Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 94134 |
|---|---|
| ensemblid | ENSG00000165322.18 |
| hgncid | 16348 |
| symbol | ARHGAP12 |
| name | Rho GTPase activating protein 12 |
| refseq_nuc | NM_018287.7 |
| refseq_prot | NP_060757.4 |
| ensembl_nuc | ENST00000344936.7 |
| ensembl_prot | ENSP00000345808.2 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 31805398 |
| end | 31928831 |
| strand | - |
| ver | v1.2 |
| region | chr10:31805398-31928831 |
| region5000 | chr10:31800398-31933831 |
| regionname0 | ARHGAP12_chr10_31805398_31928831 |
| regionname5000 | ARHGAP12_chr10_31800398_31933831 |
| 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 | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 846 | 238 | 83 | 45 | 76 | 7 | 25 | 62 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0002 | 0/0 | 846 | 79 | 3 | 13 | 53 | 1 | 9 | 43 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0003 | 0/0 | 846 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0004 | 0/0 | 846 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0005 | 0/0 | 846 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| 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 | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 2541 | 213 | 65 | 43 | 75 | 6 | 23 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| c0002 | 0/0 | 2541 | 79 | 3 | 13 | 53 | 1 | 9 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| c0003 | 0/0 | 2541 | 13 | 12 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| c0004 | 0/0 | 2541 | 3 | 2 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| c0005 | 0/0 | 2541 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| c0006 | 0/1 | 2541 | 2 | 0 | 0 | 0 | 1 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| c0007 | 0/0 | 2541 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| c0008 | 0/0 | 2541 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| c0009 | 0/0 | 2541 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| c0010 | 0/0 | 2541 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| c0011 | 0/0 | 2541 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| c0012 | 0/0 | 2541 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| c0013 | 0/0 | 2541 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| c0014 | 0/0 | 2541 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| thapid | grch38chm13v2 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 | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 2524 | 65 | 8 | 10 | 39 | 3 | 5 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| t0002 | 0/0 | 2518 | 51 | 1 | 10 | 35 | 1 | 4 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| t0003 | 0/0 | 2522 | 31 | 2 | 4 | 17 | 1 | 7 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| t0004 | 0/0 | 2516 | 18 | 4 | 7 | 0 | 1 | 6 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| t0005 | 0/0 | 2514 | 14 | 1 | 8 | 2 | 0 | 3 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| t0006 | 0/0 | 2526 | 13 | 8 | 4 | 0 | 1 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| t0007 | 0/0 | 2520 | 13 | 4 | 1 | 5 | 0 | 3 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| t0008 | 0/0 | 2522 | 12 | 3 | 4 | 4 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| t0009 | 0/0 | 2526 | 8 | 8 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| t0010 | 0/0 | 2535 | 8 | 7 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| t0011 | 0/0 | 2514 | 7 | 7 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| t0012 | 1/0 | 2520 | 6 | 1 | 2 | 1 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| t0013 | 0/0 | 2525 | 5 | 0 | 0 | 5 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| t0014 | 0/0 | 2516 | 5 | 0 | 1 | 4 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| t0015 | 0/0 | 2520 | 4 | 0 | 1 | 3 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| t0016 | 0/0 | 2533 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| t0017 | 0/0 | 2510 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| t0018 | 0/0 | 2528 | 3 | 2 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| t0019 | 0/0 | 2524 | 3 | 2 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| t0020 | 0/0 | 2522 | 3 | 0 | 2 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| t0021 | 0/0 | 2520 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| t0022 | 0/0 | 2524 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| t0023 | 0/0 | 2522 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| t0024 | 0/0 | 2526 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| t0025 | 0/0 | 2526 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| t0026 | 0/1 | 2516 | 2 | 0 | 0 | 0 | 1 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| t0027 | 0/0 | 2537 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| t0028 | 0/0 | 2522 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| t0029 | 0/0 | 2518 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| t0030 | 0/0 | 2520 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| t0031 | 0/0 | 2522 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| t0032 | 0/0 | 2528 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| t0033 | 0/0 | 2518 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| t0034 | 0/0 | 2526 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| t0035 | 0/0 | 2528 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| t0036 | 0/0 | 2522 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| t0037 | 0/0 | 2518 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| t0038 | 0/0 | 2518 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| t0039 | 0/0 | 2524 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| t0040 | 0/0 | 2536 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| t0041 | 0/0 | 2525 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| t0042 | 0/0 | 2534 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| t0043 | 0/0 | 2518 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| t0044 | 0/0 | 2524 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| t0045 | 0/0 | 2532 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| t0046 | 0/0 | 2522 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| t0047 | 0/0 | 2518 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| t0048 | 0/0 | 2521 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| t0049 | 0/0 | 2524 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| t0050 | 0/0 | 2530 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| t0051 | 0/0 | 2522 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| t0052 | 0/0 | 2522 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| t0053 | 0/0 | 2522 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| t0054 | 0/0 | 2518 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| t0055 | 0/0 | 2520 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| 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 | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0065 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0177 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| achapid | 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 | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2541 | 213 | 65 | 43 | 75 | 6 | 23 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0001c0003 | 0/0 | 2541 | 13 | 12 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0001c0005 | 0/0 | 2541 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0001c0006 | 0/1 | 2541 | 2 | 0 | 0 | 0 | 1 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0001c0007 | 0/0 | 2541 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0001c0008 | 0/0 | 2541 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0001c0010 | 0/0 | 2541 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0001c0011 | 0/0 | 2541 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0001c0013 | 0/0 | 2541 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0001c0014 | 0/0 | 2541 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0002c0002 | 0/0 | 2541 | 79 | 3 | 13 | 53 | 1 | 9 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0003c0004 | 0/0 | 2541 | 3 | 2 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0004c0012 | 0/0 | 2541 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0005c0009 | 0/0 | 2541 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5064 | 64 | 8 | 10 | 38 | 3 | 5 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0001c0001t0003 | 0/0 | 5062 | 30 | 2 | 4 | 16 | 1 | 7 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0001c0001t0004 | 0/0 | 5056 | 17 | 3 | 7 | 0 | 1 | 6 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0001c0001t0005 | 0/0 | 5054 | 12 | 1 | 8 | 2 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0001c0001t0006 | 0/0 | 5066 | 13 | 8 | 4 | 0 | 1 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0001c0001t0008 | 0/0 | 5062 | 12 | 3 | 4 | 4 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0001c0001t0009 | 0/0 | 5066 | 8 | 8 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0001c0001t0011 | 0/0 | 5054 | 7 | 7 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0001c0001t0012 | 1/0 | 5060 | 5 | 1 | 1 | 1 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0001c0001t0013 | 0/0 | 5065 | 5 | 0 | 0 | 5 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0001c0001t0015 | 0/0 | 5060 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0001c0001t0017 | 0/0 | 5050 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0001c0001t0018 | 0/0 | 5068 | 3 | 2 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0001c0001t0019 | 0/0 | 5064 | 3 | 2 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0001c0001t0022 | 0/0 | 5064 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0001c0001t0023 | 0/0 | 5062 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0001c0001t0024 | 0/0 | 5066 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0001c0001t0025 | 0/0 | 5066 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0001c0001t0031 | 0/0 | 5062 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0001c0001t0032 | 0/0 | 5068 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0001c0001t0033 | 0/0 | 5058 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0001c0001t0034 | 0/0 | 5066 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0001c0001t0035 | 0/0 | 5068 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0001c0001t0036 | 0/0 | 5062 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0001c0001t0037 | 0/0 | 5058 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0001c0001t0038 | 0/0 | 5058 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0001c0001t0039 | 0/0 | 5064 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0001c0001t0040 | 0/0 | 5076 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0001c0001t0041 | 0/0 | 5065 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0001c0001t0042 | 0/0 | 5074 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0001c0001t0043 | 0/0 | 5058 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0001c0001t0044 | 0/0 | 5064 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0001c0001t0045 | 0/0 | 5072 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0001c0001t0046 | 0/0 | 5062 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0001c0001t0049 | 0/0 | 5064 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0001c0001t0050 | 0/0 | 5070 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0001c0001t0051 | 0/0 | 5062 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0001c0001t0052 | 0/0 | 5062 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0001c0003t0010 | 0/0 | 5075 | 8 | 7 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0001c0003t0016 | 0/0 | 5073 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0001c0003t0027 | 0/0 | 5077 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0001c0003t0048 | 0/0 | 5061 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0001c0005t0016 | 0/0 | 5073 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0001c0006t0026 | 0/1 | 5056 | 2 | 0 | 0 | 0 | 1 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0001c0007t0028 | 0/0 | 5062 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0001c0008t0005 | 0/0 | 5054 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0001c0010t0053 | 0/0 | 5062 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0001c0011t0001 | 0/0 | 5064 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0001c0013t0015 | 0/0 | 5060 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0001c0014t0004 | 0/0 | 5056 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0002c0002t0002 | 0/0 | 5058 | 51 | 1 | 10 | 35 | 1 | 4 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0002c0002t0007 | 0/0 | 5060 | 10 | 2 | 0 | 5 | 0 | 3 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0002c0002t0014 | 0/0 | 5056 | 5 | 0 | 1 | 4 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0002c0002t0020 | 0/0 | 5062 | 3 | 0 | 2 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0002c0002t0021 | 0/0 | 5060 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0002c0002t0029 | 0/0 | 5058 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0002c0002t0030 | 0/0 | 5060 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0002c0002t0047 | 0/0 | 5058 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0002c0002t0054 | 0/0 | 5058 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0002c0002t0055 | 0/0 | 5060 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0003c0004t0007 | 0/0 | 5060 | 3 | 2 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0004c0012t0003 | 0/0 | 5062 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| a0005c0009t0012 | 0/0 | 5060 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | copy fasta | chr10 | 31800398 | 31933831 |
| actghapid | 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 | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0003g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0004g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0004g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0004g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0004g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0004g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0004g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0004g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0004g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0004g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0004g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0004g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0004g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0004g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0004g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0004g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0004g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0005g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0005g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0005g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0005g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0005g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0005g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0005g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0005g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0005g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0005g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0005g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0005g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0006g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0006g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0006g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0006g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0006g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0006g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0006g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0006g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0006g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0006g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0006g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0006g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0006g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0008g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0008g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0008g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0008g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0008g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0008g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0008g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0008g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0008g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0008g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0008g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0008g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0009g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0009g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0009g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0009g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0009g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0009g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0009g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0009g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0011g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0011g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0011g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0011g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0011g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0011g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0011g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0012g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0012g0177 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0012g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0012g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0012g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0013g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0013g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0013g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0013g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0013g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0015g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0015g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0015g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0017g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0017g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0017g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0018g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0018g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0018g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0019g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0019g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0019g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0022g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0022g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0023g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0023g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0024g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0024g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0025g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0025g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0031g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0032g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0033g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0034g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0035g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0036g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0037g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0038g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0039g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0040g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0041g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0042g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0043g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0044g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0045g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0046g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0049g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0050g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0051g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0052g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0003t0010g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0003t0010g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0003t0010g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0003t0010g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0003t0010g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0003t0010g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0003t0010g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0003t0010g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0003t0016g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0003t0016g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0003t0027g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0003t0027g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0003t0048g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0005t0016g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0005t0016g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0006t0026g0065 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0006t0026g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0007t0028g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0007t0028g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0008t0005g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0008t0005g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0010t0053g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0011t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0013t0015g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0014t0004g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0002g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0002g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0002g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0002g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0002g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0002g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0002g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0002g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0007g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0007g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0007g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0007g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0007g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0007g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0007g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0007g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0007g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0007g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0014g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0014g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0014g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0014g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0014g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0020g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0020g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0020g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0021g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0021g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0021g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0029g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0029g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0030g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0030g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0047g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0054g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0055g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0003c0004t0007g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0003c0004t0007g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0003c0004t0007g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0004c0012t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0005c0009t0012g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0204 | EUR | GBR | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG00099 | hp2 | a0001 | c0006 | t0026 | g0067 | EUR | GBR | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG00280 | hp1 | a0001 | c0001 | t0006 | g0159 | EUR | FIN | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0172 | EUR | FIN | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0181 | EAS | CHS | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG00597 | hp1 | a0002 | c0002 | t0002 | g0295 | EAS | CHS | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | CHS | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG00621 | hp1 | a0002 | c0002 | t0030 | g0294 | EAS | CHS | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0201 | AMR | PUR | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG00639 | hp2 | a0002 | c0002 | t0014 | g0300 | AMR | PUR | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG00673 | hp1 | a0002 | c0002 | t0002 | g0292 | EAS | CHS | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | CHS | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG00733 | hp2 | a0001 | c0001 | t0052 | g0318 | AMR | PUR | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG00735 | hp2 | a0001 | c0003 | t0010 | g0016 | AMR | PUR | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG00738 | hp2 | a0002 | c0002 | t0002 | g0267 | AMR | PUR | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG00741 | hp1 | a0001 | c0001 | t0006 | g0221 | AMR | PUR | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01071 | hp1 | a0001 | c0013 | t0015 | g0154 | AMR | PUR | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01071 | hp2 | a0002 | c0002 | t0002 | g0258 | AMR | PUR | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01081 | hp1 | a0002 | c0002 | t0002 | g0293 | AMR | PUR | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01081 | hp2 | a0001 | c0001 | t0004 | g0064 | AMR | PUR | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01099 | hp1 | a0002 | c0002 | t0002 | g0301 | AMR | PUR | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01106 | hp1 | a0001 | c0001 | t0006 | g0158 | AMR | PUR | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01106 | hp2 | a0002 | c0002 | t0002 | g0290 | AMR | PUR | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01109 | hp1 | a0001 | c0001 | t0005 | g0047 | AMR | PUR | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01109 | hp2 | a0003 | c0004 | t0007 | g0310 | AMR | PUR | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01167 | hp1 | a0001 | c0001 | t0019 | g0166 | AMR | PUR | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01167 | hp2 | a0001 | c0001 | t0004 | g0022 | AMR | PUR | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01168 | hp1 | a0001 | c0001 | t0005 | g0054 | AMR | PUR | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01168 | hp2 | a0001 | c0001 | t0004 | g0037 | AMR | PUR | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01175 | hp1 | a0001 | c0001 | t0004 | g0024 | AMR | PUR | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01192 | hp2 | a0001 | c0001 | t0005 | g0045 | AMR | PUR | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01257 | hp1 | a0002 | c0002 | t0020 | g0270 | AMR | CLM | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01257 | hp2 | a0001 | c0001 | t0005 | g0046 | AMR | CLM | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01258 | hp1 | a0001 | c0001 | t0006 | g0206 | AMR | CLM | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01258 | hp2 | a0001 | c0001 | t0005 | g0051 | AMR | CLM | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01346 | hp1 | a0001 | c0001 | t0008 | g0131 | AMR | CLM | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01346 | hp2 | a0001 | c0001 | t0004 | g0039 | AMR | CLM | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01358 | hp2 | a0002 | c0002 | t0002 | g0269 | AMR | CLM | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0178 | AMR | CLM | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0083 | EUR | IBS | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01515 | hp2 | a0002 | c0002 | t0002 | g0268 | EUR | IBS | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0099 | EUR | IBS | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01516 | hp2 | a0001 | c0001 | t0004 | g0038 | EUR | IBS | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01884 | hp1 | a0001 | c0001 | t0011 | g0071 | AFR | ACB | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | ACB | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01891 | hp2 | a0001 | c0001 | t0011 | g0057 | AFR | ACB | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01928 | hp1 | a0001 | c0001 | t0008 | g0139 | AMR | PEL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01928 | hp2 | a0002 | c0002 | t0002 | g0307 | AMR | PEL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01934 | hp1 | a0001 | c0001 | t0022 | g0002 | AMR | PEL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01934 | hp2 | a0001 | c0001 | t0005 | g0235 | AMR | PEL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01978 | hp1 | a0005 | c0009 | t0012 | g0179 | AMR | PEL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01978 | hp2 | a0001 | c0001 | t0004 | g0044 | AMR | PEL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01981 | hp1 | a0001 | c0001 | t0051 | g0237 | AMR | PEL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PEL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0176 | AMR | PEL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01993 | hp2 | a0001 | c0001 | t0004 | g0019 | AMR | PEL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02004 | hp1 | a0002 | c0002 | t0002 | g0304 | AMR | PEL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02004 | hp2 | a0001 | c0001 | t0005 | g0043 | AMR | PEL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02015 | hp1 | a0001 | c0011 | t0001 | g0112 | EAS | KHV | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02015 | hp2 | a0002 | c0002 | t0007 | g0254 | EAS | KHV | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02027 | hp1 | a0001 | c0001 | t0008 | g0136 | EAS | KHV | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02027 | hp2 | a0002 | c0002 | t0002 | g0299 | EAS | KHV | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02040 | hp1 | a0002 | c0002 | t0002 | g0298 | EAS | KHV | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02040 | hp2 | a0001 | c0001 | t0038 | g0205 | EAS | KHV | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02055 | hp1 | a0001 | c0001 | t0018 | g0087 | AFR | ACB | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02055 | hp2 | a0002 | c0002 | t0002 | g0253 | AFR | ACB | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02071 | hp1 | a0001 | c0001 | t0039 | g0089 | EAS | KHV | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02071 | hp2 | a0002 | c0002 | t0002 | g0282 | EAS | KHV | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0184 | EAS | KHV | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02074 | hp2 | a0002 | c0002 | t0007 | g0314 | EAS | KHV | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02135 | hp2 | a0001 | c0001 | t0031 | g0001 | EAS | KHV | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02145 | hp1 | a0001 | c0001 | t0009 | g0073 | AFR | ACB | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02145 | hp2 | a0001 | c0001 | t0050 | g0028 | AFR | ACB | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02148 | hp1 | a0001 | c0001 | t0012 | g0197 | AMR | PEL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02148 | hp2 | a0002 | c0002 | t0002 | g0303 | AMR | PEL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02155 | hp1 | a0002 | c0002 | t0002 | g0302 | EAS | CDX | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | CDX | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02257 | hp1 | a0001 | c0001 | t0009 | g0080 | AFR | ACB | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02257 | hp2 | a0001 | c0003 | t0010 | g0005 | AFR | ACB | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02258 | hp1 | a0001 | c0001 | t0025 | g0202 | AFR | ACB | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0036 | AFR | ACB | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02273 | hp1 | a0001 | c0001 | t0008 | g0095 | AMR | PEL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02273 | hp2 | a0001 | c0001 | t0022 | g0174 | AMR | PEL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02280 | hp1 | a0001 | c0001 | t0011 | g0056 | AFR | ACB | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02280 | hp2 | a0001 | c0001 | t0034 | g0033 | AFR | ACB | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02293 | hp1 | a0001 | c0001 | t0005 | g0048 | AMR | PEL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0194 | AMR | PEL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02300 | hp1 | a0002 | c0002 | t0002 | g0266 | AMR | PEL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02300 | hp2 | a0001 | c0001 | t0008 | g0222 | AMR | PEL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02451 | hp1 | a0001 | c0003 | t0010 | g0009 | AFR | ACB | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02451 | hp2 | a0001 | c0001 | t0006 | g0165 | AFR | ACB | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02572 | hp1 | a0001 | c0007 | t0028 | g0239 | AFR | GWD | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02572 | hp2 | a0001 | c0001 | t0023 | g0069 | AFR | GWD | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02602 | hp1 | a0001 | c0001 | t0004 | g0068 | SAS | PJL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02602 | hp2 | a0001 | c0008 | t0005 | g0074 | SAS | PJL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02615 | hp1 | a0001 | c0003 | t0010 | g0018 | AFR | GWD | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02615 | hp2 | a0001 | c0001 | t0037 | g0035 | AFR | GWD | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02622 | hp1 | a0001 | c0001 | t0009 | g0077 | AFR | GWD | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02622 | hp2 | a0001 | c0001 | t0036 | g0041 | AFR | GWD | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02630 | hp1 | a0001 | c0003 | t0010 | g0010 | AFR | GWD | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0070 | AFR | GWD | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02647 | hp1 | a0001 | c0001 | t0009 | g0072 | AFR | GWD | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02647 | hp2 | a0001 | c0001 | t0006 | g0216 | AFR | GWD | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02698 | hp2 | a0002 | c0002 | t0029 | g0244 | SAS | PJL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02717 | hp1 | a0001 | c0001 | t0011 | g0059 | AFR | GWD | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02717 | hp2 | a0001 | c0003 | t0010 | g0011 | AFR | GWD | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02723 | hp2 | a0001 | c0003 | t0048 | g0015 | AFR | GWD | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0171 | SAS | PJL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02735 | hp2 | a0001 | c0008 | t0005 | g0075 | SAS | PJL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0198 | SAS | PJL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02818 | hp1 | a0001 | c0003 | t0027 | g0014 | AFR | GWD | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02886 | hp2 | a0001 | c0010 | t0053 | g0238 | AFR | GWD | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02895 | hp1 | a0001 | c0005 | t0016 | g0008 | AFR | GWD | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02895 | hp2 | a0001 | c0001 | t0006 | g0167 | AFR | GWD | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02896 | hp1 | a0001 | c0001 | t0006 | g0160 | AFR | GWD | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02896 | hp2 | a0001 | c0007 | t0028 | g0240 | AFR | GWD | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02897 | hp1 | a0001 | c0005 | t0016 | g0007 | AFR | GWD | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02897 | hp2 | a0001 | c0001 | t0006 | g0161 | AFR | GWD | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02965 | hp1 | a0001 | c0001 | t0023 | g0040 | AFR | ESN | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02965 | hp2 | a0001 | c0001 | t0011 | g0061 | AFR | ESN | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02970 | hp1 | a0001 | c0001 | t0019 | g0162 | AFR | ESN | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02970 | hp2 | a0001 | c0001 | t0017 | g0050 | AFR | ESN | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02976 | hp1 | a0001 | c0001 | t0009 | g0082 | AFR | ESN | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02976 | hp2 | a0001 | c0001 | t0032 | g0151 | AFR | ESN | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03017 | hp1 | a0001 | c0001 | t0005 | g0063 | SAS | PJL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0173 | SAS | PJL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03041 | hp1 | a0001 | c0001 | t0008 | g0155 | AFR | GWD | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0034 | AFR | GWD | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03098 | hp1 | a0001 | c0001 | t0044 | g0079 | AFR | MSL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03098 | hp2 | a0001 | c0003 | t0010 | g0006 | AFR | MSL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03130 | hp1 | a0003 | c0004 | t0007 | g0309 | AFR | ESN | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03130 | hp2 | a0001 | c0001 | t0009 | g0078 | AFR | ESN | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03209 | hp1 | a0001 | c0001 | t0024 | g0042 | AFR | MSL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03209 | hp2 | a0001 | c0001 | t0009 | g0032 | AFR | MSL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03225 | hp1 | a0001 | c0001 | t0011 | g0058 | AFR | MSL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03225 | hp2 | a0001 | c0001 | t0040 | g0212 | AFR | MSL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03239 | hp1 | a0002 | c0002 | t0002 | g0264 | SAS | PJL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03453 | hp1 | a0002 | c0002 | t0007 | g0308 | AFR | MSL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03453 | hp2 | a0001 | c0003 | t0016 | g0003 | AFR | MSL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03486 | hp1 | a0001 | c0001 | t0017 | g0062 | AFR | MSL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03486 | hp2 | a0001 | c0001 | t0008 | g0152 | AFR | MSL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03492 | hp1 | a0002 | c0002 | t0002 | g0319 | SAS | PJL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03492 | hp2 | a0001 | c0001 | t0008 | g0133 | SAS | PJL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0026 | AFR | ESN | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03516 | hp2 | a0001 | c0003 | t0010 | g0017 | AFR | ESN | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03540 | hp1 | a0001 | c0001 | t0043 | g0025 | AFR | GWD | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03540 | hp2 | a0001 | c0001 | t0017 | g0053 | AFR | GWD | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03579 | hp1 | a0001 | c0001 | t0012 | g0027 | AFR | MSL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03579 | hp2 | a0001 | c0001 | t0006 | g0150 | AFR | MSL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03654 | hp1 | a0002 | c0002 | t0007 | g0246 | SAS | PJL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0234 | SAS | PJL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0168 | SAS | PJL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03669 | hp2 | a0001 | c0001 | t0004 | g0066 | SAS | PJL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | STU | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0233 | SAS | STU | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03704 | hp1 | a0001 | c0001 | t0004 | g0031 | SAS | PJL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03704 | hp2 | a0002 | c0002 | t0007 | g0280 | SAS | PJL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03710 | hp1 | a0001 | c0001 | t0046 | g0223 | SAS | PJL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03710 | hp2 | a0001 | c0001 | t0004 | g0020 | SAS | PJL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03834 | hp1 | a0002 | c0002 | t0007 | g0313 | SAS | BEB | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | BEB | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG04184 | hp1 | a0001 | c0001 | t0033 | g0175 | SAS | BEB | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG04184 | hp2 | a0002 | c0002 | t0029 | g0284 | SAS | BEB | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG04199 | hp1 | a0001 | c0001 | t0012 | g0187 | SAS | STU | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG04199 | hp2 | a0002 | c0002 | t0002 | g0245 | SAS | STU | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG04204 | hp1 | a0002 | c0002 | t0002 | g0289 | SAS | STU | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG04204 | hp2 | a0001 | c0001 | t0004 | g0023 | SAS | STU | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18522 | hp1 | a0001 | c0001 | t0042 | g0085 | AFR | YRI | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18522 | hp2 | a0001 | c0001 | t0045 | g0076 | AFR | YRI | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18747 | hp1 | a0002 | c0002 | t0007 | g0316 | EAS | CHB | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CHB | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18906 | hp1 | a0003 | c0004 | t0007 | g0311 | AFR | YRI | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18906 | hp2 | a0001 | c0001 | t0049 | g0029 | AFR | YRI | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18940 | hp1 | a0002 | c0002 | t0002 | g0252 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18941 | hp1 | a0002 | c0002 | t0002 | g0243 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18944 | hp1 | a0001 | c0001 | t0005 | g0052 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18944 | hp2 | a0002 | c0002 | t0002 | g0259 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18945 | hp1 | a0002 | c0002 | t0002 | g0306 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0191 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18947 | hp2 | a0002 | c0002 | t0014 | g0271 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18948 | hp1 | a0002 | c0002 | t0002 | g0247 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18951 | hp1 | a0002 | c0002 | t0002 | g0291 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18951 | hp2 | a0001 | c0001 | t0015 | g0090 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18952 | hp1 | a0001 | c0001 | t0013 | g0093 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18952 | hp2 | a0002 | c0002 | t0002 | g0250 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18954 | hp1 | a0002 | c0002 | t0002 | g0281 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18954 | hp2 | a0001 | c0001 | t0013 | g0091 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18957 | hp1 | a0002 | c0002 | t0002 | g0262 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18959 | hp2 | a0001 | c0001 | t0005 | g0049 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18960 | hp1 | a0004 | c0012 | t0003 | g0192 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18960 | hp2 | a0001 | c0001 | t0008 | g0098 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18961 | hp2 | a0002 | c0002 | t0002 | g0285 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18965 | hp1 | a0001 | c0001 | t0015 | g0116 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18965 | hp2 | a0001 | c0001 | t0003 | g0189 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18966 | hp2 | a0002 | c0002 | t0002 | g0261 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18967 | hp1 | a0002 | c0002 | t0030 | g0241 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18967 | hp2 | a0001 | c0001 | t0013 | g0092 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18969 | hp2 | a0002 | c0002 | t0002 | g0260 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18974 | hp1 | a0002 | c0002 | t0055 | g0321 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18975 | hp1 | a0001 | c0001 | t0012 | g0227 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18975 | hp2 | a0002 | c0002 | t0047 | g0125 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0200 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18979 | hp2 | a0002 | c0002 | t0002 | g0263 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18980 | hp1 | a0001 | c0001 | t0013 | g0094 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18980 | hp2 | a0002 | c0002 | t0021 | g0279 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18982 | hp1 | a0001 | c0001 | t0003 | g0188 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18982 | hp2 | a0002 | c0002 | t0014 | g0273 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18985 | hp1 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18988 | hp2 | a0001 | c0001 | t0003 | g0196 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18993 | hp1 | a0002 | c0002 | t0054 | g0322 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18994 | hp1 | a0001 | c0001 | t0013 | g0149 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18994 | hp2 | a0002 | c0002 | t0014 | g0242 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18998 | hp1 | a0002 | c0002 | t0002 | g0275 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0180 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0199 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19000 | hp2 | a0002 | c0002 | t0002 | g0296 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19002 | hp1 | a0001 | c0001 | t0035 | g0183 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19002 | hp2 | a0002 | c0002 | t0007 | g0312 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19006 | hp1 | a0002 | c0002 | t0002 | g0287 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19007 | hp1 | a0002 | c0002 | t0021 | g0249 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0120 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19009 | hp2 | a0001 | c0001 | t0015 | g0193 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19030 | hp1 | a0001 | c0001 | t0019 | g0163 | AFR | LWK | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | LWK | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | LWK | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0030 | AFR | LWK | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19056 | hp2 | a0002 | c0002 | t0002 | g0265 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19057 | hp1 | a0002 | c0002 | t0002 | g0251 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19058 | hp1 | a0002 | c0002 | t0002 | g0257 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19060 | hp1 | a0002 | c0002 | t0002 | g0276 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19062 | hp1 | a0001 | c0001 | t0008 | g0134 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19062 | hp2 | a0002 | c0002 | t0002 | g0305 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19063 | hp2 | a0002 | c0002 | t0002 | g0256 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19065 | hp2 | a0002 | c0002 | t0002 | g0317 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19070 | hp1 | a0002 | c0002 | t0021 | g0248 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19072 | hp1 | a0001 | c0001 | t0008 | g0105 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19072 | hp2 | a0002 | c0002 | t0007 | g0297 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19076 | hp1 | a0002 | c0002 | t0020 | g0315 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19077 | hp2 | a0002 | c0002 | t0002 | g0283 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19078 | hp1 | a0001 | c0001 | t0041 | g0144 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19078 | hp2 | a0002 | c0002 | t0002 | g0274 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19079 | hp2 | a0002 | c0002 | t0002 | g0278 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19084 | hp2 | a0002 | c0002 | t0002 | g0286 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19086 | hp2 | a0002 | c0002 | t0014 | g0272 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19089 | hp1 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19091 | hp1 | a0002 | c0002 | t0002 | g0277 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19091 | hp2 | a0001 | c0001 | t0018 | g0097 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA20129 | hp1 | a0001 | c0001 | t0006 | g0231 | AFR | ASW | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | ASW | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0182 | SAS | GIH | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA20905 | hp2 | a0001 | c0001 | t0004 | g0021 | SAS | GIH | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01123 | hp1 | a0001 | c0001 | t0006 | g0214 | AMR | CLM | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01123 | hp2 | a0002 | c0002 | t0020 | g0255 | AMR | CLM | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02486 | hp1 | a0001 | c0001 | t0011 | g0055 | AFR | ACB | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02486 | hp2 | a0001 | c0001 | t0008 | g0140 | AFR | ACB | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02559 | hp1 | a0001 | c0001 | t0009 | g0081 | AFR | ACB | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02559 | hp2 | a0001 | c0001 | t0006 | g0153 | AFR | ACB | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03471 | hp1 | a0001 | c0001 | t0025 | g0156 | AFR | MSL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03471 | hp2 | a0001 | c0014 | t0004 | g0013 | AFR | MSL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG06807 | hp1 | a0001 | c0001 | t0024 | g0060 | AFR | USA | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG06807 | hp2 | a0001 | c0003 | t0016 | g0004 | AFR | USA | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18955 | hp1 | a0002 | c0002 | t0002 | g0288 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0186 | AFR | USA | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA20300 | hp2 | a0001 | c0003 | t0027 | g0012 | AFR | USA | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA21309 | hp1 | a0001 | c0001 | t0018 | g0219 | AFR | LWK | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA21309 | hp2 | a0002 | c0002 | t0007 | g0320 | AFR | LWK | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0006 | t0026 | g0065 | REF | REF | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0012 | g0177 | REF | REF | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:31812781
|
G | T | 1 | a0004 | 1 | NA18960.hp1 | missense_variant | MODERATE | c.1877C>A | p.Thr626Asn | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 15/20 | 2136/5060 | 1877/2541 | 626/846 | chr10 | 31812781 | ||
| chr10:31839649
|
C | A | 1 | a0003 | 3 | HG01109.hp2 HG03130.hp1 NA18906.hp1 |
missense_variant | MODERATE | c.1359G>T | p.Lys453Asn | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 8/20 | 1618/5060 | 1359/2541 | 453/846 | chr10 | 31839649 | ||
| chr10:31839683
|
A | G | 2 | a0002a0003 | 82 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(79): Show |
missense_variant | MODERATE | c.1325T>C | p.Phe442Ser | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 8/20 | 1584/5060 | 1325/2541 | 442/846 | chr10 | 31839683 | ||
| chr10:31908252
|
C | T | 1 | a0005 | 1 | HG01978.hp1 | missense_variant | MODERATE | c.604G>A | p.Ala202Thr | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/20 | 863/5060 | 604/2541 | 202/846 | chr10 | 31908252 | ||
| chr10:31908926
|
G | C | 1 | a0001 | 2 | HG02145.hp2 NA18906.hp2 |
splice_region_variant | LOW | c.-71C>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/20 | chr10 | 31908926 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:31808681
|
G | A | 1 | a0001c0013 | 1 | HG01071.hp1 | synonymous_variant | LOW | c.2334C>T | p.Asp778Asp | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 19/20 | 2593/5060 | 2334/2541 | 778/846 | chr10 | 31808681 | ||
| chr10:31814263
|
A | C | 2 | a0001c0003a0001c0005 | 15 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
synonymous_variant | LOW | c.1830T>G | p.Leu610Leu | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 14/20 | 2089/5060 | 1830/2541 | 610/846 | chr10 | 31814263 | ||
| chr10:31826358
|
C | T | 1 | a0001c0011 | 1 | HG02015.hp1 | synonymous_variant | LOW | c.1476G>A | p.Val492Val | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 11/20 | 1735/5060 | 1476/2541 | 492/846 | chr10 | 31826358 | ||
| chr10:31831750
|
C | T | 4 | a0001c0007a0001c0010a0002c0002others(1): Show | 85 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(82): Show |
synonymous_variant | LOW | c.1437G>A | p.Gly479Gly | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 10/20 | 1696/5060 | 1437/2541 | 479/846 | chr10 | 31831750 | ||
| chr10:31852532
|
T | C | 2 | a0002c0002a0003c0004 | 82 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(79): Show |
synonymous_variant | LOW | c.1155A>G | p.Glu385Glu | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 6/20 | 1414/5060 | 1155/2541 | 385/846 | chr10 | 31852532 | ||
| chr10:31854116
|
A | G | 1 | a0001c0006 | 2 | HG00099.hp2 homoSapiens_chm13v2.hp1 |
synonymous_variant | LOW | c.1039T>C | p.Leu347Leu | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 5/20 | 1298/5060 | 1039/2541 | 347/846 | chr10 | 31854116 | ||
| chr10:31861575
|
A | G | 1 | a0001c0010 | 1 | HG02886.hp2 | synonymous_variant | LOW | c.768T>C | p.Leu256Leu | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/20 | 1027/5060 | 768/2541 | 256/846 | chr10 | 31861575 | ||
| chr10:31908175
|
T | G | 3 | a0001c0003a0001c0005a0001c0014 | 16 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(13): Show |
synonymous_variant | LOW | c.681A>C | p.Ile227Ile | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/20 | 940/5060 | 681/2541 | 227/846 | chr10 | 31908175 | ||
| chr10:31908811
|
C | T | 1 | a0001c0005 | 2 | HG02895.hp1 HG02897.hp1 |
synonymous_variant | LOW | c.45G>A | p.Val15Val | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/20 | 304/5060 | 45/2541 | 15/846 | chr10 | 31908811 | ||
| chr10:31908840
|
T | G | 1 | a0001c0008 | 2 | HG02602.hp2 HG02735.hp2 |
synonymous_variant | LOW | c.16A>C | p.Arg6Arg | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/20 | 275/5060 | 16/2541 | 6/846 | chr10 | 31908840 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:31805406
|
A | G | 1 | a0002c0002t0030 | 2 | HG00621.hp1 NA18967.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2252T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 20/20 | 2252 | chr10 | 31805406 | |||||
| chr10:31805436
|
A | G | 1 | a0001c0001t0039 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2222T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 20/20 | 2222 | chr10 | 31805436 | |||||
| chr10:31805485
|
T | C | 5 | a0001c0003t0010a0001c0003t0016a0001c0003t0027others(2): Show | 15 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2173A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 20/20 | 2173 | chr10 | 31805485 | |||||
| chr10:31805572
|
G | A | 5 | a0001c0003t0010a0001c0003t0016a0001c0003t0027others(2): Show | 15 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2086C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 20/20 | 2086 | chr10 | 31805572 | |||||
| chr10:31805648
|
T | TCA | 12 | a0001c0001t0003a0001c0001t0008a0001c0001t0023others(9): Show | 56 | HG00280.hp2 HG00544.hp1 HG00639.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*2008_*2009dupTG | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 20/20 | 2009 | chr10 | 31805648 | |||||
| chr10:31805648
|
T | TCACA | 9 | a0001c0001t0001a0001c0001t0013a0001c0001t0019others(6): Show | 79 | HG00099.hp1 HG00544.hp2 HG00597.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*2006_*2009dupTGTG | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 20/20 | 2009 | chr10 | 31805648 | |||||
| chr10:31805648
|
T | TCACACA | 5 | a0001c0001t0006a0001c0001t0009a0001c0001t0024others(2): Show | 26 | HG00280.hp1 HG00741.hp1 HG01106.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*2004_*2009dupTGTG others(2): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 20/20 | 2009 | chr10 | 31805648 | |||||
| chr10:31805648
|
T | TCACACAC others(1): Show |
3 | a0001c0001t0018a0001c0001t0032a0001c0001t0035 | 5 | HG02055.hp1 HG02976.hp2 NA19002.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2002_*2009dupTGTG others(4): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 20/20 | 2009 | chr10 | 31805648 | |||||
| chr10:31805648
|
T | TCACACAC others(3): Show |
1 | a0001c0001t0050 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2000_*2009dupTGTG others(6): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 20/20 | 2009 | chr10 | 31805648 | |||||
| chr10:31805648
|
T | TCACACAC others(5): Show |
3 | a0001c0001t0045a0001c0003t0016a0001c0005t0016 | 5 | HG02895.hp1 HG02897.hp1 HG03453.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1998_*2009dupTGTG others(8): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 20/20 | 2009 | chr10 | 31805648 | |||||
| chr10:31805648
|
T | TCACACAC others(7): Show |
2 | a0001c0001t0042a0001c0003t0010 | 9 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1996_*2009dupTGTG others(10): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 20/20 | 2009 | chr10 | 31805648 | |||||
| chr10:31805648
|
T | TCACACAC others(9): Show |
2 | a0001c0001t0040a0001c0003t0027 | 3 | HG02818.hp1 HG03225.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1994_*2009dupTGTG others(12): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 20/20 | 2009 | chr10 | 31805648 | |||||
| chr10:31805648
|
TCA | T | 8 | a0001c0001t0033a0001c0001t0037a0001c0001t0038others(5): Show | 59 | HG00597.hp1 HG00673.hp1 HG00738.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*2008_*2009delTG | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 20/20 | 2008 | chr10 | 31805648 | |||||
| chr10:31805648
|
TCACA | T | 4 | a0001c0001t0004a0001c0006t0026a0001c0014t0004others(1): Show | 25 | HG00099.hp2 HG00639.hp2 HG01081.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*2006_*2009delTGTG | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 20/20 | 2006 | chr10 | 31805648 | |||||
| chr10:31805648
|
TCACACA | T | 3 | a0001c0001t0005a0001c0001t0011a0001c0008t0005 | 21 | HG01109.hp1 HG01168.hp1 HG01192.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2004_*2009delTGTG others(2): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 20/20 | 2004 | chr10 | 31805648 | |||||
| chr10:31805648
|
TCACACAC others(3): Show |
T | 1 | a0001c0001t0017 | 3 | HG02970.hp2 HG03486.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2000_*2009delTGTG others(6): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 20/20 | 2000 | chr10 | 31805648 | |||||
| chr10:31805822
|
A | T | 1 | a0001c0001t0036 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1836T>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 20/20 | 1836 | chr10 | 31805822 | |||||
| chr10:31805823
|
T | C | 13 | a0001c0007t0028a0001c0010t0053a0002c0002t0002others(10): Show | 85 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*1835A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 20/20 | 1835 | chr10 | 31805823 | |||||
| chr10:31805840
|
T | A | 16 | a0001c0001t0001a0001c0001t0006a0001c0001t0008others(13): Show | 113 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*1818A>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 20/20 | 1818 | chr10 | 31805840 | |||||
| chr10:31805889
|
G | A | 5 | a0001c0003t0010a0001c0003t0016a0001c0003t0027others(2): Show | 15 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1769C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 20/20 | 1769 | chr10 | 31805889 | |||||
| chr10:31805940
|
C | T | 1 | a0001c0001t0025 | 2 | HG02258.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1718G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 20/20 | 1718 | chr10 | 31805940 | |||||
| chr10:31805962
|
C | A | 33 | a0001c0001t0004a0001c0001t0005a0001c0001t0009others(30): Show | 161 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(158): Show |
3_prime_UTR_variant | MODIFIER | c.*1696G>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 20/20 | 1696 | chr10 | 31805962 | |||||
| chr10:31806063
|
G | GA | 6 | a0001c0001t0041a0001c0003t0010a0001c0003t0016others(3): Show | 16 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1594dupT | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 20/20 | 1594 | chr10 | 31806063 | |||||
| chr10:31806127
|
G | A | 1 | a0001c0001t0011 | 7 | HG01884.hp1 HG01891.hp2 HG02280.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1531C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 20/20 | 1531 | chr10 | 31806127 | |||||
| chr10:31806247
|
G | A | 5 | a0001c0003t0010a0001c0003t0016a0001c0003t0027others(2): Show | 15 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1411C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 20/20 | 1411 | chr10 | 31806247 | |||||
| chr10:31806256
|
T | C | 2 | a0001c0001t0019a0001c0001t0042 | 4 | HG01167.hp1 HG02970.hp1 NA18522.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1402A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 20/20 | 1402 | chr10 | 31806256 | |||||
| chr10:31806274
|
A | G | 1 | a0002c0002t0029 | 2 | HG02698.hp2 HG04184.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1384T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 20/20 | 1384 | chr10 | 31806274 | |||||
| chr10:31806321
|
T | G | 16 | a0001c0001t0001a0001c0001t0006a0001c0001t0008others(13): Show | 113 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*1337A>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 20/20 | 1337 | chr10 | 31806321 | |||||
| chr10:31806560
|
A | C | 1 | a0001c0001t0032 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1098T>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 20/20 | 1098 | chr10 | 31806560 | |||||
| chr10:31806595
|
C | A | 1 | a0001c0006t0026 | 2 | HG00099.hp2 homoSapiens_chm13v2.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1063G>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 20/20 | 1063 | chr10 | 31806595 | |||||
| chr10:31806615
|
G | A | 4 | a0001c0001t0009a0001c0001t0043a0001c0001t0044others(1): Show | 11 | HG02145.hp1 HG02257.hp1 HG02559.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1043C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 20/20 | 1043 | chr10 | 31806615 | |||||
| chr10:31806733
|
C | T | 1 | a0001c0007t0028 | 2 | HG02572.hp1 HG02896.hp2 |
3_prime_UTR_variant | MODIFIER | c.*925G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 20/20 | 925 | chr10 | 31806733 | |||||
| chr10:31806734
|
G | A | 1 | a0001c0001t0046 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*924C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 20/20 | 924 | chr10 | 31806734 | |||||
| chr10:31806738
|
T | C | 11 | a0002c0002t0002a0002c0002t0007a0002c0002t0014others(8): Show | 82 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*920A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 20/20 | 920 | chr10 | 31806738 | |||||
| chr10:31807003
|
G | A | 1 | a0002c0002t0021 | 3 | NA18980.hp2 NA19007.hp1 NA19070.hp1 |
3_prime_UTR_variant | MODIFIER | c.*655C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 20/20 | 655 | chr10 | 31807003 | |||||
| chr10:31807076
|
T | C | 5 | a0001c0003t0010a0001c0003t0016a0001c0003t0027others(2): Show | 15 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*582A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 20/20 | 582 | chr10 | 31807076 | |||||
| chr10:31807537
|
C | CA | 1 | a0001c0001t0013 | 5 | NA18952.hp1 NA18954.hp2 NA18967.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*120dupT | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 20/20 | 120 | chr10 | 31807537 | |||||
| chr10:31928731
|
C | T | 1 | a0001c0001t0031 | 1 | HG02135.hp2 | 5_prime_UTR_variant | MODIFIER | c.-159G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/20 | 19876 | chr10 | 31928731 | |||||
| chr10:31928762
|
G | T | 2 | a0002c0002t0054a0002c0002t0055 | 2 | NA18974.hp1 NA18993.hp1 |
5_prime_UTR_variant | MODIFIER | c.-190C>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/20 | 19907 | chr10 | 31928762 | |||||
| chr10:31928763
|
A | C | 2 | a0002c0002t0054a0002c0002t0055 | 2 | NA18974.hp1 NA18993.hp1 |
5_prime_UTR_variant | MODIFIER | c.-191T>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/20 | 19908 | chr10 | 31928763 | |||||
| chr10:31928777
|
T | C | 1 | a0001c0001t0051 | 1 | HG01981.hp1 | 5_prime_UTR_variant | MODIFIER | c.-205A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/20 | 19922 | chr10 | 31928777 | |||||
| chr10:31928794
|
C | A | 13 | a0001c0001t0052a0001c0007t0028a0001c0010t0053others(10): Show | 85 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(82): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-222G>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/20 | chr10 | 31928794 | ||||||
| chr10:31928817
|
G | A | 2 | a0002c0002t0054a0002c0002t0055 | 2 | NA18974.hp1 NA18993.hp1 |
5_prime_UTR_variant | MODIFIER | c.-245C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/20 | 19962 | chr10 | 31928817 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:31807875
|
G | C | 113 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0088others(110): Show | 113 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.2367-43C>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 19/19 | chr10 | 31807875 | ||||||
| chr10:31808037
|
C | A | 1 | a0001c0001t0003g0201 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2367-205G>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 19/19 | chr10 | 31808037 | ||||||
| chr10:31808216
|
C | CT | 77 | a0002c0002t0002g0243a0002c0002t0002g0245a0002c0002t0002g0247others(74): Show | 77 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.2367-385dupA | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 19/19 | chr10 | 31808216 | ||||||
| chr10:31808219
|
T | TA | 12 | a0001c0001t0009g0032a0001c0001t0009g0072a0001c0001t0009g0073others(9): Show | 12 | HG02145.hp1 HG02257.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.2367-388dupT | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 19/19 | chr10 | 31808219 | ||||||
| chr10:31808219
|
TA | T | 18 | a0001c0001t0003g0189a0001c0003t0010g0005a0001c0003t0010g0006others(15): Show | 18 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.2367-388delT | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 19/19 | chr10 | 31808219 | ||||||
| chr10:31808220
|
A | T | 4 | a0002c0002t0007g0308a0003c0004t0007g0309a0003c0004t0007g0310others(1): Show | 4 | HG01109.hp2 HG03130.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2367-388T>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 19/19 | chr10 | 31808220 | ||||||
| chr10:31808506
|
G | T | 15 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(12): Show | 15 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.2366+143C>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 19/19 | chr10 | 31808506 | ||||||
| chr10:31808622
|
C | T | 1 | a0001c0001t0001g0213 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2366+27G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 19/19 | chr10 | 31808622 | ||||||
| chr10:31808776
|
T | A | 1 | a0001c0001t0001g0100 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2264-25A>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 18/19 | chr10 | 31808776 | ||||||
| chr10:31808878
|
A | T | 85 | a0001c0007t0028g0239a0001c0007t0028g0240a0001c0010t0053g0238others(82): Show | 85 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.2263+116T>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 18/19 | chr10 | 31808878 | ||||||
| chr10:31808923
|
A | G | 85 | a0001c0007t0028g0239a0001c0007t0028g0240a0001c0010t0053g0238others(82): Show | 85 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.2263+71T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 18/19 | chr10 | 31808923 | ||||||
| chr10:31809187
|
T | C | 2 | a0002c0002t0002g0281a0002c0002t0047g0125 | 2 | NA18954.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.2128+43A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 17/19 | chr10 | 31809187 | ||||||
| chr10:31809720
|
G | A | 15 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(12): Show | 15 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.2051-413C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 16/19 | chr10 | 31809720 | ||||||
| chr10:31809774
|
T | C | 2 | a0001c0003t0016g0003a0001c0003t0016g0004 | 2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2051-467A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 16/19 | chr10 | 31809774 | ||||||
| chr10:31810003
|
G | A | 15 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(12): Show | 15 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.2050+646C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 16/19 | chr10 | 31810003 | ||||||
| chr10:31810020
|
T | C | 2 | a0001c0001t0001g0228a0001c0001t0001g0230 | 2 | HG01175.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.2050+629A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 16/19 | chr10 | 31810020 | ||||||
| chr10:31810108
|
A | G | 1 | a0001c0001t0001g0145 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2050+541T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 16/19 | chr10 | 31810108 | ||||||
| chr10:31810223
|
G | A | 3 | a0001c0001t0001g0099a0001c0001t0001g0129a0001c0001t0001g0130 | 3 | HG00741.hp2 HG01516.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.2050+426C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 16/19 | chr10 | 31810223 | ||||||
| chr10:31810448
|
C | T | 15 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(12): Show | 15 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.2050+201G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 16/19 | chr10 | 31810448 | ||||||
| chr10:31810459
|
A | T | 112 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0088others(109): Show | 112 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.2050+190T>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 16/19 | chr10 | 31810459 | ||||||
| chr10:31810528
|
A | C | 15 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(12): Show | 15 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.2050+121T>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 16/19 | chr10 | 31810528 | ||||||
| chr10:31810619
|
TA | T | 83 | a0001c0001t0008g0098a0002c0002t0002g0243a0002c0002t0002g0245others(80): Show | 83 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.2050+29delT | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 16/19 | chr10 | 31810619 | ||||||
| chr10:31810819
|
G | A | 2 | a0001c0001t0001g0135a0001c0001t0001g0142 | 2 | NA18969.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.1952-72C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 15/19 | chr10 | 31810819 | ||||||
| chr10:31811003
|
T | C | 15 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(12): Show | 15 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1952-256A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 15/19 | chr10 | 31811003 | ||||||
| chr10:31811200
|
A | C | 258 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0088others(255): Show | 258 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.1952-453T>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 15/19 | chr10 | 31811200 | ||||||
| chr10:31811200
|
A | T | 15 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(12): Show | 15 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1952-453T>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 15/19 | chr10 | 31811200 | ||||||
| chr10:31811207
|
C | T | 1 | a0001c0001t0040g0212 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1952-460G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 15/19 | chr10 | 31811207 | ||||||
| chr10:31811402
|
T | C | 11 | a0001c0001t0009g0032a0001c0001t0009g0072a0001c0001t0009g0073others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1952-655A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 15/19 | chr10 | 31811402 | ||||||
| chr10:31811542
|
C | CT | 6 | a0001c0001t0001g0104a0001c0001t0006g0159a0001c0001t0008g0222others(3): Show | 6 | HG00280.hp1 HG00597.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1952-796dupA | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 15/19 | chr10 | 31811542 | ||||||
| chr10:31811542
|
CT | C | 151 | a0001c0001t0001g0121a0001c0001t0001g0203a0001c0001t0001g0217others(148): Show | 151 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(148): Show |
intron_variant | MODIFIER | c.1952-796delA | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 15/19 | chr10 | 31811542 | ||||||
| chr10:31811542
|
CTTT | C | 15 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(12): Show | 15 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1952-798_1952-796d others(5): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 15/19 | chr10 | 31811542 | ||||||
| chr10:31811551
|
T | G | 1 | a0001c0001t0043g0025 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1952-804A>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 15/19 | chr10 | 31811551 | ||||||
| chr10:31811606
|
T | C | 1 | a0001c0001t0001g0157 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1952-859A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 15/19 | chr10 | 31811606 | ||||||
| chr10:31811607
|
TG | T | 15 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(12): Show | 15 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1952-861delC | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 15/19 | chr10 | 31811607 | ||||||
| chr10:31811622
|
T | G | 2 | a0002c0002t0002g0302a0002c0002t0002g0305 | 2 | HG02155.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.1952-875A>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 15/19 | chr10 | 31811622 | ||||||
| chr10:31811639
|
T | C | 1 | a0002c0002t0029g0284 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1952-892A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 15/19 | chr10 | 31811639 | ||||||
| chr10:31811665
|
T | TTTTTA | 50 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(47): Show | 50 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.1952-923_1952-919d others(7): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 15/19 | chr10 | 31811665 | ||||||
| chr10:31811665
|
T | TTTTTATT others(3): Show |
215 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0088others(212): Show | 215 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(212): Show |
intron_variant | MODIFIER | c.1952-928_1952-919d others(12): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 15/19 | chr10 | 31811665 | ||||||
| chr10:31811665
|
T | TTTTTATT others(8): Show |
8 | a0001c0001t0008g0134a0001c0001t0008g0136a0001c0001t0015g0090others(5): Show | 8 | HG00639.hp2 HG01099.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.1952-933_1952-919d others(17): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 15/19 | chr10 | 31811665 | ||||||
| chr10:31811772
|
C | T | 1 | a0001c0001t0001g0118 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1951+935G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 15/19 | chr10 | 31811772 | ||||||
| chr10:31811829
|
C | G | 2 | a0001c0001t0004g0036a0001c0001t0037g0035 | 2 | HG02258.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1951+878G>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 15/19 | chr10 | 31811829 | ||||||
| chr10:31811962
|
C | G | 15 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(12): Show | 15 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1951+745G>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 15/19 | chr10 | 31811962 | ||||||
| chr10:31812227
|
T | G | 1 | a0002c0002t0007g0246 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1951+480A>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 15/19 | chr10 | 31812227 | ||||||
| chr10:31812261
|
G | A | 160 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(157): Show | 160 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.1951+446C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 15/19 | chr10 | 31812261 | ||||||
| chr10:31812294
|
G | C | 2 | a0002c0002t0002g0302a0002c0002t0002g0305 | 2 | HG02155.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.1951+413C>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 15/19 | chr10 | 31812294 | ||||||
| chr10:31812576
|
A | G | 11 | a0001c0001t0009g0032a0001c0001t0009g0072a0001c0001t0009g0073others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1951+131T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 15/19 | chr10 | 31812576 | ||||||
| chr10:31812664
|
T | C | 1 | a0002c0002t0020g0270 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1951+43A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 15/19 | chr10 | 31812664 | ||||||
| chr10:31813037
|
T | C | 1 | a0001c0010t0053g0238 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1835-214A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 14/19 | chr10 | 31813037 | ||||||
| chr10:31813182
|
G | A | 145 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(142): Show | 145 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(142): Show |
intron_variant | MODIFIER | c.1835-359C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 14/19 | chr10 | 31813182 | ||||||
| chr10:31813295
|
A | C | 1 | a0002c0002t0002g0268 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1835-472T>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 14/19 | chr10 | 31813295 | ||||||
| chr10:31813491
|
T | C | 15 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(12): Show | 15 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1835-668A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 14/19 | chr10 | 31813491 | ||||||
| chr10:31813645
|
C | CAT | 278 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0088others(275): Show | 278 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.1834+613_1834+614i others(4): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 14/19 | chr10 | 31813645 | ||||||
| chr10:31813661
|
T | C | 10 | a0001c0001t0009g0032a0001c0001t0009g0072a0001c0001t0009g0073others(7): Show | 10 | HG02145.hp1 HG02257.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1834+598A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 14/19 | chr10 | 31813661 | ||||||
| chr10:31813694
|
C | T | 1 | a0001c0001t0008g0136 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1834+565G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 14/19 | chr10 | 31813694 | ||||||
| chr10:31813703
|
T | C | 101 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0088others(98): Show | 101 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.1834+556A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 14/19 | chr10 | 31813703 | ||||||
| chr10:31813723
|
G | A | 1 | a0001c0001t0004g0019 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1834+536C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 14/19 | chr10 | 31813723 | ||||||
| chr10:31813766
|
G | A | 5 | a0001c0001t0004g0037a0001c0001t0004g0038a0001c0001t0004g0039others(2): Show | 5 | HG01168.hp2 HG01346.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1834+493C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 14/19 | chr10 | 31813766 | ||||||
| chr10:31813804
|
C | T | 15 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(12): Show | 15 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1834+455G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 14/19 | chr10 | 31813804 | ||||||
| chr10:31813901
|
T | A | 3 | a0002c0002t0002g0247a0002c0002t0002g0251a0002c0002t0002g0252 | 3 | NA18940.hp1 NA18948.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.1834+358A>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 14/19 | chr10 | 31813901 | ||||||
| chr10:31814022
|
G | A | 1 | a0002c0002t0002g0306 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1834+237C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 14/19 | chr10 | 31814022 | ||||||
| chr10:31814149
|
C | T | 161 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(158): Show | 161 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(158): Show |
intron_variant | MODIFIER | c.1834+110G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 14/19 | chr10 | 31814149 | ||||||
| chr10:31814588
|
G | T | 15 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(12): Show | 15 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1732-227C>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 13/19 | chr10 | 31814588 | ||||||
| chr10:31814733
|
G | A | 5 | a0001c0001t0023g0040a0001c0001t0023g0069a0001c0001t0024g0042others(2): Show | 5 | HG02572.hp2 HG02622.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1732-372C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 13/19 | chr10 | 31814733 | ||||||
| chr10:31815050
|
G | A | 15 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(12): Show | 15 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1732-689C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 13/19 | chr10 | 31815050 | ||||||
| chr10:31815077
|
C | T | 1 | a0002c0002t0055g0321 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1732-716G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 13/19 | chr10 | 31815077 | ||||||
| chr10:31815120
|
CA | C | 127 | a0001c0001t0003g0185a0001c0001t0004g0019a0001c0001t0004g0020others(124): Show | 127 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(124): Show |
intron_variant | MODIFIER | c.1732-760delT | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 13/19 | chr10 | 31815120 | ||||||
| chr10:31815120
|
CAA | C | 17 | a0001c0001t0004g0022a0001c0003t0010g0005a0001c0003t0010g0006others(14): Show | 17 | HG00735.hp2 HG01167.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.1732-761_1732-760d others(4): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 13/19 | chr10 | 31815120 | ||||||
| chr10:31815132
|
A | G | 1 | a0001c0001t0001g0119 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1732-771T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 13/19 | chr10 | 31815132 | ||||||
| chr10:31815132
|
AAAAAG | A | 9 | a0001c0001t0009g0032a0001c0001t0009g0072a0001c0001t0009g0073others(6): Show | 9 | HG02145.hp1 HG02257.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1732-776_1732-772d others(7): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 13/19 | chr10 | 31815132 | ||||||
| chr10:31815303
|
G | A | 1 | a0001c0001t0003g0026 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1732-942C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 13/19 | chr10 | 31815303 | ||||||
| chr10:31815339
|
C | T | 85 | a0001c0007t0028g0239a0001c0007t0028g0240a0001c0010t0053g0238others(82): Show | 85 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.1732-978G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 13/19 | chr10 | 31815339 | ||||||
| chr10:31815587
|
T | C | 2 | a0002c0002t0002g0281a0002c0002t0047g0125 | 2 | NA18954.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.1732-1226A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 13/19 | chr10 | 31815587 | ||||||
| chr10:31815602
|
A | G | 15 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(12): Show | 15 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1732-1241T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 13/19 | chr10 | 31815602 | ||||||
| chr10:31815775
|
A | C | 1 | a0002c0002t0007g0308 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1732-1414T>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 13/19 | chr10 | 31815775 | ||||||
| chr10:31815805
|
T | C | 15 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(12): Show | 15 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1732-1444A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 13/19 | chr10 | 31815805 | ||||||
| chr10:31815939
|
G | C | 273 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0088others(270): Show | 273 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.1732-1578C>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 13/19 | chr10 | 31815939 | ||||||
| chr10:31815970
|
T | C | 1 | a0001c0001t0034g0033 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1732-1609A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 13/19 | chr10 | 31815970 | ||||||
| chr10:31816037
|
G | C | 15 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(12): Show | 15 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1732-1676C>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 13/19 | chr10 | 31816037 | ||||||
| chr10:31816168
|
C | CGT | 43 | a0001c0001t0001g0226a0001c0001t0003g0120a0001c0001t0003g0168others(40): Show | 43 | HG00099.hp2 HG00280.hp1 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.1731+1618_1731+161 others(6): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 13/19 | chr10 | 31816168 | ||||||
| chr10:31816168
|
C | CGTGT | 29 | a0001c0001t0001g0114a0001c0001t0001g0137a0001c0001t0001g0146others(26): Show | 29 | HG00735.hp1 HG01346.hp2 HG01358.hp1 others(26): Show |
intron_variant | MODIFIER | c.1731+1616_1731+161 others(8): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 13/19 | chr10 | 31816168 | ||||||
| chr10:31816168
|
C | CGTGTGT | 31 | a0001c0001t0001g0119a0001c0001t0001g0135a0001c0001t0001g0142others(28): Show | 31 | HG00099.hp1 HG00639.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.1731+1614_1731+161 others(10): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 13/19 | chr10 | 31816168 | ||||||
| chr10:31816168
|
C | CGTGTGTG others(1): Show |
73 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0088others(70): Show | 73 | HG00597.hp1 HG00621.hp1 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.1731+1612_1731+161 others(12): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 13/19 | chr10 | 31816168 | ||||||
| chr10:31816168
|
C | CGTGTGTG others(3): Show |
45 | a0001c0001t0001g0096a0001c0001t0001g0099a0001c0001t0001g0101others(42): Show | 45 | HG00544.hp2 HG00597.hp2 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.1731+1610_1731+161 others(14): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 13/19 | chr10 | 31816168 | ||||||
| chr10:31816168
|
C | CGTGTGTG others(5): Show |
11 | a0001c0001t0001g0100a0001c0001t0001g0111a0001c0001t0001g0126others(8): Show | 11 | HG02055.hp1 HG02451.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.1731+1608_1731+161 others(16): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 13/19 | chr10 | 31816168 | ||||||
| chr10:31816168
|
C | CGTGTGTG others(7): Show |
5 | a0001c0001t0001g0130a0001c0001t0001g0220a0002c0002t0002g0266others(2): Show | 5 | HG00741.hp2 HG02300.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1731+1606_1731+161 others(18): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 13/19 | chr10 | 31816168 | ||||||
| chr10:31816168
|
C | CGTGTGTG others(9): Show |
1 | a0001c0001t0008g0136 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1731+1604_1731+161 others(20): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 13/19 | chr10 | 31816168 | ||||||
| chr10:31816168
|
C | CGTGTGTG others(11): Show |
3 | a0001c0001t0001g0228a0001c0001t0001g0230a0002c0002t0055g0321 | 3 | HG01175.hp2 HG01192.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.1731+1602_1731+161 others(22): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 13/19 | chr10 | 31816168 | ||||||
| chr10:31816168
|
C | CGTGTGTG others(15): Show |
1 | a0001c0001t0001g0232 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1731+1598_1731+161 others(26): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 13/19 | chr10 | 31816168 | ||||||
| chr10:31816168
|
CGT | C | 22 | a0001c0001t0003g0233a0001c0001t0003g0234a0001c0001t0004g0030others(19): Show | 22 | HG01081.hp2 HG01257.hp2 HG01258.hp2 others(19): Show |
intron_variant | MODIFIER | c.1731+1618_1731+161 others(6): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 13/19 | chr10 | 31816168 | ||||||
| chr10:31816168
|
CGTGT | C | 12 | a0001c0001t0003g0026a0001c0001t0004g0044a0001c0001t0005g0045others(9): Show | 12 | HG01109.hp1 HG01168.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.1731+1616_1731+161 others(8): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 13/19 | chr10 | 31816168 | ||||||
| chr10:31816168
|
CGTGTGTG others(7): Show |
C | 1 | a0001c0001t0017g0050 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1731+1606_1731+161 others(18): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 13/19 | chr10 | 31816168 | ||||||
| chr10:31816316
|
T | C | 2 | a0001c0001t0049g0029a0001c0001t0050g0028 | 2 | HG02145.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1731+1472A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 13/19 | chr10 | 31816316 | ||||||
| chr10:31816365
|
C | A | 15 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(12): Show | 15 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1731+1423G>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 13/19 | chr10 | 31816365 | ||||||
| chr10:31816452
|
T | C | 278 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0088others(275): Show | 278 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.1731+1336A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 13/19 | chr10 | 31816452 | ||||||
| chr10:31816475
|
T | C | 2 | a0001c0001t0005g0063a0001c0001t0005g0235 | 2 | HG01934.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.1731+1313A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 13/19 | chr10 | 31816475 | ||||||
| chr10:31816641
|
G | A | 1 | a0001c0014t0004g0013 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1731+1147C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 13/19 | chr10 | 31816641 | ||||||
| chr10:31816642
|
C | T | 161 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(158): Show | 161 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(158): Show |
intron_variant | MODIFIER | c.1731+1146G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 13/19 | chr10 | 31816642 | ||||||
| chr10:31816734
|
A | G | 1 | a0002c0002t0002g0247 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1731+1054T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 13/19 | chr10 | 31816734 | ||||||
| chr10:31816739
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1731+1049C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 13/19 | chr10 | 31816739 | ||||||
| chr10:31816790
|
T | C | 50 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(47): Show | 50 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.1731+998A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 13/19 | chr10 | 31816790 | ||||||
| chr10:31817168
|
G | A | 1 | a0001c0001t0001g0088 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1731+620C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 13/19 | chr10 | 31817168 | ||||||
| chr10:31817190
|
T | G | 1 | a0001c0001t0001g0148 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1731+598A>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 13/19 | chr10 | 31817190 | ||||||
| chr10:31817213
|
A | G | 11 | a0001c0001t0009g0032a0001c0001t0009g0072a0001c0001t0009g0073others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1731+575T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 13/19 | chr10 | 31817213 | ||||||
| chr10:31817435
|
C | T | 1 | a0001c0001t0043g0025 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1731+353G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 13/19 | chr10 | 31817435 | ||||||
| chr10:31817647
|
C | T | 146 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(143): Show | 146 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(143): Show |
intron_variant | MODIFIER | c.1731+141G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 13/19 | chr10 | 31817647 | ||||||
| chr10:31817729
|
T | TA | 16 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(13): Show | 16 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.1731+58dupT | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 13/19 | chr10 | 31817729 | ||||||
| chr10:31817780
|
C | A | 15 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(12): Show | 15 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
splice_region_variant&intron_variant | LOW | c.1731+8G>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 13/19 | chr10 | 31817780 | ||||||
| chr10:31817923
|
A | G | 161 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(158): Show | 161 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(158): Show |
intron_variant | MODIFIER | c.1633-37T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 12/19 | chr10 | 31817923 | ||||||
| chr10:31817974
|
A | T | 15 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(12): Show | 15 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1633-88T>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 12/19 | chr10 | 31817974 | ||||||
| chr10:31818031
|
C | T | 1 | a0002c0002t0007g0316 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1633-145G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 12/19 | chr10 | 31818031 | ||||||
| chr10:31818073
|
G | A | 1 | a0001c0001t0040g0212 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1633-187C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 12/19 | chr10 | 31818073 | ||||||
| chr10:31818136
|
C | T | 1 | a0001c0001t0011g0071 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1633-250G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 12/19 | chr10 | 31818136 | ||||||
| chr10:31818536
|
A | G | 15 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(12): Show | 15 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1633-650T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 12/19 | chr10 | 31818536 | ||||||
| chr10:31818784
|
C | T | 146 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(143): Show | 146 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(143): Show |
intron_variant | MODIFIER | c.1633-898G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 12/19 | chr10 | 31818784 | ||||||
| chr10:31818969
|
C | T | 15 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(12): Show | 15 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1633-1083G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 12/19 | chr10 | 31818969 | ||||||
| chr10:31819062
|
C | G | 15 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(12): Show | 15 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1633-1176G>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 12/19 | chr10 | 31819062 | ||||||
| chr10:31819150
|
A | G | 15 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(12): Show | 15 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1632+1237T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 12/19 | chr10 | 31819150 | ||||||
| chr10:31819235
|
G | A | 11 | a0001c0001t0009g0032a0001c0001t0009g0072a0001c0001t0009g0073others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1632+1152C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 12/19 | chr10 | 31819235 | ||||||
| chr10:31819261
|
C | T | 1 | a0001c0001t0001g0110 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1632+1126G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 12/19 | chr10 | 31819261 | ||||||
| chr10:31819490
|
C | T | 2 | a0001c0001t0004g0036a0001c0001t0037g0035 | 2 | HG02258.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1632+897G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 12/19 | chr10 | 31819490 | ||||||
| chr10:31819586
|
C | T | 4 | a0001c0001t0023g0040a0001c0001t0023g0069a0001c0001t0024g0060others(1): Show | 4 | HG02572.hp2 HG02622.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1632+801G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 12/19 | chr10 | 31819586 | ||||||
| chr10:31819675
|
C | T | 7 | a0002c0002t0002g0250a0002c0002t0002g0260a0002c0002t0002g0261others(4): Show | 7 | HG01123.hp2 HG01257.hp1 NA18952.hp2 others(4): Show |
intron_variant | MODIFIER | c.1632+712G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 12/19 | chr10 | 31819675 | ||||||
| chr10:31819710
|
A | G | 1 | a0001c0001t0006g0159 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1632+677T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 12/19 | chr10 | 31819710 | ||||||
| chr10:31819786
|
A | C | 1 | a0002c0002t0007g0297 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1632+601T>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 12/19 | chr10 | 31819786 | ||||||
| chr10:31819955
|
TA | T | 90 | a0001c0001t0023g0040a0001c0001t0023g0069a0001c0001t0024g0042others(87): Show | 90 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(87): Show |
intron_variant | MODIFIER | c.1632+431delT | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 12/19 | chr10 | 31819955 | ||||||
| chr10:31819989
|
T | G | 50 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(47): Show | 50 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.1632+398A>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 12/19 | chr10 | 31819989 | ||||||
| chr10:31820086
|
T | C | 15 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(12): Show | 15 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1632+301A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 12/19 | chr10 | 31820086 | ||||||
| chr10:31820339
|
C | T | 2 | a0001c0001t0005g0063a0001c0001t0005g0235 | 2 | HG01934.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.1632+48G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 12/19 | chr10 | 31820339 | ||||||
| chr10:31820349
|
A | G | 3 | a0003c0004t0007g0309a0003c0004t0007g0310a0003c0004t0007g0311 | 3 | HG01109.hp2 HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1632+38T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 12/19 | chr10 | 31820349 | ||||||
| chr10:31820641
|
A | G | 2 | a0001c0001t0049g0029a0001c0001t0050g0028 | 2 | HG02145.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1531-153T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 11/19 | chr10 | 31820641 | ||||||
| chr10:31820683
|
G | A | 11 | a0001c0001t0009g0032a0001c0001t0009g0072a0001c0001t0009g0073others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1531-195C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 11/19 | chr10 | 31820683 | ||||||
| chr10:31820712
|
T | TTA | 5 | a0001c0001t0012g0027a0001c0001t0012g0227a0001c0001t0034g0033others(2): Show | 5 | HG02280.hp2 HG03579.hp1 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.1531-226_1531-225d others(4): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 11/19 | chr10 | 31820712 | ||||||
| chr10:31820712
|
TTA | T | 77 | a0001c0001t0001g0104a0001c0001t0001g0118a0001c0001t0001g0121others(74): Show | 77 | HG00597.hp1 HG00597.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.1531-226_1531-225d others(4): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 11/19 | chr10 | 31820712 | ||||||
| chr10:31820712
|
TTATA | T | 111 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0088others(108): Show | 111 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.1531-228_1531-225d others(6): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 11/19 | chr10 | 31820712 | ||||||
| chr10:31820712
|
TTATATA | T | 66 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(63): Show | 66 | HG00099.hp2 HG00735.hp2 HG01081.hp2 others(63): Show |
intron_variant | MODIFIER | c.1531-230_1531-225d others(8): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 11/19 | chr10 | 31820712 | ||||||
| chr10:31820720
|
A | T | 50 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(47): Show | 50 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.1531-232T>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 11/19 | chr10 | 31820720 | ||||||
| chr10:31820832
|
C | T | 15 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(12): Show | 15 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1531-344G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 11/19 | chr10 | 31820832 | ||||||
| chr10:31820913
|
C | A | 2 | a0002c0002t0002g0251a0002c0002t0002g0252 | 2 | NA18940.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.1531-425G>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 11/19 | chr10 | 31820913 | ||||||
| chr10:31820923
|
G | C | 3 | a0001c0001t0017g0050a0001c0001t0017g0053a0001c0001t0017g0062 | 3 | HG02970.hp2 HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1531-435C>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 11/19 | chr10 | 31820923 | ||||||
| chr10:31820966
|
T | A | 2 | a0002c0002t0002g0245a0002c0002t0002g0289 | 2 | HG04199.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1531-478A>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 11/19 | chr10 | 31820966 | ||||||
| chr10:31821208
|
G | C | 15 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(12): Show | 15 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1531-720C>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 11/19 | chr10 | 31821208 | ||||||
| chr10:31821412
|
C | T | 3 | a0001c0001t0003g0169a0001c0001t0003g0181a0001c0001t0031g0001 | 3 | HG00544.hp1 HG02135.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.1531-924G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 11/19 | chr10 | 31821412 | ||||||
| chr10:31821427
|
G | C | 50 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(47): Show | 50 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.1531-939C>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 11/19 | chr10 | 31821427 | ||||||
| chr10:31821511
|
T | C | 2 | a0001c0001t0049g0029a0001c0001t0050g0028 | 2 | HG02145.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1531-1023A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 11/19 | chr10 | 31821511 | ||||||
| chr10:31821704
|
T | C | 1 | a0001c0001t0001g0226 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1531-1216A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 11/19 | chr10 | 31821704 | ||||||
| chr10:31821792
|
A | G | 1 | a0002c0002t0002g0302 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1531-1304T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 11/19 | chr10 | 31821792 | ||||||
| chr10:31821869
|
C | G | 2 | a0001c0001t0003g0181a0001c0001t0031g0001 | 2 | HG00544.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.1531-1381G>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 11/19 | chr10 | 31821869 | ||||||
| chr10:31821979
|
C | T | 161 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(158): Show | 161 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(158): Show |
intron_variant | MODIFIER | c.1531-1491G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 11/19 | chr10 | 31821979 | ||||||
| chr10:31821989
|
G | A | 1 | a0002c0002t0002g0301 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1531-1501C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 11/19 | chr10 | 31821989 | ||||||
| chr10:31822079
|
T | TAA | 15 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(12): Show | 15 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1531-1593_1531-159 others(6): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 11/19 | chr10 | 31822079 | ||||||
| chr10:31822119
|
G | A | 11 | a0001c0001t0009g0032a0001c0001t0009g0072a0001c0001t0009g0073others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1531-1631C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 11/19 | chr10 | 31822119 | ||||||
| chr10:31822163
|
T | C | 9 | a0001c0001t0001g0215a0001c0001t0001g0217a0001c0001t0001g0218others(6): Show | 9 | HG00738.hp1 HG00741.hp1 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.1531-1675A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 11/19 | chr10 | 31822163 | ||||||
| chr10:31822170
|
C | T | 18 | a0001c0001t0004g0044a0001c0001t0005g0043a0001c0001t0005g0045others(15): Show | 18 | HG01109.hp1 HG01168.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.1531-1682G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 11/19 | chr10 | 31822170 | ||||||
| chr10:31822270
|
T | G | 1 | a0002c0002t0002g0258 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1531-1782A>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 11/19 | chr10 | 31822270 | ||||||
| chr10:31822290
|
G | A | 1 | a0001c0001t0040g0212 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1531-1802C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 11/19 | chr10 | 31822290 | ||||||
| chr10:31822354
|
T | C | 1 | a0002c0002t0002g0277 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1531-1866A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 11/19 | chr10 | 31822354 | ||||||
| chr10:31822459
|
A | G | 15 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(12): Show | 15 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1531-1971T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 11/19 | chr10 | 31822459 | ||||||
| chr10:31822464
|
T | C | 113 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0088others(110): Show | 113 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.1531-1976A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 11/19 | chr10 | 31822464 | ||||||
| chr10:31822663
|
G | T | 1 | a0001c0001t0003g0173 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1531-2175C>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 11/19 | chr10 | 31822663 | ||||||
| chr10:31822873
|
T | C | 2 | a0001c0001t0013g0093a0001c0001t0013g0094 | 2 | NA18952.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.1531-2385A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 11/19 | chr10 | 31822873 | ||||||
| chr10:31822996
|
G | T | 2 | a0001c0001t0003g0026a0001c0001t0012g0027 | 2 | HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1531-2508C>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 11/19 | chr10 | 31822996 | ||||||
| chr10:31823045
|
A | G | 1 | a0001c0001t0009g0032 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1531-2557T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 11/19 | chr10 | 31823045 | ||||||
| chr10:31823238
|
A | T | 101 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0088others(98): Show | 101 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.1531-2750T>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 11/19 | chr10 | 31823238 | ||||||
| chr10:31823250
|
A | G | 11 | a0001c0001t0009g0032a0001c0001t0009g0072a0001c0001t0009g0073others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1531-2762T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 11/19 | chr10 | 31823250 | ||||||
| chr10:31823476
|
C | CAAA | 14 | a0001c0003t0010g0005a0001c0003t0010g0009a0001c0003t0010g0010others(11): Show | 14 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1530+2825_1530+282 others(7): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 11/19 | chr10 | 31823476 | ||||||
| chr10:31823504
|
T | C | 1 | a0001c0001t0022g0002 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1530+2800A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 11/19 | chr10 | 31823504 | ||||||
| chr10:31823573
|
C | A | 1 | a0003c0004t0007g0309 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1530+2731G>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 11/19 | chr10 | 31823573 | ||||||
| chr10:31823790
|
A | G | 1 | a0002c0002t0007g0297 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1530+2514T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 11/19 | chr10 | 31823790 | ||||||
| chr10:31823800
|
C | T | 82 | a0002c0002t0002g0243a0002c0002t0002g0245a0002c0002t0002g0247others(79): Show | 82 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.1530+2504G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 11/19 | chr10 | 31823800 | ||||||
| chr10:31823952
|
C | T | 2 | a0001c0001t0049g0029a0001c0001t0050g0028 | 2 | HG02145.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1530+2352G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 11/19 | chr10 | 31823952 | ||||||
| chr10:31824101
|
A | G | 110 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0088others(107): Show | 110 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.1530+2203T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 11/19 | chr10 | 31824101 | ||||||
| chr10:31824195
|
A | T | 15 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(12): Show | 15 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1530+2109T>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 11/19 | chr10 | 31824195 | ||||||
| chr10:31824230
|
G | A | 1 | a0001c0001t0001g0215 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1530+2074C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 11/19 | chr10 | 31824230 | ||||||
| chr10:31824238
|
C | T | 15 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(12): Show | 15 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1530+2066G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 11/19 | chr10 | 31824238 | ||||||
| chr10:31824461
|
G | C | 1 | a0001c0013t0015g0154 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1530+1843C>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 11/19 | chr10 | 31824461 | ||||||
| chr10:31824506
|
A | G | 3 | a0002c0002t0007g0313a0002c0002t0007g0314a0002c0002t0007g0316 | 3 | HG02074.hp2 HG03834.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.1530+1798T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 11/19 | chr10 | 31824506 | ||||||
| chr10:31825193
|
T | C | 100 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(97): Show | 100 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(97): Show |
intron_variant | MODIFIER | c.1530+1111A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 11/19 | chr10 | 31825193 | ||||||
| chr10:31825388
|
G | A | 50 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(47): Show | 50 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.1530+916C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 11/19 | chr10 | 31825388 | ||||||
| chr10:31825603
|
C | T | 3 | a0002c0002t0002g0256a0002c0002t0002g0257a0002c0002t0002g0259 | 3 | NA18944.hp2 NA19058.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1530+701G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 11/19 | chr10 | 31825603 | ||||||
| chr10:31825651
|
C | T | 112 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0088others(109): Show | 112 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.1530+653G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 11/19 | chr10 | 31825651 | ||||||
| chr10:31825832
|
T | C | 15 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(12): Show | 15 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1530+472A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 11/19 | chr10 | 31825832 | ||||||
| chr10:31825999
|
C | T | 1 | a0001c0001t0003g0234 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1530+305G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 11/19 | chr10 | 31825999 | ||||||
| chr10:31826022
|
A | G | 85 | a0001c0007t0028g0239a0001c0007t0028g0240a0001c0010t0053g0238others(82): Show | 85 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.1530+282T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 11/19 | chr10 | 31826022 | ||||||
| chr10:31826205
|
A | G | 273 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0088others(270): Show | 273 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.1530+99T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 11/19 | chr10 | 31826205 | ||||||
| chr10:31826212
|
T | C | 1 | a0001c0001t0022g0174 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1530+92A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 11/19 | chr10 | 31826212 | ||||||
| chr10:31826419
|
A | G | 11 | a0001c0001t0009g0032a0001c0001t0009g0072a0001c0001t0009g0073others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1449-34T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 10/19 | chr10 | 31826419 | ||||||
| chr10:31826619
|
A | G | 1 | a0002c0002t0002g0278 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1449-234T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 10/19 | chr10 | 31826619 | ||||||
| chr10:31826649
|
T | C | 1 | a0001c0001t0049g0029 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1449-264A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 10/19 | chr10 | 31826649 | ||||||
| chr10:31826655
|
C | A | 5 | a0001c0001t0003g0185a0001c0001t0003g0189a0001c0001t0003g0190others(2): Show | 5 | NA18947.hp1 NA18957.hp2 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1449-270G>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 10/19 | chr10 | 31826655 | ||||||
| chr10:31826725
|
T | C | 1 | a0001c0001t0043g0025 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1449-340A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 10/19 | chr10 | 31826725 | ||||||
| chr10:31827073
|
C | A | 110 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0088others(107): Show | 110 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.1449-688G>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 10/19 | chr10 | 31827073 | ||||||
| chr10:31827357
|
A | C | 1 | a0001c0001t0012g0027 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1449-972T>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 10/19 | chr10 | 31827357 | ||||||
| chr10:31827545
|
A | C | 1 | a0001c0003t0016g0004 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1449-1160T>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 10/19 | chr10 | 31827545 | ||||||
| chr10:31827622
|
T | C | 1 | a0001c0001t0001g0204 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1449-1237A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 10/19 | chr10 | 31827622 | ||||||
| chr10:31827794
|
G | GA | 6 | a0001c0001t0003g0180a0001c0001t0003g0198a0001c0001t0012g0187others(3): Show | 6 | HG02071.hp2 HG02738.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1449-1410dupT | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 10/19 | chr10 | 31827794 | ||||||
| chr10:31827803
|
AC | A | 8 | a0001c0003t0010g0005a0001c0003t0010g0009a0001c0003t0010g0010others(5): Show | 8 | HG02257.hp2 HG02451.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1449-1419delG | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 10/19 | chr10 | 31827803 | ||||||
| chr10:31827804
|
C | A | 7 | a0001c0003t0010g0006a0001c0003t0010g0016a0001c0003t0010g0017others(4): Show | 7 | HG00735.hp2 HG02723.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1449-1419G>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 10/19 | chr10 | 31827804 | ||||||
| chr10:31827810
|
C | A | 15 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(12): Show | 15 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1449-1425G>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 10/19 | chr10 | 31827810 | ||||||
| chr10:31827913
|
C | G | 1 | a0002c0002t0021g0279 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1449-1528G>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 10/19 | chr10 | 31827913 | ||||||
| chr10:31827937
|
T | G | 15 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(12): Show | 15 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1449-1552A>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 10/19 | chr10 | 31827937 | ||||||
| chr10:31827938
|
AAGTGAAA others(17): Show |
A | 7 | a0001c0001t0003g0185a0001c0001t0003g0188a0001c0001t0003g0189others(4): Show | 7 | NA18947.hp1 NA18957.hp2 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1449-1577_1449-155 others(28): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 10/19 | chr10 | 31827938 | ||||||
| chr10:31827971
|
A | G | 9 | a0001c0001t0001g0215a0001c0001t0001g0217a0001c0001t0001g0218others(6): Show | 9 | HG00738.hp1 HG00741.hp1 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.1449-1586T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 10/19 | chr10 | 31827971 | ||||||
| chr10:31828219
|
C | CT | 163 | a0001c0001t0001g0135a0001c0001t0001g0142a0001c0001t0004g0019others(160): Show | 163 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(160): Show |
intron_variant | MODIFIER | c.1449-1835dupA | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 10/19 | chr10 | 31828219 | ||||||
| chr10:31828219
|
C | CTT | 111 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0088others(108): Show | 111 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.1449-1836_1449-183 others(6): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 10/19 | chr10 | 31828219 | ||||||
| chr10:31828629
|
A | G | 15 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(12): Show | 15 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1449-2244T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 10/19 | chr10 | 31828629 | ||||||
| chr10:31828670
|
C | G | 2 | a0001c0001t0001g0226a0001c0001t0008g0152 | 2 | HG01884.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1449-2285G>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 10/19 | chr10 | 31828670 | ||||||
| chr10:31828694
|
C | T | 1 | a0001c0001t0001g0226 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1449-2309G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 10/19 | chr10 | 31828694 | ||||||
| chr10:31828821
|
A | T | 146 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(143): Show | 146 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(143): Show |
intron_variant | MODIFIER | c.1449-2436T>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 10/19 | chr10 | 31828821 | ||||||
| chr10:31828881
|
G | A | 10 | a0001c0001t0009g0032a0001c0001t0009g0072a0001c0001t0009g0073others(7): Show | 10 | HG02145.hp1 HG02257.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1449-2496C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 10/19 | chr10 | 31828881 | ||||||
| chr10:31828981
|
G | A | 4 | a0002c0002t0007g0308a0003c0004t0007g0309a0003c0004t0007g0310others(1): Show | 4 | HG01109.hp2 HG03130.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1449-2596C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 10/19 | chr10 | 31828981 | ||||||
| chr10:31829117
|
A | C | 1 | a0001c0001t0043g0025 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1448+2622T>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 10/19 | chr10 | 31829117 | ||||||
| chr10:31829154
|
A | AAAC | 104 | a0001c0001t0003g0120a0001c0001t0003g0182a0001c0001t0009g0032others(101): Show | 104 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(101): Show |
intron_variant | MODIFIER | c.1448+2582_1448+258 others(7): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 10/19 | chr10 | 31829154 | ||||||
| chr10:31829154
|
AAACAACA others(5): Show |
A | 1 | a0001c0001t0003g0168 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1448+2573_1448+258 others(16): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 10/19 | chr10 | 31829154 | ||||||
| chr10:31829581
|
GACAGTAC others(14): Show |
G | 1 | a0001c0001t0049g0029 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1448+2137_1448+215 others(25): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 10/19 | chr10 | 31829581 | ||||||
| chr10:31829666
|
T | C | 1 | a0001c0001t0001g0121 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1448+2073A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 10/19 | chr10 | 31829666 | ||||||
| chr10:31829842
|
G | A | 1 | a0001c0001t0025g0202 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1448+1897C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 10/19 | chr10 | 31829842 | ||||||
| chr10:31829886
|
T | C | 15 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(12): Show | 15 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1448+1853A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 10/19 | chr10 | 31829886 | ||||||
| chr10:31830010
|
CA | C | 128 | a0001c0001t0004g0034a0001c0001t0004g0044a0001c0001t0005g0043others(125): Show | 128 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(125): Show |
intron_variant | MODIFIER | c.1448+1728delT | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 10/19 | chr10 | 31830010 | ||||||
| chr10:31830042
|
T | C | 1 | a0001c0001t0034g0033 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1448+1697A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 10/19 | chr10 | 31830042 | ||||||
| chr10:31830080
|
A | T | 1 | a0001c0003t0010g0009 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1448+1659T>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 10/19 | chr10 | 31830080 | ||||||
| chr10:31830194
|
C | G | 1 | a0001c0001t0001g0138 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1448+1545G>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 10/19 | chr10 | 31830194 | ||||||
| chr10:31830436
|
C | T | 1 | a0005c0009t0012g0179 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1448+1303G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 10/19 | chr10 | 31830436 | ||||||
| chr10:31830523
|
T | C | 2 | a0001c0007t0028g0239a0001c0007t0028g0240 | 2 | HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1448+1216A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 10/19 | chr10 | 31830523 | ||||||
| chr10:31830533
|
A | C | 15 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(12): Show | 15 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1448+1206T>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 10/19 | chr10 | 31830533 | ||||||
| chr10:31830612
|
C | T | 1 | a0002c0002t0002g0245 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1448+1127G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 10/19 | chr10 | 31830612 | ||||||
| chr10:31830685
|
G | C | 1 | a0001c0003t0010g0016 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1448+1054C>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 10/19 | chr10 | 31830685 | ||||||
| chr10:31830845
|
A | T | 101 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0088others(98): Show | 101 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.1448+894T>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 10/19 | chr10 | 31830845 | ||||||
| chr10:31831124
|
T | C | 1 | a0001c0001t0004g0066 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1448+615A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 10/19 | chr10 | 31831124 | ||||||
| chr10:31831127
|
C | T | 3 | a0001c0001t0001g0132a0001c0001t0008g0098a0001c0001t0041g0144 | 3 | NA18960.hp2 NA19065.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.1448+612G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 10/19 | chr10 | 31831127 | ||||||
| chr10:31831325
|
T | C | 5 | a0002c0002t0002g0250a0002c0002t0002g0260a0002c0002t0002g0261others(2): Show | 5 | NA18952.hp2 NA18961.hp2 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.1448+414A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 10/19 | chr10 | 31831325 | ||||||
| chr10:31831395
|
G | A | 1 | a0001c0003t0048g0015 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1448+344C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 10/19 | chr10 | 31831395 | ||||||
| chr10:31831428
|
C | T | 1 | a0001c0001t0034g0033 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1448+311G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 10/19 | chr10 | 31831428 | ||||||
| chr10:31831481
|
G | GA | 21 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(18): Show | 21 | HG00099.hp2 HG01081.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.1448+257dupT | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 10/19 | chr10 | 31831481 | ||||||
| chr10:31831654
|
T | C | 15 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(12): Show | 15 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1448+85A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 10/19 | chr10 | 31831654 | ||||||
| chr10:31831862
|
C | T | 15 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(12): Show | 15 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1387-62G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31831862 | ||||||
| chr10:31831928
|
A | G | 1 | a0001c0001t0052g0318 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1387-128T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31831928 | ||||||
| chr10:31831939
|
T | C | 5 | a0002c0002t0002g0267a0002c0002t0002g0268a0002c0002t0002g0269others(2): Show | 5 | HG00738.hp2 HG01081.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.1387-139A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31831939 | ||||||
| chr10:31831979
|
G | A | 1 | a0001c0001t0004g0034 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1387-179C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31831979 | ||||||
| chr10:31832215
|
C | T | 5 | a0001c0001t0023g0040a0001c0001t0023g0069a0001c0001t0024g0042others(2): Show | 5 | HG02572.hp2 HG02622.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1387-415G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31832215 | ||||||
| chr10:31832275
|
A | C | 101 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0088others(98): Show | 101 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.1387-475T>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31832275 | ||||||
| chr10:31832411
|
T | G | 1 | a0001c0001t0006g0150 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1387-611A>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31832411 | ||||||
| chr10:31832659
|
G | A | 15 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(12): Show | 15 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1387-859C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31832659 | ||||||
| chr10:31832906
|
G | A | 7 | a0001c0001t0011g0055a0001c0001t0011g0056a0001c0001t0011g0057others(4): Show | 7 | HG01884.hp1 HG01891.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1387-1106C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31832906 | ||||||
| chr10:31832907
|
G | A | 1 | a0001c0001t0043g0025 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1387-1107C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31832907 | ||||||
| chr10:31832982
|
A | G | 1 | a0001c0001t0025g0156 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1387-1182T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31832982 | ||||||
| chr10:31833086
|
T | A | 3 | a0001c0001t0001g0228a0001c0001t0001g0230a0001c0001t0006g0206 | 3 | HG01175.hp2 HG01192.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1387-1286A>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31833086 | ||||||
| chr10:31833280
|
G | A | 1 | a0001c0001t0001g0213 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1387-1480C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31833280 | ||||||
| chr10:31833332
|
A | AT | 55 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(52): Show | 55 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(52): Show |
intron_variant | MODIFIER | c.1387-1533dupA | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31833332 | ||||||
| chr10:31833334
|
T | TTA | 91 | a0001c0001t0009g0032a0001c0001t0009g0072a0001c0001t0009g0073others(88): Show | 91 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(88): Show |
intron_variant | MODIFIER | c.1387-1535_1387-153 others(6): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31833334 | ||||||
| chr10:31833334
|
TA | T | 15 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(12): Show | 15 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1387-1535delT | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31833334 | ||||||
| chr10:31833491
|
T | C | 161 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(158): Show | 161 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(158): Show |
intron_variant | MODIFIER | c.1387-1691A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31833491 | ||||||
| chr10:31834172
|
C | T | 1 | a0002c0002t0002g0262 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1387-2372G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31834172 | ||||||
| chr10:31834271
|
G | A | 15 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(12): Show | 15 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1387-2471C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31834271 | ||||||
| chr10:31834280
|
T | C | 101 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0088others(98): Show | 101 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.1387-2480A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31834280 | ||||||
| chr10:31834300
|
C | T | 112 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0088others(109): Show | 112 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.1387-2500G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31834300 | ||||||
| chr10:31834342
|
G | T | 3 | a0002c0002t0002g0274a0002c0002t0002g0277a0002c0002t0002g0296 | 3 | NA19000.hp2 NA19078.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1387-2542C>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31834342 | ||||||
| chr10:31834557
|
A | G | 1 | a0002c0002t0020g0315 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1387-2757T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31834557 | ||||||
| chr10:31834627
|
C | T | 50 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(47): Show | 50 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.1387-2827G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31834627 | ||||||
| chr10:31834969
|
C | T | 2 | a0001c0001t0004g0066a0001c0001t0004g0068 | 2 | HG02602.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.1387-3169G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31834969 | ||||||
| chr10:31835025
|
C | T | 10 | a0001c0001t0009g0032a0001c0001t0009g0072a0001c0001t0009g0073others(7): Show | 10 | HG02145.hp1 HG02257.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1387-3225G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31835025 | ||||||
| chr10:31835192
|
C | T | 18 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(15): Show | 18 | HG00099.hp2 HG01081.hp2 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.1387-3392G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31835192 | ||||||
| chr10:31835202
|
G | GA | 6 | a0001c0001t0001g0119a0001c0001t0003g0198a0001c0001t0019g0162others(3): Show | 6 | HG00733.hp1 HG01167.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1387-3403dupT | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31835202 | ||||||
| chr10:31835215
|
AAAG | A | 6 | a0001c0001t0004g0034a0001c0001t0023g0040a0001c0001t0023g0069others(3): Show | 6 | HG02572.hp2 HG02622.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1387-3418_1387-341 others(7): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31835215 | ||||||
| chr10:31835216
|
AAG | A | 43 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(40): Show | 43 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.1387-3418_1387-341 others(6): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31835216 | ||||||
| chr10:31835236
|
T | C | 50 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(47): Show | 50 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.1387-3436A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31835236 | ||||||
| chr10:31835349
|
A | G | 1 | a0001c0003t0010g0006 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1387-3549T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31835349 | ||||||
| chr10:31835606
|
A | G | 1 | a0001c0001t0036g0041 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1386+3699T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31835606 | ||||||
| chr10:31835719
|
T | C | 1 | a0001c0001t0043g0025 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1386+3586A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31835719 | ||||||
| chr10:31835931
|
C | T | 1 | a0002c0002t0002g0317 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1386+3374G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31835931 | ||||||
| chr10:31835966
|
C | T | 161 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(158): Show | 161 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(158): Show |
intron_variant | MODIFIER | c.1386+3339G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31835966 | ||||||
| chr10:31836325
|
A | G | 15 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(12): Show | 15 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1386+2980T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31836325 | ||||||
| chr10:31836386
|
AAATAT | A | 5 | a0001c0001t0003g0026a0001c0001t0012g0027a0001c0001t0045g0076others(2): Show | 5 | HG02145.hp2 HG03516.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1386+2914_1386+291 others(9): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31836386 | ||||||
| chr10:31836419
|
C | G | 2 | a0001c0001t0004g0020a0001c0001t0004g0021 | 2 | HG03710.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1386+2886G>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31836419 | ||||||
| chr10:31836588
|
A | AG | 272 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0088others(269): Show | 272 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.1386+2716dupC | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31836588 | ||||||
| chr10:31836594
|
G | A | 272 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0088others(269): Show | 272 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.1386+2711C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31836594 | ||||||
| chr10:31836664
|
A | G | 1 | a0002c0002t0002g0266 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1386+2641T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31836664 | ||||||
| chr10:31836668
|
A | G | 112 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0088others(109): Show | 112 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.1386+2637T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31836668 | ||||||
| chr10:31836685
|
A | C | 1 | a0002c0002t0029g0244 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1386+2620T>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31836685 | ||||||
| chr10:31836768
|
G | C | 1 | a0001c0001t0046g0223 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1386+2537C>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31836768 | ||||||
| chr10:31836875
|
A | G | 277 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0088others(274): Show | 277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.1386+2430T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31836875 | ||||||
| chr10:31836957
|
G | T | 6 | a0001c0001t0001g0215a0001c0001t0001g0218a0001c0001t0006g0214others(3): Show | 6 | HG00741.hp1 HG01123.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1386+2348C>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31836957 | ||||||
| chr10:31836964
|
A | C | 1 | a0001c0014t0004g0013 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1386+2341T>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31836964 | ||||||
| chr10:31837374
|
A | G | 5 | a0001c0001t0023g0040a0001c0001t0023g0069a0001c0001t0024g0042others(2): Show | 5 | HG02572.hp2 HG02622.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1386+1931T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31837374 | ||||||
| chr10:31837538
|
G | A | 3 | a0001c0007t0028g0239a0001c0007t0028g0240a0001c0010t0053g0238 | 3 | HG02572.hp1 HG02886.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1386+1767C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31837538 | ||||||
| chr10:31837582
|
T | C | 1 | a0001c0010t0053g0238 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1386+1723A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31837582 | ||||||
| chr10:31837730
|
G | C | 112 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0088others(109): Show | 112 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.1386+1575C>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31837730 | ||||||
| chr10:31837921
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1386+1384C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31837921 | ||||||
| chr10:31838053
|
A | C | 112 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0088others(109): Show | 112 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.1386+1252T>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31838053 | ||||||
| chr10:31838141
|
C | G | 3 | a0001c0001t0001g0103a0001c0001t0001g0127a0001c0001t0001g0203 | 3 | NA18940.hp2 NA19058.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.1386+1164G>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31838141 | ||||||
| chr10:31838404
|
G | A | 2 | a0001c0007t0028g0239a0001c0007t0028g0240 | 2 | HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1386+901C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31838404 | ||||||
| chr10:31838589
|
G | C | 1 | a0002c0002t0007g0254 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1386+716C>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31838589 | ||||||
| chr10:31838830
|
CA | C | 168 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0088others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.1386+474delT | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31838830 | ||||||
| chr10:31838830
|
CAA | C | 98 | a0001c0001t0001g0135a0001c0001t0004g0066a0001c0001t0005g0063others(95): Show | 98 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.1386+473_1386+474d others(4): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31838830 | ||||||
| chr10:31838884
|
C | A | 3 | a0001c0001t0005g0045a0001c0001t0005g0047a0001c0001t0005g0048 | 3 | HG01109.hp1 HG01192.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.1386+421G>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31838884 | ||||||
| chr10:31839025
|
A | C | 82 | a0002c0002t0002g0243a0002c0002t0002g0245a0002c0002t0002g0247others(79): Show | 82 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.1386+280T>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31839025 | ||||||
| chr10:31839095
|
A | G | 273 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0088others(270): Show | 273 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.1386+210T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31839095 | ||||||
| chr10:31839923
|
C | T | 275 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0088others(272): Show | 275 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(272): Show |
intron_variant | MODIFIER | c.1297-212G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 7/19 | chr10 | 31839923 | ||||||
| chr10:31839931
|
T | G | 3 | a0001c0007t0028g0239a0001c0007t0028g0240a0001c0010t0053g0238 | 3 | HG02572.hp1 HG02886.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1297-220A>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 7/19 | chr10 | 31839931 | ||||||
| chr10:31840175
|
T | C | 1 | a0001c0001t0043g0025 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1297-464A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 7/19 | chr10 | 31840175 | ||||||
| chr10:31840215
|
T | C | 50 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(47): Show | 50 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.1297-504A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 7/19 | chr10 | 31840215 | ||||||
| chr10:31840306
|
T | A | 18 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(15): Show | 18 | HG00099.hp2 HG01081.hp2 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.1297-595A>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 7/19 | chr10 | 31840306 | ||||||
| chr10:31840355
|
G | GT | 90 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0088others(87): Show | 90 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.1297-645dupA | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 7/19 | chr10 | 31840355 | ||||||
| chr10:31840410
|
A | G | 1 | a0001c0003t0010g0005 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1297-699T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 7/19 | chr10 | 31840410 | ||||||
| chr10:31840680
|
G | A | 1 | a0001c0001t0001g0213 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1297-969C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 7/19 | chr10 | 31840680 | ||||||
| chr10:31840888
|
A | G | 1 | a0001c0001t0003g0026 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1297-1177T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 7/19 | chr10 | 31840888 | ||||||
| chr10:31840925
|
TTAAG | T | 3 | a0001c0001t0001g0226a0001c0001t0008g0152a0001c0001t0025g0202 | 3 | HG01884.hp2 HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1297-1218_1297-121 others(8): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 7/19 | chr10 | 31840925 | ||||||
| chr10:31840932
|
T | C | 1 | a0001c0001t0034g0033 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1297-1221A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 7/19 | chr10 | 31840932 | ||||||
| chr10:31841043
|
GAATAAAA others(6): Show |
G | 2 | a0001c0007t0028g0239a0001c0007t0028g0240 | 2 | HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1297-1345_1297-133 others(17): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 7/19 | chr10 | 31841043 | ||||||
| chr10:31841058
|
T | G | 2 | a0001c0007t0028g0239a0001c0007t0028g0240 | 2 | HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1297-1347A>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 7/19 | chr10 | 31841058 | ||||||
| chr10:31841059
|
A | C | 2 | a0001c0007t0028g0239a0001c0007t0028g0240 | 2 | HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1297-1348T>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 7/19 | chr10 | 31841059 | ||||||
| chr10:31841222
|
A | T | 18 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(15): Show | 18 | HG00099.hp2 HG01081.hp2 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.1297-1511T>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 7/19 | chr10 | 31841222 | ||||||
| chr10:31841445
|
G | C | 2 | a0001c0007t0028g0239a0001c0007t0028g0240 | 2 | HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1297-1734C>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 7/19 | chr10 | 31841445 | ||||||
| chr10:31841456
|
G | T | 11 | a0001c0001t0009g0032a0001c0001t0009g0072a0001c0001t0009g0073others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1297-1745C>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 7/19 | chr10 | 31841456 | ||||||
| chr10:31841815
|
G | A | 1 | a0001c0001t0024g0042 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1296+1646C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 7/19 | chr10 | 31841815 | ||||||
| chr10:31842048
|
G | A | 1 | a0001c0001t0004g0034 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1296+1413C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 7/19 | chr10 | 31842048 | ||||||
| chr10:31842109
|
T | C | 1 | a0001c0001t0018g0087 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1296+1352A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 7/19 | chr10 | 31842109 | ||||||
| chr10:31842189
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1296+1272A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 7/19 | chr10 | 31842189 | ||||||
| chr10:31842237
|
G | A | 1 | a0001c0001t0024g0042 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1296+1224C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 7/19 | chr10 | 31842237 | ||||||
| chr10:31842237
|
G | T | 1 | a0001c0001t0001g0096 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1296+1224C>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 7/19 | chr10 | 31842237 | ||||||
| chr10:31842259
|
G | C | 1 | a0001c0001t0025g0202 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1296+1202C>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 7/19 | chr10 | 31842259 | ||||||
| chr10:31842304
|
G | T | 2 | a0001c0001t0008g0134a0001c0001t0008g0136 | 2 | HG02027.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1296+1157C>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 7/19 | chr10 | 31842304 | ||||||
| chr10:31842810
|
C | G | 1 | a0001c0001t0005g0070 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1296+651G>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 7/19 | chr10 | 31842810 | ||||||
| chr10:31842821
|
A | G | 4 | a0001c0003t0010g0010a0001c0003t0010g0018a0001c0003t0027g0012others(1): Show | 4 | HG02615.hp1 HG02630.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1296+640T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 7/19 | chr10 | 31842821 | ||||||
| chr10:31842860
|
C | G | 2 | a0001c0001t0008g0134a0001c0001t0008g0136 | 2 | HG02027.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1296+601G>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 7/19 | chr10 | 31842860 | ||||||
| chr10:31843165
|
A | G | 1 | a0002c0002t0020g0255 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1296+296T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 7/19 | chr10 | 31843165 | ||||||
| chr10:31843384
|
A | G | 2 | a0001c0001t0001g0109a0001c0001t0001g0110 | 2 | NA18986.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.1296+77T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 7/19 | chr10 | 31843384 | ||||||
| chr10:31843402
|
G | T | 2 | a0001c0001t0049g0029a0001c0001t0050g0028 | 2 | HG02145.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1296+59C>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 7/19 | chr10 | 31843402 | ||||||
| chr10:31843458
|
T | C | 2 | a0001c0001t0001g0157a0001c0013t0015g0154 | 2 | HG00735.hp1 HG01071.hp1 |
splice_region_variant&intron_variant | LOW | c.1296+3A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 7/19 | chr10 | 31843458 | ||||||
| chr10:31843633
|
T | C | 1 | a0002c0002t0007g0313 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1171-47A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 6/19 | chr10 | 31843633 | ||||||
| chr10:31844082
|
A | G | 1 | a0001c0001t0005g0043 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1171-496T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 6/19 | chr10 | 31844082 | ||||||
| chr10:31844104
|
G | T | 1 | a0001c0001t0012g0027 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1171-518C>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 6/19 | chr10 | 31844104 | ||||||
| chr10:31844166
|
T | G | 1 | a0001c0001t0001g0110 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1171-580A>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 6/19 | chr10 | 31844166 | ||||||
| chr10:31844170
|
C | A | 3 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024 | 3 | HG01167.hp2 HG01175.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1171-584G>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 6/19 | chr10 | 31844170 | ||||||
| chr10:31844518
|
C | T | 5 | a0001c0001t0023g0040a0001c0001t0023g0069a0001c0001t0024g0042others(2): Show | 5 | HG02572.hp2 HG02622.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1171-932G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 6/19 | chr10 | 31844518 | ||||||
| chr10:31844583
|
G | C | 7 | a0001c0001t0011g0055a0001c0001t0011g0056a0001c0001t0011g0057others(4): Show | 7 | HG01884.hp1 HG01891.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1171-997C>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 6/19 | chr10 | 31844583 | ||||||
| chr10:31844697
|
C | CT | 11 | a0001c0001t0001g0111a0001c0001t0001g0114a0001c0001t0003g0182others(8): Show | 11 | HG02071.hp1 HG02074.hp1 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.1171-1112dupA | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 6/19 | chr10 | 31844697 | ||||||
| chr10:31844697
|
CT | C | 94 | a0001c0001t0009g0032a0001c0001t0009g0072a0001c0001t0009g0073others(91): Show | 94 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.1171-1112delA | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 6/19 | chr10 | 31844697 | ||||||
| chr10:31844739
|
C | T | 18 | a0001c0001t0004g0044a0001c0001t0005g0043a0001c0001t0005g0045others(15): Show | 18 | HG01109.hp1 HG01168.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.1171-1153G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 6/19 | chr10 | 31844739 | ||||||
| chr10:31844828
|
T | C | 146 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(143): Show | 146 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(143): Show |
intron_variant | MODIFIER | c.1171-1242A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 6/19 | chr10 | 31844828 | ||||||
| chr10:31845272
|
T | G | 1 | a0001c0001t0008g0152 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1171-1686A>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 6/19 | chr10 | 31845272 | ||||||
| chr10:31845554
|
A | G | 2 | a0002c0002t0002g0245a0002c0002t0002g0289 | 2 | HG04199.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1171-1968T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 6/19 | chr10 | 31845554 | ||||||
| chr10:31845613
|
T | A | 2 | a0001c0001t0001g0111a0001c0001t0001g0138 | 2 | NA18974.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.1171-2027A>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 6/19 | chr10 | 31845613 | ||||||
| chr10:31845630
|
C | T | 1 | a0002c0002t0007g0254 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1171-2044G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 6/19 | chr10 | 31845630 | ||||||
| chr10:31845667
|
C | A | 3 | a0002c0002t0007g0313a0002c0002t0007g0314a0002c0002t0007g0316 | 3 | HG02074.hp2 HG03834.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.1171-2081G>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 6/19 | chr10 | 31845667 | ||||||
| chr10:31845780
|
G | A | 11 | a0001c0001t0009g0032a0001c0001t0009g0072a0001c0001t0009g0073others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1171-2194C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 6/19 | chr10 | 31845780 | ||||||
| chr10:31845834
|
T | A | 1 | a0001c0001t0003g0120 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1171-2248A>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 6/19 | chr10 | 31845834 | ||||||
| chr10:31846004
|
T | C | 6 | a0001c0001t0003g0026a0001c0001t0012g0027a0001c0001t0025g0156others(3): Show | 6 | HG02145.hp2 HG02280.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.1171-2418A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 6/19 | chr10 | 31846004 | ||||||
| chr10:31846043
|
G | A | 11 | a0001c0001t0009g0032a0001c0001t0009g0072a0001c0001t0009g0073others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1171-2457C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 6/19 | chr10 | 31846043 | ||||||
| chr10:31846132
|
TA | T | 146 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(143): Show | 146 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(143): Show |
intron_variant | MODIFIER | c.1171-2547delT | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 6/19 | chr10 | 31846132 | ||||||
| chr10:31846417
|
C | A | 1 | a0001c0001t0040g0212 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1171-2831G>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 6/19 | chr10 | 31846417 | ||||||
| chr10:31846535
|
C | A | 1 | a0002c0002t0007g0246 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1171-2949G>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 6/19 | chr10 | 31846535 | ||||||
| chr10:31846536
|
C | A | 1 | a0002c0002t0007g0246 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1171-2950G>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 6/19 | chr10 | 31846536 | ||||||
| chr10:31846564
|
A | G | 1 | a0001c0001t0004g0024 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1171-2978T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 6/19 | chr10 | 31846564 | ||||||
| chr10:31846683
|
A | G | 1 | a0001c0001t0003g0185 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1171-3097T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 6/19 | chr10 | 31846683 | ||||||
| chr10:31846899
|
A | AT | 120 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0096others(117): Show | 120 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.1171-3314dupA | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 6/19 | chr10 | 31846899 | ||||||
| chr10:31846899
|
A | ATT | 12 | a0001c0001t0001g0088a0001c0001t0001g0126a0001c0001t0001g0164others(9): Show | 12 | HG00673.hp2 HG01071.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1171-3315_1171-331 others(6): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 6/19 | chr10 | 31846899 | ||||||
| chr10:31846899
|
AT | A | 29 | a0001c0001t0003g0188a0001c0001t0004g0037a0001c0001t0009g0032others(26): Show | 29 | HG00735.hp2 HG01168.hp2 HG02257.hp1 others(26): Show |
intron_variant | MODIFIER | c.1171-3314delA | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 6/19 | chr10 | 31846899 | ||||||
| chr10:31847037
|
G | C | 1 | a0001c0001t0001g0213 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1171-3451C>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 6/19 | chr10 | 31847037 | ||||||
| chr10:31847255
|
T | G | 1 | a0001c0001t0001g0083 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1171-3669A>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 6/19 | chr10 | 31847255 | ||||||
| chr10:31847744
|
C | G | 1 | a0002c0002t0002g0281 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1171-4158G>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 6/19 | chr10 | 31847744 | ||||||
| chr10:31847897
|
A | G | 1 | a0001c0001t0001g0224 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1171-4311T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 6/19 | chr10 | 31847897 | ||||||
| chr10:31848070
|
A | G | 1 | a0001c0001t0004g0034 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1170+4447T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 6/19 | chr10 | 31848070 | ||||||
| chr10:31848263
|
T | C | 1 | a0001c0001t0003g0026 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1170+4254A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 6/19 | chr10 | 31848263 | ||||||
| chr10:31848270
|
C | T | 146 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(143): Show | 146 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(143): Show |
intron_variant | MODIFIER | c.1170+4247G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 6/19 | chr10 | 31848270 | ||||||
| chr10:31848715
|
T | C | 2 | a0001c0001t0001g0164a0001c0001t0006g0159 | 2 | HG00280.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1170+3802A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 6/19 | chr10 | 31848715 | ||||||
| chr10:31848745
|
C | G | 11 | a0001c0001t0009g0032a0001c0001t0009g0072a0001c0001t0009g0073others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1170+3772G>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 6/19 | chr10 | 31848745 | ||||||
| chr10:31848791
|
G | A | 50 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(47): Show | 50 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.1170+3726C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 6/19 | chr10 | 31848791 | ||||||
| chr10:31848956
|
A | C | 4 | a0001c0001t0003g0026a0001c0001t0012g0027a0001c0001t0049g0029others(1): Show | 4 | HG02145.hp2 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1170+3561T>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 6/19 | chr10 | 31848956 | ||||||
| chr10:31849025
|
T | C | 101 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0088others(98): Show | 101 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.1170+3492A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 6/19 | chr10 | 31849025 | ||||||
| chr10:31849169
|
G | A | 3 | a0001c0001t0013g0092a0001c0001t0013g0093a0001c0001t0013g0094 | 3 | NA18952.hp1 NA18967.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.1170+3348C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 6/19 | chr10 | 31849169 | ||||||
| chr10:31849265
|
T | C | 1 | a0001c0001t0006g0221 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1170+3252A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 6/19 | chr10 | 31849265 | ||||||
| chr10:31849389
|
GGTAAAGA others(4): Show |
G | 1 | a0002c0002t0007g0297 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1170+3117_1170+312 others(15): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 6/19 | chr10 | 31849389 | ||||||
| chr10:31849477
|
A | G | 1 | a0002c0002t0007g0320 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1170+3040T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 6/19 | chr10 | 31849477 | ||||||
| chr10:31849780
|
C | T | 1 | a0001c0001t0004g0031 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1170+2737G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 6/19 | chr10 | 31849780 | ||||||
| chr10:31849951
|
A | G | 1 | a0001c0001t0003g0176 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1170+2566T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 6/19 | chr10 | 31849951 | ||||||
| chr10:31850131
|
G | C | 1 | a0001c0001t0006g0221 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1170+2386C>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 6/19 | chr10 | 31850131 | ||||||
| chr10:31850563
|
T | C | 1 | a0001c0010t0053g0238 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1170+1954A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 6/19 | chr10 | 31850563 | ||||||
| chr10:31850612
|
G | A | 1 | a0001c0001t0025g0202 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1170+1905C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 6/19 | chr10 | 31850612 | ||||||
| chr10:31850998
|
T | C | 50 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(47): Show | 50 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.1170+1519A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 6/19 | chr10 | 31850998 | ||||||
| chr10:31851182
|
T | C | 1 | a0002c0002t0002g0283 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1170+1335A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 6/19 | chr10 | 31851182 | ||||||
| chr10:31851294
|
C | T | 1 | a0001c0001t0011g0071 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1170+1223G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 6/19 | chr10 | 31851294 | ||||||
| chr10:31851681
|
A | C | 1 | a0002c0002t0002g0258 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1170+836T>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 6/19 | chr10 | 31851681 | ||||||
| chr10:31851707
|
C | T | 15 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(12): Show | 15 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1170+810G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 6/19 | chr10 | 31851707 | ||||||
| chr10:31851739
|
A | AT | 8 | a0001c0001t0003g0084a0001c0001t0003g0169a0001c0001t0003g0181others(5): Show | 8 | HG00544.hp1 HG01934.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.1170+777dupA | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 6/19 | chr10 | 31851739 | ||||||
| chr10:31851768
|
C | T | 1 | a0001c0001t0018g0087 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1170+749G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 6/19 | chr10 | 31851768 | ||||||
| chr10:31852025
|
G | A | 1 | a0001c0001t0018g0097 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1170+492C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 6/19 | chr10 | 31852025 | ||||||
| chr10:31852320
|
A | G | 1 | a0002c0002t0002g0319 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1170+197T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 6/19 | chr10 | 31852320 | ||||||
| chr10:31852371
|
C | T | 1 | a0001c0001t0004g0034 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1170+146G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 6/19 | chr10 | 31852371 | ||||||
| chr10:31852651
|
G | C | 1 | a0001c0008t0005g0074 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1090-54C>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 5/19 | chr10 | 31852651 | ||||||
| chr10:31852671
|
T | C | 2 | a0001c0001t0008g0133a0001c0001t0008g0140 | 2 | HG02486.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1090-74A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 5/19 | chr10 | 31852671 | ||||||
| chr10:31852729
|
C | CT | 19 | a0001c0001t0001g0218a0001c0001t0003g0026a0001c0001t0003g0184others(16): Show | 19 | HG00735.hp2 HG01934.hp1 HG02074.hp1 others(16): Show |
intron_variant | MODIFIER | c.1090-133dupA | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 5/19 | chr10 | 31852729 | ||||||
| chr10:31852729
|
CT | C | 47 | a0001c0001t0001g0088a0001c0001t0001g0114a0001c0001t0001g0146others(44): Show | 47 | HG00280.hp1 HG00673.hp1 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.1090-133delA | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 5/19 | chr10 | 31852729 | ||||||
| chr10:31852729
|
CTT | C | 192 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0096others(189): Show | 192 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(189): Show |
intron_variant | MODIFIER | c.1090-134_1090-133d others(4): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 5/19 | chr10 | 31852729 | ||||||
| chr10:31852729
|
CTTT | C | 8 | a0001c0001t0001g0099a0001c0001t0001g0101a0002c0002t0002g0243others(5): Show | 8 | HG01516.hp1 NA18747.hp2 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.1090-135_1090-133d others(5): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 5/19 | chr10 | 31852729 | ||||||
| chr10:31852886
|
C | A | 2 | a0001c0001t0001g0126a0001c0001t0001g0128 | 2 | NA18959.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.1090-289G>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 5/19 | chr10 | 31852886 | ||||||
| chr10:31852947
|
C | T | 18 | a0001c0001t0004g0044a0001c0001t0005g0043a0001c0001t0005g0045others(15): Show | 18 | HG01109.hp1 HG01168.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.1090-350G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 5/19 | chr10 | 31852947 | ||||||
| chr10:31852980
|
G | A | 1 | a0001c0001t0003g0182 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1090-383C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 5/19 | chr10 | 31852980 | ||||||
| chr10:31853003
|
T | C | 146 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(143): Show | 146 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(143): Show |
intron_variant | MODIFIER | c.1090-406A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 5/19 | chr10 | 31853003 | ||||||
| chr10:31853009
|
T | A | 1 | a0001c0001t0011g0061 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1090-412A>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 5/19 | chr10 | 31853009 | ||||||
| chr10:31853028
|
G | A | 2 | a0001c0001t0004g0036a0001c0001t0037g0035 | 2 | HG02258.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1090-431C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 5/19 | chr10 | 31853028 | ||||||
| chr10:31853055
|
C | A | 82 | a0002c0002t0002g0243a0002c0002t0002g0245a0002c0002t0002g0247others(79): Show | 82 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.1090-458G>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 5/19 | chr10 | 31853055 | ||||||
| chr10:31853055
|
C | G | 1 | a0001c0001t0024g0042 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1090-458G>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 5/19 | chr10 | 31853055 | ||||||
| chr10:31853061
|
G | T | 1 | a0002c0002t0021g0249 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1090-464C>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 5/19 | chr10 | 31853061 | ||||||
| chr10:31853062
|
C | G | 1 | a0001c0001t0004g0037 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1090-465G>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 5/19 | chr10 | 31853062 | ||||||
| chr10:31853293
|
T | C | 1 | a0001c0001t0005g0063 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1090-696A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 5/19 | chr10 | 31853293 | ||||||
| chr10:31853417
|
A | G | 85 | a0001c0007t0028g0239a0001c0007t0028g0240a0001c0010t0053g0238others(82): Show | 85 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.1089+649T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 5/19 | chr10 | 31853417 | ||||||
| chr10:31853521
|
A | C | 11 | a0001c0001t0009g0032a0001c0001t0009g0072a0001c0001t0009g0073others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1089+545T>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 5/19 | chr10 | 31853521 | ||||||
| chr10:31853723
|
T | C | 85 | a0001c0007t0028g0239a0001c0007t0028g0240a0001c0010t0053g0238others(82): Show | 85 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.1089+343A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 5/19 | chr10 | 31853723 | ||||||
| chr10:31853860
|
G | A | 4 | a0002c0002t0014g0242a0002c0002t0014g0271a0002c0002t0014g0272others(1): Show | 4 | NA18947.hp2 NA18982.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.1089+206C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 5/19 | chr10 | 31853860 | ||||||
| chr10:31853922
|
G | A | 146 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(143): Show | 146 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(143): Show |
intron_variant | MODIFIER | c.1089+144C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 5/19 | chr10 | 31853922 | ||||||
| chr10:31854263
|
T | C | 11 | a0001c0001t0009g0032a0001c0001t0009g0072a0001c0001t0009g0073others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.949-57A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31854263 | ||||||
| chr10:31854280
|
A | C | 145 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(142): Show | 145 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(142): Show |
intron_variant | MODIFIER | c.949-74T>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31854280 | ||||||
| chr10:31854365
|
G | C | 2 | a0001c0001t0003g0026a0001c0001t0012g0027 | 2 | HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.949-159C>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31854365 | ||||||
| chr10:31854379
|
G | A | 15 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(12): Show | 15 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.949-173C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31854379 | ||||||
| chr10:31854497
|
T | C | 1 | a0001c0001t0001g0117 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.949-291A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31854497 | ||||||
| chr10:31854585
|
C | T | 1 | a0001c0003t0010g0016 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.949-379G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31854585 | ||||||
| chr10:31854633
|
T | C | 1 | a0001c0001t0003g0184 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.949-427A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31854633 | ||||||
| chr10:31854649
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.949-443G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31854649 | ||||||
| chr10:31854959
|
T | A | 2 | a0001c0001t0004g0066a0001c0001t0004g0068 | 2 | HG02602.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.949-753A>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31854959 | ||||||
| chr10:31855011
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.949-805C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31855011 | ||||||
| chr10:31855086
|
C | T | 1 | a0001c0001t0011g0071 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.949-880G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31855086 | ||||||
| chr10:31855108
|
GAGGGA | G | 18 | a0001c0001t0004g0044a0001c0001t0005g0043a0001c0001t0005g0045others(15): Show | 18 | HG01109.hp1 HG01168.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.949-907_949-903del others(5): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31855108 | ||||||
| chr10:31855109
|
A | G | 1 | a0002c0002t0007g0297 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.949-903T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31855109 | ||||||
| chr10:31855113
|
A | G | 258 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0088others(255): Show | 258 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.949-907T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31855113 | ||||||
| chr10:31855115
|
A | G | 1 | a0001c0001t0034g0033 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.949-909T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31855115 | ||||||
| chr10:31855349
|
A | C | 4 | a0001c0001t0019g0162a0001c0001t0019g0163a0001c0001t0019g0166others(1): Show | 4 | HG01167.hp1 HG02970.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.949-1143T>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31855349 | ||||||
| chr10:31855379
|
G | C | 1 | a0001c0001t0011g0061 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.949-1173C>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31855379 | ||||||
| chr10:31855525
|
T | C | 1 | a0001c0001t0039g0089 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.949-1319A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31855525 | ||||||
| chr10:31855659
|
T | C | 9 | a0001c0001t0001g0215a0001c0001t0001g0217a0001c0001t0001g0218others(6): Show | 9 | HG00738.hp1 HG00741.hp1 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.949-1453A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31855659 | ||||||
| chr10:31855678
|
A | T | 1 | a0002c0002t0002g0267 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.949-1472T>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31855678 | ||||||
| chr10:31855686
|
T | C | 2 | a0001c0001t0003g0170a0001c0001t0003g0196 | 2 | NA18953.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.949-1480A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31855686 | ||||||
| chr10:31856157
|
T | C | 1 | a0001c0001t0001g0226 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.949-1951A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31856157 | ||||||
| chr10:31856184
|
A | T | 145 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(142): Show | 145 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(142): Show |
intron_variant | MODIFIER | c.949-1978T>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31856184 | ||||||
| chr10:31856460
|
T | G | 1 | a0001c0001t0024g0042 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.949-2254A>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31856460 | ||||||
| chr10:31856943
|
C | G | 1 | a0001c0001t0001g0110 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.949-2737G>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31856943 | ||||||
| chr10:31857062
|
TATCTGAT others(11): Show |
T | 15 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(12): Show | 15 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.949-2874_949-2857d others(20): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31857062 | ||||||
| chr10:31857214
|
G | A | 1 | a0001c0001t0040g0212 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.949-3008C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31857214 | ||||||
| chr10:31857222
|
A | G | 145 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(142): Show | 145 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(142): Show |
intron_variant | MODIFIER | c.949-3016T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31857222 | ||||||
| chr10:31857283
|
C | T | 1 | a0001c0001t0004g0034 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.949-3077G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31857283 | ||||||
| chr10:31857516
|
C | G | 145 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(142): Show | 145 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(142): Show |
intron_variant | MODIFIER | c.949-3310G>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31857516 | ||||||
| chr10:31857525
|
A | G | 1 | a0001c0001t0001g0213 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.949-3319T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31857525 | ||||||
| chr10:31857591
|
A | C | 1 | a0001c0001t0001g0118 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.949-3385T>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31857591 | ||||||
| chr10:31857598
|
C | T | 1 | a0001c0001t0001g0207 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.949-3392G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31857598 | ||||||
| chr10:31857655
|
T | A | 1 | a0001c0001t0008g0152 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.949-3449A>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31857655 | ||||||
| chr10:31857788
|
C | A | 1 | a0002c0002t0002g0295 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.949-3582G>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31857788 | ||||||
| chr10:31857875
|
C | G | 134 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(131): Show | 134 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(131): Show |
intron_variant | MODIFIER | c.948+3520G>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31857875 | ||||||
| chr10:31857909
|
A | G | 1 | a0002c0002t0002g0277 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.948+3486T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31857909 | ||||||
| chr10:31857928
|
G | C | 18 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(15): Show | 18 | HG00099.hp2 HG01081.hp2 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.948+3467C>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31857928 | ||||||
| chr10:31858080
|
T | C | 2 | a0001c0003t0010g0018a0001c0003t0027g0012 | 2 | HG02615.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.948+3315A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31858080 | ||||||
| chr10:31858163
|
A | G | 321 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0088others(318): Show | 321 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.948+3232T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31858163 | ||||||
| chr10:31858196
|
C | A | 7 | a0001c0001t0003g0185a0001c0001t0003g0188a0001c0001t0003g0189others(4): Show | 7 | NA18947.hp1 NA18957.hp2 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.948+3199G>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31858196 | ||||||
| chr10:31858244
|
T | A | 1 | a0001c0014t0004g0013 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.948+3151A>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31858244 | ||||||
| chr10:31858312
|
T | C | 1 | a0001c0001t0018g0219 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.948+3083A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31858312 | ||||||
| chr10:31858427
|
G | A | 1 | a0001c0001t0043g0025 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.948+2968C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31858427 | ||||||
| chr10:31858520
|
G | A | 1 | a0002c0002t0002g0265 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.948+2875C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31858520 | ||||||
| chr10:31858608
|
T | C | 1 | a0001c0001t0001g0096 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.948+2787A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31858608 | ||||||
| chr10:31858715
|
C | T | 1 | a0001c0001t0004g0034 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.948+2680G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31858715 | ||||||
| chr10:31858823
|
C | G | 1 | a0001c0001t0006g0214 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.948+2572G>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31858823 | ||||||
| chr10:31858905
|
A | G | 14 | a0001c0001t0001g0083a0001c0001t0001g0164a0001c0001t0001g0204others(11): Show | 14 | HG00099.hp1 HG00280.hp1 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.948+2490T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31858905 | ||||||
| chr10:31858994
|
AGT | A | 49 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(46): Show | 49 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(46): Show |
intron_variant | MODIFIER | c.948+2399_948+2400d others(4): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31858994 | ||||||
| chr10:31859309
|
C | A | 1 | a0001c0001t0003g0182 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.948+2086G>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31859309 | ||||||
| chr10:31859324
|
A | G | 18 | a0001c0001t0004g0044a0001c0001t0005g0043a0001c0001t0005g0045others(15): Show | 18 | HG01109.hp1 HG01168.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.948+2071T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31859324 | ||||||
| chr10:31859462
|
G | A | 1 | a0001c0003t0010g0005 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.948+1933C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31859462 | ||||||
| chr10:31859478
|
CAT | C | 145 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(142): Show | 145 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(142): Show |
intron_variant | MODIFIER | c.948+1915_948+1916d others(4): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31859478 | ||||||
| chr10:31859607
|
AT | A | 145 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(142): Show | 145 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(142): Show |
intron_variant | MODIFIER | c.948+1787delA | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31859607 | ||||||
| chr10:31859636
|
G | C | 1 | a0001c0001t0001g0236 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.948+1759C>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31859636 | ||||||
| chr10:31859671
|
C | T | 160 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(157): Show | 160 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.948+1724G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31859671 | ||||||
| chr10:31859799
|
C | CT | 49 | a0001c0001t0004g0020a0001c0001t0004g0021a0001c0001t0004g0022others(46): Show | 49 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(46): Show |
intron_variant | MODIFIER | c.948+1595dupA | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31859799 | ||||||
| chr10:31859889
|
G | A | 15 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(12): Show | 15 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.948+1506C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31859889 | ||||||
| chr10:31859970
|
C | T | 1 | a0001c0001t0001g0213 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.948+1425G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31859970 | ||||||
| chr10:31860002
|
G | A | 15 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(12): Show | 15 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.948+1393C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31860002 | ||||||
| chr10:31860075
|
T | C | 1 | a0002c0002t0002g0277 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.948+1320A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31860075 | ||||||
| chr10:31860081
|
T | C | 3 | a0001c0007t0028g0239a0001c0007t0028g0240a0001c0010t0053g0238 | 3 | HG02572.hp1 HG02886.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.948+1314A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31860081 | ||||||
| chr10:31860181
|
C | G | 1 | a0001c0001t0001g0083 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.948+1214G>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31860181 | ||||||
| chr10:31860345
|
G | A | 1 | a0001c0001t0018g0087 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.948+1050C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31860345 | ||||||
| chr10:31860469
|
A | G | 1 | a0001c0001t0006g0153 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.948+926T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31860469 | ||||||
| chr10:31860524
|
C | T | 1 | a0001c0001t0004g0034 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.948+871G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31860524 | ||||||
| chr10:31860582
|
T | C | 1 | a0001c0001t0001g0213 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.948+813A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31860582 | ||||||
| chr10:31860838
|
T | G | 15 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(12): Show | 15 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.948+557A>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31860838 | ||||||
| chr10:31860851
|
C | A | 1 | a0001c0001t0001g0099 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.948+544G>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31860851 | ||||||
| chr10:31860874
|
C | T | 2 | a0002c0002t0054g0322a0002c0002t0055g0321 | 2 | NA18974.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.948+521G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31860874 | ||||||
| chr10:31860941
|
G | A | 5 | a0001c0001t0009g0077a0001c0001t0009g0078a0001c0001t0009g0080others(2): Show | 5 | HG02257.hp1 HG02559.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.948+454C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31860941 | ||||||
| chr10:31861002
|
A | G | 1 | a0001c0001t0004g0031 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.948+393T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31861002 | ||||||
| chr10:31861141
|
G | C | 2 | a0001c0001t0001g0210a0001c0001t0001g0232 | 2 | HG01099.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.948+254C>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31861141 | ||||||
| chr10:31861827
|
A | G | 5 | a0001c0001t0011g0055a0001c0001t0011g0056a0001c0001t0011g0057others(2): Show | 5 | HG01891.hp2 HG02280.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.685-169T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31861827 | ||||||
| chr10:31862159
|
C | G | 1 | a0002c0002t0054g0322 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.685-501G>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31862159 | ||||||
| chr10:31862506
|
C | T | 15 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(12): Show | 15 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.685-848G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31862506 | ||||||
| chr10:31862550
|
A | C | 18 | a0001c0001t0004g0044a0001c0001t0005g0043a0001c0001t0005g0045others(15): Show | 18 | HG01109.hp1 HG01168.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.685-892T>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31862550 | ||||||
| chr10:31862696
|
GCACACAC others(3): Show |
G | 27 | a0001c0001t0001g0100a0001c0001t0001g0103a0001c0001t0001g0106others(24): Show | 27 | HG00099.hp1 HG00673.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.685-1048_685-1039d others(12): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31862696 | ||||||
| chr10:31862696
|
GCACACAC others(5): Show |
G | 10 | a0001c0001t0001g0083a0001c0001t0001g0101a0001c0001t0001g0109others(7): Show | 10 | HG01106.hp1 HG01258.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.685-1050_685-1039d others(14): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31862696 | ||||||
| chr10:31862696
|
GCACACAC others(7): Show |
G | 17 | a0001c0001t0001g0141a0001c0001t0001g0157a0001c0001t0001g0210others(14): Show | 17 | HG00735.hp1 HG01099.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.685-1052_685-1039d others(16): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31862696 | ||||||
| chr10:31862696
|
GCACACAC others(9): Show |
G | 4 | a0001c0001t0001g0217a0001c0001t0001g0220a0001c0001t0006g0159others(1): Show | 4 | HG00280.hp1 HG00738.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.685-1054_685-1039d others(18): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31862696 | ||||||
| chr10:31862696
|
GCACACAC others(11): Show |
G | 3 | a0001c0001t0001g0218a0001c0001t0006g0231a0001c0001t0018g0219 | 3 | HG02886.hp1 NA20129.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.685-1056_685-1039d others(20): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31862696 | ||||||
| chr10:31862696
|
GCACACAC others(13): Show |
G | 5 | a0001c0001t0001g0215a0001c0001t0006g0214a0001c0001t0006g0216others(2): Show | 5 | HG00741.hp1 HG01123.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.685-1058_685-1039d others(22): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31862696 | ||||||
| chr10:31862696
|
GCACACAC others(15): Show |
G | 3 | a0001c0001t0013g0091a0001c0001t0013g0092a0001c0001t0013g0093 | 3 | NA18952.hp1 NA18954.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.685-1060_685-1039d others(24): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31862696 | ||||||
| chr10:31862696
|
GCACACAC others(21): Show |
G | 1 | a0001c0001t0001g0147 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.685-1066_685-1039d others(30): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31862696 | ||||||
| chr10:31862697
|
CACACACA others(1): Show |
C | 12 | a0001c0001t0001g0096a0001c0001t0001g0118a0001c0001t0001g0123others(9): Show | 12 | HG00544.hp2 HG00741.hp2 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.685-1047_685-1040d others(10): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31862697 | ||||||
| chr10:31862699
|
CACACAG | C | 13 | a0001c0001t0001g0086a0001c0001t0001g0099a0001c0001t0001g0104others(10): Show | 13 | HG00597.hp2 HG00621.hp2 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.685-1047_685-1042d others(8): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31862699 | ||||||
| chr10:31862701
|
CACAG | C | 7 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0111others(4): Show | 7 | HG02135.hp1 NA18955.hp2 NA18974.hp2 others(4): Show |
intron_variant | MODIFIER | c.685-1047_685-1044d others(6): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31862701 | ||||||
| chr10:31862703
|
CAG | C | 9 | a0001c0001t0001g0102a0001c0001t0001g0113a0001c0001t0001g0115others(6): Show | 9 | HG00733.hp1 HG01891.hp1 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.685-1047_685-1046d others(4): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31862703 | ||||||
| chr10:31862705
|
G | C | 2 | a0001c0001t0001g0088a0001c0001t0001g0124 | 2 | NA19060.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.685-1047C>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31862705 | ||||||
| chr10:31862705
|
G | GAC | 14 | a0001c0001t0003g0084a0001c0001t0003g0168a0001c0001t0003g0181others(11): Show | 14 | HG00544.hp1 HG02135.hp2 HG02273.hp1 others(11): Show |
intron_variant | MODIFIER | c.685-1049_685-1048d others(4): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31862705 | ||||||
| chr10:31862705
|
G | GACAC | 9 | a0001c0001t0003g0170a0001c0001t0003g0171a0001c0001t0003g0189others(6): Show | 9 | HG01934.hp1 HG02273.hp2 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.685-1051_685-1048d others(6): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31862705 | ||||||
| chr10:31862705
|
GAC | G | 90 | a0001c0001t0003g0026a0001c0001t0003g0176a0001c0001t0003g0178others(87): Show | 90 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(87): Show |
intron_variant | MODIFIER | c.685-1049_685-1048d others(4): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31862705 | ||||||
| chr10:31862705
|
GACAC | G | 20 | a0001c0001t0003g0169a0001c0001t0004g0021a0001c0001t0005g0046others(17): Show | 20 | HG00733.hp2 HG00735.hp2 HG01257.hp2 others(17): Show |
intron_variant | MODIFIER | c.685-1051_685-1048d others(6): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31862705 | ||||||
| chr10:31862705
|
GACACAC | G | 11 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0022others(8): Show | 11 | HG01167.hp2 HG01168.hp1 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.685-1053_685-1048d others(8): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31862705 | ||||||
| chr10:31862705
|
GACACACA others(1): Show |
G | 19 | a0001c0001t0004g0039a0001c0001t0004g0044a0001c0001t0005g0043others(16): Show | 19 | HG01109.hp1 HG01192.hp2 HG01346.hp2 others(16): Show |
intron_variant | MODIFIER | c.685-1055_685-1048d others(10): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31862705 | ||||||
| chr10:31862705
|
GACACACA others(3): Show |
G | 15 | a0001c0001t0004g0030a0001c0001t0004g0031a0001c0001t0004g0034others(12): Show | 15 | HG00099.hp2 HG01081.hp2 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.685-1057_685-1048d others(12): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31862705 | ||||||
| chr10:31862705
|
GACACACA others(5): Show |
G | 6 | a0001c0001t0012g0027a0002c0002t0002g0267a0002c0002t0002g0269others(3): Show | 6 | HG00738.hp2 HG01081.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.685-1059_685-1048d others(14): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31862705 | ||||||
| chr10:31862705
|
GACACACA others(7): Show |
G | 1 | a0001c0001t0024g0042 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.685-1061_685-1048d others(16): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31862705 | ||||||
| chr10:31862705
|
GACACACA others(9): Show |
G | 1 | a0002c0002t0002g0268 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.685-1063_685-1048d others(18): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31862705 | ||||||
| chr10:31862705
|
GACACACA others(11): Show |
G | 2 | a0001c0001t0005g0049a0001c0001t0005g0052 | 2 | NA18944.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.685-1065_685-1048d others(20): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31862705 | ||||||
| chr10:31862713
|
C | G | 3 | a0001c0001t0005g0046a0001c0001t0005g0051a0001c0001t0011g0071 | 3 | HG01257.hp2 HG01258.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.685-1055G>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31862713 | ||||||
| chr10:31862715
|
C | G | 7 | a0001c0001t0005g0054a0001c0008t0005g0075a0002c0002t0002g0252others(4): Show | 7 | HG01168.hp1 HG02074.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.685-1057G>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31862715 | ||||||
| chr10:31862717
|
C | G | 98 | a0001c0001t0004g0044a0001c0001t0005g0043a0001c0001t0005g0045others(95): Show | 98 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.685-1059G>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31862717 | ||||||
| chr10:31862719
|
C | G | 1 | a0002c0002t0002g0243 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.685-1061G>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31862719 | ||||||
| chr10:31862721
|
C | G | 1 | a0001c0001t0009g0072 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.685-1063G>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31862721 | ||||||
| chr10:31862723
|
C | T | 1 | a0001c0001t0001g0215 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.685-1065G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31862723 | ||||||
| chr10:31862727
|
C | G | 3 | a0001c0001t0005g0049a0001c0001t0005g0052a0002c0002t0002g0278 | 3 | NA18944.hp1 NA18959.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.685-1069G>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31862727 | ||||||
| chr10:31862994
|
A | C | 1 | a0001c0001t0004g0024 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.685-1336T>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31862994 | ||||||
| chr10:31863086
|
T | C | 82 | a0002c0002t0002g0243a0002c0002t0002g0245a0002c0002t0002g0247others(79): Show | 82 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.685-1428A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31863086 | ||||||
| chr10:31863095
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.685-1437A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31863095 | ||||||
| chr10:31863416
|
T | C | 15 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(12): Show | 15 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.685-1758A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31863416 | ||||||
| chr10:31863702
|
G | A | 3 | a0001c0001t0006g0216a0001c0001t0006g0221a0001c0001t0006g0231 | 3 | HG00741.hp1 HG02647.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.685-2044C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31863702 | ||||||
| chr10:31863729
|
T | C | 4 | a0002c0002t0002g0278a0002c0002t0002g0281a0002c0002t0002g0283others(1): Show | 4 | NA18954.hp1 NA18975.hp2 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.685-2071A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31863729 | ||||||
| chr10:31863768
|
T | C | 11 | a0001c0001t0009g0032a0001c0001t0009g0072a0001c0001t0009g0073others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.685-2110A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31863768 | ||||||
| chr10:31864167
|
T | C | 1 | a0001c0001t0040g0212 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.685-2509A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31864167 | ||||||
| chr10:31864580
|
T | C | 18 | a0001c0001t0004g0044a0001c0001t0005g0043a0001c0001t0005g0045others(15): Show | 18 | HG01109.hp1 HG01168.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.685-2922A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31864580 | ||||||
| chr10:31864621
|
T | C | 1 | a0002c0002t0030g0241 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.685-2963A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31864621 | ||||||
| chr10:31864813
|
T | C | 4 | a0001c0001t0001g0104a0001c0001t0001g0118a0001c0001t0001g0121others(1): Show | 4 | HG00597.hp2 NA18945.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.685-3155A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31864813 | ||||||
| chr10:31864846
|
G | GT | 10 | a0001c0001t0009g0032a0001c0001t0009g0072a0001c0001t0009g0073others(7): Show | 10 | HG02145.hp1 HG02257.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.685-3189dupA | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31864846 | ||||||
| chr10:31864872
|
T | C | 15 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(12): Show | 15 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.685-3214A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31864872 | ||||||
| chr10:31864976
|
AGTTAGCC others(4): Show |
A | 6 | a0001c0003t0010g0005a0001c0003t0010g0011a0001c0003t0010g0016others(3): Show | 6 | HG00735.hp2 HG02257.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.685-3329_685-3319d others(13): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31864976 | ||||||
| chr10:31865072
|
G | A | 7 | a0001c0001t0003g0185a0001c0001t0003g0188a0001c0001t0003g0189others(4): Show | 7 | NA18947.hp1 NA18957.hp2 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.685-3414C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31865072 | ||||||
| chr10:31865208
|
G | A | 3 | a0001c0007t0028g0239a0001c0007t0028g0240a0001c0010t0053g0238 | 3 | HG02572.hp1 HG02886.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.685-3550C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31865208 | ||||||
| chr10:31865358
|
A | C | 85 | a0001c0007t0028g0239a0001c0007t0028g0240a0001c0010t0053g0238others(82): Show | 85 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.685-3700T>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31865358 | ||||||
| chr10:31865482
|
C | T | 1 | a0001c0001t0013g0091 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.685-3824G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31865482 | ||||||
| chr10:31865585
|
A | C | 1 | a0001c0001t0001g0099 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.685-3927T>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31865585 | ||||||
| chr10:31865591
|
G | A | 4 | a0001c0001t0019g0162a0001c0001t0019g0163a0001c0001t0019g0166others(1): Show | 4 | HG01167.hp1 HG02970.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.685-3933C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31865591 | ||||||
| chr10:31865613
|
C | T | 1 | a0001c0001t0001g0132 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.685-3955G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31865613 | ||||||
| chr10:31865636
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.685-3978C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31865636 | ||||||
| chr10:31865736
|
G | A | 1 | a0001c0001t0034g0033 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.685-4078C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31865736 | ||||||
| chr10:31865747
|
G | T | 1 | a0001c0001t0003g0172 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.685-4089C>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31865747 | ||||||
| chr10:31865764
|
G | C | 1 | a0001c0001t0003g0026 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.685-4106C>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31865764 | ||||||
| chr10:31865795
|
G | C | 7 | a0002c0002t0002g0274a0002c0002t0002g0277a0002c0002t0002g0278others(4): Show | 7 | NA18954.hp1 NA18975.hp2 NA19000.hp2 others(4): Show |
intron_variant | MODIFIER | c.685-4137C>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31865795 | ||||||
| chr10:31865877
|
C | CA | 130 | a0001c0001t0003g0084a0001c0001t0003g0120a0001c0001t0003g0168others(127): Show | 130 | HG00280.hp2 HG00544.hp1 HG00597.hp1 others(127): Show |
intron_variant | MODIFIER | c.685-4220dupT | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31865877 | ||||||
| chr10:31866027
|
A | G | 2 | a0001c0007t0028g0239a0001c0007t0028g0240 | 2 | HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.685-4369T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31866027 | ||||||
| chr10:31866204
|
A | C | 1 | a0002c0002t0002g0264 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.685-4546T>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31866204 | ||||||
| chr10:31866412
|
G | T | 2 | a0002c0002t0021g0248a0002c0002t0021g0279 | 2 | NA18980.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.685-4754C>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31866412 | ||||||
| chr10:31866414
|
A | T | 2 | a0002c0002t0021g0248a0002c0002t0021g0279 | 2 | NA18980.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.685-4756T>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31866414 | ||||||
| chr10:31866415
|
A | C | 2 | a0002c0002t0021g0248a0002c0002t0021g0279 | 2 | NA18980.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.685-4757T>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31866415 | ||||||
| chr10:31866498
|
G | T | 1 | a0001c0003t0010g0016 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.685-4840C>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31866498 | ||||||
| chr10:31866522
|
C | T | 1 | a0002c0002t0002g0278 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.685-4864G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31866522 | ||||||
| chr10:31866581
|
C | T | 274 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0088others(271): Show | 274 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.685-4923G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31866581 | ||||||
| chr10:31866718
|
C | G | 4 | a0001c0001t0001g0226a0001c0001t0008g0152a0001c0001t0025g0156others(1): Show | 4 | HG01884.hp2 HG02258.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.685-5060G>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31866718 | ||||||
| chr10:31867017
|
A | C | 1 | a0001c0001t0001g0218 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.685-5359T>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31867017 | ||||||
| chr10:31867024
|
A | C | 8 | a0001c0001t0006g0150a0001c0001t0006g0153a0001c0001t0006g0158others(5): Show | 8 | HG01106.hp1 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.685-5366T>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31867024 | ||||||
| chr10:31867118
|
G | GT | 24 | a0001c0001t0001g0107a0001c0001t0001g0209a0001c0001t0008g0105others(21): Show | 24 | HG01884.hp1 HG01891.hp2 HG01981.hp2 others(21): Show |
intron_variant | MODIFIER | c.685-5461dupA | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31867118 | ||||||
| chr10:31867118
|
G | T | 2 | a0001c0001t0001g0147a0001c0001t0003g0026 | 2 | HG03516.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.685-5460C>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31867118 | ||||||
| chr10:31867121
|
T | A | 1 | a0001c0001t0003g0198 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.685-5463A>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31867121 | ||||||
| chr10:31867138
|
G | A | 1 | a0001c0001t0004g0034 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.685-5480C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31867138 | ||||||
| chr10:31867437
|
T | A | 11 | a0001c0001t0009g0032a0001c0001t0009g0072a0001c0001t0009g0073others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.685-5779A>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31867437 | ||||||
| chr10:31867901
|
TA | T | 15 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(12): Show | 15 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.685-6244delT | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31867901 | ||||||
| chr10:31867913
|
A | T | 2 | a0001c0001t0001g0226a0001c0001t0008g0152 | 2 | HG01884.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.685-6255T>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31867913 | ||||||
| chr10:31868042
|
A | T | 146 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(143): Show | 146 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(143): Show |
intron_variant | MODIFIER | c.685-6384T>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31868042 | ||||||
| chr10:31868210
|
C | T | 15 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(12): Show | 15 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.685-6552G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31868210 | ||||||
| chr10:31868315
|
C | T | 1 | a0001c0001t0024g0042 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.685-6657G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31868315 | ||||||
| chr10:31868361
|
TTA | T | 4 | a0002c0002t0007g0308a0003c0004t0007g0309a0003c0004t0007g0310others(1): Show | 4 | HG01109.hp2 HG03130.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.685-6705_685-6704d others(4): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31868361 | ||||||
| chr10:31868362
|
T | G | 1 | a0001c0001t0006g0158 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.685-6704A>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31868362 | ||||||
| chr10:31868514
|
T | C | 5 | a0001c0001t0003g0176a0001c0001t0003g0178a0001c0001t0003g0186others(2): Show | 5 | HG01496.hp2 HG01993.hp1 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.685-6856A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31868514 | ||||||
| chr10:31868755
|
G | A | 1 | a0001c0001t0001g0118 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.685-7097C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31868755 | ||||||
| chr10:31869121
|
A | G | 1 | a0001c0001t0039g0089 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.685-7463T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31869121 | ||||||
| chr10:31869156
|
C | T | 6 | a0002c0002t0002g0262a0002c0002t0002g0275a0002c0002t0002g0276others(3): Show | 6 | HG00597.hp1 NA18955.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.685-7498G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31869156 | ||||||
| chr10:31869348
|
C | A | 1 | a0001c0001t0018g0087 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.685-7690G>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31869348 | ||||||
| chr10:31869504
|
T | C | 1 | a0001c0001t0043g0025 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.685-7846A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31869504 | ||||||
| chr10:31869516
|
A | G | 320 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0088others(317): Show | 320 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.685-7858T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31869516 | ||||||
| chr10:31869538
|
AAAAC | A | 108 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0088others(105): Show | 108 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.685-7884_685-7881d others(6): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31869538 | ||||||
| chr10:31869550
|
C | A | 50 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(47): Show | 50 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.685-7892G>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31869550 | ||||||
| chr10:31870230
|
C | CT | 6 | a0001c0001t0001g0121a0001c0001t0001g0228a0001c0001t0003g0184others(3): Show | 6 | HG01175.hp2 HG02074.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.685-8573dupA | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31870230 | ||||||
| chr10:31870230
|
CT | C | 49 | a0001c0001t0003g0169a0001c0001t0004g0020a0001c0001t0004g0021others(46): Show | 49 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(46): Show |
intron_variant | MODIFIER | c.685-8573delA | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31870230 | ||||||
| chr10:31870263
|
C | T | 146 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(143): Show | 146 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(143): Show |
intron_variant | MODIFIER | c.685-8605G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31870263 | ||||||
| chr10:31870265
|
C | T | 3 | a0001c0001t0001g0113a0001c0001t0001g0115a0001c0001t0015g0116 | 3 | NA18946.hp1 NA18965.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.685-8607G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31870265 | ||||||
| chr10:31870316
|
G | A | 85 | a0001c0007t0028g0239a0001c0007t0028g0240a0001c0010t0053g0238others(82): Show | 85 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.685-8658C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31870316 | ||||||
| chr10:31870344
|
C | A | 1 | a0001c0001t0001g0126 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.685-8686G>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31870344 | ||||||
| chr10:31870444
|
G | C | 1 | a0001c0001t0004g0064 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.685-8786C>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31870444 | ||||||
| chr10:31870476
|
C | T | 18 | a0001c0001t0004g0044a0001c0001t0005g0043a0001c0001t0005g0045others(15): Show | 18 | HG01109.hp1 HG01168.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.685-8818G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31870476 | ||||||
| chr10:31870658
|
G | A | 11 | a0001c0001t0009g0032a0001c0001t0009g0072a0001c0001t0009g0073others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.685-9000C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31870658 | ||||||
| chr10:31871008
|
T | C | 2 | a0001c0001t0001g0157a0001c0013t0015g0154 | 2 | HG00735.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.685-9350A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31871008 | ||||||
| chr10:31871067
|
T | C | 274 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0088others(271): Show | 274 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.685-9409A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31871067 | ||||||
| chr10:31871293
|
T | C | 1 | a0001c0003t0010g0016 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.685-9635A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31871293 | ||||||
| chr10:31871462
|
C | T | 1 | a0001c0001t0017g0053 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.685-9804G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31871462 | ||||||
| chr10:31871510
|
C | T | 1 | a0002c0002t0002g0291 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.685-9852G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31871510 | ||||||
| chr10:31871591
|
A | C | 50 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(47): Show | 50 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.685-9933T>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31871591 | ||||||
| chr10:31871697
|
T | C | 7 | a0001c0001t0011g0055a0001c0001t0011g0056a0001c0001t0011g0057others(4): Show | 7 | HG01884.hp1 HG01891.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.685-10039A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31871697 | ||||||
| chr10:31871775
|
G | A | 15 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(12): Show | 15 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.685-10117C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31871775 | ||||||
| chr10:31871871
|
G | T | 2 | a0001c0001t0003g0170a0001c0001t0003g0196 | 2 | NA18953.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.685-10213C>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31871871 | ||||||
| chr10:31871963
|
C | T | 1 | a0001c0001t0040g0212 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.685-10305G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31871963 | ||||||
| chr10:31872093
|
C | T | 2 | a0001c0001t0008g0155a0001c0001t0018g0087 | 2 | HG02055.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.685-10435G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31872093 | ||||||
| chr10:31872267
|
T | C | 1 | a0001c0001t0043g0025 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.685-10609A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31872267 | ||||||
| chr10:31872382
|
C | T | 50 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(47): Show | 50 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.685-10724G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31872382 | ||||||
| chr10:31872407
|
T | C | 2 | a0001c0001t0025g0156a0001c0001t0025g0202 | 2 | HG02258.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.685-10749A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31872407 | ||||||
| chr10:31872468
|
C | T | 1 | a0001c0014t0004g0013 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.685-10810G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31872468 | ||||||
| chr10:31872558
|
C | T | 111 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0088others(108): Show | 111 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.685-10900G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31872558 | ||||||
| chr10:31872613
|
C | T | 161 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(158): Show | 161 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(158): Show |
intron_variant | MODIFIER | c.685-10955G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31872613 | ||||||
| chr10:31872636
|
C | G | 11 | a0001c0001t0009g0032a0001c0001t0009g0072a0001c0001t0009g0073others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.685-10978G>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31872636 | ||||||
| chr10:31872647
|
C | T | 2 | a0001c0001t0025g0156a0001c0001t0025g0202 | 2 | HG02258.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.685-10989G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31872647 | ||||||
| chr10:31872657
|
C | T | 1 | a0001c0001t0018g0087 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.685-10999G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31872657 | ||||||
| chr10:31872748
|
G | A | 161 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(158): Show | 161 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(158): Show |
intron_variant | MODIFIER | c.685-11090C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31872748 | ||||||
| chr10:31873414
|
A | G | 146 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(143): Show | 146 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(143): Show |
intron_variant | MODIFIER | c.685-11756T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31873414 | ||||||
| chr10:31873513
|
T | C | 10 | a0001c0001t0009g0032a0001c0001t0009g0072a0001c0001t0009g0073others(7): Show | 10 | HG02145.hp1 HG02257.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.685-11855A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31873513 | ||||||
| chr10:31873732
|
T | C | 1 | a0001c0001t0003g0026 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.685-12074A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31873732 | ||||||
| chr10:31873803
|
A | G | 1 | a0001c0001t0052g0318 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.685-12145T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31873803 | ||||||
| chr10:31874248
|
T | C | 5 | a0001c0001t0049g0029a0001c0001t0050g0028a0001c0007t0028g0239others(2): Show | 5 | HG02145.hp2 HG02572.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.685-12590A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31874248 | ||||||
| chr10:31874336
|
G | A | 1 | a0001c0014t0004g0013 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.685-12678C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31874336 | ||||||
| chr10:31874482
|
T | A | 1 | a0001c0001t0003g0026 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.685-12824A>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31874482 | ||||||
| chr10:31874669
|
T | C | 93 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0088others(90): Show | 93 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.685-13011A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31874669 | ||||||
| chr10:31874675
|
G | GA | 16 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(13): Show | 16 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.685-13018dupT | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31874675 | ||||||
| chr10:31874740
|
G | A | 143 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(140): Show | 143 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(140): Show |
intron_variant | MODIFIER | c.685-13082C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31874740 | ||||||
| chr10:31874805
|
C | G | 18 | a0001c0001t0004g0044a0001c0001t0005g0043a0001c0001t0005g0045others(15): Show | 18 | HG01109.hp1 HG01168.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.685-13147G>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31874805 | ||||||
| chr10:31874897
|
C | T | 3 | a0001c0001t0005g0046a0001c0001t0005g0051a0001c0001t0005g0054 | 3 | HG01168.hp1 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.685-13239G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31874897 | ||||||
| chr10:31874973
|
C | A | 1 | a0001c0001t0001g0157 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.685-13315G>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31874973 | ||||||
| chr10:31874973
|
C | CA | 17 | a0001c0001t0003g0199a0001c0001t0004g0019a0001c0001t0004g0020others(14): Show | 17 | HG01081.hp2 HG01167.hp2 HG01934.hp2 others(14): Show |
intron_variant | MODIFIER | c.685-13316dupT | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31874973 | ||||||
| chr10:31874973
|
C | CAA | 14 | a0001c0001t0004g0024a0001c0001t0004g0031a0001c0001t0004g0036others(11): Show | 14 | HG00099.hp2 HG01168.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.685-13317_685-1331 others(6): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31874973 | ||||||
| chr10:31874973
|
C | CAAA | 39 | a0002c0002t0002g0243a0002c0002t0002g0250a0002c0002t0002g0251others(36): Show | 39 | HG00621.hp1 HG00639.hp2 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.685-13318_685-1331 others(7): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31874973 | ||||||
| chr10:31874973
|
C | CAAAA | 29 | a0001c0007t0028g0240a0002c0002t0002g0252a0002c0002t0002g0261others(26): Show | 29 | HG00673.hp1 HG01106.hp2 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.685-13319_685-1331 others(8): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31874973 | ||||||
| chr10:31874973
|
C | CAAAAA | 9 | a0002c0002t0002g0245a0002c0002t0002g0276a0002c0002t0002g0281others(6): Show | 9 | HG00597.hp1 HG01109.hp2 HG03453.hp1 others(6): Show |
intron_variant | MODIFIER | c.685-13320_685-1331 others(9): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31874973 | ||||||
| chr10:31874973
|
C | T | 2 | a0001c0001t0025g0156a0001c0001t0025g0202 | 2 | HG02258.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.685-13315G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31874973 | ||||||
| chr10:31874973
|
CA | C | 130 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0088others(127): Show | 130 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.685-13316delT | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31874973 | ||||||
| chr10:31874973
|
CAA | C | 13 | a0001c0001t0001g0215a0001c0001t0001g0217a0001c0001t0001g0218others(10): Show | 13 | HG00738.hp1 HG00741.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.685-13317_685-1331 others(6): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31874973 | ||||||
| chr10:31874973
|
CAAA | C | 16 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(13): Show | 16 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.685-13318_685-1331 others(7): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31874973 | ||||||
| chr10:31874973
|
CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0008g0140 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.685-13329_685-1331 others(18): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31874973 | ||||||
| chr10:31875003
|
T | A | 82 | a0001c0007t0028g0240a0001c0010t0053g0238a0002c0002t0002g0243others(79): Show | 82 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.685-13345A>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31875003 | ||||||
| chr10:31875299
|
G | A | 1 | a0001c0001t0003g0186 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.685-13641C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31875299 | ||||||
| chr10:31875306
|
C | T | 2 | a0001c0001t0001g0164a0001c0001t0006g0159 | 2 | HG00280.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.685-13648G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31875306 | ||||||
| chr10:31875308
|
C | G | 144 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(141): Show | 144 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(141): Show |
intron_variant | MODIFIER | c.685-13650G>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31875308 | ||||||
| chr10:31875787
|
G | C | 1 | a0001c0001t0003g0026 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.685-14129C>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31875787 | ||||||
| chr10:31875872
|
A | G | 1 | a0001c0001t0003g0120 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.685-14214T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31875872 | ||||||
| chr10:31876052
|
GAC | G | 49 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(46): Show | 49 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(46): Show |
intron_variant | MODIFIER | c.685-14396_685-1439 others(6): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31876052 | ||||||
| chr10:31876222
|
A | G | 2 | a0001c0001t0001g0228a0001c0001t0001g0230 | 2 | HG01175.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.685-14564T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31876222 | ||||||
| chr10:31876240
|
G | A | 16 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(13): Show | 16 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.685-14582C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31876240 | ||||||
| chr10:31876365
|
A | G | 2 | a0001c0001t0049g0029a0001c0001t0050g0028 | 2 | HG02145.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.685-14707T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31876365 | ||||||
| chr10:31876528
|
A | G | 3 | a0001c0001t0003g0026a0001c0001t0012g0027a0001c0001t0034g0033 | 3 | HG02280.hp2 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.685-14870T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31876528 | ||||||
| chr10:31876543
|
C | T | 1 | a0001c0001t0008g0222 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.685-14885G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31876543 | ||||||
| chr10:31876546
|
C | CA | 37 | a0001c0001t0001g0107a0001c0001t0001g0213a0001c0001t0001g0215others(34): Show | 37 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.685-14889dupT | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31876546 | ||||||
| chr10:31876546
|
C | CAA | 89 | a0001c0001t0009g0032a0001c0001t0009g0073a0001c0001t0009g0077others(86): Show | 89 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.685-14890_685-1488 others(6): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31876546 | ||||||
| chr10:31876888
|
G | C | 2 | a0002c0002t0002g0251a0002c0002t0002g0252 | 2 | NA18940.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.685-15230C>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31876888 | ||||||
| chr10:31876893
|
G | C | 2 | a0001c0001t0001g0101a0001c0001t0001g0122 | 2 | HG00621.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.685-15235C>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31876893 | ||||||
| chr10:31876983
|
C | A | 1 | a0001c0001t0003g0184 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.685-15325G>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31876983 | ||||||
| chr10:31877058
|
G | A | 1 | a0001c0001t0040g0212 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.685-15400C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31877058 | ||||||
| chr10:31877095
|
T | C | 2 | a0001c0005t0016g0007a0001c0005t0016g0008 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.685-15437A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31877095 | ||||||
| chr10:31877283
|
C | T | 9 | a0001c0001t0001g0215a0001c0001t0001g0217a0001c0001t0001g0218others(6): Show | 9 | HG00738.hp1 HG00741.hp1 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.685-15625G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31877283 | ||||||
| chr10:31877397
|
A | G | 1 | a0001c0001t0001g0145 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.685-15739T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31877397 | ||||||
| chr10:31877526
|
T | C | 2 | a0001c0001t0049g0029a0001c0001t0050g0028 | 2 | HG02145.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.685-15868A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31877526 | ||||||
| chr10:31877862
|
C | T | 2 | a0001c0001t0005g0049a0001c0001t0005g0052 | 2 | NA18944.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.685-16204G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31877862 | ||||||
| chr10:31877994
|
A | G | 165 | a0001c0001t0003g0026a0001c0001t0004g0019a0001c0001t0004g0020others(162): Show | 165 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(162): Show |
intron_variant | MODIFIER | c.685-16336T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31877994 | ||||||
| chr10:31878205
|
C | CAG | 141 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(138): Show | 141 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(138): Show |
intron_variant | MODIFIER | c.685-16549_685-1654 others(6): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31878205 | ||||||
| chr10:31878208
|
A | AGC | 3 | a0002c0002t0002g0298a0002c0002t0002g0299a0002c0002t0002g0306 | 3 | HG02027.hp2 HG02040.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.685-16551_685-1655 others(6): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31878208 | ||||||
| chr10:31878214
|
T | G | 9 | a0001c0001t0001g0215a0001c0001t0001g0217a0001c0001t0001g0218others(6): Show | 9 | HG00738.hp1 HG00741.hp1 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.685-16556A>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31878214 | ||||||
| chr10:31878457
|
C | T | 133 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(130): Show | 133 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(130): Show |
intron_variant | MODIFIER | c.685-16799G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31878457 | ||||||
| chr10:31878739
|
T | G | 4 | a0001c0001t0019g0162a0001c0001t0019g0163a0001c0001t0019g0166others(1): Show | 4 | HG01167.hp1 HG02970.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.685-17081A>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31878739 | ||||||
| chr10:31878747
|
T | C | 84 | a0001c0007t0028g0239a0001c0007t0028g0240a0001c0010t0053g0238others(81): Show | 84 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.685-17089A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31878747 | ||||||
| chr10:31878763
|
A | G | 2 | a0001c0001t0004g0066a0001c0001t0004g0068 | 2 | HG02602.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.685-17105T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31878763 | ||||||
| chr10:31878975
|
A | G | 1 | a0001c0001t0003g0184 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.685-17317T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31878975 | ||||||
| chr10:31879139
|
A | G | 15 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(12): Show | 15 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.685-17481T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31879139 | ||||||
| chr10:31879273
|
G | A | 5 | a0001c0001t0023g0040a0001c0001t0023g0069a0001c0001t0024g0042others(2): Show | 5 | HG02572.hp2 HG02622.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.685-17615C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31879273 | ||||||
| chr10:31879284
|
C | G | 1 | a0001c0001t0004g0038 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.685-17626G>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31879284 | ||||||
| chr10:31879325
|
T | C | 1 | a0002c0002t0007g0320 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.685-17667A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31879325 | ||||||
| chr10:31879391
|
T | G | 84 | a0001c0007t0028g0239a0001c0007t0028g0240a0001c0010t0053g0238others(81): Show | 84 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.685-17733A>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31879391 | ||||||
| chr10:31879698
|
A | G | 1 | a0001c0001t0023g0069 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.685-18040T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31879698 | ||||||
| chr10:31879875
|
T | C | 9 | a0001c0001t0001g0099a0001c0001t0001g0119a0001c0001t0001g0129others(6): Show | 9 | HG00733.hp1 HG00741.hp2 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.685-18217A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31879875 | ||||||
| chr10:31880048
|
T | C | 1 | a0002c0002t0002g0319 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.685-18390A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31880048 | ||||||
| chr10:31880289
|
C | T | 1 | a0001c0001t0008g0131 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.685-18631G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31880289 | ||||||
| chr10:31880473
|
C | CA | 29 | a0001c0001t0001g0147a0001c0001t0004g0044a0001c0001t0005g0043others(26): Show | 29 | HG01109.hp1 HG01168.hp1 HG01192.hp2 others(26): Show |
intron_variant | MODIFIER | c.685-18816dupT | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31880473 | ||||||
| chr10:31880490
|
GTTTAA | G | 53 | a0002c0002t0002g0243a0002c0002t0002g0245a0002c0002t0002g0250others(50): Show | 53 | HG00639.hp2 HG00738.hp2 HG01071.hp2 others(50): Show |
intron_variant | MODIFIER | c.685-18837_685-1883 others(9): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31880490 | ||||||
| chr10:31880530
|
A | G | 2 | a0002c0002t0002g0256a0002c0002t0002g0257 | 2 | NA19058.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.685-18872T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31880530 | ||||||
| chr10:31880534
|
G | T | 16 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(13): Show | 16 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.685-18876C>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31880534 | ||||||
| chr10:31880586
|
T | C | 3 | a0001c0001t0001g0103a0001c0001t0001g0127a0001c0001t0001g0203 | 3 | NA18940.hp2 NA19058.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.685-18928A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31880586 | ||||||
| chr10:31880706
|
A | G | 273 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0096others(270): Show | 273 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.685-19048T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31880706 | ||||||
| chr10:31880728
|
T | G | 1 | a0001c0001t0001g0207 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.685-19070A>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31880728 | ||||||
| chr10:31880757
|
A | T | 1 | a0001c0001t0012g0187 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.685-19099T>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31880757 | ||||||
| chr10:31880876
|
G | A | 4 | a0001c0001t0019g0162a0001c0001t0019g0163a0001c0001t0019g0166others(1): Show | 4 | HG01167.hp1 HG02970.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.685-19218C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31880876 | ||||||
| chr10:31880897
|
CA | C | 94 | a0001c0001t0009g0032a0001c0001t0009g0072a0001c0001t0009g0073others(91): Show | 94 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.685-19240delT | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31880897 | ||||||
| chr10:31881036
|
C | T | 9 | a0001c0001t0001g0215a0001c0001t0001g0217a0001c0001t0001g0218others(6): Show | 9 | HG00738.hp1 HG00741.hp1 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.685-19378G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31881036 | ||||||
| chr10:31881037
|
C | A | 1 | a0001c0001t0001g0101 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.685-19379G>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31881037 | ||||||
| chr10:31881064
|
C | T | 1 | a0001c0001t0003g0026 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.685-19406G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31881064 | ||||||
| chr10:31881290
|
G | C | 1 | a0001c0001t0001g0146 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.685-19632C>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31881290 | ||||||
| chr10:31881377
|
A | C | 84 | a0001c0007t0028g0239a0001c0007t0028g0240a0001c0010t0053g0238others(81): Show | 84 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.685-19719T>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31881377 | ||||||
| chr10:31881915
|
G | GT | 34 | a0001c0001t0001g0088a0001c0001t0001g0121a0001c0001t0001g0132others(31): Show | 34 | HG00544.hp1 HG00735.hp2 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.685-20258dupA | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31881915 | ||||||
| chr10:31881938
|
G | A | 1 | a0001c0001t0019g0163 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.685-20280C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31881938 | ||||||
| chr10:31881945
|
C | T | 1 | a0001c0003t0027g0014 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.685-20287G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31881945 | ||||||
| chr10:31882076
|
G | C | 11 | a0001c0001t0009g0032a0001c0001t0009g0072a0001c0001t0009g0073others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.685-20418C>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31882076 | ||||||
| chr10:31882244
|
T | C | 2 | a0002c0002t0002g0250a0002c0002t0002g0285 | 2 | NA18952.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.685-20586A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31882244 | ||||||
| chr10:31882249
|
A | G | 1 | a0001c0001t0022g0174 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.685-20591T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31882249 | ||||||
| chr10:31882328
|
G | A | 1 | a0001c0001t0003g0026 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.685-20670C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31882328 | ||||||
| chr10:31882328
|
G | T | 3 | a0001c0001t0012g0027a0001c0001t0049g0029a0001c0001t0050g0028 | 3 | HG02145.hp2 HG03579.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.685-20670C>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31882328 | ||||||
| chr10:31882334
|
T | C | 5 | a0001c0001t0003g0026a0001c0001t0012g0027a0001c0001t0034g0033others(2): Show | 5 | HG02145.hp2 HG02280.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.685-20676A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31882334 | ||||||
| chr10:31882355
|
A | C | 1 | a0001c0001t0004g0019 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.685-20697T>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31882355 | ||||||
| chr10:31882376
|
T | C | 16 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(13): Show | 16 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.685-20718A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31882376 | ||||||
| chr10:31882392
|
TAAG | T | 84 | a0001c0007t0028g0239a0001c0007t0028g0240a0001c0010t0053g0238others(81): Show | 84 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.685-20737_685-2073 others(7): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31882392 | ||||||
| chr10:31882471
|
T | C | 1 | a0001c0001t0001g0207 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.685-20813A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31882471 | ||||||
| chr10:31882668
|
G | A | 1 | a0001c0001t0001g0096 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.685-21010C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31882668 | ||||||
| chr10:31882820
|
GA | G | 177 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0096others(174): Show | 177 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(174): Show |
intron_variant | MODIFIER | c.685-21163delT | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31882820 | ||||||
| chr10:31882820
|
GAA | G | 22 | a0001c0001t0006g0150a0001c0001t0006g0153a0001c0001t0006g0158others(19): Show | 22 | HG01106.hp1 HG02145.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.685-21164_685-2116 others(6): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31882820 | ||||||
| chr10:31882820
|
GAAA | G | 49 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(46): Show | 49 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(46): Show |
intron_variant | MODIFIER | c.685-21165_685-2116 others(7): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31882820 | ||||||
| chr10:31883227
|
G | A | 1 | a0001c0001t0024g0042 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.685-21569C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31883227 | ||||||
| chr10:31883242
|
T | C | 1 | a0001c0001t0032g0151 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.685-21584A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31883242 | ||||||
| chr10:31883490
|
G | C | 10 | a0001c0001t0009g0032a0001c0001t0009g0072a0001c0001t0009g0073others(7): Show | 10 | HG02145.hp1 HG02257.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.685-21832C>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31883490 | ||||||
| chr10:31883516
|
C | T | 1 | a0001c0001t0006g0216 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.685-21858G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31883516 | ||||||
| chr10:31883600
|
A | G | 2 | a0001c0001t0049g0029a0001c0001t0050g0028 | 2 | HG02145.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.685-21942T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31883600 | ||||||
| chr10:31883624
|
C | T | 163 | a0001c0001t0003g0026a0001c0001t0004g0019a0001c0001t0004g0020others(160): Show | 163 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(160): Show |
intron_variant | MODIFIER | c.685-21966G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31883624 | ||||||
| chr10:31883713
|
C | CT | 30 | a0001c0001t0001g0236a0001c0001t0003g0198a0001c0001t0006g0150others(27): Show | 30 | HG00673.hp2 HG00735.hp2 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.685-22056dupA | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31883713 | ||||||
| chr10:31883817
|
T | C | 1 | a0001c0001t0001g0141 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.685-22159A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31883817 | ||||||
| chr10:31883869
|
G | A | 4 | a0001c0001t0019g0162a0001c0001t0019g0163a0001c0001t0019g0166others(1): Show | 4 | HG01167.hp1 HG02970.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.685-22211C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31883869 | ||||||
| chr10:31883899
|
G | C | 3 | a0001c0001t0017g0050a0001c0001t0017g0053a0001c0001t0017g0062 | 3 | HG02970.hp2 HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.685-22241C>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31883899 | ||||||
| chr10:31884007
|
G | T | 144 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(141): Show | 144 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(141): Show |
intron_variant | MODIFIER | c.685-22349C>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31884007 | ||||||
| chr10:31884094
|
T | TA | 7 | a0001c0001t0001g0100a0001c0001t0001g0106a0001c0001t0001g0114others(4): Show | 7 | HG00280.hp2 HG01978.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.685-22437dupT | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31884094 | ||||||
| chr10:31884094
|
TA | T | 154 | a0001c0001t0003g0026a0001c0001t0004g0019a0001c0001t0004g0020others(151): Show | 154 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(151): Show |
intron_variant | MODIFIER | c.685-22437delT | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31884094 | ||||||
| chr10:31884231
|
T | C | 19 | a0001c0001t0004g0044a0001c0001t0005g0043a0001c0001t0005g0045others(16): Show | 19 | HG01109.hp1 HG01168.hp1 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.685-22573A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31884231 | ||||||
| chr10:31884239
|
T | G | 16 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(13): Show | 16 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.685-22581A>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31884239 | ||||||
| chr10:31884240
|
C | T | 163 | a0001c0001t0003g0026a0001c0001t0004g0019a0001c0001t0004g0020others(160): Show | 163 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(160): Show |
intron_variant | MODIFIER | c.685-22582G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31884240 | ||||||
| chr10:31884289
|
A | T | 1 | a0001c0003t0048g0015 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.685-22631T>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31884289 | ||||||
| chr10:31884311
|
T | C | 11 | a0001c0001t0009g0032a0001c0001t0009g0072a0001c0001t0009g0073others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.685-22653A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31884311 | ||||||
| chr10:31884324
|
C | CA | 19 | a0001c0001t0001g0100a0001c0001t0001g0126a0001c0001t0001g0143others(16): Show | 19 | HG00597.hp1 HG01496.hp1 HG02071.hp1 others(16): Show |
intron_variant | MODIFIER | c.685-22667dupT | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31884324 | ||||||
| chr10:31884610
|
C | G | 1 | a0001c0001t0024g0042 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.685-22952G>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31884610 | ||||||
| chr10:31884635
|
C | G | 1 | a0001c0001t0024g0042 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.685-22977G>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31884635 | ||||||
| chr10:31884764
|
A | T | 1 | a0002c0002t0002g0305 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.685-23106T>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31884764 | ||||||
| chr10:31884876
|
C | G | 1 | a0001c0001t0009g0073 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.685-23218G>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31884876 | ||||||
| chr10:31884987
|
A | T | 1 | a0001c0001t0012g0027 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.684+23185T>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31884987 | ||||||
| chr10:31885015
|
A | C | 2 | a0001c0001t0004g0022a0001c0001t0004g0024 | 2 | HG01167.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.684+23157T>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31885015 | ||||||
| chr10:31885051
|
G | A | 1 | a0001c0003t0016g0004 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.684+23121C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31885051 | ||||||
| chr10:31885166
|
C | T | 49 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(46): Show | 49 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(46): Show |
intron_variant | MODIFIER | c.684+23006G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31885166 | ||||||
| chr10:31885169
|
T | C | 2 | a0002c0002t0002g0250a0002c0002t0002g0285 | 2 | NA18952.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.684+23003A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31885169 | ||||||
| chr10:31885379
|
T | C | 1 | a0002c0002t0020g0315 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.684+22793A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31885379 | ||||||
| chr10:31885682
|
G | A | 88 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0096others(85): Show | 88 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.684+22490C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31885682 | ||||||
| chr10:31885716
|
G | A | 16 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(13): Show | 16 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.684+22456C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31885716 | ||||||
| chr10:31885723
|
G | A | 1 | a0001c0006t0026g0067 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.684+22449C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31885723 | ||||||
| chr10:31885734
|
G | A | 16 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(13): Show | 16 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.684+22438C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31885734 | ||||||
| chr10:31885818
|
CA | C | 19 | a0001c0001t0004g0044a0001c0001t0005g0043a0001c0001t0005g0045others(16): Show | 19 | HG01109.hp1 HG01168.hp1 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.684+22353delT | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31885818 | ||||||
| chr10:31886029
|
A | G | 1 | a0001c0001t0040g0212 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.684+22143T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31886029 | ||||||
| chr10:31886035
|
G | T | 2 | a0001c0001t0004g0036a0001c0001t0037g0035 | 2 | HG02258.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.684+22137C>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31886035 | ||||||
| chr10:31886437
|
T | G | 1 | a0002c0002t0029g0284 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.684+21735A>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31886437 | ||||||
| chr10:31886613
|
G | T | 84 | a0001c0007t0028g0239a0001c0007t0028g0240a0001c0010t0053g0238others(81): Show | 84 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.684+21559C>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31886613 | ||||||
| chr10:31886625
|
T | G | 84 | a0001c0007t0028g0239a0001c0007t0028g0240a0001c0010t0053g0238others(81): Show | 84 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.684+21547A>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31886625 | ||||||
| chr10:31886968
|
A | G | 144 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(141): Show | 144 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(141): Show |
intron_variant | MODIFIER | c.684+21204T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31886968 | ||||||
| chr10:31887044
|
G | T | 1 | a0001c0001t0034g0033 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.684+21128C>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31887044 | ||||||
| chr10:31887061
|
C | T | 1 | a0002c0002t0002g0282 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.684+21111G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31887061 | ||||||
| chr10:31887187
|
G | A | 16 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(13): Show | 16 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.684+20985C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31887187 | ||||||
| chr10:31887212
|
C | T | 1 | a0002c0002t0014g0272 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.684+20960G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31887212 | ||||||
| chr10:31887482
|
G | A | 16 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(13): Show | 16 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.684+20690C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31887482 | ||||||
| chr10:31887651
|
T | G | 9 | a0001c0001t0001g0215a0001c0001t0001g0217a0001c0001t0001g0218others(6): Show | 9 | HG00738.hp1 HG00741.hp1 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.684+20521A>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31887651 | ||||||
| chr10:31887661
|
G | GT | 82 | a0001c0001t0001g0107a0001c0001t0013g0149a0001c0007t0028g0239others(79): Show | 82 | HG00597.hp1 HG00673.hp1 HG00738.hp2 others(79): Show |
intron_variant | MODIFIER | c.684+20510dupA | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31887661 | ||||||
| chr10:31887661
|
G | T | 3 | a0001c0001t0004g0044a0001c0001t0005g0047a0001c0001t0040g0212 | 3 | HG01109.hp1 HG01978.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.684+20511C>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31887661 | ||||||
| chr10:31887661
|
GT | G | 72 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(69): Show | 72 | HG00099.hp2 HG00735.hp2 HG01081.hp2 others(69): Show |
intron_variant | MODIFIER | c.684+20510delA | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31887661 | ||||||
| chr10:31887662
|
T | G | 1 | a0001c0001t0004g0044 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.684+20510A>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31887662 | ||||||
| chr10:31887663
|
T | G | 1 | a0001c0001t0040g0212 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.684+20509A>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31887663 | ||||||
| chr10:31887709
|
G | A | 10 | a0001c0001t0009g0032a0001c0001t0009g0072a0001c0001t0009g0073others(7): Show | 10 | HG02145.hp1 HG02257.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.684+20463C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31887709 | ||||||
| chr10:31887780
|
C | G | 49 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(46): Show | 49 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(46): Show |
intron_variant | MODIFIER | c.684+20392G>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31887780 | ||||||
| chr10:31887844
|
C | T | 11 | a0001c0001t0009g0032a0001c0001t0009g0072a0001c0001t0009g0073others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.684+20328G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31887844 | ||||||
| chr10:31887845
|
G | A | 1 | a0001c0001t0052g0318 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.684+20327C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31887845 | ||||||
| chr10:31887912
|
C | G | 2 | a0001c0001t0001g0210a0001c0001t0001g0232 | 2 | HG01099.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.684+20260G>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31887912 | ||||||
| chr10:31888181
|
G | C | 1 | a0002c0002t0007g0246 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.684+19991C>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31888181 | ||||||
| chr10:31888478
|
C | T | 1 | a0001c0001t0003g0169 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.684+19694G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31888478 | ||||||
| chr10:31888753
|
A | G | 2 | a0001c0007t0028g0239a0001c0007t0028g0240 | 2 | HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.684+19419T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31888753 | ||||||
| chr10:31888915
|
C | CT | 88 | a0001c0001t0001g0215a0001c0001t0011g0061a0001c0001t0017g0062others(85): Show | 88 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.684+19256dupA | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31888915 | ||||||
| chr10:31889193
|
T | C | 1 | a0001c0001t0004g0064 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.684+18979A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31889193 | ||||||
| chr10:31889328
|
C | T | 8 | a0002c0002t0002g0262a0002c0002t0002g0275a0002c0002t0002g0276others(5): Show | 8 | HG00597.hp1 HG00673.hp1 NA18951.hp1 others(5): Show |
intron_variant | MODIFIER | c.684+18844G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31889328 | ||||||
| chr10:31889549
|
C | T | 2 | a0001c0001t0003g0170a0001c0001t0003g0196 | 2 | NA18953.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.684+18623G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31889549 | ||||||
| chr10:31889619
|
G | GT | 70 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0001g0107others(67): Show | 70 | HG00099.hp2 HG00544.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.684+18552dupA | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31889619 | ||||||
| chr10:31889619
|
G | GTT | 6 | a0001c0001t0001g0122a0001c0001t0001g0130a0001c0001t0004g0024others(3): Show | 6 | HG00621.hp2 HG00741.hp2 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.684+18551_684+1855 others(6): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31889619 | ||||||
| chr10:31889619
|
GT | G | 67 | a0001c0001t0004g0034a0001c0001t0006g0160a0001c0001t0011g0056others(64): Show | 67 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.684+18552delA | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31889619 | ||||||
| chr10:31889619
|
GTTT | G | 8 | a0001c0001t0009g0032a0001c0001t0009g0072a0001c0001t0009g0073others(5): Show | 8 | HG02145.hp1 HG02559.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.684+18550_684+1855 others(7): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31889619 | ||||||
| chr10:31889644
|
T | TTG | 13 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(10): Show | 13 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.684+18527_684+1852 others(6): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31889644 | ||||||
| chr10:31890022
|
C | T | 1 | a0001c0001t0001g0229 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.684+18150G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31890022 | ||||||
| chr10:31890207
|
C | A | 1 | a0001c0001t0001g0208 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.684+17965G>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31890207 | ||||||
| chr10:31890247
|
C | T | 4 | a0001c0001t0019g0162a0001c0001t0019g0163a0001c0001t0019g0166others(1): Show | 4 | HG01167.hp1 HG02970.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.684+17925G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31890247 | ||||||
| chr10:31890256
|
A | C | 144 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(141): Show | 144 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(141): Show |
intron_variant | MODIFIER | c.684+17916T>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31890256 | ||||||
| chr10:31890331
|
T | C | 4 | a0002c0002t0014g0242a0002c0002t0014g0271a0002c0002t0014g0272others(1): Show | 4 | NA18947.hp2 NA18982.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.684+17841A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31890331 | ||||||
| chr10:31890335
|
T | C | 2 | a0001c0001t0003g0180a0001c0001t0003g0184 | 2 | HG02074.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.684+17837A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31890335 | ||||||
| chr10:31890347
|
T | C | 145 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(142): Show | 145 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(142): Show |
intron_variant | MODIFIER | c.684+17825A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31890347 | ||||||
| chr10:31890384
|
T | A | 1 | a0001c0001t0001g0213 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.684+17788A>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31890384 | ||||||
| chr10:31890459
|
C | T | 4 | a0001c0001t0001g0083a0001c0001t0001g0228a0001c0001t0001g0230others(1): Show | 4 | HG01175.hp2 HG01192.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.684+17713G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31890459 | ||||||
| chr10:31890595
|
G | A | 166 | a0001c0001t0001g0213a0001c0001t0003g0026a0001c0001t0004g0019others(163): Show | 166 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(163): Show |
intron_variant | MODIFIER | c.684+17577C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31890595 | ||||||
| chr10:31890667
|
A | G | 11 | a0001c0001t0009g0032a0001c0001t0009g0072a0001c0001t0009g0073others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.684+17505T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31890667 | ||||||
| chr10:31890843
|
A | G | 144 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(141): Show | 144 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(141): Show |
intron_variant | MODIFIER | c.684+17329T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31890843 | ||||||
| chr10:31891063
|
T | G | 1 | a0001c0001t0011g0071 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.684+17109A>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31891063 | ||||||
| chr10:31891487
|
G | A | 1 | a0001c0001t0004g0034 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.684+16685C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31891487 | ||||||
| chr10:31891614
|
TTGAA | T | 133 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(130): Show | 133 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(130): Show |
intron_variant | MODIFIER | c.684+16554_684+1655 others(8): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31891614 | ||||||
| chr10:31891643
|
G | A | 18 | a0001c0001t0004g0044a0001c0001t0005g0043a0001c0001t0005g0045others(15): Show | 18 | HG01109.hp1 HG01168.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.684+16529C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31891643 | ||||||
| chr10:31891863
|
C | G | 1 | a0001c0001t0001g0137 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.684+16309G>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31891863 | ||||||
| chr10:31891909
|
C | T | 1 | a0001c0003t0048g0015 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.684+16263G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31891909 | ||||||
| chr10:31892060
|
G | A | 81 | a0002c0002t0002g0243a0002c0002t0002g0245a0002c0002t0002g0247others(78): Show | 81 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.684+16112C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31892060 | ||||||
| chr10:31892131
|
A | G | 1 | a0001c0001t0003g0198 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.684+16041T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31892131 | ||||||
| chr10:31892185
|
G | A | 1 | a0001c0001t0050g0028 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.684+15987C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31892185 | ||||||
| chr10:31892266
|
A | C | 2 | a0001c0007t0028g0239a0001c0007t0028g0240 | 2 | HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.684+15906T>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31892266 | ||||||
| chr10:31892388
|
T | C | 1 | a0001c0001t0001g0130 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.684+15784A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31892388 | ||||||
| chr10:31892392
|
C | T | 144 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(141): Show | 144 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(141): Show |
intron_variant | MODIFIER | c.684+15780G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31892392 | ||||||
| chr10:31892510
|
A | C | 144 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(141): Show | 144 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(141): Show |
intron_variant | MODIFIER | c.684+15662T>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31892510 | ||||||
| chr10:31892877
|
T | G | 16 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(13): Show | 16 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.684+15295A>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31892877 | ||||||
| chr10:31892882
|
G | C | 16 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(13): Show | 16 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.684+15290C>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31892882 | ||||||
| chr10:31892951
|
G | C | 11 | a0001c0001t0009g0032a0001c0001t0009g0072a0001c0001t0009g0073others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.684+15221C>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31892951 | ||||||
| chr10:31892958
|
G | A | 77 | a0002c0002t0002g0243a0002c0002t0002g0245a0002c0002t0002g0247others(74): Show | 77 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.684+15214C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31892958 | ||||||
| chr10:31892996
|
G | A | 84 | a0001c0007t0028g0239a0001c0007t0028g0240a0001c0010t0053g0238others(81): Show | 84 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.684+15176C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31892996 | ||||||
| chr10:31893014
|
A | G | 144 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(141): Show | 144 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(141): Show |
intron_variant | MODIFIER | c.684+15158T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31893014 | ||||||
| chr10:31893240
|
T | C | 3 | a0001c0001t0001g0088a0001c0001t0008g0105a0001c0001t0039g0089 | 3 | HG02071.hp1 NA19072.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.684+14932A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31893240 | ||||||
| chr10:31893403
|
A | C | 1 | a0002c0002t0007g0297 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.684+14769T>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31893403 | ||||||
| chr10:31893406
|
A | G | 1 | a0002c0002t0002g0278 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.684+14766T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31893406 | ||||||
| chr10:31893415
|
T | A | 1 | a0001c0001t0004g0064 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.684+14757A>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31893415 | ||||||
| chr10:31893565
|
A | AT | 144 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(141): Show | 144 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(141): Show |
intron_variant | MODIFIER | c.684+14606dupA | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31893565 | ||||||
| chr10:31893676
|
A | C | 1 | a0001c0001t0004g0022 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.684+14496T>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31893676 | ||||||
| chr10:31893705
|
C | T | 1 | a0001c0001t0001g0147 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.684+14467G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31893705 | ||||||
| chr10:31893832
|
A | G | 144 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(141): Show | 144 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(141): Show |
intron_variant | MODIFIER | c.684+14340T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31893832 | ||||||
| chr10:31893898
|
T | C | 176 | a0001c0001t0001g0213a0001c0001t0001g0215a0001c0001t0001g0217others(173): Show | 176 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(173): Show |
intron_variant | MODIFIER | c.684+14274A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31893898 | ||||||
| chr10:31894091
|
T | C | 144 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(141): Show | 144 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(141): Show |
intron_variant | MODIFIER | c.684+14081A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31894091 | ||||||
| chr10:31894263
|
G | T | 1 | a0001c0001t0001g0141 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.684+13909C>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31894263 | ||||||
| chr10:31894321
|
G | C | 1 | a0001c0001t0040g0212 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.684+13851C>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31894321 | ||||||
| chr10:31894323
|
T | C | 16 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(13): Show | 16 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.684+13849A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31894323 | ||||||
| chr10:31894324
|
G | A | 1 | a0001c0003t0010g0017 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.684+13848C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31894324 | ||||||
| chr10:31894400
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.684+13772A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31894400 | ||||||
| chr10:31894444
|
T | C | 1 | a0001c0001t0045g0076 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.684+13728A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31894444 | ||||||
| chr10:31894466
|
A | G | 1 | a0002c0002t0002g0295 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.684+13706T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31894466 | ||||||
| chr10:31894487
|
T | C | 2 | a0001c0001t0001g0226a0001c0001t0008g0152 | 2 | HG01884.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.684+13685A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31894487 | ||||||
| chr10:31894504
|
T | C | 1 | a0001c0001t0043g0025 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.684+13668A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31894504 | ||||||
| chr10:31894554
|
C | T | 16 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(13): Show | 16 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.684+13618G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31894554 | ||||||
| chr10:31894653
|
C | T | 4 | a0002c0002t0007g0308a0003c0004t0007g0309a0003c0004t0007g0310others(1): Show | 4 | HG01109.hp2 HG03130.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.684+13519G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31894653 | ||||||
| chr10:31894694
|
T | C | 1 | a0002c0002t0002g0319 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.684+13478A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31894694 | ||||||
| chr10:31894717
|
G | A | 1 | a0001c0003t0010g0016 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.684+13455C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31894717 | ||||||
| chr10:31894719
|
G | T | 1 | a0001c0003t0010g0016 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.684+13453C>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31894719 | ||||||
| chr10:31894761
|
A | G | 1 | a0001c0003t0010g0016 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.684+13411T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31894761 | ||||||
| chr10:31894781
|
G | A | 5 | a0002c0002t0002g0301a0002c0002t0002g0303a0002c0002t0002g0304others(2): Show | 5 | HG00639.hp2 HG01099.hp1 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.684+13391C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31894781 | ||||||
| chr10:31894810
|
T | G | 85 | a0001c0001t0038g0205a0001c0007t0028g0239a0001c0007t0028g0240others(82): Show | 85 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.684+13362A>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31894810 | ||||||
| chr10:31894882
|
T | C | 9 | a0001c0001t0001g0215a0001c0001t0001g0217a0001c0001t0001g0218others(6): Show | 9 | HG00738.hp1 HG00741.hp1 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.684+13290A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31894882 | ||||||
| chr10:31894922
|
C | A | 11 | a0001c0001t0009g0032a0001c0001t0009g0072a0001c0001t0009g0073others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.684+13250G>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31894922 | ||||||
| chr10:31895035
|
T | C | 1 | a0001c0001t0008g0098 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.684+13137A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31895035 | ||||||
| chr10:31895348
|
T | C | 166 | a0001c0001t0003g0026a0001c0001t0004g0019a0001c0001t0004g0020others(163): Show | 166 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(163): Show |
intron_variant | MODIFIER | c.684+12824A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31895348 | ||||||
| chr10:31895359
|
C | T | 5 | a0001c0001t0003g0026a0001c0001t0012g0027a0001c0001t0034g0033others(2): Show | 5 | HG02145.hp2 HG02280.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.684+12813G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31895359 | ||||||
| chr10:31895799
|
T | C | 3 | a0001c0001t0017g0050a0001c0001t0017g0053a0001c0001t0017g0062 | 3 | HG02970.hp2 HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.684+12373A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31895799 | ||||||
| chr10:31895899
|
C | G | 11 | a0001c0001t0009g0032a0001c0001t0009g0072a0001c0001t0009g0073others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.684+12273G>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31895899 | ||||||
| chr10:31896005
|
C | T | 1 | a0001c0001t0003g0026 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.684+12167G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31896005 | ||||||
| chr10:31896109
|
G | C | 5 | a0001c0001t0023g0040a0001c0001t0023g0069a0001c0001t0024g0042others(2): Show | 5 | HG02572.hp2 HG02622.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.684+12063C>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31896109 | ||||||
| chr10:31896131
|
C | T | 1 | a0001c0001t0006g0153 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.684+12041G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31896131 | ||||||
| chr10:31896308
|
G | GA | 8 | a0001c0001t0003g0200a0001c0001t0011g0055a0001c0001t0011g0056others(5): Show | 8 | HG01884.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.684+11863dupT | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31896308 | ||||||
| chr10:31896308
|
GA | G | 32 | a0001c0001t0001g0128a0001c0001t0004g0031a0001c0001t0008g0155others(29): Show | 32 | HG00735.hp2 HG02145.hp1 HG02257.hp1 others(29): Show |
intron_variant | MODIFIER | c.684+11863delT | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31896308 | ||||||
| chr10:31896576
|
T | C | 1 | a0001c0001t0001g0132 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.684+11596A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31896576 | ||||||
| chr10:31896666
|
T | C | 8 | a0001c0001t0006g0150a0001c0001t0006g0153a0001c0001t0006g0158others(5): Show | 8 | HG01106.hp1 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.684+11506A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31896666 | ||||||
| chr10:31896980
|
A | AT | 167 | a0001c0001t0001g0157a0001c0001t0003g0026a0001c0001t0004g0019others(164): Show | 167 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(164): Show |
intron_variant | MODIFIER | c.684+11191_684+1119 others(5): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31896980 | ||||||
| chr10:31897177
|
G | A | 1 | a0001c0001t0001g0135 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.684+10995C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31897177 | ||||||
| chr10:31897228
|
A | G | 3 | a0002c0002t0002g0298a0002c0002t0002g0299a0002c0002t0002g0306 | 3 | HG02027.hp2 HG02040.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.684+10944T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31897228 | ||||||
| chr10:31897358
|
G | A | 2 | a0001c0001t0001g0086a0001c0001t0001g0102 | 2 | NA19057.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.684+10814C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31897358 | ||||||
| chr10:31897360
|
A | G | 1 | a0001c0001t0001g0119 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.684+10812T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31897360 | ||||||
| chr10:31897549
|
T | C | 2 | a0002c0002t0002g0262a0002c0002t0002g0295 | 2 | HG00597.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.684+10623A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31897549 | ||||||
| chr10:31897670
|
C | T | 1 | a0001c0001t0001g0225 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.684+10502G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31897670 | ||||||
| chr10:31897696
|
T | C | 1 | a0001c0008t0005g0075 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.684+10476A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31897696 | ||||||
| chr10:31897698
|
T | C | 1 | a0001c0001t0001g0137 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.684+10474A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31897698 | ||||||
| chr10:31897708
|
C | T | 3 | a0002c0002t0007g0313a0002c0002t0007g0314a0002c0002t0007g0316 | 3 | HG02074.hp2 HG03834.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.684+10464G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31897708 | ||||||
| chr10:31897855
|
A | G | 144 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(141): Show | 144 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(141): Show |
intron_variant | MODIFIER | c.684+10317T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31897855 | ||||||
| chr10:31897892
|
A | G | 3 | a0001c0001t0001g0115a0001c0001t0001g0117a0001c0001t0015g0116 | 3 | NA18946.hp2 NA18965.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.684+10280T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31897892 | ||||||
| chr10:31898123
|
C | G | 1 | a0001c0001t0006g0214 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.684+10049G>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31898123 | ||||||
| chr10:31898246
|
G | A | 1 | a0002c0002t0002g0289 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.684+9926C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31898246 | ||||||
| chr10:31898462
|
G | A | 2 | a0002c0002t0002g0302a0002c0002t0002g0305 | 2 | HG02155.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.684+9710C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31898462 | ||||||
| chr10:31898475
|
T | A | 2 | a0002c0002t0002g0291a0002c0002t0002g0292 | 2 | HG00673.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.684+9697A>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31898475 | ||||||
| chr10:31898580
|
G | A | 7 | a0001c0001t0011g0055a0001c0001t0011g0056a0001c0001t0011g0057others(4): Show | 7 | HG01884.hp1 HG01891.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.684+9592C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31898580 | ||||||
| chr10:31898774
|
C | A | 1 | a0001c0001t0001g0236 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.684+9398G>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31898774 | ||||||
| chr10:31898869
|
A | G | 2 | a0001c0001t0008g0134a0001c0001t0008g0136 | 2 | HG02027.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.684+9303T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31898869 | ||||||
| chr10:31898907
|
T | C | 11 | a0001c0001t0009g0032a0001c0001t0009g0072a0001c0001t0009g0073others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.684+9265A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31898907 | ||||||
| chr10:31899029
|
G | A | 2 | a0001c0001t0004g0044a0001c0001t0005g0043 | 2 | HG01978.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.684+9143C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31899029 | ||||||
| chr10:31899116
|
C | T | 6 | a0001c0001t0023g0040a0001c0001t0023g0069a0001c0001t0024g0060others(3): Show | 6 | HG02572.hp2 HG02622.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.684+9056G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31899116 | ||||||
| chr10:31899391
|
A | G | 84 | a0001c0007t0028g0239a0001c0007t0028g0240a0001c0010t0053g0238others(81): Show | 84 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.684+8781T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31899391 | ||||||
| chr10:31899401
|
T | G | 2 | a0001c0001t0003g0180a0001c0001t0003g0184 | 2 | HG02074.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.684+8771A>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31899401 | ||||||
| chr10:31899693
|
A | C | 5 | a0001c0001t0003g0026a0001c0001t0012g0027a0001c0001t0034g0033others(2): Show | 5 | HG02145.hp2 HG02280.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.684+8479T>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31899693 | ||||||
| chr10:31899796
|
G | A | 1 | a0001c0001t0011g0058 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.684+8376C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31899796 | ||||||
| chr10:31899853
|
G | A | 1 | a0001c0001t0004g0038 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.684+8319C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31899853 | ||||||
| chr10:31899951
|
A | C | 5 | a0001c0003t0010g0010a0001c0003t0010g0018a0001c0003t0027g0012others(2): Show | 5 | HG02615.hp1 HG02630.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.684+8221T>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31899951 | ||||||
| chr10:31900007
|
C | T | 1 | a0001c0001t0034g0033 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.684+8165G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31900007 | ||||||
| chr10:31900088
|
A | T | 15 | a0001c0001t0004g0044a0001c0001t0005g0043a0001c0001t0005g0045others(12): Show | 15 | HG01109.hp1 HG01168.hp1 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.684+8084T>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31900088 | ||||||
| chr10:31900170
|
T | C | 10 | a0001c0001t0009g0032a0001c0001t0009g0072a0001c0001t0009g0073others(7): Show | 10 | HG02145.hp1 HG02257.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.684+8002A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31900170 | ||||||
| chr10:31900282
|
T | C | 2 | a0001c0003t0016g0003a0001c0003t0016g0004 | 2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.684+7890A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31900282 | ||||||
| chr10:31900526
|
T | C | 1 | a0001c0001t0012g0227 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.684+7646A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31900526 | ||||||
| chr10:31900625
|
T | G | 3 | a0002c0002t0002g0265a0002c0002t0002g0282a0002c0002t0002g0317 | 3 | HG02071.hp2 NA19056.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.684+7547A>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31900625 | ||||||
| chr10:31900693
|
G | A | 1 | a0002c0002t0002g0319 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.684+7479C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31900693 | ||||||
| chr10:31900833
|
AT | A | 94 | a0001c0001t0009g0032a0001c0001t0009g0072a0001c0001t0009g0073others(91): Show | 94 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.684+7338delA | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31900833 | ||||||
| chr10:31900899
|
A | C | 19 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(16): Show | 19 | HG00099.hp2 HG01081.hp2 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.684+7273T>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31900899 | ||||||
| chr10:31901178
|
T | C | 50 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(47): Show | 50 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.684+6994A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31901178 | ||||||
| chr10:31901213
|
C | CA | 35 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(32): Show | 35 | HG00099.hp2 HG00735.hp2 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.684+6958dupT | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31901213 | ||||||
| chr10:31901269
|
T | C | 1 | a0002c0002t0007g0308 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.684+6903A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31901269 | ||||||
| chr10:31901352
|
T | C | 1 | a0001c0001t0043g0025 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.684+6820A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31901352 | ||||||
| chr10:31901377
|
C | T | 2 | a0001c0007t0028g0239a0001c0007t0028g0240 | 2 | HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.684+6795G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31901377 | ||||||
| chr10:31901392
|
G | A | 1 | a0001c0001t0003g0180 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.684+6780C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31901392 | ||||||
| chr10:31901500
|
T | C | 1 | a0001c0001t0038g0205 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.684+6672A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31901500 | ||||||
| chr10:31901534
|
C | CAAAAA | 11 | a0001c0003t0010g0005a0001c0003t0010g0010a0001c0003t0010g0011others(8): Show | 11 | HG02257.hp2 HG02615.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.684+6633_684+6637d others(7): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31901534 | ||||||
| chr10:31901534
|
CA | C | 218 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0088others(215): Show | 218 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(215): Show |
intron_variant | MODIFIER | c.684+6637delT | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31901534 | ||||||
| chr10:31901534
|
CAA | C | 67 | a0001c0001t0001g0119a0001c0001t0001g0126a0001c0001t0001g0128others(64): Show | 67 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.684+6636_684+6637d others(4): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31901534 | ||||||
| chr10:31901564
|
A | T | 2 | a0001c0001t0001g0226a0001c0001t0008g0152 | 2 | HG01884.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.684+6608T>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31901564 | ||||||
| chr10:31901684
|
A | G | 94 | a0001c0001t0009g0032a0001c0001t0009g0072a0001c0001t0009g0073others(91): Show | 94 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.684+6488T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31901684 | ||||||
| chr10:31901768
|
C | CTCTT | 16 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(13): Show | 16 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.684+6400_684+6403d others(6): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31901768 | ||||||
| chr10:31901792
|
T | C | 16 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(13): Show | 16 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.684+6380A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31901792 | ||||||
| chr10:31902130
|
G | A | 1 | a0002c0002t0002g0301 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.684+6042C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31902130 | ||||||
| chr10:31902131
|
A | G | 2 | a0001c0007t0028g0239a0001c0007t0028g0240 | 2 | HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.684+6041T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31902131 | ||||||
| chr10:31902324
|
A | C | 1 | a0001c0001t0004g0064 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.684+5848T>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31902324 | ||||||
| chr10:31902365
|
C | T | 1 | a0001c0003t0010g0011 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.684+5807G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31902365 | ||||||
| chr10:31902439
|
G | A | 1 | a0001c0003t0048g0015 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.684+5733C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31902439 | ||||||
| chr10:31902533
|
G | A | 1 | a0001c0003t0010g0018 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.684+5639C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31902533 | ||||||
| chr10:31902616
|
AG | A | 19 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(16): Show | 19 | HG00099.hp2 HG01081.hp2 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.684+5555delC | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31902616 | ||||||
| chr10:31902936
|
C | A | 1 | a0002c0002t0007g0297 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.684+5236G>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31902936 | ||||||
| chr10:31902988
|
A | C | 3 | a0001c0001t0001g0103a0001c0001t0001g0127a0001c0001t0001g0203 | 3 | NA18940.hp2 NA19058.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.684+5184T>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31902988 | ||||||
| chr10:31903098
|
A | C | 93 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0088others(90): Show | 93 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.684+5074T>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31903098 | ||||||
| chr10:31903108
|
A | T | 16 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(13): Show | 16 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.684+5064T>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31903108 | ||||||
| chr10:31903367
|
T | C | 1 | a0001c0001t0012g0027 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.684+4805A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31903367 | ||||||
| chr10:31903470
|
G | A | 1 | a0001c0001t0001g0209 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.684+4702C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31903470 | ||||||
| chr10:31903508
|
A | G | 1 | a0001c0001t0013g0149 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.684+4664T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31903508 | ||||||
| chr10:31903538
|
C | T | 2 | a0001c0001t0003g0026a0001c0001t0012g0027 | 2 | HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.684+4634G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31903538 | ||||||
| chr10:31903734
|
T | TA | 10 | a0001c0001t0001g0215a0001c0001t0001g0217a0001c0001t0001g0218others(7): Show | 10 | HG00738.hp1 HG00741.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.684+4437dupT | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31903734 | ||||||
| chr10:31903763
|
TA | T | 170 | a0001c0001t0001g0215a0001c0001t0001g0217a0001c0001t0001g0218others(167): Show | 170 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(167): Show |
intron_variant | MODIFIER | c.684+4408delT | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31903763 | ||||||
| chr10:31903892
|
C | G | 1 | a0002c0002t0002g0302 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.684+4280G>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31903892 | ||||||
| chr10:31903985
|
C | T | 4 | a0002c0002t0007g0308a0003c0004t0007g0309a0003c0004t0007g0310others(1): Show | 4 | HG01109.hp2 HG03130.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.684+4187G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31903985 | ||||||
| chr10:31904008
|
T | C | 1 | a0002c0002t0029g0284 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.684+4164A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31904008 | ||||||
| chr10:31904219
|
T | G | 16 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(13): Show | 16 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.684+3953A>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31904219 | ||||||
| chr10:31904334
|
C | T | 319 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0088others(316): Show | 319 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.684+3838G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31904334 | ||||||
| chr10:31904467
|
T | C | 7 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0011others(4): Show | 7 | HG00735.hp2 HG02257.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.684+3705A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31904467 | ||||||
| chr10:31904500
|
G | A | 18 | a0001c0001t0004g0044a0001c0001t0005g0043a0001c0001t0005g0045others(15): Show | 18 | HG01109.hp1 HG01168.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.684+3672C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31904500 | ||||||
| chr10:31904535
|
A | T | 1 | a0002c0002t0002g0301 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.684+3637T>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31904535 | ||||||
| chr10:31904572
|
T | C | 1 | a0001c0001t0001g0232 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.684+3600A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31904572 | ||||||
| chr10:31904599
|
T | C | 11 | a0001c0001t0009g0032a0001c0001t0009g0072a0001c0001t0009g0073others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.684+3573A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31904599 | ||||||
| chr10:31904625
|
C | A | 1 | a0001c0001t0011g0059 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.684+3547G>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31904625 | ||||||
| chr10:31904696
|
G | A | 1 | a0001c0001t0001g0207 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.684+3476C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31904696 | ||||||
| chr10:31904815
|
T | C | 1 | a0001c0001t0001g0118 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.684+3357A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31904815 | ||||||
| chr10:31905062
|
T | C | 1 | a0001c0001t0003g0182 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.684+3110A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31905062 | ||||||
| chr10:31905199
|
A | T | 166 | a0001c0001t0003g0026a0001c0001t0004g0019a0001c0001t0004g0020others(163): Show | 166 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(163): Show |
intron_variant | MODIFIER | c.684+2973T>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31905199 | ||||||
| chr10:31905234
|
T | C | 1 | a0001c0001t0044g0079 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.684+2938A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31905234 | ||||||
| chr10:31905255
|
C | T | 81 | a0002c0002t0002g0243a0002c0002t0002g0245a0002c0002t0002g0247others(78): Show | 81 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.684+2917G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31905255 | ||||||
| chr10:31905333
|
T | C | 10 | a0001c0001t0009g0032a0001c0001t0009g0072a0001c0001t0009g0073others(7): Show | 10 | HG02145.hp1 HG02257.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.684+2839A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31905333 | ||||||
| chr10:31905338
|
C | A | 1 | a0001c0001t0045g0076 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.684+2834G>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31905338 | ||||||
| chr10:31905456
|
G | A | 20 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(17): Show | 20 | HG00099.hp2 HG01081.hp2 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.684+2716C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31905456 | ||||||
| chr10:31905589
|
C | T | 1 | a0002c0002t0007g0254 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.684+2583G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31905589 | ||||||
| chr10:31905609
|
AGAGCTTT others(19): Show |
A | 1 | a0001c0001t0040g0212 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.684+2537_684+2562d others(28): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31905609 | ||||||
| chr10:31905610
|
G | A | 7 | a0001c0001t0011g0055a0001c0001t0011g0056a0001c0001t0011g0057others(4): Show | 7 | HG01884.hp1 HG01891.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.684+2562C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31905610 | ||||||
| chr10:31905850
|
C | CAGAAATA others(2600): Show |
1 | a0001c0003t0027g0014 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.684+2321_684+2322i others(2609): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31905850 | ||||||
| chr10:31905850
|
C | CAGAAATA others(2600): Show |
1 | a0001c0003t0010g0017 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.684+2321_684+2322i others(2609): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31905850 | ||||||
| chr10:31905850
|
C | CAGAAATA others(2598): Show |
1 | a0001c0003t0010g0009 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.684+2321_684+2322i others(2607): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31905850 | ||||||
| chr10:31905850
|
C | CAGAAATA others(2600): Show |
3 | a0001c0003t0010g0010a0001c0003t0027g0012a0001c0014t0004g0013 | 3 | HG02630.hp1 HG03471.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.684+2321_684+2322i others(2609): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31905850 | ||||||
| chr10:31905850
|
C | CAGAAATA others(2600): Show |
1 | a0001c0003t0010g0006 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.684+2321_684+2322i others(2609): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31905850 | ||||||
| chr10:31905850
|
C | CAGAAATA others(2598): Show |
1 | a0001c0003t0010g0005 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.684+2321_684+2322i others(2607): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31905850 | ||||||
| chr10:31905850
|
C | CAGAAATA others(2598): Show |
1 | a0001c0005t0016g0008 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.684+2321_684+2322i others(2607): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31905850 | ||||||
| chr10:31905850
|
C | CAGAAATA others(2599): Show |
5 | a0001c0003t0010g0016a0001c0003t0016g0003a0001c0003t0016g0004others(2): Show | 5 | HG00735.hp2 HG02723.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.684+2321_684+2322i others(2608): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31905850 | ||||||
| chr10:31905850
|
C | CAGAAATA others(2599): Show |
1 | a0001c0003t0010g0011 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.684+2321_684+2322i others(2608): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31905850 | ||||||
| chr10:31905850
|
C | CAGAAATA others(2602): Show |
1 | a0001c0003t0010g0018 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.684+2321_684+2322i others(2611): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31905850 | ||||||
| chr10:31906070
|
G | A | 1 | a0001c0001t0040g0212 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.684+2102C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31906070 | ||||||
| chr10:31906490
|
A | G | 2 | a0001c0001t0003g0180a0001c0001t0003g0184 | 2 | HG02074.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.684+1682T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31906490 | ||||||
| chr10:31907178
|
A | G | 279 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0088others(276): Show | 279 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.684+994T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31907178 | ||||||
| chr10:31907472
|
AAT | A | 48 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(45): Show | 48 | HG00099.hp2 HG01081.hp2 HG01123.hp1 others(45): Show |
intron_variant | MODIFIER | c.684+698_684+699del others(2): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31907472 | ||||||
| chr10:31907473
|
AT | A | 94 | a0001c0001t0001g0121a0001c0001t0009g0032a0001c0001t0009g0072others(91): Show | 94 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.684+698delA | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31907473 | ||||||
| chr10:31907564
|
G | A | 1 | a0001c0001t0042g0085 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.684+608C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31907564 | ||||||
| chr10:31907633
|
T | TA | 6 | a0001c0001t0001g0141a0001c0001t0004g0020a0001c0001t0004g0021others(3): Show | 6 | HG01167.hp2 HG01175.hp1 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.684+538dupT | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31907633 | ||||||
| chr10:31907633
|
TA | T | 100 | a0001c0001t0001g0111a0001c0001t0001g0121a0001c0001t0001g0232others(97): Show | 100 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(97): Show |
intron_variant | MODIFIER | c.684+538delT | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31907633 | ||||||
| chr10:31907693
|
T | C | 4 | a0001c0001t0023g0040a0001c0001t0023g0069a0001c0001t0024g0060others(1): Show | 4 | HG02572.hp2 HG02622.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.684+479A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31907693 | ||||||
| chr10:31908005
|
C | A | 2 | a0001c0003t0016g0003a0001c0003t0016g0004 | 2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.684+167G>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31908005 | ||||||
| chr10:31908025
|
C | T | 2 | a0001c0001t0003g0026a0001c0001t0012g0027 | 2 | HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.684+147G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31908025 | ||||||
| chr10:31908054
|
G | T | 1 | a0001c0001t0008g0098 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.684+118C>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31908054 | ||||||
| chr10:31909164
|
G | GA | 5 | a0001c0001t0003g0026a0001c0001t0012g0027a0001c0001t0034g0033others(2): Show | 5 | HG02145.hp2 HG02280.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.-71-239dupT | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 2/19 | chr10 | 31909164 | ||||||
| chr10:31909456
|
C | T | 2 | a0002c0002t0002g0253a0002c0002t0002g0290 | 2 | HG01106.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-71-530G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 2/19 | chr10 | 31909456 | ||||||
| chr10:31909545
|
G | T | 1 | a0001c0001t0001g0208 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-71-619C>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 2/19 | chr10 | 31909545 | ||||||
| chr10:31909691
|
T | G | 1 | a0001c0001t0001g0207 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-71-765A>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 2/19 | chr10 | 31909691 | ||||||
| chr10:31909905
|
A | G | 1 | a0002c0002t0054g0322 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-72+620T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 2/19 | chr10 | 31909905 | ||||||
| chr10:31909906
|
G | A | 1 | a0002c0002t0054g0322 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-72+619C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 2/19 | chr10 | 31909906 | ||||||
| chr10:31910287
|
T | C | 16 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(13): Show | 16 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.-72+238A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 2/19 | chr10 | 31910287 | ||||||
| chr10:31910442
|
T | C | 18 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(15): Show | 18 | HG00099.hp2 HG01081.hp2 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.-72+83A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 2/19 | chr10 | 31910442 | ||||||
| chr10:31910464
|
C | G | 1 | a0001c0001t0001g0135 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-72+61G>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 2/19 | chr10 | 31910464 | ||||||
| chr10:31910599
|
A | C | 1 | a0001c0001t0034g0033 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-110-36T>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31910599 | ||||||
| chr10:31910603
|
T | A | 1 | a0001c0003t0027g0014 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-110-40A>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31910603 | ||||||
| chr10:31910668
|
A | G | 2 | a0001c0001t0023g0040a0001c0001t0024g0060 | 2 | HG02965.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-110-105T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31910668 | ||||||
| chr10:31910694
|
T | A | 1 | a0001c0001t0001g0232 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-110-131A>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31910694 | ||||||
| chr10:31910923
|
T | C | 1 | a0002c0002t0002g0288 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-110-360A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31910923 | ||||||
| chr10:31911216
|
G | A | 11 | a0001c0001t0009g0032a0001c0001t0009g0072a0001c0001t0009g0073others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-110-653C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31911216 | ||||||
| chr10:31911306
|
G | A | 7 | a0001c0007t0028g0239a0001c0007t0028g0240a0001c0010t0053g0238others(4): Show | 7 | HG01109.hp2 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.-110-743C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31911306 | ||||||
| chr10:31911401
|
A | G | 18 | a0001c0001t0009g0032a0001c0001t0009g0072a0001c0001t0009g0073others(15): Show | 18 | HG01109.hp2 HG02145.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.-110-838T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31911401 | ||||||
| chr10:31911489
|
A | AT | 128 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(125): Show | 128 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(125): Show |
intron_variant | MODIFIER | c.-110-927dupA | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31911489 | ||||||
| chr10:31911741
|
A | T | 16 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(13): Show | 16 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.-110-1178T>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31911741 | ||||||
| chr10:31912075
|
C | T | 1 | a0002c0002t0002g0266 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-110-1512G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31912075 | ||||||
| chr10:31912107
|
C | T | 2 | a0001c0001t0003g0195a0001c0003t0048g0015 | 2 | HG02723.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.-110-1544G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31912107 | ||||||
| chr10:31912307
|
T | C | 1 | a0002c0002t0002g0243 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-110-1744A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31912307 | ||||||
| chr10:31912404
|
G | A | 2 | a0001c0001t0001g0157a0001c0001t0025g0156 | 2 | HG00735.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-110-1841C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31912404 | ||||||
| chr10:31912562
|
G | A | 7 | a0001c0007t0028g0239a0001c0007t0028g0240a0001c0010t0053g0238others(4): Show | 7 | HG01109.hp2 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.-110-1999C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31912562 | ||||||
| chr10:31912807
|
A | G | 16 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(13): Show | 16 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.-110-2244T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31912807 | ||||||
| chr10:31912818
|
T | G | 1 | a0001c0001t0001g0215 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-110-2255A>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31912818 | ||||||
| chr10:31912967
|
T | C | 1 | a0001c0003t0010g0006 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-110-2404A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31912967 | ||||||
| chr10:31912983
|
T | G | 2 | a0001c0001t0003g0026a0001c0001t0012g0027 | 2 | HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-110-2420A>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31912983 | ||||||
| chr10:31913057
|
C | G | 4 | a0001c0001t0001g0215a0001c0001t0006g0216a0001c0001t0006g0221others(1): Show | 4 | HG00741.hp1 HG02647.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.-110-2494G>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31913057 | ||||||
| chr10:31913072
|
G | T | 7 | a0001c0001t0011g0055a0001c0001t0011g0056a0001c0001t0011g0057others(4): Show | 7 | HG01884.hp1 HG01891.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-110-2509C>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31913072 | ||||||
| chr10:31913141
|
C | T | 148 | a0001c0001t0001g0086a0001c0001t0001g0100a0001c0001t0001g0102others(145): Show | 148 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(145): Show |
intron_variant | MODIFIER | c.-110-2578G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31913141 | ||||||
| chr10:31913436
|
T | C | 1 | a0001c0001t0001g0147 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-110-2873A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31913436 | ||||||
| chr10:31913599
|
T | C | 1 | a0002c0002t0002g0283 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-110-3036A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31913599 | ||||||
| chr10:31913634
|
C | CA | 7 | a0001c0001t0001g0121a0001c0001t0003g0173a0001c0001t0008g0140others(4): Show | 7 | HG02145.hp2 HG02280.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.-110-3072dupT | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31913634 | ||||||
| chr10:31913634
|
CA | C | 60 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(57): Show | 60 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(57): Show |
intron_variant | MODIFIER | c.-110-3072delT | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31913634 | ||||||
| chr10:31913635
|
A | C | 1 | a0001c0001t0018g0087 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-110-3072T>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31913635 | ||||||
| chr10:31913638
|
A | G | 1 | a0002c0002t0002g0253 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-110-3075T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31913638 | ||||||
| chr10:31913650
|
C | A | 85 | a0001c0001t0001g0086a0001c0001t0001g0100a0001c0001t0001g0102others(82): Show | 85 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.-110-3087G>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31913650 | ||||||
| chr10:31913666
|
A | G | 11 | a0001c0001t0009g0032a0001c0001t0009g0072a0001c0001t0009g0073others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-110-3103T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31913666 | ||||||
| chr10:31913721
|
A | G | 8 | a0001c0001t0001g0215a0001c0001t0001g0217a0001c0001t0001g0218others(5): Show | 8 | HG00738.hp1 HG00741.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.-110-3158T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31913721 | ||||||
| chr10:31913775
|
G | GC | 144 | a0001c0001t0001g0086a0001c0001t0001g0100a0001c0001t0001g0102others(141): Show | 144 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(141): Show |
intron_variant | MODIFIER | c.-110-3213_-110-321 others(5): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31913775 | ||||||
| chr10:31913775
|
G | GCT | 4 | a0001c0001t0009g0078a0001c0001t0009g0080a0001c0001t0009g0081others(1): Show | 4 | HG02257.hp1 HG02559.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-110-3213_-110-321 others(6): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31913775 | ||||||
| chr10:31913776
|
G | T | 148 | a0001c0001t0001g0086a0001c0001t0001g0100a0001c0001t0001g0102others(145): Show | 148 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(145): Show |
intron_variant | MODIFIER | c.-110-3213C>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31913776 | ||||||
| chr10:31913776
|
GT | G | 22 | a0001c0001t0001g0126a0001c0001t0003g0026a0001c0001t0012g0027others(19): Show | 22 | HG00735.hp2 HG02145.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.-110-3214delA | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31913776 | ||||||
| chr10:31913972
|
G | A | 1 | a0001c0001t0040g0212 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-110-3409C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31913972 | ||||||
| chr10:31914005
|
T | C | 20 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(17): Show | 20 | HG00099.hp2 HG01081.hp2 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.-110-3442A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31914005 | ||||||
| chr10:31914014
|
T | C | 1 | a0001c0001t0001g0213 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-110-3451A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31914014 | ||||||
| chr10:31914017
|
T | C | 7 | a0001c0001t0011g0055a0001c0001t0011g0056a0001c0001t0011g0057others(4): Show | 7 | HG01884.hp1 HG01891.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-110-3454A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31914017 | ||||||
| chr10:31914532
|
A | G | 169 | a0001c0001t0001g0086a0001c0001t0001g0100a0001c0001t0001g0102others(166): Show | 169 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(166): Show |
intron_variant | MODIFIER | c.-110-3969T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31914532 | ||||||
| chr10:31914628
|
A | G | 1 | a0002c0002t0002g0245 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-110-4065T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31914628 | ||||||
| chr10:31914651
|
G | A | 1 | a0001c0001t0018g0097 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-110-4088C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31914651 | ||||||
| chr10:31914681
|
A | G | 1 | a0002c0002t0002g0250 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-110-4118T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31914681 | ||||||
| chr10:31914869
|
G | T | 16 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(13): Show | 16 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.-110-4306C>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31914869 | ||||||
| chr10:31914870
|
C | T | 16 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(13): Show | 16 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.-110-4307G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31914870 | ||||||
| chr10:31914938
|
C | T | 6 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(3): Show | 6 | HG01167.hp2 HG01175.hp1 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.-110-4375G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31914938 | ||||||
| chr10:31915015
|
T | C | 1 | a0001c0001t0003g0084 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-110-4452A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31915015 | ||||||
| chr10:31915023
|
A | G | 1 | a0001c0001t0001g0083 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-110-4460T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31915023 | ||||||
| chr10:31915110
|
GGC | G | 10 | a0001c0001t0009g0032a0001c0001t0009g0072a0001c0001t0009g0073others(7): Show | 10 | HG02145.hp1 HG02257.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.-110-4549_-110-454 others(6): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31915110 | ||||||
| chr10:31915143
|
T | C | 8 | a0001c0001t0001g0215a0001c0001t0001g0217a0001c0001t0001g0218others(5): Show | 8 | HG00738.hp1 HG00741.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.-110-4580A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31915143 | ||||||
| chr10:31915154
|
G | C | 1 | a0001c0001t0043g0025 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-110-4591C>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31915154 | ||||||
| chr10:31915255
|
G | A | 4 | a0001c0001t0019g0162a0001c0001t0019g0163a0001c0001t0019g0166others(1): Show | 4 | HG01167.hp1 HG02970.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-110-4692C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31915255 | ||||||
| chr10:31915261
|
C | T | 2 | a0001c0001t0023g0040a0001c0001t0024g0060 | 2 | HG02965.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-110-4698G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31915261 | ||||||
| chr10:31915324
|
C | A | 50 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(47): Show | 50 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.-110-4761G>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31915324 | ||||||
| chr10:31915364
|
C | T | 1 | a0001c0001t0003g0201 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-110-4801G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31915364 | ||||||
| chr10:31915386
|
C | CA | 33 | a0001c0001t0001g0203a0001c0001t0009g0032a0001c0001t0009g0072others(30): Show | 33 | HG00735.hp2 HG00738.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.-110-4824dupT | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31915386 | ||||||
| chr10:31915499
|
G | A | 1 | a0001c0001t0034g0033 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-110-4936C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31915499 | ||||||
| chr10:31915513
|
AGATCTAT others(11): Show |
A | 5 | a0001c0001t0003g0026a0001c0001t0012g0027a0001c0001t0034g0033others(2): Show | 5 | HG02145.hp2 HG02280.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.-110-4968_-110-495 others(22): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31915513 | ||||||
| chr10:31915665
|
G | A | 1 | a0001c0001t0034g0033 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-110-5102C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31915665 | ||||||
| chr10:31915720
|
A | G | 1 | a0002c0002t0002g0281 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-110-5157T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31915720 | ||||||
| chr10:31915853
|
G | C | 50 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(47): Show | 50 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.-110-5290C>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31915853 | ||||||
| chr10:31915860
|
C | T | 1 | a0002c0002t0007g0308 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-110-5297G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31915860 | ||||||
| chr10:31915916
|
T | C | 2 | a0001c0007t0028g0239a0001c0007t0028g0240 | 2 | HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-110-5353A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31915916 | ||||||
| chr10:31915950
|
C | T | 1 | a0001c0001t0031g0001 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-110-5387G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31915950 | ||||||
| chr10:31915969
|
G | T | 1 | a0001c0001t0001g0213 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-110-5406C>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31915969 | ||||||
| chr10:31916116
|
G | A | 1 | a0001c0001t0001g0207 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-110-5553C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31916116 | ||||||
| chr10:31916384
|
C | T | 1 | a0001c0001t0043g0025 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-110-5821G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31916384 | ||||||
| chr10:31916574
|
A | G | 1 | a0001c0001t0031g0001 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-110-6011T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31916574 | ||||||
| chr10:31916576
|
A | T | 134 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(131): Show | 134 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(131): Show |
intron_variant | MODIFIER | c.-110-6013T>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31916576 | ||||||
| chr10:31916605
|
G | A | 1 | a0001c0001t0012g0197 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-110-6042C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31916605 | ||||||
| chr10:31916658
|
G | C | 142 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(139): Show | 142 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(139): Show |
intron_variant | MODIFIER | c.-110-6095C>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31916658 | ||||||
| chr10:31916687
|
G | A | 2 | a0001c0001t0004g0044a0001c0001t0005g0043 | 2 | HG01978.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.-110-6124C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31916687 | ||||||
| chr10:31916702
|
T | C | 148 | a0001c0001t0003g0026a0001c0001t0004g0019a0001c0001t0004g0020others(145): Show | 148 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(145): Show |
intron_variant | MODIFIER | c.-110-6139A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31916702 | ||||||
| chr10:31916710
|
G | C | 11 | a0001c0001t0009g0032a0001c0001t0009g0072a0001c0001t0009g0073others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-110-6147C>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31916710 | ||||||
| chr10:31916766
|
G | A | 3 | a0001c0001t0003g0170a0001c0001t0003g0196a0001c0001t0009g0032 | 3 | HG03209.hp2 NA18953.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.-110-6203C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31916766 | ||||||
| chr10:31916907
|
G | A | 11 | a0001c0001t0009g0032a0001c0001t0009g0072a0001c0001t0009g0073others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-110-6344C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31916907 | ||||||
| chr10:31917072
|
C | A | 2 | a0001c0001t0001g0086a0001c0001t0001g0102 | 2 | NA19057.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-110-6509G>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31917072 | ||||||
| chr10:31917167
|
T | TG | 16 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(13): Show | 16 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.-110-6605dupC | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31917167 | ||||||
| chr10:31917169
|
G | C | 1 | a0001c0001t0045g0076 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-110-6606C>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31917169 | ||||||
| chr10:31917180
|
C | T | 1 | a0001c0001t0004g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-110-6617G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31917180 | ||||||
| chr10:31917331
|
A | G | 145 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(142): Show | 145 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(142): Show |
intron_variant | MODIFIER | c.-110-6768T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31917331 | ||||||
| chr10:31917405
|
A | C | 1 | a0001c0011t0001g0112 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-110-6842T>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31917405 | ||||||
| chr10:31917428
|
T | G | 5 | a0001c0003t0010g0010a0001c0003t0010g0018a0001c0003t0027g0012others(2): Show | 5 | HG02615.hp1 HG02630.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.-110-6865A>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31917428 | ||||||
| chr10:31917742
|
C | G | 2 | a0002c0002t0021g0248a0002c0002t0021g0279 | 2 | NA18980.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.-110-7179G>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31917742 | ||||||
| chr10:31917780
|
T | C | 1 | a0001c0001t0012g0027 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-110-7217A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31917780 | ||||||
| chr10:31917918
|
T | G | 2 | a0001c0001t0001g0088a0001c0001t0039g0089 | 2 | HG02071.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.-110-7355A>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31917918 | ||||||
| chr10:31917953
|
C | T | 1 | a0001c0001t0034g0033 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-110-7390G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31917953 | ||||||
| chr10:31917953
|
CT | C | 20 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(17): Show | 20 | HG00099.hp2 HG01081.hp2 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.-110-7391delA | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31917953 | ||||||
| chr10:31918079
|
C | T | 1 | a0001c0001t0012g0027 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-110-7516G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31918079 | ||||||
| chr10:31918104
|
T | C | 1 | a0001c0001t0001g0126 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-110-7541A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31918104 | ||||||
| chr10:31918315
|
T | TCA | 61 | a0001c0001t0001g0088a0001c0001t0001g0096a0001c0001t0001g0100others(58): Show | 61 | HG00597.hp2 HG00733.hp1 HG00733.hp2 others(58): Show |
intron_variant | MODIFIER | c.-110-7754_-110-775 others(6): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31918315 | ||||||
| chr10:31918315
|
T | TCACA | 19 | a0001c0001t0001g0113a0001c0001t0001g0143a0001c0001t0001g0226others(16): Show | 19 | HG01175.hp2 HG01192.hp1 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.-110-7756_-110-775 others(8): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31918315 | ||||||
| chr10:31918315
|
T | TCACACA | 9 | a0001c0001t0001g0115a0001c0001t0001g0117a0001c0001t0001g0122others(6): Show | 9 | HG00544.hp2 HG00621.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.-110-7758_-110-775 others(10): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31918315 | ||||||
| chr10:31918315
|
TCA | T | 84 | a0001c0001t0001g0083a0001c0001t0001g0111a0001c0001t0001g0124others(81): Show | 84 | HG00280.hp1 HG00597.hp1 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.-110-7754_-110-775 others(6): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31918315 | ||||||
| chr10:31918315
|
TCACA | T | 18 | a0001c0001t0003g0186a0001c0001t0006g0165a0001c0001t0019g0162others(15): Show | 18 | HG01071.hp1 HG01099.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.-110-7756_-110-775 others(8): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31918315 | ||||||
| chr10:31918315
|
TCACACA | T | 10 | a0001c0001t0003g0188a0001c0001t0006g0153a0001c0001t0006g0158others(7): Show | 10 | HG01106.hp1 HG02280.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-110-7758_-110-775 others(10): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31918315 | ||||||
| chr10:31918315
|
TCACACAC others(1): Show |
T | 14 | a0001c0001t0001g0157a0001c0001t0001g0236a0001c0001t0004g0031others(11): Show | 14 | HG00673.hp2 HG00735.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.-110-7760_-110-775 others(12): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31918315 | ||||||
| chr10:31918315
|
TCACACAC others(3): Show |
T | 37 | a0001c0001t0003g0026a0001c0001t0004g0019a0001c0001t0004g0020others(34): Show | 37 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.-110-7762_-110-775 others(14): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31918315 | ||||||
| chr10:31918315
|
TCACACAC others(5): Show |
T | 6 | a0001c0001t0006g0214a0001c0001t0023g0040a0001c0001t0023g0069others(3): Show | 6 | HG01123.hp1 HG02572.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-110-7764_-110-775 others(16): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31918315 | ||||||
| chr10:31918315
|
TCACACAC others(9): Show |
T | 1 | a0001c0001t0006g0167 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-110-7768_-110-775 others(20): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31918315 | ||||||
| chr10:31918315
|
TCACACAC others(13): Show |
T | 1 | a0001c0001t0004g0037 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-110-7772_-110-775 others(24): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31918315 | ||||||
| chr10:31918439
|
A | G | 1 | a0001c0001t0003g0173 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-110-7876T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31918439 | ||||||
| chr10:31918732
|
A | G | 1 | a0001c0001t0043g0025 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-110-8169T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31918732 | ||||||
| chr10:31918781
|
G | T | 1 | a0001c0001t0013g0149 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-110-8218C>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31918781 | ||||||
| chr10:31918946
|
G | A | 1 | a0001c0001t0001g0141 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-110-8383C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31918946 | ||||||
| chr10:31918965
|
T | C | 313 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0088others(310): Show | 313 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.-110-8402A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31918965 | ||||||
| chr10:31919010
|
C | T | 1 | a0001c0001t0001g0207 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-110-8447G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31919010 | ||||||
| chr10:31919022
|
C | T | 3 | a0001c0001t0005g0046a0001c0001t0005g0051a0001c0001t0005g0054 | 3 | HG01168.hp1 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-110-8459G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31919022 | ||||||
| chr10:31919063
|
C | T | 3 | a0001c0001t0001g0157a0001c0001t0025g0156a0001c0001t0025g0202 | 3 | HG00735.hp1 HG02258.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-110-8500G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31919063 | ||||||
| chr10:31919250
|
T | C | 2 | a0001c0001t0003g0201a0001c0001t0033g0175 | 2 | HG00639.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.-110-8687A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31919250 | ||||||
| chr10:31919350
|
G | A | 2 | a0001c0001t0001g0107a0001c0001t0001g0108 | 2 | NA18985.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.-110-8787C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31919350 | ||||||
| chr10:31919463
|
T | C | 7 | a0001c0001t0011g0055a0001c0001t0011g0056a0001c0001t0011g0057others(4): Show | 7 | HG01884.hp1 HG01891.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-110-8900A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31919463 | ||||||
| chr10:31919487
|
A | T | 1 | a0001c0001t0034g0033 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-110-8924T>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31919487 | ||||||
| chr10:31919520
|
C | G | 1 | a0001c0001t0001g0100 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-110-8957G>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31919520 | ||||||
| chr10:31919563
|
T | C | 11 | a0001c0001t0009g0032a0001c0001t0009g0072a0001c0001t0009g0073others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-110-9000A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31919563 | ||||||
| chr10:31919605
|
C | T | 1 | a0002c0002t0002g0247 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-110-9042G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31919605 | ||||||
| chr10:31919630
|
A | T | 1 | a0001c0003t0048g0015 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-111+9053T>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31919630 | ||||||
| chr10:31919663
|
T | C | 7 | a0001c0001t0011g0055a0001c0001t0011g0056a0001c0001t0011g0057others(4): Show | 7 | HG01884.hp1 HG01891.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-111+9020A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31919663 | ||||||
| chr10:31919684
|
A | T | 84 | a0001c0007t0028g0239a0001c0007t0028g0240a0001c0010t0053g0238others(81): Show | 84 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.-111+8999T>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31919684 | ||||||
| chr10:31919791
|
C | CA | 10 | a0001c0001t0001g0215a0001c0001t0001g0217a0001c0001t0001g0218others(7): Show | 10 | HG00738.hp1 HG00741.hp1 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.-111+8891dupT | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31919791 | ||||||
| chr10:31919835
|
T | C | 1 | a0002c0002t0029g0284 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-111+8848A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31919835 | ||||||
| chr10:31919840
|
C | T | 1 | a0002c0002t0014g0300 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-111+8843G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31919840 | ||||||
| chr10:31919841
|
A | G | 145 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(142): Show | 145 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(142): Show |
intron_variant | MODIFIER | c.-111+8842T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31919841 | ||||||
| chr10:31919901
|
G | A | 50 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(47): Show | 50 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.-111+8782C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31919901 | ||||||
| chr10:31919939
|
A | C | 2 | a0001c0001t0001g0226a0001c0001t0008g0152 | 2 | HG01884.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-111+8744T>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31919939 | ||||||
| chr10:31919983
|
G | A | 1 | a0001c0006t0026g0067 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-111+8700C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31919983 | ||||||
| chr10:31920108
|
A | G | 1 | a0001c0001t0001g0099 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-111+8575T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31920108 | ||||||
| chr10:31920175
|
G | A | 1 | a0001c0001t0006g0214 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-111+8508C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31920175 | ||||||
| chr10:31920311
|
G | T | 3 | a0001c0001t0001g0115a0001c0001t0001g0117a0001c0001t0015g0116 | 3 | NA18946.hp2 NA18965.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.-111+8372C>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31920311 | ||||||
| chr10:31920374
|
C | A | 5 | a0001c0001t0003g0026a0001c0001t0012g0027a0001c0001t0034g0033others(2): Show | 5 | HG02145.hp2 HG02280.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.-111+8309G>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31920374 | ||||||
| chr10:31920445
|
G | A | 1 | a0001c0001t0001g0213 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-111+8238C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31920445 | ||||||
| chr10:31920449
|
C | CA | 20 | a0001c0001t0001g0088a0001c0001t0001g0109a0001c0001t0001g0110others(17): Show | 20 | HG01168.hp2 HG01346.hp2 HG01516.hp2 others(17): Show |
intron_variant | MODIFIER | c.-111+8233dupT | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31920449 | ||||||
| chr10:31920449
|
C | CAA | 15 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(12): Show | 15 | HG00099.hp2 HG01081.hp2 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.-111+8232_-111+823 others(6): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31920449 | ||||||
| chr10:31920449
|
C | CAAA | 73 | a0001c0001t0004g0068a0001c0001t0005g0043a0001c0008t0005g0074others(70): Show | 73 | HG00639.hp2 HG00673.hp1 HG00738.hp2 others(70): Show |
intron_variant | MODIFIER | c.-111+8231_-111+823 others(7): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31920449 | ||||||
| chr10:31920449
|
C | CAAAA | 13 | a0001c0001t0004g0044a0001c0007t0028g0239a0001c0007t0028g0240others(10): Show | 13 | HG00597.hp1 HG00621.hp1 HG01978.hp2 others(10): Show |
intron_variant | MODIFIER | c.-111+8230_-111+823 others(8): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31920449 | ||||||
| chr10:31920449
|
C | CAAAAAAA others(3): Show |
2 | a0001c0003t0010g0005a0001c0003t0010g0017 | 2 | HG02257.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-111+8224_-111+823 others(14): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31920449 | ||||||
| chr10:31920449
|
C | CAAAAAAA others(4): Show |
11 | a0001c0001t0009g0032a0001c0001t0009g0072a0001c0001t0009g0073others(8): Show | 11 | HG02145.hp1 HG02451.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.-111+8223_-111+823 others(15): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31920449 | ||||||
| chr10:31920449
|
C | CAAAAAAA others(5): Show |
10 | a0001c0001t0004g0034a0001c0001t0009g0080a0001c0001t0009g0081others(7): Show | 10 | HG00735.hp2 HG02257.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.-111+8222_-111+823 others(16): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31920449 | ||||||
| chr10:31920449
|
C | CAAAAAAA others(6): Show |
4 | a0001c0001t0009g0082a0001c0003t0027g0012a0001c0003t0027g0014others(1): Show | 4 | HG02818.hp1 HG02976.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-111+8221_-111+823 others(17): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31920449 | ||||||
| chr10:31920449
|
C | CAAAAAAA others(13): Show |
1 | a0001c0001t0024g0042 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-111+8214_-111+823 others(24): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31920449 | ||||||
| chr10:31920449
|
C | CAAAAAAA others(14): Show |
2 | a0001c0001t0005g0045a0001c0001t0005g0070 | 2 | HG01192.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-111+8213_-111+823 others(25): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31920449 | ||||||
| chr10:31920449
|
C | CAAAAAAA others(15): Show |
6 | a0001c0001t0005g0046a0001c0001t0005g0047a0001c0001t0005g0048others(3): Show | 6 | HG01109.hp1 HG01257.hp2 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.-111+8212_-111+823 others(26): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31920449 | ||||||
| chr10:31920449
|
C | CAAAAAAA others(16): Show |
2 | a0001c0001t0005g0051a0001c0001t0005g0052 | 2 | HG01258.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.-111+8233_-111+823 others(27): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31920449 | ||||||
| chr10:31920449
|
C | CAAAAAAA others(20): Show |
1 | a0001c0001t0005g0063 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-111+8233_-111+823 others(31): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31920449 | ||||||
| chr10:31920449
|
C | CAAAAAAA others(21): Show |
1 | a0001c0001t0017g0053 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-111+8233_-111+823 others(32): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31920449 | ||||||
| chr10:31920449
|
C | CAAAAAAA others(27): Show |
1 | a0001c0001t0005g0054 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-111+8233_-111+823 others(38): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31920449 | ||||||
| chr10:31920449
|
C | CAAAAAAA others(38): Show |
1 | a0001c0001t0005g0235 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-111+8233_-111+823 others(49): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31920449 | ||||||
| chr10:31920449
|
CA | C | 11 | a0001c0001t0001g0113a0001c0001t0003g0026a0001c0001t0003g0171others(8): Show | 11 | HG02145.hp2 HG02280.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.-111+8233delT | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31920449 | ||||||
| chr10:31920449
|
CAAAA | C | 6 | a0001c0001t0011g0055a0001c0001t0011g0056a0001c0001t0011g0057others(3): Show | 6 | HG01884.hp1 HG01891.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-111+8230_-111+823 others(8): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31920449 | ||||||
| chr10:31920526
|
C | T | 1 | a0001c0001t0025g0156 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-111+8157G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31920526 | ||||||
| chr10:31920665
|
AGTTTTTG others(5): Show |
A | 18 | a0001c0001t0004g0044a0001c0001t0005g0043a0001c0001t0005g0045others(15): Show | 18 | HG01109.hp1 HG01168.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.-111+8006_-111+801 others(16): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31920665 | ||||||
| chr10:31920964
|
T | C | 1 | a0002c0002t0002g0317 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-111+7719A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31920964 | ||||||
| chr10:31921042
|
G | A | 1 | a0001c0001t0040g0212 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-111+7641C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31921042 | ||||||
| chr10:31921065
|
C | T | 16 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(13): Show | 16 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.-111+7618G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31921065 | ||||||
| chr10:31921137
|
C | A | 13 | a0001c0001t0001g0083a0001c0001t0001g0141a0001c0001t0001g0204others(10): Show | 13 | HG00099.hp1 HG01099.hp2 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.-111+7546G>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31921137 | ||||||
| chr10:31921146
|
C | T | 2 | a0002c0002t0002g0245a0002c0002t0002g0289 | 2 | HG04199.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-111+7537G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31921146 | ||||||
| chr10:31921220
|
A | C | 2 | a0001c0001t0001g0210a0001c0001t0001g0232 | 2 | HG01099.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-111+7463T>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31921220 | ||||||
| chr10:31921270
|
C | T | 145 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(142): Show | 145 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(142): Show |
intron_variant | MODIFIER | c.-111+7413G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31921270 | ||||||
| chr10:31921475
|
G | A | 1 | a0001c0001t0040g0212 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-111+7208C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31921475 | ||||||
| chr10:31921493
|
C | T | 1 | a0001c0001t0008g0098 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-111+7190G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31921493 | ||||||
| chr10:31921541
|
G | A | 1 | a0001c0001t0001g0111 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-111+7142C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31921541 | ||||||
| chr10:31921550
|
G | T | 1 | a0001c0001t0001g0083 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-111+7133C>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31921550 | ||||||
| chr10:31921652
|
TA | T | 7 | a0001c0001t0001g0096a0001c0001t0001g0113a0001c0001t0001g0146others(4): Show | 7 | HG01358.hp1 HG02273.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.-111+7030delT | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31921652 | ||||||
| chr10:31921763
|
C | CA | 95 | a0001c0001t0001g0124a0001c0001t0001g0126a0001c0001t0001g0127others(92): Show | 95 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.-111+6919dupT | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31921763 | ||||||
| chr10:31921763
|
C | CAA | 17 | a0001c0001t0001g0213a0002c0002t0002g0277a0002c0002t0002g0278others(14): Show | 17 | HG02071.hp2 HG02074.hp2 HG03492.hp1 others(14): Show |
intron_variant | MODIFIER | c.-111+6918_-111+691 others(6): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31921763 | ||||||
| chr10:31921763
|
CA | C | 48 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0145others(45): Show | 48 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.-111+6919delT | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31921763 | ||||||
| chr10:31921763
|
CAAAA | C | 14 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(11): Show | 14 | HG02257.hp2 HG02451.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.-111+6916_-111+691 others(8): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31921763 | ||||||
| chr10:31921763
|
CAAAAAAA others(2): Show |
C | 9 | a0001c0001t0009g0032a0001c0001t0009g0072a0001c0001t0009g0077others(6): Show | 9 | HG02257.hp1 HG02559.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.-111+6911_-111+691 others(13): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31921763 | ||||||
| chr10:31921763
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0003g0233 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-111+6908_-111+691 others(16): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31921763 | ||||||
| chr10:31921785
|
A | G | 20 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(17): Show | 20 | HG00099.hp2 HG01081.hp2 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.-111+6898T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31921785 | ||||||
| chr10:31921938
|
C | T | 1 | a0001c0001t0006g0214 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-111+6745G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31921938 | ||||||
| chr10:31922076
|
C | T | 1 | a0001c0001t0001g0217 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-111+6607G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31922076 | ||||||
| chr10:31922180
|
C | CA | 8 | a0001c0001t0003g0185a0001c0001t0003g0186a0001c0001t0012g0187others(5): Show | 8 | HG01981.hp1 HG02258.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.-111+6502dupT | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31922180 | ||||||
| chr10:31922180
|
C | CAA | 8 | a0001c0001t0001g0164a0001c0001t0003g0188a0001c0001t0003g0189others(5): Show | 8 | HG03688.hp1 NA18947.hp1 NA18957.hp2 others(5): Show |
intron_variant | MODIFIER | c.-111+6501_-111+650 others(6): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31922180 | ||||||
| chr10:31922180
|
CA | C | 40 | a0001c0001t0001g0132a0001c0001t0001g0135a0001c0001t0001g0137others(37): Show | 40 | HG00280.hp2 HG00639.hp1 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.-111+6502delT | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31922180 | ||||||
| chr10:31922180
|
CAA | C | 35 | a0001c0001t0001g0083a0001c0001t0001g0088a0001c0001t0001g0113others(32): Show | 35 | HG00099.hp1 HG00544.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.-111+6501_-111+650 others(6): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31922180 | ||||||
| chr10:31922180
|
CAAA | C | 25 | a0001c0001t0001g0086a0001c0001t0001g0096a0001c0001t0001g0099others(22): Show | 25 | HG00597.hp2 HG01192.hp1 HG01516.hp1 others(22): Show |
intron_variant | MODIFIER | c.-111+6500_-111+650 others(7): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31922180 | ||||||
| chr10:31922180
|
CAAAAAAA others(6): Show |
C | 3 | a0001c0003t0010g0006a0001c0003t0010g0017a0001c0003t0010g0018 | 3 | HG02615.hp1 HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-111+6490_-111+650 others(17): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31922180 | ||||||
| chr10:31922180
|
CAAAAAAA others(7): Show |
C | 13 | a0001c0003t0010g0005a0001c0003t0010g0009a0001c0003t0010g0010others(10): Show | 13 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-111+6489_-111+650 others(18): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31922180 | ||||||
| chr10:31922180
|
CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0034g0033 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-111+6488_-111+650 others(19): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31922180 | ||||||
| chr10:31922180
|
CAAAAAAA others(10): Show |
C | 7 | a0001c0001t0003g0026a0001c0001t0013g0091a0001c0001t0013g0092others(4): Show | 7 | HG02145.hp2 HG03516.hp1 NA18906.hp2 others(4): Show |
intron_variant | MODIFIER | c.-111+6486_-111+650 others(21): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31922180 | ||||||
| chr10:31922180
|
CAAAAAAA others(11): Show |
C | 1 | a0001c0001t0012g0027 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-111+6485_-111+650 others(22): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31922180 | ||||||
| chr10:31922180
|
CAAAAAAA others(12): Show |
C | 12 | a0001c0001t0017g0062a0001c0007t0028g0239a0001c0007t0028g0240others(9): Show | 12 | HG01109.hp2 HG01928.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.-111+6484_-111+650 others(23): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31922180 | ||||||
| chr10:31922180
|
CAAAAAAA others(13): Show |
C | 132 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(129): Show | 132 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(129): Show |
intron_variant | MODIFIER | c.-111+6483_-111+650 others(24): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31922180 | ||||||
| chr10:31922180
|
CAAAAAAA others(14): Show |
C | 1 | a0002c0002t0002g0298 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-111+6482_-111+650 others(25): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31922180 | ||||||
| chr10:31922261
|
G | A | 5 | a0001c0001t0003g0026a0001c0001t0012g0027a0001c0001t0034g0033others(2): Show | 5 | HG02145.hp2 HG02280.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.-111+6422C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31922261 | ||||||
| chr10:31922315
|
C | T | 1 | a0001c0001t0004g0022 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-111+6368G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31922315 | ||||||
| chr10:31922349
|
T | C | 16 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(13): Show | 16 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.-111+6334A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31922349 | ||||||
| chr10:31922402
|
AT | A | 19 | a0001c0001t0003g0084a0001c0001t0006g0165a0001c0001t0019g0166others(16): Show | 19 | HG00735.hp2 HG01167.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.-111+6280delA | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31922402 | ||||||
| chr10:31922489
|
A | G | 1 | a0001c0001t0034g0033 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-111+6194T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31922489 | ||||||
| chr10:31922642
|
C | T | 1 | a0001c0001t0006g0214 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-111+6041G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31922642 | ||||||
| chr10:31922690
|
T | C | 1 | a0001c0001t0005g0063 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-111+5993A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31922690 | ||||||
| chr10:31922722
|
A | G | 1 | a0001c0008t0005g0074 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-111+5961T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31922722 | ||||||
| chr10:31923016
|
G | A | 1 | a0001c0001t0034g0033 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-111+5667C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31923016 | ||||||
| chr10:31923132
|
G | GA | 15 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(12): Show | 15 | HG01192.hp1 HG01358.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.-111+5550dupT | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31923132 | ||||||
| chr10:31923132
|
G | GAAA | 34 | a0001c0001t0004g0034a0001c0001t0004g0037a0001c0001t0004g0038others(31): Show | 34 | HG01109.hp1 HG01168.hp1 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.-111+5548_-111+555 others(7): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31923132 | ||||||
| chr10:31923132
|
G | GAAAA | 86 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(83): Show | 86 | HG00099.hp2 HG00639.hp2 HG00738.hp2 others(83): Show |
intron_variant | MODIFIER | c.-111+5547_-111+555 others(8): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31923132 | ||||||
| chr10:31923132
|
G | GAAAAA | 12 | a0001c0001t0004g0024a0001c0001t0034g0033a0002c0002t0002g0289others(9): Show | 12 | HG00597.hp1 HG00621.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.-111+5546_-111+555 others(9): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31923132 | ||||||
| chr10:31923132
|
G | GAAAAAA | 26 | a0001c0001t0001g0213a0001c0001t0001g0215a0001c0001t0001g0217others(23): Show | 26 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.-111+5545_-111+555 others(10): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31923132 | ||||||
| chr10:31923152
|
A | AAAAC | 9 | a0001c0001t0009g0032a0001c0001t0009g0072a0001c0001t0009g0077others(6): Show | 9 | HG02257.hp1 HG02559.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.-111+5530_-111+553 others(8): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31923152 | ||||||
| chr10:31923303
|
C | T | 2 | a0001c0003t0016g0003a0001c0003t0016g0004 | 2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-111+5380G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31923303 | ||||||
| chr10:31923321
|
T | C | 10 | a0002c0002t0002g0298a0002c0002t0002g0299a0002c0002t0002g0301others(7): Show | 10 | HG00639.hp2 HG01099.hp1 HG01928.hp2 others(7): Show |
intron_variant | MODIFIER | c.-111+5362A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31923321 | ||||||
| chr10:31923659
|
A | G | 16 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(13): Show | 16 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.-111+5024T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31923659 | ||||||
| chr10:31923694
|
C | A | 1 | a0001c0001t0025g0202 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-111+4989G>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31923694 | ||||||
| chr10:31923723
|
T | C | 1 | a0001c0001t0001g0210 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-111+4960A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31923723 | ||||||
| chr10:31923777
|
C | T | 1 | a0001c0001t0003g0168 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-111+4906G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31923777 | ||||||
| chr10:31923803
|
T | C | 1 | a0001c0001t0012g0027 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-111+4880A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31923803 | ||||||
| chr10:31923967
|
A | T | 2 | a0001c0008t0005g0074a0001c0008t0005g0075 | 2 | HG02602.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.-111+4716T>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31923967 | ||||||
| chr10:31924227
|
A | G | 1 | a0001c0001t0011g0071 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-111+4456T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31924227 | ||||||
| chr10:31924230
|
A | C | 1 | a0001c0001t0001g0088 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-111+4453T>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31924230 | ||||||
| chr10:31924288
|
G | T | 1 | a0002c0002t0014g0242 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-111+4395C>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31924288 | ||||||
| chr10:31924311
|
C | T | 160 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(157): Show | 160 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.-111+4372G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31924311 | ||||||
| chr10:31924335
|
T | C | 5 | a0001c0001t0006g0167a0002c0002t0007g0308a0003c0004t0007g0309others(2): Show | 5 | HG01109.hp2 HG02895.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-111+4348A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31924335 | ||||||
| chr10:31924387
|
A | G | 279 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0088others(276): Show | 279 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.-111+4296T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31924387 | ||||||
| chr10:31924487
|
T | C | 1 | a0001c0001t0022g0002 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-111+4196A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31924487 | ||||||
| chr10:31924702
|
TCATAA | T | 69 | a0001c0001t0001g0086a0001c0001t0001g0088a0001c0001t0001g0096others(66): Show | 69 | HG00544.hp2 HG00597.hp2 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.-111+3976_-111+398 others(9): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31924702 | ||||||
| chr10:31924768
|
A | C | 1 | a0002c0002t0030g0241 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-111+3915T>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31924768 | ||||||
| chr10:31924779
|
T | C | 11 | a0001c0001t0009g0032a0001c0001t0009g0072a0001c0001t0009g0073others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-111+3904A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31924779 | ||||||
| chr10:31925182
|
T | C | 1 | a0001c0001t0034g0033 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-111+3501A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31925182 | ||||||
| chr10:31925194
|
A | C | 49 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(46): Show | 49 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(46): Show |
intron_variant | MODIFIER | c.-111+3489T>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31925194 | ||||||
| chr10:31925209
|
T | C | 16 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(13): Show | 16 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.-111+3474A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31925209 | ||||||
| chr10:31925262
|
G | GCAGTACA others(19): Show |
1 | a0001c0001t0001g0203 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-111+3395_-111+342 others(30): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31925262 | ||||||
| chr10:31925889
|
CATT | C | 3 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0024 | 3 | HG01167.hp2 HG01175.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-111+2791_-111+279 others(7): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31925889 | ||||||
| chr10:31925903
|
C | A | 144 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(141): Show | 144 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(141): Show |
intron_variant | MODIFIER | c.-111+2780G>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31925903 | ||||||
| chr10:31926023
|
TTATA | T | 16 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(13): Show | 16 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.-111+2656_-111+265 others(8): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31926023 | ||||||
| chr10:31926163
|
G | A | 1 | a0001c0001t0003g0201 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-111+2520C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31926163 | ||||||
| chr10:31926236
|
G | A | 1 | a0001c0001t0025g0202 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-111+2447C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31926236 | ||||||
| chr10:31926272
|
T | C | 2 | a0001c0001t0049g0029a0001c0001t0050g0028 | 2 | HG02145.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-111+2411A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31926272 | ||||||
| chr10:31926325
|
A | C | 1 | a0001c0001t0004g0034 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-111+2358T>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31926325 | ||||||
| chr10:31926336
|
G | GA | 10 | a0001c0001t0001g0203a0001c0001t0001g0215a0001c0001t0001g0217others(7): Show | 10 | HG00738.hp1 HG00741.hp1 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.-111+2346dupT | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31926336 | ||||||
| chr10:31926336
|
GA | G | 133 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(130): Show | 133 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(130): Show |
intron_variant | MODIFIER | c.-111+2346delT | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31926336 | ||||||
| chr10:31926336
|
GAA | G | 10 | a0001c0001t0009g0032a0001c0001t0009g0072a0001c0001t0009g0073others(7): Show | 10 | HG02145.hp1 HG02257.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.-111+2345_-111+234 others(6): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31926336 | ||||||
| chr10:31926437
|
G | C | 12 | a0001c0001t0001g0083a0001c0001t0001g0204a0001c0001t0001g0207others(9): Show | 12 | HG00099.hp1 HG01099.hp2 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.-111+2246C>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31926437 | ||||||
| chr10:31926548
|
T | C | 1 | a0001c0001t0043g0025 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-111+2135A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31926548 | ||||||
| chr10:31926564
|
C | CCCATTTG others(3): Show |
1 | a0001c0001t0001g0086 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-111+2118_-111+211 others(14): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31926564 | ||||||
| chr10:31926581
|
G | C | 1 | a0001c0001t0001g0211 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-111+2102C>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31926581 | ||||||
| chr10:31926641
|
C | T | 49 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(46): Show | 49 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(46): Show |
intron_variant | MODIFIER | c.-111+2042G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31926641 | ||||||
| chr10:31926719
|
T | C | 2 | a0001c0008t0005g0074a0001c0008t0005g0075 | 2 | HG02602.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.-111+1964A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31926719 | ||||||
| chr10:31926728
|
G | C | 81 | a0002c0002t0002g0243a0002c0002t0002g0245a0002c0002t0002g0247others(78): Show | 81 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.-111+1955C>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31926728 | ||||||
| chr10:31926752
|
ATTCT | A | 4 | a0002c0002t0007g0313a0002c0002t0007g0314a0002c0002t0007g0316others(1): Show | 4 | HG02074.hp2 HG03834.hp1 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.-111+1927_-111+193 others(8): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31926752 | ||||||
| chr10:31926837
|
C | T | 2 | a0001c0001t0001g0088a0001c0001t0039g0089 | 2 | HG02071.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.-111+1846G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31926837 | ||||||
| chr10:31927089
|
T | C | 5 | a0001c0001t0003g0026a0001c0001t0012g0027a0001c0001t0034g0033others(2): Show | 5 | HG02145.hp2 HG02280.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.-111+1594A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31927089 | ||||||
| chr10:31927120
|
C | G | 1 | a0001c0001t0018g0087 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-111+1563G>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31927120 | ||||||
| chr10:31927228
|
C | G | 1 | a0001c0001t0001g0086 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-111+1455G>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31927228 | ||||||
| chr10:31927229
|
A | AATTTTAA others(7): Show |
176 | a0001c0001t0001g0213a0001c0001t0001g0215a0001c0001t0001g0217others(173): Show | 176 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(173): Show |
intron_variant | MODIFIER | c.-111+1453_-111+145 others(18): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31927229 | ||||||
| chr10:31927229
|
A | C | 1 | a0001c0001t0001g0086 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-111+1454T>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31927229 | ||||||
| chr10:31927233
|
T | A | 176 | a0001c0001t0001g0213a0001c0001t0001g0215a0001c0001t0001g0217others(173): Show | 176 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(173): Show |
intron_variant | MODIFIER | c.-111+1450A>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31927233 | ||||||
| chr10:31927239
|
T | TACTGTGC others(4): Show |
176 | a0001c0001t0001g0213a0001c0001t0001g0215a0001c0001t0001g0217others(173): Show | 176 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(173): Show |
intron_variant | MODIFIER | c.-111+1443_-111+144 others(15): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31927239 | ||||||
| chr10:31927322
|
C | G | 1 | a0001c0001t0043g0025 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-111+1361G>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31927322 | ||||||
| chr10:31927334
|
G | A | 165 | a0001c0001t0003g0026a0001c0001t0004g0019a0001c0001t0004g0020others(162): Show | 165 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(162): Show |
intron_variant | MODIFIER | c.-111+1349C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31927334 | ||||||
| chr10:31927343
|
C | A | 1 | a0001c0001t0008g0222 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-111+1340G>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31927343 | ||||||
| chr10:31927506
|
T | C | 1 | a0002c0002t0002g0317 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-111+1177A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31927506 | ||||||
| chr10:31927507
|
C | T | 1 | a0001c0001t0001g0086 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-111+1176G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31927507 | ||||||
| chr10:31927541
|
G | C | 81 | a0002c0002t0002g0243a0002c0002t0002g0245a0002c0002t0002g0247others(78): Show | 81 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.-111+1142C>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31927541 | ||||||
| chr10:31927618
|
A | T | 1 | a0001c0001t0001g0086 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-111+1065T>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31927618 | ||||||
| chr10:31927633
|
C | A | 1 | a0001c0001t0046g0223 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-111+1050G>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31927633 | ||||||
| chr10:31927798
|
T | A | 1 | a0001c0001t0001g0086 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-111+885A>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31927798 | ||||||
| chr10:31927838
|
T | G | 81 | a0002c0002t0002g0243a0002c0002t0002g0245a0002c0002t0002g0247others(78): Show | 81 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.-111+845A>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31927838 | ||||||
| chr10:31927912
|
T | G | 1 | a0001c0001t0001g0086 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-111+771A>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31927912 | ||||||
| chr10:31927913
|
A | T | 1 | a0001c0001t0001g0086 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-111+770T>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31927913 | ||||||
| chr10:31927959
|
T | G | 165 | a0001c0001t0003g0026a0001c0001t0004g0019a0001c0001t0004g0020others(162): Show | 165 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(162): Show |
intron_variant | MODIFIER | c.-111+724A>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31927959 | ||||||
| chr10:31928140
|
C | G | 1 | a0001c0001t0042g0085 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-111+543G>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31928140 | ||||||
| chr10:31928171
|
T | TGC | 44 | a0001c0001t0004g0030a0001c0001t0004g0034a0001c0001t0004g0036others(41): Show | 44 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(41): Show |
intron_variant | MODIFIER | c.-111+510_-111+511d others(4): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31928171 | ||||||
| chr10:31928174
|
G | GCA | 31 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0226others(28): Show | 31 | HG00735.hp2 HG01175.hp2 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.-111+507_-111+508d others(4): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31928174 | ||||||
| chr10:31928174
|
GCA | G | 7 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(4): Show | 7 | HG01167.hp2 HG01175.hp1 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.-111+507_-111+508d others(4): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31928174 | ||||||
| chr10:31928174
|
GCACA | G | 85 | a0001c0001t0001g0083a0001c0007t0028g0239a0001c0007t0028g0240others(82): Show | 85 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.-111+505_-111+508d others(6): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31928174 | ||||||
| chr10:31928176
|
A | G | 6 | a0001c0001t0003g0026a0001c0001t0003g0084a0001c0001t0004g0030others(3): Show | 6 | HG02145.hp2 HG03516.hp1 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.-111+507T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31928176 | ||||||
| chr10:31928178
|
A | G | 6 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(3): Show | 6 | HG01167.hp2 HG01175.hp1 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.-111+505T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31928178 | ||||||
| chr10:31928247
|
T | C | 2 | a0001c0001t0001g0232a0002c0002t0002g0319 | 2 | HG01099.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-111+436A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31928247 | ||||||
| chr10:31928314
|
C | A | 2 | a0001c0001t0003g0233a0001c0001t0003g0234 | 2 | HG03654.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.-111+369G>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31928314 | ||||||
| chr10:31928475
|
A | AC | 16 | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(13): Show | 16 | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.-111+207_-111+208i others(3): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31928475 | ||||||
| chr10:31928476
|
A | C | 166 | a0001c0001t0003g0026a0001c0001t0004g0019a0001c0001t0004g0020others(163): Show | 166 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(163): Show |
intron_variant | MODIFIER | c.-111+207T>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31928476 | ||||||
| chr10:31928535
|
G | GCGC | 3 | a0001c0001t0001g0236a0001c0001t0005g0235a0002c0002t0007g0320 | 3 | HG00673.hp2 HG01934.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-111+145_-111+147d others(5): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31928535 | ||||||
| chr10:31928579
|
C | G | 1 | a0001c0001t0022g0002 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-111+104G>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31928579 |