
6 | HG00140.hp2 HG01256.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.97-311G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56774127 | |||||||
chr3:56774222 | C | G | 17 | a0001c0002t0002g0032 a0001c0002t0002g0110 a0001c0007t0004g0031 others(14): Show |
17 | HG01361.hp2 HG01928.hp1 HG01952.hp1 others(14): Show |
intron_variant | MODIFIER | c.97-406G>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56774222 | |||||||
chr3:56774414 | C | T | 1 | a0002c0001t0001g0097 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.97-598G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56774414 | |||||||
chr3:56774450 | C | T | 2 | a0001c0007t0001g0076 a0001c0007t0001g0093 |
2 | HG02280.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.97-634G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56774450 | |||||||
chr3:56774563 | G | A | 1 | a0001c0002t0002g0029 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.97-747C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56774563 | |||||||
chr3:56774714 | A | G | 69 | a0001c0002t0002g0054 a0001c0002t0002g0083 a0001c0003t0001g0244 others(66): Show |
70 | HG00323.hp2 HG00733.hp2 HG01070.hp2 others(67): Show |
intron_variant | MODIFIER | c.97-898T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56774714 | |||||||
chr3:56774742 | T | C | 111 | a0001c0002t0002g0037 a0001c0002t0002g0052 a0001c0002t0002g0064 others(108): Show |
113 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.97-926A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56774742 | |||||||
chr3:56774825 | G | C | 1 | a0002c0001t0001g0085 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.97-1009C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56774825 | |||||||
chr3:56774881 | C | T | 8 | a0001c0002t0002g0079 a0002c0001t0001g0003 a0002c0001t0001g0145 others(5): Show |
10 | HG01167.hp2 HG01169.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.97-1065G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56774881 | |||||||
chr3:56774926 | C | A | 2 | a0001c0007t0001g0076 a0001c0007t0001g0093 |
2 | HG02280.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.97-1110G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56774926 | |||||||
chr3:56774926 | C | CA | 10 | a0001c0002t0002g0078 a0001c0002t0002g0139 a0001c0003t0001g0046 others(7): Show |
10 | HG03540.hp1 HG06807.hp2 NA18522.hp2 others(7): Show |
intron_variant | MODIFIER | c.97-1111dupT | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56774926 | |||||||
chr3:56774928 | A | AC | 168 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(165): Show |
173 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.97-1113_97-1112ins others(1): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56774928 | |||||||
chr3:56774929 | A | C | 74 | a0001c0002t0002g0054 a0001c0002t0002g0083 a0001c0002t0002g0127 others(71): Show |
76 | HG00323.hp2 HG00733.hp2 HG01070.hp2 others(73): Show |
intron_variant | MODIFIER | c.97-1113T>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56774929 | |||||||
chr3:56774931 | A | C | 1 | a0001c0003t0001g0241 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.97-1115T>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56774931 | |||||||
chr3:56774947 | G | A | 2 | a0001c0002t0017g0161 a0002c0001t0001g0141 |
2 | HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.97-1131C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56774947 | |||||||
chr3:56775221 | G | A | 1 | a0002c0004t0001g0283 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.97-1405C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56775221 | |||||||
chr3:56775262 | T | C | 2 | a0002c0004t0001g0309 a0002c0004t0001g0346 |
2 | HG00323.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.97-1446A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56775262 | |||||||
chr3:56775600 | A | G | 254 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(251): Show |
261 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.97-1784T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56775600 | |||||||
chr3:56775722 | A | G | 2 | a0001c0002t0002g0196 a0001c0002t0002g0197 |
2 | NA19057.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.97-1906T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56775722 | |||||||
chr3:56775768 | C | A | 28 | a0001c0002t0002g0005 a0001c0002t0002g0023 a0001c0002t0002g0026 others(25): Show |
29 | HG00621.hp1 HG00673.hp1 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.97-1952G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56775768 | |||||||
chr3:56775777 | TACACACA others(19): Show |
T | 3 | a0001c0002t0005g0142 a0001c0002t0005g0249 a0001c0002t0005g0250 |
3 | HG02055.hp1 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.97-1987_97-1962del others(26): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56775777 | |||||||
chr3:56775791 | C | T | 2 | a0001c0006t0002g0275 a0002c0004t0014g0284 |
2 | NA18950.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.97-1975G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56775791 | |||||||
chr3:56775792 | A | G | 193 | a0001c0002t0002g0022 a0001c0002t0002g0052 a0001c0002t0002g0054 others(190): Show |
198 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.97-1976T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56775792 | |||||||
chr3:56775794 | G | A | 14 | a0001c0002t0002g0025 a0001c0002t0002g0034 a0001c0002t0002g0038 others(11): Show |
14 | HG00597.hp1 HG01109.hp2 HG01981.hp2 others(11): Show |
intron_variant | MODIFIER | c.97-1978C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56775794 | |||||||
chr3:56775796 | G | A | 9 | a0001c0002t0002g0079 a0002c0001t0001g0003 a0002c0001t0001g0075 others(6): Show |
11 | HG01167.hp2 HG01169.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.97-1980C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56775796 | |||||||
chr3:56775800 | G | GCA | 181 | a0001c0002t0002g0022 a0001c0002t0002g0052 a0001c0002t0002g0054 others(178): Show |
186 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.97-1986_97-1985dup others(2): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56775800 | |||||||
chr3:56775800 | G | GCACA | 7 | a0001c0005t0001g0265 a0002c0001t0001g0132 a0002c0001t0001g0228 others(4): Show |
7 | HG00741.hp1 NA18945.hp2 NA19004.hp1 others(4): Show |
intron_variant | MODIFIER | c.97-1988_97-1985dup others(4): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56775800 | |||||||
chr3:56775800 | G | GCACACAC others(3): Show |
1 | a0001c0003t0001g0181 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.97-1994_97-1985dup others(10): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56775800 | |||||||
chr3:56775800 | GCA | G | 17 | a0001c0002t0002g0032 a0001c0002t0002g0110 a0001c0007t0004g0031 others(14): Show |
17 | HG01361.hp2 HG01928.hp1 HG01952.hp1 others(14): Show |
intron_variant | MODIFIER | c.97-1986_97-1985del others(2): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56775800 | |||||||
chr3:56775800 | GCACACA | G | 5 | a0001c0003t0001g0016 a0001c0003t0001g0017 a0001c0003t0001g0018 others(2): Show |
5 | HG01109.hp2 HG02145.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.97-1990_97-1985del others(6): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56775800 | |||||||
chr3:56776451 | C | A | 3 | a0002c0001t0001g0019 a0002c0001t0001g0095 a0002c0001t0001g0096 |
3 | HG02723.hp2 HG03225.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.97-2635G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56776451 | |||||||
chr3:56776476 | G | A | 1 | a0001c0002t0002g0127 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.97-2660C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56776476 | |||||||
chr3:56776481 | T | C | 2 | a0001c0002t0017g0161 a0002c0001t0001g0141 |
2 | HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.97-2665A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56776481 | |||||||
chr3:56776643 | G | T | 1 | a0001c0003t0001g0204 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.97-2827C>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56776643 | |||||||
chr3:56776722 | G | A | 2 | a0001c0007t0001g0098 a0001c0007t0001g0164 |
2 | HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.97-2906C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56776722 | |||||||
chr3:56776737 | G | A | 1 | a0001c0007t0004g0039 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.97-2921C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56776737 | |||||||
chr3:56776841 | C | T | 5 | a0001c0003t0001g0016 a0001c0003t0001g0017 a0001c0003t0001g0018 others(2): Show |
5 | HG01109.hp2 HG02145.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.97-3025G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56776841 | |||||||
chr3:56777290 | A | C | 1 | a0001c0006t0002g0326 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.97-3474T>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56777290 | |||||||
chr3:56777314 | G | A | 1 | a0001c0005t0001g0317 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.97-3498C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56777314 | |||||||
chr3:56777317 | G | A | 17 | a0001c0002t0002g0032 a0001c0002t0002g0110 a0001c0007t0004g0031 others(14): Show |
17 | HG01361.hp2 HG01928.hp1 HG01952.hp1 others(14): Show |
intron_variant | MODIFIER | c.97-3501C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56777317 | |||||||
chr3:56777383 | T | G | 1 | a0002c0001t0001g0094 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.97-3567A>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56777383 | |||||||
chr3:56777617 | T | G | 1 | a0001c0003t0001g0018 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.97-3801A>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56777617 | |||||||
chr3:56777665 | C | T | 5 | a0001c0002t0002g0078 a0001c0002t0002g0079 a0001c0002t0006g0011 others(2): Show |
5 | HG02723.hp1 HG03540.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.97-3849G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56777665 | |||||||
chr3:56778034 | C | G | 1 | a0001c0007t0004g0126 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.97-4218G>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56778034 | |||||||
chr3:56778131 | T | C | 30 | a0001c0002t0002g0007 a0001c0002t0002g0021 a0001c0002t0002g0022 others(27): Show |
31 | HG00544.hp2 HG00597.hp1 HG01981.hp2 others(28): Show |
intron_variant | MODIFIER | c.97-4315A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56778131 | |||||||
chr3:56778206 | A | T | 110 | a0001c0002t0002g0052 a0001c0002t0002g0064 a0001c0002t0002g0129 others(107): Show |
112 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.97-4390T>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56778206 | |||||||
chr3:56778394 | T | C | 2 | a0001c0002t0002g0127 a0004c0011t0008g0073 |
2 | HG02486.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.97-4578A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56778394 | |||||||
chr3:56778422 | T | C | 177 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(174): Show |
181 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(178): Show |
intron_variant | MODIFIER | c.97-4606A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56778422 | |||||||
chr3:56778710 | A | T | 177 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(174): Show |
181 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(178): Show |
intron_variant | MODIFIER | c.97-4894T>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56778710 | |||||||
chr3:56778983 | T | C | 2 | a0001c0007t0001g0098 a0001c0007t0001g0164 |
2 | HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.97-5167A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56778983 | |||||||
chr3:56779029 | A | G | 1 | a0001c0002t0005g0250 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.97-5213T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56779029 | |||||||
chr3:56779115 | C | G | 2 | a0001c0003t0001g0091 a0001c0005t0001g0308 |
2 | HG01496.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.97-5299G>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56779115 | |||||||
chr3:56779142 | C | T | 2 | a0001c0002t0017g0161 a0002c0001t0001g0141 |
2 | HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.97-5326G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56779142 | |||||||
chr3:56779203 | T | G | 176 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(173): Show |
180 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(177): Show |
intron_variant | MODIFIER | c.97-5387A>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56779203 | |||||||
chr3:56779253 | A | AAT | 74 | a0001c0002t0002g0054 a0001c0002t0002g0083 a0001c0002t0002g0127 others(71): Show |
77 | HG00280.hp2 HG00323.hp2 HG00733.hp2 others(74): Show |
intron_variant | MODIFIER | c.97-5439_97-5438dup others(2): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56779253 | |||||||
chr3:56779294 | G | A | 1 | a0001c0007t0004g0111 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.97-5478C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56779294 | |||||||
chr3:56779372 | T | C | 1 | a0001c0007t0001g0074 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.97-5556A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56779372 | |||||||
chr3:56779482 | T | A | 1 | a0002c0001t0001g0075 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.97-5666A>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56779482 | |||||||
chr3:56779486 | A | AT | 11 | a0001c0003t0001g0016 a0001c0003t0001g0017 a0001c0003t0001g0018 others(8): Show |
11 | HG01109.hp1 HG01109.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.97-5671dupA | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56779486 | |||||||
chr3:56779495 | T | G | 267 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(264): Show |
274 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(271): Show |
intron_variant | MODIFIER | c.97-5679A>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56779495 | |||||||
chr3:56779528 | TG | T | 5 | a0001c0002t0002g0007 a0001c0002t0002g0021 a0001c0002t0002g0028 others(2): Show |
6 | HG02165.hp1 NA18950.hp1 NA18990.hp2 others(3): Show |
intron_variant | MODIFIER | c.97-5713delC | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56779528 | |||||||
chr3:56779544 | G | A | 12 | a0001c0003t0001g0016 a0001c0003t0001g0017 a0001c0003t0001g0018 others(9): Show |
12 | HG01109.hp1 HG01109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.97-5728C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56779544 | |||||||
chr3:56779555 | C | T | 5 | a0002c0001t0001g0003 a0002c0001t0001g0145 a0002c0001t0001g0155 others(2): Show |
7 | HG01167.hp2 HG01169.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.97-5739G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56779555 | |||||||
chr3:56779600 | G | C | 17 | a0001c0002t0002g0032 a0001c0002t0002g0110 a0001c0007t0004g0031 others(14): Show |
17 | HG01361.hp2 HG01928.hp1 HG01952.hp1 others(14): Show |
intron_variant | MODIFIER | c.97-5784C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56779600 | |||||||
chr3:56779719 | T | C | 2 | a0001c0002t0002g0217 a0001c0002t0002g0218 |
2 | NA19005.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.97-5903A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56779719 | |||||||
chr3:56779727 | G | T | 2 | a0001c0002t0017g0161 a0002c0001t0001g0141 |
2 | HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.97-5911C>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56779727 | |||||||
chr3:56780085 | G | A | 2 | a0001c0003t0001g0033 a0001c0003t0001g0041 |
2 | NA18963.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.97-6269C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56780085 | |||||||
chr3:56780129 | C | G | 110 | a0001c0002t0002g0052 a0001c0002t0002g0064 a0001c0002t0002g0129 others(107): Show |
112 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.97-6313G>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56780129 | |||||||
chr3:56780130 | A | G | 179 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(176): Show |
184 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.97-6314T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56780130 | |||||||
chr3:56780303 | T | G | 2 | a0002c0001t0003g0198 a0002c0001t0003g0199 |
2 | NA18995.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.97-6487A>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56780303 | |||||||
chr3:56780632 | T | TTGTC | 69 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(66): Show |
72 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.97-6820_97-6817dup others(4): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56780632 | |||||||
chr3:56780872 | C | T | 1 | a0001c0007t0001g0074 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.97-7056G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56780872 | |||||||
chr3:56781023 | G | C | 2 | a0001c0005t0001g0322 a0001c0005t0001g0323 |
2 | HG00140.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.97-7207C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56781023 | |||||||
chr3:56781243 | CT | C | 112 | a0001c0002t0002g0032 a0001c0002t0002g0054 a0001c0002t0002g0083 others(109): Show |
116 | HG00323.hp2 HG00733.hp2 HG01070.hp2 others(113): Show |
intron_variant | MODIFIER | c.97-7428delA | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56781243 | |||||||
chr3:56781305 | T | C | 1 | a0001c0002t0002g0066 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.97-7489A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56781305 | |||||||
chr3:56781385 | TACAGGAG others(3): Show |
T | 1 | a0002c0001t0003g0208 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.97-7579_97-7570del others(10): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56781385 | |||||||
chr3:56781445 | C | T | 3 | a0002c0001t0001g0133 a0002c0001t0001g0159 a0002c0001t0001g0160 |
3 | HG02559.hp2 HG02615.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.97-7629G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56781445 | |||||||
chr3:56781446 | C | CGA | 179 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(176): Show |
184 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.97-7631_97-7630ins others(2): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56781446 | |||||||
chr3:56781486 | T | G | 2 | a0002c0001t0001g0001 a0002c0001t0001g0200 |
3 | HG02451.hp2 HG03098.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.97-7670A>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56781486 | |||||||
chr3:56781592 | C | A | 272 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(269): Show |
279 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.97-7776G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56781592 | |||||||
chr3:56781747 | G | A | 6 | a0001c0002t0002g0054 a0002c0001t0001g0210 a0002c0001t0001g0211 others(3): Show |
6 | NA18942.hp1 NA18956.hp2 NA18969.hp1 others(3): Show |
intron_variant | MODIFIER | c.97-7931C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56781747 | |||||||
chr3:56781823 | A | G | 38 | a0001c0002t0002g0007 a0001c0002t0002g0021 a0001c0002t0002g0022 others(35): Show |
40 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.97-8007T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56781823 | |||||||
chr3:56781966 | C | T | 286 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(283): Show |
295 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.97-8150G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56781966 | |||||||
chr3:56782009 | T | C | 1 | a0002c0001t0003g0035 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.97-8193A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56782009 | |||||||
chr3:56782100 | T | C | 1 | a0002c0004t0003g0331 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.97-8284A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56782100 | |||||||
chr3:56782217 | C | G | 179 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(176): Show |
184 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.97-8401G>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56782217 | |||||||
chr3:56782468 | G | A | 1 | a0001c0007t0004g0122 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.97-8652C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56782468 | |||||||
chr3:56782548 | G | A | 93 | a0001c0002t0002g0032 a0001c0002t0002g0054 a0001c0002t0002g0083 others(90): Show |
95 | HG00323.hp2 HG00733.hp2 HG01070.hp2 others(92): Show |
intron_variant | MODIFIER | c.97-8732C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56782548 | |||||||
chr3:56782649 | T | TA | 28 | a0001c0002t0002g0005 a0001c0002t0002g0023 a0001c0002t0002g0026 others(25): Show |
29 | HG00621.hp1 HG00673.hp1 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.97-8834dupT | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56782649 | |||||||
chr3:56782649 | TA | T | 75 | a0001c0002t0002g0043 a0001c0002t0002g0064 a0001c0002t0002g0065 others(72): Show |
78 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.97-8834delT | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56782649 | |||||||
chr3:56782649 | TAA | T | 94 | a0001c0002t0002g0032 a0001c0002t0002g0054 a0001c0002t0002g0083 others(91): Show |
96 | HG00323.hp2 HG00733.hp2 HG01070.hp2 others(93): Show |
intron_variant | MODIFIER | c.97-8835_97-8834del others(2): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56782649 | |||||||
chr3:56782671 | G | GTTTGT | 179 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(176): Show |
184 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.97-8860_97-8856dup others(5): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56782671 | |||||||
chr3:56782709 | C | T | 9 | a0001c0007t0001g0101 a0002c0001t0001g0003 a0002c0001t0001g0075 others(6): Show |
11 | HG01167.hp2 HG01169.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.97-8893G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56782709 | |||||||
chr3:56782814 | C | A | 91 | a0001c0002t0002g0129 a0001c0002t0002g0130 a0001c0002t0002g0131 others(88): Show |
93 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.97-8998G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56782814 | |||||||
chr3:56783126 | C | T | 1 | a0002c0001t0009g0012 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.97-9310G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56783126 | |||||||
chr3:56783368 | G | A | 1 | a0001c0007t0001g0101 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.97-9552C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56783368 | |||||||
chr3:56783400 | G | A | 32 | a0001c0002t0002g0007 a0001c0002t0002g0021 a0001c0002t0002g0025 others(29): Show |
33 | HG00544.hp2 HG00597.hp1 HG01981.hp2 others(30): Show |
intron_variant | MODIFIER | c.97-9584C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56783400 | |||||||
chr3:56783776 | C | T | 1 | a0001c0007t0001g0101 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.97-9960G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56783776 | |||||||
chr3:56783996 | A | G | 1 | a0001c0007t0004g0123 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.97-10180T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56783996 | |||||||
chr3:56784114 | C | T | 1 | a0002c0001t0001g0003 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.97-10298G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56784114 | |||||||
chr3:56784128 | G | C | 2 | a0002c0001t0001g0155 a0002c0001t0001g0156 |
2 | HG02572.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.97-10312C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56784128 | |||||||
chr3:56784216 | G | A | 2 | a0001c0002t0002g0127 a0004c0011t0008g0073 |
2 | HG02486.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.97-10400C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56784216 | |||||||
chr3:56784321 | G | A | 5 | a0001c0003t0001g0016 a0001c0003t0001g0017 a0001c0003t0001g0018 others(2): Show |
5 | HG01109.hp2 HG02145.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.97-10505C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56784321 | |||||||
chr3:56784356 | G | A | 1 | a0001c0007t0004g0126 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.97-10540C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56784356 | |||||||
chr3:56784625 | G | C | 1 | a0001c0002t0002g0138 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.97-10809C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56784625 | |||||||
chr3:56784767 | G | C | 3 | a0001c0002t0002g0129 a0001c0002t0002g0130 a0001c0002t0002g0131 |
3 | HG02080.hp1 HG02135.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.97-10951C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56784767 | |||||||
chr3:56784801 | T | C | 2 | a0001c0002t0002g0139 a0002c0001t0001g0136 |
2 | HG02109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.97-10985A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56784801 | |||||||
chr3:56785107 | A | T | 17 | a0001c0002t0002g0032 a0001c0002t0002g0110 a0001c0007t0004g0031 others(14): Show |
17 | HG01361.hp2 HG01928.hp1 HG01952.hp1 others(14): Show |
intron_variant | MODIFIER | c.97-11291T>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56785107 | |||||||
chr3:56785246 | G | C | 1 | a0004c0011t0008g0073 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.97-11430C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56785246 | |||||||
chr3:56785303 | T | C | 1 | a0001c0007t0001g0074 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.97-11487A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56785303 | |||||||
chr3:56785349 | T | C | 5 | a0001c0003t0001g0016 a0001c0003t0001g0017 a0001c0003t0001g0018 others(2): Show |
5 | HG01109.hp2 HG02145.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.97-11533A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56785349 | |||||||
chr3:56785412 | C | T | 17 | a0001c0002t0002g0032 a0001c0002t0002g0110 a0001c0007t0004g0031 others(14): Show |
17 | HG01361.hp2 HG01928.hp1 HG01952.hp1 others(14): Show |
intron_variant | MODIFIER | c.97-11596G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56785412 | |||||||
chr3:56785436 | C | T | 1 | a0001c0005t0001g0271 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.97-11620G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56785436 | |||||||
chr3:56785668 | T | G | 122 | a0001c0002t0002g0005 a0001c0002t0002g0022 a0001c0002t0002g0023 others(119): Show |
125 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.97-11852A>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56785668 | |||||||
chr3:56785715 | G | A | 9 | a0001c0007t0001g0101 a0002c0001t0001g0003 a0002c0001t0001g0075 others(6): Show |
11 | HG01167.hp2 HG01169.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.97-11899C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56785715 | |||||||
chr3:56785839 | G | A | 1 | a0001c0002t0002g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.97-12023C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56785839 | |||||||
chr3:56786097 | C | A | 1 | a0002c0001t0001g0075 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.97-12281G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56786097 | |||||||
chr3:56786164 | A | G | 121 | a0001c0002t0002g0005 a0001c0002t0002g0022 a0001c0002t0002g0023 others(118): Show |
124 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.97-12348T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56786164 | |||||||
chr3:56786290 | C | G | 92 | a0001c0002t0002g0032 a0001c0002t0002g0054 a0001c0002t0002g0083 others(89): Show |
94 | HG00323.hp2 HG00733.hp2 HG01070.hp2 others(91): Show |
intron_variant | MODIFIER | c.97-12474G>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56786290 | |||||||
chr3:56786328 | A | T | 73 | a0001c0002t0002g0054 a0001c0002t0002g0083 a0001c0002t0002g0127 others(70): Show |
75 | HG00323.hp2 HG00733.hp2 HG01070.hp2 others(72): Show |
intron_variant | MODIFIER | c.97-12512T>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56786328 | |||||||
chr3:56786805 | C | T | 94 | a0001c0002t0002g0022 a0001c0002t0002g0129 a0001c0002t0002g0130 others(91): Show |
96 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.97-12989G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56786805 | |||||||
chr3:56786834 | G | A | 1 | a0001c0007t0001g0101 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.97-13018C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56786834 | |||||||
chr3:56786903 | T | TA | 91 | a0001c0002t0002g0022 a0001c0002t0002g0130 a0001c0002t0002g0131 others(88): Show |
93 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.97-13088dupT | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56786903 | |||||||
chr3:56787072 | A | G | 1 | a0002c0001t0003g0089 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.97-13256T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56787072 | |||||||
chr3:56787080 | C | T | 2 | a0002c0001t0003g0116 a0002c0004t0003g0330 |
2 | HG01928.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.97-13264G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56787080 | |||||||
chr3:56787084 | T | C | 2 | a0002c0001t0001g0085 a0002c0001t0001g0152 |
2 | HG02896.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.97-13268A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56787084 | |||||||
chr3:56787290 | T | C | 94 | a0001c0002t0002g0022 a0001c0002t0002g0129 a0001c0002t0002g0130 others(91): Show |
96 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.97-13474A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56787290 | |||||||
chr3:56787327 | A | G | 1 | a0002c0001t0001g0143 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.97-13511T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56787327 | |||||||
chr3:56787349 | C | A | 3 | a0001c0002t0002g0077 a0001c0002t0002g0086 a0001c0002t0002g0087 |
3 | HG01099.hp1 HG02886.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.97-13533G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56787349 | |||||||
chr3:56787372 | C | T | 7 | a0001c0002t0002g0127 a0001c0002t0008g0135 a0001c0002t0010g0014 others(4): Show |
8 | HG01884.hp1 HG02258.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.97-13556G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56787372 | |||||||
chr3:56787374 | T | C | 80 | a0001c0002t0002g0054 a0001c0002t0002g0083 a0001c0002t0017g0161 others(77): Show |
82 | HG00280.hp2 HG00323.hp2 HG00733.hp2 others(79): Show |
intron_variant | MODIFIER | c.97-13558A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56787374 | |||||||
chr3:56787497 | T | C | 298 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(295): Show |
307 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(304): Show |
intron_variant | MODIFIER | c.97-13681A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56787497 | |||||||
chr3:56787498 | G | A | 286 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(283): Show |
295 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.97-13682C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56787498 | |||||||
chr3:56787516 | A | C | 286 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(283): Show |
295 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.97-13700T>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56787516 | |||||||
chr3:56787685 | G | C | 94 | a0001c0002t0002g0022 a0001c0002t0002g0129 a0001c0002t0002g0130 others(91): Show |
96 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.97-13869C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56787685 | |||||||
chr3:56787718 | G | GATAATA | 4 | a0001c0002t0002g0157 a0001c0002t0017g0161 a0001c0007t0001g0101 others(1): Show |
4 | HG03098.hp1 HG03540.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.97-13908_97-13903d others(8): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56787718 | |||||||
chr3:56787718 | G | GATAATAA others(5): Show |
33 | a0001c0002t0002g0083 a0001c0003t0001g0016 a0001c0003t0001g0017 others(30): Show |
33 | HG01109.hp1 HG01109.hp2 HG02109.hp1 others(30): Show |
intron_variant | MODIFIER | c.97-13914_97-13903d others(14): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56787718 | |||||||
chr3:56787718 | G | GATAATAA others(8): Show |
38 | a0001c0002t0002g0054 a0001c0003t0001g0251 a0001c0006t0002g0280 others(35): Show |
39 | HG00323.hp2 HG00733.hp2 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.97-13917_97-13903d others(17): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56787718 | |||||||
chr3:56787718 | G | GATAATAA others(11): Show |
1 | a0001c0006t0002g0281 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.97-13920_97-13903d others(20): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56787718 | |||||||
chr3:56787718 | G | GATAATAA others(14): Show |
1 | a0002c0001t0001g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.97-13903_97-13902i others(23): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56787718 | |||||||
chr3:56787864 | A | G | 94 | a0001c0002t0002g0022 a0001c0002t0002g0129 a0001c0002t0002g0130 others(91): Show |
96 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.96+13839T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56787864 | |||||||
chr3:56788154 | T | C | 129 | a0001c0002t0002g0005 a0001c0002t0002g0022 a0001c0002t0002g0023 others(126): Show |
134 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(131): Show |
intron_variant | MODIFIER | c.96+13549A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56788154 | |||||||
chr3:56788213 | C | T | 1 | a0001c0006t0002g0341 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.96+13490G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56788213 | |||||||
chr3:56788229 | G | A | 26 | a0001c0002t0002g0007 a0001c0002t0002g0021 a0001c0002t0002g0025 others(23): Show |
27 | HG00544.hp2 HG00597.hp1 HG01981.hp2 others(24): Show |
intron_variant | MODIFIER | c.96+13474C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56788229 | |||||||
chr3:56788289 | A | G | 6 | a0001c0003t0001g0148 a0001c0003t0001g0149 a0001c0005t0001g0322 others(3): Show |
6 | HG00140.hp2 HG01256.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.96+13414T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56788289 | |||||||
chr3:56788349 | T | C | 92 | a0001c0002t0002g0022 a0001c0002t0002g0129 a0001c0002t0002g0130 others(89): Show |
94 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.96+13354A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56788349 | |||||||
chr3:56788463 | A | G | 1 | a0001c0007t0004g0112 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.96+13240T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56788463 | |||||||
chr3:56788499 | A | G | 1 | a0002c0001t0001g0229 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.96+13204T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56788499 | |||||||
chr3:56788500 | G | A | 1 | a0002c0001t0001g0229 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.96+13203C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56788500 | |||||||
chr3:56788597 | A | G | 4 | a0001c0002t0002g0077 a0001c0002t0002g0086 a0001c0002t0002g0087 others(1): Show |
4 | HG01099.hp1 HG02886.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.96+13106T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56788597 | |||||||
chr3:56788697 | T | G | 1 | a0001c0003t0001g0184 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.96+13006A>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56788697 | |||||||
chr3:56788873 | G | C | 1 | a0001c0007t0001g0162 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.96+12830C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56788873 | |||||||
chr3:56788964 | C | T | 7 | a0001c0002t0002g0127 a0001c0002t0008g0135 a0001c0002t0010g0014 others(4): Show |
8 | HG01884.hp1 HG02258.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.96+12739G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56788964 | |||||||
chr3:56789020 | A | ATGC | 34 | a0001c0002t0002g0127 a0001c0002t0002g0157 a0001c0002t0002g0207 others(31): Show |
34 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.96+12680_96+12682d others(5): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56789020 | |||||||
chr3:56789020 | A | ATGCTGC | 41 | a0001c0002t0002g0110 a0001c0002t0002g0125 a0001c0002t0002g0129 others(38): Show |
43 | HG00544.hp1 HG00733.hp2 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.96+12677_96+12682d others(8): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56789020 | |||||||
chr3:56789020 | A | ATGCTGCT others(2): Show |
9 | a0001c0002t0002g0032 a0001c0002t0002g0124 a0001c0002t0002g0130 others(6): Show |
9 | HG02074.hp2 HG02135.hp1 HG02293.hp2 others(6): Show |
intron_variant | MODIFIER | c.96+12674_96+12682d others(11): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56789020 | |||||||
chr3:56789020 | A | ATGCTGCT others(17): Show |
1 | a0001c0003t0001g0149 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.96+12659_96+12682d others(26): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56789020 | |||||||
chr3:56789020 | ATGC | A | 44 | a0001c0002t0002g0005 a0001c0002t0002g0023 a0001c0002t0002g0026 others(41): Show |
47 | HG00621.hp1 HG00673.hp1 HG01099.hp1 others(44): Show |
intron_variant | MODIFIER | c.96+12680_96+12682d others(5): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56789020 | |||||||
chr3:56789020 | ATGCTGC | A | 12 | a0001c0002t0002g0040 a0001c0002t0002g0066 a0001c0002t0002g0078 others(9): Show |
12 | HG02055.hp1 HG02155.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.96+12677_96+12682d others(8): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56789020 | |||||||
chr3:56789020 | ATGCTGCT others(2): Show |
A | 46 | a0001c0002t0002g0007 a0001c0002t0002g0021 a0001c0002t0002g0025 others(43): Show |
47 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.96+12674_96+12682d others(11): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56789020 | |||||||
chr3:56789020 | ATGCTGCT others(5): Show |
A | 1 | a0002c0001t0001g0062 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.96+12671_96+12682d others(14): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56789020 | |||||||
chr3:56789020 | ATGCTGCT others(8): Show |
A | 2 | a0001c0003t0001g0104 a0001c0005t0001g0299 |
2 | HG00642.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.96+12668_96+12682d others(17): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56789020 | |||||||
chr3:56789020 | ATGCTGCT others(11): Show |
A | 5 | a0001c0002t0008g0135 a0001c0002t0010g0014 a0002c0001t0001g0001 others(2): Show |
6 | HG01884.hp1 HG02258.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.96+12665_96+12682d others(20): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56789020 | |||||||
chr3:56789020 | ATGCTGCT others(14): Show |
A | 1 | a0001c0005t0001g0265 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.96+12662_96+12682d others(23): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56789020 | |||||||
chr3:56789020 | ATGCTGCT others(17): Show |
A | 5 | a0001c0003t0001g0016 a0001c0003t0001g0017 a0001c0003t0001g0018 others(2): Show |
5 | HG01109.hp2 HG02145.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.96+12659_96+12682d others(26): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56789020 | |||||||
chr3:56789083 | G | A | 1 | a0001c0003t0001g0149 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.96+12620C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56789083 | |||||||
chr3:56789224 | C | T | 1 | a0001c0003t0001g0259 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.96+12479G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56789224 | |||||||
chr3:56789338 | A | G | 286 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(283): Show |
295 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.96+12365T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56789338 | |||||||
chr3:56789395 | C | T | 2 | a0002c0001t0001g0001 a0002c0001t0001g0200 |
3 | HG02451.hp2 HG03098.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.96+12308G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56789395 | |||||||
chr3:56789618 | A | G | 1 | a0001c0003t0001g0246 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.96+12085T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56789618 | |||||||
chr3:56789619 | G | C | 1 | a0001c0003t0001g0246 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.96+12084C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56789619 | |||||||
chr3:56789754 | G | A | 3 | a0002c0004t0003g0300 a0002c0004t0003g0301 a0002c0004t0003g0302 |
3 | HG00140.hp1 HG01934.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.96+11949C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56789754 | |||||||
chr3:56789910 | G | C | 1 | a0002c0001t0001g0264 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.96+11793C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56789910 | |||||||
chr3:56789978 | G | A | 2 | a0001c0002t0002g0139 a0002c0001t0001g0136 |
2 | HG02109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.96+11725C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56789978 | |||||||
chr3:56790173 | C | T | 1 | a0001c0002t0002g0242 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.96+11530G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56790173 | |||||||
chr3:56790174 | G | A | 1 | a0002c0001t0001g0097 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.96+11529C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56790174 | |||||||
chr3:56790317 | T | A | 7 | a0001c0002t0002g0127 a0001c0002t0008g0135 a0001c0002t0010g0014 others(4): Show |
8 | HG01884.hp1 HG02258.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.96+11386A>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56790317 | |||||||
chr3:56790471 | C | T | 1 | a0001c0002t0002g0069 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.96+11232G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56790471 | |||||||
chr3:56790534 | C | T | 19 | a0001c0002t0002g0032 a0001c0002t0002g0110 a0001c0002t0002g0124 others(16): Show |
19 | HG01361.hp2 HG01928.hp1 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.96+11169G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56790534 | |||||||
chr3:56790594 | T | C | 1 | a0002c0001t0001g0055 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.96+11109A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56790594 | |||||||
chr3:56790655 | G | T | 2 | a0002c0001t0003g0002 a0002c0001t0003g0035 |
3 | NA18960.hp2 NA18990.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.96+11048C>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56790655 | |||||||
chr3:56790773 | G | A | 3 | a0001c0002t0002g0077 a0001c0002t0002g0086 a0001c0002t0002g0087 |
3 | HG01099.hp1 HG02886.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.96+10930C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56790773 | |||||||
chr3:56790798 | T | C | 4 | a0002c0001t0003g0080 a0002c0001t0003g0082 a0002c0001t0003g0089 others(1): Show |
4 | HG02258.hp1 HG02486.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.96+10905A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56790798 | |||||||
chr3:56791062 | C | T | 2 | a0001c0007t0001g0076 a0001c0007t0001g0093 |
2 | HG02280.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.96+10641G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56791062 | |||||||
chr3:56791142 | C | T | 36 | a0001c0002t0002g0007 a0001c0002t0002g0021 a0001c0002t0002g0025 others(33): Show |
37 | HG00544.hp2 HG00597.hp1 HG01981.hp2 others(34): Show |
intron_variant | MODIFIER | c.96+10561G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56791142 | |||||||
chr3:56791459 | A | G | 3 | a0002c0001t0003g0024 a0002c0001t0003g0044 a0002c0001t0003g0045 |
3 | HG00544.hp1 NA18967.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.96+10244T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56791459 | |||||||
chr3:56791518 | C | T | 2 | a0001c0007t0001g0076 a0001c0007t0001g0093 |
2 | HG02280.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.96+10185G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56791518 | |||||||
chr3:56791542 | A | C | 1 | a0001c0002t0010g0014 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.96+10161T>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56791542 | |||||||
chr3:56791866 | TA | T | 294 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(291): Show |
303 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(300): Show |
intron_variant | MODIFIER | c.96+9836delT | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56791866 | |||||||
chr3:56791927 | G | T | 2 | a0001c0002t0002g0083 a0002c0001t0001g0084 |
2 | HG02280.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.96+9776C>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56791927 | |||||||
chr3:56791969 | G | A | 2 | a0001c0002t0005g0142 a0001c0002t0005g0250 |
2 | HG02055.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.96+9734C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56791969 | |||||||
chr3:56791969 | G | C | 96 | a0001c0002t0002g0052 a0001c0002t0002g0129 a0001c0002t0002g0130 others(93): Show |
98 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.96+9734C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56791969 | |||||||
chr3:56791976 | C | T | 1 | a0001c0002t0002g0086 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.96+9727G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56791976 | |||||||
chr3:56792093 | G | A | 1 | a0002c0001t0001g0097 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.96+9610C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56792093 | |||||||
chr3:56792103 | C | CA | 38 | a0001c0002t0002g0007 a0001c0002t0002g0021 a0001c0002t0002g0022 others(35): Show |
39 | HG00544.hp2 HG00597.hp1 HG01099.hp1 others(36): Show |
intron_variant | MODIFIER | c.96+9599dupT | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56792103 | |||||||
chr3:56792103 | C | CAAAAAA | 86 | a0001c0002t0002g0052 a0001c0002t0002g0129 a0001c0002t0002g0130 others(83): Show |
88 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.96+9594_96+9599dup others(6): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56792103 | |||||||
chr3:56792113 | A | AAAAAAAA others(4): Show |
1 | a0001c0006t0002g0326 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.96+9589_96+9590ins others(11): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56792113 | |||||||
chr3:56792113 | A | AAAAAAAA others(3): Show |
3 | a0001c0002t0002g0056 a0001c0002t0002g0187 a0001c0006t0002g0325 |
3 | HG02080.hp2 HG03239.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.96+9589_96+9590ins others(10): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56792113 | |||||||
chr3:56792113 | A | AAAAAAAA others(8): Show |
1 | a0002c0001t0016g0146 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.96+9589_96+9590ins others(15): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56792113 | |||||||
chr3:56792113 | A | AAAAAAAA others(13): Show |
6 | a0002c0001t0001g0003 a0002c0001t0001g0145 a0002c0001t0001g0147 others(3): Show |
8 | HG01167.hp2 HG01169.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.96+9589_96+9590ins others(20): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56792113 | |||||||
chr3:56792113 | A | AAAAAAG | 6 | a0001c0002t0002g0038 a0001c0002t0002g0078 a0001c0002t0002g0079 others(3): Show |
6 | HG02723.hp1 HG03540.hp1 NA18522.hp2 others(3): Show |
intron_variant | MODIFIER | c.96+9589_96+9590ins others(6): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56792113 | |||||||
chr3:56792113 | AAAAAG | A | 20 | a0001c0002t0002g0032 a0001c0002t0002g0110 a0001c0002t0002g0124 others(17): Show |
20 | HG01361.hp2 HG01928.hp1 HG01952.hp1 others(17): Show |
intron_variant | MODIFIER | c.96+9585_96+9589del others(5): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56792113 | |||||||
chr3:56792113 | AAAAAGAA others(3): Show |
A | 2 | a0001c0007t0001g0098 a0001c0007t0001g0164 |
2 | HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.96+9580_96+9589del others(10): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56792113 | |||||||
chr3:56792118 | G | A | 22 | a0001c0002t0002g0005 a0001c0002t0002g0023 a0001c0002t0002g0026 others(19): Show |
23 | HG00621.hp1 HG00673.hp1 HG02027.hp1 others(20): Show |
intron_variant | MODIFIER | c.96+9585C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56792118 | |||||||
chr3:56792123 | G | A | 1 | a0002c0001t0003g0224 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.96+9580C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56792123 | |||||||
chr3:56792125 | A | T | 1 | a0001c0005t0001g0310 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.96+9578T>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56792125 | |||||||
chr3:56792138 | GAAAAGAA others(3): Show |
G | 7 | a0001c0002t0017g0161 a0001c0007t0001g0101 a0002c0001t0001g0019 others(4): Show |
7 | HG02630.hp2 HG02723.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.96+9555_96+9564del others(10): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56792138 | |||||||
chr3:56792143 | GAAAAT | G | 80 | a0001c0002t0002g0054 a0001c0002t0002g0083 a0001c0002t0002g0138 others(77): Show |
82 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.96+9555_96+9559del others(5): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56792143 | |||||||
chr3:56792148 | T | G | 8 | a0001c0003t0001g0016 a0001c0003t0001g0017 a0001c0003t0001g0018 others(5): Show |
8 | HG01109.hp2 HG01884.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.96+9555A>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56792148 | |||||||
chr3:56792201 | A | T | 1 | a0002c0001t0001g0185 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.96+9502T>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56792201 | |||||||
chr3:56792296 | A | C | 128 | a0001c0002t0002g0005 a0001c0002t0002g0023 a0001c0002t0002g0026 others(125): Show |
133 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(130): Show |
intron_variant | MODIFIER | c.96+9407T>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56792296 | |||||||
chr3:56792665 | G | A | 93 | a0001c0002t0002g0054 a0001c0002t0002g0083 a0001c0002t0002g0138 others(90): Show |
95 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.96+9038C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56792665 | |||||||
chr3:56792737 | T | A | 128 | a0001c0002t0002g0005 a0001c0002t0002g0023 a0001c0002t0002g0026 others(125): Show |
133 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(130): Show |
intron_variant | MODIFIER | c.96+8966A>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56792737 | |||||||
chr3:56792763 | T | C | 92 | a0001c0002t0002g0052 a0001c0002t0002g0129 a0001c0002t0002g0130 others(89): Show |
94 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.96+8940A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56792763 | |||||||
chr3:56792819 | A | AT | 95 | a0001c0002t0002g0054 a0001c0002t0002g0083 a0001c0002t0002g0138 others(92): Show |
97 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.96+8883dupA | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56792819 | |||||||
chr3:56792820 | T | A | 128 | a0001c0002t0002g0005 a0001c0002t0002g0023 a0001c0002t0002g0026 others(125): Show |
133 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(130): Show |
intron_variant | MODIFIER | c.96+8883A>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56792820 | |||||||
chr3:56792933 | A | G | 1 | a0002c0004t0003g0335 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.96+8770T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56792933 | |||||||
chr3:56792997 | T | TG | 104 | a0001c0002t0002g0007 a0001c0002t0002g0021 a0001c0002t0002g0022 others(101): Show |
107 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.96+8705_96+8706ins others(1): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56792997 | |||||||
chr3:56792998 | T | G | 181 | a0001c0002t0002g0005 a0001c0002t0002g0023 a0001c0002t0002g0026 others(178): Show |
187 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(184): Show |
intron_variant | MODIFIER | c.96+8705A>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56792998 | |||||||
chr3:56793003 | T | A | 1 | a0001c0006t0002g0333 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.96+8700A>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56793003 | |||||||
chr3:56793008 | A | T | 1 | a0002c0001t0003g0163 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.96+8695T>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56793008 | |||||||
chr3:56793170 | A | AT | 6 | a0001c0002t0002g0069 a0001c0007t0004g0111 a0002c0001t0001g0205 others(3): Show |
6 | HG03017.hp1 HG04204.hp2 NA19000.hp1 others(3): Show |
intron_variant | MODIFIER | c.96+8532dupA | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56793170 | |||||||
chr3:56793170 | A | ATT | 34 | a0001c0002t0002g0007 a0001c0002t0002g0021 a0001c0002t0002g0022 others(31): Show |
35 | HG00544.hp2 HG00597.hp1 HG01981.hp2 others(32): Show |
intron_variant | MODIFIER | c.96+8531_96+8532dup others(2): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56793170 | |||||||
chr3:56793170 | AT | A | 135 | a0001c0002t0002g0005 a0001c0002t0002g0023 a0001c0002t0002g0026 others(132): Show |
140 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(137): Show |
intron_variant | MODIFIER | c.96+8532delA | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56793170 | |||||||
chr3:56793344 | T | A | 1 | a0001c0007t0004g0122 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.96+8359A>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56793344 | |||||||
chr3:56793411 | C | T | 36 | a0001c0002t0002g0007 a0001c0002t0002g0021 a0001c0002t0002g0025 others(33): Show |
37 | HG00544.hp2 HG00597.hp1 HG01981.hp2 others(34): Show |
intron_variant | MODIFIER | c.96+8292G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56793411 | |||||||
chr3:56793416 | G | A | 1 | a0002c0004t0001g0332 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.96+8287C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56793416 | |||||||
chr3:56793424 | T | C | 292 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(289): Show |
301 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(298): Show |
intron_variant | MODIFIER | c.96+8279A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56793424 | |||||||
chr3:56793484 | G | T | 2 | a0001c0002t0002g0127 a0004c0011t0008g0073 |
2 | HG02486.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.96+8219C>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56793484 | |||||||
chr3:56793510 | C | T | 5 | a0001c0002t0002g0078 a0001c0002t0002g0079 a0001c0002t0006g0011 others(2): Show |
5 | HG02723.hp1 HG03540.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.96+8193G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56793510 | |||||||
chr3:56793545 | C | T | 1 | a0002c0001t0001g0136 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.96+8158G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56793545 | |||||||
chr3:56793566 | G | A | 4 | a0001c0003t0001g0148 a0001c0003t0001g0149 a0001c0005t0001g0322 others(1): Show |
4 | HG00140.hp2 HG01256.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+8137C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56793566 | |||||||
chr3:56793610 | A | G | 4 | a0001c0003t0001g0244 a0001c0007t0001g0102 a0001c0013t0001g0140 others(1): Show |
4 | HG02630.hp1 HG02630.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.96+8093T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56793610 | |||||||
chr3:56793611 | T | A | 37 | a0001c0002t0002g0007 a0001c0002t0002g0021 a0001c0002t0002g0022 others(34): Show |
38 | HG00544.hp2 HG00597.hp1 HG01981.hp2 others(35): Show |
intron_variant | MODIFIER | c.96+8092A>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56793611 | |||||||
chr3:56793633 | A | G | 34 | a0001c0002t0002g0005 a0001c0002t0002g0023 a0001c0002t0002g0026 others(31): Show |
37 | HG00597.hp2 HG00621.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.96+8070T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56793633 | |||||||
chr3:56793739 | C | A | 1 | a0001c0003t0001g0018 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.96+7964G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56793739 | |||||||
chr3:56793919 | C | A | 2 | a0002c0004t0003g0305 a0002c0004t0003g0306 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.96+7784G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56793919 | |||||||
chr3:56794126 | A | G | 1 | a0001c0002t0008g0135 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.96+7577T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56794126 | |||||||
chr3:56794285 | C | T | 53 | a0001c0002t0002g0005 a0001c0002t0002g0023 a0001c0002t0002g0026 others(50): Show |
56 | HG00597.hp2 HG00621.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.96+7418G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56794285 | |||||||
chr3:56794290 | C | G | 1 | a0001c0007t0001g0164 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.96+7413G>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56794290 | |||||||
chr3:56794389 | C | G | 289 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(286): Show |
298 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(295): Show |
intron_variant | MODIFIER | c.96+7314G>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56794389 | |||||||
chr3:56794396 | G | A | 88 | a0001c0002t0002g0054 a0001c0002t0002g0083 a0001c0002t0002g0138 others(85): Show |
88 | HG00140.hp2 HG00323.hp2 HG01109.hp1 others(85): Show |
intron_variant | MODIFIER | c.96+7307C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56794396 | |||||||
chr3:56794446 | C | T | 2 | a0002c0001t0001g0205 a0002c0001t0001g0206 |
2 | NA18977.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.96+7257G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56794446 | |||||||
chr3:56794475 | C | T | 58 | a0001c0002t0002g0054 a0001c0002t0002g0083 a0001c0003t0001g0241 others(55): Show |
58 | HG00323.hp2 HG01109.hp1 HG01123.hp1 others(55): Show |
intron_variant | MODIFIER | c.96+7228G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56794475 | |||||||
chr3:56794488 | C | CA | 7 | a0001c0002t0002g0077 a0001c0002t0002g0086 a0001c0002t0002g0087 others(4): Show |
7 | HG01099.hp1 HG02886.hp1 NA19000.hp2 others(4): Show |
intron_variant | MODIFIER | c.96+7214dupT | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56794488 | |||||||
chr3:56794488 | C | CAAAAAAA others(1): Show |
10 | a0001c0002t0002g0110 a0001c0007t0004g0031 a0001c0007t0004g0111 others(7): Show |
10 | HG01928.hp1 HG02293.hp1 HG02293.hp2 others(7): Show |
intron_variant | MODIFIER | c.96+7207_96+7214dup others(8): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56794488 | |||||||
chr3:56794488 | C | CAAAAAAA others(2): Show |
6 | a0001c0002t0002g0032 a0001c0002t0010g0014 a0001c0007t0004g0112 others(3): Show |
6 | HG01361.hp2 HG01952.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.96+7206_96+7214dup others(9): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56794488 | |||||||
chr3:56794488 | C | CAAAAAAA others(3): Show |
1 | a0001c0007t0004g0123 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.96+7205_96+7214dup others(10): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56794488 | |||||||
chr3:56794488 | C | CAAAAAAA others(4): Show |
3 | a0001c0002t0002g0124 a0001c0002t0002g0125 a0001c0007t0001g0074 |
3 | HG02074.hp2 HG02083.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.96+7204_96+7214dup others(11): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56794488 | |||||||
chr3:56794488 | C | CAAAAAAA others(5): Show |
1 | a0001c0002t0008g0135 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.96+7203_96+7214dup others(12): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56794488 | |||||||
chr3:56794488 | C | CAAAAAAA others(29): Show |
1 | a0002c0001t0001g0001 | 2 | HG02451.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.96+7214_96+7215ins others(36): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56794488 | |||||||
chr3:56794488 | C | CAAAAAAA others(32): Show |
1 | a0002c0001t0001g0200 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.96+7214_96+7215ins others(39): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56794488 | |||||||
chr3:56794488 | CAAAAA | C | 22 | a0001c0002t0002g0127 a0001c0002t0002g0138 a0001c0003t0001g0148 others(19): Show |
22 | HG00140.hp2 HG01256.hp2 HG01516.hp1 others(19): Show |
intron_variant | MODIFIER | c.96+7210_96+7214del others(5): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56794488 | |||||||
chr3:56794488 | CAAAAAAA | C | 111 | a0001c0002t0002g0007 a0001c0002t0002g0021 a0001c0002t0002g0022 others(108): Show |
114 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.96+7208_96+7214del others(7): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56794488 | |||||||
chr3:56794488 | CAAAAAAA others(1): Show |
C | 38 | a0001c0002t0002g0005 a0001c0002t0002g0023 a0001c0002t0002g0026 others(35): Show |
41 | HG00597.hp2 HG00621.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.96+7207_96+7214del others(8): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56794488 | |||||||
chr3:56794488 | CAAAAAAA others(2): Show |
C | 94 | a0001c0002t0002g0052 a0001c0002t0002g0129 a0001c0002t0002g0130 others(91): Show |
96 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.96+7206_96+7214del others(9): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56794488 | |||||||
chr3:56794553 | A | G | 1 | a0002c0001t0003g0080 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.96+7150T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56794553 | |||||||
chr3:56794781 | C | T | 1 | a0001c0002t0002g0023 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.96+6922G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56794781 | |||||||
chr3:56794782 | G | A | 90 | a0001c0002t0002g0052 a0001c0002t0002g0129 a0001c0002t0002g0130 others(87): Show |
92 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.96+6921C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56794782 | |||||||
chr3:56794909 | G | C | 98 | a0001c0002t0002g0052 a0001c0002t0002g0129 a0001c0002t0002g0130 others(95): Show |
100 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.96+6794C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56794909 | |||||||
chr3:56794923 | A | G | 3 | a0002c0001t0003g0002 a0002c0001t0003g0035 a0002c0001t0003g0036 |
4 | NA18960.hp2 NA18972.hp2 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+6780T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56794923 | |||||||
chr3:56794970 | C | T | 1 | a0001c0002t0002g0063 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.96+6733G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56794970 | |||||||
chr3:56795033 | A | AT | 277 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(274): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.96+6669dupA | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795033 | |||||||
chr3:56795033 | A | ATT | 29 | a0001c0002t0002g0032 a0001c0002t0002g0034 a0001c0002t0002g0110 others(26): Show |
29 | HG01109.hp1 HG01361.hp2 HG01928.hp1 others(26): Show |
intron_variant | MODIFIER | c.96+6668_96+6669dup others(2): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795033 | |||||||
chr3:56795066 | T | G | 19 | a0001c0002t0002g0032 a0001c0002t0002g0110 a0001c0002t0002g0124 others(16): Show |
19 | HG01361.hp2 HG01928.hp1 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.96+6637A>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795066 | |||||||
chr3:56795095 | G | A | 61 | a0001c0002t0002g0054 a0001c0002t0002g0083 a0001c0002t0002g0086 others(58): Show |
61 | HG00323.hp2 HG01099.hp1 HG01109.hp1 others(58): Show |
intron_variant | MODIFIER | c.96+6608C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795095 | |||||||
chr3:56795224 | T | C | 1 | a0001c0002t0002g0056 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.96+6479A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795224 | |||||||
chr3:56795401 | C | T | 2 | a0001c0003t0001g0100 a0001c0003t0001g0255 |
2 | HG01884.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.96+6302G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795401 | |||||||
chr3:56795580 | A | G | 1 | a0001c0003t0001g0251 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.96+6123T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795580 | |||||||
chr3:56795585 | G | A | 18 | a0001c0002t0002g0022 a0001c0002t0002g0028 a0001c0002t0002g0057 others(15): Show |
18 | HG00544.hp2 HG00558.hp2 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.96+6118C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795585 | |||||||
chr3:56795633 | A | G | 239 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(236): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.96+6070T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795633 | |||||||
chr3:56795635 | T | C | 239 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(236): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.96+6068A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795635 | |||||||
chr3:56795655 | C | CTCTTTTT others(3): Show |
9 | a0001c0002t0002g0194 a0001c0002t0002g0195 a0001c0002t0005g0142 others(6): Show |
9 | HG00673.hp1 HG01169.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.96+6047_96+6048ins others(10): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795655 | |||||||
chr3:56795655 | C | CTCTTTTT others(4): Show |
86 | a0001c0002t0002g0005 a0001c0002t0002g0007 a0001c0002t0002g0021 others(83): Show |
90 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.96+6047_96+6048ins others(11): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795655 | |||||||
chr3:56795655 | C | CTCTTTTT others(5): Show |
19 | a0001c0002t0002g0023 a0001c0002t0002g0188 a0001c0005t0001g0265 others(16): Show |
20 | HG00597.hp2 HG00733.hp2 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.96+6047_96+6048ins others(12): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795655 | |||||||
chr3:56795655 | C | CTCTTTTT others(7): Show |
1 | a0001c0007t0001g0102 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.96+6047_96+6048ins others(14): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795655 | |||||||
chr3:56795655 | C | CTTTTTTT others(2): Show |
57 | a0001c0002t0002g0083 a0001c0002t0002g0086 a0001c0002t0002g0130 others(54): Show |
57 | HG00597.hp1 HG00642.hp1 HG01099.hp1 others(54): Show |
intron_variant | MODIFIER | c.96+6039_96+6047dup others(9): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795655 | |||||||
chr3:56795655 | C | CTTTTTTT others(3): Show |
3 | a0001c0002t0002g0129 a0002c0001t0001g0210 a0002c0001t0001g0211 |
3 | NA18956.hp2 NA19006.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.96+6038_96+6047dup others(10): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795655 | |||||||
chr3:56795655 | C | CTTTTTTT others(4): Show |
7 | a0001c0002t0002g0207 a0001c0003t0001g0092 a0001c0005t0001g0270 others(4): Show |
7 | HG01106.hp1 HG01256.hp1 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.96+6037_96+6047dup others(11): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795655 | |||||||
chr3:56795655 | C | CTTTTTTT others(5): Show |
11 | a0001c0002t0002g0025 a0001c0002t0002g0063 a0001c0002t0002g0066 others(8): Show |
11 | HG01981.hp2 HG02155.hp2 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.96+6036_96+6047dup others(12): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795655 | |||||||
chr3:56795655 | C | CTTTTTTT others(6): Show |
37 | a0001c0002t0002g0022 a0001c0002t0002g0028 a0001c0002t0002g0034 others(34): Show |
38 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.96+6047_96+6048ins others(13): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795655 | |||||||
chr3:56795655 | C | CTTTTTTT others(7): Show |
1 | a0001c0003t0001g0033 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.96+6047_96+6048ins others(14): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795655 | |||||||
chr3:56795655 | CT | C | 18 | a0001c0002t0002g0032 a0001c0002t0002g0124 a0001c0002t0002g0125 others(15): Show |
18 | HG01952.hp1 HG02074.hp2 HG02083.hp2 others(15): Show |
intron_variant | MODIFIER | c.96+6047delA | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795655 | |||||||
chr3:56795668 | G | T | 2 | a0001c0002t0002g0029 a0001c0002t0002g0069 |
2 | HG02735.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.96+6035C>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795668 | |||||||
chr3:56795707 | G | A | 2 | a0001c0002t0002g0196 a0001c0002t0002g0197 |
2 | NA19057.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.96+5996C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795707 | |||||||
chr3:56795737 | G | C | 53 | a0001c0002t0002g0022 a0001c0002t0002g0025 a0001c0002t0002g0028 others(50): Show |
54 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.96+5966C>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795737 | |||||||
chr3:56795790 | T | C | 74 | a0001c0002t0002g0022 a0001c0002t0002g0025 a0001c0002t0002g0029 others(71): Show |
75 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.96+5913A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795790 | |||||||
chr3:56795798 | C | T | 1 | a0001c0002t0002g0025 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.96+5905G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795798 | |||||||
chr3:56795801 | C | A | 1 | a0001c0002t0002g0066 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.96+5902G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795801 | |||||||
chr3:56795830 | T | C | 2 | a0001c0005t0001g0317 a0002c0004t0003g0318 |
2 | NA18956.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.96+5873A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795830 | |||||||
chr3:56795842 | G | A | 1 | a0001c0002t0008g0135 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.96+5861C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795842 | |||||||
chr3:56795864 | C | T | 153 | a0001c0002t0002g0022 a0001c0002t0002g0023 a0001c0002t0002g0025 others(150): Show |
158 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.96+5839G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795864 | |||||||
chr3:56795915 | C | T | 1 | a0002c0001t0003g0024 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.96+5788G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795915 | |||||||
chr3:56795916 | G | A | 2 | a0001c0002t0002g0139 a0001c0007t0001g0101 |
2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.96+5787C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795916 | |||||||
chr3:56795977 | T | TA | 57 | a0001c0002t0002g0022 a0001c0002t0002g0025 a0001c0002t0002g0026 others(54): Show |
58 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.96+5725dupT | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795977 | |||||||
chr3:56795977 | TA | T | 131 | a0001c0002t0002g0005 a0001c0002t0002g0077 a0001c0002t0002g0083 others(128): Show |
134 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.96+5725delT | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56795977 | |||||||
chr3:56796059 | C | T | 219 | a0001c0002t0002g0005 a0001c0002t0002g0077 a0001c0002t0002g0078 others(216): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.96+5644G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56796059 | |||||||
chr3:56796068 | G | A | 22 | a0001c0002t0002g0110 a0001c0002t0002g0124 a0001c0002t0002g0125 others(19): Show |
22 | HG00597.hp2 HG01361.hp2 HG01928.hp1 others(19): Show |
intron_variant | MODIFIER | c.96+5635C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56796068 | |||||||
chr3:56796360 | T | C | 1 | a0001c0003t0001g0184 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.96+5343A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56796360 | |||||||
chr3:56796375 | T | C | 24 | a0001c0002t0002g0110 a0001c0002t0002g0124 a0001c0002t0002g0125 others(21): Show |
24 | HG00597.hp2 HG01070.hp1 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.96+5328A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56796375 | |||||||
chr3:56796431 | C | T | 57 | a0001c0002t0002g0212 a0001c0002t0002g0213 a0001c0002t0002g0214 others(54): Show |
57 | HG00597.hp1 HG00673.hp2 HG01109.hp1 others(54): Show |
intron_variant | MODIFIER | c.96+5272G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56796431 | |||||||
chr3:56796471 | G | A | 2 | a0002c0001t0003g0198 a0002c0001t0003g0199 |
2 | NA18995.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.96+5232C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56796471 | |||||||
chr3:56796538 | G | A | 15 | a0001c0002t0002g0124 a0001c0002t0002g0125 a0001c0003t0001g0121 others(12): Show |
15 | HG00597.hp2 HG01361.hp2 HG01928.hp1 others(12): Show |
intron_variant | MODIFIER | c.96+5165C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56796538 | |||||||
chr3:56796551 | G | A | 40 | a0001c0002t0002g0005 a0001c0002t0002g0069 a0001c0002t0002g0129 others(37): Show |
43 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(40): Show |
intron_variant | MODIFIER | c.96+5152C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56796551 | |||||||
chr3:56797043 | C | T | 4 | a0001c0003t0001g0016 a0001c0003t0001g0017 a0001c0003t0001g0018 others(1): Show |
4 | HG01109.hp2 HG02145.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.96+4660G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56797043 | |||||||
chr3:56797094 | C | A | 59 | a0001c0002t0002g0212 a0001c0002t0002g0213 a0001c0002t0002g0214 others(56): Show |
59 | HG00597.hp1 HG00673.hp2 HG01109.hp1 others(56): Show |
intron_variant | MODIFIER | c.96+4609G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56797094 | |||||||
chr3:56797239 | T | C | 89 | a0001c0002t0002g0022 a0001c0005t0001g0010 a0001c0005t0001g0265 others(86): Show |
92 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.96+4464A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56797239 | |||||||
chr3:56797242 | T | A | 1 | a0001c0007t0001g0074 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.96+4461A>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56797242 | |||||||
chr3:56797285 | C | A | 1 | a0002c0004t0001g0342 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.96+4418G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56797285 | |||||||
chr3:56797366 | C | T | 18 | a0001c0002t0002g0007 a0001c0002t0002g0021 a0001c0002t0002g0187 others(15): Show |
19 | HG00621.hp1 HG00673.hp1 HG02735.hp2 others(16): Show |
intron_variant | MODIFIER | c.96+4337G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56797366 | |||||||
chr3:56797391 | C | A | 1 | a0001c0007t0001g0074 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.96+4312G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56797391 | |||||||
chr3:56797479 | G | A | 1 | a0002c0001t0001g0001 | 2 | HG02451.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.96+4224C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56797479 | |||||||
chr3:56797520 | G | A | 205 | a0001c0002t0002g0005 a0001c0002t0002g0023 a0001c0002t0002g0025 others(202): Show |
209 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.96+4183C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56797520 | |||||||
chr3:56797530 | C | A | 1 | a0001c0002t0002g0127 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.96+4173G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56797530 | |||||||
chr3:56797608 | T | C | 2 | a0001c0005t0001g0343 a0001c0005t0001g0344 |
2 | NA18952.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.96+4095A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56797608 | |||||||
chr3:56797676 | A | G | 1 | a0002c0001t0001g0185 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.96+4027T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56797676 | |||||||
chr3:56798342 | A | G | 1 | a0001c0003t0001g0134 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.96+3361T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56798342 | |||||||
chr3:56798503 | A | C | 1 | a0001c0007t0001g0074 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.96+3200T>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56798503 | |||||||
chr3:56798536 | CGTT | C | 3 | a0001c0003t0001g0070 a0001c0003t0001g0071 a0001c0003t0001g0072 |
3 | NA18941.hp1 NA18955.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.96+3164_96+3166del others(3): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56798536 | |||||||
chr3:56798537 | GT | G | 112 | a0001c0002t0002g0007 a0001c0002t0002g0021 a0001c0002t0002g0025 others(109): Show |
113 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(110): Show |
intron_variant | MODIFIER | c.96+3165delA | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56798537 | |||||||
chr3:56798537 | GTT | G | 127 | a0001c0002t0002g0005 a0001c0002t0002g0022 a0001c0002t0002g0023 others(124): Show |
130 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.96+3164_96+3165del others(2): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56798537 | |||||||
chr3:56798537 | GTTT | G | 7 | a0001c0002t0002g0127 a0001c0002t0002g0256 a0001c0002t0002g0257 others(4): Show |
7 | HG02486.hp2 HG02698.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.96+3163_96+3165del others(3): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56798537 | |||||||
chr3:56798537 | GTTTTTTT | G | 81 | a0001c0005t0001g0010 a0001c0005t0001g0265 a0001c0005t0001g0270 others(78): Show |
84 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.96+3159_96+3165del others(7): Show |
ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56798537 | |||||||
chr3:56798562 | C | A | 5 | a0001c0003t0001g0104 a0001c0007t0001g0101 a0001c0007t0001g0102 others(2): Show |
5 | HG00741.hp2 HG02622.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.96+3141G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56798562 | |||||||
chr3:56798563 | C | A | 5 | a0001c0003t0001g0104 a0001c0007t0001g0101 a0001c0007t0001g0102 others(2): Show |
5 | HG00741.hp2 HG02622.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.96+3140G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56798563 | |||||||
chr3:56798564 | T | C | 21 | a0001c0002t0002g0110 a0001c0002t0002g0124 a0001c0002t0002g0125 others(18): Show |
21 | HG00597.hp2 HG01361.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.96+3139A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56798564 | |||||||
chr3:56798676 | C | T | 1 | a0002c0001t0001g0133 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.96+3027G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56798676 | |||||||
chr3:56798996 | T | C | 89 | a0001c0002t0002g0077 a0001c0002t0002g0078 a0001c0002t0002g0079 others(86): Show |
89 | HG00597.hp1 HG00673.hp2 HG00741.hp2 others(86): Show |
intron_variant | MODIFIER | c.96+2707A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56798996 | |||||||
chr3:56799162 | A | G | 19 | a0001c0002t0002g0077 a0001c0002t0002g0078 a0001c0002t0002g0079 others(16): Show |
19 | HG01099.hp1 HG01496.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.96+2541T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56799162 | |||||||
chr3:56799406 | G | A | 1 | a0001c0002t0002g0127 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.96+2297C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56799406 | |||||||
chr3:56799686 | G | A | 4 | a0001c0003t0001g0104 a0001c0007t0001g0102 a0001c0012t0001g0105 others(1): Show |
4 | HG00741.hp2 HG02622.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+2017C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56799686 | |||||||
chr3:56799734 | C | A | 22 | a0001c0002t0002g0110 a0001c0002t0002g0124 a0001c0002t0002g0125 others(19): Show |
22 | HG00597.hp2 HG01361.hp2 HG01928.hp1 others(19): Show |
intron_variant | MODIFIER | c.96+1969G>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56799734 | |||||||
chr3:56799738 | T | C | 169 | a0001c0002t0002g0022 a0001c0002t0002g0023 a0001c0002t0002g0025 others(166): Show |
170 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(167): Show |
intron_variant | MODIFIER | c.96+1965A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56799738 | |||||||
chr3:56799741 | G | A | 86 | a0001c0005t0001g0010 a0001c0005t0001g0265 a0001c0005t0001g0270 others(83): Show |
89 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.96+1962C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56799741 | |||||||
chr3:56799763 | A | G | 4 | a0001c0002t0002g0129 a0001c0002t0002g0130 a0001c0002t0002g0131 others(1): Show |
4 | HG02080.hp1 HG02135.hp1 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+1940T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56799763 | |||||||
chr3:56799829 | T | C | 19 | a0001c0002t0002g0007 a0001c0002t0002g0021 a0001c0002t0002g0187 others(16): Show |
20 | HG00621.hp1 HG00673.hp1 HG02735.hp2 others(17): Show |
intron_variant | MODIFIER | c.96+1874A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56799829 | |||||||
chr3:56799947 | C | T | 1 | a0002c0004t0012g0266 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.96+1756G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56799947 | |||||||
chr3:56799951 | T | C | 87 | a0001c0005t0001g0010 a0001c0005t0001g0265 a0001c0005t0001g0270 others(84): Show |
90 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.96+1752A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56799951 | |||||||
chr3:56800167 | G | A | 3 | a0001c0002t0006g0011 a0001c0002t0006g0013 a0002c0001t0009g0012 |
3 | HG02109.hp1 HG02723.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.96+1536C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56800167 | |||||||
chr3:56800170 | G | A | 87 | a0001c0005t0001g0010 a0001c0005t0001g0265 a0001c0005t0001g0270 others(84): Show |
90 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.96+1533C>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56800170 | |||||||
chr3:56800204 | T | G | 3 | a0001c0002t0006g0011 a0001c0002t0006g0013 a0002c0001t0009g0012 |
3 | HG02109.hp1 HG02723.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.96+1499A>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56800204 | |||||||
chr3:56800255 | C | T | 1 | a0001c0003t0001g0128 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.96+1448G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56800255 | |||||||
chr3:56800261 | A | G | 169 | a0001c0002t0002g0022 a0001c0002t0002g0023 a0001c0002t0002g0025 others(166): Show |
170 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(167): Show |
intron_variant | MODIFIER | c.96+1442T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56800261 | |||||||
chr3:56800398 | T | C | 5 | a0001c0003t0001g0204 a0002c0001t0001g0200 a0002c0001t0003g0202 others(2): Show |
5 | HG00642.hp1 HG02257.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.96+1305A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56800398 | |||||||
chr3:56800496 | C | T | 87 | a0001c0005t0001g0010 a0001c0005t0001g0265 a0001c0005t0001g0270 others(84): Show |
90 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.96+1207G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56800496 | |||||||
chr3:56800771 | C | T | 87 | a0001c0005t0001g0010 a0001c0005t0001g0265 a0001c0005t0001g0270 others(84): Show |
90 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.96+932G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56800771 | |||||||
chr3:56800899 | T | C | 1 | a0002c0004t0001g0346 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.96+804A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56800899 | |||||||
chr3:56800950 | T | A | 60 | a0001c0002t0002g0207 a0001c0002t0002g0212 a0001c0002t0002g0213 others(57): Show |
60 | HG00597.hp1 HG00673.hp2 HG01109.hp1 others(57): Show |
intron_variant | MODIFIER | c.96+753A>T | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56800950 | |||||||
chr3:56800955 | C | T | 1 | a0004c0011t0008g0073 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.96+748G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56800955 | |||||||
chr3:56800984 | C | T | 52 | a0001c0002t0002g0022 a0001c0002t0002g0023 a0001c0002t0002g0025 others(49): Show |
53 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.96+719G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56800984 | |||||||
chr3:56801050 | A | G | 2 | a0001c0002t0002g0021 a0001c0009t0002g0020 |
2 | NA18950.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.96+653T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56801050 | |||||||
chr3:56801051 | T | C | 3 | a0001c0002t0006g0011 a0001c0002t0006g0013 a0002c0001t0009g0012 |
3 | HG02109.hp1 HG02723.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.96+652A>G | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56801051 | |||||||
chr3:56801064 | C | T | 1 | a0001c0005t0001g0265 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.96+639G>A | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56801064 | |||||||
chr3:56801607 | A | G | 7 | a0001c0002t0010g0014 a0001c0003t0001g0016 a0001c0003t0001g0017 others(4): Show |
8 | HG01109.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.96+96T>C | ARHGEF3 | ENSG00000163947.12 | transcript | ENST00000296315.8 | protein_coding | 1/9 | chr3 | 56801607 |