Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9138 |
| ensemblid | ENSG00000076928.20 |
| hgncid | 681 |
| symbol | ARHGEF1 |
| name | Rho guanine nucleotide exchange factor 1 |
| refseq_nuc | NM_004706.4 |
| refseq_prot | NP_004697.2 |
| ensembl_nuc | ENST00000354532.8 |
| ensembl_prot | ENSP00000346532.3 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 41883184 |
| end | 41907452 |
| strand | + |
| ver | v1.2 |
| region | chr19:41883184-41907452 |
| region5000 | chr19:41878184-41912452 |
| regionname0 | ARHGEF1_chr19_41883184_41907452 |
| regionname5000 | ARHGEF1_chr19_41878184_41912452 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 912 | 225 | 65 | 43 | 82 | 8 | 25 | 53 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | MEDFA others(907): Show |
chr19 | 41878184 | 41912452 |
| a0002 | 0/0 | 912 | 4 | 0 | 0 | 4 | 0 | 0 | 3 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | MEDFA others(907): Show |
chr19 | 41878184 | 41912452 |
| a0003 | 0/0 | 912 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | MEDFA others(907): Show |
chr19 | 41878184 | 41912452 |
| a0004 | 0/0 | 907 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | MEDFA others(902): Show |
chr19 | 41878184 | 41912452 |
| a0005 | 0/0 | 912 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | MEDFA others(907): Show |
chr19 | 41878184 | 41912452 |
| a0006 | 0/0 | 912 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | MEDFA others(907): Show |
chr19 | 41878184 | 41912452 |
| a0007 | 0/0 | 912 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | MEDFA others(907): Show |
chr19 | 41878184 | 41912452 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2736 | 141 | 18 | 38 | 57 | 7 | 19 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | ATGGA others(2731): Show |
chr19 | 41878184 | 41912452 | ||
| a0001c0002 | 0/0 | 2736 | 74 | 40 | 5 | 23 | 0 | 6 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | ATGGA others(2731): Show |
chr19 | 41878184 | 41912452 | ||
| a0001c0003 | 0/0 | 2736 | 7 | 7 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | ATGGA others(2731): Show |
chr19 | 41878184 | 41912452 | ||
| a0001c0006 | 0/0 | 2736 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | ATGGA others(2731): Show |
chr19 | 41878184 | 41912452 | ||
| a0001c0007 | 0/0 | 2736 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | ATGGA others(2731): Show |
chr19 | 41878184 | 41912452 | ||
| a0001c0012 | 0/0 | 2736 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | ATGGA others(2731): Show |
chr19 | 41878184 | 41912452 | ||
| a0002c0004 | 0/0 | 2736 | 4 | 0 | 0 | 4 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | ATGGA others(2731): Show |
chr19 | 41878184 | 41912452 | ||
| a0003c0011 | 0/0 | 2736 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | ATGGA others(2731): Show |
chr19 | 41878184 | 41912452 | ||
| a0004c0005 | 0/0 | 2721 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | ATGGA others(2716): Show |
chr19 | 41878184 | 41912452 | ||
| a0005c0008 | 0/0 | 2736 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | ATGGA others(2731): Show |
chr19 | 41878184 | 41912452 | ||
| a0006c0009 | 0/0 | 2736 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | ATGGA others(2731): Show |
chr19 | 41878184 | 41912452 | ||
| a0007c0010 | 0/0 | 2736 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | ATGGA others(2731): Show |
chr19 | 41878184 | 41912452 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3229 | 140 | 18 | 38 | 56 | 7 | 19 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | GACTT others(3224): Show |
chr19 | 41878184 | 41912452 |
| a0001c0001t0003 | 0/0 | 3229 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | GACTT others(3224): Show |
chr19 | 41878184 | 41912452 |
| a0001c0002t0001 | 0/0 | 3229 | 71 | 39 | 5 | 22 | 0 | 5 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | GACTT others(3224): Show |
chr19 | 41878184 | 41912452 |
| a0001c0002t0002 | 0/0 | 3229 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | GACTT others(3224): Show |
chr19 | 41878184 | 41912452 |
| a0001c0002t0004 | 0/0 | 3229 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | GACTT others(3224): Show |
chr19 | 41878184 | 41912452 |
| a0001c0002t0005 | 0/0 | 3229 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | GACTT others(3224): Show |
chr19 | 41878184 | 41912452 |
| a0001c0003t0001 | 0/0 | 3229 | 7 | 7 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | GACTT others(3224): Show |
chr19 | 41878184 | 41912452 |
| a0001c0006t0001 | 0/0 | 3229 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | GACTT others(3224): Show |
chr19 | 41878184 | 41912452 |
| a0001c0007t0001 | 0/0 | 3229 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | GACTT others(3224): Show |
chr19 | 41878184 | 41912452 |
| a0001c0012t0001 | 0/0 | 3229 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | GACTT others(3224): Show |
chr19 | 41878184 | 41912452 |
| a0002c0004t0001 | 0/0 | 3229 | 4 | 0 | 0 | 4 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | GACTT others(3224): Show |
chr19 | 41878184 | 41912452 |
| a0003c0011t0001 | 0/0 | 3229 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | GACTT others(3224): Show |
chr19 | 41878184 | 41912452 |
| a0004c0005t0001 | 0/0 | 3214 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | GACTT others(3209): Show |
chr19 | 41878184 | 41912452 |
| a0005c0008t0001 | 0/0 | 3229 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | GACTT others(3224): Show |
chr19 | 41878184 | 41912452 |
| a0006c0009t0001 | 0/0 | 3229 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | GACTT others(3224): Show |
chr19 | 41878184 | 41912452 |
| a0007c0010t0001 | 0/0 | 3229 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | GACTT others(3224): Show |
chr19 | 41878184 | 41912452 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 10 | 1 | 3 | 6 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0003 | 0/0 | 9 | 0 | 2 | 5 | 2 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0004 | 0/0 | 9 | 0 | 2 | 2 | 1 | 4 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0005 | 1/0 | 5 | 1 | 1 | 0 | 1 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0006 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0010 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0147 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0002t0001g0001 | 0/0 | 8 | 0 | 0 | 7 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0002t0001g0007 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0002t0001g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0002t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0002t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0002t0001g0014 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0002t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0002t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0002t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0002t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0002t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0002t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0002t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0002t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0002t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0002t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0002t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0002t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0002t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0002t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0002t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0002t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0002t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0002t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0002t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0002t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0002t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0002t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0002t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0002t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0002t0005g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0003t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0003t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0003t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0003t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0003t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0003t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0003t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0006t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0007t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0001c0012t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0002c0004t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0002c0004t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0002c0004t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0003c0011t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0004c0005t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0005c0008t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0006c0009t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| a0007c0010t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0112 | EUR | GBR | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG00099 | hp2 | a0001 | c0006 | t0001 | g0154 | EUR | GBR | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | CHS | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG00423 | hp2 | a0001 | c0002 | t0001 | g0044 | EAS | CHS | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | CHS | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | CHS | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0078 | EAS | CHS | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | CHS | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | CHS | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | CHS | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG00639 | hp1 | a0003 | c0011 | t0001 | g0155 | AMR | PUR | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0058 | AMR | PUR | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG00738 | hp2 | a0004 | c0005 | t0001 | g0089 | AMR | PUR | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0011 | AMR | PUR | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0038 | AMR | PUR | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0056 | AMR | CLM | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG01361 | hp1 | a0005 | c0008 | t0001 | g0003 | AMR | CLM | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0092 | EUR | IBS | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0046 | AFR | ACB | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0065 | AMR | PEL | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0081 | EAS | KHV | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG02040 | hp1 | a0002 | c0004 | t0001 | g0001 | EAS | KHV | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0128 | AFR | ACB | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0057 | AFR | ACB | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0047 | AFR | ACB | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0070 | EAS | CDX | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | CDX | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0018 | AFR | GWD | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG02572 | hp2 | a0001 | c0002 | t0004 | g0049 | AFR | GWD | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0018 | AFR | GWD | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0052 | AFR | GWD | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0068 | AFR | GWD | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0013 | AFR | GWD | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0054 | AFR | GWD | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0067 | AFR | GWD | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG02922 | hp1 | a0001 | c0003 | t0001 | g0027 | AFR | ESN | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0033 | AFR | ESN | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0011 | AFR | ESN | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0053 | AFR | ESN | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0050 | AFR | ESN | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0036 | AFR | ESN | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0060 | AFR | ESN | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | MSL | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0082 | AFR | MSL | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0061 | AFR | ESN | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0062 | AFR | ESN | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG03195 | hp1 | a0001 | c0003 | t0001 | g0028 | AFR | ESN | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG03195 | hp2 | a0001 | c0003 | t0001 | g0025 | AFR | ESN | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0013 | AFR | MSL | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | MSL | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0040 | AFR | MSL | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | MSL | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0041 | AFR | MSL | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ESN | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0059 | AFR | ESN | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0066 | AFR | GWD | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0055 | AFR | GWD | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0064 | AFR | MSL | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | STU | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0014 | SAS | STU | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG03831 | hp1 | a0007 | c0010 | t0001 | g0161 | SAS | BEB | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | BEB | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0045 | SAS | BEB | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | BEB | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | BEB | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | STU | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | STU | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | BEB | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | STU | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | STU | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | STU | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0007 | SAS | STU | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0072 | SAS | STU | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | STU | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0012 | AFR | YRI | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0012 | AFR | YRI | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | CHB | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | CHB | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0037 | AFR | YRI | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0031 | AFR | YRI | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA18940 | hp2 | a0002 | c0004 | t0001 | g0073 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA18950 | hp2 | a0001 | c0007 | t0001 | g0015 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA18951 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA18961 | hp2 | a0001 | c0002 | t0001 | g0043 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA18965 | hp2 | a0001 | c0002 | t0002 | g0039 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0071 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA18998 | hp2 | a0002 | c0004 | t0001 | g0001 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA19001 | hp1 | a0001 | c0002 | t0001 | g0080 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0079 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA19030 | hp1 | a0001 | c0003 | t0001 | g0026 | AFR | LWK | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0083 | AFR | LWK | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0077 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA19079 | hp2 | a0001 | c0012 | t0001 | g0001 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0129 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA19086 | hp1 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA19091 | hp1 | a0002 | c0004 | t0001 | g0074 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0063 | AFR | YRI | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0118 | AFR | YRI | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA20129 | hp1 | a0001 | c0003 | t0001 | g0029 | AFR | ASW | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ASW | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | TSI | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA20905 | hp1 | a0001 | c0002 | t0005 | g0001 | SAS | GIH | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | GIH | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG02109 | hp1 | a0001 | c0003 | t0001 | g0030 | AFR | ACB | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG02109 | hp2 | a0006 | c0009 | t0001 | g0023 | AFR | ACB | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0051 | AFR | ACB | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0032 | AFR | ACB | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0048 | AFR | MSL | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0042 | AFR | MSL | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | USA | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0119 | AFR | USA | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA21309 | hp1 | a0001 | c0003 | t0001 | g0022 | AFR | LWK | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | LWK | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0147 | REF | REF | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0005 | REF | REF | ARHGEF1_chr19_41878184_41912452 | ARHGEF1 | chr19 | 41878184 | 41912452 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:41888066 | C | T | 1 | a0001 | 1 | NA20905.hp1 | splice_region_variant | LOW | c.-17C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 2/29 | chr19 | 41888066 | |||||||
| chr19:41892690 | G | T | 1 | a0003 | 1 | HG00639.hp1 | missense_variant | MODERATE | c.455G>T | p.Arg152Leu | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 7/29 | 580/3229 | 455/2739 | 152/912 | chr19 | 41892690 | |||
| chr19:41894463 | C | T | 1 | a0007 | 1 | HG03831.hp1 | missense_variant | MODERATE | c.757C>T | p.Arg253Trp | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 10/29 | 882/3229 | 757/2739 | 253/912 | chr19 | 41894463 | |||
| chr19:41898444 | C | T | 1 | a0002 | 4 | HG02040.hp1 NA18940.hp2 NA18998.hp2 others(1): Show |
missense_variant&splice_region_variant | MODERATE | c.1124C>T | p.Pro375Leu | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/29 | 1249/3229 | 1124/2739 | 375/912 | chr19 | 41898444 | |||
| chr19:41898460 | G | T | 1 | a0006 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.1140G>T | p.Glu380Asp | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/29 | 1265/3229 | 1140/2739 | 380/912 | chr19 | 41898460 | |||
| chr19:41898477 | C | T | 1 | a0005 | 1 | HG01361.hp1 | missense_variant | MODERATE | c.1157C>T | p.Ser386Leu | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/29 | 1282/3229 | 1157/2739 | 386/912 | chr19 | 41898477 | |||
| chr19:41903765 | CTATGCTG others(8): Show |
C | 1 | a0004 | 1 | HG00738.hp2 | disruptive_inframe_deletion | MODERATE | c.1899_1913delTATGCT others(9): Show |
p.Met634_Phe638del | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 20/29 | 2024/3229 | 1899/2739 | 633/912 | chr19 | 41903765 | |||
| chr19:41903767 | A | G | 1 | a0001 | 1 | HG02004.hp1 | missense_variant | MODERATE | c.1900A>G | p.Met634Val | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 20/29 | 2025/3229 | 1900/2739 | 634/912 | chr19 | 41903767 | |||
| chr19:41905015 | A | C | 1 | a0004 | 1 | HG00738.hp2 | missense_variant | MODERATE | c.2228A>C | p.Gln743Pro | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 23/29 | 2353/3229 | 2228/2739 | 743/912 | chr19 | 41905015 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:41888239 | C | T | 3 | a0001c0002 a0001c0012 a0002c0004 |
79 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(76): Show |
synonymous_variant | LOW | c.72C>T | p.Ile24Ile | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 3/29 | 197/3229 | 72/2739 | 24/912 | chr19 | 41888239 | |||
| chr19:41902293 | G | A | 1 | a0006c0009 | 1 | HG02109.hp2 | synonymous_variant | LOW | c.1434G>A | p.Leu478Leu | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 16/29 | 1559/3229 | 1434/2739 | 478/912 | chr19 | 41902293 | |||
| chr19:41904274 | G | A | 2 | a0001c0003 a0006c0009 |
8 | HG02109.hp1 HG02109.hp2 HG02922.hp1 others(5): Show |
synonymous_variant | LOW | c.2052G>A | p.Arg684Arg | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 22/29 | 2177/3229 | 2052/2739 | 684/912 | chr19 | 41904274 | |||
| chr19:41904956 | A | G | 1 | a0001c0007 | 1 | NA18950.hp2 | synonymous_variant | LOW | c.2169A>G | p.Lys723Lys | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 23/29 | 2294/3229 | 2169/2739 | 723/912 | chr19 | 41904956 | |||
| chr19:41905208 | C | A | 1 | a0001c0012 | 1 | NA19079.hp2 | synonymous_variant | LOW | c.2283C>A | p.Ser761Ser | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 24/29 | 2408/3229 | 2283/2739 | 761/912 | chr19 | 41905208 | |||
| chr19:41905814 | G | A | 1 | a0001c0006 | 1 | HG00099.hp2 | synonymous_variant | LOW | c.2391G>A | p.Thr797Thr | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 25/29 | 2516/3229 | 2391/2739 | 797/912 | chr19 | 41905814 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:41883263 | C | A | 1 | a0001c0002t0002 | 1 | NA18965.hp2 | 5_prime_UTR_variant | MODIFIER | c.-46C>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/29 | 4820 | chr19 | 41883263 | ||||||
| chr19:41907226 | G | A | 1 | a0001c0002t0002 | 1 | NA18965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*139G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 29/29 | 440 | chr19 | 41907226 | ||||||
| chr19:41907310 | A | T | 1 | a0001c0002t0004 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*223A>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 29/29 | 524 | chr19 | 41907310 | ||||||
| chr19:41907439 | A | C | 1 | a0001c0001t0003 | 1 | NA19084.hp2 | 3_prime_UTR_variant | MODIFIER | c.*352A>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 29/29 | 653 | chr19 | 41907439 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:41883427 | T | C | 2 | a0001c0003t0001g0022 a0006c0009t0001g0023 |
2 | HG02109.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-20+138T>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41883427 | |||||||
| chr19:41883736 | A | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(54): Show |
78 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.-20+447A>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41883736 | |||||||
| chr19:41884115 | G | A | 1 | a0001c0001t0001g0024 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-20+826G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41884115 | |||||||
| chr19:41884158 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-20+869C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41884158 | |||||||
| chr19:41884574 | C | A | 2 | a0001c0003t0001g0025 a0001c0003t0001g0026 |
2 | HG03195.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-20+1285C>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41884574 | |||||||
| chr19:41885063 | T | C | 6 | a0001c0003t0001g0025 a0001c0003t0001g0026 a0001c0003t0001g0027 others(3): Show |
6 | HG02109.hp1 HG02922.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20+1774T>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41885063 | |||||||
| chr19:41885094 | C | T | 6 | a0001c0003t0001g0025 a0001c0003t0001g0026 a0001c0003t0001g0027 others(3): Show |
6 | HG02109.hp1 HG02922.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20+1805C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41885094 | |||||||
| chr19:41885213 | A | T | 54 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(51): Show |
75 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.-20+1924A>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41885213 | |||||||
| chr19:41885347 | C | G | 8 | a0001c0003t0001g0022 a0001c0003t0001g0025 a0001c0003t0001g0026 others(5): Show |
8 | HG02109.hp1 HG02109.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.-20+2058C>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41885347 | |||||||
| chr19:41885454 | T | TTTTA | 57 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(54): Show |
78 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.-20+2185_-20+2188d others(6): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr19 | 41885454 | ||||||
| chr19:41885524 | C | T | 6 | a0001c0003t0001g0025 a0001c0003t0001g0026 a0001c0003t0001g0027 others(3): Show |
6 | HG02109.hp1 HG02922.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20+2235C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41885524 | |||||||
| chr19:41885912 | C | G | 3 | a0001c0002t0001g0018 a0001c0002t0001g0118 a0001c0002t0001g0119 |
4 | HG02572.hp1 HG02622.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19-2152C>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41885912 | |||||||
| chr19:41886134 | T | C | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-19-1930T>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41886134 | |||||||
| chr19:41886170 | T | C | 6 | a0001c0002t0001g0018 a0001c0002t0001g0031 a0001c0002t0001g0032 others(3): Show |
7 | HG02486.hp2 HG02572.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-19-1894T>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41886170 | |||||||
| chr19:41886176 | G | A | 1 | a0001c0001t0001g0003 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-19-1888G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41886176 | |||||||
| chr19:41886253 | T | C | 12 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(9): Show |
12 | HG02109.hp1 HG02109.hp2 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.-19-1811T>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41886253 | |||||||
| chr19:41886396 | C | T | 1 | a0006c0009t0001g0023 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-19-1668C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41886396 | |||||||
| chr19:41886405 | G | A | 1 | a0001c0001t0001g0127 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-19-1659G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41886405 | |||||||
| chr19:41886864 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-19-1200G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41886864 | |||||||
| chr19:41886957 | G | A | 1 | a0001c0001t0001g0035 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-19-1107G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41886957 | |||||||
| chr19:41887008 | G | A | 11 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(8): Show |
11 | HG02109.hp1 HG02109.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.-19-1056G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41887008 | |||||||
| chr19:41887180 | C | T | 4 | a0001c0001t0001g0009 a0001c0001t0001g0115 a0001c0001t0001g0116 others(1): Show |
6 | HG01884.hp2 HG02145.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-884C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41887180 | |||||||
| chr19:41887335 | C | T | 1 | a0001c0001t0001g0035 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-19-729C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41887335 | |||||||
| chr19:41887339 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-19-725C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41887339 | |||||||
| chr19:41887354 | G | A | 64 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0011 others(61): Show |
79 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.-19-710G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41887354 | |||||||
| chr19:41887394 | C | CTGAGAGG others(38): Show |
1 | a0001c0001t0003g0129 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-19-666_-19-665ins others(45): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr19 | 41887394 | ||||||
| chr19:41887536 | G | A | 2 | a0001c0002t0001g0036 a0001c0002t0001g0037 |
2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-19-528G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41887536 | |||||||
| chr19:41887542 | T | G | 1 | a0001c0001t0001g0170 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-19-522T>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41887542 | |||||||
| chr19:41887614 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-19-450G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41887614 | |||||||
| chr19:41887643 | C | T | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 |
3 | HG02818.hp2 HG02897.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-19-421C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41887643 | |||||||
| chr19:41887686 | T | G | 11 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(8): Show |
11 | HG02109.hp1 HG02109.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.-19-378T>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41887686 | |||||||
| chr19:41887753 | A | T | 1 | a0001c0001t0001g0170 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-19-311A>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41887753 | |||||||
| chr19:41887754 | G | A | 1 | a0001c0001t0001g0170 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-19-310G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41887754 | |||||||
| chr19:41887755 | G | T | 1 | a0001c0001t0001g0170 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-19-309G>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41887755 | |||||||
| chr19:41887756 | C | A | 1 | a0001c0001t0001g0170 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-19-308C>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41887756 | |||||||
| chr19:41887758 | C | A | 1 | a0001c0001t0001g0170 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-19-306C>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41887758 | |||||||
| chr19:41887759 | C | T | 1 | a0001c0001t0001g0170 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-19-305C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41887759 | |||||||
| chr19:41887760 | C | A | 1 | a0001c0001t0001g0170 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-19-304C>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41887760 | |||||||
| chr19:41887761 | A | G | 1 | a0001c0001t0001g0170 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-19-303A>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41887761 | |||||||
| chr19:41887762 | G | T | 1 | a0001c0001t0001g0170 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-19-302G>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41887762 | |||||||
| chr19:41887763 | C | G | 1 | a0001c0001t0001g0170 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-19-301C>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41887763 | |||||||
| chr19:41887764 | C | A | 1 | a0001c0001t0001g0170 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-19-300C>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41887764 | |||||||
| chr19:41887765 | C | T | 1 | a0001c0001t0001g0170 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-19-299C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41887765 | |||||||
| chr19:41887766 | C | G | 1 | a0001c0001t0001g0170 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-19-298C>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41887766 | |||||||
| chr19:41887767 | C | T | 1 | a0001c0001t0001g0170 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-19-297C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41887767 | |||||||
| chr19:41888059 | T | C | 72 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(69): Show |
85 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(82): Show |
splice_region_variant&intron_variant | LOW | c.-19-5T>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 1/28 | chr19 | 41888059 | |||||||
| chr19:41888133 | C | G | 10 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(7): Show |
10 | HG02109.hp1 HG02109.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.24+27C>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 2/28 | chr19 | 41888133 | |||||||
| chr19:41888299 | A | G | 1 | a0001c0001t0001g0114 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.111+21A>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 3/28 | chr19 | 41888299 | |||||||
| chr19:41888370 | T | C | 72 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(69): Show |
87 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.111+92T>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 3/28 | chr19 | 41888370 | |||||||
| chr19:41888420 | C | T | 1 | a0001c0002t0001g0083 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.111+142C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 3/28 | chr19 | 41888420 | |||||||
| chr19:41888427 | G | A | 1 | a0006c0009t0001g0023 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.111+149G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 3/28 | chr19 | 41888427 | |||||||
| chr19:41888459 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.111+181C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 3/28 | chr19 | 41888459 | |||||||
| chr19:41888483 | C | T | 4 | a0001c0003t0001g0027 a0001c0003t0001g0028 a0001c0003t0001g0029 others(1): Show |
4 | HG02109.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.111+205C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 3/28 | chr19 | 41888483 | |||||||
| chr19:41888510 | C | T | 7 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(4): Show |
7 | HG02109.hp2 HG02818.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.111+232C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 3/28 | chr19 | 41888510 | |||||||
| chr19:41888651 | A | C | 1 | a0001c0001t0001g0169 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.112-101A>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 3/28 | chr19 | 41888651 | |||||||
| chr19:41888748 | C | G | 11 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(8): Show |
11 | HG02109.hp1 HG02109.hp2 HG02818.hp2 others(8): Show |
splice_region_variant&intron_variant | LOW | c.112-4C>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 3/28 | chr19 | 41888748 | |||||||
| chr19:41888881 | G | T | 1 | a0001c0001t0001g0113 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.225+16G>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41888881 | |||||||
| chr19:41889043 | C | A | 1 | a0001c0001t0001g0130 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.225+178C>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41889043 | |||||||
| chr19:41889179 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.225+314A>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41889179 | |||||||
| chr19:41889182 | G | A | 1 | a0001c0001t0001g0131 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.225+317G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41889182 | |||||||
| chr19:41889215 | A | G | 75 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(72): Show |
90 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.225+350A>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41889215 | |||||||
| chr19:41889269 | G | A | 1 | a0001c0002t0001g0038 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.225+404G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41889269 | |||||||
| chr19:41889332 | C | T | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 |
3 | HG02818.hp2 HG02897.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.225+467C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41889332 | |||||||
| chr19:41889633 | T | G | 1 | a0001c0001t0001g0132 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.225+768T>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41889633 | |||||||
| chr19:41889664 | A | C | 2 | a0001c0001t0001g0123 a0001c0001t0001g0124 |
2 | HG02897.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.225+799A>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41889664 | |||||||
| chr19:41889675 | T | A | 1 | a0001c0001t0001g0121 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.225+810T>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41889675 | |||||||
| chr19:41889747 | C | T | 1 | a0001c0001t0001g0111 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.225+882C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41889747 | |||||||
| chr19:41889975 | G | A | 7 | a0001c0001t0001g0121 a0001c0003t0001g0025 a0001c0003t0001g0026 others(4): Show |
7 | HG02109.hp1 HG02922.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.225+1110G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41889975 | |||||||
| chr19:41889980 | C | G | 1 | a0001c0001t0001g0170 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.225+1115C>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41889980 | |||||||
| chr19:41890015 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.225+1150G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41890015 | |||||||
| chr19:41890030 | T | G | 1 | a0001c0001t0001g0170 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.225+1165T>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41890030 | |||||||
| chr19:41890149 | G | C | 1 | a0001c0001t0001g0133 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.225+1284G>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41890149 | |||||||
| chr19:41890187 | T | C | 5 | a0001c0001t0001g0015 a0001c0001t0001g0085 a0001c0001t0001g0086 others(2): Show |
5 | NA18950.hp2 NA18980.hp1 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.225+1322T>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41890187 | |||||||
| chr19:41890239 | C | T | 10 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(7): Show |
10 | HG02109.hp1 HG02818.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.225+1374C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41890239 | |||||||
| chr19:41890411 | T | A | 64 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0011 others(61): Show |
79 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.225+1546T>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41890411 | |||||||
| chr19:41890578 | C | T | 1 | a0001c0003t0001g0022 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.226-1447C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41890578 | |||||||
| chr19:41890760 | G | GA | 34 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0019 others(31): Show |
37 | HG00423.hp2 HG00438.hp2 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.226-1249dupA | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 41890760 | ||||||
| chr19:41890794 | T | C | 1 | a0001c0003t0001g0027 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.226-1231T>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41890794 | |||||||
| chr19:41890821 | G | GAGGCTGA others(3): Show |
1 | a0001c0002t0001g0083 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.226-1200_226-1191d others(12): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 41890821 | ||||||
| chr19:41890943 | A | G | 1 | a0001c0001t0001g0170 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.226-1082A>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41890943 | |||||||
| chr19:41890944 | G | T | 1 | a0001c0001t0001g0170 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.226-1081G>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41890944 | |||||||
| chr19:41890945 | T | C | 1 | a0001c0001t0001g0170 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.226-1080T>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41890945 | |||||||
| chr19:41891070 | T | C | 1 | a0001c0001t0001g0091 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.226-955T>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41891070 | |||||||
| chr19:41891223 | C | T | 2 | a0001c0003t0001g0025 a0001c0003t0001g0026 |
2 | HG03195.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.226-802C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41891223 | |||||||
| chr19:41891244 | C | G | 75 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(72): Show |
90 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.226-781C>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41891244 | |||||||
| chr19:41891336 | G | A | 65 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0011 others(62): Show |
80 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.226-689G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41891336 | |||||||
| chr19:41891349 | C | T | 1 | a0001c0002t0001g0082 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.226-676C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41891349 | |||||||
| chr19:41891446 | A | G | 75 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(72): Show |
90 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.226-579A>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41891446 | |||||||
| chr19:41891481 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.226-544G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41891481 | |||||||
| chr19:41891597 | A | AACTATAC others(6): Show |
1 | a0001c0001t0001g0170 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.226-427_226-426ins others(13): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 41891597 | ||||||
| chr19:41891599 | G | T | 1 | a0001c0001t0001g0170 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.226-426G>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41891599 | |||||||
| chr19:41891600 | C | G | 1 | a0001c0001t0001g0170 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.226-425C>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41891600 | |||||||
| chr19:41891623 | G | A | 66 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0011 others(63): Show |
81 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.226-402G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41891623 | |||||||
| chr19:41891686 | G | A | 1 | a0001c0003t0001g0022 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.226-339G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41891686 | |||||||
| chr19:41891689 | G | A | 1 | a0001c0003t0001g0022 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.226-336G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41891689 | |||||||
| chr19:41891699 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.226-326C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41891699 | |||||||
| chr19:41891726 | T | C | 1 | a0001c0001t0001g0140 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.226-299T>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41891726 | |||||||
| chr19:41891793 | C | T | 7 | a0001c0001t0001g0121 a0001c0003t0001g0025 a0001c0003t0001g0026 others(4): Show |
7 | HG02109.hp1 HG02922.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.226-232C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41891793 | |||||||
| chr19:41891899 | G | A | 64 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0011 others(61): Show |
79 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.226-126G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41891899 | |||||||
| chr19:41891929 | A | G | 1 | a0006c0009t0001g0023 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.226-96A>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41891929 | |||||||
| chr19:41891997 | G | A | 1 | a0006c0009t0001g0023 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.226-28G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 4/28 | chr19 | 41891997 | |||||||
| chr19:41892195 | G | A | 75 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(72): Show |
90 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.324+72G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 5/28 | chr19 | 41892195 | |||||||
| chr19:41892222 | C | T | 1 | a0001c0002t0001g0081 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.324+99C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 5/28 | chr19 | 41892222 | |||||||
| chr19:41892438 | G | C | 7 | a0001c0001t0001g0121 a0001c0003t0001g0025 a0001c0003t0001g0026 others(4): Show |
7 | HG02109.hp1 HG02922.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.367+65G>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 6/28 | chr19 | 41892438 | |||||||
| chr19:41892513 | A | G | 7 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0090 others(4): Show |
10 | HG00642.hp1 HG01169.hp2 HG01943.hp1 others(7): Show |
intron_variant | MODIFIER | c.368-90A>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 6/28 | chr19 | 41892513 | |||||||
| chr19:41892876 | G | A | 1 | a0001c0001t0001g0020 | 2 | NA18970.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.614+27G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 7/28 | chr19 | 41892876 | |||||||
| chr19:41893106 | A | C | 1 | a0006c0009t0001g0023 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.615-168A>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 7/28 | chr19 | 41893106 | |||||||
| chr19:41893328 | G | A | 1 | a0001c0001t0001g0141 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.644+25G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893328 | |||||||
| chr19:41893332 | TCCTGGGT others(70): Show |
T | 1 | a0001c0002t0002g0039 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.644+37_644+113delT others(76): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41893332 | ||||||
| chr19:41893340 | T | C | 21 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0014 others(18): Show |
32 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(29): Show |
intron_variant | MODIFIER | c.644+37T>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893340 | |||||||
| chr19:41893357 | TGAGGGCC others(71): Show |
T | 21 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0014 others(18): Show |
32 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(29): Show |
intron_variant | MODIFIER | c.644+56_644+133delA others(77): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41893357 | ||||||
| chr19:41893366 | G | GGACGCCT others(32): Show |
1 | a0001c0001t0001g0126 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.644+66_644+67insGC others(37): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41893366 | ||||||
| chr19:41893370 | T | G | 1 | a0001c0001t0001g0126 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.644+67T>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893370 | |||||||
| chr19:41893391 | A | G | 2 | a0001c0001t0001g0126 a0001c0002t0001g0066 |
2 | HG02559.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.644+88A>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893391 | |||||||
| chr19:41893410 | C | CCTGGGTC others(31): Show |
41 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(38): Show |
45 | HG00738.hp1 HG01109.hp1 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.644+136_644+137ins others(38): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41893410 | ||||||
| chr19:41893410 | C | CCTGGGTC others(70): Show |
1 | a0001c0003t0001g0028 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.644+136_644+137ins others(77): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41893410 | ||||||
| chr19:41893434 | TG | T | 10 | a0001c0001t0001g0121 a0001c0002t0001g0032 a0001c0002t0001g0066 others(7): Show |
10 | HG02109.hp1 HG02486.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.644+137delG | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41893434 | ||||||
| chr19:41893444 | A | G | 76 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(73): Show |
91 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.644+141A>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893444 | |||||||
| chr19:41893445 | G | A | 32 | a0001c0001t0001g0121 a0001c0002t0001g0001 a0001c0002t0001g0007 others(29): Show |
43 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.644+142G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893445 | |||||||
| chr19:41893449 | C | T | 32 | a0001c0001t0001g0121 a0001c0002t0001g0001 a0001c0002t0001g0007 others(29): Show |
43 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.644+146C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893449 | |||||||
| chr19:41893464 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.644+161G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893464 | |||||||
| chr19:41893474 | G | GGGGTCCT others(68): Show |
1 | a0001c0001t0001g0126 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.644+174_644+175ins others(75): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41893474 | ||||||
| chr19:41893484 | G | A | 4 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(1): Show |
4 | HG02109.hp2 HG02818.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.644+181G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893484 | |||||||
| chr19:41893487 | G | T | 1 | a0001c0001t0001g0126 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.644+184G>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893487 | |||||||
| chr19:41893488 | C | T | 10 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(7): Show |
10 | HG02109.hp1 HG02109.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.644+185C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893488 | |||||||
| chr19:41893506 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.644+203G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893506 | |||||||
| chr19:41893527 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.644+224C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893527 | |||||||
| chr19:41893551 | T | TG | 35 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(32): Show |
46 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.644+252dupG | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41893551 | ||||||
| chr19:41893556 | T | G | 75 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(72): Show |
90 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.644+253T>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893556 | |||||||
| chr19:41893561 | G | A | 38 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0013 others(35): Show |
42 | HG00738.hp1 HG01109.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.644+258G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893561 | |||||||
| chr19:41893565 | C | T | 39 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0013 others(36): Show |
43 | HG00738.hp1 HG01109.hp1 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.644+262C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893565 | |||||||
| chr19:41893583 | G | A | 1 | a0001c0001t0001g0143 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.644+280G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893583 | |||||||
| chr19:41893589 | T | TG | 48 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(45): Show |
52 | HG00738.hp1 HG01109.hp1 HG01243.hp1 others(49): Show |
intron_variant | MODIFIER | c.644+291dupG | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41893589 | ||||||
| chr19:41893589 | T | TGGGGGGC others(227): Show |
1 | a0001c0003t0001g0028 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.644+291_644+292ins others(234): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41893589 | ||||||
| chr19:41893590 | GGGGGCCT others(30): Show |
G | 1 | a0001c0001t0001g0143 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.644+292_644+328del others(37): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41893590 | ||||||
| chr19:41893599 | G | A | 3 | a0001c0002t0001g0032 a0001c0002t0001g0067 a0001c0002t0001g0068 |
3 | HG02486.hp2 HG02723.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.644+296G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893599 | |||||||
| chr19:41893603 | C | T | 3 | a0001c0002t0001g0032 a0001c0002t0001g0067 a0001c0002t0001g0068 |
3 | HG02486.hp2 HG02723.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.644+300C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893603 | |||||||
| chr19:41893627 | T | TG | 45 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(42): Show |
49 | HG00738.hp1 HG01109.hp1 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.644+329dupG | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41893627 | ||||||
| chr19:41893640 | T | G | 72 | a0001c0001t0001g0121 a0001c0001t0001g0143 a0001c0002t0001g0001 others(69): Show |
87 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.644+337T>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893640 | |||||||
| chr19:41893641 | C | T | 7 | a0001c0001t0001g0121 a0001c0001t0001g0143 a0001c0003t0001g0025 others(4): Show |
7 | HG02109.hp1 HG02922.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.644+338C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893641 | |||||||
| chr19:41893644 | G | A | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 |
3 | HG02818.hp2 HG02897.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.644+341G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893644 | |||||||
| chr19:41893645 | G | A | 1 | a0001c0002t0001g0046 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.644+342G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893645 | |||||||
| chr19:41893661 | A | G | 49 | a0001c0001t0001g0121 a0001c0002t0001g0011 a0001c0002t0001g0012 others(46): Show |
53 | HG00738.hp1 HG01109.hp1 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.644+358A>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893661 | |||||||
| chr19:41893661 | AGGCTGGG others(70): Show |
A | 1 | a0001c0002t0001g0066 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.644+368_644+444del others(77): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41893661 | ||||||
| chr19:41893665 | T | TG | 68 | a0001c0001t0001g0121 a0001c0002t0001g0001 a0001c0002t0001g0007 others(65): Show |
83 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.644+367dupG | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41893665 | ||||||
| chr19:41893677 | C | T | 22 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0014 others(19): Show |
33 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.644+374C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893677 | |||||||
| chr19:41893678 | T | G | 74 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(71): Show |
89 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.644+375T>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893678 | |||||||
| chr19:41893679 | C | T | 10 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(7): Show |
10 | HG02109.hp1 HG02818.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.644+376C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893679 | |||||||
| chr19:41893697 | A | AGGGGCTG others(185): Show |
1 | a0006c0009t0001g0023 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.644+405_644+406ins others(192): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41893697 | ||||||
| chr19:41893697 | A | G | 73 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(70): Show |
88 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.644+394A>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893697 | |||||||
| chr19:41893703 | TG | T | 37 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0013 others(34): Show |
41 | HG00738.hp1 HG01109.hp1 HG01243.hp1 others(38): Show |
intron_variant | MODIFIER | c.644+406delG | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41893703 | ||||||
| chr19:41893717 | GTCTGGGT others(109): Show |
G | 21 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0014 others(18): Show |
32 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(29): Show |
intron_variant | MODIFIER | c.644+415_645-374del | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893717 | |||||||
| chr19:41893718 | T | C | 49 | a0001c0001t0001g0121 a0001c0002t0001g0011 a0001c0002t0001g0012 others(46): Show |
53 | HG00738.hp1 HG01109.hp1 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.644+415T>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893718 | |||||||
| chr19:41893721 | GGGTCTGA others(108): Show |
G | 1 | a0001c0002t0001g0069 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.644+421_645-369del | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41893721 | ||||||
| chr19:41893742 | TG | T | 41 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0013 others(38): Show |
45 | HG00738.hp1 HG01109.hp1 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.644+445delG | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41893742 | ||||||
| chr19:41893755 | C | T | 1 | a0001c0002t0001g0066 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.644+452C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893755 | |||||||
| chr19:41893756 | G | T | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 |
3 | HG02818.hp2 HG02897.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.645-451G>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893756 | |||||||
| chr19:41893760 | G | A | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 |
3 | HG02818.hp2 HG02897.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.645-447G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893760 | |||||||
| chr19:41893777 | G | A | 38 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0013 others(35): Show |
42 | HG00738.hp1 HG01109.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.645-430G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893777 | |||||||
| chr19:41893781 | T | TGGGGGCC others(32): Show |
1 | a0001c0002t0001g0032 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.645-421_645-420ins others(39): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41893781 | ||||||
| chr19:41893782 | G | GGGGGCCT others(30): Show |
1 | a0001c0002t0001g0067 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.645-421_645-420ins others(37): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41893782 | ||||||
| chr19:41893788 | T | C | 53 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(50): Show |
57 | HG00738.hp1 HG01109.hp1 HG01243.hp1 others(54): Show |
intron_variant | MODIFIER | c.645-419T>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893788 | |||||||
| chr19:41893794 | C | T | 40 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0013 others(37): Show |
44 | HG00738.hp1 HG01109.hp1 HG01243.hp1 others(41): Show |
intron_variant | MODIFIER | c.645-413C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893794 | |||||||
| chr19:41893795 | T | G | 50 | a0001c0001t0001g0019 a0001c0001t0001g0121 a0001c0002t0001g0011 others(47): Show |
54 | HG00738.hp1 HG01109.hp1 HG01243.hp1 others(51): Show |
intron_variant | MODIFIER | c.645-412T>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893795 | |||||||
| chr19:41893799 | G | A | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 |
3 | HG02818.hp2 HG02897.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.645-408G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893799 | |||||||
| chr19:41893814 | G | A | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 |
3 | HG02818.hp2 HG02897.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.645-393G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893814 | |||||||
| chr19:41893814 | G | GGGGGCTG others(31): Show |
1 | a0001c0001t0001g0003 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.645-355_645-318dup others(38): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41893814 | ||||||
| chr19:41893814 | GGGGGCTG others(31): Show |
A | 1 | a0001c0002t0001g0066 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.645-393_645-356del others(38): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893814 | |||||||
| chr19:41893816 | G | A | 1 | a0001c0002t0001g0068 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.645-391G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893816 | |||||||
| chr19:41893817 | G | A | 1 | a0001c0003t0001g0022 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.645-390G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893817 | |||||||
| chr19:41893820 | T | TG | 49 | a0001c0001t0001g0121 a0001c0002t0001g0011 a0001c0002t0001g0012 others(46): Show |
53 | HG00738.hp1 HG01109.hp1 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.645-382dupG | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41893820 | ||||||
| chr19:41893832 | C | T | 1 | a0001c0002t0001g0068 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.645-375C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893832 | |||||||
| chr19:41893833 | T | G | 43 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0013 others(40): Show |
47 | HG00738.hp1 HG01109.hp1 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.645-374T>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893833 | |||||||
| chr19:41893834 | C | CCTAGGTC others(186): Show |
6 | a0001c0001t0001g0121 a0001c0003t0001g0025 a0001c0003t0001g0026 others(3): Show |
6 | HG02109.hp1 HG02922.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.645-371_645-370ins others(193): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41893834 | ||||||
| chr19:41893852 | A | G | 12 | a0001c0001t0001g0106 a0001c0001t0001g0121 a0001c0001t0001g0122 others(9): Show |
12 | HG01099.hp2 HG02109.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.645-355A>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893852 | |||||||
| chr19:41893854 | G | A | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 |
3 | HG02818.hp2 HG02897.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.645-353G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893854 | |||||||
| chr19:41893858 | T | TG | 7 | a0001c0001t0001g0121 a0001c0002t0001g0068 a0001c0003t0001g0025 others(4): Show |
7 | HG02109.hp1 HG02723.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.645-344dupG | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41893858 | ||||||
| chr19:41893858 | T | TGGGGGGC others(226): Show |
1 | a0001c0003t0001g0028 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.645-344_645-343ins others(233): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41893858 | ||||||
| chr19:41893864 | C | CCTGGACG others(110): Show |
3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 |
3 | HG02818.hp2 HG02897.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.645-337_645-336ins others(117): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41893864 | ||||||
| chr19:41893864 | C | G | 1 | a0001c0002t0001g0040 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.645-343C>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893864 | |||||||
| chr19:41893871 | T | G | 8 | a0001c0001t0001g0121 a0001c0002t0001g0068 a0001c0003t0001g0025 others(5): Show |
8 | HG02109.hp1 HG02723.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.645-336T>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893871 | |||||||
| chr19:41893890 | G | A | 6 | a0001c0001t0001g0003 a0001c0001t0001g0122 a0001c0001t0001g0123 others(3): Show |
6 | HG02109.hp2 HG02155.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.645-317G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893890 | |||||||
| chr19:41893892 | G | C | 30 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0011 others(27): Show |
42 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.645-315G>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893892 | |||||||
| chr19:41893896 | T | TG | 7 | a0001c0001t0001g0121 a0001c0003t0001g0025 a0001c0003t0001g0026 others(4): Show |
7 | HG02109.hp1 HG02922.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.645-306dupG | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41893896 | ||||||
| chr19:41893902 | C | T | 7 | a0001c0001t0001g0121 a0001c0003t0001g0025 a0001c0003t0001g0026 others(4): Show |
7 | HG02109.hp1 HG02922.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.645-305C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893902 | |||||||
| chr19:41893928 | G | A | 7 | a0001c0001t0001g0121 a0001c0003t0001g0025 a0001c0003t0001g0026 others(4): Show |
7 | HG02109.hp1 HG02922.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.645-279G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41893928 | |||||||
| chr19:41894006 | A | G | 1 | a0001c0002t0001g0046 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.645-201A>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41894006 | |||||||
| chr19:41894062 | G | A | 1 | a0001c0002t0001g0046 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.645-145G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41894062 | |||||||
| chr19:41894121 | A | AGAGAGAG others(101): Show |
1 | a0001c0001t0001g0121 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.645-83_645-82insAG others(106): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41894121 | ||||||
| chr19:41894123 | A | AGAGAGAG others(101): Show |
1 | a0001c0003t0001g0025 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.645-83_645-82insAG others(106): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41894123 | ||||||
| chr19:41894123 | A | AGAGAGAG others(107): Show |
4 | a0001c0003t0001g0027 a0001c0003t0001g0028 a0001c0003t0001g0029 others(1): Show |
4 | HG02109.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.645-83_645-82insAG others(112): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41894123 | ||||||
| chr19:41894123 | A | AGAGAGAG others(102): Show |
1 | a0001c0003t0001g0026 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.645-83_645-82insAG others(107): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41894123 | ||||||
| chr19:41894123 | A | AGAGAGAG others(101): Show |
1 | a0001c0001t0001g0123 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.645-83_645-82insAG others(106): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41894123 | ||||||
| chr19:41894123 | A | AGAGAGAG others(104): Show |
1 | a0001c0001t0001g0124 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.645-83_645-82insAG others(109): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41894123 | ||||||
| chr19:41894123 | A | AGAGAGAG others(103): Show |
1 | a0001c0001t0001g0122 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.645-83_645-82insAG others(108): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41894123 | ||||||
| chr19:41894123 | AGTGTGTG others(7): Show |
A | 2 | a0001c0002t0001g0036 a0001c0002t0001g0037 |
2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.645-72_645-59delAG others(12): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41894123 | ||||||
| chr19:41894131 | T | A | 4 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(1): Show |
4 | HG02818.hp2 HG02897.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.645-76T>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41894131 | |||||||
| chr19:41894135 | A | AGT | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG02735.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.645-41_645-40dupGT | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41894135 | ||||||
| chr19:41894135 | A | AGTGT | 58 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(55): Show |
88 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.645-43_645-40dupGT others(2): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41894135 | ||||||
| chr19:41894135 | A | AGTGTGT | 34 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(31): Show |
44 | HG00438.hp2 HG00609.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.645-45_645-40dupGT others(4): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41894135 | ||||||
| chr19:41894135 | A | AGTGTGTG others(1): Show |
16 | a0001c0001t0001g0126 a0001c0001t0001g0132 a0001c0001t0001g0139 others(13): Show |
17 | HG00597.hp1 HG01106.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.645-47_645-40dupGT others(6): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41894135 | ||||||
| chr19:41894135 | A | AGTGTGTG others(3): Show |
32 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0014 others(29): Show |
43 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.645-49_645-40dupGT others(8): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41894135 | ||||||
| chr19:41894135 | A | AGTGTGTG others(5): Show |
7 | a0001c0002t0001g0012 a0001c0002t0001g0058 a0001c0002t0001g0059 others(4): Show |
8 | HG00738.hp1 HG02027.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.645-51_645-40dupGT others(10): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41894135 | ||||||
| chr19:41894135 | A | AGTGTGTG others(7): Show |
9 | a0001c0002t0001g0013 a0001c0002t0001g0042 a0001c0002t0001g0047 others(6): Show |
10 | HG02109.hp2 HG02145.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.645-53_645-40dupGT others(12): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41894135 | ||||||
| chr19:41894135 | A | T | 5 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(2): Show |
5 | HG02818.hp2 HG02897.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.645-72A>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41894135 | |||||||
| chr19:41894137 | T | A | 1 | a0001c0001t0001g0121 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.645-70T>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41894137 | |||||||
| chr19:41894163 | T | TGTGTGTG others(4): Show |
1 | a0001c0002t0001g0069 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.645-40_645-39insGT others(9): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr19 | 41894163 | ||||||
| chr19:41894168 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.645-39C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41894168 | |||||||
| chr19:41894173 | T | A | 1 | a0001c0001t0001g0144 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.645-34T>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41894173 | |||||||
| chr19:41894180 | T | G | 1 | a0001c0001t0001g0144 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.645-27T>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41894180 | |||||||
| chr19:41894181 | G | C | 1 | a0001c0001t0001g0144 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.645-26G>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41894181 | |||||||
| chr19:41894185 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.645-22C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41894185 | |||||||
| chr19:41894187 | T | C | 1 | a0001c0001t0001g0144 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.645-20T>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41894187 | |||||||
| chr19:41894199 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA19086.hp2 | splice_region_variant&intron_variant | LOW | c.645-8C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 8/28 | chr19 | 41894199 | |||||||
| chr19:41894321 | G | C | 1 | a0001c0001t0001g0144 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.744+15G>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 9/28 | chr19 | 41894321 | |||||||
| chr19:41894322 | C | A | 1 | a0001c0001t0003g0129 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.744+16C>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 9/28 | chr19 | 41894322 | |||||||
| chr19:41894322 | C | G | 1 | a0001c0001t0001g0144 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.744+16C>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 9/28 | chr19 | 41894322 | |||||||
| chr19:41894377 | T | C | 72 | a0001c0001t0001g0121 a0001c0002t0001g0001 a0001c0002t0001g0007 others(69): Show |
87 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.744+71T>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 9/28 | chr19 | 41894377 | |||||||
| chr19:41894609 | A | T | 1 | a0001c0001t0001g0144 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.842-17A>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 10/28 | chr19 | 41894609 | |||||||
| chr19:41894610 | T | C | 1 | a0001c0001t0001g0144 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.842-16T>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 10/28 | chr19 | 41894610 | |||||||
| chr19:41894612 | C | A | 1 | a0001c0001t0001g0144 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.842-14C>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 10/28 | chr19 | 41894612 | |||||||
| chr19:41894619 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG00438.hp2 | splice_region_variant&intron_variant | LOW | c.842-7G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 10/28 | chr19 | 41894619 | |||||||
| chr19:41894732 | GTCTGAGG others(29): Show |
G | 62 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0011 others(59): Show |
77 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.877+88_877+123delC others(35): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr19 | 41894732 | ||||||
| chr19:41894747 | G | A | 10 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(7): Show |
10 | HG02109.hp1 HG02818.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.877+86G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 11/28 | chr19 | 41894747 | |||||||
| chr19:41894749 | C | A | 2 | a0001c0002t0001g0067 a0006c0009t0001g0023 |
2 | HG02109.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.877+88C>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 11/28 | chr19 | 41894749 | |||||||
| chr19:41894751 | GGGACCTG others(28): Show |
G | 1 | a0001c0002t0001g0067 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.877+93_877+127delA others(34): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr19 | 41894751 | ||||||
| chr19:41894754 | A | G | 1 | a0006c0009t0001g0023 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.877+93A>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 11/28 | chr19 | 41894754 | |||||||
| chr19:41894762 | G | A | 1 | a0006c0009t0001g0023 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.877+101G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 11/28 | chr19 | 41894762 | |||||||
| chr19:41894768 | T | C | 1 | a0006c0009t0001g0023 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.877+107T>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 11/28 | chr19 | 41894768 | |||||||
| chr19:41894799 | ACCTGGGT others(270): Show |
A | 4 | a0001c0003t0001g0027 a0001c0003t0001g0028 a0001c0003t0001g0029 others(1): Show |
4 | HG02109.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.877+170_878-242del | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr19 | 41894799 | ||||||
| chr19:41894856 | TGGGCCTG others(97): Show |
T | 70 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(67): Show |
85 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.877+215_877+318del | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr19 | 41894856 | ||||||
| chr19:41894924 | G | C | 1 | a0001c0001t0001g0144 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.877+263G>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 11/28 | chr19 | 41894924 | |||||||
| chr19:41894925 | C | G | 1 | a0001c0001t0001g0144 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.877+264C>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 11/28 | chr19 | 41894925 | |||||||
| chr19:41894999 | C | G | 1 | a0001c0002t0001g0076 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.877+338C>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 11/28 | chr19 | 41894999 | |||||||
| chr19:41895067 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.878-282G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 11/28 | chr19 | 41895067 | |||||||
| chr19:41895163 | A | C | 1 | a0001c0001t0001g0144 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.878-186A>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 11/28 | chr19 | 41895163 | |||||||
| chr19:41895556 | G | A | 64 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0011 others(61): Show |
79 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.1015+70G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 12/28 | chr19 | 41895556 | |||||||
| chr19:41895561 | C | T | 63 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0011 others(60): Show |
78 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.1015+75C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 12/28 | chr19 | 41895561 | |||||||
| chr19:41895618 | T | G | 1 | a0001c0002t0001g0065 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1015+132T>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 12/28 | chr19 | 41895618 | |||||||
| chr19:41895741 | C | T | 2 | a0001c0006t0001g0154 a0003c0011t0001g0155 |
2 | HG00099.hp2 HG00639.hp1 |
intron_variant | MODIFIER | c.1015+255C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 12/28 | chr19 | 41895741 | |||||||
| chr19:41895868 | C | G | 63 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0011 others(60): Show |
78 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.1015+382C>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 12/28 | chr19 | 41895868 | |||||||
| chr19:41895973 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1016-404C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 12/28 | chr19 | 41895973 | |||||||
| chr19:41896034 | A | G | 1 | a0006c0009t0001g0023 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1016-343A>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 12/28 | chr19 | 41896034 | |||||||
| chr19:41896185 | T | G | 4 | a0001c0001t0001g0121 a0001c0003t0001g0022 a0001c0003t0001g0025 others(1): Show |
4 | HG02976.hp2 HG03195.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1016-192T>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 12/28 | chr19 | 41896185 | |||||||
| chr19:41896234 | C | T | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 |
3 | HG02818.hp2 HG02897.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1016-143C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 12/28 | chr19 | 41896234 | |||||||
| chr19:41896261 | C | A | 1 | a0001c0002t0001g0083 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1016-116C>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 12/28 | chr19 | 41896261 | |||||||
| chr19:41896333 | G | GC | 75 | a0001c0001t0001g0087 a0001c0001t0001g0100 a0001c0001t0001g0138 others(72): Show |
90 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.1016-42dupC | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 12/28 | INFO_REALIGN_3_PRIME | chr19 | 41896333 | ||||||
| chr19:41896336 | G | A | 1 | a0001c0002t0001g0072 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1016-41G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 12/28 | chr19 | 41896336 | |||||||
| chr19:41896342 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1016-35G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 12/28 | chr19 | 41896342 | |||||||
| chr19:41896528 | G | A | 1 | a0001c0001t0001g0085 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1121+46G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41896528 | |||||||
| chr19:41896619 | G | C | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 |
3 | HG02818.hp2 HG02897.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1121+137G>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41896619 | |||||||
| chr19:41896656 | C | G | 7 | a0001c0003t0001g0022 a0001c0003t0001g0025 a0001c0003t0001g0026 others(4): Show |
7 | HG02109.hp1 HG02922.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.1121+174C>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41896656 | |||||||
| chr19:41896716 | C | T | 3 | a0001c0001t0001g0136 a0001c0001t0001g0153 a0001c0001t0001g0165 |
3 | HG01109.hp2 HG01192.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.1121+234C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41896716 | |||||||
| chr19:41896766 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1121+284A>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41896766 | |||||||
| chr19:41896787 | T | TCCCCCTC others(48): Show |
1 | a0001c0002t0001g0058 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1121+327_1121+328i others(57): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr19 | 41896787 | ||||||
| chr19:41896787 | T | TCCCCCTC others(105): Show |
3 | a0001c0002t0001g0012 a0001c0002t0001g0046 a0001c0002t0001g0082 |
4 | HG01884.hp1 HG03098.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1121+327_1121+328i others(114): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr19 | 41896787 | ||||||
| chr19:41896787 | T | TCCCCCTC others(143): Show |
1 | a0001c0002t0001g0083 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1121+327_1121+328i others(152): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr19 | 41896787 | ||||||
| chr19:41896787 | T | TCCCCCTC others(272): Show |
1 | a0001c0002t0001g0051 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1121+327_1121+328i others(281): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr19 | 41896787 | ||||||
| chr19:41896787 | T | TCCCCCTC others(31): Show |
1 | a0001c0002t0001g0128 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1121+310_1121+347d others(40): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr19 | 41896787 | ||||||
| chr19:41896787 | T | TCCCCCTC others(143): Show |
1 | a0001c0001t0001g0095 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1121+420_1121+421i others(152): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr19 | 41896787 | ||||||
| chr19:41896787 | T | TCCCCCTC others(217): Show |
2 | a0001c0002t0001g0063 a0001c0002t0001g0064 |
2 | HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1121+347_1121+348i others(226): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr19 | 41896787 | ||||||
| chr19:41896787 | T | TCCCCTCC others(49): Show |
1 | a0001c0003t0001g0028 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1121+309_1121+310i others(58): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr19 | 41896787 | ||||||
| chr19:41896787 | T | TCCCCTCC others(199): Show |
2 | a0001c0003t0001g0027 a0001c0003t0001g0029 |
2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1121+309_1121+310i others(208): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr19 | 41896787 | ||||||
| chr19:41896791 | C | CCTCCTCT others(162): Show |
12 | a0001c0002t0001g0013 a0001c0002t0001g0018 a0001c0002t0001g0031 others(9): Show |
14 | HG02145.hp2 HG02486.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.1121+327_1121+328i others(171): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr19 | 41896791 | ||||||
| chr19:41896791 | C | CCTCCTCT others(445): Show |
1 | a0001c0002t0001g0052 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1121+327_1121+328i others(454): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr19 | 41896791 | ||||||
| chr19:41896791 | C | CCTCCTCT others(86): Show |
1 | a0001c0001t0001g0130 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1121+332_1121+424d others(95): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr19 | 41896791 | ||||||
| chr19:41896791 | C | CT | 7 | a0001c0002t0001g0011 a0001c0002t0001g0038 a0001c0002t0001g0041 others(4): Show |
8 | HG01109.hp1 HG01243.hp1 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.1121+309_1121+310i others(3): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41896791 | |||||||
| chr19:41896791 | CCTCCTCT others(12): Show |
C | 1 | a0001c0003t0001g0022 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1121+328_1121+346d others(21): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr19 | 41896791 | ||||||
| chr19:41896792 | C | CTCCTCTC others(107): Show |
1 | a0001c0001t0001g0126 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1121+327_1121+328i others(116): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr19 | 41896792 | ||||||
| chr19:41896792 | CTCCTCTC others(31): Show |
C | 4 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0112 others(1): Show |
4 | HG00099.hp1 HG01099.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1121+328_1121+365d others(40): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr19 | 41896792 | ||||||
| chr19:41896796 | T | TCTCTCAC others(48): Show |
1 | a0001c0001t0001g0121 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1121+327_1121+328i others(57): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr19 | 41896796 | ||||||
| chr19:41896805 | T | TCCCCTCT others(13): Show |
1 | a0001c0002t0001g0083 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1121+328_1121+347d others(22): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr19 | 41896805 | ||||||
| chr19:41896810 | T | C | 2 | a0001c0001t0001g0126 a0001c0002t0001g0082 |
2 | HG02559.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1121+328T>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41896810 | |||||||
| chr19:41896810 | T | G | 1 | a0001c0001t0001g0121 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1121+328T>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41896810 | |||||||
| chr19:41896811 | CTCCTCTC others(12): Show |
C | 2 | a0001c0001t0001g0035 a0001c0002t0001g0056 |
2 | HG01261.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1121+348_1121+366d others(21): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr19 | 41896811 | ||||||
| chr19:41896814 | C | CTCTCTCA others(203): Show |
1 | a0001c0003t0001g0030 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1121+347_1121+348i others(212): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr19 | 41896814 | ||||||
| chr19:41896814 | C | T | 2 | a0001c0003t0001g0027 a0001c0003t0001g0029 |
2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1121+332C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41896814 | |||||||
| chr19:41896829 | C | T | 2 | a0001c0002t0001g0128 a0006c0009t0001g0023 |
2 | HG02055.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1121+347C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41896829 | |||||||
| chr19:41896830 | A | ATCCTCTC others(31): Show |
1 | a0001c0001t0001g0126 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1121+366_1121+367i others(40): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr19 | 41896830 | ||||||
| chr19:41896830 | A | ATCCTCTC others(12): Show |
2 | a0001c0001t0001g0162 a0001c0001t0001g0169 |
2 | NA19001.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1121+362_1121+380d others(21): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr19 | 41896830 | ||||||
| chr19:41896830 | A | ATCCTCTC others(86): Show |
1 | a0001c0001t0001g0124 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1121+381_1121+473d others(95): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr19 | 41896830 | ||||||
| chr19:41896830 | A | ATCCTCTC others(86): Show |
6 | a0001c0002t0001g0040 a0001c0002t0001g0055 a0001c0002t0001g0057 others(3): Show |
6 | HG02055.hp2 HG02723.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1121+380_1121+381i others(95): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr19 | 41896830 | ||||||
| chr19:41896830 | A | ATCCTCTC others(124): Show |
1 | a0001c0001t0001g0122 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1121+365_1121+366i others(133): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr19 | 41896830 | ||||||
| chr19:41896830 | A | C | 2 | a0001c0002t0001g0128 a0006c0009t0001g0023 |
2 | HG02055.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1121+348A>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41896830 | |||||||
| chr19:41896832 | C | T | 1 | a0001c0001t0001g0141 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1121+350C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41896832 | |||||||
| chr19:41896844 | C | CCCCCCTC others(85): Show |
1 | a0001c0001t0001g0123 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1121+368_1121+459d others(94): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr19 | 41896844 | ||||||
| chr19:41896844 | C | T | 1 | a0001c0002t0001g0012 | 2 | NA18522.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1121+362C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41896844 | |||||||
| chr19:41896849 | C | A | 1 | a0001c0001t0001g0126 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1121+367C>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41896849 | |||||||
| chr19:41896849 | C | CTCCTCTC others(102): Show |
1 | a0001c0003t0001g0025 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1121+401_1121+402i others(111): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr19 | 41896849 | ||||||
| chr19:41896850 | T | C | 1 | a0001c0002t0001g0043 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1121+368T>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41896850 | |||||||
| chr19:41896851 | C | T | 1 | a0001c0002t0001g0043 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1121+369C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41896851 | |||||||
| chr19:41896862 | TAC | T | 3 | a0001c0001t0001g0009 a0001c0001t0001g0116 a0001c0001t0001g0117 |
5 | HG02145.hp1 HG03098.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1121+381_1121+382d others(4): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41896862 | |||||||
| chr19:41896863 | A | C | 3 | a0001c0002t0001g0036 a0001c0002t0001g0037 a0006c0009t0001g0023 |
3 | HG02109.hp2 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1121+381A>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41896863 | |||||||
| chr19:41896869 | T | C | 1 | a0001c0001t0001g0159 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1121+387T>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41896869 | |||||||
| chr19:41896870 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1121+388C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41896870 | |||||||
| chr19:41896870 | CCTCTCAC others(46): Show |
C | 3 | a0001c0001t0001g0009 a0001c0001t0001g0116 a0001c0001t0001g0117 |
5 | HG02145.hp1 HG03098.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1121+389_1121+441d others(55): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41896870 | |||||||
| chr19:41896884 | G | C | 5 | a0001c0003t0001g0022 a0001c0003t0001g0027 a0001c0003t0001g0028 others(2): Show |
5 | HG02109.hp1 HG02922.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1121+402G>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41896884 | |||||||
| chr19:41896886 | T | C | 1 | a0001c0003t0001g0026 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1121+404T>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41896886 | |||||||
| chr19:41896889 | T | C | 1 | a0001c0003t0001g0026 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1121+407T>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41896889 | |||||||
| chr19:41896891 | T | C | 1 | a0001c0003t0001g0026 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1121+409T>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41896891 | |||||||
| chr19:41896936 | T | C | 3 | a0001c0002t0001g0043 a0002c0004t0001g0073 a0002c0004t0001g0074 |
3 | NA18940.hp2 NA18961.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1121+454T>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41896936 | |||||||
| chr19:41896937 | C | T | 1 | a0001c0002t0001g0043 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1121+455C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41896937 | |||||||
| chr19:41896943 | T | G | 2 | a0002c0004t0001g0073 a0002c0004t0001g0074 |
2 | NA18940.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1121+461T>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41896943 | |||||||
| chr19:41896989 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1121+507C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41896989 | |||||||
| chr19:41897106 | C | T | 1 | a0001c0002t0001g0078 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1121+624C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41897106 | |||||||
| chr19:41897123 | C | T | 2 | a0001c0001t0001g0105 a0001c0001t0001g0164 |
2 | HG03669.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.1121+641C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41897123 | |||||||
| chr19:41897132 | G | A | 1 | a0001c0001t0001g0141 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1121+650G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41897132 | |||||||
| chr19:41897348 | G | C | 1 | a0001c0001t0001g0145 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1121+866G>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41897348 | |||||||
| chr19:41897617 | C | T | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 |
3 | HG02818.hp2 HG02897.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1122-825C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41897617 | |||||||
| chr19:41897626 | A | T | 1 | a0001c0002t0001g0043 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1122-816A>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41897626 | |||||||
| chr19:41897755 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1122-687G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41897755 | |||||||
| chr19:41898021 | G | T | 1 | a0001c0001t0001g0020 | 2 | NA18970.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.1122-421G>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41898021 | |||||||
| chr19:41898117 | T | TGTCAACC others(275): Show |
1 | a0001c0001t0001g0131 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1122-323_1122-42du others(283): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | INFO_REALIGN_3_PRIME | chr19 | 41898117 | ||||||
| chr19:41898134 | C | T | 1 | a0001c0001t0001g0163 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1122-308C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 13/28 | chr19 | 41898134 | |||||||
| chr19:41899057 | A | C | 1 | a0001c0001t0001g0151 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1267+470A>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/28 | chr19 | 41899057 | |||||||
| chr19:41899058 | T | A | 1 | a0001c0001t0001g0151 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1267+471T>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/28 | chr19 | 41899058 | |||||||
| chr19:41899367 | A | G | 1 | a0006c0009t0001g0023 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1267+780A>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/28 | chr19 | 41899367 | |||||||
| chr19:41899458 | T | G | 78 | a0001c0001t0001g0086 a0001c0001t0001g0121 a0001c0001t0001g0122 others(75): Show |
93 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.1267+871T>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/28 | chr19 | 41899458 | |||||||
| chr19:41899505 | CT | C | 72 | a0001c0001t0001g0088 a0001c0001t0001g0096 a0001c0001t0001g0108 others(69): Show |
85 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1267+939delT | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/28 | INFO_REALIGN_3_PRIME | chr19 | 41899505 | ||||||
| chr19:41899505 | CTT | C | 5 | a0001c0002t0001g0007 a0001c0002t0001g0058 a0001c0002t0001g0063 others(2): Show |
7 | HG00738.hp1 HG02897.hp2 HG04204.hp2 others(4): Show |
intron_variant | MODIFIER | c.1267+938_1267+939d others(4): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/28 | INFO_REALIGN_3_PRIME | chr19 | 41899505 | ||||||
| chr19:41899526 | T | A | 1 | a0001c0001t0001g0101 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1267+939T>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/28 | chr19 | 41899526 | |||||||
| chr19:41899533 | G | C | 1 | a0001c0002t0001g0055 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1267+946G>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/28 | chr19 | 41899533 | |||||||
| chr19:41899573 | A | G | 75 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(72): Show |
90 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.1267+986A>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/28 | chr19 | 41899573 | |||||||
| chr19:41899920 | T | TA | 65 | a0001c0001t0001g0034 a0001c0001t0001g0090 a0001c0001t0001g0097 others(62): Show |
80 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.1267+1348dupA | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/28 | INFO_REALIGN_3_PRIME | chr19 | 41899920 | ||||||
| chr19:41899920 | TA | T | 7 | a0001c0001t0001g0115 a0001c0002t0001g0040 a0001c0002t0001g0055 others(4): Show |
7 | HG01884.hp2 HG02055.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1267+1348delA | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/28 | INFO_REALIGN_3_PRIME | chr19 | 41899920 | ||||||
| chr19:41900132 | G | A | 1 | a0006c0009t0001g0023 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1267+1545G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/28 | chr19 | 41900132 | |||||||
| chr19:41900191 | A | G | 166 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(163): Show |
218 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(215): Show |
intron_variant | MODIFIER | c.1267+1604A>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/28 | chr19 | 41900191 | |||||||
| chr19:41900786 | G | GT | 25 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0015 others(22): Show |
32 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.1268-1077dupT | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/28 | INFO_REALIGN_3_PRIME | chr19 | 41900786 | ||||||
| chr19:41900786 | GT | G | 8 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0098 others(5): Show |
8 | HG01257.hp2 HG01515.hp1 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.1268-1077delT | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/28 | INFO_REALIGN_3_PRIME | chr19 | 41900786 | ||||||
| chr19:41900786 | GTT | G | 12 | a0001c0002t0001g0014 a0001c0002t0001g0036 a0001c0002t0001g0043 others(9): Show |
13 | HG00438.hp1 HG02055.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1268-1078_1268-107 others(6): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/28 | INFO_REALIGN_3_PRIME | chr19 | 41900786 | ||||||
| chr19:41900786 | GTTT | G | 50 | a0001c0001t0001g0121 a0001c0002t0001g0001 a0001c0002t0001g0007 others(47): Show |
64 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.1268-1079_1268-107 others(7): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/28 | INFO_REALIGN_3_PRIME | chr19 | 41900786 | ||||||
| chr19:41900786 | GTTTT | G | 9 | a0001c0002t0001g0045 a0001c0002t0001g0081 a0001c0002t0001g0128 others(6): Show |
9 | HG02027.hp1 HG02055.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1268-1080_1268-107 others(8): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/28 | INFO_REALIGN_3_PRIME | chr19 | 41900786 | ||||||
| chr19:41900852 | G | A | 1 | a0002c0004t0001g0073 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1268-1035G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/28 | chr19 | 41900852 | |||||||
| chr19:41900853 | T | C | 74 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(71): Show |
89 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.1268-1034T>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/28 | chr19 | 41900853 | |||||||
| chr19:41900860 | C | G | 71 | a0001c0001t0001g0121 a0001c0002t0001g0001 a0001c0002t0001g0007 others(68): Show |
86 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.1268-1027C>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/28 | chr19 | 41900860 | |||||||
| chr19:41900939 | C | T | 1 | a0001c0001t0001g0104 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1268-948C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/28 | chr19 | 41900939 | |||||||
| chr19:41901051 | A | C | 1 | a0001c0001t0001g0158 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1268-836A>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/28 | chr19 | 41901051 | |||||||
| chr19:41901086 | G | T | 74 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(71): Show |
89 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.1268-801G>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/28 | chr19 | 41901086 | |||||||
| chr19:41901224 | A | G | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 |
3 | HG02818.hp2 HG02897.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1268-663A>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/28 | chr19 | 41901224 | |||||||
| chr19:41901245 | G | A | 1 | a0007c0010t0001g0161 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1268-642G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/28 | chr19 | 41901245 | |||||||
| chr19:41901298 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1268-589C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/28 | chr19 | 41901298 | |||||||
| chr19:41901573 | C | T | 1 | a0001c0003t0001g0022 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1268-314C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 14/28 | chr19 | 41901573 | |||||||
| chr19:41902376 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1497+20C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 16/28 | chr19 | 41902376 | |||||||
| chr19:41902415 | C | T | 1 | a0006c0009t0001g0023 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1497+59C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 16/28 | chr19 | 41902415 | |||||||
| chr19:41902419 | T | A | 2 | a0001c0002t0001g0053 a0001c0002t0001g0061 |
2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1497+63T>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 16/28 | chr19 | 41902419 | |||||||
| chr19:41902444 | C | T | 1 | a0001c0003t0001g0022 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1497+88C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 16/28 | chr19 | 41902444 | |||||||
| chr19:41902493 | T | C | 2 | a0001c0002t0001g0032 a0001c0002t0001g0033 |
2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1498-40T>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 16/28 | chr19 | 41902493 | |||||||
| chr19:41903093 | G | GT | 10 | a0001c0002t0001g0011 a0001c0002t0001g0038 a0001c0002t0001g0041 others(7): Show |
11 | HG01109.hp1 HG01243.hp1 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.1739-203dupT | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr19 | 41903093 | ||||||
| chr19:41903093 | GTT | G | 8 | a0001c0001t0001g0121 a0001c0003t0001g0025 a0001c0003t0001g0026 others(5): Show |
8 | HG02109.hp1 HG02109.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.1739-204_1739-203d others(4): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr19 | 41903093 | ||||||
| chr19:41903111 | G | A | 1 | a0006c0009t0001g0023 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1739-196G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 18/28 | chr19 | 41903111 | |||||||
| chr19:41903119 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1739-188G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 18/28 | chr19 | 41903119 | |||||||
| chr19:41903217 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1739-90C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 18/28 | chr19 | 41903217 | |||||||
| chr19:41903606 | G | A | 1 | a0001c0002t0001g0056 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1840-101G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 19/28 | chr19 | 41903606 | |||||||
| chr19:41903817 | C | G | 1 | a0006c0009t0001g0023 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1917+33C>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 20/28 | chr19 | 41903817 | |||||||
| chr19:41904000 | C | A | 1 | a0004c0005t0001g0089 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1918-35C>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 20/28 | chr19 | 41904000 | |||||||
| chr19:41904033 | A | T | 1 | a0004c0005t0001g0089 | 1 | HG00738.hp2 | splice_acceptor_variant&intron_variant | HIGH | c.1918-2A>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 20/28 | chr19 | 41904033 | |||||||
| chr19:41904212 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG02735.hp1 | splice_region_variant&intron_variant | LOW | c.1994-4G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 21/28 | chr19 | 41904212 | |||||||
| chr19:41904444 | T | C | 1 | a0001c0001t0001g0156 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2161+61T>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 22/28 | chr19 | 41904444 | |||||||
| chr19:41904639 | G | C | 1 | a0001c0001t0001g0085 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2161+256G>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 22/28 | chr19 | 41904639 | |||||||
| chr19:41904724 | C | T | 72 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(69): Show |
87 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.2162-225C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 22/28 | chr19 | 41904724 | |||||||
| chr19:41904797 | G | T | 1 | a0001c0002t0001g0050 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2162-152G>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 22/28 | chr19 | 41904797 | |||||||
| chr19:41904887 | T | C | 75 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(72): Show |
90 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.2162-62T>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 22/28 | chr19 | 41904887 | |||||||
| chr19:41905075 | G | A | 6 | a0001c0001t0001g0121 a0001c0003t0001g0025 a0001c0003t0001g0026 others(3): Show |
6 | HG02109.hp1 HG02922.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.2249+39G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 23/28 | chr19 | 41905075 | |||||||
| chr19:41905379 | G | A | 8 | a0001c0001t0001g0121 a0001c0003t0001g0025 a0001c0003t0001g0026 others(5): Show |
8 | HG02109.hp1 HG02109.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.2336+118G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 24/28 | chr19 | 41905379 | |||||||
| chr19:41905381 | G | A | 3 | a0001c0001t0001g0006 a0001c0001t0001g0090 a0001c0001t0001g0108 |
6 | HG01943.hp1 HG01978.hp2 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.2336+120G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 24/28 | chr19 | 41905381 | |||||||
| chr19:41905391 | ATG | A | 2 | a0001c0001t0001g0162 a0001c0001t0001g0169 |
2 | NA19001.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.2336+136_2336+137d others(4): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr19 | 41905391 | ||||||
| chr19:41905426 | CATAT | C | 2 | a0001c0003t0001g0025 a0001c0003t0001g0026 |
2 | HG03195.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2336+169_2336+172d others(6): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr19 | 41905426 | ||||||
| chr19:41905440 | GTA | G | 4 | a0001c0003t0001g0027 a0001c0003t0001g0028 a0001c0003t0001g0029 others(1): Show |
4 | HG02109.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2336+181_2336+182d others(4): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr19 | 41905440 | ||||||
| chr19:41905442 | A | G | 7 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(4): Show |
7 | HG02109.hp2 HG02818.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.2336+181A>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 24/28 | chr19 | 41905442 | |||||||
| chr19:41905457 | C | T | 6 | a0001c0001t0001g0094 a0001c0001t0001g0102 a0001c0001t0001g0122 others(3): Show |
6 | HG01257.hp1 HG01258.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.2336+196C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 24/28 | chr19 | 41905457 | |||||||
| chr19:41905460 | G | A | 1 | a0001c0002t0001g0075 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2336+199G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 24/28 | chr19 | 41905460 | |||||||
| chr19:41905473 | C | T | 1 | a0001c0003t0001g0022 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2336+212C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 24/28 | chr19 | 41905473 | |||||||
| chr19:41905480 | GGT | G | 9 | a0001c0001t0001g0097 a0001c0001t0001g0121 a0001c0003t0001g0025 others(6): Show |
9 | HG00423.hp1 HG02109.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.2336+228_2336+229d others(4): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr19 | 41905480 | ||||||
| chr19:41905542 | T | C | 1 | a0006c0009t0001g0023 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2337-218T>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 24/28 | chr19 | 41905542 | |||||||
| chr19:41905545 | G | A | 1 | a0001c0002t0001g0076 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2337-215G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 24/28 | chr19 | 41905545 | |||||||
| chr19:41905642 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2337-118C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 24/28 | chr19 | 41905642 | |||||||
| chr19:41905710 | G | A | 9 | a0001c0001t0001g0121 a0001c0003t0001g0022 a0001c0003t0001g0025 others(6): Show |
9 | HG02109.hp1 HG02109.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.2337-50G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 24/28 | chr19 | 41905710 | |||||||
| chr19:41905872 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2404+45C>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 25/28 | chr19 | 41905872 | |||||||
| chr19:41905934 | T | C | 8 | a0001c0001t0001g0121 a0001c0003t0001g0025 a0001c0003t0001g0026 others(5): Show |
8 | HG02109.hp1 HG02109.hp2 HG02922.hp1 others(5): Show |
splice_region_variant&intron_variant | LOW | c.2405-5T>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 25/28 | chr19 | 41905934 | |||||||
| chr19:41906174 | T | G | 1 | a0001c0001t0001g0165 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2491+149T>G | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 26/28 | chr19 | 41906174 | |||||||
| chr19:41906179 | G | A | 63 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0011 others(60): Show |
78 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.2491+154G>A | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 26/28 | chr19 | 41906179 | |||||||
| chr19:41906354 | A | C | 1 | a0004c0005t0001g0089 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2492-103A>C | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 26/28 | chr19 | 41906354 | |||||||
| chr19:41906831 | G | GCTGTCCT others(85): Show |
1 | a0004c0005t0001g0089 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.*17+41_*17+42insGA others(90): Show |
ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 28/28 | INFO_REALIGN_3_PRIME | chr19 | 41906831 | ||||||
| chr19:41906920 | A | T | 64 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0011 others(61): Show |
79 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.*17+117A>T | ARHGEF1 | ENSG00000076928.20 | transcript | ENST00000354532.8 | protein_coding | 28/28 | chr19 | 41906920 |