Search by Gene
| geneid | 9824 |
|---|---|
| ensemblid | ENSG00000198826.11 |
| hgncid | 15783 |
| symbol | ARHGAP11A |
| name | Rho GTPase activating protein 11A |
| refseq_nuc | NM_014783.6 |
| refseq_prot | NP_055598.1 |
| ensembl_nuc | ENST00000361627.8 |
| ensembl_prot | ENSP00000355090.3 |
| mane_status | MANE Select |
| chr | chr15 |
| start | 32615504 |
| end | 32639941 |
| strand | + |
| ver | v1.2 |
| region | chr15:32615504-32639941 |
| region5000 | chr15:32610504-32644941 |
| regionname0 | ARHGAP11A_chr15_32615504_32639941 |
| regionname5000 | ARHGAP11A_chr15_32610504_32644941 |
Multiple Alignments (by translate haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
Multiple Alignments (by aa haplotype frequency)
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aa |
|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 1023 | 324 | 76 | 59 | 141 | 12 | 35 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| a0002 | 0/0 | 1023 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| a0003 | 0/0 | 1023 | 3 | 1 | 0 | 0 | 2 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| a0004 | 0/0 | 1023 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| a0005 | 0/0 | 1023 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| a0006 | 0/0 | 1023 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| a0007 | 0/0 | 1023 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| a0008 | 0/0 | 1023 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq |
|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 3072 | 306 | 68 | 56 | 134 | 12 | 35 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| c0002 | 0/0 | 3072 | 7 | 5 | 2 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| c0003 | 0/0 | 3072 | 5 | 0 | 1 | 4 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| c0004 | 0/0 | 3072 | 3 | 1 | 0 | 0 | 2 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| c0005 | 0/0 | 3072 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| c0006 | 0/0 | 3072 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| c0007 | 0/0 | 3072 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| c0008 | 0/0 | 3072 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| c0009 | 0/0 | 3072 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| c0010 | 0/0 | 3072 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| c0011 | 0/0 | 3072 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| c0012 | 0/0 | 3072 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| c0013 | 0/0 | 3072 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| c0014 | 0/0 | 3072 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| c0015 | 0/0 | 3072 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| thapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq |
|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 2805 | 95 | 14 | 15 | 51 | 2 | 12 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| t0002 | 0/0 | 2805 | 77 | 15 | 14 | 38 | 1 | 9 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| t0003 | 0/0 | 2805 | 76 | 30 | 14 | 23 | 2 | 7 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| t0004 | 0/0 | 2805 | 52 | 6 | 11 | 27 | 3 | 5 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| t0005 | 0/0 | 2805 | 8 | 6 | 2 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| t0006 | 0/0 | 2805 | 4 | 0 | 2 | 0 | 2 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| t0007 | 0/0 | 2805 | 2 | 0 | 0 | 0 | 2 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| t0008 | 0/0 | 2805 | 2 | 1 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| t0009 | 0/0 | 2805 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| t0010 | 0/0 | 2805 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| t0011 | 0/0 | 2805 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| t0012 | 0/0 | 2805 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| t0013 | 0/0 | 2805 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| t0014 | 0/0 | 2805 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| t0015 | 0/0 | 2805 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| t0016 | 0/0 | 2805 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| t0017 | 0/0 | 2805 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| t0018 | 0/0 | 2805 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| t0019 | 0/0 | 2805 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| t0020 | 0/0 | 2805 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| t0021 | 0/0 | 2805 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| t0022 | 0/0 | 2805 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| t0023 | 0/0 | 2805 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| t0024 | 0/0 | 2805 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/1 | 19 | 0 | 3 | 11 | 1 | 3 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0002 | 0/0 | 14 | 1 | 3 | 9 | 0 | 1 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0003 | 0/0 | 14 | 1 | 3 | 9 | 0 | 1 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0004 | 0/0 | 12 | 0 | 2 | 8 | 1 | 1 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0005 | 0/0 | 9 | 0 | 1 | 8 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0006 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0007 | 0/0 | 8 | 0 | 1 | 4 | 2 | 1 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0008 | 0/0 | 7 | 4 | 1 | 2 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0009 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0011 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0012 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0016 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0018 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0022 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0023 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0030 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0033 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0034 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0035 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0042 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0043 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| achapid | ahapid | chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | acseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | a0001 | c0001 | 0/1 | 306 | 68 | 56 | 134 | 12 | 35 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| a0001c0002 | a0001 | c0002 | 0/0 | 7 | 5 | 2 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| a0001c0003 | a0001 | c0003 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| a0001c0006 | a0001 | c0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| a0001c0008 | a0001 | c0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| a0001c0012 | a0001 | c0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| a0001c0014 | a0001 | c0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| a0001c0015 | a0001 | c0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| a0002c0005 | a0002 | c0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| a0003c0004 | a0003 | c0004 | 0/0 | 3 | 1 | 0 | 0 | 2 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| a0004c0007 | a0004 | c0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| a0005c0010 | a0005 | c0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| a0006c0011 | a0006 | c0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| a0007c0009 | a0007 | c0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| a0008c0013 | a0008 | c0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| acthapid | ahapid | chapid | thapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | actseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | a0001 | c0001 | t0001 | 0/1 | 89 | 10 | 14 | 50 | 2 | 12 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| a0001c0001t0002 | a0001 | c0001 | t0002 | 0/0 | 72 | 12 | 14 | 36 | 1 | 9 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| a0001c0001t0003 | a0001 | c0001 | t0003 | 0/0 | 69 | 30 | 13 | 18 | 2 | 6 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| a0001c0001t0004 | a0001 | c0001 | t0004 | 0/0 | 52 | 6 | 11 | 27 | 3 | 5 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| a0001c0001t0006 | a0001 | c0001 | t0006 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| a0001c0001t0008 | a0001 | c0001 | t0008 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| a0001c0001t0009 | a0001 | c0001 | t0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| a0001c0001t0010 | a0001 | c0001 | t0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| a0001c0001t0011 | a0001 | c0001 | t0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| a0001c0001t0013 | a0001 | c0001 | t0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| a0001c0001t0014 | a0001 | c0001 | t0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| a0001c0001t0015 | a0001 | c0001 | t0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| a0001c0001t0016 | a0001 | c0001 | t0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| a0001c0001t0017 | a0001 | c0001 | t0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| a0001c0001t0018 | a0001 | c0001 | t0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| a0001c0001t0019 | a0001 | c0001 | t0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| a0001c0001t0020 | a0001 | c0001 | t0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| a0001c0001t0021 | a0001 | c0001 | t0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| a0001c0001t0022 | a0001 | c0001 | t0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| a0001c0001t0023 | a0001 | c0001 | t0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| a0001c0001t0024 | a0001 | c0001 | t0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| a0001c0002t0005 | a0001 | c0002 | t0005 | 0/0 | 7 | 5 | 2 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| a0001c0003t0003 | a0001 | c0003 | t0003 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| a0001c0006t0001 | a0001 | c0006 | t0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| a0001c0008t0001 | a0001 | c0008 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| a0001c0012t0003 | a0001 | c0012 | t0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| a0001c0014t0002 | a0001 | c0014 | t0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| a0001c0015t0002 | a0001 | c0015 | t0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| a0002c0005t0002 | a0002 | c0005 | t0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| a0003c0004t0007 | a0003 | c0004 | t0007 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| a0003c0004t0012 | a0003 | c0004 | t0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| a0004c0007t0001 | a0004 | c0007 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| a0005c0010t0001 | a0005 | c0010 | t0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| a0006c0011t0003 | a0006 | c0011 | t0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| a0007c0009t0005 | a0007 | c0009 | t0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| a0008c0013t0001 | a0008 | c0013 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A | copy fasta |
| actghapid | ahapid | chapid | thapid | ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | a0001 | c0001 | t0001 | g0001 | 0/1 | 18 | 0 | 2 | 11 | 1 | 3 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0001g0005 | a0001 | c0001 | t0001 | g0005 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0001g0009 | a0001 | c0001 | t0001 | g0009 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0001g0013 | a0001 | c0001 | t0001 | g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0001g0014 | a0001 | c0001 | t0001 | g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0001g0015 | a0001 | c0001 | t0001 | g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0001g0021 | a0001 | c0001 | t0001 | g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0001g0026 | a0001 | c0001 | t0001 | g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0001g0027 | a0001 | c0001 | t0001 | g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0001g0028 | a0001 | c0001 | t0001 | g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0001g0037 | a0001 | c0001 | t0001 | g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0001g0038 | a0001 | c0001 | t0001 | g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0001g0044 | a0001 | c0001 | t0001 | g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0001g0051 | a0001 | c0001 | t0001 | g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0001g0052 | a0001 | c0001 | t0001 | g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0001g0053 | a0001 | c0001 | t0001 | g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0001g0084 | a0001 | c0001 | t0001 | g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0001g0085 | a0001 | c0001 | t0001 | g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0001g0087 | a0001 | c0001 | t0001 | g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0001g0088 | a0001 | c0001 | t0001 | g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0001g0089 | a0001 | c0001 | t0001 | g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0001g0090 | a0001 | c0001 | t0001 | g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0001g0091 | a0001 | c0001 | t0001 | g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0001g0092 | a0001 | c0001 | t0001 | g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0001g0093 | a0001 | c0001 | t0001 | g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0001g0094 | a0001 | c0001 | t0001 | g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0001g0095 | a0001 | c0001 | t0001 | g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0001g0097 | a0001 | c0001 | t0001 | g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0001g0098 | a0001 | c0001 | t0001 | g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0001g0099 | a0001 | c0001 | t0001 | g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0001g0100 | a0001 | c0001 | t0001 | g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0001g0101 | a0001 | c0001 | t0001 | g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0001g0102 | a0001 | c0001 | t0001 | g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0001g0103 | a0001 | c0001 | t0001 | g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0001g0104 | a0001 | c0001 | t0001 | g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0001g0105 | a0001 | c0001 | t0001 | g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0001g0106 | a0001 | c0001 | t0001 | g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0001g0107 | a0001 | c0001 | t0001 | g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0001g0160 | a0001 | c0001 | t0001 | g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0001g0161 | a0001 | c0001 | t0001 | g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0001g0162 | a0001 | c0001 | t0001 | g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0001g0165 | a0001 | c0001 | t0001 | g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0001g0166 | a0001 | c0001 | t0001 | g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0001g0182 | a0001 | c0001 | t0001 | g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0001g0183 | a0001 | c0001 | t0001 | g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0001g0184 | a0001 | c0001 | t0001 | g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0001g0197 | a0001 | c0001 | t0001 | g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0002g0003 | a0001 | c0001 | t0002 | g0003 | 0/0 | 12 | 1 | 2 | 8 | 0 | 1 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0002g0004 | a0001 | c0001 | t0002 | g0004 | 0/0 | 9 | 0 | 1 | 7 | 0 | 1 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0002g0011 | a0001 | c0001 | t0002 | g0011 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0002g0029 | a0001 | c0001 | t0002 | g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0002g0030 | a0001 | c0001 | t0002 | g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0002g0031 | a0001 | c0001 | t0002 | g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0002g0032 | a0001 | c0001 | t0002 | g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0002g0039 | a0001 | c0001 | t0002 | g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0002g0109 | a0001 | c0001 | t0002 | g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0002g0110 | a0001 | c0001 | t0002 | g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0002g0111 | a0001 | c0001 | t0002 | g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0002g0112 | a0001 | c0001 | t0002 | g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0002g0113 | a0001 | c0001 | t0002 | g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0002g0114 | a0001 | c0001 | t0002 | g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0002g0115 | a0001 | c0001 | t0002 | g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0002g0116 | a0001 | c0001 | t0002 | g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0002g0117 | a0001 | c0001 | t0002 | g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0002g0118 | a0001 | c0001 | t0002 | g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0002g0120 | a0001 | c0001 | t0002 | g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0002g0121 | a0001 | c0001 | t0002 | g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0002g0123 | a0001 | c0001 | t0002 | g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0002g0124 | a0001 | c0001 | t0002 | g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0002g0125 | a0001 | c0001 | t0002 | g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0002g0126 | a0001 | c0001 | t0002 | g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0002g0127 | a0001 | c0001 | t0002 | g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0002g0128 | a0001 | c0001 | t0002 | g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0002g0129 | a0001 | c0001 | t0002 | g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0002g0131 | a0001 | c0001 | t0002 | g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0002g0132 | a0001 | c0001 | t0002 | g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0002g0133 | a0001 | c0001 | t0002 | g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0002g0134 | a0001 | c0001 | t0002 | g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0002g0135 | a0001 | c0001 | t0002 | g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0002g0136 | a0001 | c0001 | t0002 | g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0002g0138 | a0001 | c0001 | t0002 | g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0002g0139 | a0001 | c0001 | t0002 | g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0002g0140 | a0001 | c0001 | t0002 | g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0002g0141 | a0001 | c0001 | t0002 | g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0002g0142 | a0001 | c0001 | t0002 | g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0002g0144 | a0001 | c0001 | t0002 | g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0002g0145 | a0001 | c0001 | t0002 | g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0002g0167 | a0001 | c0001 | t0002 | g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0002g0168 | a0001 | c0001 | t0002 | g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0002g0169 | a0001 | c0001 | t0002 | g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0002g0192 | a0001 | c0001 | t0002 | g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0002g0193 | a0001 | c0001 | t0002 | g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0002g0194 | a0001 | c0001 | t0002 | g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0003g0002 | a0001 | c0001 | t0003 | g0002 | 0/0 | 13 | 1 | 3 | 8 | 0 | 1 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0003g0008 | a0001 | c0001 | t0003 | g0008 | 0/0 | 7 | 4 | 1 | 2 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0003g0010 | a0001 | c0001 | t0003 | g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0003g0022 | a0001 | c0001 | t0003 | g0022 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0003g0024 | a0001 | c0001 | t0003 | g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0003g0025 | a0001 | c0001 | t0003 | g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0003g0034 | a0001 | c0001 | t0003 | g0034 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0003g0035 | a0001 | c0001 | t0003 | g0035 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0003g0055 | a0001 | c0001 | t0003 | g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0003g0056 | a0001 | c0001 | t0003 | g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0003g0057 | a0001 | c0001 | t0003 | g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0003g0058 | a0001 | c0001 | t0003 | g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0003g0059 | a0001 | c0001 | t0003 | g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0003g0060 | a0001 | c0001 | t0003 | g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0003g0061 | a0001 | c0001 | t0003 | g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0003g0062 | a0001 | c0001 | t0003 | g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0003g0063 | a0001 | c0001 | t0003 | g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0003g0064 | a0001 | c0001 | t0003 | g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0003g0065 | a0001 | c0001 | t0003 | g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0003g0066 | a0001 | c0001 | t0003 | g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0003g0067 | a0001 | c0001 | t0003 | g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0003g0070 | a0001 | c0001 | t0003 | g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0003g0073 | a0001 | c0001 | t0003 | g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0003g0074 | a0001 | c0001 | t0003 | g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0003g0075 | a0001 | c0001 | t0003 | g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0003g0076 | a0001 | c0001 | t0003 | g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0003g0077 | a0001 | c0001 | t0003 | g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0003g0078 | a0001 | c0001 | t0003 | g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0003g0079 | a0001 | c0001 | t0003 | g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0003g0080 | a0001 | c0001 | t0003 | g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0003g0081 | a0001 | c0001 | t0003 | g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0003g0082 | a0001 | c0001 | t0003 | g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0003g0083 | a0001 | c0001 | t0003 | g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0003g0146 | a0001 | c0001 | t0003 | g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0003g0147 | a0001 | c0001 | t0003 | g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0003g0148 | a0001 | c0001 | t0003 | g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0003g0149 | a0001 | c0001 | t0003 | g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0003g0150 | a0001 | c0001 | t0003 | g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0003g0151 | a0001 | c0001 | t0003 | g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0003g0152 | a0001 | c0001 | t0003 | g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0003g0153 | a0001 | c0001 | t0003 | g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0003g0154 | a0001 | c0001 | t0003 | g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0003g0155 | a0001 | c0001 | t0003 | g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0003g0156 | a0001 | c0001 | t0003 | g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0003g0170 | a0001 | c0001 | t0003 | g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0004g0006 | a0001 | c0001 | t0004 | g0006 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0004g0007 | a0001 | c0001 | t0004 | g0007 | 0/0 | 8 | 0 | 1 | 4 | 2 | 1 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0004g0012 | a0001 | c0001 | t0004 | g0012 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0004g0016 | a0001 | c0001 | t0004 | g0016 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0004g0017 | a0001 | c0001 | t0004 | g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0004g0036 | a0001 | c0001 | t0004 | g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0004g0040 | a0001 | c0001 | t0004 | g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0004g0041 | a0001 | c0001 | t0004 | g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0004g0042 | a0001 | c0001 | t0004 | g0042 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0004g0043 | a0001 | c0001 | t0004 | g0043 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0004g0157 | a0001 | c0001 | t0004 | g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0004g0158 | a0001 | c0001 | t0004 | g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0004g0159 | a0001 | c0001 | t0004 | g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0004g0171 | a0001 | c0001 | t0004 | g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0004g0172 | a0001 | c0001 | t0004 | g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0004g0173 | a0001 | c0001 | t0004 | g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0004g0174 | a0001 | c0001 | t0004 | g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0004g0175 | a0001 | c0001 | t0004 | g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0004g0176 | a0001 | c0001 | t0004 | g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0004g0177 | a0001 | c0001 | t0004 | g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0004g0178 | a0001 | c0001 | t0004 | g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0004g0179 | a0001 | c0001 | t0004 | g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0004g0180 | a0001 | c0001 | t0004 | g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0004g0181 | a0001 | c0001 | t0004 | g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0004g0185 | a0001 | c0001 | t0004 | g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0004g0186 | a0001 | c0001 | t0004 | g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0006g0003 | a0001 | c0001 | t0006 | g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0006g0004 | a0001 | c0001 | t0006 | g0004 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0006g0030 | a0001 | c0001 | t0006 | g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0008g0096 | a0001 | c0001 | t0008 | g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0008g0108 | a0001 | c0001 | t0008 | g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0009g0018 | a0001 | c0001 | t0009 | g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0010g0187 | a0001 | c0001 | t0010 | g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0010g0188 | a0001 | c0001 | t0010 | g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0011g0189 | a0001 | c0001 | t0011 | g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0011g0191 | a0001 | c0001 | t0011 | g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0013g0119 | a0001 | c0001 | t0013 | g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0014g0018 | a0001 | c0001 | t0014 | g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0015g0196 | a0001 | c0001 | t0015 | g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0016g0003 | a0001 | c0001 | t0016 | g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0017g0004 | a0001 | c0001 | t0017 | g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0018g0190 | a0001 | c0001 | t0018 | g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0019g0005 | a0001 | c0001 | t0019 | g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0020g0001 | a0001 | c0001 | t0020 | g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0021g0036 | a0001 | c0001 | t0021 | g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0022g0122 | a0001 | c0001 | t0022 | g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0023g0025 | a0001 | c0001 | t0023 | g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0001t0024g0024 | a0001 | c0001 | t0024 | g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0002t0005g0020 | a0001 | c0002 | t0005 | g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0002t0005g0045 | a0001 | c0002 | t0005 | g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0002t0005g0046 | a0001 | c0002 | t0005 | g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0002t0005g0048 | a0001 | c0002 | t0005 | g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0002t0005g0049 | a0001 | c0002 | t0005 | g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0002t0005g0050 | a0001 | c0002 | t0005 | g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0003t0003g0023 | a0001 | c0003 | t0003 | g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0003t0003g0068 | a0001 | c0003 | t0003 | g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0003t0003g0069 | a0001 | c0003 | t0003 | g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0003t0003g0071 | a0001 | c0003 | t0003 | g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0003t0003g0072 | a0001 | c0003 | t0003 | g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0006t0001g0163 | a0001 | c0006 | t0001 | g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0006t0001g0164 | a0001 | c0006 | t0001 | g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0008t0001g0086 | a0001 | c0008 | t0001 | g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0012t0003g0002 | a0001 | c0012 | t0003 | g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0014t0002g0137 | a0001 | c0014 | t0002 | g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0001c0015t0002g0130 | a0001 | c0015 | t0002 | g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0002c0005t0002g0019 | a0002 | c0005 | t0002 | g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0003c0004t0007g0033 | a0003 | c0004 | t0007 | g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0003c0004t0007g0143 | a0003 | c0004 | t0007 | g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0003c0004t0012g0033 | a0003 | c0004 | t0012 | g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0004c0007t0001g0195 | a0004 | c0007 | t0001 | g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0005c0010t0001g0054 | a0005 | c0010 | t0001 | g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0006c0011t0003g0023 | a0006 | c0011 | t0003 | g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0007c0009t0005g0047 | a0007 | c0009 | t0005 | g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| a0008c0013t0001g0013 | a0008 | c0013 | t0001 | g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0004 | g0007 | EUR | GBR | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG00099 | hp2 | a0003 | c0004 | t0007 | g0033 | EUR | GBR | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0034 | EUR | GBR | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG00140 | hp2 | a0001 | c0001 | t0013 | g0119 | EUR | GBR | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG00280 | hp1 | a0001 | c0001 | t0014 | g0018 | EUR | FIN | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG00280 | hp2 | a0001 | c0001 | t0004 | g0016 | EUR | FIN | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0153 | EUR | FIN | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0100 | EUR | FIN | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | CHS | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | CHS | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG00438 | hp1 | a0001 | c0003 | t0003 | g0071 | EAS | CHS | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG00558 | hp1 | a0008 | c0013 | t0001 | g0013 | EAS | CHS | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG00558 | hp2 | a0001 | c0001 | t0008 | g0096 | EAS | CHS | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | CHS | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG00639 | hp2 | a0001 | c0001 | t0004 | g0158 | AMR | PUR | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG00673 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | CHS | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG00733 | hp1 | a0001 | c0001 | t0004 | g0016 | AMR | PUR | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0132 | AMR | PUR | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0109 | AMR | PUR | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0149 | AMR | PUR | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG01070 | hp1 | a0001 | c0002 | t0005 | g0020 | AMR | PUR | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG01070 | hp2 | a0001 | c0001 | t0004 | g0012 | AMR | PUR | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG01071 | hp1 | a0001 | c0002 | t0005 | g0020 | AMR | PUR | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG01071 | hp2 | a0001 | c0001 | t0004 | g0012 | AMR | PUR | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0133 | AMR | PUR | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0035 | AMR | PUR | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0126 | AMR | PUR | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG01081 | hp2 | a0001 | c0001 | t0004 | g0012 | AMR | PUR | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG01099 | hp1 | a0001 | c0001 | t0006 | g0003 | AMR | PUR | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0114 | AMR | PUR | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0156 | AMR | PUR | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG01106 | hp2 | a0001 | c0001 | t0004 | g0041 | AMR | PUR | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0178 | AMR | PUR | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0146 | AMR | PUR | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG01169 | hp1 | a0001 | c0001 | t0004 | g0016 | AMR | PUR | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG01175 | hp2 | a0001 | c0001 | t0004 | g0174 | AMR | PUR | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0062 | AMR | PUR | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0070 | AMR | CLM | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0154 | AMR | CLM | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG01261 | hp2 | a0001 | c0001 | t0006 | g0004 | AMR | CLM | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG01346 | hp1 | a0001 | c0001 | t0004 | g0007 | AMR | CLM | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0155 | AMR | CLM | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG01361 | hp1 | a0001 | c0001 | t0020 | g0001 | AMR | CLM | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG01361 | hp2 | a0001 | c0001 | t0004 | g0041 | AMR | CLM | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0034 | AMR | CLM | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0117 | AMR | CLM | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0169 | AMR | CLM | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG01516 | hp1 | a0003 | c0004 | t0007 | g0143 | EUR | IBS | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG01516 | hp2 | a0001 | c0001 | t0006 | g0004 | EUR | IBS | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0127 | EUR | IBS | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG01517 | hp2 | a0001 | c0001 | t0006 | g0030 | EUR | IBS | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0142 | AFR | ACB | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG01884 | hp2 | a0002 | c0005 | t0002 | g0019 | AFR | ACB | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0123 | AFR | ACB | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0148 | AFR | ACB | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0008 | AMR | PEL | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG01978 | hp1 | a0005 | c0010 | t0001 | g0054 | AMR | PEL | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02004 | hp1 | a0001 | c0003 | t0003 | g0069 | AMR | PEL | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | KHV | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | KHV | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | KHV | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0060 | AFR | ACB | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0194 | AFR | ACB | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02071 | hp2 | a0001 | c0001 | t0004 | g0017 | EAS | KHV | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | KHV | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | KHV | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0063 | EAS | KHV | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | KHV | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | KHV | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02129 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | KHV | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02135 | hp1 | a0001 | c0001 | t0004 | g0172 | EAS | KHV | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02145 | hp1 | a0001 | c0002 | t0005 | g0045 | AFR | ACB | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0152 | AFR | ACB | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | CDX | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02165 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | CDX | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0055 | AFR | ACB | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0036 | AFR | ACB | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02258 | hp1 | a0001 | c0001 | t0011 | g0191 | AFR | ACB | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0075 | AFR | ACB | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0043 | AFR | ACB | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02451 | hp2 | a0004 | c0007 | t0001 | g0195 | AFR | ACB | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | KHV | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0066 | AFR | GWD | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0067 | AFR | GWD | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0118 | SAS | PJL | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02602 | hp2 | a0006 | c0011 | t0003 | g0023 | SAS | PJL | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0073 | AFR | GWD | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02615 | hp2 | a0001 | c0006 | t0001 | g0164 | AFR | GWD | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0079 | AFR | GWD | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | GWD | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02630 | hp1 | a0001 | c0002 | t0005 | g0050 | AFR | GWD | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02630 | hp2 | a0001 | c0001 | t0018 | g0190 | AFR | GWD | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0125 | AFR | GWD | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0059 | AFR | GWD | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0151 | SAS | PJL | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0193 | AFR | GWD | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0081 | AFR | GWD | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02723 | hp2 | a0001 | c0002 | t0005 | g0046 | AFR | GWD | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02809 | hp1 | a0001 | c0001 | t0021 | g0036 | AFR | GWD | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0074 | AFR | GWD | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0008 | AFR | GWD | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02818 | hp2 | a0001 | c0008 | t0001 | g0086 | AFR | GWD | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02886 | hp2 | a0001 | c0001 | t0024 | g0024 | AFR | GWD | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0077 | AFR | GWD | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0024 | AFR | GWD | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02896 | hp1 | a0001 | c0001 | t0010 | g0187 | AFR | GWD | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0040 | AFR | GWD | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | ESN | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02970 | hp1 | a0001 | c0001 | t0011 | g0189 | AFR | ESN | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02970 | hp2 | a0001 | c0001 | t0023 | g0025 | AFR | ESN | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02976 | hp1 | a0001 | c0002 | t0005 | g0048 | AFR | ESN | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | ESN | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG03017 | hp1 | a0001 | c0001 | t0004 | g0157 | SAS | PJL | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG03041 | hp1 | a0001 | c0001 | t0008 | g0108 | AFR | GWD | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0138 | AFR | GWD | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | MSL | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0080 | AFR | ESN | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG03139 | hp1 | a0001 | c0002 | t0005 | g0049 | AFR | ESN | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | ESN | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0147 | AFR | ESN | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG03209 | hp1 | a0001 | c0001 | t0015 | g0196 | AFR | MSL | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0040 | AFR | MSL | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0124 | AFR | MSL | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG03453 | hp1 | a0001 | c0006 | t0001 | g0163 | AFR | MSL | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | MSL | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG03490 | hp1 | a0001 | c0001 | t0004 | g0042 | SAS | PJL | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG03490 | hp2 | a0001 | c0001 | t0022 | g0122 | SAS | PJL | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0039 | SAS | PJL | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0042 | SAS | PJL | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0039 | SAS | PJL | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0010 | AFR | GWD | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0176 | AFR | GWD | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0025 | AFR | MSL | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0139 | AFR | MSL | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0111 | SAS | PJL | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG03710 | hp1 | a0001 | c0001 | t0004 | g0012 | SAS | PJL | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG03834 | hp1 | a0001 | c0001 | t0009 | g0018 | SAS | BEB | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0135 | SAS | BEB | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | BEB | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | BEB | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | BEB | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0121 | SAS | BEB | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0022 | SAS | STU | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | STU | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0035 | SAS | BEB | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | BEB | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | STU | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | STU | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0082 | SAS | STU | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0112 | SAS | STU | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0058 | SAS | STU | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | STU | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18612 | hp1 | a0001 | c0001 | t0004 | g0173 | EAS | CHB | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | CHB | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18747 | hp1 | a0001 | c0012 | t0003 | g0002 | EAS | CHB | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | CHB | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18939 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18943 | hp1 | a0001 | c0001 | t0004 | g0179 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18944 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18948 | hp1 | a0001 | c0001 | t0004 | g0180 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18952 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18961 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18963 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18967 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18967 | hp2 | a0001 | c0001 | t0004 | g0186 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18971 | hp2 | a0001 | c0003 | t0003 | g0068 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18973 | hp2 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18974 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18975 | hp1 | a0001 | c0001 | t0004 | g0017 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18975 | hp2 | a0001 | c0015 | t0002 | g0130 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18977 | hp1 | a0001 | c0001 | t0004 | g0181 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18978 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18979 | hp1 | a0001 | c0001 | t0004 | g0043 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18986 | hp2 | a0001 | c0014 | t0002 | g0137 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18988 | hp1 | a0001 | c0001 | t0017 | g0004 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18989 | hp1 | a0001 | c0001 | t0004 | g0171 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18989 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18991 | hp1 | a0001 | c0003 | t0003 | g0072 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18992 | hp2 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA19000 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA19002 | hp1 | a0001 | c0001 | t0004 | g0177 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA19006 | hp1 | a0001 | c0001 | t0004 | g0185 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA19012 | hp1 | a0001 | c0003 | t0003 | g0023 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0140 | AFR | LWK | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0078 | AFR | LWK | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0159 | AFR | LWK | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | LWK | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA19055 | hp1 | a0001 | c0001 | t0004 | g0017 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA19067 | hp1 | a0001 | c0001 | t0004 | g0175 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA19074 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA19075 | hp1 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA19078 | hp1 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA19083 | hp1 | a0001 | c0001 | t0016 | g0003 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA19085 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA19091 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA20129 | hp1 | a0002 | c0005 | t0002 | g0019 | AFR | ASW | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | ASW | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA20805 | hp1 | a0001 | c0001 | t0004 | g0007 | EUR | TSI | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA20905 | hp1 | a0001 | c0001 | t0009 | g0018 | SAS | GIH | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA20905 | hp2 | a0001 | c0001 | t0004 | g0007 | SAS | GIH | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG01123 | hp2 | a0001 | c0001 | t0019 | g0005 | AMR | CLM | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0008 | AFR | ACB | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02486 | hp1 | a0007 | c0009 | t0005 | g0047 | AFR | ACB | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0150 | AFR | ACB | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0061 | AFR | ACB | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0192 | AFR | ACB | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0168 | AFR | MSL | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG03471 | hp2 | a0001 | c0001 | t0010 | g0188 | AFR | MSL | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0008 | AFR | USA | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| HG06807 | hp2 | a0003 | c0004 | t0012 | g0033 | AFR | USA | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA20300 | hp1 | a0002 | c0005 | t0002 | g0019 | AFR | USA | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0076 | AFR | USA | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0001 | REF | REF | ARHGAP11A_chr15_32610504_32644941 | ARHGAP11A |
| chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:32616234
|
G | A | 1 | a0004 | 1 | HG02451.hp2 | missense_variant | MODERATE | c.23G>A | p.Arg8Lys | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/12 | 731/5876 | 23/3072 | 8/1023 | chr15 | 32616234 | ||
| chr15:32629642
|
A | G | 1 | a0002 | 3 | HG01884.hp2 NA20129.hp1 NA20300.hp1 |
missense_variant | MODERATE | c.985A>G | p.Thr329Ala | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 8/12 | 1693/5876 | 985/3072 | 329/1023 | chr15 | 32629642 | ||
| chr15:32636270
|
C | G | 1 | a0008 | 1 | HG00558.hp1 | missense_variant | MODERATE | c.1497C>G | p.Ile499Met | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 12/12 | 2205/5876 | 1497/3072 | 499/1023 | chr15 | 32636270 | ||
| chr15:32636434
|
T | C | 1 | a0007 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.1661T>C | p.Ile554Thr | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 12/12 | 2369/5876 | 1661/3072 | 554/1023 | chr15 | 32636434 | ||
| chr15:32636785
|
A | G | 1 | a0006 | 1 | HG02602.hp2 | missense_variant | MODERATE | c.2012A>G | p.Glu671Gly | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 12/12 | 2720/5876 | 2012/3072 | 671/1023 | chr15 | 32636785 | ||
| chr15:32637423
|
A | G | 1 | a0003 | 3 | HG00099.hp2 HG01516.hp1 HG06807.hp2 |
missense_variant | MODERATE | c.2650A>G | p.Ile884Val | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 12/12 | 3358/5876 | 2650/3072 | 884/1023 | chr15 | 32637423 | ||
| chr15:32637690
|
C | G | 1 | a0005 | 1 | HG01978.hp1 | missense_variant | MODERATE | c.2917C>G | p.Pro973Ala | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 12/12 | 3625/5876 | 2917/3072 | 973/1023 | chr15 | 32637690 |
| chr:pos | ref | alt | # # of chapid
|
chapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:32616334
|
A | G | 1 | a0001c0015 | 1 | NA18975.hp2 | synonymous_variant | LOW | c.123A>G | p.Glu41Glu | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/12 | 831/5876 | 123/3072 | 41/1023 | chr15 | 32616334 | ||
| chr15:32623501
|
C | A | 1 | a0001c0008 | 1 | HG02818.hp2 | synonymous_variant | LOW | c.210C>A | p.Val70Val | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 3/12 | 918/5876 | 210/3072 | 70/1023 | chr15 | 32623501 | ||
| chr15:32623537
|
C | T | 1 | a0001c0014 | 1 | NA18986.hp2 | synonymous_variant | LOW | c.246C>T | p.Thr82Thr | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 3/12 | 954/5876 | 246/3072 | 82/1023 | chr15 | 32623537 | ||
| chr15:32629755
|
G | A | 2 | a0001c0002a0007c0009 | 8 | HG01070.hp1 HG01071.hp1 HG02145.hp1 others(5): Show |
synonymous_variant | LOW | c.1098G>A | p.Pro366Pro | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 8/12 | 1806/5876 | 1098/3072 | 366/1023 | chr15 | 32629755 | ||
| chr15:32633073
|
G | A | 2 | a0001c0002a0007c0009 | 8 | HG01070.hp1 HG01071.hp1 HG02145.hp1 others(5): Show |
synonymous_variant | LOW | c.1200G>A | p.Arg400Arg | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 9/12 | 1908/5876 | 1200/3072 | 400/1023 | chr15 | 32633073 | ||
| chr15:32636700
|
C | T | 1 | a0001c0012 | 1 | NA18747.hp1 | synonymous_variant | LOW | c.1927C>T | p.Leu643Leu | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 12/12 | 2635/5876 | 1927/3072 | 643/1023 | chr15 | 32636700 | ||
| chr15:32637335
|
A | G | 1 | a0001c0006 | 2 | HG02615.hp2 HG03453.hp1 |
synonymous_variant | LOW | c.2562A>G | p.Gln854Gln | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 12/12 | 3270/5876 | 2562/3072 | 854/1023 | chr15 | 32637335 | ||
| chr15:32637482
|
G | A | 1 | a0001c0003 | 5 | HG00438.hp1 HG02004.hp1 NA18971.hp2 others(2): Show |
synonymous_variant | LOW | c.2709G>A | p.Gln903Gln | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 12/12 | 3417/5876 | 2709/3072 | 903/1023 | chr15 | 32637482 | ||
| chr15:32637707
|
C | T | 3 | a0001c0002a0002c0005a0007c0009 | 11 | HG01070.hp1 HG01071.hp1 HG01884.hp2 others(8): Show |
synonymous_variant | LOW | c.2934C>T | p.Asn978Asn | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 12/12 | 3642/5876 | 2934/3072 | 978/1023 | chr15 | 32637707 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:32615511
|
C | T | 6 | a0001c0001t0003a0001c0001t0023a0001c0001t0024others(3): Show | 78 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(75): Show |
5_prime_UTR_variant | MODIFIER | c.-701C>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/12 | 701 | chr15 | 32615511 | |||||
| chr15:32615523
|
T | C | 4 | a0001c0001t0008a0001c0001t0013a0003c0004t0007others(1): Show | 6 | HG00099.hp2 HG00140.hp2 HG00558.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-689T>C | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/12 | 689 | chr15 | 32615523 | |||||
| chr15:32615534
|
G | A | 3 | a0001c0001t0008a0003c0004t0007a0003c0004t0012 | 5 | HG00099.hp2 HG00558.hp2 HG01516.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-678G>A | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/12 | 678 | chr15 | 32615534 | |||||
| chr15:32615536
|
A | T | 3 | a0001c0001t0008a0003c0004t0007a0003c0004t0012 | 5 | HG00099.hp2 HG00558.hp2 HG01516.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-676A>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/12 | 676 | chr15 | 32615536 | |||||
| chr15:32615589
|
G | A | 2 | a0001c0001t0009a0001c0001t0014 | 3 | HG00280.hp1 HG03834.hp1 NA20905.hp1 |
5_prime_UTR_variant | MODIFIER | c.-623G>A | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/12 | 623 | chr15 | 32615589 | |||||
| chr15:32615614
|
G | A | 1 | a0001c0001t0015 | 1 | HG03209.hp1 | 5_prime_UTR_variant | MODIFIER | c.-598G>A | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/12 | 598 | chr15 | 32615614 | |||||
| chr15:32615636
|
G | A | 1 | a0001c0001t0016 | 1 | NA19083.hp1 | 5_prime_UTR_variant | MODIFIER | c.-576G>A | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/12 | 576 | chr15 | 32615636 | |||||
| chr15:32615816
|
C | T | 1 | a0001c0001t0022 | 1 | HG03490.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-396C>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/12 | chr15 | 32615816 | ||||||
| chr15:32616100
|
G | A | 2 | a0003c0004t0007a0003c0004t0012 | 3 | HG00099.hp2 HG01516.hp1 HG06807.hp2 |
5_prime_UTR_variant | MODIFIER | c.-112G>A | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/12 | 112 | chr15 | 32616100 | |||||
| chr15:32616159
|
G | A | 1 | a0001c0001t0017 | 1 | NA18988.hp1 | 5_prime_UTR_variant | MODIFIER | c.-53G>A | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/12 | 53 | chr15 | 32616159 | |||||
| chr15:32637873
|
G | A | 3 | a0001c0001t0010a0001c0001t0011a0001c0001t0018 | 5 | HG02258.hp1 HG02630.hp2 HG02896.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*28G>A | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 12/12 | 28 | chr15 | 32637873 | |||||
| chr15:32637963
|
A | G | 1 | a0001c0001t0011 | 2 | HG02258.hp1 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*118A>G | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 12/12 | 118 | chr15 | 32637963 | |||||
| chr15:32638150
|
T | C | 1 | a0001c0001t0006 | 4 | HG01099.hp1 HG01261.hp2 HG01516.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*305T>C | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 12/12 | 305 | chr15 | 32638150 | |||||
| chr15:32638304
|
G | C | 25 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(22): Show | 247 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(244): Show |
3_prime_UTR_variant | MODIFIER | c.*459G>C | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 12/12 | 459 | chr15 | 32638304 | |||||
| chr15:32638312
|
C | T | 1 | a0001c0001t0021 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*467C>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 12/12 | 467 | chr15 | 32638312 | |||||
| chr15:32638313
|
C | T | 1 | a0001c0001t0020 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*468C>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 12/12 | 468 | chr15 | 32638313 | |||||
| chr15:32638317
|
C | T | 1 | a0001c0001t0011 | 2 | HG02258.hp1 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*472C>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 12/12 | 472 | chr15 | 32638317 | |||||
| chr15:32638362
|
C | T | 2 | a0001c0002t0005a0007c0009t0005 | 8 | HG01070.hp1 HG01071.hp1 HG02145.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*517C>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 12/12 | 517 | chr15 | 32638362 | |||||
| chr15:32638495
|
G | T | 1 | a0003c0004t0007 | 2 | HG00099.hp2 HG01516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*650G>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 12/12 | 650 | chr15 | 32638495 | |||||
| chr15:32639090
|
G | T | 1 | a0001c0001t0018 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1245G>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 12/12 | 1245 | chr15 | 32639090 | |||||
| chr15:32639518
|
G | A | 1 | a0001c0001t0023 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1673G>A | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 12/12 | 1673 | chr15 | 32639518 | |||||
| chr15:32639703
|
T | A | 25 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(22): Show | 247 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(244): Show |
3_prime_UTR_variant | MODIFIER | c.*1858T>A | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 12/12 | 1858 | chr15 | 32639703 | |||||
| chr15:32639720
|
G | A | 2 | a0001c0001t0004a0001c0001t0021 | 53 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*1875G>A | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 12/12 | 1875 | chr15 | 32639720 | |||||
| chr15:32639785
|
T | A | 1 | a0001c0001t0019 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1940T>A | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 12/12 | 1940 | chr15 | 32639785 | |||||
| chr15:32639879
|
C | T | 1 | a0001c0001t0014 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2034C>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 12/12 | 2034 | chr15 | 32639879 | |||||
| chr15:32639897
|
G | C | 22 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(19): Show | 238 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(235): Show |
3_prime_UTR_variant | MODIFIER | c.*2052G>C | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 12/12 | 2052 | chr15 | 32639897 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:32616476
|
C | T | 1 | a0002c0005t0002g0019 | 3 | HG01884.hp2 NA20129.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.129+136C>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | chr15 | 32616476 | ||||||
| chr15:32616516
|
C | T | 1 | a0001c0001t0001g0197 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.129+176C>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | chr15 | 32616516 | ||||||
| chr15:32616570
|
A | T | 1 | a0001c0001t0015g0196 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.129+230A>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | chr15 | 32616570 | ||||||
| chr15:32616639
|
T | A | 7 | a0001c0002t0005g0020a0001c0002t0005g0045a0001c0002t0005g0046others(4): Show | 8 | HG01070.hp1 HG01071.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.129+299T>A | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | chr15 | 32616639 | ||||||
| chr15:32616798
|
A | G | 1 | a0004c0007t0001g0195 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.129+458A>G | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | chr15 | 32616798 | ||||||
| chr15:32616837
|
C | T | 3 | a0001c0001t0002g0192a0001c0001t0002g0193a0001c0001t0002g0194 | 3 | HG02055.hp2 HG02559.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.129+497C>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | chr15 | 32616837 | ||||||
| chr15:32617014
|
T | A | 1 | a0001c0001t0001g0051 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.129+674T>A | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | chr15 | 32617014 | ||||||
| chr15:32617244
|
C | A | 1 | a0001c0002t0005g0045 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.129+904C>A | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | chr15 | 32617244 | ||||||
| chr15:32617306
|
G | T | 5 | a0001c0001t0010g0187a0001c0001t0010g0188a0001c0001t0011g0189others(2): Show | 5 | HG02258.hp1 HG02630.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.129+966G>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | chr15 | 32617306 | ||||||
| chr15:32617319
|
T | C | 4 | a0001c0001t0001g0021a0001c0001t0001g0052a0001c0001t0001g0053others(1): Show | 5 | HG01255.hp2 HG01258.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.129+979T>C | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | chr15 | 32617319 | ||||||
| chr15:32617340
|
C | T | 1 | a0002c0005t0002g0019 | 3 | HG01884.hp2 NA20129.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.129+1000C>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | chr15 | 32617340 | ||||||
| chr15:32617350
|
G | GCTACAGT others(326): Show |
2 | a0001c0002t0005g0020a0001c0002t0005g0046 | 3 | HG01070.hp1 HG01071.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.129+1026_129+1027i others(335): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 32617350 | |||||
| chr15:32617350
|
G | GCTACAGT others(327): Show |
2 | a0001c0002t0005g0048a0007c0009t0005g0047 | 2 | HG02486.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.129+1026_129+1027i others(336): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 32617350 | |||||
| chr15:32617350
|
G | GCTACAGT others(328): Show |
2 | a0001c0002t0005g0045a0001c0002t0005g0049 | 2 | HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.129+1026_129+1027i others(337): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 32617350 | |||||
| chr15:32617350
|
G | GCTACAGT others(329): Show |
1 | a0001c0002t0005g0050 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.129+1026_129+1027i others(338): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 32617350 | |||||
| chr15:32617471
|
C | CT | 36 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0160others(33): Show | 46 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.129+1149dupT | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 32617471 | |||||
| chr15:32617471
|
C | CTT | 29 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0044others(26): Show | 59 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.129+1148_129+1149d others(4): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 32617471 | |||||
| chr15:32617471
|
C | CTTT | 9 | a0001c0001t0004g0185a0001c0001t0004g0186a0001c0002t0005g0020others(6): Show | 10 | HG01070.hp1 HG01071.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.129+1147_129+1149d others(5): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 32617471 | |||||
| chr15:32617496
|
G | A | 1 | a0001c0001t0003g0055 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.129+1156G>A | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | chr15 | 32617496 | ||||||
| chr15:32617518
|
C | G | 1 | a0001c0001t0001g0015 | 3 | NA18943.hp2 NA18983.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.129+1178C>G | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | chr15 | 32617518 | ||||||
| chr15:32617540
|
T | C | 5 | a0001c0001t0010g0187a0001c0001t0010g0188a0001c0001t0011g0189others(2): Show | 5 | HG02258.hp1 HG02630.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.129+1200T>C | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | chr15 | 32617540 | ||||||
| chr15:32617557
|
T | C | 154 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(151): Show | 250 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.129+1217T>C | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | chr15 | 32617557 | ||||||
| chr15:32617560
|
C | T | 38 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0014others(35): Show | 72 | HG00323.hp2 HG00438.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.129+1220C>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | chr15 | 32617560 | ||||||
| chr15:32617904
|
A | G | 2 | a0001c0006t0001g0163a0001c0006t0001g0164 | 2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.129+1564A>G | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | chr15 | 32617904 | ||||||
| chr15:32617920
|
C | T | 1 | a0001c0001t0002g0145 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.129+1580C>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | chr15 | 32617920 | ||||||
| chr15:32617968
|
T | C | 1 | a0001c0001t0002g0193 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.129+1628T>C | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | chr15 | 32617968 | ||||||
| chr15:32617993
|
A | C | 1 | a0001c0001t0002g0144 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.129+1653A>C | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | chr15 | 32617993 | ||||||
| chr15:32618067
|
A | T | 1 | a0001c0001t0015g0196 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.129+1727A>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | chr15 | 32618067 | ||||||
| chr15:32618275
|
C | T | 5 | a0001c0001t0010g0187a0001c0001t0010g0188a0001c0001t0011g0189others(2): Show | 5 | HG02258.hp1 HG02630.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.130-1833C>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | chr15 | 32618275 | ||||||
| chr15:32618281
|
G | GA | 55 | a0001c0001t0001g0051a0001c0001t0003g0002a0001c0001t0003g0008others(52): Show | 79 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.130-1820dupA | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 32618281 | |||||
| chr15:32618313
|
G | A | 8 | a0001c0002t0005g0020a0001c0002t0005g0045a0001c0002t0005g0046others(5): Show | 11 | HG01070.hp1 HG01071.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.130-1795G>A | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | chr15 | 32618313 | ||||||
| chr15:32618397
|
C | T | 3 | a0001c0001t0001g0028a0001c0001t0001g0038a0001c0001t0001g0166 | 5 | NA18963.hp1 NA18969.hp2 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.130-1711C>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | chr15 | 32618397 | ||||||
| chr15:32618429
|
T | A | 27 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0012others(24): Show | 53 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.130-1679T>A | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | chr15 | 32618429 | ||||||
| chr15:32618436
|
G | A | 1 | a0001c0001t0002g0145 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.130-1672G>A | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | chr15 | 32618436 | ||||||
| chr15:32618643
|
G | A | 8 | a0001c0002t0005g0020a0001c0002t0005g0045a0001c0002t0005g0046others(5): Show | 11 | HG01070.hp1 HG01071.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.130-1465G>A | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | chr15 | 32618643 | ||||||
| chr15:32618663
|
C | A | 2 | a0001c0001t0002g0011a0001c0001t0002g0109 | 5 | HG00735.hp2 HG01169.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.130-1445C>A | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | chr15 | 32618663 | ||||||
| chr15:32618674
|
G | T | 1 | a0001c0001t0008g0108 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.130-1434G>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | chr15 | 32618674 | ||||||
| chr15:32618718
|
G | A | 8 | a0001c0002t0005g0020a0001c0002t0005g0045a0001c0002t0005g0046others(5): Show | 11 | HG01070.hp1 HG01071.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.130-1390G>A | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | chr15 | 32618718 | ||||||
| chr15:32618758
|
A | AC | 30 | a0001c0001t0002g0003a0001c0001t0002g0029a0001c0001t0002g0110others(27): Show | 42 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(39): Show |
intron_variant | MODIFIER | c.130-1337dupC | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 32618758 | |||||
| chr15:32618758
|
AC | A | 15 | a0001c0001t0001g0051a0001c0001t0001g0084a0001c0001t0001g0085others(12): Show | 16 | HG00099.hp2 HG01106.hp2 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.130-1337delC | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 32618758 | |||||
| chr15:32618758
|
ACC | A | 32 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0090others(29): Show | 57 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.130-1338_130-1337d others(4): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 32618758 | |||||
| chr15:32618758
|
ACCC | A | 110 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(107): Show | 180 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.130-1339_130-1337d others(5): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 32618758 | |||||
| chr15:32618760
|
C | A | 1 | a0001c0001t0004g0171 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.130-1348C>A | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | chr15 | 32618760 | ||||||
| chr15:32618763
|
C | A | 1 | a0001c0001t0004g0040 | 2 | HG02896.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.130-1345C>A | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | chr15 | 32618763 | ||||||
| chr15:32618764
|
C | G | 2 | a0001c0001t0002g0011a0001c0001t0002g0109 | 5 | HG00735.hp2 HG01169.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.130-1344C>G | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | chr15 | 32618764 | ||||||
| chr15:32618771
|
C | T | 1 | a0001c0001t0003g0083 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.130-1337C>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | chr15 | 32618771 | ||||||
| chr15:32618825
|
G | A | 1 | a0001c0001t0003g0061 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.130-1283G>A | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | chr15 | 32618825 | ||||||
| chr15:32618863
|
A | T | 3 | a0001c0001t0002g0029a0001c0001t0002g0128a0001c0001t0002g0141 | 4 | HG00621.hp2 HG02165.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.130-1245A>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | chr15 | 32618863 | ||||||
| chr15:32618904
|
T | C | 55 | a0001c0001t0001g0051a0001c0001t0003g0002a0001c0001t0003g0008others(52): Show | 79 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.130-1204T>C | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | chr15 | 32618904 | ||||||
| chr15:32618907
|
C | T | 11 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0044others(8): Show | 20 | HG00280.hp1 HG00558.hp1 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.130-1201C>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | chr15 | 32618907 | ||||||
| chr15:32619085
|
T | C | 1 | a0001c0001t0004g0176 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.130-1023T>C | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | chr15 | 32619085 | ||||||
| chr15:32619155
|
C | T | 1 | a0001c0001t0003g0061 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.130-953C>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | chr15 | 32619155 | ||||||
| chr15:32619162
|
CAT | C | 7 | a0001c0002t0005g0020a0001c0002t0005g0045a0001c0002t0005g0046others(4): Show | 8 | HG01070.hp1 HG01071.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.130-944_130-943del others(2): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 32619162 | |||||
| chr15:32619263
|
A | G | 1 | a0002c0005t0002g0019 | 3 | HG01884.hp2 NA20129.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.130-845A>G | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | chr15 | 32619263 | ||||||
| chr15:32619326
|
A | G | 1 | a0001c0001t0003g0082 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.130-782A>G | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | chr15 | 32619326 | ||||||
| chr15:32619426
|
T | C | 1 | a0001c0001t0001g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.130-682T>C | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | chr15 | 32619426 | ||||||
| chr15:32619539
|
T | C | 154 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(151): Show | 250 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.130-569T>C | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | chr15 | 32619539 | ||||||
| chr15:32619603
|
ACTT | A | 28 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0012others(25): Show | 56 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.130-499_130-497del others(3): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 32619603 | |||||
| chr15:32619748
|
C | CCT | 96 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0014others(93): Show | 154 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.130-359_130-358dup others(2): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 32619748 | |||||
| chr15:32619768
|
A | G | 1 | a0001c0001t0001g0090 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.130-340A>G | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | chr15 | 32619768 | ||||||
| chr15:32619818
|
C | G | 27 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0012others(24): Show | 53 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.130-290C>G | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | chr15 | 32619818 | ||||||
| chr15:32619865
|
A | T | 1 | a0001c0001t0001g0107 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.130-243A>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | chr15 | 32619865 | ||||||
| chr15:32619962
|
A | C | 5 | a0001c0001t0010g0187a0001c0001t0010g0188a0001c0001t0011g0189others(2): Show | 5 | HG02258.hp1 HG02630.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.130-146A>C | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | chr15 | 32619962 | ||||||
| chr15:32620007
|
AT | A | 14 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0022others(11): Show | 33 | HG00597.hp2 HG00741.hp1 HG01192.hp1 others(30): Show |
intron_variant | MODIFIER | c.130-92delT | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 32620007 | |||||
| chr15:32620280
|
C | G | 1 | a0001c0001t0002g0145 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.200+102C>G | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 2/11 | chr15 | 32620280 | ||||||
| chr15:32620310
|
C | A | 41 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0011others(38): Show | 68 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.200+132C>A | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 2/11 | chr15 | 32620310 | ||||||
| chr15:32620316
|
C | T | 1 | a0001c0001t0008g0108 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.200+138C>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 2/11 | chr15 | 32620316 | ||||||
| chr15:32620325
|
T | C | 1 | a0001c0001t0002g0110 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.200+147T>C | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 2/11 | chr15 | 32620325 | ||||||
| chr15:32620467
|
A | G | 4 | a0001c0001t0003g0035a0001c0001t0003g0154a0001c0001t0003g0155others(1): Show | 5 | HG01074.hp2 HG01106.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.200+289A>G | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 2/11 | chr15 | 32620467 | ||||||
| chr15:32620708
|
C | A | 1 | a0001c0008t0001g0086 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.200+530C>A | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 2/11 | chr15 | 32620708 | ||||||
| chr15:32620783
|
T | C | 1 | a0001c0001t0002g0128 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.200+605T>C | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 2/11 | chr15 | 32620783 | ||||||
| chr15:32620829
|
G | C | 27 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0012others(24): Show | 53 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.200+651G>C | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 2/11 | chr15 | 32620829 | ||||||
| chr15:32621129
|
A | AATGTATT | 154 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(151): Show | 250 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.200+957_200+958ins others(7): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 32621129 | |||||
| chr15:32621174
|
C | G | 11 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0044others(8): Show | 20 | HG00280.hp1 HG00558.hp1 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.200+996C>G | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 2/11 | chr15 | 32621174 | ||||||
| chr15:32621183
|
CT | C | 78 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0014others(75): Show | 138 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.200+1028delT | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 32621183 | |||||
| chr15:32621183
|
CTT | C | 53 | a0001c0001t0001g0087a0001c0001t0001g0092a0001c0001t0003g0002others(50): Show | 77 | HG00140.hp1 HG00438.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.200+1027_200+1028d others(4): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 32621183 | |||||
| chr15:32621221
|
A | G | 1 | a0001c0001t0010g0187 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.200+1043A>G | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 2/11 | chr15 | 32621221 | ||||||
| chr15:32621230
|
G | A | 5 | a0001c0001t0004g0006a0001c0001t0004g0171a0001c0001t0004g0172others(2): Show | 13 | HG00673.hp1 HG02129.hp2 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.200+1052G>A | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 2/11 | chr15 | 32621230 | ||||||
| chr15:32621305
|
C | T | 1 | a0001c0001t0003g0170 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.200+1127C>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 2/11 | chr15 | 32621305 | ||||||
| chr15:32621315
|
G | C | 2 | a0001c0001t0003g0067a0004c0007t0001g0195 | 2 | HG02451.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.200+1137G>C | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 2/11 | chr15 | 32621315 | ||||||
| chr15:32621554
|
C | G | 1 | a0001c0001t0001g0051 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.200+1376C>G | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 2/11 | chr15 | 32621554 | ||||||
| chr15:32621816
|
C | T | 3 | a0001c0001t0001g0087a0001c0001t0015g0196a0001c0008t0001g0086 | 3 | HG02818.hp2 HG03139.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.200+1638C>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 2/11 | chr15 | 32621816 | ||||||
| chr15:32621821
|
C | CA | 17 | a0001c0001t0001g0051a0001c0001t0001g0084a0001c0001t0001g0085others(14): Show | 19 | HG00408.hp2 HG00621.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.201-1653dupA | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 32621821 | |||||
| chr15:32621821
|
CAAAAA | C | 54 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0010others(51): Show | 78 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.200+1657_201-1653d others(7): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 32621821 | |||||
| chr15:32621821
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0027 | 2 | HG03195.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.200+1651_201-1653d others(13): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | 32621821 | |||||
| chr15:32621871
|
A | G | 1 | a0002c0005t0002g0019 | 3 | HG01884.hp2 NA20129.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.201-1621A>G | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 2/11 | chr15 | 32621871 | ||||||
| chr15:32621958
|
T | C | 1 | a0001c0001t0004g0042 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.201-1534T>C | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 2/11 | chr15 | 32621958 | ||||||
| chr15:32621987
|
C | T | 1 | a0005c0010t0001g0054 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.201-1505C>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 2/11 | chr15 | 32621987 | ||||||
| chr15:32622022
|
T | A | 2 | a0001c0001t0001g0084a0001c0001t0001g0085 | 2 | HG03704.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.201-1470T>A | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 2/11 | chr15 | 32622022 | ||||||
| chr15:32622064
|
A | G | 1 | a0001c0014t0002g0137 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.201-1428A>G | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 2/11 | chr15 | 32622064 | ||||||
| chr15:32622466
|
A | G | 1 | a0001c0001t0003g0080 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.201-1026A>G | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 2/11 | chr15 | 32622466 | ||||||
| chr15:32622544
|
T | G | 1 | a0001c0006t0001g0163 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.201-948T>G | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 2/11 | chr15 | 32622544 | ||||||
| chr15:32622612
|
G | T | 7 | a0001c0002t0005g0020a0001c0002t0005g0045a0001c0002t0005g0046others(4): Show | 8 | HG01070.hp1 HG01071.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.201-880G>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 2/11 | chr15 | 32622612 | ||||||
| chr15:32622647
|
C | T | 119 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(116): Show | 186 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.201-845C>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 2/11 | chr15 | 32622647 | ||||||
| chr15:32622679
|
C | G | 1 | a0001c0001t0001g0044 | 2 | HG00735.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.201-813C>G | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 2/11 | chr15 | 32622679 | ||||||
| chr15:32623068
|
A | C | 2 | a0001c0001t0011g0189a0001c0001t0011g0191 | 2 | HG02258.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.201-424A>C | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 2/11 | chr15 | 32623068 | ||||||
| chr15:32623145
|
G | C | 5 | a0001c0001t0010g0187a0001c0001t0010g0188a0001c0001t0011g0189others(2): Show | 5 | HG02258.hp1 HG02630.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.201-347G>C | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 2/11 | chr15 | 32623145 | ||||||
| chr15:32623294
|
G | T | 1 | a0002c0005t0002g0019 | 3 | HG01884.hp2 NA20129.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.201-198G>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 2/11 | chr15 | 32623294 | ||||||
| chr15:32623321
|
A | G | 1 | a0001c0001t0003g0079 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.201-171A>G | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 2/11 | chr15 | 32623321 | ||||||
| chr15:32623353
|
C | T | 1 | a0002c0005t0002g0019 | 3 | HG01884.hp2 NA20129.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.201-139C>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 2/11 | chr15 | 32623353 | ||||||
| chr15:32623595
|
A | G | 3 | a0003c0004t0007g0033a0003c0004t0007g0143a0003c0004t0012g0033 | 3 | HG00099.hp2 HG01516.hp1 HG06807.hp2 |
splice_region_variant&intron_variant | LOW | c.297+7A>G | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 3/11 | chr15 | 32623595 | ||||||
| chr15:32623744
|
G | A | 96 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0014others(93): Show | 154 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.297+156G>A | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 3/11 | chr15 | 32623744 | ||||||
| chr15:32623880
|
G | T | 2 | a0001c0001t0001g0084a0001c0001t0001g0085 | 2 | HG03704.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.297+292G>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 3/11 | chr15 | 32623880 | ||||||
| chr15:32623965
|
C | G | 8 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0149others(5): Show | 10 | HG00140.hp1 HG00738.hp1 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.298-208C>G | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 3/11 | chr15 | 32623965 | ||||||
| chr15:32624078
|
TAAAGA | T | 1 | a0002c0005t0002g0019 | 3 | HG01884.hp2 NA20129.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.298-90_298-86delAA others(3): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 32624078 | |||||
| chr15:32624618
|
T | G | 8 | a0001c0002t0005g0020a0001c0002t0005g0045a0001c0002t0005g0046others(5): Show | 11 | HG01070.hp1 HG01071.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.551+192T>G | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 4/11 | chr15 | 32624618 | ||||||
| chr15:32624776
|
G | A | 1 | a0001c0001t0001g0093 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.552-304G>A | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 4/11 | chr15 | 32624776 | ||||||
| chr15:32624838
|
G | T | 5 | a0001c0001t0001g0021a0001c0001t0001g0052a0001c0001t0001g0053others(2): Show | 6 | HG01255.hp2 HG01258.hp1 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.552-242G>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 4/11 | chr15 | 32624838 | ||||||
| chr15:32624853
|
G | A | 1 | a0001c0003t0003g0068 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.552-227G>A | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 4/11 | chr15 | 32624853 | ||||||
| chr15:32624890
|
T | C | 41 | a0001c0001t0003g0002a0001c0001t0003g0008a0001c0001t0003g0022others(38): Show | 62 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.552-190T>C | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 4/11 | chr15 | 32624890 | ||||||
| chr15:32625015
|
C | T | 2 | a0001c0001t0010g0187a0001c0001t0018g0190 | 2 | HG02630.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.552-65C>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 4/11 | chr15 | 32625015 | ||||||
| chr15:32625294
|
C | G | 1 | a0001c0001t0022g0122 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.715+51C>G | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 5/11 | chr15 | 32625294 | ||||||
| chr15:32625365
|
A | G | 14 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0044others(11): Show | 23 | HG00280.hp1 HG00558.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.715+122A>G | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 5/11 | chr15 | 32625365 | ||||||
| chr15:32625374
|
G | T | 2 | a0001c0001t0001g0014a0001c0001t0001g0104 | 4 | HG02965.hp1 HG03098.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.716-113G>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 5/11 | chr15 | 32625374 | ||||||
| chr15:32625760
|
C | T | 1 | a0001c0001t0004g0180 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.862+127C>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 6/11 | chr15 | 32625760 | ||||||
| chr15:32625785
|
A | G | 37 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0014others(34): Show | 71 | HG00323.hp2 HG00438.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.862+152A>G | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 6/11 | chr15 | 32625785 | ||||||
| chr15:32625822
|
C | T | 1 | a0001c0001t0003g0067 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.862+189C>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 6/11 | chr15 | 32625822 | ||||||
| chr15:32626081
|
G | A | 1 | a0001c0001t0004g0177 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.862+448G>A | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 6/11 | chr15 | 32626081 | ||||||
| chr15:32626090
|
T | G | 1 | a0001c0003t0003g0069 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.862+457T>G | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 6/11 | chr15 | 32626090 | ||||||
| chr15:32626251
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.862+618C>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 6/11 | chr15 | 32626251 | ||||||
| chr15:32626266
|
C | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(151): Show | 250 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.862+633C>G | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 6/11 | chr15 | 32626266 | ||||||
| chr15:32626343
|
G | A | 1 | a0001c0001t0015g0196 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.862+710G>A | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 6/11 | chr15 | 32626343 | ||||||
| chr15:32626422
|
C | T | 7 | a0001c0002t0005g0020a0001c0002t0005g0045a0001c0002t0005g0046others(4): Show | 8 | HG01070.hp1 HG01071.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.862+789C>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 6/11 | chr15 | 32626422 | ||||||
| chr15:32626685
|
C | T | 1 | a0001c0001t0001g0102 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.862+1052C>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 6/11 | chr15 | 32626685 | ||||||
| chr15:32626926
|
C | T | 18 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0044others(15): Show | 27 | HG00280.hp1 HG00558.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.862+1293C>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 6/11 | chr15 | 32626926 | ||||||
| chr15:32627028
|
A | G | 7 | a0001c0002t0005g0020a0001c0002t0005g0045a0001c0002t0005g0046others(4): Show | 8 | HG01070.hp1 HG01071.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.862+1395A>G | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 6/11 | chr15 | 32627028 | ||||||
| chr15:32627130
|
A | T | 1 | a0002c0005t0002g0019 | 3 | HG01884.hp2 NA20129.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.862+1497A>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 6/11 | chr15 | 32627130 | ||||||
| chr15:32627147
|
G | A | 4 | a0001c0001t0004g0017a0001c0001t0004g0173a0001c0001t0004g0177others(1): Show | 6 | HG02071.hp2 NA18612.hp1 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.862+1514G>A | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 6/11 | chr15 | 32627147 | ||||||
| chr15:32627264
|
A | C | 1 | a0002c0005t0002g0019 | 3 | HG01884.hp2 NA20129.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.863-1464A>C | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 6/11 | chr15 | 32627264 | ||||||
| chr15:32627327
|
T | TA | 3 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0002g0129 | 3 | HG03704.hp1 HG04199.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.863-1400dupA | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr15 | 32627327 | |||||
| chr15:32627387
|
C | T | 6 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0002g0129others(3): Show | 6 | HG02055.hp2 HG02257.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.863-1341C>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 6/11 | chr15 | 32627387 | ||||||
| chr15:32627388
|
A | G | 6 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0002g0129others(3): Show | 6 | HG02055.hp2 HG02257.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.863-1340A>G | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 6/11 | chr15 | 32627388 | ||||||
| chr15:32627389
|
T | G | 1 | a0001c0001t0004g0159 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.863-1339T>G | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 6/11 | chr15 | 32627389 | ||||||
| chr15:32627393
|
G | A | 54 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0002g0003others(51): Show | 81 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.863-1335G>A | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 6/11 | chr15 | 32627393 | ||||||
| chr15:32627411
|
G | A | 48 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0015others(45): Show | 82 | HG00323.hp2 HG00438.hp2 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.863-1317G>A | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 6/11 | chr15 | 32627411 | ||||||
| chr15:32627455
|
C | T | 5 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0002g0129others(2): Show | 5 | HG02055.hp2 HG02559.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.863-1273C>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 6/11 | chr15 | 32627455 | ||||||
| chr15:32627459
|
A | G | 2 | a0001c0001t0001g0101a0001c0001t0003g0074 | 2 | HG02809.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.863-1269A>G | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 6/11 | chr15 | 32627459 | ||||||
| chr15:32627465
|
C | T | 211 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(208): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.863-1263C>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 6/11 | chr15 | 32627465 | ||||||
| chr15:32627486
|
T | C | 3 | a0001c0001t0002g0129a0001c0001t0002g0192a0001c0001t0002g0194 | 3 | HG02055.hp2 HG02559.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.863-1242T>C | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 6/11 | chr15 | 32627486 | ||||||
| chr15:32627493
|
G | A | 3 | a0001c0001t0002g0129a0001c0001t0002g0192a0001c0001t0002g0194 | 3 | HG02055.hp2 HG02559.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.863-1235G>A | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 6/11 | chr15 | 32627493 | ||||||
| chr15:32627504
|
C | T | 1 | a0001c0001t0002g0144 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.863-1224C>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 6/11 | chr15 | 32627504 | ||||||
| chr15:32627530
|
C | A | 1 | a0007c0009t0005g0047 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.863-1198C>A | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 6/11 | chr15 | 32627530 | ||||||
| chr15:32627532
|
A | G | 2 | a0001c0001t0001g0084a0001c0001t0001g0085 | 2 | HG03704.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.863-1196A>G | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 6/11 | chr15 | 32627532 | ||||||
| chr15:32627536
|
T | C | 2 | a0001c0001t0002g0192a0001c0001t0002g0194 | 2 | HG02055.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.863-1192T>C | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 6/11 | chr15 | 32627536 | ||||||
| chr15:32627537
|
A | G | 50 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0044others(47): Show | 78 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.863-1191A>G | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 6/11 | chr15 | 32627537 | ||||||
| chr15:32627670
|
A | C | 3 | a0001c0001t0002g0126a0001c0001t0002g0169a0001c0008t0001g0086 | 3 | HG01081.hp1 HG01496.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.863-1058A>C | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 6/11 | chr15 | 32627670 | ||||||
| chr15:32627788
|
C | T | 1 | a0001c0001t0002g0125 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.863-940C>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 6/11 | chr15 | 32627788 | ||||||
| chr15:32627791
|
C | T | 1 | a0001c0001t0001g0099 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.863-937C>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 6/11 | chr15 | 32627791 | ||||||
| chr15:32627811
|
C | CT | 156 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0014others(153): Show | 269 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.863-901dupT | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr15 | 32627811 | |||||
| chr15:32627811
|
C | CTT | 7 | a0001c0001t0001g0098a0001c0001t0001g0166a0001c0001t0002g0121others(4): Show | 7 | HG00438.hp1 HG03834.hp2 HG03942.hp2 others(4): Show |
intron_variant | MODIFIER | c.863-902_863-901dup others(2): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr15 | 32627811 | |||||
| chr15:32627832
|
C | T | 41 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0011others(38): Show | 68 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.863-896C>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 6/11 | chr15 | 32627832 | ||||||
| chr15:32627863
|
G | A | 27 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0012others(24): Show | 53 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.863-865G>A | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 6/11 | chr15 | 32627863 | ||||||
| chr15:32627902
|
T | C | 1 | a0001c0001t0001g0094 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.863-826T>C | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 6/11 | chr15 | 32627902 | ||||||
| chr15:32627967
|
G | A | 18 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0044others(15): Show | 27 | HG00280.hp1 HG00558.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.863-761G>A | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 6/11 | chr15 | 32627967 | ||||||
| chr15:32628228
|
C | G | 2 | a0001c0001t0003g0063a0001c0001t0003g0083 | 2 | HG02083.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.863-500C>G | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 6/11 | chr15 | 32628228 | ||||||
| chr15:32628380
|
C | T | 1 | a0001c0001t0001g0183 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.863-348C>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 6/11 | chr15 | 32628380 | ||||||
| chr15:32628459
|
A | G | 1 | a0001c0008t0001g0086 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.863-269A>G | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 6/11 | chr15 | 32628459 | ||||||
| chr15:32628460
|
C | T | 1 | a0001c0001t0002g0120 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.863-268C>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 6/11 | chr15 | 32628460 | ||||||
| chr15:32628844
|
A | G | 2 | a0001c0001t0002g0120a0001c0001t0002g0134 | 2 | HG00408.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.937+42A>G | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 7/11 | chr15 | 32628844 | ||||||
| chr15:32628868
|
C | A | 1 | a0001c0001t0008g0108 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.937+66C>A | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 7/11 | chr15 | 32628868 | ||||||
| chr15:32629079
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.937+277C>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 7/11 | chr15 | 32629079 | ||||||
| chr15:32629151
|
T | C | 159 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(156): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.937+349T>C | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 7/11 | chr15 | 32629151 | ||||||
| chr15:32629318
|
T | C | 146 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(143): Show | 239 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.938-277T>C | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 7/11 | chr15 | 32629318 | ||||||
| chr15:32629410
|
A | G | 3 | a0001c0001t0002g0124a0001c0001t0002g0125a0001c0001t0002g0139 | 3 | HG02647.hp1 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.938-185A>G | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 7/11 | chr15 | 32629410 | ||||||
| chr15:32629550
|
A | G | 5 | a0001c0001t0010g0187a0001c0001t0010g0188a0001c0001t0011g0189others(2): Show | 5 | HG02258.hp1 HG02630.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.938-45A>G | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 7/11 | chr15 | 32629550 | ||||||
| chr15:32629921
|
A | G | 1 | a0001c0001t0002g0140 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1105+159A>G | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 8/11 | chr15 | 32629921 | ||||||
| chr15:32629929
|
C | G | 1 | a0001c0001t0015g0196 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1105+167C>G | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 8/11 | chr15 | 32629929 | ||||||
| chr15:32629941
|
A | AGAGTGTG others(7): Show |
1 | a0001c0001t0015g0196 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1105+180_1105+181i others(16): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 32629941 | |||||
| chr15:32629941
|
A | AGT | 17 | a0001c0001t0001g0014a0001c0001t0001g0104a0001c0001t0001g0165others(14): Show | 23 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.1105+212_1105+213d others(4): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 32629941 | |||||
| chr15:32629941
|
A | AGTGT | 32 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0027others(29): Show | 56 | HG00323.hp2 HG00558.hp2 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.1105+210_1105+213d others(6): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 32629941 | |||||
| chr15:32629941
|
A | AGTGTGT | 19 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0087others(16): Show | 29 | HG00438.hp2 HG00621.hp1 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.1105+208_1105+213d others(8): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 32629941 | |||||
| chr15:32629941
|
A | AGTGTGTG others(1): Show |
9 | a0001c0001t0003g0008a0001c0001t0003g0025a0001c0001t0003g0055others(6): Show | 15 | HG01255.hp1 HG01943.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1105+206_1105+213d others(10): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 32629941 | |||||
| chr15:32629941
|
A | AGTGTGTG others(3): Show |
17 | a0001c0001t0003g0002a0001c0001t0003g0010a0001c0001t0003g0057others(14): Show | 32 | HG00597.hp2 HG00741.hp1 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.1105+204_1105+213d others(12): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 32629941 | |||||
| chr15:32629941
|
A | AGTGTGTG others(5): Show |
18 | a0001c0001t0003g0022a0001c0001t0003g0056a0001c0001t0003g0058others(15): Show | 19 | HG00438.hp1 HG01258.hp2 HG02004.hp1 others(16): Show |
intron_variant | MODIFIER | c.1105+202_1105+213d others(14): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 32629941 | |||||
| chr15:32629941
|
A | AGTGTGTG others(7): Show |
3 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0153 | 5 | HG00140.hp1 HG00323.hp1 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1105+200_1105+213d others(16): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 32629941 | |||||
| chr15:32629941
|
A | AGTGTGTG others(9): Show |
3 | a0001c0001t0003g0061a0001c0001t0003g0146a0001c0001t0003g0149 | 3 | HG00738.hp1 HG01109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1105+198_1105+213d others(18): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 32629941 | |||||
| chr15:32629941
|
A | AGTGTGTG others(15): Show |
1 | a0001c0001t0001g0051 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1105+192_1105+213d others(24): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 32629941 | |||||
| chr15:32629941
|
AGT | A | 17 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0026others(14): Show | 26 | HG00140.hp2 HG00558.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.1105+212_1105+213d others(4): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 32629941 | |||||
| chr15:32629955
|
T | C | 1 | a0001c0001t0015g0196 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1105+193T>C | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 8/11 | chr15 | 32629955 | ||||||
| chr15:32629981
|
C | T | 2 | a0001c0001t0001g0084a0001c0001t0001g0085 | 2 | HG03704.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1105+219C>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 8/11 | chr15 | 32629981 | ||||||
| chr15:32630020
|
T | C | 7 | a0001c0002t0005g0020a0001c0002t0005g0045a0001c0002t0005g0046others(4): Show | 8 | HG01070.hp1 HG01071.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1105+258T>C | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 8/11 | chr15 | 32630020 | ||||||
| chr15:32630179
|
C | T | 84 | a0001c0001t0001g0051a0001c0001t0003g0002a0001c0001t0003g0008others(81): Show | 136 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.1105+417C>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 8/11 | chr15 | 32630179 | ||||||
| chr15:32630233
|
T | C | 34 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0015others(31): Show | 65 | HG00323.hp2 HG00438.hp2 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.1105+471T>C | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 8/11 | chr15 | 32630233 | ||||||
| chr15:32630326
|
A | G | 1 | a0001c0001t0001g0051 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1105+564A>G | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 8/11 | chr15 | 32630326 | ||||||
| chr15:32630366
|
A | G | 7 | a0001c0002t0005g0020a0001c0002t0005g0045a0001c0002t0005g0046others(4): Show | 8 | HG01070.hp1 HG01071.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1105+604A>G | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 8/11 | chr15 | 32630366 | ||||||
| chr15:32630440
|
A | T | 7 | a0001c0002t0005g0020a0001c0002t0005g0045a0001c0002t0005g0046others(4): Show | 8 | HG01070.hp1 HG01071.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1105+678A>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 8/11 | chr15 | 32630440 | ||||||
| chr15:32630483
|
A | G | 1 | a0001c0001t0001g0044 | 2 | HG00735.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.1105+721A>G | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 8/11 | chr15 | 32630483 | ||||||
| chr15:32630570
|
AT | A | 23 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0044others(20): Show | 32 | HG00280.hp1 HG00558.hp1 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.1105+814delT | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 32630570 | |||||
| chr15:32630622
|
A | G | 4 | a0001c0001t0001g0013a0001c0001t0001g0184a0001c0001t0001g0197others(1): Show | 6 | HG00558.hp1 NA18942.hp2 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.1105+860A>G | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 8/11 | chr15 | 32630622 | ||||||
| chr15:32630679
|
G | T | 1 | a0003c0004t0007g0143 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1105+917G>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 8/11 | chr15 | 32630679 | ||||||
| chr15:32630746
|
T | G | 141 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(138): Show | 234 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.1105+984T>G | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 8/11 | chr15 | 32630746 | ||||||
| chr15:32630880
|
G | T | 1 | a0001c0001t0010g0188 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1105+1118G>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 8/11 | chr15 | 32630880 | ||||||
| chr15:32630992
|
T | G | 1 | a0001c0001t0008g0108 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1105+1230T>G | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 8/11 | chr15 | 32630992 | ||||||
| chr15:32631083
|
T | A | 7 | a0001c0002t0005g0020a0001c0002t0005g0045a0001c0002t0005g0046others(4): Show | 8 | HG01070.hp1 HG01071.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1105+1321T>A | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 8/11 | chr15 | 32631083 | ||||||
| chr15:32631187
|
A | G | 1 | a0001c0001t0001g0097 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1105+1425A>G | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 8/11 | chr15 | 32631187 | ||||||
| chr15:32631298
|
C | CT | 7 | a0001c0002t0005g0020a0001c0002t0005g0045a0001c0002t0005g0046others(4): Show | 8 | HG01070.hp1 HG01071.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1105+1550dupT | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 32631298 | |||||
| chr15:32631298
|
CT | C | 141 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(138): Show | 234 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.1105+1550delT | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 32631298 | |||||
| chr15:32631398
|
C | T | 7 | a0001c0002t0005g0020a0001c0002t0005g0045a0001c0002t0005g0046others(4): Show | 8 | HG01070.hp1 HG01071.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1106-1581C>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 8/11 | chr15 | 32631398 | ||||||
| chr15:32631503
|
T | C | 1 | a0001c0001t0003g0077 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1106-1476T>C | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 8/11 | chr15 | 32631503 | ||||||
| chr15:32631531
|
A | G | 2 | a0001c0001t0002g0118a0001c0001t0002g0133 | 2 | HG01074.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.1106-1448A>G | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 8/11 | chr15 | 32631531 | ||||||
| chr15:32631533
|
T | C | 1 | a0001c0001t0002g0109 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1106-1446T>C | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 8/11 | chr15 | 32631533 | ||||||
| chr15:32631698
|
C | T | 5 | a0001c0001t0002g0118a0001c0001t0002g0132a0001c0001t0002g0133others(2): Show | 5 | HG00140.hp2 HG00733.hp2 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.1106-1281C>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 8/11 | chr15 | 32631698 | ||||||
| chr15:32631867
|
G | T | 5 | a0001c0001t0010g0187a0001c0001t0010g0188a0001c0001t0011g0189others(2): Show | 5 | HG02258.hp1 HG02630.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1106-1112G>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 8/11 | chr15 | 32631867 | ||||||
| chr15:32631953
|
A | G | 1 | a0001c0001t0003g0073 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1106-1026A>G | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 8/11 | chr15 | 32631953 | ||||||
| chr15:32631954
|
C | T | 7 | a0001c0002t0005g0020a0001c0002t0005g0045a0001c0002t0005g0046others(4): Show | 8 | HG01070.hp1 HG01071.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1106-1025C>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 8/11 | chr15 | 32631954 | ||||||
| chr15:32631996
|
A | G | 3 | a0003c0004t0007g0033a0003c0004t0007g0143a0003c0004t0012g0033 | 3 | HG00099.hp2 HG01516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1106-983A>G | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 8/11 | chr15 | 32631996 | ||||||
| chr15:32632033
|
T | G | 1 | a0001c0001t0001g0087 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1106-946T>G | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 8/11 | chr15 | 32632033 | ||||||
| chr15:32632038
|
G | A | 1 | a0001c0008t0001g0086 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1106-941G>A | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 8/11 | chr15 | 32632038 | ||||||
| chr15:32632206
|
T | A | 2 | a0001c0001t0010g0187a0001c0001t0018g0190 | 2 | HG02630.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1106-773T>A | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 8/11 | chr15 | 32632206 | ||||||
| chr15:32632290
|
GT | G | 41 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0014others(38): Show | 75 | HG00323.hp2 HG00438.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.1106-687delT | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 32632290 | |||||
| chr15:32632429
|
G | A | 5 | a0001c0001t0002g0115a0001c0001t0002g0120a0001c0001t0002g0131others(2): Show | 5 | HG00408.hp1 HG02027.hp2 HG02074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1106-550G>A | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 8/11 | chr15 | 32632429 | ||||||
| chr15:32632448
|
G | A | 27 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0012others(24): Show | 53 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.1106-531G>A | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 8/11 | chr15 | 32632448 | ||||||
| chr15:32632515
|
G | A | 2 | a0001c0003t0003g0069a0001c0003t0003g0071 | 2 | HG00438.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.1106-464G>A | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 8/11 | chr15 | 32632515 | ||||||
| chr15:32632537
|
A | G | 7 | a0001c0002t0005g0020a0001c0002t0005g0045a0001c0002t0005g0046others(4): Show | 8 | HG01070.hp1 HG01071.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1106-442A>G | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 8/11 | chr15 | 32632537 | ||||||
| chr15:32632599
|
T | C | 6 | a0001c0001t0010g0187a0001c0001t0010g0188a0001c0001t0011g0189others(3): Show | 8 | HG01884.hp2 HG02258.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1106-380T>C | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 8/11 | chr15 | 32632599 | ||||||
| chr15:32632720
|
CAG | C | 7 | a0001c0002t0005g0020a0001c0002t0005g0045a0001c0002t0005g0046others(4): Show | 8 | HG01070.hp1 HG01071.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1106-256_1106-255d others(4): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 32632720 | |||||
| chr15:32633113
|
T | G | 7 | a0001c0002t0005g0020a0001c0002t0005g0045a0001c0002t0005g0046others(4): Show | 8 | HG01070.hp1 HG01071.hp1 HG02145.hp1 others(5): Show |
splice_region_variant&intron_variant | LOW | c.1235+5T>G | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 9/11 | chr15 | 32633113 | ||||||
| chr15:32633247
|
A | G | 1 | a0001c0001t0008g0108 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1235+139A>G | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 9/11 | chr15 | 32633247 | ||||||
| chr15:32633406
|
T | C | 1 | a0001c0001t0010g0188 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1235+298T>C | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 9/11 | chr15 | 32633406 | ||||||
| chr15:32633414
|
G | T | 7 | a0001c0002t0005g0020a0001c0002t0005g0045a0001c0002t0005g0046others(4): Show | 8 | HG01070.hp1 HG01071.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1235+306G>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 9/11 | chr15 | 32633414 | ||||||
| chr15:32633591
|
A | C | 1 | a0001c0001t0004g0178 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1236-342A>C | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 9/11 | chr15 | 32633591 | ||||||
| chr15:32633591
|
A | T | 153 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(150): Show | 249 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.1236-342A>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 9/11 | chr15 | 32633591 | ||||||
| chr15:32633660
|
G | A | 27 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0012others(24): Show | 53 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.1236-273G>A | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 9/11 | chr15 | 32633660 | ||||||
| chr15:32633673
|
G | T | 27 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0012others(24): Show | 53 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.1236-260G>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 9/11 | chr15 | 32633673 | ||||||
| chr15:32633864
|
A | C | 18 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0044others(15): Show | 27 | HG00280.hp1 HG00558.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.1236-69A>C | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 9/11 | chr15 | 32633864 | ||||||
| chr15:32633875
|
C | T | 123 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0014others(120): Show | 207 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.1236-58C>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 9/11 | chr15 | 32633875 | ||||||
| chr15:32634171
|
T | C | 1 | a0001c0003t0003g0071 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1344+130T>C | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 10/11 | chr15 | 32634171 | ||||||
| chr15:32634275
|
CA | C | 7 | a0001c0002t0005g0020a0001c0002t0005g0045a0001c0002t0005g0046others(4): Show | 8 | HG01070.hp1 HG01071.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1344+235delA | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 10/11 | chr15 | 32634275 | ||||||
| chr15:32634342
|
T | C | 2 | a0001c0001t0001g0084a0001c0001t0001g0085 | 2 | HG03704.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1344+301T>C | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 10/11 | chr15 | 32634342 | ||||||
| chr15:32634594
|
T | C | 1 | a0001c0001t0001g0160 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1344+553T>C | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 10/11 | chr15 | 32634594 | ||||||
| chr15:32634701
|
A | C | 1 | a0002c0005t0002g0019 | 3 | HG01884.hp2 NA20129.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1344+660A>C | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 10/11 | chr15 | 32634701 | ||||||
| chr15:32634774
|
G | C | 2 | a0001c0001t0001g0095a0001c0001t0001g0100 | 2 | HG00323.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.1344+733G>C | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 10/11 | chr15 | 32634774 | ||||||
| chr15:32634794
|
A | G | 1 | a0001c0001t0010g0188 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1344+753A>G | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 10/11 | chr15 | 32634794 | ||||||
| chr15:32634822
|
A | G | 1 | a0001c0001t0008g0096 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1344+781A>G | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 10/11 | chr15 | 32634822 | ||||||
| chr15:32634870
|
C | T | 1 | a0001c0001t0004g0042 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1344+829C>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 10/11 | chr15 | 32634870 | ||||||
| chr15:32635115
|
A | C | 1 | a0001c0001t0002g0117 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1345-662A>C | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 10/11 | chr15 | 32635115 | ||||||
| chr15:32635147
|
T | A | 18 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0044others(15): Show | 27 | HG00280.hp1 HG00558.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.1345-630T>A | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 10/11 | chr15 | 32635147 | ||||||
| chr15:32635275
|
C | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(151): Show | 250 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.1345-502C>T | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 10/11 | chr15 | 32635275 | ||||||
| chr15:32635449
|
G | A | 1 | a0002c0005t0002g0019 | 3 | HG01884.hp2 NA20129.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1345-328G>A | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 10/11 | chr15 | 32635449 | ||||||
| chr15:32635487
|
A | G | 7 | a0001c0002t0005g0020a0001c0002t0005g0045a0001c0002t0005g0046others(4): Show | 8 | HG01070.hp1 HG01071.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1345-290A>G | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 10/11 | chr15 | 32635487 | ||||||
| chr15:32635544
|
T | G | 1 | a0001c0001t0002g0131 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1345-233T>G | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 10/11 | chr15 | 32635544 | ||||||
| chr15:32635570
|
C | A | 1 | a0001c0001t0002g0116 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1345-207C>A | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 10/11 | chr15 | 32635570 | ||||||
| chr15:32635621
|
G | A | 1 | a0001c0002t0005g0020 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1345-156G>A | ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 10/11 | chr15 | 32635621 |