Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | 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 | MKMAD others(841): Show |
chr10 | 31800398 | 31933831 |
| a0002 | 0/0 | 846 | 79 | 3 | 13 | 53 | 1 | 9 | 43 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | MKMAD others(841): Show |
chr10 | 31800398 | 31933831 |
| a0003 | 0/0 | 846 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | MKMAD others(841): Show |
chr10 | 31800398 | 31933831 |
| a0004 | 0/0 | 846 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | MKMAD others(841): Show |
chr10 | 31800398 | 31933831 |
| a0005 | 0/0 | 846 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | MKMAD others(841): Show |
chr10 | 31800398 | 31933831 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2538 | 213 | 65 | 43 | 75 | 6 | 23 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | ATGAA others(2533): Show |
chr10 | 31800398 | 31933831 | ||
| a0001c0003 | 0/0 | 2538 | 13 | 12 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | ATGAA others(2533): Show |
chr10 | 31800398 | 31933831 | ||
| a0001c0005 | 0/0 | 2538 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | ATGAA others(2533): Show |
chr10 | 31800398 | 31933831 | ||
| a0001c0006 | 0/1 | 2538 | 2 | 0 | 0 | 0 | 1 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | ATGAA others(2533): Show |
chr10 | 31800398 | 31933831 | ||
| a0001c0007 | 0/0 | 2538 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | ATGAA others(2533): Show |
chr10 | 31800398 | 31933831 | ||
| a0001c0008 | 0/0 | 2538 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | ATGAA others(2533): Show |
chr10 | 31800398 | 31933831 | ||
| a0001c0010 | 0/0 | 2538 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | ATGAA others(2533): Show |
chr10 | 31800398 | 31933831 | ||
| a0001c0011 | 0/0 | 2538 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | ATGAA others(2533): Show |
chr10 | 31800398 | 31933831 | ||
| a0001c0013 | 0/0 | 2538 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | ATGAA others(2533): Show |
chr10 | 31800398 | 31933831 | ||
| a0001c0014 | 0/0 | 2538 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | ATGAA others(2533): Show |
chr10 | 31800398 | 31933831 | ||
| a0002c0002 | 0/0 | 2538 | 79 | 3 | 13 | 53 | 1 | 9 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | ATGAA others(2533): Show |
chr10 | 31800398 | 31933831 | ||
| a0003c0004 | 0/0 | 2538 | 3 | 2 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | ATGAA others(2533): Show |
chr10 | 31800398 | 31933831 | ||
| a0004c0009 | 0/0 | 2538 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | ATGAA others(2533): Show |
chr10 | 31800398 | 31933831 | ||
| a0005c0012 | 0/0 | 2538 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | ATGAA others(2533): Show |
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 | GTAAC others(5059): Show |
chr10 | 31800398 | 31933831 |
| a0001c0001t0003 | 0/0 | 5062 | 30 | 2 | 4 | 16 | 1 | 7 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | GTAAC others(5057): Show |
chr10 | 31800398 | 31933831 |
| a0001c0001t0004 | 0/0 | 5056 | 17 | 3 | 7 | 0 | 1 | 6 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | GTAAC others(5051): Show |
chr10 | 31800398 | 31933831 |
| a0001c0001t0005 | 0/0 | 5054 | 12 | 1 | 8 | 2 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | GTAAC others(5049): Show |
chr10 | 31800398 | 31933831 |
| a0001c0001t0006 | 0/0 | 5066 | 13 | 8 | 4 | 0 | 1 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | GTAAC others(5061): Show |
chr10 | 31800398 | 31933831 |
| a0001c0001t0008 | 0/0 | 5062 | 12 | 3 | 4 | 4 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | GTAAC others(5057): Show |
chr10 | 31800398 | 31933831 |
| a0001c0001t0009 | 0/0 | 5066 | 8 | 8 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | GTAAC others(5061): Show |
chr10 | 31800398 | 31933831 |
| a0001c0001t0011 | 0/0 | 5054 | 7 | 7 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | GTAAC others(5049): Show |
chr10 | 31800398 | 31933831 |
| a0001c0001t0012 | 1/0 | 5060 | 5 | 1 | 1 | 1 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | GTAAC others(5055): Show |
chr10 | 31800398 | 31933831 |
| a0001c0001t0013 | 0/0 | 5065 | 5 | 0 | 0 | 5 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | GTAAC others(5060): Show |
chr10 | 31800398 | 31933831 |
| a0001c0001t0015 | 0/0 | 5060 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | GTAAC others(5055): Show |
chr10 | 31800398 | 31933831 |
| a0001c0001t0017 | 0/0 | 5050 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | GTAAC others(5045): Show |
chr10 | 31800398 | 31933831 |
| a0001c0001t0018 | 0/0 | 5068 | 3 | 2 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | GTAAC others(5063): Show |
chr10 | 31800398 | 31933831 |
| a0001c0001t0019 | 0/0 | 5064 | 3 | 2 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | GTAAC others(5059): Show |
chr10 | 31800398 | 31933831 |
| a0001c0001t0022 | 0/0 | 5064 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | GTAAC others(5059): Show |
chr10 | 31800398 | 31933831 |
| a0001c0001t0023 | 0/0 | 5062 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | GTAAC others(5057): Show |
chr10 | 31800398 | 31933831 |
| a0001c0001t0024 | 0/0 | 5066 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | GTAAC others(5061): Show |
chr10 | 31800398 | 31933831 |
| a0001c0001t0025 | 0/0 | 5066 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | GTAAC others(5061): Show |
chr10 | 31800398 | 31933831 |
| a0001c0001t0031 | 0/0 | 5062 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | GTAAC others(5057): Show |
chr10 | 31800398 | 31933831 |
| a0001c0001t0032 | 0/0 | 5068 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | GTAAC others(5063): Show |
chr10 | 31800398 | 31933831 |
| a0001c0001t0033 | 0/0 | 5058 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | GTAAC others(5053): Show |
chr10 | 31800398 | 31933831 |
| a0001c0001t0034 | 0/0 | 5066 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | GTAAC others(5061): Show |
chr10 | 31800398 | 31933831 |
| a0001c0001t0035 | 0/0 | 5068 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | GTAAC others(5063): Show |
chr10 | 31800398 | 31933831 |
| a0001c0001t0036 | 0/0 | 5062 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | GTAAC others(5057): Show |
chr10 | 31800398 | 31933831 |
| a0001c0001t0037 | 0/0 | 5058 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | GTAAC others(5053): Show |
chr10 | 31800398 | 31933831 |
| a0001c0001t0038 | 0/0 | 5058 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | GTAAC others(5053): Show |
chr10 | 31800398 | 31933831 |
| a0001c0001t0039 | 0/0 | 5064 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | GTAAC others(5059): Show |
chr10 | 31800398 | 31933831 |
| a0001c0001t0040 | 0/0 | 5076 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | GTAAC others(5071): Show |
chr10 | 31800398 | 31933831 |
| a0001c0001t0041 | 0/0 | 5065 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | GTAAC others(5060): Show |
chr10 | 31800398 | 31933831 |
| a0001c0001t0042 | 0/0 | 5074 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | GTAAC others(5069): Show |
chr10 | 31800398 | 31933831 |
| a0001c0001t0043 | 0/0 | 5058 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | GTAAC others(5053): Show |
chr10 | 31800398 | 31933831 |
| a0001c0001t0044 | 0/0 | 5064 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | GTAAC others(5059): Show |
chr10 | 31800398 | 31933831 |
| a0001c0001t0045 | 0/0 | 5072 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | GTAAC others(5067): Show |
chr10 | 31800398 | 31933831 |
| a0001c0001t0046 | 0/0 | 5062 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | GTAAC others(5057): Show |
chr10 | 31800398 | 31933831 |
| a0001c0001t0049 | 0/0 | 5064 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | GTAAC others(5059): Show |
chr10 | 31800398 | 31933831 |
| a0001c0001t0050 | 0/0 | 5070 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | GTAAC others(5065): Show |
chr10 | 31800398 | 31933831 |
| a0001c0001t0051 | 0/0 | 5062 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | GTAAC others(5057): Show |
chr10 | 31800398 | 31933831 |
| a0001c0001t0052 | 0/0 | 5062 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | GTAAC others(5057): Show |
chr10 | 31800398 | 31933831 |
| a0001c0003t0010 | 0/0 | 5075 | 8 | 7 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | GTAAC others(5070): Show |
chr10 | 31800398 | 31933831 |
| a0001c0003t0016 | 0/0 | 5073 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | GTAAC others(5068): Show |
chr10 | 31800398 | 31933831 |
| a0001c0003t0027 | 0/0 | 5077 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | GTAAC others(5072): Show |
chr10 | 31800398 | 31933831 |
| a0001c0003t0048 | 0/0 | 5061 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | GTAAC others(5056): Show |
chr10 | 31800398 | 31933831 |
| a0001c0005t0016 | 0/0 | 5073 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | GTAAC others(5068): Show |
chr10 | 31800398 | 31933831 |
| a0001c0006t0026 | 0/1 | 5056 | 2 | 0 | 0 | 0 | 1 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | GTAAC others(5051): Show |
chr10 | 31800398 | 31933831 |
| a0001c0007t0028 | 0/0 | 5062 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | GTAAC others(5057): Show |
chr10 | 31800398 | 31933831 |
| a0001c0008t0005 | 0/0 | 5054 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | GTAAC others(5049): Show |
chr10 | 31800398 | 31933831 |
| a0001c0010t0053 | 0/0 | 5062 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | GTAAC others(5057): Show |
chr10 | 31800398 | 31933831 |
| a0001c0011t0001 | 0/0 | 5064 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | GTAAC others(5059): Show |
chr10 | 31800398 | 31933831 |
| a0001c0013t0015 | 0/0 | 5060 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | GTAAC others(5055): Show |
chr10 | 31800398 | 31933831 |
| a0001c0014t0004 | 0/0 | 5056 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | GTAAC others(5051): Show |
chr10 | 31800398 | 31933831 |
| a0002c0002t0002 | 0/0 | 5058 | 51 | 1 | 10 | 35 | 1 | 4 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | GTAAC others(5053): Show |
chr10 | 31800398 | 31933831 |
| a0002c0002t0007 | 0/0 | 5060 | 10 | 2 | 0 | 5 | 0 | 3 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | GTAAC others(5055): Show |
chr10 | 31800398 | 31933831 |
| a0002c0002t0014 | 0/0 | 5056 | 5 | 0 | 1 | 4 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | GTAAC others(5051): Show |
chr10 | 31800398 | 31933831 |
| a0002c0002t0020 | 0/0 | 5062 | 3 | 0 | 2 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | GTAAC others(5057): Show |
chr10 | 31800398 | 31933831 |
| a0002c0002t0021 | 0/0 | 5060 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | GTAAC others(5055): Show |
chr10 | 31800398 | 31933831 |
| a0002c0002t0029 | 0/0 | 5058 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | GTAAC others(5053): Show |
chr10 | 31800398 | 31933831 |
| a0002c0002t0030 | 0/0 | 5060 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | GTAAC others(5055): Show |
chr10 | 31800398 | 31933831 |
| a0002c0002t0047 | 0/0 | 5058 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | GTAAC others(5053): Show |
chr10 | 31800398 | 31933831 |
| a0002c0002t0054 | 0/0 | 5058 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | GTAAC others(5053): Show |
chr10 | 31800398 | 31933831 |
| a0002c0002t0055 | 0/0 | 5060 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | GTAAC others(5055): Show |
chr10 | 31800398 | 31933831 |
| a0003c0004t0007 | 0/0 | 5060 | 3 | 2 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | GTAAC others(5055): Show |
chr10 | 31800398 | 31933831 |
| a0004c0009t0012 | 0/0 | 5060 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | GTAAC others(5055): Show |
chr10 | 31800398 | 31933831 |
| a0005c0012t0003 | 0/0 | 5062 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | GTAAC others(5057): Show |
chr10 | 31800398 | 31933831 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0112 | 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 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0125 | 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 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0133 | 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 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0144 | 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 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0003g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0004g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0004g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0004g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0004g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0004g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0004g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0004g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 |
| a0001c0001t0004g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0004g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0004g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0004g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0004g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0004g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0004g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0005g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 |
| a0001c0001t0005g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0005g0045 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0005g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0005g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0005g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0005g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0005g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0005g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0006g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0006g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0006g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0006g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0006g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0006g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0006g0163 | 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 |
| a0001c0001t0006g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0006g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0006g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0006g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0006g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0008g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0008g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0008g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0008g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0008g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0008g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0008g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0008g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0008g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0008g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0008g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0009g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0009g0071 | 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 |
| a0001c0001t0009g0076 | 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 |
| a0001c0001t0009g0079 | 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 |
| a0001c0001t0011g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0011g0054 | 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 |
| a0001c0001t0011g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0011g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0012g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0012g0175 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0012g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0012g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0012g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0013g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0013g0090 | 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 |
| a0001c0001t0013g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0015g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0015g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0015g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0017g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0017g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0017g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0018g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0018g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0018g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0019g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0019g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0019g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0022g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0022g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0023g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0023g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0024g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0024g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0025g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0025g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0031g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0032g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0033g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0034g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0035g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0036g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0037g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0038g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0039g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0040g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0041g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0042g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0043g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0044g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0045g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0046g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0049g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0050g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0051g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0001t0052g0317 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0003t0010g0007 | 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 |
| a0001c0003t0010g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0003t0010g0017 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0003t0010g0019 | 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 |
| a0001c0003t0016g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0003t0027g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0003t0027g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0003t0048g0016 | 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 |
| a0001c0005t0016g0009 | 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 |
| a0001c0006t0026g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0007t0028g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 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 |
| a0001c0008t0005g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0010t0053g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0011t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0013t0015g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0001c0014t0004g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 0 | 1 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0002c0002t0002g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0007g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0007g0251 | 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 |
| a0002c0002t0007g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0014g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0014g0270 | 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 |
| a0002c0002t0014g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0020g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0020g0269 | 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 |
| a0002c0002t0021g0247 | 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 |
| a0002c0002t0021g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0029g0243 | 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 |
| a0002c0002t0030g0240 | 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 |
| a0002c0002t0047g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0054g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0002c0002t0055g0320 | 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 |
| a0004c0009t0012g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| a0005c0012t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 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 | g0203 | EUR | GBR | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG00099 | hp2 | a0001 | c0006 | t0026 | g0066 | EUR | GBR | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG00280 | hp1 | a0001 | c0001 | t0006 | g0157 | EUR | FIN | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0170 | EUR | FIN | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0179 | EAS | CHS | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0120 | 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 | g0102 | 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 | g0121 | EAS | CHS | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0200 | 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 | g0235 | EAS | CHS | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG00733 | hp2 | a0001 | c0001 | t0052 | g0317 | AMR | PUR | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG00735 | hp2 | a0001 | c0003 | t0010 | g0017 | AMR | PUR | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG00738 | hp2 | a0002 | c0002 | t0002 | g0266 | AMR | PUR | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG00741 | hp1 | a0001 | c0001 | t0006 | g0220 | AMR | PUR | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01071 | hp1 | a0001 | c0013 | t0015 | g0152 | AMR | PUR | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01071 | hp2 | a0002 | c0002 | t0002 | g0257 | 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 | g0063 | 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 | g0231 | AMR | PUR | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01106 | hp1 | a0001 | c0001 | t0006 | g0156 | 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 | g0046 | 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 | g0164 | AMR | PUR | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01167 | hp2 | a0001 | c0001 | t0004 | g0021 | AMR | PUR | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01168 | hp1 | a0001 | c0001 | t0005 | g0052 | AMR | PUR | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01168 | hp2 | a0001 | c0001 | t0004 | g0035 | AMR | PUR | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01175 | hp1 | a0001 | c0001 | t0004 | g0023 | AMR | PUR | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01192 | hp2 | a0001 | c0001 | t0005 | g0043 | AMR | PUR | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01257 | hp1 | a0002 | c0002 | t0020 | g0269 | AMR | CLM | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01257 | hp2 | a0001 | c0001 | t0005 | g0044 | AMR | CLM | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01258 | hp1 | a0001 | c0001 | t0006 | g0205 | AMR | CLM | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01258 | hp2 | a0001 | c0001 | t0005 | g0049 | AMR | CLM | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01346 | hp1 | a0001 | c0001 | t0008 | g0129 | AMR | CLM | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01346 | hp2 | a0001 | c0001 | t0004 | g0037 | AMR | CLM | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01358 | hp2 | a0002 | c0002 | t0002 | g0268 | AMR | CLM | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0176 | AMR | CLM | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0082 | EUR | IBS | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01515 | hp2 | a0002 | c0002 | t0002 | g0267 | EUR | IBS | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0097 | EUR | IBS | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01516 | hp2 | a0001 | c0001 | t0004 | g0036 | EUR | IBS | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01884 | hp1 | a0001 | c0001 | t0011 | g0070 | AFR | ACB | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | ACB | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01891 | hp2 | a0001 | c0001 | t0011 | g0055 | AFR | ACB | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01928 | hp1 | a0001 | c0001 | t0008 | g0137 | 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 | g0003 | AMR | PEL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01934 | hp2 | a0001 | c0001 | t0005 | g0234 | AMR | PEL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01978 | hp1 | a0004 | c0009 | t0012 | g0177 | AMR | PEL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01978 | hp2 | a0001 | c0001 | t0004 | g0042 | AMR | PEL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01981 | hp1 | a0001 | c0001 | t0051 | g0236 | AMR | PEL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PEL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0174 | AMR | PEL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01993 | hp2 | a0001 | c0001 | t0004 | g0020 | 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 | g0041 | AMR | PEL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02015 | hp1 | a0001 | c0011 | t0001 | g0110 | EAS | KHV | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02015 | hp2 | a0002 | c0002 | t0007 | g0251 | EAS | KHV | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02027 | hp1 | a0001 | c0001 | t0008 | g0134 | 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 | g0204 | EAS | KHV | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02055 | hp1 | a0001 | c0001 | t0018 | g0085 | AFR | ACB | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02055 | hp2 | a0002 | c0002 | t0002 | g0250 | AFR | ACB | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02071 | hp1 | a0001 | c0001 | t0039 | g0087 | 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 | g0182 | 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 | g0112 | EAS | KHV | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02135 | hp2 | a0001 | c0001 | t0031 | g0002 | EAS | KHV | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02145 | hp1 | a0001 | c0001 | t0009 | g0072 | AFR | ACB | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02145 | hp2 | a0001 | c0001 | t0050 | g0030 | AFR | ACB | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02148 | hp1 | a0001 | c0001 | t0012 | g0196 | 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 | g0223 | EAS | CDX | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02257 | hp1 | a0001 | c0001 | t0009 | g0079 | AFR | ACB | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02257 | hp2 | a0001 | c0003 | t0010 | g0006 | AFR | ACB | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02258 | hp1 | a0001 | c0001 | t0025 | g0201 | AFR | ACB | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0034 | AFR | ACB | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02273 | hp1 | a0001 | c0001 | t0008 | g0093 | AMR | PEL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02273 | hp2 | a0001 | c0001 | t0022 | g0172 | AMR | PEL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02280 | hp1 | a0001 | c0001 | t0011 | g0054 | AFR | ACB | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02280 | hp2 | a0001 | c0001 | t0034 | g0029 | AFR | ACB | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02293 | hp1 | a0001 | c0001 | t0005 | g0047 | AMR | PEL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0193 | AMR | PEL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02300 | hp1 | a0002 | c0002 | t0002 | g0265 | AMR | PEL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02300 | hp2 | a0001 | c0001 | t0008 | g0221 | AMR | PEL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02451 | hp1 | a0001 | c0003 | t0010 | g0010 | AFR | ACB | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02451 | hp2 | a0001 | c0001 | t0006 | g0163 | AFR | ACB | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02572 | hp1 | a0001 | c0007 | t0028 | g0238 | AFR | GWD | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02572 | hp2 | a0001 | c0001 | t0023 | g0068 | AFR | GWD | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02602 | hp1 | a0001 | c0001 | t0004 | g0067 | SAS | PJL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02602 | hp2 | a0001 | c0008 | t0005 | g0073 | SAS | PJL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02615 | hp1 | a0001 | c0003 | t0010 | g0019 | AFR | GWD | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02615 | hp2 | a0001 | c0001 | t0037 | g0033 | AFR | GWD | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02622 | hp1 | a0001 | c0001 | t0009 | g0076 | AFR | GWD | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02622 | hp2 | a0001 | c0001 | t0036 | g0039 | AFR | GWD | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02630 | hp1 | a0001 | c0003 | t0010 | g0011 | AFR | GWD | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0069 | AFR | GWD | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02647 | hp1 | a0001 | c0001 | t0009 | g0071 | AFR | GWD | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02647 | hp2 | a0001 | c0001 | t0006 | g0215 | AFR | GWD | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02698 | hp2 | a0002 | c0002 | t0029 | g0243 | SAS | PJL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02717 | hp1 | a0001 | c0001 | t0011 | g0057 | AFR | GWD | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02717 | hp2 | a0001 | c0003 | t0010 | g0012 | AFR | GWD | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02723 | hp2 | a0001 | c0003 | t0048 | g0016 | AFR | GWD | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0169 | SAS | PJL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02735 | hp2 | a0001 | c0008 | t0005 | g0074 | SAS | PJL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0197 | SAS | PJL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02818 | hp1 | a0001 | c0003 | t0027 | g0015 | AFR | GWD | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | GWD | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02886 | hp2 | a0001 | c0010 | t0053 | g0237 | AFR | GWD | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02895 | hp1 | a0001 | c0005 | t0016 | g0009 | AFR | GWD | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02895 | hp2 | a0001 | c0001 | t0006 | g0165 | AFR | GWD | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02896 | hp1 | a0001 | c0001 | t0006 | g0158 | AFR | GWD | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02896 | hp2 | a0001 | c0007 | t0028 | g0239 | AFR | GWD | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02897 | hp1 | a0001 | c0005 | t0016 | g0008 | AFR | GWD | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02897 | hp2 | a0001 | c0001 | t0006 | g0159 | AFR | GWD | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02965 | hp1 | a0001 | c0001 | t0023 | g0038 | AFR | ESN | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02965 | hp2 | a0001 | c0001 | t0011 | g0059 | AFR | ESN | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02970 | hp1 | a0001 | c0001 | t0019 | g0160 | AFR | ESN | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02970 | hp2 | a0001 | c0001 | t0017 | g0048 | AFR | ESN | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02976 | hp1 | a0001 | c0001 | t0009 | g0081 | AFR | ESN | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02976 | hp2 | a0001 | c0001 | t0032 | g0149 | AFR | ESN | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03017 | hp1 | a0001 | c0001 | t0005 | g0061 | SAS | PJL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0171 | SAS | PJL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03041 | hp1 | a0001 | c0001 | t0008 | g0153 | AFR | GWD | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0032 | AFR | GWD | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03098 | hp1 | a0001 | c0001 | t0044 | g0078 | AFR | MSL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03098 | hp2 | a0001 | c0003 | t0010 | g0007 | 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 | g0077 | AFR | ESN | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03209 | hp1 | a0001 | c0001 | t0024 | g0040 | AFR | MSL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03209 | hp2 | a0001 | c0001 | t0009 | g0026 | AFR | MSL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03225 | hp1 | a0001 | c0001 | t0011 | g0056 | AFR | MSL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03225 | hp2 | a0001 | c0001 | t0040 | g0211 | AFR | MSL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03239 | hp1 | a0002 | c0002 | t0002 | g0263 | SAS | PJL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0206 | 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 | g0004 | AFR | MSL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03486 | hp1 | a0001 | c0001 | t0017 | g0060 | AFR | MSL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03486 | hp2 | a0001 | c0001 | t0008 | g0150 | AFR | MSL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03492 | hp1 | a0002 | c0002 | t0002 | g0318 | SAS | PJL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03492 | hp2 | a0001 | c0001 | t0008 | g0131 | SAS | PJL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0027 | AFR | ESN | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03516 | hp2 | a0001 | c0003 | t0010 | g0018 | AFR | ESN | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03540 | hp1 | a0001 | c0001 | t0043 | g0024 | AFR | GWD | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03540 | hp2 | a0001 | c0001 | t0017 | g0051 | AFR | GWD | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03579 | hp1 | a0001 | c0001 | t0012 | g0028 | AFR | MSL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03579 | hp2 | a0001 | c0001 | t0006 | g0148 | AFR | MSL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03654 | hp1 | a0002 | c0002 | t0007 | g0245 | SAS | PJL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0233 | SAS | PJL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0166 | SAS | PJL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03669 | hp2 | a0001 | c0001 | t0004 | g0064 | SAS | PJL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | STU | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0232 | SAS | STU | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03704 | hp1 | a0001 | c0001 | t0004 | g0025 | 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 | g0222 | SAS | PJL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03710 | hp2 | a0001 | c0001 | t0004 | g0001 | 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 | g0104 | SAS | BEB | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG04184 | hp1 | a0001 | c0001 | t0033 | g0173 | 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 | g0185 | SAS | STU | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG04199 | hp2 | a0002 | c0002 | t0002 | g0244 | 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 | g0022 | SAS | STU | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18522 | hp1 | a0001 | c0001 | t0042 | g0083 | AFR | YRI | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18522 | hp2 | a0001 | c0001 | t0045 | g0075 | 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 | g0099 | 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 | g0031 | AFR | YRI | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18940 | hp1 | a0002 | c0002 | t0002 | g0254 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18941 | hp1 | a0002 | c0002 | t0002 | g0242 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18944 | hp1 | a0001 | c0001 | t0005 | g0050 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18944 | hp2 | a0002 | c0002 | t0002 | g0258 | 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 | g0116 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0189 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18947 | hp2 | a0002 | c0002 | t0014 | g0270 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18948 | hp1 | a0002 | c0002 | t0002 | g0246 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0094 | 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 | g0088 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18952 | hp1 | a0001 | c0001 | t0013 | g0091 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18952 | hp2 | a0002 | c0002 | t0002 | g0249 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0168 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0098 | 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 | g0089 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18957 | hp1 | a0002 | c0002 | t0002 | g0261 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0188 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18959 | hp2 | a0001 | c0001 | t0005 | g0045 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18960 | hp1 | a0005 | c0012 | t0003 | g0190 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18960 | hp2 | a0001 | c0001 | t0008 | g0096 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0146 | 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 | g0114 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18965 | hp2 | a0001 | c0001 | t0003 | g0187 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0194 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18966 | hp2 | a0002 | c0002 | t0002 | g0260 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18967 | hp1 | a0002 | c0002 | t0030 | g0240 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18967 | hp2 | a0001 | c0001 | t0013 | g0090 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18969 | hp2 | a0002 | c0002 | t0002 | g0259 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18974 | hp1 | a0002 | c0002 | t0055 | g0320 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18975 | hp1 | a0001 | c0001 | t0012 | g0226 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18975 | hp2 | a0002 | c0002 | t0047 | g0123 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0199 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18979 | hp2 | a0002 | c0002 | t0002 | g0262 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18980 | hp1 | a0001 | c0001 | t0013 | g0092 | 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 | g0186 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18982 | hp2 | a0002 | c0002 | t0014 | g0272 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18985 | hp1 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0191 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18988 | hp2 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18993 | hp1 | a0002 | c0002 | t0054 | g0321 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18994 | hp1 | a0001 | c0001 | t0013 | g0147 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18994 | hp2 | a0002 | c0002 | t0014 | g0241 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18998 | hp1 | a0002 | c0002 | t0002 | g0274 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0178 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0198 | 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 | g0181 | 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 | g0124 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19007 | hp1 | a0002 | c0002 | t0021 | g0248 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0118 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19009 | hp2 | a0001 | c0001 | t0015 | g0192 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19030 | hp1 | a0001 | c0001 | t0019 | g0161 | AFR | LWK | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | LWK | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | LWK | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0062 | AFR | LWK | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19056 | hp2 | a0002 | c0002 | t0002 | g0264 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19057 | hp1 | a0002 | c0002 | t0002 | g0253 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19058 | hp1 | a0002 | c0002 | t0002 | g0256 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19060 | hp1 | a0002 | c0002 | t0002 | g0275 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19062 | hp1 | a0001 | c0001 | t0008 | g0132 | 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 | g0202 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19063 | hp2 | a0002 | c0002 | t0002 | g0255 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19065 | hp2 | a0002 | c0002 | t0002 | g0276 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19070 | hp1 | a0002 | c0002 | t0021 | g0247 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19072 | hp1 | a0001 | c0001 | t0008 | g0103 | 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 | g0133 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0119 | 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 | g0142 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19078 | hp2 | a0002 | c0002 | t0002 | g0273 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0086 | 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 | g0135 | 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 | g0210 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19086 | hp2 | a0002 | c0002 | t0014 | g0271 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19089 | hp1 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0107 | 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 | g0095 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA20129 | hp1 | a0001 | c0001 | t0006 | g0230 | AFR | ASW | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | ASW | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0180 | SAS | GIH | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA20905 | hp2 | a0001 | c0001 | t0004 | g0001 | SAS | GIH | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01123 | hp1 | a0001 | c0001 | t0006 | g0213 | AMR | CLM | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG01123 | hp2 | a0002 | c0002 | t0020 | g0252 | AMR | CLM | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02486 | hp1 | a0001 | c0001 | t0011 | g0053 | AFR | ACB | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02486 | hp2 | a0001 | c0001 | t0008 | g0138 | AFR | ACB | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02559 | hp1 | a0001 | c0001 | t0009 | g0080 | AFR | ACB | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG02559 | hp2 | a0001 | c0001 | t0006 | g0151 | AFR | ACB | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03471 | hp1 | a0001 | c0001 | t0025 | g0154 | AFR | MSL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG03471 | hp2 | a0001 | c0014 | t0004 | g0014 | AFR | MSL | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG06807 | hp1 | a0001 | c0001 | t0024 | g0058 | AFR | USA | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| HG06807 | hp2 | a0001 | c0003 | t0016 | g0005 | 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 | g0143 | EAS | JPT | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0184 | AFR | USA | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA20300 | hp2 | a0001 | c0003 | t0027 | g0013 | AFR | USA | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA21309 | hp1 | a0001 | c0001 | t0018 | g0218 | AFR | LWK | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| NA21309 | hp2 | a0002 | c0002 | t0007 | g0319 | AFR | LWK | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| homoSapiens | chm13v2 | a0001 | c0006 | t0026 | g0065 | REF | REF | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0012 | g0175 | REF | REF | ARHGAP12_chr10_31800398_31933831 | ARHGAP12 | chr10 | 31800398 | 31933831 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:31812781 | G | T | 1 | a0005 | 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 | a0002 a0003 |
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 | a0004 | 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 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | a0001c0003 a0001c0005 |
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 | a0001c0007 a0001c0010 a0002c0002 others(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 | a0002c0002 a0003c0004 |
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 | 1 | HG00099.hp2 | 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 | a0001c0003 a0001c0005 a0001c0014 |
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 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | a0001c0003t0010 a0001c0003t0016 a0001c0003t0027 others(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 | a0001c0003t0010 a0001c0003t0016 a0001c0003t0027 others(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 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0023 others(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 | a0001c0001t0001 a0001c0001t0013 a0001c0001t0019 others(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 | a0001c0001t0006 a0001c0001t0009 a0001c0001t0024 others(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 | a0001c0001t0018 a0001c0001t0032 a0001c0001t0035 |
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 | a0001c0001t0045 a0001c0003t0016 a0001c0005t0016 |
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 | a0001c0001t0042 a0001c0003t0010 |
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 | a0001c0001t0040 a0001c0003t0027 |
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 | a0001c0001t0033 a0001c0001t0037 a0001c0001t0038 others(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 | a0001c0001t0004 a0001c0006t0026 a0001c0014t0004 others(1): Show |
24 | HG00099.hp2 HG00639.hp2 HG01081.hp2 others(21): 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 | a0001c0001t0005 a0001c0001t0011 a0001c0008t0005 |
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 | a0001c0007t0028 a0001c0010t0053 a0002c0002t0002 others(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 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0008 others(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 | a0001c0003t0010 a0001c0003t0016 a0001c0003t0027 others(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 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0009 others(30): Show |
160 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(157): 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 | a0001c0001t0041 a0001c0003t0010 a0001c0003t0016 others(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 | a0001c0003t0010 a0001c0003t0016 a0001c0003t0027 others(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 | a0001c0001t0019 a0001c0001t0042 |
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 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0008 others(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 | 1 | HG00099.hp2 | 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 | a0001c0001t0009 a0001c0001t0043 a0001c0001t0044 others(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 | a0002c0002t0002 a0002c0002t0007 a0002c0002t0014 others(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 | a0001c0003t0010 a0001c0003t0016 a0001c0003t0027 others(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 | a0002c0002t0054 a0002c0002t0055 |
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 | a0002c0002t0054 a0002c0002t0055 |
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 | a0001c0001t0052 a0001c0007t0028 a0001c0010t0053 others(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 | a0002c0002t0054 a0002c0002t0055 |
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 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:31807875 | G | C | 113 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0086 others(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 | a0001c0001t0003g0200 | 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 | a0002c0002t0002g0242 a0002c0002t0002g0244 a0002c0002t0002g0246 others(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 | a0001c0001t0009g0026 a0001c0001t0009g0071 a0001c0001t0009g0072 others(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 | a0001c0001t0003g0187 a0001c0003t0010g0006 a0001c0003t0010g0007 others(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 | a0002c0002t0007g0308 a0003c0004t0007g0309 a0003c0004t0007g0310 others(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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0001t0001g0212 | 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 | a0001c0001t0001g0098 | 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 | a0001c0007t0028g0238 a0001c0007t0028g0239 a0001c0010t0053g0237 others(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 | a0001c0007t0028g0238 a0001c0007t0028g0239 a0001c0010t0053g0237 others(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 | a0002c0002t0002g0281 a0002c0002t0047g0123 |
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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0003t0016g0004 a0001c0003t0016g0005 |
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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0001t0001g0227 a0001c0001t0001g0229 |
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 | a0001c0001t0001g0143 | 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 | a0001c0001t0001g0097 a0001c0001t0001g0127 a0001c0001t0001g0128 |
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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0086 others(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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0001t0008g0096 a0002c0002t0002g0242 a0002c0002t0002g0244 others(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 | a0001c0001t0001g0133 a0001c0001t0001g0140 |
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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | 256 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0086 others(253): Show |
257 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(254): 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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0001t0040g0211 | 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 | a0001c0001t0009g0026 a0001c0001t0009g0071 a0001c0001t0009g0072 others(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 | a0001c0001t0001g0102 a0001c0001t0006g0157 a0001c0001t0008g0221 others(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 | 149 | a0001c0001t0001g0119 a0001c0001t0001g0202 a0001c0001t0001g0216 others(146): Show |
150 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(147): Show |
intron_variant | MODIFIER | c.1952-796delA | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 15/19 | chr10 | 31811542 | |||||||
| chr10:31811542 | CTTT | C | 15 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0001t0043g0024 | 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 | a0001c0001t0001g0155 | 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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0002c0002t0002g0302 a0002c0002t0002g0305 |
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 | 48 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(45): Show |
49 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(46): 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 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0086 others(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 | a0001c0001t0008g0132 a0001c0001t0008g0134 a0001c0001t0015g0088 others(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 | a0001c0001t0001g0116 | 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 | a0001c0001t0004g0034 a0001c0001t0037g0033 |
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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0002c0002t0007g0245 | 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 | 158 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(155): Show |
159 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(156): 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 | a0002c0002t0002g0302 a0002c0002t0002g0305 |
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 | a0001c0001t0009g0026 a0001c0001t0009g0071 a0001c0001t0009g0072 others(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 | a0002c0002t0020g0269 | 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 | a0001c0010t0053g0237 | 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 | 143 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(140): Show |
144 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(141): 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 | a0002c0002t0002g0267 | 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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | 276 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0086 others(273): Show |
277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): 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 | a0001c0001t0009g0026 a0001c0001t0009g0071 a0001c0001t0009g0072 others(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 | a0001c0001t0008g0134 | 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 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0086 others(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 | a0001c0001t0004g0020 | 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 | a0001c0001t0004g0035 a0001c0001t0004g0036 a0001c0001t0004g0037 others(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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0002c0002t0002g0246 a0002c0002t0002g0253 a0002c0002t0002g0254 |
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 | 159 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(156): Show |
160 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(157): 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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0001t0023g0038 a0001c0001t0023g0068 a0001c0001t0024g0040 others(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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0002c0002t0055g0320 | 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 | 125 | a0001c0001t0003g0183 a0001c0001t0004g0001 a0001c0001t0004g0020 others(122): Show |
126 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(123): Show |
intron_variant | MODIFIER | c.1732-760delT | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 13/19 | chr10 | 31815120 | |||||||
| chr10:31815120 | CAA | C | 17 | a0001c0001t0004g0021 a0001c0003t0010g0006 a0001c0003t0010g0007 others(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 | a0001c0001t0001g0117 | 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 | a0001c0001t0009g0026 a0001c0001t0009g0071 a0001c0001t0009g0072 others(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 | a0001c0001t0003g0027 | 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 | a0001c0007t0028g0238 a0001c0007t0028g0239 a0001c0010t0053g0237 others(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 | a0002c0002t0002g0281 a0002c0002t0047g0123 |
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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | 271 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0086 others(268): Show |
272 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(269): 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 | a0001c0001t0034g0029 | 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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | 41 | a0001c0001t0001g0225 a0001c0001t0003g0118 a0001c0001t0003g0166 others(38): Show |
42 | HG00099.hp2 HG00280.hp1 HG00733.hp2 others(39): 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 | a0001c0001t0001g0112 a0001c0001t0001g0135 a0001c0001t0001g0144 others(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 | a0001c0001t0001g0117 a0001c0001t0001g0133 a0001c0001t0001g0140 others(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 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0086 others(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 | a0001c0001t0001g0094 a0001c0001t0001g0097 a0001c0001t0001g0099 others(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 | a0001c0001t0001g0098 a0001c0001t0001g0109 a0001c0001t0001g0124 others(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 | a0001c0001t0001g0128 a0001c0001t0001g0219 a0002c0002t0002g0265 others(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 | a0001c0001t0008g0134 | 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 | a0001c0001t0001g0227 a0001c0001t0001g0229 a0002c0002t0055g0320 |
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 | a0001c0001t0001g0231 | 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 | a0001c0001t0003g0232 a0001c0001t0003g0233 a0001c0001t0004g0062 others(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 | a0001c0001t0003g0027 a0001c0001t0004g0042 a0001c0001t0005g0043 others(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 | a0001c0001t0017g0048 | 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 | a0001c0001t0049g0031 a0001c0001t0050g0030 |
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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | 276 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0086 others(273): Show |
277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): 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 | a0001c0001t0005g0061 a0001c0001t0005g0234 |
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 | a0001c0014t0004g0014 | 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 | 159 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(156): Show |
160 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(157): 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 | a0002c0002t0002g0246 | 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 | a0001c0001t0001g0127 | 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 | 48 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(45): Show |
49 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(46): 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 | a0001c0001t0001g0086 | 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 | a0001c0001t0001g0146 | 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 | a0001c0001t0009g0026 a0001c0001t0009g0071 a0001c0001t0009g0072 others(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 | a0001c0001t0043g0024 | 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 | 144 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(141): Show |
145 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(142): 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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | 159 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(156): Show |
160 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(157): 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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0001t0040g0211 | 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 | a0001c0001t0011g0070 | 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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | 144 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(141): Show |
145 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(142): 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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0001t0009g0026 a0001c0001t0009g0071 a0001c0001t0009g0072 others(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 | a0001c0001t0001g0108 | 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 | a0001c0001t0004g0034 a0001c0001t0037g0033 |
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 | a0001c0001t0023g0038 a0001c0001t0023g0068 a0001c0001t0024g0058 others(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 | a0002c0002t0002g0249 a0002c0002t0002g0259 a0002c0002t0002g0260 others(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 | a0001c0001t0006g0157 | 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 | a0001c0001t0023g0038 a0001c0001t0023g0068 a0001c0001t0024g0040 others(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 | 48 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(45): Show |
49 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(46): 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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0001t0005g0061 a0001c0001t0005g0234 |
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 | a0003c0004t0007g0309 a0003c0004t0007g0310 a0003c0004t0007g0311 |
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 | a0001c0001t0049g0031 a0001c0001t0050g0030 |
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 | a0001c0001t0009g0026 a0001c0001t0009g0071 a0001c0001t0009g0072 others(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 | a0001c0001t0012g0028 a0001c0001t0012g0226 a0001c0001t0034g0029 others(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 | a0001c0001t0001g0102 a0001c0001t0001g0116 a0001c0001t0001g0119 others(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 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0086 others(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 | 64 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(61): Show |
65 | HG00099.hp2 HG00735.hp2 HG01081.hp2 others(62): 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 | 48 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(45): Show |
49 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(46): 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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0002c0002t0002g0253 a0002c0002t0002g0254 |
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 | a0001c0001t0017g0048 a0001c0001t0017g0051 a0001c0001t0017g0060 |
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 | a0002c0002t0002g0244 a0002c0002t0002g0289 |
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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0001t0003g0167 a0001c0001t0003g0179 a0001c0001t0031g0002 |
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 | 48 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(45): Show |
49 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(46): 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 | a0001c0001t0049g0031 a0001c0001t0050g0030 |
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 | a0001c0001t0001g0225 | 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 | a0001c0001t0003g0179 a0001c0001t0031g0002 |
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 | 159 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(156): Show |
160 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(157): 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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0001t0009g0026 a0001c0001t0009g0071 a0001c0001t0009g0072 others(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 | a0001c0001t0001g0214 a0001c0001t0001g0216 a0001c0001t0001g0217 others(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 | a0001c0001t0004g0042 a0001c0001t0005g0041 a0001c0001t0005g0043 others(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 | a0002c0002t0002g0257 | 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 | a0001c0001t0040g0211 | 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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0086 others(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 | a0001c0001t0003g0171 | 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 | a0001c0001t0013g0091 a0001c0001t0013g0092 |
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 | a0001c0001t0003g0027 a0001c0001t0012g0028 |
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 | a0001c0001t0009g0026 | 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 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0086 others(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 | a0001c0001t0009g0026 a0001c0001t0009g0071 a0001c0001t0009g0072 others(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 | a0001c0003t0010g0006 a0001c0003t0010g0010 a0001c0003t0010g0011 others(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 | a0001c0001t0022g0003 | 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 | a0002c0002t0002g0242 a0002c0002t0002g0244 a0002c0002t0002g0246 others(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 | a0001c0001t0049g0031 a0001c0001t0050g0030 |
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 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0086 others(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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0001t0001g0214 | 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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0013t0015g0152 | 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 | a0002c0002t0007g0313 a0002c0002t0007g0314 a0002c0002t0007g0316 |
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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | 48 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(45): Show |
49 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(46): 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 | a0002c0002t0002g0255 a0002c0002t0002g0256 a0002c0002t0002g0258 |
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 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0086 others(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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0001t0003g0233 | 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 | a0001c0007t0028g0238 a0001c0007t0028g0239 a0001c0010t0053g0237 others(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 | 271 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0086 others(268): Show |
272 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(269): 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 | a0001c0001t0022g0172 | 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 | a0001c0001t0009g0026 a0001c0001t0009g0071 a0001c0001t0009g0072 others(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 | a0001c0001t0049g0031 | 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 | a0001c0001t0003g0183 a0001c0001t0003g0187 a0001c0001t0003g0188 others(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 | a0001c0001t0043g0024 | 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 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0086 others(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 | a0001c0001t0012g0028 | 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 | a0001c0003t0016g0005 | 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 | a0001c0001t0001g0203 | 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 | a0001c0001t0003g0178 a0001c0001t0003g0197 a0001c0001t0012g0185 others(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 | a0001c0003t0010g0006 a0001c0003t0010g0010 a0001c0003t0010g0011 others(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 | a0001c0003t0010g0007 a0001c0003t0010g0017 a0001c0003t0010g0018 others(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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0001t0003g0183 a0001c0001t0003g0186 a0001c0001t0003g0187 others(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 | a0001c0001t0001g0214 a0001c0001t0001g0216 a0001c0001t0001g0217 others(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 | 161 | a0001c0001t0001g0133 a0001c0001t0001g0140 a0001c0001t0004g0001 others(158): Show |
162 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(159): Show |
intron_variant | MODIFIER | c.1449-1835dupA | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 10/19 | chr10 | 31828219 | |||||||
| chr10:31828219 | C | CTT | 111 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0086 others(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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0001t0001g0225 a0001c0001t0008g0150 |
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 | a0001c0001t0001g0225 | 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 | 144 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(141): Show |
145 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(142): 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 | a0001c0001t0009g0026 a0001c0001t0009g0071 a0001c0001t0009g0072 others(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 | a0002c0002t0007g0308 a0003c0004t0007g0309 a0003c0004t0007g0310 others(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 | a0001c0001t0043g0024 | 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 | a0001c0001t0003g0118 a0001c0001t0003g0180 a0001c0001t0009g0026 others(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 | a0001c0001t0003g0166 | 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 | a0001c0001t0049g0031 | 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 | a0001c0001t0001g0119 | 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 | a0001c0001t0025g0201 | 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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0001t0004g0032 a0001c0001t0004g0042 a0001c0001t0005g0041 others(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 | a0001c0001t0034g0029 | 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 | a0001c0003t0010g0010 | 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 | a0001c0001t0001g0136 | 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 | a0004c0009t0012g0177 | 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 | a0001c0007t0028g0238 a0001c0007t0028g0239 |
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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0002c0002t0002g0244 | 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 | a0001c0003t0010g0017 | 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 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0086 others(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 | a0001c0001t0004g0064 | 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 | a0001c0001t0001g0130 a0001c0001t0008g0096 a0001c0001t0041g0142 |
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 | a0002c0002t0002g0249 a0002c0002t0002g0259 a0002c0002t0002g0260 others(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 | a0001c0003t0048g0016 | 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 | a0001c0001t0034g0029 | 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 | 19 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(16): Show |
20 | HG00099.hp2 HG01081.hp2 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.1448+257dupT | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 10/19 | chr10 | 31831481 | |||||||
| chr10:31831654 | T | C | 15 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0001t0052g0317 | 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 | a0002c0002t0002g0266 a0002c0002t0002g0267 a0002c0002t0002g0268 others(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 | a0001c0001t0004g0032 | 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 | a0001c0001t0023g0038 a0001c0001t0023g0068 a0001c0001t0024g0040 others(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 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0086 others(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 | a0001c0001t0006g0148 | 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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0001t0011g0053 a0001c0001t0011g0054 a0001c0001t0011g0055 others(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 | a0001c0001t0043g0024 | 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 | a0001c0001t0025g0154 | 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 | a0001c0001t0001g0227 a0001c0001t0001g0229 a0001c0001t0006g0205 |
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 | a0001c0001t0001g0212 | 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 | 53 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(50): Show |
54 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(51): Show |
intron_variant | MODIFIER | c.1387-1533dupA | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31833332 | |||||||
| chr10:31833334 | T | TTA | 91 | a0001c0001t0009g0026 a0001c0001t0009g0071 a0001c0001t0009g0072 others(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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | 159 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(156): Show |
160 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(157): 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 | a0002c0002t0002g0261 | 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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0086 others(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 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0086 others(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 | a0002c0002t0002g0273 a0002c0002t0002g0277 a0002c0002t0002g0296 |
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 | 48 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(45): Show |
49 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(46): 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 | a0001c0001t0004g0064 a0001c0001t0004g0067 |
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 | a0001c0001t0009g0026 a0001c0001t0009g0071 a0001c0001t0009g0072 others(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 | 16 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(13): Show |
17 | HG00099.hp2 HG01081.hp2 HG01167.hp2 others(14): 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 | a0001c0001t0001g0117 a0001c0001t0003g0197 a0001c0001t0019g0160 others(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 | a0001c0001t0004g0032 a0001c0001t0023g0038 a0001c0001t0023g0068 others(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 | 41 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(38): Show |
42 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(39): 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 | 48 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(45): Show |
49 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(46): 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 | a0001c0003t0010g0007 | 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 | a0001c0001t0036g0039 | 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 | a0001c0001t0043g0024 | 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 | a0002c0002t0002g0276 | 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 | 159 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(156): Show |
160 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(157): 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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0001t0003g0027 a0001c0001t0012g0028 a0001c0001t0045g0075 others(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 | 1 | a0001c0001t0004g0001 | 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 | 270 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0086 others(267): Show |
271 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.1386+2716dupC | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31836588 | |||||||
| chr10:31836594 | G | A | 270 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0086 others(267): Show |
271 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(268): 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 | a0002c0002t0002g0265 | 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 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0086 others(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 | a0002c0002t0029g0243 | 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 | a0001c0001t0046g0222 | 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 | 275 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0086 others(272): Show |
276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): 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 | a0001c0001t0001g0214 a0001c0001t0001g0217 a0001c0001t0006g0213 others(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 | a0001c0014t0004g0014 | 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 | a0001c0001t0023g0038 a0001c0001t0023g0068 a0001c0001t0024g0040 others(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 | a0001c0007t0028g0238 a0001c0007t0028g0239 a0001c0010t0053g0237 |
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 | a0001c0010t0053g0237 | 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 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0086 others(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 | a0001c0001t0001g0155 | 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 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0086 others(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 | a0001c0001t0001g0101 a0001c0001t0001g0125 a0001c0001t0001g0202 |
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 | a0001c0007t0028g0238 a0001c0007t0028g0239 |
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 | a0002c0002t0007g0251 | 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 | 166 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0086 others(163): Show |
167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.1386+474delT | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31838830 | |||||||
| chr10:31838830 | CAA | C | 98 | a0001c0001t0001g0133 a0001c0001t0004g0064 a0001c0001t0005g0061 others(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 | a0001c0001t0005g0043 a0001c0001t0005g0046 a0001c0001t0005g0047 |
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 | a0002c0002t0002g0242 a0002c0002t0002g0244 a0002c0002t0002g0246 others(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 | 271 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0086 others(268): Show |
272 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.1386+210T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 9/19 | chr10 | 31839095 | |||||||
| chr10:31839923 | C | T | 274 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0086 others(271): 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 | a0001c0007t0028g0238 a0001c0007t0028g0239 a0001c0010t0053g0237 |
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 | a0001c0001t0043g0024 | 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 | 48 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(45): Show |
49 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(46): Show |
intron_variant | MODIFIER | c.1297-504A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 7/19 | chr10 | 31840215 | |||||||
| chr10:31840306 | T | A | 16 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(13): Show |
17 | HG00099.hp2 HG01081.hp2 HG01167.hp2 others(14): 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 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0086 others(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 | a0001c0003t0010g0006 | 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 | a0001c0001t0001g0212 | 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 | a0001c0001t0003g0027 | 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 | a0001c0001t0001g0225 a0001c0001t0008g0150 a0001c0001t0025g0201 |
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 | a0001c0001t0034g0029 | 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 | a0001c0007t0028g0238 a0001c0007t0028g0239 |
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 | a0001c0007t0028g0238 a0001c0007t0028g0239 |
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 | a0001c0007t0028g0238 a0001c0007t0028g0239 |
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 | 16 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(13): Show |
17 | HG00099.hp2 HG01081.hp2 HG01167.hp2 others(14): 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 | a0001c0007t0028g0238 a0001c0007t0028g0239 |
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 | a0001c0001t0009g0026 a0001c0001t0009g0071 a0001c0001t0009g0072 others(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 | a0001c0001t0024g0040 | 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 | a0001c0001t0004g0032 | 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 | a0001c0001t0018g0085 | 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 | a0001c0001t0001g0144 | 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 | a0001c0001t0024g0040 | 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 | a0001c0001t0001g0094 | 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 | a0001c0001t0025g0201 | 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 | a0001c0001t0008g0132 a0001c0001t0008g0134 |
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 | a0001c0001t0005g0069 | 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 | a0001c0003t0010g0011 a0001c0003t0010g0019 a0001c0003t0027g0013 others(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 | a0001c0001t0008g0132 a0001c0001t0008g0134 |
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 | a0002c0002t0020g0252 | 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 | a0001c0001t0001g0107 a0001c0001t0001g0108 |
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 | a0001c0001t0049g0031 a0001c0001t0050g0030 |
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 | a0001c0001t0001g0155 a0001c0013t0015g0152 |
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 | a0001c0001t0005g0041 | 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 | a0001c0001t0012g0028 | 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 | a0001c0001t0001g0108 | 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 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0023 |
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 | a0001c0001t0023g0038 a0001c0001t0023g0068 a0001c0001t0024g0040 others(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 | a0001c0001t0011g0053 a0001c0001t0011g0054 a0001c0001t0011g0055 others(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 | a0001c0001t0001g0109 a0001c0001t0001g0112 a0001c0001t0003g0180 others(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 | a0001c0001t0009g0026 a0001c0001t0009g0071 a0001c0001t0009g0072 others(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 | a0001c0001t0004g0042 a0001c0001t0005g0041 a0001c0001t0005g0043 others(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 | 144 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(141): Show |
145 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(142): 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 | a0001c0001t0008g0150 | 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 | a0002c0002t0002g0244 a0002c0002t0002g0289 |
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 | a0001c0001t0001g0109 a0001c0001t0001g0136 |
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 | a0002c0002t0007g0251 | 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 | a0002c0002t0007g0313 a0002c0002t0007g0314 a0002c0002t0007g0316 |
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 | a0001c0001t0009g0026 a0001c0001t0009g0071 a0001c0001t0009g0072 others(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 | a0001c0001t0003g0118 | 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 | a0001c0001t0003g0027 a0001c0001t0012g0028 a0001c0001t0025g0154 others(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 | a0001c0001t0009g0026 a0001c0001t0009g0071 a0001c0001t0009g0072 others(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 | 144 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(141): Show |
145 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(142): Show |
intron_variant | MODIFIER | c.1171-2547delT | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 6/19 | chr10 | 31846132 | |||||||
| chr10:31846417 | C | A | 1 | a0001c0001t0040g0211 | 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 | a0002c0002t0007g0245 | 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 | a0002c0002t0007g0245 | 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 | a0001c0001t0004g0023 | 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 | a0001c0001t0003g0183 | 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 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0094 others(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 | a0001c0001t0001g0086 a0001c0001t0001g0124 a0001c0001t0001g0162 others(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 | a0001c0001t0003g0186 a0001c0001t0004g0035 a0001c0001t0009g0026 others(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 | a0001c0001t0001g0212 | 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 | a0001c0001t0001g0082 | 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 | a0001c0001t0001g0223 | 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 | a0001c0001t0004g0032 | 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 | a0001c0001t0003g0027 | 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 | 144 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(141): Show |
145 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(142): 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 | a0001c0001t0001g0162 a0001c0001t0006g0157 |
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 | a0001c0001t0009g0026 a0001c0001t0009g0071 a0001c0001t0009g0072 others(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 | 48 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(45): Show |
49 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(46): 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 | a0001c0001t0003g0027 a0001c0001t0012g0028 a0001c0001t0049g0031 others(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 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0086 others(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 | a0001c0001t0013g0090 a0001c0001t0013g0091 a0001c0001t0013g0092 |
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 | a0001c0001t0006g0220 | 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 | a0002c0002t0007g0319 | 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 | a0001c0001t0004g0025 | 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 | a0001c0001t0003g0174 | 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 | a0001c0001t0006g0220 | 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 | a0001c0010t0053g0237 | 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 | a0001c0001t0025g0201 | 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 | 48 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(45): Show |
49 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(46): 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 | a0001c0001t0011g0070 | 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 | a0002c0002t0002g0257 | 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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0001t0003g0167 a0001c0001t0003g0179 a0001c0001t0003g0191 others(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 | a0001c0001t0018g0085 | 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 | a0001c0001t0018g0095 | 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 | a0002c0002t0002g0318 | 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 | a0001c0001t0004g0032 | 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 | a0001c0008t0005g0073 | 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 | a0001c0001t0008g0131 a0001c0001t0008g0138 |
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 | a0001c0001t0001g0217 a0001c0001t0003g0027 a0001c0001t0003g0182 others(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 | a0001c0001t0001g0086 a0001c0001t0001g0112 a0001c0001t0001g0144 others(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 | 190 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0094 others(187): Show |
191 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(188): 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 | a0001c0001t0001g0097 a0001c0001t0001g0099 a0002c0002t0002g0242 others(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 | a0001c0001t0001g0124 a0001c0001t0001g0126 |
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 | a0001c0001t0004g0042 a0001c0001t0005g0041 a0001c0001t0005g0043 others(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 | a0001c0001t0003g0180 | 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 | 144 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(141): Show |
145 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(142): 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 | a0001c0001t0011g0059 | 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 | a0001c0001t0004g0034 a0001c0001t0037g0033 |
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 | a0002c0002t0002g0242 a0002c0002t0002g0244 a0002c0002t0002g0246 others(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 | a0001c0001t0024g0040 | 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 | a0002c0002t0021g0248 | 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 | a0001c0001t0004g0035 | 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 | a0001c0001t0005g0061 | 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 | a0001c0007t0028g0238 a0001c0007t0028g0239 a0001c0010t0053g0237 others(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 | a0001c0001t0009g0026 a0001c0001t0009g0071 a0001c0001t0009g0072 others(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 | a0001c0007t0028g0238 a0001c0007t0028g0239 a0001c0010t0053g0237 others(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 | a0002c0002t0014g0241 a0002c0002t0014g0270 a0002c0002t0014g0271 others(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 | 144 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(141): Show |
145 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(142): 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 | a0001c0001t0009g0026 a0001c0001t0009g0071 a0001c0001t0009g0072 others(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 | 143 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(140): Show |
144 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(141): 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 | a0001c0001t0003g0027 a0001c0001t0012g0028 |
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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0001t0001g0115 | 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 | a0001c0003t0010g0017 | 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 | a0001c0001t0003g0182 | 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 | a0001c0001t0001g0097 | 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 | a0001c0001t0004g0064 a0001c0001t0004g0067 |
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 | a0001c0001t0001g0155 | 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 | a0001c0001t0011g0070 | 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 | a0001c0001t0004g0042 a0001c0001t0005g0041 a0001c0001t0005g0043 others(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 | 256 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0086 others(253): Show |
257 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(254): 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 | a0001c0001t0034g0029 | 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 | a0001c0001t0019g0160 a0001c0001t0019g0161 a0001c0001t0019g0164 others(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 | a0001c0001t0011g0059 | 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 | a0001c0001t0039g0087 | 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 | a0001c0001t0001g0214 a0001c0001t0001g0216 a0001c0001t0001g0217 others(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 | a0002c0002t0002g0266 | 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 | a0001c0001t0003g0168 a0001c0001t0003g0195 |
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 | a0001c0001t0001g0225 | 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 | 143 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(140): Show |
144 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(141): 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 | a0001c0001t0024g0040 | 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 | a0001c0001t0001g0108 | 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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0001t0040g0211 | 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 | 143 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(140): Show |
144 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(141): 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 | a0001c0001t0004g0032 | 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 | 143 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(140): Show |
144 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(141): 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 | a0001c0001t0001g0212 | 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 | a0001c0001t0001g0116 | 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 | a0001c0001t0001g0206 | 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 | a0001c0001t0008g0150 | 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 | 132 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(129): Show |
133 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(130): 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 | 16 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(13): Show |
17 | HG00099.hp2 HG01081.hp2 HG01167.hp2 others(14): 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 | a0001c0003t0010g0019 a0001c0003t0027g0013 |
2 | HG02615.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.948+3315A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31858080 | |||||||
| chr10:31858196 | C | A | 7 | a0001c0001t0003g0183 a0001c0001t0003g0186 a0001c0001t0003g0187 others(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 | a0001c0014t0004g0014 | 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 | a0001c0001t0018g0218 | 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 | a0001c0001t0043g0024 | 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 | a0002c0002t0002g0264 | 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 | a0001c0001t0001g0094 | 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 | a0001c0001t0004g0032 | 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 | a0001c0001t0006g0213 | 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 | a0001c0001t0001g0082 a0001c0001t0001g0162 a0001c0001t0001g0203 others(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 | 47 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(44): Show |
48 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(45): 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 | a0001c0001t0003g0180 | 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 | a0001c0001t0004g0042 a0001c0001t0005g0041 a0001c0001t0005g0043 others(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 | a0001c0003t0010g0006 | 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 | 143 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(140): Show |
144 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(141): 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 | 143 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(140): Show |
144 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(141): Show |
intron_variant | MODIFIER | c.948+1787delA | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31859607 | |||||||
| chr10:31859636 | G | C | 1 | a0001c0001t0001g0235 | 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 | 158 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(155): Show |
159 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(156): Show |
intron_variant | MODIFIER | c.948+1724G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31859671 | |||||||
| chr10:31859799 | C | CT | 47 | a0001c0001t0004g0001 a0001c0001t0004g0021 a0001c0001t0004g0022 others(44): Show |
48 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.948+1595dupA | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4/19 | chr10 | 31859799 | |||||||
| chr10:31859889 | G | A | 15 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0001t0001g0212 | 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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0007t0028g0238 a0001c0007t0028g0239 a0001c0010t0053g0237 |
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 | a0001c0001t0001g0082 | 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 | a0001c0001t0018g0085 | 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 | a0001c0001t0006g0151 | 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 | a0001c0001t0004g0032 | 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 | a0001c0001t0001g0212 | 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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0001t0001g0097 | 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 | a0002c0002t0054g0321 a0002c0002t0055g0320 |
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 | a0001c0001t0009g0076 a0001c0001t0009g0077 a0001c0001t0009g0079 others(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 | a0001c0001t0004g0025 | 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 | a0001c0001t0001g0209 a0001c0001t0001g0231 |
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 | a0001c0001t0011g0053 a0001c0001t0011g0054 a0001c0001t0011g0055 others(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 | a0002c0002t0054g0321 | 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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0001t0004g0042 a0001c0001t0005g0041 a0001c0001t0005g0043 others(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 | a0001c0001t0001g0098 a0001c0001t0001g0101 a0001c0001t0001g0104 others(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 | a0001c0001t0001g0082 a0001c0001t0001g0099 a0001c0001t0001g0107 others(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 | a0001c0001t0001g0139 a0001c0001t0001g0155 a0001c0001t0001g0209 others(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 | a0001c0001t0001g0216 a0001c0001t0001g0219 a0001c0001t0006g0157 others(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 | a0001c0001t0001g0217 a0001c0001t0006g0230 a0001c0001t0018g0218 |
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 | a0001c0001t0001g0214 a0001c0001t0006g0213 a0001c0001t0006g0215 others(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 | a0001c0001t0013g0089 a0001c0001t0013g0090 a0001c0001t0013g0091 |
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 | a0001c0001t0001g0145 | 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 | a0001c0001t0001g0094 a0001c0001t0001g0116 a0001c0001t0001g0120 others(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 | a0001c0001t0001g0084 a0001c0001t0001g0097 a0001c0001t0001g0102 others(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 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0100 a0001c0001t0001g0111 a0001c0001t0001g0113 others(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 | a0001c0001t0001g0086 a0001c0001t0001g0122 |
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 | a0001c0001t0003g0166 a0001c0001t0003g0179 a0001c0001t0003g0183 others(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 | a0001c0001t0003g0168 a0001c0001t0003g0169 a0001c0001t0003g0187 others(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 | a0001c0001t0003g0027 a0001c0001t0003g0174 a0001c0001t0003g0176 others(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 | a0001c0001t0003g0167 a0001c0001t0004g0001 a0001c0001t0005g0044 others(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 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(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 | a0001c0001t0004g0037 a0001c0001t0004g0042 a0001c0001t0005g0041 others(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 | 14 | a0001c0001t0004g0025 a0001c0001t0004g0032 a0001c0001t0004g0035 others(11): Show |
14 | HG00099.hp2 HG01081.hp2 HG01168.hp2 others(11): 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 | a0001c0001t0012g0028 a0002c0002t0002g0266 a0002c0002t0002g0268 others(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 | a0001c0001t0024g0040 | 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 | a0002c0002t0002g0267 | 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 | a0001c0001t0005g0045 a0001c0001t0005g0050 |
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 | a0001c0001t0005g0044 a0001c0001t0005g0049 a0001c0001t0011g0070 |
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 | a0001c0001t0005g0052 a0001c0008t0005g0074 a0002c0002t0002g0254 others(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 | a0001c0001t0004g0042 a0001c0001t0005g0041 a0001c0001t0005g0043 others(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 | a0002c0002t0002g0242 | 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 | a0001c0001t0009g0071 | 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 | a0001c0001t0001g0214 | 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 | a0001c0001t0005g0045 a0001c0001t0005g0050 a0002c0002t0002g0278 |
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 | a0001c0001t0004g0023 | 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 | a0002c0002t0002g0242 a0002c0002t0002g0244 a0002c0002t0002g0246 others(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 | a0001c0001t0001g0104 | 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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0001t0006g0215 a0001c0001t0006g0220 a0001c0001t0006g0230 |
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 | a0002c0002t0002g0278 a0002c0002t0002g0281 a0002c0002t0002g0283 others(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 | a0001c0001t0009g0026 a0001c0001t0009g0071 a0001c0001t0009g0072 others(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 | a0001c0001t0040g0211 | 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 | a0001c0001t0004g0042 a0001c0001t0005g0041 a0001c0001t0005g0043 others(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 | a0002c0002t0030g0240 | 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 | a0001c0001t0001g0102 a0001c0001t0001g0116 a0001c0001t0001g0119 others(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 | a0001c0001t0009g0026 a0001c0001t0009g0071 a0001c0001t0009g0072 others(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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0003t0010g0006 a0001c0003t0010g0012 a0001c0003t0010g0017 others(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 | a0001c0001t0003g0183 a0001c0001t0003g0186 a0001c0001t0003g0187 others(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 | a0001c0007t0028g0238 a0001c0007t0028g0239 a0001c0010t0053g0237 |
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 | a0001c0007t0028g0238 a0001c0007t0028g0239 a0001c0010t0053g0237 others(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 | a0001c0001t0013g0089 | 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 | a0001c0001t0001g0097 | 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 | a0001c0001t0019g0160 a0001c0001t0019g0161 a0001c0001t0019g0164 others(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 | a0001c0001t0001g0130 | 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 | a0001c0001t0001g0082 | 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 | a0001c0001t0034g0029 | 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 | a0001c0001t0003g0170 | 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 | a0001c0001t0003g0027 | 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 | a0002c0002t0002g0273 a0002c0002t0002g0277 a0002c0002t0002g0278 others(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 | a0001c0001t0003g0118 a0001c0001t0003g0166 a0001c0001t0003g0167 others(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 | a0001c0007t0028g0238 a0001c0007t0028g0239 |
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 | a0002c0002t0002g0263 | 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 | a0002c0002t0021g0247 a0002c0002t0021g0279 |
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 | a0002c0002t0021g0247 a0002c0002t0021g0279 |
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 | a0002c0002t0021g0247 a0002c0002t0021g0279 |
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 | a0001c0003t0010g0017 | 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 | 272 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0086 others(269): Show |
273 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(270): 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 | a0001c0001t0001g0225 a0001c0001t0008g0150 a0001c0001t0025g0154 others(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 | a0001c0001t0001g0217 | 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 | a0001c0001t0006g0148 a0001c0001t0006g0151 a0001c0001t0006g0156 others(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 | a0001c0001t0001g0105 a0001c0001t0001g0208 a0001c0001t0008g0103 others(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 | a0001c0001t0001g0145 a0001c0001t0003g0027 |
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 | a0001c0001t0003g0197 | 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 | a0001c0001t0004g0032 | 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 | a0001c0001t0009g0026 a0001c0001t0009g0071 a0001c0001t0009g0072 others(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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0001t0001g0225 a0001c0001t0008g0150 |
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 | 144 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(141): Show |
145 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(142): 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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0001t0024g0040 | 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 | a0002c0002t0007g0308 a0003c0004t0007g0309 a0003c0004t0007g0310 others(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 | a0001c0001t0006g0156 | 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 | a0001c0001t0003g0174 a0001c0001t0003g0176 a0001c0001t0003g0184 others(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 | a0001c0001t0001g0116 | 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 | a0001c0001t0039g0087 | 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 | a0002c0002t0002g0261 a0002c0002t0002g0274 a0002c0002t0002g0275 others(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 | a0001c0001t0018g0085 | 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 | a0001c0001t0043g0024 | 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 | 318 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0086 others(315): Show |
319 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(316): 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 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0086 others(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 | 48 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(45): Show |
49 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(46): 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 | a0001c0001t0001g0119 a0001c0001t0001g0227 a0001c0001t0003g0182 others(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 | 47 | a0001c0001t0003g0167 a0001c0001t0004g0001 a0001c0001t0004g0021 others(44): Show |
48 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.685-8573delA | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31870230 | |||||||
| chr10:31870263 | C | T | 144 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(141): Show |
145 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(142): 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 | a0001c0001t0001g0111 a0001c0001t0001g0113 a0001c0001t0015g0114 |
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 | a0001c0007t0028g0238 a0001c0007t0028g0239 a0001c0010t0053g0237 others(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 | a0001c0001t0001g0124 | 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 | a0001c0001t0004g0063 | 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 | a0001c0001t0004g0042 a0001c0001t0005g0041 a0001c0001t0005g0043 others(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 | a0001c0001t0009g0026 a0001c0001t0009g0071 a0001c0001t0009g0072 others(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 | a0001c0001t0001g0155 a0001c0013t0015g0152 |
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 | 272 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0086 others(269): Show |
273 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(270): 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 | a0001c0003t0010g0017 | 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 | a0001c0001t0017g0051 | 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 | 48 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(45): Show |
49 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(46): 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 | a0001c0001t0011g0053 a0001c0001t0011g0054 a0001c0001t0011g0055 others(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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0001t0003g0168 a0001c0001t0003g0195 |
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 | a0001c0001t0040g0211 | 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 | a0001c0001t0008g0153 a0001c0001t0018g0085 |
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 | a0001c0001t0043g0024 | 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 | 48 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(45): Show |
49 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(46): 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 | a0001c0001t0025g0154 a0001c0001t0025g0201 |
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 | a0001c0014t0004g0014 | 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 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0086 others(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 | 159 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(156): Show |
160 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(157): 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 | a0001c0001t0009g0026 a0001c0001t0009g0071 a0001c0001t0009g0072 others(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 | a0001c0001t0025g0154 a0001c0001t0025g0201 |
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 | a0001c0001t0018g0085 | 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 | 159 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(156): Show |
160 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.685-11090C>T | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31872748 | |||||||
| chr10:31873414 | A | G | 144 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(141): Show |
145 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(142): 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 | a0001c0001t0009g0026 a0001c0001t0009g0071 a0001c0001t0009g0072 others(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 | a0001c0001t0003g0027 | 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 | a0001c0001t0052g0317 | 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 | a0001c0001t0049g0031 a0001c0001t0050g0030 a0001c0007t0028g0238 others(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 | a0001c0014t0004g0014 | 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 | a0001c0001t0003g0027 | 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 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0086 others(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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | 141 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(138): Show |
142 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(139): 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 | a0001c0001t0004g0042 a0001c0001t0005g0041 a0001c0001t0005g0043 others(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 | a0001c0001t0005g0044 a0001c0001t0005g0049 a0001c0001t0005g0052 |
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 | a0001c0001t0001g0155 | 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 | 16 | a0001c0001t0003g0198 a0001c0001t0004g0001 a0001c0001t0004g0020 others(13): 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 | 13 | a0001c0001t0004g0023 a0001c0001t0004g0025 a0001c0001t0004g0034 others(10): Show |
13 | HG00099.hp2 HG01168.hp2 HG01175.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 | C | CAAA | 39 | a0002c0002t0002g0242 a0002c0002t0002g0249 a0002c0002t0002g0250 others(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 | a0001c0007t0028g0239 a0002c0002t0002g0254 a0002c0002t0002g0260 others(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 | a0002c0002t0002g0244 a0002c0002t0002g0275 a0002c0002t0002g0281 others(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 | a0001c0001t0025g0154 a0001c0001t0025g0201 |
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 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0086 others(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 | a0001c0001t0001g0214 a0001c0001t0001g0216 a0001c0001t0001g0217 others(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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0001t0008g0138 | 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 | a0001c0007t0028g0239 a0001c0010t0053g0237 a0002c0002t0002g0242 others(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 | a0001c0001t0003g0184 | 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 | a0001c0001t0001g0162 a0001c0001t0006g0157 |
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 | 142 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(139): Show |
143 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(140): 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 | a0001c0001t0003g0027 | 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 | a0001c0001t0003g0118 | 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 | 47 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(44): Show |
48 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(45): 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 | a0001c0001t0001g0227 a0001c0001t0001g0229 |
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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0001t0049g0031 a0001c0001t0050g0030 |
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 | a0001c0001t0003g0027 a0001c0001t0012g0028 a0001c0001t0034g0029 |
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 | a0001c0001t0008g0221 | 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 | a0001c0001t0001g0105 a0001c0001t0001g0212 a0001c0001t0001g0214 others(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 | a0001c0001t0009g0026 a0001c0001t0009g0072 a0001c0001t0009g0076 others(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 | a0002c0002t0002g0253 a0002c0002t0002g0254 |
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 | a0001c0001t0001g0099 a0001c0001t0001g0121 |
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 | a0001c0001t0003g0182 | 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 | a0001c0001t0040g0211 | 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 | a0001c0005t0016g0008 a0001c0005t0016g0009 |
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 | a0001c0001t0001g0214 a0001c0001t0001g0216 a0001c0001t0001g0217 others(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 | a0001c0001t0001g0143 | 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 | a0001c0001t0049g0031 a0001c0001t0050g0030 |
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 | a0001c0001t0005g0045 a0001c0001t0005g0050 |
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 | 163 | a0001c0001t0003g0027 a0001c0001t0004g0001 a0001c0001t0004g0020 others(160): Show |
164 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(161): Show |
intron_variant | MODIFIER | c.685-16336T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31877994 | |||||||
| chr10:31878205 | C | CAG | 139 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(136): Show |
140 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(137): 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 | a0002c0002t0002g0298 a0002c0002t0002g0299 a0002c0002t0002g0306 |
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 | a0001c0001t0001g0214 a0001c0001t0001g0216 a0001c0001t0001g0217 others(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 | 131 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(128): Show |
132 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(129): 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 | a0001c0001t0019g0160 a0001c0001t0019g0161 a0001c0001t0019g0164 others(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 | a0001c0007t0028g0238 a0001c0007t0028g0239 a0001c0010t0053g0237 others(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 | a0001c0001t0004g0064 a0001c0001t0004g0067 |
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 | a0001c0001t0003g0182 | 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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0001t0023g0038 a0001c0001t0023g0068 a0001c0001t0024g0040 others(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 | a0001c0001t0004g0036 | 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 | a0002c0002t0007g0319 | 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 | a0001c0007t0028g0238 a0001c0007t0028g0239 a0001c0010t0053g0237 others(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 | a0001c0001t0023g0068 | 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 | a0001c0001t0001g0097 a0001c0001t0001g0117 a0001c0001t0001g0127 others(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 | a0002c0002t0002g0318 | 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 | a0001c0001t0008g0129 | 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 | a0001c0001t0001g0145 a0001c0001t0004g0042 a0001c0001t0005g0041 others(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 | a0002c0002t0002g0242 a0002c0002t0002g0244 a0002c0002t0002g0249 others(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 | a0002c0002t0002g0255 a0002c0002t0002g0256 |
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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0001t0001g0101 a0001c0001t0001g0125 a0001c0001t0001g0202 |
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 | 271 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0094 others(268): Show |
272 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(269): 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 | a0001c0001t0001g0206 | 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 | a0001c0001t0012g0185 | 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 | a0001c0001t0019g0160 a0001c0001t0019g0161 a0001c0001t0019g0164 others(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 | a0001c0001t0009g0026 a0001c0001t0009g0071 a0001c0001t0009g0072 others(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 | a0001c0001t0001g0214 a0001c0001t0001g0216 a0001c0001t0001g0217 others(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 | a0001c0001t0001g0099 | 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 | a0001c0001t0003g0027 | 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 | a0001c0001t0001g0144 | 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 | a0001c0007t0028g0238 a0001c0007t0028g0239 a0001c0010t0053g0237 others(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 | a0001c0001t0001g0086 a0001c0001t0001g0119 a0001c0001t0001g0130 others(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 | a0001c0001t0019g0161 | 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 | a0001c0003t0027g0015 | 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 | a0001c0001t0009g0026 a0001c0001t0009g0071 a0001c0001t0009g0072 others(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 | a0002c0002t0002g0249 a0002c0002t0002g0285 |
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 | a0001c0001t0022g0172 | 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 | a0001c0001t0003g0027 | 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 | a0001c0001t0012g0028 a0001c0001t0049g0031 a0001c0001t0050g0030 |
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 | a0001c0001t0003g0027 a0001c0001t0012g0028 a0001c0001t0034g0029 others(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 | a0001c0001t0004g0020 | 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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0007t0028g0238 a0001c0007t0028g0239 a0001c0010t0053g0237 others(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 | a0001c0001t0001g0206 | 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 | a0001c0001t0001g0094 | 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 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0094 others(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 | a0001c0001t0006g0148 a0001c0001t0006g0151 a0001c0001t0006g0156 others(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 | 47 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(44): Show |
48 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(45): 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 | a0001c0001t0024g0040 | 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 | a0001c0001t0032g0149 | 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 | a0001c0001t0009g0026 a0001c0001t0009g0071 a0001c0001t0009g0072 others(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 | a0001c0001t0006g0215 | 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 | a0001c0001t0049g0031 a0001c0001t0050g0030 |
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 | 161 | a0001c0001t0003g0027 a0001c0001t0004g0001 a0001c0001t0004g0020 others(158): Show |
162 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(159): 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 | a0001c0001t0001g0235 a0001c0001t0003g0197 a0001c0001t0006g0148 others(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 | a0001c0001t0001g0139 | 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 | a0001c0001t0019g0160 a0001c0001t0019g0161 a0001c0001t0019g0164 others(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 | a0001c0001t0017g0048 a0001c0001t0017g0051 a0001c0001t0017g0060 |
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 | 142 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(139): Show |
143 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(140): 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 | a0001c0001t0001g0098 a0001c0001t0001g0104 a0001c0001t0001g0112 others(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 | 152 | a0001c0001t0003g0027 a0001c0001t0004g0001 a0001c0001t0004g0020 others(149): Show |
153 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(150): Show |
intron_variant | MODIFIER | c.685-22437delT | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31884094 | |||||||
| chr10:31884231 | T | C | 19 | a0001c0001t0004g0042 a0001c0001t0005g0041 a0001c0001t0005g0043 others(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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | 161 | a0001c0001t0003g0027 a0001c0001t0004g0001 a0001c0001t0004g0020 others(158): Show |
162 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(159): 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 | a0001c0003t0048g0016 | 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 | a0001c0001t0009g0026 a0001c0001t0009g0071 a0001c0001t0009g0072 others(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 | a0001c0001t0001g0098 a0001c0001t0001g0124 a0001c0001t0001g0141 others(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 | a0001c0001t0024g0040 | 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 | a0001c0001t0024g0040 | 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 | a0001c0001t0009g0072 | 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 | a0001c0001t0012g0028 | 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 | a0001c0001t0004g0021 a0001c0001t0004g0023 |
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 | a0001c0003t0016g0005 | 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 | 47 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(44): Show |
48 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(45): 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 | a0002c0002t0002g0249 a0002c0002t0002g0285 |
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 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0094 others(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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0006t0026g0066 | 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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0001t0004g0042 a0001c0001t0005g0041 a0001c0001t0005g0043 others(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 | a0001c0001t0040g0211 | 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 | a0001c0001t0004g0034 a0001c0001t0037g0033 |
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 | a0001c0007t0028g0238 a0001c0007t0028g0239 a0001c0010t0053g0237 others(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 | a0001c0007t0028g0238 a0001c0007t0028g0239 a0001c0010t0053g0237 others(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 | 142 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(139): Show |
143 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(140): 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 | a0001c0001t0034g0029 | 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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0002c0002t0014g0271 | 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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0001t0001g0214 a0001c0001t0001g0216 a0001c0001t0001g0217 others(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 | a0001c0001t0001g0105 a0001c0001t0013g0147 a0001c0007t0028g0238 others(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 | a0001c0001t0004g0042 a0001c0001t0005g0046 a0001c0001t0040g0211 |
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 | 70 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(67): Show |
71 | HG00099.hp2 HG00735.hp2 HG01081.hp2 others(68): Show |
intron_variant | MODIFIER | c.684+20510delA | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31887661 | |||||||
| chr10:31887662 | T | G | 1 | a0001c0001t0004g0042 | 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 | a0001c0001t0040g0211 | 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 | a0001c0001t0009g0026 a0001c0001t0009g0071 a0001c0001t0009g0072 others(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 | 47 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(44): Show |
48 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(45): 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 | a0001c0001t0009g0026 a0001c0001t0009g0071 a0001c0001t0009g0072 others(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 | a0001c0001t0052g0317 | 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 | a0001c0001t0001g0209 a0001c0001t0001g0231 |
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 | a0002c0002t0007g0245 | 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 | a0001c0001t0003g0167 | 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 | a0001c0007t0028g0238 a0001c0007t0028g0239 |
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 | a0001c0001t0001g0214 a0001c0001t0011g0059 a0001c0001t0017g0060 others(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 | a0001c0001t0004g0063 | 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 | a0002c0002t0002g0261 a0002c0002t0002g0274 a0002c0002t0002g0275 others(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 | a0001c0001t0003g0168 a0001c0001t0003g0195 |
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 | 69 | a0001c0001t0001g0097 a0001c0001t0001g0099 a0001c0001t0001g0105 others(66): 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 | GT | G | 67 | a0001c0001t0004g0032 a0001c0001t0006g0158 a0001c0001t0011g0054 others(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 | a0001c0001t0009g0026 a0001c0001t0009g0071 a0001c0001t0009g0072 others(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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0001t0001g0228 | 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 | a0001c0001t0001g0207 | 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 | a0001c0001t0019g0160 a0001c0001t0019g0161 a0001c0001t0019g0164 others(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 | 142 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(139): Show |
143 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(140): 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 | a0002c0002t0014g0241 a0002c0002t0014g0270 a0002c0002t0014g0271 others(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 | a0001c0001t0003g0178 a0001c0001t0003g0182 |
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 | 143 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(140): Show |
144 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(141): 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 | a0001c0001t0001g0212 | 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 | a0001c0001t0001g0082 a0001c0001t0001g0227 a0001c0001t0001g0229 others(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 | 164 | a0001c0001t0001g0212 a0001c0001t0003g0027 a0001c0001t0004g0001 others(161): Show |
165 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(162): 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 | a0001c0001t0009g0026 a0001c0001t0009g0071 a0001c0001t0009g0072 others(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 | 142 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(139): Show |
143 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(140): 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 | a0001c0001t0011g0070 | 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 | a0001c0001t0004g0032 | 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 | 131 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(128): Show |
132 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(129): 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 | a0001c0001t0004g0042 a0001c0001t0005g0041 a0001c0001t0005g0043 others(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 | a0001c0001t0001g0135 | 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 | a0001c0003t0048g0016 | 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 | a0002c0002t0002g0242 a0002c0002t0002g0244 a0002c0002t0002g0246 others(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 | a0001c0001t0003g0197 | 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 | a0001c0001t0050g0030 | 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 | a0001c0007t0028g0238 a0001c0007t0028g0239 |
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 | a0001c0001t0001g0128 | 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 | 142 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(139): Show |
143 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(140): Show |
intron_variant | MODIFIER | c.684+15780G>A | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31892392 | |||||||
| chr10:31892510 | A | C | 142 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(139): Show |
143 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(140): 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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0001t0009g0026 a0001c0001t0009g0071 a0001c0001t0009g0072 others(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 | a0002c0002t0002g0242 a0002c0002t0002g0244 a0002c0002t0002g0246 others(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 | a0001c0007t0028g0238 a0001c0007t0028g0239 a0001c0010t0053g0237 others(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 | 142 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(139): Show |
143 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(140): 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 | a0001c0001t0001g0086 a0001c0001t0008g0103 a0001c0001t0039g0087 |
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 | a0001c0001t0004g0063 | 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 | 142 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(139): Show |
143 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(140): Show |
intron_variant | MODIFIER | c.684+14606dupA | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31893565 | |||||||
| chr10:31893676 | A | C | 1 | a0001c0001t0004g0021 | 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 | a0001c0001t0001g0145 | 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 | 142 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(139): Show |
143 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(140): Show |
intron_variant | MODIFIER | c.684+14340T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31893832 | |||||||
| chr10:31893898 | T | C | 174 | a0001c0001t0001g0212 a0001c0001t0001g0214 a0001c0001t0001g0216 others(171): Show |
175 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(172): Show |
intron_variant | MODIFIER | c.684+14274A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31893898 | |||||||
| chr10:31894091 | T | C | 142 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(139): Show |
143 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(140): 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 | a0001c0001t0001g0139 | 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 | a0001c0001t0040g0211 | 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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0003t0010g0018 | 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 | a0001c0001t0001g0104 | 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 | a0001c0001t0045g0075 | 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 | a0001c0001t0001g0225 a0001c0001t0008g0150 |
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 | a0001c0001t0043g0024 | 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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0002c0002t0007g0308 a0003c0004t0007g0309 a0003c0004t0007g0310 others(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 | a0002c0002t0002g0318 | 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 | a0001c0003t0010g0017 | 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 | a0001c0003t0010g0017 | 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 | a0001c0003t0010g0017 | 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 | a0002c0002t0002g0301 a0002c0002t0002g0303 a0002c0002t0002g0304 others(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 | a0001c0001t0038g0204 a0001c0007t0028g0238 a0001c0007t0028g0239 others(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 | a0001c0001t0001g0214 a0001c0001t0001g0216 a0001c0001t0001g0217 others(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 | a0001c0001t0009g0026 a0001c0001t0009g0071 a0001c0001t0009g0072 others(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 | a0001c0001t0008g0096 | 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 | 164 | a0001c0001t0003g0027 a0001c0001t0004g0001 a0001c0001t0004g0020 others(161): Show |
165 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(162): 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 | a0001c0001t0003g0027 a0001c0001t0012g0028 a0001c0001t0034g0029 others(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 | a0001c0001t0017g0048 a0001c0001t0017g0051 a0001c0001t0017g0060 |
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 | a0001c0001t0009g0026 a0001c0001t0009g0071 a0001c0001t0009g0072 others(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 | a0001c0001t0003g0027 | 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 | a0001c0001t0023g0038 a0001c0001t0023g0068 a0001c0001t0024g0040 others(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 | a0001c0001t0006g0151 | 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 | a0001c0001t0003g0199 a0001c0001t0011g0053 a0001c0001t0011g0054 others(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 | a0001c0001t0001g0126 a0001c0001t0004g0025 a0001c0001t0008g0153 others(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 | a0001c0001t0001g0130 | 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 | a0001c0001t0006g0148 a0001c0001t0006g0151 a0001c0001t0006g0156 others(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 | 165 | a0001c0001t0001g0155 a0001c0001t0003g0027 a0001c0001t0004g0001 others(162): Show |
166 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(163): 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 | a0001c0001t0001g0133 | 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 | a0002c0002t0002g0298 a0002c0002t0002g0299 a0002c0002t0002g0306 |
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 | a0001c0001t0001g0084 a0001c0001t0001g0100 |
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 | a0001c0001t0001g0117 | 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 | a0002c0002t0002g0261 a0002c0002t0002g0295 |
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 | a0001c0001t0001g0224 | 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 | a0001c0008t0005g0074 | 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 | a0001c0001t0001g0135 | 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 | a0002c0002t0007g0313 a0002c0002t0007g0314 a0002c0002t0007g0316 |
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 | 142 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(139): Show |
143 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(140): 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 | a0001c0001t0001g0113 a0001c0001t0001g0115 a0001c0001t0015g0114 |
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 | a0001c0001t0006g0213 | 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 | a0002c0002t0002g0302 a0002c0002t0002g0305 |
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 | a0002c0002t0002g0291 a0002c0002t0002g0292 |
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 | a0001c0001t0011g0053 a0001c0001t0011g0054 a0001c0001t0011g0055 others(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 | a0001c0001t0001g0235 | 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 | a0001c0001t0008g0132 a0001c0001t0008g0134 |
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 | a0001c0001t0009g0026 a0001c0001t0009g0071 a0001c0001t0009g0072 others(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 | a0001c0001t0004g0042 a0001c0001t0005g0041 |
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 | a0001c0001t0023g0038 a0001c0001t0023g0068 a0001c0001t0024g0058 others(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 | a0001c0007t0028g0238 a0001c0007t0028g0239 a0001c0010t0053g0237 others(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 | a0001c0001t0003g0178 a0001c0001t0003g0182 |
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 | a0001c0001t0003g0027 a0001c0001t0012g0028 a0001c0001t0034g0029 others(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 | a0001c0001t0011g0056 | 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 | a0001c0001t0004g0036 | 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 | a0001c0003t0010g0011 a0001c0003t0010g0019 a0001c0003t0027g0013 others(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 | a0001c0001t0034g0029 | 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 | a0001c0001t0004g0042 a0001c0001t0005g0041 a0001c0001t0005g0043 others(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 | a0001c0001t0009g0026 a0001c0001t0009g0071 a0001c0001t0009g0072 others(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 | a0001c0003t0016g0004 a0001c0003t0016g0005 |
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 | a0001c0001t0012g0226 | 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 | a0002c0002t0002g0264 a0002c0002t0002g0276 a0002c0002t0002g0282 |
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 | a0002c0002t0002g0318 | 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 | a0001c0001t0009g0026 a0001c0001t0009g0071 a0001c0001t0009g0072 others(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 | 17 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(14): Show |
18 | HG00099.hp2 HG01081.hp2 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.684+7273T>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31900899 | |||||||
| chr10:31901178 | T | C | 48 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(45): Show |
49 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(46): Show |
intron_variant | MODIFIER | c.684+6994A>G | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31901178 | |||||||
| chr10:31901213 | C | CA | 33 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(30): Show |
34 | HG00099.hp2 HG00735.hp2 HG01081.hp2 others(31): 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 | a0001c0001t0043g0024 | 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 | a0001c0007t0028g0238 a0001c0007t0028g0239 |
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 | a0001c0001t0003g0178 | 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 | a0001c0001t0038g0204 | 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 | a0001c0003t0010g0006 a0001c0003t0010g0011 a0001c0003t0010g0012 others(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 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0086 others(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 | 65 | a0001c0001t0001g0117 a0001c0001t0001g0124 a0001c0001t0001g0126 others(62): Show |
66 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(63): 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 | a0001c0001t0001g0225 a0001c0001t0008g0150 |
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 | a0001c0001t0009g0026 a0001c0001t0009g0071 a0001c0001t0009g0072 others(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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0007t0028g0238 a0001c0007t0028g0239 |
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 | a0001c0001t0004g0063 | 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 | a0001c0003t0010g0012 | 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 | a0001c0003t0048g0016 | 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 | a0001c0003t0010g0019 | 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 | 17 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(14): Show |
18 | HG00099.hp2 HG01081.hp2 HG01167.hp2 others(15): 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 | a0001c0001t0001g0101 a0001c0001t0001g0125 a0001c0001t0001g0202 |
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 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0086 others(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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0001t0012g0028 | 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 | a0001c0001t0001g0208 | 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 | a0001c0001t0013g0147 | 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 | a0001c0001t0003g0027 a0001c0001t0012g0028 |
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 | a0001c0001t0001g0214 a0001c0001t0001g0216 a0001c0001t0001g0217 others(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 | 168 | a0001c0001t0001g0214 a0001c0001t0001g0216 a0001c0001t0001g0217 others(165): Show |
169 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(166): 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 | a0002c0002t0007g0308 a0003c0004t0007g0309 a0003c0004t0007g0310 others(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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | 317 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0086 others(314): Show |
318 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(315): 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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0012 others(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 | a0001c0001t0004g0042 a0001c0001t0005g0041 a0001c0001t0005g0043 others(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 | a0001c0001t0001g0231 | 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 | a0001c0001t0009g0026 a0001c0001t0009g0071 a0001c0001t0009g0072 others(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 | a0001c0001t0011g0057 | 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 | a0001c0001t0001g0206 | 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 | a0001c0001t0001g0116 | 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 | a0001c0001t0003g0180 | 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 | 164 | a0001c0001t0003g0027 a0001c0001t0004g0001 a0001c0001t0004g0020 others(161): Show |
165 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(162): 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 | a0001c0001t0044g0078 | 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 | a0002c0002t0002g0242 a0002c0002t0002g0244 a0002c0002t0002g0246 others(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 | a0001c0001t0009g0026 a0001c0001t0009g0071 a0001c0001t0009g0072 others(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 | a0001c0001t0045g0075 | 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 | 18 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(15): Show |
19 | HG00099.hp2 HG01081.hp2 HG01123.hp1 others(16): 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 | a0002c0002t0007g0251 | 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 | a0001c0001t0040g0211 | 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 | a0001c0001t0011g0053 a0001c0001t0011g0054 a0001c0001t0011g0055 others(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 | a0001c0003t0027g0015 | 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 | a0001c0003t0010g0018 | 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 | a0001c0003t0010g0010 | 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 | a0001c0003t0010g0011 a0001c0003t0027g0013 a0001c0014t0004g0014 |
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 | a0001c0003t0010g0007 | 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 | a0001c0003t0010g0006 | 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 | a0001c0005t0016g0009 | 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 | a0001c0003t0010g0017 a0001c0003t0016g0004 a0001c0003t0016g0005 others(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 | a0001c0003t0010g0012 | 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 | a0001c0003t0010g0019 | 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 | a0001c0001t0040g0211 | 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 | a0001c0001t0003g0178 a0001c0001t0003g0182 |
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 | 277 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0086 others(274): Show |
278 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.684+994T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | 31907178 | |||||||
| chr10:31907472 | AAT | A | 46 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(43): Show |
47 | HG00099.hp2 HG01081.hp2 HG01123.hp1 others(44): 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 | a0001c0001t0001g0119 a0001c0001t0009g0026 a0001c0001t0009g0071 others(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 | a0001c0001t0042g0083 | 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 | 5 | a0001c0001t0001g0139 a0001c0001t0004g0001 a0001c0001t0004g0021 others(2): 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 | a0001c0001t0001g0109 a0001c0001t0001g0119 a0001c0001t0001g0231 others(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 | a0001c0001t0023g0038 a0001c0001t0023g0068 a0001c0001t0024g0058 others(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 | a0001c0003t0016g0004 a0001c0003t0016g0005 |
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 | a0001c0001t0003g0027 a0001c0001t0012g0028 |
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 | a0001c0001t0008g0096 | 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 | a0001c0001t0003g0027 a0001c0001t0012g0028 a0001c0001t0034g0029 others(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 | a0002c0002t0002g0250 a0002c0002t0002g0290 |
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 | a0001c0001t0001g0207 | 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 | a0001c0001t0001g0206 | 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 | a0002c0002t0054g0321 | 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 | a0002c0002t0054g0321 | 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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | 16 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(13): Show |
17 | HG00099.hp2 HG01081.hp2 HG01167.hp2 others(14): 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 | a0001c0001t0001g0133 | 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 | a0001c0001t0034g0029 | 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 | a0001c0003t0027g0015 | 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 | a0001c0001t0023g0038 a0001c0001t0024g0058 |
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 | a0001c0001t0001g0231 | 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 | a0001c0001t0009g0026 a0001c0001t0009g0071 a0001c0001t0009g0072 others(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 | a0001c0007t0028g0238 a0001c0007t0028g0239 a0001c0010t0053g0237 others(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 | a0001c0001t0009g0026 a0001c0001t0009g0071 a0001c0001t0009g0072 others(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 | 126 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(123): Show |
127 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(124): Show |
intron_variant | MODIFIER | c.-110-927dupA | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31911489 | |||||||
| chr10:31911741 | A | T | 16 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0002c0002t0002g0265 | 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 | a0001c0001t0003g0194 a0001c0003t0048g0016 |
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 | a0002c0002t0002g0242 | 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 | a0001c0001t0001g0155 a0001c0001t0025g0154 |
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 | a0001c0007t0028g0238 a0001c0007t0028g0239 a0001c0010t0053g0237 others(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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0001t0001g0214 | 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 | a0001c0003t0010g0007 | 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 | a0001c0001t0003g0027 a0001c0001t0012g0028 |
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 | a0001c0001t0001g0214 a0001c0001t0006g0215 a0001c0001t0006g0220 others(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 | a0001c0001t0011g0053 a0001c0001t0011g0054 a0001c0001t0011g0055 others(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 | 146 | a0001c0001t0001g0084 a0001c0001t0001g0098 a0001c0001t0001g0100 others(143): Show |
147 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(144): 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 | a0001c0001t0001g0145 | 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 | a0001c0001t0001g0119 a0001c0001t0003g0171 a0001c0001t0008g0138 others(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 | 58 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(55): Show |
59 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(56): Show |
intron_variant | MODIFIER | c.-110-3072delT | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31913634 | |||||||
| chr10:31913635 | A | C | 1 | a0001c0001t0018g0085 | 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 | a0002c0002t0002g0250 | 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 | a0001c0001t0001g0084 a0001c0001t0001g0098 a0001c0001t0001g0100 others(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 | a0001c0001t0009g0026 a0001c0001t0009g0071 a0001c0001t0009g0072 others(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 | a0001c0001t0001g0214 a0001c0001t0001g0216 a0001c0001t0001g0217 others(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 | 142 | a0001c0001t0001g0084 a0001c0001t0001g0098 a0001c0001t0001g0100 others(139): Show |
143 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(140): 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 | a0001c0001t0009g0077 a0001c0001t0009g0079 a0001c0001t0009g0080 others(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 | 146 | a0001c0001t0001g0084 a0001c0001t0001g0098 a0001c0001t0001g0100 others(143): Show |
147 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(144): 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 | a0001c0001t0001g0124 a0001c0001t0003g0027 a0001c0001t0012g0028 others(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 | a0001c0001t0040g0211 | 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 | 18 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(15): Show |
19 | HG00099.hp2 HG01081.hp2 HG01123.hp1 others(16): 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 | a0001c0001t0001g0212 | 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 | a0001c0001t0011g0053 a0001c0001t0011g0054 a0001c0001t0011g0055 others(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 | 167 | a0001c0001t0001g0084 a0001c0001t0001g0098 a0001c0001t0001g0100 others(164): Show |
168 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(165): 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 | a0002c0002t0002g0244 | 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 | a0001c0001t0018g0095 | 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 | a0002c0002t0002g0249 | 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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | 5 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(2): 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 | a0001c0001t0003g0191 | 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 | a0001c0001t0001g0082 | 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 | a0001c0001t0009g0026 a0001c0001t0009g0071 a0001c0001t0009g0072 others(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 | a0001c0001t0001g0214 a0001c0001t0001g0216 a0001c0001t0001g0217 others(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 | a0001c0001t0043g0024 | 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 | a0001c0001t0019g0160 a0001c0001t0019g0161 a0001c0001t0019g0164 others(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 | a0001c0001t0023g0038 a0001c0001t0024g0058 |
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 | 48 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(45): Show |
49 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(46): 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 | a0001c0001t0003g0200 | 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 | a0001c0001t0001g0202 a0001c0001t0009g0026 a0001c0001t0009g0071 others(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 | a0001c0001t0034g0029 | 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 | a0001c0001t0003g0027 a0001c0001t0012g0028 a0001c0001t0034g0029 others(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 | a0001c0001t0034g0029 | 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 | 48 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(45): Show |
49 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(46): 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 | a0001c0007t0028g0238 a0001c0007t0028g0239 |
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 | a0001c0001t0031g0002 | 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 | a0001c0001t0001g0212 | 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 | a0001c0001t0001g0206 | 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 | a0001c0001t0043g0024 | 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 | a0001c0001t0031g0002 | 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 | 132 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(129): Show |
133 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(130): 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 | a0001c0001t0012g0196 | 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 | 140 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(137): Show |
141 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(138): 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 | a0001c0001t0004g0042 a0001c0001t0005g0041 |
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 | 146 | a0001c0001t0003g0027 a0001c0001t0004g0001 a0001c0001t0004g0020 others(143): Show |
147 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(144): 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 | a0001c0001t0009g0026 a0001c0001t0009g0071 a0001c0001t0009g0072 others(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 | a0001c0001t0003g0168 a0001c0001t0003g0195 a0001c0001t0009g0026 |
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 | a0001c0001t0009g0026 a0001c0001t0009g0071 a0001c0001t0009g0072 others(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 | a0001c0001t0001g0084 a0001c0001t0001g0100 |
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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0001t0045g0075 | 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 | a0001c0001t0004g0062 | 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 | 143 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(140): Show |
144 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(141): 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 | a0001c0011t0001g0110 | 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 | a0001c0003t0010g0011 a0001c0003t0010g0019 a0001c0003t0027g0013 others(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 | a0002c0002t0021g0247 a0002c0002t0021g0279 |
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 | a0001c0001t0012g0028 | 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 | a0001c0001t0001g0086 a0001c0001t0039g0087 |
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 | a0001c0001t0034g0029 | 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 | 18 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(15): Show |
19 | HG00099.hp2 HG01081.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.-110-7391delA | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31917953 | |||||||
| chr10:31918079 | C | T | 1 | a0001c0001t0012g0028 | 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 | a0001c0001t0001g0124 | 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 | a0001c0001t0001g0086 a0001c0001t0001g0094 a0001c0001t0001g0098 others(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 | a0001c0001t0001g0111 a0001c0001t0001g0141 a0001c0001t0001g0225 others(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 | a0001c0001t0001g0113 a0001c0001t0001g0115 a0001c0001t0001g0120 others(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 | a0001c0001t0001g0082 a0001c0001t0001g0109 a0001c0001t0001g0122 others(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 | a0001c0001t0003g0184 a0001c0001t0006g0163 a0001c0001t0019g0160 others(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 | a0001c0001t0003g0186 a0001c0001t0006g0151 a0001c0001t0006g0156 others(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 | a0001c0001t0001g0155 a0001c0001t0001g0235 a0001c0001t0004g0025 others(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 | 35 | a0001c0001t0003g0027 a0001c0001t0004g0001 a0001c0001t0004g0020 others(32): Show |
36 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(33): 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 | a0001c0001t0006g0213 a0001c0001t0023g0038 a0001c0001t0023g0068 others(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 | a0001c0001t0006g0165 | 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 | a0001c0001t0004g0035 | 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 | a0001c0001t0003g0171 | 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 | a0001c0001t0043g0024 | 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 | a0001c0001t0013g0147 | 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 | a0001c0001t0001g0139 | 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 | 311 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0086 others(308): Show |
312 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(309): 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 | a0001c0001t0001g0206 | 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 | a0001c0001t0005g0044 a0001c0001t0005g0049 a0001c0001t0005g0052 |
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 | a0001c0001t0001g0155 a0001c0001t0025g0154 a0001c0001t0025g0201 |
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 | a0001c0001t0003g0200 a0001c0001t0033g0173 |
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 | a0001c0001t0001g0105 a0001c0001t0001g0106 |
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 | a0001c0001t0011g0053 a0001c0001t0011g0054 a0001c0001t0011g0055 others(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 | a0001c0001t0034g0029 | 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 | a0001c0001t0001g0098 | 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 | a0001c0001t0009g0026 a0001c0001t0009g0071 a0001c0001t0009g0072 others(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 | a0002c0002t0002g0246 | 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 | a0001c0003t0048g0016 | 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 | a0001c0001t0011g0053 a0001c0001t0011g0054 a0001c0001t0011g0055 others(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 | a0001c0007t0028g0238 a0001c0007t0028g0239 a0001c0010t0053g0237 others(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 | a0001c0001t0001g0214 a0001c0001t0001g0216 a0001c0001t0001g0217 others(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 | 143 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(140): Show |
144 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(141): Show |
intron_variant | MODIFIER | c.-111+8842T>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31919841 | |||||||
| chr10:31919901 | G | A | 48 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(45): Show |
49 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(46): 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 | a0001c0001t0001g0225 a0001c0001t0008g0150 |
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 | a0001c0006t0026g0066 | 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 | a0001c0001t0001g0097 | 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 | a0001c0001t0006g0213 | 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 | a0001c0001t0001g0113 a0001c0001t0001g0115 a0001c0001t0015g0114 |
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 | a0001c0001t0003g0027 a0001c0001t0012g0028 a0001c0001t0034g0029 others(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 | a0001c0001t0001g0212 | 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 | a0001c0001t0001g0086 a0001c0001t0001g0107 a0001c0001t0001g0108 others(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 | 13 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(10): Show |
14 | HG00099.hp2 HG01081.hp2 HG01123.hp1 others(11): 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 | a0001c0001t0004g0067 a0001c0001t0005g0041 a0001c0008t0005g0073 others(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 | a0001c0001t0004g0042 a0001c0007t0028g0238 a0001c0007t0028g0239 others(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 | a0001c0003t0010g0006 a0001c0003t0010g0018 |
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 | a0001c0001t0009g0026 a0001c0001t0009g0071 a0001c0001t0009g0072 others(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 | a0001c0001t0004g0032 a0001c0001t0009g0079 a0001c0001t0009g0080 others(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 | a0001c0001t0009g0081 a0001c0003t0027g0013 a0001c0003t0027g0015 others(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 | a0001c0001t0024g0040 | 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 | a0001c0001t0005g0043 a0001c0001t0005g0069 |
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 | a0001c0001t0005g0044 a0001c0001t0005g0045 a0001c0001t0005g0046 others(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 | a0001c0001t0005g0049 a0001c0001t0005g0050 |
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 | a0001c0001t0005g0061 | 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 | a0001c0001t0017g0051 | 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 | a0001c0001t0005g0052 | 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 | a0001c0001t0005g0234 | 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 | a0001c0001t0001g0111 a0001c0001t0003g0027 a0001c0001t0003g0169 others(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 | a0001c0001t0011g0053 a0001c0001t0011g0054 a0001c0001t0011g0055 others(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 | a0001c0001t0025g0154 | 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 | a0001c0001t0004g0042 a0001c0001t0005g0041 a0001c0001t0005g0043 others(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 | a0002c0002t0002g0276 | 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 | a0001c0001t0040g0211 | 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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0001t0001g0082 a0001c0001t0001g0139 a0001c0001t0001g0203 others(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 | a0002c0002t0002g0244 a0002c0002t0002g0289 |
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 | a0001c0001t0001g0209 a0001c0001t0001g0231 |
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 | 143 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(140): Show |
144 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(141): 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 | a0001c0001t0040g0211 | 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 | a0001c0001t0008g0096 | 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 | a0001c0001t0001g0109 | 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 | a0001c0001t0001g0082 | 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 | a0001c0001t0001g0094 a0001c0001t0001g0111 a0001c0001t0001g0144 others(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 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0125 others(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 | a0001c0001t0001g0212 a0002c0002t0002g0277 a0002c0002t0002g0278 others(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 | 46 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0143 others(43): Show |
47 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.-111+6919delT | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31921763 | |||||||
| chr10:31921763 | CAAAA | C | 14 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0001t0009g0026 a0001c0001t0009g0071 a0001c0001t0009g0076 others(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 | a0001c0001t0003g0232 | 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 | 18 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(15): Show |
19 | HG00099.hp2 HG01081.hp2 HG01123.hp1 others(16): 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 | a0001c0001t0006g0213 | 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 | a0001c0001t0001g0216 | 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 | a0001c0001t0003g0183 a0001c0001t0003g0184 a0001c0001t0012g0185 others(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 | a0001c0001t0001g0162 a0001c0001t0003g0186 a0001c0001t0003g0187 others(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 | a0001c0001t0001g0130 a0001c0001t0001g0133 a0001c0001t0001g0135 others(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 | a0001c0001t0001g0082 a0001c0001t0001g0086 a0001c0001t0001g0111 others(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 | a0001c0001t0001g0084 a0001c0001t0001g0094 a0001c0001t0001g0097 others(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 | a0001c0003t0010g0007 a0001c0003t0010g0018 a0001c0003t0010g0019 |
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 | a0001c0003t0010g0006 a0001c0003t0010g0010 a0001c0003t0010g0011 others(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 | a0001c0001t0034g0029 | 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 | a0001c0001t0003g0027 a0001c0001t0013g0089 a0001c0001t0013g0090 others(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 | a0001c0001t0012g0028 | 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 | a0001c0001t0017g0060 a0001c0007t0028g0238 a0001c0007t0028g0239 others(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 | 130 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(127): Show |
131 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(128): 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 | a0001c0001t0003g0027 a0001c0001t0012g0028 a0001c0001t0034g0029 others(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 | a0001c0001t0004g0021 | 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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0001t0003g0191 a0001c0001t0006g0163 a0001c0001t0019g0164 others(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 | a0001c0001t0034g0029 | 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 | a0001c0001t0006g0213 | 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 | a0001c0001t0005g0061 | 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 | a0001c0008t0005g0073 | 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 | a0001c0001t0034g0029 | 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 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(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 | a0001c0001t0004g0032 a0001c0001t0004g0035 a0001c0001t0004g0036 others(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 | 84 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(81): Show |
85 | HG00099.hp2 HG00639.hp2 HG00738.hp2 others(82): 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 | a0001c0001t0004g0023 a0001c0001t0034g0029 a0002c0002t0002g0289 others(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 | a0001c0001t0001g0212 a0001c0001t0001g0214 a0001c0001t0001g0216 others(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 | a0001c0001t0009g0026 a0001c0001t0009g0071 a0001c0001t0009g0076 others(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 | a0001c0003t0016g0004 a0001c0003t0016g0005 |
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 | a0002c0002t0002g0298 a0002c0002t0002g0299 a0002c0002t0002g0301 others(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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0001t0025g0201 | 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 | a0001c0001t0001g0209 | 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 | a0001c0001t0003g0166 | 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 | a0001c0001t0012g0028 | 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 | a0001c0008t0005g0073 a0001c0008t0005g0074 |
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 | a0001c0001t0011g0070 | 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 | a0001c0001t0001g0086 | 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 | a0002c0002t0014g0241 | 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 | 158 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(155): Show |
159 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(156): 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 | a0001c0001t0006g0165 a0002c0002t0007g0308 a0003c0004t0007g0309 others(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 | 277 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0086 others(274): Show |
278 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(275): 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 | a0001c0001t0022g0003 | 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 | a0001c0001t0001g0084 a0001c0001t0001g0086 a0001c0001t0001g0094 others(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 | a0002c0002t0030g0240 | 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 | a0001c0001t0009g0026 a0001c0001t0009g0071 a0001c0001t0009g0072 others(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 | a0001c0001t0034g0029 | 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 | 47 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(44): Show |
48 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(45): 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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0001t0001g0202 | 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 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0023 |
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 | 142 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(139): Show |
143 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(140): 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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | a0001c0001t0003g0200 | 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 | a0001c0001t0025g0201 | 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 | a0001c0001t0049g0031 a0001c0001t0050g0030 |
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 | a0001c0001t0004g0032 | 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 | a0001c0001t0001g0202 a0001c0001t0001g0214 a0001c0001t0001g0216 others(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 | 131 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(128): Show |
132 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(129): Show |
intron_variant | MODIFIER | c.-111+2346delT | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31926336 | |||||||
| chr10:31926336 | GAA | G | 10 | a0001c0001t0009g0026 a0001c0001t0009g0071 a0001c0001t0009g0072 others(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 | a0001c0001t0001g0082 a0001c0001t0001g0203 a0001c0001t0001g0206 others(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 | a0001c0001t0043g0024 | 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 | a0001c0001t0001g0084 | 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 | a0001c0001t0001g0210 | 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 | 47 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(44): Show |
48 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(45): 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 | a0001c0008t0005g0073 a0001c0008t0005g0074 |
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 | a0002c0002t0002g0242 a0002c0002t0002g0244 a0002c0002t0002g0246 others(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 | a0002c0002t0007g0313 a0002c0002t0007g0314 a0002c0002t0007g0316 others(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 | a0001c0001t0001g0086 a0001c0001t0039g0087 |
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 | a0001c0001t0003g0027 a0001c0001t0012g0028 a0001c0001t0034g0029 others(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 | a0001c0001t0018g0085 | 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 | a0001c0001t0001g0084 | 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 |
174 | a0001c0001t0001g0212 a0001c0001t0001g0214 a0001c0001t0001g0216 others(171): Show |
175 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(172): 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 | a0001c0001t0001g0084 | 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 | 174 | a0001c0001t0001g0212 a0001c0001t0001g0214 a0001c0001t0001g0216 others(171): Show |
175 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(172): 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 |
174 | a0001c0001t0001g0212 a0001c0001t0001g0214 a0001c0001t0001g0216 others(171): Show |
175 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(172): 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 | a0001c0001t0043g0024 | 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 | 163 | a0001c0001t0003g0027 a0001c0001t0004g0001 a0001c0001t0004g0020 others(160): Show |
164 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(161): 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 | a0001c0001t0008g0221 | 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 | a0002c0002t0002g0276 | 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 | a0001c0001t0001g0084 | 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 | a0002c0002t0002g0242 a0002c0002t0002g0244 a0002c0002t0002g0246 others(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 | a0001c0001t0001g0084 | 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 | a0001c0001t0046g0222 | 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 | a0001c0001t0001g0084 | 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 | a0002c0002t0002g0242 a0002c0002t0002g0244 a0002c0002t0002g0246 others(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 | a0001c0001t0001g0084 | 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 | a0001c0001t0001g0084 | 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 | 163 | a0001c0001t0003g0027 a0001c0001t0004g0001 a0001c0001t0004g0020 others(160): Show |
164 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(161): 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 | a0001c0001t0042g0083 | 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 | 43 | a0001c0001t0004g0032 a0001c0001t0004g0034 a0001c0001t0004g0035 others(40): Show |
43 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(40): 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 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(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 | 6 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(3): 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 | a0001c0001t0001g0082 a0001c0007t0028g0238 a0001c0007t0028g0239 others(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 | a0001c0001t0003g0027 a0001c0001t0003g0191 a0001c0001t0004g0062 others(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 | 5 | a0001c0001t0004g0001 a0001c0001t0004g0020 a0001c0001t0004g0021 others(2): 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 | a0001c0001t0001g0231 a0002c0002t0002g0318 |
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 | a0001c0001t0003g0232 a0001c0001t0003g0233 |
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 | a0001c0003t0010g0006 a0001c0003t0010g0007 a0001c0003t0010g0010 others(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 | 164 | a0001c0001t0003g0027 a0001c0001t0004g0001 a0001c0001t0004g0020 others(161): Show |
165 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(162): 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 | a0001c0001t0001g0235 a0001c0001t0005g0234 a0002c0002t0007g0319 |
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 | a0001c0001t0022g0003 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-111+104G>C | ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | 31928579 |