Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 89839 |
| ensemblid | ENSG00000285077.4 |
| hgncid | 15782 |
| symbol | ARHGAP11B |
| name | Rho GTPase activating protein 11B |
| refseq_nuc | NM_001039841.3 |
| refseq_prot | NP_001034930.1 |
| ensembl_nuc | ENST00000697964.2 |
| ensembl_prot | ENSP00000513489.1 |
| mane_status | MANE Select |
| chr | chr15 |
| start | 30626128 |
| end | 30638810 |
| strand | + |
| ver | v1.2 |
| region | chr15:30626128-30638810 |
| region5000 | chr15:30621128-30643810 |
| regionname0 | ARHGAP11B_chr15_30626128_30638810 |
| regionname5000 | ARHGAP11B_chr15_30621128_30643810 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 267 | 237 | 84 | 46 | 61 | 14 | 31 | 32 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | MWDQR others(262): Show |
chr15 | 30621128 | 30643810 |
| a0002 | 0/0 | 267 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | MWDQR others(262): Show |
chr15 | 30621128 | 30643810 |
| a0003 | 0/0 | 267 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | MWDQR others(262): Show |
chr15 | 30621128 | 30643810 |
| a0004 | 0/0 | 267 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | MWDQR others(262): Show |
chr15 | 30621128 | 30643810 |
| a0005 | 0/0 | 267 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | MWDQR others(262): Show |
chr15 | 30621128 | 30643810 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 801 | 237 | 84 | 46 | 61 | 14 | 31 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | ATGTG others(796): Show |
chr15 | 30621128 | 30643810 | ||
| a0002c0002 | 0/0 | 801 | 7 | 6 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | ATGTG others(796): Show |
chr15 | 30621128 | 30643810 | ||
| a0003c0003 | 0/0 | 801 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | ATGTG others(796): Show |
chr15 | 30621128 | 30643810 | ||
| a0004c0005 | 0/0 | 801 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | ATGTG others(796): Show |
chr15 | 30621128 | 30643810 | ||
| a0005c0004 | 0/0 | 801 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | ATGTG others(796): Show |
chr15 | 30621128 | 30643810 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1565 | 228 | 80 | 45 | 59 | 14 | 29 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | GGTGG others(1560): Show |
chr15 | 30621128 | 30643810 |
| a0001c0001t0002 | 0/0 | 1565 | 6 | 4 | 1 | 0 | 0 | 1 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | GGTGG others(1560): Show |
chr15 | 30621128 | 30643810 |
| a0001c0001t0003 | 0/0 | 1565 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | GGTGG others(1560): Show |
chr15 | 30621128 | 30643810 |
| a0001c0001t0004 | 0/0 | 1565 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | GGTGG others(1560): Show |
chr15 | 30621128 | 30643810 |
| a0001c0001t0005 | 0/0 | 1565 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | GGTGG others(1560): Show |
chr15 | 30621128 | 30643810 |
| a0002c0002t0001 | 0/0 | 1565 | 7 | 6 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | GGTGG others(1560): Show |
chr15 | 30621128 | 30643810 |
| a0003c0003t0001 | 0/0 | 1565 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | GGTGG others(1560): Show |
chr15 | 30621128 | 30643810 |
| a0004c0005t0001 | 0/0 | 1565 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | GGTGG others(1560): Show |
chr15 | 30621128 | 30643810 |
| a0005c0004t0001 | 0/0 | 1565 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | GGTGG others(1560): Show |
chr15 | 30621128 | 30643810 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 45 | 3 | 14 | 16 | 4 | 8 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0002 | 0/0 | 15 | 1 | 4 | 3 | 5 | 2 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0003 | 0/0 | 14 | 13 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0004 | 0/0 | 12 | 3 | 1 | 4 | 1 | 3 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0005 | 0/0 | 9 | 9 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0006 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0007 | 0/0 | 6 | 0 | 2 | 0 | 1 | 3 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0008 | 0/0 | 6 | 2 | 1 | 0 | 2 | 1 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 1 | 0 | 1 | 2 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0012 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0044 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0004g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0001c0001t0005g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0002c0002t0001g0009 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0002c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0002c0002t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0002c0002t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0003c0003t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0004c0005t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| a0005c0004t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | FIN | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | CHS | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG00673 | hp2 | a0003 | c0003 | t0001 | g0018 | EAS | CHS | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0009 | AMR | PUR | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0046 | AMR | PUR | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | ACB | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG01952 | hp2 | a0004 | c0005 | t0001 | g0004 | AMR | PEL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | KHV | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | KHV | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CDX | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02615 | hp1 | a0002 | c0002 | t0001 | g0058 | AFR | GWD | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02622 | hp1 | a0002 | c0002 | t0001 | g0009 | AFR | GWD | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02895 | hp1 | a0002 | c0002 | t0001 | g0087 | AFR | GWD | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG03017 | hp2 | a0001 | c0001 | t0004 | g0084 | SAS | PJL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | MSL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0023 | SAS | PJL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | ESN | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG03579 | hp2 | a0002 | c0002 | t0001 | g0009 | AFR | MSL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | STU | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | STU | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | BEB | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | STU | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | STU | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG04204 | hp1 | a0005 | c0004 | t0001 | g0007 | SAS | STU | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | STU | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | STU | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| NA18522 | hp1 | a0002 | c0002 | t0001 | g0009 | AFR | YRI | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0082 | AFR | YRI | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | YRI | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| NA19001 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | LWK | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | LWK | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | LWK | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | LWK | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ASW | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ASW | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | TSI | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0047 | AFR | ACB | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG03471 | hp1 | a0002 | c0002 | t0001 | g0083 | AFR | MSL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | USA | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | USA | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | USA | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | USA | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | LWK | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0044 | REF | REF | ARHGAP11B_chr15_30621128_30643810 | ARHGAP11B | chr15 | 30621128 | 30643810 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:30626947 | G | C | 1 | a0002 | 7 | HG01081.hp2 HG02615.hp1 HG02622.hp1 others(4): Show |
missense_variant&splice_region_variant | MODERATE | c.127G>C | p.Gly43Arg | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/7 | 820/1565 | 127/804 | 43/267 | chr15 | 30626947 | |||
| chr15:30633523 | A | C | 1 | a0004 | 1 | HG01952.hp2 | missense_variant | MODERATE | c.234A>C | p.Glu78Asp | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 3/7 | 927/1565 | 234/804 | 78/267 | chr15 | 30633523 | |||
| chr15:30635148 | G | A | 1 | a0003 | 1 | HG00673.hp2 | missense_variant | MODERATE | c.620G>A | p.Ser207Asn | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 5/7 | 1313/1565 | 620/804 | 207/267 | chr15 | 30635148 | |||
| chr15:30635624 | C | A | 1 | a0005 | 1 | HG04204.hp1 | missense_variant | MODERATE | c.798C>A | p.Asn266Lys | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 6/7 | 1491/1565 | 798/804 | 266/267 | chr15 | 30635624 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:30626400 | G | T | 1 | a0001c0001t0005 | 1 | NA19001.hp2 | 5_prime_UTR_variant | MODIFIER | c.-421G>T | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/7 | 421 | chr15 | 30626400 | ||||||
| chr15:30626570 | C | G | 1 | a0001c0001t0002 | 6 | HG01109.hp1 HG01891.hp2 HG02109.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-251C>G | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/7 | 251 | chr15 | 30626570 | ||||||
| chr15:30626589 | G | A | 1 | a0001c0001t0003 | 1 | NA18986.hp1 | 5_prime_UTR_variant | MODIFIER | c.-232G>A | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/7 | 232 | chr15 | 30626589 | ||||||
| chr15:30626689 | G | T | 1 | a0001c0001t0004 | 1 | HG03017.hp2 | 5_prime_UTR_variant | MODIFIER | c.-132G>T | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/7 | 132 | chr15 | 30626689 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:30627116 | G | GT | 4 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0001g0101 others(1): Show |
8 | HG01070.hp1 HG01071.hp2 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.129+177dupT | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 30627116 | ||||||
| chr15:30627134 | G | A | 1 | a0001c0001t0001g0029 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.129+185G>A | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/6 | chr15 | 30627134 | |||||||
| chr15:30627147 | TGAGA | T | 5 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0031 others(2): Show |
6 | HG01256.hp2 HG01258.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.129+201_129+204del others(4): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 30627147 | ||||||
| chr15:30627335 | A | T | 1 | a0001c0001t0001g0100 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.129+386A>T | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/6 | chr15 | 30627335 | |||||||
| chr15:30627566 | A | AT | 11 | a0001c0001t0001g0018 a0001c0001t0001g0033 a0001c0001t0001g0093 others(8): Show |
11 | HG00423.hp1 HG00673.hp2 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.129+628dupT | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 30627566 | ||||||
| chr15:30627758 | G | T | 1 | a0001c0001t0001g0092 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.129+809G>T | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/6 | chr15 | 30627758 | |||||||
| chr15:30627931 | G | T | 1 | a0001c0001t0001g0092 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.129+982G>T | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/6 | chr15 | 30627931 | |||||||
| chr15:30628079 | C | CT | 18 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0011 others(15): Show |
40 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.129+1143dupT | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 30628079 | ||||||
| chr15:30628195 | C | G | 1 | a0001c0001t0001g0025 | 2 | HG02647.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.129+1246C>G | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/6 | chr15 | 30628195 | |||||||
| chr15:30628275 | G | A | 42 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(39): Show |
76 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.129+1326G>A | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/6 | chr15 | 30628275 | |||||||
| chr15:30628282 | T | C | 42 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(39): Show |
76 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.129+1333T>C | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/6 | chr15 | 30628282 | |||||||
| chr15:30628515 | C | A | 1 | a0001c0001t0001g0056 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.129+1566C>A | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/6 | chr15 | 30628515 | |||||||
| chr15:30628715 | T | A | 1 | a0001c0001t0001g0092 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.129+1766T>A | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/6 | chr15 | 30628715 | |||||||
| chr15:30628716 | G | A | 72 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(69): Show |
142 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.129+1767G>A | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/6 | chr15 | 30628716 | |||||||
| chr15:30629055 | T | A | 1 | a0001c0001t0001g0034 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.130-1648T>A | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/6 | chr15 | 30629055 | |||||||
| chr15:30629067 | G | T | 1 | a0001c0001t0001g0063 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.130-1636G>T | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/6 | chr15 | 30629067 | |||||||
| chr15:30629167 | A | G | 2 | a0001c0001t0001g0054 a0001c0001t0001g0055 |
2 | HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.130-1536A>G | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/6 | chr15 | 30629167 | |||||||
| chr15:30629310 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.130-1393G>A | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/6 | chr15 | 30629310 | |||||||
| chr15:30629365 | AC | A | 60 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(57): Show |
118 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.130-1330delC | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 30629365 | ||||||
| chr15:30629375 | C | G | 1 | a0001c0001t0004g0084 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.130-1328C>G | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/6 | chr15 | 30629375 | |||||||
| chr15:30629426 | C | T | 5 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0052 others(2): Show |
13 | HG00280.hp1 HG01071.hp1 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.130-1277C>T | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/6 | chr15 | 30629426 | |||||||
| chr15:30629508 | G | A | 1 | a0001c0001t0001g0021 | 2 | HG00438.hp1 HG00621.hp1 |
intron_variant | MODIFIER | c.130-1195G>A | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/6 | chr15 | 30629508 | |||||||
| chr15:30629602 | C | T | 4 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0001g0101 others(1): Show |
8 | HG01070.hp1 HG01071.hp2 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.130-1101C>T | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/6 | chr15 | 30629602 | |||||||
| chr15:30629765 | G | A | 1 | a0001c0001t0001g0093 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.130-938G>A | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/6 | chr15 | 30629765 | |||||||
| chr15:30630143 | A | G | 3 | a0001c0001t0001g0027 a0001c0001t0001g0090 a0001c0001t0001g0091 |
4 | HG02572.hp1 HG02615.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.130-560A>G | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/6 | chr15 | 30630143 | |||||||
| chr15:30630181 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.130-522G>A | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/6 | chr15 | 30630181 | |||||||
| chr15:30630267 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.130-436C>T | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/6 | chr15 | 30630267 | |||||||
| chr15:30630295 | G | T | 1 | a0001c0001t0001g0080 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.130-408G>T | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/6 | chr15 | 30630295 | |||||||
| chr15:30630401 | TACTG | T | 2 | a0001c0001t0001g0003 a0001c0001t0001g0065 |
15 | HG01981.hp1 HG02145.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.130-298_130-295del others(4): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 30630401 | ||||||
| chr15:30630673 | G | A | 1 | a0001c0001t0001g0014 | 3 | HG00558.hp1 HG02132.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.130-30G>A | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1/6 | chr15 | 30630673 | |||||||
| chr15:30630888 | T | C | 1 | a0001c0001t0001g0015 | 3 | HG02622.hp2 HG02809.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.200+115T>C | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30630888 | |||||||
| chr15:30630933 | T | C | 1 | a0001c0001t0001g0064 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.200+160T>C | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30630933 | |||||||
| chr15:30630970 | G | C | 1 | a0001c0001t0001g0066 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.200+197G>C | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30630970 | |||||||
| chr15:30631131 | A | T | 4 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0001g0101 others(1): Show |
8 | HG01070.hp1 HG01071.hp2 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.200+358A>T | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30631131 | |||||||
| chr15:30631151 | A | T | 1 | a0001c0001t0001g0080 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.200+378A>T | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30631151 | |||||||
| chr15:30631152 | T | A | 1 | a0001c0001t0001g0080 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.200+379T>A | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30631152 | |||||||
| chr15:30631153 | A | T | 1 | a0001c0001t0001g0080 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.200+380A>T | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30631153 | |||||||
| chr15:30631256 | T | C | 1 | a0001c0001t0001g0067 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.200+483T>C | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30631256 | |||||||
| chr15:30631285 | A | G | 6 | a0001c0001t0001g0018 a0001c0001t0001g0096 a0001c0001t0001g0097 others(3): Show |
6 | HG00423.hp1 HG00673.hp2 NA18944.hp1 others(3): Show |
intron_variant | MODIFIER | c.200+512A>G | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30631285 | |||||||
| chr15:30631352 | C | A | 2 | a0001c0001t0001g0025 a0001c0001t0001g0039 |
3 | HG01975.hp2 HG02647.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.200+579C>A | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30631352 | |||||||
| chr15:30631353 | C | CT | 1 | a0001c0001t0001g0005 | 9 | HG01884.hp2 HG01891.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.200+588dupT | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 30631353 | ||||||
| chr15:30631415 | A | G | 3 | a0001c0001t0001g0013 a0001c0001t0001g0029 a0001c0001t0001g0062 |
5 | HG02258.hp1 HG02451.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.200+642A>G | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30631415 | |||||||
| chr15:30631440 | C | T | 1 | a0001c0001t0001g0050 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.200+667C>T | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30631440 | |||||||
| chr15:30631475 | A | G | 1 | a0001c0001t0001g0079 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.200+702A>G | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30631475 | |||||||
| chr15:30631504 | T | A | 42 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(39): Show |
76 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.200+731T>A | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30631504 | |||||||
| chr15:30631537 | A | G | 72 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(69): Show |
142 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.200+764A>G | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30631537 | |||||||
| chr15:30631626 | C | A | 1 | a0001c0001t0001g0068 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.200+853C>A | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30631626 | |||||||
| chr15:30631784 | G | A | 72 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(69): Show |
142 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.200+1011G>A | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30631784 | |||||||
| chr15:30631787 | C | CT | 6 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0078 others(3): Show |
6 | HG01261.hp1 HG01358.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.200+1030dupT | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 30631787 | ||||||
| chr15:30631803 | T | G | 1 | a0001c0001t0001g0096 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.200+1030T>G | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30631803 | |||||||
| chr15:30631816 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.200+1043C>T | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30631816 | |||||||
| chr15:30631911 | C | G | 1 | a0001c0001t0001g0049 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.200+1138C>G | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30631911 | |||||||
| chr15:30632144 | G | A | 1 | a0001c0001t0002g0040 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.201-1346G>A | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30632144 | |||||||
| chr15:30632166 | A | AATCCCAG others(587): Show |
1 | a0001c0001t0001g0050 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.201-1312_201-1311i others(596): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 30632166 | ||||||
| chr15:30632166 | A | AATCCCAG others(588): Show |
1 | a0001c0001t0001g0099 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.201-1312_201-1311i others(597): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 30632166 | ||||||
| chr15:30632166 | A | AATCCCAG others(586): Show |
1 | a0001c0001t0001g0092 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.201-1312_201-1311i others(595): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 30632166 | ||||||
| chr15:30632166 | A | AATCCCAG others(586): Show |
1 | a0001c0001t0001g0069 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.201-1312_201-1311i others(595): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 30632166 | ||||||
| chr15:30632166 | A | AATCCCAG others(589): Show |
2 | a0001c0001t0001g0020 a0001c0001t0001g0081 |
3 | HG00544.hp2 HG02040.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.201-1312_201-1311i others(598): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 30632166 | ||||||
| chr15:30632166 | A | AATCCCAG others(588): Show |
5 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0042 others(2): Show |
5 | HG00741.hp1 HG01261.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.201-1312_201-1311i others(597): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 30632166 | ||||||
| chr15:30632166 | A | AATCCCAG others(588): Show |
1 | a0002c0002t0001g0058 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.201-1312_201-1311i others(597): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 30632166 | ||||||
| chr15:30632166 | A | AATCCCAG others(587): Show |
1 | a0001c0001t0001g0022 | 2 | NA18975.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.201-1312_201-1311i others(596): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 30632166 | ||||||
| chr15:30632166 | A | AATCCCAG others(587): Show |
43 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(40): Show |
103 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.201-1312_201-1311i others(596): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 30632166 | ||||||
| chr15:30632166 | A | AATCCCAG others(585): Show |
1 | a0001c0001t0001g0038 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.201-1312_201-1311i others(594): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 30632166 | ||||||
| chr15:30632166 | A | AATCCCAG others(587): Show |
4 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0002c0002t0001g0009 others(1): Show |
10 | HG01081.hp2 HG02559.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.201-1312_201-1311i others(596): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 30632166 | ||||||
| chr15:30632166 | A | AATCCCAG others(586): Show |
2 | a0001c0001t0001g0048 a0001c0001t0001g0049 |
2 | HG02083.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.201-1312_201-1311i others(595): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 30632166 | ||||||
| chr15:30632166 | A | AATCCCAG others(586): Show |
1 | a0002c0002t0001g0087 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.201-1312_201-1311i others(595): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 30632166 | ||||||
| chr15:30632166 | A | AATCCCAG others(586): Show |
30 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0014 others(27): Show |
95 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.201-1312_201-1311i others(595): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 30632166 | ||||||
| chr15:30632166 | A | AATCCCAG others(586): Show |
4 | a0001c0001t0001g0088 a0001c0001t0001g0091 a0001c0001t0001g0101 others(1): Show |
4 | HG01070.hp1 HG01496.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.201-1312_201-1311i others(595): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 30632166 | ||||||
| chr15:30632166 | A | AATCCCAG others(585): Show |
1 | a0001c0001t0001g0077 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.201-1312_201-1311i others(594): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 30632166 | ||||||
| chr15:30632166 | A | AATCCCAG others(585): Show |
2 | a0001c0001t0001g0017 a0001c0001t0001g0098 |
4 | HG02735.hp1 HG03490.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.201-1312_201-1311i others(594): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 30632166 | ||||||
| chr15:30632166 | A | AATCCCAG others(587): Show |
2 | a0001c0001t0001g0056 a0001c0001t0001g0060 |
2 | HG02630.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.201-1312_201-1311i others(596): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 30632166 | ||||||
| chr15:30632166 | A | AATCCCAG others(586): Show |
1 | a0001c0001t0001g0061 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.201-1312_201-1311i others(595): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 30632166 | ||||||
| chr15:30632166 | A | AATCCCAG others(588): Show |
1 | a0001c0001t0001g0052 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.201-1317_201-1316i others(597): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 30632166 | ||||||
| chr15:30632166 | A | AATCCCAG others(587): Show |
2 | a0001c0001t0001g0010 a0001c0001t0001g0053 |
5 | HG00280.hp1 HG01258.hp1 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.201-1317_201-1316i others(596): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 30632166 | ||||||
| chr15:30632169 | C | CCCAGCAC others(587): Show |
1 | a0001c0001t0001g0068 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.201-1312_201-1311i others(596): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 30632169 | ||||||
| chr15:30632211 | A | G | 1 | a0001c0001t0001g0064 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.201-1279A>G | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30632211 | |||||||
| chr15:30632220 | A | G | 2 | a0001c0001t0001g0005 a0001c0001t0001g0057 |
10 | HG01346.hp1 HG01884.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.201-1270A>G | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30632220 | |||||||
| chr15:30632427 | GA | G | 4 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0076 others(1): Show |
12 | HG01346.hp1 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.201-1052delA | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 30632427 | ||||||
| chr15:30632429 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.201-1061A>G | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30632429 | |||||||
| chr15:30632451 | C | T | 3 | a0001c0001t0001g0056 a0001c0001t0001g0060 a0001c0001t0001g0061 |
3 | HG02630.hp1 HG02896.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.201-1039C>T | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30632451 | |||||||
| chr15:30632527 | T | G | 1 | a0001c0001t0001g0063 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.201-963T>G | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30632527 | |||||||
| chr15:30632558 | C | A | 1 | a0001c0001t0001g0029 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.201-932C>A | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30632558 | |||||||
| chr15:30632574 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.201-916C>T | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30632574 | |||||||
| chr15:30632798 | G | GA | 8 | a0001c0001t0001g0033 a0001c0001t0001g0041 a0001c0001t0001g0049 others(5): Show |
8 | HG02109.hp2 HG02300.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.201-684dupA | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 30632798 | ||||||
| chr15:30632968 | G | C | 1 | a0001c0001t0001g0071 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.201-522G>C | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30632968 | |||||||
| chr15:30633076 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.201-414G>A | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30633076 | |||||||
| chr15:30633170 | G | C | 1 | a0001c0001t0001g0067 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.201-320G>C | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30633170 | |||||||
| chr15:30633246 | G | A | 2 | a0001c0001t0001g0012 a0001c0001t0001g0102 |
5 | HG01070.hp1 HG01071.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.201-244G>A | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30633246 | |||||||
| chr15:30633331 | A | G | 1 | a0001c0001t0001g0074 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.201-159A>G | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30633331 | |||||||
| chr15:30633366 | A | T | 6 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0002c0002t0001g0009 others(3): Show |
12 | HG01081.hp2 HG02559.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.201-124A>T | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | chr15 | 30633366 | |||||||
| chr15:30633471 | G | GA | 3 | a0001c0001t0001g0027 a0001c0001t0001g0090 a0001c0001t0001g0091 |
4 | HG02572.hp1 HG02615.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.201-13dupA | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 30633471 | ||||||
| chr15:30633718 | A | AT | 70 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(67): Show |
139 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.297+143dupT | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr15 | 30633718 | ||||||
| chr15:30633877 | T | G | 3 | a0001c0001t0001g0013 a0001c0001t0001g0029 a0001c0001t0001g0062 |
5 | HG02258.hp1 HG02451.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.297+291T>G | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 3/6 | chr15 | 30633877 | |||||||
| chr15:30634106 | G | C | 1 | a0001c0001t0001g0045 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.298-64G>C | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 3/6 | chr15 | 30634106 | |||||||
| chr15:30634802 | G | A | 1 | a0001c0001t0001g0003 | 14 | HG01981.hp1 HG02145.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.552-278G>A | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 4/6 | chr15 | 30634802 | |||||||
| chr15:30634862 | C | CTT | 1 | a0001c0001t0001g0015 | 3 | HG02622.hp2 HG02809.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.552-217_552-216ins others(2): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr15 | 30634862 | ||||||
| chr15:30635007 | A | C | 2 | a0001c0001t0001g0005 a0001c0001t0001g0057 |
10 | HG01346.hp1 HG01884.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.552-73A>C | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 4/6 | chr15 | 30635007 | |||||||
| chr15:30635211 | TAC | T | 4 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0001g0101 others(1): Show |
8 | HG01070.hp1 HG01071.hp2 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.660+25_660+26delCA | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr15 | 30635211 | ||||||
| chr15:30635428 | T | C | 2 | a0001c0001t0001g0005 a0001c0001t0001g0057 |
10 | HG01346.hp1 HG01884.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.661-59T>C | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 5/6 | chr15 | 30635428 | |||||||
| chr15:30635642 | T | C | 1 | a0001c0001t0001g0072 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.*3+9T>C | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 6/6 | chr15 | 30635642 | |||||||
| chr15:30635664 | A | G | 17 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0011 others(14): Show |
39 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.*3+31A>G | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 6/6 | chr15 | 30635664 | |||||||
| chr15:30635776 | G | T | 1 | a0001c0001t0001g0085 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.*3+143G>T | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 6/6 | chr15 | 30635776 | |||||||
| chr15:30635852 | C | T | 72 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(69): Show |
142 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.*3+219C>T | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 6/6 | chr15 | 30635852 | |||||||
| chr15:30636249 | G | A | 1 | a0001c0001t0001g0031 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.*3+616G>A | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 6/6 | chr15 | 30636249 | |||||||
| chr15:30636373 | T | A | 2 | a0001c0001t0001g0005 a0001c0001t0001g0057 |
10 | HG01346.hp1 HG01884.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.*3+740T>A | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 6/6 | chr15 | 30636373 | |||||||
| chr15:30636813 | A | G | 1 | a0001c0001t0001g0093 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.*3+1180A>G | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 6/6 | chr15 | 30636813 | |||||||
| chr15:30636930 | C | T | 1 | a0001c0001t0001g0068 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.*3+1297C>T | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 6/6 | chr15 | 30636930 | |||||||
| chr15:30637121 | A | G | 12 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0034 others(9): Show |
24 | HG01099.hp2 HG01109.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.*3+1488A>G | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 6/6 | chr15 | 30637121 | |||||||
| chr15:30637542 | G | A | 3 | a0001c0001t0001g0056 a0001c0001t0001g0060 a0001c0001t0001g0061 |
3 | HG02630.hp1 HG02896.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.*4-1204G>A | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 6/6 | chr15 | 30637542 | |||||||
| chr15:30637666 | G | A | 4 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0001g0101 others(1): Show |
8 | HG01070.hp1 HG01071.hp2 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.*4-1080G>A | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 6/6 | chr15 | 30637666 | |||||||
| chr15:30637722 | A | T | 4 | a0001c0001t0001g0008 a0001c0001t0001g0034 a0001c0001t0001g0038 others(1): Show |
9 | HG01099.hp2 HG01243.hp1 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.*4-1024A>T | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 6/6 | chr15 | 30637722 | |||||||
| chr15:30637781 | C | T | 23 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0011 others(20): Show |
47 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.*4-965C>T | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 6/6 | chr15 | 30637781 | |||||||
| chr15:30637816 | C | CT | 4 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0057 others(1): Show |
13 | HG00544.hp1 HG01346.hp1 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.*4-909dupT | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr15 | 30637816 | ||||||
| chr15:30637816 | CT | C | 49 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(46): Show |
102 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.*4-909delT | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr15 | 30637816 | ||||||
| chr15:30637816 | CTT | C | 11 | a0001c0001t0001g0009 a0001c0001t0001g0032 a0001c0001t0001g0052 others(8): Show |
14 | HG01081.hp2 HG01256.hp2 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.*4-910_*4-909delTT | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr15 | 30637816 | ||||||
| chr15:30637902 | C | T | 3 | a0001c0001t0001g0013 a0001c0001t0001g0029 a0001c0001t0001g0062 |
5 | HG02258.hp1 HG02451.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.*4-844C>T | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 6/6 | chr15 | 30637902 | |||||||
| chr15:30638046 | C | T | 33 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0019 others(30): Show |
51 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.*4-700C>T | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 6/6 | chr15 | 30638046 | |||||||
| chr15:30638280 | A | C | 1 | a0001c0001t0001g0073 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.*4-466A>C | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 6/6 | chr15 | 30638280 | |||||||
| chr15:30638297 | G | T | 72 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(69): Show |
142 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.*4-449G>T | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 6/6 | chr15 | 30638297 | |||||||
| chr15:30638453 | A | G | 4 | a0001c0001t0001g0016 a0001c0001t0001g0021 a0001c0001t0001g0067 others(1): Show |
7 | HG00438.hp1 HG00621.hp1 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.*4-293A>G | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 6/6 | chr15 | 30638453 | |||||||
| chr15:30638522 | A | G | 1 | a0001c0001t0001g0025 | 2 | HG02647.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.*4-224A>G | ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 6/6 | chr15 | 30638522 |