Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 389337 |
| ensemblid | ENSG00000183111.12 |
| hgncid | 34430 |
| symbol | ARHGEF37 |
| name | Rho guanine nucleotide exchange factor 37 |
| refseq_nuc | NM_001001669.3 |
| refseq_prot | NP_001001669.2 |
| ensembl_nuc | ENST00000333677.7 |
| ensembl_prot | ENSP00000328083.6 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 149581498 |
| end | 149634968 |
| strand | + |
| ver | v1.2 |
| region | chr5:149581498-149634968 |
| region5000 | chr5:149576498-149639968 |
| regionname0 | ARHGEF37_chr5_149581498_149634968 |
| regionname5000 | ARHGEF37_chr5_149576498_149639968 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 675 | 96 | 17 | 14 | 42 | 11 | 12 | 36 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | MAKHG others(670): Show |
chr5 | 149576498 | 149639968 |
| a0002 | 0/1 | 675 | 74 | 5 | 21 | 33 | 4 | 10 | 24 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | MAKHG others(670): Show |
chr5 | 149576498 | 149639968 |
| a0003 | 0/0 | 675 | 67 | 2 | 10 | 52 | 2 | 1 | 40 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | MAKHG others(670): Show |
chr5 | 149576498 | 149639968 |
| a0004 | 0/0 | 675 | 55 | 23 | 4 | 23 | 1 | 4 | 18 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | MAKHG others(670): Show |
chr5 | 149576498 | 149639968 |
| a0005 | 0/0 | 675 | 24 | 7 | 0 | 16 | 0 | 1 | 13 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | MAKHG others(670): Show |
chr5 | 149576498 | 149639968 |
| a0006 | 0/0 | 675 | 18 | 18 | 0 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | MAKHG others(670): Show |
chr5 | 149576498 | 149639968 |
| a0007 | 0/0 | 675 | 14 | 0 | 0 | 14 | 0 | 0 | 12 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | MAKHG others(670): Show |
chr5 | 149576498 | 149639968 |
| a0008 | 0/0 | 675 | 11 | 9 | 2 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | MAKHG others(670): Show |
chr5 | 149576498 | 149639968 |
| a0009 | 0/0 | 675 | 9 | 6 | 3 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | MAKHG others(670): Show |
chr5 | 149576498 | 149639968 |
| a0010 | 0/0 | 675 | 4 | 1 | 3 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | MAKHG others(670): Show |
chr5 | 149576498 | 149639968 |
| a0011 | 0/0 | 675 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | MAKHG others(670): Show |
chr5 | 149576498 | 149639968 |
| a0012 | 0/0 | 675 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | MAKHG others(670): Show |
chr5 | 149576498 | 149639968 |
| a0013 | 0/0 | 675 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | MAKHG others(670): Show |
chr5 | 149576498 | 149639968 |
| a0014 | 0/0 | 675 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | MAKHG others(670): Show |
chr5 | 149576498 | 149639968 |
| a0015 | 0/0 | 675 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | MAKHG others(670): Show |
chr5 | 149576498 | 149639968 |
| a0016 | 0/0 | 675 | 2 | 0 | 0 | 1 | 0 | 1 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | MAKHG others(670): Show |
chr5 | 149576498 | 149639968 |
| a0017 | 0/0 | 675 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | MAKHG others(670): Show |
chr5 | 149576498 | 149639968 |
| a0018 | 0/0 | 675 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | MAKHG others(670): Show |
chr5 | 149576498 | 149639968 |
| a0019 | 1/0 | 675 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | MAKHG others(670): Show |
chr5 | 149576498 | 149639968 |
| a0020 | 0/0 | 320 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | MAKHG others(315): Show |
chr5 | 149576498 | 149639968 |
| a0021 | 0/0 | 675 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | MAKHG others(670): Show |
chr5 | 149576498 | 149639968 |
| a0022 | 0/0 | 675 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | MAKHG others(670): Show |
chr5 | 149576498 | 149639968 |
| a0023 | 0/0 | 675 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | MAKHG others(670): Show |
chr5 | 149576498 | 149639968 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 0/0 | 2025 | 61 | 9 | 3 | 41 | 4 | 4 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | ATGGC others(2020): Show |
chr5 | 149576498 | 149639968 | ||
| a0001c0005 | 0/0 | 2025 | 34 | 8 | 11 | 0 | 7 | 8 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | ATGGC others(2020): Show |
chr5 | 149576498 | 149639968 | ||
| a0001c0030 | 0/0 | 2025 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | ATGGC others(2020): Show |
chr5 | 149576498 | 149639968 | ||
| a0002c0001 | 0/1 | 2025 | 72 | 5 | 20 | 33 | 4 | 9 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | ATGGC others(2020): Show |
chr5 | 149576498 | 149639968 | ||
| a0002c0024 | 0/0 | 2025 | 2 | 0 | 1 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | ATGGC others(2020): Show |
chr5 | 149576498 | 149639968 | ||
| a0003c0003 | 0/0 | 2025 | 60 | 2 | 10 | 46 | 2 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | ATGGC others(2020): Show |
chr5 | 149576498 | 149639968 | ||
| a0003c0012 | 0/0 | 2025 | 6 | 0 | 0 | 5 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | ATGGC others(2020): Show |
chr5 | 149576498 | 149639968 | ||
| a0003c0029 | 0/0 | 2025 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | ATGGC others(2020): Show |
chr5 | 149576498 | 149639968 | ||
| a0004c0004 | 0/0 | 2025 | 47 | 16 | 4 | 22 | 1 | 4 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | ATGGC others(2020): Show |
chr5 | 149576498 | 149639968 | ||
| a0004c0010 | 0/0 | 2025 | 7 | 7 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | ATGGC others(2020): Show |
chr5 | 149576498 | 149639968 | ||
| a0004c0036 | 0/0 | 2025 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | ATGGC others(2020): Show |
chr5 | 149576498 | 149639968 | ||
| a0005c0007 | 0/0 | 2025 | 15 | 0 | 0 | 14 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | ATGGC others(2020): Show |
chr5 | 149576498 | 149639968 | ||
| a0005c0011 | 0/0 | 2025 | 6 | 6 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | ATGGC others(2020): Show |
chr5 | 149576498 | 149639968 | ||
| a0005c0027 | 0/0 | 2025 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | ATGGC others(2020): Show |
chr5 | 149576498 | 149639968 | ||
| a0005c0033 | 0/0 | 2025 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | ATGGC others(2020): Show |
chr5 | 149576498 | 149639968 | ||
| a0005c0035 | 0/0 | 2025 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | ATGGC others(2020): Show |
chr5 | 149576498 | 149639968 | ||
| a0006c0006 | 0/0 | 2025 | 16 | 16 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | ATGGC others(2020): Show |
chr5 | 149576498 | 149639968 | ||
| a0006c0023 | 0/0 | 2025 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | ATGGC others(2020): Show |
chr5 | 149576498 | 149639968 | ||
| a0007c0008 | 0/0 | 2025 | 14 | 0 | 0 | 14 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | ATGGC others(2020): Show |
chr5 | 149576498 | 149639968 | ||
| a0008c0009 | 0/0 | 2025 | 8 | 6 | 2 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | ATGGC others(2020): Show |
chr5 | 149576498 | 149639968 | ||
| a0008c0017 | 0/0 | 2025 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | ATGGC others(2020): Show |
chr5 | 149576498 | 149639968 | ||
| a0009c0013 | 0/0 | 2025 | 5 | 2 | 3 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | ATGGC others(2020): Show |
chr5 | 149576498 | 149639968 | ||
| a0009c0014 | 0/0 | 2025 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | ATGGC others(2020): Show |
chr5 | 149576498 | 149639968 | ||
| a0010c0015 | 0/0 | 2025 | 4 | 1 | 3 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | ATGGC others(2020): Show |
chr5 | 149576498 | 149639968 | ||
| a0011c0016 | 0/0 | 2025 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | ATGGC others(2020): Show |
chr5 | 149576498 | 149639968 | ||
| a0012c0026 | 0/0 | 2025 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | ATGGC others(2020): Show |
chr5 | 149576498 | 149639968 | ||
| a0013c0022 | 0/0 | 2025 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | ATGGC others(2020): Show |
chr5 | 149576498 | 149639968 | ||
| a0014c0025 | 0/0 | 2025 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | ATGGC others(2020): Show |
chr5 | 149576498 | 149639968 | ||
| a0015c0020 | 0/0 | 2025 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | ATGGC others(2020): Show |
chr5 | 149576498 | 149639968 | ||
| a0016c0019 | 0/0 | 2025 | 2 | 0 | 0 | 1 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | ATGGC others(2020): Show |
chr5 | 149576498 | 149639968 | ||
| a0017c0021 | 0/0 | 2025 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | ATGGC others(2020): Show |
chr5 | 149576498 | 149639968 | ||
| a0018c0018 | 0/0 | 2025 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | ATGGC others(2020): Show |
chr5 | 149576498 | 149639968 | ||
| a0019c0028 | 1/0 | 2025 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | ATGGC others(2020): Show |
chr5 | 149576498 | 149639968 | ||
| a0020c0034 | 0/0 | 2025 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | ATGGC others(2020): Show |
chr5 | 149576498 | 149639968 | ||
| a0021c0037 | 0/0 | 2025 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | ATGGC others(2020): Show |
chr5 | 149576498 | 149639968 | ||
| a0022c0031 | 0/0 | 2025 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | ATGGC others(2020): Show |
chr5 | 149576498 | 149639968 | ||
| a0023c0032 | 0/0 | 2025 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | ATGGC others(2020): Show |
chr5 | 149576498 | 149639968 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0004 | 0/0 | 4943 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0001c0002t0005 | 0/0 | 4943 | 4 | 0 | 0 | 0 | 2 | 2 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0001c0002t0006 | 0/0 | 4943 | 31 | 1 | 2 | 24 | 2 | 2 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0001c0002t0008 | 0/0 | 4943 | 13 | 1 | 0 | 12 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0001c0002t0010 | 0/0 | 4943 | 5 | 0 | 0 | 5 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0001c0002t0011 | 0/0 | 4943 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0001c0002t0015 | 0/0 | 4943 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0001c0002t0020 | 0/0 | 4943 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0001c0002t0027 | 0/0 | 4943 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0001c0005t0004 | 0/0 | 4943 | 6 | 6 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0001c0005t0005 | 0/0 | 4943 | 25 | 1 | 9 | 0 | 7 | 8 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0001c0005t0019 | 0/0 | 4943 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0001c0005t0029 | 0/0 | 4943 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0001c0030t0006 | 0/0 | 4943 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0002c0001t0001 | 0/1 | 4943 | 62 | 2 | 16 | 32 | 3 | 8 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0002c0001t0003 | 0/0 | 4943 | 9 | 2 | 4 | 1 | 1 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0002c0001t0018 | 0/0 | 4943 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0002c0024t0003 | 0/0 | 4943 | 2 | 0 | 1 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0003c0003t0002 | 0/0 | 4943 | 55 | 2 | 9 | 42 | 2 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0003c0003t0008 | 0/0 | 4943 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0003c0003t0012 | 0/0 | 4943 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0003c0003t0016 | 0/0 | 4943 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0003c0003t0018 | 0/0 | 4943 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0003c0012t0002 | 0/0 | 4943 | 5 | 0 | 0 | 4 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0003c0012t0012 | 0/0 | 4943 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0003c0029t0002 | 0/0 | 4943 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0004c0004t0002 | 0/0 | 4943 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0004c0004t0004 | 0/0 | 4943 | 32 | 5 | 4 | 20 | 1 | 2 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0004c0004t0009 | 0/0 | 4943 | 10 | 10 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0004c0004t0024 | 0/0 | 4943 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0004c0004t0028 | 0/0 | 4943 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0004c0004t0030 | 0/0 | 4943 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0004c0004t0033 | 0/0 | 4943 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0004c0010t0009 | 0/0 | 4943 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0004c0010t0014 | 0/0 | 4943 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0004c0010t0022 | 0/0 | 4943 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0004c0036t0004 | 0/0 | 4943 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0005c0007t0003 | 0/0 | 4943 | 15 | 0 | 0 | 14 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0005c0011t0001 | 0/0 | 4943 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0005c0011t0003 | 0/0 | 4943 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0005c0027t0003 | 0/0 | 4943 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0005c0033t0003 | 0/0 | 4943 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0005c0035t0003 | 0/0 | 4943 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0006c0006t0007 | 0/0 | 4943 | 14 | 14 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0006c0006t0032 | 0/0 | 4943 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0006c0006t0034 | 0/0 | 4943 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0006c0023t0007 | 0/0 | 4943 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0007c0008t0001 | 0/0 | 4943 | 10 | 0 | 0 | 10 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0007c0008t0003 | 0/0 | 4943 | 4 | 0 | 0 | 4 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0008c0009t0002 | 0/0 | 4943 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0008c0009t0003 | 0/0 | 4943 | 5 | 3 | 2 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0008c0009t0025 | 0/0 | 4943 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0008c0009t0026 | 0/0 | 4943 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0008c0017t0013 | 0/0 | 4943 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0008c0017t0031 | 0/0 | 4943 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0009c0013t0011 | 0/0 | 4943 | 3 | 1 | 2 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0009c0013t0021 | 0/0 | 4943 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0009c0014t0011 | 0/0 | 4943 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0009c0014t0023 | 0/0 | 4943 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0009c0014t0035 | 0/0 | 4943 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0010c0015t0005 | 0/0 | 4943 | 4 | 1 | 3 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0011c0016t0012 | 0/0 | 4943 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0012c0026t0003 | 0/0 | 4943 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0013c0022t0004 | 0/0 | 4943 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0014c0025t0013 | 0/0 | 4943 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0015c0020t0017 | 0/0 | 4943 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0016c0019t0002 | 0/0 | 4943 | 2 | 0 | 0 | 1 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0017c0021t0006 | 0/0 | 4943 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0018c0018t0001 | 0/0 | 4943 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0019c0028t0003 | 1/0 | 4943 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0020c0034t0005 | 0/0 | 4943 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0021c0037t0003 | 0/0 | 4943 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0022c0031t0001 | 0/0 | 4943 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| a0023c0032t0009 | 0/0 | 4943 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | GGGCA others(4938): Show |
chr5 | 149576498 | 149639968 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0004g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0005g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0005g0358 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0005g0359 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0005g0363 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0006g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0006g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0006g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0006g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0006g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0006g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0006g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0006g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0006g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0006g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0006g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0006g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0006g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0006g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0006g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0006g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0006g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0006g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0006g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0006g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0006g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0006g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0006g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0006g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0006g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0006g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0006g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0006g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0006g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0006g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0008g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0008g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0008g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0008g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0008g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0008g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0008g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0008g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0008g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0008g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0008g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0010g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0010g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0010g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0010g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0011g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0015g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0015g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0015g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0020g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0020g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0002t0027g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0005t0004g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0005t0004g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0005t0004g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0005t0004g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0005t0004g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0005t0004g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0005t0005g0003 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0005t0005g0004 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0005t0005g0011 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0005t0005g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0005t0005g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0005t0005g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0005t0005g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0005t0005g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0005t0005g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0005t0005g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0005t0005g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0005t0005g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0005t0005g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0005t0005g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0005t0005g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0005t0005g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0005t0005g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0005t0005g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0005t0005g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0005t0005g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0005t0005g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0005t0019g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0005t0019g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0005t0029g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0001c0030t0006g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0002 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0046 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0003g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0003g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0003g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0003g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0003g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0001t0018g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0024t0003g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0002c0024t0003g0367 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0001 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0018 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0336 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0002g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0008g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0012g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0016g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0016g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0003t0018g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0012t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0012t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0012t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0012t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0012t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0012t0012g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0003c0029t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0004g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0004g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0004g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0004g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0004g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0004g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0004g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0004g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0004g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0004g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0004g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0004g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0004g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0004g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0004g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0004g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0004g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0004g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0004g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0004g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0004g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0004g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0004g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0004g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0004g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0004g0362 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0004g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0004g0365 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0009g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0009g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0009g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0009g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0009g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0009g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0009g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0009g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0009g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0024g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0028g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0030g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0004t0033g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0010t0009g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0010t0009g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0010t0014g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0010t0014g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0010t0014g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0010t0022g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0010t0022g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0004c0036t0004g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0005c0007t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0005c0007t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0005c0007t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0005c0007t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0005c0007t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0005c0007t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0005c0007t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0005c0007t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0005c0007t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0005c0007t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0005c0007t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0005c0007t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0005c0007t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0005c0007t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0005c0007t0003g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0005c0011t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0005c0011t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0005c0011t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0005c0011t0003g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0005c0011t0003g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0005c0011t0003g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0005c0027t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0005c0033t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0005c0035t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0006c0006t0007g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0006c0006t0007g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0006c0006t0007g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0006c0006t0007g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0006c0006t0007g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0006c0006t0007g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0006c0006t0007g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0006c0006t0007g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0006c0006t0007g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0006c0006t0007g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0006c0006t0007g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0006c0006t0007g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0006c0006t0007g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0006c0006t0007g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0006c0006t0032g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0006c0006t0034g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0006c0023t0007g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0006c0023t0007g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0007c0008t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0007c0008t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0007c0008t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0007c0008t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0007c0008t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0007c0008t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0007c0008t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0007c0008t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0007c0008t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0007c0008t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0007c0008t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0007c0008t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0007c0008t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0007c0008t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0008c0009t0002g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0008c0009t0003g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0008c0009t0003g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0008c0009t0003g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0008c0009t0003g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0008c0009t0003g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0008c0009t0025g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0008c0009t0026g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0008c0017t0013g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0008c0017t0013g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0008c0017t0031g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0009c0013t0011g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0009c0013t0011g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0009c0013t0021g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0009c0013t0021g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0009c0014t0011g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0009c0014t0023g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0009c0014t0035g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0010c0015t0005g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0010c0015t0005g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0010c0015t0005g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0010c0015t0005g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0011c0016t0012g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0011c0016t0012g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0011c0016t0012g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0012c0026t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0012c0026t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0013c0022t0004g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0013c0022t0004g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0014c0025t0013g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0014c0025t0013g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0015c0020t0017g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0015c0020t0017g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0016c0019t0002g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0016c0019t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0017c0021t0006g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0017c0021t0006g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0018c0018t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0018c0018t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0019c0028t0003g0194 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0020c0034t0005g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0021c0037t0003g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0022c0031t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| a0023c0032t0009g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0005 | t0005 | g0011 | EUR | GBR | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00099 | hp2 | a0003 | c0003 | t0002 | g0018 | EUR | GBR | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00140 | hp1 | a0003 | c0003 | t0002 | g0336 | EUR | GBR | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00140 | hp2 | a0002 | c0001 | t0001 | g0054 | EUR | GBR | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00280 | hp1 | a0001 | c0005 | t0005 | g0187 | EUR | FIN | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00280 | hp2 | a0004 | c0004 | t0004 | g0362 | EUR | FIN | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00323 | hp1 | a0002 | c0001 | t0003 | g0214 | EUR | FIN | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00323 | hp2 | a0001 | c0005 | t0005 | g0191 | EUR | FIN | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00408 | hp1 | a0003 | c0029 | t0002 | g0271 | EAS | CHS | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00408 | hp2 | a0001 | c0002 | t0006 | g0125 | EAS | CHS | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00423 | hp1 | a0003 | c0003 | t0002 | g0291 | EAS | CHS | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00423 | hp2 | a0002 | c0001 | t0001 | g0048 | EAS | CHS | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00438 | hp1 | a0004 | c0036 | t0004 | g0235 | EAS | CHS | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00438 | hp2 | a0003 | c0003 | t0002 | g0307 | EAS | CHS | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00544 | hp1 | a0001 | c0002 | t0008 | g0253 | EAS | CHS | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00544 | hp2 | a0002 | c0001 | t0003 | g0166 | EAS | CHS | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00558 | hp1 | a0012 | c0026 | t0003 | g0233 | EAS | CHS | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00558 | hp2 | a0002 | c0001 | t0001 | g0032 | EAS | CHS | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00597 | hp1 | a0005 | c0007 | t0003 | g0152 | EAS | CHS | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00597 | hp2 | a0004 | c0004 | t0004 | g0247 | EAS | CHS | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00609 | hp1 | a0005 | c0007 | t0003 | g0161 | EAS | CHS | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00609 | hp2 | a0002 | c0001 | t0001 | g0035 | EAS | CHS | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00621 | hp1 | a0007 | c0008 | t0001 | g0100 | EAS | CHS | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00621 | hp2 | a0003 | c0003 | t0016 | g0288 | EAS | CHS | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00639 | hp1 | a0001 | c0005 | t0005 | g0003 | AMR | PUR | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00639 | hp2 | a0002 | c0001 | t0003 | g0360 | AMR | PUR | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00673 | hp1 | a0013 | c0022 | t0004 | g0331 | EAS | CHS | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00673 | hp2 | a0002 | c0001 | t0001 | g0034 | EAS | CHS | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00735 | hp1 | a0008 | c0009 | t0003 | g0315 | AMR | PUR | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00735 | hp2 | a0003 | c0003 | t0002 | g0321 | AMR | PUR | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00738 | hp1 | a0001 | c0002 | t0006 | g0106 | AMR | PUR | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00738 | hp2 | a0001 | c0002 | t0020 | g0135 | AMR | PUR | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00741 | hp1 | a0002 | c0001 | t0001 | g0132 | AMR | PUR | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG00741 | hp2 | a0001 | c0005 | t0005 | g0195 | AMR | PUR | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01069 | hp1 | a0003 | c0003 | t0002 | g0277 | AMR | PUR | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01069 | hp2 | a0009 | c0013 | t0011 | g0017 | AMR | PUR | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01071 | hp1 | a0009 | c0013 | t0011 | g0017 | AMR | PUR | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01071 | hp2 | a0001 | c0005 | t0005 | g0004 | AMR | PUR | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01074 | hp1 | a0004 | c0004 | t0004 | g0364 | AMR | PUR | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01074 | hp2 | a0001 | c0005 | t0005 | g0003 | AMR | PUR | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01081 | hp1 | a0002 | c0001 | t0003 | g0290 | AMR | PUR | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01081 | hp2 | a0003 | c0003 | t0002 | g0246 | AMR | PUR | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01099 | hp1 | a0002 | c0001 | t0001 | g0065 | AMR | PUR | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01099 | hp2 | a0001 | c0005 | t0005 | g0190 | AMR | PUR | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01106 | hp1 | a0001 | c0005 | t0019 | g0193 | AMR | PUR | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01106 | hp2 | a0003 | c0003 | t0018 | g0335 | AMR | PUR | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01167 | hp1 | a0001 | c0005 | t0005 | g0203 | AMR | PUR | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01167 | hp2 | a0014 | c0025 | t0013 | g0260 | AMR | PUR | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01169 | hp1 | a0020 | c0034 | t0005 | g0004 | AMR | PUR | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01169 | hp2 | a0014 | c0025 | t0013 | g0261 | AMR | PUR | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01175 | hp1 | a0002 | c0001 | t0003 | g0343 | AMR | PUR | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01175 | hp2 | a0003 | c0003 | t0002 | g0337 | AMR | PUR | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01243 | hp1 | a0009 | c0013 | t0021 | g0108 | AMR | PUR | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01243 | hp2 | a0004 | c0004 | t0004 | g0179 | AMR | PUR | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01255 | hp1 | a0002 | c0001 | t0001 | g0039 | AMR | CLM | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01255 | hp2 | a0001 | c0005 | t0005 | g0198 | AMR | CLM | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01256 | hp1 | a0010 | c0015 | t0005 | g0182 | AMR | CLM | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01256 | hp2 | a0002 | c0001 | t0001 | g0064 | AMR | CLM | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01257 | hp1 | a0003 | c0003 | t0002 | g0366 | AMR | CLM | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01257 | hp2 | a0004 | c0004 | t0004 | g0020 | AMR | CLM | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01258 | hp1 | a0004 | c0004 | t0004 | g0020 | AMR | CLM | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01258 | hp2 | a0010 | c0015 | t0005 | g0183 | AMR | CLM | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01261 | hp1 | a0002 | c0001 | t0001 | g0075 | AMR | CLM | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01261 | hp2 | a0001 | c0002 | t0006 | g0130 | AMR | CLM | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01346 | hp1 | a0002 | c0001 | t0001 | g0007 | AMR | CLM | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01346 | hp2 | a0001 | c0005 | t0005 | g0245 | AMR | CLM | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01358 | hp1 | a0001 | c0005 | t0019 | g0188 | AMR | CLM | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01358 | hp2 | a0002 | c0001 | t0001 | g0007 | AMR | CLM | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01361 | hp1 | a0002 | c0001 | t0001 | g0133 | AMR | CLM | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01361 | hp2 | a0003 | c0003 | t0002 | g0018 | AMR | CLM | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01433 | hp1 | a0002 | c0001 | t0001 | g0080 | AMR | CLM | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01433 | hp2 | a0002 | c0001 | t0001 | g0002 | AMR | CLM | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01496 | hp1 | a0008 | c0009 | t0003 | g0311 | AMR | CLM | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01496 | hp2 | a0002 | c0001 | t0001 | g0023 | AMR | CLM | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01515 | hp1 | a0002 | c0001 | t0001 | g0081 | EUR | IBS | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01515 | hp2 | a0001 | c0005 | t0005 | g0199 | EUR | IBS | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01516 | hp1 | a0001 | c0002 | t0006 | g0129 | EUR | IBS | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01516 | hp2 | a0001 | c0002 | t0005 | g0358 | EUR | IBS | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01517 | hp1 | a0001 | c0002 | t0006 | g0127 | EUR | IBS | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01517 | hp2 | a0002 | c0001 | t0001 | g0076 | EUR | IBS | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01884 | hp1 | a0004 | c0010 | t0022 | g0045 | AFR | ACB | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01884 | hp2 | a0004 | c0004 | t0009 | g0015 | AFR | ACB | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01891 | hp1 | a0001 | c0005 | t0005 | g0011 | AFR | ACB | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01891 | hp2 | a0015 | c0020 | t0017 | g0176 | AFR | ACB | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01934 | hp1 | a0010 | c0015 | t0005 | g0201 | AMR | PEL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01934 | hp2 | a0002 | c0001 | t0001 | g0072 | AMR | PEL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01943 | hp1 | a0002 | c0001 | t0003 | g0215 | AMR | PEL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01943 | hp2 | a0001 | c0005 | t0005 | g0192 | AMR | PEL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01952 | hp1 | a0003 | c0003 | t0002 | g0275 | AMR | PEL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01952 | hp2 | a0002 | c0001 | t0001 | g0060 | AMR | PEL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01975 | hp1 | a0003 | c0003 | t0002 | g0001 | AMR | PEL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01975 | hp2 | a0002 | c0001 | t0001 | g0024 | AMR | PEL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01978 | hp1 | a0003 | c0003 | t0002 | g0001 | AMR | PEL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01978 | hp2 | a0002 | c0001 | t0001 | g0067 | AMR | PEL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01993 | hp1 | a0002 | c0001 | t0001 | g0002 | AMR | PEL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG01993 | hp2 | a0002 | c0024 | t0003 | g0205 | AMR | PEL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02015 | hp1 | a0003 | c0003 | t0002 | g0332 | EAS | KHV | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02015 | hp2 | a0003 | c0012 | t0002 | g0162 | EAS | KHV | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02027 | hp1 | a0011 | c0016 | t0012 | g0058 | EAS | KHV | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02027 | hp2 | a0005 | c0007 | t0003 | g0155 | EAS | KHV | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02040 | hp1 | a0001 | c0002 | t0008 | g0169 | EAS | KHV | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02040 | hp2 | a0003 | c0003 | t0002 | g0005 | EAS | KHV | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02055 | hp1 | a0001 | c0005 | t0004 | g0212 | AFR | ACB | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02055 | hp2 | a0004 | c0004 | t0009 | g0265 | AFR | ACB | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02071 | hp1 | a0001 | c0002 | t0006 | g0118 | EAS | KHV | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02071 | hp2 | a0002 | c0001 | t0001 | g0111 | EAS | KHV | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02074 | hp1 | a0007 | c0008 | t0001 | g0101 | EAS | KHV | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02074 | hp2 | a0003 | c0003 | t0002 | g0016 | EAS | KHV | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02129 | hp1 | a0001 | c0002 | t0006 | g0112 | EAS | KHV | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02129 | hp2 | a0013 | c0022 | t0004 | g0357 | EAS | KHV | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02132 | hp1 | a0016 | c0019 | t0002 | g0294 | EAS | KHV | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02132 | hp2 | a0004 | c0004 | t0004 | g0238 | EAS | KHV | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02135 | hp1 | a0001 | c0002 | t0006 | g0050 | EAS | KHV | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02135 | hp2 | a0003 | c0003 | t0012 | g0053 | EAS | KHV | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02145 | hp1 | a0004 | c0004 | t0004 | g0241 | AFR | ACB | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02145 | hp2 | a0002 | c0001 | t0018 | g0269 | AFR | ACB | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02155 | hp1 | a0004 | c0004 | t0004 | g0222 | EAS | CDX | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02155 | hp2 | a0003 | c0003 | t0002 | g0285 | EAS | CDX | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02257 | hp1 | a0004 | c0004 | t0004 | g0338 | AFR | ACB | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02257 | hp2 | a0010 | c0015 | t0005 | g0204 | AFR | ACB | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02280 | hp1 | a0006 | c0006 | t0007 | g0351 | AFR | ACB | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02280 | hp2 | a0005 | c0011 | t0001 | g0041 | AFR | ACB | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02451 | hp1 | a0006 | c0006 | t0007 | g0322 | AFR | ACB | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02451 | hp2 | a0008 | c0009 | t0003 | g0314 | AFR | ACB | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02523 | hp1 | a0003 | c0012 | t0002 | g0165 | EAS | KHV | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02523 | hp2 | a0002 | c0001 | t0001 | g0069 | EAS | KHV | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02572 | hp1 | a0006 | c0006 | t0007 | g0353 | AFR | GWD | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02572 | hp2 | a0004 | c0004 | t0009 | g0255 | AFR | GWD | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02602 | hp1 | a0002 | c0024 | t0003 | g0367 | SAS | PJL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02602 | hp2 | a0003 | c0012 | t0002 | g0213 | SAS | PJL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02615 | hp1 | a0009 | c0014 | t0011 | g0273 | AFR | GWD | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02615 | hp2 | a0005 | c0011 | t0003 | g0361 | AFR | GWD | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02622 | hp1 | a0005 | c0011 | t0003 | g0316 | AFR | GWD | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02622 | hp2 | a0006 | c0023 | t0007 | g0264 | AFR | GWD | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02630 | hp1 | a0006 | c0006 | t0007 | g0344 | AFR | GWD | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02630 | hp2 | a0005 | c0035 | t0003 | g0239 | AFR | GWD | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02647 | hp1 | a0006 | c0006 | t0007 | g0348 | AFR | GWD | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02647 | hp2 | a0001 | c0002 | t0011 | g0356 | AFR | GWD | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02683 | hp1 | a0002 | c0001 | t0001 | g0061 | SAS | PJL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02683 | hp2 | a0001 | c0002 | t0005 | g0363 | SAS | PJL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02717 | hp1 | a0004 | c0004 | t0009 | g0257 | AFR | GWD | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02717 | hp2 | a0001 | c0002 | t0004 | g0350 | AFR | GWD | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02735 | hp1 | a0001 | c0005 | t0005 | g0185 | SAS | PJL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02735 | hp2 | a0002 | c0001 | t0001 | g0059 | SAS | PJL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02738 | hp1 | a0002 | c0001 | t0001 | g0074 | SAS | PJL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02738 | hp2 | a0001 | c0005 | t0005 | g0196 | SAS | PJL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02809 | hp1 | a0004 | c0004 | t0009 | g0256 | AFR | GWD | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02809 | hp2 | a0008 | c0009 | t0026 | g0309 | AFR | GWD | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02818 | hp1 | a0005 | c0011 | t0001 | g0042 | AFR | GWD | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02818 | hp2 | a0004 | c0004 | t0004 | g0240 | AFR | GWD | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02886 | hp1 | a0009 | c0013 | t0011 | g0320 | AFR | GWD | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02886 | hp2 | a0001 | c0002 | t0008 | g0308 | AFR | GWD | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02895 | hp1 | a0009 | c0014 | t0023 | g0006 | AFR | GWD | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02895 | hp2 | a0005 | c0011 | t0001 | g0043 | AFR | GWD | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02896 | hp1 | a0001 | c0005 | t0004 | g0210 | AFR | GWD | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02896 | hp2 | a0001 | c0002 | t0015 | g0038 | AFR | GWD | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02897 | hp1 | a0009 | c0014 | t0023 | g0006 | AFR | GWD | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02897 | hp2 | a0001 | c0002 | t0015 | g0037 | AFR | GWD | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02922 | hp1 | a0004 | c0004 | t0009 | g0263 | AFR | ESN | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02922 | hp2 | a0006 | c0006 | t0032 | g0105 | AFR | ESN | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02965 | hp1 | a0006 | c0006 | t0007 | g0341 | AFR | ESN | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02965 | hp2 | a0001 | c0005 | t0004 | g0207 | AFR | ESN | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02970 | hp1 | a0006 | c0006 | t0007 | g0323 | AFR | ESN | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02970 | hp2 | a0004 | c0010 | t0009 | g0339 | AFR | ESN | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03041 | hp1 | a0008 | c0009 | t0025 | g0318 | AFR | GWD | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03041 | hp2 | a0001 | c0002 | t0015 | g0036 | AFR | GWD | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03098 | hp1 | a0006 | c0006 | t0007 | g0347 | AFR | MSL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03098 | hp2 | a0006 | c0006 | t0007 | g0368 | AFR | MSL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03130 | hp1 | a0004 | c0010 | t0022 | g0044 | AFR | ESN | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03130 | hp2 | a0004 | c0004 | t0009 | g0015 | AFR | ESN | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03139 | hp1 | a0008 | c0017 | t0031 | g0109 | AFR | ESN | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03139 | hp2 | a0001 | c0005 | t0029 | g0208 | AFR | ESN | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03195 | hp1 | a0003 | c0003 | t0002 | g0334 | AFR | ESN | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03195 | hp2 | a0008 | c0009 | t0003 | g0313 | AFR | ESN | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03209 | hp1 | a0009 | c0013 | t0021 | g0126 | AFR | MSL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03209 | hp2 | a0006 | c0006 | t0007 | g0349 | AFR | MSL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03225 | hp1 | a0008 | c0009 | t0002 | g0329 | AFR | MSL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03225 | hp2 | a0004 | c0004 | t0033 | g0266 | AFR | MSL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03239 | hp1 | a0002 | c0001 | t0003 | g0217 | SAS | PJL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03239 | hp2 | a0001 | c0005 | t0005 | g0197 | SAS | PJL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03453 | hp1 | a0004 | c0004 | t0009 | g0262 | AFR | MSL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03453 | hp2 | a0006 | c0006 | t0007 | g0355 | AFR | MSL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03486 | hp1 | a0005 | c0011 | t0003 | g0326 | AFR | MSL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03486 | hp2 | a0008 | c0017 | t0013 | g0250 | AFR | MSL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03490 | hp1 | a0002 | c0001 | t0001 | g0079 | SAS | PJL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03490 | hp2 | a0001 | c0005 | t0005 | g0174 | SAS | PJL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03491 | hp1 | a0002 | c0001 | t0001 | g0073 | SAS | PJL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03491 | hp2 | a0017 | c0021 | t0006 | g0141 | SAS | PJL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03492 | hp1 | a0001 | c0005 | t0005 | g0175 | SAS | PJL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03492 | hp2 | a0017 | c0021 | t0006 | g0142 | SAS | PJL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03516 | hp1 | a0001 | c0005 | t0004 | g0211 | AFR | ESN | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03516 | hp2 | a0006 | c0006 | t0007 | g0346 | AFR | ESN | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03540 | hp1 | a0004 | c0010 | t0009 | g0340 | AFR | GWD | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03540 | hp2 | a0001 | c0002 | t0006 | g0131 | AFR | GWD | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03579 | hp1 | a0009 | c0014 | t0035 | g0029 | AFR | MSL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03579 | hp2 | a0004 | c0010 | t0014 | g0317 | AFR | MSL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03654 | hp1 | a0002 | c0001 | t0001 | g0138 | SAS | PJL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03654 | hp2 | a0004 | c0004 | t0030 | g0243 | SAS | PJL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03669 | hp1 | a0016 | c0019 | t0002 | g0284 | SAS | PJL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03669 | hp2 | a0001 | c0005 | t0005 | g0202 | SAS | PJL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03831 | hp1 | a0002 | c0001 | t0001 | g0062 | SAS | BEB | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03831 | hp2 | a0001 | c0002 | t0006 | g0128 | SAS | BEB | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03942 | hp1 | a0001 | c0002 | t0005 | g0342 | SAS | BEB | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03942 | hp2 | a0001 | c0002 | t0006 | g0051 | SAS | BEB | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG04199 | hp1 | a0004 | c0004 | t0028 | g0244 | SAS | STU | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG04199 | hp2 | a0005 | c0007 | t0003 | g0181 | SAS | STU | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG04204 | hp1 | a0022 | c0031 | t0001 | g0077 | SAS | STU | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG04204 | hp2 | a0001 | c0005 | t0005 | g0189 | SAS | STU | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG04228 | hp1 | a0004 | c0004 | t0004 | g0365 | SAS | STU | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG04228 | hp2 | a0001 | c0005 | t0005 | g0186 | SAS | STU | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18522 | hp1 | a0002 | c0001 | t0003 | g0270 | AFR | YRI | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18522 | hp2 | a0001 | c0005 | t0004 | g0206 | AFR | YRI | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18612 | hp1 | a0003 | c0003 | t0002 | g0001 | EAS | CHB | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18612 | hp2 | a0002 | c0001 | t0001 | g0136 | EAS | CHB | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18747 | hp1 | a0004 | c0004 | t0004 | g0178 | EAS | CHB | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18747 | hp2 | a0002 | c0001 | t0001 | g0049 | EAS | CHB | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18906 | hp1 | a0004 | c0004 | t0009 | g0259 | AFR | YRI | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18906 | hp2 | a0004 | c0010 | t0014 | g0312 | AFR | YRI | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18939 | hp1 | a0001 | c0002 | t0006 | g0123 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18939 | hp2 | a0003 | c0003 | t0002 | g0297 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18940 | hp1 | a0002 | c0001 | t0001 | g0091 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18940 | hp2 | a0005 | c0033 | t0003 | g0151 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18941 | hp1 | a0004 | c0004 | t0004 | g0230 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18941 | hp2 | a0001 | c0002 | t0008 | g0171 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18942 | hp1 | a0007 | c0008 | t0001 | g0097 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18942 | hp2 | a0002 | c0001 | t0001 | g0055 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18943 | hp1 | a0002 | c0001 | t0001 | g0033 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18943 | hp2 | a0001 | c0002 | t0006 | g0086 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18944 | hp1 | a0002 | c0001 | t0001 | g0104 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18944 | hp2 | a0001 | c0002 | t0008 | g0170 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18945 | hp1 | a0001 | c0002 | t0008 | g0014 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18945 | hp2 | a0001 | c0002 | t0006 | g0117 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18946 | hp1 | a0002 | c0001 | t0001 | g0052 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18946 | hp2 | a0005 | c0007 | t0003 | g0145 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18948 | hp1 | a0003 | c0003 | t0002 | g0280 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18948 | hp2 | a0005 | c0007 | t0003 | g0148 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18949 | hp1 | a0004 | c0004 | t0004 | g0219 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18949 | hp2 | a0003 | c0003 | t0002 | g0324 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18950 | hp1 | a0001 | c0002 | t0006 | g0116 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18950 | hp2 | a0002 | c0001 | t0001 | g0082 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18951 | hp1 | a0003 | c0003 | t0002 | g0019 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18951 | hp2 | a0003 | c0003 | t0002 | g0302 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18954 | hp1 | a0001 | c0002 | t0006 | g0120 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18954 | hp2 | a0001 | c0002 | t0010 | g0167 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18956 | hp1 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18956 | hp2 | a0002 | c0001 | t0001 | g0139 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18957 | hp1 | a0004 | c0004 | t0004 | g0012 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18957 | hp2 | a0003 | c0003 | t0002 | g0281 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18959 | hp1 | a0004 | c0004 | t0004 | g0226 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18959 | hp2 | a0003 | c0003 | t0002 | g0016 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18960 | hp1 | a0001 | c0002 | t0008 | g0009 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18960 | hp2 | a0003 | c0003 | t0002 | g0282 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18961 | hp1 | a0007 | c0008 | t0001 | g0056 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18961 | hp2 | a0003 | c0012 | t0002 | g0274 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18962 | hp1 | a0007 | c0008 | t0003 | g0149 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18962 | hp2 | a0003 | c0003 | t0002 | g0013 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18965 | hp1 | a0003 | c0003 | t0002 | g0272 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18965 | hp2 | a0001 | c0002 | t0010 | g0172 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18966 | hp1 | a0003 | c0003 | t0002 | g0019 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18966 | hp2 | a0001 | c0002 | t0006 | g0028 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18967 | hp1 | a0001 | c0002 | t0006 | g0134 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18967 | hp2 | a0002 | c0001 | t0001 | g0027 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18969 | hp1 | a0003 | c0003 | t0002 | g0300 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18969 | hp2 | a0001 | c0002 | t0010 | g0010 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18970 | hp1 | a0002 | c0001 | t0001 | g0066 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18970 | hp2 | a0001 | c0002 | t0006 | g0088 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18972 | hp1 | a0004 | c0004 | t0004 | g0223 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18972 | hp2 | a0003 | c0012 | t0002 | g0163 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18973 | hp1 | a0002 | c0001 | t0001 | g0026 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18973 | hp2 | a0003 | c0003 | t0002 | g0333 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18975 | hp1 | a0002 | c0001 | t0001 | g0092 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18975 | hp2 | a0003 | c0003 | t0002 | g0306 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18978 | hp1 | a0018 | c0018 | t0001 | g0093 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18978 | hp2 | a0001 | c0002 | t0006 | g0087 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18980 | hp1 | a0003 | c0003 | t0002 | g0005 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18980 | hp2 | a0004 | c0004 | t0004 | g0227 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18982 | hp1 | a0007 | c0008 | t0001 | g0057 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18982 | hp2 | a0002 | c0001 | t0001 | g0078 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18984 | hp1 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18984 | hp2 | a0007 | c0008 | t0001 | g0103 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18986 | hp1 | a0005 | c0007 | t0003 | g0150 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18986 | hp2 | a0004 | c0004 | t0004 | g0232 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18989 | hp1 | a0011 | c0016 | t0012 | g0095 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18989 | hp2 | a0003 | c0003 | t0002 | g0268 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18991 | hp1 | a0002 | c0001 | t0001 | g0047 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18991 | hp2 | a0003 | c0003 | t0002 | g0304 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18992 | hp1 | a0004 | c0004 | t0024 | g0220 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18992 | hp2 | a0007 | c0008 | t0001 | g0096 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18993 | hp1 | a0001 | c0002 | t0006 | g0114 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18993 | hp2 | a0005 | c0007 | t0003 | g0160 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18994 | hp1 | a0018 | c0018 | t0001 | g0089 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18994 | hp2 | a0004 | c0004 | t0004 | g0221 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18995 | hp1 | a0001 | c0002 | t0008 | g0014 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18995 | hp2 | a0003 | c0003 | t0002 | g0325 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18997 | hp1 | a0007 | c0008 | t0003 | g0237 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18997 | hp2 | a0001 | c0002 | t0008 | g0168 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18998 | hp1 | a0003 | c0003 | t0002 | g0298 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA18998 | hp2 | a0001 | c0002 | t0006 | g0122 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19000 | hp1 | a0005 | c0007 | t0003 | g0146 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19000 | hp2 | a0002 | c0001 | t0001 | g0025 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19001 | hp1 | a0003 | c0003 | t0002 | g0278 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19001 | hp2 | a0002 | c0001 | t0001 | g0022 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19003 | hp1 | a0001 | c0002 | t0006 | g0121 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19003 | hp2 | a0001 | c0002 | t0010 | g0010 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19005 | hp1 | a0001 | c0002 | t0008 | g0009 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19005 | hp2 | a0002 | c0001 | t0001 | g0071 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19006 | hp1 | a0002 | c0001 | t0001 | g0085 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19006 | hp2 | a0001 | c0002 | t0010 | g0173 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19007 | hp1 | a0005 | c0007 | t0003 | g0153 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19007 | hp2 | a0003 | c0003 | t0002 | g0295 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19009 | hp1 | a0003 | c0003 | t0002 | g0299 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19009 | hp2 | a0002 | c0001 | t0001 | g0070 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19010 | hp1 | a0007 | c0008 | t0001 | g0030 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19010 | hp2 | a0003 | c0003 | t0002 | g0005 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19011 | hp1 | a0002 | c0001 | t0001 | g0090 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19011 | hp2 | a0001 | c0002 | t0008 | g0252 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19012 | hp1 | a0005 | c0007 | t0003 | g0164 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19012 | hp2 | a0007 | c0008 | t0001 | g0102 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19030 | hp1 | a0001 | c0002 | t0027 | g0327 | AFR | LWK | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19030 | hp2 | a0006 | c0006 | t0007 | g0352 | AFR | LWK | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19043 | hp1 | a0004 | c0004 | t0004 | g0248 | AFR | LWK | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19043 | hp2 | a0006 | c0023 | t0007 | g0180 | AFR | LWK | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19054 | hp1 | a0007 | c0008 | t0003 | g0158 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19054 | hp2 | a0003 | c0003 | t0002 | g0292 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19056 | hp1 | a0004 | c0004 | t0004 | g0012 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19056 | hp2 | a0003 | c0003 | t0002 | g0328 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19057 | hp1 | a0003 | c0003 | t0002 | g0013 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19057 | hp2 | a0012 | c0026 | t0003 | g0234 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19058 | hp1 | a0004 | c0004 | t0004 | g0231 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19058 | hp2 | a0003 | c0003 | t0002 | g0276 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19060 | hp1 | a0005 | c0007 | t0003 | g0156 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19060 | hp2 | a0003 | c0003 | t0016 | g0303 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19062 | hp1 | a0003 | c0003 | t0002 | g0279 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19062 | hp2 | a0004 | c0004 | t0004 | g0218 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19063 | hp1 | a0003 | c0003 | t0002 | g0283 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19063 | hp2 | a0001 | c0002 | t0006 | g0008 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19064 | hp1 | a0001 | c0002 | t0006 | g0063 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19064 | hp2 | a0004 | c0004 | t0002 | g0229 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19065 | hp1 | a0001 | c0002 | t0006 | g0113 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19065 | hp2 | a0001 | c0002 | t0008 | g0254 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19066 | hp1 | a0002 | c0001 | t0001 | g0031 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19066 | hp2 | a0005 | c0007 | t0003 | g0157 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19067 | hp1 | a0001 | c0002 | t0006 | g0107 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19067 | hp2 | a0003 | c0003 | t0002 | g0289 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19068 | hp1 | a0002 | c0001 | t0001 | g0084 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19068 | hp2 | a0004 | c0004 | t0004 | g0228 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19070 | hp1 | a0005 | c0007 | t0003 | g0159 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19070 | hp2 | a0002 | c0001 | t0001 | g0094 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19072 | hp1 | a0001 | c0002 | t0006 | g0137 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19072 | hp2 | a0007 | c0008 | t0001 | g0098 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19074 | hp1 | a0002 | c0001 | t0001 | g0068 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19074 | hp2 | a0003 | c0003 | t0008 | g0293 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19077 | hp1 | a0001 | c0002 | t0008 | g0251 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19077 | hp2 | a0004 | c0004 | t0004 | g0224 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19079 | hp1 | a0003 | c0012 | t0012 | g0099 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19079 | hp2 | a0005 | c0007 | t0003 | g0144 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19080 | hp1 | a0004 | c0004 | t0004 | g0225 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19080 | hp2 | a0003 | c0003 | t0002 | g0296 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19084 | hp1 | a0001 | c0002 | t0006 | g0008 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19084 | hp2 | a0004 | c0004 | t0004 | g0147 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19085 | hp1 | a0003 | c0003 | t0002 | g0287 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19085 | hp2 | a0005 | c0027 | t0003 | g0236 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19086 | hp1 | a0001 | c0030 | t0006 | g0115 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19086 | hp2 | a0004 | c0004 | t0004 | g0143 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19088 | hp1 | a0007 | c0008 | t0003 | g0154 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19088 | hp2 | a0003 | c0003 | t0002 | g0286 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19090 | hp1 | a0001 | c0002 | t0006 | g0124 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19090 | hp2 | a0003 | c0003 | t0002 | g0301 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19091 | hp1 | a0011 | c0016 | t0012 | g0083 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19091 | hp2 | a0001 | c0002 | t0006 | g0119 | EAS | JPT | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19240 | hp1 | a0001 | c0002 | t0020 | g0110 | AFR | YRI | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA19240 | hp2 | a0004 | c0004 | t0009 | g0258 | AFR | YRI | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA20129 | hp1 | a0004 | c0010 | t0014 | g0319 | AFR | ASW | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA20129 | hp2 | a0003 | c0003 | t0002 | g0330 | AFR | ASW | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA20752 | hp1 | a0001 | c0002 | t0005 | g0359 | EUR | TSI | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA20752 | hp2 | a0001 | c0005 | t0005 | g0003 | EUR | TSI | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA20805 | hp1 | a0001 | c0005 | t0005 | g0200 | EUR | TSI | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA20805 | hp2 | a0001 | c0005 | t0005 | g0004 | EUR | TSI | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA20905 | hp1 | a0004 | c0004 | t0004 | g0184 | SAS | GIH | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA20905 | hp2 | a0002 | c0001 | t0001 | g0140 | SAS | GIH | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02486 | hp1 | a0004 | c0004 | t0004 | g0242 | AFR | ACB | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02486 | hp2 | a0008 | c0017 | t0013 | g0249 | AFR | ACB | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02559 | hp1 | a0002 | c0001 | t0003 | g0216 | AFR | ACB | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG02559 | hp2 | a0006 | c0006 | t0034 | g0267 | AFR | ACB | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03471 | hp1 | a0021 | c0037 | t0003 | g0354 | AFR | MSL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG03471 | hp2 | a0008 | c0009 | t0003 | g0310 | AFR | MSL | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG06807 | hp1 | a0015 | c0020 | t0017 | g0177 | AFR | USA | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| HG06807 | hp2 | a0002 | c0001 | t0001 | g0040 | AFR | USA | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA20300 | hp1 | a0006 | c0006 | t0007 | g0345 | AFR | USA | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA20300 | hp2 | a0002 | c0001 | t0001 | g0021 | AFR | USA | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA21309 | hp1 | a0001 | c0005 | t0004 | g0209 | AFR | LWK | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| NA21309 | hp2 | a0023 | c0032 | t0009 | g0305 | AFR | LWK | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| homoSapiens | chm13v2 | a0002 | c0001 | t0001 | g0046 | REF | REF | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| homoSapiens | grch38p0 | a0019 | c0028 | t0003 | g0194 | REF | REF | ARHGEF37_chr5_149576498_149639968 | ARHGEF37 | chr5 | 149576498 | 149639968 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:149597844 | C | G | 1 | a0021 | 1 | HG03471.hp1 | missense_variant | MODERATE | c.75C>G | p.Asp25Glu | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/13 | 213/4943 | 75/2028 | 25/675 | chr5 | 149597844 | |||
| chr5:149609652 | C | T | 1 | a0009 | 4 | HG02615.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
missense_variant | MODERATE | c.415C>T | p.Pro139Ser | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/13 | 553/4943 | 415/2028 | 139/675 | chr5 | 149609652 | |||
| chr5:149609653 | C | T | 3 | a0009 a0012 a0023 |
8 | HG00558.hp1 HG01069.hp2 HG01071.hp1 others(5): Show |
missense_variant | MODERATE | c.416C>T | p.Pro139Leu | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/13 | 554/4943 | 416/2028 | 139/675 | chr5 | 149609653 | |||
| chr5:149616569 | C | T | 1 | a0013 | 2 | HG00673.hp1 HG02129.hp2 |
missense_variant&splice_region_variant | MODERATE | c.461C>T | p.Pro154Leu | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 5/13 | 599/4943 | 461/2028 | 154/675 | chr5 | 149616569 | |||
| chr5:149618234 | C | A | 1 | a0018 | 2 | NA18978.hp1 NA18994.hp1 |
missense_variant | MODERATE | c.717C>A | p.Asn239Lys | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 6/13 | 855/4943 | 717/2028 | 239/675 | chr5 | 149618234 | |||
| chr5:149619019 | G | A | 1 | a0007 | 14 | HG00621.hp1 HG02074.hp1 NA18942.hp1 others(11): Show |
missense_variant | MODERATE | c.871G>A | p.Ala291Thr | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 7/13 | 1009/4943 | 871/2028 | 291/675 | chr5 | 149619019 | |||
| chr5:149620422 | C | A | 1 | a0020 | 1 | HG01169.hp1 | stop_gained | HIGH | c.963C>A | p.Cys321* | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 8/13 | 1101/4943 | 963/2028 | 321/675 | chr5 | 149620422 | |||
| chr5:149621790 | C | T | 1 | a0014 | 2 | HG01167.hp2 HG01169.hp2 |
missense_variant | MODERATE | c.1063C>T | p.Leu355Phe | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 9/13 | 1201/4943 | 1063/2028 | 355/675 | chr5 | 149621790 | |||
| chr5:149621988 | A | C | 12 | a0002 a0004 a0005 others(9): Show |
180 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(177): Show |
missense_variant | MODERATE | c.1261A>C | p.Met421Leu | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 9/13 | 1399/4943 | 1261/2028 | 421/675 | chr5 | 149621988 | |||
| chr5:149624027 | G | T | 1 | a0011 | 3 | HG02027.hp1 NA18989.hp1 NA19091.hp1 |
missense_variant | MODERATE | c.1351G>T | p.Val451Phe | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/13 | 1489/4943 | 1351/2028 | 451/675 | chr5 | 149624027 | |||
| chr5:149624063 | G | A | 1 | a0010 | 4 | HG01256.hp1 HG01258.hp2 HG01934.hp1 others(1): Show |
missense_variant | MODERATE | c.1387G>A | p.Ala463Thr | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/13 | 1525/4943 | 1387/2028 | 463/675 | chr5 | 149624063 | |||
| chr5:149624064 | C | T | 2 | a0004 a0023 |
56 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(53): Show |
missense_variant | MODERATE | c.1388C>T | p.Ala463Val | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/13 | 1526/4943 | 1388/2028 | 463/675 | chr5 | 149624064 | |||
| chr5:149627077 | C | T | 6 | a0001 a0006 a0009 others(3): Show |
130 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(127): Show |
missense_variant&splice_region_variant | MODERATE | c.1466C>T | p.Pro489Leu | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/13 | 1604/4943 | 1466/2028 | 489/675 | chr5 | 149627077 | |||
| chr5:149627163 | A | C | 3 | a0004 a0015 a0023 |
58 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(55): Show |
missense_variant | MODERATE | c.1552A>C | p.Ser518Arg | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/13 | 1690/4943 | 1552/2028 | 518/675 | chr5 | 149627163 | |||
| chr5:149627164 | G | T | 1 | a0016 | 2 | HG02132.hp1 HG03669.hp1 |
missense_variant | MODERATE | c.1553G>T | p.Ser518Ile | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/13 | 1691/4943 | 1553/2028 | 518/675 | chr5 | 149627164 | |||
| chr5:149628904 | C | A | 4 | a0003 a0011 a0013 others(1): Show |
74 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(71): Show |
missense_variant | MODERATE | c.1756C>A | p.Pro586Thr | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/13 | 1894/4943 | 1756/2028 | 586/675 | chr5 | 149628904 | |||
| chr5:149628914 | T | C | 1 | a0022 | 1 | HG04204.hp1 | missense_variant | MODERATE | c.1766T>C | p.Leu589Pro | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/13 | 1904/4943 | 1766/2028 | 589/675 | chr5 | 149628914 | |||
| chr5:149628958 | A | G | 18 | a0001 a0003 a0004 others(15): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
missense_variant | MODERATE | c.1810A>G | p.Met604Val | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/13 | 1948/4943 | 1810/2028 | 604/675 | chr5 | 149628958 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:149609559 | C | T | 15 | a0001c0005 a0002c0024 a0003c0012 others(12): Show |
135 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(132): Show |
synonymous_variant | LOW | c.322C>T | p.Leu108Leu | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/13 | 460/4943 | 322/2028 | 108/675 | chr5 | 149609559 | |||
| chr5:149616765 | G | A | 5 | a0005c0007 a0005c0027 a0005c0033 others(2): Show |
33 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(30): Show |
splice_region_variant&synonymous_variant | LOW | c.657G>A | p.Val219Val | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 5/13 | 795/4943 | 657/2028 | 219/675 | chr5 | 149616765 | |||
| chr5:149620377 | C | T | 1 | a0005c0033 | 1 | NA18940.hp2 | synonymous_variant | LOW | c.918C>T | p.His306His | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 8/13 | 1056/4943 | 918/2028 | 306/675 | chr5 | 149620377 | |||
| chr5:149624062 | C | T | 1 | a0001c0030 | 1 | NA19086.hp1 | synonymous_variant | LOW | c.1386C>T | p.Asp462Asp | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/13 | 1524/4943 | 1386/2028 | 462/675 | chr5 | 149624062 | |||
| chr5:149627246 | C | T | 1 | a0003c0029 | 1 | HG00408.hp1 | synonymous_variant | LOW | c.1635C>T | p.Ser545Ser | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/13 | 1773/4943 | 1635/2028 | 545/675 | chr5 | 149627246 | |||
| chr5:149628840 | A | G | 27 | a0001c0002 a0001c0005 a0001c0030 others(24): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
synonymous_variant | LOW | c.1692A>G | p.Leu564Leu | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/13 | 1830/4943 | 1692/2028 | 564/675 | chr5 | 149628840 | |||
| chr5:149628921 | G | A | 5 | a0005c0007 a0005c0027 a0005c0033 others(2): Show |
33 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(30): Show |
synonymous_variant | LOW | c.1773G>A | p.Pro591Pro | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/13 | 1911/4943 | 1773/2028 | 591/675 | chr5 | 149628921 | |||
| chr5:149632134 | T | C | 1 | a0004c0036 | 1 | HG00438.hp1 | synonymous_variant | LOW | c.1971T>C | p.Ser657Ser | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 13/13 | 2109/4943 | 1971/2028 | 657/675 | chr5 | 149632134 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:149581555 | C | T | 2 | a0009c0014t0023 a0009c0014t0035 |
3 | HG02895.hp1 HG02897.hp1 HG03579.hp1 |
5_prime_UTR_variant | MODIFIER | c.-81C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/13 | 16215 | chr5 | 149581555 | ||||||
| chr5:149581558 | C | T | 1 | a0006c0006t0034 | 1 | HG02559.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-78C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/13 | chr5 | 149581558 | |||||||
| chr5:149581578 | C | G | 20 | a0001c0002t0006 a0001c0002t0015 a0001c0002t0020 others(17): Show |
131 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(128): Show |
5_prime_UTR_variant | MODIFIER | c.-58C>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/13 | 16192 | chr5 | 149581578 | ||||||
| chr5:149632239 | A | T | 1 | a0004c0010t0014 | 3 | HG03579.hp2 NA18906.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*48A>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 13/13 | 48 | chr5 | 149632239 | ||||||
| chr5:149632372 | G | C | 1 | a0004c0004t0024 | 1 | NA18992.hp1 | 3_prime_UTR_variant | MODIFIER | c.*181G>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 13/13 | 181 | chr5 | 149632372 | ||||||
| chr5:149632485 | C | T | 1 | a0004c0004t0030 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*294C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 13/13 | 294 | chr5 | 149632485 | ||||||
| chr5:149632488 | C | G | 25 | a0001c0002t0004 a0001c0002t0005 a0001c0002t0011 others(22): Show |
110 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*297C>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 13/13 | 297 | chr5 | 149632488 | ||||||
| chr5:149632490 | T | C | 9 | a0001c0002t0006 a0001c0002t0008 a0001c0002t0010 others(6): Show |
58 | HG00408.hp2 HG00544.hp1 HG00621.hp2 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*299T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 13/13 | 299 | chr5 | 149632490 | ||||||
| chr5:149632540 | G | A | 1 | a0009c0014t0035 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*349G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 13/13 | 349 | chr5 | 149632540 | ||||||
| chr5:149632654 | A | G | 3 | a0004c0010t0014 a0008c0017t0013 a0014c0025t0013 |
7 | HG01167.hp2 HG01169.hp2 HG02486.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*463A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 13/13 | 463 | chr5 | 149632654 | ||||||
| chr5:149632896 | G | T | 1 | a0001c0002t0010 | 5 | NA18954.hp2 NA18965.hp2 NA18969.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*705G>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 13/13 | 705 | chr5 | 149632896 | ||||||
| chr5:149632897 | G | A | 4 | a0001c0002t0011 a0009c0013t0011 a0009c0013t0021 others(1): Show |
7 | HG01069.hp2 HG01071.hp1 HG01243.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*706G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 13/13 | 706 | chr5 | 149632897 | ||||||
| chr5:149632911 | T | C | 1 | a0004c0010t0022 | 2 | HG01884.hp1 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*720T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 13/13 | 720 | chr5 | 149632911 | ||||||
| chr5:149633044 | C | T | 1 | a0004c0010t0022 | 2 | HG01884.hp1 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*853C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 13/13 | 853 | chr5 | 149633044 | ||||||
| chr5:149633104 | G | A | 1 | a0008c0009t0026 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*913G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 13/13 | 913 | chr5 | 149633104 | ||||||
| chr5:149633219 | G | A | 16 | a0001c0002t0004 a0001c0002t0005 a0001c0005t0004 others(13): Show |
85 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*1028G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 13/13 | 1028 | chr5 | 149633219 | ||||||
| chr5:149633322 | C | T | 2 | a0008c0017t0013 a0014c0025t0013 |
4 | HG01167.hp2 HG01169.hp2 HG02486.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1131C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 13/13 | 1131 | chr5 | 149633322 | ||||||
| chr5:149633427 | C | T | 1 | a0004c0010t0014 | 3 | HG03579.hp2 NA18906.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1236C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 13/13 | 1236 | chr5 | 149633427 | ||||||
| chr5:149633481 | C | A | 1 | a0004c0004t0028 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1290C>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 13/13 | 1290 | chr5 | 149633481 | ||||||
| chr5:149633498 | G | C | 2 | a0008c0017t0013 a0014c0025t0013 |
4 | HG01167.hp2 HG01169.hp2 HG02486.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1307G>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 13/13 | 1307 | chr5 | 149633498 | ||||||
| chr5:149633644 | C | A | 1 | a0001c0005t0029 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1453C>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 13/13 | 1453 | chr5 | 149633644 | ||||||
| chr5:149633851 | A | G | 4 | a0006c0006t0007 a0006c0006t0032 a0006c0006t0034 others(1): Show |
18 | HG02280.hp1 HG02451.hp1 HG02559.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1660A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 13/13 | 1660 | chr5 | 149633851 | ||||||
| chr5:149633998 | A | C | 1 | a0001c0005t0019 | 2 | HG01106.hp1 HG01358.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1807A>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 13/13 | 1807 | chr5 | 149633998 | ||||||
| chr5:149634024 | G | A | 12 | a0003c0003t0002 a0003c0003t0012 a0003c0003t0016 others(9): Show |
75 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*1833G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 13/13 | 1833 | chr5 | 149634024 | ||||||
| chr5:149634277 | G | A | 1 | a0015c0020t0017 | 2 | HG01891.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2086G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 13/13 | 2086 | chr5 | 149634277 | ||||||
| chr5:149634281 | T | A | 5 | a0001c0002t0005 a0001c0005t0005 a0001c0005t0019 others(2): Show |
36 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*2090T>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 13/13 | 2090 | chr5 | 149634281 | ||||||
| chr5:149634378 | A | T | 2 | a0001c0002t0027 a0009c0014t0035 |
2 | HG03579.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2187A>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 13/13 | 2187 | chr5 | 149634378 | ||||||
| chr5:149634409 | T | C | 2 | a0008c0017t0013 a0014c0025t0013 |
4 | HG01167.hp2 HG01169.hp2 HG02486.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2218T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 13/13 | 2218 | chr5 | 149634409 | ||||||
| chr5:149634430 | T | C | 1 | a0004c0010t0014 | 3 | HG03579.hp2 NA18906.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2239T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 13/13 | 2239 | chr5 | 149634430 | ||||||
| chr5:149634487 | G | C | 1 | a0008c0017t0031 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2296G>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 13/13 | 2296 | chr5 | 149634487 | ||||||
| chr5:149634855 | A | G | 19 | a0001c0002t0006 a0001c0002t0008 a0001c0002t0010 others(16): Show |
82 | HG00408.hp2 HG00544.hp1 HG00738.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*2664A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 13/13 | 2664 | chr5 | 149634855 | ||||||
| chr5:149634865 | A | C | 2 | a0008c0017t0013 a0014c0025t0013 |
4 | HG01167.hp2 HG01169.hp2 HG02486.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2674A>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 13/13 | 2674 | chr5 | 149634865 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:149581750 | G | T | 108 | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(105): Show |
118 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.-12+126G>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149581750 | |||||||
| chr5:149581997 | G | C | 9 | a0001c0002t0006g0028 a0002c0001t0001g0002 a0002c0001t0001g0021 others(6): Show |
11 | HG01433.hp2 HG01496.hp2 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.-12+373G>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149581997 | |||||||
| chr5:149582180 | A | G | 1 | a0006c0006t0034g0267 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-12+556A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149582180 | |||||||
| chr5:149582191 | C | T | 1 | a0004c0004t0033g0266 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-12+567C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149582191 | |||||||
| chr5:149582215 | G | A | 126 | a0001c0002t0006g0008 a0001c0002t0006g0028 a0001c0002t0006g0050 others(123): Show |
131 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.-12+591G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149582215 | |||||||
| chr5:149582333 | C | G | 126 | a0001c0002t0006g0008 a0001c0002t0006g0028 a0001c0002t0006g0050 others(123): Show |
131 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.-12+709C>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149582333 | |||||||
| chr5:149582346 | G | T | 13 | a0004c0004t0009g0015 a0004c0004t0009g0255 a0004c0004t0009g0256 others(10): Show |
14 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-12+722G>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149582346 | |||||||
| chr5:149582459 | C | T | 5 | a0001c0002t0008g0014 a0001c0002t0008g0251 a0001c0002t0008g0252 others(2): Show |
6 | HG00544.hp1 NA18945.hp1 NA18995.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12+835C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149582459 | |||||||
| chr5:149582487 | G | T | 1 | a0006c0006t0007g0368 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-12+863G>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149582487 | |||||||
| chr5:149582498 | C | G | 1 | a0002c0024t0003g0367 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-12+874C>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149582498 | |||||||
| chr5:149582668 | T | TAAAGA | 235 | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(232): Show |
250 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.-12+1045_-12+1049d others(7): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 149582668 | ||||||
| chr5:149583226 | T | C | 37 | a0001c0002t0008g0009 a0001c0002t0008g0014 a0001c0002t0008g0168 others(34): Show |
40 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.-12+1602T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149583226 | |||||||
| chr5:149583229 | C | T | 2 | a0008c0017t0013g0249 a0008c0017t0013g0250 |
2 | HG02486.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-12+1605C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149583229 | |||||||
| chr5:149583230 | G | A | 126 | a0001c0002t0006g0008 a0001c0002t0006g0028 a0001c0002t0006g0050 others(123): Show |
131 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.-12+1606G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149583230 | |||||||
| chr5:149583320 | A | C | 14 | a0004c0004t0009g0015 a0004c0004t0009g0255 a0004c0004t0009g0256 others(11): Show |
15 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.-12+1696A>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149583320 | |||||||
| chr5:149583411 | C | T | 1 | a0003c0003t0002g0366 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-12+1787C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149583411 | |||||||
| chr5:149583425 | T | C | 126 | a0001c0002t0006g0008 a0001c0002t0006g0028 a0001c0002t0006g0050 others(123): Show |
131 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.-12+1801T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149583425 | |||||||
| chr5:149583591 | G | A | 37 | a0001c0002t0008g0009 a0001c0002t0008g0014 a0001c0002t0008g0168 others(34): Show |
40 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.-12+1967G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149583591 | |||||||
| chr5:149583610 | C | T | 126 | a0001c0002t0006g0008 a0001c0002t0006g0028 a0001c0002t0006g0050 others(123): Show |
131 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.-12+1986C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149583610 | |||||||
| chr5:149583768 | GT | G | 2 | a0009c0014t0023g0006 a0009c0014t0035g0029 |
3 | HG02895.hp1 HG02897.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-12+2147delT | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 149583768 | ||||||
| chr5:149583823 | C | T | 1 | a0004c0004t0004g0248 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-12+2199C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149583823 | |||||||
| chr5:149583861 | A | C | 2 | a0017c0021t0006g0141 a0017c0021t0006g0142 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-12+2237A>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149583861 | |||||||
| chr5:149583949 | G | A | 1 | a0007c0008t0001g0030 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-12+2325G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149583949 | |||||||
| chr5:149584017 | C | T | 64 | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(61): Show |
67 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.-12+2393C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149584017 | |||||||
| chr5:149584187 | T | C | 2 | a0001c0005t0005g0174 a0001c0005t0005g0175 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-12+2563T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149584187 | |||||||
| chr5:149584364 | AAGAG | A | 127 | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(124): Show |
138 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.-12+2748_-12+2751d others(6): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 149584364 | ||||||
| chr5:149584427 | C | T | 5 | a0001c0002t0005g0363 a0004c0004t0004g0020 a0004c0004t0004g0362 others(2): Show |
6 | HG00280.hp2 HG01074.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.-12+2803C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149584427 | |||||||
| chr5:149584428 | G | A | 2 | a0015c0020t0017g0176 a0015c0020t0017g0177 |
2 | HG01891.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-12+2804G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149584428 | |||||||
| chr5:149584462 | G | A | 37 | a0001c0002t0008g0009 a0001c0002t0008g0014 a0001c0002t0008g0168 others(34): Show |
40 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.-12+2838G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149584462 | |||||||
| chr5:149584648 | C | T | 2 | a0002c0001t0001g0140 a0004c0004t0004g0247 |
2 | HG00597.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.-12+3024C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149584648 | |||||||
| chr5:149584918 | G | A | 13 | a0004c0004t0009g0015 a0004c0004t0009g0255 a0004c0004t0009g0256 others(10): Show |
14 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-12+3294G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149584918 | |||||||
| chr5:149585159 | C | T | 1 | a0005c0011t0003g0361 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-12+3535C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149585159 | |||||||
| chr5:149585308 | G | A | 3 | a0001c0002t0015g0036 a0001c0002t0015g0037 a0001c0002t0015g0038 |
3 | HG02896.hp2 HG02897.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-12+3684G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149585308 | |||||||
| chr5:149585334 | G | A | 287 | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(284): Show |
306 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(303): Show |
intron_variant | MODIFIER | c.-12+3710G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149585334 | |||||||
| chr5:149585435 | C | A | 1 | a0004c0004t0004g0178 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-12+3811C>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149585435 | |||||||
| chr5:149585448 | G | A | 64 | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(61): Show |
67 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.-12+3824G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149585448 | |||||||
| chr5:149585490 | A | G | 13 | a0004c0004t0009g0015 a0004c0004t0009g0255 a0004c0004t0009g0256 others(10): Show |
14 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-12+3866A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149585490 | |||||||
| chr5:149585516 | A | ATTAT | 37 | a0001c0002t0008g0009 a0001c0002t0008g0014 a0001c0002t0008g0168 others(34): Show |
40 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.-12+3908_-12+3911d others(6): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 149585516 | ||||||
| chr5:149585540 | C | T | 50 | a0001c0002t0008g0009 a0001c0002t0008g0014 a0001c0002t0008g0168 others(47): Show |
54 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.-12+3916C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149585540 | |||||||
| chr5:149585662 | T | A | 234 | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(231): Show |
249 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.-12+4038T>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149585662 | |||||||
| chr5:149585665 | C | A | 234 | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(231): Show |
249 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.-12+4041C>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149585665 | |||||||
| chr5:149585674 | C | T | 234 | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(231): Show |
249 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.-12+4050C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149585674 | |||||||
| chr5:149585684 | AT | A | 234 | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(231): Show |
249 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.-12+4066delT | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 149585684 | ||||||
| chr5:149585787 | C | T | 1 | a0002c0001t0001g0139 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-12+4163C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149585787 | |||||||
| chr5:149585849 | G | T | 1 | a0002c0001t0001g0138 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-12+4225G>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149585849 | |||||||
| chr5:149585902 | C | A | 1 | a0003c0003t0002g0268 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-12+4278C>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149585902 | |||||||
| chr5:149585965 | T | C | 13 | a0001c0002t0008g0308 a0004c0010t0014g0312 a0004c0010t0014g0317 others(10): Show |
13 | HG00735.hp1 HG01496.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.-12+4341T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149585965 | |||||||
| chr5:149586001 | C | A | 126 | a0001c0002t0006g0008 a0001c0002t0006g0028 a0001c0002t0006g0050 others(123): Show |
131 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.-12+4377C>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149586001 | |||||||
| chr5:149586234 | GAAGTA | G | 109 | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(106): Show |
119 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.-12+4615_-12+4619d others(7): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 149586234 | ||||||
| chr5:149586286 | A | T | 1 | a0001c0002t0006g0137 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-12+4662A>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149586286 | |||||||
| chr5:149586399 | C | T | 1 | a0001c0005t0005g0245 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-12+4775C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149586399 | |||||||
| chr5:149586442 | CA | C | 13 | a0004c0004t0009g0015 a0004c0004t0009g0255 a0004c0004t0009g0256 others(10): Show |
14 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-12+4819delA | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149586442 | |||||||
| chr5:149586482 | C | T | 1 | a0004c0004t0028g0244 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-12+4858C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149586482 | |||||||
| chr5:149586515 | G | A | 2 | a0003c0003t0002g0018 a0003c0003t0002g0366 |
3 | HG00099.hp2 HG01257.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.-12+4891G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149586515 | |||||||
| chr5:149586530 | C | T | 128 | a0001c0002t0006g0008 a0001c0002t0006g0028 a0001c0002t0006g0050 others(125): Show |
133 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.-12+4906C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149586530 | |||||||
| chr5:149586531 | G | A | 64 | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(61): Show |
67 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.-12+4907G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149586531 | |||||||
| chr5:149586649 | G | A | 13 | a0004c0004t0009g0015 a0004c0004t0009g0255 a0004c0004t0009g0256 others(10): Show |
14 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-12+5025G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149586649 | |||||||
| chr5:149586661 | C | A | 2 | a0004c0004t0004g0179 a0006c0023t0007g0180 |
2 | HG01243.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-12+5037C>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149586661 | |||||||
| chr5:149586734 | A | G | 1 | a0004c0004t0028g0244 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-12+5110A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149586734 | |||||||
| chr5:149586900 | C | T | 37 | a0001c0002t0008g0009 a0001c0002t0008g0014 a0001c0002t0008g0168 others(34): Show |
40 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.-12+5276C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149586900 | |||||||
| chr5:149587043 | G | T | 322 | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(319): Show |
343 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(340): Show |
intron_variant | MODIFIER | c.-12+5419G>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149587043 | |||||||
| chr5:149587065 | G | A | 1 | a0002c0001t0001g0039 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-12+5441G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149587065 | |||||||
| chr5:149587306 | G | A | 1 | a0004c0004t0004g0218 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-12+5682G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149587306 | |||||||
| chr5:149587326 | C | A | 1 | a0002c0001t0001g0040 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-12+5702C>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149587326 | |||||||
| chr5:149587339 | A | G | 117 | a0001c0002t0006g0008 a0001c0002t0006g0028 a0001c0002t0006g0050 others(114): Show |
121 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.-12+5715A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149587339 | |||||||
| chr5:149587403 | A | G | 1 | a0002c0001t0003g0360 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-12+5779A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149587403 | |||||||
| chr5:149587540 | T | C | 2 | a0004c0010t0022g0044 a0004c0010t0022g0045 |
2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-12+5916T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149587540 | |||||||
| chr5:149587575 | C | T | 2 | a0015c0020t0017g0176 a0015c0020t0017g0177 |
2 | HG01891.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-12+5951C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149587575 | |||||||
| chr5:149587689 | C | G | 1 | a0004c0004t0004g0248 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-12+6065C>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149587689 | |||||||
| chr5:149587748 | A | C | 1 | a0004c0004t0030g0243 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-12+6124A>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149587748 | |||||||
| chr5:149587887 | C | G | 1 | a0002c0001t0001g0136 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-12+6263C>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149587887 | |||||||
| chr5:149587894 | C | CT | 17 | a0001c0002t0008g0168 a0004c0004t0009g0015 a0004c0004t0009g0255 others(14): Show |
18 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.-12+6289dupT | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 149587894 | ||||||
| chr5:149587894 | CT | C | 149 | a0001c0002t0006g0008 a0001c0002t0006g0028 a0001c0002t0006g0050 others(146): Show |
155 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.-12+6289delT | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 149587894 | ||||||
| chr5:149587894 | CTTT | C | 106 | a0001c0002t0004g0350 a0001c0002t0005g0358 a0001c0002t0005g0359 others(103): Show |
116 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.-12+6287_-12+6289d others(5): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 149587894 | ||||||
| chr5:149587895 | T | C | 5 | a0001c0002t0006g0134 a0001c0002t0020g0135 a0002c0001t0001g0035 others(2): Show |
5 | HG00609.hp2 HG00738.hp2 HG00741.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12+6271T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149587895 | |||||||
| chr5:149587896 | T | C | 119 | a0001c0002t0006g0008 a0001c0002t0006g0028 a0001c0002t0006g0050 others(116): Show |
123 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.-12+6272T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149587896 | |||||||
| chr5:149587897 | T | A | 1 | a0005c0011t0003g0361 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-12+6273T>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149587897 | |||||||
| chr5:149587897 | T | C | 2 | a0009c0014t0023g0006 a0009c0014t0035g0029 |
3 | HG02895.hp1 HG02897.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-12+6273T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149587897 | |||||||
| chr5:149587927 | C | T | 13 | a0001c0002t0008g0308 a0004c0010t0014g0312 a0004c0010t0014g0317 others(10): Show |
13 | HG00735.hp1 HG01496.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.-12+6303C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149587927 | |||||||
| chr5:149587939 | C | G | 1 | a0004c0004t0004g0242 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-12+6315C>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149587939 | |||||||
| chr5:149587953 | G | A | 109 | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(106): Show |
119 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.-12+6329G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149587953 | |||||||
| chr5:149587982 | C | T | 109 | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(106): Show |
119 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.-12+6358C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149587982 | |||||||
| chr5:149588129 | C | T | 36 | a0003c0003t0002g0013 a0004c0004t0002g0229 a0004c0004t0004g0012 others(33): Show |
38 | HG00438.hp1 HG00558.hp1 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.-12+6505C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149588129 | |||||||
| chr5:149588133 | G | A | 2 | a0002c0001t0001g0047 a0002c0001t0001g0048 |
2 | HG00423.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.-12+6509G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149588133 | |||||||
| chr5:149588186 | G | A | 109 | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(106): Show |
119 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.-12+6562G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149588186 | |||||||
| chr5:149588198 | T | TTTTG | 116 | a0001c0002t0006g0008 a0001c0002t0006g0028 a0001c0002t0006g0051 others(113): Show |
120 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.-12+6603_-12+6606d others(6): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 149588198 | ||||||
| chr5:149588227 | T | C | 1 | a0003c0003t0002g0321 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-12+6603T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149588227 | |||||||
| chr5:149588227 | T | TTTGC | 108 | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(105): Show |
118 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.-12+6606_-12+6609d others(6): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 149588227 | ||||||
| chr5:149588301 | C | A | 13 | a0001c0002t0008g0308 a0004c0010t0014g0312 a0004c0010t0014g0317 others(10): Show |
13 | HG00735.hp1 HG01496.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.-12+6677C>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149588301 | |||||||
| chr5:149588416 | C | A | 37 | a0001c0002t0008g0009 a0001c0002t0008g0014 a0001c0002t0008g0168 others(34): Show |
40 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.-12+6792C>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149588416 | |||||||
| chr5:149588546 | G | A | 1 | a0006c0006t0007g0322 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-12+6922G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149588546 | |||||||
| chr5:149588611 | A | G | 6 | a0001c0002t0006g0127 a0001c0002t0006g0128 a0001c0002t0006g0129 others(3): Show |
6 | HG00738.hp2 HG01261.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12+6987A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149588611 | |||||||
| chr5:149588704 | T | C | 126 | a0001c0002t0006g0008 a0001c0002t0006g0028 a0001c0002t0006g0050 others(123): Show |
131 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.-12+7080T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149588704 | |||||||
| chr5:149588729 | G | T | 235 | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(232): Show |
250 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.-12+7105G>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149588729 | |||||||
| chr5:149588761 | A | G | 2 | a0015c0020t0017g0176 a0015c0020t0017g0177 |
2 | HG01891.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-12+7137A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149588761 | |||||||
| chr5:149588808 | G | A | 2 | a0002c0001t0003g0270 a0002c0001t0018g0269 |
2 | HG02145.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-12+7184G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149588808 | |||||||
| chr5:149588812 | G | A | 109 | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(106): Show |
119 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.-12+7188G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149588812 | |||||||
| chr5:149588816 | G | A | 30 | a0003c0003t0002g0013 a0004c0004t0002g0229 a0004c0004t0004g0012 others(27): Show |
32 | HG00438.hp1 HG00558.hp1 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.-12+7192G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149588816 | |||||||
| chr5:149589040 | G | A | 37 | a0001c0002t0008g0009 a0001c0002t0008g0014 a0001c0002t0008g0168 others(34): Show |
40 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.-12+7416G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149589040 | |||||||
| chr5:149589107 | T | C | 126 | a0001c0002t0006g0008 a0001c0002t0006g0028 a0001c0002t0006g0050 others(123): Show |
131 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.-12+7483T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149589107 | |||||||
| chr5:149589115 | G | C | 1 | a0004c0004t0033g0266 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-12+7491G>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149589115 | |||||||
| chr5:149589128 | A | G | 126 | a0001c0002t0006g0008 a0001c0002t0006g0028 a0001c0002t0006g0050 others(123): Show |
131 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.-12+7504A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149589128 | |||||||
| chr5:149589194 | TA | T | 65 | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(62): Show |
68 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.-12+7583delA | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 149589194 | ||||||
| chr5:149589323 | T | TATTA | 124 | a0001c0002t0006g0008 a0001c0002t0006g0028 a0001c0002t0006g0050 others(121): Show |
128 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.-12+7715_-12+7718d others(6): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 149589323 | ||||||
| chr5:149589339 | A | T | 1 | a0004c0004t0009g0015 | 2 | HG01884.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-12+7715A>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149589339 | |||||||
| chr5:149589420 | A | G | 321 | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(318): Show |
342 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(339): Show |
intron_variant | MODIFIER | c.-12+7796A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149589420 | |||||||
| chr5:149589656 | C | A | 2 | a0009c0014t0023g0006 a0009c0014t0035g0029 |
3 | HG02895.hp1 HG02897.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-12+8032C>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149589656 | |||||||
| chr5:149589811 | G | A | 2 | a0003c0003t0002g0324 a0003c0003t0002g0325 |
2 | NA18949.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.-11-7948G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149589811 | |||||||
| chr5:149589853 | G | A | 117 | a0001c0002t0006g0008 a0001c0002t0006g0028 a0001c0002t0006g0050 others(114): Show |
121 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.-11-7906G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149589853 | |||||||
| chr5:149590174 | C | T | 2 | a0002c0001t0003g0270 a0002c0001t0018g0269 |
2 | HG02145.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-11-7585C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149590174 | |||||||
| chr5:149590184 | CAGAAG | C | 124 | a0001c0002t0006g0008 a0001c0002t0006g0028 a0001c0002t0006g0050 others(121): Show |
129 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.-11-7566_-11-7562d others(7): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 149590184 | ||||||
| chr5:149590244 | G | C | 1 | a0004c0004t0004g0362 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-11-7515G>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149590244 | |||||||
| chr5:149590282 | C | CT | 153 | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(150): Show |
165 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.-11-7460dupT | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 149590282 | ||||||
| chr5:149590328 | C | T | 2 | a0001c0002t0005g0358 a0001c0002t0005g0359 |
2 | HG01516.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-11-7431C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149590328 | |||||||
| chr5:149590369 | C | T | 32 | a0004c0004t0002g0229 a0004c0004t0004g0012 a0004c0004t0004g0143 others(29): Show |
33 | HG00438.hp1 HG00558.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.-11-7390C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149590369 | |||||||
| chr5:149590466 | G | T | 1 | a0009c0014t0023g0006 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-11-7293G>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149590466 | |||||||
| chr5:149590502 | G | A | 4 | a0004c0004t0004g0240 a0004c0004t0004g0241 a0004c0004t0004g0248 others(1): Show |
4 | HG02145.hp1 HG02630.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11-7257G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149590502 | |||||||
| chr5:149590558 | G | A | 2 | a0009c0014t0023g0006 a0009c0014t0035g0029 |
3 | HG02895.hp1 HG02897.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-11-7201G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149590558 | |||||||
| chr5:149590575 | T | A | 1 | a0009c0014t0011g0273 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-11-7184T>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149590575 | |||||||
| chr5:149590593 | C | CT | 150 | a0001c0002t0006g0008 a0001c0002t0006g0028 a0001c0002t0006g0050 others(147): Show |
158 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.-11-7152dupT | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 149590593 | ||||||
| chr5:149590701 | T | C | 1 | a0005c0035t0003g0239 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-11-7058T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149590701 | |||||||
| chr5:149590772 | T | C | 7 | a0001c0002t0006g0051 a0001c0002t0015g0036 a0001c0002t0015g0037 others(4): Show |
7 | HG02280.hp2 HG02818.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11-6987T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149590772 | |||||||
| chr5:149590848 | C | T | 2 | a0015c0020t0017g0176 a0015c0020t0017g0177 |
2 | HG01891.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-11-6911C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149590848 | |||||||
| chr5:149590934 | C | G | 248 | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(245): Show |
266 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.-11-6825C>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149590934 | |||||||
| chr5:149591063 | G | T | 327 | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(324): Show |
348 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(345): Show |
intron_variant | MODIFIER | c.-11-6696G>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149591063 | |||||||
| chr5:149591160 | C | T | 103 | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(100): Show |
113 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.-11-6599C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149591160 | |||||||
| chr5:149591226 | C | CA | 63 | a0001c0002t0005g0363 a0002c0001t0003g0166 a0003c0003t0002g0246 others(60): Show |
65 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.-11-6518dupA | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 149591226 | ||||||
| chr5:149591226 | CA | C | 111 | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(108): Show |
122 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.-11-6518delA | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 149591226 | ||||||
| chr5:149591226 | CAA | C | 135 | a0001c0002t0006g0008 a0001c0002t0006g0028 a0001c0002t0006g0050 others(132): Show |
142 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.-11-6519_-11-6518d others(4): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 149591226 | ||||||
| chr5:149591238 | A | G | 2 | a0002c0001t0001g0104 a0002c0001t0001g0139 |
2 | NA18944.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.-11-6521A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149591238 | |||||||
| chr5:149591362 | C | T | 144 | a0001c0002t0006g0008 a0001c0002t0006g0028 a0001c0002t0006g0050 others(141): Show |
152 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.-11-6397C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149591362 | |||||||
| chr5:149591387 | T | A | 98 | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(95): Show |
107 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.-11-6372T>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149591387 | |||||||
| chr5:149591420 | A | G | 248 | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(245): Show |
266 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.-11-6339A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149591420 | |||||||
| chr5:149591681 | A | G | 1 | a0008c0017t0013g0250 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-11-6078A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149591681 | |||||||
| chr5:149591742 | A | C | 1 | a0005c0011t0001g0041 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-11-6017A>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149591742 | |||||||
| chr5:149591742 | A | G | 326 | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(323): Show |
347 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(344): Show |
intron_variant | MODIFIER | c.-11-6017A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149591742 | |||||||
| chr5:149591777 | C | A | 1 | a0002c0001t0001g0054 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-11-5982C>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149591777 | |||||||
| chr5:149591782 | T | C | 1 | a0002c0001t0001g0055 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-11-5977T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149591782 | |||||||
| chr5:149591831 | A | T | 15 | a0004c0004t0009g0015 a0004c0004t0009g0255 a0004c0004t0009g0256 others(12): Show |
16 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.-11-5928A>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149591831 | |||||||
| chr5:149591962 | C | T | 38 | a0001c0002t0005g0363 a0003c0003t0002g0246 a0004c0004t0002g0229 others(35): Show |
40 | HG00280.hp2 HG00438.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.-11-5797C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149591962 | |||||||
| chr5:149592062 | C | T | 327 | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(324): Show |
348 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(345): Show |
intron_variant | MODIFIER | c.-11-5697C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149592062 | |||||||
| chr5:149592100 | A | G | 2 | a0015c0020t0017g0176 a0015c0020t0017g0177 |
2 | HG01891.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-11-5659A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149592100 | |||||||
| chr5:149592238 | T | A | 144 | a0001c0002t0006g0008 a0001c0002t0006g0028 a0001c0002t0006g0050 others(141): Show |
152 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.-11-5521T>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149592238 | |||||||
| chr5:149592396 | A | G | 2 | a0001c0005t0005g0174 a0001c0005t0005g0175 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-11-5363A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149592396 | |||||||
| chr5:149592577 | A | G | 104 | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(101): Show |
114 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.-11-5182A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149592577 | |||||||
| chr5:149592626 | A | G | 2 | a0015c0020t0017g0176 a0015c0020t0017g0177 |
2 | HG01891.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-11-5133A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149592626 | |||||||
| chr5:149592739 | C | T | 15 | a0004c0004t0009g0015 a0004c0004t0009g0255 a0004c0004t0009g0256 others(12): Show |
16 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.-11-5020C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149592739 | |||||||
| chr5:149592859 | T | C | 12 | a0004c0010t0014g0312 a0004c0010t0014g0317 a0004c0010t0014g0319 others(9): Show |
12 | HG00735.hp1 HG01496.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.-11-4900T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149592859 | |||||||
| chr5:149593148 | T | G | 327 | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(324): Show |
348 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(345): Show |
intron_variant | MODIFIER | c.-11-4611T>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149593148 | |||||||
| chr5:149593403 | T | C | 145 | a0001c0002t0006g0008 a0001c0002t0006g0028 a0001c0002t0006g0050 others(142): Show |
153 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.-11-4356T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149593403 | |||||||
| chr5:149593491 | C | T | 1 | a0013c0022t0004g0357 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-11-4268C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149593491 | |||||||
| chr5:149593577 | C | G | 144 | a0001c0002t0006g0008 a0001c0002t0006g0028 a0001c0002t0006g0050 others(141): Show |
152 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.-11-4182C>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149593577 | |||||||
| chr5:149593678 | T | C | 3 | a0001c0002t0027g0327 a0009c0014t0023g0006 a0009c0014t0035g0029 |
4 | HG02895.hp1 HG02897.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11-4081T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149593678 | |||||||
| chr5:149593741 | A | G | 28 | a0004c0004t0002g0229 a0004c0004t0004g0012 a0004c0004t0004g0143 others(25): Show |
29 | HG00438.hp1 HG00558.hp1 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.-11-4018A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149593741 | |||||||
| chr5:149594008 | G | T | 7 | a0001c0005t0004g0206 a0001c0005t0004g0207 a0001c0005t0004g0209 others(4): Show |
7 | HG02055.hp1 HG02896.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11-3751G>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149594008 | |||||||
| chr5:149594027 | A | G | 1 | a0003c0003t0002g0304 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-11-3732A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149594027 | |||||||
| chr5:149594056 | C | T | 1 | a0002c0001t0001g0054 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-11-3703C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149594056 | |||||||
| chr5:149594394 | C | T | 1 | a0001c0005t0004g0212 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-11-3365C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149594394 | |||||||
| chr5:149594566 | T | G | 4 | a0004c0010t0022g0044 a0004c0010t0022g0045 a0017c0021t0006g0141 others(1): Show |
4 | HG01884.hp1 HG03130.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11-3193T>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149594566 | |||||||
| chr5:149594698 | G | A | 124 | a0001c0002t0005g0358 a0001c0002t0005g0359 a0001c0002t0005g0363 others(121): Show |
136 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.-11-3061G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149594698 | |||||||
| chr5:149594964 | A | G | 1 | a0007c0008t0001g0103 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-11-2795A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149594964 | |||||||
| chr5:149595019 | A | T | 1 | a0003c0003t0016g0303 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-11-2740A>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149595019 | |||||||
| chr5:149595059 | A | T | 2 | a0001c0002t0011g0356 a0003c0003t0002g0302 |
2 | HG02647.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.-11-2700A>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149595059 | |||||||
| chr5:149595285 | C | T | 33 | a0003c0012t0002g0162 a0003c0012t0002g0163 a0003c0012t0002g0165 others(30): Show |
33 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.-11-2474C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149595285 | |||||||
| chr5:149595354 | T | A | 11 | a0004c0010t0014g0312 a0004c0010t0014g0317 a0004c0010t0014g0319 others(8): Show |
11 | HG00735.hp1 HG01496.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.-11-2405T>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149595354 | |||||||
| chr5:149595739 | G | T | 5 | a0009c0013t0011g0017 a0009c0013t0011g0320 a0009c0013t0021g0108 others(2): Show |
6 | HG01069.hp2 HG01071.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11-2020G>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149595739 | |||||||
| chr5:149595792 | C | T | 1 | a0006c0006t0007g0322 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-11-1967C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149595792 | |||||||
| chr5:149595800 | C | T | 28 | a0001c0002t0004g0350 a0001c0002t0011g0356 a0002c0001t0003g0270 others(25): Show |
29 | HG00639.hp2 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.-11-1959C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149595800 | |||||||
| chr5:149595899 | C | T | 1 | a0001c0002t0008g0254 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-11-1860C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149595899 | |||||||
| chr5:149595945 | A | AT | 26 | a0002c0001t0001g0048 a0004c0004t0009g0015 a0004c0004t0009g0256 others(23): Show |
27 | HG00423.hp2 HG00735.hp1 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.-11-1799dupT | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 149595945 | ||||||
| chr5:149595945 | AT | A | 71 | a0001c0002t0004g0350 a0001c0002t0011g0356 a0002c0001t0001g0022 others(68): Show |
73 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.-11-1799delT | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 149595945 | ||||||
| chr5:149595994 | T | TG | 137 | a0001c0002t0005g0342 a0001c0002t0006g0008 a0001c0002t0006g0028 others(134): Show |
145 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.-11-1758dupG | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 149595994 | ||||||
| chr5:149596079 | A | G | 1 | a0003c0003t0002g0301 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-11-1680A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149596079 | |||||||
| chr5:149596102 | C | T | 138 | a0001c0002t0005g0342 a0001c0002t0006g0008 a0001c0002t0006g0028 others(135): Show |
146 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.-11-1657C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149596102 | |||||||
| chr5:149596118 | A | G | 1 | a0001c0002t0006g0125 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-11-1641A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149596118 | |||||||
| chr5:149596235 | G | A | 2 | a0010c0015t0005g0182 a0010c0015t0005g0183 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.-11-1524G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149596235 | |||||||
| chr5:149596482 | T | G | 1 | a0003c0012t0002g0213 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-11-1277T>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149596482 | |||||||
| chr5:149596524 | C | T | 1 | a0005c0035t0003g0239 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-11-1235C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149596524 | |||||||
| chr5:149596594 | C | T | 127 | a0001c0002t0005g0342 a0001c0002t0006g0008 a0001c0002t0006g0028 others(124): Show |
135 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.-11-1165C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149596594 | |||||||
| chr5:149596600 | C | T | 1 | a0002c0001t0001g0094 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-11-1159C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149596600 | |||||||
| chr5:149596751 | G | A | 1 | a0001c0002t0006g0137 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-11-1008G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149596751 | |||||||
| chr5:149596924 | A | T | 1 | a0004c0010t0014g0319 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-11-835A>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149596924 | |||||||
| chr5:149596941 | G | A | 124 | a0001c0002t0005g0358 a0001c0002t0005g0359 a0001c0002t0005g0363 others(121): Show |
136 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.-11-818G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149596941 | |||||||
| chr5:149597194 | G | T | 1 | a0004c0004t0004g0238 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-11-565G>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149597194 | |||||||
| chr5:149597235 | A | C | 1 | a0005c0011t0003g0361 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-11-524A>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149597235 | |||||||
| chr5:149597266 | A | T | 5 | a0002c0001t0001g0090 a0002c0001t0001g0091 a0002c0001t0001g0092 others(2): Show |
5 | NA18940.hp1 NA18975.hp1 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.-11-493A>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149597266 | |||||||
| chr5:149597267 | A | T | 116 | a0001c0002t0005g0342 a0001c0002t0006g0008 a0001c0002t0006g0028 others(113): Show |
123 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.-11-492A>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149597267 | |||||||
| chr5:149597268 | A | T | 261 | a0001c0002t0005g0342 a0001c0002t0005g0358 a0001c0002t0005g0359 others(258): Show |
281 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.-11-491A>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149597268 | |||||||
| chr5:149597269 | A | T | 262 | a0001c0002t0005g0342 a0001c0002t0005g0358 a0001c0002t0005g0359 others(259): Show |
282 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.-11-490A>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149597269 | |||||||
| chr5:149597350 | C | T | 1 | a0015c0020t0017g0177 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-11-409C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149597350 | |||||||
| chr5:149597402 | G | C | 11 | a0004c0010t0014g0312 a0004c0010t0014g0317 a0004c0010t0014g0319 others(8): Show |
11 | HG00735.hp1 HG01496.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.-11-357G>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149597402 | |||||||
| chr5:149597408 | G | A | 64 | a0001c0002t0005g0358 a0001c0002t0005g0359 a0001c0002t0005g0363 others(61): Show |
73 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.-11-351G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149597408 | |||||||
| chr5:149597478 | C | G | 2 | a0003c0003t0002g0299 a0003c0003t0002g0300 |
2 | NA18969.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.-11-281C>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149597478 | |||||||
| chr5:149597588 | T | A | 2 | a0005c0011t0003g0326 a0006c0006t0032g0105 |
2 | HG02922.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-11-171T>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149597588 | |||||||
| chr5:149597652 | C | T | 6 | a0001c0002t0008g0170 a0001c0002t0008g0171 a0001c0002t0010g0010 others(3): Show |
7 | NA18941.hp2 NA18944.hp2 NA18954.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11-107C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149597652 | |||||||
| chr5:149597670 | C | T | 24 | a0001c0002t0006g0008 a0001c0002t0006g0050 a0001c0002t0006g0051 others(21): Show |
25 | HG00408.hp2 HG00738.hp1 HG02071.hp1 others(22): Show |
intron_variant | MODIFIER | c.-11-89C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 1/12 | chr5 | 149597670 | |||||||
| chr5:149598034 | C | G | 1 | a0003c0012t0002g0165 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.186+79C>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598034 | |||||||
| chr5:149598050 | C | T | 260 | a0001c0002t0005g0342 a0001c0002t0005g0358 a0001c0002t0005g0359 others(257): Show |
280 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.186+95C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598050 | |||||||
| chr5:149598188 | G | A | 3 | a0004c0010t0009g0339 a0004c0010t0009g0340 a0008c0009t0002g0329 |
3 | HG02970.hp2 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.186+233G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598188 | |||||||
| chr5:149598262 | A | ACTC | 8 | a0001c0002t0005g0342 a0001c0002t0006g0086 a0001c0002t0008g0252 others(5): Show |
8 | HG00558.hp2 HG02818.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.186+308_186+310dup others(3): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598262 | ||||||
| chr5:149598263 | C | CTCCTCT | 15 | a0001c0002t0008g0014 a0001c0002t0008g0251 a0001c0002t0027g0327 others(12): Show |
16 | HG01496.hp2 HG01952.hp2 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.186+310_186+311ins others(6): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598263 | ||||||
| chr5:149598263 | C | CTCT | 27 | a0001c0002t0005g0363 a0001c0005t0005g0004 a0001c0005t0005g0011 others(24): Show |
29 | HG00099.hp1 HG00323.hp2 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.186+370_186+372dup others(3): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598263 | ||||||
| chr5:149598263 | C | CTCTTCT | 22 | a0001c0005t0004g0207 a0001c0005t0004g0209 a0001c0005t0004g0210 others(19): Show |
25 | HG00280.hp1 HG00597.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.186+367_186+372dup others(6): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598263 | ||||||
| chr5:149598263 | C | CTCTTCTT others(2): Show |
16 | a0001c0005t0004g0206 a0001c0005t0005g0185 a0001c0005t0005g0186 others(13): Show |
18 | HG01069.hp2 HG01071.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.186+364_186+372dup others(9): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598263 | ||||||
| chr5:149598263 | C | CTCTTCTT others(5): Show |
12 | a0001c0002t0011g0356 a0002c0001t0003g0343 a0004c0004t0004g0184 others(9): Show |
12 | HG00558.hp1 HG00597.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.186+361_186+372dup others(12): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598263 | ||||||
| chr5:149598263 | C | CTCTTCTT others(8): Show |
6 | a0003c0012t0002g0274 a0004c0004t0004g0147 a0005c0007t0003g0148 others(3): Show |
6 | NA18940.hp2 NA18948.hp2 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.186+358_186+372dup others(15): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598263 | ||||||
| chr5:149598263 | C | CTCTTCTT others(11): Show |
3 | a0002c0001t0003g0360 a0005c0007t0003g0146 a0009c0013t0021g0126 |
3 | HG00639.hp2 HG03209.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.186+355_186+372dup others(18): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598263 | ||||||
| chr5:149598263 | C | CTCTTCTT others(14): Show |
1 | a0005c0007t0003g0145 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.186+352_186+372dup others(21): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598263 | ||||||
| chr5:149598263 | C | CTCTTCTT others(17): Show |
1 | a0005c0007t0003g0144 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.186+349_186+372dup others(24): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598263 | ||||||
| chr5:149598263 | CTCT | C | 22 | a0001c0005t0005g0200 a0001c0005t0005g0202 a0001c0005t0005g0203 others(19): Show |
24 | HG00673.hp2 HG00735.hp2 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.186+370_186+372del others(3): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598263 | ||||||
| chr5:149598263 | CTCTTCT | C | 12 | a0003c0003t0002g0298 a0004c0004t0004g0232 a0004c0004t0004g0241 others(9): Show |
12 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.186+367_186+372del others(6): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598263 | ||||||
| chr5:149598263 | CTCTTCTT others(2): Show |
C | 7 | a0003c0012t0012g0099 a0004c0004t0009g0262 a0004c0004t0009g0263 others(4): Show |
7 | HG00621.hp1 HG02074.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.186+364_186+372del others(9): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598263 | ||||||
| chr5:149598263 | CTCTTCTT others(5): Show |
C | 5 | a0004c0004t0009g0015 a0004c0004t0009g0255 a0004c0004t0009g0265 others(2): Show |
6 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.186+361_186+372del others(12): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598263 | ||||||
| chr5:149598263 | CTCTTCTT others(8): Show |
C | 3 | a0005c0007t0003g0164 a0005c0011t0003g0361 a0007c0008t0001g0102 |
3 | HG02615.hp2 NA19012.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.186+358_186+372del others(15): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598263 | ||||||
| chr5:149598266 | T | C | 109 | a0001c0002t0006g0008 a0001c0002t0006g0028 a0001c0002t0006g0050 others(106): Show |
115 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.186+311T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598266 | |||||||
| chr5:149598269 | T | C | 2 | a0002c0001t0001g0034 a0009c0014t0023g0006 |
3 | HG00673.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.186+314T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598269 | |||||||
| chr5:149598272 | T | C | 1 | a0004c0010t0022g0045 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.186+317T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598272 | |||||||
| chr5:149598303 | TCTTCTTC others(29): Show |
T | 1 | a0008c0009t0025g0318 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.186+349_186+384del others(36): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598303 | |||||||
| chr5:149598312 | TCTTCTTC others(20): Show |
T | 2 | a0004c0010t0014g0312 a0004c0010t0014g0319 |
2 | NA18906.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.186+358_186+384del others(27): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598312 | |||||||
| chr5:149598322 | CTTCT | C | 36 | a0001c0002t0005g0359 a0001c0002t0006g0106 a0001c0002t0006g0107 others(33): Show |
38 | HG00140.hp1 HG00621.hp2 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.186+373_186+376del others(4): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598322 | ||||||
| chr5:149598323 | TTCTTTCT others(3): Show |
T | 1 | a0001c0002t0006g0134 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.186+373_186+382del others(10): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598323 | ||||||
| chr5:149598323 | TTCTTTCT others(9): Show |
T | 2 | a0002c0001t0001g0066 a0002c0001t0001g0068 |
2 | NA18970.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.186+373_186+388del others(16): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598323 | ||||||
| chr5:149598325 | CT | C | 81 | a0001c0002t0005g0358 a0001c0002t0006g0008 a0001c0002t0006g0050 others(78): Show |
84 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.186+373delT | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598325 | ||||||
| chr5:149598326 | T | TTC | 8 | a0001c0002t0004g0350 a0003c0003t0002g0001 a0004c0004t0004g0227 others(5): Show |
9 | HG01074.hp1 HG01975.hp1 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.186+372_186+373ins others(2): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598326 | ||||||
| chr5:149598326 | TTTCTTCC | T | 36 | a0001c0002t0006g0028 a0001c0002t0006g0051 a0001c0002t0006g0122 others(33): Show |
37 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.186+373_186+379del others(7): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598326 | ||||||
| chr5:149598327 | TTCTTCCT others(4): Show |
T | 1 | a0005c0027t0003g0236 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.186+373_186+383del others(11): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598327 | |||||||
| chr5:149598333 | C | T | 124 | a0001c0002t0004g0350 a0001c0002t0005g0358 a0001c0002t0005g0359 others(121): Show |
132 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.186+378C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598333 | |||||||
| chr5:149598337 | TCC | T | 27 | a0001c0002t0005g0359 a0002c0001t0003g0290 a0003c0003t0002g0001 others(24): Show |
32 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(29): Show |
intron_variant | MODIFIER | c.186+383_186+384del others(2): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598337 | |||||||
| chr5:149598338 | C | CT | 24 | a0001c0002t0005g0358 a0003c0003t0002g0001 a0003c0003t0002g0286 others(21): Show |
25 | HG00438.hp1 HG01074.hp1 HG01516.hp2 others(22): Show |
intron_variant | MODIFIER | c.186+383_186+384ins others(1): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598338 | |||||||
| chr5:149598339 | C | T | 129 | a0001c0002t0005g0358 a0001c0002t0006g0008 a0001c0002t0006g0028 others(126): Show |
136 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.186+384C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598339 | |||||||
| chr5:149598343 | TCC | T | 67 | a0001c0002t0006g0008 a0001c0002t0006g0028 a0001c0002t0006g0051 others(64): Show |
72 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.186+389_186+390del others(2): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598343 | |||||||
| chr5:149598344 | C | CT | 4 | a0003c0003t0002g0275 a0004c0004t0004g0226 a0004c0004t0004g0362 others(1): Show |
4 | HG00280.hp2 HG01952.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.186+389_186+390ins others(1): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598344 | |||||||
| chr5:149598344 | CCTCTT | C | 16 | a0001c0002t0006g0050 a0001c0002t0006g0087 a0001c0002t0006g0088 others(13): Show |
16 | HG00323.hp1 HG01099.hp1 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.186+392_186+396del others(5): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598344 | ||||||
| chr5:149598345 | C | T | 24 | a0001c0002t0006g0113 a0001c0002t0006g0118 a0001c0002t0006g0119 others(21): Show |
24 | HG00140.hp2 HG00280.hp2 HG01256.hp2 others(21): Show |
intron_variant | MODIFIER | c.186+390C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598345 | |||||||
| chr5:149598348 | TTC | T | 6 | a0001c0002t0006g0119 a0001c0002t0006g0120 a0001c0002t0006g0121 others(3): Show |
6 | HG01943.hp1 NA18944.hp1 NA18954.hp1 others(3): Show |
intron_variant | MODIFIER | c.186+395_186+396del others(2): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598348 | ||||||
| chr5:149598348 | TTCTTCTT others(8): Show |
T | 65 | a0001c0002t0005g0363 a0003c0003t0002g0013 a0003c0003t0002g0016 others(62): Show |
70 | HG00408.hp1 HG00597.hp2 HG00673.hp1 others(67): Show |
intron_variant | MODIFIER | c.186+427_186+441del others(15): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598348 | ||||||
| chr5:149598348 | TTCTTCTT others(23): Show |
T | 31 | a0001c0002t0005g0342 a0001c0002t0006g0063 a0001c0002t0006g0086 others(28): Show |
33 | HG00544.hp2 HG00558.hp2 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.186+412_186+441del others(30): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598348 | ||||||
| chr5:149598350 | C | CT | 6 | a0001c0002t0006g0118 a0002c0001t0001g0047 a0002c0001t0001g0054 others(3): Show |
6 | HG00140.hp2 HG01256.hp2 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.186+397dupT | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598350 | ||||||
| chr5:149598350 | C | T | 16 | a0001c0002t0006g0050 a0001c0002t0006g0087 a0001c0002t0006g0088 others(13): Show |
16 | HG00323.hp1 HG01099.hp1 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.186+395C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598350 | |||||||
| chr5:149598351 | T | C | 128 | a0001c0002t0005g0358 a0001c0002t0005g0359 a0001c0002t0006g0008 others(125): Show |
140 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.186+396T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598351 | |||||||
| chr5:149598355 | TCC | T | 3 | a0002c0001t0001g0040 a0002c0001t0001g0066 a0002c0001t0001g0068 |
3 | HG06807.hp2 NA18970.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.186+401_186+402del others(2): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598355 | |||||||
| chr5:149598357 | C | T | 2 | a0002c0001t0001g0139 a0005c0011t0003g0326 |
2 | HG03486.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.186+402C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598357 | |||||||
| chr5:149598360 | TTCC | T | 55 | a0001c0002t0005g0358 a0001c0002t0005g0359 a0002c0001t0003g0290 others(52): Show |
62 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.186+408_186+410del others(3): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598360 | ||||||
| chr5:149598363 | C | CTCT | 4 | a0003c0003t0002g0275 a0004c0004t0004g0226 a0004c0004t0004g0362 others(1): Show |
4 | HG00280.hp2 HG01952.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.186+414_186+416dup others(3): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598363 | ||||||
| chr5:149598363 | CTCT | C | 34 | a0001c0002t0006g0050 a0001c0002t0006g0087 a0001c0002t0006g0088 others(31): Show |
35 | HG00140.hp2 HG00323.hp1 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.186+414_186+416del others(3): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598363 | ||||||
| chr5:149598366 | TTCTTCCT others(5): Show |
T | 67 | a0001c0002t0006g0008 a0001c0002t0006g0028 a0001c0002t0006g0051 others(64): Show |
72 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.186+417_186+428del others(12): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598366 | ||||||
| chr5:149598369 | T | C | 2 | a0002c0001t0001g0040 a0002c0001t0001g0139 |
2 | HG06807.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.186+414T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598369 | |||||||
| chr5:149598372 | C | T | 2 | a0002c0001t0001g0040 a0002c0001t0001g0139 |
2 | HG06807.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.186+417C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598372 | |||||||
| chr5:149598375 | T | C | 2 | a0002c0001t0001g0040 a0002c0001t0001g0139 |
2 | HG06807.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.186+420T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598375 | |||||||
| chr5:149598375 | TTCC | T | 31 | a0001c0002t0006g0050 a0001c0002t0006g0087 a0001c0002t0006g0088 others(28): Show |
32 | HG00140.hp2 HG00323.hp1 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.186+423_186+425del others(3): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598375 | ||||||
| chr5:149598378 | C | T | 2 | a0002c0001t0001g0040 a0002c0001t0001g0139 |
2 | HG06807.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.186+423C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598378 | |||||||
| chr5:149598439 | CCTTCCTC others(12): Show |
C | 5 | a0002c0001t0001g0132 a0002c0001t0003g0214 a0002c0001t0003g0215 others(2): Show |
5 | HG00323.hp1 HG00741.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.186+486_186+504del others(19): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598439 | ||||||
| chr5:149598542 | T | C | 136 | a0001c0002t0005g0342 a0001c0002t0006g0008 a0001c0002t0006g0028 others(133): Show |
144 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.186+587T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598542 | |||||||
| chr5:149598544 | A | G | 260 | a0001c0002t0005g0342 a0001c0002t0005g0358 a0001c0002t0005g0359 others(257): Show |
280 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.186+589A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598544 | |||||||
| chr5:149598554 | T | C | 1 | a0004c0010t0014g0317 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.186+599T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598554 | |||||||
| chr5:149598560 | C | A | 1 | a0009c0014t0023g0006 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.186+605C>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598560 | |||||||
| chr5:149598737 | C | CAT | 4 | a0001c0002t0027g0327 a0009c0014t0011g0273 a0009c0014t0023g0006 others(1): Show |
5 | HG02615.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.186+793_186+794dup others(2): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598737 | ||||||
| chr5:149598744 | A | C | 2 | a0015c0020t0017g0176 a0015c0020t0017g0177 |
2 | HG01891.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.186+789A>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598744 | |||||||
| chr5:149598745 | TATATCTA others(7): Show |
T | 5 | a0002c0001t0001g0027 a0002c0001t0001g0052 a0002c0001t0001g0070 others(2): Show |
5 | NA18946.hp1 NA18967.hp2 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.186+795_186+808del others(14): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598745 | ||||||
| chr5:149598747 | TATCTATA others(5): Show |
T | 110 | a0001c0002t0005g0358 a0001c0002t0005g0359 a0001c0002t0005g0363 others(107): Show |
122 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.186+795_186+806del others(12): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598747 | ||||||
| chr5:149598747 | TATCTATA others(11): Show |
T | 2 | a0004c0004t0004g0221 a0004c0004t0004g0230 |
2 | NA18941.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.186+795_186+812del others(18): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598747 | ||||||
| chr5:149598747 | TATCTATA others(17): Show |
T | 1 | a0016c0019t0002g0294 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.186+795_186+818del others(24): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598747 | ||||||
| chr5:149598748 | ATC | A | 112 | a0001c0002t0005g0342 a0001c0002t0006g0008 a0001c0002t0006g0028 others(109): Show |
118 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.186+795_186+796del others(2): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598748 | ||||||
| chr5:149598750 | C | A | 28 | a0001c0002t0006g0063 a0001c0002t0015g0036 a0001c0002t0020g0135 others(25): Show |
30 | HG00735.hp1 HG00738.hp2 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.186+795C>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598750 | |||||||
| chr5:149598753 | T | TATATAGA others(5): Show |
1 | a0005c0007t0003g0146 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.186+816_186+827dup others(12): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598753 | ||||||
| chr5:149598753 | TATATAG | T | 5 | a0001c0005t0005g0174 a0001c0005t0005g0175 a0002c0001t0003g0270 others(2): Show |
5 | HG01891.hp2 HG02145.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.186+822_186+827del others(6): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598753 | ||||||
| chr5:149598757 | TAGATATA others(7): Show |
T | 5 | a0002c0001t0001g0007 a0002c0001t0001g0040 a0002c0001t0001g0060 others(2): Show |
6 | HG01346.hp1 HG01358.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.186+804_186+817del others(14): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598757 | ||||||
| chr5:149598759 | G | T | 13 | a0001c0002t0015g0037 a0001c0002t0015g0038 a0004c0010t0014g0312 others(10): Show |
13 | HG00735.hp1 HG01496.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.186+804G>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598759 | |||||||
| chr5:149598759 | GATATAGA others(13): Show |
G | 1 | a0001c0002t0008g0169 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.186+822_186+841del others(20): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598759 | ||||||
| chr5:149598761 | T | G | 110 | a0001c0002t0005g0358 a0001c0002t0005g0359 a0001c0002t0005g0363 others(107): Show |
122 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.186+806T>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598761 | |||||||
| chr5:149598761 | T | TATATATA others(17): Show |
1 | a0008c0009t0003g0315 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.186+809_186+810ins others(24): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598761 | ||||||
| chr5:149598761 | T | TATATATA others(21): Show |
1 | a0004c0010t0014g0312 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.186+809_186+810ins others(28): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598761 | ||||||
| chr5:149598761 | T | TATATATA others(19): Show |
1 | a0008c0009t0003g0310 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.186+809_186+810ins others(26): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598761 | ||||||
| chr5:149598761 | T | TATATATA others(23): Show |
1 | a0004c0010t0014g0317 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.186+809_186+810ins others(30): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598761 | ||||||
| chr5:149598761 | T | TATATATA others(27): Show |
1 | a0004c0010t0014g0319 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.186+809_186+810ins others(34): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598761 | ||||||
| chr5:149598761 | T | TATATATA others(21): Show |
1 | a0008c0009t0003g0311 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.186+809_186+810ins others(28): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598761 | ||||||
| chr5:149598761 | T | TATATATA others(23): Show |
1 | a0008c0009t0025g0318 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.186+809_186+810ins others(30): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598761 | ||||||
| chr5:149598761 | T | TATATATA others(27): Show |
1 | a0008c0009t0003g0313 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.186+809_186+810ins others(34): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598761 | ||||||
| chr5:149598761 | T | TATATATA others(25): Show |
1 | a0005c0011t0003g0316 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.186+809_186+810ins others(32): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598761 | ||||||
| chr5:149598761 | T | TATATATA others(29): Show |
2 | a0008c0009t0003g0314 a0008c0009t0026g0309 |
2 | HG02451.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.186+809_186+810ins others(36): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598761 | ||||||
| chr5:149598763 | T | C | 1 | a0008c0017t0031g0109 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.186+808T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598763 | |||||||
| chr5:149598765 | GATATAGA others(7): Show |
G | 107 | a0001c0002t0006g0008 a0001c0002t0006g0028 a0001c0002t0006g0050 others(104): Show |
113 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.186+836_186+849del others(14): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598765 | ||||||
| chr5:149598767 | T | G | 2 | a0004c0004t0004g0221 a0004c0004t0004g0230 |
2 | NA18941.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.186+812T>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598767 | |||||||
| chr5:149598773 | T | G | 1 | a0016c0019t0002g0294 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.186+818T>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598773 | |||||||
| chr5:149598777 | GAT | G | 13 | a0001c0002t0015g0037 a0001c0002t0015g0038 a0002c0001t0001g0007 others(10): Show |
14 | HG01346.hp1 HG01358.hp2 HG01934.hp2 others(11): Show |
intron_variant | MODIFIER | c.186+828_186+829del others(2): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598777 | ||||||
| chr5:149598779 | T | G | 8 | a0005c0011t0003g0316 a0008c0009t0003g0310 a0008c0009t0003g0311 others(5): Show |
8 | HG00735.hp1 HG01496.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.186+824T>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598779 | |||||||
| chr5:149598785 | GATATAGA others(9): Show |
G | 1 | a0001c0002t0005g0342 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.186+836_186+851del others(16): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598785 | ||||||
| chr5:149598787 | TATAGATA others(5): Show |
T | 1 | a0001c0002t0020g0110 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.186+836_186+847del others(12): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598787 | ||||||
| chr5:149598808 | A | G | 1 | a0001c0002t0020g0110 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.186+853A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598808 | |||||||
| chr5:149598808 | ATG | A | 38 | a0001c0005t0019g0193 a0003c0012t0002g0162 a0003c0012t0002g0163 others(35): Show |
38 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.186+867_186+868del others(2): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149598808 | ||||||
| chr5:149598810 | G | A | 1 | a0001c0002t0005g0342 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.186+855G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598810 | |||||||
| chr5:149598822 | G | A | 191 | a0001c0002t0004g0350 a0001c0002t0005g0358 a0001c0002t0005g0359 others(188): Show |
204 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.186+867G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598822 | |||||||
| chr5:149598867 | T | G | 11 | a0004c0010t0014g0312 a0004c0010t0014g0317 a0004c0010t0014g0319 others(8): Show |
11 | HG00735.hp1 HG01496.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.186+912T>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598867 | |||||||
| chr5:149598959 | G | A | 1 | a0001c0005t0005g0200 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.186+1004G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149598959 | |||||||
| chr5:149599290 | A | T | 1 | a0002c0001t0001g0085 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.186+1335A>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149599290 | |||||||
| chr5:149599299 | C | T | 7 | a0001c0005t0004g0206 a0001c0005t0004g0207 a0001c0005t0004g0209 others(4): Show |
7 | HG02055.hp1 HG02896.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.186+1344C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149599299 | |||||||
| chr5:149599314 | G | A | 260 | a0001c0002t0005g0342 a0001c0002t0005g0358 a0001c0002t0005g0359 others(257): Show |
280 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.186+1359G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149599314 | |||||||
| chr5:149599434 | C | CTTACTTA others(17): Show |
7 | a0005c0011t0003g0316 a0008c0009t0003g0310 a0008c0009t0003g0311 others(4): Show |
7 | HG00735.hp1 HG01496.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.186+1482_186+1483i others(26): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149599434 | ||||||
| chr5:149599434 | C | CTTACTTA others(21): Show |
3 | a0004c0010t0014g0312 a0004c0010t0014g0317 a0008c0009t0003g0313 |
3 | HG03195.hp2 HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.186+1482_186+1483i others(30): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149599434 | ||||||
| chr5:149599434 | C | CTTACTTA others(25): Show |
1 | a0004c0010t0014g0319 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.186+1482_186+1483i others(34): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149599434 | ||||||
| chr5:149599434 | C | CTTATTTA others(1): Show |
3 | a0001c0002t0006g0051 a0001c0002t0006g0106 a0004c0004t0004g0218 |
3 | HG00738.hp1 HG03942.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.186+1495_186+1502d others(10): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149599434 | ||||||
| chr5:149599434 | C | CTTATTTA others(5): Show |
10 | a0002c0001t0001g0061 a0002c0001t0001g0064 a0002c0001t0001g0074 others(7): Show |
10 | HG00323.hp1 HG00741.hp1 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.186+1491_186+1502d others(14): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149599434 | ||||||
| chr5:149599434 | C | CTTATTTA others(9): Show |
1 | a0003c0003t0002g0283 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.186+1487_186+1502d others(18): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149599434 | ||||||
| chr5:149599434 | C | CTTATTTA others(13): Show |
158 | a0001c0002t0005g0342 a0001c0002t0006g0008 a0001c0002t0006g0028 others(155): Show |
167 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.186+1483_186+1502d others(22): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149599434 | ||||||
| chr5:149599434 | C | CTTATTTA others(17): Show |
81 | a0001c0002t0004g0350 a0001c0002t0005g0358 a0001c0002t0006g0063 others(78): Show |
84 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.186+1502_186+1503i others(26): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149599434 | ||||||
| chr5:149599434 | C | CTTATTTA others(21): Show |
18 | a0001c0002t0015g0037 a0001c0002t0015g0038 a0003c0003t0002g0005 others(15): Show |
20 | HG00140.hp1 HG00735.hp2 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.186+1502_186+1503i others(30): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149599434 | ||||||
| chr5:149599434 | C | CTTATTTA others(25): Show |
35 | a0001c0002t0005g0363 a0001c0002t0011g0356 a0003c0003t0002g0001 others(32): Show |
40 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.186+1502_186+1503i others(34): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149599434 | ||||||
| chr5:149599434 | C | CTTATTTA others(29): Show |
7 | a0001c0002t0005g0359 a0002c0001t0003g0290 a0003c0003t0002g0013 others(4): Show |
9 | HG00423.hp1 HG01081.hp1 HG02074.hp2 others(6): Show |
intron_variant | MODIFIER | c.186+1502_186+1503i others(38): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149599434 | ||||||
| chr5:149599434 | C | CTTATTTA others(33): Show |
3 | a0003c0003t0002g0282 a0003c0003t0002g0298 a0003c0003t0008g0293 |
3 | NA18960.hp2 NA18998.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.186+1502_186+1503i others(42): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149599434 | ||||||
| chr5:149599702 | A | T | 1 | a0004c0004t0004g0240 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.187-1406A>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149599702 | |||||||
| chr5:149599864 | T | A | 6 | a0001c0002t0006g0087 a0001c0002t0006g0112 a0001c0002t0006g0124 others(3): Show |
6 | HG00408.hp2 HG02129.hp1 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.187-1244T>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149599864 | |||||||
| chr5:149600097 | A | G | 363 | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(360): Show |
388 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(385): Show |
intron_variant | MODIFIER | c.187-1011A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149600097 | |||||||
| chr5:149600214 | A | G | 2 | a0002c0001t0003g0270 a0002c0001t0018g0269 |
2 | HG02145.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.187-894A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149600214 | |||||||
| chr5:149600265 | C | T | 2 | a0004c0004t0004g0242 a0004c0004t0030g0243 |
2 | HG02486.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.187-843C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149600265 | |||||||
| chr5:149600350 | G | A | 12 | a0004c0004t0009g0015 a0004c0004t0009g0255 a0004c0004t0009g0256 others(9): Show |
13 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.187-758G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149600350 | |||||||
| chr5:149600546 | G | A | 1 | a0005c0011t0003g0316 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.187-562G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149600546 | |||||||
| chr5:149600585 | T | C | 327 | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(324): Show |
348 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(345): Show |
intron_variant | MODIFIER | c.187-523T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149600585 | |||||||
| chr5:149600597 | A | C | 1 | a0001c0005t0005g0200 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.187-511A>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149600597 | |||||||
| chr5:149600604 | C | T | 2 | a0002c0001t0003g0270 a0002c0001t0018g0269 |
2 | HG02145.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.187-504C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149600604 | |||||||
| chr5:149600605 | G | A | 48 | a0004c0004t0002g0229 a0004c0004t0004g0012 a0004c0004t0004g0020 others(45): Show |
51 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.187-503G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149600605 | |||||||
| chr5:149600644 | A | AT | 223 | a0001c0002t0005g0342 a0001c0002t0005g0358 a0001c0002t0005g0359 others(220): Show |
239 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.187-450dupT | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149600644 | ||||||
| chr5:149600644 | A | ATT | 13 | a0003c0003t0002g0280 a0003c0003t0002g0281 a0003c0003t0002g0324 others(10): Show |
14 | HG00280.hp2 HG01074.hp1 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.187-451_187-450dup others(2): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 149600644 | ||||||
| chr5:149600738 | T | A | 2 | a0003c0003t0002g0330 a0003c0003t0002g0334 |
2 | HG03195.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.187-370T>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149600738 | |||||||
| chr5:149600768 | T | C | 2 | a0012c0026t0003g0233 a0012c0026t0003g0234 |
2 | HG00558.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.187-340T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149600768 | |||||||
| chr5:149600799 | C | T | 14 | a0001c0002t0008g0009 a0001c0002t0008g0014 a0001c0002t0008g0168 others(11): Show |
17 | HG00544.hp1 HG02040.hp1 NA18941.hp2 others(14): Show |
intron_variant | MODIFIER | c.187-309C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149600799 | |||||||
| chr5:149600803 | C | A | 2 | a0012c0026t0003g0233 a0012c0026t0003g0234 |
2 | HG00558.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.187-305C>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149600803 | |||||||
| chr5:149600805 | A | G | 1 | a0004c0004t0004g0228 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.187-303A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149600805 | |||||||
| chr5:149600889 | A | G | 325 | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(322): Show |
346 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(343): Show |
intron_variant | MODIFIER | c.187-219A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149600889 | |||||||
| chr5:149601048 | C | T | 3 | a0004c0004t0004g0226 a0004c0004t0004g0227 a0004c0004t0004g0228 |
3 | NA18959.hp1 NA18980.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.187-60C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | chr5 | 149601048 | |||||||
| chr5:149601253 | T | C | 1 | a0005c0011t0003g0361 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.310+22T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149601253 | |||||||
| chr5:149601265 | G | A | 9 | a0004c0004t0004g0020 a0004c0004t0004g0240 a0004c0004t0004g0241 others(6): Show |
10 | HG00280.hp2 HG01074.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.310+34G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149601265 | |||||||
| chr5:149601265 | G | C | 1 | a0001c0002t0027g0327 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.310+34G>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149601265 | |||||||
| chr5:149601317 | G | C | 1 | a0001c0002t0006g0137 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.310+86G>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149601317 | |||||||
| chr5:149601466 | A | G | 124 | a0001c0002t0005g0358 a0001c0002t0005g0359 a0001c0002t0005g0363 others(121): Show |
136 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.310+235A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149601466 | |||||||
| chr5:149601471 | C | T | 1 | a0002c0001t0001g0069 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.310+240C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149601471 | |||||||
| chr5:149601483 | T | C | 262 | a0001c0002t0005g0342 a0001c0002t0005g0358 a0001c0002t0005g0359 others(259): Show |
282 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.310+252T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149601483 | |||||||
| chr5:149601533 | C | T | 2 | a0014c0025t0013g0260 a0014c0025t0013g0261 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.310+302C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149601533 | |||||||
| chr5:149601564 | G | C | 1 | a0003c0003t0002g0337 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.310+333G>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149601564 | |||||||
| chr5:149601606 | G | A | 1 | a0002c0001t0001g0140 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.310+375G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149601606 | |||||||
| chr5:149601645 | A | G | 2 | a0012c0026t0003g0233 a0012c0026t0003g0234 |
2 | HG00558.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.310+414A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149601645 | |||||||
| chr5:149601704 | G | A | 35 | a0003c0012t0002g0162 a0003c0012t0002g0163 a0003c0012t0002g0165 others(32): Show |
35 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.310+473G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149601704 | |||||||
| chr5:149601859 | G | A | 2 | a0005c0007t0003g0146 a0005c0007t0003g0159 |
2 | NA19000.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.310+628G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149601859 | |||||||
| chr5:149601902 | T | C | 1 | a0001c0005t0004g0207 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.310+671T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149601902 | |||||||
| chr5:149602031 | C | T | 1 | a0003c0003t0002g0272 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.310+800C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149602031 | |||||||
| chr5:149602059 | CTT | C | 244 | a0001c0002t0005g0342 a0001c0002t0005g0358 a0001c0002t0005g0359 others(241): Show |
264 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.310+842_310+843del others(2): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 149602059 | ||||||
| chr5:149602143 | G | A | 1 | a0002c0001t0001g0082 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.310+912G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149602143 | |||||||
| chr5:149602182 | G | A | 135 | a0001c0002t0005g0342 a0001c0002t0006g0008 a0001c0002t0006g0028 others(132): Show |
143 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.310+951G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149602182 | |||||||
| chr5:149602202 | G | A | 1 | a0006c0006t0007g0368 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.310+971G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149602202 | |||||||
| chr5:149602205 | C | T | 18 | a0001c0002t0004g0350 a0001c0002t0011g0356 a0005c0011t0003g0361 others(15): Show |
18 | HG02280.hp1 HG02451.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.310+974C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149602205 | |||||||
| chr5:149602257 | G | A | 260 | a0001c0002t0005g0342 a0001c0002t0005g0358 a0001c0002t0005g0359 others(257): Show |
280 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.310+1026G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149602257 | |||||||
| chr5:149602262 | G | T | 1 | a0001c0005t0005g0189 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.310+1031G>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149602262 | |||||||
| chr5:149602492 | A | AT | 48 | a0004c0004t0002g0229 a0004c0004t0004g0012 a0004c0004t0004g0020 others(45): Show |
51 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.310+1274dupT | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 149602492 | ||||||
| chr5:149602492 | AT | A | 133 | a0001c0002t0005g0342 a0001c0002t0006g0008 a0001c0002t0006g0028 others(130): Show |
141 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.310+1274delT | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 149602492 | ||||||
| chr5:149602534 | C | A | 1 | a0005c0035t0003g0239 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.310+1303C>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149602534 | |||||||
| chr5:149602621 | A | C | 1 | a0005c0007t0003g0150 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.310+1390A>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149602621 | |||||||
| chr5:149602721 | G | A | 29 | a0001c0002t0004g0350 a0001c0002t0011g0356 a0002c0001t0003g0270 others(26): Show |
30 | HG01069.hp2 HG01071.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.310+1490G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149602721 | |||||||
| chr5:149602798 | A | T | 133 | a0001c0002t0005g0342 a0001c0002t0006g0008 a0001c0002t0006g0028 others(130): Show |
141 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.310+1567A>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149602798 | |||||||
| chr5:149602800 | T | A | 18 | a0001c0002t0004g0350 a0001c0002t0011g0356 a0005c0011t0003g0361 others(15): Show |
18 | HG02280.hp1 HG02451.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.310+1569T>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149602800 | |||||||
| chr5:149602982 | G | A | 1 | a0003c0003t0002g0330 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.310+1751G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149602982 | |||||||
| chr5:149602987 | C | T | 260 | a0001c0002t0005g0342 a0001c0002t0005g0358 a0001c0002t0005g0359 others(257): Show |
280 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.310+1756C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149602987 | |||||||
| chr5:149602988 | G | A | 3 | a0005c0011t0003g0326 a0006c0006t0032g0105 a0008c0017t0031g0109 |
3 | HG02922.hp2 HG03139.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.310+1757G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149602988 | |||||||
| chr5:149603036 | G | A | 11 | a0004c0010t0014g0312 a0004c0010t0014g0317 a0004c0010t0014g0319 others(8): Show |
11 | HG00735.hp1 HG01496.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.310+1805G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149603036 | |||||||
| chr5:149603051 | A | G | 328 | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(325): Show |
349 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(346): Show |
intron_variant | MODIFIER | c.310+1820A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149603051 | |||||||
| chr5:149603114 | G | A | 4 | a0001c0002t0027g0327 a0009c0014t0011g0273 a0009c0014t0023g0006 others(1): Show |
5 | HG02615.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.310+1883G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149603114 | |||||||
| chr5:149603142 | A | G | 126 | a0001c0002t0005g0342 a0001c0002t0006g0008 a0001c0002t0006g0028 others(123): Show |
133 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.310+1911A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149603142 | |||||||
| chr5:149603222 | C | T | 3 | a0005c0011t0003g0326 a0006c0006t0032g0105 a0008c0017t0031g0109 |
3 | HG02922.hp2 HG03139.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.310+1991C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149603222 | |||||||
| chr5:149603692 | T | G | 121 | a0001c0002t0005g0342 a0001c0002t0006g0008 a0001c0002t0006g0028 others(118): Show |
128 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.310+2461T>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149603692 | |||||||
| chr5:149603725 | C | T | 1 | a0001c0005t0005g0187 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.310+2494C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149603725 | |||||||
| chr5:149603872 | G | T | 2 | a0008c0009t0003g0313 a0008c0009t0003g0314 |
2 | HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.310+2641G>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149603872 | |||||||
| chr5:149604082 | G | A | 1 | a0003c0003t0002g0286 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.310+2851G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149604082 | |||||||
| chr5:149604239 | C | T | 1 | a0008c0009t0025g0318 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.310+3008C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149604239 | |||||||
| chr5:149604438 | C | A | 260 | a0001c0002t0005g0342 a0001c0002t0005g0358 a0001c0002t0005g0359 others(257): Show |
280 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.310+3207C>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149604438 | |||||||
| chr5:149604556 | A | C | 2 | a0012c0026t0003g0233 a0012c0026t0003g0234 |
2 | HG00558.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.310+3325A>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149604556 | |||||||
| chr5:149604603 | C | T | 1 | a0002c0001t0001g0059 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.310+3372C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149604603 | |||||||
| chr5:149604676 | A | AT | 27 | a0001c0002t0004g0350 a0001c0002t0011g0356 a0001c0005t0004g0206 others(24): Show |
28 | HG01069.hp2 HG01071.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.310+3469dupT | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 149604676 | ||||||
| chr5:149604676 | A | ATT | 7 | a0001c0005t0004g0211 a0001c0005t0004g0212 a0004c0004t0033g0266 others(4): Show |
7 | HG02055.hp1 HG02280.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.310+3468_310+3469d others(4): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 149604676 | ||||||
| chr5:149604676 | AT | A | 70 | a0001c0002t0006g0008 a0001c0002t0006g0050 a0001c0002t0006g0051 others(67): Show |
71 | HG00408.hp2 HG00558.hp1 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.310+3469delT | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 149604676 | ||||||
| chr5:149604676 | ATT | A | 175 | a0001c0002t0005g0342 a0001c0002t0005g0358 a0001c0002t0005g0359 others(172): Show |
192 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.310+3468_310+3469d others(4): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 149604676 | ||||||
| chr5:149604676 | ATTT | A | 51 | a0001c0002t0027g0327 a0002c0001t0001g0065 a0002c0001t0001g0072 others(48): Show |
53 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.310+3467_310+3469d others(5): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 149604676 | ||||||
| chr5:149604708 | AATCT | A | 133 | a0001c0002t0005g0342 a0001c0002t0006g0008 a0001c0002t0006g0028 others(130): Show |
141 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.310+3478_310+3481d others(6): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149604708 | |||||||
| chr5:149604709 | ATCTC | A | 127 | a0001c0002t0005g0358 a0001c0002t0005g0359 a0001c0002t0005g0363 others(124): Show |
139 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.310+3484_310+3487d others(6): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 149604709 | ||||||
| chr5:149604713 | C | T | 133 | a0001c0002t0005g0342 a0001c0002t0006g0008 a0001c0002t0006g0028 others(130): Show |
141 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.310+3482C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149604713 | |||||||
| chr5:149604785 | C | T | 133 | a0001c0002t0005g0342 a0001c0002t0006g0008 a0001c0002t0006g0028 others(130): Show |
141 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.310+3554C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149604785 | |||||||
| chr5:149604828 | G | A | 1 | a0002c0001t0001g0059 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.310+3597G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149604828 | |||||||
| chr5:149604832 | G | A | 11 | a0004c0010t0014g0312 a0004c0010t0014g0317 a0004c0010t0014g0319 others(8): Show |
11 | HG00735.hp1 HG01496.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.310+3601G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149604832 | |||||||
| chr5:149604844 | G | A | 7 | a0001c0002t0006g0050 a0001c0002t0006g0122 a0009c0013t0011g0017 others(4): Show |
8 | HG01069.hp2 HG01071.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.310+3613G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149604844 | |||||||
| chr5:149604891 | C | T | 3 | a0001c0005t0005g0187 a0001c0005t0005g0195 a0004c0004t0004g0184 |
3 | HG00280.hp1 HG00741.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.310+3660C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149604891 | |||||||
| chr5:149604965 | G | A | 1 | a0003c0003t0016g0303 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.310+3734G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149604965 | |||||||
| chr5:149605078 | T | G | 1 | a0003c0003t0002g0268 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.310+3847T>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149605078 | |||||||
| chr5:149605169 | G | A | 1 | a0003c0003t0002g0268 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.310+3938G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149605169 | |||||||
| chr5:149605196 | C | A | 1 | a0003c0003t0002g0286 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.310+3965C>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149605196 | |||||||
| chr5:149605226 | CA | C | 204 | a0001c0002t0005g0358 a0001c0002t0005g0359 a0001c0002t0005g0363 others(201): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.310+4010delA | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 149605226 | ||||||
| chr5:149605301 | A | G | 261 | a0001c0002t0005g0342 a0001c0002t0005g0358 a0001c0002t0005g0359 others(258): Show |
281 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.310+4070A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149605301 | |||||||
| chr5:149605461 | G | A | 1 | a0002c0001t0001g0068 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.311-4087G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149605461 | |||||||
| chr5:149605505 | T | C | 2 | a0015c0020t0017g0176 a0015c0020t0017g0177 |
2 | HG01891.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.311-4043T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149605505 | |||||||
| chr5:149605511 | C | T | 3 | a0005c0011t0003g0326 a0006c0006t0032g0105 a0008c0017t0031g0109 |
3 | HG02922.hp2 HG03139.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.311-4037C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149605511 | |||||||
| chr5:149605885 | T | C | 4 | a0004c0004t0009g0256 a0004c0004t0009g0257 a0004c0004t0009g0258 others(1): Show |
4 | HG02717.hp1 HG02809.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.311-3663T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149605885 | |||||||
| chr5:149605986 | G | A | 1 | a0002c0001t0001g0066 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.311-3562G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149605986 | |||||||
| chr5:149606197 | C | T | 1 | a0003c0003t0002g0279 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.311-3351C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149606197 | |||||||
| chr5:149606228 | C | T | 39 | a0001c0005t0004g0206 a0001c0005t0004g0207 a0001c0005t0004g0209 others(36): Show |
43 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.311-3320C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149606228 | |||||||
| chr5:149606298 | T | TG | 3 | a0005c0011t0003g0326 a0006c0006t0032g0105 a0008c0017t0031g0109 |
3 | HG02922.hp2 HG03139.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.311-3249dupG | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 149606298 | ||||||
| chr5:149606381 | C | T | 2 | a0003c0003t0002g0306 a0003c0003t0002g0307 |
2 | HG00438.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.311-3167C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149606381 | |||||||
| chr5:149606436 | G | A | 260 | a0001c0002t0005g0342 a0001c0002t0005g0358 a0001c0002t0005g0359 others(257): Show |
280 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.311-3112G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149606436 | |||||||
| chr5:149606462 | T | A | 63 | a0001c0002t0005g0358 a0001c0002t0005g0359 a0001c0002t0005g0363 others(60): Show |
72 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.311-3086T>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149606462 | |||||||
| chr5:149606518 | C | T | 7 | a0002c0001t0001g0039 a0002c0001t0001g0065 a0002c0001t0001g0067 others(4): Show |
7 | HG01099.hp1 HG01255.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.311-3030C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149606518 | |||||||
| chr5:149606681 | G | C | 144 | a0001c0002t0005g0342 a0001c0002t0006g0008 a0001c0002t0006g0028 others(141): Show |
152 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.311-2867G>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149606681 | |||||||
| chr5:149606781 | G | A | 5 | a0009c0013t0011g0017 a0009c0013t0011g0320 a0009c0013t0021g0108 others(2): Show |
6 | HG01069.hp2 HG01071.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.311-2767G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149606781 | |||||||
| chr5:149606813 | C | G | 39 | a0001c0005t0004g0206 a0001c0005t0004g0207 a0001c0005t0004g0209 others(36): Show |
43 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.311-2735C>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149606813 | |||||||
| chr5:149606980 | A | G | 79 | a0001c0005t0004g0206 a0001c0005t0004g0207 a0001c0005t0004g0209 others(76): Show |
83 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.311-2568A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149606980 | |||||||
| chr5:149607017 | G | A | 1 | a0002c0001t0001g0140 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.311-2531G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149607017 | |||||||
| chr5:149607365 | T | C | 11 | a0004c0010t0014g0312 a0004c0010t0014g0317 a0004c0010t0014g0319 others(8): Show |
11 | HG00735.hp1 HG01496.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.311-2183T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149607365 | |||||||
| chr5:149607455 | A | C | 9 | a0004c0004t0004g0020 a0004c0004t0004g0240 a0004c0004t0004g0241 others(6): Show |
10 | HG00280.hp2 HG01074.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.311-2093A>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149607455 | |||||||
| chr5:149607505 | A | G | 3 | a0009c0014t0011g0273 a0009c0014t0023g0006 a0009c0014t0035g0029 |
4 | HG02615.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.311-2043A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149607505 | |||||||
| chr5:149607755 | C | CT | 20 | a0001c0002t0006g0008 a0001c0002t0006g0086 a0001c0002t0006g0128 others(17): Show |
20 | HG01175.hp2 HG01358.hp2 HG01517.hp2 others(17): Show |
intron_variant | MODIFIER | c.311-1768dupT | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 149607755 | ||||||
| chr5:149607755 | CT | C | 67 | a0001c0002t0006g0129 a0001c0002t0006g0137 a0002c0001t0001g0052 others(64): Show |
70 | HG00280.hp2 HG00438.hp1 HG00735.hp1 others(67): Show |
intron_variant | MODIFIER | c.311-1768delT | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 149607755 | ||||||
| chr5:149607755 | CTTTT | C | 34 | a0001c0005t0004g0206 a0001c0005t0004g0207 a0001c0005t0004g0209 others(31): Show |
37 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.311-1771_311-1768d others(6): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 149607755 | ||||||
| chr5:149607755 | CTTTTTTT others(3): Show |
C | 37 | a0003c0012t0002g0162 a0003c0012t0002g0163 a0003c0012t0002g0165 others(34): Show |
37 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.311-1777_311-1768d others(12): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 149607755 | ||||||
| chr5:149607755 | CTTTTTTT others(6): Show |
C | 1 | a0009c0013t0011g0017 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.311-1780_311-1768d others(15): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 149607755 | ||||||
| chr5:149607890 | C | T | 39 | a0001c0005t0004g0206 a0001c0005t0004g0207 a0001c0005t0004g0209 others(36): Show |
43 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.311-1658C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149607890 | |||||||
| chr5:149607958 | C | T | 63 | a0001c0002t0005g0358 a0001c0002t0005g0359 a0001c0002t0005g0363 others(60): Show |
72 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.311-1590C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149607958 | |||||||
| chr5:149607976 | G | A | 3 | a0001c0002t0015g0036 a0001c0002t0015g0037 a0001c0002t0015g0038 |
3 | HG02896.hp2 HG02897.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.311-1572G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149607976 | |||||||
| chr5:149608262 | CTGACATA others(27): Show |
C | 356 | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(353): Show |
381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.311-1243_311-1210d others(36): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 149608262 | ||||||
| chr5:149608376 | T | A | 76 | a0001c0005t0004g0206 a0001c0005t0004g0207 a0001c0005t0004g0209 others(73): Show |
80 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.311-1172T>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149608376 | |||||||
| chr5:149608377 | T | A | 1 | a0007c0008t0001g0103 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.311-1171T>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149608377 | |||||||
| chr5:149608397 | G | A | 2 | a0017c0021t0006g0141 a0017c0021t0006g0142 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.311-1151G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149608397 | |||||||
| chr5:149608402 | G | C | 1 | a0006c0006t0007g0352 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.311-1146G>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149608402 | |||||||
| chr5:149608537 | T | A | 39 | a0001c0005t0004g0206 a0001c0005t0004g0207 a0001c0005t0004g0209 others(36): Show |
43 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.311-1011T>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149608537 | |||||||
| chr5:149608560 | G | A | 77 | a0001c0005t0004g0206 a0001c0005t0004g0207 a0001c0005t0004g0209 others(74): Show |
81 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.311-988G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149608560 | |||||||
| chr5:149608665 | C | T | 1 | a0001c0002t0006g0124 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.311-883C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149608665 | |||||||
| chr5:149609108 | T | C | 1 | a0004c0004t0009g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.311-440T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149609108 | |||||||
| chr5:149609161 | G | A | 1 | a0008c0017t0031g0109 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.311-387G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149609161 | |||||||
| chr5:149609168 | G | C | 2 | a0001c0002t0015g0037 a0001c0002t0015g0038 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.311-380G>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149609168 | |||||||
| chr5:149609205 | A | AAAACAAA others(1): Show |
37 | a0003c0012t0002g0162 a0003c0012t0002g0163 a0003c0012t0002g0165 others(34): Show |
37 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.311-337_311-336ins others(8): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 149609205 | ||||||
| chr5:149609208 | A | G | 10 | a0001c0002t0006g0063 a0002c0001t0001g0007 a0002c0001t0001g0040 others(7): Show |
11 | HG01346.hp1 HG01358.hp2 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.311-340A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149609208 | |||||||
| chr5:149609237 | A | G | 1 | a0002c0024t0003g0205 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.311-311A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149609237 | |||||||
| chr5:149609260 | G | A | 196 | a0001c0002t0005g0342 a0001c0002t0005g0358 a0001c0002t0005g0359 others(193): Show |
213 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.311-288G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149609260 | |||||||
| chr5:149609366 | C | T | 4 | a0001c0002t0010g0010 a0001c0002t0010g0167 a0001c0002t0010g0172 others(1): Show |
5 | NA18954.hp2 NA18965.hp2 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.311-182C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149609366 | |||||||
| chr5:149609370 | T | C | 2 | a0002c0001t0001g0140 a0022c0031t0001g0077 |
2 | HG04204.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.311-178T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149609370 | |||||||
| chr5:149609414 | G | T | 2 | a0006c0006t0007g0355 a0021c0037t0003g0354 |
2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.311-134G>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149609414 | |||||||
| chr5:149609534 | G | A | 5 | a0001c0002t0015g0036 a0001c0002t0015g0037 a0001c0002t0015g0038 others(2): Show |
5 | HG00423.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.311-14G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 3/12 | chr5 | 149609534 | |||||||
| chr5:149609740 | C | T | 12 | a0004c0004t0009g0015 a0004c0004t0009g0255 a0004c0004t0009g0256 others(9): Show |
13 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.458+45C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149609740 | |||||||
| chr5:149609749 | A | G | 128 | a0001c0005t0004g0206 a0001c0005t0004g0207 a0001c0005t0004g0209 others(125): Show |
135 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.458+54A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149609749 | |||||||
| chr5:149609757 | T | C | 128 | a0001c0005t0004g0206 a0001c0005t0004g0207 a0001c0005t0004g0209 others(125): Show |
135 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.458+62T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149609757 | |||||||
| chr5:149609795 | C | T | 51 | a0004c0004t0002g0229 a0004c0004t0004g0012 a0004c0004t0004g0020 others(48): Show |
54 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.458+100C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149609795 | |||||||
| chr5:149609844 | G | A | 11 | a0004c0010t0014g0312 a0004c0010t0014g0317 a0004c0010t0014g0319 others(8): Show |
11 | HG00735.hp1 HG01496.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.458+149G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149609844 | |||||||
| chr5:149609847 | A | G | 299 | a0001c0002t0005g0342 a0001c0002t0005g0358 a0001c0002t0005g0359 others(296): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.458+152A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149609847 | |||||||
| chr5:149609847 | A | T | 51 | a0004c0004t0002g0229 a0004c0004t0004g0012 a0004c0004t0004g0020 others(48): Show |
54 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.458+152A>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149609847 | |||||||
| chr5:149609999 | AGTAACTG others(10): Show |
A | 1 | a0001c0002t0008g0168 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.458+305_458+321del others(17): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149609999 | |||||||
| chr5:149610000 | G | A | 2 | a0002c0001t0001g0104 a0002c0001t0001g0139 |
2 | NA18944.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.458+305G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149610000 | |||||||
| chr5:149610034 | G | A | 11 | a0004c0010t0014g0312 a0004c0010t0014g0317 a0004c0010t0014g0319 others(8): Show |
11 | HG00735.hp1 HG01496.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.458+339G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149610034 | |||||||
| chr5:149610087 | C | T | 2 | a0015c0020t0017g0176 a0015c0020t0017g0177 |
2 | HG01891.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.458+392C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149610087 | |||||||
| chr5:149610164 | A | G | 1 | a0007c0008t0001g0102 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.458+469A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149610164 | |||||||
| chr5:149610178 | G | A | 128 | a0001c0005t0004g0206 a0001c0005t0004g0207 a0001c0005t0004g0209 others(125): Show |
135 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.458+483G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149610178 | |||||||
| chr5:149610183 | C | G | 121 | a0001c0002t0005g0342 a0001c0002t0006g0008 a0001c0002t0006g0028 others(118): Show |
128 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.458+488C>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149610183 | |||||||
| chr5:149610325 | G | A | 1 | a0002c0001t0001g0022 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.458+630G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149610325 | |||||||
| chr5:149610396 | A | G | 2 | a0012c0026t0003g0233 a0012c0026t0003g0234 |
2 | HG00558.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.458+701A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149610396 | |||||||
| chr5:149610418 | C | T | 3 | a0003c0012t0002g0274 a0005c0007t0003g0144 a0005c0007t0003g0160 |
3 | NA18961.hp2 NA18993.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.458+723C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149610418 | |||||||
| chr5:149610444 | G | A | 127 | a0001c0005t0004g0206 a0001c0005t0004g0207 a0001c0005t0004g0209 others(124): Show |
134 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.458+749G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149610444 | |||||||
| chr5:149610630 | G | A | 27 | a0004c0004t0002g0229 a0004c0004t0004g0012 a0004c0004t0004g0143 others(24): Show |
28 | HG00438.hp1 HG00597.hp2 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.458+935G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149610630 | |||||||
| chr5:149610650 | T | G | 39 | a0001c0005t0004g0206 a0001c0005t0004g0207 a0001c0005t0004g0209 others(36): Show |
43 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.458+955T>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149610650 | |||||||
| chr5:149610869 | C | T | 4 | a0001c0002t0027g0327 a0009c0014t0011g0273 a0009c0014t0023g0006 others(1): Show |
5 | HG02615.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.458+1174C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149610869 | |||||||
| chr5:149611087 | G | A | 1 | a0001c0005t0005g0200 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.458+1392G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149611087 | |||||||
| chr5:149611207 | C | T | 1 | a0008c0009t0025g0318 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.458+1512C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149611207 | |||||||
| chr5:149611301 | A | T | 2 | a0017c0021t0006g0141 a0017c0021t0006g0142 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.458+1606A>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149611301 | |||||||
| chr5:149611307 | G | T | 349 | a0001c0002t0005g0342 a0001c0002t0005g0358 a0001c0002t0005g0359 others(346): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.458+1612G>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149611307 | |||||||
| chr5:149611443 | C | T | 1 | a0008c0017t0031g0109 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.458+1748C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149611443 | |||||||
| chr5:149611496 | A | G | 1 | a0001c0002t0006g0130 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.458+1801A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149611496 | |||||||
| chr5:149611598 | G | A | 1 | a0002c0001t0001g0023 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.458+1903G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149611598 | |||||||
| chr5:149611802 | C | T | 126 | a0001c0002t0005g0342 a0001c0002t0006g0008 a0001c0002t0006g0028 others(123): Show |
133 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.458+2107C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149611802 | |||||||
| chr5:149611927 | G | T | 128 | a0001c0005t0004g0206 a0001c0005t0004g0207 a0001c0005t0004g0209 others(125): Show |
135 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.458+2232G>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149611927 | |||||||
| chr5:149612177 | C | CT | 41 | a0001c0005t0004g0206 a0001c0005t0004g0207 a0001c0005t0004g0209 others(38): Show |
45 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.458+2490dupT | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr5 | 149612177 | ||||||
| chr5:149612190 | T | C | 2 | a0005c0011t0003g0326 a0006c0006t0032g0105 |
2 | HG02922.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.458+2495T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149612190 | |||||||
| chr5:149612292 | C | T | 125 | a0001c0002t0005g0342 a0001c0002t0006g0008 a0001c0002t0006g0028 others(122): Show |
132 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.458+2597C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149612292 | |||||||
| chr5:149612316 | G | C | 4 | a0004c0004t0004g0147 a0005c0007t0003g0152 a0005c0007t0003g0155 others(1): Show |
4 | HG00597.hp1 HG02027.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.458+2621G>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149612316 | |||||||
| chr5:149612413 | C | A | 1 | a0009c0013t0011g0017 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.458+2718C>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149612413 | |||||||
| chr5:149612424 | C | T | 5 | a0001c0005t0004g0206 a0001c0005t0004g0209 a0001c0005t0004g0210 others(2): Show |
5 | HG02055.hp1 HG02896.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.458+2729C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149612424 | |||||||
| chr5:149612834 | G | C | 1 | a0009c0013t0011g0017 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.458+3139G>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149612834 | |||||||
| chr5:149612873 | A | C | 3 | a0005c0011t0001g0041 a0005c0011t0001g0042 a0005c0011t0001g0043 |
3 | HG02280.hp2 HG02818.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.458+3178A>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149612873 | |||||||
| chr5:149612880 | C | T | 2 | a0002c0001t0003g0270 a0002c0001t0018g0269 |
2 | HG02145.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.458+3185C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149612880 | |||||||
| chr5:149613041 | G | A | 230 | a0001c0002t0005g0342 a0001c0002t0005g0358 a0001c0002t0006g0008 others(227): Show |
248 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.458+3346G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149613041 | |||||||
| chr5:149613097 | G | A | 1 | a0006c0006t0007g0368 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.458+3402G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149613097 | |||||||
| chr5:149613177 | A | G | 8 | a0005c0011t0003g0316 a0008c0009t0003g0310 a0008c0009t0003g0311 others(5): Show |
8 | HG00735.hp1 HG01496.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.459-3390A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149613177 | |||||||
| chr5:149613187 | T | C | 8 | a0005c0011t0003g0316 a0008c0009t0003g0310 a0008c0009t0003g0311 others(5): Show |
8 | HG00735.hp1 HG01496.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.459-3380T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149613187 | |||||||
| chr5:149613349 | A | AT | 199 | a0001c0002t0004g0350 a0001c0002t0005g0358 a0001c0002t0005g0359 others(196): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.459-3203dupT | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr5 | 149613349 | ||||||
| chr5:149613403 | G | A | 150 | a0001c0002t0005g0358 a0001c0002t0006g0008 a0001c0002t0006g0050 others(147): Show |
166 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.459-3164G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149613403 | |||||||
| chr5:149613404 | T | C | 2 | a0009c0014t0023g0006 a0009c0014t0035g0029 |
3 | HG02895.hp1 HG02897.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.459-3163T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149613404 | |||||||
| chr5:149613507 | C | T | 64 | a0003c0003t0002g0001 a0003c0003t0002g0005 a0003c0003t0002g0013 others(61): Show |
73 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.459-3060C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149613507 | |||||||
| chr5:149613518 | T | C | 2 | a0004c0004t0004g0143 a0007c0008t0003g0237 |
2 | NA18997.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.459-3049T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149613518 | |||||||
| chr5:149613663 | C | T | 55 | a0001c0002t0006g0008 a0001c0002t0006g0028 a0001c0002t0006g0050 others(52): Show |
60 | HG00408.hp2 HG00544.hp1 HG00738.hp1 others(57): Show |
intron_variant | MODIFIER | c.459-2904C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149613663 | |||||||
| chr5:149613715 | T | C | 7 | a0008c0009t0003g0310 a0008c0009t0003g0311 a0008c0009t0003g0313 others(4): Show |
7 | HG00735.hp1 HG01496.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.459-2852T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149613715 | |||||||
| chr5:149613764 | C | CT | 5 | a0001c0002t0027g0327 a0001c0005t0005g0196 a0004c0004t0004g0218 others(2): Show |
6 | HG02738.hp2 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.459-2786dupT | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr5 | 149613764 | ||||||
| chr5:149613764 | CT | C | 117 | a0001c0002t0006g0129 a0001c0002t0015g0037 a0002c0001t0001g0002 others(114): Show |
120 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.459-2786delT | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr5 | 149613764 | ||||||
| chr5:149613841 | G | A | 1 | a0006c0006t0007g0348 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.459-2726G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149613841 | |||||||
| chr5:149614012 | C | T | 1 | a0001c0002t0015g0036 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.459-2555C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149614012 | |||||||
| chr5:149614039 | C | T | 115 | a0002c0001t0001g0002 a0002c0001t0001g0007 a0002c0001t0001g0021 others(112): Show |
118 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.459-2528C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149614039 | |||||||
| chr5:149614068 | G | GT | 7 | a0008c0009t0003g0310 a0008c0009t0003g0311 a0008c0009t0003g0313 others(4): Show |
7 | HG00735.hp1 HG01496.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.459-2491dupT | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr5 | 149614068 | ||||||
| chr5:149614123 | A | AT | 122 | a0002c0001t0001g0002 a0002c0001t0001g0007 a0002c0001t0001g0021 others(119): Show |
125 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.459-2442dupT | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr5 | 149614123 | ||||||
| chr5:149614327 | A | G | 1 | a0009c0013t0011g0320 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.459-2240A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149614327 | |||||||
| chr5:149614395 | T | C | 2 | a0003c0003t0002g0019 a0003c0012t0012g0099 |
3 | NA18951.hp1 NA18966.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.459-2172T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149614395 | |||||||
| chr5:149614718 | G | A | 1 | a0008c0009t0026g0309 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.459-1849G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149614718 | |||||||
| chr5:149614812 | G | A | 3 | a0008c0009t0003g0313 a0008c0009t0003g0314 a0008c0009t0003g0315 |
3 | HG00735.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.459-1755G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149614812 | |||||||
| chr5:149614858 | C | T | 1 | a0004c0004t0030g0243 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.459-1709C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149614858 | |||||||
| chr5:149614859 | G | A | 1 | a0003c0003t0002g0283 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.459-1708G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149614859 | |||||||
| chr5:149614866 | A | G | 1 | a0001c0002t0020g0110 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.459-1701A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149614866 | |||||||
| chr5:149614951 | C | T | 5 | a0002c0001t0001g0090 a0002c0001t0001g0091 a0002c0001t0001g0092 others(2): Show |
5 | NA18940.hp1 NA18975.hp1 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.459-1616C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149614951 | |||||||
| chr5:149615102 | T | C | 76 | a0002c0001t0001g0002 a0002c0001t0001g0007 a0002c0001t0001g0021 others(73): Show |
79 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.459-1465T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149615102 | |||||||
| chr5:149615244 | T | G | 1 | a0001c0002t0008g0170 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.459-1323T>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149615244 | |||||||
| chr5:149615280 | G | T | 1 | a0003c0003t0002g0272 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.459-1287G>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149615280 | |||||||
| chr5:149615305 | A | AT | 98 | a0002c0001t0001g0002 a0002c0001t0001g0007 a0002c0001t0001g0021 others(95): Show |
102 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.459-1247dupT | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr5 | 149615305 | ||||||
| chr5:149615305 | AT | A | 6 | a0001c0002t0006g0114 a0001c0002t0010g0167 a0003c0003t0002g0304 others(3): Show |
6 | HG01169.hp2 NA18954.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.459-1247delT | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr5 | 149615305 | ||||||
| chr5:149615551 | A | G | 2 | a0001c0002t0006g0127 a0001c0002t0006g0129 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.459-1016A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149615551 | |||||||
| chr5:149615616 | G | A | 65 | a0003c0003t0002g0001 a0003c0003t0002g0005 a0003c0003t0002g0013 others(62): Show |
74 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.459-951G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149615616 | |||||||
| chr5:149615658 | G | A | 1 | a0006c0006t0007g0353 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.459-909G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149615658 | |||||||
| chr5:149615698 | T | C | 33 | a0005c0007t0003g0144 a0005c0007t0003g0145 a0005c0007t0003g0146 others(30): Show |
33 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.459-869T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149615698 | |||||||
| chr5:149615792 | T | C | 69 | a0003c0003t0002g0001 a0003c0003t0002g0005 a0003c0003t0002g0013 others(66): Show |
78 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.459-775T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149615792 | |||||||
| chr5:149615829 | T | C | 1 | a0005c0007t0003g0161 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.459-738T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149615829 | |||||||
| chr5:149615914 | AC | A | 8 | a0005c0011t0001g0041 a0005c0011t0001g0042 a0005c0011t0001g0043 others(5): Show |
8 | HG02280.hp2 HG02615.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.459-652delC | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149615914 | |||||||
| chr5:149615946 | C | G | 40 | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(37): Show |
44 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.459-621C>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149615946 | |||||||
| chr5:149615972 | C | T | 1 | a0001c0002t0006g0137 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.459-595C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149615972 | |||||||
| chr5:149616067 | G | A | 4 | a0002c0001t0001g0136 a0011c0016t0012g0058 a0011c0016t0012g0083 others(1): Show |
4 | HG02027.hp1 NA18612.hp2 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.459-500G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149616067 | |||||||
| chr5:149616303 | G | A | 1 | a0015c0020t0017g0176 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.459-264G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149616303 | |||||||
| chr5:149616316 | C | T | 224 | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(221): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.459-251C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149616316 | |||||||
| chr5:149616388 | C | T | 7 | a0008c0009t0003g0310 a0008c0009t0003g0311 a0008c0009t0003g0313 others(4): Show |
7 | HG00735.hp1 HG01496.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.459-179C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149616388 | |||||||
| chr5:149616459 | G | T | 33 | a0005c0007t0003g0144 a0005c0007t0003g0145 a0005c0007t0003g0146 others(30): Show |
33 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.459-108G>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149616459 | |||||||
| chr5:149616539 | C | T | 2 | a0001c0002t0006g0127 a0001c0002t0006g0129 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.459-28C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 4/12 | chr5 | 149616539 | |||||||
| chr5:149617052 | C | T | 7 | a0008c0009t0003g0310 a0008c0009t0003g0311 a0008c0009t0003g0313 others(4): Show |
7 | HG00735.hp1 HG01496.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.658+286C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 5/12 | chr5 | 149617052 | |||||||
| chr5:149617110 | T | C | 1 | a0005c0007t0003g0155 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.658+344T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 5/12 | chr5 | 149617110 | |||||||
| chr5:149617295 | T | C | 10 | a0001c0002t0006g0008 a0001c0002t0006g0088 a0001c0002t0006g0107 others(7): Show |
11 | NA18939.hp1 NA18950.hp1 NA18954.hp1 others(8): Show |
intron_variant | MODIFIER | c.658+529T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 5/12 | chr5 | 149617295 | |||||||
| chr5:149617628 | G | A | 349 | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(346): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.659-548G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 5/12 | chr5 | 149617628 | |||||||
| chr5:149617687 | C | T | 1 | a0004c0004t0009g0256 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.659-489C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 5/12 | chr5 | 149617687 | |||||||
| chr5:149617744 | A | G | 14 | a0007c0008t0001g0030 a0007c0008t0001g0056 a0007c0008t0001g0057 others(11): Show |
14 | HG00621.hp1 HG02074.hp1 NA18942.hp1 others(11): Show |
intron_variant | MODIFIER | c.659-432A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 5/12 | chr5 | 149617744 | |||||||
| chr5:149617903 | T | C | 2 | a0001c0002t0011g0356 a0009c0014t0011g0273 |
2 | HG02615.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.659-273T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 5/12 | chr5 | 149617903 | |||||||
| chr5:149618097 | C | T | 7 | a0008c0009t0003g0310 a0008c0009t0003g0311 a0008c0009t0003g0313 others(4): Show |
7 | HG00735.hp1 HG01496.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.659-79C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 5/12 | chr5 | 149618097 | |||||||
| chr5:149618123 | A | G | 349 | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(346): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.659-53A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 5/12 | chr5 | 149618123 | |||||||
| chr5:149618132 | A | T | 1 | a0004c0004t0004g0218 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.659-44A>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 5/12 | chr5 | 149618132 | |||||||
| chr5:149618584 | C | T | 9 | a0004c0004t0004g0020 a0004c0004t0004g0240 a0004c0004t0004g0241 others(6): Show |
10 | HG00280.hp2 HG01074.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.789+278C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 6/12 | chr5 | 149618584 | |||||||
| chr5:149618685 | G | A | 84 | a0002c0001t0001g0002 a0002c0001t0001g0007 a0002c0001t0001g0021 others(81): Show |
87 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.790-253G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 6/12 | chr5 | 149618685 | |||||||
| chr5:149618687 | G | A | 84 | a0002c0001t0001g0002 a0002c0001t0001g0007 a0002c0001t0001g0021 others(81): Show |
87 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.790-251G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 6/12 | chr5 | 149618687 | |||||||
| chr5:149618725 | G | A | 1 | a0004c0004t0028g0244 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.790-213G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 6/12 | chr5 | 149618725 | |||||||
| chr5:149618814 | T | G | 1 | a0002c0001t0001g0021 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.790-124T>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 6/12 | chr5 | 149618814 | |||||||
| chr5:149618816 | C | T | 7 | a0008c0009t0003g0310 a0008c0009t0003g0311 a0008c0009t0003g0313 others(4): Show |
7 | HG00735.hp1 HG01496.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.790-122C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 6/12 | chr5 | 149618816 | |||||||
| chr5:149618817 | G | A | 51 | a0001c0002t0006g0008 a0001c0002t0006g0028 a0001c0002t0006g0050 others(48): Show |
56 | HG00408.hp2 HG00544.hp1 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.790-121G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 6/12 | chr5 | 149618817 | |||||||
| chr5:149619161 | G | T | 33 | a0005c0007t0003g0144 a0005c0007t0003g0145 a0005c0007t0003g0146 others(30): Show |
33 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.894+119G>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 7/12 | chr5 | 149619161 | |||||||
| chr5:149619229 | G | C | 8 | a0005c0011t0001g0041 a0005c0011t0001g0042 a0005c0011t0001g0043 others(5): Show |
8 | HG02280.hp2 HG02615.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.894+187G>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 7/12 | chr5 | 149619229 | |||||||
| chr5:149619284 | G | A | 55 | a0004c0004t0002g0229 a0004c0004t0004g0012 a0004c0004t0004g0020 others(52): Show |
58 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.894+242G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 7/12 | chr5 | 149619284 | |||||||
| chr5:149619716 | G | A | 9 | a0001c0002t0011g0356 a0001c0002t0015g0036 a0001c0002t0015g0037 others(6): Show |
10 | HG01069.hp2 HG01071.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.895-638G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 7/12 | chr5 | 149619716 | |||||||
| chr5:149619822 | A | C | 249 | a0002c0001t0001g0002 a0002c0001t0001g0007 a0002c0001t0001g0021 others(246): Show |
264 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.895-532A>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 7/12 | chr5 | 149619822 | |||||||
| chr5:149619840 | C | T | 1 | a0004c0004t0004g0184 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.895-514C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 7/12 | chr5 | 149619840 | |||||||
| chr5:149620014 | A | C | 16 | a0004c0004t0009g0015 a0004c0004t0009g0255 a0004c0004t0009g0256 others(13): Show |
17 | HG01884.hp1 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.895-340A>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 7/12 | chr5 | 149620014 | |||||||
| chr5:149620072 | C | CA | 7 | a0003c0003t0002g0013 a0003c0003t0002g0287 a0003c0012t0002g0274 others(4): Show |
8 | HG03225.hp2 HG03579.hp2 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.895-267dupA | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr5 | 149620072 | ||||||
| chr5:149620072 | CA | C | 133 | a0001c0002t0006g0087 a0001c0002t0008g0171 a0002c0001t0001g0002 others(130): Show |
137 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.895-267delA | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr5 | 149620072 | ||||||
| chr5:149620118 | T | C | 1 | a0005c0011t0003g0326 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.895-236T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 7/12 | chr5 | 149620118 | |||||||
| chr5:149620171 | A | G | 2 | a0015c0020t0017g0176 a0015c0020t0017g0177 |
2 | HG01891.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.895-183A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 7/12 | chr5 | 149620171 | |||||||
| chr5:149620180 | C | T | 1 | a0003c0003t0002g0246 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.895-174C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 7/12 | chr5 | 149620180 | |||||||
| chr5:149620246 | G | T | 4 | a0001c0005t0005g0185 a0001c0005t0005g0191 a0001c0005t0005g0192 others(1): Show |
4 | HG00323.hp2 HG01943.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.895-108G>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 7/12 | chr5 | 149620246 | |||||||
| chr5:149620318 | G | GC | 249 | a0002c0001t0001g0002 a0002c0001t0001g0007 a0002c0001t0001g0021 others(246): Show |
264 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.895-35dupC | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr5 | 149620318 | ||||||
| chr5:149620476 | C | T | 249 | a0002c0001t0001g0002 a0002c0001t0001g0007 a0002c0001t0001g0021 others(246): Show |
264 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.1005+12C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 8/12 | chr5 | 149620476 | |||||||
| chr5:149620567 | C | T | 1 | a0003c0003t0002g0018 | 2 | HG00099.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.1005+103C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 8/12 | chr5 | 149620567 | |||||||
| chr5:149620633 | C | A | 1 | a0004c0010t0014g0312 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1005+169C>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 8/12 | chr5 | 149620633 | |||||||
| chr5:149620688 | G | A | 174 | a0002c0001t0001g0002 a0002c0001t0001g0007 a0002c0001t0001g0021 others(171): Show |
180 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.1005+224G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 8/12 | chr5 | 149620688 | |||||||
| chr5:149620692 | A | G | 249 | a0002c0001t0001g0002 a0002c0001t0001g0007 a0002c0001t0001g0021 others(246): Show |
264 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.1005+228A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 8/12 | chr5 | 149620692 | |||||||
| chr5:149620714 | C | T | 1 | a0005c0007t0003g0164 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1005+250C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 8/12 | chr5 | 149620714 | |||||||
| chr5:149620780 | G | A | 48 | a0001c0002t0006g0008 a0001c0002t0006g0028 a0001c0002t0006g0050 others(45): Show |
52 | HG00408.hp2 HG00544.hp1 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.1005+316G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 8/12 | chr5 | 149620780 | |||||||
| chr5:149620829 | C | CAAAAAAA others(3): Show |
13 | a0002c0001t0001g0052 a0002c0001t0001g0064 a0002c0001t0001g0081 others(10): Show |
13 | HG00323.hp1 HG01256.hp2 HG01515.hp1 others(10): Show |
intron_variant | MODIFIER | c.1005+372_1005+373i others(12): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr5 | 149620829 | ||||||
| chr5:149620829 | C | CAAAAAAA others(4): Show |
140 | a0002c0001t0001g0002 a0002c0001t0001g0007 a0002c0001t0001g0021 others(137): Show |
145 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.1005+372_1005+373i others(13): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr5 | 149620829 | ||||||
| chr5:149620829 | C | CAAAAAAA others(5): Show |
21 | a0002c0001t0001g0091 a0004c0004t0009g0015 a0004c0004t0009g0255 others(18): Show |
22 | HG01884.hp1 HG01884.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.1005+372_1005+373i others(14): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr5 | 149620829 | ||||||
| chr5:149620837 | G | A | 1 | a0004c0004t0004g0218 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1005+373G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 8/12 | chr5 | 149620837 | |||||||
| chr5:149620841 | T | C | 84 | a0002c0001t0001g0002 a0002c0001t0001g0007 a0002c0001t0001g0021 others(81): Show |
87 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.1005+377T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 8/12 | chr5 | 149620841 | |||||||
| chr5:149620982 | G | A | 1 | a0004c0004t0004g0179 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1005+518G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 8/12 | chr5 | 149620982 | |||||||
| chr5:149621378 | C | T | 68 | a0003c0003t0002g0001 a0003c0003t0002g0005 a0003c0003t0002g0013 others(65): Show |
77 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.1006-355C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 8/12 | chr5 | 149621378 | |||||||
| chr5:149621379 | G | A | 119 | a0002c0001t0001g0002 a0002c0001t0001g0007 a0002c0001t0001g0021 others(116): Show |
122 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.1006-354G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 8/12 | chr5 | 149621379 | |||||||
| chr5:149621432 | T | A | 2 | a0015c0020t0017g0176 a0015c0020t0017g0177 |
2 | HG01891.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1006-301T>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 8/12 | chr5 | 149621432 | |||||||
| chr5:149621449 | C | A | 16 | a0004c0004t0009g0015 a0004c0004t0009g0255 a0004c0004t0009g0256 others(13): Show |
17 | HG01884.hp1 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1006-284C>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 8/12 | chr5 | 149621449 | |||||||
| chr5:149621455 | A | G | 33 | a0005c0007t0003g0144 a0005c0007t0003g0145 a0005c0007t0003g0146 others(30): Show |
33 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.1006-278A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 8/12 | chr5 | 149621455 | |||||||
| chr5:149621540 | C | T | 100 | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(97): Show |
110 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.1006-193C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 8/12 | chr5 | 149621540 | |||||||
| chr5:149621720 | T | C | 64 | a0003c0003t0002g0001 a0003c0003t0002g0005 a0003c0003t0002g0013 others(61): Show |
73 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.1006-13T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 8/12 | chr5 | 149621720 | |||||||
| chr5:149622128 | C | CACACACA others(4): Show |
7 | a0004c0004t0009g0015 a0004c0004t0009g0255 a0004c0004t0009g0262 others(4): Show |
8 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1335+67_1335+68ins others(11): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 149622128 | ||||||
| chr5:149622334 | A | G | 22 | a0001c0002t0006g0063 a0001c0002t0006g0127 a0001c0002t0006g0128 others(19): Show |
25 | HG00544.hp1 HG00738.hp2 HG01261.hp2 others(22): Show |
intron_variant | MODIFIER | c.1335+272A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 9/12 | chr5 | 149622334 | |||||||
| chr5:149622387 | A | G | 100 | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(97): Show |
110 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.1335+325A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 9/12 | chr5 | 149622387 | |||||||
| chr5:149622411 | A | C | 1 | a0003c0003t0002g0298 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1335+349A>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 9/12 | chr5 | 149622411 | |||||||
| chr5:149622504 | C | G | 226 | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(223): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.1335+442C>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 9/12 | chr5 | 149622504 | |||||||
| chr5:149622568 | T | A | 1 | a0003c0003t0002g0285 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1335+506T>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 9/12 | chr5 | 149622568 | |||||||
| chr5:149622666 | C | T | 1 | a0005c0011t0003g0361 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1335+604C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 9/12 | chr5 | 149622666 | |||||||
| chr5:149622850 | A | G | 2 | a0002c0001t0003g0270 a0002c0001t0018g0269 |
2 | HG02145.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1335+788A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 9/12 | chr5 | 149622850 | |||||||
| chr5:149622937 | C | G | 18 | a0003c0003t0002g0013 a0003c0003t0002g0016 a0003c0003t0002g0272 others(15): Show |
20 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.1335+875C>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 9/12 | chr5 | 149622937 | |||||||
| chr5:149622969 | A | T | 1 | a0003c0003t0002g0292 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1335+907A>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 9/12 | chr5 | 149622969 | |||||||
| chr5:149623008 | C | G | 7 | a0005c0011t0001g0041 a0005c0011t0001g0042 a0005c0011t0001g0043 others(4): Show |
7 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1335+946C>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 9/12 | chr5 | 149623008 | |||||||
| chr5:149623198 | A | G | 1 | a0001c0002t0006g0116 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1336-814A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 9/12 | chr5 | 149623198 | |||||||
| chr5:149623232 | C | T | 5 | a0001c0002t0006g0087 a0001c0002t0006g0112 a0001c0002t0006g0124 others(2): Show |
5 | HG00408.hp2 HG02129.hp1 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.1336-780C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 9/12 | chr5 | 149623232 | |||||||
| chr5:149623615 | C | T | 1 | a0001c0005t0005g0199 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1336-397C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 9/12 | chr5 | 149623615 | |||||||
| chr5:149623718 | A | C | 2 | a0014c0025t0013g0260 a0014c0025t0013g0261 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1336-294A>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 9/12 | chr5 | 149623718 | |||||||
| chr5:149623934 | A | G | 1 | a0001c0002t0006g0028 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1336-78A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 9/12 | chr5 | 149623934 | |||||||
| chr5:149623966 | T | C | 7 | a0008c0009t0003g0310 a0008c0009t0003g0311 a0008c0009t0003g0313 others(4): Show |
7 | HG00735.hp1 HG01496.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1336-46T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 9/12 | chr5 | 149623966 | |||||||
| chr5:149624288 | A | C | 248 | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(245): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1464+148A>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149624288 | |||||||
| chr5:149624299 | G | A | 1 | a0006c0006t0007g0347 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1464+159G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149624299 | |||||||
| chr5:149624302 | G | A | 18 | a0006c0006t0007g0322 a0006c0006t0007g0323 a0006c0006t0007g0341 others(15): Show |
18 | HG02280.hp1 HG02451.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.1464+162G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149624302 | |||||||
| chr5:149624302 | G | T | 16 | a0004c0004t0009g0015 a0004c0004t0009g0255 a0004c0004t0009g0256 others(13): Show |
17 | HG01884.hp1 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1464+162G>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149624302 | |||||||
| chr5:149624419 | C | T | 16 | a0004c0004t0009g0015 a0004c0004t0009g0255 a0004c0004t0009g0256 others(13): Show |
17 | HG01884.hp1 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1464+279C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149624419 | |||||||
| chr5:149624480 | A | G | 7 | a0006c0006t0007g0322 a0006c0006t0007g0323 a0006c0006t0007g0347 others(4): Show |
7 | HG02451.hp1 HG02572.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1464+340A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149624480 | |||||||
| chr5:149624538 | C | T | 1 | a0015c0020t0017g0177 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1464+398C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149624538 | |||||||
| chr5:149624539 | C | T | 27 | a0004c0004t0002g0229 a0004c0004t0004g0012 a0004c0004t0004g0143 others(24): Show |
28 | HG00438.hp1 HG00597.hp2 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.1464+399C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149624539 | |||||||
| chr5:149624553 | C | T | 100 | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(97): Show |
110 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.1464+413C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149624553 | |||||||
| chr5:149624582 | T | C | 7 | a0008c0009t0003g0310 a0008c0009t0003g0311 a0008c0009t0003g0313 others(4): Show |
7 | HG00735.hp1 HG01496.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1464+442T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149624582 | |||||||
| chr5:149624634 | C | T | 2 | a0015c0020t0017g0176 a0015c0020t0017g0177 |
2 | HG01891.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1464+494C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149624634 | |||||||
| chr5:149624649 | C | CTGTAA | 247 | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(244): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.1464+510_1464+511i others(7): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr5 | 149624649 | ||||||
| chr5:149624688 | T | G | 293 | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(290): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.1464+548T>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149624688 | |||||||
| chr5:149624819 | G | A | 1 | a0013c0022t0004g0331 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1464+679G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149624819 | |||||||
| chr5:149624900 | G | GT | 51 | a0002c0001t0001g0027 a0002c0001t0001g0084 a0004c0004t0002g0229 others(48): Show |
53 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.1464+776dupT | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr5 | 149624900 | ||||||
| chr5:149624900 | G | GTT | 87 | a0001c0002t0004g0350 a0001c0002t0006g0008 a0001c0002t0006g0028 others(84): Show |
93 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.1464+775_1464+776d others(4): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr5 | 149624900 | ||||||
| chr5:149624900 | G | GTTT | 104 | a0001c0002t0005g0342 a0001c0002t0005g0358 a0001c0002t0005g0359 others(101): Show |
117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.1464+774_1464+776d others(5): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr5 | 149624900 | ||||||
| chr5:149624900 | G | GTTTT | 10 | a0001c0002t0010g0172 a0001c0002t0010g0173 a0001c0005t0005g0190 others(7): Show |
11 | HG00735.hp1 HG01099.hp2 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.1464+773_1464+776d others(6): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr5 | 149624900 | ||||||
| chr5:149624938 | G | A | 1 | a0001c0002t0008g0014 | 2 | NA18945.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.1464+798G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149624938 | |||||||
| chr5:149624938 | G | T | 75 | a0003c0003t0002g0001 a0003c0003t0002g0005 a0003c0003t0002g0013 others(72): Show |
84 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.1464+798G>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149624938 | |||||||
| chr5:149625015 | C | G | 1 | a0005c0011t0003g0361 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1464+875C>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149625015 | |||||||
| chr5:149625135 | T | A | 7 | a0008c0009t0003g0310 a0008c0009t0003g0311 a0008c0009t0003g0313 others(4): Show |
7 | HG00735.hp1 HG01496.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1464+995T>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149625135 | |||||||
| chr5:149625135 | T | C | 276 | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(273): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.1464+995T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149625135 | |||||||
| chr5:149625180 | C | T | 53 | a0004c0004t0002g0229 a0004c0004t0004g0012 a0004c0004t0004g0020 others(50): Show |
56 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.1464+1040C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149625180 | |||||||
| chr5:149625184 | C | T | 33 | a0005c0007t0003g0144 a0005c0007t0003g0145 a0005c0007t0003g0146 others(30): Show |
33 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.1464+1044C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149625184 | |||||||
| chr5:149625185 | G | A | 64 | a0003c0003t0002g0001 a0003c0003t0002g0005 a0003c0003t0002g0013 others(61): Show |
73 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.1464+1045G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149625185 | |||||||
| chr5:149625264 | A | C | 248 | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(245): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1464+1124A>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149625264 | |||||||
| chr5:149625434 | A | G | 248 | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(245): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1464+1294A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149625434 | |||||||
| chr5:149625526 | G | T | 1 | a0004c0004t0004g0240 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1464+1386G>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149625526 | |||||||
| chr5:149625611 | T | A | 1 | a0001c0002t0010g0173 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1465-1465T>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149625611 | |||||||
| chr5:149625650 | C | T | 2 | a0001c0002t0008g0251 a0004c0004t0004g0179 |
2 | HG01243.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1465-1426C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149625650 | |||||||
| chr5:149625675 | G | A | 7 | a0008c0009t0003g0310 a0008c0009t0003g0311 a0008c0009t0003g0313 others(4): Show |
7 | HG00735.hp1 HG01496.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1465-1401G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149625675 | |||||||
| chr5:149625682 | G | A | 1 | a0002c0001t0001g0061 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1465-1394G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149625682 | |||||||
| chr5:149625761 | C | CCACA | 74 | a0003c0003t0002g0001 a0003c0003t0002g0005 a0003c0003t0002g0013 others(71): Show |
83 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.1465-1300_1465-129 others(8): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr5 | 149625761 | ||||||
| chr5:149625849 | G | A | 2 | a0001c0002t0011g0356 a0009c0014t0011g0273 |
2 | HG02615.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1465-1227G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149625849 | |||||||
| chr5:149625951 | G | T | 3 | a0005c0011t0003g0316 a0005c0011t0003g0326 a0021c0037t0003g0354 |
3 | HG02622.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1465-1125G>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149625951 | |||||||
| chr5:149625997 | A | G | 1 | a0002c0001t0001g0071 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1465-1079A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149625997 | |||||||
| chr5:149626211 | C | T | 248 | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(245): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1465-865C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149626211 | |||||||
| chr5:149626241 | A | AAC | 25 | a0001c0002t0005g0359 a0001c0005t0004g0206 a0001c0005t0004g0209 others(22): Show |
28 | HG00423.hp1 HG00558.hp2 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.1465-790_1465-789d others(4): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr5 | 149626241 | ||||||
| chr5:149626241 | A | AACAC | 6 | a0001c0005t0005g0189 a0002c0001t0001g0035 a0002c0001t0001g0066 others(3): Show |
6 | HG00609.hp2 HG04204.hp2 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1465-792_1465-789d others(6): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr5 | 149626241 | ||||||
| chr5:149626241 | A | AACACAC | 6 | a0002c0001t0001g0067 a0002c0001t0001g0078 a0002c0001t0001g0079 others(3): Show |
6 | HG01978.hp2 HG02602.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1465-794_1465-789d others(8): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr5 | 149626241 | ||||||
| chr5:149626241 | AAC | A | 45 | a0001c0002t0005g0358 a0001c0002t0006g0028 a0001c0002t0006g0050 others(42): Show |
45 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.1465-790_1465-789d others(4): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr5 | 149626241 | ||||||
| chr5:149626241 | AACAC | A | 52 | a0001c0002t0005g0342 a0001c0002t0005g0363 a0001c0002t0006g0118 others(49): Show |
55 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.1465-792_1465-789d others(6): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr5 | 149626241 | ||||||
| chr5:149626241 | AACACAC | A | 62 | a0001c0002t0006g0008 a0001c0002t0006g0086 a0001c0002t0006g0088 others(59): Show |
63 | HG00280.hp2 HG00609.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.1465-794_1465-789d others(8): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr5 | 149626241 | ||||||
| chr5:149626241 | AACACACA others(1): Show |
A | 13 | a0001c0002t0027g0327 a0004c0004t0004g0020 a0004c0004t0004g0238 others(10): Show |
15 | HG01257.hp2 HG01258.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.1465-796_1465-789d others(10): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr5 | 149626241 | ||||||
| chr5:149626241 | AACACACA others(3): Show |
A | 12 | a0006c0006t0007g0341 a0006c0006t0007g0344 a0006c0006t0007g0345 others(9): Show |
12 | HG01891.hp2 HG02280.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1465-798_1465-789d others(12): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr5 | 149626241 | ||||||
| chr5:149626241 | AACACACA others(7): Show |
A | 7 | a0008c0009t0003g0310 a0008c0009t0003g0311 a0008c0009t0003g0313 others(4): Show |
7 | HG00735.hp1 HG01496.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1465-802_1465-789d others(16): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr5 | 149626241 | ||||||
| chr5:149626244 | A | C | 1 | a0001c0002t0010g0173 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1465-832A>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149626244 | |||||||
| chr5:149626282 | ACACACG | A | 3 | a0003c0003t0002g0019 a0003c0003t0002g0302 a0008c0009t0002g0329 |
4 | HG03225.hp1 NA18951.hp1 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.1465-792_1465-787d others(8): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr5 | 149626282 | ||||||
| chr5:149626284 | ACACG | A | 31 | a0003c0003t0002g0001 a0003c0003t0002g0018 a0003c0003t0002g0246 others(28): Show |
32 | HG00099.hp2 HG00140.hp1 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.1465-790_1465-787d others(6): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr5 | 149626284 | ||||||
| chr5:149626286 | ACG | A | 8 | a0003c0003t0002g0001 a0003c0003t0002g0005 a0003c0003t0002g0277 others(5): Show |
9 | HG00438.hp2 HG00735.hp2 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.1465-788_1465-787d others(4): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr5 | 149626286 | ||||||
| chr5:149626288 | G | A | 24 | a0003c0003t0002g0001 a0003c0003t0002g0005 a0003c0003t0002g0013 others(21): Show |
27 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.1465-788G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149626288 | |||||||
| chr5:149626288 | G | T | 1 | a0007c0008t0001g0030 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1465-788G>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149626288 | |||||||
| chr5:149626473 | C | G | 53 | a0004c0004t0002g0229 a0004c0004t0004g0012 a0004c0004t0004g0020 others(50): Show |
56 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.1465-603C>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149626473 | |||||||
| chr5:149626772 | C | G | 195 | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(192): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.1465-304C>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149626772 | |||||||
| chr5:149626782 | A | G | 8 | a0005c0011t0001g0041 a0005c0011t0001g0042 a0005c0011t0001g0043 others(5): Show |
8 | HG02280.hp2 HG02615.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1465-294A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149626782 | |||||||
| chr5:149626845 | G | A | 55 | a0004c0004t0002g0229 a0004c0004t0004g0012 a0004c0004t0004g0020 others(52): Show |
58 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.1465-231G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149626845 | |||||||
| chr5:149626863 | A | G | 120 | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(117): Show |
130 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.1465-213A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149626863 | |||||||
| chr5:149626883 | A | G | 55 | a0004c0004t0002g0229 a0004c0004t0004g0012 a0004c0004t0004g0020 others(52): Show |
58 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.1465-193A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149626883 | |||||||
| chr5:149626912 | A | G | 1 | a0002c0001t0001g0079 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1465-164A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | chr5 | 149626912 | |||||||
| chr5:149626955 | TCAGTGG | T | 102 | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(99): Show |
112 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.1465-117_1465-112d others(8): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr5 | 149626955 | ||||||
| chr5:149627274 | A | G | 235 | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(232): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
splice_region_variant&intron_variant | LOW | c.1660+3A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/12 | chr5 | 149627274 | |||||||
| chr5:149627275 | C | T | 1 | a0002c0001t0001g0138 | 1 | HG03654.hp1 | splice_region_variant&intron_variant | LOW | c.1660+4C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/12 | chr5 | 149627275 | |||||||
| chr5:149627279 | A | G | 55 | a0004c0004t0002g0229 a0004c0004t0004g0012 a0004c0004t0004g0020 others(52): Show |
58 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(55): Show |
splice_region_variant&intron_variant | LOW | c.1660+8A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/12 | chr5 | 149627279 | |||||||
| chr5:149627316 | A | G | 235 | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(232): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.1660+45A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/12 | chr5 | 149627316 | |||||||
| chr5:149627323 | A | G | 1 | a0008c0017t0013g0249 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1660+52A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/12 | chr5 | 149627323 | |||||||
| chr5:149627330 | G | A | 1 | a0004c0004t0028g0244 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1660+59G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/12 | chr5 | 149627330 | |||||||
| chr5:149627333 | G | A | 2 | a0004c0010t0022g0044 a0004c0010t0022g0045 |
2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1660+62G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/12 | chr5 | 149627333 | |||||||
| chr5:149627342 | C | T | 2 | a0015c0020t0017g0176 a0015c0020t0017g0177 |
2 | HG01891.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1660+71C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/12 | chr5 | 149627342 | |||||||
| chr5:149627462 | A | C | 9 | a0001c0002t0011g0356 a0001c0002t0015g0036 a0001c0002t0015g0037 others(6): Show |
10 | HG01069.hp2 HG01071.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.1660+191A>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/12 | chr5 | 149627462 | |||||||
| chr5:149627496 | C | T | 155 | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(152): Show |
168 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.1660+225C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/12 | chr5 | 149627496 | |||||||
| chr5:149627499 | T | G | 7 | a0001c0002t0005g0358 a0001c0005t0005g0003 a0001c0005t0005g0004 others(4): Show |
10 | HG00639.hp1 HG01071.hp2 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1660+228T>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/12 | chr5 | 149627499 | |||||||
| chr5:149627619 | A | G | 16 | a0004c0004t0002g0229 a0004c0004t0004g0012 a0004c0004t0004g0143 others(13): Show |
17 | HG00597.hp2 HG02155.hp1 NA18747.hp1 others(14): Show |
intron_variant | MODIFIER | c.1660+348A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/12 | chr5 | 149627619 | |||||||
| chr5:149627646 | C | T | 78 | a0003c0003t0002g0001 a0003c0003t0002g0005 a0003c0003t0002g0013 others(75): Show |
87 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.1660+375C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/12 | chr5 | 149627646 | |||||||
| chr5:149627663 | C | T | 53 | a0004c0004t0002g0229 a0004c0004t0004g0012 a0004c0004t0004g0020 others(50): Show |
56 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.1660+392C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/12 | chr5 | 149627663 | |||||||
| chr5:149627778 | G | A | 1 | a0001c0005t0005g0202 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1660+507G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/12 | chr5 | 149627778 | |||||||
| chr5:149628043 | A | C | 3 | a0004c0010t0014g0312 a0004c0010t0014g0317 a0004c0010t0014g0319 |
3 | HG03579.hp2 NA18906.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1661-766A>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/12 | chr5 | 149628043 | |||||||
| chr5:149628109 | C | A | 133 | a0003c0003t0002g0001 a0003c0003t0002g0005 a0003c0003t0002g0013 others(130): Show |
145 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.1661-700C>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/12 | chr5 | 149628109 | |||||||
| chr5:149628134 | C | T | 1 | a0002c0001t0001g0054 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1661-675C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/12 | chr5 | 149628134 | |||||||
| chr5:149628139 | G | A | 1 | a0001c0002t0010g0173 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1661-670G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/12 | chr5 | 149628139 | |||||||
| chr5:149628179 | G | A | 53 | a0004c0004t0002g0229 a0004c0004t0004g0012 a0004c0004t0004g0020 others(50): Show |
56 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.1661-630G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/12 | chr5 | 149628179 | |||||||
| chr5:149628186 | G | A | 102 | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(99): Show |
112 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.1661-623G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/12 | chr5 | 149628186 | |||||||
| chr5:149628223 | C | T | 1 | a0004c0004t0030g0243 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1661-586C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/12 | chr5 | 149628223 | |||||||
| chr5:149628297 | G | C | 33 | a0005c0007t0003g0144 a0005c0007t0003g0145 a0005c0007t0003g0146 others(30): Show |
33 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.1661-512G>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/12 | chr5 | 149628297 | |||||||
| chr5:149628311 | G | A | 1 | a0002c0001t0001g0085 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1661-498G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/12 | chr5 | 149628311 | |||||||
| chr5:149628403 | C | G | 155 | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(152): Show |
168 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.1661-406C>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/12 | chr5 | 149628403 | |||||||
| chr5:149628439 | A | G | 235 | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(232): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.1661-370A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/12 | chr5 | 149628439 | |||||||
| chr5:149628459 | G | A | 67 | a0003c0003t0002g0001 a0003c0003t0002g0005 a0003c0003t0002g0013 others(64): Show |
76 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.1661-350G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/12 | chr5 | 149628459 | |||||||
| chr5:149628485 | A | G | 33 | a0005c0007t0003g0144 a0005c0007t0003g0145 a0005c0007t0003g0146 others(30): Show |
33 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.1661-324A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/12 | chr5 | 149628485 | |||||||
| chr5:149628510 | G | A | 33 | a0005c0007t0003g0144 a0005c0007t0003g0145 a0005c0007t0003g0146 others(30): Show |
33 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.1661-299G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/12 | chr5 | 149628510 | |||||||
| chr5:149628587 | C | T | 7 | a0001c0002t0015g0036 a0001c0002t0015g0037 a0001c0002t0015g0038 others(4): Show |
8 | HG01069.hp2 HG01071.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.1661-222C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/12 | chr5 | 149628587 | |||||||
| chr5:149628751 | T | A | 4 | a0008c0017t0013g0249 a0008c0017t0013g0250 a0014c0025t0013g0260 others(1): Show |
4 | HG01167.hp2 HG01169.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1661-58T>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/12 | chr5 | 149628751 | |||||||
| chr5:149628777 | C | T | 1 | a0001c0005t0005g0199 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1661-32C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 11/12 | chr5 | 149628777 | |||||||
| chr5:149628998 | C | T | 33 | a0005c0007t0003g0144 a0005c0007t0003g0145 a0005c0007t0003g0146 others(30): Show |
33 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.1818+32C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149628998 | |||||||
| chr5:149629004 | G | A | 2 | a0015c0020t0017g0176 a0015c0020t0017g0177 |
2 | HG01891.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1818+38G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149629004 | |||||||
| chr5:149629188 | C | G | 102 | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(99): Show |
112 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.1818+222C>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149629188 | |||||||
| chr5:149629215 | G | GATTC | 17 | a0002c0001t0003g0270 a0002c0001t0018g0269 a0005c0011t0001g0041 others(14): Show |
17 | HG02145.hp2 HG02280.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.1818+279_1818+282d others(6): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr5 | 149629215 | ||||||
| chr5:149629215 | G | GATTCATT others(1): Show |
5 | a0005c0011t0001g0043 a0005c0011t0003g0316 a0005c0011t0003g0326 others(2): Show |
5 | HG02622.hp1 HG02630.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1818+275_1818+282d others(10): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr5 | 149629215 | ||||||
| chr5:149629215 | G | GATTCATT others(5): Show |
3 | a0005c0011t0001g0042 a0005c0011t0003g0361 a0006c0006t0034g0267 |
3 | HG02559.hp2 HG02615.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1818+271_1818+282d others(14): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr5 | 149629215 | ||||||
| chr5:149629215 | GATTC | G | 154 | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(151): Show |
165 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.1818+279_1818+282d others(6): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr5 | 149629215 | ||||||
| chr5:149629215 | GATTCATT others(1): Show |
G | 109 | a0003c0003t0002g0001 a0003c0003t0002g0005 a0003c0003t0002g0013 others(106): Show |
120 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.1818+275_1818+282d others(10): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr5 | 149629215 | ||||||
| chr5:149629281 | A | G | 8 | a0004c0004t0004g0020 a0004c0004t0004g0240 a0004c0004t0004g0241 others(5): Show |
9 | HG00280.hp2 HG01074.hp1 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1818+315A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149629281 | |||||||
| chr5:149629352 | T | A | 33 | a0005c0007t0003g0144 a0005c0007t0003g0145 a0005c0007t0003g0146 others(30): Show |
33 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.1818+386T>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149629352 | |||||||
| chr5:149629380 | T | G | 1 | a0005c0007t0003g0181 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1818+414T>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149629380 | |||||||
| chr5:149629419 | T | G | 1 | a0005c0011t0003g0316 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1818+453T>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149629419 | |||||||
| chr5:149629458 | G | A | 268 | a0001c0002t0004g0350 a0001c0002t0005g0342 a0001c0002t0005g0358 others(265): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.1818+492G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149629458 | |||||||
| chr5:149629553 | C | A | 1 | a0005c0011t0001g0042 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1818+587C>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149629553 | |||||||
| chr5:149629573 | G | A | 1 | a0009c0013t0021g0126 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1818+607G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149629573 | |||||||
| chr5:149629581 | T | A | 1 | a0001c0002t0010g0173 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1818+615T>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149629581 | |||||||
| chr5:149629590 | G | A | 1 | a0004c0004t0028g0244 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1818+624G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149629590 | |||||||
| chr5:149629755 | G | A | 7 | a0006c0006t0007g0322 a0006c0006t0007g0323 a0006c0006t0007g0347 others(4): Show |
7 | HG02451.hp1 HG02572.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1818+789G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149629755 | |||||||
| chr5:149629769 | C | T | 1 | a0004c0004t0004g0240 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1818+803C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149629769 | |||||||
| chr5:149629796 | G | A | 50 | a0001c0002t0006g0008 a0001c0002t0006g0028 a0001c0002t0006g0050 others(47): Show |
54 | HG00408.hp2 HG00544.hp1 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.1818+830G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149629796 | |||||||
| chr5:149629877 | C | T | 39 | a0004c0004t0002g0229 a0004c0004t0004g0012 a0004c0004t0004g0020 others(36): Show |
41 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.1818+911C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149629877 | |||||||
| chr5:149629933 | T | A | 7 | a0008c0009t0003g0310 a0008c0009t0003g0311 a0008c0009t0003g0313 others(4): Show |
7 | HG00735.hp1 HG01496.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1818+967T>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149629933 | |||||||
| chr5:149629947 | C | T | 14 | a0004c0004t0009g0015 a0004c0004t0009g0255 a0004c0004t0009g0256 others(11): Show |
15 | HG01884.hp1 HG01884.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.1818+981C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149629947 | |||||||
| chr5:149629958 | T | C | 8 | a0005c0011t0001g0041 a0005c0011t0001g0042 a0005c0011t0001g0043 others(5): Show |
8 | HG02280.hp2 HG02615.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1818+992T>C | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149629958 | |||||||
| chr5:149629970 | A | G | 3 | a0004c0004t0004g0219 a0004c0004t0004g0231 a0004c0004t0004g0232 |
3 | NA18949.hp1 NA18986.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.1818+1004A>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149629970 | |||||||
| chr5:149630010 | G | A | 2 | a0015c0020t0017g0176 a0015c0020t0017g0177 |
2 | HG01891.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1818+1044G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149630010 | |||||||
| chr5:149630130 | C | A | 1 | a0023c0032t0009g0305 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1818+1164C>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149630130 | |||||||
| chr5:149630188 | G | A | 41 | a0004c0004t0002g0229 a0004c0004t0004g0012 a0004c0004t0004g0020 others(38): Show |
43 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.1818+1222G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149630188 | |||||||
| chr5:149630252 | T | G | 1 | a0004c0004t0004g0231 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1818+1286T>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149630252 | |||||||
| chr5:149630334 | C | T | 3 | a0002c0001t0001g0059 a0002c0001t0001g0062 a0002c0001t0001g0073 |
3 | HG02735.hp2 HG03491.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1818+1368C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149630334 | |||||||
| chr5:149630529 | C | A | 1 | a0004c0004t0009g0015 | 2 | HG01884.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1819-1453C>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149630529 | |||||||
| chr5:149630615 | C | G | 41 | a0004c0004t0002g0229 a0004c0004t0004g0012 a0004c0004t0004g0020 others(38): Show |
43 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.1819-1367C>G | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149630615 | |||||||
| chr5:149630650 | C | T | 2 | a0014c0025t0013g0260 a0014c0025t0013g0261 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1819-1332C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149630650 | |||||||
| chr5:149631070 | C | T | 2 | a0001c0002t0015g0037 a0001c0002t0015g0038 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1819-912C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149631070 | |||||||
| chr5:149631116 | T | TTTTC | 5 | a0005c0011t0001g0041 a0005c0011t0001g0042 a0005c0011t0001g0043 others(2): Show |
5 | HG02280.hp2 HG02622.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1819-847_1819-844d others(6): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr5 | 149631116 | ||||||
| chr5:149631132 | CTTTCTTC others(9): Show |
C | 4 | a0003c0012t0002g0165 a0011c0016t0012g0058 a0011c0016t0012g0083 others(1): Show |
4 | HG02027.hp1 HG02523.hp1 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.1819-847_1819-832d others(18): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr5 | 149631132 | ||||||
| chr5:149631135 | TCTTCCTT others(9): Show |
T | 2 | a0003c0003t0002g0280 a0003c0003t0002g0281 |
2 | NA18948.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.1819-834_1819-819d others(18): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr5 | 149631135 | ||||||
| chr5:149631136 | CTTCCTTC others(5): Show |
C | 64 | a0003c0003t0002g0001 a0003c0003t0002g0005 a0003c0003t0002g0013 others(61): Show |
74 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.1819-834_1819-823d others(14): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr5 | 149631136 | ||||||
| chr5:149631139 | C | T | 3 | a0001c0002t0015g0036 a0001c0002t0015g0037 a0001c0002t0015g0038 |
3 | HG02896.hp2 HG02897.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1819-843C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149631139 | |||||||
| chr5:149631140 | CTTCCTTC others(1): Show |
C | 3 | a0001c0002t0015g0036 a0001c0002t0015g0037 a0001c0002t0015g0038 |
3 | HG02896.hp2 HG02897.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1819-834_1819-827d others(10): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr5 | 149631140 | ||||||
| chr5:149631151 | C | T | 1 | a0005c0035t0003g0239 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1819-831C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149631151 | |||||||
| chr5:149631167 | CCTTT | C | 49 | a0002c0001t0001g0054 a0004c0004t0002g0229 a0004c0004t0004g0012 others(46): Show |
51 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.1819-810_1819-807d others(6): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr5 | 149631167 | ||||||
| chr5:149631172 | CTTTT | C | 4 | a0003c0003t0002g0282 a0003c0003t0002g0298 a0003c0003t0008g0293 others(1): Show |
4 | NA18960.hp2 NA18961.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.1819-806_1819-803d others(6): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr5 | 149631172 | ||||||
| chr5:149631180 | CT | C | 42 | a0001c0005t0005g0191 a0004c0004t0002g0229 a0004c0004t0004g0012 others(39): Show |
44 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.1819-789delT | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr5 | 149631180 | ||||||
| chr5:149631195 | G | A | 1 | a0003c0012t0002g0162 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1819-787G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149631195 | |||||||
| chr5:149631235 | G | A | 4 | a0009c0013t0011g0017 a0009c0013t0011g0320 a0009c0013t0021g0108 others(1): Show |
5 | HG01069.hp2 HG01071.hp1 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.1819-747G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149631235 | |||||||
| chr5:149631240 | C | T | 72 | a0001c0002t0015g0036 a0001c0002t0015g0037 a0001c0002t0015g0038 others(69): Show |
82 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.1819-742C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149631240 | |||||||
| chr5:149631568 | C | T | 1 | a0003c0003t0002g0287 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1819-414C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149631568 | |||||||
| chr5:149631681 | T | TCCTTGAC others(3): Show |
33 | a0005c0007t0003g0144 a0005c0007t0003g0145 a0005c0007t0003g0146 others(30): Show |
33 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.1819-300_1819-291d others(12): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr5 | 149631681 | ||||||
| chr5:149631748 | G | A | 1 | a0001c0002t0005g0359 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1819-234G>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149631748 | |||||||
| chr5:149631789 | C | A | 2 | a0008c0017t0013g0249 a0008c0017t0013g0250 |
2 | HG02486.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1819-193C>A | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149631789 | |||||||
| chr5:149631861 | C | T | 1 | a0002c0001t0001g0026 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1819-121C>T | ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 12/12 | chr5 | 149631861 |